| geneid | 348980 |
|---|---|
| ensemblid | ENSG00000164588.8 |
| hgncid | 4845 |
| symbol | HCN1 |
| name | hyperpolarization activated cyclic nucleotide gated potassium channel 1 |
| refseq_nuc | NM_021072.4 |
| refseq_prot | NP_066550.2 |
| ensembl_nuc | ENST00000303230.6 |
| ensembl_prot | ENSP00000307342.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 45254948 |
| end | 45696380 |
| strand | - |
| ver | v1.2 |
| region | chr5:45254948-45696380 |
| region5000 | chr5:45249948-45701380 |
| regionname0 | HCN1_chr5_45254948_45696380 |
| regionname5000 | HCN1_chr5_45249948_45701380 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 890 | 219 | 52 | 47 | 92 | 8 | 18 | 66 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0002 | 0/0 | 887 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0003 | 0/0 | 890 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2673 | 216 | 52 | 45 | 92 | 8 | 17 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| c0002 | 0/0 | 2664 | 5 | 4 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| c0003 | 0/0 | 2673 | 2 | 2 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| c0004 | 0/0 | 2673 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| c0005 | 0/0 | 2673 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| c0006 | 0/0 | 2673 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 7261 | 66 | 14 | 16 | 29 | 1 | 5 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0002 | 0/0 | 7260 | 57 | 13 | 11 | 21 | 4 | 8 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0003 | 0/0 | 7261 | 30 | 1 | 13 | 12 | 1 | 3 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0004 | 0/0 | 7260 | 15 | 0 | 0 | 15 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0005 | 0/0 | 7258 | 11 | 10 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0006 | 0/0 | 7557 | 3 | 2 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0007 | 0/0 | 7262 | 3 | 2 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0008 | 0/0 | 7261 | 3 | 3 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0009 | 0/0 | 7264 | 2 | 0 | 0 | 0 | 1 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0010 | 0/0 | 7261 | 2 | 0 | 0 | 2 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0011 | 0/0 | 7261 | 2 | 0 | 0 | 2 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0012 | 0/0 | 7261 | 2 | 2 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0013 | 0/0 | 7261 | 2 | 0 | 0 | 2 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0014 | 0/0 | 7261 | 2 | 1 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0015 | 0/0 | 7260 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0016 | 0/0 | 7260 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0017 | 0/0 | 7261 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0018 | 0/0 | 7261 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0019 | 0/0 | 7262 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0020 | 0/0 | 7260 | 1 | 0 | 0 | 0 | 1 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0021 | 0/0 | 7261 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0022 | 0/0 | 7261 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0023 | 0/0 | 7556 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0024 | 0/0 | 7555 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0025 | 0/0 | 7554 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0026 | 0/0 | 7553 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0027 | 0/0 | 7260 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0028 | 0/0 | 7261 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0029 | 0/0 | 7260 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0030 | 0/1 | 7261 | 1 | 0 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0031 | 0/0 | 7576 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0032 | 0/0 | 7575 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0033 | 0/0 | 7261 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0034 | 0/0 | 7261 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0035 | 0/0 | 7260 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0036 | 0/0 | 7261 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0037 | 0/0 | 7260 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0038 | 0/0 | 7261 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0039 | 0/0 | 7260 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| t0040 | 0/0 | 7260 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0008 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0145 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2673 | 216 | 52 | 45 | 92 | 8 | 17 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0004 | 0/0 | 2673 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0005 | 0/0 | 2673 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0006 | 0/0 | 2673 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0002c0002 | 0/0 | 2664 | 5 | 4 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0003c0003 | 0/0 | 2673 | 2 | 2 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 9933 | 66 | 14 | 16 | 29 | 1 | 5 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0002 | 0/0 | 9932 | 53 | 12 | 9 | 21 | 4 | 7 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0003 | 0/0 | 9933 | 30 | 1 | 13 | 12 | 1 | 3 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0004 | 0/0 | 9932 | 15 | 0 | 0 | 15 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0005 | 0/0 | 9930 | 11 | 10 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0006 | 0/0 | 10229 | 3 | 2 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0007 | 0/0 | 9934 | 3 | 2 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0009 | 0/0 | 9936 | 2 | 0 | 0 | 0 | 1 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0010 | 0/0 | 9933 | 2 | 0 | 0 | 2 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0011 | 0/0 | 9933 | 2 | 0 | 0 | 2 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0012 | 0/0 | 9933 | 2 | 2 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0013 | 0/0 | 9933 | 2 | 0 | 0 | 2 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0015 | 0/0 | 9932 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0016 | 0/0 | 9932 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0017 | 0/0 | 9933 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0018 | 0/0 | 9933 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0019 | 0/0 | 9934 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0020 | 0/0 | 9932 | 1 | 0 | 0 | 0 | 1 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0021 | 0/0 | 9933 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0022 | 0/0 | 9933 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0023 | 0/0 | 10228 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0024 | 0/0 | 10227 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0025 | 0/0 | 10226 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0026 | 0/0 | 10225 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0027 | 0/0 | 9932 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0028 | 0/0 | 9933 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0029 | 0/0 | 9932 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0030 | 0/1 | 9933 | 1 | 0 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0031 | 0/0 | 10248 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0032 | 0/0 | 10247 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0033 | 0/0 | 9933 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0034 | 0/0 | 9933 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0036 | 0/0 | 9933 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0037 | 0/0 | 9932 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0038 | 0/0 | 9933 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0039 | 0/0 | 9932 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0001t0040 | 0/0 | 9932 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0004t0002 | 0/0 | 9932 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0005t0002 | 0/0 | 9932 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0001c0006t0002 | 0/0 | 9932 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0002c0002t0008 | 0/0 | 9924 | 3 | 3 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0002c0002t0014 | 0/0 | 9924 | 2 | 1 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0003c0003t0002 | 0/0 | 9932 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| a0003c0003t0035 | 0/0 | 9932 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | copy fasta | chr5 | 45249948 | 45701380 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0145 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0006g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0006g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0007g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0007g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0009g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0009g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0010g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0010g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0011g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0011g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0012g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0012g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0013g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0013g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0015g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0016g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0017g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0018g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0019g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0020g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0021g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0022g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0023g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0024g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0025g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0026g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0027g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0028g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0029g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0030g0008 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0031g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0032g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0033g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0034g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0036g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0037g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0038g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0039g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0001t0040g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0004t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0005t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0001c0006t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0002c0002t0008g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0002c0002t0008g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0002c0002t0008g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0002c0002t0014g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0002c0002t0014g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0003c0003t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| a0003c0003t0035g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0019 | EUR | GBR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG00099 | hp2 | a0001 | c0001 | t0009 | g0002 | EUR | GBR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0047 | EUR | FIN | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0178 | EUR | FIN | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0177 | EUR | FIN | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0083 | EUR | FIN | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | CHS | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG00438 | hp2 | a0001 | c0001 | t0007 | g0100 | EAS | CHS | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | CHS | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | CHS | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0055 | EAS | CHS | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0053 | AMR | PUR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | CHS | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0120 | AMR | PUR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0118 | AMR | PUR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG00741 | hp2 | a0001 | c0001 | t0034 | g0172 | AMR | PUR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0094 | AMR | PUR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0063 | AMR | PUR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0117 | AMR | PUR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0087 | AMR | PUR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01109 | hp2 | a0001 | c0001 | t0006 | g0057 | AMR | PUR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01167 | hp1 | a0001 | c0001 | t0031 | g0009 | AMR | PUR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01167 | hp2 | a0001 | c0005 | t0002 | g0199 | AMR | PUR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01169 | hp2 | a0001 | c0001 | t0032 | g0010 | AMR | PUR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01192 | hp2 | a0001 | c0001 | t0025 | g0217 | AMR | PUR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01243 | hp1 | a0001 | c0004 | t0002 | g0006 | AMR | PUR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0158 | AMR | CLM | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | CLM | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | CLM | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01257 | hp2 | a0001 | c0001 | t0037 | g0148 | AMR | CLM | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0183 | AMR | CLM | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | CLM | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0125 | AMR | CLM | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | CLM | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | CLM | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0099 | AMR | CLM | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01433 | hp2 | a0002 | c0002 | t0014 | g0223 | AMR | CLM | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0069 | EUR | IBS | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01516 | hp2 | a0001 | c0001 | t0020 | g0196 | EUR | IBS | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0127 | AFR | ACB | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01891 | hp2 | a0003 | c0003 | t0002 | g0221 | AFR | ACB | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0093 | AMR | PEL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PEL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0095 | AMR | PEL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PEL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0215 | AMR | PEL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0048 | EAS | KHV | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02040 | hp2 | a0001 | c0001 | t0027 | g0022 | EAS | KHV | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0123 | AFR | ACB | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02055 | hp2 | a0002 | c0002 | t0008 | g0225 | AFR | ACB | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | KHV | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0020 | EAS | KHV | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | KHV | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | KHV | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | ACB | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02155 | hp1 | a0001 | c0001 | t0028 | g0174 | EAS | CDX | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CDX | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | CDX | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | CDX | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02257 | hp1 | a0001 | c0001 | t0026 | g0071 | AFR | ACB | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02257 | hp2 | a0002 | c0002 | t0008 | g0226 | AFR | ACB | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02258 | hp2 | a0001 | c0001 | t0022 | g0080 | AFR | ACB | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02451 | hp1 | a0001 | c0001 | t0007 | g0214 | AFR | ACB | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02451 | hp2 | a0001 | c0001 | t0019 | g0114 | AFR | ACB | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0119 | SAS | PJL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02615 | hp1 | a0001 | c0001 | t0016 | g0014 | AFR | GWD | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02622 | hp2 | a0003 | c0003 | t0035 | g0220 | AFR | GWD | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0089 | AFR | GWD | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0124 | AFR | GWD | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0115 | AFR | GWD | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0142 | AFR | GWD | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02897 | hp1 | a0002 | c0002 | t0014 | g0222 | AFR | GWD | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0130 | AFR | GWD | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02965 | hp2 | a0001 | c0001 | t0039 | g0218 | AFR | ESN | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | ESN | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0143 | AFR | ESN | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03139 | hp1 | a0002 | c0002 | t0008 | g0224 | AFR | ESN | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | ESN | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | MSL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | MSL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0129 | AFR | MSL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03486 | hp1 | a0001 | c0001 | t0012 | g0137 | AFR | MSL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | MSL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0128 | AFR | GWD | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03540 | hp2 | a0001 | c0001 | t0024 | g0007 | AFR | GWD | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03579 | hp1 | a0001 | c0001 | t0033 | g0213 | AFR | MSL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0122 | AFR | MSL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0194 | SAS | PJL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0098 | SAS | BEB | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03927 | hp1 | a0001 | c0001 | t0038 | g0016 | SAS | BEB | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0165 | SAS | BEB | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0104 | SAS | STU | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | STU | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHB | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | CHB | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0126 | AFR | YRI | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | YRI | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18939 | hp1 | a0001 | c0001 | t0018 | g0018 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18942 | hp1 | a0001 | c0001 | t0029 | g0070 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18959 | hp1 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18992 | hp1 | a0001 | c0001 | t0011 | g0164 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18992 | hp2 | a0001 | c0001 | t0013 | g0079 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19003 | hp2 | a0001 | c0001 | t0013 | g0078 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19009 | hp1 | a0001 | c0001 | t0010 | g0005 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0189 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19011 | hp1 | a0001 | c0001 | t0011 | g0163 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | LWK | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19030 | hp2 | a0001 | c0001 | t0017 | g0081 | AFR | LWK | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19070 | hp1 | a0001 | c0001 | t0036 | g0186 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19072 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19078 | hp1 | a0001 | c0001 | t0021 | g0138 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19080 | hp2 | a0001 | c0001 | t0040 | g0175 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19085 | hp1 | a0001 | c0001 | t0010 | g0004 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19240 | hp1 | a0001 | c0001 | t0023 | g0075 | AFR | YRI | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | YRI | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA20905 | hp1 | a0001 | c0006 | t0002 | g0219 | SAS | GIH | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA20905 | hp2 | a0001 | c0001 | t0009 | g0003 | SAS | GIH | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0203 | AFR | ACB | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG02559 | hp2 | a0001 | c0001 | t0012 | g0064 | AFR | ACB | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | MSL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | USA | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | USA | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0030 | g0008 | REF | REF | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0145 | REF | REF | HCN1_chr5_45249948_45701380 | HCN1 | chr5 | 45249948 | 45701380 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:45695884
|
GCCGCCGC others(2): Show |
G | 1 | a0002 | 5 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(2): Show |
disruptive_inframe_deletion | MODERATE | c.201_209delTGGCGGCG others(1): Show |
p.Gly68_Gly70del | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/8 | 496/9933 | 201/2673 | 67/890 | chr5 | 45695884 | ||
| chr5:45695935
|
G | C | 1 | a0003 | 2 | HG01891.hp2 HG02622.hp2 |
missense_variant | MODERATE | c.159C>G | p.His53Gln | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/8 | 446/9933 | 159/2673 | 53/890 | chr5 | 45695935 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:45262692
|
C | T | 1 | a0001c0005 | 1 | HG01167.hp2 | synonymous_variant | LOW | c.1902G>A | p.Gln634Gln | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 2189/9933 | 1902/2673 | 634/890 | chr5 | 45262692 | ||
| chr5:45695833
|
G | C | 1 | a0001c0006 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.261C>G | p.Pro87Pro | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/8 | 548/9933 | 261/2673 | 87/890 | chr5 | 45695833 | ||
| chr5:45695893
|
A | G | 1 | a0001c0004 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.201T>C | p.Gly67Gly | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/8 | 488/9933 | 201/2673 | 67/890 | chr5 | 45695893 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:45254957
|
C | T | 1 | a0001c0001t0039 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6964G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 6964 | chr5 | 45254957 | |||||
| chr5:45255168
|
G | A | 1 | a0001c0001t0030 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6753C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 6753 | chr5 | 45255168 | |||||
| chr5:45255269
|
G | C | 1 | a0001c0001t0034 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6652C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 6652 | chr5 | 45255269 | |||||
| chr5:45255376
|
A | T | 5 | a0001c0001t0003a0001c0001t0009a0001c0001t0012others(2): Show | 36 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*6545T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 6545 | chr5 | 45255376 | |||||
| chr5:45255546
|
C | T | 1 | a0002c0002t0008 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6375G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 6375 | chr5 | 45255546 | |||||
| chr5:45255674
|
T | G | 1 | a0001c0001t0029 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6247A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 6247 | chr5 | 45255674 | |||||
| chr5:45255764
|
T | C | 1 | a0001c0001t0017 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6157A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 6157 | chr5 | 45255764 | |||||
| chr5:45255772
|
C | T | 1 | a0001c0001t0013 | 2 | NA18992.hp2 NA19003.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6149G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 6149 | chr5 | 45255772 | |||||
| chr5:45255873
|
C | T | 1 | a0001c0001t0025 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6048G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 6048 | chr5 | 45255873 | |||||
| chr5:45255875
|
GT | G | 8 | a0001c0001t0003a0001c0001t0009a0001c0001t0012others(5): Show | 40 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*6045delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 6045 | chr5 | 45255875 | |||||
| chr5:45256087
|
A | G | 2 | a0001c0001t0031a0001c0001t0032 | 2 | HG01167.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5834T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 5834 | chr5 | 45256087 | |||||
| chr5:45256145
|
C | T | 1 | a0001c0001t0012 | 2 | HG02559.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5776G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 5776 | chr5 | 45256145 | |||||
| chr5:45256175
|
G | A | 4 | a0001c0001t0023a0001c0001t0024a0001c0001t0031others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5746C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 5746 | chr5 | 45256175 | |||||
| chr5:45256372
|
T | TA | 7 | a0001c0001t0003a0001c0001t0007a0001c0001t0009others(4): Show | 41 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*5548dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 5548 | chr5 | 45256372 | |||||
| chr5:45256372
|
TA | T | 12 | a0001c0001t0002a0001c0001t0004a0001c0001t0015others(9): Show | 78 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*5548delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 5548 | chr5 | 45256372 | |||||
| chr5:45256372
|
TAAA | T | 1 | a0001c0001t0005 | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5546_*5548delTTT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 5546 | chr5 | 45256372 | |||||
| chr5:45256379
|
A | T | 1 | a0001c0001t0005 | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5542T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 5542 | chr5 | 45256379 | |||||
| chr5:45256380
|
A | T | 1 | a0001c0001t0005 | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5541T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 5541 | chr5 | 45256380 | |||||
| chr5:45256381
|
A | T | 1 | a0001c0001t0005 | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5540T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 5540 | chr5 | 45256381 | |||||
| chr5:45256382
|
A | T | 1 | a0001c0001t0005 | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5539T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 5539 | chr5 | 45256382 | |||||
| chr5:45256383
|
A | T | 1 | a0001c0001t0005 | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5538T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 5538 | chr5 | 45256383 | |||||
| chr5:45256384
|
A | T | 1 | a0001c0001t0005 | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5537T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 5537 | chr5 | 45256384 | |||||
| chr5:45256385
|
A | T | 1 | a0001c0001t0005 | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5536T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 5536 | chr5 | 45256385 | |||||
| chr5:45256386
|
A | T | 1 | a0001c0001t0005 | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5535T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 5535 | chr5 | 45256386 | |||||
| chr5:45256387
|
A | T | 1 | a0001c0001t0005 | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5534T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 5534 | chr5 | 45256387 | |||||
| chr5:45256388
|
A | T | 1 | a0001c0001t0005 | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5533T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 5533 | chr5 | 45256388 | |||||
| chr5:45256389
|
A | T | 1 | a0001c0001t0005 | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5532T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 5532 | chr5 | 45256389 | |||||
| chr5:45256710
|
A | G | 2 | a0001c0001t0025a0001c0001t0026 | 2 | HG01192.hp2 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5211T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 5211 | chr5 | 45256710 | |||||
| chr5:45256742
|
A | T | 1 | a0001c0001t0028 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5179T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 5179 | chr5 | 45256742 | |||||
| chr5:45256843
|
A | G | 2 | a0001c0001t0013a0001c0001t0039 | 3 | HG02965.hp2 NA18992.hp2 NA19003.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5078T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 5078 | chr5 | 45256843 | |||||
| chr5:45256984
|
C | T | 5 | a0001c0001t0003a0001c0001t0009a0001c0001t0012others(2): Show | 36 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*4937G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 4937 | chr5 | 45256984 | |||||
| chr5:45257264
|
A | G | 1 | a0001c0001t0023 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4657T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 4657 | chr5 | 45257264 | |||||
| chr5:45257352
|
T | G | 1 | a0001c0001t0013 | 2 | NA18992.hp2 NA19003.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4569A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 4569 | chr5 | 45257352 | |||||
| chr5:45257587
|
A | T | 1 | a0001c0001t0027 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4334T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 4334 | chr5 | 45257587 | |||||
| chr5:45257602
|
C | T | 1 | a0001c0001t0022 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4319G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 4319 | chr5 | 45257602 | |||||
| chr5:45257627
|
G | C | 1 | a0001c0001t0026 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4294C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 4294 | chr5 | 45257627 | |||||
| chr5:45257679
|
T | A | 1 | a0001c0001t0025 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4242A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 4242 | chr5 | 45257679 | |||||
| chr5:45257948
|
C | CAGTATGA others(285): Show |
1 | a0001c0001t0026 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3972_*3973insAATC others(288): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 3972 | chr5 | 45257948 | |||||
| chr5:45257948
|
C | CAGTATGA others(286): Show |
1 | a0001c0001t0025 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3972_*3973insAATC others(289): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 3972 | chr5 | 45257948 | |||||
| chr5:45257948
|
C | CAGTATGA others(287): Show |
1 | a0001c0001t0024 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3972_*3973insAATC others(290): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 3972 | chr5 | 45257948 | |||||
| chr5:45257948
|
C | CAGTATGA others(288): Show |
1 | a0001c0001t0023 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3972_*3973insAATC others(291): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 3972 | chr5 | 45257948 | |||||
| chr5:45257948
|
C | CAGTATGA others(289): Show |
1 | a0001c0001t0006 | 3 | HG01109.hp2 HG02559.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3972_*3973insAATC others(292): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 3972 | chr5 | 45257948 | |||||
| chr5:45257948
|
C | CAGTATGA others(307): Show |
1 | a0001c0001t0032 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3972_*3973insAATC others(310): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 3972 | chr5 | 45257948 | |||||
| chr5:45257948
|
C | CAGTATGA others(308): Show |
1 | a0001c0001t0031 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3972_*3973insAATC others(311): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 3972 | chr5 | 45257948 | |||||
| chr5:45257974
|
G | A | 1 | a0001c0001t0039 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3947C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 3947 | chr5 | 45257974 | |||||
| chr5:45258061
|
A | G | 1 | a0001c0001t0036 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3860T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 3860 | chr5 | 45258061 | |||||
| chr5:45258125
|
G | T | 1 | a0001c0001t0022 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3796C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 3796 | chr5 | 45258125 | |||||
| chr5:45258147
|
T | C | 2 | a0001c0001t0031a0001c0001t0032 | 2 | HG01167.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3774A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 3774 | chr5 | 45258147 | |||||
| chr5:45258324
|
C | T | 1 | a0001c0001t0021 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3597G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 3597 | chr5 | 45258324 | |||||
| chr5:45258521
|
C | A | 1 | a0001c0001t0033 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3400G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 3400 | chr5 | 45258521 | |||||
| chr5:45258571
|
C | T | 1 | a0001c0001t0011 | 2 | NA18992.hp1 NA19011.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3350G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 3350 | chr5 | 45258571 | |||||
| chr5:45258648
|
G | A | 1 | a0001c0001t0034 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3273C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 3273 | chr5 | 45258648 | |||||
| chr5:45258666
|
G | A | 1 | a0003c0003t0035 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3255C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 3255 | chr5 | 45258666 | |||||
| chr5:45258916
|
G | A | 1 | a0001c0001t0005 | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3005C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 3005 | chr5 | 45258916 | |||||
| chr5:45259261
|
T | C | 5 | a0001c0001t0003a0001c0001t0009a0001c0001t0012others(2): Show | 36 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2660A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 2660 | chr5 | 45259261 | |||||
| chr5:45259460
|
C | T | 1 | a0001c0001t0013 | 2 | NA18992.hp2 NA19003.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2461G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 2461 | chr5 | 45259460 | |||||
| chr5:45259551
|
A | C | 1 | a0001c0001t0020 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2370T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 2370 | chr5 | 45259551 | |||||
| chr5:45259728
|
C | G | 1 | a0001c0001t0019 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2193G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 2193 | chr5 | 45259728 | |||||
| chr5:45259964
|
T | C | 1 | a0001c0001t0013 | 2 | NA18992.hp2 NA19003.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1957A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 1957 | chr5 | 45259964 | |||||
| chr5:45259984
|
G | A | 1 | a0001c0001t0038 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1937C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 1937 | chr5 | 45259984 | |||||
| chr5:45259997
|
C | T | 1 | a0001c0001t0017 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1924G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 1924 | chr5 | 45259997 | |||||
| chr5:45260122
|
G | T | 1 | a0001c0001t0019 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1799C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 1799 | chr5 | 45260122 | |||||
| chr5:45260421
|
G | A | 2 | a0001c0001t0013a0001c0001t0039 | 3 | HG02965.hp2 NA18992.hp2 NA19003.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1500C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 1500 | chr5 | 45260421 | |||||
| chr5:45260435
|
A | T | 2 | a0001c0001t0004a0001c0001t0018 | 16 | HG00438.hp1 HG00609.hp2 HG02027.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1486T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 1486 | chr5 | 45260435 | |||||
| chr5:45260916
|
G | T | 1 | a0001c0001t0017 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1005C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 1005 | chr5 | 45260916 | |||||
| chr5:45261353
|
C | T | 1 | a0001c0001t0016 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*568G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 568 | chr5 | 45261353 | |||||
| chr5:45261586
|
T | G | 1 | a0001c0001t0040 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*335A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 8/8 | 335 | chr5 | 45261586 | |||||
| chr5:45696148
|
C | A | 2 | a0002c0002t0008a0002c0002t0014 | 5 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-55G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/8 | 55 | chr5 | 45696148 | |||||
| chr5:45696189
|
C | T | 1 | a0001c0001t0010 | 2 | NA19009.hp1 NA19085.hp1 |
5_prime_UTR_variant | MODIFIER | c.-96G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/8 | 96 | chr5 | 45696189 | |||||
| chr5:45696213
|
C | CGCG | 1 | a0001c0001t0009 | 2 | HG00099.hp2 NA20905.hp2 |
5_prime_UTR_variant | MODIFIER | c.-123_-121dupCGC | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/8 | 121 | chr5 | 45696213 | |||||
| chr5:45696378
|
C | T | 1 | a0001c0001t0015 | 1 | NA18959.hp1 | 5_prime_UTR_variant | MODIFIER | c.-285G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/8 | 285 | chr5 | 45696378 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:45262855
|
C | G | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1784-45G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45262855 | ||||||
| chr5:45263057
|
C | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1784-247G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45263057 | ||||||
| chr5:45263263
|
C | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1784-453G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45263263 | ||||||
| chr5:45263267
|
C | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1784-457G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45263267 | ||||||
| chr5:45263307
|
T | C | 1 | a0001c0001t0003g0093 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1784-497A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45263307 | ||||||
| chr5:45263333
|
C | G | 69 | a0001c0001t0001g0011a0001c0001t0001g0074a0001c0001t0002g0050others(66): Show | 69 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.1784-523G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45263333 | ||||||
| chr5:45263422
|
C | T | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1784-612G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45263422 | ||||||
| chr5:45263526
|
T | G | 3 | a0001c0001t0002g0050a0001c0001t0007g0115a0001c0001t0007g0214 | 3 | HG02451.hp1 HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1784-716A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45263526 | ||||||
| chr5:45263688
|
C | A | 1 | a0001c0001t0001g0202 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1784-878G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45263688 | ||||||
| chr5:45263805
|
T | G | 5 | a0001c0001t0001g0051a0001c0001t0002g0049a0001c0001t0002g0140others(2): Show | 5 | HG01891.hp2 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1784-995A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45263805 | ||||||
| chr5:45263896
|
C | T | 2 | a0001c0001t0023g0075a0001c0001t0024g0007 | 2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1784-1086G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45263896 | ||||||
| chr5:45263949
|
G | A | 3 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0039g0218 | 3 | HG02965.hp2 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1784-1139C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45263949 | ||||||
| chr5:45263997
|
G | T | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG01952.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1784-1187C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45263997 | ||||||
| chr5:45264229
|
C | G | 3 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0039g0218 | 3 | HG02965.hp2 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1784-1419G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45264229 | ||||||
| chr5:45264329
|
T | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1784-1519A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45264329 | ||||||
| chr5:45264442
|
C | T | 2 | a0001c0001t0003g0098a0001c0001t0003g0099 | 2 | HG01361.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1784-1632G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45264442 | ||||||
| chr5:45264670
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1784-1860A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45264670 | ||||||
| chr5:45264918
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1784-2108G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45264918 | ||||||
| chr5:45264933
|
G | A | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1784-2123C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45264933 | ||||||
| chr5:45264992
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1783+2097G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45264992 | ||||||
| chr5:45265189
|
T | TA | 10 | a0001c0001t0001g0051a0001c0001t0003g0087a0001c0001t0003g0093others(7): Show | 10 | HG00099.hp2 HG01071.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.1783+1899dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45265189 | ||||||
| chr5:45265189
|
TA | T | 10 | a0001c0001t0001g0176a0001c0001t0002g0056a0001c0001t0003g0083others(7): Show | 10 | HG00323.hp2 HG00438.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1783+1899delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45265189 | ||||||
| chr5:45265205
|
T | A | 1 | a0001c0004t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1783+1884A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45265205 | ||||||
| chr5:45265309
|
T | C | 1 | a0001c0001t0004g0048 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1783+1780A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45265309 | ||||||
| chr5:45265370
|
A | G | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1783+1719T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45265370 | ||||||
| chr5:45265408
|
C | T | 217 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1783+1681G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45265408 | ||||||
| chr5:45265467
|
A | G | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1783+1622T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45265467 | ||||||
| chr5:45265520
|
A | T | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1783+1569T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45265520 | ||||||
| chr5:45265649
|
A | G | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1783+1440T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45265649 | ||||||
| chr5:45265666
|
T | C | 60 | a0001c0001t0001g0034a0001c0001t0002g0012a0001c0001t0002g0019others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1783+1423A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45265666 | ||||||
| chr5:45265806
|
T | C | 3 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0121 | 3 | HG01346.hp2 HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1783+1283A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45265806 | ||||||
| chr5:45265977
|
C | A | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1783+1112G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45265977 | ||||||
| chr5:45266010
|
G | C | 2 | a0001c0001t0025g0217a0001c0001t0026g0071 | 2 | HG01192.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1783+1079C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45266010 | ||||||
| chr5:45266089
|
C | G | 1 | a0001c0001t0002g0069 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1783+1000G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45266089 | ||||||
| chr5:45266487
|
A | G | 45 | a0001c0001t0001g0011a0001c0001t0001g0085a0001c0001t0001g0102others(42): Show | 45 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.1783+602T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45266487 | ||||||
| chr5:45266676
|
A | T | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1783+413T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45266676 | ||||||
| chr5:45266704
|
A | AC | 5 | a0001c0001t0003g0086a0001c0001t0006g0143a0001c0001t0006g0203others(2): Show | 5 | HG00558.hp1 HG02559.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1783+384_1783+385i others(3): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45266704 | ||||||
| chr5:45266704
|
AT | A | 10 | a0001c0001t0001g0076a0001c0001t0001g0202a0001c0001t0002g0041others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1783+384delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45266704 | ||||||
| chr5:45266705
|
T | C | 60 | a0001c0001t0001g0074a0001c0001t0003g0053a0001c0001t0003g0063others(57): Show | 60 | HG00099.hp2 HG00323.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1783+384A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45266705 | ||||||
| chr5:45266706
|
T | C | 3 | a0001c0001t0005g0126a0001c0001t0005g0142a0001c0001t0022g0080 | 3 | HG02258.hp2 HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1783+383A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45266706 | ||||||
| chr5:45266755
|
C | T | 3 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0039g0218 | 3 | HG02965.hp2 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1783+334G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45266755 | ||||||
| chr5:45266756
|
G | A | 2 | a0001c0001t0002g0067a0001c0001t0002g0131 | 2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1783+333C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45266756 | ||||||
| chr5:45266831
|
T | G | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1783+258A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45266831 | ||||||
| chr5:45267001
|
T | G | 3 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0039g0218 | 3 | HG02965.hp2 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1783+88A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45267001 | ||||||
| chr5:45267012
|
TTTGGGAC others(6): Show |
T | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1783+64_1783+76del others(13): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45267012 | ||||||
| chr5:45267081
|
T | TA | 9 | a0001c0001t0006g0057a0001c0001t0006g0143a0001c0001t0006g0203others(6): Show | 9 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.1783+7dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 7/7 | chr5 | 45267081 | ||||||
| chr5:45267399
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1619-146A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45267399 | ||||||
| chr5:45267463
|
T | A | 10 | a0001c0001t0003g0087a0001c0001t0003g0093a0001c0001t0003g0094others(7): Show | 10 | HG00099.hp2 HG01071.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.1619-210A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45267463 | ||||||
| chr5:45267463
|
T | TA | 12 | a0001c0001t0001g0034a0001c0001t0001g0135a0001c0001t0001g0136others(9): Show | 12 | HG00597.hp1 HG01109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1619-211dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45267463 | ||||||
| chr5:45267464
|
A | T | 2 | a0001c0001t0001g0013a0001c0001t0005g0130 | 2 | HG00741.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1619-211T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45267464 | ||||||
| chr5:45267507
|
C | T | 1 | a0001c0001t0003g0094 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1619-254G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45267507 | ||||||
| chr5:45267654
|
G | T | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1619-401C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45267654 | ||||||
| chr5:45268904
|
T | C | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1619-1651A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45268904 | ||||||
| chr5:45269026
|
T | G | 1 | a0001c0001t0001g0102 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1619-1773A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45269026 | ||||||
| chr5:45269302
|
C | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1619-2049G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45269302 | ||||||
| chr5:45269318
|
T | C | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1619-2065A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45269318 | ||||||
| chr5:45269343
|
T | G | 1 | a0001c0001t0002g0025 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1619-2090A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45269343 | ||||||
| chr5:45269474
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1619-2221G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45269474 | ||||||
| chr5:45269590
|
A | G | 2 | a0001c0001t0012g0064a0001c0001t0012g0137 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1619-2337T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45269590 | ||||||
| chr5:45269631
|
G | C | 1 | a0001c0001t0001g0180 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1619-2378C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45269631 | ||||||
| chr5:45270103
|
C | T | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1619-2850G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45270103 | ||||||
| chr5:45270201
|
C | G | 1 | a0001c0001t0003g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1619-2948G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45270201 | ||||||
| chr5:45270231
|
C | T | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1619-2978G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45270231 | ||||||
| chr5:45270247
|
C | G | 11 | a0001c0001t0005g0089a0001c0001t0005g0122a0001c0001t0005g0123others(8): Show | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1619-2994G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45270247 | ||||||
| chr5:45270363
|
G | A | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1619-3110C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45270363 | ||||||
| chr5:45270381
|
T | G | 1 | a0001c0001t0002g0038 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1619-3128A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45270381 | ||||||
| chr5:45270424
|
G | A | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1619-3171C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45270424 | ||||||
| chr5:45270551
|
T | C | 3 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0039g0218 | 3 | HG02965.hp2 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1619-3298A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45270551 | ||||||
| chr5:45270612
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1619-3359C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45270612 | ||||||
| chr5:45271304
|
G | A | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1619-4051C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45271304 | ||||||
| chr5:45271359
|
T | TAC | 21 | a0001c0001t0001g0051a0001c0001t0001g0074a0001c0001t0001g0151others(18): Show | 21 | HG00735.hp1 HG01081.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.1619-4108_1619-410 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45271359 | ||||||
| chr5:45271359
|
T | TACAC | 27 | a0001c0001t0002g0027a0001c0001t0002g0038a0001c0001t0002g0052others(24): Show | 27 | HG00323.hp2 HG00642.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1619-4110_1619-410 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45271359 | ||||||
| chr5:45271359
|
T | TACACAC | 9 | a0001c0001t0003g0063a0001c0001t0003g0094a0001c0001t0003g0108others(6): Show | 9 | HG00738.hp1 HG01071.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1619-4112_1619-410 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45271359 | ||||||
| chr5:45271359
|
T | TACACACA others(3): Show |
1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1619-4116_1619-410 others(14): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45271359 | ||||||
| chr5:45271359
|
TAC | T | 77 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0045others(74): Show | 77 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1619-4108_1619-410 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45271359 | ||||||
| chr5:45271359
|
TACAC | T | 16 | a0001c0001t0001g0102a0001c0001t0001g0192a0001c0001t0001g0204others(13): Show | 16 | HG01257.hp1 HG01258.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1619-4110_1619-410 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45271359 | ||||||
| chr5:45271359
|
TACACAC | T | 5 | a0001c0001t0001g0116a0001c0001t0001g0195a0001c0001t0002g0015others(2): Show | 5 | HG00642.hp1 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1619-4112_1619-410 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45271359 | ||||||
| chr5:45271359
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1619-4116_1619-410 others(14): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45271359 | ||||||
| chr5:45271403
|
G | C | 3 | a0001c0001t0003g0158a0001c0001t0003g0183a0001c0006t0002g0219 | 3 | HG01256.hp1 HG01258.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1619-4150C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45271403 | ||||||
| chr5:45271684
|
G | A | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1619-4431C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45271684 | ||||||
| chr5:45271688
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1619-4435A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45271688 | ||||||
| chr5:45271713
|
G | A | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1619-4460C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45271713 | ||||||
| chr5:45271813
|
G | C | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1619-4560C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45271813 | ||||||
| chr5:45272080
|
C | T | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1619-4827G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45272080 | ||||||
| chr5:45272307
|
A | T | 3 | a0001c0001t0006g0057a0001c0001t0006g0143a0001c0001t0006g0203 | 3 | HG01109.hp2 HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1619-5054T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45272307 | ||||||
| chr5:45272316
|
T | C | 1 | a0001c0001t0003g0117 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1619-5063A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45272316 | ||||||
| chr5:45272323
|
C | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1619-5070G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45272323 | ||||||
| chr5:45272428
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1619-5175A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45272428 | ||||||
| chr5:45272491
|
T | C | 3 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0039g0218 | 3 | HG02965.hp2 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1619-5238A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45272491 | ||||||
| chr5:45272504
|
A | G | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1619-5251T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45272504 | ||||||
| chr5:45272533
|
T | A | 1 | a0001c0001t0009g0003 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1619-5280A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45272533 | ||||||
| chr5:45272725
|
T | C | 1 | a0001c0001t0007g0214 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1619-5472A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45272725 | ||||||
| chr5:45273060
|
G | T | 2 | a0001c0001t0023g0075a0001c0001t0024g0007 | 2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1619-5807C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45273060 | ||||||
| chr5:45273112
|
A | T | 1 | a0001c0001t0002g0056 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1619-5859T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45273112 | ||||||
| chr5:45273118
|
ATGGGGAC others(117): Show |
A | 1 | a0001c0001t0002g0056 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1619-5989_1619-586 others(4): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45273118 | ||||||
| chr5:45273277
|
T | C | 3 | a0001c0001t0006g0057a0001c0001t0006g0143a0001c0001t0006g0203 | 3 | HG01109.hp2 HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1619-6024A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45273277 | ||||||
| chr5:45273445
|
C | T | 3 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0039g0218 | 3 | HG02965.hp2 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1619-6192G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45273445 | ||||||
| chr5:45273718
|
A | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1619-6465T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45273718 | ||||||
| chr5:45274277
|
T | C | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1619-7024A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45274277 | ||||||
| chr5:45274379
|
C | A | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1619-7126G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45274379 | ||||||
| chr5:45274382
|
G | A | 7 | a0001c0001t0001g0065a0001c0001t0001g0134a0001c0001t0001g0160others(4): Show | 7 | HG02132.hp2 HG02155.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.1619-7129C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45274382 | ||||||
| chr5:45274509
|
T | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1619-7256A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45274509 | ||||||
| chr5:45274632
|
A | G | 1 | a0001c0001t0001g0073 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1619-7379T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45274632 | ||||||
| chr5:45274642
|
A | G | 1 | a0001c0001t0003g0103 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1619-7389T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45274642 | ||||||
| chr5:45274773
|
G | T | 1 | a0001c0001t0029g0070 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1619-7520C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45274773 | ||||||
| chr5:45274931
|
A | G | 4 | a0001c0001t0023g0075a0001c0001t0024g0007a0001c0001t0031g0009others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1619-7678T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45274931 | ||||||
| chr5:45274993
|
T | C | 1 | a0001c0001t0020g0196 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1619-7740A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45274993 | ||||||
| chr5:45275091
|
C | T | 1 | a0001c0001t0015g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1619-7838G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45275091 | ||||||
| chr5:45275226
|
A | T | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1619-7973T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45275226 | ||||||
| chr5:45275262
|
G | A | 3 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0039g0218 | 3 | HG02965.hp2 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1619-8009C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45275262 | ||||||
| chr5:45275337
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1619-8084G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45275337 | ||||||
| chr5:45275918
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1619-8665C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45275918 | ||||||
| chr5:45276094
|
C | T | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1619-8841G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45276094 | ||||||
| chr5:45276222
|
A | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1619-8969T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45276222 | ||||||
| chr5:45276503
|
A | T | 1 | a0001c0001t0007g0100 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1619-9250T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45276503 | ||||||
| chr5:45276596
|
T | G | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1619-9343A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45276596 | ||||||
| chr5:45276677
|
T | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1619-9424A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45276677 | ||||||
| chr5:45276734
|
C | T | 1 | a0001c0001t0028g0174 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1619-9481G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45276734 | ||||||
| chr5:45276896
|
G | T | 1 | a0001c0001t0001g0074 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1619-9643C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45276896 | ||||||
| chr5:45277010
|
A | G | 70 | a0001c0001t0001g0045a0001c0001t0001g0074a0001c0001t0003g0053others(67): Show | 70 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1619-9757T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45277010 | ||||||
| chr5:45277091
|
C | G | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1619-9838G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45277091 | ||||||
| chr5:45277152
|
G | A | 2 | a0001c0001t0002g0039a0001c0001t0002g0040 | 2 | HG00639.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1619-9899C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45277152 | ||||||
| chr5:45277164
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1619-9911A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45277164 | ||||||
| chr5:45277855
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1619-10602A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45277855 | ||||||
| chr5:45278050
|
C | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1619-10797G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45278050 | ||||||
| chr5:45278251
|
T | C | 2 | a0001c0001t0001g0153a0001c0001t0015g0001 | 2 | NA18939.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1619-10998A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45278251 | ||||||
| chr5:45278550
|
A | T | 2 | a0001c0001t0002g0052a0001c0001t0002g0165 | 2 | HG03669.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1619-11297T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45278550 | ||||||
| chr5:45278626
|
T | C | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1619-11373A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45278626 | ||||||
| chr5:45278751
|
A | G | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1619-11498T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45278751 | ||||||
| chr5:45278822
|
G | A | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1619-11569C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45278822 | ||||||
| chr5:45278908
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1619-11655T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45278908 | ||||||
| chr5:45278912
|
G | A | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1619-11659C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45278912 | ||||||
| chr5:45279150
|
T | C | 1 | a0001c0001t0034g0172 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1619-11897A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45279150 | ||||||
| chr5:45279176
|
T | C | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1619-11923A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45279176 | ||||||
| chr5:45279375
|
C | T | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1619-12122G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45279375 | ||||||
| chr5:45279444
|
A | C | 1 | a0001c0001t0001g0074 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1619-12191T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45279444 | ||||||
| chr5:45279556
|
A | G | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1619-12303T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45279556 | ||||||
| chr5:45279648
|
C | T | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1619-12395G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45279648 | ||||||
| chr5:45279756
|
A | C | 37 | a0001c0001t0001g0045a0001c0001t0003g0053a0001c0001t0003g0063others(34): Show | 37 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1619-12503T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45279756 | ||||||
| chr5:45279837
|
A | G | 2 | a0001c0001t0003g0098a0001c0001t0003g0099 | 2 | HG01361.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1619-12584T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45279837 | ||||||
| chr5:45279852
|
A | C | 3 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0039g0218 | 3 | HG02965.hp2 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1619-12599T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45279852 | ||||||
| chr5:45279994
|
A | ATAAT | 3 | a0001c0001t0005g0130a0002c0002t0014g0222a0002c0002t0014g0223 | 3 | HG01433.hp2 HG02897.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1619-12745_1619-12 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45279994 | ||||||
| chr5:45280110
|
A | C | 37 | a0001c0001t0001g0045a0001c0001t0003g0053a0001c0001t0003g0063others(34): Show | 37 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1619-12857T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45280110 | ||||||
| chr5:45280181
|
T | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1619-12928A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45280181 | ||||||
| chr5:45280286
|
G | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1619-13033C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45280286 | ||||||
| chr5:45280341
|
T | C | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1619-13088A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45280341 | ||||||
| chr5:45280462
|
A | T | 54 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0002g0012others(51): Show | 54 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1619-13209T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45280462 | ||||||
| chr5:45281016
|
C | CA | 8 | a0001c0001t0001g0051a0001c0001t0002g0049a0001c0001t0002g0050others(5): Show | 8 | HG01891.hp2 HG02258.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1619-13764dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45281016 | ||||||
| chr5:45281016
|
CA | C | 15 | a0001c0001t0001g0065a0001c0001t0001g0073a0001c0001t0001g0134others(12): Show | 15 | HG00673.hp2 HG02056.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.1619-13764delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45281016 | ||||||
| chr5:45281156
|
A | C | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1619-13903T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45281156 | ||||||
| chr5:45281170
|
T | C | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1619-13917A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45281170 | ||||||
| chr5:45281293
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1619-14040G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45281293 | ||||||
| chr5:45281369
|
C | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1619-14116G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45281369 | ||||||
| chr5:45281468
|
C | T | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1619-14215G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45281468 | ||||||
| chr5:45281525
|
A | G | 70 | a0001c0001t0001g0045a0001c0001t0001g0074a0001c0001t0003g0053others(67): Show | 70 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1619-14272T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45281525 | ||||||
| chr5:45281579
|
C | CT | 44 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0051others(41): Show | 44 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1619-14327dupA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45281579 | ||||||
| chr5:45281579
|
C | CTT | 33 | a0001c0001t0001g0045a0001c0001t0003g0053a0001c0001t0003g0063others(30): Show | 33 | HG00099.hp2 HG00642.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1619-14328_1619-14 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45281579 | ||||||
| chr5:45281579
|
CT | C | 7 | a0001c0001t0001g0074a0001c0001t0001g0177a0001c0001t0001g0212others(4): Show | 7 | HG00323.hp1 HG01256.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.1619-14327delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45281579 | ||||||
| chr5:45281627
|
T | C | 3 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0039g0218 | 3 | HG02965.hp2 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1619-14374A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45281627 | ||||||
| chr5:45281628
|
G | A | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1619-14375C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45281628 | ||||||
| chr5:45281630
|
C | T | 3 | a0001c0001t0007g0115a0001c0001t0007g0214a0001c0001t0033g0213 | 3 | HG02451.hp1 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1619-14377G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45281630 | ||||||
| chr5:45281631
|
G | A | 3 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0039g0218 | 3 | HG02965.hp2 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1619-14378C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45281631 | ||||||
| chr5:45281690
|
C | T | 1 | a0001c0001t0002g0181 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1619-14437G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45281690 | ||||||
| chr5:45281737
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1619-14484C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45281737 | ||||||
| chr5:45281923
|
G | A | 1 | a0001c0001t0027g0022 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1619-14670C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45281923 | ||||||
| chr5:45281929
|
T | C | 3 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0039g0218 | 3 | HG02965.hp2 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1619-14676A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45281929 | ||||||
| chr5:45282069
|
T | G | 1 | a0001c0001t0001g0210 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1619-14816A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45282069 | ||||||
| chr5:45282235
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1619-14982A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45282235 | ||||||
| chr5:45282280
|
C | T | 1 | a0001c0001t0001g0200 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1619-15027G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45282280 | ||||||
| chr5:45282298
|
T | C | 2 | a0001c0001t0002g0067a0001c0001t0002g0131 | 2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1619-15045A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45282298 | ||||||
| chr5:45282579
|
A | G | 1 | a0001c0001t0002g0025 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1619-15326T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45282579 | ||||||
| chr5:45282706
|
A | C | 37 | a0001c0001t0001g0045a0001c0001t0003g0053a0001c0001t0003g0063others(34): Show | 37 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1619-15453T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45282706 | ||||||
| chr5:45282738
|
C | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1619-15485G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45282738 | ||||||
| chr5:45282907
|
C | G | 4 | a0001c0001t0001g0034a0001c0001t0002g0023a0001c0001t0002g0024others(1): Show | 4 | NA18949.hp2 NA18977.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.1619-15654G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45282907 | ||||||
| chr5:45282959
|
T | C | 4 | a0001c0001t0023g0075a0001c0001t0024g0007a0001c0001t0031g0009others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1619-15706A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45282959 | ||||||
| chr5:45283126
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1619-15873C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45283126 | ||||||
| chr5:45283176
|
A | G | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1619-15923T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45283176 | ||||||
| chr5:45283356
|
A | C | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1619-16103T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45283356 | ||||||
| chr5:45283452
|
A | G | 18 | a0001c0001t0001g0013a0001c0001t0001g0037a0001c0001t0001g0060others(15): Show | 18 | HG00642.hp1 HG00673.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.1619-16199T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45283452 | ||||||
| chr5:45283551
|
C | G | 3 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0039g0218 | 3 | HG02965.hp2 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1619-16298G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45283551 | ||||||
| chr5:45283884
|
G | A | 3 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0039g0218 | 3 | HG02965.hp2 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1619-16631C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45283884 | ||||||
| chr5:45283898
|
C | T | 3 | a0001c0001t0007g0115a0001c0001t0007g0214a0001c0001t0033g0213 | 3 | HG02451.hp1 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1619-16645G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45283898 | ||||||
| chr5:45283981
|
G | A | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1619-16728C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45283981 | ||||||
| chr5:45284335
|
T | C | 1 | a0001c0001t0003g0083 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1619-17082A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45284335 | ||||||
| chr5:45284432
|
A | G | 1 | a0001c0001t0002g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1619-17179T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45284432 | ||||||
| chr5:45284862
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1619-17609A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45284862 | ||||||
| chr5:45285076
|
C | A | 6 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0156others(3): Show | 6 | HG00597.hp1 NA18939.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.1619-17823G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45285076 | ||||||
| chr5:45285093
|
C | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1619-17840G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45285093 | ||||||
| chr5:45285217
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0190 | 2 | NA18971.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1619-17964G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45285217 | ||||||
| chr5:45285379
|
C | CCATTT | 41 | a0001c0001t0001g0045a0001c0001t0003g0053a0001c0001t0003g0063others(38): Show | 41 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1619-18127_1619-18 others(11): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45285379 | ||||||
| chr5:45285490
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1618+18109G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45285490 | ||||||
| chr5:45285572
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1618+18027C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45285572 | ||||||
| chr5:45285616
|
A | C | 45 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(42): Show | 45 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.1618+17983T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45285616 | ||||||
| chr5:45285650
|
A | G | 142 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0045others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.1618+17949T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45285650 | ||||||
| chr5:45285701
|
A | G | 3 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0039g0218 | 3 | HG02965.hp2 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1618+17898T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45285701 | ||||||
| chr5:45285895
|
C | G | 3 | a0001c0001t0006g0057a0001c0001t0006g0143a0001c0001t0006g0203 | 3 | HG01109.hp2 HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1618+17704G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45285895 | ||||||
| chr5:45285910
|
T | A | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1618+17689A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45285910 | ||||||
| chr5:45285995
|
T | C | 37 | a0001c0001t0001g0034a0001c0001t0002g0012a0001c0001t0002g0023others(34): Show | 37 | HG00280.hp1 HG00438.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.1618+17604A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45285995 | ||||||
| chr5:45286020
|
T | TA | 7 | a0001c0001t0003g0090a0001c0001t0003g0092a0001c0001t0003g0109others(4): Show | 7 | HG02056.hp2 HG02129.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.1618+17578dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45286020 | ||||||
| chr5:45286186
|
T | A | 6 | a0001c0001t0001g0159a0001c0001t0001g0182a0001c0001t0001g0184others(3): Show | 6 | HG00639.hp1 HG01169.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1618+17413A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45286186 | ||||||
| chr5:45286256
|
T | C | 2 | a0001c0001t0001g0074a0001c0001t0002g0178 | 2 | HG00280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1618+17343A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45286256 | ||||||
| chr5:45286450
|
A | G | 3 | a0001c0001t0002g0015a0001c0001t0002g0082a0001c0001t0016g0014 | 3 | HG02615.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1618+17149T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45286450 | ||||||
| chr5:45286606
|
C | T | 4 | a0001c0001t0001g0073a0001c0001t0001g0205a0001c0001t0001g0210others(1): Show | 4 | HG02165.hp1 NA18612.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+16993G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45286606 | ||||||
| chr5:45286738
|
T | C | 1 | a0001c0001t0002g0066 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1618+16861A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45286738 | ||||||
| chr5:45286875
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1618+16724G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45286875 | ||||||
| chr5:45286928
|
TCTGA | T | 3 | a0001c0001t0002g0015a0001c0001t0002g0082a0001c0001t0016g0014 | 3 | HG02615.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1618+16667_1618+16 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45286928 | ||||||
| chr5:45286940
|
T | A | 1 | a0001c0001t0019g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1618+16659A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45286940 | ||||||
| chr5:45286995
|
T | C | 7 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(4): Show | 7 | HG01167.hp2 HG01192.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1618+16604A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45286995 | ||||||
| chr5:45287050
|
ATAT | A | 12 | a0001c0001t0005g0089a0001c0001t0005g0122a0001c0001t0005g0123others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1618+16546_1618+16 others(9): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45287050 | ||||||
| chr5:45287080
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1618+16519G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45287080 | ||||||
| chr5:45287099
|
CTGTGTGT others(9): Show |
C | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1618+16484_1618+16 others(22): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45287099 | ||||||
| chr5:45287254
|
C | T | 5 | a0001c0001t0001g0051a0001c0001t0002g0050a0001c0001t0002g0140others(2): Show | 5 | HG01891.hp2 HG03139.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1618+16345G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45287254 | ||||||
| chr5:45287307
|
G | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1618+16292C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45287307 | ||||||
| chr5:45287338
|
C | T | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1618+16261G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45287338 | ||||||
| chr5:45287510
|
C | T | 3 | a0002c0002t0014g0222a0002c0002t0014g0223a0003c0003t0035g0220 | 3 | HG01433.hp2 HG02622.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1618+16089G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45287510 | ||||||
| chr5:45288007
|
A | T | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1618+15592T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45288007 | ||||||
| chr5:45288103
|
T | A | 1 | a0001c0001t0002g0091 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1618+15496A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45288103 | ||||||
| chr5:45288136
|
C | G | 1 | a0001c0001t0001g0060 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1618+15463G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45288136 | ||||||
| chr5:45288329
|
G | A | 1 | a0001c0001t0005g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1618+15270C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45288329 | ||||||
| chr5:45288354
|
A | G | 2 | a0001c0001t0017g0081a0001c0001t0019g0114 | 2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1618+15245T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45288354 | ||||||
| chr5:45288401
|
C | G | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1618+15198G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45288401 | ||||||
| chr5:45288437
|
C | T | 1 | a0001c0001t0023g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1618+15162G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45288437 | ||||||
| chr5:45288913
|
G | C | 1 | a0001c0001t0001g0207 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1618+14686C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45288913 | ||||||
| chr5:45288962
|
T | C | 225 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1618+14637A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45288962 | ||||||
| chr5:45288963
|
G | A | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1618+14636C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45288963 | ||||||
| chr5:45289074
|
T | A | 3 | a0001c0001t0003g0084a0001c0001t0003g0101a0001c0001t0036g0186 | 3 | NA19003.hp1 NA19011.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1618+14525A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45289074 | ||||||
| chr5:45289195
|
A | T | 3 | a0001c0001t0002g0015a0001c0001t0002g0082a0001c0001t0016g0014 | 3 | HG02615.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1618+14404T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45289195 | ||||||
| chr5:45289475
|
C | T | 1 | a0001c0001t0013g0078 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1618+14124G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45289475 | ||||||
| chr5:45289751
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1618+13848C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45289751 | ||||||
| chr5:45290005
|
C | A | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1618+13594G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45290005 | ||||||
| chr5:45290026
|
G | T | 3 | a0001c0001t0001g0167a0001c0001t0013g0078a0001c0001t0013g0079 | 3 | HG02056.hp1 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1618+13573C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45290026 | ||||||
| chr5:45290097
|
C | T | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1618+13502G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45290097 | ||||||
| chr5:45290307
|
T | G | 1 | a0001c0001t0001g0201 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1618+13292A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45290307 | ||||||
| chr5:45290361
|
C | T | 10 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(7): Show | 10 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1618+13238G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45290361 | ||||||
| chr5:45290374
|
C | T | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1618+13225G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45290374 | ||||||
| chr5:45290538
|
T | C | 9 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.1618+13061A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45290538 | ||||||
| chr5:45290584
|
T | A | 3 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0142 | 3 | HG02886.hp2 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1618+13015A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45290584 | ||||||
| chr5:45290621
|
T | G | 3 | a0001c0001t0001g0167a0001c0001t0013g0078a0001c0001t0013g0079 | 3 | HG02056.hp1 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1618+12978A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45290621 | ||||||
| chr5:45290884
|
G | T | 1 | a0001c0001t0001g0139 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1618+12715C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45290884 | ||||||
| chr5:45290944
|
A | C | 3 | a0001c0001t0001g0167a0001c0001t0013g0078a0001c0001t0013g0079 | 3 | HG02056.hp1 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1618+12655T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45290944 | ||||||
| chr5:45291085
|
TTCA | T | 3 | a0001c0001t0001g0167a0001c0001t0013g0078a0001c0001t0013g0079 | 3 | HG02056.hp1 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1618+12511_1618+12 others(9): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45291085 | ||||||
| chr5:45291325
|
T | C | 1 | a0001c0001t0002g0019 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1618+12274A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45291325 | ||||||
| chr5:45291371
|
C | T | 1 | a0001c0001t0002g0194 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1618+12228G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45291371 | ||||||
| chr5:45291412
|
T | C | 82 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(79): Show | 82 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.1618+12187A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45291412 | ||||||
| chr5:45291619
|
G | A | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1618+11980C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45291619 | ||||||
| chr5:45291628
|
T | G | 12 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1618+11971A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45291628 | ||||||
| chr5:45291808
|
G | A | 38 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(35): Show | 38 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1618+11791C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45291808 | ||||||
| chr5:45291811
|
C | T | 225 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1618+11788G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45291811 | ||||||
| chr5:45292172
|
T | A | 3 | a0001c0001t0001g0167a0001c0001t0013g0078a0001c0001t0013g0079 | 3 | HG02056.hp1 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1618+11427A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45292172 | ||||||
| chr5:45292304
|
A | G | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1618+11295T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45292304 | ||||||
| chr5:45292451
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1618+11148T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45292451 | ||||||
| chr5:45292953
|
C | T | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1618+10646G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45292953 | ||||||
| chr5:45293178
|
C | G | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1618+10421G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45293178 | ||||||
| chr5:45293236
|
T | C | 1 | a0001c0001t0002g0140 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1618+10363A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45293236 | ||||||
| chr5:45293409
|
G | A | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1618+10190C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45293409 | ||||||
| chr5:45293479
|
A | AAAAAC | 5 | a0001c0001t0001g0204a0001c0001t0002g0091a0001c0001t0002g0096others(2): Show | 5 | HG02615.hp2 NA18945.hp2 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.1618+10115_1618+10 others(11): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45293479 | ||||||
| chr5:45293479
|
A | AAAAACAA others(3): Show |
2 | a0001c0001t0002g0121a0001c0001t0033g0213 | 2 | HG01346.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1618+10110_1618+10 others(16): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45293479 | ||||||
| chr5:45293479
|
A | AAAAACAA others(8): Show |
3 | a0001c0001t0001g0167a0001c0001t0013g0078a0001c0001t0013g0079 | 3 | HG02056.hp1 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1618+10105_1618+10 others(21): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45293479 | ||||||
| chr5:45293479
|
AAAAACAA others(3): Show |
A | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1618+10110_1618+10 others(16): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45293479 | ||||||
| chr5:45293956
|
G | C | 3 | a0001c0001t0001g0167a0001c0001t0013g0078a0001c0001t0013g0079 | 3 | HG02056.hp1 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1618+9643C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45293956 | ||||||
| chr5:45294252
|
T | A | 1 | a0001c0001t0003g0119 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1618+9347A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45294252 | ||||||
| chr5:45294350
|
C | T | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1618+9249G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45294350 | ||||||
| chr5:45294623
|
G | T | 3 | a0001c0001t0001g0167a0001c0001t0013g0078a0001c0001t0013g0079 | 3 | HG02056.hp1 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1618+8976C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45294623 | ||||||
| chr5:45295081
|
C | CACCCCAA others(11): Show |
3 | a0001c0001t0001g0167a0001c0001t0013g0078a0001c0001t0013g0079 | 3 | HG02056.hp1 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1618+8500_1618+851 others(22): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45295081 | ||||||
| chr5:45295178
|
T | C | 34 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(31): Show | 34 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1618+8421A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45295178 | ||||||
| chr5:45295209
|
G | A | 5 | a0001c0001t0001g0051a0001c0001t0002g0050a0001c0001t0002g0140others(2): Show | 5 | HG01891.hp2 HG03139.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1618+8390C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45295209 | ||||||
| chr5:45295833
|
G | C | 3 | a0001c0001t0001g0167a0001c0001t0013g0078a0001c0001t0013g0079 | 3 | HG02056.hp1 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1618+7766C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45295833 | ||||||
| chr5:45296299
|
A | C | 3 | a0001c0001t0001g0167a0001c0001t0013g0078a0001c0001t0013g0079 | 3 | HG02056.hp1 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1618+7300T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45296299 | ||||||
| chr5:45296752
|
A | T | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1618+6847T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45296752 | ||||||
| chr5:45296865
|
T | A | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1618+6734A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45296865 | ||||||
| chr5:45297047
|
A | G | 3 | a0001c0001t0001g0167a0001c0001t0013g0078a0001c0001t0013g0079 | 3 | HG02056.hp1 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1618+6552T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45297047 | ||||||
| chr5:45297289
|
G | A | 3 | a0001c0001t0001g0167a0001c0001t0013g0078a0001c0001t0013g0079 | 3 | HG02056.hp1 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1618+6310C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45297289 | ||||||
| chr5:45297304
|
C | A | 1 | a0001c0001t0002g0091 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1618+6295G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45297304 | ||||||
| chr5:45297304
|
C | T | 1 | a0001c0001t0006g0203 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1618+6295G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45297304 | ||||||
| chr5:45297495
|
C | T | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1618+6104G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45297495 | ||||||
| chr5:45297846
|
G | A | 1 | a0001c0001t0002g0069 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1618+5753C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45297846 | ||||||
| chr5:45297984
|
G | GA | 111 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0037others(108): Show | 111 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1618+5614dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45297984 | ||||||
| chr5:45297984
|
G | GAA | 31 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0157others(28): Show | 31 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.1618+5613_1618+561 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45297984 | ||||||
| chr5:45297991
|
A | AC | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1618+5607_1618+560 others(5): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45297991 | ||||||
| chr5:45298220
|
T | C | 1 | a0001c0001t0038g0016 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1618+5379A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45298220 | ||||||
| chr5:45298281
|
G | C | 3 | a0001c0001t0002g0026a0001c0001t0002g0028a0001c0001t0002g0097 | 3 | HG00673.hp1 NA18962.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1618+5318C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45298281 | ||||||
| chr5:45298509
|
G | C | 132 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.1618+5090C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45298509 | ||||||
| chr5:45298531
|
C | G | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1618+5068G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45298531 | ||||||
| chr5:45298733
|
A | C | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1618+4866T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45298733 | ||||||
| chr5:45298916
|
C | T | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1618+4683G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45298916 | ||||||
| chr5:45298929
|
A | T | 1 | a0001c0001t0003g0118 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1618+4670T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45298929 | ||||||
| chr5:45299373
|
G | A | 8 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(5): Show | 8 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1618+4226C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45299373 | ||||||
| chr5:45299415
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1618+4184G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45299415 | ||||||
| chr5:45299811
|
G | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1618+3788C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45299811 | ||||||
| chr5:45299866
|
A | G | 1 | a0001c0001t0003g0090 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1618+3733T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45299866 | ||||||
| chr5:45299894
|
A | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1618+3705T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45299894 | ||||||
| chr5:45299999
|
A | G | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1618+3600T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45299999 | ||||||
| chr5:45300722
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1618+2877G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45300722 | ||||||
| chr5:45300907
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1618+2692G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45300907 | ||||||
| chr5:45300933
|
T | G | 132 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.1618+2666A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45300933 | ||||||
| chr5:45300950
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1618+2649T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45300950 | ||||||
| chr5:45301270
|
T | C | 3 | a0001c0001t0001g0167a0001c0001t0013g0078a0001c0001t0013g0079 | 3 | HG02056.hp1 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1618+2329A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45301270 | ||||||
| chr5:45301330
|
T | TTTAGAAT others(20): Show |
40 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(37): Show | 40 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1618+2268_1618+226 others(31): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45301330 | ||||||
| chr5:45301353
|
A | G | 1 | a0001c0001t0019g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1618+2246T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45301353 | ||||||
| chr5:45301497
|
T | C | 1 | a0001c0001t0004g0032 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1618+2102A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45301497 | ||||||
| chr5:45301507
|
C | T | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1618+2092G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45301507 | ||||||
| chr5:45301722
|
T | TA | 104 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1618+1876dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45301722 | ||||||
| chr5:45301722
|
TA | T | 9 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(6): Show | 9 | HG01109.hp2 HG01169.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1618+1876delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45301722 | ||||||
| chr5:45301964
|
G | A | 3 | a0001c0001t0001g0167a0001c0001t0013g0078a0001c0001t0013g0079 | 3 | HG02056.hp1 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1618+1635C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45301964 | ||||||
| chr5:45302020
|
C | T | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1618+1579G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45302020 | ||||||
| chr5:45302099
|
G | T | 1 | a0001c0001t0003g0087 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1618+1500C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45302099 | ||||||
| chr5:45302203
|
C | T | 1 | a0001c0001t0016g0014 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1618+1396G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45302203 | ||||||
| chr5:45302277
|
A | AAGTGGC | 133 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1618+1321_1618+132 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45302277 | ||||||
| chr5:45302374
|
C | A | 6 | a0001c0001t0001g0159a0001c0001t0001g0182a0001c0001t0001g0184others(3): Show | 6 | HG00639.hp1 HG01169.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1618+1225G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45302374 | ||||||
| chr5:45302402
|
G | A | 1 | a0001c0001t0024g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1618+1197C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45302402 | ||||||
| chr5:45302514
|
C | T | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1618+1085G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45302514 | ||||||
| chr5:45302545
|
T | C | 3 | a0001c0001t0003g0083a0001c0001t0003g0098a0001c0001t0003g0099 | 3 | HG00323.hp2 HG01361.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1618+1054A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45302545 | ||||||
| chr5:45302562
|
A | T | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1618+1037T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45302562 | ||||||
| chr5:45302567
|
C | T | 7 | a0001c0001t0003g0090a0001c0001t0003g0092a0001c0001t0003g0109others(4): Show | 7 | HG02056.hp2 HG02129.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.1618+1032G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45302567 | ||||||
| chr5:45302631
|
T | A | 1 | a0001c0001t0027g0022 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1618+968A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45302631 | ||||||
| chr5:45302640
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1618+959A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45302640 | ||||||
| chr5:45302756
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1618+843A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45302756 | ||||||
| chr5:45302782
|
A | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0190 | 2 | NA18971.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1618+817T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45302782 | ||||||
| chr5:45302836
|
G | T | 1 | a0001c0001t0003g0103 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1618+763C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45302836 | ||||||
| chr5:45303026
|
A | T | 1 | a0001c0001t0005g0142 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1618+573T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45303026 | ||||||
| chr5:45303398
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1618+201G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45303398 | ||||||
| chr5:45303570
|
T | C | 7 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1618+29A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 6/7 | chr5 | 45303570 | ||||||
| chr5:45303907
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-68T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45303907 | ||||||
| chr5:45304048
|
A | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1378-209T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45304048 | ||||||
| chr5:45304192
|
T | C | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1378-353A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45304192 | ||||||
| chr5:45304297
|
GT | G | 90 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(87): Show | 90 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1378-459delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45304297 | ||||||
| chr5:45304390
|
T | C | 2 | a0001c0001t0011g0163a0001c0001t0011g0164 | 2 | NA18992.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1378-551A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45304390 | ||||||
| chr5:45304403
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-564A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45304403 | ||||||
| chr5:45304542
|
G | T | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1378-703C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45304542 | ||||||
| chr5:45304680
|
G | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-841C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45304680 | ||||||
| chr5:45304688
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1378-849T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45304688 | ||||||
| chr5:45304994
|
A | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-1155T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45304994 | ||||||
| chr5:45305044
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-1205G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45305044 | ||||||
| chr5:45305071
|
T | C | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1378-1232A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45305071 | ||||||
| chr5:45305118
|
G | T | 1 | a0001c0001t0001g0216 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1378-1279C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45305118 | ||||||
| chr5:45305196
|
C | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-1357G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45305196 | ||||||
| chr5:45305285
|
C | T | 1 | a0001c0001t0003g0117 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1378-1446G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45305285 | ||||||
| chr5:45305309
|
A | G | 1 | a0001c0001t0002g0193 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1378-1470T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45305309 | ||||||
| chr5:45305383
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1378-1544C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45305383 | ||||||
| chr5:45305419
|
T | C | 17 | a0001c0001t0001g0065a0001c0001t0004g0017a0001c0001t0004g0020others(14): Show | 17 | HG00438.hp1 HG00609.hp2 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.1378-1580A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45305419 | ||||||
| chr5:45305458
|
G | C | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1378-1619C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45305458 | ||||||
| chr5:45305513
|
A | G | 133 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1378-1674T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45305513 | ||||||
| chr5:45305601
|
A | C | 1 | a0001c0001t0002g0026 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1378-1762T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45305601 | ||||||
| chr5:45305613
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1378-1774C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45305613 | ||||||
| chr5:45305635
|
G | C | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1378-1796C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45305635 | ||||||
| chr5:45305774
|
AAAGG | A | 4 | a0001c0001t0002g0012a0001c0001t0003g0104a0001c0001t0023g0075others(1): Show | 4 | HG02257.hp2 HG04204.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.1378-1939_1378-193 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45305774 | ||||||
| chr5:45306179
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-2340T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45306179 | ||||||
| chr5:45306387
|
C | A | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1378-2548G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45306387 | ||||||
| chr5:45306426
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1378-2587G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45306426 | ||||||
| chr5:45306548
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1378-2709T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45306548 | ||||||
| chr5:45306927
|
C | T | 1 | a0001c0001t0007g0100 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1378-3088G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45306927 | ||||||
| chr5:45307010
|
C | A | 38 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(35): Show | 38 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1378-3171G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45307010 | ||||||
| chr5:45307131
|
C | T | 131 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1378-3292G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45307131 | ||||||
| chr5:45307375
|
G | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG01934.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.1378-3536C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45307375 | ||||||
| chr5:45307491
|
G | A | 2 | a0001c0001t0003g0118a0001c0001t0003g0120 | 2 | HG00735.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.1378-3652C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45307491 | ||||||
| chr5:45307550
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1378-3711G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45307550 | ||||||
| chr5:45307557
|
C | T | 5 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(2): Show | 5 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378-3718G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45307557 | ||||||
| chr5:45307596
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1378-3757G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45307596 | ||||||
| chr5:45307667
|
A | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1378-3828T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45307667 | ||||||
| chr5:45307799
|
G | A | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1378-3960C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45307799 | ||||||
| chr5:45307824
|
T | G | 68 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(65): Show | 68 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.1378-3985A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45307824 | ||||||
| chr5:45307855
|
C | T | 1 | a0001c0001t0021g0138 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1378-4016G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45307855 | ||||||
| chr5:45308085
|
G | C | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1378-4246C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45308085 | ||||||
| chr5:45308113
|
C | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-4274G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45308113 | ||||||
| chr5:45308139
|
T | C | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1378-4300A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45308139 | ||||||
| chr5:45308143
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-4304A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45308143 | ||||||
| chr5:45308273
|
C | A | 3 | a0001c0001t0003g0110a0001c0001t0003g0111a0001c0001t0003g0112 | 3 | HG02056.hp2 NA19001.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1378-4434G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45308273 | ||||||
| chr5:45308286
|
A | C | 1 | a0001c0001t0002g0019 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1378-4447T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45308286 | ||||||
| chr5:45308315
|
T | C | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1378-4476A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45308315 | ||||||
| chr5:45308622
|
T | C | 1 | a0001c0001t0003g0087 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1378-4783A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45308622 | ||||||
| chr5:45308911
|
C | A | 1 | a0001c0001t0002g0049 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1378-5072G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45308911 | ||||||
| chr5:45308911
|
C | T | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1378-5072G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45308911 | ||||||
| chr5:45308985
|
T | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-5146A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45308985 | ||||||
| chr5:45309375
|
T | C | 131 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1378-5536A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45309375 | ||||||
| chr5:45309411
|
A | G | 131 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1378-5572T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45309411 | ||||||
| chr5:45309592
|
T | C | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1378-5753A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45309592 | ||||||
| chr5:45309662
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1378-5823G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45309662 | ||||||
| chr5:45309723
|
G | C | 7 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1378-5884C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45309723 | ||||||
| chr5:45309910
|
C | T | 3 | a0001c0001t0003g0063a0001c0001t0003g0158a0001c0001t0003g0183 | 3 | HG01071.hp2 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1378-6071G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45309910 | ||||||
| chr5:45309982
|
A | G | 1 | a0001c0001t0002g0046 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1378-6143T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45309982 | ||||||
| chr5:45310187
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1378-6348G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45310187 | ||||||
| chr5:45310334
|
C | T | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1378-6495G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45310334 | ||||||
| chr5:45310422
|
C | T | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1378-6583G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45310422 | ||||||
| chr5:45310549
|
G | A | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1378-6710C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45310549 | ||||||
| chr5:45310559
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-6720G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45310559 | ||||||
| chr5:45310651
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1378-6812T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45310651 | ||||||
| chr5:45310655
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-6816G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45310655 | ||||||
| chr5:45310726
|
C | A | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1378-6887G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45310726 | ||||||
| chr5:45311093
|
C | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-7254G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45311093 | ||||||
| chr5:45311413
|
T | G | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1378-7574A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45311413 | ||||||
| chr5:45311476
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1378-7637C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45311476 | ||||||
| chr5:45311545
|
T | G | 1 | a0001c0001t0004g0030 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1378-7706A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45311545 | ||||||
| chr5:45311663
|
C | T | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1378-7824G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45311663 | ||||||
| chr5:45312216
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-8377G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45312216 | ||||||
| chr5:45312402
|
A | G | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1378-8563T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45312402 | ||||||
| chr5:45312452
|
C | T | 28 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0157others(25): Show | 28 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.1378-8613G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45312452 | ||||||
| chr5:45312511
|
C | G | 2 | a0001c0001t0002g0121a0001c0001t0002g0165 | 2 | HG01346.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1378-8672G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45312511 | ||||||
| chr5:45312511
|
C | T | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1378-8672G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45312511 | ||||||
| chr5:45312649
|
A | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1378-8810T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45312649 | ||||||
| chr5:45312663
|
C | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1378-8824G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45312663 | ||||||
| chr5:45312720
|
T | A | 3 | a0001c0001t0002g0015a0001c0001t0002g0082a0001c0001t0016g0014 | 3 | HG02615.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1378-8881A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45312720 | ||||||
| chr5:45312747
|
G | A | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1378-8908C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45312747 | ||||||
| chr5:45312799
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1378-8960C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45312799 | ||||||
| chr5:45312845
|
G | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-9006C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45312845 | ||||||
| chr5:45312966
|
C | A | 1 | a0001c0001t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1378-9127G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45312966 | ||||||
| chr5:45313085
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-9246G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45313085 | ||||||
| chr5:45313367
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-9528G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45313367 | ||||||
| chr5:45313378
|
T | C | 1 | a0001c0001t0002g0097 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1378-9539A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45313378 | ||||||
| chr5:45313415
|
A | G | 3 | a0001c0001t0002g0012a0001c0001t0002g0025a0001c0001t0002g0072 | 3 | HG02165.hp1 NA18612.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1378-9576T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45313415 | ||||||
| chr5:45313426
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1378-9587C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45313426 | ||||||
| chr5:45313499
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-9660T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45313499 | ||||||
| chr5:45313702
|
G | A | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1378-9863C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45313702 | ||||||
| chr5:45313715
|
C | A | 1 | a0001c0001t0002g0047 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1378-9876G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45313715 | ||||||
| chr5:45313716
|
G | A | 3 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0019g0114 | 3 | HG02451.hp2 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-9877C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45313716 | ||||||
| chr5:45313721
|
C | T | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1378-9882G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45313721 | ||||||
| chr5:45313803
|
G | C | 23 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0156others(20): Show | 23 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.1378-9964C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45313803 | ||||||
| chr5:45313884
|
C | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1378-10045G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45313884 | ||||||
| chr5:45314018
|
G | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-10179C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45314018 | ||||||
| chr5:45314096
|
G | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-10257C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45314096 | ||||||
| chr5:45314158
|
G | A | 1 | a0001c0001t0040g0175 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1378-10319C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45314158 | ||||||
| chr5:45314311
|
C | T | 34 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(31): Show | 34 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1378-10472G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45314311 | ||||||
| chr5:45314383
|
G | A | 5 | a0001c0001t0001g0216a0001c0001t0007g0115a0001c0001t0007g0214others(2): Show | 5 | HG00558.hp2 HG02451.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1378-10544C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45314383 | ||||||
| chr5:45314413
|
A | G | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1378-10574T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45314413 | ||||||
| chr5:45314427
|
G | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-10588C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45314427 | ||||||
| chr5:45314446
|
T | A | 1 | a0001c0001t0003g0111 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1378-10607A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45314446 | ||||||
| chr5:45314447
|
G | T | 1 | a0001c0001t0004g0029 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1378-10608C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45314447 | ||||||
| chr5:45314542
|
G | T | 1 | a0001c0001t0003g0084 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1378-10703C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45314542 | ||||||
| chr5:45314710
|
T | C | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1378-10871A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45314710 | ||||||
| chr5:45314758
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1378-10919C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45314758 | ||||||
| chr5:45314788
|
A | C | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1378-10949T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45314788 | ||||||
| chr5:45314880
|
T | C | 7 | a0001c0001t0001g0051a0001c0001t0002g0049a0001c0001t0002g0050others(4): Show | 7 | HG01891.hp2 HG03041.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1378-11041A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45314880 | ||||||
| chr5:45314927
|
A | G | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1378-11088T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45314927 | ||||||
| chr5:45314976
|
C | A | 1 | a0001c0001t0001g0168 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1378-11137G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45314976 | ||||||
| chr5:45315002
|
C | A | 1 | a0001c0001t0005g0130 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1378-11163G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45315002 | ||||||
| chr5:45315004
|
A | T | 8 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(5): Show | 8 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1378-11165T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45315004 | ||||||
| chr5:45315027
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-11188A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45315027 | ||||||
| chr5:45315046
|
G | C | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1378-11207C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45315046 | ||||||
| chr5:45315059
|
C | T | 1 | a0001c0001t0005g0129 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1378-11220G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45315059 | ||||||
| chr5:45315218
|
C | T | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1378-11379G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45315218 | ||||||
| chr5:45315371
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1378-11532T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45315371 | ||||||
| chr5:45315582
|
G | T | 1 | a0001c0001t0003g0090 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1378-11743C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45315582 | ||||||
| chr5:45315615
|
T | C | 3 | a0001c0001t0002g0027a0001c0001t0002g0036a0001c0001t0002g0054 | 3 | NA18959.hp2 NA18982.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1378-11776A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45315615 | ||||||
| chr5:45315897
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1378-12058C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45315897 | ||||||
| chr5:45315929
|
A | G | 1 | a0001c0001t0001g0102 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1378-12090T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45315929 | ||||||
| chr5:45315945
|
A | C | 217 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1378-12106T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45315945 | ||||||
| chr5:45316045
|
A | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-12206T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45316045 | ||||||
| chr5:45316160
|
T | C | 131 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1378-12321A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45316160 | ||||||
| chr5:45316287
|
A | T | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1378-12448T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45316287 | ||||||
| chr5:45316313
|
C | T | 34 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(31): Show | 34 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1378-12474G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45316313 | ||||||
| chr5:45316363
|
C | A | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1378-12524G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45316363 | ||||||
| chr5:45316425
|
G | C | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1378-12586C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45316425 | ||||||
| chr5:45316555
|
T | C | 1 | a0001c0001t0002g0067 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1378-12716A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45316555 | ||||||
| chr5:45316978
|
G | T | 1 | a0001c0001t0021g0138 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1378-13139C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45316978 | ||||||
| chr5:45317114
|
G | T | 131 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1378-13275C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45317114 | ||||||
| chr5:45317116
|
C | G | 1 | a0001c0001t0002g0041 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1378-13277G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45317116 | ||||||
| chr5:45317122
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-13283G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45317122 | ||||||
| chr5:45317205
|
G | A | 23 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0156others(20): Show | 23 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.1378-13366C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45317205 | ||||||
| chr5:45317339
|
G | A | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1378-13500C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45317339 | ||||||
| chr5:45317552
|
C | A | 2 | a0001c0001t0002g0039a0001c0001t0003g0103 | 2 | HG00639.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1378-13713G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45317552 | ||||||
| chr5:45317700
|
G | A | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1378-13861C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45317700 | ||||||
| chr5:45317755
|
G | T | 2 | a0001c0001t0002g0067a0001c0001t0002g0131 | 2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1378-13916C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45317755 | ||||||
| chr5:45317784
|
C | T | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1378-13945G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45317784 | ||||||
| chr5:45317858
|
C | G | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1378-14019G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45317858 | ||||||
| chr5:45317892
|
G | A | 131 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1378-14053C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45317892 | ||||||
| chr5:45317993
|
G | T | 1 | a0001c0001t0003g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1378-14154C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45317993 | ||||||
| chr5:45318018
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0003g0117 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1378-14179C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45318018 | ||||||
| chr5:45318109
|
C | T | 6 | a0001c0001t0001g0102a0001c0001t0001g0107a0001c0001t0001g0216others(3): Show | 6 | HG00438.hp2 HG00558.hp2 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.1378-14270G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45318109 | ||||||
| chr5:45318211
|
T | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1378-14372A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45318211 | ||||||
| chr5:45318228
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1378-14389A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45318228 | ||||||
| chr5:45318303
|
C | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1378-14464G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45318303 | ||||||
| chr5:45318351
|
G | T | 1 | a0001c0001t0019g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1378-14512C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45318351 | ||||||
| chr5:45318383
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-14544T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45318383 | ||||||
| chr5:45318573
|
A | G | 1 | a0001c0006t0002g0219 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1378-14734T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45318573 | ||||||
| chr5:45318785
|
T | A | 1 | a0001c0001t0002g0036 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1378-14946A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45318785 | ||||||
| chr5:45318793
|
C | T | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1378-14954G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45318793 | ||||||
| chr5:45318798
|
G | A | 1 | a0001c0001t0028g0174 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1378-14959C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45318798 | ||||||
| chr5:45318880
|
A | G | 1 | a0001c0001t0002g0012 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1378-15041T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45318880 | ||||||
| chr5:45318947
|
C | T | 2 | a0001c0001t0001g0209a0001c0001t0002g0178 | 2 | HG00280.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1378-15108G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45318947 | ||||||
| chr5:45319190
|
C | T | 1 | a0001c0001t0019g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1378-15351G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45319190 | ||||||
| chr5:45319241
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-15402T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45319241 | ||||||
| chr5:45319348
|
A | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1378-15509T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45319348 | ||||||
| chr5:45319410
|
T | A | 1 | a0001c0001t0020g0196 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1378-15571A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45319410 | ||||||
| chr5:45319549
|
C | G | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1378-15710G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45319549 | ||||||
| chr5:45319561
|
T | C | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1378-15722A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45319561 | ||||||
| chr5:45319594
|
T | G | 5 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(2): Show | 5 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378-15755A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45319594 | ||||||
| chr5:45320025
|
T | G | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1378-16186A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45320025 | ||||||
| chr5:45320034
|
C | T | 2 | a0001c0001t0001g0187a0001c0001t0040g0175 | 2 | NA18977.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1378-16195G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45320034 | ||||||
| chr5:45320259
|
T | G | 1 | a0001c0001t0001g0192 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1378-16420A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45320259 | ||||||
| chr5:45320317
|
A | T | 2 | a0001c0001t0001g0187a0001c0001t0040g0175 | 2 | NA18977.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1378-16478T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45320317 | ||||||
| chr5:45320533
|
A | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-16694T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45320533 | ||||||
| chr5:45320551
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1378-16712T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45320551 | ||||||
| chr5:45320751
|
T | C | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1378-16912A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45320751 | ||||||
| chr5:45320890
|
G | A | 1 | a0001c0001t0002g0096 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1378-17051C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45320890 | ||||||
| chr5:45320895
|
T | C | 1 | a0001c0001t0013g0079 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1378-17056A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45320895 | ||||||
| chr5:45320948
|
G | T | 1 | a0001c0001t0001g0190 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1378-17109C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45320948 | ||||||
| chr5:45321141
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-17302G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45321141 | ||||||
| chr5:45321146
|
C | T | 12 | a0001c0001t0001g0179a0001c0001t0005g0122a0001c0001t0005g0123others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1378-17307G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45321146 | ||||||
| chr5:45321163
|
C | T | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1378-17324G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45321163 | ||||||
| chr5:45321172
|
C | T | 1 | a0001c0001t0003g0053 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1378-17333G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45321172 | ||||||
| chr5:45321254
|
C | A | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1378-17415G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45321254 | ||||||
| chr5:45321306
|
G | A | 131 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1378-17467C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45321306 | ||||||
| chr5:45321310
|
A | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1378-17471T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45321310 | ||||||
| chr5:45321323
|
T | G | 11 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(8): Show | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1378-17484A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45321323 | ||||||
| chr5:45321497
|
T | TTAGCACG others(92): Show |
3 | a0001c0001t0002g0015a0001c0001t0002g0082a0001c0001t0016g0014 | 3 | HG02615.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1378-17757_1378-17 others(105): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45321497 | ||||||
| chr5:45321550
|
A | C | 2 | a0001c0001t0001g0034a0001c0001t0002g0035 | 2 | NA18949.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1378-17711T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45321550 | ||||||
| chr5:45321808
|
T | G | 1 | a0001c0001t0001g0192 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1378-17969A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45321808 | ||||||
| chr5:45321990
|
G | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1378-18151C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45321990 | ||||||
| chr5:45322038
|
CTAAA | C | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1378-18203_1378-18 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45322038 | ||||||
| chr5:45322337
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1378-18498G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45322337 | ||||||
| chr5:45322396
|
T | A | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1378-18557A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45322396 | ||||||
| chr5:45322454
|
G | C | 91 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(88): Show | 91 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1378-18615C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45322454 | ||||||
| chr5:45322488
|
C | T | 1 | a0001c0001t0002g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1378-18649G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45322488 | ||||||
| chr5:45322575
|
C | T | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1378-18736G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45322575 | ||||||
| chr5:45322772
|
A | C | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1378-18933T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45322772 | ||||||
| chr5:45322844
|
T | A | 1 | a0001c0001t0003g0086 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1378-19005A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45322844 | ||||||
| chr5:45322904
|
G | A | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1378-19065C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45322904 | ||||||
| chr5:45322911
|
G | T | 1 | a0001c0001t0002g0052 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1378-19072C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45322911 | ||||||
| chr5:45322912
|
T | C | 1 | a0001c0001t0002g0052 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1378-19073A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45322912 | ||||||
| chr5:45323000
|
G | A | 3 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0043 | 3 | HG00597.hp2 HG00639.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1378-19161C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45323000 | ||||||
| chr5:45323035
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-19196G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45323035 | ||||||
| chr5:45323053
|
T | C | 1 | a0001c0001t0002g0157 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1378-19214A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45323053 | ||||||
| chr5:45323214
|
C | A | 1 | a0001c0001t0023g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1378-19375G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45323214 | ||||||
| chr5:45323261
|
C | T | 41 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(38): Show | 41 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1378-19422G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45323261 | ||||||
| chr5:45323450
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1378-19611A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45323450 | ||||||
| chr5:45323492
|
T | A | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1378-19653A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45323492 | ||||||
| chr5:45323532
|
G | A | 8 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(5): Show | 8 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1378-19693C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45323532 | ||||||
| chr5:45323713
|
C | G | 1 | a0001c0001t0001g0207 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1378-19874G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45323713 | ||||||
| chr5:45323726
|
C | T | 1 | a0001c0001t0019g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1378-19887G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45323726 | ||||||
| chr5:45324053
|
T | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1378-20214A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45324053 | ||||||
| chr5:45324084
|
G | A | 1 | a0001c0001t0002g0052 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1378-20245C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45324084 | ||||||
| chr5:45324088
|
GC | G | 80 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(77): Show | 80 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.1378-20250delG | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45324088 | ||||||
| chr5:45324410
|
A | G | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1378-20571T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45324410 | ||||||
| chr5:45324656
|
T | A | 1 | a0001c0001t0002g0019 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1378-20817A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45324656 | ||||||
| chr5:45324801
|
A | T | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1378-20962T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45324801 | ||||||
| chr5:45324803
|
C | T | 1 | a0003c0003t0002g0221 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1378-20964G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45324803 | ||||||
| chr5:45324804
|
T | C | 1 | a0001c0001t0002g0058 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1378-20965A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45324804 | ||||||
| chr5:45324838
|
T | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-20999A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45324838 | ||||||
| chr5:45325095
|
C | T | 1 | a0001c0001t0002g0027 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1378-21256G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45325095 | ||||||
| chr5:45325198
|
G | C | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1378-21359C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45325198 | ||||||
| chr5:45325221
|
G | T | 1 | a0001c0001t0001g0180 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1378-21382C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45325221 | ||||||
| chr5:45325310
|
T | A | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1378-21471A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45325310 | ||||||
| chr5:45325602
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1378-21763C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45325602 | ||||||
| chr5:45325806
|
G | A | 1 | a0001c0001t0003g0053 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1378-21967C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45325806 | ||||||
| chr5:45325813
|
G | A | 131 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1378-21974C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45325813 | ||||||
| chr5:45326055
|
A | G | 1 | a0001c0001t0002g0015 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1378-22216T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45326055 | ||||||
| chr5:45326231
|
A | C | 34 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(31): Show | 34 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1378-22392T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45326231 | ||||||
| chr5:45326295
|
T | G | 6 | a0001c0001t0001g0051a0001c0001t0002g0049a0001c0001t0002g0050others(3): Show | 6 | HG01891.hp2 HG03041.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1378-22456A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45326295 | ||||||
| chr5:45326583
|
T | C | 1 | a0001c0001t0011g0164 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1378-22744A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45326583 | ||||||
| chr5:45326618
|
T | A | 1 | a0001c0001t0007g0100 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1378-22779A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45326618 | ||||||
| chr5:45326671
|
T | G | 131 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1378-22832A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45326671 | ||||||
| chr5:45326788
|
C | T | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1378-22949G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45326788 | ||||||
| chr5:45327055
|
T | C | 6 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0156others(3): Show | 6 | HG00597.hp1 NA18939.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.1378-23216A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45327055 | ||||||
| chr5:45327741
|
G | T | 1 | a0001c0001t0003g0086 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1378-23902C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45327741 | ||||||
| chr5:45327845
|
G | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1378-24006C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45327845 | ||||||
| chr5:45327963
|
C | T | 1 | a0001c0001t0019g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1378-24124G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45327963 | ||||||
| chr5:45328164
|
C | T | 1 | a0001c0001t0005g0129 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1378-24325G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45328164 | ||||||
| chr5:45328228
|
G | A | 39 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(36): Show | 39 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.1378-24389C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45328228 | ||||||
| chr5:45328257
|
AT | A | 14 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1378-24419delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45328257 | ||||||
| chr5:45328311
|
C | T | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1378-24472G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45328311 | ||||||
| chr5:45328631
|
C | A | 1 | a0001c0001t0002g0082 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1377+24469G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45328631 | ||||||
| chr5:45328631
|
C | T | 1 | a0001c0001t0010g0005 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1377+24469G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45328631 | ||||||
| chr5:45328632
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1377+24468C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45328632 | ||||||
| chr5:45328674
|
A | G | 1 | a0001c0001t0001g0153 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1377+24426T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45328674 | ||||||
| chr5:45328821
|
T | C | 1 | a0001c0001t0023g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1377+24279A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45328821 | ||||||
| chr5:45328936
|
A | G | 1 | a0001c0001t0002g0052 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1377+24164T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45328936 | ||||||
| chr5:45329085
|
A | G | 2 | a0001c0001t0001g0107a0001c0001t0007g0100 | 2 | HG00438.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.1377+24015T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45329085 | ||||||
| chr5:45329167
|
T | TCAGTACA others(3): Show |
1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1377+23923_1377+23 others(16): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45329167 | ||||||
| chr5:45329247
|
T | C | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1377+23853A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45329247 | ||||||
| chr5:45329391
|
G | C | 1 | a0001c0001t0002g0036 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1377+23709C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45329391 | ||||||
| chr5:45329473
|
A | T | 1 | a0001c0001t0003g0188 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1377+23627T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45329473 | ||||||
| chr5:45329708
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1377+23392G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45329708 | ||||||
| chr5:45329726
|
G | A | 1 | a0001c0001t0021g0138 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1377+23374C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45329726 | ||||||
| chr5:45330040
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1377+23060C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45330040 | ||||||
| chr5:45330134
|
A | G | 1 | a0001c0001t0003g0084 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1377+22966T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45330134 | ||||||
| chr5:45330325
|
G | A | 2 | a0001c0001t0001g0209a0001c0001t0002g0178 | 2 | HG00280.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1377+22775C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45330325 | ||||||
| chr5:45330433
|
A | G | 7 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1377+22667T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45330433 | ||||||
| chr5:45330457
|
T | C | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1377+22643A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45330457 | ||||||
| chr5:45330666
|
C | A | 1 | a0001c0001t0001g0202 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1377+22434G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45330666 | ||||||
| chr5:45330720
|
A | T | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1377+22380T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45330720 | ||||||
| chr5:45330762
|
A | C | 1 | a0001c0001t0001g0177 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1377+22338T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45330762 | ||||||
| chr5:45330805
|
T | A | 1 | a0001c0001t0001g0182 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1377+22295A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45330805 | ||||||
| chr5:45330987
|
G | T | 1 | a0001c0001t0005g0130 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1377+22113C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45330987 | ||||||
| chr5:45331144
|
A | C | 1 | a0001c0001t0005g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1377+21956T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45331144 | ||||||
| chr5:45331158
|
T | C | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG00323.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1377+21942A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45331158 | ||||||
| chr5:45331184
|
T | C | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1377+21916A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45331184 | ||||||
| chr5:45331195
|
A | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1377+21905T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45331195 | ||||||
| chr5:45331620
|
T | C | 18 | a0001c0001t0001g0065a0001c0001t0002g0024a0001c0001t0004g0017others(15): Show | 18 | HG00438.hp1 HG00609.hp2 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.1377+21480A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45331620 | ||||||
| chr5:45331678
|
C | T | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1377+21422G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45331678 | ||||||
| chr5:45331853
|
T | G | 3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0002g0194 | 3 | HG01952.hp1 HG03669.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1377+21247A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45331853 | ||||||
| chr5:45332068
|
A | G | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1377+21032T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45332068 | ||||||
| chr5:45332096
|
T | G | 1 | a0001c0001t0001g0107 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1377+21004A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45332096 | ||||||
| chr5:45332110
|
A | G | 4 | a0001c0001t0001g0045a0001c0001t0003g0063a0001c0001t0003g0158others(1): Show | 4 | HG01071.hp2 HG01081.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.1377+20990T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45332110 | ||||||
| chr5:45332452
|
C | T | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1377+20648G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45332452 | ||||||
| chr5:45332510
|
T | A | 67 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1377+20590A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45332510 | ||||||
| chr5:45332547
|
G | A | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1377+20553C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45332547 | ||||||
| chr5:45332547
|
G | C | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1377+20553C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45332547 | ||||||
| chr5:45332588
|
A | C | 11 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(8): Show | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1377+20512T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45332588 | ||||||
| chr5:45332707
|
T | G | 1 | a0001c0001t0024g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1377+20393A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45332707 | ||||||
| chr5:45332718
|
C | G | 1 | a0001c0001t0015g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1377+20382G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45332718 | ||||||
| chr5:45332722
|
A | T | 131 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1377+20378T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45332722 | ||||||
| chr5:45332774
|
CAG | C | 2 | a0001c0001t0012g0064a0001c0001t0012g0137 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1377+20324_1377+20 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45332774 | ||||||
| chr5:45332975
|
T | C | 11 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(8): Show | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1377+20125A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45332975 | ||||||
| chr5:45333038
|
A | C | 1 | a0001c0001t0002g0133 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1377+20062T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45333038 | ||||||
| chr5:45333048
|
T | C | 1 | a0001c0001t0002g0096 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1377+20052A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45333048 | ||||||
| chr5:45333467
|
C | T | 1 | a0001c0001t0003g0092 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1377+19633G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45333467 | ||||||
| chr5:45333476
|
G | A | 1 | a0001c0001t0006g0143 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1377+19624C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45333476 | ||||||
| chr5:45333519
|
G | A | 1 | a0003c0003t0002g0221 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1377+19581C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45333519 | ||||||
| chr5:45333692
|
T | A | 1 | a0001c0001t0001g0060 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1377+19408A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45333692 | ||||||
| chr5:45333758
|
T | C | 11 | a0001c0001t0001g0159a0001c0001t0001g0161a0001c0001t0001g0162others(8): Show | 11 | HG00280.hp2 HG00639.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.1377+19342A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45333758 | ||||||
| chr5:45333760
|
T | G | 1 | a0001c0001t0002g0025 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1377+19340A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45333760 | ||||||
| chr5:45333848
|
G | T | 39 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(36): Show | 39 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.1377+19252C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45333848 | ||||||
| chr5:45333930
|
A | G | 1 | a0003c0003t0002g0221 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1377+19170T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45333930 | ||||||
| chr5:45333952
|
G | A | 1 | a0001c0001t0029g0070 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1377+19148C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45333952 | ||||||
| chr5:45333987
|
T | C | 1 | a0001c0005t0002g0199 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1377+19113A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45333987 | ||||||
| chr5:45334015
|
A | T | 3 | a0001c0001t0002g0027a0001c0001t0002g0036a0001c0001t0002g0054 | 3 | NA18959.hp2 NA18982.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1377+19085T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45334015 | ||||||
| chr5:45334170
|
A | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1377+18930T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45334170 | ||||||
| chr5:45334279
|
G | A | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1377+18821C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45334279 | ||||||
| chr5:45334419
|
C | T | 1 | a0001c0001t0002g0047 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1377+18681G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45334419 | ||||||
| chr5:45334467
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1377+18633G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45334467 | ||||||
| chr5:45334511
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1377+18589A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45334511 | ||||||
| chr5:45334616
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1377+18484A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45334616 | ||||||
| chr5:45334706
|
C | T | 7 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(4): Show | 7 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1377+18394G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45334706 | ||||||
| chr5:45334987
|
T | A | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1377+18113A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45334987 | ||||||
| chr5:45334997
|
A | C | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1377+18103T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45334997 | ||||||
| chr5:45335007
|
G | A | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1377+18093C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45335007 | ||||||
| chr5:45335022
|
A | G | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1377+18078T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45335022 | ||||||
| chr5:45335023
|
T | A | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1377+18077A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45335023 | ||||||
| chr5:45335026
|
C | A | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1377+18074G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45335026 | ||||||
| chr5:45335028
|
C | G | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1377+18072G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45335028 | ||||||
| chr5:45335029
|
T | TAAATGGA others(26): Show |
1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1377+18070_1377+18 others(39): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45335029 | ||||||
| chr5:45335030
|
C | A | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1377+18070G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45335030 | ||||||
| chr5:45335032
|
C | G | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1377+18068G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45335032 | ||||||
| chr5:45335040
|
T | A | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1377+18060A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45335040 | ||||||
| chr5:45335042
|
C | G | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1377+18058G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45335042 | ||||||
| chr5:45335044
|
T | A | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1377+18056A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45335044 | ||||||
| chr5:45335045
|
G | A | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1377+18055C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45335045 | ||||||
| chr5:45335046
|
C | G | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1377+18054G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45335046 | ||||||
| chr5:45335048
|
C | A | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1377+18052G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45335048 | ||||||
| chr5:45335050
|
G | T | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1377+18050C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45335050 | ||||||
| chr5:45335051
|
T | A | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1377+18049A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45335051 | ||||||
| chr5:45335062
|
T | A | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1377+18038A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45335062 | ||||||
| chr5:45335063
|
A | T | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1377+18037T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45335063 | ||||||
| chr5:45335113
|
G | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1377+17987C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45335113 | ||||||
| chr5:45335314
|
A | G | 2 | a0001c0001t0003g0118a0001c0001t0003g0120 | 2 | HG00735.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.1377+17786T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45335314 | ||||||
| chr5:45335498
|
T | C | 1 | a0001c0001t0001g0011 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1377+17602A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45335498 | ||||||
| chr5:45335503
|
T | C | 1 | a0001c0001t0002g0047 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1377+17597A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45335503 | ||||||
| chr5:45335657
|
T | C | 131 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1377+17443A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45335657 | ||||||
| chr5:45335690
|
T | C | 1 | a0001c0001t0002g0091 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1377+17410A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45335690 | ||||||
| chr5:45335961
|
G | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1377+17139C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45335961 | ||||||
| chr5:45336295
|
G | A | 8 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(5): Show | 8 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1377+16805C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45336295 | ||||||
| chr5:45336369
|
T | C | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1377+16731A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45336369 | ||||||
| chr5:45336399
|
G | T | 7 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1377+16701C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45336399 | ||||||
| chr5:45336687
|
T | A | 55 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0065others(52): Show | 55 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1377+16413A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45336687 | ||||||
| chr5:45336852
|
G | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1377+16248C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45336852 | ||||||
| chr5:45337062
|
T | C | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1377+16038A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45337062 | ||||||
| chr5:45337139
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1377+15961T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45337139 | ||||||
| chr5:45337228
|
A | G | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1377+15872T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45337228 | ||||||
| chr5:45337245
|
T | TA | 6 | a0001c0001t0001g0013a0001c0001t0001g0037a0001c0001t0001g0045others(3): Show | 6 | HG00735.hp2 HG00741.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.1377+15854dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45337245 | ||||||
| chr5:45337339
|
T | A | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1377+15761A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45337339 | ||||||
| chr5:45337401
|
T | C | 2 | a0001c0001t0025g0217a0001c0001t0026g0071 | 2 | HG01192.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1377+15699A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45337401 | ||||||
| chr5:45337817
|
C | G | 1 | a0001c0001t0002g0194 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1377+15283G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45337817 | ||||||
| chr5:45337870
|
T | C | 34 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(31): Show | 34 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1377+15230A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45337870 | ||||||
| chr5:45337926
|
A | G | 1 | a0001c0001t0002g0193 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1377+15174T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45337926 | ||||||
| chr5:45338033
|
G | T | 2 | a0001c0001t0002g0067a0001c0001t0002g0131 | 2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1377+15067C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45338033 | ||||||
| chr5:45338114
|
C | G | 81 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.1377+14986G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45338114 | ||||||
| chr5:45338415
|
G | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1377+14685C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45338415 | ||||||
| chr5:45338621
|
ATAACAG | A | 80 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(77): Show | 80 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.1377+14473_1377+14 others(12): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45338621 | ||||||
| chr5:45338739
|
T | C | 1 | a0001c0001t0005g0125 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1377+14361A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45338739 | ||||||
| chr5:45338931
|
A | C | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1377+14169T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45338931 | ||||||
| chr5:45339141
|
C | G | 80 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(77): Show | 80 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.1377+13959G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45339141 | ||||||
| chr5:45339165
|
G | T | 1 | a0001c0001t0002g0023 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1377+13935C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45339165 | ||||||
| chr5:45339205
|
A | G | 1 | a0001c0001t0002g0096 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1377+13895T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45339205 | ||||||
| chr5:45339210
|
C | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1377+13890G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45339210 | ||||||
| chr5:45339289
|
T | C | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1377+13811A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45339289 | ||||||
| chr5:45339486
|
T | C | 1 | a0001c0001t0001g0191 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1377+13614A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45339486 | ||||||
| chr5:45339506
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1377+13594G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45339506 | ||||||
| chr5:45339932
|
T | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1377+13168A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45339932 | ||||||
| chr5:45339940
|
C | T | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1377+13160G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45339940 | ||||||
| chr5:45339980
|
A | G | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1377+13120T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45339980 | ||||||
| chr5:45340039
|
C | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1377+13061G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45340039 | ||||||
| chr5:45340068
|
A | G | 64 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(61): Show | 64 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1377+13032T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45340068 | ||||||
| chr5:45340135
|
G | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1377+12965C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45340135 | ||||||
| chr5:45340141
|
G | A | 11 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(8): Show | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1377+12959C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45340141 | ||||||
| chr5:45340174
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1377+12926T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45340174 | ||||||
| chr5:45340216
|
C | T | 3 | a0001c0001t0002g0015a0001c0001t0002g0082a0001c0001t0016g0014 | 3 | HG02615.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1377+12884G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45340216 | ||||||
| chr5:45340279
|
T | C | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1377+12821A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45340279 | ||||||
| chr5:45340648
|
GT | G | 9 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(6): Show | 9 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1377+12451delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45340648 | ||||||
| chr5:45340847
|
C | A | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1377+12253G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45340847 | ||||||
| chr5:45341060
|
T | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1377+12040A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45341060 | ||||||
| chr5:45341192
|
A | C | 1 | a0001c0001t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1377+11908T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45341192 | ||||||
| chr5:45341259
|
C | T | 1 | a0001c0001t0002g0019 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1377+11841G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45341259 | ||||||
| chr5:45341281
|
G | A | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1377+11819C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45341281 | ||||||
| chr5:45341328
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1377+11772T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45341328 | ||||||
| chr5:45341423
|
C | A | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1377+11677G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45341423 | ||||||
| chr5:45341464
|
TG | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1377+11635delC | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45341464 | ||||||
| chr5:45341575
|
T | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1377+11525A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45341575 | ||||||
| chr5:45341614
|
C | T | 1 | a0001c0001t0005g0127 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1377+11486G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45341614 | ||||||
| chr5:45341699
|
G | C | 80 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(77): Show | 80 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.1377+11401C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45341699 | ||||||
| chr5:45341850
|
C | A | 67 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1377+11250G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45341850 | ||||||
| chr5:45341904
|
A | C | 1 | a0001c0001t0027g0022 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1377+11196T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45341904 | ||||||
| chr5:45341942
|
A | G | 133 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1377+11158T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45341942 | ||||||
| chr5:45341992
|
A | G | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1377+11108T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45341992 | ||||||
| chr5:45342010
|
T | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1377+11090A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45342010 | ||||||
| chr5:45342043
|
G | A | 3 | a0001c0001t0003g0084a0001c0001t0003g0101a0001c0001t0036g0186 | 3 | NA19003.hp1 NA19011.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1377+11057C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45342043 | ||||||
| chr5:45342138
|
G | T | 1 | a0001c0001t0001g0116 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1377+10962C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45342138 | ||||||
| chr5:45342207
|
T | A | 2 | a0001c0001t0001g0156a0001c0001t0002g0154 | 2 | NA18949.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.1377+10893A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45342207 | ||||||
| chr5:45342281
|
A | T | 225 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1377+10819T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45342281 | ||||||
| chr5:45342344
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1377+10756G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45342344 | ||||||
| chr5:45342346
|
T | G | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1377+10754A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45342346 | ||||||
| chr5:45342395
|
A | AT | 45 | a0001c0001t0001g0011a0001c0001t0001g0171a0001c0001t0001g0180others(42): Show | 45 | HG00099.hp1 HG00597.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1377+10704dupA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45342395 | ||||||
| chr5:45342395
|
A | ATT | 10 | a0001c0001t0001g0051a0001c0001t0002g0049a0001c0001t0002g0050others(7): Show | 10 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1377+10703_1377+10 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45342395 | ||||||
| chr5:45342395
|
A | ATTT | 5 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(2): Show | 5 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1377+10702_1377+10 others(9): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45342395 | ||||||
| chr5:45342649
|
C | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1377+10451G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45342649 | ||||||
| chr5:45343071
|
G | T | 1 | a0001c0001t0001g0216 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1377+10029C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45343071 | ||||||
| chr5:45343241
|
A | C | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1377+9859T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45343241 | ||||||
| chr5:45343341
|
G | A | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1377+9759C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45343341 | ||||||
| chr5:45343405
|
T | A | 1 | a0003c0003t0002g0221 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1377+9695A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45343405 | ||||||
| chr5:45343481
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1377+9619C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45343481 | ||||||
| chr5:45343528
|
C | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1377+9572G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45343528 | ||||||
| chr5:45343553
|
G | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1377+9547C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45343553 | ||||||
| chr5:45343597
|
A | T | 1 | a0001c0001t0004g0029 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1377+9503T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45343597 | ||||||
| chr5:45343664
|
T | C | 3 | a0001c0001t0002g0121a0001c0001t0013g0078a0001c0001t0013g0079 | 3 | HG01346.hp2 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1377+9436A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45343664 | ||||||
| chr5:45343708
|
G | A | 130 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1377+9392C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45343708 | ||||||
| chr5:45343839
|
A | C | 12 | a0001c0001t0001g0073a0001c0001t0001g0134a0001c0001t0001g0160others(9): Show | 12 | HG00673.hp2 HG02056.hp1 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1377+9261T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45343839 | ||||||
| chr5:45343869
|
A | AT | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1377+9230_1377+923 others(5): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45343869 | ||||||
| chr5:45343869
|
A | T | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1377+9231T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45343869 | ||||||
| chr5:45343876
|
A | T | 1 | a0001c0001t0002g0038 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1377+9224T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45343876 | ||||||
| chr5:45344054
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1377+9046T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45344054 | ||||||
| chr5:45344178
|
T | A | 1 | a0001c0001t0001g0212 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1377+8922A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45344178 | ||||||
| chr5:45344196
|
C | A | 67 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1377+8904G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45344196 | ||||||
| chr5:45344225
|
G | A | 10 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(7): Show | 10 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1377+8875C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45344225 | ||||||
| chr5:45344319
|
G | T | 34 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(31): Show | 34 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1377+8781C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45344319 | ||||||
| chr5:45344389
|
A | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1377+8711T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45344389 | ||||||
| chr5:45344615
|
C | T | 2 | a0001c0001t0005g0122a0001c0001t0005g0123 | 2 | HG02055.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1377+8485G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45344615 | ||||||
| chr5:45344681
|
T | A | 1 | a0001c0001t0019g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1377+8419A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45344681 | ||||||
| chr5:45344718
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1377+8382G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45344718 | ||||||
| chr5:45344721
|
G | A | 11 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(8): Show | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1377+8379C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45344721 | ||||||
| chr5:45344751
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1377+8349A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45344751 | ||||||
| chr5:45344881
|
C | T | 6 | a0001c0001t0003g0087a0001c0001t0003g0093a0001c0001t0003g0094others(3): Show | 6 | HG01071.hp1 HG01081.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1377+8219G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45344881 | ||||||
| chr5:45345372
|
C | T | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1377+7728G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45345372 | ||||||
| chr5:45345565
|
C | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1377+7535G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45345565 | ||||||
| chr5:45345654
|
T | A | 2 | a0002c0002t0008g0224a0002c0002t0008g0225 | 2 | HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1377+7446A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45345654 | ||||||
| chr5:45345756
|
C | G | 67 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1377+7344G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45345756 | ||||||
| chr5:45345761
|
C | T | 1 | a0001c0001t0002g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1377+7339G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45345761 | ||||||
| chr5:45345796
|
G | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1377+7304C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45345796 | ||||||
| chr5:45346070
|
C | G | 1 | a0001c0001t0004g0030 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1377+7030G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45346070 | ||||||
| chr5:45346087
|
A | G | 67 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1377+7013T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45346087 | ||||||
| chr5:45346153
|
C | A | 1 | a0001c0001t0003g0053 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1377+6947G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45346153 | ||||||
| chr5:45346298
|
G | T | 5 | a0001c0001t0001g0051a0001c0001t0002g0050a0001c0001t0002g0140others(2): Show | 5 | HG01891.hp2 HG03139.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1377+6802C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45346298 | ||||||
| chr5:45346305
|
T | C | 36 | a0001c0001t0001g0034a0001c0001t0001g0065a0001c0001t0002g0012others(33): Show | 36 | HG00280.hp1 HG00438.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.1377+6795A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45346305 | ||||||
| chr5:45346327
|
G | A | 1 | a0001c0001t0002g0096 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1377+6773C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45346327 | ||||||
| chr5:45346476
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1377+6624G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45346476 | ||||||
| chr5:45346580
|
C | G | 1 | a0001c0001t0001g0167 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1377+6520G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45346580 | ||||||
| chr5:45346580
|
C | T | 1 | a0001c0001t0005g0142 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1377+6520G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45346580 | ||||||
| chr5:45346581
|
G | A | 3 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0017g0081 | 3 | NA18992.hp2 NA19003.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1377+6519C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45346581 | ||||||
| chr5:45346658
|
C | G | 67 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1377+6442G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45346658 | ||||||
| chr5:45346670
|
G | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1377+6430C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45346670 | ||||||
| chr5:45346721
|
C | A | 1 | a0001c0001t0001g0139 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1377+6379G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45346721 | ||||||
| chr5:45346726
|
T | C | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1377+6374A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45346726 | ||||||
| chr5:45346795
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1377+6305T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45346795 | ||||||
| chr5:45346882
|
C | A | 1 | a0001c0001t0001g0171 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1377+6218G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45346882 | ||||||
| chr5:45347091
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1377+6009C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45347091 | ||||||
| chr5:45347113
|
C | A | 8 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(5): Show | 8 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1377+5987G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45347113 | ||||||
| chr5:45347114
|
T | C | 217 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1377+5986A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45347114 | ||||||
| chr5:45347233
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1377+5867G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45347233 | ||||||
| chr5:45347424
|
G | T | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1377+5676C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45347424 | ||||||
| chr5:45347442
|
C | A | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1377+5658G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45347442 | ||||||
| chr5:45347460
|
C | G | 1 | a0001c0006t0002g0219 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1377+5640G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45347460 | ||||||
| chr5:45347527
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1377+5573A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45347527 | ||||||
| chr5:45347552
|
C | T | 22 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(19): Show | 22 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1377+5548G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45347552 | ||||||
| chr5:45347668
|
A | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1377+5432T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45347668 | ||||||
| chr5:45347690
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1377+5410C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45347690 | ||||||
| chr5:45347708
|
C | T | 3 | a0001c0001t0002g0067a0001c0001t0002g0131a0001c0004t0002g0006 | 3 | HG01243.hp1 HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1377+5392G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45347708 | ||||||
| chr5:45347709
|
G | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1377+5391C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45347709 | ||||||
| chr5:45347871
|
G | T | 2 | a0001c0001t0001g0197a0001c0001t0020g0196 | 2 | HG01516.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1377+5229C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45347871 | ||||||
| chr5:45347908
|
C | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1377+5192G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45347908 | ||||||
| chr5:45347991
|
T | C | 1 | a0001c0001t0003g0113 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1377+5109A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45347991 | ||||||
| chr5:45348148
|
C | A | 3 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0043 | 3 | HG00597.hp2 HG00639.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1377+4952G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45348148 | ||||||
| chr5:45348166
|
C | T | 2 | a0001c0001t0003g0118a0001c0001t0003g0120 | 2 | HG00735.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.1377+4934G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45348166 | ||||||
| chr5:45348182
|
C | T | 1 | a0003c0003t0002g0221 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1377+4918G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45348182 | ||||||
| chr5:45348217
|
T | A | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1377+4883A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45348217 | ||||||
| chr5:45348263
|
G | A | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1377+4837C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45348263 | ||||||
| chr5:45348331
|
C | T | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1377+4769G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45348331 | ||||||
| chr5:45348390
|
C | T | 12 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1377+4710G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45348390 | ||||||
| chr5:45348463
|
A | G | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1377+4637T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45348463 | ||||||
| chr5:45348472
|
A | C | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1377+4628T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45348472 | ||||||
| chr5:45348530
|
T | A | 67 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1377+4570A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45348530 | ||||||
| chr5:45348713
|
G | T | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1377+4387C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45348713 | ||||||
| chr5:45348724
|
T | G | 7 | a0001c0001t0003g0090a0001c0001t0003g0092a0001c0001t0003g0109others(4): Show | 7 | HG02056.hp2 HG02129.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.1377+4376A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45348724 | ||||||
| chr5:45348744
|
G | C | 2 | a0001c0001t0003g0098a0001c0001t0003g0099 | 2 | HG01361.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1377+4356C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45348744 | ||||||
| chr5:45348744
|
G | T | 1 | a0001c0001t0001g0051 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1377+4356C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45348744 | ||||||
| chr5:45348937
|
C | A | 1 | a0001c0001t0003g0090 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1377+4163G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45348937 | ||||||
| chr5:45348960
|
T | C | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1377+4140A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45348960 | ||||||
| chr5:45348964
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1377+4136G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45348964 | ||||||
| chr5:45349036
|
A | C | 1 | a0001c0001t0005g0129 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1377+4064T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45349036 | ||||||
| chr5:45349096
|
C | A | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1377+4004G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45349096 | ||||||
| chr5:45349116
|
C | G | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1377+3984G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45349116 | ||||||
| chr5:45349140
|
A | T | 55 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0065others(52): Show | 55 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1377+3960T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45349140 | ||||||
| chr5:45349194
|
A | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1377+3906T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45349194 | ||||||
| chr5:45349195
|
A | T | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1377+3905T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45349195 | ||||||
| chr5:45349225
|
A | T | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1377+3875T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45349225 | ||||||
| chr5:45349253
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1377+3847G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45349253 | ||||||
| chr5:45349267
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1377+3833T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45349267 | ||||||
| chr5:45349381
|
G | C | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1377+3719C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45349381 | ||||||
| chr5:45349449
|
T | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG02647.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1377+3651A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45349449 | ||||||
| chr5:45349559
|
C | T | 8 | a0001c0001t0001g0116a0001c0001t0003g0063a0001c0001t0003g0117others(5): Show | 8 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1377+3541G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45349559 | ||||||
| chr5:45349743
|
C | T | 1 | a0001c0001t0024g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1377+3357G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45349743 | ||||||
| chr5:45349854
|
AC | A | 7 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(4): Show | 7 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1377+3245delG | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45349854 | ||||||
| chr5:45349874
|
A | G | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1377+3226T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45349874 | ||||||
| chr5:45349893
|
A | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1377+3207T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45349893 | ||||||
| chr5:45350029
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1377+3071T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45350029 | ||||||
| chr5:45350033
|
C | T | 8 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(5): Show | 8 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1377+3067G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45350033 | ||||||
| chr5:45350142
|
C | A | 2 | a0001c0001t0001g0209a0001c0001t0002g0178 | 2 | HG00280.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1377+2958G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45350142 | ||||||
| chr5:45350177
|
C | T | 39 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(36): Show | 39 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.1377+2923G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45350177 | ||||||
| chr5:45350210
|
C | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1377+2890G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45350210 | ||||||
| chr5:45350210
|
C | T | 3 | a0001c0001t0003g0084a0001c0001t0003g0101a0001c0001t0036g0186 | 3 | NA19003.hp1 NA19011.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1377+2890G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45350210 | ||||||
| chr5:45350274
|
T | G | 1 | a0001c0001t0004g0033 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1377+2826A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45350274 | ||||||
| chr5:45350311
|
A | T | 1 | a0001c0001t0003g0090 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1377+2789T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45350311 | ||||||
| chr5:45350326
|
T | C | 39 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(36): Show | 39 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.1377+2774A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45350326 | ||||||
| chr5:45350369
|
G | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1377+2731C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45350369 | ||||||
| chr5:45350511
|
G | T | 1 | a0001c0001t0001g0045 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1377+2589C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45350511 | ||||||
| chr5:45350555
|
T | C | 11 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(8): Show | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1377+2545A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45350555 | ||||||
| chr5:45350571
|
G | T | 1 | a0001c0001t0001g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1377+2529C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45350571 | ||||||
| chr5:45350646
|
C | A | 7 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1377+2454G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45350646 | ||||||
| chr5:45350672
|
C | G | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG01934.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.1377+2428G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45350672 | ||||||
| chr5:45350713
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1377+2387G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45350713 | ||||||
| chr5:45350729
|
C | T | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1377+2371G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45350729 | ||||||
| chr5:45350749
|
A | T | 1 | a0001c0001t0021g0138 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1377+2351T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45350749 | ||||||
| chr5:45350787
|
A | G | 1 | a0001c0001t0019g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1377+2313T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45350787 | ||||||
| chr5:45350809
|
A | G | 34 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(31): Show | 34 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1377+2291T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45350809 | ||||||
| chr5:45350889
|
T | G | 1 | a0001c0001t0002g0038 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1377+2211A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45350889 | ||||||
| chr5:45351000
|
G | T | 11 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(8): Show | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1377+2100C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351000 | ||||||
| chr5:45351057
|
C | T | 1 | a0001c0001t0003g0101 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1377+2043G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351057 | ||||||
| chr5:45351106
|
C | T | 67 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1377+1994G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351106 | ||||||
| chr5:45351107
|
G | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1377+1993C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351107 | ||||||
| chr5:45351220
|
C | T | 1 | a0001c0001t0028g0174 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1377+1880G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351220 | ||||||
| chr5:45351260
|
A | G | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1377+1840T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351260 | ||||||
| chr5:45351292
|
A | G | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1377+1808T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351292 | ||||||
| chr5:45351311
|
G | C | 2 | a0001c0001t0001g0147a0001c0001t0003g0063 | 2 | HG01071.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.1377+1789C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351311 | ||||||
| chr5:45351333
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0190 | 2 | NA18971.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1377+1767G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351333 | ||||||
| chr5:45351350
|
T | C | 133 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1377+1750A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351350 | ||||||
| chr5:45351370
|
TCAA | T | 133 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1377+1727_1377+172 others(7): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351370 | ||||||
| chr5:45351375
|
T | A | 133 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1377+1725A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351375 | ||||||
| chr5:45351376
|
C | T | 133 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1377+1724G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351376 | ||||||
| chr5:45351382
|
G | A | 133 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1377+1718C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351382 | ||||||
| chr5:45351385
|
T | C | 133 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1377+1715A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351385 | ||||||
| chr5:45351392
|
T | C | 133 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1377+1708A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351392 | ||||||
| chr5:45351398
|
C | T | 133 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1377+1702G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351398 | ||||||
| chr5:45351432
|
A | G | 133 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1377+1668T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351432 | ||||||
| chr5:45351439
|
A | G | 133 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1377+1661T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351439 | ||||||
| chr5:45351442
|
T | A | 133 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1377+1658A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351442 | ||||||
| chr5:45351462
|
G | A | 133 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1377+1638C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351462 | ||||||
| chr5:45351473
|
C | G | 133 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1377+1627G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351473 | ||||||
| chr5:45351482
|
C | T | 133 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1377+1618G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351482 | ||||||
| chr5:45351506
|
A | C | 133 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1377+1594T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351506 | ||||||
| chr5:45351511
|
A | C | 133 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1377+1589T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351511 | ||||||
| chr5:45351514
|
A | C | 133 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1377+1586T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351514 | ||||||
| chr5:45351564
|
G | T | 133 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1377+1536C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351564 | ||||||
| chr5:45351598
|
C | A | 133 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1377+1502G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351598 | ||||||
| chr5:45351619
|
C | A | 11 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(8): Show | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1377+1481G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351619 | ||||||
| chr5:45351783
|
T | C | 131 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1377+1317A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351783 | ||||||
| chr5:45351828
|
C | T | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1377+1272G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351828 | ||||||
| chr5:45351843
|
G | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1377+1257C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45351843 | ||||||
| chr5:45352089
|
C | A | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1377+1011G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45352089 | ||||||
| chr5:45352091
|
G | T | 1 | a0001c0001t0003g0215 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1377+1009C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45352091 | ||||||
| chr5:45352196
|
A | G | 67 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1377+904T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45352196 | ||||||
| chr5:45352268
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1377+832G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45352268 | ||||||
| chr5:45352285
|
G | T | 35 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(32): Show | 35 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1377+815C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45352285 | ||||||
| chr5:45352378
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1377+722T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45352378 | ||||||
| chr5:45352388
|
G | A | 2 | a0001c0001t0001g0149a0001c0001t0002g0152 | 2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1377+712C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45352388 | ||||||
| chr5:45352601
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1377+499C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45352601 | ||||||
| chr5:45352632
|
A | G | 2 | a0001c0001t0003g0118a0001c0001t0003g0120 | 2 | HG00735.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.1377+468T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45352632 | ||||||
| chr5:45352693
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1377+407A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45352693 | ||||||
| chr5:45352967
|
A | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1377+133T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45352967 | ||||||
| chr5:45353067
|
T | C | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1377+33A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 5/7 | chr5 | 45353067 | ||||||
| chr5:45353344
|
TCA | T | 8 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(5): Show | 8 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1231-100_1231-99de others(3): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45353344 | ||||||
| chr5:45353451
|
C | G | 1 | a0001c0001t0002g0041 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1231-205G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45353451 | ||||||
| chr5:45353491
|
T | C | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1231-245A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45353491 | ||||||
| chr5:45353574
|
T | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1231-328A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45353574 | ||||||
| chr5:45353631
|
C | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1231-385G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45353631 | ||||||
| chr5:45354029
|
C | T | 2 | a0001c0001t0002g0121a0001c0006t0002g0219 | 2 | HG01346.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1231-783G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45354029 | ||||||
| chr5:45354697
|
G | A | 131 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1231-1451C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45354697 | ||||||
| chr5:45354828
|
A | C | 3 | a0001c0001t0003g0084a0001c0001t0003g0101a0001c0001t0036g0186 | 3 | NA19003.hp1 NA19011.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1231-1582T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45354828 | ||||||
| chr5:45355077
|
T | C | 3 | a0001c0001t0002g0015a0001c0001t0002g0082a0001c0001t0016g0014 | 3 | HG02615.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1231-1831A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45355077 | ||||||
| chr5:45355229
|
T | C | 1 | a0001c0001t0002g0025 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1231-1983A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45355229 | ||||||
| chr5:45355263
|
C | A | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1231-2017G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45355263 | ||||||
| chr5:45355379
|
C | T | 1 | a0001c0001t0002g0058 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1231-2133G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45355379 | ||||||
| chr5:45355411
|
C | A | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1231-2165G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45355411 | ||||||
| chr5:45355772
|
T | A | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1231-2526A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45355772 | ||||||
| chr5:45356004
|
C | A | 8 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(5): Show | 8 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1231-2758G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45356004 | ||||||
| chr5:45356115
|
C | T | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1231-2869G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45356115 | ||||||
| chr5:45356162
|
C | A | 1 | a0001c0001t0002g0040 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1231-2916G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45356162 | ||||||
| chr5:45356208
|
T | C | 1 | a0001c0001t0002g0026 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1231-2962A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45356208 | ||||||
| chr5:45356366
|
T | C | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1231-3120A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45356366 | ||||||
| chr5:45356473
|
A | G | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1231-3227T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45356473 | ||||||
| chr5:45356532
|
C | T | 131 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1231-3286G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45356532 | ||||||
| chr5:45356535
|
G | A | 2 | a0001c0001t0011g0163a0001c0001t0011g0164 | 2 | NA18992.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1231-3289C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45356535 | ||||||
| chr5:45356630
|
G | T | 1 | a0001c0001t0002g0026 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1231-3384C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45356630 | ||||||
| chr5:45357009
|
G | C | 2 | a0001c0001t0001g0085a0001c0001t0001g0190 | 2 | NA18971.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1231-3763C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45357009 | ||||||
| chr5:45357116
|
A | G | 1 | a0001c0001t0040g0175 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1231-3870T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45357116 | ||||||
| chr5:45357304
|
C | G | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1231-4058G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45357304 | ||||||
| chr5:45358115
|
T | A | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1231-4869A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45358115 | ||||||
| chr5:45358398
|
T | C | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1231-5152A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45358398 | ||||||
| chr5:45358445
|
C | A | 1 | a0001c0001t0002g0019 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1231-5199G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45358445 | ||||||
| chr5:45358469
|
T | G | 1 | a0001c0001t0005g0126 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1231-5223A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45358469 | ||||||
| chr5:45358547
|
C | T | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG00323.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1231-5301G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45358547 | ||||||
| chr5:45358644
|
A | G | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1231-5398T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45358644 | ||||||
| chr5:45358924
|
C | T | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1231-5678G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45358924 | ||||||
| chr5:45359258
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG01952.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1231-6012C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45359258 | ||||||
| chr5:45359404
|
CA | C | 32 | a0001c0001t0001g0065a0001c0001t0001g0135a0001c0001t0001g0204others(29): Show | 32 | HG00438.hp1 HG00609.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.1231-6159delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45359404 | ||||||
| chr5:45359412
|
A | T | 1 | a0001c0001t0004g0020 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1231-6166T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45359412 | ||||||
| chr5:45359414
|
A | AT | 2 | a0001c0001t0002g0052a0001c0001t0002g0067 | 2 | HG01884.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1231-6169_1231-616 others(5): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45359414 | ||||||
| chr5:45359414
|
A | T | 25 | a0001c0001t0001g0034a0001c0001t0001g0065a0001c0001t0002g0012others(22): Show | 25 | HG00438.hp1 HG00609.hp2 HG01516.hp1 others(22): Show |
intron_variant | MODIFIER | c.1231-6168T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45359414 | ||||||
| chr5:45359416
|
A | AT | 9 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG00597.hp1 HG01109.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.1231-6171_1231-617 others(5): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45359416 | ||||||
| chr5:45359416
|
A | ATAT | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1231-6171_1231-617 others(7): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45359416 | ||||||
| chr5:45359416
|
A | T | 76 | a0001c0001t0001g0034a0001c0001t0001g0051a0001c0001t0001g0065others(73): Show | 76 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.1231-6170T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45359416 | ||||||
| chr5:45359416
|
AAT | A | 6 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(3): Show | 6 | HG01261.hp2 HG02055.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-6172_1231-617 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45359416 | ||||||
| chr5:45359417
|
AT | A | 3 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0142 | 3 | HG02886.hp2 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1231-6172delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45359417 | ||||||
| chr5:45359418
|
T | A | 6 | a0001c0001t0001g0147a0001c0001t0002g0146a0001c0001t0003g0109others(3): Show | 6 | HG02027.hp2 HG02165.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1231-6172A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45359418 | ||||||
| chr5:45359420
|
T | A | 9 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(6): Show | 9 | HG01261.hp2 HG02055.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1231-6174A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45359420 | ||||||
| chr5:45359574
|
T | A | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1231-6328A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45359574 | ||||||
| chr5:45359742
|
C | G | 1 | a0001c0001t0029g0070 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1231-6496G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45359742 | ||||||
| chr5:45359941
|
G | GTA | 3 | a0001c0001t0001g0167a0001c0001t0001g0208a0001c0001t0033g0213 | 3 | HG02056.hp1 HG03579.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.1231-6697_1231-669 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45359941 | ||||||
| chr5:45359941
|
GTA | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1231-6697_1231-669 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45359941 | ||||||
| chr5:45359956
|
T | C | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1231-6710A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45359956 | ||||||
| chr5:45359959
|
A | T | 13 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(10): Show | 13 | HG00735.hp1 HG00738.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1231-6713T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45359959 | ||||||
| chr5:45359961
|
T | A | 2 | a0001c0001t0025g0217a0003c0003t0035g0220 | 2 | HG01192.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1231-6715A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45359961 | ||||||
| chr5:45361073
|
T | C | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1231-7827A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45361073 | ||||||
| chr5:45361112
|
T | G | 5 | a0001c0001t0001g0013a0001c0001t0001g0037a0001c0001t0001g0045others(2): Show | 5 | HG00735.hp2 HG00741.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231-7866A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45361112 | ||||||
| chr5:45361401
|
C | T | 1 | a0001c0001t0002g0043 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1231-8155G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45361401 | ||||||
| chr5:45361406
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1231-8160G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45361406 | ||||||
| chr5:45361478
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1231-8232T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45361478 | ||||||
| chr5:45361599
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1231-8353C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45361599 | ||||||
| chr5:45361671
|
C | A | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1231-8425G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45361671 | ||||||
| chr5:45361693
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1231-8447T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45361693 | ||||||
| chr5:45362078
|
A | T | 34 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(31): Show | 34 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1231-8832T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45362078 | ||||||
| chr5:45362143
|
GGTGTGTG others(7): Show |
G | 1 | a0001c0001t0002g0019 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1231-8911_1231-889 others(18): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45362143 | ||||||
| chr5:45362154
|
T | TTG | 18 | a0001c0001t0001g0179a0001c0001t0001g0192a0001c0001t0002g0027others(15): Show | 18 | HG00735.hp1 HG01109.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.1231-8910_1231-890 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45362154 | ||||||
| chr5:45362154
|
TTG | T | 27 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0157others(24): Show | 27 | HG00099.hp2 HG00323.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1231-8910_1231-890 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45362154 | ||||||
| chr5:45362154
|
TTGTG | T | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0003g0086 | 3 | HG00558.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1231-8912_1231-890 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45362154 | ||||||
| chr5:45362184
|
GTATC | G | 8 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(5): Show | 8 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1231-8942_1231-893 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45362184 | ||||||
| chr5:45362694
|
A | G | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1231-9448T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45362694 | ||||||
| chr5:45362961
|
C | T | 217 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1231-9715G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45362961 | ||||||
| chr5:45363132
|
TTATATAT others(13): Show |
T | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1231-9906_1231-988 others(24): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45363132 | ||||||
| chr5:45363132
|
TTATATAT others(15): Show |
T | 7 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1231-9908_1231-988 others(26): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45363132 | ||||||
| chr5:45363141
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1231-9895A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45363141 | ||||||
| chr5:45363145
|
C | CAT | 18 | a0001c0001t0001g0013a0001c0001t0001g0037a0001c0001t0001g0045others(15): Show | 18 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.1231-9901_1231-990 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45363145 | ||||||
| chr5:45363145
|
C | CATATAT | 2 | a0001c0001t0005g0122a0001c0001t0005g0123 | 2 | HG02055.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1231-9905_1231-990 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45363145 | ||||||
| chr5:45363145
|
C | CATATATA others(1): Show |
4 | a0001c0001t0005g0126a0001c0001t0005g0129a0001c0001t0005g0130others(1): Show | 4 | HG02886.hp2 HG02897.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1231-9907_1231-990 others(12): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45363145 | ||||||
| chr5:45363145
|
C | CATATATA others(3): Show |
4 | a0001c0001t0005g0124a0001c0001t0005g0125a0001c0001t0005g0127others(1): Show | 4 | HG01261.hp2 HG01891.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1231-9909_1231-990 others(14): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45363145 | ||||||
| chr5:45363145
|
C | CATATATA others(7): Show |
1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1231-9913_1231-990 others(18): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45363145 | ||||||
| chr5:45363145
|
CAT | C | 51 | a0001c0001t0001g0085a0001c0001t0001g0150a0001c0001t0001g0151others(48): Show | 51 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.1231-9901_1231-990 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45363145 | ||||||
| chr5:45363145
|
CATAT | C | 68 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(65): Show | 68 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.1231-9903_1231-990 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45363145 | ||||||
| chr5:45363154
|
A | T | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1231-9908T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45363154 | ||||||
| chr5:45363409
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1231-10163T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45363409 | ||||||
| chr5:45363531
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1231-10285T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45363531 | ||||||
| chr5:45363549
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1231-10303T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45363549 | ||||||
| chr5:45363755
|
G | T | 1 | a0001c0001t0003g0087 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1231-10509C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45363755 | ||||||
| chr5:45363757
|
T | C | 1 | a0001c0001t0003g0087 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1231-10511A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45363757 | ||||||
| chr5:45363774
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1231-10528G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45363774 | ||||||
| chr5:45363816
|
C | A | 8 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(5): Show | 8 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1231-10570G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45363816 | ||||||
| chr5:45363831
|
C | T | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1231-10585G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45363831 | ||||||
| chr5:45364123
|
C | T | 11 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(8): Show | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1231-10877G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45364123 | ||||||
| chr5:45364226
|
AC | A | 2 | a0001c0001t0011g0163a0001c0001t0011g0164 | 2 | NA18992.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1231-10981delG | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45364226 | ||||||
| chr5:45364504
|
T | C | 1 | a0001c0001t0005g0127 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1231-11258A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45364504 | ||||||
| chr5:45364550
|
T | C | 2 | a0001c0001t0001g0187a0001c0001t0040g0175 | 2 | NA18977.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1231-11304A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45364550 | ||||||
| chr5:45364773
|
T | C | 131 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1231-11527A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45364773 | ||||||
| chr5:45364969
|
A | G | 32 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0157others(29): Show | 32 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1231-11723T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45364969 | ||||||
| chr5:45365086
|
T | A | 2 | a0001c0001t0006g0143a0001c0001t0006g0203 | 2 | HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1231-11840A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45365086 | ||||||
| chr5:45365282
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1231-12036A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45365282 | ||||||
| chr5:45365321
|
A | G | 3 | a0001c0001t0002g0042a0001c0001t0002g0046a0001c0001t0030g0008 | 3 | HG00738.hp2 HG02258.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1231-12075T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45365321 | ||||||
| chr5:45365429
|
A | C | 8 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(5): Show | 8 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1231-12183T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45365429 | ||||||
| chr5:45365561
|
T | A | 1 | a0001c0001t0003g0188 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1231-12315A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45365561 | ||||||
| chr5:45365602
|
T | G | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1231-12356A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45365602 | ||||||
| chr5:45365887
|
T | A | 1 | a0001c0001t0003g0087 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1231-12641A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45365887 | ||||||
| chr5:45365955
|
T | C | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG01952.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1231-12709A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45365955 | ||||||
| chr5:45366009
|
A | G | 8 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(5): Show | 8 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1231-12763T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45366009 | ||||||
| chr5:45366164
|
T | TTG | 38 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(35): Show | 38 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1231-12920_1231-12 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45366164 | ||||||
| chr5:45366164
|
T | TTGTG | 3 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0033g0213 | 3 | HG03579.hp1 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1231-12922_1231-12 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45366164 | ||||||
| chr5:45366164
|
TTG | T | 50 | a0001c0001t0001g0011a0001c0001t0001g0051a0001c0001t0001g0074others(47): Show | 50 | HG00099.hp1 HG00597.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1231-12920_1231-12 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45366164 | ||||||
| chr5:45366164
|
TTGTG | T | 3 | a0001c0001t0001g0060a0001c0001t0007g0115a0001c0001t0007g0214 | 3 | HG02451.hp1 HG02809.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1231-12922_1231-12 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45366164 | ||||||
| chr5:45366241
|
T | C | 6 | a0001c0001t0001g0051a0001c0001t0002g0049a0001c0001t0002g0050others(3): Show | 6 | HG01891.hp2 HG03041.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1231-12995A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45366241 | ||||||
| chr5:45366441
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0039g0218 | 2 | HG01081.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1231-13195G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45366441 | ||||||
| chr5:45366442
|
G | A | 1 | a0001c0001t0002g0019 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1231-13196C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45366442 | ||||||
| chr5:45366686
|
T | C | 34 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(31): Show | 34 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1231-13440A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45366686 | ||||||
| chr5:45366687
|
A | C | 1 | a0001c0001t0003g0087 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1231-13441T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45366687 | ||||||
| chr5:45366824
|
T | C | 39 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(36): Show | 39 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-13578A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45366824 | ||||||
| chr5:45366937
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1231-13691G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45366937 | ||||||
| chr5:45366963
|
C | T | 1 | a0001c0001t0019g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1231-13717G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45366963 | ||||||
| chr5:45367007
|
C | T | 35 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(32): Show | 35 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1231-13761G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45367007 | ||||||
| chr5:45367317
|
A | G | 1 | a0001c0001t0003g0090 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1231-14071T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45367317 | ||||||
| chr5:45367634
|
G | A | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1231-14388C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45367634 | ||||||
| chr5:45367806
|
G | A | 2 | a0001c0001t0012g0064a0001c0001t0012g0137 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1231-14560C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45367806 | ||||||
| chr5:45367905
|
G | C | 1 | a0001c0001t0001g0207 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1231-14659C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45367905 | ||||||
| chr5:45368155
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1231-14909A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45368155 | ||||||
| chr5:45368282
|
A | G | 1 | a0001c0001t0019g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1231-15036T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45368282 | ||||||
| chr5:45368397
|
G | A | 1 | a0001c0001t0005g0124 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1231-15151C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45368397 | ||||||
| chr5:45368701
|
C | A | 1 | a0001c0001t0003g0188 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1231-15455G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45368701 | ||||||
| chr5:45368713
|
A | ACT | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1231-15468_1231-15 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45368713 | ||||||
| chr5:45368713
|
A | ATT | 132 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.1231-15468_1231-15 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45368713 | ||||||
| chr5:45368802
|
C | G | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1231-15556G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45368802 | ||||||
| chr5:45368944
|
C | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1231-15698G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45368944 | ||||||
| chr5:45369099
|
C | CT | 8 | a0001c0001t0001g0074a0001c0001t0001g0170a0001c0001t0013g0078others(5): Show | 8 | HG01261.hp1 HG02055.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1231-15854dupA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45369099 | ||||||
| chr5:45369373
|
C | T | 7 | a0001c0001t0001g0051a0001c0001t0002g0049a0001c0001t0002g0050others(4): Show | 7 | HG01891.hp2 HG03041.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1231-16127G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45369373 | ||||||
| chr5:45369374
|
C | A | 7 | a0001c0001t0001g0051a0001c0001t0002g0049a0001c0001t0002g0050others(4): Show | 7 | HG01891.hp2 HG03041.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1231-16128G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45369374 | ||||||
| chr5:45369375
|
C | A | 7 | a0001c0001t0001g0051a0001c0001t0002g0049a0001c0001t0002g0050others(4): Show | 7 | HG01891.hp2 HG03041.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1231-16129G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45369375 | ||||||
| chr5:45369377
|
T | TC | 7 | a0001c0001t0001g0051a0001c0001t0002g0049a0001c0001t0002g0050others(4): Show | 7 | HG01891.hp2 HG03041.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1231-16132_1231-16 others(7): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45369377 | ||||||
| chr5:45369378
|
G | T | 7 | a0001c0001t0001g0051a0001c0001t0002g0049a0001c0001t0002g0050others(4): Show | 7 | HG01891.hp2 HG03041.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1231-16132C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45369378 | ||||||
| chr5:45369380
|
C | T | 7 | a0001c0001t0001g0051a0001c0001t0002g0049a0001c0001t0002g0050others(4): Show | 7 | HG01891.hp2 HG03041.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1231-16134G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45369380 | ||||||
| chr5:45369382
|
T | A | 7 | a0001c0001t0001g0051a0001c0001t0002g0049a0001c0001t0002g0050others(4): Show | 7 | HG01891.hp2 HG03041.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1231-16136A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45369382 | ||||||
| chr5:45369808
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1231-16562C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45369808 | ||||||
| chr5:45370301
|
C | G | 1 | a0001c0001t0002g0040 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1231-17055G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45370301 | ||||||
| chr5:45370318
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1231-17072A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45370318 | ||||||
| chr5:45370629
|
T | TTTTTTAT others(39): Show |
1 | a0001c0001t0002g0140 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1231-17384_1231-17 others(52): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45370629 | ||||||
| chr5:45370630
|
C | A | 1 | a0001c0001t0002g0140 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1231-17384G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45370630 | ||||||
| chr5:45370632
|
C | A | 1 | a0001c0001t0002g0140 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1231-17386G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45370632 | ||||||
| chr5:45370634
|
A | T | 1 | a0001c0001t0002g0140 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1231-17388T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45370634 | ||||||
| chr5:45370635
|
G | T | 1 | a0001c0001t0002g0140 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1231-17389C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45370635 | ||||||
| chr5:45370739
|
T | C | 11 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(8): Show | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1231-17493A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45370739 | ||||||
| chr5:45371027
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1231-17781T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45371027 | ||||||
| chr5:45371191
|
T | A | 1 | a0001c0001t0024g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1231-17945A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45371191 | ||||||
| chr5:45371265
|
T | C | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1231-18019A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45371265 | ||||||
| chr5:45371525
|
G | A | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1231-18279C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45371525 | ||||||
| chr5:45371554
|
T | G | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1231-18308A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45371554 | ||||||
| chr5:45371594
|
T | C | 1 | a0001c0001t0003g0188 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1231-18348A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45371594 | ||||||
| chr5:45371595
|
A | T | 1 | a0001c0001t0003g0188 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1231-18349T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45371595 | ||||||
| chr5:45371625
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1231-18379G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45371625 | ||||||
| chr5:45371626
|
G | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1231-18380C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45371626 | ||||||
| chr5:45371766
|
A | AT | 9 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(6): Show | 9 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1231-18521_1231-18 others(7): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45371766 | ||||||
| chr5:45371766
|
A | T | 47 | a0001c0001t0001g0051a0001c0001t0001g0065a0001c0001t0001g0160others(44): Show | 47 | HG00438.hp1 HG00609.hp2 HG01192.hp2 others(44): Show |
intron_variant | MODIFIER | c.1231-18520T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45371766 | ||||||
| chr5:45371768
|
T | A | 3 | a0001c0001t0001g0167a0001c0001t0002g0028a0001c0006t0002g0219 | 3 | HG02056.hp1 NA18962.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1231-18522A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45371768 | ||||||
| chr5:45371776
|
T | C | 3 | a0001c0001t0001g0173a0001c0001t0011g0163a0001c0001t0011g0164 | 3 | NA18992.hp1 NA19000.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1231-18530A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45371776 | ||||||
| chr5:45371796
|
C | G | 1 | a0001c0001t0024g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1231-18550G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45371796 | ||||||
| chr5:45371898
|
A | ATTAT | 130 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1231-18656_1231-18 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45371898 | ||||||
| chr5:45371947
|
A | T | 67 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1231-18701T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45371947 | ||||||
| chr5:45371990
|
T | G | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1231-18744A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45371990 | ||||||
| chr5:45372002
|
A | ATT | 224 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(221): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1231-18757_1231-18 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372002 | ||||||
| chr5:45372002
|
A | T | 1 | a0001c0001t0001g0216 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1231-18756T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372002 | ||||||
| chr5:45372037
|
T | C | 80 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(77): Show | 80 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.1231-18791A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372037 | ||||||
| chr5:45372041
|
TATTATAT others(21): Show |
T | 6 | a0001c0001t0003g0087a0001c0001t0003g0093a0001c0001t0003g0094others(3): Show | 6 | HG01071.hp1 HG01081.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1231-18823_1231-18 others(34): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372041 | ||||||
| chr5:45372044
|
T | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1231-18798A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372044 | ||||||
| chr5:45372044
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1231-18798A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372044 | ||||||
| chr5:45372045
|
ATATATAT others(20): Show |
A | 29 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(26): Show | 29 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.1231-18826_1231-18 others(33): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372045 | ||||||
| chr5:45372052
|
TAATATAA others(49): Show |
T | 3 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG02647.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1231-18862_1231-18 others(62): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372052 | ||||||
| chr5:45372060
|
T | TTATACA | 9 | a0001c0001t0001g0051a0001c0001t0002g0023a0001c0001t0002g0038others(6): Show | 9 | HG00280.hp1 HG01891.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1231-18815_1231-18 others(12): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372060 | ||||||
| chr5:45372060
|
TTATATTA others(24): Show |
T | 3 | a0001c0001t0003g0092a0001c0001t0003g0098a0001c0001t0003g0099 | 3 | HG01361.hp1 HG02129.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1231-18845_1231-18 others(37): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372060 | ||||||
| chr5:45372062
|
ATATTATA others(46): Show |
A | 9 | a0001c0001t0006g0057a0001c0001t0013g0078a0001c0001t0013g0079others(6): Show | 9 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1231-18869_1231-18 others(59): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372062 | ||||||
| chr5:45372063
|
T | TACATATA others(16): Show |
3 | a0001c0001t0002g0046a0001c0001t0002g0052a0001c0001t0030g0008 | 3 | HG00738.hp2 HG03669.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1231-18818_1231-18 others(29): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372063 | ||||||
| chr5:45372063
|
T | TACATATA others(72): Show |
1 | a0001c0001t0002g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1231-18818_1231-18 others(85): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372063 | ||||||
| chr5:45372064
|
A | AC | 65 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0065others(62): Show | 65 | HG00099.hp1 HG00438.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.1231-18819_1231-18 others(7): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372064 | ||||||
| chr5:45372065
|
T | A | 65 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0065others(62): Show | 65 | HG00099.hp1 HG00438.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.1231-18819A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372065 | ||||||
| chr5:45372066
|
T | A | 1 | a0001c0001t0003g0103 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1231-18820A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372066 | ||||||
| chr5:45372066
|
T | C | 1 | a0001c0001t0005g0142 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1231-18820A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372066 | ||||||
| chr5:45372067
|
A | T | 1 | a0001c0001t0003g0103 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1231-18821T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372067 | ||||||
| chr5:45372071
|
A | ATTATATA others(21): Show |
1 | a0001c0001t0001g0102 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1231-18853_1231-18 others(34): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372071 | ||||||
| chr5:45372071
|
A | T | 66 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0065others(63): Show | 66 | HG00099.hp1 HG00438.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.1231-18825T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372071 | ||||||
| chr5:45372071
|
AT | A | 7 | a0001c0001t0003g0087a0001c0001t0003g0093a0001c0001t0003g0094others(4): Show | 7 | HG01071.hp1 HG01081.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1231-18826delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372071 | ||||||
| chr5:45372072
|
T | A | 66 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0065others(63): Show | 66 | HG00099.hp1 HG00438.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.1231-18826A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372072 | ||||||
| chr5:45372072
|
T | TATAATAT others(16): Show |
7 | a0001c0001t0002g0023a0001c0001t0002g0038a0001c0001t0002g0047others(4): Show | 7 | HG00280.hp1 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1231-18827_1231-18 others(29): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372072 | ||||||
| chr5:45372072
|
T | TATAATAT others(44): Show |
2 | a0001c0001t0001g0051a0001c0001t0002g0050 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1231-18827_1231-18 others(57): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372072 | ||||||
| chr5:45372072
|
T | TATATTA | 4 | a0001c0001t0002g0042a0001c0001t0002g0046a0001c0001t0002g0052others(1): Show | 4 | HG00738.hp2 HG02258.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-18827_1231-18 others(12): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372072 | ||||||
| chr5:45372084
|
T | C | 6 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0156others(3): Show | 6 | HG00597.hp1 NA18939.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-18838A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372084 | ||||||
| chr5:45372100
|
T | A | 118 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.1231-18854A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372100 | ||||||
| chr5:45372113
|
A | T | 1 | a0001c0001t0003g0103 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1231-18867T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372113 | ||||||
| chr5:45372116
|
T | TATATATT others(41): Show |
1 | a0001c0001t0028g0174 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1231-18871_1231-18 others(54): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372116 | ||||||
| chr5:45372121
|
A | T | 9 | a0001c0001t0006g0057a0001c0001t0013g0078a0001c0001t0013g0079others(6): Show | 9 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1231-18875T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372121 | ||||||
| chr5:45372122
|
T | A | 10 | a0001c0001t0006g0057a0001c0001t0013g0078a0001c0001t0013g0079others(7): Show | 10 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1231-18876A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372122 | ||||||
| chr5:45372122
|
T | TTA | 108 | a0001c0001t0001g0034a0001c0001t0001g0051a0001c0001t0001g0065others(105): Show | 108 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1231-18878_1231-18 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372122 | ||||||
| chr5:45372124
|
A | G | 1 | a0001c0001t0003g0103 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1231-18878T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372124 | ||||||
| chr5:45372130
|
A | G | 1 | a0001c0001t0029g0070 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1231-18884T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372130 | ||||||
| chr5:45372133
|
A | T | 2 | a0001c0001t0003g0103a0001c0001t0029g0070 | 2 | NA18942.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.1231-18887T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372133 | ||||||
| chr5:45372138
|
A | T | 1 | a0001c0001t0029g0070 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1231-18892T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372138 | ||||||
| chr5:45372140
|
A | AT | 128 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.1231-18895_1231-18 others(7): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372140 | ||||||
| chr5:45372140
|
A | T | 2 | a0001c0001t0001g0206a0001c0001t0033g0213 | 2 | HG02738.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1231-18894T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372140 | ||||||
| chr5:45372141
|
A | T | 1 | a0001c0001t0003g0103 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1231-18895T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372141 | ||||||
| chr5:45372142
|
T | A | 1 | a0001c0001t0003g0103 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1231-18896A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372142 | ||||||
| chr5:45372143
|
A | G | 1 | a0001c0001t0029g0070 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1231-18897T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372143 | ||||||
| chr5:45372145
|
A | T | 1 | a0001c0001t0003g0103 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1231-18899T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372145 | ||||||
| chr5:45372146
|
T | A | 129 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1231-18900A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372146 | ||||||
| chr5:45372146
|
T | TATATTAT others(105): Show |
1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1231-18901_1231-18 others(118): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372146 | ||||||
| chr5:45372151
|
T | A | 17 | a0001c0001t0001g0065a0001c0001t0004g0017a0001c0001t0004g0020others(14): Show | 17 | HG00438.hp1 HG00609.hp2 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.1231-18905A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372151 | ||||||
| chr5:45372152
|
A | T | 1 | a0001c0001t0029g0070 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1231-18906T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372152 | ||||||
| chr5:45372156
|
T | A | 1 | a0001c0001t0003g0103 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1231-18910A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372156 | ||||||
| chr5:45372157
|
G | A | 1 | a0001c0001t0029g0070 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1231-18911C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372157 | ||||||
| chr5:45372157
|
G | C | 1 | a0001c0001t0003g0103 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1231-18911C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372157 | ||||||
| chr5:45372157
|
GT | G | 128 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.1231-18912delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372157 | ||||||
| chr5:45372158
|
T | A | 1 | a0001c0001t0003g0103 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1231-18912A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372158 | ||||||
| chr5:45372159
|
T | A | 1 | a0001c0001t0029g0070 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1231-18913A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372159 | ||||||
| chr5:45372166
|
TA | T | 129 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1231-18921delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372166 | ||||||
| chr5:45372172
|
T | A | 1 | a0001c0001t0029g0070 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1231-18926A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372172 | ||||||
| chr5:45372173
|
A | G | 129 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1231-18927T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372173 | ||||||
| chr5:45372181
|
A | T | 128 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.1231-18935T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372181 | ||||||
| chr5:45372189
|
C | T | 130 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1231-18943G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372189 | ||||||
| chr5:45372193
|
T | A | 2 | a0001c0001t0002g0121a0001c0001t0029g0070 | 2 | HG01346.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.1231-18947A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372193 | ||||||
| chr5:45372194
|
A | AT | 128 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.1231-18949_1231-18 others(7): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372194 | ||||||
| chr5:45372194
|
A | T | 2 | a0001c0001t0002g0121a0001c0001t0029g0070 | 2 | HG01346.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.1231-18948T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372194 | ||||||
| chr5:45372196
|
T | C | 1 | a0001c0001t0002g0058 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1231-18950A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372196 | ||||||
| chr5:45372198
|
T | A | 17 | a0001c0001t0001g0065a0001c0001t0004g0017a0001c0001t0004g0020others(14): Show | 17 | HG00438.hp1 HG00609.hp2 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.1231-18952A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372198 | ||||||
| chr5:45372200
|
A | T | 1 | a0001c0001t0003g0103 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1231-18954T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372200 | ||||||
| chr5:45372201
|
T | TA | 64 | a0001c0001t0001g0060a0001c0001t0001g0074a0001c0001t0001g0076others(61): Show | 64 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1231-18956dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372201 | ||||||
| chr5:45372203
|
C | A | 66 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(63): Show | 66 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1231-18957G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372203 | ||||||
| chr5:45372203
|
C | T | 2 | a0001c0001t0003g0103a0001c0001t0029g0070 | 2 | NA18942.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.1231-18957G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372203 | ||||||
| chr5:45372206
|
A | T | 1 | a0001c0001t0003g0103 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1231-18960T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372206 | ||||||
| chr5:45372207
|
T | TTA | 129 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1231-18963_1231-18 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372207 | ||||||
| chr5:45372225
|
A | G | 6 | a0001c0001t0001g0051a0001c0001t0002g0049a0001c0001t0002g0050others(3): Show | 6 | HG01891.hp2 HG03041.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1231-18979T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372225 | ||||||
| chr5:45372227
|
A | T | 1 | a0001c0001t0003g0103 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1231-18981T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372227 | ||||||
| chr5:45372234
|
ATTATATT others(29): Show |
A | 8 | a0001c0001t0003g0087a0001c0001t0003g0093a0001c0001t0003g0094others(5): Show | 8 | HG00099.hp2 HG01071.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.1231-19024_1231-18 others(42): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372234 | ||||||
| chr5:45372242
|
T | A | 3 | a0001c0001t0003g0103a0001c0001t0003g0110a0001c0001t0003g0111 | 3 | HG02056.hp2 NA18942.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1231-18996A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372242 | ||||||
| chr5:45372257
|
AT | A | 101 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(98): Show | 101 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1231-19012delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372257 | ||||||
| chr5:45372258
|
T | C | 1 | a0001c0001t0002g0082 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1231-19012A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372258 | ||||||
| chr5:45372269
|
AT | A | 20 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0157others(17): Show | 20 | HG00323.hp2 HG00558.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.1231-19024delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372269 | ||||||
| chr5:45372279
|
AT | A | 4 | a0001c0001t0001g0045a0001c0001t0003g0063a0001c0001t0003g0158others(1): Show | 4 | HG01071.hp2 HG01081.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.1231-19034delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372279 | ||||||
| chr5:45372283
|
T | C | 4 | a0001c0001t0002g0026a0001c0001t0002g0028a0001c0001t0002g0097others(1): Show | 4 | HG00673.hp1 HG02040.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-19037A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372283 | ||||||
| chr5:45372301
|
T | A | 1 | a0001c0001t0002g0044 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1231-19055A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372301 | ||||||
| chr5:45372313
|
G | A | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1231-19067C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372313 | ||||||
| chr5:45372328
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1231-19082A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372328 | ||||||
| chr5:45372333
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1231-19087A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372333 | ||||||
| chr5:45372351
|
T | C | 1 | a0001c0001t0007g0214 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1231-19105A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372351 | ||||||
| chr5:45372351
|
T | G | 1 | a0001c0001t0002g0049 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1231-19105A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372351 | ||||||
| chr5:45372365
|
A | T | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1231-19119T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372365 | ||||||
| chr5:45372369
|
CAT | C | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1231-19125_1231-19 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372369 | ||||||
| chr5:45372390
|
T | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1231-19144A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372390 | ||||||
| chr5:45372404
|
T | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1231-19158A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372404 | ||||||
| chr5:45372423
|
A | G | 8 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(5): Show | 8 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1231-19177T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372423 | ||||||
| chr5:45372436
|
C | A | 11 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(8): Show | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1231-19190G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372436 | ||||||
| chr5:45372440
|
T | C | 1 | a0001c0001t0019g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1231-19194A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372440 | ||||||
| chr5:45372440
|
T | TATATAAA others(18): Show |
8 | a0001c0001t0001g0116a0001c0001t0001g0185a0001c0001t0003g0117others(5): Show | 8 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1231-19219_1231-19 others(31): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372440 | ||||||
| chr5:45372440
|
T | TATATAAA others(43): Show |
2 | a0001c0001t0010g0004a0001c0001t0010g0005 | 2 | NA19009.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1231-19244_1231-19 others(56): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372440 | ||||||
| chr5:45372440
|
TATATAAA others(18): Show |
T | 17 | a0001c0001t0001g0013a0001c0001t0001g0037a0001c0001t0001g0134others(14): Show | 17 | HG00280.hp2 HG00735.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.1231-19219_1231-19 others(31): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372440 | ||||||
| chr5:45372440
|
TATATAAA others(43): Show |
T | 1 | a0001c0001t0002g0146 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1231-19244_1231-19 others(56): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372440 | ||||||
| chr5:45372469
|
T | TAAAAATA others(19): Show |
1 | a0001c0001t0004g0030 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1231-19249_1231-19 others(32): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372469 | ||||||
| chr5:45372540
|
CATATAAA others(67): Show |
C | 7 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0003g0103others(4): Show | 7 | HG02145.hp2 HG02451.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1231-19368_1231-19 others(80): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372540 | ||||||
| chr5:45372561
|
T | C | 1 | a0001c0001t0009g0003 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1231-19315A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372561 | ||||||
| chr5:45372565
|
CATATAAA others(42): Show |
C | 28 | a0001c0001t0003g0086a0001c0001t0003g0087a0001c0001t0003g0090others(25): Show | 28 | HG00099.hp2 HG00558.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.1231-19368_1231-19 others(55): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372565 | ||||||
| chr5:45372602
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1231-19356A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372602 | ||||||
| chr5:45372613
|
T | TA | 20 | a0001c0001t0001g0176a0001c0001t0002g0015a0001c0001t0002g0028others(17): Show | 20 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.1231-19368_1231-19 others(7): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372613 | ||||||
| chr5:45372613
|
T | TACATATA others(19): Show |
54 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0065others(51): Show | 54 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1231-19368_1231-19 others(32): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372613 | ||||||
| chr5:45372613
|
T | TACATATA others(69): Show |
1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1231-19368_1231-19 others(82): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372613 | ||||||
| chr5:45372614
|
T | C | 75 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0065others(72): Show | 75 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1231-19368A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372614 | ||||||
| chr5:45372634
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1231-19388T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372634 | ||||||
| chr5:45372637
|
TTATATAA others(2): Show |
T | 23 | a0001c0001t0001g0051a0001c0001t0002g0050a0001c0001t0002g0066others(20): Show | 23 | HG00323.hp2 HG01243.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.1231-19400_1231-19 others(15): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372637 | ||||||
| chr5:45372653
|
AAAACATT others(7): Show |
A | 23 | a0001c0001t0001g0051a0001c0001t0002g0050a0001c0001t0002g0066others(20): Show | 23 | HG00323.hp2 HG01243.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.1231-19421_1231-19 others(20): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372653 | ||||||
| chr5:45372667
|
T | TA | 108 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0065others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1231-19422dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372667 | ||||||
| chr5:45372698
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1231-19452A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372698 | ||||||
| chr5:45372757
|
T | A | 1 | a0001c0001t0002g0046 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1231-19511A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372757 | ||||||
| chr5:45372772
|
ACGTATTC others(68): Show |
A | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1231-19601_1231-19 others(81): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372772 | ||||||
| chr5:45372790
|
A | T | 11 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(8): Show | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1231-19544T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372790 | ||||||
| chr5:45372795
|
T | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1231-19549A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372795 | ||||||
| chr5:45372795
|
T | G | 11 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(8): Show | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1231-19549A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372795 | ||||||
| chr5:45372799
|
G | A | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1231-19553C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372799 | ||||||
| chr5:45372898
|
C | T | 2 | a0001c0001t0001g0135a0001c0001t0002g0193 | 2 | HG02145.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1231-19652G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372898 | ||||||
| chr5:45372899
|
G | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1231-19653C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372899 | ||||||
| chr5:45372899
|
G | C | 1 | a0001c0001t0001g0074 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1231-19653C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372899 | ||||||
| chr5:45372935
|
A | G | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1231-19689T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372935 | ||||||
| chr5:45372942
|
T | G | 1 | a0001c0001t0004g0030 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1231-19696A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45372942 | ||||||
| chr5:45373061
|
AAT | A | 3 | a0001c0001t0002g0067a0001c0001t0002g0131a0001c0004t0002g0006 | 3 | HG01243.hp1 HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1231-19817_1231-19 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373061 | ||||||
| chr5:45373070
|
A | T | 1 | a0001c0001t0001g0191 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1231-19824T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373070 | ||||||
| chr5:45373159
|
ATATG | A | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1231-19917_1231-19 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373159 | ||||||
| chr5:45373163
|
G | A | 89 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(86): Show | 89 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1231-19917C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373163 | ||||||
| chr5:45373227
|
T | C | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1231-19981A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373227 | ||||||
| chr5:45373244
|
AATATATA others(16): Show |
A | 1 | a0001c0001t0001g0204 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1231-20021_1231-19 others(29): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373244 | ||||||
| chr5:45373257
|
T | C | 2 | a0001c0001t0001g0179a0001c0001t0005g0142 | 2 | HG02886.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1231-20011A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373257 | ||||||
| chr5:45373267
|
T | A | 1 | a0001c0001t0021g0138 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1231-20021A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373267 | ||||||
| chr5:45373277
|
T | A | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1231-20031A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373277 | ||||||
| chr5:45373280
|
T | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1231-20034A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373280 | ||||||
| chr5:45373294
|
T | C | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1231-20048A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373294 | ||||||
| chr5:45373310
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1231-20064A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373310 | ||||||
| chr5:45373390
|
A | G | 1 | a0001c0001t0037g0148 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1231-20144T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373390 | ||||||
| chr5:45373399
|
T | TAA | 131 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1231-20154_1231-20 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373399 | ||||||
| chr5:45373452
|
T | G | 1 | a0001c0001t0019g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1231-20206A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373452 | ||||||
| chr5:45373552
|
T | TATATATT others(25): Show |
2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1231-20307_1231-20 others(38): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373552 | ||||||
| chr5:45373556
|
T | C | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1231-20310A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373556 | ||||||
| chr5:45373566
|
A | G | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1231-20320T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373566 | ||||||
| chr5:45373567
|
T | G | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1231-20321A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373567 | ||||||
| chr5:45373567
|
T | TTATATAC others(25): Show |
3 | a0001c0001t0003g0118a0001c0001t0003g0120a0001c0001t0027g0022 | 3 | HG00735.hp1 HG00738.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.1231-20353_1231-20 others(38): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373567 | ||||||
| chr5:45373567
|
T | TTATATAC others(57): Show |
1 | a0001c0001t0028g0174 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1231-20385_1231-20 others(70): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373567 | ||||||
| chr5:45373567
|
TTATATAC others(57): Show |
T | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1231-20385_1231-20 others(70): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373567 | ||||||
| chr5:45373567
|
TTATATAC others(181): Show |
T | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1231-20509_1231-20 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373567 | ||||||
| chr5:45373567
|
TTATATAC others(245): Show |
T | 10 | a0001c0001t0001g0051a0001c0001t0002g0015a0001c0001t0002g0049others(7): Show | 10 | HG01891.hp2 HG02615.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1231-20573_1231-20 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373567 | ||||||
| chr5:45373594
|
A | ATACGGTA others(117): Show |
1 | a0001c0001t0001g0135 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1231-20472_1231-20 others(130): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373594 | ||||||
| chr5:45373611
|
T | C | 1 | a0001c0001t0002g0052 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1231-20365A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373611 | ||||||
| chr5:45373626
|
ATACGGTA others(85): Show |
A | 33 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(30): Show | 33 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.1231-20472_1231-20 others(98): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373626 | ||||||
| chr5:45373643
|
T | C | 1 | a0001c0001t0002g0052 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1231-20397A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373643 | ||||||
| chr5:45373658
|
ATACGGTA others(53): Show |
A | 1 | a0001c0001t0005g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1231-20472_1231-20 others(66): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373658 | ||||||
| chr5:45373662
|
G | GGTATATA others(25): Show |
1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1231-20417_1231-20 others(38): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373662 | ||||||
| chr5:45373670
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1231-20424G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373670 | ||||||
| chr5:45373671
|
G | A | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1231-20425C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373671 | ||||||
| chr5:45373680
|
AATATATT others(240): Show |
A | 1 | a0001c0001t0002g0052 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1231-20681_1231-20 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373680 | ||||||
| chr5:45373690
|
ATACGGTA others(21): Show |
A | 3 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0195 | 3 | HG00323.hp1 HG01433.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1231-20472_1231-20 others(34): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373690 | ||||||
| chr5:45373718
|
T | TTACGGTA others(25): Show |
1 | a0001c0001t0023g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1231-20504_1231-20 others(38): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373718 | ||||||
| chr5:45373718
|
TTACGGTA others(25): Show |
T | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1231-20504_1231-20 others(38): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373718 | ||||||
| chr5:45373719
|
T | A | 1 | a0001c0001t0001g0205 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1231-20473A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373719 | ||||||
| chr5:45373794
|
C | T | 1 | a0001c0001t0003g0188 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1231-20548G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373794 | ||||||
| chr5:45373798
|
A | T | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1231-20552T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373798 | ||||||
| chr5:45373817
|
C | T | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1231-20571G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373817 | ||||||
| chr5:45373826
|
C | T | 1 | a0001c0001t0005g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1231-20580G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373826 | ||||||
| chr5:45373858
|
C | CGTCATCT others(25): Show |
1 | a0001c0001t0028g0174 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1231-20644_1231-20 others(38): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373858 | ||||||
| chr5:45373858
|
C | T | 39 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(36): Show | 39 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-20612G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373858 | ||||||
| chr5:45373858
|
CGTCATCT others(25): Show |
C | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1231-20644_1231-20 others(38): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373858 | ||||||
| chr5:45373863
|
T | C | 66 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(63): Show | 66 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1231-20617A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373863 | ||||||
| chr5:45373890
|
T | C | 12 | a0001c0001t0005g0089a0001c0001t0005g0122a0001c0001t0005g0123others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1231-20644A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373890 | ||||||
| chr5:45373891
|
G | A | 1 | a0001c0001t0005g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1231-20645C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373891 | ||||||
| chr5:45373913
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1231-20667G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373913 | ||||||
| chr5:45373923
|
A | G | 12 | a0001c0001t0001g0208a0001c0001t0005g0122a0001c0001t0005g0123others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1231-20677T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373923 | ||||||
| chr5:45373927
|
T | TCTATA | 11 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(8): Show | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1231-20682_1231-20 others(11): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373927 | ||||||
| chr5:45373949
|
C | T | 5 | a0001c0001t0005g0127a0001c0001t0005g0129a0001c0001t0005g0130others(2): Show | 5 | HG01891.hp1 HG02258.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231-20703G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373949 | ||||||
| chr5:45373950
|
A | G | 11 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(8): Show | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1231-20704T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373950 | ||||||
| chr5:45373955
|
A | C | 11 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(8): Show | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1231-20709T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373955 | ||||||
| chr5:45373973
|
A | G | 11 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(8): Show | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1231-20727T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373973 | ||||||
| chr5:45373977
|
G | GATACATA others(20): Show |
2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1231-20732_1231-20 others(33): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373977 | ||||||
| chr5:45373977
|
G | T | 11 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(8): Show | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1231-20731C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373977 | ||||||
| chr5:45373977
|
GATACATA others(20): Show |
G | 3 | a0001c0001t0001g0212a0001c0001t0007g0115a0001c0001t0007g0214 | 3 | HG02451.hp1 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1231-20758_1231-20 others(33): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373977 | ||||||
| chr5:45373984
|
A | C | 11 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(8): Show | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1231-20738T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373984 | ||||||
| chr5:45373986
|
T | TATATATT others(18): Show |
10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1231-20741_1231-20 others(31): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373986 | ||||||
| chr5:45373993
|
A | AATATATA others(20): Show |
1 | a0001c0001t0002g0067 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1231-20774_1231-20 others(33): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373993 | ||||||
| chr5:45373993
|
A | AATATATA others(47): Show |
1 | a0001c0001t0002g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1231-20801_1231-20 others(60): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373993 | ||||||
| chr5:45373993
|
A | T | 3 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0022g0080 | 3 | HG02258.hp2 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1231-20747T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373993 | ||||||
| chr5:45373995
|
T | C | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1231-20749A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373995 | ||||||
| chr5:45373999
|
T | C | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1231-20753A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373999 | ||||||
| chr5:45373999
|
T | TTACATAC | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1231-20754_1231-20 others(13): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45373999 | ||||||
| chr5:45374000
|
A | G | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1231-20754T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374000 | ||||||
| chr5:45374001
|
T | G | 11 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(8): Show | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1231-20755A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374001 | ||||||
| chr5:45374004
|
T | G | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1231-20758A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374004 | ||||||
| chr5:45374011
|
A | C | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1231-20765T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374011 | ||||||
| chr5:45374020
|
T | AATATATA others(20): Show |
1 | a0001c0001t0003g0053 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1231-20774_1231-20 others(33): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374020 | ||||||
| chr5:45374022
|
T | C | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1231-20776A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374022 | ||||||
| chr5:45374026
|
T | C | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1231-20780A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374026 | ||||||
| chr5:45374028
|
T | G | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1231-20782A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374028 | ||||||
| chr5:45374031
|
T | G | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1231-20785A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374031 | ||||||
| chr5:45374032
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1231-20786T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374032 | ||||||
| chr5:45374036
|
A | G | 1 | a0001c0001t0002g0193 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1231-20790T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374036 | ||||||
| chr5:45374040
|
T | C | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1231-20794A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374040 | ||||||
| chr5:45374047
|
T | A | 14 | a0001c0001t0001g0184a0001c0001t0002g0193a0001c0001t0005g0122others(11): Show | 14 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1231-20801A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374047 | ||||||
| chr5:45374059
|
A | G | 3 | a0001c0001t0001g0206a0001c0001t0002g0056a0001c0001t0002g0193 | 3 | HG01975.hp2 HG02738.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1231-20813T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374059 | ||||||
| chr5:45374062
|
T | C | 6 | a0001c0001t0006g0057a0001c0001t0013g0078a0001c0001t0013g0079others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-20816A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374062 | ||||||
| chr5:45374074
|
A | T | 3 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0017g0081 | 3 | NA18992.hp2 NA19003.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1231-20828T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374074 | ||||||
| chr5:45374076
|
T | C | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1231-20830A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374076 | ||||||
| chr5:45374079
|
C | A | 4 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0157others(1): Show | 4 | NA18945.hp2 NA19030.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.1231-20833G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374079 | ||||||
| chr5:45374080
|
T | C | 1 | a0001c0001t0003g0092 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1231-20834A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374080 | ||||||
| chr5:45374092
|
G | GTATATAA others(20): Show |
3 | a0001c0001t0001g0159a0001c0001t0025g0217a0001c0001t0026g0071 | 3 | HG01192.hp2 HG01361.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1231-20873_1231-20 others(33): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374092 | ||||||
| chr5:45374101
|
A | G | 67 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1231-20855T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374101 | ||||||
| chr5:45374104
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1231-20858A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374104 | ||||||
| chr5:45374117
|
A | T | 67 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1231-20871T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374117 | ||||||
| chr5:45374131
|
T | C | 67 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1231-20885A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374131 | ||||||
| chr5:45374171
|
A | T | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1231-20925T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374171 | ||||||
| chr5:45374189
|
A | ATACATTA others(22): Show |
2 | a0001c0001t0003g0158a0001c0001t0003g0183 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1231-20972_1231-20 others(35): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374189 | ||||||
| chr5:45374189
|
ATACATTA others(51): Show |
A | 3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0002g0194 | 3 | HG01952.hp1 HG03669.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1231-21001_1231-20 others(64): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374189 | ||||||
| chr5:45374198
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1231-20952T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374198 | ||||||
| chr5:45374206
|
CAT | C | 2 | a0001c0001t0025g0217a0001c0001t0026g0071 | 2 | HG01192.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1231-20962_1231-20 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374206 | ||||||
| chr5:45374207
|
A | ATATAT | 2 | a0001c0001t0012g0064a0001c0001t0012g0137 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1231-20966_1231-20 others(11): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374207 | ||||||
| chr5:45374218
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1231-20972C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374218 | ||||||
| chr5:45374219
|
T | C | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1231-20973A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374219 | ||||||
| chr5:45374229
|
A | T | 1 | a0001c0001t0034g0172 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1231-20983T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374229 | ||||||
| chr5:45374264
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1231-21018G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374264 | ||||||
| chr5:45374270
|
TATTATAT others(29): Show |
T | 1 | a0001c0001t0002g0044 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1231-21060_1231-21 others(42): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374270 | ||||||
| chr5:45374276
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1231-21030T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374276 | ||||||
| chr5:45374283
|
A | T | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1231-21037T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374283 | ||||||
| chr5:45374290
|
T | TAA | 31 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(28): Show | 31 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.1231-21045_1231-21 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374290 | ||||||
| chr5:45374290
|
T | TAACATAT others(53): Show |
2 | a0001c0001t0012g0064a0001c0001t0012g0137 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1231-21045_1231-21 others(66): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374290 | ||||||
| chr5:45374290
|
T | TAATATAT others(24): Show |
31 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(28): Show | 31 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.1231-21045_1231-21 others(37): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374290 | ||||||
| chr5:45374291
|
T | A | 66 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(63): Show | 66 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1231-21045A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374291 | ||||||
| chr5:45374291
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1231-21045A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374291 | ||||||
| chr5:45374299
|
TTGTATAC | T | 66 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(63): Show | 66 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1231-21060_1231-21 others(13): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374299 | ||||||
| chr5:45374301
|
G | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1231-21055C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374301 | ||||||
| chr5:45374301
|
GTATACAT others(2): Show |
G | 5 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0202others(2): Show | 5 | HG01192.hp1 HG01884.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1231-21064_1231-21 others(15): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374301 | ||||||
| chr5:45374310
|
A | ATATACAT others(13): Show |
1 | a0001c0001t0009g0003 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1231-21065_1231-21 others(26): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374310 | ||||||
| chr5:45374310
|
A | G | 66 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(63): Show | 66 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1231-21064T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374310 | ||||||
| chr5:45374317
|
T | TAA | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1231-21072_1231-21 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374317 | ||||||
| chr5:45374324
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1231-21078G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374324 | ||||||
| chr5:45374328
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1231-21082T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374328 | ||||||
| chr5:45374497
|
A | T | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1231-21251T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374497 | ||||||
| chr5:45374512
|
C | G | 1 | a0001c0001t0037g0148 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1231-21266G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374512 | ||||||
| chr5:45374574
|
A | G | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1231-21328T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374574 | ||||||
| chr5:45374769
|
AAT | A | 116 | a0001c0001t0001g0013a0001c0001t0001g0037a0001c0001t0001g0045others(113): Show | 116 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.1231-21525_1231-21 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374769 | ||||||
| chr5:45374782
|
A | G | 108 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1231-21536T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374782 | ||||||
| chr5:45374786
|
G | GTA | 3 | a0001c0001t0001g0180a0001c0001t0002g0012a0001c0001t0005g0089 | 3 | HG02647.hp1 NA18961.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1231-21541_1231-21 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374786 | ||||||
| chr5:45374788
|
G | A | 108 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1231-21542C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374788 | ||||||
| chr5:45374886
|
A | G | 67 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1230+21606T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374886 | ||||||
| chr5:45374894
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1230+21598T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374894 | ||||||
| chr5:45374897
|
CAGAG | C | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1230+21591_1230+21 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374897 | ||||||
| chr5:45374998
|
A | T | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1230+21494T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45374998 | ||||||
| chr5:45375026
|
T | C | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1230+21466A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375026 | ||||||
| chr5:45375038
|
T | C | 34 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(31): Show | 34 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1230+21454A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375038 | ||||||
| chr5:45375072
|
TATTATAT others(3): Show |
T | 8 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(5): Show | 8 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1230+21410_1230+21 others(16): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375072 | ||||||
| chr5:45375094
|
TATA | T | 35 | a0001c0001t0001g0179a0001c0001t0002g0091a0001c0001t0002g0096others(32): Show | 35 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1230+21395_1230+21 others(9): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375094 | ||||||
| chr5:45375097
|
A | ATTTTATA others(23): Show |
1 | a0001c0001t0005g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1230+21394_1230+21 others(36): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375097 | ||||||
| chr5:45375097
|
AATATTTT others(26): Show |
A | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1230+21362_1230+21 others(39): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375097 | ||||||
| chr5:45375117
|
A | ATATTATA others(26): Show |
1 | a0001c0001t0001g0166 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1230+21342_1230+21 others(39): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375117 | ||||||
| chr5:45375117
|
A | G | 2 | a0001c0001t0002g0193a0001c0001t0003g0111 | 2 | NA19057.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1230+21375T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375117 | ||||||
| chr5:45375117
|
ATATTATA others(26): Show |
A | 1 | a0001c0001t0001g0153 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1230+21342_1230+21 others(39): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375117 | ||||||
| chr5:45375132
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1230+21360A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375132 | ||||||
| chr5:45375156
|
T | C | 8 | a0001c0001t0001g0159a0001c0001t0001g0161a0001c0001t0001g0162others(5): Show | 8 | HG00639.hp1 HG01074.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1230+21336A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375156 | ||||||
| chr5:45375183
|
G | A | 3 | a0001c0001t0002g0121a0001c0001t0013g0078a0001c0001t0013g0079 | 3 | HG01346.hp2 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1230+21309C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375183 | ||||||
| chr5:45375186
|
T | C | 1 | a0001c0001t0002g0096 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1230+21306A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375186 | ||||||
| chr5:45375187
|
T | TATATATA others(15): Show |
1 | a0001c0001t0027g0022 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1230+21283_1230+21 others(28): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375187 | ||||||
| chr5:45375187
|
TATATATA others(15): Show |
T | 1 | a0001c0001t0040g0175 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1230+21283_1230+21 others(28): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375187 | ||||||
| chr5:45375213
|
T | TATAATAT others(29): Show |
2 | a0001c0001t0003g0118a0001c0001t0003g0120 | 2 | HG00735.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.1230+21278_1230+21 others(42): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375213 | ||||||
| chr5:45375219
|
A | G | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1230+21273T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375219 | ||||||
| chr5:45375222
|
A | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1230+21270T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375222 | ||||||
| chr5:45375227
|
T | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1230+21265A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375227 | ||||||
| chr5:45375233
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1230+21259A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375233 | ||||||
| chr5:45375235
|
T | G | 7 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(4): Show | 7 | HG00642.hp1 HG01071.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1230+21257A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375235 | ||||||
| chr5:45375239
|
A | G | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1230+21253T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375239 | ||||||
| chr5:45375239
|
A | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1230+21253T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375239 | ||||||
| chr5:45375241
|
A | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1230+21251T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375241 | ||||||
| chr5:45375245
|
T | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1230+21247A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375245 | ||||||
| chr5:45375249
|
C | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1230+21243G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375249 | ||||||
| chr5:45375290
|
T | TATA | 6 | a0001c0001t0003g0119a0001c0001t0007g0115a0001c0001t0007g0214others(3): Show | 6 | HG02451.hp1 HG02602.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1230+21199_1230+21 others(9): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375290 | ||||||
| chr5:45375297
|
C | T | 6 | a0001c0001t0003g0119a0001c0001t0007g0115a0001c0001t0007g0214others(3): Show | 6 | HG02451.hp1 HG02602.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1230+21195G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375297 | ||||||
| chr5:45375297
|
CATGATAT others(24): Show |
C | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1230+21164_1230+21 others(37): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375297 | ||||||
| chr5:45375300
|
G | A | 6 | a0001c0001t0003g0119a0001c0001t0007g0115a0001c0001t0007g0214others(3): Show | 6 | HG02451.hp1 HG02602.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1230+21192C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375300 | ||||||
| chr5:45375306
|
C | T | 6 | a0001c0001t0003g0119a0001c0001t0007g0115a0001c0001t0007g0214others(3): Show | 6 | HG02451.hp1 HG02602.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1230+21186G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375306 | ||||||
| chr5:45375312
|
A | AT | 6 | a0001c0001t0003g0119a0001c0001t0007g0115a0001c0001t0007g0214others(3): Show | 6 | HG02451.hp1 HG02602.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1230+21179dupA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375312 | ||||||
| chr5:45375316
|
A | AC | 6 | a0001c0001t0003g0119a0001c0001t0007g0115a0001c0001t0007g0214others(3): Show | 6 | HG02451.hp1 HG02602.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1230+21175_1230+21 others(7): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375316 | ||||||
| chr5:45375317
|
A | C | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1230+21175T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375317 | ||||||
| chr5:45375320
|
T | A | 6 | a0001c0001t0003g0119a0001c0001t0007g0115a0001c0001t0007g0214others(3): Show | 6 | HG02451.hp1 HG02602.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1230+21172A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375320 | ||||||
| chr5:45375321
|
A | T | 6 | a0001c0001t0003g0119a0001c0001t0007g0115a0001c0001t0007g0214others(3): Show | 6 | HG02451.hp1 HG02602.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1230+21171T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375321 | ||||||
| chr5:45375328
|
T | C | 6 | a0001c0001t0003g0119a0001c0001t0007g0115a0001c0001t0007g0214others(3): Show | 6 | HG02451.hp1 HG02602.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1230+21164A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375328 | ||||||
| chr5:45375352
|
AATATTTT others(86): Show |
A | 6 | a0001c0001t0002g0012a0001c0001t0002g0025a0001c0001t0003g0108others(3): Show | 6 | HG01433.hp2 HG02897.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1230+21047_1230+21 others(99): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375352 | ||||||
| chr5:45375352
|
AATATTTT others(117): Show |
A | 32 | a0001c0001t0002g0091a0001c0001t0002g0105a0001c0001t0002g0106others(29): Show | 32 | HG00099.hp2 HG00558.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1230+21016_1230+21 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375352 | ||||||
| chr5:45375352
|
AATATTTT others(148): Show |
A | 2 | a0001c0001t0002g0096a0001c0001t0003g0083 | 2 | HG00323.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.1230+20985_1230+21 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375352 | ||||||
| chr5:45375366
|
T | C | 1 | a0001c0001t0006g0203 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1230+21126A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375366 | ||||||
| chr5:45375368
|
C | T | 1 | a0001c0001t0006g0203 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1230+21124G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375368 | ||||||
| chr5:45375370
|
A | T | 1 | a0001c0001t0006g0203 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1230+21122T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375370 | ||||||
| chr5:45375370
|
ATATATAT others(148): Show |
A | 1 | a0001c0001t0002g0193 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1230+20967_1230+21 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375370 | ||||||
| chr5:45375380
|
T | G | 1 | a0001c0001t0006g0203 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1230+21112A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375380 | ||||||
| chr5:45375383
|
A | AATATTTT others(55): Show |
3 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0195 | 3 | HG01074.hp2 HG01109.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1230+21047_1230+21 others(68): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375383 | ||||||
| chr5:45375383
|
A | C | 1 | a0001c0001t0006g0203 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1230+21109T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375383 | ||||||
| chr5:45375383
|
AATATTTT others(86): Show |
A | 41 | a0001c0001t0001g0034a0001c0001t0001g0051a0001c0001t0001g0065others(38): Show | 41 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.1230+21016_1230+21 others(99): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375383 | ||||||
| chr5:45375383
|
AATATTTT others(117): Show |
A | 4 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0036others(1): Show | 4 | NA18959.hp2 NA18962.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.1230+20985_1230+21 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375383 | ||||||
| chr5:45375395
|
TACATATT others(53): Show |
T | 2 | a0001c0001t0002g0023a0001c0001t0002g0024 | 2 | NA18977.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1230+21037_1230+21 others(66): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375395 | ||||||
| chr5:45375395
|
TACATATT others(115): Show |
T | 1 | a0001c0001t0013g0079 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1230+20975_1230+21 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375395 | ||||||
| chr5:45375397
|
C | T | 5 | a0001c0001t0003g0119a0001c0001t0006g0057a0001c0001t0007g0115others(2): Show | 5 | HG01109.hp2 HG02451.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.1230+21095G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375397 | ||||||
| chr5:45375399
|
T | C | 5 | a0001c0001t0003g0119a0001c0001t0006g0057a0001c0001t0007g0115others(2): Show | 5 | HG01109.hp2 HG02451.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.1230+21093A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375399 | ||||||
| chr5:45375401
|
T | A | 5 | a0001c0001t0003g0119a0001c0001t0006g0057a0001c0001t0007g0115others(2): Show | 5 | HG01109.hp2 HG02451.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.1230+21091A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375401 | ||||||
| chr5:45375402
|
T | TATATATA others(55): Show |
1 | a0001c0001t0007g0100 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1230+21089_1230+21 others(68): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375402 | ||||||
| chr5:45375402
|
TATATATA others(55): Show |
T | 5 | a0001c0001t0002g0015a0001c0001t0002g0026a0001c0001t0002g0097others(2): Show | 5 | HG00673.hp1 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1230+21028_1230+21 others(68): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375402 | ||||||
| chr5:45375411
|
G | T | 5 | a0001c0001t0003g0119a0001c0001t0006g0057a0001c0001t0007g0115others(2): Show | 5 | HG01109.hp2 HG02451.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.1230+21081C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375411 | ||||||
| chr5:45375414
|
C | A | 4 | a0001c0001t0003g0119a0001c0001t0006g0057a0001c0001t0007g0115others(1): Show | 4 | HG01109.hp2 HG02602.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1230+21078G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375414 | ||||||
| chr5:45375420
|
TTATGATA others(26): Show |
T | 2 | a0001c0001t0023g0075a0001c0001t0024g0007 | 2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1230+21039_1230+21 others(39): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375420 | ||||||
| chr5:45375420
|
TTATGATA others(57): Show |
T | 5 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+21008_1230+21 others(70): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375420 | ||||||
| chr5:45375433
|
T | G | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0006g0203 | 3 | HG02145.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1230+21059A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375433 | ||||||
| chr5:45375433
|
T | TATATATA others(24): Show |
8 | a0001c0001t0001g0013a0001c0001t0001g0045a0001c0001t0001g0202others(5): Show | 8 | HG00280.hp2 HG00741.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.1230+21028_1230+21 others(37): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375433 | ||||||
| chr5:45375433
|
TATATATA others(24): Show |
T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1230+21028_1230+21 others(37): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375433 | ||||||
| chr5:45375460
|
AT | A | 2 | a0001c0001t0002g0023a0001c0001t0002g0024 | 2 | NA18977.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1230+21031delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375460 | ||||||
| chr5:45375463
|
TG | T | 2 | a0001c0001t0002g0023a0001c0001t0002g0024 | 2 | NA18977.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1230+21028delC | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375463 | ||||||
| chr5:45375464
|
G | GATATATA others(55): Show |
1 | a0001c0001t0001g0180 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1230+21027_1230+21 others(68): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375464 | ||||||
| chr5:45375464
|
G | GATATATA others(24): Show |
28 | a0001c0001t0001g0060a0001c0001t0001g0073a0001c0001t0001g0107others(25): Show | 28 | HG00642.hp2 HG00673.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.1230+20997_1230+21 others(37): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375464 | ||||||
| chr5:45375464
|
G | GATATATA others(55): Show |
26 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0135others(23): Show | 26 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.1230+20966_1230+21 others(68): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375464 | ||||||
| chr5:45375464
|
G | GATATATA others(86): Show |
8 | a0001c0001t0001g0136a0001c0001t0001g0153a0001c0001t0001g0155others(5): Show | 8 | HG00597.hp1 HG02738.hp2 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.1230+20935_1230+21 others(99): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375464 | ||||||
| chr5:45375464
|
G | T | 44 | a0001c0001t0001g0011a0001c0001t0001g0161a0001c0001t0001g0162others(41): Show | 44 | HG00438.hp2 HG00609.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.1230+21028C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375464 | ||||||
| chr5:45375473
|
G | T | 2 | a0001c0001t0002g0023a0001c0001t0002g0024 | 2 | NA18977.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1230+21019C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375473 | ||||||
| chr5:45375476
|
C | A | 2 | a0001c0001t0002g0023a0001c0001t0002g0024 | 2 | NA18977.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1230+21016G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375476 | ||||||
| chr5:45375494
|
T | TTATATAT others(52): Show |
1 | a0001c0001t0034g0172 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1230+20939_1230+20 others(65): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375494 | ||||||
| chr5:45375495
|
T | G | 11 | a0001c0001t0001g0116a0001c0001t0001g0184a0001c0001t0001g0209others(8): Show | 11 | HG00280.hp2 HG00642.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.1230+20997A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375495 | ||||||
| chr5:45375525
|
T | A | 1 | a0001c0001t0013g0079 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1230+20967A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375525 | ||||||
| chr5:45375526
|
T | G | 2 | a0001c0001t0003g0119a0001c0001t0003g0120 | 2 | HG00735.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1230+20966A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375526 | ||||||
| chr5:45375535
|
G | T | 1 | a0001c0001t0013g0079 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1230+20957C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375535 | ||||||
| chr5:45375538
|
C | A | 1 | a0001c0001t0013g0079 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1230+20954G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375538 | ||||||
| chr5:45375556
|
TTATATAT others(57): Show |
T | 1 | a0001c0001t0002g0082 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1230+20872_1230+20 others(70): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375556 | ||||||
| chr5:45375584
|
ATATTATA others(27): Show |
A | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1230+20874_1230+20 others(40): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375584 | ||||||
| chr5:45375586
|
ATTATATA others(148): Show |
A | 8 | a0001c0001t0004g0031a0001c0001t0004g0032a0001c0001t0004g0033others(5): Show | 8 | HG00609.hp2 NA18953.hp2 NA18971.hp2 others(5): Show |
intron_variant | MODIFIER | c.1230+20751_1230+20 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375586 | ||||||
| chr5:45375588
|
T | C | 1 | a0001c0001t0002g0024 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1230+20904A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375588 | ||||||
| chr5:45375597
|
G | T | 10 | a0001c0001t0001g0011a0001c0001t0001g0074a0001c0001t0001g0076others(7): Show | 10 | HG01167.hp1 HG01169.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1230+20895C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375597 | ||||||
| chr5:45375597
|
GATCATAT others(148): Show |
G | 1 | a0001c0001t0004g0062 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1230+20740_1230+20 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375597 | ||||||
| chr5:45375628
|
G | T | 23 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(20): Show | 23 | HG01167.hp1 HG01169.hp2 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.1230+20864C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375628 | ||||||
| chr5:45375648
|
ATTATATA others(86): Show |
A | 2 | a0001c0001t0001g0011a0003c0003t0035g0220 | 2 | HG02622.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1230+20751_1230+20 others(99): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375648 | ||||||
| chr5:45375648
|
ATTATATA others(117): Show |
A | 2 | a0001c0001t0002g0058a0001c0001t0013g0078 | 2 | HG02738.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1230+20720_1230+20 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375648 | ||||||
| chr5:45375654
|
TATAAGAT others(58): Show |
T | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1230+20773_1230+20 others(71): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375654 | ||||||
| chr5:45375654
|
TATAAGAT others(89): Show |
T | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1230+20742_1230+20 others(102): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375654 | ||||||
| chr5:45375658
|
AGATCATA others(27): Show |
A | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1230+20800_1230+20 others(40): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375658 | ||||||
| chr5:45375659
|
G | T | 11 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(8): Show | 11 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1230+20833C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375659 | ||||||
| chr5:45375679
|
ATTATATA others(86): Show |
A | 1 | a0001c0006t0002g0219 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1230+20720_1230+20 others(99): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375679 | ||||||
| chr5:45375690
|
G | T | 91 | a0001c0001t0001g0034a0001c0001t0001g0051a0001c0001t0001g0065others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1230+20802C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375690 | ||||||
| chr5:45375690
|
GATCATAT others(24): Show |
G | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1230+20771_1230+20 others(37): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375690 | ||||||
| chr5:45375693
|
C | A | 2 | a0001c0001t0023g0075a0001c0001t0024g0007 | 2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1230+20799G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375693 | ||||||
| chr5:45375693
|
C | T | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1230+20799G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375693 | ||||||
| chr5:45375707
|
C | T | 8 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1230+20785G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375707 | ||||||
| chr5:45375710
|
A | ATTATATA others(24): Show |
1 | a0001c0001t0002g0088 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1230+20751_1230+20 others(37): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375710 | ||||||
| chr5:45375710
|
A | C | 9 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1230+20782T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375710 | ||||||
| chr5:45375710
|
ATTATATA others(24): Show |
A | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1230+20751_1230+20 others(37): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375710 | ||||||
| chr5:45375721
|
T | G | 18 | a0001c0001t0001g0045a0001c0001t0001g0060a0001c0001t0001g0073others(15): Show | 18 | HG00280.hp2 HG00642.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.1230+20771A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375721 | ||||||
| chr5:45375724
|
C | A | 8 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1230+20768G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375724 | ||||||
| chr5:45375738
|
T | C | 70 | a0001c0001t0001g0034a0001c0001t0001g0051a0001c0001t0001g0065others(67): Show | 70 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.1230+20754A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375738 | ||||||
| chr5:45375741
|
C | A | 69 | a0001c0001t0001g0034a0001c0001t0001g0051a0001c0001t0001g0065others(66): Show | 69 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.1230+20751G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375741 | ||||||
| chr5:45375752
|
T | G | 3 | a0001c0001t0001g0184a0001c0001t0001g0209a0001c0001t0002g0178 | 3 | HG00280.hp2 HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1230+20740A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375752 | ||||||
| chr5:45375755
|
C | A | 57 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(54): Show | 57 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1230+20737G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375755 | ||||||
| chr5:45375769
|
T | C | 2 | a0001c0001t0001g0209a0001c0001t0002g0178 | 2 | HG00280.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1230+20723A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375769 | ||||||
| chr5:45375772
|
C | A | 2 | a0001c0001t0001g0209a0001c0001t0002g0178 | 2 | HG00280.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1230+20720G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375772 | ||||||
| chr5:45375782
|
A | C | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1230+20710T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375782 | ||||||
| chr5:45375783
|
T | C | 1 | a0001c0001t0011g0163 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1230+20709A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375783 | ||||||
| chr5:45375786
|
A | C | 88 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(85): Show | 88 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.1230+20706T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375786 | ||||||
| chr5:45375804
|
T | TTATATAT others(86): Show |
1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1230+20687_1230+20 others(99): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375804 | ||||||
| chr5:45375817
|
A | C | 13 | a0001c0001t0001g0051a0001c0001t0002g0015a0001c0001t0002g0049others(10): Show | 13 | HG01192.hp2 HG01891.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.1230+20675T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375817 | ||||||
| chr5:45375848
|
A | C | 11 | a0001c0001t0001g0051a0001c0001t0002g0015a0001c0001t0002g0049others(8): Show | 11 | HG01891.hp2 HG02615.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1230+20644T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375848 | ||||||
| chr5:45375865
|
C | G | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1230+20627G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375865 | ||||||
| chr5:45375871
|
TATATTTT others(24): Show |
T | 1 | a0001c0001t0003g0090 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1230+20590_1230+20 others(37): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375871 | ||||||
| chr5:45375910
|
A | C | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1230+20582T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375910 | ||||||
| chr5:45375963
|
A | T | 11 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(8): Show | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1230+20529T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375963 | ||||||
| chr5:45375977
|
ATATAT | A | 11 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(8): Show | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1230+20510_1230+20 others(11): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375977 | ||||||
| chr5:45375994
|
T | A | 1 | a0001c0001t0004g0048 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1230+20498A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45375994 | ||||||
| chr5:45376065
|
AAT | A | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1230+20425_1230+20 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376065 | ||||||
| chr5:45376071
|
TTATAA | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1230+20416_1230+20 others(11): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376071 | ||||||
| chr5:45376080
|
ATAT | A | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1230+20409_1230+20 others(9): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376080 | ||||||
| chr5:45376135
|
A | G | 1 | a0001c0001t0002g0096 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1230+20357T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376135 | ||||||
| chr5:45376238
|
ATATATTC others(25): Show |
A | 1 | a0001c0001t0001g0197 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1230+20222_1230+20 others(38): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376238 | ||||||
| chr5:45376245
|
C | CTATATGG others(82): Show |
1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1230+20246_1230+20 others(95): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376245 | ||||||
| chr5:45376245
|
C | CTATATGG others(100): Show |
2 | a0001c0001t0017g0081a0001c0001t0033g0213 | 2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1230+20246_1230+20 others(113): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376245 | ||||||
| chr5:45376245
|
C | CTATATGG others(100): Show |
30 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0157others(27): Show | 30 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.1230+20246_1230+20 others(113): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376245 | ||||||
| chr5:45376245
|
C | CTATATGG others(100): Show |
2 | a0001c0001t0003g0095a0001c0001t0019g0114 | 2 | HG01975.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1230+20246_1230+20 others(113): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376245 | ||||||
| chr5:45376245
|
C | CTATATGG others(100): Show |
2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1230+20246_1230+20 others(113): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376245 | ||||||
| chr5:45376245
|
C | CTATATGG others(114): Show |
2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1230+20246_1230+20 others(127): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376245 | ||||||
| chr5:45376251
|
A | AGAATATA others(293): Show |
1 | a0001c0001t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1230+20240_1230+20 others(306): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(261): Show |
1 | a0001c0001t0001g0074 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1230+20240_1230+20 others(274): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(243): Show |
1 | a0001c0001t0024g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1230+20240_1230+20 others(256): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(293): Show |
1 | a0001c0001t0001g0076 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1230+20240_1230+20 others(306): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(218): Show |
1 | a0001c0001t0023g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1230+20240_1230+20 others(231): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(25): Show |
1 | a0001c0006t0002g0219 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1230+20240_1230+20 others(38): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(243): Show |
2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1230+20240_1230+20 others(256): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(100): Show |
1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1230+20240_1230+20 others(113): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(100): Show |
88 | a0001c0001t0001g0013a0001c0001t0001g0037a0001c0001t0001g0045others(85): Show | 88 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1230+20240_1230+20 others(113): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(100): Show |
1 | a0001c0001t0001g0211 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1230+20240_1230+20 others(113): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(100): Show |
1 | a0001c0001t0003g0053 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1230+20240_1230+20 others(113): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(431): Show |
1 | a0001c0001t0007g0214 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1230+20240_1230+20 others(444): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(431): Show |
1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1230+20240_1230+20 others(444): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(43): Show |
62 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(59): Show | 62 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.1230+20240_1230+20 others(56): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(690): Show |
1 | a0001c0001t0013g0078 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1230+20240_1230+20 others(703): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(672): Show |
1 | a0001c0001t0013g0079 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1230+20240_1230+20 others(685): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(297): Show |
1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1230+20240_1230+20 others(310): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(494): Show |
1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1230+20240_1230+20 others(507): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(256): Show |
1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1230+20240_1230+20 others(269): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(281): Show |
5 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(2): Show | 5 | HG01261.hp2 HG02055.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1230+20240_1230+20 others(294): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(313): Show |
1 | a0001c0001t0005g0127 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1230+20240_1230+20 others(326): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(281): Show |
1 | a0001c0001t0005g0142 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1230+20240_1230+20 others(294): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(281): Show |
2 | a0001c0001t0005g0129a0001c0001t0005g0130 | 2 | HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1230+20240_1230+20 others(294): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(77): Show |
1 | a0001c0001t0002g0036 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1230+20240_1230+20 others(90): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(159): Show |
1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1230+20240_1230+20 others(172): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(75): Show |
2 | a0001c0001t0001g0167a0001c0001t0020g0196 | 2 | HG01516.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.1230+20240_1230+20 others(88): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(272): Show |
1 | a0001c0001t0005g0128 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1230+20240_1230+20 others(285): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(45): Show |
1 | a0001c0001t0002g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1230+20240_1230+20 others(58): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | AGAATATA others(18): Show |
1 | a0001c0001t0029g0070 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1230+20240_1230+20 others(31): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376251
|
A | G | 39 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(36): Show | 39 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.1230+20241T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376251 | ||||||
| chr5:45376252
|
G | GAATATAG others(43): Show |
1 | a0001c0001t0002g0026 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1230+20239_1230+20 others(56): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376252 | ||||||
| chr5:45376319
|
A | G | 1 | a0001c0001t0003g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1230+20173T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376319 | ||||||
| chr5:45376338
|
T | TTA | 4 | a0001c0001t0002g0121a0001c0001t0013g0078a0001c0001t0013g0079others(1): Show | 4 | HG01346.hp2 NA18992.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.1230+20152_1230+20 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376338 | ||||||
| chr5:45376347
|
T | G | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1230+20145A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376347 | ||||||
| chr5:45376349
|
T | G | 9 | a0001c0001t0001g0169a0001c0001t0001g0201a0001c0001t0001g0202others(6): Show | 9 | HG01192.hp1 HG02451.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1230+20143A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376349 | ||||||
| chr5:45376349
|
T | TAG | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1230+20141_1230+20 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376349 | ||||||
| chr5:45376349
|
TAGAGAGA others(1): Show |
T | 3 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0157 | 3 | NA18945.hp2 NA19064.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1230+20135_1230+20 others(14): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376349 | ||||||
| chr5:45376351
|
G | T | 154 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1230+20141C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376351 | ||||||
| chr5:45376353
|
G | T | 100 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(97): Show | 100 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1230+20139C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376353 | ||||||
| chr5:45376355
|
G | T | 10 | a0001c0001t0001g0034a0001c0001t0001g0179a0001c0001t0001g0206others(7): Show | 10 | HG01167.hp1 HG01169.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1230+20137C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376355 | ||||||
| chr5:45376387
|
C | T | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1230+20105G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376387 | ||||||
| chr5:45376473
|
G | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0190 | 2 | NA18971.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1230+20019C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376473 | ||||||
| chr5:45376490
|
T | C | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1230+20002A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376490 | ||||||
| chr5:45376501
|
C | T | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1230+19991G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376501 | ||||||
| chr5:45376677
|
A | T | 2 | a0002c0002t0008g0224a0002c0002t0008g0225 | 2 | HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1230+19815T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376677 | ||||||
| chr5:45376770
|
G | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1230+19722C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376770 | ||||||
| chr5:45376913
|
G | T | 11 | a0001c0001t0001g0051a0001c0001t0002g0015a0001c0001t0002g0049others(8): Show | 11 | HG01891.hp2 HG02615.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1230+19579C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376913 | ||||||
| chr5:45376990
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1230+19502G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45376990 | ||||||
| chr5:45377337
|
T | C | 3 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0142 | 3 | HG02886.hp2 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1230+19155A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45377337 | ||||||
| chr5:45377449
|
AT | A | 5 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(2): Show | 5 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+19042delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45377449 | ||||||
| chr5:45377487
|
T | G | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1230+19005A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45377487 | ||||||
| chr5:45377555
|
G | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1230+18937C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45377555 | ||||||
| chr5:45377568
|
A | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1230+18924T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45377568 | ||||||
| chr5:45377569
|
T | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1230+18923A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45377569 | ||||||
| chr5:45377623
|
G | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG00323.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1230+18869C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45377623 | ||||||
| chr5:45377675
|
G | A | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1230+18817C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45377675 | ||||||
| chr5:45377763
|
A | G | 1 | a0001c0001t0001g0180 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1230+18729T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45377763 | ||||||
| chr5:45377944
|
T | C | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1230+18548A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45377944 | ||||||
| chr5:45378053
|
T | G | 1 | a0001c0001t0024g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1230+18439A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45378053 | ||||||
| chr5:45378105
|
C | T | 133 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1230+18387G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45378105 | ||||||
| chr5:45378522
|
C | T | 2 | a0001c0001t0002g0039a0001c0001t0002g0040 | 2 | HG00639.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1230+17970G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45378522 | ||||||
| chr5:45378635
|
A | G | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1230+17857T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45378635 | ||||||
| chr5:45378683
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1230+17809G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45378683 | ||||||
| chr5:45378686
|
A | T | 5 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(2): Show | 5 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+17806T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45378686 | ||||||
| chr5:45379479
|
A | C | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1230+17013T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45379479 | ||||||
| chr5:45379488
|
CA | C | 133 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1230+17003delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45379488 | ||||||
| chr5:45379689
|
G | A | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1230+16803C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45379689 | ||||||
| chr5:45379797
|
A | T | 1 | a0001c0001t0003g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1230+16695T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45379797 | ||||||
| chr5:45379956
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1230+16536G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45379956 | ||||||
| chr5:45379992
|
G | T | 3 | a0001c0001t0002g0067a0001c0001t0002g0131a0001c0004t0002g0006 | 3 | HG01243.hp1 HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1230+16500C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45379992 | ||||||
| chr5:45380249
|
A | T | 13 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(10): Show | 13 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1230+16243T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45380249 | ||||||
| chr5:45380259
|
G | T | 1 | a0001c0001t0004g0017 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1230+16233C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45380259 | ||||||
| chr5:45380585
|
G | T | 7 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1230+15907C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45380585 | ||||||
| chr5:45380591
|
A | G | 2 | a0001c0001t0002g0027a0001c0001t0002g0054 | 2 | NA18959.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.1230+15901T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45380591 | ||||||
| chr5:45380634
|
A | T | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1230+15858T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45380634 | ||||||
| chr5:45380844
|
G | A | 3 | a0001c0001t0002g0015a0001c0001t0002g0082a0001c0001t0016g0014 | 3 | HG02615.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1230+15648C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45380844 | ||||||
| chr5:45381328
|
G | A | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1230+15164C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45381328 | ||||||
| chr5:45381574
|
A | G | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1230+14918T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45381574 | ||||||
| chr5:45381975
|
C | T | 1 | a0001c0001t0034g0172 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1230+14517G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45381975 | ||||||
| chr5:45381984
|
C | A | 1 | a0001c0001t0019g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1230+14508G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45381984 | ||||||
| chr5:45382307
|
C | A | 1 | a0001c0001t0002g0019 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1230+14185G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45382307 | ||||||
| chr5:45382420
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1230+14072T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45382420 | ||||||
| chr5:45382516
|
C | A | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1230+13976G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45382516 | ||||||
| chr5:45382631
|
A | G | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1230+13861T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45382631 | ||||||
| chr5:45382816
|
G | A | 32 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0157others(29): Show | 32 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1230+13676C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45382816 | ||||||
| chr5:45382871
|
A | G | 1 | a0001c0001t0006g0143 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1230+13621T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45382871 | ||||||
| chr5:45382892
|
T | A | 1 | a0001c0001t0002g0038 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1230+13600A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45382892 | ||||||
| chr5:45383394
|
A | C | 1 | a0001c0001t0001g0190 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1230+13098T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45383394 | ||||||
| chr5:45383470
|
C | A | 1 | a0001c0001t0001g0156 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1230+13022G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45383470 | ||||||
| chr5:45383722
|
C | CA | 81 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.1230+12769dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45383722 | ||||||
| chr5:45383804
|
T | A | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1230+12688A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45383804 | ||||||
| chr5:45383825
|
A | T | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1230+12667T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45383825 | ||||||
| chr5:45383838
|
T | C | 1 | a0001c0001t0023g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1230+12654A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45383838 | ||||||
| chr5:45384192
|
G | A | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1230+12300C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45384192 | ||||||
| chr5:45384390
|
C | T | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1230+12102G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45384390 | ||||||
| chr5:45384631
|
G | A | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1230+11861C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45384631 | ||||||
| chr5:45385012
|
T | C | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1230+11480A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45385012 | ||||||
| chr5:45385106
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1230+11386T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45385106 | ||||||
| chr5:45385204
|
G | T | 32 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0157others(29): Show | 32 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1230+11288C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45385204 | ||||||
| chr5:45385275
|
T | A | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1230+11217A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45385275 | ||||||
| chr5:45385297
|
C | G | 1 | a0001c0001t0003g0083 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1230+11195G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45385297 | ||||||
| chr5:45385362
|
T | A | 1 | a0001c0001t0003g0083 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1230+11130A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45385362 | ||||||
| chr5:45385397
|
T | G | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1230+11095A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45385397 | ||||||
| chr5:45385551
|
T | C | 1 | a0001c0001t0002g0015 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1230+10941A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45385551 | ||||||
| chr5:45385618
|
A | AACAATAT others(10): Show |
10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1230+10873_1230+10 others(23): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45385618 | ||||||
| chr5:45385875
|
C | T | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1230+10617G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45385875 | ||||||
| chr5:45385933
|
C | G | 1 | a0001c0001t0019g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1230+10559G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45385933 | ||||||
| chr5:45386012
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1230+10480C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45386012 | ||||||
| chr5:45386083
|
T | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1230+10409A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45386083 | ||||||
| chr5:45386179
|
A | AT | 35 | a0001c0001t0001g0107a0001c0001t0002g0091a0001c0001t0002g0096others(32): Show | 35 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1230+10312dupA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45386179 | ||||||
| chr5:45386179
|
A | ATT | 68 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(65): Show | 68 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.1230+10311_1230+10 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45386179 | ||||||
| chr5:45386315
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1230+10177T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45386315 | ||||||
| chr5:45386543
|
T | C | 1 | a0001c0001t0004g0033 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1230+9949A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45386543 | ||||||
| chr5:45386669
|
A | C | 1 | a0001c0001t0001g0134 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1230+9823T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45386669 | ||||||
| chr5:45386711
|
G | A | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1230+9781C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45386711 | ||||||
| chr5:45386860
|
A | G | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1230+9632T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45386860 | ||||||
| chr5:45387382
|
C | T | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1230+9110G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45387382 | ||||||
| chr5:45387588
|
T | A | 1 | a0001c0001t0001g0211 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1230+8904A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45387588 | ||||||
| chr5:45387665
|
T | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1230+8827A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45387665 | ||||||
| chr5:45387752
|
C | T | 133 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1230+8740G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45387752 | ||||||
| chr5:45387893
|
T | A | 7 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(4): Show | 7 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1230+8599A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45387893 | ||||||
| chr5:45388146
|
A | G | 36 | a0001c0001t0001g0034a0001c0001t0001g0065a0001c0001t0002g0012others(33): Show | 36 | HG00280.hp1 HG00438.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.1230+8346T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45388146 | ||||||
| chr5:45388152
|
T | C | 1 | a0001c0001t0002g0028 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1230+8340A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45388152 | ||||||
| chr5:45388368
|
G | C | 1 | a0001c0001t0036g0186 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1230+8124C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45388368 | ||||||
| chr5:45388387
|
C | T | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1230+8105G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45388387 | ||||||
| chr5:45388390
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0015g0001 | 2 | NA18939.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1230+8102C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45388390 | ||||||
| chr5:45388687
|
T | C | 131 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1230+7805A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45388687 | ||||||
| chr5:45388859
|
A | G | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1230+7633T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45388859 | ||||||
| chr5:45389122
|
G | C | 2 | a0001c0001t0007g0115a0001c0001t0007g0214 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1230+7370C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45389122 | ||||||
| chr5:45389418
|
T | C | 13 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(10): Show | 13 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1230+7074A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45389418 | ||||||
| chr5:45389472
|
A | T | 130 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1230+7020T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45389472 | ||||||
| chr5:45389512
|
G | A | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1230+6980C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45389512 | ||||||
| chr5:45389529
|
T | C | 11 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(8): Show | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1230+6963A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45389529 | ||||||
| chr5:45389747
|
C | G | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1230+6745G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45389747 | ||||||
| chr5:45389772
|
T | G | 1 | a0001c0001t0001g0180 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1230+6720A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45389772 | ||||||
| chr5:45389937
|
C | A | 1 | a0001c0001t0019g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1230+6555G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45389937 | ||||||
| chr5:45389939
|
C | T | 1 | a0001c0001t0020g0196 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1230+6553G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45389939 | ||||||
| chr5:45389946
|
C | G | 1 | a0001c0001t0004g0030 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1230+6546G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45389946 | ||||||
| chr5:45390117
|
T | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1230+6375A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45390117 | ||||||
| chr5:45390256
|
G | T | 1 | a0001c0001t0003g0094 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1230+6236C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45390256 | ||||||
| chr5:45390354
|
A | C | 1 | a0001c0001t0003g0215 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1230+6138T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45390354 | ||||||
| chr5:45390448
|
A | T | 2 | a0001c0001t0002g0023a0001c0001t0002g0024 | 2 | NA18977.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1230+6044T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45390448 | ||||||
| chr5:45390495
|
TA | T | 12 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1230+5996delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45390495 | ||||||
| chr5:45390496
|
A | C | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1230+5996T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45390496 | ||||||
| chr5:45391032
|
C | T | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1230+5460G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45391032 | ||||||
| chr5:45391074
|
TAG | T | 13 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(10): Show | 13 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1230+5416_1230+541 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45391074 | ||||||
| chr5:45391078
|
C | A | 13 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(10): Show | 13 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1230+5414G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45391078 | ||||||
| chr5:45391079
|
T | A | 13 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(10): Show | 13 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1230+5413A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45391079 | ||||||
| chr5:45391082
|
T | A | 13 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(10): Show | 13 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1230+5410A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45391082 | ||||||
| chr5:45391083
|
A | T | 13 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(10): Show | 13 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1230+5409T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45391083 | ||||||
| chr5:45391346
|
G | A | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1230+5146C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45391346 | ||||||
| chr5:45391382
|
A | C | 1 | a0001c0001t0003g0084 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1230+5110T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45391382 | ||||||
| chr5:45391821
|
C | G | 130 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1230+4671G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45391821 | ||||||
| chr5:45392440
|
A | T | 123 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.1230+4052T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45392440 | ||||||
| chr5:45392460
|
T | C | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1230+4032A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45392460 | ||||||
| chr5:45392583
|
C | T | 130 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1230+3909G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45392583 | ||||||
| chr5:45392612
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1230+3880C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45392612 | ||||||
| chr5:45392670
|
C | G | 1 | a0001c0001t0001g0200 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1230+3822G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45392670 | ||||||
| chr5:45392805
|
C | T | 1 | a0001c0006t0002g0219 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1230+3687G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45392805 | ||||||
| chr5:45392891
|
T | G | 1 | a0001c0001t0003g0103 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1230+3601A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45392891 | ||||||
| chr5:45393121
|
A | G | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1230+3371T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45393121 | ||||||
| chr5:45393158
|
C | T | 37 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0105others(34): Show | 37 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1230+3334G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45393158 | ||||||
| chr5:45393159
|
G | A | 24 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(21): Show | 24 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1230+3333C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45393159 | ||||||
| chr5:45393391
|
T | C | 1 | a0001c0004t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1230+3101A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45393391 | ||||||
| chr5:45393396
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1230+3096C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45393396 | ||||||
| chr5:45393450
|
G | C | 129 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1230+3042C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45393450 | ||||||
| chr5:45393486
|
A | T | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1230+3006T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45393486 | ||||||
| chr5:45393652
|
G | C | 123 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0051others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.1230+2840C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45393652 | ||||||
| chr5:45393808
|
T | C | 11 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(8): Show | 11 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1230+2684A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45393808 | ||||||
| chr5:45394237
|
C | T | 22 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(19): Show | 22 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1230+2255G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45394237 | ||||||
| chr5:45394359
|
C | T | 1 | a0001c0001t0002g0088 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1230+2133G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45394359 | ||||||
| chr5:45394707
|
T | C | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1230+1785A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45394707 | ||||||
| chr5:45394750
|
A | G | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1230+1742T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45394750 | ||||||
| chr5:45394874
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1230+1618T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45394874 | ||||||
| chr5:45395197
|
C | G | 1 | a0001c0001t0001g0168 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1230+1295G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45395197 | ||||||
| chr5:45395354
|
G | C | 5 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(2): Show | 5 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+1138C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45395354 | ||||||
| chr5:45395574
|
A | C | 1 | a0001c0001t0002g0181 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1230+918T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45395574 | ||||||
| chr5:45395576
|
T | G | 1 | a0001c0001t0001g0107 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1230+916A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45395576 | ||||||
| chr5:45395759
|
C | A | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1230+733G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45395759 | ||||||
| chr5:45395849
|
G | GA | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1230+642dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45395849 | ||||||
| chr5:45395863
|
A | G | 1 | a0001c0004t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1230+629T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45395863 | ||||||
| chr5:45396180
|
A | C | 4 | a0001c0001t0001g0034a0001c0001t0002g0023a0001c0001t0002g0024others(1): Show | 4 | NA18949.hp2 NA18977.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.1230+312T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45396180 | ||||||
| chr5:45396216
|
C | T | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1230+276G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45396216 | ||||||
| chr5:45396311
|
A | C | 1 | a0001c0001t0034g0172 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1230+181T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45396311 | ||||||
| chr5:45396326
|
C | T | 4 | a0001c0001t0002g0012a0001c0001t0002g0025a0001c0001t0002g0026others(1): Show | 4 | HG00673.hp1 NA18612.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.1230+166G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45396326 | ||||||
| chr5:45396337
|
C | G | 1 | a0001c0001t0003g0103 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1230+155G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45396337 | ||||||
| chr5:45396354
|
G | A | 1 | a0001c0001t0002g0046 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1230+138C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45396354 | ||||||
| chr5:45396386
|
C | CT | 46 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0002g0038others(43): Show | 46 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.1230+105dupA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45396386 | ||||||
| chr5:45396388
|
T | C | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1230+104A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45396388 | ||||||
| chr5:45396396
|
T | G | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1230+96A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 4/7 | chr5 | 45396396 | ||||||
| chr5:45396724
|
T | C | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1012-14A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45396724 | ||||||
| chr5:45396882
|
A | G | 1 | a0001c0001t0002g0046 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1012-172T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45396882 | ||||||
| chr5:45396894
|
T | C | 1 | a0001c0001t0038g0016 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1012-184A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45396894 | ||||||
| chr5:45396924
|
T | C | 7 | a0001c0001t0007g0115a0001c0004t0002g0006a0002c0002t0008g0224others(4): Show | 7 | HG01243.hp1 HG01433.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1012-214A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45396924 | ||||||
| chr5:45397006
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1012-296T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45397006 | ||||||
| chr5:45397107
|
C | A | 1 | a0001c0001t0002g0178 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1012-397G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45397107 | ||||||
| chr5:45397929
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1012-1219A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45397929 | ||||||
| chr5:45397974
|
A | T | 1 | a0001c0001t0001g0192 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1012-1264T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45397974 | ||||||
| chr5:45397976
|
A | T | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1012-1266T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45397976 | ||||||
| chr5:45398013
|
C | T | 1 | a0003c0003t0002g0221 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1012-1303G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45398013 | ||||||
| chr5:45398085
|
G | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1012-1375C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45398085 | ||||||
| chr5:45398319
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1012-1609G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45398319 | ||||||
| chr5:45398325
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1012-1615G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45398325 | ||||||
| chr5:45398523
|
A | G | 9 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(6): Show | 9 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1012-1813T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45398523 | ||||||
| chr5:45398640
|
C | A | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1012-1930G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45398640 | ||||||
| chr5:45399022
|
A | G | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG01074.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1012-2312T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45399022 | ||||||
| chr5:45399036
|
T | C | 2 | a0001c0001t0002g0121a0001c0001t0025g0217 | 2 | HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1012-2326A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45399036 | ||||||
| chr5:45399195
|
C | G | 2 | a0001c0001t0002g0121a0001c0001t0025g0217 | 2 | HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1012-2485G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45399195 | ||||||
| chr5:45399206
|
A | C | 16 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(13): Show | 16 | HG01167.hp1 HG01169.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.1012-2496T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45399206 | ||||||
| chr5:45399263
|
A | G | 1 | a0001c0001t0002g0040 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1012-2553T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45399263 | ||||||
| chr5:45399444
|
G | T | 4 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(1): Show | 4 | HG02055.hp2 HG02257.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1012-2734C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45399444 | ||||||
| chr5:45399467
|
G | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1012-2757C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45399467 | ||||||
| chr5:45399564
|
C | A | 1 | a0001c0001t0003g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1012-2854G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45399564 | ||||||
| chr5:45399709
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1012-2999G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45399709 | ||||||
| chr5:45400155
|
A | G | 2 | a0001c0001t0002g0121a0001c0001t0025g0217 | 2 | HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1012-3445T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45400155 | ||||||
| chr5:45400394
|
C | CT | 16 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(13): Show | 16 | HG01952.hp1 HG02027.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1012-3685dupA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45400394 | ||||||
| chr5:45400394
|
CT | C | 21 | a0001c0001t0001g0153a0001c0001t0002g0049a0001c0001t0002g0105others(18): Show | 21 | HG01169.hp2 HG01257.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.1012-3685delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45400394 | ||||||
| chr5:45400545
|
C | G | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1012-3835G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45400545 | ||||||
| chr5:45400856
|
C | T | 1 | a0001c0001t0007g0214 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1012-4146G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45400856 | ||||||
| chr5:45401098
|
G | A | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1012-4388C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45401098 | ||||||
| chr5:45401192
|
T | A | 1 | a0001c0001t0001g0073 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1012-4482A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45401192 | ||||||
| chr5:45401392
|
C | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1012-4682G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45401392 | ||||||
| chr5:45401431
|
A | C | 1 | a0001c0001t0002g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1012-4721T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45401431 | ||||||
| chr5:45401446
|
T | C | 1 | a0001c0001t0002g0028 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1012-4736A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45401446 | ||||||
| chr5:45401581
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1012-4871G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45401581 | ||||||
| chr5:45401584
|
A | G | 35 | a0001c0001t0002g0072a0001c0001t0002g0091a0001c0001t0002g0096others(32): Show | 35 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1012-4874T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45401584 | ||||||
| chr5:45401657
|
G | GT | 16 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0001g0156others(13): Show | 16 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.1012-4948dupA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45401657 | ||||||
| chr5:45401657
|
GT | G | 20 | a0001c0001t0001g0085a0001c0001t0001g0179a0001c0001t0001g0180others(17): Show | 20 | HG01167.hp2 HG01192.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1012-4948delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45401657 | ||||||
| chr5:45401679
|
G | A | 1 | a0001c0001t0003g0188 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1012-4969C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45401679 | ||||||
| chr5:45401715
|
A | T | 144 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1012-5005T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45401715 | ||||||
| chr5:45401756
|
G | A | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1012-5046C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45401756 | ||||||
| chr5:45401870
|
G | T | 11 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(8): Show | 11 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1012-5160C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45401870 | ||||||
| chr5:45401871
|
TTTTAATT others(8): Show |
T | 1 | a0001c0001t0001g0011 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1012-5176_1012-516 others(19): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45401871 | ||||||
| chr5:45401921
|
G | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1012-5211C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45401921 | ||||||
| chr5:45401984
|
A | G | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1012-5274T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45401984 | ||||||
| chr5:45402262
|
G | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG01934.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.1012-5552C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45402262 | ||||||
| chr5:45402429
|
G | A | 2 | a0001c0001t0002g0072a0001c0001t0002g0097 | 2 | HG00673.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1012-5719C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45402429 | ||||||
| chr5:45402457
|
G | A | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1012-5747C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45402457 | ||||||
| chr5:45402791
|
T | A | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1012-6081A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45402791 | ||||||
| chr5:45402813
|
C | CTCCT | 84 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0065others(81): Show | 84 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.1012-6107_1012-610 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45402813 | ||||||
| chr5:45402813
|
C | CTCCTTCC others(1): Show |
26 | a0001c0001t0001g0011a0001c0001t0001g0073a0001c0001t0001g0147others(23): Show | 26 | HG00280.hp2 HG00609.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.1012-6111_1012-610 others(12): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45402813 | ||||||
| chr5:45402813
|
C | CTCCTTCC others(5): Show |
7 | a0001c0001t0002g0019a0001c0001t0002g0044a0001c0001t0003g0053others(4): Show | 7 | HG00099.hp1 HG00642.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.1012-6115_1012-610 others(16): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45402813 | ||||||
| chr5:45402813
|
C | CTCCTTCC others(9): Show |
3 | a0001c0001t0002g0069a0001c0001t0002g0121a0001c0001t0007g0115 | 3 | HG01346.hp2 HG01516.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1012-6119_1012-610 others(20): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45402813 | ||||||
| chr5:45402813
|
C | CTCCTTCC others(17): Show |
1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1012-6127_1012-610 others(28): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45402813 | ||||||
| chr5:45402813
|
CTCCT | C | 37 | a0001c0001t0001g0116a0001c0001t0001g0201a0001c0001t0002g0015others(34): Show | 37 | HG00099.hp2 HG00323.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1012-6107_1012-610 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45402813 | ||||||
| chr5:45402813
|
CTCCTTCC others(1): Show |
C | 8 | a0001c0001t0002g0082a0001c0001t0002g0132a0001c0001t0002g0133others(5): Show | 8 | HG01257.hp1 HG01258.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1012-6111_1012-610 others(12): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45402813 | ||||||
| chr5:45402813
|
CTCCTTCC others(5): Show |
C | 4 | a0001c0001t0019g0114a0002c0002t0008g0224a0002c0002t0008g0225others(1): Show | 4 | HG02055.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1012-6115_1012-610 others(16): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45402813 | ||||||
| chr5:45402813
|
CTCCTTCC others(9): Show |
C | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0023g0075 | 3 | HG02647.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1012-6119_1012-610 others(20): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45402813 | ||||||
| chr5:45402813
|
CTCCTTCC others(17): Show |
C | 1 | a0001c0001t0001g0074 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1012-6127_1012-610 others(28): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45402813 | ||||||
| chr5:45403102
|
T | A | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1012-6392A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45403102 | ||||||
| chr5:45403423
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1012-6713G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45403423 | ||||||
| chr5:45403633
|
T | C | 143 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1012-6923A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45403633 | ||||||
| chr5:45403726
|
G | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1012-7016C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45403726 | ||||||
| chr5:45403792
|
T | C | 2 | a0001c0001t0003g0098a0001c0001t0003g0099 | 2 | HG01361.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1012-7082A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45403792 | ||||||
| chr5:45403811
|
G | A | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1012-7101C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45403811 | ||||||
| chr5:45403901
|
G | A | 9 | a0001c0001t0001g0051a0001c0001t0002g0015a0001c0001t0002g0049others(6): Show | 9 | HG01109.hp2 HG02615.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1012-7191C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45403901 | ||||||
| chr5:45404053
|
C | T | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1012-7343G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45404053 | ||||||
| chr5:45404077
|
T | C | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1012-7367A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45404077 | ||||||
| chr5:45404272
|
G | A | 1 | a0001c0001t0012g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1012-7562C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45404272 | ||||||
| chr5:45404359
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1012-7649T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45404359 | ||||||
| chr5:45404496
|
TA | T | 2 | a0001c0001t0002g0015a0001c0001t0016g0014 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1012-7787delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45404496 | ||||||
| chr5:45404498
|
AT | A | 136 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0037others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.1012-7789delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45404498 | ||||||
| chr5:45404619
|
T | C | 1 | a0001c0001t0021g0138 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1012-7909A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45404619 | ||||||
| chr5:45404634
|
T | G | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1012-7924A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45404634 | ||||||
| chr5:45404693
|
C | CA | 33 | a0001c0001t0001g0073a0001c0001t0001g0147a0001c0001t0001g0151others(30): Show | 33 | HG00280.hp2 HG01192.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.1012-7984dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45404693 | ||||||
| chr5:45404693
|
C | CAAAA | 8 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(5): Show | 8 | HG00642.hp1 HG00738.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1012-7987_1012-798 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45404693 | ||||||
| chr5:45404693
|
CA | C | 17 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0015others(14): Show | 17 | HG00438.hp1 HG01109.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.1012-7984delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45404693 | ||||||
| chr5:45404693
|
CAA | C | 50 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(47): Show | 50 | HG00099.hp1 HG00597.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1012-7985_1012-798 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45404693 | ||||||
| chr5:45404693
|
CAAAAAAA others(3): Show |
C | 36 | a0001c0001t0002g0072a0001c0001t0002g0091a0001c0001t0002g0096others(33): Show | 36 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.1012-7993_1012-798 others(14): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45404693 | ||||||
| chr5:45404693
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1012-7994_1012-798 others(15): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45404693 | ||||||
| chr5:45404693
|
CAAAAAAA others(9): Show |
C | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1012-7999_1012-798 others(20): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45404693 | ||||||
| chr5:45404957
|
G | T | 16 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(13): Show | 16 | HG01167.hp1 HG01169.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.1012-8247C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45404957 | ||||||
| chr5:45404973
|
T | C | 1 | a0001c0001t0002g0041 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1012-8263A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45404973 | ||||||
| chr5:45405011
|
T | C | 2 | a0001c0001t0002g0121a0001c0001t0025g0217 | 2 | HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1012-8301A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45405011 | ||||||
| chr5:45405047
|
G | C | 5 | a0001c0001t0003g0109a0001c0001t0003g0110a0001c0001t0003g0111others(2): Show | 5 | HG02056.hp2 NA18980.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.1012-8337C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45405047 | ||||||
| chr5:45405552
|
C | T | 1 | a0001c0001t0003g0092 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1012-8842G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45405552 | ||||||
| chr5:45405653
|
G | A | 1 | a0002c0002t0014g0223 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1012-8943C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45405653 | ||||||
| chr5:45405997
|
G | A | 2 | a0001c0001t0003g0118a0001c0001t0003g0120 | 2 | HG00735.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.1012-9287C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45405997 | ||||||
| chr5:45406131
|
C | A | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1012-9421G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45406131 | ||||||
| chr5:45406163
|
T | C | 1 | a0001c0001t0002g0152 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1012-9453A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45406163 | ||||||
| chr5:45406190
|
G | T | 1 | a0001c0001t0003g0094 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1012-9480C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45406190 | ||||||
| chr5:45406219
|
T | C | 143 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1012-9509A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45406219 | ||||||
| chr5:45406231
|
T | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1012-9521A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45406231 | ||||||
| chr5:45406907
|
A | T | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1012-10197T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45406907 | ||||||
| chr5:45407180
|
T | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1012-10470A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45407180 | ||||||
| chr5:45407191
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1012-10481A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45407191 | ||||||
| chr5:45407214
|
C | T | 1 | a0001c0001t0003g0053 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1012-10504G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45407214 | ||||||
| chr5:45407452
|
T | C | 1 | a0001c0001t0002g0023 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1012-10742A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45407452 | ||||||
| chr5:45407713
|
G | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1012-11003C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45407713 | ||||||
| chr5:45407791
|
T | C | 2 | a0001c0001t0001g0034a0001c0001t0002g0035 | 2 | NA18949.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1012-11081A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45407791 | ||||||
| chr5:45407854
|
C | T | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1012-11144G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45407854 | ||||||
| chr5:45408158
|
G | A | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1012-11448C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45408158 | ||||||
| chr5:45408475
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1012-11765G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45408475 | ||||||
| chr5:45408567
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1012-11857G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45408567 | ||||||
| chr5:45408754
|
G | A | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1012-12044C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45408754 | ||||||
| chr5:45408764
|
C | T | 1 | a0001c0006t0002g0219 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1012-12054G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45408764 | ||||||
| chr5:45408797
|
T | C | 6 | a0001c0001t0001g0159a0001c0001t0001g0182a0001c0001t0001g0184others(3): Show | 6 | HG00639.hp1 HG01169.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1012-12087A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45408797 | ||||||
| chr5:45408894
|
C | T | 139 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.1012-12184G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45408894 | ||||||
| chr5:45408933
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0003g0063 | 2 | HG01071.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.1012-12223G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45408933 | ||||||
| chr5:45409222
|
A | G | 2 | a0001c0001t0002g0121a0001c0001t0025g0217 | 2 | HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1012-12512T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45409222 | ||||||
| chr5:45409344
|
G | T | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1012-12634C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45409344 | ||||||
| chr5:45409367
|
C | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1012-12657G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45409367 | ||||||
| chr5:45409798
|
T | C | 143 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1012-13088A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45409798 | ||||||
| chr5:45410461
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1012-13751G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45410461 | ||||||
| chr5:45410504
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1012-13794G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45410504 | ||||||
| chr5:45410518
|
A | G | 1 | a0001c0001t0003g0118 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1012-13808T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45410518 | ||||||
| chr5:45410792
|
T | A | 1 | a0001c0001t0003g0188 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1012-14082A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45410792 | ||||||
| chr5:45410852
|
G | A | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1012-14142C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45410852 | ||||||
| chr5:45411005
|
G | C | 1 | a0001c0001t0002g0027 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1012-14295C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45411005 | ||||||
| chr5:45411359
|
G | GT | 7 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(4): Show | 7 | HG02615.hp2 HG02647.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1012-14650dupA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45411359 | ||||||
| chr5:45411359
|
GT | G | 5 | a0001c0001t0001g0034a0001c0001t0002g0027a0001c0001t0002g0035others(2): Show | 5 | NA18949.hp2 NA18959.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.1012-14650delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45411359 | ||||||
| chr5:45411458
|
G | C | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1012-14748C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45411458 | ||||||
| chr5:45411459
|
A | G | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1012-14749T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45411459 | ||||||
| chr5:45411574
|
AT | A | 65 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(62): Show | 65 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1012-14865delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45411574 | ||||||
| chr5:45411576
|
T | C | 65 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(62): Show | 65 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1012-14866A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45411576 | ||||||
| chr5:45411824
|
A | G | 40 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(37): Show | 40 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1012-15114T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45411824 | ||||||
| chr5:45411870
|
T | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1012-15160A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45411870 | ||||||
| chr5:45412020
|
A | G | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1012-15310T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45412020 | ||||||
| chr5:45412102
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1012-15392G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45412102 | ||||||
| chr5:45412185
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1012-15475C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45412185 | ||||||
| chr5:45412494
|
T | A | 2 | a0001c0001t0002g0023a0001c0001t0002g0024 | 2 | NA18977.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1012-15784A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45412494 | ||||||
| chr5:45412571
|
G | A | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1012-15861C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45412571 | ||||||
| chr5:45412753
|
AGAGGCTG | A | 106 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.1012-16050_1012-16 others(13): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45412753 | ||||||
| chr5:45412764
|
C | T | 1 | a0001c0001t0018g0018 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1012-16054G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45412764 | ||||||
| chr5:45412887
|
C | T | 1 | a0001c0005t0002g0199 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1012-16177G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45412887 | ||||||
| chr5:45413257
|
T | C | 67 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1012-16547A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45413257 | ||||||
| chr5:45413332
|
C | A | 1 | a0001c0001t0002g0044 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1012-16622G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45413332 | ||||||
| chr5:45413402
|
G | A | 5 | a0001c0001t0001g0034a0001c0001t0002g0027a0001c0001t0002g0035others(2): Show | 5 | NA18949.hp2 NA18959.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.1012-16692C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45413402 | ||||||
| chr5:45413761
|
T | C | 1 | a0001c0001t0003g0099 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1012-17051A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45413761 | ||||||
| chr5:45413768
|
G | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1012-17058C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45413768 | ||||||
| chr5:45413965
|
T | C | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1012-17255A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45413965 | ||||||
| chr5:45413999
|
G | A | 4 | a0001c0001t0002g0066a0001c0001t0002g0067a0001c0001t0002g0131others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1012-17289C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45413999 | ||||||
| chr5:45414108
|
C | T | 1 | a0001c0001t0001g0205 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1012-17398G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45414108 | ||||||
| chr5:45414171
|
A | G | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1012-17461T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45414171 | ||||||
| chr5:45414256
|
T | C | 40 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(37): Show | 40 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1012-17546A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45414256 | ||||||
| chr5:45414440
|
C | T | 1 | a0001c0006t0002g0219 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1012-17730G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45414440 | ||||||
| chr5:45414466
|
A | G | 67 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1012-17756T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45414466 | ||||||
| chr5:45414493
|
G | T | 1 | a0001c0001t0001g0209 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1012-17783C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45414493 | ||||||
| chr5:45414507
|
T | C | 1 | a0001c0001t0003g0117 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1012-17797A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45414507 | ||||||
| chr5:45414595
|
C | A | 1 | a0001c0001t0024g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1012-17885G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45414595 | ||||||
| chr5:45414600
|
CAGA | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1012-17893_1012-17 others(9): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45414600 | ||||||
| chr5:45414775
|
T | C | 4 | a0001c0001t0002g0066a0001c0001t0002g0067a0001c0001t0002g0131others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1012-18065A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45414775 | ||||||
| chr5:45414905
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1012-18195A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45414905 | ||||||
| chr5:45415216
|
A | G | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1012-18506T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45415216 | ||||||
| chr5:45415419
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1012-18709G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45415419 | ||||||
| chr5:45415590
|
T | C | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1012-18880A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45415590 | ||||||
| chr5:45416227
|
G | A | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1012-19517C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45416227 | ||||||
| chr5:45416401
|
T | C | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1012-19691A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45416401 | ||||||
| chr5:45416433
|
T | C | 1 | a0001c0001t0002g0072 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1012-19723A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45416433 | ||||||
| chr5:45416513
|
G | A | 16 | a0001c0001t0001g0065a0001c0001t0004g0017a0001c0001t0004g0020others(13): Show | 16 | HG00438.hp1 HG00609.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.1012-19803C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45416513 | ||||||
| chr5:45416692
|
T | C | 144 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1012-19982A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45416692 | ||||||
| chr5:45416795
|
A | T | 1 | a0001c0001t0001g0151 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1012-20085T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45416795 | ||||||
| chr5:45417046
|
C | T | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1012-20336G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45417046 | ||||||
| chr5:45417211
|
A | T | 1 | a0001c0001t0021g0138 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1012-20501T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45417211 | ||||||
| chr5:45417588
|
C | T | 14 | a0001c0001t0001g0073a0001c0001t0001g0134a0001c0001t0001g0160others(11): Show | 14 | HG00642.hp2 HG00673.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.1012-20878G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45417588 | ||||||
| chr5:45417728
|
A | C | 1 | a0001c0001t0007g0214 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1012-21018T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45417728 | ||||||
| chr5:45417751
|
C | CA | 44 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0074others(41): Show | 44 | HG00099.hp2 HG00438.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1012-21042dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45417751 | ||||||
| chr5:45417751
|
CA | C | 10 | a0001c0001t0001g0073a0001c0001t0001g0085a0001c0001t0002g0025others(7): Show | 10 | HG01256.hp2 HG01257.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.1012-21042delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45417751 | ||||||
| chr5:45417822
|
A | G | 2 | a0001c0001t0002g0121a0001c0001t0025g0217 | 2 | HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1012-21112T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45417822 | ||||||
| chr5:45417918
|
G | T | 1 | a0001c0001t0005g0129 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1012-21208C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45417918 | ||||||
| chr5:45418084
|
T | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1012-21374A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45418084 | ||||||
| chr5:45418194
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1012-21484A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45418194 | ||||||
| chr5:45418300
|
C | G | 1 | a0001c0001t0002g0082 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1012-21590G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45418300 | ||||||
| chr5:45418319
|
C | T | 67 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1012-21609G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45418319 | ||||||
| chr5:45418645
|
C | T | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1012-21935G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45418645 | ||||||
| chr5:45418649
|
G | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1012-21939C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45418649 | ||||||
| chr5:45418838
|
A | C | 16 | a0001c0001t0001g0065a0001c0001t0004g0017a0001c0001t0004g0020others(13): Show | 16 | HG00438.hp1 HG00609.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.1012-22128T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45418838 | ||||||
| chr5:45418916
|
C | G | 6 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0156others(3): Show | 6 | HG00597.hp1 NA18939.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.1012-22206G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45418916 | ||||||
| chr5:45419006
|
C | T | 1 | a0001c0001t0019g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1012-22296G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45419006 | ||||||
| chr5:45419246
|
T | C | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1012-22536A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45419246 | ||||||
| chr5:45419317
|
C | A | 1 | a0001c0001t0007g0214 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1012-22607G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45419317 | ||||||
| chr5:45419394
|
C | T | 2 | a0001c0001t0002g0039a0001c0001t0002g0040 | 2 | HG00639.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1012-22684G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45419394 | ||||||
| chr5:45419443
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1012-22733G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45419443 | ||||||
| chr5:45419486
|
C | T | 2 | a0001c0001t0002g0069a0001c0006t0002g0219 | 2 | HG01516.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1012-22776G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45419486 | ||||||
| chr5:45419657
|
C | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1012-22947G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45419657 | ||||||
| chr5:45419823
|
A | G | 11 | a0001c0001t0002g0121a0001c0001t0005g0122a0001c0001t0005g0123others(8): Show | 11 | HG01261.hp2 HG01346.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1012-23113T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45419823 | ||||||
| chr5:45419884
|
T | C | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1012-23174A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45419884 | ||||||
| chr5:45420216
|
C | A | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1012-23506G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45420216 | ||||||
| chr5:45420308
|
T | TG | 4 | a0001c0001t0001g0134a0001c0001t0001g0136a0001c0001t0002g0027others(1): Show | 4 | HG00673.hp1 NA18959.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1012-23599dupC | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45420308 | ||||||
| chr5:45420482
|
C | T | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1012-23772G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45420482 | ||||||
| chr5:45420659
|
A | C | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1012-23949T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45420659 | ||||||
| chr5:45420715
|
C | T | 1 | a0001c0001t0002g0193 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1012-24005G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45420715 | ||||||
| chr5:45421068
|
C | T | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1012-24358G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45421068 | ||||||
| chr5:45421128
|
T | A | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1012-24418A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45421128 | ||||||
| chr5:45421138
|
A | C | 223 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1012-24428T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45421138 | ||||||
| chr5:45421208
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1012-24498C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45421208 | ||||||
| chr5:45421429
|
A | G | 1 | a0001c0001t0002g0019 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1012-24719T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45421429 | ||||||
| chr5:45421507
|
C | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1012-24797G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45421507 | ||||||
| chr5:45421511
|
G | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1012-24801C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45421511 | ||||||
| chr5:45421516
|
A | G | 3 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0157 | 3 | NA18945.hp2 NA19064.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1012-24806T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45421516 | ||||||
| chr5:45421570
|
C | A | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1012-24860G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45421570 | ||||||
| chr5:45421648
|
A | C | 2 | a0001c0001t0002g0015a0001c0001t0016g0014 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1012-24938T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45421648 | ||||||
| chr5:45422088
|
G | T | 1 | a0001c0001t0001g0180 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1012-25378C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45422088 | ||||||
| chr5:45422384
|
T | C | 4 | a0001c0001t0002g0052a0001c0001t0006g0057a0002c0002t0014g0222others(1): Show | 4 | HG01109.hp2 HG01433.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1012-25674A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45422384 | ||||||
| chr5:45422712
|
A | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1012-26002T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45422712 | ||||||
| chr5:45422718
|
T | A | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1012-26008A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45422718 | ||||||
| chr5:45422728
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1012-26018T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45422728 | ||||||
| chr5:45423041
|
A | T | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1012-26331T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45423041 | ||||||
| chr5:45423418
|
A | G | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1012-26708T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45423418 | ||||||
| chr5:45423504
|
C | G | 1 | a0001c0001t0001g0139 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1012-26794G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45423504 | ||||||
| chr5:45423575
|
CA | C | 4 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(1): Show | 4 | HG02055.hp2 HG02257.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1012-26866delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45423575 | ||||||
| chr5:45423793
|
A | G | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1012-27083T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45423793 | ||||||
| chr5:45423844
|
A | G | 11 | a0001c0001t0002g0121a0001c0001t0005g0122a0001c0001t0005g0123others(8): Show | 11 | HG01261.hp2 HG01346.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1012-27134T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45423844 | ||||||
| chr5:45424117
|
T | TA | 64 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0037others(61): Show | 64 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.1012-27408_1012-27 others(7): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45424117 | ||||||
| chr5:45424118
|
C | A | 159 | a0001c0001t0001g0011a0001c0001t0001g0045a0001c0001t0001g0073others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.1012-27408G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45424118 | ||||||
| chr5:45424119
|
C | A | 64 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0037others(61): Show | 64 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.1012-27409G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45424119 | ||||||
| chr5:45424119
|
C | CAA | 10 | a0001c0001t0002g0015a0001c0001t0002g0058a0001c0001t0002g0066others(7): Show | 10 | HG00438.hp1 HG02027.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1012-27411_1012-27 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45424119 | ||||||
| chr5:45424119
|
CA | C | 49 | a0001c0001t0001g0184a0001c0001t0001g0204a0001c0001t0002g0049others(46): Show | 49 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1012-27410delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45424119 | ||||||
| chr5:45424121
|
A | C | 2 | a0001c0001t0005g0124a0001c0001t0019g0114 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1012-27411T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45424121 | ||||||
| chr5:45424850
|
C | T | 3 | a0001c0001t0003g0084a0001c0001t0003g0101a0001c0001t0036g0186 | 3 | NA19003.hp1 NA19011.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1012-28140G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45424850 | ||||||
| chr5:45424977
|
C | A | 40 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(37): Show | 40 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1012-28267G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45424977 | ||||||
| chr5:45424992
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1012-28282C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45424992 | ||||||
| chr5:45425058
|
A | G | 35 | a0001c0001t0002g0072a0001c0001t0002g0082a0001c0001t0002g0091others(32): Show | 35 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1012-28348T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45425058 | ||||||
| chr5:45425077
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1012-28367C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45425077 | ||||||
| chr5:45425303
|
G | T | 1 | a0001c0001t0028g0174 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1012-28593C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45425303 | ||||||
| chr5:45425704
|
A | C | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1012-28994T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45425704 | ||||||
| chr5:45425781
|
T | G | 1 | a0001c0001t0004g0062 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1012-29071A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45425781 | ||||||
| chr5:45425854
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1012-29144C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45425854 | ||||||
| chr5:45425936
|
A | C | 1 | a0001c0001t0002g0050 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1012-29226T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45425936 | ||||||
| chr5:45426115
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1012-29405T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45426115 | ||||||
| chr5:45426158
|
A | G | 4 | a0001c0001t0001g0102a0001c0001t0001g0107a0001c0001t0001g0160others(1): Show | 4 | HG00438.hp2 HG02040.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1012-29448T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45426158 | ||||||
| chr5:45426193
|
T | C | 1 | a0001c0001t0002g0012 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1012-29483A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45426193 | ||||||
| chr5:45426552
|
G | A | 1 | a0001c0001t0005g0142 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1012-29842C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45426552 | ||||||
| chr5:45426600
|
A | G | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1012-29890T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45426600 | ||||||
| chr5:45426712
|
T | C | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1012-30002A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45426712 | ||||||
| chr5:45426765
|
C | T | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1012-30055G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45426765 | ||||||
| chr5:45426926
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1012-30216G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45426926 | ||||||
| chr5:45426952
|
C | T | 1 | a0001c0001t0006g0143 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1012-30242G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45426952 | ||||||
| chr5:45426979
|
T | G | 1 | a0001c0001t0003g0083 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1012-30269A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45426979 | ||||||
| chr5:45427035
|
A | G | 141 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.1012-30325T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45427035 | ||||||
| chr5:45427071
|
C | T | 140 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1012-30361G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45427071 | ||||||
| chr5:45427188
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1012-30478A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45427188 | ||||||
| chr5:45427273
|
A | G | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1012-30563T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45427273 | ||||||
| chr5:45427284
|
A | G | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1012-30574T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45427284 | ||||||
| chr5:45427431
|
T | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1012-30721A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45427431 | ||||||
| chr5:45427544
|
A | G | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1012-30834T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45427544 | ||||||
| chr5:45427651
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1012-30941C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45427651 | ||||||
| chr5:45427835
|
C | T | 6 | a0001c0001t0001g0159a0001c0001t0001g0182a0001c0001t0001g0184others(3): Show | 6 | HG00639.hp1 HG01169.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1012-31125G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45427835 | ||||||
| chr5:45427888
|
A | G | 1 | a0001c0001t0002g0028 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1012-31178T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45427888 | ||||||
| chr5:45427992
|
T | C | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1012-31282A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45427992 | ||||||
| chr5:45428102
|
TTATC | T | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1012-31396_1012-31 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45428102 | ||||||
| chr5:45428175
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1012-31465C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45428175 | ||||||
| chr5:45428433
|
T | C | 140 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1012-31723A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45428433 | ||||||
| chr5:45428538
|
T | C | 35 | a0001c0001t0002g0072a0001c0001t0002g0082a0001c0001t0002g0091others(32): Show | 35 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1012-31828A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45428538 | ||||||
| chr5:45428690
|
T | G | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1012-31980A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45428690 | ||||||
| chr5:45428855
|
A | G | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1012-32145T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45428855 | ||||||
| chr5:45429075
|
T | A | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1012-32365A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45429075 | ||||||
| chr5:45429493
|
G | C | 1 | a0001c0001t0012g0137 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1011+32353C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45429493 | ||||||
| chr5:45429888
|
G | C | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1011+31958C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45429888 | ||||||
| chr5:45430071
|
A | C | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1011+31775T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45430071 | ||||||
| chr5:45430326
|
T | G | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1011+31520A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45430326 | ||||||
| chr5:45430413
|
G | GT | 9 | a0001c0001t0001g0206a0001c0001t0002g0019a0001c0001t0002g0121others(6): Show | 9 | HG00099.hp1 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1011+31432dupA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45430413 | ||||||
| chr5:45430672
|
T | A | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1011+31174A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45430672 | ||||||
| chr5:45430746
|
T | C | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1011+31100A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45430746 | ||||||
| chr5:45430776
|
C | T | 2 | a0001c0001t0001g0187a0001c0001t0040g0175 | 2 | NA18977.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1011+31070G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45430776 | ||||||
| chr5:45430800
|
C | T | 1 | a0001c0001t0003g0053 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1011+31046G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45430800 | ||||||
| chr5:45430808
|
C | A | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1011+31038G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45430808 | ||||||
| chr5:45430810
|
A | G | 1 | a0001c0001t0001g0102 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1011+31036T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45430810 | ||||||
| chr5:45431106
|
A | G | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1011+30740T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45431106 | ||||||
| chr5:45431123
|
T | C | 1 | a0001c0001t0002g0096 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1011+30723A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45431123 | ||||||
| chr5:45431149
|
T | C | 6 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(3): Show | 6 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1011+30697A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45431149 | ||||||
| chr5:45431289
|
G | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1011+30557C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45431289 | ||||||
| chr5:45431339
|
A | T | 1 | a0001c0001t0034g0172 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1011+30507T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45431339 | ||||||
| chr5:45431733
|
A | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1011+30113T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45431733 | ||||||
| chr5:45431816
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1011+30030T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45431816 | ||||||
| chr5:45431902
|
G | A | 33 | a0001c0001t0002g0072a0001c0001t0002g0091a0001c0001t0002g0096others(30): Show | 33 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.1011+29944C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45431902 | ||||||
| chr5:45431920
|
C | T | 1 | a0001c0001t0028g0174 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1011+29926G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45431920 | ||||||
| chr5:45431990
|
TACAAATA others(14): Show |
T | 1 | a0001c0001t0002g0039 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1011+29835_1011+29 others(27): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45431990 | ||||||
| chr5:45432042
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0190 | 2 | NA18971.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1011+29804C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45432042 | ||||||
| chr5:45432287
|
C | G | 1 | a0001c0001t0001g0179 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1011+29559G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45432287 | ||||||
| chr5:45432391
|
C | T | 1 | a0001c0001t0002g0054 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1011+29455G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45432391 | ||||||
| chr5:45432443
|
T | G | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1011+29403A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45432443 | ||||||
| chr5:45432606
|
A | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1011+29240T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45432606 | ||||||
| chr5:45432860
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1011+28986G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45432860 | ||||||
| chr5:45433018
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0002g0181 | 2 | HG01346.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1011+28828G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45433018 | ||||||
| chr5:45433019
|
G | A | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1011+28827C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45433019 | ||||||
| chr5:45433059
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1011+28787G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45433059 | ||||||
| chr5:45433369
|
G | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1011+28477C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45433369 | ||||||
| chr5:45433377
|
G | T | 4 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0031g0009others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.1011+28469C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45433377 | ||||||
| chr5:45434381
|
A | T | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1011+27465T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45434381 | ||||||
| chr5:45434384
|
C | T | 5 | a0001c0001t0001g0134a0001c0001t0001g0166a0001c0001t0002g0088others(2): Show | 5 | HG02165.hp2 NA18961.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1011+27462G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45434384 | ||||||
| chr5:45434419
|
T | C | 1 | a0001c0001t0002g0069 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1011+27427A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45434419 | ||||||
| chr5:45434434
|
G | T | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1011+27412C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45434434 | ||||||
| chr5:45434827
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1011+27019T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45434827 | ||||||
| chr5:45434842
|
A | G | 2 | a0001c0001t0002g0082a0001c0001t0019g0114 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1011+27004T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45434842 | ||||||
| chr5:45434917
|
T | C | 139 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.1011+26929A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45434917 | ||||||
| chr5:45434956
|
T | C | 16 | a0001c0001t0001g0065a0001c0001t0004g0017a0001c0001t0004g0020others(13): Show | 16 | HG00438.hp1 HG00609.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.1011+26890A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45434956 | ||||||
| chr5:45434964
|
A | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1011+26882T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45434964 | ||||||
| chr5:45435021
|
G | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1011+26825C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45435021 | ||||||
| chr5:45435104
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1011+26742T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45435104 | ||||||
| chr5:45435239
|
A | G | 1 | a0001c0001t0003g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1011+26607T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45435239 | ||||||
| chr5:45435268
|
T | C | 1 | a0002c0002t0014g0222 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1011+26578A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45435268 | ||||||
| chr5:45435664
|
A | G | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1011+26182T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45435664 | ||||||
| chr5:45435698
|
G | A | 1 | a0001c0001t0007g0214 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1011+26148C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45435698 | ||||||
| chr5:45435884
|
T | A | 140 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1011+25962A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45435884 | ||||||
| chr5:45435957
|
C | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1011+25889G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45435957 | ||||||
| chr5:45436148
|
C | T | 1 | a0001c0001t0003g0119 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1011+25698G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45436148 | ||||||
| chr5:45436472
|
C | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1011+25374G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45436472 | ||||||
| chr5:45436518
|
T | A | 1 | a0001c0001t0002g0096 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1011+25328A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45436518 | ||||||
| chr5:45436534
|
T | A | 225 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1011+25312A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45436534 | ||||||
| chr5:45436634
|
A | G | 1 | a0001c0001t0024g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1011+25212T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45436634 | ||||||
| chr5:45436760
|
T | A | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1011+25086A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45436760 | ||||||
| chr5:45436792
|
T | G | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1011+25054A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45436792 | ||||||
| chr5:45436795
|
T | C | 95 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.1011+25051A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45436795 | ||||||
| chr5:45436887
|
A | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1011+24959T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45436887 | ||||||
| chr5:45436908
|
C | T | 4 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(1): Show | 4 | HG02055.hp2 HG02257.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1011+24938G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45436908 | ||||||
| chr5:45436909
|
G | A | 1 | a0001c0001t0002g0152 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1011+24937C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45436909 | ||||||
| chr5:45436959
|
G | A | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1011+24887C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45436959 | ||||||
| chr5:45437001
|
C | T | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1011+24845G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45437001 | ||||||
| chr5:45437027
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1011+24819A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45437027 | ||||||
| chr5:45437628
|
G | T | 1 | a0001c0001t0001g0074 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1011+24218C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45437628 | ||||||
| chr5:45437680
|
G | A | 1 | a0001c0001t0028g0174 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1011+24166C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45437680 | ||||||
| chr5:45437756
|
T | C | 1 | a0002c0002t0014g0222 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1011+24090A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45437756 | ||||||
| chr5:45437815
|
C | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1011+24031G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45437815 | ||||||
| chr5:45437908
|
G | T | 1 | a0001c0001t0003g0053 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1011+23938C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45437908 | ||||||
| chr5:45438032
|
G | C | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1011+23814C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45438032 | ||||||
| chr5:45438044
|
C | T | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1011+23802G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45438044 | ||||||
| chr5:45438080
|
T | C | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1011+23766A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45438080 | ||||||
| chr5:45438121
|
A | T | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1011+23725T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45438121 | ||||||
| chr5:45438194
|
A | G | 1 | a0001c0001t0027g0022 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1011+23652T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45438194 | ||||||
| chr5:45438375
|
C | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1011+23471G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45438375 | ||||||
| chr5:45438447
|
C | T | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1011+23399G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45438447 | ||||||
| chr5:45438468
|
G | C | 1 | a0001c0001t0023g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1011+23378C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45438468 | ||||||
| chr5:45438506
|
G | C | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1011+23340C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45438506 | ||||||
| chr5:45438576
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1011+23270G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45438576 | ||||||
| chr5:45438579
|
G | A | 10 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1011+23267C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45438579 | ||||||
| chr5:45438589
|
C | CA | 10 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(7): Show | 10 | HG01257.hp2 HG01891.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1011+23256dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45438589 | ||||||
| chr5:45438591
|
A | T | 1 | a0001c0001t0019g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1011+23255T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45438591 | ||||||
| chr5:45438640
|
A | G | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1011+23206T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45438640 | ||||||
| chr5:45438649
|
A | G | 1 | a0001c0001t0002g0046 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1011+23197T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45438649 | ||||||
| chr5:45438680
|
T | C | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1011+23166A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45438680 | ||||||
| chr5:45438718
|
T | G | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1011+23128A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45438718 | ||||||
| chr5:45439331
|
G | A | 140 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1011+22515C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45439331 | ||||||
| chr5:45439655
|
C | T | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1011+22191G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45439655 | ||||||
| chr5:45439800
|
GA | G | 2 | a0002c0002t0008g0224a0002c0002t0008g0225 | 2 | HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1011+22045delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45439800 | ||||||
| chr5:45439855
|
C | G | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1011+21991G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45439855 | ||||||
| chr5:45439937
|
T | C | 1 | a0001c0001t0019g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1011+21909A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45439937 | ||||||
| chr5:45440002
|
T | C | 1 | a0001c0001t0006g0143 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1011+21844A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45440002 | ||||||
| chr5:45440117
|
A | G | 1 | a0001c0001t0003g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1011+21729T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45440117 | ||||||
| chr5:45440241
|
G | T | 140 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1011+21605C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45440241 | ||||||
| chr5:45440587
|
T | C | 10 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1011+21259A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45440587 | ||||||
| chr5:45440627
|
G | A | 4 | a0001c0001t0001g0045a0001c0001t0003g0063a0001c0001t0003g0158others(1): Show | 4 | HG01071.hp2 HG01081.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.1011+21219C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45440627 | ||||||
| chr5:45440649
|
T | A | 65 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(62): Show | 65 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1011+21197A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45440649 | ||||||
| chr5:45440713
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1011+21133T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45440713 | ||||||
| chr5:45440925
|
C | G | 140 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1011+20921G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45440925 | ||||||
| chr5:45441035
|
G | C | 1 | a0001c0001t0004g0032 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1011+20811C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45441035 | ||||||
| chr5:45441266
|
G | T | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1011+20580C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45441266 | ||||||
| chr5:45441352
|
T | G | 5 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0031g0009others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1011+20494A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45441352 | ||||||
| chr5:45441362
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1011+20484T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45441362 | ||||||
| chr5:45441535
|
A | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1011+20311T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45441535 | ||||||
| chr5:45441638
|
T | C | 5 | a0001c0001t0001g0073a0001c0001t0001g0167a0001c0001t0001g0169others(2): Show | 5 | HG02056.hp1 NA18612.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.1011+20208A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45441638 | ||||||
| chr5:45441686
|
C | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1011+20160G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45441686 | ||||||
| chr5:45442085
|
C | T | 3 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0043 | 3 | HG00597.hp2 HG00639.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1011+19761G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45442085 | ||||||
| chr5:45442186
|
G | A | 1 | a0001c0001t0018g0018 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1011+19660C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45442186 | ||||||
| chr5:45442296
|
T | C | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1011+19550A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45442296 | ||||||
| chr5:45442530
|
C | T | 1 | a0001c0001t0001g0011 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1011+19316G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45442530 | ||||||
| chr5:45442533
|
G | T | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1011+19313C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45442533 | ||||||
| chr5:45442865
|
C | T | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1011+18981G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45442865 | ||||||
| chr5:45443138
|
T | C | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1011+18708A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45443138 | ||||||
| chr5:45443227
|
T | G | 3 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0157 | 3 | NA18945.hp2 NA19064.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1011+18619A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45443227 | ||||||
| chr5:45443426
|
G | T | 1 | a0001c0001t0001g0211 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1011+18420C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45443426 | ||||||
| chr5:45443671
|
T | C | 1 | a0001c0001t0009g0002 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1011+18175A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45443671 | ||||||
| chr5:45443727
|
A | G | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1011+18119T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45443727 | ||||||
| chr5:45443876
|
G | A | 1 | a0001c0001t0002g0036 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1011+17970C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45443876 | ||||||
| chr5:45444149
|
T | C | 1 | a0001c0001t0002g0027 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1011+17697A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45444149 | ||||||
| chr5:45444455
|
C | T | 225 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1011+17391G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45444455 | ||||||
| chr5:45444662
|
A | G | 10 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1011+17184T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45444662 | ||||||
| chr5:45444800
|
TTTA | T | 11 | a0001c0001t0002g0121a0001c0001t0005g0122a0001c0001t0005g0123others(8): Show | 11 | HG01261.hp2 HG01346.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1011+17043_1011+17 others(9): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45444800 | ||||||
| chr5:45444817
|
T | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG01952.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1011+17029A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45444817 | ||||||
| chr5:45444845
|
A | C | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1011+17001T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45444845 | ||||||
| chr5:45444967
|
G | A | 141 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.1011+16879C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45444967 | ||||||
| chr5:45445057
|
G | A | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1011+16789C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45445057 | ||||||
| chr5:45445061
|
G | A | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1011+16785C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45445061 | ||||||
| chr5:45445190
|
C | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1011+16656G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45445190 | ||||||
| chr5:45445191
|
A | G | 140 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1011+16655T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45445191 | ||||||
| chr5:45445238
|
G | A | 1 | a0001c0001t0003g0099 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1011+16608C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45445238 | ||||||
| chr5:45445260
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1011+16586G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45445260 | ||||||
| chr5:45445367
|
C | T | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1011+16479G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45445367 | ||||||
| chr5:45445481
|
T | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1011+16365A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45445481 | ||||||
| chr5:45445519
|
C | T | 4 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(1): Show | 4 | HG02055.hp2 HG02257.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1011+16327G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45445519 | ||||||
| chr5:45445578
|
G | T | 3 | a0001c0001t0003g0083a0001c0001t0003g0098a0001c0001t0003g0099 | 3 | HG00323.hp2 HG01361.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1011+16268C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45445578 | ||||||
| chr5:45445611
|
C | T | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1011+16235G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45445611 | ||||||
| chr5:45445778
|
G | C | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1011+16068C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45445778 | ||||||
| chr5:45445916
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1011+15930C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45445916 | ||||||
| chr5:45445931
|
A | C | 1 | a0001c0001t0012g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1011+15915T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45445931 | ||||||
| chr5:45445931
|
A | G | 1 | a0001c0001t0003g0053 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1011+15915T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45445931 | ||||||
| chr5:45445973
|
C | T | 1 | a0001c0001t0003g0109 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1011+15873G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45445973 | ||||||
| chr5:45446013
|
C | A | 3 | a0001c0001t0003g0083a0001c0001t0003g0098a0001c0001t0003g0099 | 3 | HG00323.hp2 HG01361.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1011+15833G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45446013 | ||||||
| chr5:45446050
|
C | T | 67 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1011+15796G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45446050 | ||||||
| chr5:45446093
|
C | A | 1 | a0001c0001t0009g0003 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1011+15753G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45446093 | ||||||
| chr5:45446223
|
G | A | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1011+15623C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45446223 | ||||||
| chr5:45446259
|
A | G | 1 | a0001c0001t0003g0104 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1011+15587T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45446259 | ||||||
| chr5:45446336
|
C | T | 1 | a0001c0001t0002g0043 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1011+15510G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45446336 | ||||||
| chr5:45446419
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1011+15427G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45446419 | ||||||
| chr5:45446431
|
G | A | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1011+15415C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45446431 | ||||||
| chr5:45446505
|
G | A | 2 | a0001c0001t0002g0015a0001c0001t0016g0014 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1011+15341C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45446505 | ||||||
| chr5:45446644
|
C | T | 1 | a0001c0004t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1011+15202G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45446644 | ||||||
| chr5:45446645
|
C | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1011+15201G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45446645 | ||||||
| chr5:45446646
|
G | A | 1 | a0001c0001t0023g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1011+15200C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45446646 | ||||||
| chr5:45446659
|
G | C | 10 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1011+15187C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45446659 | ||||||
| chr5:45446663
|
A | T | 1 | a0001c0001t0002g0050 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1011+15183T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45446663 | ||||||
| chr5:45446816
|
C | A | 2 | a0001c0001t0002g0082a0001c0001t0019g0114 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1011+15030G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45446816 | ||||||
| chr5:45446935
|
T | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1011+14911A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45446935 | ||||||
| chr5:45446952
|
A | T | 2 | a0001c0001t0002g0023a0001c0001t0002g0024 | 2 | NA18977.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1011+14894T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45446952 | ||||||
| chr5:45447147
|
C | T | 9 | a0001c0001t0001g0051a0001c0001t0002g0015a0001c0001t0002g0049others(6): Show | 9 | HG01109.hp2 HG02615.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1011+14699G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45447147 | ||||||
| chr5:45447184
|
G | C | 10 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1011+14662C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45447184 | ||||||
| chr5:45447548
|
A | T | 1 | a0001c0001t0001g0171 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1011+14298T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45447548 | ||||||
| chr5:45447575
|
A | T | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1011+14271T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45447575 | ||||||
| chr5:45447881
|
GAT | G | 10 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1011+13963_1011+13 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45447881 | ||||||
| chr5:45447959
|
A | T | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1011+13887T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45447959 | ||||||
| chr5:45448375
|
G | T | 2 | a0001c0001t0003g0101a0001c0001t0036g0186 | 2 | NA19011.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1011+13471C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45448375 | ||||||
| chr5:45448419
|
A | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1011+13427T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45448419 | ||||||
| chr5:45448478
|
C | G | 40 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(37): Show | 40 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1011+13368G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45448478 | ||||||
| chr5:45448679
|
T | G | 2 | a0001c0001t0002g0067a0001c0001t0002g0131 | 2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1011+13167A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45448679 | ||||||
| chr5:45449087
|
G | A | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1011+12759C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45449087 | ||||||
| chr5:45449481
|
C | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1011+12365G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45449481 | ||||||
| chr5:45449500
|
A | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1011+12346T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45449500 | ||||||
| chr5:45449608
|
CT | C | 10 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1011+12237delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45449608 | ||||||
| chr5:45449627
|
C | T | 1 | a0001c0001t0028g0174 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1011+12219G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45449627 | ||||||
| chr5:45449681
|
T | C | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1011+12165A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45449681 | ||||||
| chr5:45449858
|
C | T | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1011+11988G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45449858 | ||||||
| chr5:45449990
|
G | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1011+11856C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45449990 | ||||||
| chr5:45450011
|
T | G | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1011+11835A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45450011 | ||||||
| chr5:45450121
|
G | A | 2 | a0001c0001t0001g0156a0001c0001t0003g0108 | 2 | HG03225.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.1011+11725C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45450121 | ||||||
| chr5:45450245
|
A | G | 1 | a0001c0001t0007g0100 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1011+11601T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45450245 | ||||||
| chr5:45450420
|
A | G | 1 | a0001c0001t0005g0127 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1011+11426T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45450420 | ||||||
| chr5:45450895
|
C | G | 1 | a0001c0001t0001g0065 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1011+10951G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45450895 | ||||||
| chr5:45450950
|
G | A | 33 | a0001c0001t0002g0072a0001c0001t0002g0091a0001c0001t0002g0096others(30): Show | 33 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.1011+10896C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45450950 | ||||||
| chr5:45451094
|
T | C | 13 | a0001c0001t0002g0121a0001c0001t0005g0122a0001c0001t0005g0123others(10): Show | 13 | HG01261.hp2 HG01346.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1011+10752A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45451094 | ||||||
| chr5:45451130
|
A | T | 4 | a0001c0001t0002g0019a0001c0001t0002g0042a0001c0001t0002g0046others(1): Show | 4 | HG00099.hp1 HG00738.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1011+10716T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45451130 | ||||||
| chr5:45451337
|
G | T | 1 | a0001c0001t0003g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1011+10509C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45451337 | ||||||
| chr5:45451393
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1011+10453T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45451393 | ||||||
| chr5:45451673
|
T | A | 225 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1011+10173A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45451673 | ||||||
| chr5:45451805
|
G | A | 1 | a0001c0001t0005g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1011+10041C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45451805 | ||||||
| chr5:45451982
|
A | G | 1 | a0001c0001t0023g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1011+9864T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45451982 | ||||||
| chr5:45452038
|
A | C | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1011+9808T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45452038 | ||||||
| chr5:45452044
|
C | T | 135 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1011+9802G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45452044 | ||||||
| chr5:45452508
|
G | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1011+9338C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45452508 | ||||||
| chr5:45452848
|
A | G | 3 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0157 | 3 | NA18945.hp2 NA19064.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1011+8998T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45452848 | ||||||
| chr5:45453233
|
G | A | 29 | a0001c0001t0002g0072a0001c0001t0002g0091a0001c0001t0002g0096others(26): Show | 29 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.1011+8613C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45453233 | ||||||
| chr5:45453537
|
A | G | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1011+8309T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45453537 | ||||||
| chr5:45453580
|
G | C | 1 | a0001c0001t0005g0142 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1011+8266C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45453580 | ||||||
| chr5:45453590
|
T | G | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1011+8256A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45453590 | ||||||
| chr5:45453599
|
C | T | 7 | a0001c0001t0003g0090a0001c0001t0003g0092a0001c0001t0003g0109others(4): Show | 7 | HG02056.hp2 HG02129.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.1011+8247G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45453599 | ||||||
| chr5:45453618
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1011+8228C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45453618 | ||||||
| chr5:45453660
|
C | A | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1011+8186G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45453660 | ||||||
| chr5:45453778
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG01074.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1011+8068C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45453778 | ||||||
| chr5:45453836
|
A | T | 216 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1011+8010T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45453836 | ||||||
| chr5:45454011
|
C | T | 1 | a0001c0001t0003g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1011+7835G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45454011 | ||||||
| chr5:45454117
|
T | C | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1011+7729A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45454117 | ||||||
| chr5:45454122
|
G | T | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1011+7724C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45454122 | ||||||
| chr5:45454330
|
G | A | 93 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(90): Show | 93 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.1011+7516C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45454330 | ||||||
| chr5:45454495
|
A | AT | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1011+7350_1011+735 others(5): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45454495 | ||||||
| chr5:45454496
|
A | T | 2 | a0001c0001t0001g0073a0001c0001t0017g0081 | 2 | NA18982.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1011+7350T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45454496 | ||||||
| chr5:45454506
|
A | T | 1 | a0001c0001t0029g0070 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1011+7340T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45454506 | ||||||
| chr5:45454643
|
A | C | 1 | a0001c0001t0002g0027 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1011+7203T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45454643 | ||||||
| chr5:45454658
|
A | G | 6 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(3): Show | 6 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1011+7188T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45454658 | ||||||
| chr5:45454679
|
A | G | 1 | a0001c0001t0002g0038 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1011+7167T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45454679 | ||||||
| chr5:45454860
|
G | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1011+6986C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45454860 | ||||||
| chr5:45455037
|
A | G | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1011+6809T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45455037 | ||||||
| chr5:45455078
|
T | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1011+6768A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45455078 | ||||||
| chr5:45455099
|
C | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1011+6747G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45455099 | ||||||
| chr5:45455148
|
T | C | 4 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(1): Show | 4 | HG02055.hp2 HG02257.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1011+6698A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45455148 | ||||||
| chr5:45455316
|
T | C | 4 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(1): Show | 4 | HG02055.hp2 HG02257.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1011+6530A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45455316 | ||||||
| chr5:45455679
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1011+6167G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45455679 | ||||||
| chr5:45455714
|
G | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1011+6132C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45455714 | ||||||
| chr5:45455760
|
C | CA | 9 | a0001c0001t0001g0176a0001c0001t0001g0200a0001c0001t0002g0026others(6): Show | 9 | HG01192.hp2 HG01433.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.1011+6085dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45455760 | ||||||
| chr5:45455760
|
CA | C | 23 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(20): Show | 23 | HG01256.hp2 HG01257.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1011+6085delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45455760 | ||||||
| chr5:45455760
|
CAAA | C | 14 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1011+6083_1011+608 others(7): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45455760 | ||||||
| chr5:45455970
|
T | G | 1 | a0001c0001t0002g0056 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1011+5876A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45455970 | ||||||
| chr5:45456154
|
G | A | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1011+5692C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45456154 | ||||||
| chr5:45456404
|
A | C | 1 | a0001c0001t0002g0019 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1011+5442T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45456404 | ||||||
| chr5:45456530
|
A | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1011+5316T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45456530 | ||||||
| chr5:45456975
|
T | C | 144 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1011+4871A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45456975 | ||||||
| chr5:45457074
|
G | A | 10 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1011+4772C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45457074 | ||||||
| chr5:45457216
|
A | G | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1011+4630T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45457216 | ||||||
| chr5:45457237
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1011+4609G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45457237 | ||||||
| chr5:45457605
|
G | T | 1 | a0001c0001t0001g0191 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1011+4241C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45457605 | ||||||
| chr5:45457612
|
C | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1011+4234G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45457612 | ||||||
| chr5:45458406
|
C | G | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1011+3440G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45458406 | ||||||
| chr5:45458422
|
G | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1011+3424C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45458422 | ||||||
| chr5:45458472
|
T | C | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1011+3374A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45458472 | ||||||
| chr5:45458539
|
A | T | 1 | a0001c0001t0007g0100 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1011+3307T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45458539 | ||||||
| chr5:45458651
|
A | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1011+3195T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45458651 | ||||||
| chr5:45458907
|
A | T | 1 | a0001c0001t0002g0026 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1011+2939T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45458907 | ||||||
| chr5:45459190
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1011+2656G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45459190 | ||||||
| chr5:45459367
|
A | G | 7 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(4): Show | 7 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1011+2479T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45459367 | ||||||
| chr5:45459401
|
C | CA | 50 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(47): Show | 50 | HG00099.hp1 HG00280.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.1011+2444dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45459401 | ||||||
| chr5:45459401
|
C | CAA | 16 | a0001c0001t0001g0065a0001c0001t0002g0026a0001c0001t0004g0017others(13): Show | 16 | HG00438.hp1 HG00609.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.1011+2443_1011+244 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45459401 | ||||||
| chr5:45459455
|
A | G | 6 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(3): Show | 6 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1011+2391T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45459455 | ||||||
| chr5:45459511
|
TACAC | T | 65 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(62): Show | 65 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1011+2331_1011+233 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45459511 | ||||||
| chr5:45459597
|
C | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1011+2249G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45459597 | ||||||
| chr5:45459667
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1011+2179A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45459667 | ||||||
| chr5:45459749
|
A | C | 1 | a0001c0001t0029g0070 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1011+2097T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45459749 | ||||||
| chr5:45459768
|
A | G | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1011+2078T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45459768 | ||||||
| chr5:45459801
|
T | C | 1 | a0001c0001t0003g0095 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1011+2045A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45459801 | ||||||
| chr5:45460160
|
T | G | 13 | a0001c0001t0002g0121a0001c0001t0005g0122a0001c0001t0005g0123others(10): Show | 13 | HG01261.hp2 HG01346.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1011+1686A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45460160 | ||||||
| chr5:45460271
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1011+1575G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45460271 | ||||||
| chr5:45460286
|
T | C | 10 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1011+1560A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45460286 | ||||||
| chr5:45460392
|
C | G | 35 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0037others(32): Show | 35 | HG00280.hp1 HG00438.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.1011+1454G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45460392 | ||||||
| chr5:45460450
|
C | A | 1 | a0001c0001t0002g0028 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1011+1396G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45460450 | ||||||
| chr5:45460505
|
G | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1011+1341C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45460505 | ||||||
| chr5:45460621
|
G | A | 1 | a0001c0001t0002g0096 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1011+1225C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45460621 | ||||||
| chr5:45460694
|
G | A | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1011+1152C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45460694 | ||||||
| chr5:45460753
|
G | C | 6 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(3): Show | 6 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1011+1093C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45460753 | ||||||
| chr5:45460990
|
C | T | 1 | a0001c0001t0007g0214 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1011+856G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45460990 | ||||||
| chr5:45461083
|
C | G | 2 | a0001c0001t0002g0023a0001c0001t0002g0024 | 2 | NA18977.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1011+763G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45461083 | ||||||
| chr5:45461096
|
C | T | 64 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(61): Show | 64 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1011+750G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45461096 | ||||||
| chr5:45461135
|
T | G | 14 | a0001c0001t0001g0045a0001c0001t0001g0074a0001c0001t0001g0076others(11): Show | 14 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.1011+711A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45461135 | ||||||
| chr5:45461159
|
C | A | 4 | a0001c0001t0001g0045a0001c0001t0003g0063a0001c0001t0003g0158others(1): Show | 4 | HG01071.hp2 HG01081.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.1011+687G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45461159 | ||||||
| chr5:45461390
|
T | A | 2 | a0001c0001t0002g0023a0001c0001t0002g0024 | 2 | NA18977.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1011+456A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45461390 | ||||||
| chr5:45461391
|
T | G | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1011+455A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45461391 | ||||||
| chr5:45461427
|
G | A | 1 | a0001c0001t0003g0053 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1011+419C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45461427 | ||||||
| chr5:45461494
|
T | G | 1 | a0001c0001t0001g0179 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1011+352A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45461494 | ||||||
| chr5:45461529
|
C | T | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1011+317G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45461529 | ||||||
| chr5:45461534
|
T | G | 1 | a0001c0001t0002g0012 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1011+312A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 3/7 | chr5 | 45461534 | ||||||
| chr5:45462349
|
A | G | 12 | a0001c0001t0001g0073a0001c0001t0001g0134a0001c0001t0001g0160others(9): Show | 12 | HG00673.hp2 HG02056.hp1 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.850-342T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45462349 | ||||||
| chr5:45462486
|
T | A | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.850-479A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45462486 | ||||||
| chr5:45462535
|
G | T | 32 | a0001c0001t0002g0072a0001c0001t0002g0091a0001c0001t0002g0096others(29): Show | 32 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.850-528C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45462535 | ||||||
| chr5:45462927
|
T | A | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-920A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45462927 | ||||||
| chr5:45463011
|
T | A | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-1004A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45463011 | ||||||
| chr5:45463176
|
T | A | 1 | a0001c0001t0002g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.850-1169A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45463176 | ||||||
| chr5:45463215
|
T | C | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.850-1208A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45463215 | ||||||
| chr5:45463600
|
T | C | 3 | a0001c0001t0002g0012a0001c0001t0002g0025a0001c0001t0002g0026 | 3 | NA18612.hp2 NA18961.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.850-1593A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45463600 | ||||||
| chr5:45463780
|
C | G | 2 | a0001c0001t0002g0027a0001c0001t0002g0054 | 2 | NA18959.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.850-1773G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45463780 | ||||||
| chr5:45463908
|
T | C | 1 | a0001c0001t0004g0020 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.850-1901A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45463908 | ||||||
| chr5:45464312
|
T | C | 6 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(3): Show | 6 | HG01192.hp1 HG01884.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-2305A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45464312 | ||||||
| chr5:45464495
|
T | C | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.850-2488A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45464495 | ||||||
| chr5:45464579
|
G | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-2572C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45464579 | ||||||
| chr5:45464680
|
GTGA | G | 13 | a0001c0001t0002g0121a0001c0001t0005g0122a0001c0001t0005g0123others(10): Show | 13 | HG01261.hp2 HG01346.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.850-2676_850-2674d others(5): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45464680 | ||||||
| chr5:45464691
|
G | A | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-2684C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45464691 | ||||||
| chr5:45464694
|
A | T | 1 | a0001c0001t0002g0047 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.850-2687T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45464694 | ||||||
| chr5:45464812
|
CTT | C | 64 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(61): Show | 64 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.850-2807_850-2806d others(4): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45464812 | ||||||
| chr5:45464842
|
G | C | 50 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(47): Show | 50 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.850-2835C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45464842 | ||||||
| chr5:45464864
|
A | G | 1 | a0001c0001t0013g0078 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.850-2857T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45464864 | ||||||
| chr5:45464972
|
A | T | 2 | a0001c0001t0002g0023a0001c0001t0002g0024 | 2 | NA18977.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.850-2965T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45464972 | ||||||
| chr5:45465345
|
G | C | 2 | a0001c0001t0002g0023a0001c0001t0002g0024 | 2 | NA18977.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.850-3338C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45465345 | ||||||
| chr5:45465464
|
G | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-3457C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45465464 | ||||||
| chr5:45465480
|
G | A | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.850-3473C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45465480 | ||||||
| chr5:45465621
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-3614C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45465621 | ||||||
| chr5:45465710
|
A | G | 140 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.850-3703T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45465710 | ||||||
| chr5:45465722
|
T | C | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-3715A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45465722 | ||||||
| chr5:45465818
|
T | C | 1 | a0001c0001t0004g0189 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.850-3811A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45465818 | ||||||
| chr5:45465824
|
T | C | 67 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.850-3817A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45465824 | ||||||
| chr5:45465885
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-3878T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45465885 | ||||||
| chr5:45465927
|
T | C | 2 | a0001c0001t0002g0082a0001c0001t0019g0114 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.850-3920A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45465927 | ||||||
| chr5:45466060
|
C | T | 3 | a0001c0001t0003g0103a0001c0001t0003g0188a0001c0001t0004g0030 | 3 | NA18942.hp2 NA18943.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.850-4053G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45466060 | ||||||
| chr5:45466281
|
T | G | 1 | a0001c0001t0002g0157 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.850-4274A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45466281 | ||||||
| chr5:45466355
|
A | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-4348T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45466355 | ||||||
| chr5:45466385
|
T | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-4378A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45466385 | ||||||
| chr5:45466507
|
G | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-4500C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45466507 | ||||||
| chr5:45466514
|
C | G | 143 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.850-4507G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45466514 | ||||||
| chr5:45466606
|
T | C | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-4599A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45466606 | ||||||
| chr5:45466631
|
T | TA | 11 | a0001c0001t0002g0121a0001c0001t0005g0122a0001c0001t0005g0123others(8): Show | 11 | HG01261.hp2 HG01346.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.850-4625dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45466631 | ||||||
| chr5:45466863
|
C | A | 1 | a0001c0001t0002g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850-4856G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45466863 | ||||||
| chr5:45467090
|
C | A | 2 | a0001c0001t0001g0153a0001c0001t0015g0001 | 2 | NA18939.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.850-5083G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45467090 | ||||||
| chr5:45467324
|
G | A | 2 | a0001c0001t0001g0184a0001c0001t0001g0191 | 2 | HG02717.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.850-5317C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45467324 | ||||||
| chr5:45467436
|
C | T | 66 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(63): Show | 66 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.850-5429G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45467436 | ||||||
| chr5:45467687
|
C | T | 2 | a0001c0001t0002g0082a0001c0001t0019g0114 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.850-5680G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45467687 | ||||||
| chr5:45467715
|
C | A | 1 | a0001c0001t0023g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.850-5708G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45467715 | ||||||
| chr5:45467833
|
A | C | 1 | a0001c0001t0003g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.850-5826T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45467833 | ||||||
| chr5:45467881
|
T | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-5874A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45467881 | ||||||
| chr5:45467910
|
C | T | 2 | a0001c0001t0001g0209a0001c0001t0002g0178 | 2 | HG00280.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.850-5903G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45467910 | ||||||
| chr5:45468132
|
G | T | 16 | a0001c0001t0001g0065a0001c0001t0004g0017a0001c0001t0004g0020others(13): Show | 16 | HG00438.hp1 HG00609.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.850-6125C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45468132 | ||||||
| chr5:45468149
|
A | T | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.850-6142T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45468149 | ||||||
| chr5:45468472
|
T | TA | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-6466dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45468472 | ||||||
| chr5:45468474
|
T | C | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-6467A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45468474 | ||||||
| chr5:45469040
|
GA | G | 4 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(1): Show | 4 | HG02055.hp2 HG02257.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-7034delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45469040 | ||||||
| chr5:45469043
|
A | T | 4 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(1): Show | 4 | HG02055.hp2 HG02257.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-7036T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45469043 | ||||||
| chr5:45469051
|
T | C | 107 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.850-7044A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45469051 | ||||||
| chr5:45469078
|
T | C | 10 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-7071A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45469078 | ||||||
| chr5:45469254
|
G | A | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-7247C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45469254 | ||||||
| chr5:45469379
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.850-7372A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45469379 | ||||||
| chr5:45469505
|
G | A | 7 | a0001c0001t0003g0087a0001c0001t0003g0093a0001c0001t0003g0094others(4): Show | 7 | HG00099.hp2 HG01071.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.850-7498C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45469505 | ||||||
| chr5:45469525
|
T | C | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-7518A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45469525 | ||||||
| chr5:45469556
|
G | A | 31 | a0001c0001t0002g0072a0001c0001t0002g0091a0001c0001t0002g0096others(28): Show | 31 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.850-7549C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45469556 | ||||||
| chr5:45469728
|
T | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-7721A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45469728 | ||||||
| chr5:45469745
|
C | T | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.850-7738G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45469745 | ||||||
| chr5:45469767
|
A | T | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-7760T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45469767 | ||||||
| chr5:45469784
|
A | AGT | 34 | a0001c0001t0001g0051a0001c0001t0001g0065a0001c0001t0001g0116others(31): Show | 34 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.850-7779_850-7778d others(4): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45469784 | ||||||
| chr5:45469784
|
AGT | A | 8 | a0001c0001t0001g0045a0001c0001t0001g0139a0001c0001t0001g0204others(5): Show | 8 | HG00609.hp1 HG01071.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.850-7779_850-7778d others(4): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45469784 | ||||||
| chr5:45469815
|
G | T | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.850-7808C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45469815 | ||||||
| chr5:45469921
|
T | C | 1 | a0001c0001t0001g0180 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.850-7914A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45469921 | ||||||
| chr5:45469979
|
A | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-7972T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45469979 | ||||||
| chr5:45470182
|
C | T | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-8175G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45470182 | ||||||
| chr5:45470286
|
G | A | 1 | a0001c0001t0003g0086 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.850-8279C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45470286 | ||||||
| chr5:45470321
|
C | T | 50 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(47): Show | 50 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.850-8314G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45470321 | ||||||
| chr5:45470485
|
A | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-8478T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45470485 | ||||||
| chr5:45470578
|
T | A | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.850-8571A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45470578 | ||||||
| chr5:45470617
|
ATACT | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0190 | 2 | NA18971.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.850-8614_850-8611d others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45470617 | ||||||
| chr5:45470703
|
T | C | 1 | a0001c0001t0020g0196 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.850-8696A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45470703 | ||||||
| chr5:45470703
|
T | G | 1 | a0001c0001t0001g0191 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.850-8696A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45470703 | ||||||
| chr5:45470824
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-8817G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45470824 | ||||||
| chr5:45471547
|
T | C | 1 | a0001c0001t0002g0041 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.850-9540A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45471547 | ||||||
| chr5:45471783
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.850-9776C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45471783 | ||||||
| chr5:45471856
|
T | A | 1 | a0001c0001t0001g0155 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.850-9849A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45471856 | ||||||
| chr5:45471891
|
A | T | 40 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(37): Show | 40 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.850-9884T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45471891 | ||||||
| chr5:45472509
|
A | T | 1 | a0001c0001t0002g0019 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.850-10502T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45472509 | ||||||
| chr5:45472571
|
A | AGAAG | 3 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0026g0071 | 3 | HG01257.hp1 HG01258.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.850-10568_850-1056 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45472571 | ||||||
| chr5:45472571
|
AGAAG | A | 7 | a0001c0001t0003g0086a0001c0001t0007g0115a0001c0001t0031g0009others(4): Show | 7 | HG00558.hp1 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.850-10568_850-1056 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45472571 | ||||||
| chr5:45472651
|
G | GGA | 144 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.850-10646_850-1064 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45472651 | ||||||
| chr5:45472797
|
A | C | 1 | a0001c0001t0005g0126 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.850-10790T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45472797 | ||||||
| chr5:45472970
|
A | G | 1 | a0001c0001t0005g0130 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.850-10963T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45472970 | ||||||
| chr5:45473088
|
C | G | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-11081G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45473088 | ||||||
| chr5:45473137
|
T | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-11130A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45473137 | ||||||
| chr5:45473285
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.850-11278T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45473285 | ||||||
| chr5:45473371
|
C | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-11364G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45473371 | ||||||
| chr5:45473386
|
A | G | 1 | a0001c0001t0003g0188 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.850-11379T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45473386 | ||||||
| chr5:45473449
|
G | GA | 5 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(2): Show | 5 | HG02647.hp1 HG02647.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-11443dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45473449 | ||||||
| chr5:45473943
|
A | C | 1 | a0001c0001t0001g0060 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.850-11936T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45473943 | ||||||
| chr5:45473980
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.850-11973C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45473980 | ||||||
| chr5:45474081
|
T | C | 1 | a0001c0001t0002g0152 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.850-12074A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45474081 | ||||||
| chr5:45474403
|
T | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-12396A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45474403 | ||||||
| chr5:45474406
|
T | G | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.850-12399A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45474406 | ||||||
| chr5:45474436
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-12429A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45474436 | ||||||
| chr5:45474511
|
G | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-12504C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45474511 | ||||||
| chr5:45474712
|
A | C | 144 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.850-12705T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45474712 | ||||||
| chr5:45474809
|
C | T | 225 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.850-12802G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45474809 | ||||||
| chr5:45474857
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-12850G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45474857 | ||||||
| chr5:45474886
|
G | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-12879C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45474886 | ||||||
| chr5:45474985
|
C | A | 11 | a0001c0001t0002g0121a0001c0001t0005g0122a0001c0001t0005g0123others(8): Show | 11 | HG01261.hp2 HG01346.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.850-12978G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45474985 | ||||||
| chr5:45475011
|
C | A | 1 | a0001c0001t0023g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.850-13004G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45475011 | ||||||
| chr5:45475067
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-13060T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45475067 | ||||||
| chr5:45475401
|
T | G | 1 | a0001c0001t0006g0203 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.850-13394A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45475401 | ||||||
| chr5:45475416
|
T | C | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-13409A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45475416 | ||||||
| chr5:45475829
|
A | G | 1 | a0001c0006t0002g0219 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.850-13822T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45475829 | ||||||
| chr5:45475841
|
T | C | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.850-13834A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45475841 | ||||||
| chr5:45475879
|
C | T | 1 | a0001c0001t0002g0181 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.850-13872G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45475879 | ||||||
| chr5:45475901
|
A | T | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-13894T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45475901 | ||||||
| chr5:45475982
|
T | C | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.850-13975A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45475982 | ||||||
| chr5:45476337
|
A | G | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.850-14330T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45476337 | ||||||
| chr5:45476346
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.850-14339A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45476346 | ||||||
| chr5:45476575
|
A | G | 1 | a0001c0001t0002g0066 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.850-14568T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45476575 | ||||||
| chr5:45476679
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-14672G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45476679 | ||||||
| chr5:45476751
|
A | C | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.850-14744T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45476751 | ||||||
| chr5:45476785
|
G | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-14778C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45476785 | ||||||
| chr5:45476904
|
T | C | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.850-14897A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45476904 | ||||||
| chr5:45476971
|
A | G | 1 | a0001c0001t0003g0053 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.850-14964T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45476971 | ||||||
| chr5:45477001
|
C | A | 64 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(61): Show | 64 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.850-14994G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45477001 | ||||||
| chr5:45477007
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.850-15000T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45477007 | ||||||
| chr5:45477286
|
A | G | 1 | a0001c0001t0006g0203 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.850-15279T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45477286 | ||||||
| chr5:45477347
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.850-15340T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45477347 | ||||||
| chr5:45477398
|
G | A | 1 | a0001c0001t0003g0110 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.850-15391C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45477398 | ||||||
| chr5:45477426
|
T | C | 1 | a0001c0001t0013g0079 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.850-15419A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45477426 | ||||||
| chr5:45477433
|
T | G | 67 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.850-15426A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45477433 | ||||||
| chr5:45477541
|
G | T | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-15534C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45477541 | ||||||
| chr5:45477689
|
A | G | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.850-15682T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45477689 | ||||||
| chr5:45477702
|
G | A | 1 | a0001c0001t0001g0011 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.850-15695C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45477702 | ||||||
| chr5:45477906
|
A | C | 67 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.850-15899T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45477906 | ||||||
| chr5:45478103
|
G | C | 1 | a0001c0001t0002g0019 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.850-16096C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45478103 | ||||||
| chr5:45478145
|
C | T | 1 | a0002c0002t0014g0223 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.850-16138G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45478145 | ||||||
| chr5:45478490
|
C | G | 1 | a0001c0001t0001g0180 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.850-16483G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45478490 | ||||||
| chr5:45478542
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.850-16535A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45478542 | ||||||
| chr5:45478547
|
T | G | 1 | a0001c0001t0002g0041 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.850-16540A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45478547 | ||||||
| chr5:45478593
|
T | A | 1 | a0001c0001t0019g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.850-16586A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45478593 | ||||||
| chr5:45478650
|
C | A | 1 | a0001c0001t0003g0117 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.850-16643G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45478650 | ||||||
| chr5:45478669
|
G | A | 143 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.850-16662C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45478669 | ||||||
| chr5:45478717
|
G | T | 1 | a0001c0001t0003g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.850-16710C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45478717 | ||||||
| chr5:45478940
|
G | T | 1 | a0001c0001t0005g0124 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.850-16933C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45478940 | ||||||
| chr5:45478984
|
G | A | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.850-16977C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45478984 | ||||||
| chr5:45479124
|
T | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-17117A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45479124 | ||||||
| chr5:45479124
|
T | TA | 19 | a0001c0001t0002g0121a0001c0001t0005g0122a0001c0001t0005g0123others(16): Show | 19 | HG01261.hp2 HG01346.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.850-17118dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45479124 | ||||||
| chr5:45479124
|
TA | T | 9 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0155others(6): Show | 9 | HG00280.hp1 HG02145.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.850-17118delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45479124 | ||||||
| chr5:45479125
|
A | T | 1 | a0001c0001t0003g0103 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.850-17118T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45479125 | ||||||
| chr5:45479168
|
C | T | 1 | a0001c0001t0002g0015 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.850-17161G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45479168 | ||||||
| chr5:45479253
|
G | C | 1 | a0001c0001t0003g0110 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.850-17246C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45479253 | ||||||
| chr5:45479323
|
C | T | 64 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(61): Show | 64 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.850-17316G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45479323 | ||||||
| chr5:45479526
|
C | A | 1 | a0001c0001t0002g0091 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.850-17519G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45479526 | ||||||
| chr5:45479553
|
G | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-17546C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45479553 | ||||||
| chr5:45479971
|
C | T | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.850-17964G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45479971 | ||||||
| chr5:45479978
|
A | G | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.850-17971T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45479978 | ||||||
| chr5:45480089
|
C | T | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-18082G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45480089 | ||||||
| chr5:45480092
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.850-18085T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45480092 | ||||||
| chr5:45480290
|
C | A | 1 | a0001c0001t0002g0012 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.850-18283G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45480290 | ||||||
| chr5:45480312
|
G | T | 11 | a0001c0001t0002g0121a0001c0001t0005g0122a0001c0001t0005g0123others(8): Show | 11 | HG01261.hp2 HG01346.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.850-18305C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45480312 | ||||||
| chr5:45480473
|
T | C | 1 | a0001c0001t0002g0193 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.850-18466A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45480473 | ||||||
| chr5:45480668
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.850-18661C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45480668 | ||||||
| chr5:45481146
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-19139C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45481146 | ||||||
| chr5:45481284
|
G | A | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.850-19277C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45481284 | ||||||
| chr5:45481674
|
T | C | 225 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.850-19667A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45481674 | ||||||
| chr5:45481768
|
CATGATGC others(12): Show |
C | 10 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-19780_850-1976 others(23): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45481768 | ||||||
| chr5:45481966
|
A | G | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-19959T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45481966 | ||||||
| chr5:45481971
|
CA | C | 135 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.850-19965delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45481971 | ||||||
| chr5:45482013
|
G | T | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-20006C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45482013 | ||||||
| chr5:45482099
|
T | C | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.850-20092A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45482099 | ||||||
| chr5:45482133
|
A | G | 42 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(39): Show | 42 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.850-20126T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45482133 | ||||||
| chr5:45482364
|
C | T | 1 | a0001c0001t0002g0056 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.850-20357G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45482364 | ||||||
| chr5:45482648
|
T | C | 5 | a0001c0001t0001g0051a0001c0001t0002g0049a0001c0001t0002g0050others(2): Show | 5 | HG03041.hp1 HG03139.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-20641A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45482648 | ||||||
| chr5:45482649
|
G | A | 2 | a0001c0001t0002g0072a0001c0001t0002g0097 | 2 | HG00673.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.850-20642C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45482649 | ||||||
| chr5:45482884
|
T | C | 6 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0156others(3): Show | 6 | HG00597.hp1 NA18939.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-20877A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45482884 | ||||||
| chr5:45482930
|
A | G | 1 | a0001c0001t0002g0028 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.850-20923T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45482930 | ||||||
| chr5:45482954
|
G | T | 1 | a0001c0001t0001g0065 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.850-20947C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45482954 | ||||||
| chr5:45483081
|
T | G | 1 | a0001c0001t0024g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.850-21074A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45483081 | ||||||
| chr5:45483215
|
C | T | 11 | a0001c0001t0002g0121a0001c0001t0005g0122a0001c0001t0005g0123others(8): Show | 11 | HG01261.hp2 HG01346.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.850-21208G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45483215 | ||||||
| chr5:45483274
|
G | A | 2 | a0001c0001t0002g0082a0001c0001t0019g0114 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.850-21267C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45483274 | ||||||
| chr5:45483345
|
T | C | 1 | a0001c0001t0001g0102 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.850-21338A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45483345 | ||||||
| chr5:45483410
|
G | T | 139 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.850-21403C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45483410 | ||||||
| chr5:45483447
|
G | T | 12 | a0001c0001t0001g0073a0001c0001t0001g0134a0001c0001t0001g0160others(9): Show | 12 | HG00673.hp2 HG02056.hp1 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.850-21440C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45483447 | ||||||
| chr5:45483774
|
C | T | 2 | a0001c0001t0005g0129a0001c0001t0005g0130 | 2 | HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.850-21767G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45483774 | ||||||
| chr5:45483791
|
C | A | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.850-21784G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45483791 | ||||||
| chr5:45483955
|
C | T | 2 | a0001c0001t0003g0098a0001c0001t0003g0099 | 2 | HG01361.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.850-21948G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45483955 | ||||||
| chr5:45484166
|
C | T | 1 | a0001c0001t0007g0214 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.850-22159G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45484166 | ||||||
| chr5:45484248
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.850-22241G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45484248 | ||||||
| chr5:45484287
|
T | C | 1 | a0001c0001t0004g0189 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.850-22280A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45484287 | ||||||
| chr5:45484448
|
G | A | 2 | a0001c0001t0002g0025a0001c0001t0033g0213 | 2 | HG03579.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.850-22441C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45484448 | ||||||
| chr5:45484506
|
A | G | 7 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0156others(4): Show | 7 | HG00597.hp1 NA18939.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.850-22499T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45484506 | ||||||
| chr5:45484526
|
C | T | 16 | a0001c0001t0001g0065a0001c0001t0004g0017a0001c0001t0004g0020others(13): Show | 16 | HG00438.hp1 HG00609.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.850-22519G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45484526 | ||||||
| chr5:45484753
|
A | G | 1 | a0002c0002t0008g0226 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.850-22746T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45484753 | ||||||
| chr5:45484767
|
C | T | 1 | a0001c0001t0013g0079 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.850-22760G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45484767 | ||||||
| chr5:45484942
|
G | A | 2 | a0001c0001t0002g0015a0001c0001t0016g0014 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.850-22935C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45484942 | ||||||
| chr5:45485139
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.850-23132G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45485139 | ||||||
| chr5:45485233
|
C | T | 1 | a0001c0001t0003g0117 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.850-23226G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45485233 | ||||||
| chr5:45485286
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.850-23279T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45485286 | ||||||
| chr5:45485619
|
T | C | 1 | a0001c0001t0002g0069 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.850-23612A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45485619 | ||||||
| chr5:45485650
|
C | T | 8 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(5): Show | 8 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.850-23643G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45485650 | ||||||
| chr5:45486114
|
C | T | 1 | a0001c0001t0002g0178 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.850-24107G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45486114 | ||||||
| chr5:45486235
|
C | T | 1 | a0001c0001t0003g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.850-24228G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45486235 | ||||||
| chr5:45486393
|
A | G | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.850-24386T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45486393 | ||||||
| chr5:45486507
|
G | A | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-24500C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45486507 | ||||||
| chr5:45486828
|
T | A | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.850-24821A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45486828 | ||||||
| chr5:45486987
|
T | C | 1 | a0001c0001t0002g0069 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.850-24980A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45486987 | ||||||
| chr5:45487018
|
G | A | 1 | a0001c0001t0005g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.850-25011C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45487018 | ||||||
| chr5:45487111
|
C | T | 1 | a0001c0001t0002g0082 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.850-25104G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45487111 | ||||||
| chr5:45487457
|
T | C | 1 | a0001c0001t0003g0090 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.850-25450A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45487457 | ||||||
| chr5:45487534
|
C | CATATACT others(1): Show |
9 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(6): Show | 9 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.850-25535_850-2552 others(12): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45487534 | ||||||
| chr5:45487666
|
C | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.850-25659G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45487666 | ||||||
| chr5:45487923
|
C | T | 1 | a0002c0002t0008g0226 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.850-25916G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45487923 | ||||||
| chr5:45488186
|
G | A | 1 | a0001c0001t0012g0137 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.850-26179C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45488186 | ||||||
| chr5:45488448
|
T | G | 1 | a0001c0001t0001g0150 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.850-26441A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45488448 | ||||||
| chr5:45488528
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-26521T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45488528 | ||||||
| chr5:45488553
|
C | A | 65 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(62): Show | 65 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.850-26546G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45488553 | ||||||
| chr5:45488553
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.850-26546G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45488553 | ||||||
| chr5:45488979
|
T | A | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.850-26972A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45488979 | ||||||
| chr5:45489164
|
G | A | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-27157C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45489164 | ||||||
| chr5:45489342
|
G | T | 1 | a0001c0001t0002g0193 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.850-27335C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45489342 | ||||||
| chr5:45489393
|
A | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-27386T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45489393 | ||||||
| chr5:45489427
|
A | G | 1 | a0001c0001t0002g0028 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.850-27420T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45489427 | ||||||
| chr5:45489458
|
A | T | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-27451T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45489458 | ||||||
| chr5:45489472
|
T | C | 1 | a0001c0001t0002g0049 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.850-27465A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45489472 | ||||||
| chr5:45489556
|
GCT | G | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-27551_850-2755 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45489556 | ||||||
| chr5:45489638
|
C | T | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-27631G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45489638 | ||||||
| chr5:45489725
|
A | C | 1 | a0001c0001t0013g0078 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.850-27718T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45489725 | ||||||
| chr5:45489733
|
C | T | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-27726G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45489733 | ||||||
| chr5:45489761
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-27754G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45489761 | ||||||
| chr5:45490086
|
A | C | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.850-28079T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45490086 | ||||||
| chr5:45490152
|
A | T | 2 | a0002c0002t0008g0224a0002c0002t0008g0225 | 2 | HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.850-28145T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45490152 | ||||||
| chr5:45490281
|
T | C | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.850-28274A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45490281 | ||||||
| chr5:45490534
|
G | T | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.850-28527C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45490534 | ||||||
| chr5:45490606
|
C | T | 1 | a0001c0001t0024g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.850-28599G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45490606 | ||||||
| chr5:45490639
|
T | C | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.850-28632A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45490639 | ||||||
| chr5:45490731
|
C | T | 1 | a0001c0001t0003g0084 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.850-28724G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45490731 | ||||||
| chr5:45490806
|
T | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG01074.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.850-28799A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45490806 | ||||||
| chr5:45491044
|
A | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-29037T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45491044 | ||||||
| chr5:45491154
|
A | C | 1 | a0001c0001t0002g0044 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.850-29147T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45491154 | ||||||
| chr5:45491224
|
T | C | 10 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-29217A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45491224 | ||||||
| chr5:45491345
|
T | C | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-29338A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45491345 | ||||||
| chr5:45491470
|
C | T | 1 | a0001c0001t0029g0070 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.850-29463G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45491470 | ||||||
| chr5:45491621
|
A | T | 10 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-29614T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45491621 | ||||||
| chr5:45491622
|
G | T | 10 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-29615C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45491622 | ||||||
| chr5:45491655
|
T | G | 1 | a0001c0001t0002g0012 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.850-29648A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45491655 | ||||||
| chr5:45491837
|
A | G | 50 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(47): Show | 50 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.850-29830T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45491837 | ||||||
| chr5:45492075
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.850-30068G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492075 | ||||||
| chr5:45492103
|
A | G | 141 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.850-30096T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492103 | ||||||
| chr5:45492137
|
C | T | 2 | a0001c0001t0003g0098a0001c0001t0003g0099 | 2 | HG01361.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.850-30130G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492137 | ||||||
| chr5:45492160
|
T | G | 10 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-30153A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492160 | ||||||
| chr5:45492296
|
A | ATG | 43 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0002g0025others(40): Show | 43 | HG00323.hp2 HG00558.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.850-30291_850-3029 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492296 | ||||||
| chr5:45492296
|
A | ATGTG | 9 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(6): Show | 9 | HG00099.hp2 HG01071.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.850-30293_850-3029 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492296 | ||||||
| chr5:45492296
|
ATG | A | 7 | a0001c0001t0001g0013a0001c0001t0001g0037a0001c0001t0001g0060others(4): Show | 7 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.850-30291_850-3029 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492296 | ||||||
| chr5:45492296
|
ATGTG | A | 2 | a0001c0001t0006g0057a0001c0001t0033g0213 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.850-30293_850-3029 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492296 | ||||||
| chr5:45492317
|
T | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-30310A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492317 | ||||||
| chr5:45492319
|
T | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-30312A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492319 | ||||||
| chr5:45492321
|
T | A | 6 | a0001c0001t0001g0011a0001c0001t0001g0177a0001c0001t0002g0026others(3): Show | 6 | HG00323.hp1 HG03704.hp2 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-30314A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492321 | ||||||
| chr5:45492392
|
A | AAT | 15 | a0001c0001t0001g0116a0001c0001t0001g0187a0001c0001t0002g0019others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.850-30387_850-3038 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492392 | ||||||
| chr5:45492392
|
A | AATAT | 28 | a0001c0001t0001g0034a0001c0001t0001g0045a0001c0001t0002g0015others(25): Show | 28 | HG00597.hp2 HG00639.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.850-30389_850-3038 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492392 | ||||||
| chr5:45492392
|
A | AATATAT | 22 | a0001c0001t0001g0013a0001c0001t0001g0037a0001c0001t0001g0065others(19): Show | 22 | HG00438.hp1 HG00609.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.850-30391_850-3038 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492392 | ||||||
| chr5:45492392
|
A | AATATATA others(1): Show |
7 | a0001c0001t0001g0011a0001c0001t0002g0056a0001c0001t0002g0066others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.850-30393_850-3038 others(12): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492392 | ||||||
| chr5:45492392
|
A | AATATATA others(3): Show |
10 | a0001c0001t0001g0051a0001c0001t0001g0060a0001c0001t0002g0023others(7): Show | 10 | HG03041.hp1 HG03139.hp2 HG03225.hp2 others(7): Show |
intron_variant | MODIFIER | c.850-30395_850-3038 others(14): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492392 | ||||||
| chr5:45492392
|
A | AATATATA others(5): Show |
1 | a0001c0001t0002g0047 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.850-30397_850-3038 others(16): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492392 | ||||||
| chr5:45492392
|
A | AATATATA others(7): Show |
1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.850-30399_850-3038 others(18): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492392 | ||||||
| chr5:45492392
|
AAT | A | 86 | a0001c0001t0001g0074a0001c0001t0001g0085a0001c0001t0001g0102others(83): Show | 86 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.850-30387_850-3038 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492392 | ||||||
| chr5:45492392
|
AATAT | A | 30 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0121others(27): Show | 30 | HG00099.hp2 HG00323.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.850-30389_850-3038 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492392 | ||||||
| chr5:45492392
|
AATATAT | A | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0023g0075 | 3 | HG02647.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.850-30391_850-3038 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492392 | ||||||
| chr5:45492392
|
AATATATA others(1): Show |
A | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-30393_850-3038 others(12): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492392 | ||||||
| chr5:45492461
|
G | A | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.850-30454C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492461 | ||||||
| chr5:45492498
|
G | A | 2 | a0001c0001t0005g0122a0001c0001t0005g0123 | 2 | HG02055.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.850-30491C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492498 | ||||||
| chr5:45492519
|
G | GT | 92 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0037others(89): Show | 92 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.850-30513dupA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492519 | ||||||
| chr5:45492519
|
G | GTT | 36 | a0001c0001t0001g0011a0001c0001t0002g0023a0001c0001t0002g0052others(33): Show | 36 | HG00099.hp2 HG00323.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.850-30514_850-3051 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492519 | ||||||
| chr5:45492519
|
G | T | 6 | a0001c0001t0003g0118a0001c0001t0003g0120a0001c0001t0004g0061others(3): Show | 6 | HG00735.hp1 HG00738.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-30512C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492519 | ||||||
| chr5:45492523
|
T | TG | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-30517_850-3051 others(5): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492523 | ||||||
| chr5:45492683
|
G | A | 40 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(37): Show | 40 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.850-30676C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492683 | ||||||
| chr5:45492730
|
G | A | 7 | a0001c0001t0003g0090a0001c0001t0003g0092a0001c0001t0003g0109others(4): Show | 7 | HG02056.hp2 HG02129.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.850-30723C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492730 | ||||||
| chr5:45492960
|
T | C | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-30953A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45492960 | ||||||
| chr5:45493234
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-31227T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45493234 | ||||||
| chr5:45493363
|
G | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-31356C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45493363 | ||||||
| chr5:45493406
|
C | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-31399G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45493406 | ||||||
| chr5:45493497
|
T | C | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.850-31490A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45493497 | ||||||
| chr5:45493593
|
AT | A | 4 | a0001c0001t0002g0052a0001c0001t0002g0067a0003c0003t0002g0221others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-31587delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45493593 | ||||||
| chr5:45493658
|
G | C | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-31651C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45493658 | ||||||
| chr5:45493666
|
T | C | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.850-31659A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45493666 | ||||||
| chr5:45493689
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.850-31682G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45493689 | ||||||
| chr5:45493715
|
G | C | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-31708C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45493715 | ||||||
| chr5:45493734
|
A | G | 1 | a0001c0001t0002g0178 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.850-31727T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45493734 | ||||||
| chr5:45493806
|
A | C | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-31799T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45493806 | ||||||
| chr5:45493806
|
A | T | 142 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.850-31799T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45493806 | ||||||
| chr5:45493869
|
C | T | 1 | a0001c0001t0003g0084 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.850-31862G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45493869 | ||||||
| chr5:45493908
|
T | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-31901A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45493908 | ||||||
| chr5:45493949
|
C | T | 1 | a0001c0001t0003g0188 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.850-31942G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45493949 | ||||||
| chr5:45494049
|
C | T | 1 | a0001c0001t0034g0172 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.850-32042G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45494049 | ||||||
| chr5:45494084
|
A | G | 1 | a0001c0001t0001g0134 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.850-32077T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45494084 | ||||||
| chr5:45494137
|
A | C | 1 | a0001c0001t0001g0171 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.850-32130T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45494137 | ||||||
| chr5:45494250
|
T | A | 66 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(63): Show | 66 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.850-32243A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45494250 | ||||||
| chr5:45494279
|
G | T | 140 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.850-32272C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45494279 | ||||||
| chr5:45494285
|
T | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-32278A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45494285 | ||||||
| chr5:45494386
|
C | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-32379G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45494386 | ||||||
| chr5:45494426
|
C | T | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.850-32419G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45494426 | ||||||
| chr5:45494508
|
A | T | 35 | a0001c0001t0002g0072a0001c0001t0002g0082a0001c0001t0002g0091others(32): Show | 35 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.850-32501T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45494508 | ||||||
| chr5:45494524
|
C | T | 10 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-32517G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45494524 | ||||||
| chr5:45494597
|
G | T | 128 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.850-32590C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45494597 | ||||||
| chr5:45494625
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.850-32618A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45494625 | ||||||
| chr5:45494736
|
T | G | 1 | a0001c0001t0001g0177 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.850-32729A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45494736 | ||||||
| chr5:45494917
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.850-32910A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45494917 | ||||||
| chr5:45494933
|
G | C | 1 | a0001c0001t0004g0020 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.850-32926C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45494933 | ||||||
| chr5:45494955
|
C | G | 1 | a0001c0001t0001g0102 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.850-32948G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45494955 | ||||||
| chr5:45494956
|
T | G | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-32949A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45494956 | ||||||
| chr5:45495073
|
G | C | 6 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(3): Show | 6 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-33066C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45495073 | ||||||
| chr5:45495136
|
G | T | 1 | a0001c0001t0001g0202 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.850-33129C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45495136 | ||||||
| chr5:45495319
|
C | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.850-33312G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45495319 | ||||||
| chr5:45495340
|
G | T | 40 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(37): Show | 40 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.850-33333C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45495340 | ||||||
| chr5:45495363
|
T | C | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.850-33356A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45495363 | ||||||
| chr5:45495409
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.850-33402T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45495409 | ||||||
| chr5:45495608
|
A | G | 1 | a0001c0001t0002g0047 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.850-33601T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45495608 | ||||||
| chr5:45495717
|
C | G | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG00323.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.850-33710G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45495717 | ||||||
| chr5:45495769
|
C | T | 2 | a0001c0001t0002g0082a0001c0001t0019g0114 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.850-33762G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45495769 | ||||||
| chr5:45495777
|
G | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-33770C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45495777 | ||||||
| chr5:45495964
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-33957C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45495964 | ||||||
| chr5:45495995
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.850-33988G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45495995 | ||||||
| chr5:45496081
|
G | T | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-34074C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45496081 | ||||||
| chr5:45496106
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.850-34099G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45496106 | ||||||
| chr5:45496110
|
C | A | 3 | a0001c0001t0003g0083a0001c0001t0003g0098a0001c0001t0003g0099 | 3 | HG00323.hp2 HG01361.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.850-34103G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45496110 | ||||||
| chr5:45496111
|
C | T | 1 | a0001c0001t0003g0087 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.850-34104G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45496111 | ||||||
| chr5:45496198
|
G | C | 1 | a0001c0001t0002g0054 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.850-34191C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45496198 | ||||||
| chr5:45496246
|
T | G | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.850-34239A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45496246 | ||||||
| chr5:45496345
|
G | A | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.850-34338C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45496345 | ||||||
| chr5:45496392
|
G | A | 1 | a0001c0001t0002g0178 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.850-34385C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45496392 | ||||||
| chr5:45496461
|
A | G | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.850-34454T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45496461 | ||||||
| chr5:45496573
|
C | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-34566G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45496573 | ||||||
| chr5:45496586
|
C | T | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-34579G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45496586 | ||||||
| chr5:45496640
|
C | T | 6 | a0001c0001t0001g0134a0001c0001t0001g0160a0001c0001t0001g0166others(3): Show | 6 | HG02132.hp2 HG02165.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-34633G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45496640 | ||||||
| chr5:45496641
|
C | T | 1 | a0001c0001t0002g0039 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.850-34634G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45496641 | ||||||
| chr5:45496741
|
T | G | 1 | a0001c0001t0006g0143 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.850-34734A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45496741 | ||||||
| chr5:45496845
|
C | CT | 33 | a0001c0001t0002g0072a0001c0001t0002g0091a0001c0001t0002g0096others(30): Show | 33 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.850-34839_850-3483 others(5): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45496845 | ||||||
| chr5:45497011
|
C | T | 138 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.850-35004G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45497011 | ||||||
| chr5:45497068
|
T | G | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-35061A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45497068 | ||||||
| chr5:45497234
|
T | G | 1 | a0001c0001t0002g0097 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.850-35227A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45497234 | ||||||
| chr5:45497273
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-35266G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45497273 | ||||||
| chr5:45497284
|
C | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-35277G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45497284 | ||||||
| chr5:45497515
|
G | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-35508C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45497515 | ||||||
| chr5:45497571
|
C | G | 10 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-35564G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45497571 | ||||||
| chr5:45497660
|
C | T | 1 | a0001c0001t0002g0015 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.850-35653G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45497660 | ||||||
| chr5:45497677
|
T | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-35670A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45497677 | ||||||
| chr5:45497747
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.850-35740G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45497747 | ||||||
| chr5:45497748
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.850-35741T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45497748 | ||||||
| chr5:45497991
|
G | C | 1 | a0001c0001t0002g0082 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.850-35984C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45497991 | ||||||
| chr5:45498206
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-36199T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45498206 | ||||||
| chr5:45498312
|
A | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-36305T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45498312 | ||||||
| chr5:45498380
|
G | C | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG00323.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.850-36373C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45498380 | ||||||
| chr5:45498390
|
C | G | 3 | a0001c0001t0001g0102a0001c0001t0001g0107a0001c0001t0007g0100 | 3 | HG00438.hp2 HG02040.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.850-36383G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45498390 | ||||||
| chr5:45498450
|
C | G | 35 | a0001c0001t0002g0072a0001c0001t0002g0082a0001c0001t0002g0091others(32): Show | 35 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.850-36443G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45498450 | ||||||
| chr5:45498543
|
G | T | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.850-36536C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45498543 | ||||||
| chr5:45498547
|
G | A | 1 | a0001c0001t0003g0103 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.850-36540C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45498547 | ||||||
| chr5:45498642
|
T | C | 1 | a0001c0001t0028g0174 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.850-36635A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45498642 | ||||||
| chr5:45498717
|
T | A | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.850-36710A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45498717 | ||||||
| chr5:45498725
|
T | C | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-36718A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45498725 | ||||||
| chr5:45498766
|
G | T | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-36759C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45498766 | ||||||
| chr5:45498838
|
G | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-36831C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45498838 | ||||||
| chr5:45498985
|
A | T | 1 | a0001c0001t0004g0031 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.850-36978T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45498985 | ||||||
| chr5:45499031
|
C | CT | 33 | a0001c0001t0002g0072a0001c0001t0002g0091a0001c0001t0002g0096others(30): Show | 33 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.850-37025dupA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45499031 | ||||||
| chr5:45499189
|
C | T | 9 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(6): Show | 9 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.850-37182G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45499189 | ||||||
| chr5:45499237
|
C | G | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.850-37230G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45499237 | ||||||
| chr5:45499242
|
C | T | 3 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0026g0071 | 3 | HG01257.hp1 HG01258.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.850-37235G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45499242 | ||||||
| chr5:45499311
|
T | C | 1 | a0001c0001t0002g0039 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.850-37304A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45499311 | ||||||
| chr5:45499433
|
C | T | 2 | a0001c0001t0011g0163a0001c0001t0011g0164 | 2 | NA18992.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.850-37426G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45499433 | ||||||
| chr5:45499477
|
C | T | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.850-37470G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45499477 | ||||||
| chr5:45499622
|
T | C | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.850-37615A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45499622 | ||||||
| chr5:45500272
|
G | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.850-38265C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45500272 | ||||||
| chr5:45500370
|
T | C | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.850-38363A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45500370 | ||||||
| chr5:45500480
|
G | T | 1 | a0001c0001t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.850-38473C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45500480 | ||||||
| chr5:45500662
|
C | G | 40 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(37): Show | 40 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.850-38655G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45500662 | ||||||
| chr5:45500679
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.850-38672C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45500679 | ||||||
| chr5:45500687
|
G | A | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.850-38680C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45500687 | ||||||
| chr5:45500932
|
A | G | 1 | a0001c0001t0024g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.850-38925T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45500932 | ||||||
| chr5:45501200
|
A | G | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-39193T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45501200 | ||||||
| chr5:45501215
|
T | C | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.850-39208A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45501215 | ||||||
| chr5:45501530
|
G | A | 1 | a0001c0001t0019g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.850-39523C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45501530 | ||||||
| chr5:45501558
|
C | A | 3 | a0001c0001t0001g0134a0001c0001t0001g0160a0001c0001t0001g0166 | 3 | HG02132.hp2 NA18962.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.850-39551G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45501558 | ||||||
| chr5:45501686
|
C | A | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.850-39679G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45501686 | ||||||
| chr5:45501687
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.850-39680C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45501687 | ||||||
| chr5:45501735
|
C | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.850-39728G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45501735 | ||||||
| chr5:45501947
|
T | G | 1 | a0001c0001t0002g0025 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.850-39940A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45501947 | ||||||
| chr5:45502197
|
G | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-40190C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45502197 | ||||||
| chr5:45502239
|
G | A | 1 | a0001c0001t0019g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.850-40232C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45502239 | ||||||
| chr5:45502341
|
C | G | 10 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(7): Show | 10 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-40334G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45502341 | ||||||
| chr5:45502529
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-40522C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45502529 | ||||||
| chr5:45502651
|
C | T | 1 | a0001c0001t0002g0066 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.850-40644G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45502651 | ||||||
| chr5:45502801
|
T | C | 1 | a0001c0001t0002g0146 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.850-40794A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45502801 | ||||||
| chr5:45503002
|
G | T | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-40995C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45503002 | ||||||
| chr5:45503176
|
G | A | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.850-41169C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45503176 | ||||||
| chr5:45503396
|
A | C | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-41389T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45503396 | ||||||
| chr5:45503473
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-41466T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45503473 | ||||||
| chr5:45503495
|
A | T | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-41488T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45503495 | ||||||
| chr5:45503519
|
A | T | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.850-41512T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45503519 | ||||||
| chr5:45503807
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.850-41800G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45503807 | ||||||
| chr5:45503888
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-41881G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45503888 | ||||||
| chr5:45503917
|
C | T | 217 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.850-41910G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45503917 | ||||||
| chr5:45503925
|
A | G | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-41918T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45503925 | ||||||
| chr5:45503940
|
C | T | 36 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(33): Show | 36 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.850-41933G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45503940 | ||||||
| chr5:45504099
|
A | ATTC | 2 | a0001c0001t0001g0185a0001c0001t0002g0091 | 2 | HG00639.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.850-42095_850-4209 others(7): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45504099 | ||||||
| chr5:45504102
|
C | A | 1 | a0001c0001t0003g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.850-42095G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45504102 | ||||||
| chr5:45504108
|
C | A | 7 | a0001c0001t0001g0205a0001c0001t0002g0019a0001c0001t0002g0047others(4): Show | 7 | HG00099.hp1 HG00280.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.850-42101G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45504108 | ||||||
| chr5:45504148
|
T | C | 59 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(56): Show | 59 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.850-42141A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45504148 | ||||||
| chr5:45504221
|
G | C | 6 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(3): Show | 6 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-42214C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45504221 | ||||||
| chr5:45504304
|
A | T | 8 | a0001c0001t0001g0159a0001c0001t0001g0182a0001c0001t0001g0184others(5): Show | 8 | HG00639.hp1 HG01169.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.850-42297T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45504304 | ||||||
| chr5:45504345
|
T | G | 1 | a0001c0001t0003g0053 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.850-42338A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45504345 | ||||||
| chr5:45504347
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.850-42340C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45504347 | ||||||
| chr5:45504473
|
C | A | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.850-42466G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45504473 | ||||||
| chr5:45504581
|
G | C | 1 | a0001c0001t0001g0135 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.850-42574C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45504581 | ||||||
| chr5:45504723
|
A | G | 5 | a0001c0001t0003g0087a0001c0001t0003g0093a0001c0001t0003g0094others(2): Show | 5 | HG01071.hp1 HG01081.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-42716T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45504723 | ||||||
| chr5:45505003
|
C | T | 2 | a0001c0001t0011g0163a0001c0001t0011g0164 | 2 | NA18992.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.850-42996G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45505003 | ||||||
| chr5:45505008
|
A | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.850-43001T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45505008 | ||||||
| chr5:45505032
|
T | G | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.850-43025A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45505032 | ||||||
| chr5:45505052
|
C | T | 12 | a0001c0001t0001g0073a0001c0001t0001g0134a0001c0001t0001g0160others(9): Show | 12 | HG00673.hp2 HG02056.hp1 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.850-43045G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45505052 | ||||||
| chr5:45505112
|
T | C | 35 | a0001c0001t0001g0107a0001c0001t0002g0072a0001c0001t0002g0091others(32): Show | 35 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-43105A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45505112 | ||||||
| chr5:45505271
|
T | C | 66 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(63): Show | 66 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.850-43264A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45505271 | ||||||
| chr5:45505426
|
A | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.850-43419T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45505426 | ||||||
| chr5:45505546
|
G | A | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG01952.hp1 HG03704.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-43539C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45505546 | ||||||
| chr5:45505665
|
GA | G | 3 | a0001c0001t0001g0173a0001c0001t0011g0163a0001c0001t0011g0164 | 3 | NA18992.hp1 NA19000.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.850-43659delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45505665 | ||||||
| chr5:45505682
|
T | C | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-43675A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45505682 | ||||||
| chr5:45505753
|
A | C | 1 | a0001c0001t0002g0028 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.850-43746T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45505753 | ||||||
| chr5:45505844
|
T | C | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.850-43837A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45505844 | ||||||
| chr5:45505864
|
C | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-43857G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45505864 | ||||||
| chr5:45506068
|
C | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-44061G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45506068 | ||||||
| chr5:45506101
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-44094G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45506101 | ||||||
| chr5:45506156
|
T | C | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-44149A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45506156 | ||||||
| chr5:45506328
|
G | A | 1 | a0001c0001t0002g0025 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.850-44321C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45506328 | ||||||
| chr5:45506405
|
C | T | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.850-44398G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45506405 | ||||||
| chr5:45506677
|
T | C | 1 | a0001c0006t0002g0219 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.850-44670A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45506677 | ||||||
| chr5:45506716
|
T | C | 62 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(59): Show | 62 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.850-44709A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45506716 | ||||||
| chr5:45506775
|
T | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-44768A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45506775 | ||||||
| chr5:45506810
|
A | T | 1 | a0001c0001t0013g0079 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.850-44803T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45506810 | ||||||
| chr5:45506884
|
C | G | 54 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(51): Show | 54 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.850-44877G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45506884 | ||||||
| chr5:45507168
|
C | T | 1 | a0001c0001t0002g0082 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.850-45161G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45507168 | ||||||
| chr5:45507218
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG01074.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.850-45211G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45507218 | ||||||
| chr5:45507249
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.850-45242G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45507249 | ||||||
| chr5:45507565
|
G | A | 4 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(1): Show | 4 | HG01257.hp1 HG01258.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-45558C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45507565 | ||||||
| chr5:45507657
|
T | G | 2 | a0001c0001t0001g0187a0001c0001t0040g0175 | 2 | NA18977.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.850-45650A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45507657 | ||||||
| chr5:45507950
|
G | A | 6 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(3): Show | 6 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-45943C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45507950 | ||||||
| chr5:45507963
|
T | A | 1 | a0001c0001t0005g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.850-45956A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45507963 | ||||||
| chr5:45507965
|
T | A | 1 | a0001c0001t0002g0056 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.850-45958A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45507965 | ||||||
| chr5:45508521
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-46514T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45508521 | ||||||
| chr5:45508680
|
T | C | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.850-46673A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45508680 | ||||||
| chr5:45508929
|
G | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-46922C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45508929 | ||||||
| chr5:45508929
|
G | T | 1 | a0002c0002t0014g0223 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.850-46922C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45508929 | ||||||
| chr5:45509031
|
C | A | 3 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0142 | 3 | HG02886.hp2 HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.850-47024G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45509031 | ||||||
| chr5:45509048
|
T | C | 1 | a0001c0001t0002g0038 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.850-47041A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45509048 | ||||||
| chr5:45509081
|
G | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-47074C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45509081 | ||||||
| chr5:45509185
|
A | T | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.850-47178T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45509185 | ||||||
| chr5:45509233
|
T | G | 2 | a0001c0001t0002g0072a0001c0001t0002g0097 | 2 | HG00673.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.850-47226A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45509233 | ||||||
| chr5:45509247
|
C | T | 1 | a0001c0001t0002g0056 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.850-47240G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45509247 | ||||||
| chr5:45509253
|
T | C | 1 | a0001c0001t0002g0178 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.850-47246A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45509253 | ||||||
| chr5:45509473
|
G | A | 62 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(59): Show | 62 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.850-47466C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45509473 | ||||||
| chr5:45509740
|
A | T | 1 | a0001c0001t0005g0127 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.850-47733T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45509740 | ||||||
| chr5:45509769
|
T | A | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-47762A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45509769 | ||||||
| chr5:45509816
|
A | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-47809T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45509816 | ||||||
| chr5:45509836
|
A | G | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.850-47829T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45509836 | ||||||
| chr5:45510094
|
C | T | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-48087G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45510094 | ||||||
| chr5:45510191
|
G | A | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.850-48184C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45510191 | ||||||
| chr5:45510251
|
A | G | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.850-48244T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45510251 | ||||||
| chr5:45510257
|
C | T | 4 | a0001c0001t0001g0102a0001c0001t0001g0216a0001c0001t0010g0004others(1): Show | 4 | HG00558.hp2 NA19009.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-48250G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45510257 | ||||||
| chr5:45510331
|
C | T | 2 | a0001c0001t0002g0082a0001c0001t0019g0114 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.850-48324G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45510331 | ||||||
| chr5:45510630
|
G | C | 1 | a0001c0001t0002g0043 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.850-48623C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45510630 | ||||||
| chr5:45510631
|
T | C | 1 | a0001c0001t0002g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.850-48624A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45510631 | ||||||
| chr5:45510891
|
TC | T | 62 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(59): Show | 62 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.850-48885delG | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45510891 | ||||||
| chr5:45510897
|
T | A | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-48890A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45510897 | ||||||
| chr5:45511031
|
T | TTAG | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.850-49027_850-4902 others(7): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45511031 | ||||||
| chr5:45511192
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-49185T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45511192 | ||||||
| chr5:45511246
|
A | G | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.850-49239T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45511246 | ||||||
| chr5:45511365
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-49358G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45511365 | ||||||
| chr5:45511366
|
G | A | 49 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0139others(46): Show | 49 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.850-49359C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45511366 | ||||||
| chr5:45511508
|
C | G | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.850-49501G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45511508 | ||||||
| chr5:45511708
|
G | A | 2 | a0001c0001t0002g0015a0001c0001t0016g0014 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.850-49701C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45511708 | ||||||
| chr5:45511721
|
A | T | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.850-49714T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45511721 | ||||||
| chr5:45512164
|
A | G | 2 | a0001c0001t0002g0015a0001c0001t0016g0014 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.850-50157T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45512164 | ||||||
| chr5:45512211
|
A | T | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.850-50204T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45512211 | ||||||
| chr5:45512242
|
A | C | 6 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(3): Show | 6 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-50235T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45512242 | ||||||
| chr5:45512248
|
A | G | 37 | a0001c0001t0001g0107a0001c0001t0002g0072a0001c0001t0002g0082others(34): Show | 37 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.850-50241T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45512248 | ||||||
| chr5:45512442
|
T | G | 1 | a0001c0001t0003g0104 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.850-50435A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45512442 | ||||||
| chr5:45512487
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-50480A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45512487 | ||||||
| chr5:45512541
|
A | G | 2 | a0001c0001t0002g0015a0001c0001t0016g0014 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.850-50534T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45512541 | ||||||
| chr5:45512925
|
T | C | 2 | a0001c0001t0001g0085a0001c0001t0001g0190 | 2 | NA18971.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.850-50918A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45512925 | ||||||
| chr5:45513010
|
T | C | 9 | a0001c0001t0001g0107a0001c0001t0003g0090a0001c0001t0003g0092others(6): Show | 9 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.850-51003A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45513010 | ||||||
| chr5:45513076
|
C | T | 2 | a0001c0001t0002g0082a0001c0001t0019g0114 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.850-51069G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45513076 | ||||||
| chr5:45513447
|
C | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.850-51440G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45513447 | ||||||
| chr5:45513518
|
C | T | 62 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(59): Show | 62 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.850-51511G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45513518 | ||||||
| chr5:45513651
|
C | T | 6 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(3): Show | 6 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-51644G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45513651 | ||||||
| chr5:45513676
|
G | A | 5 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226others(2): Show | 5 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-51669C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45513676 | ||||||
| chr5:45513741
|
C | T | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.850-51734G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45513741 | ||||||
| chr5:45513817
|
T | C | 1 | a0001c0001t0001g0156 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.850-51810A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45513817 | ||||||
| chr5:45513890
|
C | A | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.850-51883G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45513890 | ||||||
| chr5:45513952
|
A | G | 1 | a0001c0001t0002g0040 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.850-51945T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45513952 | ||||||
| chr5:45513957
|
G | A | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.850-51950C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45513957 | ||||||
| chr5:45514063
|
C | T | 1 | a0001c0001t0002g0194 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.850-52056G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45514063 | ||||||
| chr5:45514195
|
T | C | 3 | a0001c0001t0001g0184a0001c0001t0003g0158a0001c0001t0003g0183 | 3 | HG01256.hp1 HG01258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.850-52188A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45514195 | ||||||
| chr5:45514245
|
T | C | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-52238A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45514245 | ||||||
| chr5:45514454
|
A | C | 6 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(3): Show | 6 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-52447T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45514454 | ||||||
| chr5:45514517
|
G | C | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-52510C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45514517 | ||||||
| chr5:45514629
|
A | T | 1 | a0001c0001t0005g0128 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.850-52622T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45514629 | ||||||
| chr5:45514687
|
A | T | 1 | a0001c0001t0004g0030 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.850-52680T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45514687 | ||||||
| chr5:45514872
|
T | A | 62 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(59): Show | 62 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.850-52865A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45514872 | ||||||
| chr5:45514965
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.850-52958C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45514965 | ||||||
| chr5:45514982
|
T | A | 62 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(59): Show | 62 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.850-52975A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45514982 | ||||||
| chr5:45515158
|
A | AAAATATG others(1): Show |
62 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(59): Show | 62 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.850-53159_850-5315 others(12): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45515158 | ||||||
| chr5:45515322
|
G | C | 62 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(59): Show | 62 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.850-53315C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45515322 | ||||||
| chr5:45515655
|
A | T | 1 | a0001c0001t0001g0173 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.850-53648T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45515655 | ||||||
| chr5:45515741
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-53734T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45515741 | ||||||
| chr5:45515800
|
C | A | 1 | a0001c0001t0003g0104 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.850-53793G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45515800 | ||||||
| chr5:45516162
|
G | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-54155C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45516162 | ||||||
| chr5:45516176
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-54169C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45516176 | ||||||
| chr5:45516262
|
T | C | 35 | a0001c0001t0001g0107a0001c0001t0002g0072a0001c0001t0002g0091others(32): Show | 35 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-54255A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45516262 | ||||||
| chr5:45516383
|
T | C | 2 | a0001c0001t0002g0121a0001c0005t0002g0199 | 2 | HG01167.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.850-54376A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45516383 | ||||||
| chr5:45516763
|
C | G | 62 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(59): Show | 62 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.850-54756G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45516763 | ||||||
| chr5:45516893
|
A | ATG | 138 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.850-54888_850-5488 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45516893 | ||||||
| chr5:45516907
|
G | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-54900C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45516907 | ||||||
| chr5:45516966
|
G | A | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.850-54959C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45516966 | ||||||
| chr5:45517152
|
T | G | 1 | a0001c0001t0001g0166 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.850-55145A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45517152 | ||||||
| chr5:45517271
|
G | T | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.850-55264C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45517271 | ||||||
| chr5:45517520
|
T | TA | 82 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0045others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.850-55514dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45517520 | ||||||
| chr5:45517520
|
T | TAA | 32 | a0001c0001t0001g0051a0001c0001t0001g0074a0001c0001t0001g0076others(29): Show | 32 | HG01257.hp1 HG01891.hp1 HG01975.hp1 others(29): Show |
intron_variant | MODIFIER | c.850-55515_850-5551 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45517520 | ||||||
| chr5:45517520
|
T | TAAA | 39 | a0001c0001t0001g0107a0001c0001t0001g0155a0001c0001t0001g0173others(36): Show | 39 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.850-55516_850-5551 others(7): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45517520 | ||||||
| chr5:45517520
|
TA | T | 14 | a0001c0001t0001g0034a0001c0001t0002g0025a0001c0001t0002g0027others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.850-55514delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45517520 | ||||||
| chr5:45517858
|
T | C | 2 | a0001c0001t0002g0082a0001c0001t0019g0114 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.850-55851A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45517858 | ||||||
| chr5:45517871
|
C | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.850-55864G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45517871 | ||||||
| chr5:45517911
|
T | C | 1 | a0001c0001t0002g0067 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.850-55904A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45517911 | ||||||
| chr5:45518315
|
C | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-56308G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45518315 | ||||||
| chr5:45518452
|
G | C | 1 | a0001c0001t0002g0067 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.850-56445C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45518452 | ||||||
| chr5:45518609
|
G | T | 1 | a0001c0001t0002g0041 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.850-56602C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45518609 | ||||||
| chr5:45518748
|
G | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-56741C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45518748 | ||||||
| chr5:45519329
|
T | C | 3 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133 | 3 | HG01257.hp1 HG01258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.850-57322A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45519329 | ||||||
| chr5:45519526
|
A | G | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.850-57519T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45519526 | ||||||
| chr5:45519809
|
A | AT | 6 | a0001c0001t0002g0026a0001c0001t0002g0131a0001c0001t0002g0132others(3): Show | 6 | HG01071.hp1 HG01257.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-57803dupA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45519809 | ||||||
| chr5:45519979
|
A | G | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-57972T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45519979 | ||||||
| chr5:45519994
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.850-57987A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45519994 | ||||||
| chr5:45520031
|
A | C | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-58024T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45520031 | ||||||
| chr5:45520241
|
C | G | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-58234G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45520241 | ||||||
| chr5:45520317
|
A | T | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-58310T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45520317 | ||||||
| chr5:45520383
|
G | C | 62 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(59): Show | 62 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.850-58376C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45520383 | ||||||
| chr5:45520414
|
A | T | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.850-58407T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45520414 | ||||||
| chr5:45520442
|
G | C | 1 | a0001c0001t0002g0069 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.850-58435C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45520442 | ||||||
| chr5:45520680
|
A | G | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.850-58673T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45520680 | ||||||
| chr5:45520783
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.850-58776A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45520783 | ||||||
| chr5:45521358
|
C | A | 7 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(4): Show | 7 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.850-59351G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45521358 | ||||||
| chr5:45521688
|
A | G | 1 | a0001c0001t0006g0203 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.850-59681T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45521688 | ||||||
| chr5:45521710
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.850-59703G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45521710 | ||||||
| chr5:45521784
|
G | A | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-59777C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45521784 | ||||||
| chr5:45521924
|
A | T | 1 | a0001c0001t0001g0051 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.850-59917T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45521924 | ||||||
| chr5:45522371
|
T | G | 7 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(4): Show | 7 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.850-60364A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45522371 | ||||||
| chr5:45522602
|
CT | C | 51 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(48): Show | 51 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.850-60596delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45522602 | ||||||
| chr5:45522822
|
C | T | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-60815G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45522822 | ||||||
| chr5:45522837
|
C | A | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.850-60830G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45522837 | ||||||
| chr5:45522877
|
C | A | 8 | a0001c0001t0001g0159a0001c0001t0001g0182a0001c0001t0001g0184others(5): Show | 8 | HG00639.hp1 HG01169.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.850-60870G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45522877 | ||||||
| chr5:45522893
|
A | G | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-60886T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45522893 | ||||||
| chr5:45522937
|
C | G | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-60930G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45522937 | ||||||
| chr5:45523082
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0002g0181 | 2 | HG01346.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.850-61075G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45523082 | ||||||
| chr5:45523183
|
T | C | 2 | a0001c0001t0004g0017a0001c0001t0018g0018 | 2 | HG00438.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.850-61176A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45523183 | ||||||
| chr5:45523225
|
A | G | 2 | a0001c0001t0001g0149a0001c0001t0002g0152 | 2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.850-61218T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45523225 | ||||||
| chr5:45523320
|
C | T | 64 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(61): Show | 64 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.850-61313G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45523320 | ||||||
| chr5:45523635
|
T | G | 1 | a0001c0001t0009g0003 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.850-61628A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45523635 | ||||||
| chr5:45523686
|
C | T | 2 | a0001c0001t0002g0082a0001c0001t0019g0114 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.850-61679G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45523686 | ||||||
| chr5:45523687
|
G | A | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.850-61680C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45523687 | ||||||
| chr5:45523698
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.850-61691C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45523698 | ||||||
| chr5:45523704
|
T | G | 225 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.850-61697A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45523704 | ||||||
| chr5:45523864
|
A | G | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.850-61857T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45523864 | ||||||
| chr5:45524074
|
T | C | 1 | a0001c0001t0002g0194 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.850-62067A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45524074 | ||||||
| chr5:45524076
|
C | T | 1 | a0001c0001t0002g0194 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.850-62069G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45524076 | ||||||
| chr5:45524167
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-62160A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45524167 | ||||||
| chr5:45524176
|
C | T | 1 | a0001c0001t0029g0070 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.850-62169G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45524176 | ||||||
| chr5:45524292
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-62285G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45524292 | ||||||
| chr5:45524304
|
C | A | 9 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(6): Show | 9 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.850-62297G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45524304 | ||||||
| chr5:45524341
|
A | C | 1 | a0001c0001t0001g0197 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.850-62334T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45524341 | ||||||
| chr5:45524532
|
T | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-62525A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45524532 | ||||||
| chr5:45524563
|
G | A | 3 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0043 | 3 | HG00597.hp2 HG00639.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.850-62556C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45524563 | ||||||
| chr5:45524622
|
G | A | 2 | a0001c0001t0005g0122a0001c0001t0005g0123 | 2 | HG02055.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.850-62615C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45524622 | ||||||
| chr5:45524631
|
C | A | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.850-62624G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45524631 | ||||||
| chr5:45524633
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.850-62626A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45524633 | ||||||
| chr5:45524868
|
G | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG01074.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.850-62861C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45524868 | ||||||
| chr5:45524966
|
C | T | 2 | a0001c0001t0002g0072a0001c0001t0002g0097 | 2 | HG00673.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.850-62959G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45524966 | ||||||
| chr5:45525001
|
A | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-62994T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45525001 | ||||||
| chr5:45525024
|
T | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-63017A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45525024 | ||||||
| chr5:45525053
|
A | T | 1 | a0001c0001t0002g0067 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.850-63046T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45525053 | ||||||
| chr5:45525060
|
A | G | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-63053T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45525060 | ||||||
| chr5:45525071
|
C | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-63064G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45525071 | ||||||
| chr5:45525177
|
G | A | 1 | a0001c0001t0009g0002 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.850-63170C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45525177 | ||||||
| chr5:45525447
|
T | TAA | 6 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(3): Show | 6 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-63441_850-6344 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45525447 | ||||||
| chr5:45525448
|
C | T | 6 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(3): Show | 6 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-63441G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45525448 | ||||||
| chr5:45525449
|
G | A | 6 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(3): Show | 6 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-63442C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45525449 | ||||||
| chr5:45525473
|
G | T | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.850-63466C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45525473 | ||||||
| chr5:45525500
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.850-63493A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45525500 | ||||||
| chr5:45525771
|
T | C | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.850-63764A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45525771 | ||||||
| chr5:45525772
|
G | T | 1 | a0001c0001t0005g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.850-63765C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45525772 | ||||||
| chr5:45525898
|
G | A | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.850-63891C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45525898 | ||||||
| chr5:45525903
|
G | A | 3 | a0001c0001t0001g0134a0001c0001t0001g0160a0001c0001t0001g0166 | 3 | HG02132.hp2 NA18962.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.850-63896C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45525903 | ||||||
| chr5:45525974
|
T | G | 8 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(5): Show | 8 | HG01167.hp2 HG01192.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.850-63967A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45525974 | ||||||
| chr5:45526096
|
A | G | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.850-64089T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45526096 | ||||||
| chr5:45526150
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0033g0213 | 2 | HG01361.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.850-64143G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45526150 | ||||||
| chr5:45526362
|
C | A | 2 | a0001c0001t0001g0209a0001c0001t0002g0178 | 2 | HG00280.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.850-64355G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45526362 | ||||||
| chr5:45526600
|
T | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-64593A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45526600 | ||||||
| chr5:45526869
|
TATCAGCT others(493): Show |
T | 62 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(59): Show | 62 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.850-65362_850-6486 others(4): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45526869 | ||||||
| chr5:45526971
|
T | C | 1 | a0001c0001t0024g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.850-64964A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45526971 | ||||||
| chr5:45527019
|
C | T | 1 | a0001c0001t0002g0082 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.850-65012G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45527019 | ||||||
| chr5:45527229
|
T | C | 7 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(4): Show | 7 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.850-65222A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45527229 | ||||||
| chr5:45527266
|
G | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-65259C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45527266 | ||||||
| chr5:45527366
|
TATC | T | 154 | a0001c0001t0001g0045a0001c0001t0001g0073a0001c0001t0001g0074others(151): Show | 154 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.850-65362_850-6536 others(7): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45527366 | ||||||
| chr5:45527608
|
T | C | 1 | a0001c0001t0012g0137 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.850-65601A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45527608 | ||||||
| chr5:45527642
|
A | C | 1 | a0001c0001t0002g0019 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.850-65635T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45527642 | ||||||
| chr5:45527667
|
C | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-65660G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45527667 | ||||||
| chr5:45527724
|
C | T | 216 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.850-65717G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45527724 | ||||||
| chr5:45527932
|
G | GT | 11 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(8): Show | 11 | HG01167.hp2 HG01192.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.850-65926dupA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45527932 | ||||||
| chr5:45527932
|
GT | G | 98 | a0001c0001t0001g0073a0001c0001t0001g0102a0001c0001t0001g0134others(95): Show | 98 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.850-65926delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45527932 | ||||||
| chr5:45527946
|
T | A | 1 | a0001c0001t0002g0082 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.850-65939A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45527946 | ||||||
| chr5:45528323
|
T | C | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.850-66316A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45528323 | ||||||
| chr5:45528474
|
G | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-66467C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45528474 | ||||||
| chr5:45528810
|
T | A | 16 | a0001c0001t0001g0065a0001c0001t0004g0017a0001c0001t0004g0020others(13): Show | 16 | HG00438.hp1 HG00609.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.850-66803A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45528810 | ||||||
| chr5:45529183
|
C | A | 3 | a0001c0001t0002g0072a0001c0001t0002g0097a0001c0001t0003g0086 | 3 | HG00558.hp1 HG00673.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.850-67176G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45529183 | ||||||
| chr5:45529226
|
CACTA | C | 3 | a0001c0001t0002g0046a0003c0003t0002g0221a0003c0003t0035g0220 | 3 | HG00738.hp2 HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-67223_850-6722 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45529226 | ||||||
| chr5:45529404
|
T | A | 1 | a0001c0001t0012g0137 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.850-67397A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45529404 | ||||||
| chr5:45529536
|
G | A | 3 | a0001c0001t0002g0072a0001c0001t0002g0097a0001c0001t0003g0086 | 3 | HG00558.hp1 HG00673.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.850-67529C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45529536 | ||||||
| chr5:45529619
|
G | C | 3 | a0001c0001t0003g0110a0001c0001t0003g0111a0001c0001t0003g0112 | 3 | HG02056.hp2 NA19001.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.850-67612C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45529619 | ||||||
| chr5:45529701
|
C | G | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.850-67694G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45529701 | ||||||
| chr5:45530059
|
G | A | 154 | a0001c0001t0001g0045a0001c0001t0001g0073a0001c0001t0001g0074others(151): Show | 154 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.850-68052C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45530059 | ||||||
| chr5:45530257
|
A | T | 1 | a0001c0001t0001g0206 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.850-68250T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45530257 | ||||||
| chr5:45530410
|
T | TTATA | 3 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0142 | 3 | HG02886.hp2 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.850-68404_850-6840 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45530410 | ||||||
| chr5:45530412
|
T | A | 5 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0129others(2): Show | 5 | HG02886.hp2 HG02897.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-68405A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45530412 | ||||||
| chr5:45530412
|
T | TTA | 3 | a0001c0001t0001g0185a0001c0001t0031g0009a0001c0001t0032g0010 | 3 | HG00639.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.850-68407_850-6840 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45530412 | ||||||
| chr5:45530412
|
T | TTATA | 7 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(4): Show | 7 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.850-68409_850-6840 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45530412 | ||||||
| chr5:45530414
|
A | G | 2 | a0001c0001t0002g0082a0001c0001t0019g0114 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.850-68407T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45530414 | ||||||
| chr5:45530448
|
T | A | 1 | a0001c0001t0001g0051 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.850-68441A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45530448 | ||||||
| chr5:45530449
|
A | T | 18 | a0001c0001t0001g0013a0001c0001t0003g0093a0001c0001t0003g0101others(15): Show | 18 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.850-68442T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45530449 | ||||||
| chr5:45530520
|
C | A | 1 | a0001c0001t0002g0178 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.850-68513G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45530520 | ||||||
| chr5:45530542
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-68535T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45530542 | ||||||
| chr5:45530720
|
T | A | 62 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(59): Show | 62 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.850-68713A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45530720 | ||||||
| chr5:45530860
|
C | T | 2 | a0001c0001t0003g0109a0001c0001t0003g0113 | 2 | NA18980.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.850-68853G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45530860 | ||||||
| chr5:45530886
|
A | C | 6 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(3): Show | 6 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-68879T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45530886 | ||||||
| chr5:45530951
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.850-68944C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45530951 | ||||||
| chr5:45531057
|
T | C | 7 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(4): Show | 7 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.850-69050A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45531057 | ||||||
| chr5:45531057
|
T | TAC | 13 | a0001c0001t0002g0044a0001c0001t0002g0069a0001c0001t0002g0082others(10): Show | 13 | HG01192.hp2 HG01256.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.850-69052_850-6905 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45531057 | ||||||
| chr5:45531057
|
T | TACAC | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-69054_850-6905 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45531057 | ||||||
| chr5:45531255
|
C | T | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.850-69248G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45531255 | ||||||
| chr5:45531415
|
C | T | 1 | a0001c0001t0004g0059 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.850-69408G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45531415 | ||||||
| chr5:45531637
|
C | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-69630G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45531637 | ||||||
| chr5:45531741
|
C | T | 1 | a0001c0001t0002g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.850-69734G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45531741 | ||||||
| chr5:45531912
|
C | T | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.850-69905G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45531912 | ||||||
| chr5:45531950
|
G | T | 15 | a0001c0001t0001g0011a0001c0001t0002g0019a0001c0001t0002g0039others(12): Show | 15 | HG00099.hp1 HG00597.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.850-69943C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45531950 | ||||||
| chr5:45532035
|
G | A | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.850-70028C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45532035 | ||||||
| chr5:45532058
|
C | T | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.850-70051G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45532058 | ||||||
| chr5:45532181
|
T | C | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.850-70174A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45532181 | ||||||
| chr5:45532246
|
C | A | 21 | a0001c0001t0001g0139a0001c0001t0001g0147a0001c0001t0001g0173others(18): Show | 21 | HG00558.hp2 HG00609.hp1 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.850-70239G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45532246 | ||||||
| chr5:45532340
|
TG | T | 2 | a0001c0001t0002g0082a0001c0001t0019g0114 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.850-70334delC | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45532340 | ||||||
| chr5:45532421
|
T | C | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.850-70414A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45532421 | ||||||
| chr5:45532572
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.850-70565G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45532572 | ||||||
| chr5:45532706
|
T | C | 8 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(5): Show | 8 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.850-70699A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45532706 | ||||||
| chr5:45533362
|
C | G | 7 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(4): Show | 7 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.850-71355G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45533362 | ||||||
| chr5:45533386
|
G | T | 8 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(5): Show | 8 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.850-71379C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45533386 | ||||||
| chr5:45533387
|
A | T | 8 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0003g0063others(5): Show | 8 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.850-71380T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45533387 | ||||||
| chr5:45533530
|
T | A | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.850-71523A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45533530 | ||||||
| chr5:45533780
|
C | A | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.850-71773G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45533780 | ||||||
| chr5:45533807
|
G | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-71800C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45533807 | ||||||
| chr5:45533865
|
C | A | 1 | a0001c0001t0002g0056 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.850-71858G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45533865 | ||||||
| chr5:45534042
|
G | A | 4 | a0001c0001t0004g0059a0001c0001t0004g0061a0001c0001t0004g0062others(1): Show | 4 | NA18953.hp2 NA18971.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-72035C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534042 | ||||||
| chr5:45534100
|
A | C | 1 | a0001c0001t0005g0123 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.850-72093T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534100 | ||||||
| chr5:45534269
|
C | T | 1 | a0001c0001t0007g0214 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.850-72262G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534269 | ||||||
| chr5:45534289
|
C | T | 1 | a0001c0001t0027g0022 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.850-72282G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534289 | ||||||
| chr5:45534321
|
C | G | 139 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.850-72314G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534321 | ||||||
| chr5:45534404
|
C | CA | 19 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0156others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.850-72398dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534404 | ||||||
| chr5:45534404
|
C | CAA | 9 | a0001c0001t0001g0167a0001c0001t0001g0195a0001c0001t0002g0140others(6): Show | 9 | HG02056.hp1 HG02897.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.850-72399_850-7239 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534404 | ||||||
| chr5:45534404
|
C | CAAA | 13 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0190others(10): Show | 13 | HG00639.hp1 HG01261.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.850-72400_850-7239 others(7): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534404 | ||||||
| chr5:45534404
|
C | CAAAA | 9 | a0001c0001t0001g0159a0001c0001t0001g0170a0001c0001t0001g0176others(6): Show | 9 | HG00323.hp1 HG01169.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.850-72401_850-7239 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534404 | ||||||
| chr5:45534404
|
C | CAAAAAAA others(3): Show |
3 | a0001c0001t0001g0171a0001c0001t0003g0117a0002c0002t0014g0222 | 3 | HG01074.hp1 HG01978.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.850-72407_850-7239 others(14): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534404 | ||||||
| chr5:45534404
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.850-72408_850-7239 others(15): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534404 | ||||||
| chr5:45534404
|
C | CAAAAAAA others(8): Show |
2 | a0002c0002t0008g0224a0002c0002t0008g0225 | 2 | HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.850-72412_850-7239 others(19): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534404 | ||||||
| chr5:45534404
|
C | CAAAAAAA others(14): Show |
1 | a0002c0002t0008g0226 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.850-72418_850-7239 others(25): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534404 | ||||||
| chr5:45534404
|
CA | C | 5 | a0001c0001t0001g0209a0001c0001t0002g0043a0001c0001t0002g0178others(2): Show | 5 | HG00280.hp2 HG00597.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-72398delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534404 | ||||||
| chr5:45534404
|
CAAAA | C | 8 | a0001c0001t0001g0037a0001c0001t0002g0026a0001c0001t0002g0052others(5): Show | 8 | HG00735.hp2 HG01258.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.850-72401_850-7239 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534404 | ||||||
| chr5:45534404
|
CAAAAA | C | 19 | a0001c0001t0001g0065a0001c0001t0002g0035a0001c0001t0002g0036others(16): Show | 19 | HG00280.hp1 HG00639.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.850-72402_850-7239 others(9): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534404 | ||||||
| chr5:45534404
|
CAAAAAA | C | 31 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0045others(28): Show | 31 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.850-72403_850-7239 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534404 | ||||||
| chr5:45534404
|
CAAAAAAA | C | 8 | a0001c0001t0001g0013a0001c0001t0002g0015a0001c0001t0002g0023others(5): Show | 8 | HG00741.hp1 HG01256.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.850-72404_850-7239 others(11): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534404 | ||||||
| chr5:45534404
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0002g0152a0001c0001t0009g0003 | 2 | HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.850-72407_850-7239 others(14): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534404 | ||||||
| chr5:45534404
|
CAAAAAAA others(4): Show |
C | 4 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0003g0110others(1): Show | 4 | HG02056.hp2 HG02145.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-72408_850-7239 others(15): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534404 | ||||||
| chr5:45534404
|
CAAAAAAA others(5): Show |
C | 35 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(32): Show | 35 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-72409_850-7239 others(16): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534404 | ||||||
| chr5:45534404
|
CAAAAAAA others(7): Show |
C | 2 | a0001c0001t0002g0025a0001c0001t0003g0108 | 2 | HG03225.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.850-72411_850-7239 others(18): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534404 | ||||||
| chr5:45534404
|
CAAAAAAA others(8): Show |
C | 3 | a0001c0001t0031g0009a0001c0001t0032g0010a0001c0001t0033g0213 | 3 | HG01167.hp1 HG01169.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.850-72412_850-7239 others(19): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534404 | ||||||
| chr5:45534404
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0003g0053 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.850-72414_850-7239 others(21): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534404 | ||||||
| chr5:45534404
|
CAAAAAAA others(12): Show |
C | 2 | a0001c0001t0003g0118a0001c0001t0003g0120 | 2 | HG00735.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.850-72416_850-7239 others(23): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534404 | ||||||
| chr5:45534404
|
CAAAAAAA others(13): Show |
C | 3 | a0001c0001t0002g0042a0001c0001t0002g0046a0001c0001t0030g0008 | 3 | HG00738.hp2 HG02258.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.850-72417_850-7239 others(24): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534404 | ||||||
| chr5:45534404
|
CAAAAAAA others(16): Show |
C | 1 | a0001c0001t0001g0151 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.850-72420_850-7239 others(27): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534404 | ||||||
| chr5:45534404
|
CAAAAAAA others(17): Show |
C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-72421_850-7239 others(28): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534404 | ||||||
| chr5:45534418
|
A | G | 1 | a0001c0001t0004g0029 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.850-72411T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534418 | ||||||
| chr5:45534541
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-72534T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534541 | ||||||
| chr5:45534553
|
A | G | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.850-72546T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534553 | ||||||
| chr5:45534655
|
C | T | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.850-72648G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534655 | ||||||
| chr5:45534656
|
G | A | 1 | a0001c0001t0003g0099 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.850-72649C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534656 | ||||||
| chr5:45534668
|
C | CA | 8 | a0001c0001t0001g0159a0001c0001t0001g0182a0001c0001t0001g0184others(5): Show | 8 | HG00639.hp1 HG01169.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.850-72662dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534668 | ||||||
| chr5:45534691
|
T | C | 1 | a0001c0001t0037g0148 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.850-72684A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534691 | ||||||
| chr5:45534715
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.850-72708C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45534715 | ||||||
| chr5:45535144
|
A | G | 1 | a0001c0001t0016g0014 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.850-73137T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45535144 | ||||||
| chr5:45535381
|
T | C | 2 | a0001c0001t0002g0144a0001c0001t0002g0146 | 2 | HG02165.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.850-73374A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45535381 | ||||||
| chr5:45535494
|
T | C | 2 | a0001c0001t0003g0118a0001c0001t0003g0120 | 2 | HG00735.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.850-73487A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45535494 | ||||||
| chr5:45535512
|
C | T | 1 | a0001c0001t0003g0113 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.850-73505G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45535512 | ||||||
| chr5:45535553
|
G | A | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-73546C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45535553 | ||||||
| chr5:45535603
|
A | G | 1 | a0001c0001t0002g0088 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.850-73596T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45535603 | ||||||
| chr5:45535675
|
A | G | 1 | a0001c0001t0001g0011 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.850-73668T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45535675 | ||||||
| chr5:45535734
|
CCAT | C | 6 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(3): Show | 6 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-73730_850-7372 others(7): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45535734 | ||||||
| chr5:45535877
|
T | A | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-73870A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45535877 | ||||||
| chr5:45536070
|
T | A | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.850-74063A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45536070 | ||||||
| chr5:45536232
|
G | C | 1 | a0001c0001t0006g0143 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.850-74225C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45536232 | ||||||
| chr5:45536807
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.850-74800T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45536807 | ||||||
| chr5:45537197
|
T | G | 73 | a0001c0001t0001g0073a0001c0001t0001g0134a0001c0001t0001g0135others(70): Show | 73 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.850-75190A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537197 | ||||||
| chr5:45537259
|
A | T | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-75252T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537259 | ||||||
| chr5:45537265
|
A | T | 3 | a0001c0001t0001g0173a0001c0001t0011g0163a0001c0001t0011g0164 | 3 | NA18992.hp1 NA19000.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.850-75258T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537265 | ||||||
| chr5:45537402
|
G | T | 2 | a0001c0001t0001g0147a0001c0001t0025g0217 | 2 | HG01192.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.850-75395C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537402 | ||||||
| chr5:45537402
|
GT | G | 150 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(147): Show | 150 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.850-75396delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537402 | ||||||
| chr5:45537403
|
T | G | 2 | a0001c0001t0001g0147a0001c0001t0025g0217 | 2 | HG01192.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.850-75396A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537403 | ||||||
| chr5:45537420
|
C | T | 1 | a0001c0001t0002g0066 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.850-75413G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537420 | ||||||
| chr5:45537518
|
T | C | 73 | a0001c0001t0001g0073a0001c0001t0001g0134a0001c0001t0001g0135others(70): Show | 73 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.850-75511A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537518 | ||||||
| chr5:45537523
|
C | CT | 45 | a0001c0001t0001g0013a0001c0001t0001g0073a0001c0001t0001g0074others(42): Show | 45 | HG00099.hp2 HG00438.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.850-75517dupA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537523 | ||||||
| chr5:45537523
|
C | CTT | 43 | a0001c0001t0001g0034a0001c0001t0001g0060a0001c0001t0001g0065others(40): Show | 43 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.850-75518_850-7551 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537523 | ||||||
| chr5:45537523
|
C | CTTT | 19 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0147others(16): Show | 19 | HG00323.hp1 HG00642.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.850-75519_850-7551 others(7): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537523 | ||||||
| chr5:45537523
|
C | CTTTT | 12 | a0001c0001t0001g0139a0001c0001t0001g0180a0001c0001t0001g0184others(9): Show | 12 | HG00609.hp1 HG00639.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.850-75520_850-7551 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537523 | ||||||
| chr5:45537523
|
C | CTTTTT | 6 | a0001c0001t0001g0173a0001c0001t0012g0137a0001c0001t0021g0138others(3): Show | 6 | HG00741.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-75521_850-7551 others(9): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537523 | ||||||
| chr5:45537523
|
C | CTTTTTT | 7 | a0001c0001t0001g0116a0001c0001t0002g0178a0001c0001t0003g0117others(4): Show | 7 | HG00280.hp2 HG00642.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.850-75522_850-7551 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537523 | ||||||
| chr5:45537523
|
C | CTTTTTTT others(3): Show |
1 | a0002c0002t0014g0223 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.850-75526_850-7551 others(14): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537523 | ||||||
| chr5:45537523
|
CT | C | 13 | a0001c0001t0001g0051a0001c0001t0001g0085a0001c0001t0002g0015others(10): Show | 13 | HG00099.hp1 HG01256.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.850-75517delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537523 | ||||||
| chr5:45537523
|
CTTTT | C | 9 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(6): Show | 9 | HG01891.hp1 HG02055.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.850-75520_850-7551 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537523 | ||||||
| chr5:45537523
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.850-75527_850-7551 others(15): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537523 | ||||||
| chr5:45537523
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0003g0092 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.850-75531_850-7551 others(19): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537523 | ||||||
| chr5:45537523
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0009g0003 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.850-75532_850-7551 others(20): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537523 | ||||||
| chr5:45537565
|
G | C | 35 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(32): Show | 35 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-75558C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537565 | ||||||
| chr5:45537686
|
C | T | 1 | a0001c0001t0003g0109 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.850-75679G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537686 | ||||||
| chr5:45537753
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-75746G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537753 | ||||||
| chr5:45537767
|
G | A | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.850-75760C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537767 | ||||||
| chr5:45537828
|
C | A | 1 | a0001c0001t0012g0137 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.850-75821G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537828 | ||||||
| chr5:45537850
|
A | G | 43 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(40): Show | 43 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.850-75843T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537850 | ||||||
| chr5:45537921
|
A | T | 1 | a0001c0001t0001g0073 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.850-75914T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537921 | ||||||
| chr5:45537944
|
G | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-75937C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45537944 | ||||||
| chr5:45538008
|
T | C | 2 | a0001c0001t0002g0015a0001c0001t0016g0014 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.850-76001A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45538008 | ||||||
| chr5:45538033
|
T | TA | 39 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(36): Show | 39 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.850-76027dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45538033 | ||||||
| chr5:45538033
|
TA | T | 149 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0037others(146): Show | 149 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.850-76027delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45538033 | ||||||
| chr5:45538033
|
TAA | T | 17 | a0001c0001t0001g0073a0001c0001t0001g0134a0001c0001t0001g0160others(14): Show | 17 | HG00642.hp2 HG00673.hp2 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.850-76028_850-7602 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45538033 | ||||||
| chr5:45538099
|
T | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-76092A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45538099 | ||||||
| chr5:45538245
|
T | C | 1 | a0001c0001t0028g0174 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.850-76238A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45538245 | ||||||
| chr5:45538270
|
C | T | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-76263G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45538270 | ||||||
| chr5:45538282
|
G | A | 152 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(149): Show | 152 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.850-76275C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45538282 | ||||||
| chr5:45538297
|
C | A | 1 | a0001c0001t0001g0139 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.850-76290G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45538297 | ||||||
| chr5:45538370
|
T | C | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-76363A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45538370 | ||||||
| chr5:45538392
|
G | T | 1 | a0001c0001t0002g0066 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.850-76385C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45538392 | ||||||
| chr5:45538657
|
G | C | 1 | a0001c0001t0002g0026 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.850-76650C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45538657 | ||||||
| chr5:45538858
|
T | C | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.850-76851A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45538858 | ||||||
| chr5:45538909
|
T | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-76902A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45538909 | ||||||
| chr5:45539213
|
A | G | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-77206T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539213 | ||||||
| chr5:45539314
|
A | G | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-77307T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539314 | ||||||
| chr5:45539400
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-77393G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539400 | ||||||
| chr5:45539463
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0002g0152 | 2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.850-77456G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539463 | ||||||
| chr5:45539477
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-77470T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539477 | ||||||
| chr5:45539584
|
G | A | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.850-77577C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539584 | ||||||
| chr5:45539613
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-77606A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539613 | ||||||
| chr5:45539652
|
G | A | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-77645C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539652 | ||||||
| chr5:45539672
|
A | G | 1 | a0001c0001t0001g0156 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.850-77665T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539672 | ||||||
| chr5:45539692
|
A | T | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.850-77685T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539692 | ||||||
| chr5:45539697
|
A | ATATTATT others(28): Show |
3 | a0001c0001t0001g0173a0001c0001t0011g0163a0001c0001t0011g0164 | 3 | NA18992.hp1 NA19000.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.850-77725_850-7769 others(39): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539697 | ||||||
| chr5:45539757
|
A | T | 152 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(149): Show | 152 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.850-77750T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539757 | ||||||
| chr5:45539919
|
G | GAT | 4 | a0001c0001t0001g0034a0001c0001t0005g0125a0001c0004t0002g0006others(1): Show | 4 | HG01243.hp1 HG01261.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-77914_850-7791 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539919 | ||||||
| chr5:45539919
|
G | GATAT | 3 | a0001c0001t0005g0126a0001c0001t0005g0127a0001c0001t0019g0114 | 3 | HG01891.hp1 HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.850-77916_850-7791 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539919 | ||||||
| chr5:45539919
|
G | GATATAT | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.850-77918_850-7791 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539919 | ||||||
| chr5:45539919
|
G | GATATATA others(1): Show |
7 | a0001c0001t0002g0121a0001c0001t0005g0122a0001c0001t0005g0123others(4): Show | 7 | HG01346.hp2 HG02055.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.850-77920_850-7791 others(12): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539919 | ||||||
| chr5:45539919
|
G | GATATATA others(3): Show |
1 | a0001c0001t0005g0129 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.850-77922_850-7791 others(14): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539919 | ||||||
| chr5:45539919
|
GAT | G | 4 | a0001c0001t0003g0083a0001c0001t0003g0108a0001c0001t0006g0203others(1): Show | 4 | HG00323.hp2 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-77914_850-7791 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539919 | ||||||
| chr5:45539919
|
GATAT | G | 9 | a0001c0001t0002g0041a0001c0001t0002g0052a0001c0001t0002g0066others(6): Show | 9 | HG01167.hp2 HG01934.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.850-77916_850-7791 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539919 | ||||||
| chr5:45539919
|
GATATAT | G | 18 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0202others(15): Show | 18 | HG00558.hp1 HG00738.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.850-77918_850-7791 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539919 | ||||||
| chr5:45539919
|
GATATATA others(1): Show |
G | 78 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0037others(75): Show | 78 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.850-77920_850-7791 others(12): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539919 | ||||||
| chr5:45539919
|
GATATATA others(3): Show |
G | 7 | a0001c0001t0001g0051a0001c0001t0001g0073a0001c0001t0002g0040others(4): Show | 7 | HG00099.hp2 HG01884.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.850-77922_850-7791 others(14): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539919 | ||||||
| chr5:45539919
|
GATATATA others(5): Show |
G | 16 | a0001c0001t0001g0116a0001c0001t0001g0150a0001c0001t0001g0156others(13): Show | 16 | HG00642.hp1 HG00741.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.850-77924_850-7791 others(16): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539919 | ||||||
| chr5:45539919
|
GATATATA others(7): Show |
G | 60 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.850-77926_850-7791 others(18): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539919 | ||||||
| chr5:45539919
|
GATATATA others(9): Show |
G | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG00735.hp1 HG00738.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.850-77928_850-7791 others(20): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539919 | ||||||
| chr5:45539919
|
GATATATA others(11): Show |
G | 2 | a0001c0001t0022g0080a0001c0001t0026g0071 | 2 | HG02257.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.850-77930_850-7791 others(22): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539919 | ||||||
| chr5:45539919
|
GATATATA others(15): Show |
G | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-77934_850-7791 others(26): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539919 | ||||||
| chr5:45539919
|
GATATATA others(21): Show |
G | 1 | a0001c0001t0001g0201 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.850-77940_850-7791 others(32): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539919 | ||||||
| chr5:45539947
|
TATATATA others(6): Show |
T | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.850-77953_850-7794 others(17): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45539947 | ||||||
| chr5:45540024
|
TTTGTTAT others(40): Show |
T | 1 | a0001c0001t0003g0063 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.850-78064_850-7801 others(51): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45540024 | ||||||
| chr5:45540037
|
A | G | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG01952.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.850-78030T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45540037 | ||||||
| chr5:45540073
|
C | T | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.850-78066G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45540073 | ||||||
| chr5:45540077
|
G | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-78070C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45540077 | ||||||
| chr5:45540207
|
A | C | 41 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(38): Show | 41 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.850-78200T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45540207 | ||||||
| chr5:45540305
|
T | A | 35 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(32): Show | 35 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-78298A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45540305 | ||||||
| chr5:45540326
|
A | AT | 10 | a0001c0001t0001g0073a0001c0001t0001g0159a0001c0001t0002g0082others(7): Show | 10 | HG01257.hp2 HG01361.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.850-78320dupA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45540326 | ||||||
| chr5:45540326
|
AT | A | 85 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(82): Show | 85 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.850-78320delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45540326 | ||||||
| chr5:45540529
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-78522G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45540529 | ||||||
| chr5:45540581
|
T | C | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.850-78574A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45540581 | ||||||
| chr5:45540632
|
T | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-78625A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45540632 | ||||||
| chr5:45540711
|
C | G | 64 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(61): Show | 64 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.850-78704G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45540711 | ||||||
| chr5:45540723
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.850-78716G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45540723 | ||||||
| chr5:45540892
|
A | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-78885T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45540892 | ||||||
| chr5:45540907
|
A | G | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-78900T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45540907 | ||||||
| chr5:45540934
|
G | A | 1 | a0001c0001t0023g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.850-78927C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45540934 | ||||||
| chr5:45541079
|
T | C | 43 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(40): Show | 43 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.850-79072A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45541079 | ||||||
| chr5:45541089
|
A | C | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-79082T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45541089 | ||||||
| chr5:45541198
|
T | C | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.850-79191A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45541198 | ||||||
| chr5:45541317
|
G | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-79310C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45541317 | ||||||
| chr5:45541338
|
T | C | 1 | a0001c0001t0002g0067 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.850-79331A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45541338 | ||||||
| chr5:45541355
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.850-79348G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45541355 | ||||||
| chr5:45541497
|
G | T | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-79490C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45541497 | ||||||
| chr5:45541509
|
C | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-79502G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45541509 | ||||||
| chr5:45541605
|
A | AAAACATG others(15): Show |
5 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226others(2): Show | 5 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-79620_850-7959 others(26): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45541605 | ||||||
| chr5:45541953
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.850-79946C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45541953 | ||||||
| chr5:45542064
|
A | C | 6 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(3): Show | 6 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-80057T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45542064 | ||||||
| chr5:45542087
|
C | A | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.850-80080G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45542087 | ||||||
| chr5:45542454
|
A | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-80447T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45542454 | ||||||
| chr5:45542894
|
G | A | 1 | a0001c0001t0005g0129 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.850-80887C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45542894 | ||||||
| chr5:45542950
|
G | A | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.850-80943C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45542950 | ||||||
| chr5:45542954
|
C | T | 1 | a0001c0001t0003g0090 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.850-80947G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45542954 | ||||||
| chr5:45542992
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.850-80985T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45542992 | ||||||
| chr5:45544170
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.850-82163T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45544170 | ||||||
| chr5:45544403
|
T | G | 2 | a0001c0001t0002g0023a0001c0001t0002g0024 | 2 | NA18977.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.850-82396A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45544403 | ||||||
| chr5:45544524
|
C | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.850-82517G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45544524 | ||||||
| chr5:45544634
|
T | C | 1 | a0001c0001t0002g0067 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.850-82627A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45544634 | ||||||
| chr5:45544711
|
T | C | 5 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226others(2): Show | 5 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-82704A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45544711 | ||||||
| chr5:45544899
|
G | A | 1 | a0001c0001t0002g0019 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.850-82892C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45544899 | ||||||
| chr5:45544957
|
A | G | 32 | a0001c0001t0001g0102a0001c0001t0001g0107a0001c0001t0002g0072others(29): Show | 32 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.850-82950T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45544957 | ||||||
| chr5:45545019
|
G | A | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.850-83012C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45545019 | ||||||
| chr5:45545032
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.850-83025G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45545032 | ||||||
| chr5:45545134
|
C | T | 1 | a0001c0001t0002g0082 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.850-83127G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45545134 | ||||||
| chr5:45545244
|
C | A | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.850-83237G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45545244 | ||||||
| chr5:45545349
|
T | C | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.850-83342A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45545349 | ||||||
| chr5:45545357
|
A | G | 5 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226others(2): Show | 5 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-83350T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45545357 | ||||||
| chr5:45545419
|
T | C | 41 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(38): Show | 41 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.850-83412A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45545419 | ||||||
| chr5:45545444
|
T | G | 9 | a0001c0001t0031g0009a0001c0001t0032g0010a0002c0002t0008g0224others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.850-83437A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45545444 | ||||||
| chr5:45545491
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-83484G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45545491 | ||||||
| chr5:45545504
|
A | G | 3 | a0001c0001t0002g0121a0003c0003t0002g0221a0003c0003t0035g0220 | 3 | HG01346.hp2 HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-83497T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45545504 | ||||||
| chr5:45545506
|
T | A | 3 | a0001c0001t0002g0121a0003c0003t0002g0221a0003c0003t0035g0220 | 3 | HG01346.hp2 HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-83499A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45545506 | ||||||
| chr5:45545548
|
C | A | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-83541G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45545548 | ||||||
| chr5:45545549
|
T | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-83542A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45545549 | ||||||
| chr5:45545725
|
T | C | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.850-83718A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45545725 | ||||||
| chr5:45545949
|
C | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-83942G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45545949 | ||||||
| chr5:45546406
|
T | C | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.850-84399A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45546406 | ||||||
| chr5:45546545
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG01074.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.850-84538G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45546545 | ||||||
| chr5:45546596
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-84589A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45546596 | ||||||
| chr5:45546705
|
G | A | 1 | a0001c0001t0002g0072 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.850-84698C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45546705 | ||||||
| chr5:45546714
|
C | T | 1 | a0001c0001t0002g0058 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.850-84707G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45546714 | ||||||
| chr5:45546786
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-84779A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45546786 | ||||||
| chr5:45546834
|
A | G | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-84827T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45546834 | ||||||
| chr5:45546911
|
C | T | 2 | a0001c0001t0001g0107a0001c0001t0007g0100 | 2 | HG00438.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.850-84904G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45546911 | ||||||
| chr5:45546944
|
C | T | 6 | a0001c0001t0001g0102a0001c0001t0002g0088a0001c0001t0002g0091others(3): Show | 6 | NA18945.hp2 NA19003.hp1 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-84937G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45546944 | ||||||
| chr5:45546961
|
C | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.850-84954G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45546961 | ||||||
| chr5:45547176
|
A | G | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.850-85169T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45547176 | ||||||
| chr5:45547445
|
C | T | 43 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(40): Show | 43 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.850-85438G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45547445 | ||||||
| chr5:45547704
|
A | G | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.850-85697T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45547704 | ||||||
| chr5:45547860
|
C | T | 41 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(38): Show | 41 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.850-85853G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45547860 | ||||||
| chr5:45547905
|
A | G | 3 | a0001c0001t0001g0102a0001c0001t0003g0084a0001c0001t0003g0101 | 3 | NA19003.hp1 NA19011.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.850-85898T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45547905 | ||||||
| chr5:45547932
|
G | A | 3 | a0001c0001t0002g0121a0003c0003t0002g0221a0003c0003t0035g0220 | 3 | HG01346.hp2 HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-85925C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45547932 | ||||||
| chr5:45547979
|
T | C | 2 | a0001c0001t0001g0107a0001c0001t0007g0100 | 2 | HG00438.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.850-85972A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45547979 | ||||||
| chr5:45548109
|
C | G | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.850-86102G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45548109 | ||||||
| chr5:45548157
|
G | T | 1 | a0001c0001t0024g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.850-86150C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45548157 | ||||||
| chr5:45548389
|
G | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-86382C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45548389 | ||||||
| chr5:45548427
|
C | T | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.850-86420G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45548427 | ||||||
| chr5:45548454
|
C | T | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.850-86447G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45548454 | ||||||
| chr5:45548474
|
A | C | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.850-86467T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45548474 | ||||||
| chr5:45548572
|
T | C | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-86565A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45548572 | ||||||
| chr5:45548649
|
T | A | 1 | a0001c0001t0001g0085 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.850-86642A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45548649 | ||||||
| chr5:45548652
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.850-86645G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45548652 | ||||||
| chr5:45548658
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.850-86651T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45548658 | ||||||
| chr5:45548683
|
C | T | 1 | a0001c0001t0003g0083 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.850-86676G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45548683 | ||||||
| chr5:45548719
|
G | C | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-86712C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45548719 | ||||||
| chr5:45548857
|
C | A | 78 | a0001c0001t0001g0073a0001c0001t0001g0134a0001c0001t0001g0135others(75): Show | 78 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.850-86850G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45548857 | ||||||
| chr5:45548911
|
A | G | 1 | a0001c0005t0002g0199 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.850-86904T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45548911 | ||||||
| chr5:45548985
|
T | G | 1 | a0001c0001t0001g0200 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.850-86978A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45548985 | ||||||
| chr5:45549104
|
T | G | 37 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(34): Show | 37 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.850-87097A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45549104 | ||||||
| chr5:45549105
|
C | G | 1 | a0001c0001t0001g0116 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.850-87098G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45549105 | ||||||
| chr5:45549249
|
C | T | 1 | a0001c0001t0004g0048 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.850-87242G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45549249 | ||||||
| chr5:45549638
|
T | C | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.850-87631A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45549638 | ||||||
| chr5:45549678
|
A | C | 1 | a0001c0001t0002g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.850-87671T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45549678 | ||||||
| chr5:45549718
|
G | A | 6 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(3): Show | 6 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-87711C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45549718 | ||||||
| chr5:45549719
|
A | C | 6 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(3): Show | 6 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-87712T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45549719 | ||||||
| chr5:45549808
|
G | T | 41 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(38): Show | 41 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.850-87801C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45549808 | ||||||
| chr5:45549842
|
C | T | 1 | a0001c0001t0021g0138 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.850-87835G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45549842 | ||||||
| chr5:45549843
|
G | A | 6 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(3): Show | 6 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-87836C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45549843 | ||||||
| chr5:45549846
|
C | A | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.850-87839G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45549846 | ||||||
| chr5:45549912
|
G | C | 194 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.850-87905C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45549912 | ||||||
| chr5:45550177
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.850-88170T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45550177 | ||||||
| chr5:45550210
|
C | A | 1 | a0001c0004t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.850-88203G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45550210 | ||||||
| chr5:45550335
|
A | C | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-88328T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45550335 | ||||||
| chr5:45550512
|
G | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-88505C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45550512 | ||||||
| chr5:45550542
|
T | C | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-88535A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45550542 | ||||||
| chr5:45550652
|
A | G | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-88645T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45550652 | ||||||
| chr5:45550685
|
G | C | 1 | a0001c0001t0002g0044 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.850-88678C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45550685 | ||||||
| chr5:45550747
|
A | T | 2 | a0001c0001t0001g0209a0001c0001t0002g0178 | 2 | HG00280.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.850-88740T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45550747 | ||||||
| chr5:45551274
|
C | T | 1 | a0001c0001t0002g0026 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.850-89267G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45551274 | ||||||
| chr5:45551298
|
G | T | 1 | a0001c0001t0005g0142 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.850-89291C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45551298 | ||||||
| chr5:45551474
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.850-89467T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45551474 | ||||||
| chr5:45551595
|
G | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-89588C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45551595 | ||||||
| chr5:45551624
|
T | C | 6 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(3): Show | 6 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-89617A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45551624 | ||||||
| chr5:45551632
|
C | T | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.850-89625G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45551632 | ||||||
| chr5:45551633
|
G | A | 37 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(34): Show | 37 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.850-89626C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45551633 | ||||||
| chr5:45551736
|
T | C | 1 | a0001c0001t0009g0003 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.850-89729A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45551736 | ||||||
| chr5:45551975
|
T | G | 1 | a0001c0001t0004g0189 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.850-89968A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45551975 | ||||||
| chr5:45552005
|
T | C | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.850-89998A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45552005 | ||||||
| chr5:45552022
|
T | G | 37 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(34): Show | 37 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.850-90015A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45552022 | ||||||
| chr5:45552087
|
T | C | 1 | a0001c0001t0013g0079 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.850-90080A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45552087 | ||||||
| chr5:45552174
|
C | T | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.850-90167G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45552174 | ||||||
| chr5:45552326
|
A | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.850-90319T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45552326 | ||||||
| chr5:45552573
|
A | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-90566T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45552573 | ||||||
| chr5:45552663
|
G | T | 143 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.850-90656C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45552663 | ||||||
| chr5:45553092
|
A | T | 1 | a0001c0001t0001g0204 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.850-91085T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45553092 | ||||||
| chr5:45553233
|
G | T | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-91226C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45553233 | ||||||
| chr5:45553285
|
C | T | 138 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.850-91278G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45553285 | ||||||
| chr5:45553631
|
A | G | 43 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(40): Show | 43 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.849+91554T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45553631 | ||||||
| chr5:45553651
|
C | T | 2 | a0001c0001t0002g0091a0001c0001t0002g0096 | 2 | NA18945.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.849+91534G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45553651 | ||||||
| chr5:45553705
|
C | T | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849+91480G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45553705 | ||||||
| chr5:45553903
|
T | C | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.849+91282A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45553903 | ||||||
| chr5:45554014
|
C | A | 1 | a0001c0001t0002g0052 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.849+91171G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45554014 | ||||||
| chr5:45554079
|
T | C | 3 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0033g0213 | 3 | HG03579.hp1 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+91106A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45554079 | ||||||
| chr5:45554126
|
G | T | 2 | a0001c0001t0002g0193a0001c0001t0004g0189 | 2 | NA19010.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.849+91059C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45554126 | ||||||
| chr5:45554186
|
G | A | 3 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133 | 3 | HG01257.hp1 HG01258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.849+90999C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45554186 | ||||||
| chr5:45554241
|
C | T | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+90944G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45554241 | ||||||
| chr5:45554338
|
C | T | 5 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226others(2): Show | 5 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+90847G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45554338 | ||||||
| chr5:45555033
|
G | A | 6 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(3): Show | 6 | HG01261.hp2 HG02055.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+90152C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45555033 | ||||||
| chr5:45555075
|
G | T | 1 | a0001c0001t0002g0049 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.849+90110C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45555075 | ||||||
| chr5:45555076
|
C | T | 1 | a0001c0001t0002g0049 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.849+90109G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45555076 | ||||||
| chr5:45555112
|
A | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.849+90073T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45555112 | ||||||
| chr5:45555313
|
T | C | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.849+89872A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45555313 | ||||||
| chr5:45555538
|
A | G | 1 | a0001c0001t0009g0002 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.849+89647T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45555538 | ||||||
| chr5:45555627
|
T | C | 1 | a0001c0001t0034g0172 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.849+89558A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45555627 | ||||||
| chr5:45555755
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.849+89430G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45555755 | ||||||
| chr5:45555812
|
C | A | 1 | a0001c0001t0001g0074 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.849+89373G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45555812 | ||||||
| chr5:45555863
|
T | C | 1 | a0001c0001t0006g0143 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.849+89322A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45555863 | ||||||
| chr5:45555888
|
C | A | 1 | a0001c0001t0001g0156 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.849+89297G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45555888 | ||||||
| chr5:45555935
|
G | A | 1 | a0001c0001t0003g0120 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.849+89250C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45555935 | ||||||
| chr5:45555944
|
C | T | 1 | a0001c0001t0004g0030 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.849+89241G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45555944 | ||||||
| chr5:45556140
|
T | C | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+89045A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45556140 | ||||||
| chr5:45556188
|
C | A | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.849+88997G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45556188 | ||||||
| chr5:45556201
|
G | A | 2 | a0001c0001t0001g0209a0001c0001t0002g0178 | 2 | HG00280.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.849+88984C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45556201 | ||||||
| chr5:45556256
|
A | G | 1 | a0001c0001t0002g0091 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.849+88929T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45556256 | ||||||
| chr5:45556276
|
C | T | 72 | a0001c0001t0001g0073a0001c0001t0001g0134a0001c0001t0001g0135others(69): Show | 72 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.849+88909G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45556276 | ||||||
| chr5:45556424
|
A | G | 1 | a0001c0001t0007g0100 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.849+88761T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45556424 | ||||||
| chr5:45556594
|
C | G | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.849+88591G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45556594 | ||||||
| chr5:45556629
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.849+88556A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45556629 | ||||||
| chr5:45556919
|
A | C | 1 | a0001c0001t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.849+88266T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45556919 | ||||||
| chr5:45556955
|
C | A | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.849+88230G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45556955 | ||||||
| chr5:45557310
|
T | C | 3 | a0001c0001t0002g0088a0001c0001t0002g0091a0001c0001t0002g0096 | 3 | NA18945.hp2 NA19064.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.849+87875A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45557310 | ||||||
| chr5:45557316
|
T | C | 5 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226others(2): Show | 5 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+87869A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45557316 | ||||||
| chr5:45557545
|
G | C | 1 | a0001c0001t0001g0187 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.849+87640C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45557545 | ||||||
| chr5:45557702
|
T | C | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+87483A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45557702 | ||||||
| chr5:45557773
|
A | C | 1 | a0001c0001t0036g0186 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.849+87412T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45557773 | ||||||
| chr5:45557804
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.849+87381A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45557804 | ||||||
| chr5:45557870
|
G | A | 1 | a0001c0001t0003g0099 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.849+87315C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45557870 | ||||||
| chr5:45558146
|
AAG | A | 8 | a0001c0001t0001g0107a0001c0001t0001g0191a0001c0001t0002g0121others(5): Show | 8 | HG01256.hp1 HG01258.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.849+87037_849+8703 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45558146 | ||||||
| chr5:45558147
|
AG | A | 143 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(140): Show | 143 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.849+87037delC | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45558147 | ||||||
| chr5:45558455
|
T | C | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.849+86730A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45558455 | ||||||
| chr5:45558633
|
C | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849+86552G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45558633 | ||||||
| chr5:45558671
|
T | G | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.849+86514A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45558671 | ||||||
| chr5:45558739
|
G | T | 1 | a0001c0001t0034g0172 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.849+86446C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45558739 | ||||||
| chr5:45558771
|
T | C | 6 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(3): Show | 6 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+86414A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45558771 | ||||||
| chr5:45558801
|
C | G | 1 | a0001c0001t0001g0159 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.849+86384G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45558801 | ||||||
| chr5:45558843
|
A | G | 3 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0142 | 3 | HG02886.hp2 HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.849+86342T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45558843 | ||||||
| chr5:45558918
|
A | AT | 37 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0201others(34): Show | 37 | HG00673.hp1 HG01192.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.849+86266dupA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45558918 | ||||||
| chr5:45558918
|
AT | A | 5 | a0001c0001t0001g0076a0001c0001t0003g0083a0001c0001t0003g0092others(2): Show | 5 | HG00323.hp2 HG02129.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+86266delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45558918 | ||||||
| chr5:45558927
|
T | TG | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+86257_849+8625 others(5): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45558927 | ||||||
| chr5:45558931
|
T | G | 6 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(3): Show | 6 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+86254A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45558931 | ||||||
| chr5:45559050
|
CACACCCA others(4): Show |
C | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.849+86124_849+8613 others(15): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45559050 | ||||||
| chr5:45559065
|
C | T | 1 | a0001c0001t0005g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.849+86120G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45559065 | ||||||
| chr5:45559193
|
T | C | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+85992A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45559193 | ||||||
| chr5:45559327
|
T | C | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.849+85858A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45559327 | ||||||
| chr5:45559430
|
T | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849+85755A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45559430 | ||||||
| chr5:45559541
|
G | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+85644C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45559541 | ||||||
| chr5:45559644
|
G | C | 5 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226others(2): Show | 5 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+85541C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45559644 | ||||||
| chr5:45560098
|
C | T | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.849+85087G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45560098 | ||||||
| chr5:45560450
|
A | T | 1 | a0001c0001t0027g0022 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.849+84735T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45560450 | ||||||
| chr5:45560671
|
C | A | 35 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(32): Show | 35 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.849+84514G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45560671 | ||||||
| chr5:45560760
|
G | C | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+84425C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45560760 | ||||||
| chr5:45560761
|
C | T | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+84424G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45560761 | ||||||
| chr5:45560762
|
T | A | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+84423A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45560762 | ||||||
| chr5:45560777
|
A | T | 2 | a0001c0001t0001g0116a0001c0001t0003g0117 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.849+84408T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45560777 | ||||||
| chr5:45560779
|
T | C | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849+84406A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45560779 | ||||||
| chr5:45560846
|
G | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849+84339C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45560846 | ||||||
| chr5:45560872
|
C | A | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.849+84313G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45560872 | ||||||
| chr5:45560952
|
C | T | 1 | a0001c0001t0002g0194 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.849+84233G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45560952 | ||||||
| chr5:45560977
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+84208A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45560977 | ||||||
| chr5:45561008
|
T | G | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+84177A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561008 | ||||||
| chr5:45561048
|
T | C | 1 | a0001c0001t0001g0155 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.849+84137A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561048 | ||||||
| chr5:45561051
|
A | G | 5 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226others(2): Show | 5 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+84134T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561051 | ||||||
| chr5:45561121
|
T | A | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+84064A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561121 | ||||||
| chr5:45561124
|
T | A | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+84061A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561124 | ||||||
| chr5:45561125
|
T | C | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+84060A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561125 | ||||||
| chr5:45561128
|
A | T | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+84057T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561128 | ||||||
| chr5:45561130
|
A | C | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+84055T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561130 | ||||||
| chr5:45561131
|
A | T | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+84054T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561131 | ||||||
| chr5:45561134
|
C | A | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+84051G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561134 | ||||||
| chr5:45561141
|
T | A | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+84044A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561141 | ||||||
| chr5:45561150
|
G | A | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+84035C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561150 | ||||||
| chr5:45561151
|
A | C | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+84034T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561151 | ||||||
| chr5:45561286
|
C | A | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.849+83899G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561286 | ||||||
| chr5:45561332
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.849+83853A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561332 | ||||||
| chr5:45561371
|
AAT | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+83812_849+8381 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561371 | ||||||
| chr5:45561462
|
A | G | 1 | a0001c0001t0003g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.849+83723T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561462 | ||||||
| chr5:45561598
|
G | GA | 39 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(36): Show | 39 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.849+83586dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561598 | ||||||
| chr5:45561598
|
GA | G | 64 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(61): Show | 64 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.849+83586delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561598 | ||||||
| chr5:45561682
|
T | A | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.849+83503A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561682 | ||||||
| chr5:45561699
|
G | A | 64 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(61): Show | 64 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.849+83486C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561699 | ||||||
| chr5:45561801
|
G | A | 143 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.849+83384C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561801 | ||||||
| chr5:45561802
|
G | A | 1 | a0001c0001t0003g0086 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.849+83383C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561802 | ||||||
| chr5:45561805
|
A | T | 1 | a0001c0001t0002g0028 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.849+83380T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561805 | ||||||
| chr5:45561931
|
G | A | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+83254C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561931 | ||||||
| chr5:45561937
|
G | T | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+83248C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561937 | ||||||
| chr5:45561938
|
A | T | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+83247T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561938 | ||||||
| chr5:45561940
|
T | A | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+83245A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561940 | ||||||
| chr5:45561943
|
G | A | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+83242C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561943 | ||||||
| chr5:45561944
|
C | A | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+83241G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561944 | ||||||
| chr5:45561948
|
T | A | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+83237A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561948 | ||||||
| chr5:45561949
|
G | A | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+83236C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561949 | ||||||
| chr5:45561950
|
G | T | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+83235C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561950 | ||||||
| chr5:45561953
|
G | A | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+83232C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561953 | ||||||
| chr5:45561963
|
T | G | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+83222A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561963 | ||||||
| chr5:45561972
|
T | A | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+83213A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561972 | ||||||
| chr5:45561973
|
A | T | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+83212T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561973 | ||||||
| chr5:45561977
|
T | C | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+83208A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561977 | ||||||
| chr5:45561978
|
AAAACTGT others(3): Show |
A | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+83197_849+8320 others(14): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561978 | ||||||
| chr5:45561989
|
C | G | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+83196G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561989 | ||||||
| chr5:45561992
|
A | C | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+83193T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561992 | ||||||
| chr5:45561999
|
G | A | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+83186C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45561999 | ||||||
| chr5:45562003
|
T | C | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.849+83182A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45562003 | ||||||
| chr5:45562058
|
G | A | 1 | a0001c0001t0003g0110 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.849+83127C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45562058 | ||||||
| chr5:45562133
|
G | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+83052C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45562133 | ||||||
| chr5:45562158
|
C | T | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.849+83027G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45562158 | ||||||
| chr5:45562290
|
G | T | 1 | a0001c0001t0007g0214 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.849+82895C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45562290 | ||||||
| chr5:45562409
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.849+82776A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45562409 | ||||||
| chr5:45562428
|
T | C | 2 | a0001c0001t0002g0082a0001c0001t0019g0114 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.849+82757A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45562428 | ||||||
| chr5:45562490
|
A | G | 1 | a0001c0001t0002g0194 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.849+82695T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45562490 | ||||||
| chr5:45562509
|
A | AAAAC | 5 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(2): Show | 5 | HG01192.hp2 HG01257.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+82672_849+8267 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45562509 | ||||||
| chr5:45562521
|
C | CAAACAAA others(4): Show |
137 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.849+82663_849+8266 others(15): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45562521 | ||||||
| chr5:45562525
|
C | CAAACAAA others(5): Show |
1 | a0001c0001t0002g0035 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.849+82659_849+8266 others(16): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45562525 | ||||||
| chr5:45562721
|
C | G | 1 | a0001c0001t0003g0188 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.849+82464G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45562721 | ||||||
| chr5:45562727
|
T | G | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.849+82458A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45562727 | ||||||
| chr5:45562744
|
T | C | 1 | a0001c0001t0003g0053 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.849+82441A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45562744 | ||||||
| chr5:45562868
|
G | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849+82317C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45562868 | ||||||
| chr5:45562940
|
A | G | 6 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(3): Show | 6 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+82245T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45562940 | ||||||
| chr5:45563177
|
C | T | 1 | a0001c0001t0023g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.849+82008G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45563177 | ||||||
| chr5:45563311
|
G | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849+81874C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45563311 | ||||||
| chr5:45563345
|
G | A | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+81840C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45563345 | ||||||
| chr5:45563745
|
AAT | A | 64 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(61): Show | 64 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.849+81438_849+8143 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45563745 | ||||||
| chr5:45563753
|
T | C | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.849+81432A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45563753 | ||||||
| chr5:45564197
|
A | T | 1 | a0001c0001t0001g0011 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.849+80988T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45564197 | ||||||
| chr5:45564538
|
T | A | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.849+80647A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45564538 | ||||||
| chr5:45564710
|
T | C | 1 | a0001c0001t0005g0130 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.849+80475A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45564710 | ||||||
| chr5:45565108
|
G | T | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.849+80077C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45565108 | ||||||
| chr5:45565519
|
G | T | 1 | a0001c0001t0002g0058 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.849+79666C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45565519 | ||||||
| chr5:45565545
|
T | G | 1 | a0001c0001t0003g0086 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.849+79640A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45565545 | ||||||
| chr5:45565561
|
A | C | 37 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(34): Show | 37 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.849+79624T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45565561 | ||||||
| chr5:45565630
|
C | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+79555G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45565630 | ||||||
| chr5:45565696
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0002g0038 | 2 | HG03710.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.849+79489G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45565696 | ||||||
| chr5:45565774
|
G | A | 3 | a0001c0001t0001g0034a0001c0001t0002g0035a0001c0001t0002g0036 | 3 | NA18949.hp2 NA19078.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.849+79411C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45565774 | ||||||
| chr5:45566516
|
C | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849+78669G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45566516 | ||||||
| chr5:45566523
|
A | C | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849+78662T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45566523 | ||||||
| chr5:45566695
|
C | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+78490G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45566695 | ||||||
| chr5:45566696
|
C | G | 1 | a0001c0001t0019g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.849+78489G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45566696 | ||||||
| chr5:45567214
|
A | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+77971T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45567214 | ||||||
| chr5:45567214
|
AT | A | 63 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(60): Show | 63 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.849+77970delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45567214 | ||||||
| chr5:45567219
|
T | C | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.849+77966A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45567219 | ||||||
| chr5:45567349
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.849+77836C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45567349 | ||||||
| chr5:45567558
|
T | TAC | 3 | a0001c0001t0002g0133a0001c0001t0017g0081a0001c0001t0039g0218 | 3 | HG01258.hp2 HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.849+77625_849+7762 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45567558 | ||||||
| chr5:45567558
|
TAC | T | 21 | a0001c0001t0001g0107a0001c0001t0001g0176a0001c0001t0001g0190others(18): Show | 21 | HG00673.hp1 HG01071.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.849+77625_849+7762 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45567558 | ||||||
| chr5:45567558
|
TACAC | T | 85 | a0001c0001t0001g0034a0001c0001t0001g0045a0001c0001t0001g0051others(82): Show | 85 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.849+77623_849+7762 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45567558 | ||||||
| chr5:45567558
|
TACACAC | T | 87 | a0001c0001t0001g0013a0001c0001t0001g0037a0001c0001t0001g0060others(84): Show | 87 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.849+77621_849+7762 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45567558 | ||||||
| chr5:45567558
|
TACACACA others(1): Show |
T | 19 | a0001c0001t0001g0011a0001c0001t0001g0085a0001c0001t0001g0153others(16): Show | 19 | HG00597.hp2 HG01109.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.849+77619_849+7762 others(12): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45567558 | ||||||
| chr5:45567558
|
TACACACA others(3): Show |
T | 4 | a0001c0001t0001g0167a0001c0001t0002g0106a0001c0001t0031g0009others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+77617_849+7762 others(14): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45567558 | ||||||
| chr5:45567613
|
A | G | 1 | a0001c0001t0001g0034 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.849+77572T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45567613 | ||||||
| chr5:45567738
|
G | T | 3 | a0001c0001t0002g0121a0003c0003t0002g0221a0003c0003t0035g0220 | 3 | HG01346.hp2 HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.849+77447C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45567738 | ||||||
| chr5:45567911
|
TAC | T | 113 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0037others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.849+77272_849+7727 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45567911 | ||||||
| chr5:45567911
|
TACAC | T | 67 | a0001c0001t0001g0073a0001c0001t0001g0134a0001c0001t0001g0135others(64): Show | 67 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.849+77270_849+7727 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45567911 | ||||||
| chr5:45567911
|
TACACAC | T | 7 | a0001c0001t0001g0187a0001c0001t0003g0053a0001c0001t0012g0137others(4): Show | 7 | HG00642.hp2 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.849+77268_849+7727 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45567911 | ||||||
| chr5:45567911
|
TACACACA others(1): Show |
T | 13 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(10): Show | 13 | HG01192.hp2 HG01261.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.849+77266_849+7727 others(12): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45567911 | ||||||
| chr5:45567911
|
TACACACA others(7): Show |
T | 1 | a0001c0001t0034g0172 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.849+77260_849+7727 others(18): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45567911 | ||||||
| chr5:45568459
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.849+76726G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45568459 | ||||||
| chr5:45568567
|
A | C | 1 | a0001c0001t0037g0148 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.849+76618T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45568567 | ||||||
| chr5:45568921
|
T | C | 3 | a0001c0001t0031g0009a0001c0001t0032g0010a0001c0001t0033g0213 | 3 | HG01167.hp1 HG01169.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.849+76264A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45568921 | ||||||
| chr5:45569025
|
G | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849+76160C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45569025 | ||||||
| chr5:45569674
|
T | C | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.849+75511A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45569674 | ||||||
| chr5:45570000
|
C | T | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.849+75185G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45570000 | ||||||
| chr5:45570005
|
T | C | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.849+75180A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45570005 | ||||||
| chr5:45570339
|
T | C | 1 | a0001c0001t0002g0069 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.849+74846A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45570339 | ||||||
| chr5:45570421
|
C | A | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.849+74764G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45570421 | ||||||
| chr5:45570915
|
A | T | 152 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(149): Show | 152 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.849+74270T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45570915 | ||||||
| chr5:45570983
|
C | T | 2 | a0001c0001t0003g0158a0001c0001t0003g0183 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.849+74202G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45570983 | ||||||
| chr5:45571008
|
T | C | 4 | a0001c0001t0002g0019a0001c0001t0002g0042a0001c0001t0002g0046others(1): Show | 4 | HG00099.hp1 HG00738.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+74177A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45571008 | ||||||
| chr5:45571769
|
C | A | 8 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(5): Show | 8 | HG01167.hp2 HG01192.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.849+73416G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45571769 | ||||||
| chr5:45571850
|
G | T | 1 | a0001c0001t0001g0206 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.849+73335C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45571850 | ||||||
| chr5:45571997
|
C | T | 138 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.849+73188G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45571997 | ||||||
| chr5:45572020
|
T | C | 3 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0033g0213 | 3 | HG03579.hp1 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+73165A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45572020 | ||||||
| chr5:45572443
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0020g0196 | 2 | HG01516.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.849+72742G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45572443 | ||||||
| chr5:45572519
|
T | G | 1 | a0001c0001t0002g0050 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.849+72666A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45572519 | ||||||
| chr5:45572552
|
C | T | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.849+72633G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45572552 | ||||||
| chr5:45572726
|
T | C | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.849+72459A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45572726 | ||||||
| chr5:45572748
|
G | A | 1 | a0001c0001t0002g0194 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.849+72437C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45572748 | ||||||
| chr5:45572863
|
T | C | 1 | a0001c0001t0007g0214 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.849+72322A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45572863 | ||||||
| chr5:45572963
|
G | A | 1 | a0003c0003t0002g0221 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.849+72222C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45572963 | ||||||
| chr5:45573326
|
A | C | 61 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(58): Show | 61 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.849+71859T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45573326 | ||||||
| chr5:45573436
|
T | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+71749A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45573436 | ||||||
| chr5:45573471
|
C | A | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.849+71714G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45573471 | ||||||
| chr5:45573486
|
T | C | 1 | a0001c0001t0003g0119 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.849+71699A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45573486 | ||||||
| chr5:45573489
|
TA | T | 139 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.849+71695delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45573489 | ||||||
| chr5:45573707
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+71478T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45573707 | ||||||
| chr5:45573895
|
A | G | 16 | a0001c0001t0001g0065a0001c0001t0004g0017a0001c0001t0004g0020others(13): Show | 16 | HG00438.hp1 HG00609.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.849+71290T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45573895 | ||||||
| chr5:45573981
|
C | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849+71204G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45573981 | ||||||
| chr5:45574107
|
A | G | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.849+71078T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45574107 | ||||||
| chr5:45574111
|
T | G | 3 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0033g0213 | 3 | HG03579.hp1 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+71074A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45574111 | ||||||
| chr5:45574295
|
C | T | 3 | a0001c0001t0002g0121a0003c0003t0002g0221a0003c0003t0035g0220 | 3 | HG01346.hp2 HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.849+70890G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45574295 | ||||||
| chr5:45574408
|
G | A | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.849+70777C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45574408 | ||||||
| chr5:45574442
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.849+70743A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45574442 | ||||||
| chr5:45574585
|
A | T | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.849+70600T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45574585 | ||||||
| chr5:45574777
|
T | C | 1 | a0001c0001t0002g0091 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.849+70408A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45574777 | ||||||
| chr5:45575025
|
C | A | 6 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(3): Show | 6 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+70160G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45575025 | ||||||
| chr5:45575103
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.849+70082T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45575103 | ||||||
| chr5:45575420
|
G | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849+69765C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45575420 | ||||||
| chr5:45575689
|
C | T | 6 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(3): Show | 6 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+69496G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45575689 | ||||||
| chr5:45575733
|
T | C | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.849+69452A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45575733 | ||||||
| chr5:45575802
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.849+69383A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45575802 | ||||||
| chr5:45575986
|
A | G | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.849+69199T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45575986 | ||||||
| chr5:45576096
|
C | T | 2 | a0001c0001t0003g0118a0001c0001t0003g0120 | 2 | HG00735.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.849+69089G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45576096 | ||||||
| chr5:45576170
|
C | A | 35 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(32): Show | 35 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.849+69015G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45576170 | ||||||
| chr5:45576684
|
C | T | 22 | a0001c0001t0001g0085a0001c0001t0001g0107a0001c0001t0002g0072others(19): Show | 22 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.849+68501G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45576684 | ||||||
| chr5:45576786
|
T | G | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.849+68399A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45576786 | ||||||
| chr5:45576951
|
C | A | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+68234G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45576951 | ||||||
| chr5:45577103
|
C | T | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+68082G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45577103 | ||||||
| chr5:45577289
|
G | A | 1 | a0001c0001t0005g0129 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.849+67896C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45577289 | ||||||
| chr5:45577453
|
C | G | 1 | a0001c0001t0001g0011 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.849+67732G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45577453 | ||||||
| chr5:45577463
|
A | G | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.849+67722T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45577463 | ||||||
| chr5:45577598
|
C | A | 1 | a0001c0001t0002g0049 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.849+67587G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45577598 | ||||||
| chr5:45577825
|
TTGAAC | T | 41 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(38): Show | 41 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.849+67355_849+6735 others(9): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45577825 | ||||||
| chr5:45577870
|
C | T | 64 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(61): Show | 64 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.849+67315G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45577870 | ||||||
| chr5:45578038
|
T | A | 5 | a0001c0001t0001g0034a0001c0001t0002g0027a0001c0001t0002g0035others(2): Show | 5 | NA18949.hp2 NA18959.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+67147A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45578038 | ||||||
| chr5:45578149
|
T | C | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.849+67036A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45578149 | ||||||
| chr5:45578173
|
G | A | 1 | a0001c0001t0016g0014 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.849+67012C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45578173 | ||||||
| chr5:45578308
|
T | A | 5 | a0001c0001t0001g0034a0001c0001t0002g0027a0001c0001t0002g0035others(2): Show | 5 | NA18949.hp2 NA18959.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+66877A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45578308 | ||||||
| chr5:45578555
|
A | C | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.849+66630T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45578555 | ||||||
| chr5:45578896
|
A | G | 35 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(32): Show | 35 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.849+66289T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45578896 | ||||||
| chr5:45579196
|
C | T | 3 | a0001c0001t0001g0173a0001c0001t0011g0163a0001c0001t0011g0164 | 3 | NA18992.hp1 NA19000.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.849+65989G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45579196 | ||||||
| chr5:45579402
|
C | T | 1 | a0001c0001t0003g0113 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.849+65783G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45579402 | ||||||
| chr5:45579590
|
C | T | 77 | a0001c0001t0001g0073a0001c0001t0001g0134a0001c0001t0001g0135others(74): Show | 77 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.849+65595G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45579590 | ||||||
| chr5:45579691
|
A | G | 43 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(40): Show | 43 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.849+65494T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45579691 | ||||||
| chr5:45580094
|
T | C | 37 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(34): Show | 37 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.849+65091A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45580094 | ||||||
| chr5:45580114
|
A | G | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.849+65071T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45580114 | ||||||
| chr5:45580390
|
G | A | 1 | a0001c0001t0004g0029 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.849+64795C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45580390 | ||||||
| chr5:45580461
|
C | A | 1 | a0001c0001t0002g0052 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.849+64724G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45580461 | ||||||
| chr5:45580780
|
C | T | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.849+64405G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45580780 | ||||||
| chr5:45580788
|
G | A | 4 | a0001c0001t0004g0059a0001c0001t0004g0061a0001c0001t0004g0062others(1): Show | 4 | NA18953.hp2 NA18971.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+64397C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45580788 | ||||||
| chr5:45580800
|
G | C | 3 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133 | 3 | HG01257.hp1 HG01258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.849+64385C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45580800 | ||||||
| chr5:45580825
|
G | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849+64360C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45580825 | ||||||
| chr5:45580833
|
C | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849+64352G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45580833 | ||||||
| chr5:45581107
|
C | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849+64078G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45581107 | ||||||
| chr5:45581390
|
C | G | 1 | a0001c0001t0037g0148 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.849+63795G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45581390 | ||||||
| chr5:45581421
|
C | A | 1 | a0002c0002t0008g0226 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.849+63764G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45581421 | ||||||
| chr5:45581590
|
T | A | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.849+63595A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45581590 | ||||||
| chr5:45581695
|
G | A | 1 | a0001c0001t0004g0032 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.849+63490C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45581695 | ||||||
| chr5:45581723
|
A | T | 43 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(40): Show | 43 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.849+63462T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45581723 | ||||||
| chr5:45581809
|
T | C | 1 | a0001c0001t0005g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.849+63376A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45581809 | ||||||
| chr5:45581880
|
A | G | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.849+63305T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45581880 | ||||||
| chr5:45581998
|
A | T | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.849+63187T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45581998 | ||||||
| chr5:45582021
|
T | C | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.849+63164A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45582021 | ||||||
| chr5:45582337
|
A | G | 6 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0156others(3): Show | 6 | HG00597.hp1 NA18939.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+62848T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45582337 | ||||||
| chr5:45582341
|
G | A | 2 | a0001c0001t0001g0102a0001c0001t0003g0101 | 2 | NA19011.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.849+62844C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45582341 | ||||||
| chr5:45582425
|
G | A | 5 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226others(2): Show | 5 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+62760C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45582425 | ||||||
| chr5:45582425
|
G | C | 1 | a0001c0001t0013g0078 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.849+62760C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45582425 | ||||||
| chr5:45582427
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.849+62758A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45582427 | ||||||
| chr5:45582597
|
G | C | 1 | a0001c0001t0001g0191 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.849+62588C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45582597 | ||||||
| chr5:45582657
|
T | C | 2 | a0001c0001t0002g0069a0001c0006t0002g0219 | 2 | HG01516.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.849+62528A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45582657 | ||||||
| chr5:45582676
|
T | G | 1 | a0001c0001t0009g0003 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.849+62509A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45582676 | ||||||
| chr5:45582709
|
T | C | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.849+62476A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45582709 | ||||||
| chr5:45582763
|
A | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849+62422T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45582763 | ||||||
| chr5:45582876
|
G | T | 1 | a0001c0001t0002g0015 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.849+62309C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45582876 | ||||||
| chr5:45582981
|
CT | C | 90 | a0001c0001t0001g0073a0001c0001t0001g0116a0001c0001t0001g0134others(87): Show | 90 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.849+62203delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45582981 | ||||||
| chr5:45582981
|
CTT | C | 61 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(58): Show | 61 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.849+62202_849+6220 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45582981 | ||||||
| chr5:45583005
|
G | C | 1 | a0001c0001t0001g0139 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.849+62180C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45583005 | ||||||
| chr5:45583011
|
G | A | 2 | a0001c0001t0002g0082a0001c0001t0019g0114 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.849+62174C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45583011 | ||||||
| chr5:45583011
|
G | T | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0012g0137others(1): Show | 4 | HG02145.hp1 HG03486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+62174C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45583011 | ||||||
| chr5:45583272
|
G | A | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.849+61913C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45583272 | ||||||
| chr5:45583523
|
T | C | 2 | a0001c0001t0001g0149a0001c0001t0002g0152 | 2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.849+61662A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45583523 | ||||||
| chr5:45583537
|
A | C | 2 | a0001c0001t0001g0149a0001c0001t0002g0152 | 2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.849+61648T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45583537 | ||||||
| chr5:45583542
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0002g0152 | 2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.849+61643G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45583542 | ||||||
| chr5:45583551
|
T | C | 4 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(1): Show | 4 | HG01257.hp1 HG01258.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+61634A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45583551 | ||||||
| chr5:45583722
|
T | G | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.849+61463A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45583722 | ||||||
| chr5:45584046
|
C | T | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+61139G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45584046 | ||||||
| chr5:45584180
|
C | T | 1 | a0001c0006t0002g0219 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.849+61005G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45584180 | ||||||
| chr5:45584355
|
T | C | 1 | a0001c0001t0002g0043 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.849+60830A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45584355 | ||||||
| chr5:45584419
|
G | C | 1 | a0001c0001t0002g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.849+60766C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45584419 | ||||||
| chr5:45584507
|
T | C | 1 | a0001c0001t0019g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.849+60678A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45584507 | ||||||
| chr5:45584514
|
G | A | 216 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.849+60671C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45584514 | ||||||
| chr5:45584596
|
C | A | 1 | a0001c0001t0001g0153 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.849+60589G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45584596 | ||||||
| chr5:45584615
|
T | C | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.849+60570A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45584615 | ||||||
| chr5:45584617
|
C | T | 73 | a0001c0001t0001g0073a0001c0001t0001g0134a0001c0001t0001g0135others(70): Show | 73 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.849+60568G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45584617 | ||||||
| chr5:45584818
|
G | T | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+60367C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45584818 | ||||||
| chr5:45584993
|
G | A | 4 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(1): Show | 4 | HG01257.hp1 HG01258.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+60192C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45584993 | ||||||
| chr5:45585085
|
T | C | 1 | a0001c0001t0001g0187 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.849+60100A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45585085 | ||||||
| chr5:45585090
|
C | T | 34 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(31): Show | 34 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.849+60095G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45585090 | ||||||
| chr5:45585106
|
A | G | 12 | a0001c0001t0001g0073a0001c0001t0001g0134a0001c0001t0001g0160others(9): Show | 12 | HG00673.hp2 HG02056.hp1 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.849+60079T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45585106 | ||||||
| chr5:45585162
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.849+60023G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45585162 | ||||||
| chr5:45585173
|
T | C | 1 | a0001c0001t0012g0137 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.849+60012A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45585173 | ||||||
| chr5:45585339
|
A | C | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.849+59846T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45585339 | ||||||
| chr5:45585426
|
C | T | 2 | a0001c0001t0001g0102a0001c0001t0003g0101 | 2 | NA19011.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.849+59759G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45585426 | ||||||
| chr5:45585526
|
A | G | 1 | a0001c0001t0004g0048 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.849+59659T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45585526 | ||||||
| chr5:45585575
|
C | T | 6 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(3): Show | 6 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.849+59610G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45585575 | ||||||
| chr5:45585621
|
C | T | 138 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.849+59564G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45585621 | ||||||
| chr5:45585706
|
G | T | 1 | a0001c0001t0002g0049 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.849+59479C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45585706 | ||||||
| chr5:45585749
|
G | A | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.849+59436C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45585749 | ||||||
| chr5:45585852
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+59333G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45585852 | ||||||
| chr5:45585936
|
C | T | 1 | a0001c0001t0002g0181 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.849+59249G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45585936 | ||||||
| chr5:45586011
|
C | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849+59174G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45586011 | ||||||
| chr5:45586029
|
A | T | 1 | a0001c0001t0023g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.849+59156T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45586029 | ||||||
| chr5:45586225
|
C | T | 225 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.849+58960G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45586225 | ||||||
| chr5:45586326
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.849+58859C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45586326 | ||||||
| chr5:45586473
|
G | A | 1 | a0001c0001t0003g0090 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.849+58712C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45586473 | ||||||
| chr5:45586511
|
G | A | 3 | a0001c0001t0003g0118a0001c0001t0031g0009a0001c0001t0032g0010 | 3 | HG00738.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.849+58674C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45586511 | ||||||
| chr5:45586565
|
A | T | 1 | a0001c0001t0005g0130 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.849+58620T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45586565 | ||||||
| chr5:45586570
|
G | A | 1 | a0001c0001t0003g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.849+58615C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45586570 | ||||||
| chr5:45586801
|
A | C | 1 | a0001c0001t0001g0182 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.849+58384T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45586801 | ||||||
| chr5:45586815
|
C | T | 143 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.849+58370G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45586815 | ||||||
| chr5:45587075
|
C | A | 1 | a0001c0001t0002g0026 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.849+58110G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45587075 | ||||||
| chr5:45587076
|
A | T | 1 | a0001c0001t0002g0026 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.849+58109T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45587076 | ||||||
| chr5:45587105
|
C | T | 3 | a0001c0001t0002g0044a0001c0001t0002g0069a0001c0006t0002g0219 | 3 | HG01256.hp2 HG01516.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.849+58080G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45587105 | ||||||
| chr5:45587370
|
C | CA | 3 | a0001c0001t0002g0072a0001c0001t0002g0097a0001c0001t0003g0086 | 3 | HG00558.hp1 HG00673.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.849+57814dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45587370 | ||||||
| chr5:45587418
|
A | T | 1 | a0001c0001t0003g0090 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.849+57767T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45587418 | ||||||
| chr5:45587601
|
T | A | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.849+57584A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45587601 | ||||||
| chr5:45587660
|
G | A | 34 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0037others(31): Show | 34 | HG00280.hp1 HG00438.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.849+57525C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45587660 | ||||||
| chr5:45587694
|
A | C | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.849+57491T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45587694 | ||||||
| chr5:45587896
|
C | T | 1 | a0003c0003t0002g0221 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.849+57289G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45587896 | ||||||
| chr5:45587918
|
GCT | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.849+57265_849+5726 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45587918 | ||||||
| chr5:45588039
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.849+57146A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45588039 | ||||||
| chr5:45588175
|
A | G | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.849+57010T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45588175 | ||||||
| chr5:45588301
|
G | A | 6 | a0001c0001t0001g0013a0001c0001t0001g0037a0001c0001t0001g0060others(3): Show | 6 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+56884C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45588301 | ||||||
| chr5:45588720
|
G | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+56465C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45588720 | ||||||
| chr5:45589104
|
G | A | 63 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(60): Show | 63 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.849+56081C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45589104 | ||||||
| chr5:45589165
|
G | GT | 2 | a0001c0001t0003g0158a0001c0001t0003g0183 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.849+56019dupA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45589165 | ||||||
| chr5:45589581
|
T | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+55604A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45589581 | ||||||
| chr5:45589838
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+55347G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45589838 | ||||||
| chr5:45589977
|
G | C | 3 | a0001c0001t0001g0184a0001c0001t0003g0158a0001c0001t0003g0183 | 3 | HG01256.hp1 HG01258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.849+55208C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45589977 | ||||||
| chr5:45590207
|
A | T | 3 | a0001c0001t0001g0034a0001c0001t0002g0035a0001c0001t0002g0036 | 3 | NA18949.hp2 NA19078.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.849+54978T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45590207 | ||||||
| chr5:45590437
|
A | G | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+54748T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45590437 | ||||||
| chr5:45590567
|
T | C | 6 | a0001c0001t0001g0134a0001c0001t0001g0160a0001c0001t0001g0166others(3): Show | 6 | HG02132.hp2 HG02165.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.849+54618A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45590567 | ||||||
| chr5:45591182
|
T | G | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+54003A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45591182 | ||||||
| chr5:45591202
|
T | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849+53983A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45591202 | ||||||
| chr5:45591299
|
T | C | 41 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(38): Show | 41 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.849+53886A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45591299 | ||||||
| chr5:45591342
|
C | T | 1 | a0001c0001t0007g0214 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.849+53843G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45591342 | ||||||
| chr5:45591360
|
G | T | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.849+53825C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45591360 | ||||||
| chr5:45591433
|
T | A | 1 | a0001c0001t0002g0058 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.849+53752A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45591433 | ||||||
| chr5:45591510
|
C | T | 6 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(3): Show | 6 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+53675G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45591510 | ||||||
| chr5:45591610
|
A | G | 6 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(3): Show | 6 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+53575T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45591610 | ||||||
| chr5:45591990
|
AGATT | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+53191_849+5319 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45591990 | ||||||
| chr5:45591995
|
A | AT | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0003g0093others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.849+53189dupA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45591995 | ||||||
| chr5:45592330
|
TGATTAAA | T | 50 | a0001c0001t0001g0139a0001c0001t0001g0147a0001c0001t0001g0153others(47): Show | 50 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.849+52848_849+5285 others(11): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45592330 | ||||||
| chr5:45592478
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.849+52707G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45592478 | ||||||
| chr5:45592707
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+52478G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45592707 | ||||||
| chr5:45592816
|
T | C | 1 | a0001c0001t0005g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.849+52369A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45592816 | ||||||
| chr5:45593096
|
A | C | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849+52089T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593096 | ||||||
| chr5:45593197
|
C | T | 1 | a0001c0001t0021g0138 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.849+51988G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593197 | ||||||
| chr5:45593212
|
G | GCA | 2 | a0001c0001t0001g0011a0001c0001t0002g0049 | 2 | HG03041.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.849+51971_849+5197 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593212 | ||||||
| chr5:45593212
|
GCA | G | 58 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(55): Show | 58 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.849+51971_849+5197 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593212 | ||||||
| chr5:45593212
|
GCACA | G | 78 | a0001c0001t0001g0073a0001c0001t0001g0134a0001c0001t0001g0135others(75): Show | 78 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.849+51969_849+5197 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593212 | ||||||
| chr5:45593212
|
GCACACAC others(1): Show |
G | 3 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133 | 3 | HG01257.hp1 HG01258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.849+51965_849+5197 others(12): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593212 | ||||||
| chr5:45593214
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.849+51971T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593214 | ||||||
| chr5:45593286
|
G | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849+51899C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593286 | ||||||
| chr5:45593291
|
T | TTC | 4 | a0001c0001t0003g0117a0001c0001t0003g0119a0001c0001t0004g0062others(1): Show | 4 | HG01074.hp1 HG02602.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+51892_849+5189 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593291 | ||||||
| chr5:45593291
|
T | TTCTC | 3 | a0001c0001t0003g0118a0001c0001t0003g0120a0001c0001t0005g0124 | 3 | HG00735.hp1 HG00738.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.849+51890_849+5189 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593291 | ||||||
| chr5:45593291
|
TTCTCTCT others(1): Show |
T | 5 | a0001c0001t0001g0147a0001c0001t0001g0192a0001c0001t0001g0208others(2): Show | 5 | HG00642.hp2 HG01192.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+51886_849+5189 others(12): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593291 | ||||||
| chr5:45593310
|
TCTCTCTC others(5): Show |
T | 1 | a0001c0001t0024g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.849+51863_849+5187 others(16): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593310 | ||||||
| chr5:45593312
|
TCTCTCTC others(3): Show |
T | 64 | a0001c0001t0001g0073a0001c0001t0001g0134a0001c0001t0001g0135others(61): Show | 64 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.849+51863_849+5187 others(14): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593312 | ||||||
| chr5:45593314
|
T | C | 7 | a0001c0001t0001g0159a0001c0001t0001g0169a0001c0001t0001g0182others(4): Show | 7 | HG00639.hp1 HG01169.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.849+51871A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593314 | ||||||
| chr5:45593314
|
TCTCTCTC others(1): Show |
T | 2 | a0001c0001t0001g0136a0001c0001t0001g0206 | 2 | HG02738.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.849+51863_849+5187 others(12): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593314 | ||||||
| chr5:45593316
|
T | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849+51869A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593316 | ||||||
| chr5:45593316
|
TCTCTCC | T | 7 | a0001c0001t0001g0159a0001c0001t0001g0169a0001c0001t0001g0182others(4): Show | 7 | HG00639.hp1 HG01169.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.849+51863_849+5186 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593316 | ||||||
| chr5:45593317
|
C | CTCTCTCT others(4): Show |
1 | a0001c0001t0013g0078 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.849+51867_849+5186 others(15): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593317 | ||||||
| chr5:45593320
|
T | C | 3 | a0001c0001t0007g0115a0001c0001t0031g0009a0001c0001t0032g0010 | 3 | HG01167.hp1 HG01169.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.849+51865A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593320 | ||||||
| chr5:45593320
|
T | TCTCC | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.849+51864_849+5186 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593320 | ||||||
| chr5:45593322
|
C | T | 21 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(18): Show | 21 | HG01167.hp1 HG01169.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.849+51863G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593322 | ||||||
| chr5:45593322
|
CCT | C | 6 | a0001c0001t0002g0015a0001c0001t0002g0082a0001c0001t0002g0121others(3): Show | 6 | HG01346.hp2 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.849+51861_849+5186 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593322 | ||||||
| chr5:45593322
|
CCTCT | C | 3 | a0001c0001t0003g0093a0001c0001t0003g0095a0001c0001t0005g0089 | 3 | HG01934.hp2 HG01975.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.849+51859_849+5186 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593322 | ||||||
| chr5:45593324
|
T | C | 73 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0077others(70): Show | 73 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.849+51861A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593324 | ||||||
| chr5:45593324
|
T | TCC | 11 | a0001c0001t0002g0066a0001c0001t0002g0067a0001c0001t0002g0140others(8): Show | 11 | HG01261.hp2 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.849+51860_849+5186 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593324 | ||||||
| chr5:45593326
|
T | C | 2 | a0001c0001t0001g0074a0001c0001t0024g0007 | 2 | HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.849+51859A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593326 | ||||||
| chr5:45593330
|
T | C | 1 | a0001c0001t0013g0079 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.849+51855A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593330 | ||||||
| chr5:45593336
|
T | A | 10 | a0001c0001t0001g0159a0001c0001t0001g0182a0001c0001t0001g0184others(7): Show | 10 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.849+51849A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593336 | ||||||
| chr5:45593336
|
TCTCTCA | T | 31 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(28): Show | 31 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.849+51843_849+5184 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593336 | ||||||
| chr5:45593338
|
T | A | 24 | a0001c0001t0001g0116a0001c0001t0001g0147a0001c0001t0001g0159others(21): Show | 24 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.849+51847A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593338 | ||||||
| chr5:45593338
|
T | TCACACA | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.849+51846_849+5184 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593338 | ||||||
| chr5:45593338
|
T | TCACACAC others(3): Show |
1 | a0001c0001t0013g0078 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.849+51846_849+5184 others(14): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593338 | ||||||
| chr5:45593340
|
T | A | 87 | a0001c0001t0001g0116a0001c0001t0001g0135a0001c0001t0001g0136others(84): Show | 87 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.849+51845A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593340 | ||||||
| chr5:45593340
|
T | TCACA | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.849+51841_849+5184 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593340 | ||||||
| chr5:45593340
|
T | TCTCTCTC others(7): Show |
1 | a0001c0001t0013g0079 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.849+51844_849+5184 others(18): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593340 | ||||||
| chr5:45593340
|
TCA | T | 58 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(55): Show | 58 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.849+51843_849+5184 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593340 | ||||||
| chr5:45593342
|
A | T | 8 | a0001c0001t0001g0204a0001c0001t0002g0035a0001c0001t0002g0066others(5): Show | 8 | HG01884.hp1 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.849+51843T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593342 | ||||||
| chr5:45593370
|
A | C | 8 | a0001c0001t0002g0121a0001c0001t0003g0087a0001c0001t0003g0093others(5): Show | 8 | HG00099.hp2 HG01071.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.849+51815T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593370 | ||||||
| chr5:45593370
|
AC | A | 4 | a0001c0001t0001g0208a0001c0001t0005g0089a0001c0001t0016g0014others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+51814delG | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593370 | ||||||
| chr5:45593433
|
C | A | 1 | a0001c0001t0001g0180 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.849+51752G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593433 | ||||||
| chr5:45593644
|
C | CATT | 30 | a0001c0001t0001g0011a0001c0001t0001g0116a0001c0001t0002g0121others(27): Show | 30 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.849+51538_849+5154 others(7): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593644 | ||||||
| chr5:45593644
|
C | CATTATT | 129 | a0001c0001t0001g0013a0001c0001t0001g0037a0001c0001t0001g0045others(126): Show | 129 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.849+51535_849+5154 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593644 | ||||||
| chr5:45593644
|
C | CATTATTA others(2): Show |
62 | a0001c0001t0001g0034a0001c0001t0001g0085a0001c0001t0001g0102others(59): Show | 62 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.849+51532_849+5154 others(13): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593644 | ||||||
| chr5:45593644
|
C | CATTATTA others(8): Show |
2 | a0001c0001t0001g0065a0001c0001t0018g0018 | 2 | HG02155.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.849+51526_849+5154 others(19): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593644 | ||||||
| chr5:45593903
|
T | C | 1 | a0001c0001t0002g0097 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.849+51282A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45593903 | ||||||
| chr5:45594082
|
G | A | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.849+51103C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45594082 | ||||||
| chr5:45594866
|
A | G | 1 | a0001c0001t0001g0179 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.849+50319T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45594866 | ||||||
| chr5:45594908
|
A | C | 2 | a0001c0001t0002g0082a0001c0001t0019g0114 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.849+50277T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45594908 | ||||||
| chr5:45595009
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.849+50176G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45595009 | ||||||
| chr5:45595429
|
C | T | 20 | a0001c0001t0001g0073a0001c0001t0001g0134a0001c0001t0001g0135others(17): Show | 20 | HG00642.hp2 HG00673.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.849+49756G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45595429 | ||||||
| chr5:45595499
|
G | C | 1 | a0001c0001t0002g0072 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.849+49686C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45595499 | ||||||
| chr5:45595892
|
T | C | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.849+49293A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45595892 | ||||||
| chr5:45596038
|
G | C | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+49147C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45596038 | ||||||
| chr5:45596057
|
G | A | 79 | a0001c0001t0001g0073a0001c0001t0001g0134a0001c0001t0001g0135others(76): Show | 79 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.849+49128C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45596057 | ||||||
| chr5:45596101
|
T | G | 1 | a0001c0001t0034g0172 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.849+49084A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45596101 | ||||||
| chr5:45596244
|
C | A | 2 | a0001c0001t0010g0004a0001c0001t0010g0005 | 2 | NA19009.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.849+48941G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45596244 | ||||||
| chr5:45596256
|
T | C | 79 | a0001c0001t0001g0073a0001c0001t0001g0134a0001c0001t0001g0135others(76): Show | 79 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.849+48929A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45596256 | ||||||
| chr5:45596511
|
T | C | 1 | a0001c0001t0002g0027 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.849+48674A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45596511 | ||||||
| chr5:45596937
|
C | T | 79 | a0001c0001t0001g0073a0001c0001t0001g0134a0001c0001t0001g0135others(76): Show | 79 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.849+48248G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45596937 | ||||||
| chr5:45597099
|
C | A | 1 | a0001c0001t0003g0087 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.849+48086G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45597099 | ||||||
| chr5:45597317
|
A | C | 1 | a0001c0001t0002g0028 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.849+47868T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45597317 | ||||||
| chr5:45597385
|
C | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849+47800G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45597385 | ||||||
| chr5:45597572
|
A | T | 1 | a0001c0001t0002g0050 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.849+47613T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45597572 | ||||||
| chr5:45597587
|
G | A | 153 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(150): Show | 153 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.849+47598C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45597587 | ||||||
| chr5:45597803
|
A | T | 153 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(150): Show | 153 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.849+47382T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45597803 | ||||||
| chr5:45597818
|
C | T | 79 | a0001c0001t0001g0073a0001c0001t0001g0134a0001c0001t0001g0135others(76): Show | 79 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.849+47367G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45597818 | ||||||
| chr5:45597917
|
A | C | 1 | a0001c0001t0003g0063 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.849+47268T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45597917 | ||||||
| chr5:45597938
|
T | A | 4 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(1): Show | 4 | HG01257.hp1 HG01258.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+47247A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45597938 | ||||||
| chr5:45597939
|
T | C | 78 | a0001c0001t0001g0073a0001c0001t0001g0134a0001c0001t0001g0135others(75): Show | 78 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.849+47246A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45597939 | ||||||
| chr5:45597966
|
C | A | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.849+47219G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45597966 | ||||||
| chr5:45598037
|
C | T | 9 | a0001c0001t0001g0107a0001c0001t0003g0090a0001c0001t0003g0092others(6): Show | 9 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.849+47148G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45598037 | ||||||
| chr5:45598131
|
A | C | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.849+47054T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45598131 | ||||||
| chr5:45598154
|
G | A | 1 | a0001c0001t0002g0154 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.849+47031C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45598154 | ||||||
| chr5:45598263
|
G | A | 78 | a0001c0001t0001g0073a0001c0001t0001g0134a0001c0001t0001g0135others(75): Show | 78 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.849+46922C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45598263 | ||||||
| chr5:45598341
|
G | T | 1 | a0001c0001t0019g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.849+46844C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45598341 | ||||||
| chr5:45598376
|
A | T | 2 | a0001c0001t0001g0149a0001c0001t0002g0152 | 2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.849+46809T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45598376 | ||||||
| chr5:45598982
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.849+46203G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45598982 | ||||||
| chr5:45599007
|
G | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+46178C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45599007 | ||||||
| chr5:45599037
|
C | T | 63 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(60): Show | 63 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.849+46148G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45599037 | ||||||
| chr5:45599185
|
G | A | 1 | a0001c0001t0007g0100 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.849+46000C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45599185 | ||||||
| chr5:45599362
|
G | A | 1 | a0001c0001t0002g0026 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.849+45823C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45599362 | ||||||
| chr5:45599410
|
G | A | 1 | a0001c0001t0015g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.849+45775C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45599410 | ||||||
| chr5:45599534
|
A | G | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+45651T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45599534 | ||||||
| chr5:45599578
|
G | T | 1 | a0001c0001t0001g0200 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.849+45607C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45599578 | ||||||
| chr5:45599668
|
T | G | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.849+45517A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45599668 | ||||||
| chr5:45599794
|
C | T | 1 | a0001c0001t0004g0189 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.849+45391G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45599794 | ||||||
| chr5:45599973
|
C | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849+45212G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45599973 | ||||||
| chr5:45600008
|
T | C | 1 | a0001c0001t0003g0111 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.849+45177A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45600008 | ||||||
| chr5:45600403
|
T | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849+44782A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45600403 | ||||||
| chr5:45600422
|
T | C | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.849+44763A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45600422 | ||||||
| chr5:45600482
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.849+44703T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45600482 | ||||||
| chr5:45600526
|
T | C | 41 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(38): Show | 41 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.849+44659A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45600526 | ||||||
| chr5:45600573
|
C | T | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+44612G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45600573 | ||||||
| chr5:45600835
|
G | A | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.849+44350C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45600835 | ||||||
| chr5:45600981
|
T | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+44204A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45600981 | ||||||
| chr5:45601044
|
T | C | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.849+44141A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45601044 | ||||||
| chr5:45601363
|
A | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849+43822T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45601363 | ||||||
| chr5:45601364
|
G | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849+43821C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45601364 | ||||||
| chr5:45601649
|
T | C | 1 | a0001c0001t0003g0117 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.849+43536A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45601649 | ||||||
| chr5:45601763
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+43422T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45601763 | ||||||
| chr5:45601829
|
C | G | 1 | a0001c0001t0034g0172 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.849+43356G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45601829 | ||||||
| chr5:45601951
|
T | C | 2 | a0001c0001t0003g0104a0001c0001t0029g0070 | 2 | HG04204.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.849+43234A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45601951 | ||||||
| chr5:45602456
|
G | T | 1 | a0001c0001t0036g0186 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.849+42729C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45602456 | ||||||
| chr5:45602469
|
A | G | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.849+42716T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45602469 | ||||||
| chr5:45602874
|
T | C | 52 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(49): Show | 52 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.849+42311A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45602874 | ||||||
| chr5:45602878
|
C | G | 3 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0043 | 3 | HG00597.hp2 HG00639.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.849+42307G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45602878 | ||||||
| chr5:45602929
|
T | A | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.849+42256A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45602929 | ||||||
| chr5:45603104
|
C | T | 137 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.849+42081G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45603104 | ||||||
| chr5:45603297
|
C | T | 1 | a0001c0001t0002g0058 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.849+41888G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45603297 | ||||||
| chr5:45603400
|
G | A | 1 | a0001c0001t0037g0148 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.849+41785C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45603400 | ||||||
| chr5:45603490
|
A | C | 1 | a0001c0001t0003g0111 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.849+41695T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45603490 | ||||||
| chr5:45603502
|
G | T | 1 | a0001c0001t0003g0111 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.849+41683C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45603502 | ||||||
| chr5:45603599
|
A | G | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.849+41586T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45603599 | ||||||
| chr5:45603905
|
G | A | 1 | a0001c0001t0005g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.849+41280C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45603905 | ||||||
| chr5:45603909
|
T | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849+41276A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45603909 | ||||||
| chr5:45604038
|
T | C | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.849+41147A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45604038 | ||||||
| chr5:45604111
|
T | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849+41074A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45604111 | ||||||
| chr5:45604389
|
GC | G | 4 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(1): Show | 4 | HG01257.hp1 HG01258.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+40795delG | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45604389 | ||||||
| chr5:45604515
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.849+40670C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45604515 | ||||||
| chr5:45604574
|
T | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849+40611A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45604574 | ||||||
| chr5:45605231
|
T | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+39954A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45605231 | ||||||
| chr5:45605248
|
T | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG01074.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.849+39937A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45605248 | ||||||
| chr5:45605402
|
G | C | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.849+39783C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45605402 | ||||||
| chr5:45605573
|
T | C | 4 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(1): Show | 4 | HG01257.hp1 HG01258.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+39612A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45605573 | ||||||
| chr5:45606003
|
T | TCCTTTAA others(318): Show |
1 | a0001c0006t0002g0219 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.849+39181_849+3918 others(329): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45606003 | ||||||
| chr5:45606003
|
T | TCCTTTAA others(330): Show |
1 | a0001c0001t0002g0069 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.849+39181_849+3918 others(341): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45606003 | ||||||
| chr5:45606262
|
G | A | 5 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226others(2): Show | 5 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+38923C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45606262 | ||||||
| chr5:45606357
|
A | G | 1 | a0001c0001t0005g0124 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.849+38828T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45606357 | ||||||
| chr5:45606526
|
C | A | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.849+38659G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45606526 | ||||||
| chr5:45606597
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.849+38588G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45606597 | ||||||
| chr5:45606708
|
C | T | 1 | a0001c0001t0003g0092 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.849+38477G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45606708 | ||||||
| chr5:45606826
|
C | G | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.849+38359G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45606826 | ||||||
| chr5:45606835
|
C | A | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.849+38350G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45606835 | ||||||
| chr5:45607058
|
C | T | 1 | a0001c0001t0002g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.849+38127G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45607058 | ||||||
| chr5:45607172
|
T | C | 2 | a0001c0001t0011g0163a0001c0001t0011g0164 | 2 | NA18992.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.849+38013A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45607172 | ||||||
| chr5:45607207
|
T | C | 1 | a0001c0001t0005g0127 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.849+37978A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45607207 | ||||||
| chr5:45607274
|
T | G | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.849+37911A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45607274 | ||||||
| chr5:45607292
|
C | T | 1 | a0001c0001t0005g0130 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.849+37893G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45607292 | ||||||
| chr5:45607555
|
A | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849+37630T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45607555 | ||||||
| chr5:45607578
|
A | ATT | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+37605_849+3760 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45607578 | ||||||
| chr5:45607579
|
T | TTA | 12 | a0001c0001t0001g0139a0001c0001t0001g0184a0001c0001t0002g0105others(9): Show | 12 | HG00609.hp1 HG01256.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.849+37604_849+3760 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45607579 | ||||||
| chr5:45607579
|
T | TTATA | 30 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(27): Show | 30 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.849+37602_849+3760 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45607579 | ||||||
| chr5:45607579
|
TTA | T | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.849+37604_849+3760 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45607579 | ||||||
| chr5:45607597
|
C | A | 116 | a0001c0001t0001g0073a0001c0001t0001g0085a0001c0001t0001g0102others(113): Show | 116 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.849+37588G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45607597 | ||||||
| chr5:45607598
|
T | G | 4 | a0001c0001t0002g0193a0001c0001t0004g0189a0001c0001t0019g0114others(1): Show | 4 | HG01192.hp2 HG02451.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+37587A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45607598 | ||||||
| chr5:45607602
|
G | T | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0012g0137others(1): Show | 4 | HG02145.hp1 HG03486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+37583C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45607602 | ||||||
| chr5:45607962
|
T | C | 1 | a0001c0001t0003g0104 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.849+37223A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45607962 | ||||||
| chr5:45608220
|
T | C | 137 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.849+36965A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45608220 | ||||||
| chr5:45608293
|
T | C | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.849+36892A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45608293 | ||||||
| chr5:45608357
|
A | ATG | 36 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0085others(33): Show | 36 | HG00323.hp2 HG00597.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.849+36826_849+3682 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45608357 | ||||||
| chr5:45608357
|
A | ATGTG | 19 | a0001c0001t0001g0107a0001c0001t0001g0156a0001c0001t0002g0105others(16): Show | 19 | HG00099.hp2 HG00438.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.849+36824_849+3682 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45608357 | ||||||
| chr5:45608357
|
A | ATGTGTG | 17 | a0001c0001t0001g0013a0001c0001t0001g0037a0001c0001t0001g0060others(14): Show | 17 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.849+36822_849+3682 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45608357 | ||||||
| chr5:45608357
|
A | ATGTGTGT others(1): Show |
7 | a0001c0001t0001g0051a0001c0001t0001g0065a0001c0001t0002g0027others(4): Show | 7 | HG00738.hp2 HG01975.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.849+36820_849+3682 others(12): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45608357 | ||||||
| chr5:45608357
|
A | ATGTGTGT others(3): Show |
35 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0045others(32): Show | 35 | HG00099.hp1 HG00438.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.849+36818_849+3682 others(14): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45608357 | ||||||
| chr5:45608357
|
A | ATGTGTGT others(5): Show |
7 | a0001c0001t0002g0023a0001c0001t0002g0035a0001c0001t0002g0044others(4): Show | 7 | HG01256.hp2 NA18953.hp2 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.849+36816_849+3682 others(16): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45608357 | ||||||
| chr5:45608357
|
A | ATGTGTGT others(7): Show |
1 | a0001c0001t0002g0026 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.849+36814_849+3682 others(18): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45608357 | ||||||
| chr5:45608357
|
A | ATGTGTGT others(9): Show |
1 | a0001c0004t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.849+36812_849+3682 others(20): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45608357 | ||||||
| chr5:45608357
|
ATG | A | 5 | a0001c0001t0001g0184a0001c0001t0001g0202a0001c0001t0003g0158others(2): Show | 5 | HG01256.hp1 HG01258.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+36826_849+3682 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45608357 | ||||||
| chr5:45608394
|
T | G | 64 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(61): Show | 64 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.849+36791A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45608394 | ||||||
| chr5:45608426
|
ACTT | A | 67 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.849+36756_849+3675 others(7): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45608426 | ||||||
| chr5:45608545
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.849+36640C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45608545 | ||||||
| chr5:45608686
|
A | T | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.849+36499T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45608686 | ||||||
| chr5:45609063
|
G | A | 1 | a0001c0001t0005g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.849+36122C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45609063 | ||||||
| chr5:45609140
|
CG | C | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.849+36044delC | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45609140 | ||||||
| chr5:45609141
|
G | A | 3 | a0001c0001t0007g0115a0002c0002t0014g0222a0002c0002t0014g0223 | 3 | HG01433.hp2 HG02809.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.849+36044C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45609141 | ||||||
| chr5:45609143
|
T | A | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.849+36042A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45609143 | ||||||
| chr5:45609188
|
C | T | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.849+35997G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45609188 | ||||||
| chr5:45609247
|
A | C | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849+35938T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45609247 | ||||||
| chr5:45609272
|
T | C | 2 | a0001c0001t0001g0187a0001c0001t0040g0175 | 2 | NA18977.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.849+35913A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45609272 | ||||||
| chr5:45609412
|
A | C | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.849+35773T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45609412 | ||||||
| chr5:45609574
|
A | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG01074.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.849+35611T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45609574 | ||||||
| chr5:45610327
|
C | A | 1 | a0001c0001t0004g0055 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.849+34858G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45610327 | ||||||
| chr5:45610429
|
A | G | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849+34756T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45610429 | ||||||
| chr5:45610454
|
A | G | 2 | a0001c0001t0001g0190a0001c0001t0003g0188 | 2 | NA18971.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.849+34731T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45610454 | ||||||
| chr5:45610602
|
C | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.849+34583G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45610602 | ||||||
| chr5:45610989
|
C | T | 1 | a0001c0001t0002g0054 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.849+34196G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45610989 | ||||||
| chr5:45611002
|
G | C | 1 | a0001c0001t0005g0126 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.849+34183C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45611002 | ||||||
| chr5:45611057
|
CT | C | 142 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.849+34127delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45611057 | ||||||
| chr5:45611143
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG01074.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.849+34042G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45611143 | ||||||
| chr5:45611257
|
T | TA | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+33927_849+3392 others(5): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45611257 | ||||||
| chr5:45611260
|
T | TA | 37 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(34): Show | 37 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.849+33924dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45611260 | ||||||
| chr5:45611269
|
C | CT | 7 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0037others(4): Show | 7 | HG00735.hp2 HG00741.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.849+33915dupA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45611269 | ||||||
| chr5:45611269
|
CT | C | 8 | a0001c0001t0001g0045a0001c0001t0001g0073a0001c0001t0001g0139others(5): Show | 8 | HG00558.hp2 HG00609.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.849+33915delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45611269 | ||||||
| chr5:45611274
|
T | C | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.849+33911A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45611274 | ||||||
| chr5:45611309
|
T | C | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.849+33876A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45611309 | ||||||
| chr5:45611505
|
C | A | 2 | a0001c0001t0002g0193a0001c0001t0004g0189 | 2 | NA19010.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.849+33680G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45611505 | ||||||
| chr5:45611509
|
T | A | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.849+33676A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45611509 | ||||||
| chr5:45611548
|
A | G | 3 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0033g0213 | 3 | HG03579.hp1 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+33637T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45611548 | ||||||
| chr5:45611886
|
T | C | 53 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(50): Show | 53 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.849+33299A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45611886 | ||||||
| chr5:45611931
|
A | T | 131 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.849+33254T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45611931 | ||||||
| chr5:45612681
|
G | A | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.849+32504C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45612681 | ||||||
| chr5:45612694
|
A | T | 1 | a0001c0001t0002g0041 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.849+32491T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45612694 | ||||||
| chr5:45612781
|
C | A | 1 | a0001c0001t0001g0195 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.849+32404G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45612781 | ||||||
| chr5:45612978
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+32207T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45612978 | ||||||
| chr5:45613155
|
T | C | 1 | a0001c0001t0021g0138 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.849+32030A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45613155 | ||||||
| chr5:45613571
|
C | T | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.849+31614G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45613571 | ||||||
| chr5:45613793
|
C | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849+31392G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45613793 | ||||||
| chr5:45613823
|
A | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849+31362T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45613823 | ||||||
| chr5:45613909
|
C | T | 2 | a0001c0001t0001g0195a0001c0001t0002g0088 | 2 | HG04204.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.849+31276G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45613909 | ||||||
| chr5:45613934
|
C | T | 2 | a0001c0001t0001g0190a0001c0001t0003g0188 | 2 | NA18971.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.849+31251G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45613934 | ||||||
| chr5:45613951
|
G | C | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.849+31234C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45613951 | ||||||
| chr5:45613992
|
A | G | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.849+31193T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45613992 | ||||||
| chr5:45614021
|
T | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+31164A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45614021 | ||||||
| chr5:45614028
|
T | A | 1 | a0001c0001t0005g0129 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.849+31157A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45614028 | ||||||
| chr5:45614115
|
G | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.849+31070C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45614115 | ||||||
| chr5:45614123
|
T | C | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+31062A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45614123 | ||||||
| chr5:45614210
|
G | A | 37 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(34): Show | 37 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.849+30975C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45614210 | ||||||
| chr5:45614434
|
C | G | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.849+30751G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45614434 | ||||||
| chr5:45614494
|
G | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849+30691C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45614494 | ||||||
| chr5:45614649
|
C | T | 5 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226others(2): Show | 5 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+30536G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45614649 | ||||||
| chr5:45614873
|
T | C | 50 | a0001c0001t0001g0139a0001c0001t0001g0147a0001c0001t0001g0153others(47): Show | 50 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.849+30312A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45614873 | ||||||
| chr5:45614971
|
GA | G | 6 | a0001c0001t0002g0040a0001c0001t0027g0022a0001c0001t0031g0009others(3): Show | 6 | HG01167.hp1 HG01433.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.849+30213delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45614971 | ||||||
| chr5:45615095
|
CA | C | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.849+30089delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45615095 | ||||||
| chr5:45615553
|
A | G | 1 | a0001c0001t0007g0100 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.849+29632T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45615553 | ||||||
| chr5:45615596
|
C | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.849+29589G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45615596 | ||||||
| chr5:45615851
|
T | C | 1 | a0001c0001t0030g0008 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.849+29334A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45615851 | ||||||
| chr5:45615886
|
AAC | A | 2 | a0001c0001t0002g0082a0001c0001t0019g0114 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.849+29297_849+2929 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45615886 | ||||||
| chr5:45616189
|
A | G | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.849+28996T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45616189 | ||||||
| chr5:45616236
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.849+28949G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45616236 | ||||||
| chr5:45616373
|
G | T | 1 | a0001c0005t0002g0199 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.849+28812C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45616373 | ||||||
| chr5:45616658
|
T | C | 5 | a0001c0001t0001g0034a0001c0001t0002g0027a0001c0001t0002g0035others(2): Show | 5 | NA18949.hp2 NA18959.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+28527A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45616658 | ||||||
| chr5:45616721
|
A | C | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.849+28464T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45616721 | ||||||
| chr5:45616809
|
C | T | 2 | a0001c0001t0005g0122a0001c0001t0005g0123 | 2 | HG02055.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.849+28376G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45616809 | ||||||
| chr5:45616911
|
G | A | 64 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(61): Show | 64 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.849+28274C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45616911 | ||||||
| chr5:45617051
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.849+28134A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45617051 | ||||||
| chr5:45617840
|
A | G | 1 | a0001c0001t0027g0022 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.849+27345T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45617840 | ||||||
| chr5:45617847
|
A | ATTAATTT others(126): Show |
5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+27205_849+2733 others(137): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45617847 | ||||||
| chr5:45618135
|
AG | A | 77 | a0001c0001t0001g0073a0001c0001t0001g0134a0001c0001t0001g0135others(74): Show | 77 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.849+27049delC | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45618135 | ||||||
| chr5:45618316
|
G | A | 5 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226others(2): Show | 5 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+26869C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45618316 | ||||||
| chr5:45618377
|
A | T | 1 | a0001c0001t0002g0097 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.849+26808T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45618377 | ||||||
| chr5:45618494
|
T | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+26691A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45618494 | ||||||
| chr5:45618775
|
G | A | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.849+26410C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45618775 | ||||||
| chr5:45618795
|
T | A | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.849+26390A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45618795 | ||||||
| chr5:45619217
|
C | A | 15 | a0001c0001t0002g0121a0001c0001t0002g0140a0001c0001t0002g0141others(12): Show | 15 | HG01261.hp2 HG01346.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.849+25968G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45619217 | ||||||
| chr5:45619280
|
A | C | 5 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226others(2): Show | 5 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+25905T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45619280 | ||||||
| chr5:45619435
|
G | A | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.849+25750C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45619435 | ||||||
| chr5:45619637
|
G | A | 6 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(3): Show | 6 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+25548C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45619637 | ||||||
| chr5:45619810
|
G | A | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.849+25375C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45619810 | ||||||
| chr5:45619812
|
C | T | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.849+25373G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45619812 | ||||||
| chr5:45619845
|
G | C | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.849+25340C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45619845 | ||||||
| chr5:45619963
|
C | T | 4 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(1): Show | 4 | HG01934.hp1 NA18945.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+25222G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45619963 | ||||||
| chr5:45620024
|
C | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849+25161G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45620024 | ||||||
| chr5:45620104
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.849+25081G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45620104 | ||||||
| chr5:45620234
|
T | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG00323.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.849+24951A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45620234 | ||||||
| chr5:45620324
|
GTACAATG others(7): Show |
G | 1 | a0001c0001t0030g0008 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.849+24847_849+2486 others(18): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45620324 | ||||||
| chr5:45620363
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.849+24822C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45620363 | ||||||
| chr5:45620396
|
A | G | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849+24789T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45620396 | ||||||
| chr5:45620650
|
TAAATACA others(4): Show |
T | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849+24524_849+2453 others(15): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45620650 | ||||||
| chr5:45620736
|
A | G | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.849+24449T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45620736 | ||||||
| chr5:45620987
|
T | C | 37 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(34): Show | 37 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.849+24198A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45620987 | ||||||
| chr5:45621084
|
C | G | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.849+24101G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45621084 | ||||||
| chr5:45621321
|
TC | T | 125 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.849+23863delG | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45621321 | ||||||
| chr5:45621455
|
T | C | 1 | a0001c0001t0023g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.849+23730A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45621455 | ||||||
| chr5:45621576
|
C | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849+23609G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45621576 | ||||||
| chr5:45621809
|
T | C | 1 | a0001c0001t0002g0025 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.849+23376A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45621809 | ||||||
| chr5:45621820
|
T | A | 1 | a0001c0001t0018g0018 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.849+23365A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45621820 | ||||||
| chr5:45621942
|
C | T | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.849+23243G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45621942 | ||||||
| chr5:45621978
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.849+23207A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45621978 | ||||||
| chr5:45622034
|
C | T | 3 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133 | 3 | HG01257.hp1 HG01258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.849+23151G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45622034 | ||||||
| chr5:45622095
|
G | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0208 | 2 | NA18953.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.849+23090C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45622095 | ||||||
| chr5:45622155
|
G | A | 1 | a0001c0001t0006g0203 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.849+23030C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45622155 | ||||||
| chr5:45622162
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.849+23023G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45622162 | ||||||
| chr5:45622345
|
T | G | 1 | a0001c0001t0002g0019 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.849+22840A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45622345 | ||||||
| chr5:45622394
|
C | A | 140 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.849+22791G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45622394 | ||||||
| chr5:45622490
|
C | A | 1 | a0001c0001t0001g0135 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.849+22695G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45622490 | ||||||
| chr5:45622539
|
G | A | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.849+22646C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45622539 | ||||||
| chr5:45622732
|
T | C | 1 | a0001c0001t0002g0026 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.849+22453A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45622732 | ||||||
| chr5:45622979
|
G | T | 1 | a0001c0001t0001g0060 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.849+22206C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45622979 | ||||||
| chr5:45623074
|
T | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+22111A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45623074 | ||||||
| chr5:45623827
|
C | T | 1 | a0001c0001t0002g0050 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.849+21358G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45623827 | ||||||
| chr5:45623882
|
G | A | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.849+21303C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45623882 | ||||||
| chr5:45623889
|
A | T | 6 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(3): Show | 6 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.849+21296T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45623889 | ||||||
| chr5:45624294
|
G | A | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.849+20891C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45624294 | ||||||
| chr5:45624531
|
G | T | 1 | a0001c0001t0002g0012 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.849+20654C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45624531 | ||||||
| chr5:45624887
|
G | T | 1 | a0001c0001t0024g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.849+20298C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45624887 | ||||||
| chr5:45625017
|
A | G | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.849+20168T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45625017 | ||||||
| chr5:45625023
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.849+20162A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45625023 | ||||||
| chr5:45625045
|
T | A | 1 | a0001c0001t0024g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.849+20140A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45625045 | ||||||
| chr5:45625073
|
G | C | 1 | a0001c0001t0005g0129 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.849+20112C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45625073 | ||||||
| chr5:45625076
|
C | T | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849+20109G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45625076 | ||||||
| chr5:45625093
|
G | A | 2 | a0001c0001t0002g0193a0001c0001t0004g0189 | 2 | NA19010.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.849+20092C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45625093 | ||||||
| chr5:45625171
|
C | A | 6 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(3): Show | 6 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.849+20014G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45625171 | ||||||
| chr5:45625269
|
C | T | 3 | a0001c0001t0001g0073a0001c0001t0001g0205a0001c0001t0001g0210 | 3 | NA18612.hp1 NA18982.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.849+19916G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45625269 | ||||||
| chr5:45625284
|
C | T | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849+19901G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45625284 | ||||||
| chr5:45625301
|
T | TCAAAA | 2 | a0001c0001t0017g0081a0001c0001t0033g0213 | 2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.849+19879_849+1988 others(9): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45625301 | ||||||
| chr5:45625301
|
TCAAAACA others(3): Show |
T | 52 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(49): Show | 52 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.849+19874_849+1988 others(14): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45625301 | ||||||
| chr5:45625684
|
T | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+19501A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45625684 | ||||||
| chr5:45625685
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+19500T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45625685 | ||||||
| chr5:45626058
|
C | T | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.849+19127G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45626058 | ||||||
| chr5:45626293
|
A | G | 3 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133 | 3 | HG01257.hp1 HG01258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.849+18892T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45626293 | ||||||
| chr5:45626311
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.849+18874G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45626311 | ||||||
| chr5:45626526
|
C | A | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.849+18659G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45626526 | ||||||
| chr5:45626530
|
T | A | 1 | a0001c0001t0002g0082 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.849+18655A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45626530 | ||||||
| chr5:45626752
|
G | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+18433C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45626752 | ||||||
| chr5:45626822
|
G | A | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.849+18363C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45626822 | ||||||
| chr5:45626898
|
ATATG | A | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.849+18283_849+1828 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45626898 | ||||||
| chr5:45626958
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+18227A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45626958 | ||||||
| chr5:45626958
|
TAC | T | 2 | a0001c0001t0001g0107a0001c0001t0007g0100 | 2 | HG00438.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.849+18225_849+1822 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45626958 | ||||||
| chr5:45627637
|
C | A | 1 | a0001c0001t0005g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.849+17548G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45627637 | ||||||
| chr5:45627872
|
A | C | 2 | a0001c0001t0002g0082a0001c0001t0019g0114 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.849+17313T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45627872 | ||||||
| chr5:45628018
|
C | T | 1 | a0001c0001t0002g0026 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.849+17167G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45628018 | ||||||
| chr5:45628384
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.849+16801G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45628384 | ||||||
| chr5:45628521
|
A | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849+16664T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45628521 | ||||||
| chr5:45628627
|
A | AAAC | 3 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0033g0213 | 3 | HG03579.hp1 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+16557_849+1655 others(7): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45628627 | ||||||
| chr5:45628696
|
C | T | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.849+16489G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45628696 | ||||||
| chr5:45628769
|
C | T | 6 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(3): Show | 6 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.849+16416G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45628769 | ||||||
| chr5:45628890
|
A | G | 1 | a0001c0001t0002g0041 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.849+16295T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45628890 | ||||||
| chr5:45628908
|
A | G | 126 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.849+16277T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45628908 | ||||||
| chr5:45628985
|
T | TA | 41 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(38): Show | 41 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.849+16199dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45628985 | ||||||
| chr5:45629003
|
T | G | 4 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0031g0009others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+16182A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45629003 | ||||||
| chr5:45629164
|
A | G | 1 | a0001c0001t0023g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.849+16021T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45629164 | ||||||
| chr5:45629340
|
T | A | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.849+15845A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45629340 | ||||||
| chr5:45629468
|
A | G | 4 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(1): Show | 4 | HG01257.hp1 HG01258.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+15717T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45629468 | ||||||
| chr5:45629515
|
T | C | 1 | a0001c0001t0002g0026 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.849+15670A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45629515 | ||||||
| chr5:45629708
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+15477A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45629708 | ||||||
| chr5:45629822
|
G | A | 2 | a0001c0001t0005g0129a0001c0001t0005g0130 | 2 | HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.849+15363C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45629822 | ||||||
| chr5:45629998
|
A | ACCCCAGA others(18): Show |
2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+15162_849+1518 others(29): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45629998 | ||||||
| chr5:45630098
|
G | C | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.849+15087C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45630098 | ||||||
| chr5:45630175
|
C | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+15010G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45630175 | ||||||
| chr5:45630223
|
T | C | 3 | a0001c0001t0002g0072a0001c0001t0002g0097a0001c0001t0003g0086 | 3 | HG00558.hp1 HG00673.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.849+14962A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45630223 | ||||||
| chr5:45630288
|
A | G | 41 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(38): Show | 41 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.849+14897T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45630288 | ||||||
| chr5:45630483
|
T | C | 2 | a0001c0001t0002g0015a0001c0001t0016g0014 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.849+14702A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45630483 | ||||||
| chr5:45630486
|
G | C | 1 | a0001c0001t0003g0113 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.849+14699C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45630486 | ||||||
| chr5:45630787
|
C | T | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+14398G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45630787 | ||||||
| chr5:45630991
|
C | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.849+14194G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45630991 | ||||||
| chr5:45630996
|
A | T | 1 | a0001c0001t0007g0100 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.849+14189T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45630996 | ||||||
| chr5:45631249
|
T | C | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+13936A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45631249 | ||||||
| chr5:45631464
|
G | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+13721C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45631464 | ||||||
| chr5:45631907
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.849+13278T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45631907 | ||||||
| chr5:45631946
|
G | T | 2 | a0001c0001t0002g0052a0001c0001t0006g0057 | 2 | HG01109.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.849+13239C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45631946 | ||||||
| chr5:45632197
|
T | C | 1 | a0001c0001t0002g0082 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.849+12988A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45632197 | ||||||
| chr5:45632279
|
T | TTG | 9 | a0001c0001t0001g0116a0001c0001t0001g0139a0001c0001t0002g0088others(6): Show | 9 | HG00609.hp1 HG00642.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.849+12904_849+1290 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45632279 | ||||||
| chr5:45632279
|
T | TTGTG | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.849+12902_849+1290 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45632279 | ||||||
| chr5:45633141
|
A | G | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.849+12044T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45633141 | ||||||
| chr5:45633255
|
C | A | 65 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(62): Show | 65 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.849+11930G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45633255 | ||||||
| chr5:45633306
|
AT | A | 6 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(3): Show | 6 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+11878delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45633306 | ||||||
| chr5:45633661
|
T | A | 1 | a0001c0001t0005g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.849+11524A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45633661 | ||||||
| chr5:45633898
|
T | G | 140 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.849+11287A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45633898 | ||||||
| chr5:45634658
|
G | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+10527C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45634658 | ||||||
| chr5:45634795
|
G | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849+10390C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45634795 | ||||||
| chr5:45634915
|
A | C | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.849+10270T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45634915 | ||||||
| chr5:45634960
|
T | C | 6 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0156others(3): Show | 6 | HG00597.hp1 NA18939.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+10225A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45634960 | ||||||
| chr5:45635077
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.849+10108G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45635077 | ||||||
| chr5:45635527
|
G | T | 1 | a0001c0001t0002g0052 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.849+9658C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45635527 | ||||||
| chr5:45635774
|
T | C | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.849+9411A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45635774 | ||||||
| chr5:45635839
|
C | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.849+9346G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45635839 | ||||||
| chr5:45635911
|
G | A | 2 | a0001c0001t0002g0082a0001c0001t0019g0114 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.849+9274C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45635911 | ||||||
| chr5:45636199
|
C | T | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.849+8986G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45636199 | ||||||
| chr5:45636345
|
G | T | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849+8840C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45636345 | ||||||
| chr5:45636372
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.849+8813G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45636372 | ||||||
| chr5:45636584
|
G | A | 2 | a0001c0001t0003g0098a0001c0001t0003g0099 | 2 | HG01361.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.849+8601C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45636584 | ||||||
| chr5:45636672
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.849+8513T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45636672 | ||||||
| chr5:45636684
|
C | A | 65 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(62): Show | 65 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.849+8501G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45636684 | ||||||
| chr5:45636743
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.849+8442A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45636743 | ||||||
| chr5:45637173
|
T | C | 1 | a0001c0001t0038g0016 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.849+8012A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45637173 | ||||||
| chr5:45637245
|
A | C | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.849+7940T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45637245 | ||||||
| chr5:45637404
|
T | C | 2 | a0001c0001t0011g0163a0001c0001t0011g0164 | 2 | NA18992.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.849+7781A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45637404 | ||||||
| chr5:45637451
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.849+7734T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45637451 | ||||||
| chr5:45637553
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.849+7632C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45637553 | ||||||
| chr5:45637941
|
T | A | 3 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133 | 3 | HG01257.hp1 HG01258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.849+7244A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45637941 | ||||||
| chr5:45637996
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.849+7189C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45637996 | ||||||
| chr5:45638068
|
CA | C | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.849+7116delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45638068 | ||||||
| chr5:45638327
|
T | C | 2 | a0001c0001t0001g0149a0001c0001t0002g0152 | 2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.849+6858A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45638327 | ||||||
| chr5:45638409
|
T | A | 65 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(62): Show | 65 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.849+6776A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45638409 | ||||||
| chr5:45638434
|
A | G | 35 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(32): Show | 35 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.849+6751T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45638434 | ||||||
| chr5:45638527
|
G | A | 138 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.849+6658C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45638527 | ||||||
| chr5:45638699
|
T | C | 2 | a0001c0001t0005g0129a0001c0001t0005g0130 | 2 | HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.849+6486A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45638699 | ||||||
| chr5:45638828
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.849+6357C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45638828 | ||||||
| chr5:45639004
|
C | T | 1 | a0001c0001t0002g0058 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.849+6181G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45639004 | ||||||
| chr5:45639931
|
A | G | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.849+5254T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45639931 | ||||||
| chr5:45640108
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.849+5077G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45640108 | ||||||
| chr5:45640250
|
G | C | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.849+4935C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45640250 | ||||||
| chr5:45640484
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.849+4701C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45640484 | ||||||
| chr5:45640520
|
G | A | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+4665C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45640520 | ||||||
| chr5:45640524
|
C | T | 1 | a0001c0001t0002g0091 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.849+4661G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45640524 | ||||||
| chr5:45640535
|
G | A | 1 | a0001c0001t0003g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.849+4650C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45640535 | ||||||
| chr5:45640562
|
A | G | 1 | a0001c0001t0002g0019 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.849+4623T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45640562 | ||||||
| chr5:45640577
|
C | CT | 6 | a0001c0001t0002g0046a0001c0001t0003g0118a0001c0001t0007g0214others(3): Show | 6 | HG00738.hp1 HG00738.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+4607dupA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45640577 | ||||||
| chr5:45640704
|
A | C | 1 | a0001c0001t0011g0163 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.849+4481T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45640704 | ||||||
| chr5:45640754
|
T | C | 4 | a0001c0001t0001g0045a0001c0001t0002g0044a0001c0001t0003g0063others(1): Show | 4 | HG01071.hp2 HG01081.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+4431A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45640754 | ||||||
| chr5:45640837
|
A | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+4348T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45640837 | ||||||
| chr5:45640858
|
G | GA | 18 | a0001c0001t0001g0134a0001c0001t0001g0155a0001c0001t0001g0160others(15): Show | 18 | HG00673.hp2 HG01257.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.849+4326dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45640858 | ||||||
| chr5:45640858
|
GA | G | 43 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(40): Show | 43 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.849+4326delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45640858 | ||||||
| chr5:45640865
|
A | T | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.849+4320T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45640865 | ||||||
| chr5:45640888
|
G | A | 16 | a0001c0001t0002g0121a0001c0001t0002g0140a0001c0001t0002g0141others(13): Show | 16 | HG01261.hp2 HG01346.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.849+4297C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45640888 | ||||||
| chr5:45641050
|
A | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849+4135T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45641050 | ||||||
| chr5:45641158
|
T | G | 1 | a0001c0001t0002g0046 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.849+4027A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45641158 | ||||||
| chr5:45641193
|
T | C | 1 | a0001c0001t0036g0186 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.849+3992A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45641193 | ||||||
| chr5:45641355
|
A | G | 1 | a0001c0001t0020g0196 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.849+3830T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45641355 | ||||||
| chr5:45641507
|
A | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+3678T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45641507 | ||||||
| chr5:45641540
|
G | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+3645C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45641540 | ||||||
| chr5:45641592
|
G | T | 2 | a0001c0001t0002g0052a0001c0001t0003g0053 | 2 | HG00642.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.849+3593C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45641592 | ||||||
| chr5:45641596
|
T | C | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.849+3589A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45641596 | ||||||
| chr5:45641633
|
A | G | 1 | a0001c0001t0002g0157 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.849+3552T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45641633 | ||||||
| chr5:45641650
|
C | T | 1 | a0001c0001t0006g0143 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.849+3535G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45641650 | ||||||
| chr5:45642063
|
A | T | 2 | a0001c0001t0001g0149a0001c0001t0002g0152 | 2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.849+3122T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45642063 | ||||||
| chr5:45642083
|
C | A | 1 | a0001c0001t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.849+3102G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45642083 | ||||||
| chr5:45642121
|
T | C | 1 | a0001c0001t0002g0036 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.849+3064A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45642121 | ||||||
| chr5:45642179
|
T | C | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849+3006A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45642179 | ||||||
| chr5:45642364
|
T | A | 1 | a0001c0001t0002g0194 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.849+2821A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45642364 | ||||||
| chr5:45642386
|
A | G | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.849+2799T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45642386 | ||||||
| chr5:45642454
|
G | GA | 35 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(32): Show | 35 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.849+2730dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45642454 | ||||||
| chr5:45642522
|
T | C | 2 | a0001c0001t0001g0171a0001c0001t0037g0148 | 2 | HG01257.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.849+2663A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45642522 | ||||||
| chr5:45643261
|
T | C | 15 | a0001c0001t0002g0121a0001c0001t0002g0140a0001c0001t0002g0141others(12): Show | 15 | HG01261.hp2 HG01346.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.849+1924A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45643261 | ||||||
| chr5:45643379
|
T | C | 1 | a0001c0001t0003g0119 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.849+1806A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45643379 | ||||||
| chr5:45643491
|
G | A | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.849+1694C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45643491 | ||||||
| chr5:45643601
|
T | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849+1584A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45643601 | ||||||
| chr5:45643656
|
C | A | 1 | a0001c0001t0002g0178 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.849+1529G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45643656 | ||||||
| chr5:45643771
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.849+1414T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45643771 | ||||||
| chr5:45643793
|
C | T | 1 | a0003c0003t0002g0221 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.849+1392G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45643793 | ||||||
| chr5:45644233
|
G | T | 1 | a0001c0001t0002g0049 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.849+952C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45644233 | ||||||
| chr5:45644240
|
T | A | 37 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(34): Show | 37 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.849+945A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45644240 | ||||||
| chr5:45644260
|
A | G | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.849+925T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45644260 | ||||||
| chr5:45644293
|
C | T | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.849+892G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45644293 | ||||||
| chr5:45644469
|
C | T | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.849+716G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45644469 | ||||||
| chr5:45644483
|
A | G | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.849+702T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45644483 | ||||||
| chr5:45644556
|
T | C | 2 | a0001c0001t0002g0025a0001c0001t0002g0026 | 2 | NA18612.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.849+629A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45644556 | ||||||
| chr5:45644577
|
T | C | 1 | a0001c0001t0013g0079 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.849+608A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45644577 | ||||||
| chr5:45644630
|
A | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+555T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45644630 | ||||||
| chr5:45644683
|
T | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.849+502A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45644683 | ||||||
| chr5:45644721
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.849+464T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45644721 | ||||||
| chr5:45644958
|
A | T | 1 | a0003c0003t0002g0221 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.849+227T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 2/7 | chr5 | 45644958 | ||||||
| chr5:45645652
|
C | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.426-44G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45645652 | ||||||
| chr5:45645665
|
C | G | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.426-57G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45645665 | ||||||
| chr5:45645736
|
A | T | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.426-128T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45645736 | ||||||
| chr5:45645810
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.426-202C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45645810 | ||||||
| chr5:45646059
|
C | A | 1 | a0001c0001t0003g0109 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.426-451G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45646059 | ||||||
| chr5:45646077
|
A | G | 1 | a0001c0001t0016g0014 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.426-469T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45646077 | ||||||
| chr5:45646367
|
CT | C | 5 | a0001c0001t0001g0085a0001c0001t0001g0180a0001c0001t0001g0208others(2): Show | 5 | HG02897.hp1 HG03704.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.426-760delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45646367 | ||||||
| chr5:45646367
|
CTTTTT | C | 64 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0037others(61): Show | 64 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.426-764_426-760del others(5): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45646367 | ||||||
| chr5:45646371
|
T | C | 3 | a0001c0001t0001g0102a0001c0001t0003g0084a0001c0001t0003g0101 | 3 | NA19003.hp1 NA19011.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.426-763A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45646371 | ||||||
| chr5:45646550
|
T | C | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.426-942A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45646550 | ||||||
| chr5:45646659
|
G | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.426-1051C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45646659 | ||||||
| chr5:45647290
|
T | C | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.426-1682A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45647290 | ||||||
| chr5:45647394
|
C | T | 1 | a0001c0001t0002g0157 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.426-1786G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45647394 | ||||||
| chr5:45647520
|
G | A | 37 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(34): Show | 37 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.426-1912C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45647520 | ||||||
| chr5:45647890
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG01074.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.426-2282C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45647890 | ||||||
| chr5:45647926
|
C | T | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.426-2318G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45647926 | ||||||
| chr5:45648058
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.426-2450A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45648058 | ||||||
| chr5:45648072
|
C | G | 1 | a0001c0001t0005g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.426-2464G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45648072 | ||||||
| chr5:45648233
|
C | T | 1 | a0001c0001t0023g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.426-2625G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45648233 | ||||||
| chr5:45648483
|
C | T | 1 | a0001c0001t0002g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.426-2875G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45648483 | ||||||
| chr5:45648488
|
G | C | 3 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133 | 3 | HG01257.hp1 HG01258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.426-2880C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45648488 | ||||||
| chr5:45648493
|
TA | T | 3 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133 | 3 | HG01257.hp1 HG01258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.426-2886delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45648493 | ||||||
| chr5:45648600
|
A | T | 1 | a0001c0001t0002g0019 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.426-2992T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45648600 | ||||||
| chr5:45648655
|
T | C | 65 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(62): Show | 65 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.426-3047A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45648655 | ||||||
| chr5:45649094
|
T | C | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.426-3486A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45649094 | ||||||
| chr5:45649157
|
C | T | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.426-3549G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45649157 | ||||||
| chr5:45649157
|
CCCCTCAA others(16): Show |
C | 1 | a0001c0001t0002g0152 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.426-3572_426-3550d others(25): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45649157 | ||||||
| chr5:45649251
|
T | C | 1 | a0001c0001t0007g0214 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.426-3643A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45649251 | ||||||
| chr5:45649285
|
A | C | 1 | a0001c0001t0002g0052 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.426-3677T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45649285 | ||||||
| chr5:45649325
|
C | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.426-3717G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45649325 | ||||||
| chr5:45649351
|
C | T | 1 | a0001c0001t0003g0087 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.426-3743G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45649351 | ||||||
| chr5:45649412
|
C | T | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.426-3804G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45649412 | ||||||
| chr5:45649507
|
A | G | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.426-3899T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45649507 | ||||||
| chr5:45649669
|
A | G | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.426-4061T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45649669 | ||||||
| chr5:45649776
|
A | G | 1 | a0001c0001t0002g0040 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.426-4168T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45649776 | ||||||
| chr5:45649779
|
A | C | 1 | a0001c0001t0015g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.426-4171T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45649779 | ||||||
| chr5:45650035
|
T | C | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.426-4427A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45650035 | ||||||
| chr5:45650259
|
T | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.426-4651A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45650259 | ||||||
| chr5:45650558
|
C | A | 2 | a0001c0001t0002g0027a0001c0001t0002g0054 | 2 | NA18959.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.426-4950G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45650558 | ||||||
| chr5:45650693
|
T | C | 37 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(34): Show | 37 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.426-5085A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45650693 | ||||||
| chr5:45650726
|
C | T | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.426-5118G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45650726 | ||||||
| chr5:45651076
|
T | C | 1 | a0001c0001t0002g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.426-5468A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45651076 | ||||||
| chr5:45651121
|
G | A | 1 | a0001c0001t0002g0028 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.426-5513C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45651121 | ||||||
| chr5:45651419
|
T | C | 1 | a0001c0001t0009g0003 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.426-5811A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45651419 | ||||||
| chr5:45651460
|
G | A | 65 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(62): Show | 65 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.426-5852C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45651460 | ||||||
| chr5:45651767
|
G | A | 65 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(62): Show | 65 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.426-6159C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45651767 | ||||||
| chr5:45651873
|
A | G | 1 | a0001c0001t0003g0090 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.426-6265T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45651873 | ||||||
| chr5:45651938
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.426-6330T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45651938 | ||||||
| chr5:45652397
|
C | T | 1 | a0001c0001t0002g0012 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.426-6789G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45652397 | ||||||
| chr5:45652434
|
T | C | 1 | a0001c0001t0002g0082 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.426-6826A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45652434 | ||||||
| chr5:45652790
|
A | G | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.426-7182T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45652790 | ||||||
| chr5:45653026
|
A | G | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.426-7418T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45653026 | ||||||
| chr5:45653211
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.426-7603G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45653211 | ||||||
| chr5:45653290
|
T | C | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.426-7682A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45653290 | ||||||
| chr5:45653532
|
A | G | 1 | a0001c0001t0004g0189 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.426-7924T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45653532 | ||||||
| chr5:45653678
|
T | A | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.426-8070A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45653678 | ||||||
| chr5:45653810
|
T | C | 139 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.426-8202A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45653810 | ||||||
| chr5:45653923
|
T | TAATA | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.426-8319_426-8316d others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45653923 | ||||||
| chr5:45654293
|
C | T | 1 | a0001c0001t0003g0053 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.426-8685G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45654293 | ||||||
| chr5:45654490
|
T | C | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.426-8882A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45654490 | ||||||
| chr5:45654530
|
G | A | 14 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(11): Show | 14 | HG01261.hp2 HG01891.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.426-8922C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45654530 | ||||||
| chr5:45654562
|
A | C | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.426-8954T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45654562 | ||||||
| chr5:45654713
|
C | T | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.426-9105G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45654713 | ||||||
| chr5:45654968
|
T | C | 139 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.426-9360A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45654968 | ||||||
| chr5:45655127
|
C | T | 1 | a0001c0001t0036g0186 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.426-9519G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45655127 | ||||||
| chr5:45655206
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.426-9598G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45655206 | ||||||
| chr5:45655651
|
G | A | 1 | a0001c0001t0004g0055 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.426-10043C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45655651 | ||||||
| chr5:45655791
|
A | G | 140 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.426-10183T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45655791 | ||||||
| chr5:45655900
|
A | AGCAAGAG others(6): Show |
1 | a0001c0001t0003g0188 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.426-10305_426-1029 others(17): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45655900 | ||||||
| chr5:45656095
|
TAA | T | 13 | a0001c0001t0001g0073a0001c0001t0001g0134a0001c0001t0001g0160others(10): Show | 13 | HG00673.hp2 HG02056.hp1 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.426-10489_426-1048 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45656095 | ||||||
| chr5:45656515
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.426-10907G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45656515 | ||||||
| chr5:45656821
|
C | A | 140 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.426-11213G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45656821 | ||||||
| chr5:45657543
|
T | C | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.426-11935A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45657543 | ||||||
| chr5:45657634
|
T | C | 1 | a0001c0001t0005g0142 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.426-12026A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45657634 | ||||||
| chr5:45657680
|
C | A | 15 | a0001c0001t0002g0121a0001c0001t0002g0140a0001c0001t0002g0141others(12): Show | 15 | HG01261.hp2 HG01346.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.426-12072G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45657680 | ||||||
| chr5:45657861
|
A | G | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.426-12253T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45657861 | ||||||
| chr5:45657960
|
C | T | 12 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0122others(9): Show | 12 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.426-12352G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45657960 | ||||||
| chr5:45658079
|
C | T | 1 | a0001c0001t0002g0019 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.426-12471G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45658079 | ||||||
| chr5:45658083
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.426-12475C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45658083 | ||||||
| chr5:45658105
|
T | A | 1 | a0001c0001t0002g0047 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.426-12497A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45658105 | ||||||
| chr5:45658187
|
G | A | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.426-12579C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45658187 | ||||||
| chr5:45658288
|
G | A | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.426-12680C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45658288 | ||||||
| chr5:45658319
|
T | C | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.426-12711A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45658319 | ||||||
| chr5:45658406
|
A | G | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.426-12798T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45658406 | ||||||
| chr5:45658441
|
G | A | 35 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(32): Show | 35 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.426-12833C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45658441 | ||||||
| chr5:45658602
|
G | A | 1 | a0001c0001t0003g0120 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.426-12994C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45658602 | ||||||
| chr5:45658603
|
T | A | 1 | a0001c0001t0002g0152 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.426-12995A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45658603 | ||||||
| chr5:45658673
|
G | T | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.426-13065C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45658673 | ||||||
| chr5:45658692
|
G | C | 139 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.426-13084C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45658692 | ||||||
| chr5:45658746
|
C | T | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.426-13138G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45658746 | ||||||
| chr5:45658804
|
C | G | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.426-13196G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45658804 | ||||||
| chr5:45658860
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.426-13252C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45658860 | ||||||
| chr5:45658866
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.426-13258C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45658866 | ||||||
| chr5:45658924
|
G | A | 6 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(3): Show | 6 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.426-13316C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45658924 | ||||||
| chr5:45659099
|
A | G | 1 | a0001c0001t0003g0110 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.426-13491T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45659099 | ||||||
| chr5:45659190
|
G | A | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.426-13582C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45659190 | ||||||
| chr5:45659217
|
A | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.426-13609T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45659217 | ||||||
| chr5:45659297
|
C | A | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.426-13689G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45659297 | ||||||
| chr5:45659305
|
C | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.426-13697G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45659305 | ||||||
| chr5:45659310
|
A | C | 127 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.426-13702T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45659310 | ||||||
| chr5:45659394
|
C | T | 2 | a0001c0001t0011g0163a0001c0001t0011g0164 | 2 | NA18992.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.426-13786G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45659394 | ||||||
| chr5:45659413
|
G | C | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.426-13805C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45659413 | ||||||
| chr5:45659436
|
G | A | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.426-13828C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45659436 | ||||||
| chr5:45659491
|
T | C | 139 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.426-13883A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45659491 | ||||||
| chr5:45659674
|
C | T | 13 | a0001c0001t0002g0121a0001c0001t0002g0140a0001c0001t0002g0141others(10): Show | 13 | HG01261.hp2 HG01346.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.426-14066G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45659674 | ||||||
| chr5:45659762
|
T | G | 1 | a0001c0001t0002g0066 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.426-14154A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45659762 | ||||||
| chr5:45659821
|
C | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.426-14213G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45659821 | ||||||
| chr5:45659825
|
T | C | 3 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133 | 3 | HG01257.hp1 HG01258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.426-14217A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45659825 | ||||||
| chr5:45659972
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.426-14364G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45659972 | ||||||
| chr5:45659981
|
A | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.426-14373T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45659981 | ||||||
| chr5:45660046
|
G | GC | 127 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.426-14439dupG | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45660046 | ||||||
| chr5:45660070
|
T | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.426-14462A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45660070 | ||||||
| chr5:45660139
|
G | A | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.426-14531C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45660139 | ||||||
| chr5:45660150
|
A | C | 65 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(62): Show | 65 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.426-14542T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45660150 | ||||||
| chr5:45660261
|
T | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.426-14653A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45660261 | ||||||
| chr5:45660271
|
G | C | 144 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.426-14663C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45660271 | ||||||
| chr5:45660295
|
T | C | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.426-14687A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45660295 | ||||||
| chr5:45660326
|
C | G | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.426-14718G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45660326 | ||||||
| chr5:45660338
|
G | A | 1 | a0001c0001t0003g0083 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.426-14730C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45660338 | ||||||
| chr5:45660409
|
C | A | 3 | a0001c0001t0001g0051a0001c0001t0002g0049a0001c0001t0002g0050 | 3 | HG03041.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.426-14801G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45660409 | ||||||
| chr5:45660512
|
T | G | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.426-14904A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45660512 | ||||||
| chr5:45660708
|
G | A | 1 | a0001c0001t0036g0186 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.426-15100C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45660708 | ||||||
| chr5:45660713
|
T | C | 1 | a0001c0001t0003g0118 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.426-15105A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45660713 | ||||||
| chr5:45660800
|
A | G | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.426-15192T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45660800 | ||||||
| chr5:45660808
|
T | A | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.426-15200A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45660808 | ||||||
| chr5:45660816
|
G | A | 1 | a0001c0001t0002g0157 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.426-15208C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45660816 | ||||||
| chr5:45660822
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.426-15214G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45660822 | ||||||
| chr5:45660855
|
G | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.426-15247C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45660855 | ||||||
| chr5:45660896
|
G | A | 1 | a0001c0006t0002g0219 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.426-15288C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45660896 | ||||||
| chr5:45660909
|
A | C | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.426-15301T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45660909 | ||||||
| chr5:45660913
|
A | C | 1 | a0001c0001t0029g0070 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.426-15305T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45660913 | ||||||
| chr5:45660919
|
C | T | 1 | a0001c0001t0037g0148 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.426-15311G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45660919 | ||||||
| chr5:45660949
|
C | T | 17 | a0001c0001t0001g0116a0001c0001t0002g0140a0001c0001t0002g0141others(14): Show | 17 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.426-15341G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45660949 | ||||||
| chr5:45661218
|
G | A | 1 | a0001c0001t0003g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.426-15610C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45661218 | ||||||
| chr5:45661504
|
A | G | 13 | a0001c0001t0002g0121a0001c0001t0002g0140a0001c0001t0002g0141others(10): Show | 13 | HG01261.hp2 HG01346.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.426-15896T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45661504 | ||||||
| chr5:45661553
|
G | A | 1 | a0001c0001t0002g0181 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.426-15945C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45661553 | ||||||
| chr5:45661631
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG01074.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.426-16023G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45661631 | ||||||
| chr5:45661682
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.426-16074G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45661682 | ||||||
| chr5:45661730
|
A | T | 1 | a0001c0001t0005g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.426-16122T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45661730 | ||||||
| chr5:45661960
|
C | T | 1 | a0001c0001t0003g0119 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.426-16352G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45661960 | ||||||
| chr5:45661973
|
G | C | 1 | a0001c0001t0036g0186 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.426-16365C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45661973 | ||||||
| chr5:45662072
|
A | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.426-16464T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45662072 | ||||||
| chr5:45662216
|
C | A | 16 | a0001c0001t0001g0065a0001c0001t0004g0017a0001c0001t0004g0020others(13): Show | 16 | HG00438.hp1 HG00609.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.426-16608G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45662216 | ||||||
| chr5:45662234
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.426-16626T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45662234 | ||||||
| chr5:45662299
|
C | T | 1 | a0001c0001t0003g0103 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.426-16691G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45662299 | ||||||
| chr5:45662352
|
C | G | 1 | a0001c0001t0003g0109 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.426-16744G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45662352 | ||||||
| chr5:45662420
|
G | A | 9 | a0001c0001t0001g0159a0001c0001t0001g0182a0001c0001t0001g0184others(6): Show | 9 | HG00639.hp1 HG01169.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.426-16812C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45662420 | ||||||
| chr5:45662491
|
A | G | 1 | a0001c0001t0004g0021 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.426-16883T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45662491 | ||||||
| chr5:45662597
|
C | T | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.426-16989G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45662597 | ||||||
| chr5:45662822
|
G | T | 1 | a0001c0001t0002g0052 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.426-17214C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45662822 | ||||||
| chr5:45662983
|
G | C | 1 | a0001c0001t0005g0127 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.426-17375C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45662983 | ||||||
| chr5:45663009
|
A | T | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.426-17401T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45663009 | ||||||
| chr5:45663184
|
C | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.426-17576G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45663184 | ||||||
| chr5:45663188
|
G | C | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.426-17580C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45663188 | ||||||
| chr5:45663242
|
C | G | 1 | a0001c0001t0001g0159 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.426-17634G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45663242 | ||||||
| chr5:45663243
|
T | G | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.426-17635A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45663243 | ||||||
| chr5:45663365
|
C | T | 6 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(3): Show | 6 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.426-17757G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45663365 | ||||||
| chr5:45663529
|
C | A | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.426-17921G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45663529 | ||||||
| chr5:45663611
|
G | GA | 5 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226others(2): Show | 5 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.426-18004dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45663611 | ||||||
| chr5:45663639
|
T | G | 3 | a0001c0001t0001g0034a0001c0001t0002g0035a0001c0001t0002g0036 | 3 | NA18949.hp2 NA19078.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.426-18031A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45663639 | ||||||
| chr5:45663697
|
A | T | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.426-18089T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45663697 | ||||||
| chr5:45663769
|
C | A | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.426-18161G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45663769 | ||||||
| chr5:45663847
|
C | T | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.426-18239G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45663847 | ||||||
| chr5:45663957
|
G | T | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.426-18349C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45663957 | ||||||
| chr5:45664224
|
C | G | 66 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(63): Show | 66 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.426-18616G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45664224 | ||||||
| chr5:45664268
|
T | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0037a0001c0001t0001g0060others(3): Show | 6 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.426-18660A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45664268 | ||||||
| chr5:45664424
|
ATGTGCAC others(984): Show |
A | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.426-19807_426-1881 others(4): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45664424 | ||||||
| chr5:45664472
|
G | GA | 8 | a0001c0001t0001g0116a0001c0001t0001g0187a0001c0001t0002g0058others(5): Show | 8 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.426-18865dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45664472 | ||||||
| chr5:45664472
|
GA | G | 21 | a0001c0001t0002g0039a0001c0001t0002g0088a0001c0001t0002g0140others(18): Show | 21 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.426-18865delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45664472 | ||||||
| chr5:45664503
|
G | C | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.426-18895C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45664503 | ||||||
| chr5:45664762
|
C | G | 1 | a0001c0001t0021g0138 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.426-19154G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45664762 | ||||||
| chr5:45664763
|
T | G | 15 | a0001c0001t0002g0121a0001c0001t0002g0140a0001c0001t0002g0141others(12): Show | 15 | HG01261.hp2 HG01346.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.426-19155A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45664763 | ||||||
| chr5:45664844
|
G | A | 6 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(3): Show | 6 | HG01934.hp1 NA18945.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.426-19236C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45664844 | ||||||
| chr5:45664847
|
G | A | 1 | a0001c0001t0003g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.426-19239C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45664847 | ||||||
| chr5:45664903
|
C | G | 1 | a0001c0001t0001g0085 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.426-19295G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45664903 | ||||||
| chr5:45665061
|
A | G | 1 | a0001c0001t0002g0066 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.426-19453T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45665061 | ||||||
| chr5:45665130
|
G | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.426-19522C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45665130 | ||||||
| chr5:45665192
|
G | A | 1 | a0001c0001t0013g0078 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.426-19584C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45665192 | ||||||
| chr5:45665311
|
G | T | 6 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0156others(3): Show | 6 | HG00597.hp1 NA18939.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.426-19703C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45665311 | ||||||
| chr5:45665317
|
A | T | 1 | a0001c0001t0021g0138 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.426-19709T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45665317 | ||||||
| chr5:45665594
|
C | T | 1 | a0001c0001t0003g0087 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.426-19986G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45665594 | ||||||
| chr5:45665647
|
G | T | 1 | a0001c0001t0002g0058 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.426-20039C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45665647 | ||||||
| chr5:45665699
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.426-20091G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45665699 | ||||||
| chr5:45665702
|
A | T | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.426-20094T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45665702 | ||||||
| chr5:45665914
|
A | C | 1 | a0001c0001t0001g0209 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.426-20306T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45665914 | ||||||
| chr5:45666044
|
A | G | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG01952.hp1 HG03704.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.426-20436T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45666044 | ||||||
| chr5:45666060
|
C | A | 2 | a0001c0001t0004g0017a0001c0001t0018g0018 | 2 | HG00438.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.426-20452G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45666060 | ||||||
| chr5:45666088
|
C | A | 1 | a0001c0001t0002g0194 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.426-20480G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45666088 | ||||||
| chr5:45666136
|
T | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.426-20528A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45666136 | ||||||
| chr5:45666432
|
C | T | 1 | a0001c0001t0013g0078 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.426-20824G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45666432 | ||||||
| chr5:45666463
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.426-20855C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45666463 | ||||||
| chr5:45666549
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.426-20941A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45666549 | ||||||
| chr5:45666669
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.426-21061G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45666669 | ||||||
| chr5:45666917
|
T | G | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.426-21309A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45666917 | ||||||
| chr5:45667117
|
C | G | 1 | a0001c0001t0009g0003 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.426-21509G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45667117 | ||||||
| chr5:45667122
|
G | T | 1 | a0001c0001t0009g0003 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.426-21514C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45667122 | ||||||
| chr5:45667212
|
C | T | 1 | a0001c0001t0037g0148 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.426-21604G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45667212 | ||||||
| chr5:45667302
|
G | T | 1 | a0001c0001t0003g0118 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.426-21694C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45667302 | ||||||
| chr5:45667404
|
T | C | 6 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(3): Show | 6 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.426-21796A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45667404 | ||||||
| chr5:45667573
|
A | G | 1 | a0001c0001t0003g0084 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.426-21965T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45667573 | ||||||
| chr5:45668366
|
A | C | 1 | a0001c0001t0004g0020 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.426-22758T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45668366 | ||||||
| chr5:45668558
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.426-22950G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45668558 | ||||||
| chr5:45668809
|
C | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.426-23201G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45668809 | ||||||
| chr5:45668885
|
C | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.426-23277G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45668885 | ||||||
| chr5:45668936
|
A | G | 36 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0037others(33): Show | 36 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.426-23328T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45668936 | ||||||
| chr5:45668942
|
T | G | 41 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(38): Show | 41 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.426-23334A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45668942 | ||||||
| chr5:45669006
|
A | G | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.426-23398T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45669006 | ||||||
| chr5:45669034
|
T | G | 7 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(4): Show | 7 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.426-23426A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45669034 | ||||||
| chr5:45669166
|
T | G | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.426-23558A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45669166 | ||||||
| chr5:45669865
|
G | T | 1 | a0001c0001t0002g0019 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.426-24257C>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45669865 | ||||||
| chr5:45670283
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.426-24675G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45670283 | ||||||
| chr5:45670513
|
T | C | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.426-24905A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45670513 | ||||||
| chr5:45670627
|
T | C | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.426-25019A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45670627 | ||||||
| chr5:45670632
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.426-25024A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45670632 | ||||||
| chr5:45670815
|
A | G | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.425+24854T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45670815 | ||||||
| chr5:45670982
|
A | G | 1 | a0003c0003t0002g0221 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.425+24687T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45670982 | ||||||
| chr5:45671083
|
A | T | 10 | a0001c0001t0002g0121a0001c0001t0005g0122a0001c0001t0005g0123others(7): Show | 10 | HG01261.hp2 HG01346.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.425+24586T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45671083 | ||||||
| chr5:45671103
|
T | G | 2 | a0001c0001t0001g0197a0001c0001t0020g0196 | 2 | HG01516.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.425+24566A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45671103 | ||||||
| chr5:45671435
|
G | A | 1 | a0001c0001t0006g0143 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.425+24234C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45671435 | ||||||
| chr5:45671565
|
T | G | 65 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(62): Show | 65 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.425+24104A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45671565 | ||||||
| chr5:45671682
|
A | T | 1 | a0001c0001t0002g0144 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.425+23987T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45671682 | ||||||
| chr5:45672019
|
C | T | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.425+23650G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45672019 | ||||||
| chr5:45672380
|
A | C | 215 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.425+23289T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45672380 | ||||||
| chr5:45672420
|
C | T | 1 | a0001c0001t0005g0129 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.425+23249G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45672420 | ||||||
| chr5:45672431
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.425+23238G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45672431 | ||||||
| chr5:45672520
|
A | G | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.425+23149T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45672520 | ||||||
| chr5:45672567
|
TA | T | 7 | a0001c0001t0001g0085a0001c0001t0001g0116a0001c0001t0003g0117others(4): Show | 7 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.425+23101delT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45672567 | ||||||
| chr5:45672774
|
T | C | 1 | a0001c0001t0002g0047 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.425+22895A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45672774 | ||||||
| chr5:45672790
|
T | C | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.425+22879A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45672790 | ||||||
| chr5:45672791
|
C | G | 1 | a0001c0001t0002g0146 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.425+22878G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45672791 | ||||||
| chr5:45672807
|
T | C | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.425+22862A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45672807 | ||||||
| chr5:45672868
|
T | C | 225 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.425+22801A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45672868 | ||||||
| chr5:45672916
|
C | A | 41 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(38): Show | 41 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.425+22753G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45672916 | ||||||
| chr5:45672937
|
A | T | 1 | a0001c0001t0001g0212 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.425+22732T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45672937 | ||||||
| chr5:45672972
|
CT | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.425+22696delA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45672972 | ||||||
| chr5:45673175
|
G | C | 1 | a0001c0001t0002g0058 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.425+22494C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45673175 | ||||||
| chr5:45673197
|
T | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.425+22472A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45673197 | ||||||
| chr5:45673624
|
A | G | 1 | a0001c0001t0002g0144 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.425+22045T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45673624 | ||||||
| chr5:45673676
|
T | G | 66 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(63): Show | 66 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.425+21993A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45673676 | ||||||
| chr5:45673782
|
C | G | 52 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(49): Show | 52 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.425+21887G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45673782 | ||||||
| chr5:45673799
|
T | C | 2 | a0001c0001t0002g0082a0001c0001t0019g0114 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.425+21870A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45673799 | ||||||
| chr5:45673822
|
C | T | 2 | a0001c0001t0002g0082a0001c0001t0019g0114 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.425+21847G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45673822 | ||||||
| chr5:45673909
|
C | G | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.425+21760G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45673909 | ||||||
| chr5:45674513
|
ATATT | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.425+21152_425+2115 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45674513 | ||||||
| chr5:45674601
|
C | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.425+21068G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45674601 | ||||||
| chr5:45674763
|
G | A | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.425+20906C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45674763 | ||||||
| chr5:45674816
|
G | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.425+20853C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45674816 | ||||||
| chr5:45674909
|
A | ATT | 37 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(34): Show | 37 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.425+20759_425+2076 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45674909 | ||||||
| chr5:45675083
|
A | T | 1 | a0001c0001t0002g0054 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.425+20586T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45675083 | ||||||
| chr5:45675086
|
C | A | 1 | a0001c0001t0002g0054 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.425+20583G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45675086 | ||||||
| chr5:45675088
|
G | C | 1 | a0001c0001t0002g0054 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.425+20581C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45675088 | ||||||
| chr5:45675090
|
T | G | 1 | a0001c0001t0002g0054 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.425+20579A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45675090 | ||||||
| chr5:45675091
|
GGAACCAG others(507): Show |
G | 1 | a0001c0001t0002g0054 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.425+20064_425+2057 others(4): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45675091 | ||||||
| chr5:45675337
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0003g0117 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.425+20332G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45675337 | ||||||
| chr5:45675416
|
G | A | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.425+20253C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45675416 | ||||||
| chr5:45675460
|
G | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.425+20209C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45675460 | ||||||
| chr5:45675696
|
T | G | 2 | a0001c0001t0004g0017a0001c0001t0018g0018 | 2 | HG00438.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.425+19973A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45675696 | ||||||
| chr5:45676012
|
T | C | 6 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(3): Show | 6 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.425+19657A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45676012 | ||||||
| chr5:45676090
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.425+19579A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45676090 | ||||||
| chr5:45676155
|
T | C | 1 | a0001c0001t0003g0053 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.425+19514A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45676155 | ||||||
| chr5:45676182
|
C | T | 2 | a0001c0001t0002g0082a0001c0001t0019g0114 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.425+19487G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45676182 | ||||||
| chr5:45676223
|
C | T | 1 | a0001c0001t0003g0084 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.425+19446G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45676223 | ||||||
| chr5:45676272
|
G | A | 9 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(6): Show | 9 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.425+19397C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45676272 | ||||||
| chr5:45676475
|
T | A | 1 | a0001c0001t0001g0205 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.425+19194A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45676475 | ||||||
| chr5:45676484
|
T | C | 12 | a0001c0001t0002g0121a0001c0001t0005g0122a0001c0001t0005g0123others(9): Show | 12 | HG01261.hp2 HG01346.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.425+19185A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45676484 | ||||||
| chr5:45676774
|
A | T | 3 | a0001c0001t0001g0051a0001c0001t0002g0049a0001c0001t0002g0050 | 3 | HG03041.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.425+18895T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45676774 | ||||||
| chr5:45676895
|
G | A | 35 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(32): Show | 35 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.425+18774C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45676895 | ||||||
| chr5:45677020
|
T | C | 2 | a0001c0001t0001g0011a0001c0001t0029g0070 | 2 | NA18942.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.425+18649A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45677020 | ||||||
| chr5:45677058
|
A | T | 2 | a0001c0001t0002g0082a0001c0001t0019g0114 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.425+18611T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45677058 | ||||||
| chr5:45677077
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.425+18592A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45677077 | ||||||
| chr5:45677147
|
A | G | 1 | a0001c0001t0002g0072 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.425+18522T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45677147 | ||||||
| chr5:45677186
|
T | C | 1 | a0001c0001t0002g0069 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.425+18483A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45677186 | ||||||
| chr5:45677349
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.425+18320G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45677349 | ||||||
| chr5:45677977
|
TACACACA others(19): Show |
T | 66 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(63): Show | 66 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.425+17666_425+1769 others(30): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45677977 | ||||||
| chr5:45677988
|
A | G | 4 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0005g0142others(1): Show | 4 | HG02886.hp2 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.425+17681T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45677988 | ||||||
| chr5:45677989
|
T | TAC | 62 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(59): Show | 62 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.425+17678_425+1767 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45677989 | ||||||
| chr5:45677989
|
T | TACACACA others(1): Show |
5 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226others(2): Show | 5 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.425+17672_425+1767 others(12): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45677989 | ||||||
| chr5:45677989
|
T | TACACACA others(5): Show |
1 | a0001c0001t0001g0207 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.425+17668_425+1767 others(16): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45677989 | ||||||
| chr5:45678015
|
T | C | 6 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(3): Show | 6 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.425+17654A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45678015 | ||||||
| chr5:45678135
|
C | T | 6 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(3): Show | 6 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.425+17534G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45678135 | ||||||
| chr5:45678170
|
A | G | 1 | a0001c0001t0017g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.425+17499T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45678170 | ||||||
| chr5:45678201
|
G | A | 1 | a0001c0001t0004g0048 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.425+17468C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45678201 | ||||||
| chr5:45678259
|
C | T | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.425+17410G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45678259 | ||||||
| chr5:45678274
|
T | C | 1 | a0001c0001t0003g0103 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.425+17395A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45678274 | ||||||
| chr5:45678276
|
G | C | 56 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(53): Show | 56 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.425+17393C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45678276 | ||||||
| chr5:45678402
|
T | C | 1 | a0001c0001t0001g0208 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.425+17267A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45678402 | ||||||
| chr5:45678505
|
C | T | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.425+17164G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45678505 | ||||||
| chr5:45678784
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.425+16885A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45678784 | ||||||
| chr5:45678871
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.425+16798T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45678871 | ||||||
| chr5:45678947
|
T | C | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.425+16722A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45678947 | ||||||
| chr5:45679327
|
C | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.425+16342G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45679327 | ||||||
| chr5:45679534
|
A | G | 65 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(62): Show | 65 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.425+16135T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45679534 | ||||||
| chr5:45679562
|
T | C | 1 | a0001c0001t0001g0210 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.425+16107A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45679562 | ||||||
| chr5:45679723
|
A | C | 2 | a0001c0001t0004g0017a0001c0001t0018g0018 | 2 | HG00438.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.425+15946T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45679723 | ||||||
| chr5:45679800
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.425+15869G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45679800 | ||||||
| chr5:45679867
|
C | T | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.425+15802G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45679867 | ||||||
| chr5:45680215
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.425+15454C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45680215 | ||||||
| chr5:45680312
|
G | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.425+15357C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45680312 | ||||||
| chr5:45680866
|
A | T | 53 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(50): Show | 53 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.425+14803T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45680866 | ||||||
| chr5:45680990
|
T | C | 9 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(6): Show | 9 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.425+14679A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45680990 | ||||||
| chr5:45681079
|
G | C | 1 | a0001c0001t0003g0104 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.425+14590C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45681079 | ||||||
| chr5:45681190
|
C | G | 1 | a0001c0001t0001g0139 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.425+14479G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45681190 | ||||||
| chr5:45681340
|
G | A | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.425+14329C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45681340 | ||||||
| chr5:45681467
|
C | A | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.425+14202G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45681467 | ||||||
| chr5:45681775
|
C | A | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.425+13894G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45681775 | ||||||
| chr5:45682198
|
C | T | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.425+13471G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45682198 | ||||||
| chr5:45682255
|
T | TCATATAT others(11): Show |
1 | a0001c0001t0002g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.425+13413_425+1341 others(22): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45682255 | ||||||
| chr5:45682270
|
TACATATA others(13): Show |
T | 1 | a0001c0001t0002g0106 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.425+13379_425+1339 others(24): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45682270 | ||||||
| chr5:45682272
|
C | CAT | 2 | a0001c0001t0022g0080a0001c0001t0025g0217 | 2 | HG01192.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.425+13395_425+1339 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45682272 | ||||||
| chr5:45682272
|
C | T | 13 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(10): Show | 13 | HG01261.hp2 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.425+13397G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45682272 | ||||||
| chr5:45682272
|
CAT | C | 2 | a0001c0001t0002g0067a0001c0001t0012g0137 | 2 | HG01884.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.425+13395_425+1339 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45682272 | ||||||
| chr5:45682274
|
T | C | 14 | a0001c0001t0002g0121a0001c0001t0005g0122a0001c0001t0005g0123others(11): Show | 14 | HG01261.hp2 HG01346.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.425+13395A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45682274 | ||||||
| chr5:45682276
|
T | TATATATA others(19): Show |
1 | a0001c0001t0005g0128 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.425+13392_425+1339 others(30): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45682276 | ||||||
| chr5:45682284
|
TATATAC | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.425+13379_425+1338 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45682284 | ||||||
| chr5:45682286
|
TATAC | T | 9 | a0001c0001t0001g0107a0001c0001t0001g0116a0001c0001t0003g0117others(6): Show | 9 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.425+13379_425+1338 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45682286 | ||||||
| chr5:45682288
|
TAC | T | 104 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0037others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.425+13379_425+1338 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45682288 | ||||||
| chr5:45682290
|
C | CATATATA others(5): Show |
2 | a0001c0001t0005g0129a0001c0001t0005g0130 | 2 | HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.425+13378_425+1337 others(16): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45682290 | ||||||
| chr5:45682290
|
C | CATATATA others(23): Show |
6 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(3): Show | 6 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.425+13378_425+1337 others(34): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45682290 | ||||||
| chr5:45682290
|
C | CATATATA others(87): Show |
1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.425+13378_425+1337 others(98): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45682290 | ||||||
| chr5:45682290
|
C | CATATATA others(57): Show |
1 | a0003c0003t0002g0221 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.425+13378_425+1337 others(68): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45682290 | ||||||
| chr5:45682290
|
C | T | 14 | a0001c0001t0001g0011a0001c0001t0002g0121a0001c0001t0002g0131others(11): Show | 14 | HG01192.hp2 HG01257.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.425+13379G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45682290 | ||||||
| chr5:45682293
|
A | G | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.425+13376T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45682293 | ||||||
| chr5:45682439
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.425+13230A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45682439 | ||||||
| chr5:45682527
|
T | C | 1 | a0001c0001t0019g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.425+13142A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45682527 | ||||||
| chr5:45682684
|
T | G | 1 | a0001c0001t0007g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.425+12985A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45682684 | ||||||
| chr5:45682794
|
G | A | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.425+12875C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45682794 | ||||||
| chr5:45683132
|
TTTTA | T | 64 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(61): Show | 64 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.425+12533_425+1253 others(8): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45683132 | ||||||
| chr5:45683355
|
T | C | 1 | a0001c0001t0009g0003 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.425+12314A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45683355 | ||||||
| chr5:45683368
|
G | A | 1 | a0001c0001t0003g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.425+12301C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45683368 | ||||||
| chr5:45683478
|
T | C | 12 | a0001c0001t0002g0121a0001c0001t0005g0122a0001c0001t0005g0123others(9): Show | 12 | HG01261.hp2 HG01346.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.425+12191A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45683478 | ||||||
| chr5:45683484
|
G | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.425+12185C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45683484 | ||||||
| chr5:45683548
|
C | T | 1 | a0001c0001t0004g0059 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.425+12121G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45683548 | ||||||
| chr5:45683644
|
T | TAC | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.425+12024_425+1202 others(6): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45683644 | ||||||
| chr5:45683646
|
T | C | 3 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133 | 3 | HG01257.hp1 HG01258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.425+12023A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45683646 | ||||||
| chr5:45683650
|
C | T | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.425+12019G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45683650 | ||||||
| chr5:45683689
|
C | T | 1 | a0001c0001t0021g0138 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.425+11980G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45683689 | ||||||
| chr5:45683793
|
CCCAAGT | C | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0012g0137 | 3 | HG02145.hp1 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.425+11870_425+1187 others(10): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45683793 | ||||||
| chr5:45683882
|
G | A | 1 | a0001c0001t0004g0055 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.425+11787C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45683882 | ||||||
| chr5:45683933
|
AGTGCTAG others(20): Show |
A | 1 | a0001c0001t0002g0056 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.425+11709_425+1173 others(31): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45683933 | ||||||
| chr5:45684029
|
G | A | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.425+11640C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45684029 | ||||||
| chr5:45684414
|
T | A | 65 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(62): Show | 65 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.425+11255A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45684414 | ||||||
| chr5:45684950
|
T | A | 5 | a0001c0001t0003g0109a0001c0001t0003g0110a0001c0001t0003g0111others(2): Show | 5 | HG02056.hp2 NA18980.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.425+10719A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45684950 | ||||||
| chr5:45685377
|
C | G | 2 | a0001c0001t0002g0015a0001c0001t0016g0014 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.425+10292G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45685377 | ||||||
| chr5:45685436
|
G | A | 1 | a0001c0001t0006g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.425+10233C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45685436 | ||||||
| chr5:45685485
|
G | A | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.425+10184C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45685485 | ||||||
| chr5:45685489
|
G | A | 64 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(61): Show | 64 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.425+10180C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45685489 | ||||||
| chr5:45685672
|
A | G | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.425+9997T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45685672 | ||||||
| chr5:45685674
|
T | C | 1 | a0001c0001t0002g0058 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.425+9995A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45685674 | ||||||
| chr5:45685859
|
A | G | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0012g0137 | 3 | HG02145.hp1 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.425+9810T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45685859 | ||||||
| chr5:45685922
|
G | C | 2 | a0002c0002t0014g0222a0002c0002t0014g0223 | 2 | HG01433.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.425+9747C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45685922 | ||||||
| chr5:45686042
|
T | C | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.425+9627A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45686042 | ||||||
| chr5:45686123
|
A | AT | 50 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0107others(47): Show | 50 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.425+9545dupA | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45686123 | ||||||
| chr5:45686123
|
A | T | 57 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(54): Show | 57 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.425+9546T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45686123 | ||||||
| chr5:45686124
|
T | TA | 3 | a0001c0001t0007g0214a0001c0001t0013g0078a0001c0001t0013g0079 | 3 | HG02451.hp1 NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.425+9544_425+9545i others(3): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45686124 | ||||||
| chr5:45686125
|
T | A | 1 | a0002c0002t0008g0226 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.425+9544A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45686125 | ||||||
| chr5:45686292
|
C | T | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.425+9377G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45686292 | ||||||
| chr5:45686296
|
C | T | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.425+9373G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45686296 | ||||||
| chr5:45686438
|
T | G | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.425+9231A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45686438 | ||||||
| chr5:45686862
|
A | G | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.425+8807T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45686862 | ||||||
| chr5:45686867
|
T | A | 1 | a0001c0001t0019g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.425+8802A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45686867 | ||||||
| chr5:45686943
|
T | C | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.425+8726A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45686943 | ||||||
| chr5:45687002
|
TAG | T | 64 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(61): Show | 64 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.425+8665_425+8666d others(4): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45687002 | ||||||
| chr5:45687125
|
G | A | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.425+8544C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45687125 | ||||||
| chr5:45687228
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.425+8441A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45687228 | ||||||
| chr5:45687306
|
T | C | 1 | a0001c0001t0004g0068 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.425+8363A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45687306 | ||||||
| chr5:45687578
|
T | C | 41 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(38): Show | 41 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.425+8091A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45687578 | ||||||
| chr5:45688186
|
T | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.425+7483A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45688186 | ||||||
| chr5:45688374
|
C | T | 1 | a0001c0001t0002g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.425+7295G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45688374 | ||||||
| chr5:45688505
|
C | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.425+7164G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45688505 | ||||||
| chr5:45688746
|
G | A | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.425+6923C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45688746 | ||||||
| chr5:45688892
|
A | G | 1 | a0001c0001t0022g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.425+6777T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45688892 | ||||||
| chr5:45688938
|
T | C | 2 | a0003c0003t0002g0221a0003c0003t0035g0220 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.425+6731A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45688938 | ||||||
| chr5:45688981
|
C | T | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.425+6688G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45688981 | ||||||
| chr5:45689154
|
C | CA | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.425+6514dupT | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45689154 | ||||||
| chr5:45689334
|
G | C | 1 | a0001c0001t0001g0212 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.425+6335C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45689334 | ||||||
| chr5:45689345
|
C | A | 2 | a0001c0001t0002g0069a0001c0006t0002g0219 | 2 | HG01516.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.425+6324G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45689345 | ||||||
| chr5:45689615
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.425+6054G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45689615 | ||||||
| chr5:45689732
|
T | C | 1 | a0001c0001t0029g0070 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.425+5937A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45689732 | ||||||
| chr5:45689863
|
G | A | 6 | a0001c0001t0007g0115a0002c0002t0008g0224a0002c0002t0008g0225others(3): Show | 6 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.425+5806C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45689863 | ||||||
| chr5:45689877
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.425+5792G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45689877 | ||||||
| chr5:45690085
|
A | G | 141 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.425+5584T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45690085 | ||||||
| chr5:45690316
|
T | C | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.425+5353A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45690316 | ||||||
| chr5:45690892
|
G | A | 5 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226others(2): Show | 5 | HG01433.hp2 HG02055.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.425+4777C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45690892 | ||||||
| chr5:45691028
|
G | A | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.425+4641C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45691028 | ||||||
| chr5:45691044
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.425+4625T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45691044 | ||||||
| chr5:45691220
|
CG | C | 5 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.425+4448delC | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45691220 | ||||||
| chr5:45691291
|
T | C | 1 | a0001c0001t0030g0008 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.425+4378A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45691291 | ||||||
| chr5:45691627
|
T | C | 10 | a0001c0001t0002g0121a0001c0001t0005g0122a0001c0001t0005g0123others(7): Show | 10 | HG01261.hp2 HG01346.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.425+4042A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45691627 | ||||||
| chr5:45692044
|
T | G | 1 | a0001c0001t0007g0214 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.425+3625A>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45692044 | ||||||
| chr5:45692142
|
C | T | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.425+3527G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45692142 | ||||||
| chr5:45692204
|
A | C | 1 | a0001c0001t0002g0012 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.425+3465T>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45692204 | ||||||
| chr5:45692206
|
C | T | 136 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.425+3463G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45692206 | ||||||
| chr5:45692384
|
A | G | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.425+3285T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45692384 | ||||||
| chr5:45692418
|
T | TCGAGCTA others(315): Show |
2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.425+3250_425+3251i others(324): Show |
HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45692418 | ||||||
| chr5:45692528
|
C | T | 2 | a0001c0001t0013g0078a0001c0001t0013g0079 | 2 | NA18992.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.425+3141G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45692528 | ||||||
| chr5:45692753
|
A | T | 1 | a0001c0004t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.425+2916T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45692753 | ||||||
| chr5:45692755
|
C | T | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.425+2914G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45692755 | ||||||
| chr5:45692831
|
G | C | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.425+2838C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45692831 | ||||||
| chr5:45692948
|
C | A | 1 | a0001c0001t0033g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.425+2721G>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45692948 | ||||||
| chr5:45693181
|
C | T | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.425+2488G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45693181 | ||||||
| chr5:45693684
|
T | A | 3 | a0002c0002t0008g0224a0002c0002t0008g0225a0002c0002t0008g0226 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.425+1985A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45693684 | ||||||
| chr5:45693686
|
C | T | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.425+1983G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45693686 | ||||||
| chr5:45693991
|
T | C | 1 | a0001c0001t0007g0214 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.425+1678A>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45693991 | ||||||
| chr5:45694164
|
A | G | 1 | a0001c0001t0001g0073 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.425+1505T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45694164 | ||||||
| chr5:45694170
|
A | T | 1 | a0001c0001t0001g0011 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.425+1499T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45694170 | ||||||
| chr5:45694184
|
A | T | 1 | a0001c0001t0002g0072 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.425+1485T>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45694184 | ||||||
| chr5:45694254
|
A | G | 1 | a0001c0001t0026g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.425+1415T>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45694254 | ||||||
| chr5:45694473
|
C | G | 64 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(61): Show | 64 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.425+1196G>C | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45694473 | ||||||
| chr5:45694476
|
T | A | 1 | a0001c0001t0007g0214 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.425+1193A>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45694476 | ||||||
| chr5:45694722
|
C | T | 2 | a0001c0001t0031g0009a0001c0001t0032g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.425+947G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45694722 | ||||||
| chr5:45694734
|
G | C | 1 | a0001c0001t0003g0215 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.425+935C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45694734 | ||||||
| chr5:45694878
|
C | T | 1 | a0001c0001t0030g0008 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.425+791G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45694878 | ||||||
| chr5:45695013
|
C | T | 1 | a0001c0001t0024g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.425+656G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45695013 | ||||||
| chr5:45695014
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.425+655C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45695014 | ||||||
| chr5:45695052
|
C | T | 1 | a0003c0003t0035g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.425+617G>A | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45695052 | ||||||
| chr5:45695200
|
G | C | 1 | a0001c0001t0025g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.425+469C>G | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45695200 | ||||||
| chr5:45695511
|
G | A | 1 | a0001c0001t0039g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.425+158C>T | HCN1 | ENSG00000164588.8 | transcript | ENST00000303230.6 | protein_coding | 1/7 | chr5 | 45695511 |