| geneid | 163882 |
|---|---|
| ensemblid | ENSG00000162852.14 |
| hgncid | 26486 |
| symbol | CNST |
| name | consortin, connexin sorting protein |
| refseq_nuc | NM_152609.3 |
| refseq_prot | NP_689822.2 |
| ensembl_nuc | ENST00000366513.9 |
| ensembl_prot | ENSP00000355470.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 246566456 |
| end | 246668595 |
| strand | + |
| ver | v1.2 |
| region | chr1:246566456-246668595 |
| region5000 | chr1:246561456-246673595 |
| regionname0 | CNST_chr1_246566456_246668595 |
| regionname5000 | CNST_chr1_246561456_246673595 |
| 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 | 0/1 | 725 | 253 | 59 | 64 | 85 | 13 | 31 | 58 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0002 | 1/0 | 725 | 43 | 13 | 6 | 18 | 3 | 2 | 11 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0003 | 0/0 | 725 | 12 | 10 | 2 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0004 | 0/0 | 725 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0005 | 0/0 | 725 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0006 | 0/0 | 725 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0007 | 0/0 | 725 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0008 | 0/0 | 725 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0009 | 0/0 | 725 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0010 | 0/0 | 725 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| 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 | 0/1 | 2178 | 250 | 58 | 64 | 83 | 13 | 31 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| c0002 | 1/0 | 2178 | 43 | 13 | 6 | 18 | 3 | 2 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| c0003 | 0/0 | 2178 | 12 | 10 | 2 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| c0004 | 0/0 | 2178 | 6 | 6 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| c0005 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| c0006 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| c0007 | 0/0 | 2178 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| c0008 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| c0009 | 0/0 | 2178 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| c0010 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| c0011 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| c0012 | 0/0 | 2178 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| c0013 | 0/0 | 2178 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| 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 | 0/0 | 2950 | 133 | 36 | 28 | 50 | 9 | 10 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| t0002 | 1/1 | 2950 | 67 | 4 | 23 | 24 | 4 | 10 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| t0003 | 0/0 | 2950 | 53 | 7 | 13 | 19 | 3 | 11 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| t0004 | 0/0 | 2950 | 26 | 24 | 2 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| t0005 | 0/0 | 2950 | 5 | 4 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| t0006 | 0/0 | 2950 | 3 | 3 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| t0007 | 0/0 | 2950 | 3 | 0 | 0 | 3 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| t0008 | 0/0 | 2950 | 3 | 3 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| t0009 | 0/0 | 2950 | 3 | 3 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| t0010 | 0/0 | 2950 | 3 | 0 | 0 | 3 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| t0011 | 0/0 | 2950 | 3 | 1 | 1 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| t0012 | 0/0 | 2950 | 2 | 0 | 2 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| t0013 | 0/0 | 2950 | 2 | 2 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| t0014 | 0/0 | 2950 | 2 | 0 | 0 | 2 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| t0015 | 0/0 | 2950 | 2 | 2 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| t0016 | 0/0 | 2950 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| t0017 | 0/0 | 2950 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| t0018 | 0/0 | 2950 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| t0019 | 0/0 | 2950 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| t0020 | 0/0 | 2950 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| t0021 | 0/0 | 2950 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| t0022 | 0/0 | 2950 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| t0023 | 0/0 | 2950 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| t0024 | 0/0 | 2950 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| t0025 | 0/0 | 2950 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| 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 | 2 | 0 | 2 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0107 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0178 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| 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 | 0/1 | 2178 | 250 | 58 | 64 | 83 | 13 | 31 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0001c0006 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0001c0009 | 0/0 | 2178 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0001c0012 | 0/0 | 2178 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0002c0002 | 1/0 | 2178 | 43 | 13 | 6 | 18 | 3 | 2 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0003c0003 | 0/0 | 2178 | 12 | 10 | 2 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0004c0004 | 0/0 | 2178 | 6 | 6 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0005c0013 | 0/0 | 2178 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0006c0005 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0007c0011 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0008c0007 | 0/0 | 2178 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0009c0008 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0010c0010 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5127 | 89 | 19 | 21 | 34 | 7 | 8 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0001c0001t0002 | 0/1 | 5127 | 61 | 3 | 23 | 21 | 3 | 10 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0001c0001t0003 | 0/0 | 5127 | 47 | 2 | 13 | 19 | 3 | 10 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0001c0001t0004 | 0/0 | 5127 | 22 | 21 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0001c0001t0005 | 0/0 | 5127 | 5 | 4 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0001c0001t0007 | 0/0 | 5127 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0001c0001t0008 | 0/0 | 5127 | 3 | 3 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0001c0001t0009 | 0/0 | 5127 | 3 | 3 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0001c0001t0010 | 0/0 | 5127 | 3 | 0 | 0 | 3 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0001c0001t0011 | 0/0 | 5127 | 3 | 1 | 1 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0001c0001t0012 | 0/0 | 5127 | 2 | 0 | 2 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0001c0001t0013 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0001c0001t0014 | 0/0 | 5127 | 2 | 0 | 0 | 2 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0001c0001t0016 | 0/0 | 5127 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0001c0001t0017 | 0/0 | 5127 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0001c0001t0018 | 0/0 | 5127 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0001c0001t0019 | 0/0 | 5127 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0001c0001t0020 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0001c0001t0022 | 0/0 | 5127 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0001c0001t0024 | 0/0 | 5127 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0001c0001t0025 | 0/0 | 5127 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0001c0006t0001 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0001c0009t0001 | 0/0 | 5127 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0001c0012t0002 | 0/0 | 5127 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0002c0002t0001 | 0/0 | 5127 | 32 | 8 | 6 | 14 | 2 | 2 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0002c0002t0002 | 1/0 | 5127 | 4 | 0 | 0 | 2 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0002c0002t0006 | 0/0 | 5127 | 3 | 3 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0002c0002t0007 | 0/0 | 5127 | 2 | 0 | 0 | 2 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0002c0002t0013 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0002c0002t0015 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0003c0003t0001 | 0/0 | 5127 | 8 | 7 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0003c0003t0004 | 0/0 | 5127 | 4 | 3 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0004c0004t0003 | 0/0 | 5127 | 5 | 5 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0004c0004t0021 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0005c0013t0001 | 0/0 | 5127 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0006c0005t0023 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0007c0011t0015 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0008c0007t0003 | 0/0 | 5127 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0009c0008t0001 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| a0010c0010t0002 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | copy fasta | chr1 | 246561456 | 246673595 |
| 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 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0107 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0005g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0007g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0008g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0008g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0008g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0009g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0009g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0009g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0010g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0010g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0010g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0011g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0011g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0011g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0012g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0013g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0014g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0014g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0016g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0017g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0018g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0019g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0020g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0022g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0024g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0025g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0006t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0009t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0012t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0002g0178 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0007g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0013g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0015g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0003c0003t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0003c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0003c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0003c0003t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0003c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0003c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0003c0003t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0003c0003t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0003c0003t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0003c0003t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0003c0003t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0003c0003t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0004c0004t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0004c0004t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0004c0004t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0004c0004t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0004c0004t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0004c0004t0021g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0005c0013t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0006c0005t0023g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0007c0011t0015g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0008c0007t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0009c0008t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0010c0010t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | GBR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0103 | EUR | GBR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0056 | EUR | FIN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0265 | EUR | FIN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0200 | EUR | FIN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0306 | EUR | FIN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | CHS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | CHS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | CHS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00423 | hp2 | a0001 | c0001 | t0014 | g0165 | EAS | CHS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | CHS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00558 | hp2 | a0001 | c0001 | t0010 | g0229 | EAS | CHS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0126 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0276 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | CHS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | CHS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00733 | hp1 | a0003 | c0003 | t0001 | g0041 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0096 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01069 | hp2 | a0001 | c0001 | t0012 | g0001 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01071 | hp1 | a0001 | c0001 | t0012 | g0001 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0108 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0158 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0104 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0151 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0067 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0285 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01243 | hp1 | a0003 | c0003 | t0004 | g0035 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01243 | hp2 | a0001 | c0001 | t0016 | g0136 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0065 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0047 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0048 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0268 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0204 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | IBS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0055 | EUR | IBS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | IBS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0282 | EUR | IBS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | IBS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0174 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01891 | hp2 | a0003 | c0003 | t0001 | g0039 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01934 | hp1 | a0001 | c0001 | t0011 | g0212 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0050 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0247 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0092 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01981 | hp1 | a0001 | c0001 | t0017 | g0008 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0069 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0068 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0118 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02080 | hp2 | a0001 | c0001 | t0010 | g0286 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02083 | hp1 | a0001 | c0001 | t0007 | g0062 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02129 | hp2 | a0001 | c0001 | t0010 | g0230 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0297 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0181 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0070 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0275 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02257 | hp2 | a0003 | c0003 | t0001 | g0040 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0150 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0157 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0051 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0066 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02451 | hp1 | a0003 | c0003 | t0001 | g0033 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02451 | hp2 | a0004 | c0004 | t0003 | g0192 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0105 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02615 | hp1 | a0002 | c0002 | t0006 | g0030 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02622 | hp1 | a0002 | c0002 | t0015 | g0168 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02622 | hp2 | a0002 | c0002 | t0006 | g0031 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02630 | hp2 | a0004 | c0004 | t0021 | g0152 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02647 | hp2 | a0001 | c0001 | t0008 | g0021 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0146 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0262 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0109 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02717 | hp1 | a0003 | c0003 | t0004 | g0162 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02723 | hp1 | a0003 | c0003 | t0001 | g0038 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0145 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02818 | hp2 | a0004 | c0004 | t0003 | g0119 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02896 | hp1 | a0003 | c0003 | t0004 | g0036 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02896 | hp2 | a0004 | c0004 | t0003 | g0184 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0134 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02897 | hp2 | a0004 | c0004 | t0003 | g0185 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02922 | hp2 | a0010 | c0010 | t0002 | g0028 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02965 | hp1 | a0001 | c0001 | t0013 | g0196 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02965 | hp2 | a0001 | c0001 | t0008 | g0176 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0010 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0317 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03017 | hp2 | a0008 | c0007 | t0003 | g0267 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0013 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03098 | hp1 | a0003 | c0003 | t0001 | g0037 | AFR | MSL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0155 | AFR | MSL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03130 | hp1 | a0003 | c0003 | t0001 | g0044 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03139 | hp1 | a0001 | c0001 | t0009 | g0012 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0203 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0130 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03209 | hp1 | a0001 | c0001 | t0020 | g0024 | AFR | MSL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03209 | hp2 | a0006 | c0005 | t0023 | g0043 | AFR | MSL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0122 | AFR | MSL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03225 | hp2 | a0002 | c0002 | t0013 | g0179 | AFR | MSL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03239 | hp2 | a0001 | c0001 | t0022 | g0085 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03486 | hp1 | a0007 | c0011 | t0015 | g0213 | AFR | MSL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03486 | hp2 | a0002 | c0002 | t0006 | g0029 | AFR | MSL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0154 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0180 | AFR | MSL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03579 | hp2 | a0003 | c0003 | t0001 | g0032 | AFR | MSL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0238 | SAS | STU | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0220 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0259 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | BEB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0270 | SAS | BEB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0131 | SAS | BEB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0209 | SAS | STU | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0284 | SAS | STU | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0281 | SAS | BEB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0258 | SAS | STU | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0250 | SAS | STU | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0206 | SAS | STU | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0316 | SAS | STU | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG04228 | hp1 | a0001 | c0001 | t0019 | g0106 | SAS | STU | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0084 | SAS | STU | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18522 | hp2 | a0003 | c0003 | t0004 | g0034 | AFR | YRI | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | CHB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18612 | hp2 | a0002 | c0002 | t0007 | g0143 | EAS | CHB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | CHB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0124 | EAS | CHB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0020 | AFR | YRI | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0127 | AFR | YRI | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18943 | hp2 | a0001 | c0012 | t0002 | g0278 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0113 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0251 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18952 | hp1 | a0001 | c0009 | t0001 | g0191 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18960 | hp1 | a0001 | c0001 | t0025 | g0288 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18971 | hp1 | a0001 | c0001 | t0011 | g0221 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18979 | hp2 | a0002 | c0002 | t0007 | g0142 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19009 | hp1 | a0001 | c0001 | t0014 | g0164 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0294 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | LWK | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0100 | AFR | LWK | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | LWK | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0133 | AFR | LWK | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19085 | hp2 | a0005 | c0013 | t0001 | g0138 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0205 | AFR | YRI | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ASW | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0292 | AFR | ASW | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0148 | EUR | TSI | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0123 | EUR | TSI | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0057 | EUR | TSI | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0163 | EUR | TSI | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0063 | SAS | GIH | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA20905 | hp2 | a0001 | c0001 | t0024 | g0269 | SAS | GIH | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0153 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0171 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02486 | hp2 | a0001 | c0006 | t0001 | g0009 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0147 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0159 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03471 | hp2 | a0004 | c0004 | t0003 | g0193 | AFR | MSL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0117 | AFR | USA | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | USA | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18955 | hp2 | a0001 | c0001 | t0018 | g0256 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0173 | AFR | USA | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA20300 | hp2 | a0001 | c0001 | t0011 | g0208 | AFR | USA | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA21309 | hp1 | a0009 | c0008 | t0001 | g0161 | AFR | LWK | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | LWK | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0107 | REF | REF | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0178 | REF | REF | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:246591579
|
C | G | 1 | a0005 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.17C>G | p.Thr6Ser | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/11 | 276/5127 | 17/2178 | 6/725 | chr1 | 246591579 | ||
| chr1:246591645
|
G | A | 2 | a0003a0006 | 13 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
missense_variant | MODERATE | c.83G>A | p.Ser28Asn | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/11 | 342/5127 | 83/2178 | 28/725 | chr1 | 246591645 | ||
| chr1:246591822
|
T | C | 5 | a0001a0004a0008others(2): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
missense_variant | MODERATE | c.260T>C | p.Leu87Ser | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/11 | 519/5127 | 260/2178 | 87/725 | chr1 | 246591822 | ||
| chr1:246591902
|
C | T | 1 | a0010 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.340C>T | p.Pro114Ser | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/11 | 599/5127 | 340/2178 | 114/725 | chr1 | 246591902 | ||
| chr1:246621597
|
A | G | 1 | a0004 | 6 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
missense_variant | MODERATE | c.548A>G | p.Gln183Arg | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/11 | 807/5127 | 548/2178 | 183/725 | chr1 | 246621597 | ||
| chr1:246634514
|
C | G | 1 | a0007 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.745C>G | p.Leu249Val | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/11 | 1004/5127 | 745/2178 | 249/725 | chr1 | 246634514 | ||
| chr1:246641963
|
A | G | 1 | a0009 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.863A>G | p.Gln288Arg | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/11 | 1122/5127 | 863/2178 | 288/725 | chr1 | 246641963 | ||
| chr1:246647186
|
A | C | 1 | a0006 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.985A>C | p.Thr329Pro | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/11 | 1244/5127 | 985/2178 | 329/725 | chr1 | 246647186 | ||
| chr1:246647396
|
C | T | 1 | a0004 | 6 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
missense_variant | MODERATE | c.1195C>T | p.Arg399Cys | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/11 | 1454/5127 | 1195/2178 | 399/725 | chr1 | 246647396 | ||
| chr1:246660289
|
A | C | 1 | a0008 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.1927A>C | p.Lys643Gln | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/11 | 2186/5127 | 1927/2178 | 643/725 | chr1 | 246660289 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:246591718
|
C | T | 1 | a0001c0012 | 1 | NA18943.hp2 | synonymous_variant | LOW | c.156C>T | p.Thr52Thr | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/11 | 415/5127 | 156/2178 | 52/725 | chr1 | 246591718 | ||
| chr1:246633994
|
C | T | 1 | a0001c0009 | 1 | NA18952.hp1 | synonymous_variant | LOW | c.687C>T | p.Ala229Ala | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 5/11 | 946/5127 | 687/2178 | 229/725 | chr1 | 246633994 | ||
| chr1:246647290
|
G | A | 1 | a0001c0006 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.1089G>A | p.Leu363Leu | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/11 | 1348/5127 | 1089/2178 | 363/725 | chr1 | 246647290 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:246566584
|
G | A | 1 | a0001c0001t0016 | 1 | HG01243.hp2 | 5_prime_UTR_variant | MODIFIER | c.-131G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/11 | 24979 | chr1 | 246566584 | |||||
| chr1:246566590
|
C | A | 2 | a0001c0001t0017a0002c0002t0006 | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-125C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/11 | 24973 | chr1 | 246566590 | |||||
| chr1:246666020
|
G | A | 2 | a0001c0001t0007a0002c0002t0007 | 3 | HG02083.hp1 NA18612.hp2 NA18979.hp2 |
3_prime_UTR_variant | MODIFIER | c.*115G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 115 | chr1 | 246666020 | |||||
| chr1:246666168
|
T | G | 1 | a0001c0001t0018 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*263T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 263 | chr1 | 246666168 | |||||
| chr1:246666307
|
A | G | 1 | a0001c0001t0025 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*402A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 402 | chr1 | 246666307 | |||||
| chr1:246666314
|
T | C | 22 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(19): Show | 205 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*409T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 409 | chr1 | 246666314 | |||||
| chr1:246666380
|
T | A | 1 | a0001c0001t0008 | 3 | HG02647.hp2 HG02965.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*475T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 475 | chr1 | 246666380 | |||||
| chr1:246666440
|
T | C | 31 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(28): Show | 244 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*535T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 535 | chr1 | 246666440 | |||||
| chr1:246666459
|
A | G | 1 | a0001c0001t0009 | 3 | HG02976.hp1 HG03041.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*554A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 554 | chr1 | 246666459 | |||||
| chr1:246666468
|
C | T | 1 | a0001c0001t0011 | 3 | HG01934.hp1 NA18971.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*563C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 563 | chr1 | 246666468 | |||||
| chr1:246666553
|
T | C | 1 | a0001c0001t0012 | 2 | HG01069.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*648T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 648 | chr1 | 246666553 | |||||
| chr1:246666571
|
G | A | 22 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(19): Show | 205 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*666G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 666 | chr1 | 246666571 | |||||
| chr1:246666656
|
A | T | 1 | a0001c0001t0008 | 3 | HG02647.hp2 HG02965.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*751A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 751 | chr1 | 246666656 | |||||
| chr1:246666715
|
C | T | 5 | a0001c0001t0004a0001c0001t0009a0001c0001t0016others(2): Show | 33 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*810C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 810 | chr1 | 246666715 | |||||
| chr1:246666732
|
G | C | 1 | a0001c0001t0019 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*827G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 827 | chr1 | 246666732 | |||||
| chr1:246666991
|
A | G | 31 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(28): Show | 244 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*1086A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 1086 | chr1 | 246666991 | |||||
| chr1:246666999
|
A | G | 1 | a0001c0001t0014 | 2 | HG00423.hp2 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1094A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 1094 | chr1 | 246666999 | |||||
| chr1:246667186
|
T | C | 31 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(28): Show | 244 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*1281T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 1281 | chr1 | 246667186 | |||||
| chr1:246667325
|
T | C | 3 | a0001c0001t0005a0001c0001t0013a0002c0002t0013 | 7 | HG01433.hp1 HG02965.hp1 HG03098.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1420T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 1420 | chr1 | 246667325 | |||||
| chr1:246667422
|
C | T | 2 | a0001c0001t0022a0004c0004t0021 | 2 | HG02630.hp2 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1517C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 1517 | chr1 | 246667422 | |||||
| chr1:246667725
|
A | G | 1 | a0001c0001t0020 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1820A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 1820 | chr1 | 246667725 | |||||
| chr1:246667751
|
C | T | 1 | a0001c0001t0010 | 3 | HG00558.hp2 HG02080.hp2 HG02129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1846C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 1846 | chr1 | 246667751 | |||||
| chr1:246667752
|
A | G | 2 | a0001c0001t0013a0002c0002t0013 | 2 | HG02965.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1847A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 1847 | chr1 | 246667752 | |||||
| chr1:246667946
|
C | T | 3 | a0001c0001t0008a0002c0002t0015a0007c0011t0015 | 5 | HG02622.hp1 HG02647.hp2 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2041C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 2041 | chr1 | 246667946 | |||||
| chr1:246668054
|
G | A | 6 | a0001c0001t0003a0001c0001t0012a0001c0001t0014others(3): Show | 58 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*2149G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 2149 | chr1 | 246668054 | |||||
| chr1:246668060
|
G | A | 1 | a0001c0001t0024 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2155G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 2155 | chr1 | 246668060 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:246566688
|
A | G | 125 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0001g0198others(122): Show | 125 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.-52+25A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246566688 | ||||||
| chr1:246566777
|
C | T | 1 | a0001c0001t0001g0318 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-52+114C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246566777 | ||||||
| chr1:246566788
|
G | C | 291 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(288): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.-52+125G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246566788 | ||||||
| chr1:246566872
|
C | G | 1 | a0001c0001t0001g0166 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-52+209C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246566872 | ||||||
| chr1:246566931
|
C | A | 1 | a0001c0001t0003g0003 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-52+268C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246566931 | ||||||
| chr1:246567059
|
T | G | 1 | a0001c0001t0004g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-52+396T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246567059 | ||||||
| chr1:246567062
|
C | T | 2 | a0001c0001t0014g0164a0001c0001t0014g0165 | 2 | HG00423.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-52+399C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246567062 | ||||||
| chr1:246567090
|
G | A | 5 | a0001c0001t0001g0167a0001c0001t0001g0169a0001c0001t0001g0170others(2): Show | 5 | HG02486.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+427G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246567090 | ||||||
| chr1:246567165
|
A | G | 2 | a0001c0001t0003g0316a0001c0001t0003g0317 | 2 | HG03017.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-52+502A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246567165 | ||||||
| chr1:246567353
|
C | CT | 132 | a0001c0001t0001g0156a0001c0001t0001g0160a0001c0001t0001g0202others(129): Show | 132 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.-52+701dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246567353 | |||||
| chr1:246567384
|
A | G | 2 | a0001c0001t0001g0314a0001c0001t0002g0315 | 2 | HG00673.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.-52+721A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246567384 | ||||||
| chr1:246567435
|
C | G | 23 | a0001c0001t0001g0198a0001c0001t0001g0293a0001c0001t0001g0295others(20): Show | 23 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(20): Show |
intron_variant | MODIFIER | c.-52+772C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246567435 | ||||||
| chr1:246567435
|
C | T | 52 | a0001c0001t0001g0121a0001c0001t0001g0128a0001c0001t0001g0132others(49): Show | 53 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.-52+772C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246567435 | ||||||
| chr1:246567591
|
C | T | 1 | a0001c0001t0003g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-52+928C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246567591 | ||||||
| chr1:246567614
|
C | T | 3 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0002g0097 | 3 | HG00642.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-52+951C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246567614 | ||||||
| chr1:246567782
|
C | T | 1 | a0002c0002t0001g0149 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-52+1119C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246567782 | ||||||
| chr1:246567788
|
GAC | G | 4 | a0001c0001t0001g0167a0001c0001t0001g0169a0001c0001t0001g0170others(1): Show | 4 | HG02622.hp1 HG02809.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+1127_-52+1128d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246567788 | |||||
| chr1:246567807
|
CTT | C | 5 | a0001c0001t0001g0293a0001c0001t0001g0295a0001c0001t0001g0296others(2): Show | 5 | HG00621.hp1 HG02135.hp1 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.-52+1146_-52+1147d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246567807 | |||||
| chr1:246568001
|
T | A | 135 | a0001c0001t0001g0156a0001c0001t0001g0160a0001c0001t0001g0194others(132): Show | 135 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.-52+1338T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246568001 | ||||||
| chr1:246568039
|
G | A | 1 | a0001c0001t0001g0298 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-52+1376G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246568039 | ||||||
| chr1:246568202
|
A | G | 1 | a0001c0001t0003g0096 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-52+1539A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246568202 | ||||||
| chr1:246568520
|
G | T | 1 | a0001c0001t0001g0291 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-52+1857G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246568520 | ||||||
| chr1:246568624
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-52+1961C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246568624 | ||||||
| chr1:246568625
|
G | A | 1 | a0001c0001t0004g0007 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-52+1962G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246568625 | ||||||
| chr1:246568668
|
C | T | 13 | a0001c0001t0001g0312a0001c0001t0002g0186a0001c0001t0002g0187others(10): Show | 13 | HG00423.hp1 HG02451.hp2 HG02896.hp2 others(10): Show |
intron_variant | MODIFIER | c.-52+2005C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246568668 | ||||||
| chr1:246568947
|
T | C | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-52+2284T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246568947 | ||||||
| chr1:246569022
|
C | T | 1 | a0001c0001t0025g0288 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-52+2359C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246569022 | ||||||
| chr1:246569156
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-52+2493A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246569156 | ||||||
| chr1:246569175
|
C | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-52+2512C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246569175 | ||||||
| chr1:246569208
|
G | A | 139 | a0001c0001t0001g0156a0001c0001t0001g0160a0001c0001t0001g0194others(136): Show | 139 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.-52+2545G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246569208 | ||||||
| chr1:246569511
|
C | T | 44 | a0001c0001t0001g0121a0001c0001t0001g0128a0001c0001t0001g0132others(41): Show | 44 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.-52+2848C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246569511 | ||||||
| chr1:246569645
|
G | A | 8 | a0001c0001t0002g0002a0001c0001t0002g0101a0001c0001t0002g0102others(5): Show | 9 | HG00140.hp2 HG00733.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.-52+2982G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246569645 | ||||||
| chr1:246569755
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-52+3092C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246569755 | ||||||
| chr1:246569776
|
A | C | 4 | a0001c0001t0002g0172a0001c0001t0002g0175a0001c0001t0004g0173others(1): Show | 4 | HG01884.hp2 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+3113A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246569776 | ||||||
| chr1:246570069
|
A | G | 13 | a0001c0001t0001g0312a0001c0001t0002g0186a0001c0001t0002g0187others(10): Show | 13 | HG00423.hp1 HG02451.hp2 HG02896.hp2 others(10): Show |
intron_variant | MODIFIER | c.-52+3406A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246570069 | ||||||
| chr1:246570177
|
A | G | 1 | a0001c0001t0003g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-52+3514A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246570177 | ||||||
| chr1:246570266
|
C | T | 1 | a0004c0004t0003g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-52+3603C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246570266 | ||||||
| chr1:246570568
|
A | C | 76 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(73): Show | 77 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.-52+3905A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246570568 | ||||||
| chr1:246570674
|
G | T | 89 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(86): Show | 90 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.-52+4011G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246570674 | ||||||
| chr1:246570679
|
A | G | 89 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(86): Show | 90 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.-52+4016A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246570679 | ||||||
| chr1:246570680
|
T | TGA | 89 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(86): Show | 90 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.-52+4017_-52+4018i others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246570680 | ||||||
| chr1:246570681
|
A | G | 89 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(86): Show | 90 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.-52+4018A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246570681 | ||||||
| chr1:246570697
|
T | A | 1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-52+4034T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246570697 | ||||||
| chr1:246570795
|
A | C | 4 | a0001c0001t0002g0172a0001c0001t0002g0175a0001c0001t0004g0173others(1): Show | 4 | HG01884.hp2 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+4132A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246570795 | ||||||
| chr1:246570897
|
C | T | 2 | a0002c0002t0001g0147a0002c0002t0001g0148 | 2 | HG02559.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-52+4234C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246570897 | ||||||
| chr1:246571185
|
C | T | 135 | a0001c0001t0001g0156a0001c0001t0001g0160a0001c0001t0001g0194others(132): Show | 135 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.-52+4522C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246571185 | ||||||
| chr1:246571350
|
A | G | 8 | a0001c0001t0002g0002a0001c0001t0002g0101a0001c0001t0002g0102others(5): Show | 9 | HG00140.hp2 HG00733.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.-52+4687A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246571350 | ||||||
| chr1:246571452
|
A | G | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+4789A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246571452 | ||||||
| chr1:246571685
|
ATTTACTT others(9): Show |
A | 1 | a0001c0001t0002g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-52+5023_-52+5038d others(18): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246571685 | ||||||
| chr1:246572093
|
C | T | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-52+5430C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246572093 | ||||||
| chr1:246572162
|
G | A | 1 | a0001c0001t0002g0201 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-52+5499G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246572162 | ||||||
| chr1:246572224
|
G | T | 7 | a0001c0001t0004g0042a0003c0003t0001g0038a0003c0003t0001g0039others(4): Show | 7 | HG00733.hp1 HG01891.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-52+5561G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246572224 | ||||||
| chr1:246572251
|
A | G | 1 | a0010c0010t0002g0028 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-52+5588A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246572251 | ||||||
| chr1:246572262
|
A | G | 1 | a0001c0001t0003g0092 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-52+5599A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246572262 | ||||||
| chr1:246572532
|
T | TTAAA | 308 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(305): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.-52+5871_-52+5872i others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246572532 | |||||
| chr1:246572601
|
T | C | 53 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(50): Show | 54 | HG00280.hp1 HG00423.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.-52+5938T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246572601 | ||||||
| chr1:246572631
|
G | A | 1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-52+5968G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246572631 | ||||||
| chr1:246572722
|
T | A | 1 | a0001c0001t0009g0010 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-52+6059T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246572722 | ||||||
| chr1:246572831
|
G | A | 2 | a0001c0001t0001g0011a0010c0010t0002g0028 | 2 | HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-52+6168G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246572831 | ||||||
| chr1:246572917
|
T | C | 12 | a0001c0001t0004g0042a0003c0003t0001g0032a0003c0003t0001g0033others(9): Show | 12 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-52+6254T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246572917 | ||||||
| chr1:246572968
|
C | T | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+6305C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246572968 | ||||||
| chr1:246573018
|
G | T | 3 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0002g0097 | 3 | HG00642.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-52+6355G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246573018 | ||||||
| chr1:246573025
|
C | T | 13 | a0001c0001t0004g0042a0003c0003t0001g0032a0003c0003t0001g0033others(10): Show | 13 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-52+6362C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246573025 | ||||||
| chr1:246573113
|
C | A | 3 | a0001c0001t0003g0109a0002c0002t0001g0108a0002c0002t0001g0200 | 3 | HG00323.hp1 HG01074.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.-52+6450C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246573113 | ||||||
| chr1:246573270
|
A | G | 1 | a0001c0001t0004g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-52+6607A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246573270 | ||||||
| chr1:246573280
|
C | T | 2 | a0001c0001t0001g0011a0010c0010t0002g0028 | 2 | HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-52+6617C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246573280 | ||||||
| chr1:246573521
|
T | G | 1 | a0001c0001t0001g0194 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-52+6858T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246573521 | ||||||
| chr1:246573624
|
G | A | 306 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(303): Show | 308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.-52+6961G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246573624 | ||||||
| chr1:246573687
|
T | C | 1 | a0001c0001t0004g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-52+7024T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246573687 | ||||||
| chr1:246573784
|
C | T | 4 | a0002c0002t0001g0145a0002c0002t0001g0146a0002c0002t0001g0147others(1): Show | 4 | HG02559.hp1 HG02683.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+7121C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246573784 | ||||||
| chr1:246573785
|
G | A | 4 | a0001c0001t0001g0202a0001c0001t0005g0203a0001c0001t0005g0204others(1): Show | 4 | HG01261.hp1 HG01433.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+7122G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246573785 | ||||||
| chr1:246573861
|
G | GA | 53 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(50): Show | 54 | HG00280.hp1 HG00423.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.-52+7204dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246573861 | |||||
| chr1:246573992
|
C | T | 2 | a0001c0001t0001g0011a0010c0010t0002g0028 | 2 | HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-52+7329C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246573992 | ||||||
| chr1:246574047
|
T | C | 1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-52+7384T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574047 | ||||||
| chr1:246574171
|
G | A | 1 | a0001c0001t0001g0293 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-52+7508G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574171 | ||||||
| chr1:246574185
|
G | A | 1 | a0002c0002t0001g0110 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-52+7522G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574185 | ||||||
| chr1:246574235
|
A | C | 1 | a0002c0002t0001g0110 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-52+7572A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574235 | ||||||
| chr1:246574275
|
T | C | 13 | a0001c0001t0004g0042a0003c0003t0001g0032a0003c0003t0001g0033others(10): Show | 13 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-52+7612T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574275 | ||||||
| chr1:246574331
|
G | A | 2 | a0001c0001t0001g0314a0001c0001t0002g0315 | 2 | HG00673.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.-52+7668G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574331 | ||||||
| chr1:246574434
|
A | T | 1 | a0001c0001t0010g0286 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-52+7771A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574434 | ||||||
| chr1:246574438
|
T | G | 1 | a0001c0001t0003g0206 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-52+7775T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574438 | ||||||
| chr1:246574445
|
A | G | 1 | a0001c0001t0002g0285 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-52+7782A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574445 | ||||||
| chr1:246574530
|
A | G | 1 | a0001c0001t0002g0083 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-52+7867A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574530 | ||||||
| chr1:246574530
|
A | T | 1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-52+7867A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574530 | ||||||
| chr1:246574808
|
GTCCT | G | 6 | a0001c0001t0002g0097a0001c0001t0002g0101a0001c0001t0002g0102others(3): Show | 6 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52+8150_-52+8153d others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246574808 | |||||
| chr1:246574827
|
T | C | 13 | a0001c0001t0001g0312a0001c0001t0002g0186a0001c0001t0002g0187others(10): Show | 13 | HG00423.hp1 HG02451.hp2 HG02896.hp2 others(10): Show |
intron_variant | MODIFIER | c.-52+8164T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574827 | ||||||
| chr1:246574839
|
T | C | 7 | a0002c0002t0001g0111a0002c0002t0001g0112a0002c0002t0001g0114others(4): Show | 7 | HG02040.hp1 HG02074.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.-52+8176T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574839 | ||||||
| chr1:246574842
|
C | T | 314 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(311): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.-52+8179C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574842 | ||||||
| chr1:246574908
|
A | G | 2 | a0001c0001t0003g0081a0001c0001t0003g0082 | 2 | NA18943.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-52+8245A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574908 | ||||||
| chr1:246574938
|
C | G | 8 | a0001c0001t0003g0144a0002c0002t0001g0110a0002c0002t0001g0139others(5): Show | 8 | HG02129.hp1 NA18612.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.-52+8275C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574938 | ||||||
| chr1:246574972
|
T | TTTTA | 61 | a0001c0001t0001g0076a0001c0001t0001g0089a0001c0001t0001g0090others(58): Show | 61 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.-52+8345_-52+8348d others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246574972 | |||||
| chr1:246574972
|
T | TTTTATTT others(1): Show |
132 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(129): Show | 133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-52+8341_-52+8348d others(10): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246574972 | |||||
| chr1:246574972
|
T | TTTTATTT others(5): Show |
90 | a0001c0001t0001g0210a0001c0001t0001g0215a0001c0001t0001g0216others(87): Show | 91 | HG00558.hp1 HG00558.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.-52+8337_-52+8348d others(14): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246574972 | |||||
| chr1:246574972
|
T | TTTTATTT others(9): Show |
2 | a0001c0001t0001g0207a0001c0001t0011g0208 | 2 | HG02040.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-52+8333_-52+8348d others(18): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246574972 | |||||
| chr1:246574972
|
TTTTA | T | 14 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0177others(11): Show | 14 | HG00735.hp1 HG00741.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-52+8345_-52+8348d others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246574972 | |||||
| chr1:246574972
|
TTTTATTT others(1): Show |
T | 4 | a0001c0001t0004g0004a0003c0003t0004g0034a0003c0003t0004g0035others(1): Show | 4 | HG01243.hp1 HG02896.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+8341_-52+8348d others(10): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246574972 | |||||
| chr1:246574972
|
TTTTATTT others(5): Show |
T | 1 | a0001c0001t0010g0286 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-52+8337_-52+8348d others(14): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246574972 | |||||
| chr1:246574976
|
A | ATTTATTT others(5): Show |
1 | a0001c0001t0002g0080 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-52+8324_-52+8325i others(14): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246574976 | |||||
| chr1:246575057
|
A | G | 44 | a0001c0001t0001g0121a0001c0001t0001g0128a0001c0001t0001g0132others(41): Show | 44 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.-52+8394A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246575057 | ||||||
| chr1:246575376
|
C | A | 1 | a0010c0010t0002g0028 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-52+8713C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246575376 | ||||||
| chr1:246575411
|
A | C | 1 | a0001c0001t0001g0177 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-52+8748A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246575411 | ||||||
| chr1:246575432
|
G | C | 2 | a0001c0001t0001g0011a0010c0010t0002g0028 | 2 | HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-52+8769G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246575432 | ||||||
| chr1:246575624
|
A | G | 1 | a0001c0001t0004g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-52+8961A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246575624 | ||||||
| chr1:246575631
|
C | T | 1 | a0004c0004t0003g0119 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-52+8968C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246575631 | ||||||
| chr1:246575739
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-52+9076C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246575739 | ||||||
| chr1:246575785
|
A | G | 1 | a0001c0001t0004g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-52+9122A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246575785 | ||||||
| chr1:246575853
|
A | C | 4 | a0001c0001t0001g0166a0001c0001t0009g0010a0001c0001t0009g0012others(1): Show | 4 | HG02976.hp1 HG03041.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+9190A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246575853 | ||||||
| chr1:246575876
|
T | C | 16 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0177others(13): Show | 16 | HG00735.hp1 HG00741.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-52+9213T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246575876 | ||||||
| chr1:246575881
|
T | C | 1 | a0001c0001t0002g0209 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-52+9218T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246575881 | ||||||
| chr1:246575903
|
T | C | 13 | a0001c0001t0001g0312a0001c0001t0002g0186a0001c0001t0002g0187others(10): Show | 13 | HG00423.hp1 HG02451.hp2 HG02896.hp2 others(10): Show |
intron_variant | MODIFIER | c.-52+9240T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246575903 | ||||||
| chr1:246575973
|
G | A | 1 | a0001c0001t0001g0293 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-52+9310G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246575973 | ||||||
| chr1:246576007
|
A | G | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9344A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576007 | ||||||
| chr1:246576010
|
A | G | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9347A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576010 | ||||||
| chr1:246576016
|
CTT | C | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9354_-52+9355d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576016 | ||||||
| chr1:246576029
|
A | G | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9366A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576029 | ||||||
| chr1:246576030
|
T | A | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9367T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576030 | ||||||
| chr1:246576033
|
A | G | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9370A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576033 | ||||||
| chr1:246576040
|
G | T | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9377G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576040 | ||||||
| chr1:246576042
|
C | G | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9379C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576042 | ||||||
| chr1:246576047
|
C | T | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9384C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576047 | ||||||
| chr1:246576052
|
T | C | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9389T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576052 | ||||||
| chr1:246576062
|
G | C | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9399G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576062 | ||||||
| chr1:246576063
|
T | C | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9400T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576063 | ||||||
| chr1:246576067
|
C | T | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9404C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576067 | ||||||
| chr1:246576079
|
G | A | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9416G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576079 | ||||||
| chr1:246576080
|
C | CA | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9422dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576080 | |||||
| chr1:246576091
|
C | T | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9428C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576091 | ||||||
| chr1:246576092
|
A | G | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9429A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576092 | ||||||
| chr1:246576096
|
A | G | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9433A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576096 | ||||||
| chr1:246576098
|
G | A | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9435G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576098 | ||||||
| chr1:246576113
|
T | C | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9450T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576113 | ||||||
| chr1:246576115
|
A | G | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9452A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576115 | ||||||
| chr1:246576122
|
A | C | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9459A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576122 | ||||||
| chr1:246576128
|
T | G | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9465T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576128 | ||||||
| chr1:246576149
|
T | G | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9486T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576149 | ||||||
| chr1:246576151
|
G | C | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9488G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576151 | ||||||
| chr1:246576152
|
T | G | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9489T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576152 | ||||||
| chr1:246576166
|
T | C | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9503T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576166 | ||||||
| chr1:246576183
|
C | T | 1 | a0001c0001t0011g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-52+9520C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576183 | ||||||
| chr1:246576186
|
A | G | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9523A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576186 | ||||||
| chr1:246576187
|
A | G | 1 | a0001c0001t0002g0258 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-52+9524A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576187 | ||||||
| chr1:246576189
|
G | C | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9526G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576189 | ||||||
| chr1:246576190
|
G | C | 4 | a0001c0001t0017g0008a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9527G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576190 | ||||||
| chr1:246576190
|
G | GCGCCACC others(412): Show |
1 | a0001c0001t0011g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-52+9532_-52+9533i others(421): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576190 | |||||
| chr1:246576190
|
G | GCGCCACC others(410): Show |
1 | a0001c0001t0014g0164 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-52+9532_-52+9533i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576190 | |||||
| chr1:246576195
|
A | ACCGCACT others(411): Show |
1 | a0001c0001t0001g0197 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-52+9532_-52+9533i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576195 | ||||||
| chr1:246576195
|
A | ACCGCACT others(410): Show |
2 | a0001c0001t0003g0073a0001c0001t0003g0074 | 2 | HG02071.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.-52+9532_-52+9533i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576195 | ||||||
| chr1:246576195
|
A | ACCGCACT others(410): Show |
1 | a0001c0001t0003g0051 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-52+9532_-52+9533i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576195 | ||||||
| chr1:246576195
|
A | ACCGCACT others(412): Show |
1 | a0001c0001t0003g0081 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-52+9532_-52+9533i others(421): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576195 | ||||||
| chr1:246576195
|
A | ACCGCACT others(411): Show |
3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0003g0082 | 3 | HG00738.hp1 HG01978.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.-52+9532_-52+9533i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576195 | ||||||
| chr1:246576195
|
A | ACCGCACT others(409): Show |
4 | a0001c0001t0001g0076a0001c0001t0002g0183a0001c0001t0003g0054others(1): Show | 4 | HG01891.hp1 HG01934.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+9532_-52+9533i others(418): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576195 | ||||||
| chr1:246576195
|
A | ACCGCACT others(410): Show |
1 | a0001c0001t0003g0055 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-52+9532_-52+9533i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576195 | ||||||
| chr1:246576195
|
A | ACCGCACT others(410): Show |
23 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(20): Show | 24 | HG00280.hp1 HG00423.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.-52+9532_-52+9533i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576195 | ||||||
| chr1:246576195
|
A | ACCGCACT others(410): Show |
1 | a0001c0001t0002g0080 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-52+9532_-52+9533i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576195 | ||||||
| chr1:246576195
|
A | ACCGCACT others(410): Show |
1 | a0001c0001t0002g0078 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-52+9532_-52+9533i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576195 | ||||||
| chr1:246576195
|
A | ACCGCACT others(409): Show |
8 | a0001c0001t0002g0071a0001c0001t0003g0050a0001c0001t0003g0066others(5): Show | 8 | HG01192.hp1 HG01943.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.-52+9532_-52+9533i others(418): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576195 | ||||||
| chr1:246576195
|
A | ACCGCACT others(410): Show |
2 | a0001c0001t0002g0072a0001c0001t0003g0079 | 2 | HG01099.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.-52+9532_-52+9533i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576195 | ||||||
| chr1:246576196
|
T | C | 54 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(51): Show | 55 | HG00280.hp1 HG00423.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.-52+9533T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576196 | ||||||
| chr1:246576196
|
T | TTGCACTC others(411): Show |
1 | a0003c0003t0001g0039 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576196 | |||||
| chr1:246576196
|
T | TTGCACTC others(411): Show |
1 | a0003c0003t0001g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576196 | |||||
| chr1:246576196
|
T | TTGCACTC others(412): Show |
1 | a0007c0011t0015g0213 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(421): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576196 | |||||
| chr1:246576196
|
T | TTGCACTC others(411): Show |
1 | a0001c0001t0003g0259 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576196 | |||||
| chr1:246576196
|
T | TTGCACTC others(410): Show |
3 | a0001c0001t0004g0042a0003c0003t0001g0040a0003c0003t0001g0041 | 3 | HG00733.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576196 | |||||
| chr1:246576196
|
T | TTGCACTC others(410): Show |
4 | a0003c0003t0001g0033a0003c0003t0004g0034a0003c0003t0004g0035others(1): Show | 4 | HG01243.hp1 HG02451.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576196 | |||||
| chr1:246576196
|
T | TTGCACTC others(411): Show |
1 | a0003c0003t0001g0038 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576196 | |||||
| chr1:246576196
|
T | TTGCACTC others(411): Show |
1 | a0001c0001t0003g0220 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576196 | |||||
| chr1:246576196
|
T | TTGCACTC others(409): Show |
1 | a0003c0003t0004g0036 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(418): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576196 | |||||
| chr1:246576196
|
T | TTGCACTC others(410): Show |
1 | a0004c0004t0003g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576196 | |||||
| chr1:246576196
|
T | TTGCACTC others(412): Show |
1 | a0001c0001t0001g0166 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(421): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576196 | |||||
| chr1:246576196
|
T | TTGCACTC others(410): Show |
1 | a0004c0004t0003g0192 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576196 | |||||
| chr1:246576196
|
T | TTGCACTC others(410): Show |
1 | a0003c0003t0001g0037 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576196 | |||||
| chr1:246576200
|
A | ACTCAAGC others(415): Show |
1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-52+9540_-52+9541i others(424): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(417): Show |
1 | a0001c0001t0002g0097 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(426): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(413): Show |
2 | a0001c0001t0001g0156a0002c0002t0001g0151 | 2 | HG01175.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(422): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(414): Show |
1 | a0001c0001t0019g0106 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(423): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(415): Show |
5 | a0001c0001t0002g0002a0001c0001t0002g0101a0001c0001t0002g0102others(2): Show | 6 | HG00140.hp2 HG00733.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(424): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(416): Show |
1 | a0001c0001t0002g0105 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(425): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(412): Show |
11 | a0001c0001t0001g0210a0001c0001t0001g0314a0001c0001t0002g0315others(8): Show | 11 | HG00673.hp2 HG01934.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(421): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(412): Show |
4 | a0001c0001t0001g0160a0001c0001t0004g0157a0001c0001t0004g0158others(1): Show | 4 | HG01109.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(421): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(413): Show |
1 | a0001c0001t0002g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(422): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(413): Show |
6 | a0001c0001t0001g0215a0001c0001t0001g0289a0001c0001t0001g0299others(3): Show | 6 | HG01175.hp1 HG02145.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(422): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(412): Show |
1 | a0001c0001t0002g0186 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(421): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(410): Show |
6 | a0001c0001t0001g0293a0001c0001t0004g0016a0001c0001t0004g0017others(3): Show | 6 | HG02630.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(411): Show |
9 | a0001c0001t0001g0207a0001c0001t0001g0216a0001c0001t0001g0217others(6): Show | 9 | HG00558.hp1 HG00673.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(411): Show |
82 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0177others(79): Show | 82 | HG00280.hp2 HG00558.hp2 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(412): Show |
2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | NA18969.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(421): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(412): Show |
19 | a0001c0001t0001g0198a0001c0001t0001g0255a0001c0001t0001g0274others(16): Show | 19 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(16): Show |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(421): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(411): Show |
1 | a0001c0001t0004g0275 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(411): Show |
2 | a0001c0001t0003g0206a0001c0001t0013g0196 | 2 | HG02965.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(411): Show |
1 | a0001c0001t0002g0276 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(412): Show |
1 | a0001c0001t0003g0282 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(421): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(411): Show |
1 | a0001c0001t0002g0285 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(409): Show |
1 | a0001c0001t0002g0187 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(418): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(410): Show |
2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(410): Show |
3 | a0001c0001t0001g0277a0001c0001t0001g0283a0001c0001t0002g0172 | 3 | HG02886.hp2 HG03491.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(411): Show |
3 | a0001c0001t0004g0173a0001c0001t0004g0174a0001c0001t0009g0010 | 3 | HG01884.hp2 HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(412): Show |
2 | a0001c0001t0002g0175a0001c0001t0009g0013 | 2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(421): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(413): Show |
1 | a0001c0001t0009g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(422): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(410): Show |
2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(410): Show |
4 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0091others(1): Show | 4 | HG01261.hp2 HG01433.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(410): Show |
2 | a0004c0004t0003g0184a0004c0004t0003g0185 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(410): Show |
6 | a0001c0001t0001g0312a0001c0001t0002g0188a0001c0001t0002g0189others(3): Show | 6 | NA18950.hp2 NA18952.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(408): Show |
35 | a0001c0001t0001g0121a0001c0001t0001g0128a0001c0001t0002g0129others(32): Show | 35 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(417): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(408): Show |
3 | a0001c0001t0001g0135a0001c0001t0004g0134a0001c0001t0016g0136 | 3 | HG01243.hp2 HG02897.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(417): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(409): Show |
4 | a0001c0001t0001g0257a0001c0001t0003g0137a0002c0002t0001g0139others(1): Show | 4 | HG01884.hp1 NA18960.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(418): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(409): Show |
1 | a0001c0001t0001g0088 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(418): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(409): Show |
1 | a0001c0001t0002g0311 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(418): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(412): Show |
1 | a0001c0001t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(421): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(413): Show |
1 | a0010c0010t0002g0028 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(422): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(407): Show |
1 | a0001c0001t0002g0131 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(416): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | ACTCCAGC others(407): Show |
2 | a0001c0001t0001g0132a0002c0002t0001g0141 | 2 | HG02735.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(416): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | |||||
| chr1:246576200
|
A | G | 54 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(51): Show | 55 | HG00280.hp1 HG00423.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.-52+9537A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576200 | ||||||
| chr1:246576213
|
C | A | 2 | a0001c0001t0003g0220a0001c0001t0003g0259 | 2 | HG03704.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-52+9550C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576213 | ||||||
| chr1:246576213
|
C | T | 57 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(54): Show | 58 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.-52+9550C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576213 | ||||||
| chr1:246576214
|
G | T | 2 | a0004c0004t0003g0192a0004c0004t0003g0193 | 2 | HG02451.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-52+9551G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576214 | ||||||
| chr1:246576219
|
A | G | 6 | a0001c0001t0004g0150a0001c0001t0004g0153a0001c0001t0004g0154others(3): Show | 6 | HG01175.hp2 HG02109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52+9556A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576219 | ||||||
| chr1:246576222
|
C | G | 21 | a0001c0001t0002g0172a0001c0001t0003g0297a0001c0001t0004g0042others(18): Show | 21 | HG00733.hp1 HG01175.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.-52+9559C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576222 | ||||||
| chr1:246576229
|
C | T | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+9566C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576229 | ||||||
| chr1:246576234
|
C | A | 1 | a0003c0003t0004g0162 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-52+9571C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576234 | ||||||
| chr1:246576234
|
C | CA | 174 | a0001c0001t0001g0011a0001c0001t0001g0121a0001c0001t0001g0128others(171): Show | 175 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-52+9590dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576234 | |||||
| chr1:246576234
|
C | CAA | 49 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0135others(46): Show | 49 | HG00642.hp1 HG00733.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.-52+9589_-52+9590d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576234 | |||||
| chr1:246576234
|
C | CAAA | 72 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(69): Show | 73 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.-52+9588_-52+9590d others(5): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576234 | |||||
| chr1:246576234
|
C | G | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-52+9571C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576234 | ||||||
| chr1:246576258
|
C | A | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+9595C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576258 | ||||||
| chr1:246576265
|
TTCTCAGT others(1650): Show |
T | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+9606_-52+11262 others(3): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576265 | |||||
| chr1:246576445
|
TTTTGGTT others(8): Show |
T | 137 | a0001c0001t0001g0156a0001c0001t0001g0160a0001c0001t0001g0194others(134): Show | 137 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.-52+9785_-52+9799d others(17): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576445 | |||||
| chr1:246576605
|
C | T | 1 | a0001c0001t0002g0071 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-52+9942C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576605 | ||||||
| chr1:246576610
|
C | G | 2 | a0001c0001t0014g0164a0001c0001t0014g0165 | 2 | HG00423.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-52+9947C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576610 | ||||||
| chr1:246576677
|
A | G | 84 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(81): Show | 85 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.-52+10014A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576677 | ||||||
| chr1:246576735
|
C | G | 1 | a0001c0001t0004g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-52+10072C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576735 | ||||||
| chr1:246576990
|
T | C | 4 | a0001c0001t0002g0225a0001c0001t0003g0226a0001c0001t0003g0227others(1): Show | 4 | NA18985.hp1 NA18999.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+10327T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576990 | ||||||
| chr1:246577069
|
G | A | 1 | a0001c0012t0002g0278 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-52+10406G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577069 | ||||||
| chr1:246577114
|
G | T | 3 | a0001c0001t0009g0010a0001c0001t0009g0012a0001c0001t0009g0013 | 3 | HG02976.hp1 HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-52+10451G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577114 | ||||||
| chr1:246577245
|
C | T | 5 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(2): Show | 5 | HG02145.hp1 HG02647.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+10582C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577245 | ||||||
| chr1:246577295
|
G | A | 1 | a0001c0001t0004g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-52+10632G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577295 | ||||||
| chr1:246577301
|
C | A | 1 | a0001c0001t0002g0281 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-52+10638C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577301 | ||||||
| chr1:246577351
|
C | T | 53 | a0001c0001t0001g0053a0001c0001t0001g0061a0001c0001t0001g0076others(50): Show | 53 | HG00140.hp1 HG00423.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.-52+10688C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577351 | ||||||
| chr1:246577361
|
T | C | 4 | a0001c0001t0001g0160a0001c0001t0004g0157a0001c0001t0004g0158others(1): Show | 4 | HG01109.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+10698T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577361 | ||||||
| chr1:246577373
|
A | G | 1 | a0001c0001t0003g0084 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-52+10710A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577373 | ||||||
| chr1:246577455
|
T | C | 1 | a0003c0003t0001g0037 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-52+10792T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577455 | ||||||
| chr1:246577553
|
G | A | 1 | a0001c0001t0004g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-52+10890G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577553 | ||||||
| chr1:246577637
|
G | T | 3 | a0002c0002t0006g0029a0002c0002t0006g0030a0002c0002t0006g0031 | 3 | HG02615.hp1 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-52+10974G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577637 | ||||||
| chr1:246577798
|
G | T | 1 | a0001c0001t0002g0072 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-52+11135G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577798 | ||||||
| chr1:246577803
|
A | G | 10 | a0001c0001t0001g0135a0001c0001t0002g0172a0001c0001t0002g0175others(7): Show | 10 | HG01243.hp2 HG01884.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-52+11140A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577803 | ||||||
| chr1:246577808
|
A | G | 1 | a0001c0001t0002g0224 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-52+11145A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577808 | ||||||
| chr1:246577845
|
C | T | 16 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0177others(13): Show | 16 | HG00735.hp1 HG00741.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-52+11182C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577845 | ||||||
| chr1:246577925
|
T | A | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11262T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577925 | ||||||
| chr1:246577928
|
T | G | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11265T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577928 | ||||||
| chr1:246577935
|
T | G | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11272T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577935 | ||||||
| chr1:246577938
|
C | G | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11275C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577938 | ||||||
| chr1:246577939
|
C | T | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11276C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577939 | ||||||
| chr1:246577940
|
C | A | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11277C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577940 | ||||||
| chr1:246577967
|
T | G | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11304T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577967 | ||||||
| chr1:246577973
|
T | G | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11310T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577973 | ||||||
| chr1:246577974
|
T | G | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11311T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577974 | ||||||
| chr1:246577975
|
T | G | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11312T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577975 | ||||||
| chr1:246577976
|
T | G | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11313T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577976 | ||||||
| chr1:246577976
|
TTTG | T | 10 | a0001c0001t0001g0135a0001c0001t0002g0172a0001c0001t0002g0175others(7): Show | 10 | HG01243.hp2 HG01884.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-52+11319_-52+1132 others(7): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246577976 | |||||
| chr1:246577977
|
T | G | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11314T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577977 | ||||||
| chr1:246577978
|
T | G | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11315T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577978 | ||||||
| chr1:246577980
|
T | G | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11317T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577980 | ||||||
| chr1:246577981
|
T | A | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11318T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577981 | ||||||
| chr1:246577987
|
G | A | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11324G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577987 | ||||||
| chr1:246577989
|
A | T | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11326A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577989 | ||||||
| chr1:246577990
|
C | A | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11327C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577990 | ||||||
| chr1:246577995
|
T | TGCCTTTG others(4): Show |
1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11332_-52+1133 others(15): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577995 | ||||||
| chr1:246578005
|
C | G | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11342C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578005 | ||||||
| chr1:246578010
|
G | T | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11347G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578010 | ||||||
| chr1:246578014
|
T | A | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11351T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578014 | ||||||
| chr1:246578016
|
T | C | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11353T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578016 | ||||||
| chr1:246578019
|
C | A | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11356C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578019 | ||||||
| chr1:246578024
|
TTTTTCTA others(356): Show |
T | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11364_-52+1172 others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246578024 | |||||
| chr1:246578290
|
A | G | 1 | a0001c0001t0004g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-52+11627A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578290 | ||||||
| chr1:246578388
|
T | C | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11725T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578388 | ||||||
| chr1:246578391
|
G | A | 2 | a0001c0001t0001g0279a0001c0001t0002g0201 | 2 | HG00673.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-52+11728G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578391 | ||||||
| chr1:246578394
|
T | C | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11731T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578394 | ||||||
| chr1:246578400
|
T | C | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11737T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578400 | ||||||
| chr1:246578438
|
T | C | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11775T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578438 | ||||||
| chr1:246578443
|
T | C | 4 | a0001c0001t0001g0166a0001c0001t0009g0010a0001c0001t0009g0012others(1): Show | 4 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+11780T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578443 | ||||||
| chr1:246578454
|
T | C | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11791T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578454 | ||||||
| chr1:246578468
|
G | A | 305 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0052others(302): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.-52+11805G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578468 | ||||||
| chr1:246578477
|
C | G | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11814C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578477 | ||||||
| chr1:246578490
|
T | C | 9 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG00140.hp1 HG01261.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.-52+11827T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578490 | ||||||
| chr1:246578511
|
C | A | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11848C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578511 | ||||||
| chr1:246578527
|
T | C | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11864T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578527 | ||||||
| chr1:246578531
|
T | C | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11868T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578531 | ||||||
| chr1:246578532
|
G | A | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11869G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578532 | ||||||
| chr1:246578540
|
A | G | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11877A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578540 | ||||||
| chr1:246578541
|
C | G | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11878C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578541 | ||||||
| chr1:246578542
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-52+11879G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578542 | ||||||
| chr1:246578543
|
T | C | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11880T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578543 | ||||||
| chr1:246578569
|
G | T | 69 | a0001c0001t0001g0053a0001c0001t0001g0061a0001c0001t0001g0076others(66): Show | 69 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.-52+11906G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578569 | ||||||
| chr1:246578621
|
A | G | 3 | a0001c0001t0003g0084a0001c0001t0003g0250a0001c0001t0003g0270 | 3 | HG03942.hp1 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-52+11958A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578621 | ||||||
| chr1:246578658
|
G | C | 175 | a0001c0001t0001g0121a0001c0001t0001g0128a0001c0001t0001g0132others(172): Show | 175 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.-52+11995G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578658 | ||||||
| chr1:246578668
|
C | CA | 12 | a0001c0001t0001g0135a0001c0001t0001g0156a0001c0001t0001g0210others(9): Show | 12 | HG01243.hp2 HG01884.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-52+12018dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246578668 | |||||
| chr1:246578827
|
A | G | 1 | a0001c0001t0001g0249 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-52+12164A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578827 | ||||||
| chr1:246578855
|
C | T | 21 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(18): Show | 23 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.-52+12192C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578855 | ||||||
| chr1:246578886
|
G | A | 6 | a0001c0001t0004g0150a0001c0001t0004g0153a0001c0001t0004g0154others(3): Show | 6 | HG01175.hp2 HG02109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52+12223G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578886 | ||||||
| chr1:246578922
|
A | G | 2 | a0001c0001t0003g0047a0001c0001t0003g0048 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-52+12259A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578922 | ||||||
| chr1:246579148
|
T | A | 21 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(18): Show | 23 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.-51-12364T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246579148 | ||||||
| chr1:246579250
|
T | A | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-51-12262T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246579250 | ||||||
| chr1:246579307
|
T | C | 1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-51-12205T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246579307 | ||||||
| chr1:246579435
|
G | C | 1 | a0001c0001t0004g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-51-12077G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246579435 | ||||||
| chr1:246579499
|
T | C | 10 | a0001c0001t0001g0135a0001c0001t0002g0172a0001c0001t0002g0175others(7): Show | 10 | HG01243.hp2 HG01884.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-51-12013T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246579499 | ||||||
| chr1:246579555
|
G | A | 1 | a0003c0003t0001g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-51-11957G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246579555 | ||||||
| chr1:246579733
|
C | T | 1 | a0001c0001t0002g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-51-11779C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246579733 | ||||||
| chr1:246579818
|
G | A | 1 | a0001c0001t0004g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-51-11694G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246579818 | ||||||
| chr1:246580076
|
G | A | 1 | a0002c0002t0001g0120 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-51-11436G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246580076 | ||||||
| chr1:246580374
|
C | A | 1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-51-11138C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246580374 | ||||||
| chr1:246580389
|
TACAG | T | 3 | a0002c0002t0006g0029a0002c0002t0006g0030a0002c0002t0006g0031 | 3 | HG02615.hp1 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-51-11118_-51-1111 others(8): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246580389 | |||||
| chr1:246580428
|
C | CT | 65 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0086others(62): Show | 65 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.-51-11075dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246580428 | |||||
| chr1:246580432
|
T | C | 1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-51-11080T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246580432 | ||||||
| chr1:246580465
|
G | C | 10 | a0001c0001t0001g0135a0001c0001t0002g0172a0001c0001t0002g0175others(7): Show | 10 | HG01243.hp2 HG01884.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-51-11047G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246580465 | ||||||
| chr1:246580514
|
G | T | 85 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(82): Show | 87 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.-51-10998G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246580514 | ||||||
| chr1:246580740
|
T | C | 1 | a0001c0001t0001g0312 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-51-10772T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246580740 | ||||||
| chr1:246580751
|
C | T | 1 | a0001c0001t0001g0299 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-51-10761C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246580751 | ||||||
| chr1:246580832
|
C | T | 1 | a0001c0001t0003g0054 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-51-10680C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246580832 | ||||||
| chr1:246580985
|
C | A | 1 | a0001c0001t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-51-10527C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246580985 | ||||||
| chr1:246581030
|
C | T | 1 | a0002c0002t0001g0118 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-51-10482C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246581030 | ||||||
| chr1:246581054
|
A | G | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-51-10458A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246581054 | ||||||
| chr1:246581246
|
T | C | 12 | a0001c0001t0004g0042a0003c0003t0001g0032a0003c0003t0001g0033others(9): Show | 12 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-51-10266T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246581246 | ||||||
| chr1:246581263
|
C | G | 1 | a0001c0001t0003g0096 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-51-10249C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246581263 | ||||||
| chr1:246581358
|
G | C | 21 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(18): Show | 23 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.-51-10154G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246581358 | ||||||
| chr1:246581455
|
G | T | 42 | a0001c0001t0001g0128a0001c0001t0001g0132a0001c0001t0001g0287others(39): Show | 42 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.-51-10057G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246581455 | ||||||
| chr1:246581683
|
A | G | 2 | a0001c0001t0004g0006a0004c0004t0003g0119 | 2 | HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-51-9829A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246581683 | ||||||
| chr1:246581699
|
T | C | 306 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0052others(303): Show | 308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.-51-9813T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246581699 | ||||||
| chr1:246581709
|
A | G | 1 | a0001c0001t0004g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-51-9803A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246581709 | ||||||
| chr1:246581792
|
G | A | 48 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0086others(45): Show | 48 | HG00140.hp1 HG00423.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.-51-9720G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246581792 | ||||||
| chr1:246581877
|
T | G | 1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-51-9635T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246581877 | ||||||
| chr1:246581957
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-51-9555G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246581957 | ||||||
| chr1:246582001
|
G | A | 4 | a0002c0002t0001g0145a0002c0002t0001g0146a0002c0002t0001g0147others(1): Show | 4 | HG02559.hp1 HG02683.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-9511G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582001 | ||||||
| chr1:246582169
|
C | T | 1 | a0001c0001t0003g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-51-9343C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582169 | ||||||
| chr1:246582261
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-51-9251C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582261 | ||||||
| chr1:246582356
|
C | CT | 20 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0177others(17): Show | 20 | HG00735.hp1 HG00741.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.-51-9142dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246582356 | |||||
| chr1:246582356
|
CT | C | 119 | a0001c0001t0001g0088a0001c0001t0001g0121a0001c0001t0001g0156others(116): Show | 119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.-51-9142delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246582356 | |||||
| chr1:246582419
|
G | GCTCCCTG others(10): Show |
4 | a0001c0001t0001g0160a0001c0001t0004g0157a0001c0001t0004g0158others(1): Show | 4 | HG01109.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-9087_-51-9071d others(19): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246582419 | |||||
| chr1:246582675
|
T | C | 1 | a0001c0001t0004g0275 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-51-8837T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582675 | ||||||
| chr1:246582707
|
A | G | 1 | a0001c0001t0004g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-51-8805A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582707 | ||||||
| chr1:246582715
|
G | A | 27 | a0001c0001t0001g0022a0001c0001t0001g0177a0001c0001t0004g0014others(24): Show | 27 | HG00733.hp1 HG00735.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.-51-8797G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582715 | ||||||
| chr1:246582763
|
C | T | 1 | a0001c0001t0002g0129 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-51-8749C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582763 | ||||||
| chr1:246582799
|
C | G | 2 | a0001c0001t0003g0047a0001c0001t0003g0048 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-51-8713C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582799 | ||||||
| chr1:246582799
|
C | T | 120 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0052others(117): Show | 121 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.-51-8713C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582799 | ||||||
| chr1:246582831
|
G | A | 1 | a0001c0001t0004g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-51-8681G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582831 | ||||||
| chr1:246582849
|
C | T | 1 | a0001c0001t0001g0298 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-51-8663C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582849 | ||||||
| chr1:246582869
|
A | G | 81 | a0001c0001t0001g0011a0001c0001t0001g0061a0001c0001t0001g0076others(78): Show | 81 | HG00423.hp2 HG00642.hp1 HG00738.hp2 others(78): Show |
intron_variant | MODIFIER | c.-51-8643A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582869 | ||||||
| chr1:246582931
|
G | A | 1 | a0001c0001t0004g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-51-8581G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582931 | ||||||
| chr1:246582995
|
G | C | 1 | a0001c0001t0001g0299 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-51-8517G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582995 | ||||||
| chr1:246582996
|
C | G | 1 | a0001c0001t0001g0299 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-51-8516C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582996 | ||||||
| chr1:246583110
|
A | C | 2 | a0001c0001t0004g0018a0001c0001t0004g0019 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-51-8402A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246583110 | ||||||
| chr1:246583157
|
T | TTTGGTGG others(23): Show |
1 | a0001c0001t0001g0299 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-51-8353_-51-8324d others(32): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246583157 | |||||
| chr1:246583301
|
A | G | 11 | a0001c0001t0001g0025a0001c0001t0004g0006a0001c0001t0004g0026others(8): Show | 11 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-51-8211A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246583301 | ||||||
| chr1:246583435
|
A | C | 13 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0169others(10): Show | 13 | HG01884.hp2 HG01981.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-51-8077A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246583435 | ||||||
| chr1:246583639
|
G | A | 16 | a0001c0001t0001g0076a0001c0001t0001g0121a0001c0001t0001g0304others(13): Show | 16 | HG00558.hp2 HG01934.hp2 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-51-7873G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246583639 | ||||||
| chr1:246583836
|
G | A | 13 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0169others(10): Show | 13 | HG01884.hp2 HG01981.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-51-7676G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246583836 | ||||||
| chr1:246583880
|
T | G | 3 | a0002c0002t0001g0027a0002c0002t0001g0122a0002c0002t0001g0130 | 3 | HG00741.hp2 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-51-7632T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246583880 | ||||||
| chr1:246583929
|
G | T | 11 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0037others(8): Show | 11 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-51-7583G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246583929 | ||||||
| chr1:246583930
|
C | T | 11 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0037others(8): Show | 11 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-51-7582C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246583930 | ||||||
| chr1:246583986
|
G | T | 95 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(92): Show | 97 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.-51-7526G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246583986 | ||||||
| chr1:246584036
|
CT | C | 276 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(273): Show | 278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.-51-7473delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246584036 | |||||
| chr1:246584039
|
T | C | 276 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(273): Show | 278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.-51-7473T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246584039 | ||||||
| chr1:246584179
|
C | T | 1 | a0001c0001t0004g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-51-7333C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246584179 | ||||||
| chr1:246584250
|
C | T | 1 | a0001c0001t0003g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-51-7262C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246584250 | ||||||
| chr1:246584278
|
G | A | 2 | a0001c0001t0017g0008a0001c0006t0001g0009 | 2 | HG01981.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-51-7234G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246584278 | ||||||
| chr1:246584284
|
G | A | 129 | a0001c0001t0001g0022a0001c0001t0001g0135a0001c0001t0001g0156others(126): Show | 129 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.-51-7228G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246584284 | ||||||
| chr1:246584388
|
T | G | 1 | a0001c0001t0002g0224 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-51-7124T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246584388 | ||||||
| chr1:246584419
|
G | A | 1 | a0001c0001t0002g0002 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-51-7093G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246584419 | ||||||
| chr1:246584576
|
T | C | 1 | a0001c0001t0001g0295 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-51-6936T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246584576 | ||||||
| chr1:246584640
|
G | A | 10 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(7): Show | 10 | HG00735.hp1 HG02630.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-51-6872G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246584640 | ||||||
| chr1:246584812
|
G | A | 41 | a0001c0001t0001g0011a0001c0001t0001g0166a0001c0001t0001g0167others(38): Show | 41 | HG00733.hp1 HG00735.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.-51-6700G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246584812 | ||||||
| chr1:246584828
|
A | G | 2 | a0001c0001t0002g0284a0002c0002t0001g0133 | 2 | HG04115.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-51-6684A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246584828 | ||||||
| chr1:246585034
|
T | A | 2 | a0002c0002t0001g0108a0002c0002t0002g0123 | 2 | HG01074.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-51-6478T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585034 | ||||||
| chr1:246585140
|
C | T | 1 | a0002c0002t0001g0108 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-51-6372C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585140 | ||||||
| chr1:246585175
|
C | T | 87 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0061others(84): Show | 89 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.-51-6337C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585175 | ||||||
| chr1:246585382
|
CACATCTG others(426): Show |
C | 1 | a0001c0001t0001g0248 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-51-6116_-51-5684d others(2): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585382 | |||||
| chr1:246585552
|
C | T | 4 | a0001c0001t0003g0054a0001c0001t0003g0073a0001c0001t0003g0074others(1): Show | 4 | HG02071.hp1 HG02074.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-5960C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585552 | ||||||
| chr1:246585561
|
C | G | 2 | a0002c0002t0015g0168a0007c0011t0015g0213 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-51-5951C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585561 | ||||||
| chr1:246585590
|
G | A | 1 | a0001c0001t0002g0231 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-51-5922G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585590 | ||||||
| chr1:246585641
|
C | CA | 13 | a0001c0001t0001g0194a0001c0001t0001g0253a0001c0001t0001g0293others(10): Show | 13 | HG00140.hp2 HG00621.hp1 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.-51-5849dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585641 | |||||
| chr1:246585641
|
CA | C | 21 | a0001c0001t0001g0156a0001c0001t0001g0166a0001c0001t0001g0202others(18): Show | 21 | HG00558.hp1 HG01074.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.-51-5849delA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585641 | |||||
| chr1:246585641
|
CAA | C | 7 | a0001c0001t0001g0135a0001c0001t0004g0004a0001c0001t0004g0134others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-51-5850_-51-5849d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585641 | |||||
| chr1:246585641
|
CAAA | C | 11 | a0001c0001t0001g0291a0001c0001t0004g0042a0001c0001t0004g0150others(8): Show | 11 | HG01175.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-51-5851_-51-5849d others(5): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585641 | |||||
| chr1:246585641
|
CAAAAA | C | 9 | a0001c0001t0004g0174a0001c0001t0005g0155a0001c0001t0005g0203others(6): Show | 9 | HG01433.hp1 HG01884.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51-5853_-51-5849d others(7): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585641 | |||||
| chr1:246585656
|
A | T | 2 | a0001c0001t0004g0006a0003c0003t0004g0034 | 2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-51-5856A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585656 | ||||||
| chr1:246585658
|
A | T | 9 | a0001c0001t0004g0006a0003c0003t0001g0037a0003c0003t0001g0038others(6): Show | 9 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51-5854A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585658 | ||||||
| chr1:246585660
|
A | T | 21 | a0001c0001t0001g0025a0001c0001t0003g0292a0001c0001t0004g0006others(18): Show | 21 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-51-5852A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585660 | ||||||
| chr1:246585661
|
AAAT | A | 16 | a0001c0001t0001g0167a0001c0001t0002g0078a0001c0001t0002g0101others(13): Show | 16 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.-51-5849_-51-5847d others(5): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585661 | |||||
| chr1:246585661
|
AAATATAC others(4): Show |
A | 8 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0170others(5): Show | 8 | HG01515.hp1 HG01517.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-51-5849_-51-5839d others(13): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585661 | |||||
| chr1:246585661
|
AAATATAC others(18): Show |
A | 2 | a0001c0001t0001g0128a0002c0002t0001g0117 | 2 | HG03688.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-51-5849_-51-5825d others(27): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585661 | |||||
| chr1:246585662
|
A | AT | 3 | a0001c0001t0001g0301a0001c0001t0003g0079a0002c0002t0001g0111 | 3 | HG02015.hp2 HG02074.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.-51-5850_-51-5849i others(3): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585662 | ||||||
| chr1:246585662
|
A | T | 23 | a0001c0001t0001g0025a0001c0001t0003g0292a0001c0001t0004g0006others(20): Show | 23 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.-51-5850A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585662 | ||||||
| chr1:246585663
|
ATATAC | A | 8 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0182others(5): Show | 8 | HG01257.hp2 HG01346.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-51-5848_-51-5844d others(7): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585663 | ||||||
| chr1:246585663
|
ATATACAC others(10): Show |
A | 2 | a0001c0001t0001g0011a0001c0001t0001g0177 | 2 | HG00735.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-51-5848_-51-5832d others(19): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585663 | ||||||
| chr1:246585664
|
T | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0290 | 2 | HG01978.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-51-5848T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585664 | ||||||
| chr1:246585664
|
T | C | 3 | a0001c0001t0001g0301a0001c0001t0003g0079a0002c0002t0001g0111 | 3 | HG02015.hp2 HG02074.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.-51-5848T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585664 | ||||||
| chr1:246585664
|
TATAC | T | 4 | a0001c0001t0002g0005a0001c0001t0002g0131a0001c0001t0002g0284others(1): Show | 4 | HG00741.hp1 HG03942.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-5846_-51-5843d others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585664 | |||||
| chr1:246585664
|
TATACACA others(3): Show |
T | 3 | a0001c0001t0001g0169a0001c0001t0003g0066a0002c0002t0006g0029 | 3 | HG02300.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-51-5846_-51-5837d others(12): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585664 | |||||
| chr1:246585666
|
T | C | 15 | a0001c0001t0001g0202a0001c0001t0001g0301a0001c0001t0002g0072others(12): Show | 15 | HG01099.hp2 HG01261.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.-51-5846T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585666 | ||||||
| chr1:246585666
|
TAC | T | 19 | a0001c0001t0001g0234a0001c0001t0001g0257a0001c0001t0001g0260others(16): Show | 19 | HG00280.hp1 HG00558.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.-51-5801_-51-5800d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585666 | |||||
| chr1:246585666
|
TACAC | T | 47 | a0001c0001t0001g0053a0001c0001t0001g0076a0001c0001t0001g0087others(44): Show | 48 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.-51-5803_-51-5800d others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585666 | |||||
| chr1:246585666
|
TACACAC | T | 99 | a0001c0001t0001g0052a0001c0001t0001g0059a0001c0001t0001g0094others(96): Show | 100 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.-51-5805_-51-5800d others(8): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585666 | |||||
| chr1:246585666
|
TACACACA others(1): Show |
T | 24 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0086others(21): Show | 24 | HG01070.hp2 HG01074.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.-51-5807_-51-5800d others(10): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585666 | |||||
| chr1:246585666
|
TACACACA others(3): Show |
T | 5 | a0001c0001t0001g0160a0001c0001t0002g0315a0001c0001t0003g0144others(2): Show | 5 | HG02015.hp1 HG02257.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-5809_-51-5800d others(12): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585666 | |||||
| chr1:246585666
|
TACACACA others(5): Show |
T | 7 | a0001c0001t0001g0210a0001c0001t0001g0246a0001c0001t0004g0275others(4): Show | 7 | HG02257.hp1 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-51-5811_-51-5800d others(14): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585666 | |||||
| chr1:246585666
|
TACACACA others(7): Show |
T | 15 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0016others(12): Show | 15 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.-51-5813_-51-5800d others(16): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585666 | |||||
| chr1:246585666
|
TACACACA others(9): Show |
T | 6 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0002g0188others(3): Show | 6 | HG02647.hp1 HG02976.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51-5815_-51-5800d others(18): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585666 | |||||
| chr1:246585666
|
TACACACA others(11): Show |
T | 4 | a0001c0001t0001g0156a0001c0001t0001g0166a0003c0003t0004g0162others(1): Show | 4 | HG02717.hp1 HG03209.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-5817_-51-5800d others(20): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585666 | |||||
| chr1:246585666
|
TACACACA others(13): Show |
T | 1 | a0001c0001t0003g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-51-5819_-51-5800d others(22): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585666 | |||||
| chr1:246585668
|
C | T | 9 | a0001c0001t0001g0025a0001c0001t0002g0183a0001c0001t0004g0006others(6): Show | 9 | HG01891.hp1 HG01981.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51-5844C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585668 | ||||||
| chr1:246585670
|
C | T | 18 | a0001c0001t0001g0025a0001c0001t0001g0061a0001c0001t0001g0088others(15): Show | 18 | HG00140.hp1 HG01257.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.-51-5842C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585670 | ||||||
| chr1:246585672
|
C | T | 16 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0061others(13): Show | 16 | HG01257.hp2 HG01346.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.-51-5840C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585672 | ||||||
| chr1:246585674
|
C | T | 13 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0170others(10): Show | 13 | HG01515.hp1 HG01517.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51-5838C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585674 | ||||||
| chr1:246585676
|
C | T | 5 | a0001c0001t0009g0010a0001c0001t0009g0012a0001c0001t0017g0008others(2): Show | 5 | HG01981.hp1 HG02486.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-5836C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585676 | ||||||
| chr1:246585678
|
C | T | 6 | a0001c0001t0009g0010a0001c0001t0009g0012a0001c0001t0017g0008others(3): Show | 6 | HG01981.hp1 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51-5834C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585678 | ||||||
| chr1:246585680
|
C | T | 4 | a0001c0006t0001g0009a0002c0002t0006g0030a0002c0002t0006g0031others(1): Show | 4 | HG02257.hp2 HG02486.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-5832C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585680 | ||||||
| chr1:246585682
|
C | T | 11 | a0001c0001t0001g0011a0001c0001t0001g0177a0003c0003t0001g0037others(8): Show | 11 | HG00733.hp1 HG00735.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.-51-5830C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585682 | ||||||
| chr1:246585684
|
C | T | 13 | a0001c0001t0001g0011a0001c0001t0001g0177a0001c0001t0001g0290others(10): Show | 13 | HG00733.hp1 HG00735.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51-5828C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585684 | ||||||
| chr1:246585686
|
C | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0156a0001c0001t0001g0166others(4): Show | 7 | HG00735.hp1 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-51-5826C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585686 | ||||||
| chr1:246585688
|
C | T | 2 | a0001c0001t0001g0128a0002c0002t0001g0117 | 2 | HG03688.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-51-5824C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585688 | ||||||
| chr1:246585709
|
A | T | 1 | a0002c0002t0001g0093 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-51-5803A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585709 | ||||||
| chr1:246585767
|
G | A | 1 | a0001c0001t0002g0201 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-51-5745G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585767 | ||||||
| chr1:246586105
|
A | ATGTGTGT others(3): Show |
1 | a0003c0003t0004g0162 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-51-5406_-51-5405i others(12): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586105 | |||||
| chr1:246586107
|
A | ATGTGTGT others(1): Show |
6 | a0001c0001t0004g0004a0001c0001t0004g0026a0001c0001t0004g0173others(3): Show | 6 | HG02818.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51-5404_-51-5403i others(10): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586107 | |||||
| chr1:246586107
|
A | ATGTGTGT others(5): Show |
4 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(1): Show | 4 | HG01515.hp1 HG01517.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-5404_-51-5403i others(14): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586107 | |||||
| chr1:246586107
|
A | ATGTGTGT others(7): Show |
1 | a0001c0001t0001g0088 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-51-5404_-51-5403i others(16): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586107 | |||||
| chr1:246586107
|
A | G | 1 | a0003c0003t0004g0162 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-51-5405A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246586107 | ||||||
| chr1:246586109
|
A | ATG | 50 | a0001c0001t0001g0076a0001c0001t0001g0087a0001c0001t0001g0094others(47): Show | 50 | HG00423.hp2 HG01099.hp2 HG01169.hp1 others(47): Show |
intron_variant | MODIFIER | c.-51-5402_-51-5401i others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586109 | |||||
| chr1:246586109
|
A | ATGTG | 30 | a0001c0001t0001g0053a0001c0001t0001g0059a0001c0001t0001g0060others(27): Show | 31 | HG00140.hp2 HG00423.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.-51-5402_-51-5401i others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586109 | |||||
| chr1:246586109
|
A | ATGTGTG | 4 | a0001c0001t0001g0170a0001c0001t0001g0312a0001c0001t0002g0097others(1): Show | 4 | HG00642.hp2 HG01515.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-5402_-51-5401i others(8): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586109 | |||||
| chr1:246586109
|
A | ATGTGTGT others(1): Show |
3 | a0001c0001t0002g0172a0001c0001t0003g0181a0001c0001t0003g0316 | 3 | HG02145.hp2 HG02886.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-51-5402_-51-5401i others(10): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586109 | |||||
| chr1:246586109
|
A | ATGTGTGT others(3): Show |
3 | a0001c0001t0002g0175a0001c0001t0004g0174a0002c0002t0001g0171 | 3 | HG01884.hp2 HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-51-5402_-51-5401i others(12): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586109 | |||||
| chr1:246586109
|
A | ATGTGTGT others(7): Show |
1 | a0001c0001t0002g0077 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-51-5402_-51-5401i others(16): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586109 | |||||
| chr1:246586109
|
A | G | 16 | a0001c0001t0001g0025a0001c0001t0001g0088a0001c0001t0001g0089others(13): Show | 17 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-51-5403A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246586109 | ||||||
| chr1:246586109
|
ATATG | A | 10 | a0001c0001t0001g0207a0001c0001t0002g0285a0001c0001t0002g0302others(7): Show | 10 | HG00558.hp2 HG01192.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.-51-5401_-51-5398d others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586109 | |||||
| chr1:246586109
|
ATATGTG | A | 111 | a0001c0001t0001g0022a0001c0001t0001g0135a0001c0001t0001g0156others(108): Show | 111 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.-51-5401_-51-5396d others(8): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586109 | |||||
| chr1:246586111
|
A | ATATATGT others(3): Show |
1 | a0003c0003t0004g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-51-5400_-51-5399i others(12): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586111 | |||||
| chr1:246586111
|
A | ATATATGT others(5): Show |
2 | a0003c0003t0004g0034a0003c0003t0004g0036 | 2 | HG02896.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-51-5400_-51-5399i others(14): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586111 | |||||
| chr1:246586111
|
A | ATATATGT others(7): Show |
1 | a0003c0003t0001g0033 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-51-5400_-51-5399i others(16): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586111 | |||||
| chr1:246586111
|
A | ATATATGT others(9): Show |
5 | a0003c0003t0001g0038a0003c0003t0001g0039a0003c0003t0001g0040others(2): Show | 5 | HG00733.hp1 HG01891.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.-51-5400_-51-5399i others(18): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586111 | |||||
| chr1:246586111
|
A | ATATATGT others(11): Show |
1 | a0003c0003t0001g0037 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-51-5400_-51-5399i others(20): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586111 | |||||
| chr1:246586111
|
A | ATATGTGT others(9): Show |
1 | a0002c0002t0006g0030 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-51-5400_-51-5399i others(18): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586111 | |||||
| chr1:246586111
|
A | ATGTGTG | 6 | a0001c0001t0001g0011a0001c0001t0001g0052a0001c0001t0001g0167others(3): Show | 6 | HG00738.hp1 HG02647.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51-5375_-51-5370d others(8): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586111 | |||||
| chr1:246586111
|
A | ATGTGTGT others(1): Show |
7 | a0001c0001t0001g0182a0001c0001t0004g0014a0001c0001t0004g0015others(4): Show | 7 | HG01981.hp1 HG02630.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-51-5377_-51-5370d others(10): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586111 | |||||
| chr1:246586111
|
A | ATGTGTGT others(3): Show |
2 | a0001c0001t0001g0177a0001c0001t0004g0017 | 2 | HG00735.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-51-5379_-51-5370d others(12): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586111 | |||||
| chr1:246586111
|
A | ATGTGTGT others(7): Show |
2 | a0002c0002t0006g0029a0002c0002t0006g0031 | 2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-51-5383_-51-5370d others(16): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586111 | |||||
| chr1:246586111
|
A | G | 113 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0059others(110): Show | 115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.-51-5401A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246586111 | ||||||
| chr1:246586141
|
G | A | 120 | a0001c0001t0001g0022a0001c0001t0001g0135a0001c0001t0001g0156others(117): Show | 120 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.-51-5371G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246586141 | ||||||
| chr1:246586141
|
G | GTA | 6 | a0001c0001t0002g0056a0004c0004t0003g0119a0004c0004t0003g0184others(3): Show | 6 | HG00280.hp1 HG02451.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51-5365_-51-5364d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586141 | |||||
| chr1:246586143
|
A | G | 10 | a0001c0001t0002g0049a0002c0002t0001g0145a0002c0002t0001g0146others(7): Show | 10 | HG01256.hp1 HG02486.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-51-5369A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246586143 | ||||||
| chr1:246586213
|
G | C | 13 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0037others(10): Show | 13 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-51-5299G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246586213 | ||||||
| chr1:246586224
|
A | G | 2 | a0001c0001t0001g0025a0001c0001t0004g0026 | 2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-51-5288A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246586224 | ||||||
| chr1:246586285
|
C | A | 1 | a0001c0001t0001g0166 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-51-5227C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246586285 | ||||||
| chr1:246586397
|
A | G | 1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-51-5115A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246586397 | ||||||
| chr1:246586405
|
CAT | C | 14 | a0001c0001t0001g0234a0003c0003t0001g0032a0003c0003t0001g0033others(11): Show | 14 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-51-5104_-51-5103d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586405 | |||||
| chr1:246586408
|
A | G | 1 | a0001c0001t0005g0155 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-51-5104A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246586408 | ||||||
| chr1:246587097
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-51-4415T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246587097 | ||||||
| chr1:246587327
|
T | C | 29 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(26): Show | 30 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.-51-4185T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246587327 | ||||||
| chr1:246587695
|
C | T | 13 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0037others(10): Show | 13 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-51-3817C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246587695 | ||||||
| chr1:246587790
|
G | A | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-51-3722G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246587790 | ||||||
| chr1:246587864
|
T | C | 7 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(4): Show | 7 | HG00140.hp1 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.-51-3648T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246587864 | ||||||
| chr1:246587885
|
T | C | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0002c0002t0001g0133 | 3 | HG02970.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-51-3627T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246587885 | ||||||
| chr1:246587953
|
G | A | 2 | a0001c0001t0003g0047a0001c0001t0003g0048 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-51-3559G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246587953 | ||||||
| chr1:246588159
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0169 | 2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-51-3353G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246588159 | ||||||
| chr1:246588488
|
A | G | 137 | a0001c0001t0001g0022a0001c0001t0001g0135a0001c0001t0001g0156others(134): Show | 137 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.-51-3024A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246588488 | ||||||
| chr1:246588502
|
A | T | 1 | a0001c0001t0002g0310 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-51-3010A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246588502 | ||||||
| chr1:246588555
|
A | G | 10 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(7): Show | 10 | HG00735.hp1 HG02630.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-51-2957A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246588555 | ||||||
| chr1:246588702
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-51-2810A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246588702 | ||||||
| chr1:246588828
|
A | G | 2 | a0001c0001t0001g0166a0001c0001t0003g0292 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-51-2684A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246588828 | ||||||
| chr1:246589004
|
T | C | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-51-2508T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589004 | ||||||
| chr1:246589222
|
G | A | 2 | a0001c0001t0001g0304a0001c0001t0003g0199 | 2 | NA18969.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-51-2290G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589222 | ||||||
| chr1:246589265
|
T | TC | 13 | a0001c0001t0001g0128a0001c0001t0002g0187a0001c0001t0002g0233others(10): Show | 13 | HG01099.hp1 HG01192.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51-2241dupC | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246589265 | |||||
| chr1:246589402
|
A | G | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-51-2110A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589402 | ||||||
| chr1:246589410
|
C | T | 8 | a0002c0002t0001g0110a0002c0002t0001g0126a0002c0002t0001g0139others(5): Show | 8 | HG00639.hp2 HG02129.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.-51-2102C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589410 | ||||||
| chr1:246589421
|
A | T | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-51-2091A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589421 | ||||||
| chr1:246589427
|
C | T | 1 | a0001c0001t0002g0244 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-51-2085C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589427 | ||||||
| chr1:246589449
|
A | C | 1 | a0008c0007t0003g0267 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-51-2063A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589449 | ||||||
| chr1:246589460
|
A | C | 7 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(4): Show | 7 | HG00140.hp1 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.-51-2052A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589460 | ||||||
| chr1:246589507
|
T | C | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-51-2005T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589507 | ||||||
| chr1:246589516
|
G | T | 13 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0037others(10): Show | 13 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-51-1996G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589516 | ||||||
| chr1:246589528
|
C | G | 273 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(270): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.-51-1984C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589528 | ||||||
| chr1:246589551
|
T | C | 1 | a0001c0001t0001g0135 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-51-1961T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589551 | ||||||
| chr1:246589587
|
G | A | 13 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0037others(10): Show | 13 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-51-1925G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589587 | ||||||
| chr1:246589641
|
G | A | 1 | a0001c0001t0024g0269 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-51-1871G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589641 | ||||||
| chr1:246589832
|
C | G | 10 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(7): Show | 10 | HG00735.hp1 HG02630.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-51-1680C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589832 | ||||||
| chr1:246589832
|
C | T | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-51-1680C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589832 | ||||||
| chr1:246589908
|
G | A | 8 | a0001c0001t0001g0312a0001c0001t0002g0186a0001c0001t0002g0187others(5): Show | 8 | HG00423.hp1 NA18950.hp2 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.-51-1604G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589908 | ||||||
| chr1:246589941
|
C | T | 6 | a0004c0004t0003g0119a0004c0004t0003g0184a0004c0004t0003g0185others(3): Show | 6 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51-1571C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589941 | ||||||
| chr1:246589998
|
G | A | 2 | a0001c0001t0001g0240a0001c0001t0001g0283 | 2 | NA18945.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-51-1514G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589998 | ||||||
| chr1:246590078
|
C | T | 1 | a0006c0005t0023g0043 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-51-1434C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246590078 | ||||||
| chr1:246590237
|
C | T | 2 | a0002c0002t0015g0168a0007c0011t0015g0213 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-51-1275C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246590237 | ||||||
| chr1:246590282
|
G | A | 1 | a0001c0001t0004g0007 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-51-1230G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246590282 | ||||||
| chr1:246590450
|
T | G | 1 | a0001c0001t0001g0121 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-51-1062T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246590450 | ||||||
| chr1:246590488
|
G | A | 1 | a0007c0011t0015g0213 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-51-1024G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246590488 | ||||||
| chr1:246590512
|
C | T | 8 | a0001c0001t0001g0135a0001c0001t0004g0042a0001c0001t0004g0100others(5): Show | 8 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-51-1000C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246590512 | ||||||
| chr1:246590621
|
A | G | 102 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0053others(99): Show | 104 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.-51-891A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246590621 | ||||||
| chr1:246590648
|
G | GT | 316 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(313): Show | 318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.-51-857dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246590648 | |||||
| chr1:246590738
|
G | A | 1 | a0001c0001t0003g0259 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-51-774G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246590738 | ||||||
| chr1:246590859
|
C | CT | 105 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0053others(102): Show | 107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.-51-636dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246590859 | |||||
| chr1:246590859
|
CTTTT | C | 7 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(4): Show | 7 | HG00140.hp1 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.-51-639_-51-636del others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246590859 | |||||
| chr1:246590944
|
A | G | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-51-568A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246590944 | ||||||
| chr1:246590962
|
A | T | 1 | a0001c0001t0001g0052 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-51-550A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246590962 | ||||||
| chr1:246591015
|
T | A | 1 | a0001c0001t0001g0166 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-51-497T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246591015 | ||||||
| chr1:246591016
|
A | T | 149 | a0001c0001t0001g0022a0001c0001t0001g0088a0001c0001t0001g0089others(146): Show | 149 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.-51-496A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246591016 | ||||||
| chr1:246591113
|
T | C | 2 | a0002c0002t0001g0139a0002c0002t0001g0140 | 2 | NA18960.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-51-399T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246591113 | ||||||
| chr1:246591314
|
C | T | 2 | a0001c0001t0003g0047a0001c0001t0003g0048 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-51-198C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246591314 | ||||||
| chr1:246591440
|
G | A | 1 | a0001c0001t0025g0288 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-51-72G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246591440 | ||||||
| chr1:246591476
|
G | GA | 137 | a0001c0001t0001g0022a0001c0001t0001g0135a0001c0001t0001g0156others(134): Show | 137 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.-51-32dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246591476 | |||||
| chr1:246591979
|
A | T | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.379+38A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246591979 | ||||||
| chr1:246592198
|
C | G | 2 | a0001c0001t0001g0166a0001c0001t0003g0292 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.379+257C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246592198 | ||||||
| chr1:246592211
|
G | A | 1 | a0001c0001t0003g0261 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.379+270G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246592211 | ||||||
| chr1:246592217
|
G | A | 4 | a0001c0001t0002g0172a0001c0001t0002g0175a0001c0001t0004g0173others(1): Show | 4 | HG01884.hp2 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.379+276G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246592217 | ||||||
| chr1:246592226
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.379+285C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246592226 | ||||||
| chr1:246592574
|
C | T | 1 | a0001c0001t0003g0226 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.379+633C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246592574 | ||||||
| chr1:246592705
|
C | T | 1 | a0002c0002t0001g0120 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.379+764C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246592705 | ||||||
| chr1:246592813
|
T | C | 2 | a0001c0001t0001g0170a0001c0001t0003g0181 | 2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.379+872T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246592813 | ||||||
| chr1:246592822
|
G | A | 1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.379+881G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246592822 | ||||||
| chr1:246592862
|
G | C | 1 | a0001c0001t0002g0235 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.379+921G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246592862 | ||||||
| chr1:246593261
|
C | T | 243 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(240): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.379+1320C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246593261 | ||||||
| chr1:246593319
|
CT | C | 57 | a0001c0001t0001g0194a0001c0001t0001g0207a0001c0001t0001g0215others(54): Show | 57 | HG00280.hp2 HG00558.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.379+1391delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246593319 | |||||
| chr1:246593408
|
C | T | 2 | a0001c0001t0017g0008a0001c0006t0001g0009 | 2 | HG01981.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.379+1467C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246593408 | ||||||
| chr1:246593558
|
G | T | 1 | a0001c0001t0002g0201 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.379+1617G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246593558 | ||||||
| chr1:246593631
|
C | T | 1 | a0001c0001t0002g0064 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.379+1690C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246593631 | ||||||
| chr1:246593741
|
C | T | 1 | a0001c0001t0001g0249 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.379+1800C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246593741 | ||||||
| chr1:246593865
|
C | T | 2 | a0001c0001t0001g0274a0001c0001t0003g0003 | 2 | HG02109.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.379+1924C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246593865 | ||||||
| chr1:246594012
|
C | T | 2 | a0001c0001t0001g0308a0001c0001t0001g0309 | 2 | HG00408.hp1 HG00408.hp2 |
intron_variant | MODIFIER | c.379+2071C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246594012 | ||||||
| chr1:246594026
|
C | T | 1 | a0006c0005t0023g0043 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.379+2085C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246594026 | ||||||
| chr1:246594147
|
T | C | 275 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(272): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.379+2206T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246594147 | ||||||
| chr1:246594248
|
C | G | 1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.379+2307C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246594248 | ||||||
| chr1:246594281
|
C | G | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.379+2340C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246594281 | ||||||
| chr1:246594385
|
A | G | 2 | a0001c0001t0001g0194a0001c0001t0001g0207 | 2 | HG00621.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.379+2444A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246594385 | ||||||
| chr1:246594731
|
T | A | 3 | a0003c0003t0004g0034a0003c0003t0004g0035a0003c0003t0004g0036 | 3 | HG01243.hp1 HG02896.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.379+2790T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246594731 | ||||||
| chr1:246594860
|
C | T | 279 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(276): Show | 281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.379+2919C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246594860 | ||||||
| chr1:246595000
|
G | A | 1 | a0001c0001t0002g0233 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.379+3059G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246595000 | ||||||
| chr1:246595484
|
C | T | 2 | a0002c0002t0015g0168a0007c0011t0015g0213 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.379+3543C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246595484 | ||||||
| chr1:246595591
|
T | C | 2 | a0001c0001t0003g0003a0001c0001t0003g0211 | 2 | NA18962.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.379+3650T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246595591 | ||||||
| chr1:246595635
|
T | C | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG02056.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.379+3694T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246595635 | ||||||
| chr1:246595817
|
G | T | 1 | a0001c0001t0001g0087 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.379+3876G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246595817 | ||||||
| chr1:246595991
|
G | C | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.379+4050G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246595991 | ||||||
| chr1:246596151
|
C | T | 1 | a0001c0001t0003g0082 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.379+4210C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246596151 | ||||||
| chr1:246596341
|
G | A | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.379+4400G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246596341 | ||||||
| chr1:246596397
|
C | CA | 8 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(5): Show | 8 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.379+4469dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246596397 | |||||
| chr1:246596780
|
C | T | 279 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(276): Show | 281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.379+4839C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246596780 | ||||||
| chr1:246596821
|
A | T | 1 | a0001c0001t0011g0212 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.379+4880A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246596821 | ||||||
| chr1:246596829
|
A | T | 273 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(270): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.379+4888A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246596829 | ||||||
| chr1:246596910
|
T | C | 1 | a0001c0001t0003g0294 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.379+4969T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246596910 | ||||||
| chr1:246596971
|
G | C | 13 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0037others(10): Show | 13 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.379+5030G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246596971 | ||||||
| chr1:246597165
|
G | T | 9 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(6): Show | 9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.379+5224G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246597165 | ||||||
| chr1:246597250
|
C | T | 7 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(4): Show | 7 | HG00140.hp1 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.379+5309C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246597250 | ||||||
| chr1:246597268
|
C | G | 102 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0053others(99): Show | 104 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.379+5327C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246597268 | ||||||
| chr1:246597342
|
C | A | 7 | a0001c0001t0001g0025a0001c0001t0004g0004a0001c0001t0004g0006others(4): Show | 7 | HG02723.hp2 HG02818.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.379+5401C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246597342 | ||||||
| chr1:246597542
|
G | A | 1 | a0001c0001t0002g0005 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.379+5601G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246597542 | ||||||
| chr1:246597601
|
T | C | 2 | a0002c0002t0015g0168a0007c0011t0015g0213 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.379+5660T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246597601 | ||||||
| chr1:246597649
|
T | C | 6 | a0001c0001t0002g0225a0001c0001t0003g0226a0001c0001t0003g0227others(3): Show | 6 | HG00423.hp2 NA18985.hp1 NA18999.hp2 others(3): Show |
intron_variant | MODIFIER | c.379+5708T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246597649 | ||||||
| chr1:246597973
|
GTATT | G | 270 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(267): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.379+6055_379+6058d others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246597973 | |||||
| chr1:246597973
|
GTATTTAT others(5): Show |
G | 4 | a0002c0002t0001g0171a0002c0002t0006g0029a0002c0002t0006g0030others(1): Show | 4 | HG02486.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.379+6047_379+6058d others(14): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246597973 | |||||
| chr1:246598087
|
T | G | 1 | a0001c0001t0003g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.379+6146T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246598087 | ||||||
| chr1:246598149
|
A | AT | 13 | a0001c0001t0001g0169a0001c0001t0001g0299a0003c0003t0001g0032others(10): Show | 13 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.379+6224dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246598149 | |||||
| chr1:246598149
|
AT | A | 209 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(206): Show | 211 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.379+6224delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246598149 | |||||
| chr1:246598477
|
A | G | 1 | a0001c0001t0003g0206 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.379+6536A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246598477 | ||||||
| chr1:246598615
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0290 | 2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.379+6674G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246598615 | ||||||
| chr1:246598719
|
T | C | 17 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0167others(14): Show | 17 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.379+6778T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246598719 | ||||||
| chr1:246599129
|
T | A | 1 | a0001c0001t0004g0157 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.379+7188T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246599129 | ||||||
| chr1:246599176
|
GA | G | 19 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0167others(16): Show | 19 | HG01884.hp2 HG02040.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.379+7249delA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246599176 | |||||
| chr1:246599232
|
A | G | 2 | a0002c0002t0015g0168a0007c0011t0015g0213 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.379+7291A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246599232 | ||||||
| chr1:246599283
|
C | T | 1 | a0002c0002t0001g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.379+7342C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246599283 | ||||||
| chr1:246599388
|
G | A | 2 | a0001c0001t0002g0102a0001c0001t0002g0103 | 2 | HG00140.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.379+7447G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246599388 | ||||||
| chr1:246599437
|
C | G | 9 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.379+7496C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246599437 | ||||||
| chr1:246599480
|
G | C | 1 | a0001c0001t0022g0085 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.379+7539G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246599480 | ||||||
| chr1:246599552
|
G | A | 1 | a0002c0002t0001g0120 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.379+7611G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246599552 | ||||||
| chr1:246599600
|
T | C | 1 | a0002c0002t0001g0146 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.379+7659T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246599600 | ||||||
| chr1:246599680
|
A | G | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.379+7739A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246599680 | ||||||
| chr1:246599756
|
T | G | 1 | a0001c0001t0003g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.379+7815T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246599756 | ||||||
| chr1:246599837
|
A | T | 1 | a0001c0001t0003g0144 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.379+7896A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246599837 | ||||||
| chr1:246600164
|
G | A | 1 | a0001c0001t0008g0021 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.379+8223G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246600164 | ||||||
| chr1:246600191
|
G | A | 1 | a0001c0001t0004g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.379+8250G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246600191 | ||||||
| chr1:246600308
|
T | C | 1 | a0001c0012t0002g0278 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.379+8367T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246600308 | ||||||
| chr1:246600748
|
G | A | 1 | a0001c0001t0003g0055 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.379+8807G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246600748 | ||||||
| chr1:246600751
|
G | A | 1 | a0001c0001t0024g0269 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.379+8810G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246600751 | ||||||
| chr1:246601101
|
T | C | 5 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0004g0034others(2): Show | 5 | HG01243.hp1 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.379+9160T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246601101 | ||||||
| chr1:246601163
|
G | C | 1 | a0001c0001t0003g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.379+9222G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246601163 | ||||||
| chr1:246601323
|
C | T | 7 | a0001c0001t0001g0177a0001c0001t0004g0017a0001c0001t0004g0018others(4): Show | 7 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.379+9382C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246601323 | ||||||
| chr1:246601337
|
G | T | 1 | a0001c0001t0001g0266 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.379+9396G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246601337 | ||||||
| chr1:246601372
|
C | CACCAACT others(7): Show |
1 | a0001c0001t0018g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.379+9433_379+9446d others(16): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246601372 | |||||
| chr1:246601555
|
G | A | 13 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0037others(10): Show | 13 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.379+9614G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246601555 | ||||||
| chr1:246601624
|
A | G | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.379+9683A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246601624 | ||||||
| chr1:246601637
|
A | G | 1 | a0002c0002t0001g0127 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.379+9696A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246601637 | ||||||
| chr1:246601655
|
G | A | 1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.379+9714G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246601655 | ||||||
| chr1:246601660
|
G | A | 7 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(4): Show | 7 | HG00140.hp1 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.379+9719G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246601660 | ||||||
| chr1:246601700
|
G | A | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.379+9759G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246601700 | ||||||
| chr1:246601845
|
A | G | 1 | a0001c0001t0003g0081 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.379+9904A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246601845 | ||||||
| chr1:246601895
|
A | C | 8 | a0001c0001t0001g0135a0001c0001t0004g0016a0001c0001t0004g0042others(5): Show | 8 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.379+9954A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246601895 | ||||||
| chr1:246602075
|
T | G | 1 | a0001c0001t0004g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.379+10134T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246602075 | ||||||
| chr1:246602504
|
A | G | 26 | a0001c0001t0001g0198a0001c0001t0001g0210a0001c0001t0001g0219others(23): Show | 26 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(23): Show |
intron_variant | MODIFIER | c.379+10563A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246602504 | ||||||
| chr1:246602535
|
C | G | 1 | a0001c0001t0001g0283 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.379+10594C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246602535 | ||||||
| chr1:246602706
|
C | T | 7 | a0001c0001t0003g0003a0003c0003t0001g0032a0003c0003t0001g0033others(4): Show | 7 | HG00733.hp1 HG01891.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.379+10765C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246602706 | ||||||
| chr1:246602836
|
G | C | 3 | a0001c0001t0001g0217a0001c0001t0001g0254a0001c0001t0002g0201 | 3 | HG00673.hp1 NA18969.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.379+10895G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246602836 | ||||||
| chr1:246602897
|
G | GT | 150 | a0001c0001t0001g0022a0001c0001t0001g0088a0001c0001t0001g0089others(147): Show | 150 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.379+10968dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246602897 | |||||
| chr1:246602897
|
GT | G | 97 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(94): Show | 99 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.379+10968delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246602897 | |||||
| chr1:246602953
|
G | T | 1 | a0008c0007t0003g0267 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.379+11012G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246602953 | ||||||
| chr1:246602968
|
A | G | 1 | a0001c0001t0004g0157 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.379+11027A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246602968 | ||||||
| chr1:246602970
|
G | A | 7 | a0001c0001t0001g0177a0001c0001t0004g0017a0001c0001t0004g0018others(4): Show | 7 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.379+11029G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246602970 | ||||||
| chr1:246603133
|
A | G | 273 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(270): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.379+11192A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246603133 | ||||||
| chr1:246603345
|
CTAAA | C | 125 | a0001c0001t0001g0022a0001c0001t0001g0135a0001c0001t0001g0156others(122): Show | 125 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.379+11407_379+1141 others(8): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246603345 | |||||
| chr1:246603508
|
T | TTTAAACA others(11): Show |
1 | a0001c0001t0002g0302 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.379+11568_379+1158 others(22): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246603508 | |||||
| chr1:246603585
|
A | T | 2 | a0002c0002t0015g0168a0007c0011t0015g0213 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.379+11644A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246603585 | ||||||
| chr1:246603696
|
A | T | 273 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(270): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.379+11755A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246603696 | ||||||
| chr1:246603742
|
A | G | 3 | a0002c0002t0015g0168a0007c0011t0015g0213a0009c0008t0001g0161 | 3 | HG02622.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.379+11801A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246603742 | ||||||
| chr1:246603889
|
C | T | 275 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(272): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.379+11948C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246603889 | ||||||
| chr1:246603975
|
C | T | 1 | a0003c0003t0001g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.379+12034C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246603975 | ||||||
| chr1:246603994
|
C | T | 7 | a0001c0001t0001g0177a0001c0001t0004g0017a0001c0001t0004g0018others(4): Show | 7 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.379+12053C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246603994 | ||||||
| chr1:246604238
|
C | T | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.379+12297C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246604238 | ||||||
| chr1:246604272
|
A | G | 4 | a0001c0001t0003g0069a0001c0001t0003g0092a0002c0002t0015g0168others(1): Show | 4 | HG01952.hp2 HG01981.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.379+12331A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246604272 | ||||||
| chr1:246604304
|
A | AAGAAACG others(53): Show |
1 | a0001c0001t0001g0089 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.379+12365_379+1242 others(64): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246604304 | |||||
| chr1:246604628
|
A | T | 1 | a0001c0001t0013g0196 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.379+12687A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246604628 | ||||||
| chr1:246604673
|
AT | A | 4 | a0001c0001t0001g0160a0001c0001t0004g0157a0001c0001t0004g0158others(1): Show | 4 | HG01109.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.379+12734delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246604673 | |||||
| chr1:246604681
|
T | TATTTTGA others(36): Show |
2 | a0002c0002t0015g0168a0007c0011t0015g0213 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.379+12743_379+1278 others(47): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246604681 | |||||
| chr1:246604697
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.379+12756C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246604697 | ||||||
| chr1:246604723
|
C | T | 1 | a0001c0001t0003g0096 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.379+12782C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246604723 | ||||||
| chr1:246604729
|
C | T | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.379+12788C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246604729 | ||||||
| chr1:246604743
|
A | C | 2 | a0001c0001t0001g0156a0001c0001t0001g0291 | 2 | HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.379+12802A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246604743 | ||||||
| chr1:246604831
|
G | A | 1 | a0001c0001t0005g0023 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.379+12890G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246604831 | ||||||
| chr1:246604838
|
T | G | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.379+12897T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246604838 | ||||||
| chr1:246605043
|
C | A | 1 | a0001c0001t0002g0183 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.379+13102C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605043 | ||||||
| chr1:246605182
|
A | T | 2 | a0003c0003t0004g0162a0006c0005t0023g0043 | 2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.379+13241A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605182 | ||||||
| chr1:246605203
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.379+13262A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605203 | ||||||
| chr1:246605304
|
G | A | 2 | a0001c0001t0001g0170a0001c0001t0003g0181 | 2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.379+13363G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605304 | ||||||
| chr1:246605360
|
G | C | 60 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0086others(57): Show | 61 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.379+13419G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605360 | ||||||
| chr1:246605363
|
T | A | 1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.379+13422T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605363 | ||||||
| chr1:246605368
|
G | T | 5 | a0002c0002t0001g0027a0002c0002t0001g0122a0002c0002t0001g0130others(2): Show | 5 | HG00741.hp2 HG01175.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.379+13427G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605368 | ||||||
| chr1:246605437
|
C | T | 1 | a0001c0001t0004g0015 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.379+13496C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605437 | ||||||
| chr1:246605467
|
G | A | 3 | a0001c0001t0002g0258a0001c0001t0002g0262a0001c0001t0002g0284 | 3 | HG02698.hp1 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.379+13526G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605467 | ||||||
| chr1:246605487
|
T | A | 1 | a0001c0001t0003g0282 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.379+13546T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605487 | ||||||
| chr1:246605503
|
T | C | 1 | a0001c0001t0002g0281 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.379+13562T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605503 | ||||||
| chr1:246605536
|
G | A | 3 | a0002c0002t0001g0139a0002c0002t0001g0140a0002c0002t0007g0142 | 3 | NA18960.hp2 NA18979.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.379+13595G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605536 | ||||||
| chr1:246605541
|
A | G | 278 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(275): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.379+13600A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605541 | ||||||
| chr1:246605549
|
G | A | 9 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(6): Show | 9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.379+13608G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605549 | ||||||
| chr1:246605571
|
C | T | 1 | a0001c0001t0002g0005 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.379+13630C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605571 | ||||||
| chr1:246605641
|
C | T | 1 | a0001c0001t0002g0072 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.379+13700C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605641 | ||||||
| chr1:246605648
|
GGGTGTCT others(73): Show |
G | 73 | a0001c0001t0001g0025a0001c0001t0001g0061a0001c0001t0001g0076others(70): Show | 74 | HG00423.hp2 HG00558.hp2 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.379+13787_379+1386 others(84): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605648 | |||||
| chr1:246605666
|
G | T | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.379+13725G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605666 | ||||||
| chr1:246605669
|
CGTGTCTT others(13): Show |
C | 15 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(12): Show | 15 | HG00735.hp1 HG00741.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.379+13787_379+1380 others(24): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605669 | |||||
| chr1:246605688
|
A | G | 2 | a0001c0001t0001g0166a0001c0001t0003g0292 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.379+13747A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605688 | ||||||
| chr1:246605689
|
G | C | 2 | a0001c0001t0001g0166a0001c0001t0003g0292 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.379+13748G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605689 | ||||||
| chr1:246605709
|
G | GGTGTCTT others(13): Show |
4 | a0001c0001t0001g0210a0001c0001t0001g0246a0001c0001t0002g0232others(1): Show | 4 | HG00735.hp2 HG02056.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.379+13786_379+1378 others(24): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605709 | |||||
| chr1:246605709
|
GGTGTCTT others(33): Show |
G | 1 | a0001c0001t0001g0166 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.379+13807_379+1384 others(44): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605709 | |||||
| chr1:246605723
|
GGGGTAGG others(72): Show |
G | 1 | a0001c0001t0003g0068 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.379+13786_379+1386 others(83): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605723 | |||||
| chr1:246605728
|
A | G | 31 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(28): Show | 32 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.379+13787A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605728 | ||||||
| chr1:246605729
|
G | C | 31 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(28): Show | 32 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.379+13788G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605729 | ||||||
| chr1:246605729
|
GGTGTCTT others(13): Show |
G | 1 | a0001c0001t0003g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.379+13807_379+1382 others(24): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605729 | |||||
| chr1:246605738
|
C | T | 12 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0037others(9): Show | 12 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.379+13797C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605738 | ||||||
| chr1:246605748
|
G | A | 35 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(32): Show | 36 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.379+13807G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605748 | ||||||
| chr1:246605749
|
C | CGTGTCTT others(13): Show |
5 | a0001c0001t0001g0202a0001c0001t0002g0302a0001c0001t0005g0155others(2): Show | 5 | HG01261.hp1 HG01433.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.379+13847_379+1386 others(24): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605749 | |||||
| chr1:246605749
|
C | G | 35 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(32): Show | 36 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.379+13808C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605749 | ||||||
| chr1:246605758
|
C | T | 1 | a0001c0001t0002g0233 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.379+13817C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605758 | ||||||
| chr1:246605759
|
GGCCGGGG others(53): Show |
G | 31 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(28): Show | 32 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.379+13847_379+1390 others(64): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605759 | |||||
| chr1:246605762
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0169others(2): Show | 5 | HG02647.hp1 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.379+13821C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605762 | ||||||
| chr1:246605768
|
A | G | 14 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0169others(11): Show | 14 | HG01884.hp2 HG01981.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.379+13827A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605768 | ||||||
| chr1:246605769
|
G | C | 14 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0169others(11): Show | 14 | HG01884.hp2 HG01981.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.379+13828G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605769 | ||||||
| chr1:246605776
|
T | C | 1 | a0001c0001t0003g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.379+13835T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605776 | ||||||
| chr1:246605788
|
A | G | 4 | a0001c0001t0001g0210a0001c0001t0001g0246a0001c0001t0002g0232others(1): Show | 4 | HG00735.hp2 HG02056.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.379+13847A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605788 | ||||||
| chr1:246605789
|
G | C | 4 | a0001c0001t0001g0210a0001c0001t0001g0246a0001c0001t0002g0232others(1): Show | 4 | HG00735.hp2 HG02056.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.379+13848G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605789 | ||||||
| chr1:246605789
|
G | GGTGTCTT others(33): Show |
103 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(100): Show | 103 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.379+13866_379+1386 others(44): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605789 | |||||
| chr1:246605789
|
G | GGTGTCTT others(53): Show |
1 | a0001c0001t0002g0209 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.379+13866_379+1386 others(64): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605789 | |||||
| chr1:246605789
|
G | GGTGTCTT others(13): Show |
14 | a0001c0001t0005g0205a0003c0003t0001g0032a0003c0003t0001g0033others(11): Show | 14 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.379+13858_379+1387 others(24): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605789 | |||||
| chr1:246605789
|
G | GGTGTCTT others(33): Show |
9 | a0001c0001t0001g0135a0001c0001t0004g0016a0001c0001t0004g0042others(6): Show | 9 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.379+13877_379+1387 others(44): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605789 | |||||
| chr1:246605799
|
GGCCGGGG others(13): Show |
G | 2 | a0001c0001t0001g0011a0001c0001t0001g0290 | 2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.379+13867_379+1388 others(24): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605799 | |||||
| chr1:246605802
|
C | CGGGGTAG others(34): Show |
1 | a0001c0001t0003g0294 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.379+13866_379+1386 others(45): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605802 | |||||
| chr1:246605808
|
G | A | 1 | a0001c0001t0018g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.379+13867G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605808 | ||||||
| chr1:246605809
|
C | G | 1 | a0001c0001t0018g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.379+13868C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605809 | ||||||
| chr1:246605817
|
C | T | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.379+13876C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605817 | ||||||
| chr1:246605819
|
A | G | 237 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0061others(234): Show | 238 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.379+13878A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605819 | ||||||
| chr1:246605825
|
G | GGTGCGTG others(19): Show |
1 | a0001c0001t0018g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.379+13886_379+1388 others(30): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605825 | |||||
| chr1:246605828
|
A | G | 32 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(29): Show | 33 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.379+13887A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605828 | ||||||
| chr1:246605829
|
G | C | 32 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(29): Show | 33 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.379+13888G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605829 | ||||||
| chr1:246605912
|
C | T | 251 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0052others(248): Show | 253 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.379+13971C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605912 | ||||||
| chr1:246605973
|
G | A | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.379+14032G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605973 | ||||||
| chr1:246605974
|
GC | G | 5 | a0001c0001t0004g0016a0001c0001t0004g0042a0001c0001t0004g0150others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.379+14037delC | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605974 | |||||
| chr1:246605978
|
C | T | 1 | a0001c0001t0002g0183 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.379+14037C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605978 | ||||||
| chr1:246606001
|
C | T | 2 | a0004c0004t0003g0192a0004c0004t0003g0193 | 2 | HG02451.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.379+14060C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606001 | ||||||
| chr1:246606066
|
G | A | 1 | a0001c0001t0002g0311 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.379+14125G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606066 | ||||||
| chr1:246606068
|
G | A | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.379+14127G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606068 | ||||||
| chr1:246606100
|
A | T | 103 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0053others(100): Show | 105 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.379+14159A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606100 | ||||||
| chr1:246606108
|
G | A | 3 | a0001c0001t0001g0170a0001c0001t0003g0137a0001c0001t0003g0181 | 3 | HG02145.hp2 HG03195.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.379+14167G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606108 | ||||||
| chr1:246606143
|
G | A | 125 | a0001c0001t0001g0022a0001c0001t0001g0135a0001c0001t0001g0156others(122): Show | 125 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.379+14202G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606143 | ||||||
| chr1:246606207
|
G | A | 2 | a0002c0002t0015g0168a0007c0011t0015g0213 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.379+14266G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606207 | ||||||
| chr1:246606246
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.379+14305G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606246 | ||||||
| chr1:246606291
|
T | G | 13 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0037others(10): Show | 13 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.379+14350T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606291 | ||||||
| chr1:246606312
|
C | A | 1 | a0001c0001t0004g0007 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.379+14371C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606312 | ||||||
| chr1:246606364
|
C | T | 1 | a0001c0001t0003g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.379+14423C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606364 | ||||||
| chr1:246606403
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.379+14462G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606403 | ||||||
| chr1:246606417
|
A | G | 1 | a0001c0001t0003g0220 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.379+14476A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606417 | ||||||
| chr1:246606441
|
C | G | 269 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(266): Show | 271 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.379+14500C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606441 | ||||||
| chr1:246606454
|
G | C | 3 | a0001c0001t0002g0209a0004c0004t0003g0184a0004c0004t0003g0185 | 3 | HG02896.hp2 HG02897.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.379+14513G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606454 | ||||||
| chr1:246606462
|
C | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0289a0001c0001t0008g0020others(1): Show | 4 | HG02145.hp1 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.379+14521C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606462 | ||||||
| chr1:246606542
|
C | T | 9 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(6): Show | 9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.379+14601C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606542 | ||||||
| chr1:246606596
|
G | T | 103 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0053others(100): Show | 105 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.379+14655G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606596 | ||||||
| chr1:246606597
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.379+14656T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606597 | ||||||
| chr1:246606612
|
A | G | 102 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0053others(99): Show | 104 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.379+14671A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606612 | ||||||
| chr1:246606618
|
G | C | 105 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0053others(102): Show | 107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.379+14677G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606618 | ||||||
| chr1:246606674
|
C | T | 2 | a0001c0001t0004g0275a0002c0002t0001g0171 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.379+14733C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606674 | ||||||
| chr1:246606718
|
G | A | 2 | a0001c0001t0001g0166a0001c0001t0003g0292 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.380-14711G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606718 | ||||||
| chr1:246606811
|
G | A | 1 | a0002c0002t0001g0117 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.380-14618G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606811 | ||||||
| chr1:246606813
|
T | C | 1 | a0002c0002t0001g0117 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.380-14616T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606813 | ||||||
| chr1:246606864
|
C | T | 6 | a0004c0004t0003g0119a0004c0004t0003g0184a0004c0004t0003g0185others(3): Show | 6 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.380-14565C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606864 | ||||||
| chr1:246606909
|
G | A | 315 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(312): Show | 317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.380-14520G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606909 | ||||||
| chr1:246606957
|
C | G | 253 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0052others(250): Show | 255 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.380-14472C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606957 | ||||||
| chr1:246606960
|
A | G | 1 | a0001c0001t0001g0249 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.380-14469A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606960 | ||||||
| chr1:246606963
|
T | C | 1 | a0001c0001t0001g0166 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.380-14466T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606963 | ||||||
| chr1:246606974
|
TTAG | T | 103 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0053others(100): Show | 105 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.380-14453_380-1445 others(7): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246606974 | |||||
| chr1:246606999
|
C | T | 1 | a0001c0001t0002g0232 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.380-14430C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606999 | ||||||
| chr1:246607043
|
G | T | 9 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(6): Show | 9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.380-14386G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607043 | ||||||
| chr1:246607054
|
G | A | 10 | a0001c0001t0001g0132a0001c0001t0003g0063a0001c0001t0003g0065others(7): Show | 10 | HG00423.hp2 HG01255.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.380-14375G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607054 | ||||||
| chr1:246607268
|
G | T | 1 | a0001c0001t0001g0264 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.380-14161G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607268 | ||||||
| chr1:246607302
|
C | T | 6 | a0004c0004t0003g0119a0004c0004t0003g0184a0004c0004t0003g0185others(3): Show | 6 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.380-14127C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607302 | ||||||
| chr1:246607325
|
A | G | 125 | a0001c0001t0001g0022a0001c0001t0001g0135a0001c0001t0001g0156others(122): Show | 125 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.380-14104A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607325 | ||||||
| chr1:246607334
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0290 | 2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.380-14095A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607334 | ||||||
| chr1:246607407
|
G | T | 90 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(87): Show | 92 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.380-14022G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607407 | ||||||
| chr1:246607586
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.380-13843G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607586 | ||||||
| chr1:246607600
|
C | T | 7 | a0002c0002t0001g0111a0002c0002t0001g0112a0002c0002t0001g0114others(4): Show | 7 | HG02040.hp1 HG02074.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.380-13829C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607600 | ||||||
| chr1:246607678
|
A | AT | 269 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(266): Show | 271 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.380-13751_380-1375 others(5): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607678 | ||||||
| chr1:246607687
|
C | T | 102 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0053others(99): Show | 104 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.380-13742C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607687 | ||||||
| chr1:246607803
|
C | T | 1 | a0001c0001t0002g0281 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.380-13626C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607803 | ||||||
| chr1:246607881
|
G | T | 14 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0169others(11): Show | 14 | HG01884.hp2 HG01981.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.380-13548G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607881 | ||||||
| chr1:246607919
|
G | A | 1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.380-13510G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607919 | ||||||
| chr1:246607930
|
A | C | 1 | a0001c0001t0004g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.380-13499A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607930 | ||||||
| chr1:246607984
|
G | A | 13 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0037others(10): Show | 13 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.380-13445G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607984 | ||||||
| chr1:246608030
|
G | A | 1 | a0001c0001t0002g0285 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.380-13399G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246608030 | ||||||
| chr1:246608056
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.380-13373G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246608056 | ||||||
| chr1:246608136
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0004g0026 | 2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.380-13293C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246608136 | ||||||
| chr1:246608160
|
A | C | 1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.380-13269A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246608160 | ||||||
| chr1:246608165
|
AAATAAAT others(4): Show |
A | 1 | a0001c0001t0004g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.380-13249_380-1323 others(15): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246608165 | |||||
| chr1:246608178
|
AT | A | 11 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0037others(8): Show | 11 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.380-13250delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246608178 | ||||||
| chr1:246608387
|
T | C | 9 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(6): Show | 9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.380-13042T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246608387 | ||||||
| chr1:246608647
|
C | G | 1 | a0001c0001t0001g0135 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.380-12782C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246608647 | ||||||
| chr1:246608649
|
C | T | 1 | a0001c0001t0004g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.380-12780C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246608649 | ||||||
| chr1:246608702
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.380-12727G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246608702 | ||||||
| chr1:246608717
|
G | A | 104 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0053others(101): Show | 106 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.380-12712G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246608717 | ||||||
| chr1:246608909
|
C | T | 11 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0037others(8): Show | 11 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.380-12520C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246608909 | ||||||
| chr1:246609056
|
G | A | 103 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0053others(100): Show | 105 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.380-12373G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246609056 | ||||||
| chr1:246609352
|
G | T | 9 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(6): Show | 9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.380-12077G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246609352 | ||||||
| chr1:246609404
|
C | T | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.380-12025C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246609404 | ||||||
| chr1:246610102
|
G | C | 1 | a0001c0001t0001g0087 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.380-11327G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610102 | ||||||
| chr1:246610125
|
A | G | 1 | a0001c0001t0022g0085 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.380-11304A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610125 | ||||||
| chr1:246610149
|
G | A | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.380-11280G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610149 | ||||||
| chr1:246610282
|
AAAAC | A | 10 | a0001c0001t0001g0025a0001c0001t0001g0170a0001c0001t0001g0248others(7): Show | 10 | HG02083.hp2 HG02145.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.380-11131_380-1112 others(8): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246610282 | |||||
| chr1:246610441
|
A | T | 1 | a0001c0001t0001g0166 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.380-10988A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610441 | ||||||
| chr1:246610503
|
C | G | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.380-10926C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610503 | ||||||
| chr1:246610515
|
G | GT | 4 | a0001c0001t0001g0234a0001c0001t0004g0014a0001c0001t0004g0134others(1): Show | 4 | HG02074.hp2 HG02602.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.380-10907dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246610515 | |||||
| chr1:246610538
|
G | T | 104 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0053others(101): Show | 106 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.380-10891G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610538 | ||||||
| chr1:246610556
|
G | A | 2 | a0001c0001t0003g0250a0001c0001t0003g0270 | 2 | HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.380-10873G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610556 | ||||||
| chr1:246610604
|
C | G | 1 | a0001c0001t0002g0232 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.380-10825C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610604 | ||||||
| chr1:246610614
|
G | A | 1 | a0001c0001t0003g0075 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.380-10815G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610614 | ||||||
| chr1:246610770
|
C | T | 2 | a0001c0001t0010g0229a0001c0001t0010g0230 | 2 | HG00558.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.380-10659C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610770 | ||||||
| chr1:246610786
|
G | A | 2 | a0001c0001t0001g0314a0001c0001t0002g0315 | 2 | HG00673.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.380-10643G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610786 | ||||||
| chr1:246610790
|
G | A | 3 | a0001c0001t0002g0258a0001c0001t0002g0262a0001c0001t0002g0284 | 3 | HG02698.hp1 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.380-10639G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610790 | ||||||
| chr1:246610809
|
C | T | 2 | a0003c0003t0004g0162a0006c0005t0023g0043 | 2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.380-10620C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610809 | ||||||
| chr1:246610810
|
G | A | 2 | a0001c0001t0001g0312a0001c0001t0002g0313 | 2 | NA18993.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.380-10619G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610810 | ||||||
| chr1:246610826
|
T | C | 1 | a0001c0001t0004g0134 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.380-10603T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610826 | ||||||
| chr1:246610827
|
C | T | 1 | a0001c0001t0004g0134 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.380-10602C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610827 | ||||||
| chr1:246610856
|
C | T | 1 | a0001c0001t0002g0238 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.380-10573C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610856 | ||||||
| chr1:246610912
|
G | A | 2 | a0002c0002t0015g0168a0007c0011t0015g0213 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.380-10517G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610912 | ||||||
| chr1:246610926
|
C | T | 1 | a0002c0002t0001g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.380-10503C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610926 | ||||||
| chr1:246610979
|
A | G | 12 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0169others(9): Show | 12 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.380-10450A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610979 | ||||||
| chr1:246610998
|
C | T | 1 | a0003c0003t0004g0034 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.380-10431C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610998 | ||||||
| chr1:246611262
|
G | A | 1 | a0006c0005t0023g0043 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.380-10167G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246611262 | ||||||
| chr1:246611298
|
T | C | 105 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0053others(102): Show | 107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.380-10131T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246611298 | ||||||
| chr1:246611317
|
A | G | 1 | a0001c0001t0009g0013 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.380-10112A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246611317 | ||||||
| chr1:246611325
|
T | C | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.380-10104T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246611325 | ||||||
| chr1:246611339
|
G | GT | 7 | a0002c0002t0001g0141a0004c0004t0003g0119a0004c0004t0003g0184others(4): Show | 7 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.380-10081dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246611339 | |||||
| chr1:246611348
|
T | A | 3 | a0001c0001t0001g0167a0001c0001t0001g0169a0001c0001t0003g0316 | 3 | HG02809.hp1 HG03516.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.380-10081T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246611348 | ||||||
| chr1:246611349
|
A | T | 6 | a0004c0004t0003g0119a0004c0004t0003g0184a0004c0004t0003g0185others(3): Show | 6 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.380-10080A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246611349 | ||||||
| chr1:246611393
|
G | A | 9 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(6): Show | 9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.380-10036G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246611393 | ||||||
| chr1:246611459
|
G | A | 1 | a0002c0002t0001g0268 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.380-9970G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246611459 | ||||||
| chr1:246611490
|
A | C | 1 | a0001c0001t0003g0068 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.380-9939A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246611490 | ||||||
| chr1:246611607
|
G | GA | 6 | a0001c0001t0001g0217a0001c0001t0001g0307a0001c0001t0002g0101others(3): Show | 6 | HG00733.hp2 HG02083.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.380-9815dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246611607 | |||||
| chr1:246611615
|
C | A | 100 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(97): Show | 102 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.380-9814C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246611615 | ||||||
| chr1:246611778
|
C | G | 1 | a0001c0001t0001g0306 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.380-9651C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246611778 | ||||||
| chr1:246611786
|
C | CATAGCAG others(19): Show |
1 | a0001c0001t0002g0224 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.380-9641_380-9616d others(28): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246611786 | |||||
| chr1:246612124
|
G | A | 1 | a0001c0001t0001g0304 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.380-9305G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246612124 | ||||||
| chr1:246612148
|
T | C | 2 | a0001c0001t0001g0166a0001c0001t0003g0292 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.380-9281T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246612148 | ||||||
| chr1:246612183
|
T | C | 6 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.380-9246T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246612183 | ||||||
| chr1:246612328
|
A | G | 1 | a0001c0001t0002g0223 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.380-9101A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246612328 | ||||||
| chr1:246612566
|
T | A | 1 | a0001c0001t0002g0244 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.380-8863T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246612566 | ||||||
| chr1:246612569
|
GT | G | 4 | a0001c0001t0003g0046a0002c0002t0001g0139a0004c0004t0003g0119others(1): Show | 4 | HG02818.hp2 HG02896.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.380-8853delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246612569 | |||||
| chr1:246612684
|
C | T | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.380-8745C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246612684 | ||||||
| chr1:246612686
|
A | AGACCAGT others(20): Show |
1 | a0001c0001t0001g0307 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.380-8742_380-8716d others(29): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246612686 | |||||
| chr1:246612751
|
G | T | 9 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(6): Show | 9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.380-8678G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246612751 | ||||||
| chr1:246612765
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0003g0055 | 2 | HG01515.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.380-8664G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246612765 | ||||||
| chr1:246612898
|
A | T | 1 | a0001c0001t0001g0255 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.380-8531A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246612898 | ||||||
| chr1:246612899
|
T | A | 1 | a0001c0001t0001g0255 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.380-8530T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246612899 | ||||||
| chr1:246612930
|
A | G | 1 | a0001c0001t0001g0301 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.380-8499A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246612930 | ||||||
| chr1:246613055
|
C | T | 91 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(88): Show | 93 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.380-8374C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613055 | ||||||
| chr1:246613131
|
G | T | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.380-8298G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613131 | ||||||
| chr1:246613179
|
C | G | 185 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(182): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.380-8250C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613179 | ||||||
| chr1:246613428
|
G | T | 1 | a0001c0001t0002g0224 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.380-8001G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613428 | ||||||
| chr1:246613431
|
T | G | 1 | a0001c0001t0002g0224 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.380-7998T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613431 | ||||||
| chr1:246613466
|
C | T | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.380-7963C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613466 | ||||||
| chr1:246613577
|
AGGGTACT others(15): Show |
A | 1 | a0001c0001t0001g0217 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.380-7851_380-7830d others(24): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613577 | ||||||
| chr1:246613654
|
T | TCCCCCTC others(914): Show |
1 | a0001c0001t0001g0254 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.380-7774_380-7773i others(923): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613654 | |||||
| chr1:246613656
|
T | C | 1 | a0001c0001t0001g0254 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.380-7773T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613656 | ||||||
| chr1:246613656
|
T | TCTCCCCC others(1188): Show |
1 | a0002c0002t0001g0268 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.380-7770_380-7769i others(1197): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(958): Show |
1 | a0001c0001t0001g0300 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(967): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(957): Show |
2 | a0001c0001t0001g0266a0001c0001t0001g0303 | 2 | NA18942.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(966): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(949): Show |
1 | a0001c0001t0001g0301 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(958): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(990): Show |
1 | a0001c0001t0004g0007 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(999): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(977): Show |
1 | a0001c0001t0002g0225 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(986): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(971): Show |
1 | a0001c0001t0001g0095 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(980): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(960): Show |
1 | a0001c0001t0004g0275 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(969): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(965): Show |
1 | a0001c0001t0002g0190 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(974): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(964): Show |
1 | a0001c0001t0002g0103 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(973): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(961): Show |
1 | a0001c0001t0001g0257 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(970): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(1170): Show |
1 | a0003c0003t0001g0037 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1179): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(992): Show |
1 | a0001c0001t0003g0181 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1001): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(960): Show |
1 | a0001c0001t0001g0272 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(969): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(967): Show |
1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(976): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(980): Show |
1 | a0001c0001t0003g0081 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(989): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(979): Show |
1 | a0001c0001t0003g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(988): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(963): Show |
1 | a0001c0001t0004g0158 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(972): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(975): Show |
1 | a0002c0002t0001g0112 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(984): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(980): Show |
1 | a0001c0001t0003g0003 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(989): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(959): Show |
1 | a0001c0001t0001g0228 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(968): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(975): Show |
1 | a0001c0001t0003g0067 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(984): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(963): Show |
1 | a0001c0001t0002g0187 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(972): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(968): Show |
1 | a0001c0001t0001g0094 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(977): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(974): Show |
1 | a0002c0002t0001g0151 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(983): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(1362): Show |
1 | a0001c0001t0001g0307 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1371): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(931): Show |
1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(940): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(895): Show |
1 | a0001c0001t0001g0274 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(904): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(970): Show |
1 | a0001c0001t0003g0109 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(979): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(957): Show |
1 | a0001c0001t0003g0294 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(966): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(969): Show |
1 | a0001c0001t0003g0316 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(978): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(953): Show |
1 | a0001c0001t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(962): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(963): Show |
1 | a0001c0001t0002g0049 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(972): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(963): Show |
1 | a0001c0001t0002g0097 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(972): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(964): Show |
1 | a0001c0001t0019g0106 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(973): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(964): Show |
1 | a0001c0001t0002g0186 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(973): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(962): Show |
18 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(15): Show | 19 | HG00280.hp1 HG00738.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.380-7767_380-7766i others(971): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(961): Show |
1 | a0001c0001t0002g0313 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(970): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(961): Show |
1 | a0001c0001t0002g0058 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(970): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(961): Show |
1 | a0001c0001t0001g0312 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(970): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(969): Show |
1 | a0001c0001t0003g0070 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(978): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(970): Show |
1 | a0001c0001t0003g0137 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(979): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(969): Show |
1 | a0001c0001t0001g0304 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(978): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(1577): Show |
1 | a0001c0001t0008g0176 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1586): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(1579): Show |
1 | a0001c0001t0001g0289 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1588): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(998): Show |
1 | a0001c0001t0001g0022 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1007): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(970): Show |
2 | a0001c0001t0001g0011a0001c0001t0001g0290 | 2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(979): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(959): Show |
1 | a0001c0001t0001g0156 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(968): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(1469): Show |
1 | a0001c0001t0001g0296 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1478): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(958): Show |
29 | a0001c0001t0001g0160a0001c0001t0001g0198a0001c0001t0001g0202others(26): Show | 29 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.380-7767_380-7766i others(967): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(969): Show |
1 | a0001c0001t0002g0078 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(978): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(969): Show |
1 | a0001c0001t0003g0069 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(978): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(968): Show |
41 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0098others(38): Show | 41 | HG00423.hp2 HG00558.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.380-7767_380-7766i others(977): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(958): Show |
1 | a0001c0001t0002g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(967): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(950): Show |
1 | a0010c0010t0002g0028 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(959): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(932): Show |
1 | a0001c0001t0002g0183 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(941): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(978): Show |
1 | a0001c0001t0002g0175 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(987): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(957): Show |
1 | a0001c0001t0001g0293 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(966): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(968): Show |
1 | a0001c0001t0012g0001 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(977): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(969): Show |
3 | a0001c0001t0004g0016a0001c0001t0004g0042a0001c0001t0004g0150 | 3 | HG02280.hp1 HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(978): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(933): Show |
1 | a0001c0001t0001g0271 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(942): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(978): Show |
2 | a0003c0003t0001g0032a0003c0003t0001g0033 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(987): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(1403): Show |
1 | a0003c0003t0004g0036 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1412): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(1403): Show |
2 | a0003c0003t0004g0034a0003c0003t0004g0035 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(1412): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(1168): Show |
3 | a0003c0003t0001g0038a0003c0003t0001g0039a0003c0003t0001g0044 | 3 | HG01891.hp2 HG02723.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(1177): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(960): Show |
2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(969): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(973): Show |
1 | a0002c0002t0001g0125 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(982): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(973): Show |
1 | a0002c0002t0001g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(982): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(972): Show |
2 | a0002c0002t0001g0180a0002c0002t0013g0179 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(981): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(973): Show |
1 | a0002c0002t0001g0111 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(982): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(973): Show |
1 | a0002c0002t0001g0093 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(982): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(972): Show |
26 | a0002c0002t0001g0027a0002c0002t0001g0108a0002c0002t0001g0110others(23): Show | 26 | HG00639.hp2 HG00741.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.380-7767_380-7766i others(981): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(972): Show |
1 | a0002c0002t0001g0120 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(981): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(955): Show |
1 | a0001c0001t0001g0197 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(964): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(972): Show |
1 | a0002c0002t0006g0030 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(981): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(1168): Show |
1 | a0003c0003t0001g0041 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1177): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(1575): Show |
1 | a0001c0001t0008g0020 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1584): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(970): Show |
1 | a0001c0001t0003g0068 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(979): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(970): Show |
1 | a0001c0001t0022g0085 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(979): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(971): Show |
1 | a0001c0001t0001g0088 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(980): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(970): Show |
3 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0002g0077 | 3 | HG01517.hp1 HG03239.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(979): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(993): Show |
1 | a0001c0001t0004g0174 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1002): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(993): Show |
1 | a0001c0001t0001g0170 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1002): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(1031): Show |
5 | a0001c0001t0001g0025a0001c0001t0004g0026a0001c0001t0009g0010others(2): Show | 5 | HG02818.hp1 HG02976.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.380-7767_380-7766i others(1040): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(992): Show |
1 | a0001c0001t0001g0169 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1001): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(991): Show |
1 | a0001c0001t0001g0182 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1000): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(992): Show |
1 | a0001c0001t0001g0166 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1001): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(1103): Show |
1 | a0001c0001t0004g0173 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1112): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(991): Show |
1 | a0001c0001t0002g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1000): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(981): Show |
1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(990): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(983): Show |
1 | a0006c0005t0023g0043 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(992): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(1072): Show |
1 | a0003c0003t0004g0162 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1081): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(969): Show |
1 | a0001c0001t0004g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(978): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(967): Show |
1 | a0001c0001t0004g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(976): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(673): Show |
5 | a0004c0004t0003g0119a0004c0004t0003g0185a0004c0004t0003g0192others(2): Show | 5 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.380-7767_380-7766i others(682): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(961): Show |
1 | a0001c0001t0002g0102 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(970): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(965): Show |
1 | a0001c0001t0004g0014 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(974): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(964): Show |
1 | a0007c0011t0015g0213 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(973): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(963): Show |
1 | a0002c0002t0015g0168 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(972): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(965): Show |
1 | a0001c0001t0001g0177 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(974): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(988): Show |
2 | a0001c0001t0004g0018a0001c0001t0004g0019 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(997): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(964): Show |
5 | a0001c0001t0004g0015a0001c0001t0004g0017a0001c0001t0005g0023others(2): Show | 5 | HG02647.hp2 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.380-7767_380-7766i others(973): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(972): Show |
1 | a0001c0001t0001g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(981): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(964): Show |
1 | a0001c0001t0004g0154 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(973): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(968): Show |
1 | a0001c0001t0003g0104 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(977): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(973): Show |
1 | a0002c0002t0001g0141 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(982): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(955): Show |
1 | a0001c0001t0001g0219 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(964): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(944): Show |
1 | a0001c0001t0014g0164 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(953): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(967): Show |
1 | a0001c0001t0004g0153 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(976): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(968): Show |
1 | a0001c0001t0002g0101 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(977): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(971): Show |
1 | a0002c0002t0001g0200 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(980): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(677): Show |
1 | a0004c0004t0003g0184 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(686): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(933): Show |
1 | a0001c0001t0002g0224 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(942): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(1193): Show |
1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1202): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(1163): Show |
1 | a0003c0003t0001g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1172): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(959): Show |
1 | a0001c0001t0002g0195 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(968): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(961): Show |
1 | a0001c0001t0002g0231 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(970): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(998): Show |
1 | a0001c0001t0001g0215 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1007): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(959): Show |
1 | a0001c0001t0002g0223 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(968): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(960): Show |
1 | a0001c0001t0002g0238 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(969): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(959): Show |
2 | a0001c0001t0001g0194a0001c0001t0001g0236 | 2 | HG00621.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(968): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(959): Show |
1 | a0001c0001t0001g0298 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(968): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(959): Show |
1 | a0001c0001t0001g0260 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(968): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(935): Show |
1 | a0001c0001t0002g0233 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(944): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(973): Show |
1 | a0001c0001t0025g0288 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(982): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(972): Show |
2 | a0001c0001t0002g0302a0001c0001t0018g0256 | 2 | NA18955.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(981): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(959): Show |
1 | a0001c0001t0001g0241 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(968): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(959): Show |
1 | a0001c0001t0003g0297 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(968): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(959): Show |
1 | a0001c0001t0003g0222 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(968): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(958): Show |
36 | a0001c0001t0001g0207a0001c0001t0001g0216a0001c0001t0001g0237others(33): Show | 36 | HG00280.hp2 HG00642.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.380-7767_380-7766i others(967): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(957): Show |
1 | a0001c0001t0001g0234 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(966): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(958): Show |
2 | a0001c0001t0002g0258a0001c0001t0002g0262 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(967): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(958): Show |
1 | a0001c0001t0001g0318 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(967): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCCC others(966): Show |
1 | a0001c0001t0001g0255 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(975): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCTC others(986): Show |
1 | a0002c0002t0001g0139 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.380-7768_380-7767i others(995): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCTC others(978): Show |
1 | a0001c0001t0001g0128 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.380-7768_380-7767i others(987): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCTC others(964): Show |
1 | a0001c0001t0002g0285 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.380-7768_380-7767i others(973): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613656
|
T | TCTCTCTC others(982): Show |
1 | a0001c0001t0001g0217 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.380-7768_380-7767i others(991): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | |||||
| chr1:246613663
|
T | C | 5 | a0001c0001t0001g0135a0001c0001t0004g0134a0001c0001t0016g0136others(2): Show | 5 | HG01243.hp2 HG02622.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.380-7766T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613663 | ||||||
| chr1:246613666
|
T | C | 3 | a0001c0001t0001g0135a0001c0001t0004g0134a0002c0002t0006g0031 | 3 | HG02622.hp2 HG02897.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.380-7763T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613666 | ||||||
| chr1:246613670
|
T | TCTCCCTC others(953): Show |
2 | a0001c0001t0001g0135a0002c0002t0006g0031 | 2 | HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.380-7759_380-7758i others(962): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613670 | ||||||
| chr1:246613670
|
T | TCTCCCTC others(949): Show |
1 | a0001c0001t0004g0134 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.380-7759_380-7758i others(958): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613670 | ||||||
| chr1:246613671
|
A | C | 5 | a0001c0001t0001g0135a0001c0001t0004g0134a0001c0001t0016g0136others(2): Show | 5 | HG01243.hp2 HG02622.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.380-7758A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613671 | ||||||
| chr1:246613679
|
T | C | 2 | a0001c0001t0016g0136a0002c0002t0006g0029 | 2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.380-7750T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613679 | ||||||
| chr1:246613680
|
C | T | 2 | a0001c0001t0016g0136a0002c0002t0006g0029 | 2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.380-7749C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613680 | ||||||
| chr1:246613681
|
C | CACCTCCT others(958): Show |
1 | a0002c0002t0006g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.380-7748_380-7747i others(967): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613681 | ||||||
| chr1:246613681
|
C | CACCTCCT others(957): Show |
1 | a0001c0001t0016g0136 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.380-7748_380-7747i others(966): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613681 | ||||||
| chr1:246613681
|
C | CTCTCTA | 3 | a0001c0001t0001g0135a0001c0001t0004g0134a0002c0002t0006g0031 | 3 | HG02622.hp2 HG02897.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.380-7743_380-7742i others(8): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613681 | |||||
| chr1:246613734
|
T | C | 102 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(99): Show | 104 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.380-7695T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613734 | ||||||
| chr1:246613737
|
A | G | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.380-7692A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613737 | ||||||
| chr1:246613826
|
T | G | 1 | a0001c0001t0001g0277 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.380-7603T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613826 | ||||||
| chr1:246613878
|
A | T | 1 | a0004c0004t0003g0184 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.380-7551A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613878 | ||||||
| chr1:246613914
|
G | A | 1 | a0001c0001t0003g0250 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.380-7515G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613914 | ||||||
| chr1:246613939
|
C | T | 5 | a0001c0001t0001g0135a0001c0001t0004g0134a0001c0001t0016g0136others(2): Show | 5 | HG01243.hp2 HG02622.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.380-7490C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613939 | ||||||
| chr1:246613983
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.380-7446T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613983 | ||||||
| chr1:246614143
|
A | C | 1 | a0001c0001t0003g0003 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.380-7286A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614143 | ||||||
| chr1:246614147
|
T | G | 1 | a0001c0001t0003g0003 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.380-7282T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614147 | ||||||
| chr1:246614148
|
T | A | 1 | a0001c0001t0003g0003 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.380-7281T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614148 | ||||||
| chr1:246614149
|
C | G | 1 | a0001c0001t0003g0003 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.380-7280C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614149 | ||||||
| chr1:246614150
|
G | A | 1 | a0001c0001t0003g0003 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.380-7279G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614150 | ||||||
| chr1:246614151
|
C | G | 1 | a0001c0001t0003g0003 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.380-7278C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614151 | ||||||
| chr1:246614183
|
C | T | 7 | a0001c0001t0001g0170a0001c0001t0002g0172a0001c0001t0002g0175others(4): Show | 7 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.380-7246C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614183 | ||||||
| chr1:246614300
|
A | C | 2 | a0001c0001t0001g0166a0001c0001t0003g0292 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.380-7129A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614300 | ||||||
| chr1:246614315
|
G | A | 9 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(6): Show | 9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.380-7114G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614315 | ||||||
| chr1:246614512
|
AT | A | 116 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0052others(113): Show | 118 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.380-6900delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246614512 | |||||
| chr1:246614512
|
ATT | A | 151 | a0001c0001t0001g0022a0001c0001t0001g0088a0001c0001t0001g0090others(148): Show | 151 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.380-6901_380-6900d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246614512 | |||||
| chr1:246614512
|
ATTT | A | 10 | a0001c0001t0001g0228a0001c0001t0001g0265a0001c0001t0001g0266others(7): Show | 10 | HG00280.hp2 HG00558.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.380-6902_380-6900d others(5): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246614512 | |||||
| chr1:246614526
|
T | C | 2 | a0001c0001t0002g0005a0001c0001t0002g0276 | 2 | HG00642.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.380-6903T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614526 | ||||||
| chr1:246614535
|
C | T | 1 | a0001c0001t0003g0220 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.380-6894C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614535 | ||||||
| chr1:246614589
|
A | G | 1 | a0001c0001t0002g0102 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.380-6840A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614589 | ||||||
| chr1:246614611
|
A | G | 1 | a0001c0001t0003g0222 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.380-6818A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614611 | ||||||
| chr1:246614620
|
C | G | 1 | a0001c0001t0001g0219 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.380-6809C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614620 | ||||||
| chr1:246614623
|
C | T | 1 | a0001c0001t0002g0078 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.380-6806C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614623 | ||||||
| chr1:246614664
|
G | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.380-6765G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614664 | ||||||
| chr1:246614875
|
A | G | 1 | a0001c0001t0002g0102 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.380-6554A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614875 | ||||||
| chr1:246615113
|
A | G | 1 | a0001c0001t0003g0003 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.380-6316A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246615113 | ||||||
| chr1:246615121
|
A | T | 1 | a0001c0001t0001g0215 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.380-6308A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246615121 | ||||||
| chr1:246615168
|
T | C | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.380-6261T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246615168 | ||||||
| chr1:246615170
|
C | CA | 6 | a0001c0001t0001g0197a0001c0001t0001g0255a0001c0001t0002g0058others(3): Show | 6 | HG01109.hp1 HG01255.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.380-6249dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246615170 | |||||
| chr1:246615199
|
G | A | 9 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(6): Show | 9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.380-6230G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246615199 | ||||||
| chr1:246615206
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.380-6223C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246615206 | ||||||
| chr1:246615215
|
A | G | 10 | a0001c0001t0001g0135a0001c0001t0004g0016a0001c0001t0004g0042others(7): Show | 10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.380-6214A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246615215 | ||||||
| chr1:246615228
|
C | T | 10 | a0001c0001t0001g0135a0001c0001t0004g0016a0001c0001t0004g0042others(7): Show | 10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.380-6201C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246615228 | ||||||
| chr1:246615302
|
C | T | 1 | a0002c0002t0001g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.380-6127C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246615302 | ||||||
| chr1:246615470
|
C | T | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.380-5959C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246615470 | ||||||
| chr1:246615471
|
G | A | 1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.380-5958G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246615471 | ||||||
| chr1:246615673
|
G | A | 3 | a0001c0001t0017g0008a0002c0002t0015g0168a0007c0011t0015g0213 | 3 | HG01981.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.380-5756G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246615673 | ||||||
| chr1:246615818
|
C | T | 1 | a0010c0010t0002g0028 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.380-5611C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246615818 | ||||||
| chr1:246615819
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0290 | 2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.380-5610G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246615819 | ||||||
| chr1:246615879
|
C | CA | 6 | a0001c0001t0001g0236a0001c0001t0002g0072a0001c0001t0002g0103others(3): Show | 6 | HG00140.hp2 HG01099.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.380-5539dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246615879 | |||||
| chr1:246616088
|
G | A | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.380-5341G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246616088 | ||||||
| chr1:246616322
|
G | C | 1 | a0001c0001t0002g0102 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.380-5107G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246616322 | ||||||
| chr1:246616323
|
A | G | 1 | a0001c0001t0001g0303 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.380-5106A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246616323 | ||||||
| chr1:246616424
|
G | T | 9 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(6): Show | 9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.380-5005G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246616424 | ||||||
| chr1:246616511
|
T | C | 154 | a0001c0001t0001g0022a0001c0001t0001g0088a0001c0001t0001g0090others(151): Show | 154 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.380-4918T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246616511 | ||||||
| chr1:246616524
|
C | T | 3 | a0001c0001t0011g0208a0001c0001t0011g0212a0001c0001t0011g0221 | 3 | HG01934.hp1 NA18971.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.380-4905C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246616524 | ||||||
| chr1:246616755
|
A | G | 1 | a0002c0002t0013g0179 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.380-4674A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246616755 | ||||||
| chr1:246616916
|
AT | A | 3 | a0001c0001t0001g0094a0001c0001t0001g0167a0001c0001t0001g0312 | 3 | HG01516.hp1 HG02809.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.380-4507delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246616916 | |||||
| chr1:246616953
|
C | T | 6 | a0004c0004t0003g0119a0004c0004t0003g0184a0004c0004t0003g0185others(3): Show | 6 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.380-4476C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246616953 | ||||||
| chr1:246617255
|
C | G | 111 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(108): Show | 113 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.380-4174C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246617255 | ||||||
| chr1:246617317
|
T | C | 113 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(110): Show | 115 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.380-4112T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246617317 | ||||||
| chr1:246617346
|
T | C | 1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.380-4083T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246617346 | ||||||
| chr1:246617499
|
A | AG | 6 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.380-3926dupG | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246617499 | |||||
| chr1:246617725
|
C | A | 1 | a0001c0001t0002g0195 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.380-3704C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246617725 | ||||||
| chr1:246617725
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.380-3704C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246617725 | ||||||
| chr1:246617751
|
A | G | 4 | a0001c0001t0001g0160a0001c0001t0004g0157a0001c0001t0004g0158others(1): Show | 4 | HG01109.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.380-3678A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246617751 | ||||||
| chr1:246617773
|
C | T | 17 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0167others(14): Show | 17 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.380-3656C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246617773 | ||||||
| chr1:246618018
|
A | T | 1 | a0001c0001t0002g0232 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.380-3411A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246618018 | ||||||
| chr1:246618088
|
A | G | 1 | a0002c0002t0001g0146 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.380-3341A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246618088 | ||||||
| chr1:246618098
|
T | C | 1 | a0002c0002t0007g0143 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.380-3331T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246618098 | ||||||
| chr1:246618769
|
G | A | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.380-2660G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246618769 | ||||||
| chr1:246618810
|
C | T | 3 | a0002c0002t0015g0168a0007c0011t0015g0213a0009c0008t0001g0161 | 3 | HG02622.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.380-2619C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246618810 | ||||||
| chr1:246618829
|
G | A | 7 | a0001c0001t0001g0121a0001c0001t0003g0137a0001c0001t0003g0226others(4): Show | 7 | HG00423.hp2 NA18985.hp2 NA18999.hp2 others(4): Show |
intron_variant | MODIFIER | c.380-2600G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246618829 | ||||||
| chr1:246618929
|
T | C | 111 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(108): Show | 113 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.380-2500T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246618929 | ||||||
| chr1:246619104
|
A | G | 24 | a0001c0001t0001g0166a0001c0001t0001g0177a0001c0001t0003g0292others(21): Show | 24 | HG00735.hp1 HG02451.hp2 HG02622.hp1 others(21): Show |
intron_variant | MODIFIER | c.380-2325A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246619104 | ||||||
| chr1:246619154
|
G | GA | 119 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0052others(116): Show | 119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.380-2263dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246619154 | |||||
| chr1:246619154
|
G | GAA | 16 | a0001c0001t0001g0177a0001c0001t0001g0283a0001c0001t0001g0293others(13): Show | 16 | HG00735.hp1 HG00741.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.380-2264_380-2263d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246619154 | |||||
| chr1:246619154
|
G | GAAA | 8 | a0001c0001t0004g0014a0004c0004t0003g0119a0004c0004t0003g0184others(5): Show | 8 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.380-2265_380-2263d others(5): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246619154 | |||||
| chr1:246619198
|
C | T | 21 | a0001c0001t0001g0194a0001c0001t0001g0207a0001c0001t0001g0215others(18): Show | 21 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.380-2231C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246619198 | ||||||
| chr1:246619246
|
A | G | 1 | a0001c0001t0002g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.380-2183A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246619246 | ||||||
| chr1:246619248
|
G | A | 1 | a0008c0007t0003g0267 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.380-2181G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246619248 | ||||||
| chr1:246619315
|
G | A | 6 | a0004c0004t0003g0119a0004c0004t0003g0184a0004c0004t0003g0185others(3): Show | 6 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.380-2114G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246619315 | ||||||
| chr1:246619839
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.380-1590C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246619839 | ||||||
| chr1:246619852
|
GGTGCATA others(47): Show |
G | 1 | a0001c0001t0001g0177 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.380-1551_380-1498d others(56): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246619852 | |||||
| chr1:246619852
|
GGTGCATA others(153): Show |
G | 2 | a0001c0001t0001g0170a0001c0001t0003g0181 | 2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.380-1473_380-1314d others(2): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246619852 | |||||
| chr1:246619876
|
G | A | 1 | a0001c0001t0004g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.380-1553G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246619876 | ||||||
| chr1:246619878
|
CACACTCT others(369): Show |
C | 10 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0091others(7): Show | 10 | HG00140.hp1 HG01517.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.380-1205_380-830de others(1): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246619878 | |||||
| chr1:246619912
|
TAC | T | 3 | a0002c0002t0015g0168a0007c0011t0015g0213a0009c0008t0001g0161 | 3 | HG02622.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.380-1512_380-1511d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246619912 | |||||
| chr1:246619932
|
AACACTAC others(637): Show |
A | 1 | a0001c0001t0003g0220 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.380-1391_380-748de others(1): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246619932 | |||||
| chr1:246619948
|
C | T | 21 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0169others(18): Show | 21 | HG00733.hp1 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.380-1481C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246619948 | ||||||
| chr1:246619958
|
C | T | 3 | a0002c0002t0015g0168a0007c0011t0015g0213a0009c0008t0001g0161 | 3 | HG02622.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.380-1471C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246619958 | ||||||
| chr1:246619984
|
A | C | 108 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(105): Show | 110 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.380-1445A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246619984 | ||||||
| chr1:246620002
|
C | T | 108 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(105): Show | 110 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.380-1427C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620002 | ||||||
| chr1:246620024
|
C | T | 2 | a0002c0002t0001g0117a0002c0002t0001g0118 | 2 | HG02004.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.380-1405C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620024 | ||||||
| chr1:246620038
|
C | A | 3 | a0001c0001t0001g0305a0001c0001t0002g0005a0001c0001t0002g0276 | 3 | HG00642.hp1 HG00741.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.380-1391C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620038 | ||||||
| chr1:246620038
|
CACACTCT others(583): Show |
C | 1 | a0002c0002t0001g0116 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.380-1313_380-724de others(1): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620038 | |||||
| chr1:246620041
|
ACT | A | 3 | a0001c0001t0001g0305a0002c0002t0001g0127a0004c0004t0003g0184 | 3 | HG02135.hp2 HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.380-1385_380-1384d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620041 | |||||
| chr1:246620041
|
ACTCTACA others(211): Show |
A | 5 | a0004c0004t0003g0119a0004c0004t0003g0185a0004c0004t0003g0192others(2): Show | 5 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.380-1385_380-1168d others(2): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620041 | |||||
| chr1:246620043
|
TCTACAGG others(45): Show |
T | 1 | a0001c0001t0002g0281 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.380-1365_380-1314d others(54): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620043 | |||||
| chr1:246620066
|
C | G | 2 | a0002c0002t0015g0168a0007c0011t0015g0213 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.380-1363C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620066 | ||||||
| chr1:246620069
|
GCATACAC others(366): Show |
G | 1 | a0001c0001t0001g0305 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.380-1359_380-987de others(1): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620069 | ||||||
| chr1:246620092
|
A | C | 3 | a0001c0001t0002g0005a0001c0001t0002g0276a0009c0008t0001g0161 | 3 | HG00642.hp1 HG00741.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.380-1337A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620092 | ||||||
| chr1:246620095
|
A | ACT | 5 | a0001c0001t0002g0005a0001c0001t0002g0276a0002c0002t0015g0168others(2): Show | 5 | HG00642.hp1 HG00741.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.380-1333_380-1332d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620095 | |||||
| chr1:246620102
|
G | A | 1 | a0001c0001t0001g0257 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.380-1327G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620102 | ||||||
| chr1:246620106
|
G | A | 2 | a0002c0002t0015g0168a0007c0011t0015g0213 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.380-1323G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620106 | ||||||
| chr1:246620115
|
A | AG | 3 | a0001c0001t0003g0206a0001c0001t0003g0259a0008c0007t0003g0267 | 3 | HG03017.hp2 HG03704.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.380-1314_380-1313i others(3): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620115 | ||||||
| chr1:246620115
|
ATC | A | 5 | a0001c0001t0002g0005a0001c0001t0002g0276a0002c0002t0015g0168others(2): Show | 5 | HG00642.hp1 HG00741.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.380-1313_380-1312d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620115 | ||||||
| chr1:246620120
|
G | C | 5 | a0001c0001t0002g0005a0001c0001t0002g0276a0002c0002t0015g0168others(2): Show | 5 | HG00642.hp1 HG00741.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.380-1309G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620120 | ||||||
| chr1:246620126
|
T | C | 3 | a0001c0001t0003g0206a0001c0001t0003g0259a0008c0007t0003g0267 | 3 | HG03017.hp2 HG03704.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.380-1303T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620126 | ||||||
| chr1:246620146
|
A | C | 2 | a0002c0002t0015g0168a0007c0011t0015g0213 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.380-1283A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620146 | ||||||
| chr1:246620149
|
ACTACAGG others(103): Show |
A | 30 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(27): Show | 31 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.380-1259_380-1150d others(2): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620149 | |||||
| chr1:246620149
|
ACTACAGG others(209): Show |
A | 4 | a0001c0001t0003g0081a0001c0001t0003g0104a0001c0001t0014g0164others(1): Show | 4 | HG01169.hp1 HG02896.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.380-1259_380-1044d others(2): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620149 | |||||
| chr1:246620149
|
ACTACAGG others(263): Show |
A | 8 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(5): Show | 8 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.380-1259_380-990de others(1): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620149 | |||||
| chr1:246620149
|
ACTACAGG others(477): Show |
A | 1 | a0001c0001t0001g0132 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.380-1259_380-776de others(1): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620149 | |||||
| chr1:246620151
|
TACAGGGA others(582): Show |
T | 3 | a0001c0001t0003g0206a0001c0001t0003g0259a0008c0007t0003g0267 | 3 | HG03017.hp2 HG03704.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.380-1277_380-689de others(1): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620151 | ||||||
| chr1:246620162
|
C | T | 1 | a0010c0010t0002g0028 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.380-1267C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620162 | ||||||
| chr1:246620163
|
G | A | 5 | a0003c0003t0001g0038a0003c0003t0001g0039a0003c0003t0001g0040others(2): Show | 5 | HG00733.hp1 HG01891.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.380-1266G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620163 | ||||||
| chr1:246620169
|
ATCGTGGT others(49): Show |
A | 59 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0086others(56): Show | 60 | HG00423.hp2 HG00558.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.380-1259_380-1204d others(58): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620169 | ||||||
| chr1:246620171
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.380-1258C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620171 | ||||||
| chr1:246620174
|
G | C | 1 | a0001c0001t0004g0019 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.380-1255G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620174 | ||||||
| chr1:246620190
|
G | A | 121 | a0001c0001t0001g0022a0001c0001t0001g0135a0001c0001t0001g0156others(118): Show | 121 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.380-1239G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620190 | ||||||
| chr1:246620198
|
GGCACACT others(50): Show |
G | 1 | a0001c0001t0001g0307 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.380-1230_380-1174d others(59): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620198 | ||||||
| chr1:246620200
|
C | A | 4 | a0001c0001t0002g0005a0001c0001t0002g0276a0001c0001t0004g0019others(1): Show | 4 | HG00642.hp1 HG00741.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.380-1229C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620200 | ||||||
| chr1:246620203
|
A | T | 2 | a0002c0002t0015g0168a0007c0011t0015g0213 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.380-1226A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620203 | ||||||
| chr1:246620223
|
ATC | A | 122 | a0001c0001t0001g0022a0001c0001t0001g0135a0001c0001t0001g0156others(119): Show | 122 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.380-1205_380-1204d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620223 | ||||||
| chr1:246620228
|
G | C | 181 | a0001c0001t0001g0022a0001c0001t0001g0061a0001c0001t0001g0076others(178): Show | 182 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.380-1201G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620228 | ||||||
| chr1:246620228
|
GGTGCATA others(47): Show |
G | 1 | a0001c0001t0004g0019 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.380-1169_380-1116d others(56): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620228 | |||||
| chr1:246620244
|
G | A | 2 | a0001c0001t0002g0005a0001c0001t0002g0276 | 2 | HG00642.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.380-1185G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620244 | ||||||
| chr1:246620254
|
A | C | 3 | a0002c0002t0015g0168a0007c0011t0015g0213a0009c0008t0001g0161 | 3 | HG02622.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.380-1175A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620254 | ||||||
| chr1:246620257
|
ACTCTACA others(155): Show |
A | 58 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0086others(55): Show | 59 | HG00423.hp2 HG00558.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.380-1169_380-1008d others(2): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620257 | |||||
| chr1:246620259
|
T | A | 3 | a0001c0001t0001g0307a0001c0001t0002g0005a0001c0001t0002g0276 | 3 | HG00642.hp1 HG00741.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.380-1170T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620259 | ||||||
| chr1:246620259
|
TCTACAGG others(45): Show |
T | 1 | a0001c0001t0008g0176 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.380-1115_380-1064d others(54): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620259 | |||||
| chr1:246620269
|
G | A | 2 | a0002c0002t0015g0168a0007c0011t0015g0213 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.380-1160G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620269 | ||||||
| chr1:246620308
|
A | C | 1 | a0001c0001t0004g0019 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.380-1121A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620308 | ||||||
| chr1:246620311
|
A | ACT | 6 | a0001c0001t0001g0307a0001c0001t0002g0005a0001c0001t0002g0276others(3): Show | 6 | HG00642.hp1 HG00741.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.380-1117_380-1116d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620311 | |||||
| chr1:246620311
|
ACTACAGG others(315): Show |
A | 1 | a0001c0001t0001g0182 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.380-1063_380-742de others(1): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620311 | |||||
| chr1:246620324
|
C | T | 2 | a0003c0003t0004g0162a0006c0005t0023g0043 | 2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.380-1105C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620324 | ||||||
| chr1:246620331
|
A | ATC | 6 | a0001c0001t0001g0095a0004c0004t0003g0119a0004c0004t0003g0185others(3): Show | 6 | HG01517.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.380-1098_380-1097i others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620331 | ||||||
| chr1:246620334
|
C | G | 6 | a0001c0001t0001g0095a0004c0004t0003g0119a0004c0004t0003g0185others(3): Show | 6 | HG01517.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.380-1095C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620334 | ||||||
| chr1:246620337
|
GCATACAC others(44): Show |
G | 1 | a0001c0001t0011g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.380-1091_380-1041d others(53): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620337 | ||||||
| chr1:246620337
|
GCATACAC others(98): Show |
G | 118 | a0001c0001t0001g0022a0001c0001t0001g0135a0001c0001t0001g0156others(115): Show | 118 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.380-1091_380-987de others(1): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620337 | ||||||
| chr1:246620360
|
A | C | 3 | a0001c0001t0004g0019a0002c0002t0015g0168a0007c0011t0015g0213 | 3 | HG02622.hp1 HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.380-1069A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620360 | ||||||
| chr1:246620360
|
AACACTCT others(47): Show |
A | 1 | a0001c0001t0009g0010 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.380-1015_380-962de others(55): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620360 | |||||
| chr1:246620363
|
ACT | A | 40 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(37): Show | 41 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.380-1063_380-1062d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620363 | |||||
| chr1:246620365
|
T | A | 1 | a0001c0001t0001g0095 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.380-1064T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620365 | ||||||
| chr1:246620385
|
A | ATC | 30 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(27): Show | 31 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.380-1044_380-1043i others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620385 | ||||||
| chr1:246620386
|
GTCGTGCA others(152): Show |
G | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.380-1037_380-879de others(1): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620386 | |||||
| chr1:246620388
|
C | G | 30 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(27): Show | 31 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.380-1041C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620388 | ||||||
| chr1:246620391
|
GCATACAC others(44): Show |
G | 4 | a0001c0001t0001g0307a0001c0001t0002g0005a0001c0001t0002g0276others(1): Show | 4 | HG00642.hp1 HG00741.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.380-1037_380-987de others(52): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620391 | ||||||
| chr1:246620394
|
T | C | 1 | a0001c0001t0011g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.380-1035T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620394 | ||||||
| chr1:246620414
|
C | A | 11 | a0001c0001t0003g0081a0001c0001t0003g0104a0001c0001t0004g0019others(8): Show | 11 | HG01169.hp1 HG02451.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.380-1015C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620414 | ||||||
| chr1:246620417
|
ACT | A | 40 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(37): Show | 41 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.380-1009_380-1008d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620417 | |||||
| chr1:246620419
|
T | C | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.380-1010T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620419 | ||||||
| chr1:246620419
|
TCTACAGG others(153): Show |
T | 1 | a0001c0001t0001g0095 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.380-955_380-796del | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620419 | |||||
| chr1:246620440
|
G | A | 1 | a0001c0001t0011g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.380-989G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620440 | ||||||
| chr1:246620442
|
C | CGTGCATA others(209): Show |
1 | a0003c0003t0001g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.380-908_380-907ins others(216): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620442 | |||||
| chr1:246620442
|
C | G | 1 | a0001c0001t0011g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.380-987C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620442 | ||||||
| chr1:246620448
|
T | C | 123 | a0001c0001t0001g0022a0001c0001t0001g0135a0001c0001t0001g0156others(120): Show | 123 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.380-981T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620448 | ||||||
| chr1:246620468
|
A | C | 30 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(27): Show | 31 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.380-961A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620468 | ||||||
| chr1:246620471
|
A | ACT | 30 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(27): Show | 31 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.380-957_380-956dup others(2): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620471 | |||||
| chr1:246620491
|
ATC | A | 3 | a0001c0001t0004g0019a0002c0002t0015g0168a0007c0011t0015g0213 | 3 | HG02622.hp1 HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.380-937_380-936del others(2): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620491 | ||||||
| chr1:246620494
|
G | A | 110 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(107): Show | 110 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.380-935G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620494 | ||||||
| chr1:246620496
|
G | C | 3 | a0001c0001t0004g0019a0002c0002t0015g0168a0007c0011t0015g0213 | 3 | HG02622.hp1 HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.380-933G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620496 | ||||||
| chr1:246620522
|
A | C | 106 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(103): Show | 108 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.380-907A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620522 | ||||||
| chr1:246620545
|
ATC | A | 106 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(103): Show | 108 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.380-883_380-882del others(2): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620545 | ||||||
| chr1:246620550
|
G | C | 106 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(103): Show | 108 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.380-879G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620550 | ||||||
| chr1:246620556
|
T | C | 2 | a0001c0001t0011g0208a0009c0008t0001g0161 | 2 | NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.380-873T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620556 | ||||||
| chr1:246620563
|
G | T | 1 | a0001c0001t0003g0104 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.380-866G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620563 | ||||||
| chr1:246620579
|
A | ACT | 76 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0086others(73): Show | 77 | HG00423.hp2 HG00558.hp2 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.380-849_380-848dup others(2): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620579 | |||||
| chr1:246620579
|
A | ACTCTACA others(431): Show |
2 | a0002c0002t0015g0168a0007c0011t0015g0213 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.380-848_380-847ins others(438): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620579 | |||||
| chr1:246620579
|
A | T | 1 | a0001c0001t0011g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.380-850A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620579 | ||||||
| chr1:246620608
|
T | C | 123 | a0001c0001t0001g0022a0001c0001t0001g0135a0001c0001t0001g0156others(120): Show | 123 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.380-821T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620608 | ||||||
| chr1:246620628
|
A | C | 1 | a0001c0001t0003g0220 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.380-801A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620628 | ||||||
| chr1:246620630
|
C | T | 2 | a0001c0001t0001g0166a0001c0001t0003g0292 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.380-799C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620630 | ||||||
| chr1:246620656
|
CGTGCATA others(48): Show |
C | 5 | a0001c0001t0001g0025a0001c0001t0004g0026a0001c0001t0009g0010others(2): Show | 5 | HG02818.hp1 HG02976.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.380-730_380-676del others(55): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620656 | |||||
| chr1:246620662
|
T | C | 1 | a0001c0001t0011g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.380-767T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620662 | ||||||
| chr1:246620699
|
G | A | 1 | a0001c0001t0011g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.380-730G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620699 | ||||||
| chr1:246620709
|
G | A | 4 | a0001c0001t0001g0160a0001c0001t0004g0157a0001c0001t0004g0158others(1): Show | 4 | HG01109.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.380-720G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620709 | ||||||
| chr1:246620712
|
G | A | 1 | a0001c0001t0011g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.380-717G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620712 | ||||||
| chr1:246620717
|
T | C | 134 | a0001c0001t0001g0022a0001c0001t0001g0088a0001c0001t0001g0090others(131): Show | 134 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.380-712T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620717 | ||||||
| chr1:246620737
|
A | C | 1 | a0001c0001t0011g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.380-692A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620737 | ||||||
| chr1:246620740
|
A | ACT | 132 | a0001c0001t0001g0022a0001c0001t0001g0088a0001c0001t0001g0090others(129): Show | 132 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.380-688_380-687dup others(2): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620740 | |||||
| chr1:246620750
|
G | A | 1 | a0001c0001t0011g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.380-679G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620750 | ||||||
| chr1:246620754
|
A | G | 11 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(8): Show | 11 | HG00735.hp1 HG02486.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.380-675A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620754 | ||||||
| chr1:246620764
|
A | G | 1 | a0001c0001t0011g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.380-665A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620764 | ||||||
| chr1:246620768
|
A | G | 13 | a0001c0001t0001g0135a0001c0001t0004g0016a0001c0001t0004g0042others(10): Show | 13 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.380-661A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620768 | ||||||
| chr1:246620778
|
T | C | 1 | a0001c0001t0011g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.380-651T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620778 | ||||||
| chr1:246620781
|
G | A | 5 | a0001c0001t0001g0025a0001c0001t0004g0026a0001c0001t0009g0010others(2): Show | 5 | HG02818.hp1 HG02976.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.380-648G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620781 | ||||||
| chr1:246620818
|
G | A | 1 | a0001c0001t0010g0286 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.380-611G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620818 | ||||||
| chr1:246620832
|
C | T | 91 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(88): Show | 93 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.380-597C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620832 | ||||||
| chr1:246620885
|
A | G | 2 | a0001c0001t0003g0003a0001c0001t0003g0211 | 2 | NA18962.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.380-544A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620885 | ||||||
| chr1:246620965
|
G | A | 3 | a0002c0002t0015g0168a0007c0011t0015g0213a0009c0008t0001g0161 | 3 | HG02622.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.380-464G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620965 | ||||||
| chr1:246621373
|
T | C | 1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.380-56T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246621373 | ||||||
| chr1:246621723
|
A | C | 1 | a0001c0001t0003g0104 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.585+89A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246621723 | ||||||
| chr1:246621811
|
A | C | 115 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(112): Show | 115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.585+177A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246621811 | ||||||
| chr1:246621892
|
G | A | 2 | a0003c0003t0004g0162a0006c0005t0023g0043 | 2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.585+258G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246621892 | ||||||
| chr1:246621896
|
A | G | 2 | a0002c0002t0015g0168a0007c0011t0015g0213 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.585+262A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246621896 | ||||||
| chr1:246622043
|
G | C | 1 | a0002c0002t0001g0146 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.585+409G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622043 | ||||||
| chr1:246622094
|
C | T | 6 | a0001c0001t0002g0097a0001c0001t0002g0101a0001c0001t0002g0102others(3): Show | 6 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.585+460C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622094 | ||||||
| chr1:246622146
|
C | A | 99 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(96): Show | 101 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.585+512C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622146 | ||||||
| chr1:246622226
|
A | G | 277 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(274): Show | 279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.585+592A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622226 | ||||||
| chr1:246622259
|
A | C | 6 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.585+625A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622259 | ||||||
| chr1:246622309
|
C | T | 99 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(96): Show | 101 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.585+675C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622309 | ||||||
| chr1:246622444
|
G | T | 9 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(6): Show | 9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.585+810G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622444 | ||||||
| chr1:246622531
|
A | G | 1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.585+897A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622531 | ||||||
| chr1:246622575
|
G | T | 1 | a0001c0001t0003g0297 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.585+941G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622575 | ||||||
| chr1:246622681
|
G | A | 11 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0037others(8): Show | 11 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.585+1047G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622681 | ||||||
| chr1:246622731
|
C | T | 6 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.585+1097C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622731 | ||||||
| chr1:246622745
|
CT | C | 113 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(110): Show | 113 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.585+1121delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246622745 | |||||
| chr1:246622794
|
C | A | 4 | a0001c0001t0001g0160a0001c0001t0004g0157a0001c0001t0004g0158others(1): Show | 4 | HG01109.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.585+1160C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622794 | ||||||
| chr1:246622867
|
A | G | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.585+1233A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622867 | ||||||
| chr1:246622970
|
C | T | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.585+1336C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622970 | ||||||
| chr1:246623002
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.585+1368T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623002 | ||||||
| chr1:246623145
|
A | G | 99 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(96): Show | 101 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.585+1511A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623145 | ||||||
| chr1:246623213
|
A | C | 2 | a0001c0001t0001g0156a0001c0001t0001g0291 | 2 | HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.585+1579A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623213 | ||||||
| chr1:246623223
|
C | T | 29 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0167others(26): Show | 29 | HG00733.hp1 HG01243.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.585+1589C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623223 | ||||||
| chr1:246623296
|
G | A | 108 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(105): Show | 110 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.585+1662G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623296 | ||||||
| chr1:246623343
|
C | G | 109 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(106): Show | 111 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.585+1709C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623343 | ||||||
| chr1:246623473
|
A | C | 112 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(109): Show | 114 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.585+1839A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623473 | ||||||
| chr1:246623527
|
G | A | 1 | a0002c0002t0001g0122 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.585+1893G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623527 | ||||||
| chr1:246623601
|
C | T | 4 | a0003c0003t0001g0038a0003c0003t0001g0039a0003c0003t0001g0040others(1): Show | 4 | HG00733.hp1 HG01891.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.585+1967C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623601 | ||||||
| chr1:246623605
|
C | A | 1 | a0001c0001t0004g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.585+1971C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623605 | ||||||
| chr1:246623721
|
C | G | 28 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0167others(25): Show | 28 | HG00733.hp1 HG01243.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.585+2087C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623721 | ||||||
| chr1:246623797
|
T | G | 1 | a0006c0005t0023g0043 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.585+2163T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623797 | ||||||
| chr1:246623818
|
C | T | 1 | a0001c0001t0019g0106 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.585+2184C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623818 | ||||||
| chr1:246623841
|
T | C | 5 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0004g0034others(2): Show | 5 | HG01243.hp1 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.585+2207T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623841 | ||||||
| chr1:246623898
|
C | CA | 132 | a0001c0001t0001g0022a0001c0001t0001g0088a0001c0001t0001g0090others(129): Show | 132 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.585+2278dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246623898 | |||||
| chr1:246623898
|
C | CAA | 97 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(94): Show | 99 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.585+2277_585+2278d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246623898 | |||||
| chr1:246623898
|
C | CAAA | 6 | a0001c0001t0002g0057a0001c0001t0002g0103a0001c0001t0003g0054others(3): Show | 6 | HG00140.hp2 HG02071.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.585+2276_585+2278d others(5): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246623898 | |||||
| chr1:246623926
|
G | A | 28 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0167others(25): Show | 28 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.585+2292G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623926 | ||||||
| chr1:246623960
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.585+2326C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623960 | ||||||
| chr1:246623978
|
G | A | 6 | a0001c0001t0004g0016a0001c0001t0004g0042a0001c0001t0004g0150others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.585+2344G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623978 | ||||||
| chr1:246624040
|
G | A | 2 | a0001c0001t0001g0241a0001c0001t0001g0242 | 2 | HG00639.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.585+2406G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246624040 | ||||||
| chr1:246624058
|
A | G | 277 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(274): Show | 279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.585+2424A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246624058 | ||||||
| chr1:246624146
|
C | T | 99 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(96): Show | 101 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.585+2512C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246624146 | ||||||
| chr1:246624353
|
C | T | 1 | a0001c0001t0002g0102 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.585+2719C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246624353 | ||||||
| chr1:246624677
|
G | A | 6 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.585+3043G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246624677 | ||||||
| chr1:246624729
|
T | C | 99 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(96): Show | 101 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.585+3095T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246624729 | ||||||
| chr1:246624905
|
T | C | 113 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(110): Show | 115 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.585+3271T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246624905 | ||||||
| chr1:246624975
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.585+3341G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246624975 | ||||||
| chr1:246625323
|
G | A | 128 | a0001c0001t0001g0022a0001c0001t0001g0135a0001c0001t0001g0156others(125): Show | 128 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.585+3689G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246625323 | ||||||
| chr1:246625414
|
CT | C | 137 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(134): Show | 139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.585+3805delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246625414 | |||||
| chr1:246625414
|
CTT | C | 168 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(165): Show | 168 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.585+3804_585+3805d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246625414 | |||||
| chr1:246625414
|
CTTT | C | 7 | a0001c0001t0002g0223a0001c0001t0004g0007a0001c0001t0009g0013others(4): Show | 7 | HG02258.hp1 HG02622.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.585+3803_585+3805d others(5): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246625414 | |||||
| chr1:246625420
|
T | C | 2 | a0001c0001t0003g0292a0001c0001t0004g0017 | 2 | HG02809.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.585+3786T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246625420 | ||||||
| chr1:246625482
|
C | T | 4 | a0001c0001t0001g0198a0001c0001t0001g0228a0001c0001t0001g0305others(1): Show | 4 | HG00323.hp2 HG01081.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.585+3848C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246625482 | ||||||
| chr1:246625578
|
C | T | 2 | a0002c0002t0015g0168a0007c0011t0015g0213 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.585+3944C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246625578 | ||||||
| chr1:246625631
|
A | AG | 6 | a0004c0004t0003g0119a0004c0004t0003g0184a0004c0004t0003g0185others(3): Show | 6 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.585+3999dupG | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246625631 | |||||
| chr1:246625641
|
C | T | 27 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0167others(24): Show | 27 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.585+4007C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246625641 | ||||||
| chr1:246625642
|
G | A | 5 | a0001c0001t0001g0135a0001c0001t0004g0134a0001c0001t0016g0136others(2): Show | 5 | HG01243.hp2 HG02622.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.585+4008G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246625642 | ||||||
| chr1:246625662
|
C | T | 1 | a0004c0004t0003g0119 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.585+4028C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246625662 | ||||||
| chr1:246625716
|
G | A | 2 | a0001c0001t0004g0004a0001c0001t0004g0006 | 2 | HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.585+4082G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246625716 | ||||||
| chr1:246625799
|
C | T | 3 | a0002c0002t0001g0114a0002c0002t0001g0115a0002c0002t0002g0113 | 3 | NA18944.hp1 NA18948.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.585+4165C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246625799 | ||||||
| chr1:246625845
|
A | G | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.585+4211A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246625845 | ||||||
| chr1:246625934
|
C | T | 2 | a0001c0001t0004g0004a0001c0001t0004g0006 | 2 | HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.585+4300C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246625934 | ||||||
| chr1:246625951
|
A | G | 2 | a0001c0001t0009g0010a0001c0001t0009g0012 | 2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.585+4317A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246625951 | ||||||
| chr1:246626015
|
C | T | 1 | a0001c0001t0005g0205 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.585+4381C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626015 | ||||||
| chr1:246626016
|
A | G | 3 | a0002c0002t0015g0168a0007c0011t0015g0213a0009c0008t0001g0161 | 3 | HG02622.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.585+4382A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626016 | ||||||
| chr1:246626037
|
C | T | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.585+4403C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626037 | ||||||
| chr1:246626066
|
CT | C | 28 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0167others(25): Show | 28 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.585+4444delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246626066 | |||||
| chr1:246626088
|
T | C | 115 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(112): Show | 115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.585+4454T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626088 | ||||||
| chr1:246626118
|
C | T | 1 | a0001c0001t0002g0101 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.585+4484C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626118 | ||||||
| chr1:246626145
|
G | A | 1 | a0001c0001t0003g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.585+4511G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626145 | ||||||
| chr1:246626149
|
A | G | 2 | a0002c0002t0001g0108a0002c0002t0002g0123 | 2 | HG01074.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.585+4515A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626149 | ||||||
| chr1:246626271
|
G | A | 2 | a0001c0001t0005g0023a0001c0001t0020g0024 | 2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.585+4637G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626271 | ||||||
| chr1:246626438
|
C | T | 1 | a0001c0001t0002g0077 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.585+4804C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626438 | ||||||
| chr1:246626451
|
C | CT | 54 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0088others(51): Show | 54 | HG00140.hp1 HG00558.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.585+4841dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246626451 | |||||
| chr1:246626451
|
C | CTT | 89 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(86): Show | 91 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.585+4840_585+4841d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246626451 | |||||
| chr1:246626451
|
C | CTTT | 13 | a0001c0001t0002g0080a0001c0001t0003g0066a0001c0001t0003g0067others(10): Show | 13 | HG01169.hp1 HG01192.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.585+4839_585+4841d others(5): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246626451 | |||||
| chr1:246626451
|
CT | C | 6 | a0001c0001t0001g0022a0001c0001t0001g0293a0002c0002t0001g0126others(3): Show | 6 | HG00639.hp2 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.585+4841delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246626451 | |||||
| chr1:246626451
|
CTTTTTTT others(5): Show |
C | 15 | a0001c0001t0001g0135a0001c0001t0004g0016a0001c0001t0004g0042others(12): Show | 15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.585+4830_585+4841d others(14): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246626451 | |||||
| chr1:246626525
|
T | G | 3 | a0002c0002t0015g0168a0007c0011t0015g0213a0009c0008t0001g0161 | 3 | HG02622.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.585+4891T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626525 | ||||||
| chr1:246626544
|
G | A | 1 | a0001c0001t0003g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.585+4910G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626544 | ||||||
| chr1:246626603
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0257 | 2 | HG01884.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.585+4969C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626603 | ||||||
| chr1:246626604
|
G | A | 1 | a0001c0001t0002g0201 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.585+4970G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626604 | ||||||
| chr1:246626752
|
C | T | 1 | a0001c0001t0005g0205 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.585+5118C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626752 | ||||||
| chr1:246626842
|
C | A | 3 | a0002c0002t0015g0168a0007c0011t0015g0213a0009c0008t0001g0161 | 3 | HG02622.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.586-5052C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626842 | ||||||
| chr1:246626911
|
G | A | 268 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(265): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.586-4983G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626911 | ||||||
| chr1:246626946
|
G | C | 3 | a0002c0002t0015g0168a0007c0011t0015g0213a0009c0008t0001g0161 | 3 | HG02622.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.586-4948G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626946 | ||||||
| chr1:246627055
|
C | T | 9 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(6): Show | 9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.586-4839C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246627055 | ||||||
| chr1:246627072
|
A | G | 1 | a0001c0001t0012g0001 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.586-4822A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246627072 | ||||||
| chr1:246627187
|
A | G | 15 | a0001c0001t0001g0135a0001c0001t0004g0016a0001c0001t0004g0042others(12): Show | 15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.586-4707A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246627187 | ||||||
| chr1:246627225
|
C | T | 4 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0298others(1): Show | 4 | HG01257.hp2 HG01258.hp2 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.586-4669C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246627225 | ||||||
| chr1:246627269
|
C | T | 1 | a0002c0002t0002g0251 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.586-4625C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246627269 | ||||||
| chr1:246627335
|
C | T | 1 | a0001c0001t0002g0238 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.586-4559C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246627335 | ||||||
| chr1:246627400
|
C | T | 7 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0091others(4): Show | 7 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.586-4494C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246627400 | ||||||
| chr1:246627454
|
G | A | 167 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(164): Show | 167 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.586-4440G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246627454 | ||||||
| chr1:246627884
|
G | GAACTCAT others(50): Show |
2 | a0002c0002t0015g0168a0007c0011t0015g0213 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.586-3975_586-3974i others(59): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246627884 | |||||
| chr1:246627884
|
G | GAACTCAT others(68): Show |
1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.586-3964_586-3963i others(77): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246627884 | |||||
| chr1:246627893
|
G | A | 7 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0091others(4): Show | 7 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.586-4001G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246627893 | ||||||
| chr1:246627977
|
A | C | 2 | a0001c0001t0004g0004a0001c0001t0004g0006 | 2 | HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.586-3917A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246627977 | ||||||
| chr1:246628076
|
G | T | 8 | a0001c0001t0001g0215a0001c0001t0001g0236a0001c0001t0001g0237others(5): Show | 8 | HG01109.hp1 HG01175.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.586-3818G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246628076 | ||||||
| chr1:246628078
|
G | A | 4 | a0001c0001t0003g0292a0002c0002t0015g0168a0007c0011t0015g0213others(1): Show | 4 | HG02622.hp1 HG03486.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.586-3816G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246628078 | ||||||
| chr1:246628110
|
C | G | 7 | a0001c0001t0001g0170a0001c0001t0002g0172a0001c0001t0002g0175others(4): Show | 7 | HG02145.hp2 HG02258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.586-3784C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246628110 | ||||||
| chr1:246628114
|
C | T | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.586-3780C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246628114 | ||||||
| chr1:246628200
|
A | G | 1 | a0001c0001t0004g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.586-3694A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246628200 | ||||||
| chr1:246628241
|
C | T | 115 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(112): Show | 115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.586-3653C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246628241 | ||||||
| chr1:246628409
|
G | A | 1 | a0001c0001t0002g0244 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.586-3485G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246628409 | ||||||
| chr1:246628640
|
C | T | 26 | a0001c0001t0001g0135a0001c0001t0004g0016a0001c0001t0004g0042others(23): Show | 26 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.586-3254C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246628640 | ||||||
| chr1:246628830
|
C | A | 1 | a0001c0001t0001g0274 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.586-3064C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246628830 | ||||||
| chr1:246628830
|
C | G | 276 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(273): Show | 278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.586-3064C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246628830 | ||||||
| chr1:246628926
|
C | T | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.586-2968C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246628926 | ||||||
| chr1:246628933
|
T | A | 11 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0037others(8): Show | 11 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.586-2961T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246628933 | ||||||
| chr1:246629018
|
T | C | 9 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(6): Show | 9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.586-2876T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246629018 | ||||||
| chr1:246629399
|
A | ATGTC | 277 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(274): Show | 279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.586-2494_586-2493i others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246629399 | |||||
| chr1:246629439
|
A | G | 19 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0167others(16): Show | 19 | HG01981.hp1 HG02145.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.586-2455A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246629439 | ||||||
| chr1:246629511
|
G | T | 3 | a0002c0002t0015g0168a0007c0011t0015g0213a0009c0008t0001g0161 | 3 | HG02622.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.586-2383G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246629511 | ||||||
| chr1:246629628
|
A | G | 1 | a0001c0001t0003g0163 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.586-2266A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246629628 | ||||||
| chr1:246629786
|
C | G | 1 | a0001c0001t0008g0021 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.586-2108C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246629786 | ||||||
| chr1:246629838
|
T | G | 9 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(6): Show | 9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.586-2056T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246629838 | ||||||
| chr1:246629879
|
A | C | 3 | a0002c0002t0015g0168a0007c0011t0015g0213a0009c0008t0001g0161 | 3 | HG02622.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.586-2015A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246629879 | ||||||
| chr1:246629913
|
G | T | 1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.586-1981G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246629913 | ||||||
| chr1:246629928
|
C | T | 157 | a0001c0001t0001g0022a0001c0001t0001g0088a0001c0001t0001g0090others(154): Show | 157 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.586-1966C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246629928 | ||||||
| chr1:246629983
|
C | T | 7 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0091others(4): Show | 7 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.586-1911C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246629983 | ||||||
| chr1:246630027
|
C | T | 4 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0094others(1): Show | 4 | HG01261.hp2 HG01433.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.586-1867C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246630027 | ||||||
| chr1:246630257
|
T | C | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.586-1637T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246630257 | ||||||
| chr1:246630402
|
C | A | 1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.586-1492C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246630402 | ||||||
| chr1:246630447
|
A | C | 179 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(176): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.586-1447A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246630447 | ||||||
| chr1:246630481
|
C | T | 179 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(176): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.586-1413C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246630481 | ||||||
| chr1:246630578
|
A | G | 179 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(176): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.586-1316A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246630578 | ||||||
| chr1:246630653
|
G | A | 1 | a0001c0001t0003g0065 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.586-1241G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246630653 | ||||||
| chr1:246630677
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.586-1217T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246630677 | ||||||
| chr1:246630699
|
C | CT | 179 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(176): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.586-1188dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246630699 | |||||
| chr1:246630730
|
A | G | 179 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(176): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.586-1164A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246630730 | ||||||
| chr1:246630731
|
T | G | 11 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0169others(8): Show | 11 | HG02145.hp2 HG02258.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.586-1163T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246630731 | ||||||
| chr1:246630832
|
A | G | 179 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(176): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.586-1062A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246630832 | ||||||
| chr1:246630887
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.586-1007A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246630887 | ||||||
| chr1:246630993
|
A | G | 179 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(176): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.586-901A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246630993 | ||||||
| chr1:246631025
|
C | T | 2 | a0001c0001t0004g0004a0001c0001t0004g0006 | 2 | HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.586-869C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246631025 | ||||||
| chr1:246631069
|
G | A | 115 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(112): Show | 115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.586-825G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246631069 | ||||||
| chr1:246631125
|
A | G | 1 | a0001c0001t0003g0144 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.586-769A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246631125 | ||||||
| chr1:246631173
|
A | G | 1 | a0001c0001t0003g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.586-721A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246631173 | ||||||
| chr1:246631392
|
C | T | 1 | a0001c0001t0002g0311 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.586-502C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246631392 | ||||||
| chr1:246631393
|
G | A | 2 | a0004c0004t0003g0184a0004c0004t0003g0185 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.586-501G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246631393 | ||||||
| chr1:246631599
|
T | C | 1 | a0001c0001t0003g0070 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.586-295T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246631599 | ||||||
| chr1:246631645
|
G | A | 177 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(174): Show | 177 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.586-249G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246631645 | ||||||
| chr1:246632161
|
T | G | 179 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(176): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.616+237T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246632161 | ||||||
| chr1:246632581
|
A | T | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.616+657A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246632581 | ||||||
| chr1:246632591
|
G | A | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.616+667G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246632591 | ||||||
| chr1:246632796
|
G | C | 115 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(112): Show | 115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.616+872G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246632796 | ||||||
| chr1:246633147
|
C | T | 1 | a0001c0001t0002g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.617-777C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246633147 | ||||||
| chr1:246633175
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.617-749C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246633175 | ||||||
| chr1:246633187
|
C | T | 7 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0091others(4): Show | 7 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.617-737C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246633187 | ||||||
| chr1:246633301
|
G | T | 277 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(274): Show | 279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.617-623G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246633301 | ||||||
| chr1:246633305
|
C | T | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.617-619C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246633305 | ||||||
| chr1:246633341
|
C | G | 1 | a0001c0001t0001g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617-583C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246633341 | ||||||
| chr1:246633424
|
C | G | 279 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(276): Show | 281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.617-500C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246633424 | ||||||
| chr1:246633603
|
C | T | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.617-321C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246633603 | ||||||
| chr1:246633637
|
G | A | 1 | a0001c0001t0003g0211 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.617-287G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246633637 | ||||||
| chr1:246633668
|
G | A | 2 | a0001c0001t0003g0047a0001c0001t0003g0048 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.617-256G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246633668 | ||||||
| chr1:246633746
|
GA | G | 10 | a0001c0001t0002g0243a0001c0001t0004g0016a0001c0001t0004g0042others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.617-163delA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 246633746 | |||||
| chr1:246633799
|
A | G | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.617-125A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246633799 | ||||||
| chr1:246633853
|
G | A | 1 | a0001c0001t0022g0085 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.617-71G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246633853 | ||||||
| chr1:246633906
|
C | T | 1 | a0001c0001t0002g0183 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.617-18C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246633906 | ||||||
| chr1:246634123
|
A | G | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.703+113A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 5/10 | chr1 | 246634123 | ||||||
| chr1:246634343
|
T | C | 4 | a0001c0001t0003g0206a0001c0001t0003g0220a0001c0001t0003g0259others(1): Show | 4 | HG03017.hp2 HG03704.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-130T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 5/10 | chr1 | 246634343 | ||||||
| chr1:246634391
|
G | A | 1 | a0003c0003t0004g0034 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.704-82G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 5/10 | chr1 | 246634391 | ||||||
| chr1:246634408
|
G | T | 116 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(113): Show | 116 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.704-65G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 5/10 | chr1 | 246634408 | ||||||
| chr1:246634412
|
G | GT | 115 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(112): Show | 115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.704-54dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 246634412 | |||||
| chr1:246634672
|
T | A | 116 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(113): Show | 116 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.818+85T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246634672 | ||||||
| chr1:246634747
|
G | A | 115 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(112): Show | 115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.818+160G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246634747 | ||||||
| chr1:246634783
|
A | C | 24 | a0001c0001t0001g0198a0001c0001t0001g0210a0001c0001t0001g0219others(21): Show | 24 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(21): Show |
intron_variant | MODIFIER | c.818+196A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246634783 | ||||||
| chr1:246634788
|
G | A | 2 | a0002c0002t0015g0168a0007c0011t0015g0213 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.818+201G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246634788 | ||||||
| chr1:246634848
|
G | A | 115 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(112): Show | 115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.818+261G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246634848 | ||||||
| chr1:246634863
|
G | A | 2 | a0001c0001t0002g0072a0001c0001t0003g0084 | 2 | HG01099.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.818+276G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246634863 | ||||||
| chr1:246634935
|
C | T | 6 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0255others(3): Show | 6 | HG01109.hp1 HG01943.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.818+348C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246634935 | ||||||
| chr1:246634951
|
T | TGGTGGGT others(13): Show |
114 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(111): Show | 114 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.818+368_818+369ins others(20): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 246634951 | |||||
| chr1:246634951
|
T | TGGTGTGT others(13): Show |
1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.818+368_818+369ins others(20): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 246634951 | |||||
| chr1:246634951
|
TGGTGCGT others(13): Show |
T | 1 | a0002c0002t0001g0147 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.818+385_818+404del others(20): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 246634951 | |||||
| chr1:246634956
|
C | CGTGTCTT others(13): Show |
127 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0052others(124): Show | 129 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.818+387_818+388ins others(20): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 246634956 | |||||
| chr1:246634956
|
C | CGTGTCTT others(13): Show |
1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.818+377_818+378ins others(20): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 246634956 | |||||
| chr1:246634956
|
C | G | 1 | a0010c0010t0002g0028 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.818+369C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246634956 | ||||||
| chr1:246634967
|
G | T | 1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.818+380G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246634967 | ||||||
| chr1:246634969
|
C | CGGGGTAG others(13): Show |
33 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0091others(30): Show | 33 | HG00140.hp1 HG00733.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.818+387_818+388ins others(20): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 246634969 | |||||
| chr1:246634977
|
G | C | 7 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0091others(4): Show | 7 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.818+390G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246634977 | ||||||
| chr1:246634990
|
G | A | 116 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(113): Show | 116 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.818+403G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246634990 | ||||||
| chr1:246635047
|
C | T | 1 | a0001c0001t0003g0104 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.818+460C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635047 | ||||||
| chr1:246635083
|
C | T | 116 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(113): Show | 116 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.818+496C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635083 | ||||||
| chr1:246635105
|
T | C | 1 | a0002c0002t0001g0200 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.818+518T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635105 | ||||||
| chr1:246635155
|
A | G | 117 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(114): Show | 117 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.818+568A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635155 | ||||||
| chr1:246635163
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.818+576C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635163 | ||||||
| chr1:246635208
|
G | A | 115 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(112): Show | 115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.818+621G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635208 | ||||||
| chr1:246635244
|
T | A | 168 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(165): Show | 168 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.818+657T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635244 | ||||||
| chr1:246635266
|
G | A | 116 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(113): Show | 116 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.818+679G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635266 | ||||||
| chr1:246635283
|
G | A | 98 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(95): Show | 100 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.818+696G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635283 | ||||||
| chr1:246635289
|
A | G | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.818+702A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635289 | ||||||
| chr1:246635300
|
A | G | 17 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0167others(14): Show | 17 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.818+713A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635300 | ||||||
| chr1:246635358
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0002g0049 | 2 | HG01256.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.818+771G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635358 | ||||||
| chr1:246635374
|
C | G | 1 | a0002c0002t0001g0120 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.818+787C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635374 | ||||||
| chr1:246635379
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.818+792A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635379 | ||||||
| chr1:246635414
|
T | A | 115 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(112): Show | 115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.818+827T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635414 | ||||||
| chr1:246635487
|
C | T | 52 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0088others(49): Show | 52 | HG00140.hp1 HG00733.hp1 HG01243.hp1 others(49): Show |
intron_variant | MODIFIER | c.818+900C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635487 | ||||||
| chr1:246635646
|
A | G | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.818+1059A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635646 | ||||||
| chr1:246635664
|
G | A | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.818+1077G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635664 | ||||||
| chr1:246635678
|
C | G | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.818+1091C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635678 | ||||||
| chr1:246635683
|
G | A | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.818+1096G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635683 | ||||||
| chr1:246635719
|
T | G | 2 | a0001c0001t0001g0182a0001c0001t0017g0008 | 2 | HG01981.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.818+1132T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635719 | ||||||
| chr1:246635741
|
C | G | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.818+1154C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635741 | ||||||
| chr1:246635756
|
G | A | 2 | a0001c0001t0001g0240a0001c0001t0001g0283 | 2 | NA18945.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.818+1169G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635756 | ||||||
| chr1:246635758
|
G | A | 1 | a0006c0005t0023g0043 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.818+1171G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635758 | ||||||
| chr1:246635767
|
G | A | 2 | a0001c0001t0001g0170a0001c0001t0003g0181 | 2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.818+1180G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635767 | ||||||
| chr1:246635778
|
T | G | 1 | a0001c0001t0003g0316 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.818+1191T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635778 | ||||||
| chr1:246635807
|
G | A | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.818+1220G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635807 | ||||||
| chr1:246635819
|
C | T | 30 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(27): Show | 31 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.818+1232C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635819 | ||||||
| chr1:246635840
|
C | T | 8 | a0001c0001t0001g0215a0001c0001t0001g0236a0001c0001t0001g0237others(5): Show | 8 | HG01109.hp1 HG01175.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.818+1253C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635840 | ||||||
| chr1:246635903
|
C | T | 9 | a0001c0001t0001g0301a0002c0002t0001g0110a0002c0002t0001g0126others(6): Show | 9 | HG00639.hp2 HG02015.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.818+1316C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635903 | ||||||
| chr1:246635916
|
C | T | 1 | a0002c0002t0001g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.818+1329C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635916 | ||||||
| chr1:246635957
|
A | G | 118 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(115): Show | 118 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.818+1370A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635957 | ||||||
| chr1:246635982
|
G | A | 1 | a0001c0001t0002g0285 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.818+1395G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635982 | ||||||
| chr1:246636035
|
G | A | 1 | a0001c0001t0001g0301 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.818+1448G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636035 | ||||||
| chr1:246636086
|
C | T | 26 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0088others(23): Show | 26 | HG00140.hp1 HG00408.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.818+1499C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636086 | ||||||
| chr1:246636139
|
C | G | 1 | a0001c0001t0004g0007 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.818+1552C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636139 | ||||||
| chr1:246636176
|
C | T | 8 | a0001c0001t0001g0215a0001c0001t0001g0236a0001c0001t0001g0237others(5): Show | 8 | HG01109.hp1 HG01175.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.818+1589C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636176 | ||||||
| chr1:246636177
|
A | G | 116 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(113): Show | 116 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.818+1590A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636177 | ||||||
| chr1:246636235
|
CAG | C | 5 | a0003c0003t0001g0038a0003c0003t0001g0039a0003c0003t0001g0040others(2): Show | 5 | HG00733.hp1 HG01891.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.818+1649_818+1650d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636235 | ||||||
| chr1:246636252
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.818+1665G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636252 | ||||||
| chr1:246636256
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.818+1669C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636256 | ||||||
| chr1:246636275
|
A | G | 4 | a0001c0001t0001g0022a0001c0001t0001g0289a0001c0001t0008g0020others(1): Show | 4 | HG02145.hp1 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.818+1688A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636275 | ||||||
| chr1:246636281
|
G | A | 2 | a0002c0002t0015g0168a0007c0011t0015g0213 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.818+1694G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636281 | ||||||
| chr1:246636295
|
G | A | 9 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(6): Show | 9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.818+1708G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636295 | ||||||
| chr1:246636409
|
G | A | 1 | a0001c0001t0002g0101 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.818+1822G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636409 | ||||||
| chr1:246636427
|
C | T | 98 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(95): Show | 100 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.818+1840C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636427 | ||||||
| chr1:246636448
|
C | T | 3 | a0002c0002t0001g0114a0002c0002t0001g0115a0002c0002t0002g0113 | 3 | NA18944.hp1 NA18948.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.818+1861C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636448 | ||||||
| chr1:246636472
|
G | A | 4 | a0001c0001t0001g0121a0001c0001t0010g0229a0001c0001t0010g0230others(1): Show | 4 | HG00558.hp2 HG02080.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.818+1885G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636472 | ||||||
| chr1:246636504
|
T | G | 1 | a0001c0001t0004g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.818+1917T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636504 | ||||||
| chr1:246636532
|
G | A | 1 | a0001c0001t0003g0294 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.818+1945G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636532 | ||||||
| chr1:246636561
|
A | G | 1 | a0001c0001t0025g0288 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.818+1974A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636561 | ||||||
| chr1:246636605
|
T | C | 1 | a0001c0001t0001g0309 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.818+2018T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636605 | ||||||
| chr1:246636631
|
T | C | 1 | a0003c0003t0004g0162 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.818+2044T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636631 | ||||||
| chr1:246636652
|
G | A | 1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.818+2065G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636652 | ||||||
| chr1:246636654
|
G | A | 1 | a0001c0001t0002g0209 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.818+2067G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636654 | ||||||
| chr1:246636696
|
T | G | 24 | a0001c0001t0001g0198a0001c0001t0001g0210a0001c0001t0001g0219others(21): Show | 24 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(21): Show |
intron_variant | MODIFIER | c.818+2109T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636696 | ||||||
| chr1:246636708
|
A | G | 116 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(113): Show | 116 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.818+2121A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636708 | ||||||
| chr1:246636720
|
A | G | 116 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(113): Show | 116 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.818+2133A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636720 | ||||||
| chr1:246636937
|
G | A | 116 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(113): Show | 116 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.818+2350G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636937 | ||||||
| chr1:246636952
|
C | G | 7 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0091others(4): Show | 7 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.818+2365C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636952 | ||||||
| chr1:246637027
|
T | A | 115 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(112): Show | 115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.818+2440T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246637027 | ||||||
| chr1:246637106
|
G | T | 1 | a0001c0001t0003g0220 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.818+2519G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246637106 | ||||||
| chr1:246637268
|
A | G | 3 | a0001c0001t0001g0091a0001c0001t0001g0128a0001c0001t0002g0077 | 3 | HG03239.hp1 HG03688.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.818+2681A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246637268 | ||||||
| chr1:246637303
|
T | G | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.818+2716T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246637303 | ||||||
| chr1:246637479
|
G | A | 1 | a0001c0001t0003g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.818+2892G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246637479 | ||||||
| chr1:246637545
|
G | A | 9 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(6): Show | 9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.818+2958G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246637545 | ||||||
| chr1:246637687
|
C | T | 277 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(274): Show | 279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.818+3100C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246637687 | ||||||
| chr1:246637702
|
T | G | 170 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(167): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.818+3115T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246637702 | ||||||
| chr1:246637703
|
C | T | 170 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(167): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.818+3116C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246637703 | ||||||
| chr1:246637782
|
A | G | 2 | a0002c0002t0015g0168a0007c0011t0015g0213 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.818+3195A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246637782 | ||||||
| chr1:246637808
|
A | G | 7 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0091others(4): Show | 7 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.818+3221A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246637808 | ||||||
| chr1:246637887
|
G | A | 7 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0091others(4): Show | 7 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.818+3300G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246637887 | ||||||
| chr1:246637938
|
T | G | 7 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0091others(4): Show | 7 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.818+3351T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246637938 | ||||||
| chr1:246638119
|
C | T | 9 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(6): Show | 9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.818+3532C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246638119 | ||||||
| chr1:246638293
|
C | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0290 | 2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.819-3456C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246638293 | ||||||
| chr1:246638305
|
G | A | 1 | a0001c0001t0012g0001 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.819-3444G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246638305 | ||||||
| chr1:246638346
|
G | A | 277 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(274): Show | 279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.819-3403G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246638346 | ||||||
| chr1:246638356
|
C | T | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.819-3393C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246638356 | ||||||
| chr1:246638416
|
A | C | 1 | a0001c0001t0003g0226 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.819-3333A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246638416 | ||||||
| chr1:246638491
|
C | G | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.819-3258C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246638491 | ||||||
| chr1:246638558
|
T | C | 26 | a0001c0001t0001g0135a0001c0001t0004g0016a0001c0001t0004g0042others(23): Show | 26 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.819-3191T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246638558 | ||||||
| chr1:246638886
|
G | A | 1 | a0001c0001t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.819-2863G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246638886 | ||||||
| chr1:246639090
|
G | A | 2 | a0001c0001t0001g0260a0001c0001t0001g0318 | 2 | HG00558.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.819-2659G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639090 | ||||||
| chr1:246639154
|
T | C | 1 | a0001c0009t0001g0191 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.819-2595T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639154 | ||||||
| chr1:246639176
|
T | C | 115 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(112): Show | 115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.819-2573T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639176 | ||||||
| chr1:246639180
|
C | T | 1 | a0001c0001t0002g0131 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.819-2569C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639180 | ||||||
| chr1:246639183
|
C | A | 7 | a0001c0001t0004g0016a0001c0001t0004g0042a0001c0001t0004g0150others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.819-2566C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639183 | ||||||
| chr1:246639183
|
C | G | 98 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(95): Show | 100 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.819-2566C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639183 | ||||||
| chr1:246639197
|
G | A | 3 | a0003c0003t0004g0034a0003c0003t0004g0035a0003c0003t0004g0036 | 3 | HG01243.hp1 HG02896.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.819-2552G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639197 | ||||||
| chr1:246639266
|
G | A | 2 | a0001c0001t0002g0245a0001c0001t0002g0252 | 2 | HG01070.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.819-2483G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639266 | ||||||
| chr1:246639391
|
C | A | 1 | a0001c0001t0002g0238 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.819-2358C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639391 | ||||||
| chr1:246639423
|
C | T | 1 | a0001c0001t0002g0238 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.819-2326C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639423 | ||||||
| chr1:246639455
|
G | A | 4 | a0001c0001t0001g0197a0001c0001t0001g0274a0001c0001t0001g0277others(1): Show | 4 | HG02109.hp2 HG03491.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.819-2294G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639455 | ||||||
| chr1:246639566
|
A | G | 179 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(176): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.819-2183A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639566 | ||||||
| chr1:246639704
|
G | A | 4 | a0001c0001t0005g0155a0001c0001t0005g0203a0001c0001t0005g0204others(1): Show | 4 | HG01433.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.819-2045G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639704 | ||||||
| chr1:246639769
|
C | T | 2 | a0002c0002t0015g0168a0007c0011t0015g0213 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.819-1980C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639769 | ||||||
| chr1:246639915
|
T | C | 115 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(112): Show | 115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.819-1834T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639915 | ||||||
| chr1:246640074
|
T | G | 4 | a0002c0002t0001g0145a0002c0002t0001g0146a0002c0002t0001g0147others(1): Show | 4 | HG02559.hp1 HG02683.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.819-1675T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246640074 | ||||||
| chr1:246640420
|
A | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0257 | 2 | HG01884.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.819-1329A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246640420 | ||||||
| chr1:246640488
|
T | A | 1 | a0002c0002t0001g0125 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.819-1261T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246640488 | ||||||
| chr1:246640548
|
T | C | 1 | a0001c0001t0003g0067 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.819-1201T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246640548 | ||||||
| chr1:246640604
|
A | G | 1 | a0002c0002t0001g0126 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.819-1145A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246640604 | ||||||
| chr1:246640618
|
A | G | 1 | a0001c0001t0003g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.819-1131A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246640618 | ||||||
| chr1:246640918
|
G | T | 2 | a0002c0002t0015g0168a0007c0011t0015g0213 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.819-831G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246640918 | ||||||
| chr1:246640935
|
T | TGGAACAT others(54): Show |
1 | a0001c0001t0004g0007 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.819-813_819-753dup others(61): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 246640935 | |||||
| chr1:246640983
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.819-766C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246640983 | ||||||
| chr1:246640999
|
A | G | 1 | a0001c0001t0003g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.819-750A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246640999 | ||||||
| chr1:246641188
|
A | G | 9 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(6): Show | 9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.819-561A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246641188 | ||||||
| chr1:246641288
|
A | G | 3 | a0002c0002t0015g0168a0007c0011t0015g0213a0009c0008t0001g0161 | 3 | HG02622.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.819-461A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246641288 | ||||||
| chr1:246641431
|
T | A | 1 | a0001c0001t0001g0287 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.819-318T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246641431 | ||||||
| chr1:246641522
|
T | C | 115 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(112): Show | 115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.819-227T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246641522 | ||||||
| chr1:246641895
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.841-46C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 7/10 | chr1 | 246641895 | ||||||
| chr1:246642131
|
TG | T | 94 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(91): Show | 94 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.937+96delG | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642131 | |||||
| chr1:246642132
|
G | GTT | 8 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(5): Show | 8 | HG00140.hp1 HG00741.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.937+95_937+96insTT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | ||||||
| chr1:246642132
|
G | GTTTTTT | 9 | a0001c0001t0001g0135a0001c0001t0004g0042a0001c0001t0004g0134others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.937+95_937+96insTT others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | ||||||
| chr1:246642132
|
G | GTTTTTTT | 14 | a0001c0001t0004g0015a0001c0001t0004g0016a0001c0001t0004g0150others(11): Show | 14 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.937+95_937+96insTT others(5): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | ||||||
| chr1:246642132
|
G | GTTTTTTT others(1): Show |
4 | a0001c0001t0004g0100a0003c0003t0001g0032a0003c0003t0001g0040others(1): Show | 4 | HG02257.hp2 HG02896.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.937+95_937+96insTT others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | ||||||
| chr1:246642132
|
G | GTTTTTTT others(4): Show |
1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.937+95_937+96insTT others(9): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | ||||||
| chr1:246642132
|
G | GTTTTTTT others(5): Show |
3 | a0001c0001t0004g0017a0001c0001t0005g0023a0001c0001t0020g0024 | 3 | HG02809.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.937+95_937+96insTT others(10): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | ||||||
| chr1:246642132
|
G | GTTTTTTT others(6): Show |
6 | a0001c0001t0001g0177a0001c0001t0001g0182a0001c0001t0004g0014others(3): Show | 6 | HG00735.hp1 HG02647.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.937+95_937+96insTT others(11): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | ||||||
| chr1:246642132
|
G | GTTTTTTT others(8): Show |
2 | a0001c0001t0001g0170a0001c0001t0004g0007 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.937+95_937+96insTT others(13): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | ||||||
| chr1:246642132
|
G | GTTTTTTT others(9): Show |
5 | a0001c0001t0001g0167a0001c0001t0002g0172a0001c0001t0002g0175others(2): Show | 5 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.937+95_937+96insTT others(14): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | ||||||
| chr1:246642132
|
G | GTTTTTTT others(10): Show |
1 | a0001c0001t0009g0013 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.937+95_937+96insTT others(15): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | ||||||
| chr1:246642132
|
G | GTTTTTTT others(11): Show |
5 | a0001c0001t0001g0025a0001c0001t0001g0169a0001c0001t0004g0026others(2): Show | 5 | HG02818.hp1 HG02976.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.937+95_937+96insTT others(16): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | ||||||
| chr1:246642132
|
G | GTTTTTTT others(15): Show |
2 | a0001c0001t0001g0011a0001c0001t0003g0292 | 2 | NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.937+95_937+96insTT others(20): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | ||||||
| chr1:246642132
|
G | GTTTTTTT others(16): Show |
1 | a0001c0001t0001g0290 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.937+95_937+96insTT others(21): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | ||||||
| chr1:246642132
|
GGT | G | 7 | a0001c0001t0001g0234a0001c0001t0005g0155a0001c0001t0005g0203others(4): Show | 7 | HG01433.hp1 HG02602.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.937+96_937+97delGT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | ||||||
| chr1:246642133
|
G | GT | 10 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0312others(7): Show | 10 | HG01978.hp2 HG01981.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.937+117dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642133 | |||||
| chr1:246642133
|
G | T | 78 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0088others(75): Show | 78 | HG00140.hp1 HG00621.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.937+96G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642133 | ||||||
| chr1:246642143
|
T | G | 1 | a0001c0001t0002g0080 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.937+106T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642143 | ||||||
| chr1:246642259
|
A | C | 1 | a0001c0001t0001g0197 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.937+222A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642259 | ||||||
| chr1:246642379
|
A | G | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.937+342A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642379 | ||||||
| chr1:246642383
|
A | G | 1 | a0001c0001t0003g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.937+346A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642383 | ||||||
| chr1:246642764
|
T | G | 1 | a0001c0001t0002g0189 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.937+727T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642764 | ||||||
| chr1:246642780
|
A | G | 1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.937+743A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642780 | ||||||
| chr1:246642837
|
G | GGTGGTGG others(889): Show |
3 | a0001c0001t0004g0157a0001c0001t0004g0158a0001c0001t0004g0159 | 3 | HG01109.hp2 HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.937+801_937+802ins others(896): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(886): Show |
1 | a0001c0001t0001g0283 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(893): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(892): Show |
1 | a0001c0001t0002g0231 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(899): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(883): Show |
1 | a0010c0010t0002g0028 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(890): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(877): Show |
2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG02056.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.937+801_937+802ins others(884): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(880): Show |
1 | a0001c0001t0002g0232 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(887): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(886): Show |
1 | a0001c0001t0001g0260 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(893): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(889): Show |
1 | a0001c0001t0002g0209 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(896): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(892): Show |
73 | a0001c0001t0001g0022a0001c0001t0001g0166a0001c0001t0001g0194others(70): Show | 73 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.937+801_937+802ins others(899): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(883): Show |
1 | a0001c0001t0001g0314 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(890): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(889): Show |
2 | a0001c0001t0005g0155a0001c0001t0005g0204 | 2 | HG01433.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.937+801_937+802ins others(896): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(889): Show |
5 | a0001c0001t0001g0160a0001c0001t0001g0240a0001c0001t0001g0257others(2): Show | 5 | HG01884.hp1 HG03130.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.937+801_937+802ins others(896): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(889): Show |
1 | a0001c0001t0002g0238 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(896): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(892): Show |
1 | a0001c0001t0001g0291 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(899): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(891): Show |
1 | a0001c0001t0002g0201 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(898): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(892): Show |
3 | a0001c0001t0002g0225a0001c0001t0002g0245a0001c0001t0002g0252 | 3 | HG01070.hp2 HG01081.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.937+801_937+802ins others(899): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(889): Show |
1 | a0001c0001t0001g0272 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(896): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(889): Show |
1 | a0001c0001t0001g0265 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(896): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(892): Show |
1 | a0001c0001t0001g0207 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(899): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(886): Show |
1 | a0001c0001t0001g0296 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(893): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(886): Show |
4 | a0001c0001t0001g0237a0001c0001t0001g0255a0001c0001t0001g0264others(1): Show | 4 | HG01109.hp1 HG01943.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.937+801_937+802ins others(893): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(883): Show |
1 | a0001c0001t0001g0236 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(890): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(883): Show |
1 | a0001c0001t0001g0263 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(890): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(892): Show |
1 | a0001c0001t0001g0266 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(899): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(883): Show |
2 | a0001c0001t0001g0156a0001c0012t0002g0278 | 2 | NA18943.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.937+801_937+802ins others(890): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(880): Show |
1 | a0001c0001t0002g0233 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(887): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(892): Show |
1 | a0001c0001t0011g0221 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(899): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(892): Show |
1 | a0007c0011t0015g0213 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(899): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(886): Show |
1 | a0002c0002t0015g0168 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(893): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(898): Show |
1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(905): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(889): Show |
1 | a0001c0001t0001g0271 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(896): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(919): Show |
32 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(29): Show | 33 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.937+801_937+802ins others(926): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(916): Show |
1 | a0001c0001t0002g0189 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(923): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(916): Show |
1 | a0001c0001t0002g0057 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(923): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(916): Show |
1 | a0001c0001t0002g0064 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(923): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(910): Show |
7 | a0002c0002t0001g0027a0002c0002t0001g0122a0002c0002t0001g0130others(4): Show | 7 | HG00741.hp2 HG01175.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.937+801_937+802ins others(917): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(901): Show |
7 | a0002c0002t0001g0111a0002c0002t0001g0112a0002c0002t0001g0114others(4): Show | 7 | HG02040.hp1 HG02074.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.937+801_937+802ins others(908): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(904): Show |
19 | a0001c0001t0001g0301a0002c0002t0001g0108a0002c0002t0001g0110others(16): Show | 19 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.937+801_937+802ins others(911): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(904): Show |
1 | a0002c0002t0001g0268 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(911): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(958): Show |
1 | a0002c0002t0007g0143 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(965): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(901): Show |
2 | a0002c0002t0001g0093a0002c0002t0001g0124 | 2 | NA18747.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.937+801_937+802ins others(908): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(910): Show |
2 | a0002c0002t0001g0171a0002c0002t0006g0030 | 2 | HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.937+801_937+802ins others(917): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(895): Show |
1 | a0002c0002t0001g0146 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(902): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(994): Show |
1 | a0001c0001t0003g0227 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(1001): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(994): Show |
1 | a0001c0001t0010g0229 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(1001): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(982): Show |
2 | a0001c0001t0002g0072a0001c0001t0003g0084 | 2 | HG01099.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.937+801_937+802ins others(989): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(994): Show |
49 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0086others(46): Show | 50 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(47): Show |
intron_variant | MODIFIER | c.937+801_937+802ins others(1001): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(994): Show |
1 | a0001c0001t0003g0082 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(1001): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(1213): Show |
2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.937+801_937+802ins others(1220): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(991): Show |
1 | a0001c0001t0003g0054 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(998): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(991): Show |
1 | a0001c0001t0003g0003 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(998): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(991): Show |
1 | a0001c0001t0002g0183 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(998): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(991): Show |
1 | a0001c0001t0003g0270 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(998): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(874): Show |
1 | a0001c0001t0013g0196 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(881): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(784): Show |
2 | a0001c0001t0001g0170a0001c0001t0003g0181 | 2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.937+801_937+802ins others(791): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(904): Show |
1 | a0001c0001t0004g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(911): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(895): Show |
1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(902): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(910): Show |
2 | a0003c0003t0004g0162a0006c0005t0023g0043 | 2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.937+801_937+802ins others(917): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(901): Show |
9 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(6): Show | 9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.937+801_937+802ins others(908): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(883): Show |
7 | a0001c0001t0004g0016a0001c0001t0004g0042a0001c0001t0004g0150others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.937+801_937+802ins others(890): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(883): Show |
5 | a0001c0001t0001g0135a0001c0001t0004g0134a0001c0001t0016g0136others(2): Show | 5 | HG01243.hp2 HG02622.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.937+801_937+802ins others(890): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(787): Show |
1 | a0001c0001t0002g0175 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(794): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(790): Show |
1 | a0001c0001t0001g0290 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(797): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(979): Show |
1 | a0001c0001t0004g0007 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(986): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(796): Show |
2 | a0001c0001t0002g0172a0001c0001t0004g0173 | 2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.937+801_937+802ins others(803): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(793): Show |
2 | a0001c0001t0001g0167a0001c0001t0001g0169 | 2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.937+801_937+802ins others(800): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(799): Show |
1 | a0001c0001t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(806): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(796): Show |
1 | a0001c0001t0001g0182 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(803): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(820): Show |
4 | a0001c0001t0001g0025a0001c0001t0004g0026a0001c0001t0009g0012others(1): Show | 4 | HG02818.hp1 HG03041.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.937+801_937+802ins others(827): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(817): Show |
1 | a0001c0001t0009g0010 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(824): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(904): Show |
1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(911): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(811): Show |
1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(818): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(904): Show |
1 | a0001c0001t0003g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(911): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(883): Show |
1 | a0003c0003t0001g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(890): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(886): Show |
9 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0037others(6): Show | 9 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.937+801_937+802ins others(893): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(871): Show |
1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(878): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(892): Show |
5 | a0001c0001t0001g0091a0001c0001t0001g0128a0001c0001t0001g0287others(2): Show | 5 | HG03239.hp1 HG03239.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.937+801_937+802ins others(899): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(889): Show |
2 | a0001c0001t0001g0088a0001c0001t0001g0090 | 2 | HG00140.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.937+801_937+802ins others(896): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642837
|
G | GGTGGTGG others(907): Show |
1 | a0001c0001t0004g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(914): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | |||||
| chr1:246642839
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.937+802A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642839 | ||||||
| chr1:246642857
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.937+820G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642857 | ||||||
| chr1:246642858
|
T | TGGTGATG others(903): Show |
1 | a0001c0001t0001g0089 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.937+822_937+823ins others(910): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642858 | |||||
| chr1:246642887
|
CT | C | 6 | a0003c0003t0001g0037a0003c0003t0001g0038a0003c0003t0001g0039others(3): Show | 6 | HG00733.hp1 HG01891.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.937+856delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642887 | |||||
| chr1:246642900
|
T | A | 1 | a0001c0001t0001g0089 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.937+863T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642900 | ||||||
| chr1:246642925
|
G | A | 2 | a0001c0001t0001g0241a0001c0001t0001g0242 | 2 | HG00639.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.937+888G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642925 | ||||||
| chr1:246642973
|
C | T | 1 | a0003c0003t0004g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.937+936C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642973 | ||||||
| chr1:246643040
|
C | T | 2 | a0001c0001t0003g0069a0001c0001t0003g0092 | 2 | HG01952.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.937+1003C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643040 | ||||||
| chr1:246643068
|
T | G | 1 | a0001c0001t0003g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.937+1031T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643068 | ||||||
| chr1:246643084
|
G | T | 26 | a0001c0001t0001g0135a0001c0001t0004g0016a0001c0001t0004g0042others(23): Show | 26 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.937+1047G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643084 | ||||||
| chr1:246643092
|
A | G | 18 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0167others(15): Show | 18 | HG01981.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.937+1055A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643092 | ||||||
| chr1:246643128
|
G | A | 8 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(5): Show | 8 | HG00735.hp1 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.937+1091G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643128 | ||||||
| chr1:246643304
|
G | T | 1 | a0002c0002t0001g0027 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.937+1267G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643304 | ||||||
| chr1:246643312
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.937+1275G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643312 | ||||||
| chr1:246643379
|
A | T | 1 | a0001c0001t0002g0077 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.937+1342A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643379 | ||||||
| chr1:246643498
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0257 | 2 | HG01884.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.937+1461G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643498 | ||||||
| chr1:246643559
|
G | A | 9 | a0001c0001t0001g0022a0001c0001t0001g0202a0001c0001t0001g0271others(6): Show | 9 | HG01261.hp1 HG02145.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.937+1522G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643559 | ||||||
| chr1:246643637
|
C | G | 1 | a0001c0001t0002g0285 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.937+1600C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643637 | ||||||
| chr1:246643759
|
C | G | 10 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(7): Show | 10 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.937+1722C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643759 | ||||||
| chr1:246643812
|
A | G | 60 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0088others(57): Show | 60 | HG00140.hp1 HG00733.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.937+1775A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643812 | ||||||
| chr1:246643836
|
A | G | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.937+1799A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643836 | ||||||
| chr1:246643847
|
G | A | 16 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0167others(13): Show | 16 | HG01981.hp1 HG02486.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.937+1810G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643847 | ||||||
| chr1:246644124
|
G | A | 1 | a0001c0001t0003g0092 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.937+2087G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246644124 | ||||||
| chr1:246644128
|
C | T | 10 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(7): Show | 10 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.937+2091C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246644128 | ||||||
| chr1:246644176
|
G | A | 13 | a0001c0001t0001g0132a0001c0001t0002g0071a0001c0001t0003g0050others(10): Show | 13 | HG01192.hp1 HG01255.hp1 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.937+2139G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246644176 | ||||||
| chr1:246644341
|
A | G | 4 | a0001c0001t0005g0155a0001c0001t0005g0203a0001c0001t0005g0204others(1): Show | 4 | HG01433.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.937+2304A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246644341 | ||||||
| chr1:246644367
|
G | A | 1 | a0001c0001t0024g0269 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.937+2330G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246644367 | ||||||
| chr1:246644388
|
C | CA | 89 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(86): Show | 91 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.937+2374dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246644388 | |||||
| chr1:246644388
|
C | CAA | 15 | a0001c0001t0001g0060a0001c0001t0002g0064a0001c0001t0002g0105others(12): Show | 15 | HG00738.hp2 HG01358.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.937+2373_937+2374d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246644388 | |||||
| chr1:246644388
|
CA | C | 108 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0156others(105): Show | 108 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.937+2374delA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246644388 | |||||
| chr1:246644388
|
CAA | C | 13 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(10): Show | 13 | HG00140.hp1 HG01515.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.937+2373_937+2374d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246644388 | |||||
| chr1:246644388
|
CAAA | C | 32 | a0001c0001t0001g0135a0001c0001t0001g0177a0001c0001t0004g0014others(29): Show | 32 | HG00733.hp1 HG00735.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.937+2372_937+2374d others(5): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246644388 | |||||
| chr1:246644388
|
CAAAAAAA | C | 30 | a0001c0001t0001g0301a0002c0002t0001g0093a0002c0002t0001g0108others(27): Show | 30 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.937+2368_937+2374d others(9): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246644388 | |||||
| chr1:246644450
|
A | G | 1 | a0008c0007t0003g0267 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.937+2413A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246644450 | ||||||
| chr1:246644728
|
C | T | 1 | a0001c0001t0004g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.938-2411C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246644728 | ||||||
| chr1:246644766
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.938-2373T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246644766 | ||||||
| chr1:246644906
|
G | A | 1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.938-2233G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246644906 | ||||||
| chr1:246644953
|
A | G | 60 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0088others(57): Show | 60 | HG00140.hp1 HG00733.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.938-2186A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246644953 | ||||||
| chr1:246645053
|
C | T | 1 | a0001c0001t0003g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.938-2086C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645053 | ||||||
| chr1:246645111
|
A | G | 1 | a0001c0001t0016g0136 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.938-2028A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645111 | ||||||
| chr1:246645240
|
T | A | 1 | a0001c0001t0003g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.938-1899T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645240 | ||||||
| chr1:246645296
|
GA | G | 102 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(99): Show | 104 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.938-1840delA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246645296 | |||||
| chr1:246645423
|
A | ATT | 28 | a0001c0001t0001g0135a0001c0001t0004g0014a0001c0001t0004g0015others(25): Show | 28 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.938-1716_938-1715i others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645423 | ||||||
| chr1:246645423
|
A | ATTT | 7 | a0001c0001t0001g0177a0001c0001t0004g0018a0001c0001t0004g0100others(4): Show | 7 | HG00735.hp1 HG02109.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.938-1716_938-1715i others(5): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645423 | ||||||
| chr1:246645424
|
C | CT | 32 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(29): Show | 33 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.938-1694dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246645424 | |||||
| chr1:246645424
|
C | CTTTTTT | 9 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0167others(6): Show | 9 | HG02647.hp1 HG02809.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.938-1699_938-1694d others(8): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246645424 | |||||
| chr1:246645424
|
C | T | 42 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0091others(39): Show | 42 | HG00140.hp1 HG00733.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.938-1715C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645424 | ||||||
| chr1:246645426
|
T | TTTA | 113 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(110): Show | 113 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.938-1711_938-1710i others(5): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246645426 | |||||
| chr1:246645430
|
T | A | 113 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(110): Show | 113 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.938-1709T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645430 | ||||||
| chr1:246645431
|
T | A | 2 | a0001c0001t0002g0195a0001c0001t0025g0288 | 2 | HG02300.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.938-1708T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645431 | ||||||
| chr1:246645434
|
T | A | 3 | a0001c0001t0001g0198a0001c0001t0001g0228a0001c0001t0001g0306 | 3 | HG00323.hp2 HG01081.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.938-1705T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645434 | ||||||
| chr1:246645450
|
T | C | 3 | a0002c0002t0001g0116a0002c0002t0015g0168a0007c0011t0015g0213 | 3 | HG02040.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.938-1689T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645450 | ||||||
| chr1:246645466
|
C | T | 1 | a0001c0001t0003g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.938-1673C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645466 | ||||||
| chr1:246645513
|
C | T | 99 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(96): Show | 101 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.938-1626C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645513 | ||||||
| chr1:246645514
|
G | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0291 | 2 | HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.938-1625G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645514 | ||||||
| chr1:246645521
|
G | A | 277 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(274): Show | 279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.938-1618G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645521 | ||||||
| chr1:246645529
|
G | A | 277 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(274): Show | 279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.938-1610G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645529 | ||||||
| chr1:246645553
|
G | T | 5 | a0001c0001t0001g0025a0001c0001t0004g0026a0001c0001t0009g0010others(2): Show | 5 | HG02818.hp1 HG02976.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.938-1586G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645553 | ||||||
| chr1:246645583
|
G | A | 1 | a0003c0003t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.938-1556G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645583 | ||||||
| chr1:246645585
|
G | A | 115 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(112): Show | 115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.938-1554G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645585 | ||||||
| chr1:246645588
|
C | T | 1 | a0001c0001t0002g0078 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.938-1551C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645588 | ||||||
| chr1:246645695
|
G | A | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.938-1444G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645695 | ||||||
| chr1:246645717
|
G | A | 6 | a0004c0004t0003g0119a0004c0004t0003g0184a0004c0004t0003g0185others(3): Show | 6 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.938-1422G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645717 | ||||||
| chr1:246645799
|
T | C | 5 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(2): Show | 5 | HG00738.hp1 HG01255.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.938-1340T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645799 | ||||||
| chr1:246645891
|
T | C | 1 | a0001c0001t0002g0209 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.938-1248T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645891 | ||||||
| chr1:246645915
|
A | T | 2 | a0001c0001t0003g0046a0001c0001t0003g0079 | 2 | NA18942.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.938-1224A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645915 | ||||||
| chr1:246646005
|
C | T | 34 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(31): Show | 34 | HG00140.hp1 HG00621.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.938-1134C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646005 | ||||||
| chr1:246646018
|
G | A | 1 | a0001c0001t0002g0002 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.938-1121G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646018 | ||||||
| chr1:246646055
|
A | G | 60 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0088others(57): Show | 60 | HG00140.hp1 HG00733.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.938-1084A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646055 | ||||||
| chr1:246646209
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.938-930G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646209 | ||||||
| chr1:246646212
|
G | A | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.938-927G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646212 | ||||||
| chr1:246646279
|
C | CAAA | 8 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(5): Show | 8 | HG00140.hp1 HG01515.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.938-847_938-845dup others(3): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246646279 | |||||
| chr1:246646279
|
C | CAAAAAAA | 9 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(6): Show | 9 | HG00735.hp1 HG02809.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.938-851_938-845dup others(7): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246646279 | |||||
| chr1:246646279
|
C | CAAAAAAA others(3): Show |
47 | a0001c0001t0001g0207a0001c0001t0001g0215a0001c0001t0001g0216others(44): Show | 47 | HG00280.hp2 HG00558.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.938-854_938-845dup others(10): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246646279 | |||||
| chr1:246646279
|
C | CAAAAAAA others(4): Show |
62 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(59): Show | 62 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.938-855_938-845dup others(11): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246646279 | |||||
| chr1:246646279
|
C | CAAAAAAA others(5): Show |
4 | a0001c0001t0001g0197a0001c0001t0001g0272a0001c0001t0001g0299others(1): Show | 4 | HG02970.hp1 HG03017.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.938-856_938-845dup others(12): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246646279 | |||||
| chr1:246646279
|
C | CAAAAAAA others(6): Show |
26 | a0001c0001t0001g0011a0001c0001t0001g0135a0001c0001t0001g0167others(23): Show | 26 | HG00733.hp1 HG01243.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.938-857_938-845dup others(13): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246646279 | |||||
| chr1:246646279
|
C | CAAAAAAA others(7): Show |
13 | a0001c0001t0001g0025a0001c0001t0001g0290a0001c0001t0002g0172others(10): Show | 13 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.938-858_938-845dup others(14): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246646279 | |||||
| chr1:246646279
|
C | CAAAAAAA others(8): Show |
3 | a0001c0001t0004g0042a0001c0001t0004g0153a0001c0006t0001g0009 | 3 | HG02109.hp1 HG02486.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.938-859_938-845dup others(15): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246646279 | |||||
| chr1:246646361
|
C | T | 1 | a0001c0001t0003g0226 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.938-778C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646361 | ||||||
| chr1:246646427
|
T | C | 1 | a0006c0005t0023g0043 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.938-712T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646427 | ||||||
| chr1:246646445
|
C | G | 1 | a0001c0001t0001g0306 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.938-694C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646445 | ||||||
| chr1:246646541
|
C | T | 2 | a0002c0002t0001g0171a0002c0002t0006g0030 | 2 | HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.938-598C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646541 | ||||||
| chr1:246646550
|
A | C | 43 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(40): Show | 43 | HG00140.hp1 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.938-589A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646550 | ||||||
| chr1:246646566
|
C | T | 1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.938-573C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646566 | ||||||
| chr1:246646574
|
G | A | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.938-565G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646574 | ||||||
| chr1:246646575
|
G | T | 2 | a0001c0001t0018g0256a0002c0002t0002g0251 | 2 | NA18945.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.938-564G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646575 | ||||||
| chr1:246646654
|
G | A | 276 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(273): Show | 278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.938-485G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646654 | ||||||
| chr1:246646792
|
C | A | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.938-347C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646792 | ||||||
| chr1:246648394
|
A | G | 114 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(111): Show | 114 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.1836+357A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246648394 | ||||||
| chr1:246648402
|
C | T | 99 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(96): Show | 101 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1836+365C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246648402 | ||||||
| chr1:246648463
|
T | C | 1 | a0001c0001t0016g0136 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1836+426T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246648463 | ||||||
| chr1:246648648
|
C | T | 37 | a0001c0001t0001g0025a0001c0001t0001g0091a0001c0001t0001g0128others(34): Show | 37 | HG00735.hp1 HG01884.hp2 HG02109.hp1 others(34): Show |
intron_variant | MODIFIER | c.1836+611C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246648648 | ||||||
| chr1:246648888
|
A | G | 1 | a0006c0005t0023g0043 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1836+851A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246648888 | ||||||
| chr1:246648940
|
G | C | 1 | a0001c0001t0002g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1836+903G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246648940 | ||||||
| chr1:246649091
|
A | C | 1 | a0001c0001t0001g0255 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1836+1054A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246649091 | ||||||
| chr1:246649105
|
T | G | 1 | a0001c0001t0005g0205 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1836+1068T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246649105 | ||||||
| chr1:246649112
|
A | G | 26 | a0001c0001t0001g0135a0001c0001t0004g0016a0001c0001t0004g0042others(23): Show | 26 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.1836+1075A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246649112 | ||||||
| chr1:246649130
|
T | G | 1 | a0001c0001t0002g0107 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1836+1093T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246649130 | ||||||
| chr1:246649160
|
TG | T | 13 | a0001c0001t0001g0076a0001c0001t0001g0304a0001c0001t0003g0054others(10): Show | 13 | HG01934.hp2 HG02071.hp1 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1836+1124delG | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246649160 | ||||||
| chr1:246649161
|
G | T | 55 | a0001c0001t0001g0061a0001c0001t0001g0086a0001c0001t0001g0087others(52): Show | 56 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.1836+1124G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246649161 | ||||||
| chr1:246649161
|
GT | G | 219 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(216): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1836+1139delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246649161 | |||||
| chr1:246649247
|
A | G | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1836+1210A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246649247 | ||||||
| chr1:246649258
|
A | G | 26 | a0001c0001t0001g0135a0001c0001t0004g0016a0001c0001t0004g0042others(23): Show | 26 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.1836+1221A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246649258 | ||||||
| chr1:246649375
|
G | C | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1836+1338G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246649375 | ||||||
| chr1:246649576
|
C | T | 1 | a0002c0002t0001g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1836+1539C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246649576 | ||||||
| chr1:246649614
|
TGAA | T | 10 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(7): Show | 10 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1836+1585_1836+158 others(7): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246649614 | |||||
| chr1:246649808
|
C | T | 1 | a0001c0001t0003g0206 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1836+1771C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246649808 | ||||||
| chr1:246649929
|
T | C | 1 | a0001c0001t0002g0224 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1836+1892T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246649929 | ||||||
| chr1:246650162
|
G | A | 1 | a0002c0002t0001g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1836+2125G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246650162 | ||||||
| chr1:246650175
|
A | C | 227 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(224): Show | 229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1836+2138A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246650175 | ||||||
| chr1:246650676
|
C | CT | 228 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(225): Show | 229 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.1836+2658dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246650676 | |||||
| chr1:246650676
|
C | CTT | 11 | a0001c0001t0001g0197a0001c0001t0001g0265a0001c0001t0002g0102others(8): Show | 11 | HG00140.hp2 HG00280.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1836+2657_1836+265 others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246650676 | |||||
| chr1:246650676
|
C | CTTT | 7 | a0001c0001t0003g0047a0001c0001t0003g0068a0004c0004t0003g0119others(4): Show | 7 | HG01256.hp2 HG01993.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1836+2656_1836+265 others(7): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246650676 | |||||
| chr1:246650676
|
C | CTTTT | 49 | a0001c0001t0001g0061a0001c0001t0001g0086a0001c0001t0001g0087others(46): Show | 50 | HG00423.hp2 HG01069.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.1836+2655_1836+265 others(8): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246650676 | |||||
| chr1:246650735
|
C | T | 14 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0167others(11): Show | 14 | HG02486.hp2 HG02615.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.1836+2698C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246650735 | ||||||
| chr1:246650835
|
G | A | 149 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(146): Show | 150 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.1836+2798G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246650835 | ||||||
| chr1:246650992
|
C | A | 2 | a0001c0001t0003g0046a0001c0001t0003g0079 | 2 | NA18942.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1836+2955C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246650992 | ||||||
| chr1:246651070
|
T | A | 35 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(32): Show | 35 | HG00140.hp1 HG00733.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.1836+3033T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246651070 | ||||||
| chr1:246651074
|
G | C | 276 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(273): Show | 278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.1836+3037G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246651074 | ||||||
| chr1:246651136
|
AT | A | 14 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0169others(11): Show | 14 | HG01109.hp1 HG01175.hp1 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1836+3108delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246651136 | |||||
| chr1:246651254
|
GC | G | 7 | a0001c0001t0004g0016a0001c0001t0004g0042a0001c0001t0004g0150others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1836+3222delC | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246651254 | |||||
| chr1:246651399
|
G | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0291 | 2 | HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1836+3362G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246651399 | ||||||
| chr1:246651440
|
G | A | 2 | a0003c0003t0001g0032a0003c0003t0001g0033 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1836+3403G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246651440 | ||||||
| chr1:246651504
|
A | G | 59 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0088others(56): Show | 59 | HG00140.hp1 HG00733.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.1836+3467A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246651504 | ||||||
| chr1:246651644
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1836+3607A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246651644 | ||||||
| chr1:246651680
|
C | T | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1836+3643C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246651680 | ||||||
| chr1:246651774
|
A | G | 2 | a0001c0001t0001g0293a0001c0001t0001g0296 | 2 | HG00621.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.1836+3737A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246651774 | ||||||
| chr1:246651872
|
C | A | 1 | a0001c0001t0001g0061 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1836+3835C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246651872 | ||||||
| chr1:246652056
|
C | T | 1 | a0001c0001t0005g0205 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1836+4019C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652056 | ||||||
| chr1:246652119
|
G | A | 5 | a0001c0001t0001g0248a0001c0001t0001g0295a0001c0001t0001g0307others(2): Show | 5 | HG00408.hp1 HG02083.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.1836+4082G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652119 | ||||||
| chr1:246652294
|
G | T | 64 | a0001c0001t0001g0061a0001c0001t0001g0086a0001c0001t0001g0087others(61): Show | 65 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.1836+4257G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652294 | ||||||
| chr1:246652299
|
G | C | 2 | a0002c0002t0015g0168a0007c0011t0015g0213 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1836+4262G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652299 | ||||||
| chr1:246652372
|
T | C | 140 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(137): Show | 141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1836+4335T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652372 | ||||||
| chr1:246652726
|
C | T | 3 | a0001c0001t0001g0210a0001c0001t0001g0246a0001c0001t0003g0003 | 3 | NA18950.hp1 NA18983.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1836+4689C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652726 | ||||||
| chr1:246652730
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1836+4693C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652730 | ||||||
| chr1:246652731
|
A | G | 116 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(113): Show | 116 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1836+4694A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652731 | ||||||
| chr1:246652733
|
A | G | 114 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(111): Show | 114 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.1836+4696A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652733 | ||||||
| chr1:246652737
|
G | C | 1 | a0001c0001t0004g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1836+4700G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652737 | ||||||
| chr1:246652743
|
G | A | 1 | a0001c0001t0001g0303 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1836+4706G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652743 | ||||||
| chr1:246652771
|
A | G | 119 | a0001c0001t0001g0011a0001c0001t0001g0061a0001c0001t0001g0086others(116): Show | 121 | HG00140.hp1 HG00423.hp2 HG00733.hp1 others(118): Show |
intron_variant | MODIFIER | c.1836+4734A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652771 | ||||||
| chr1:246652775
|
C | A | 137 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(134): Show | 137 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.1836+4738C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652775 | ||||||
| chr1:246652779
|
C | T | 12 | a0001c0001t0001g0025a0001c0001t0001g0167a0001c0001t0001g0169others(9): Show | 12 | HG01981.hp1 HG02615.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.1836+4742C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652779 | ||||||
| chr1:246652780
|
G | A | 67 | a0001c0001t0001g0061a0001c0001t0001g0086a0001c0001t0001g0087others(64): Show | 68 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(65): Show |
intron_variant | MODIFIER | c.1836+4743G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652780 | ||||||
| chr1:246652786
|
C | CAAGGTCA others(259): Show |
1 | a0001c0001t0001g0289 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1836+4749_1836+475 others(270): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652786 | ||||||
| chr1:246652786
|
C | CAAGGTCA others(126): Show |
17 | a0001c0001t0001g0022a0001c0001t0001g0160a0001c0001t0001g0248others(14): Show | 17 | HG00408.hp2 HG01884.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.1836+4749_1836+475 others(137): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652786 | ||||||
| chr1:246652786
|
C | CAAGGTCA others(259): Show |
1 | a0001c0009t0001g0191 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1836+4749_1836+475 others(270): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652786 | ||||||
| chr1:246652786
|
C | CAAGGTCA others(126): Show |
1 | a0001c0001t0001g0253 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1836+4749_1836+475 others(137): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652786 | ||||||
| chr1:246652786
|
C | CAAGGTCA others(392): Show |
1 | a0001c0001t0001g0307 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1836+4749_1836+475 others(403): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652786 | ||||||
| chr1:246652786
|
C | CGAGGTCA others(126): Show |
5 | a0001c0001t0001g0052a0001c0001t0001g0059a0001c0001t0002g0045others(2): Show | 5 | HG00280.hp1 HG00738.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.1836+4762_1836+476 others(137): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246652786 | |||||
| chr1:246652786
|
C | CGAGGTCA others(127): Show |
1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1836+4762_1836+476 others(138): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246652786 | |||||
| chr1:246652787
|
G | A | 45 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(42): Show | 45 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.1836+4750G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652787 | ||||||
| chr1:246652792
|
C | T | 2 | a0002c0002t0001g0093a0002c0002t0001g0124 | 2 | NA18747.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1836+4755C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652792 | ||||||
| chr1:246652800
|
C | G | 68 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0088others(65): Show | 69 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.1836+4763C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652800 | ||||||
| chr1:246652801
|
G | A | 1 | a0002c0002t0001g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1836+4764G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652801 | ||||||
| chr1:246652805
|
C | A | 1 | a0001c0001t0001g0272 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1836+4768C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652805 | ||||||
| chr1:246652807
|
A | G | 26 | a0001c0001t0001g0135a0001c0001t0004g0016a0001c0001t0004g0042others(23): Show | 26 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.1836+4770A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652807 | ||||||
| chr1:246652807
|
A | T | 1 | a0001c0001t0001g0076 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1836+4770A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652807 | ||||||
| chr1:246652810
|
C | CTGGCTGA others(126): Show |
3 | a0001c0001t0001g0219a0001c0001t0001g0299a0001c0001t0001g0300 | 3 | NA18946.hp1 NA18951.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1836+4778_1836+477 others(137): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246652810 | |||||
| chr1:246652811
|
T | C | 5 | a0002c0002t0001g0027a0002c0002t0001g0122a0002c0002t0001g0133others(2): Show | 5 | HG00741.hp2 HG01175.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1836+4774T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652811 | ||||||
| chr1:246652813
|
G | A | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1836+4776G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652813 | ||||||
| chr1:246652816
|
A | G | 206 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(203): Show | 207 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.1836+4779A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652816 | ||||||
| chr1:246652820
|
C | T | 2 | a0002c0002t0001g0149a0002c0002t0007g0143 | 2 | NA18612.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.1836+4783C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652820 | ||||||
| chr1:246652821
|
G | A | 1 | a0007c0011t0015g0213 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1836+4784G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652821 | ||||||
| chr1:246652831
|
C | A | 1 | a0001c0001t0002g0105 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1836+4794C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652831 | ||||||
| chr1:246652832
|
G | A | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1836+4795G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652832 | ||||||
| chr1:246652853
|
A | C | 3 | a0001c0001t0001g0306a0001c0001t0003g0222a0002c0002t0001g0127 | 3 | HG00323.hp2 NA18906.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1836+4816A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652853 | ||||||
| chr1:246652855
|
C | T | 274 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(271): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1836+4818C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652855 | ||||||
| chr1:246652861
|
G | A | 1 | a0003c0003t0004g0162 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1836+4824G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652861 | ||||||
| chr1:246652865
|
G | A | 61 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(58): Show | 61 | HG00140.hp1 HG00408.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.1836+4828G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652865 | ||||||
| chr1:246652866
|
T | G | 26 | a0001c0001t0001g0022a0001c0001t0001g0160a0001c0001t0001g0248others(23): Show | 26 | HG00408.hp2 HG01884.hp1 HG02083.hp2 others(23): Show |
intron_variant | MODIFIER | c.1836+4829T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652866 | ||||||
| chr1:246652866
|
T | TGGCGGGC others(123): Show |
1 | a0001c0001t0002g0285 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1836+4831_1836+483 others(134): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246652866 | |||||
| chr1:246652866
|
T | TGGTGGCG others(126): Show |
3 | a0001c0001t0004g0158a0001c0001t0004g0159a0001c0001t0004g0173 | 3 | HG01109.hp2 HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1836+4846_1836+484 others(137): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246652866 | |||||
| chr1:246652866
|
T | TGGTGGCG others(126): Show |
72 | a0001c0001t0001g0053a0001c0001t0001g0121a0001c0001t0001g0166others(69): Show | 72 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.1836+4846_1836+484 others(137): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246652866 | |||||
| chr1:246652866
|
T | TGGTGGCG others(259): Show |
6 | a0001c0001t0002g0097a0001c0001t0002g0101a0001c0001t0002g0102others(3): Show | 6 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.1836+4846_1836+484 others(270): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246652866 | |||||
| chr1:246652866
|
T | TGGTGGCG others(259): Show |
16 | a0001c0001t0001g0060a0001c0001t0001g0312a0001c0001t0002g0049others(13): Show | 16 | HG00423.hp1 HG01074.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.1836+4846_1836+484 others(270): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246652866 | |||||
| chr1:246652866
|
T | TGGTGGCG others(392): Show |
1 | a0001c0001t0002g0002 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1836+4846_1836+484 others(403): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246652866 | |||||
| chr1:246652866
|
T | TGGTGGCG others(259): Show |
1 | a0001c0001t0001g0308 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1836+4846_1836+484 others(270): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246652866 | |||||
| chr1:246652866
|
T | TGGTGGCG others(126): Show |
1 | a0001c0001t0005g0205 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1836+4846_1836+484 others(137): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246652866 | |||||
| chr1:246652866
|
T | TGGTGGCG others(126): Show |
1 | a0001c0001t0002g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1836+4854_1836+485 others(137): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246652866 | |||||
| chr1:246652873
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1836+4836G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652873 | ||||||
| chr1:246652874
|
G | GGCGCCTG others(126): Show |
1 | a0001c0001t0005g0155 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1836+4846_1836+484 others(137): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246652874 | |||||
| chr1:246652877
|
G | A | 2 | a0001c0001t0003g0316a0001c0001t0003g0317 | 2 | HG03017.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1836+4840G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652877 | ||||||
| chr1:246652884
|
G | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0246 | 2 | NA18950.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1836+4847G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652884 | ||||||
| chr1:246652928
|
T | C | 13 | a0001c0001t0001g0177a0001c0001t0003g0181a0001c0001t0004g0004others(10): Show | 13 | HG00735.hp1 HG02145.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.1836+4891T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652928 | ||||||
| chr1:246652940
|
C | G | 2 | a0002c0002t0015g0168a0007c0011t0015g0213 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1836+4903C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652940 | ||||||
| chr1:246652940
|
C | T | 10 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(7): Show | 10 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1836+4903C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652940 | ||||||
| chr1:246652958
|
T | C | 2 | a0001c0001t0002g0231a0001c0006t0001g0009 | 2 | HG02486.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1836+4921T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652958 | ||||||
| chr1:246652959
|
G | A | 1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1836+4922G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652959 | ||||||
| chr1:246652961
|
A | G | 1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1836+4924A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652961 | ||||||
| chr1:246652983
|
T | G | 1 | a0001c0001t0024g0269 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1836+4946T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652983 | ||||||
| chr1:246653003
|
CA | C | 11 | a0001c0006t0001g0009a0002c0002t0006g0030a0003c0003t0004g0034others(8): Show | 11 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1836+4981delA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246653003 | |||||
| chr1:246653015
|
AAAAG | A | 9 | a0001c0001t0001g0022a0001c0001t0001g0202a0001c0001t0001g0271others(6): Show | 9 | HG01261.hp1 HG02145.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1836+4983_1836+498 others(8): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246653015 | |||||
| chr1:246653041
|
A | G | 1 | a0009c0008t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1836+5004A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246653041 | ||||||
| chr1:246653363
|
C | T | 3 | a0001c0001t0003g0181a0001c0001t0004g0004a0001c0001t0004g0006 | 3 | HG02145.hp2 HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1836+5326C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246653363 | ||||||
| chr1:246653407
|
C | T | 1 | a0001c0001t0009g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1836+5370C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246653407 | ||||||
| chr1:246653583
|
G | A | 1 | a0006c0005t0023g0043 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1836+5546G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246653583 | ||||||
| chr1:246653704
|
C | T | 13 | a0001c0001t0001g0135a0001c0001t0004g0016a0001c0001t0004g0042others(10): Show | 13 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1836+5667C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246653704 | ||||||
| chr1:246653705
|
G | A | 206 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(203): Show | 208 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1836+5668G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246653705 | ||||||
| chr1:246653771
|
C | G | 26 | a0001c0001t0001g0135a0001c0001t0004g0016a0001c0001t0004g0042others(23): Show | 26 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.1836+5734C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246653771 | ||||||
| chr1:246653879
|
C | T | 1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1836+5842C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246653879 | ||||||
| chr1:246653907
|
A | G | 1 | a0010c0010t0002g0028 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1836+5870A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246653907 | ||||||
| chr1:246653949
|
C | T | 1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1836+5912C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246653949 | ||||||
| chr1:246653995
|
C | T | 1 | a0001c0001t0005g0205 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1836+5958C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246653995 | ||||||
| chr1:246654060
|
A | T | 2 | a0002c0002t0001g0122a0002c0002t0001g0151 | 2 | HG01175.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1836+6023A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654060 | ||||||
| chr1:246654086
|
C | T | 1 | a0001c0001t0013g0196 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1836+6049C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654086 | ||||||
| chr1:246654089
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0169 | 2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1836+6052C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654089 | ||||||
| chr1:246654150
|
C | T | 1 | a0001c0001t0002g0262 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1837-6049C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654150 | ||||||
| chr1:246654166
|
A | G | 62 | a0001c0001t0001g0061a0001c0001t0001g0086a0001c0001t0001g0087others(59): Show | 63 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(60): Show |
intron_variant | MODIFIER | c.1837-6033A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654166 | ||||||
| chr1:246654236
|
C | A | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1837-5963C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654236 | ||||||
| chr1:246654253
|
C | T | 7 | a0001c0001t0004g0016a0001c0001t0004g0042a0001c0001t0004g0150others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1837-5946C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654253 | ||||||
| chr1:246654415
|
G | C | 26 | a0001c0001t0001g0135a0001c0001t0004g0016a0001c0001t0004g0042others(23): Show | 26 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.1837-5784G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654415 | ||||||
| chr1:246654468
|
C | T | 6 | a0004c0004t0003g0119a0004c0004t0003g0184a0004c0004t0003g0185others(3): Show | 6 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1837-5731C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654468 | ||||||
| chr1:246654553
|
G | A | 1 | a0002c0002t0001g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1837-5646G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654553 | ||||||
| chr1:246654580
|
A | G | 1 | a0001c0001t0020g0024 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1837-5619A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654580 | ||||||
| chr1:246654793
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1837-5406G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654793 | ||||||
| chr1:246654823
|
GT | G | 266 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(263): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1837-5365delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246654823 | |||||
| chr1:246654942
|
A | T | 62 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0088others(59): Show | 62 | HG00140.hp1 HG00733.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.1837-5257A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654942 | ||||||
| chr1:246654947
|
C | T | 3 | a0001c0001t0003g0250a0002c0002t0001g0093a0002c0002t0001g0124 | 3 | HG04199.hp2 NA18747.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1837-5252C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654947 | ||||||
| chr1:246655086
|
A | G | 1 | a0001c0001t0003g0003 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1837-5113A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246655086 | ||||||
| chr1:246655332
|
A | G | 140 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(137): Show | 141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1837-4867A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246655332 | ||||||
| chr1:246655425
|
T | A | 1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1837-4774T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246655425 | ||||||
| chr1:246655707
|
A | C | 1 | a0001c0001t0003g0109 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1837-4492A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246655707 | ||||||
| chr1:246655853
|
G | A | 62 | a0001c0001t0001g0121a0001c0001t0001g0194a0001c0001t0001g0207others(59): Show | 62 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.1837-4346G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246655853 | ||||||
| chr1:246655857
|
T | A | 15 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0304others(12): Show | 15 | HG01257.hp2 HG01258.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1837-4342T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246655857 | ||||||
| chr1:246656114
|
G | A | 1 | a0001c0001t0002g0218 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1837-4085G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246656114 | ||||||
| chr1:246656166
|
A | G | 1 | a0001c0012t0002g0278 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1837-4033A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246656166 | ||||||
| chr1:246656233
|
AG | A | 45 | a0001c0001t0001g0025a0001c0001t0001g0135a0001c0001t0001g0177others(42): Show | 45 | HG00733.hp1 HG00735.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.1837-3965delG | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246656233 | ||||||
| chr1:246656265
|
A | T | 1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1837-3934A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246656265 | ||||||
| chr1:246656293
|
C | T | 27 | a0001c0001t0001g0135a0001c0001t0004g0016a0001c0001t0004g0042others(24): Show | 27 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.1837-3906C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246656293 | ||||||
| chr1:246656417
|
T | C | 4 | a0001c0001t0005g0023a0001c0001t0020g0024a0001c0006t0001g0009others(1): Show | 4 | HG02486.hp1 HG02486.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1837-3782T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246656417 | ||||||
| chr1:246656679
|
G | A | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1837-3520G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246656679 | ||||||
| chr1:246656801
|
G | C | 269 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(266): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1837-3398G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246656801 | ||||||
| chr1:246656838
|
G | T | 2 | a0001c0001t0003g0046a0001c0001t0003g0079 | 2 | NA18942.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1837-3361G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246656838 | ||||||
| chr1:246656852
|
C | T | 1 | a0001c0001t0017g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1837-3347C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246656852 | ||||||
| chr1:246656918
|
C | T | 1 | a0001c0001t0002g0258 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1837-3281C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246656918 | ||||||
| chr1:246656919
|
G | A | 24 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0169others(21): Show | 24 | HG00558.hp1 HG00621.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.1837-3280G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246656919 | ||||||
| chr1:246656943
|
A | G | 11 | a0001c0001t0001g0177a0001c0001t0004g0014a0001c0001t0004g0015others(8): Show | 11 | HG00735.hp1 HG00741.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1837-3256A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246656943 | ||||||
| chr1:246657139
|
T | C | 1 | a0001c0001t0001g0274 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1837-3060T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246657139 | ||||||
| chr1:246657208
|
C | T | 1 | a0001c0001t0002g0002 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1837-2991C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246657208 | ||||||
| chr1:246657209
|
G | A | 1 | a0002c0002t0001g0147 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1837-2990G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246657209 | ||||||
| chr1:246657236
|
C | T | 6 | a0004c0004t0003g0119a0004c0004t0003g0184a0004c0004t0003g0185others(3): Show | 6 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1837-2963C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246657236 | ||||||
| chr1:246657512
|
C | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0246 | 2 | NA18950.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1837-2687C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246657512 | ||||||
| chr1:246657555
|
A | C | 8 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(5): Show | 8 | HG00140.hp1 HG01515.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.1837-2644A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246657555 | ||||||
| chr1:246657730
|
G | A | 28 | a0001c0001t0004g0007a0001c0001t0004g0016a0001c0001t0004g0042others(25): Show | 28 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1837-2469G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246657730 | ||||||
| chr1:246657770
|
A | G | 2 | a0002c0002t0015g0168a0007c0011t0015g0213 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1837-2429A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246657770 | ||||||
| chr1:246657807
|
A | G | 24 | a0001c0001t0001g0011a0001c0001t0001g0059a0001c0001t0001g0167others(21): Show | 24 | HG00558.hp1 HG00621.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.1837-2392A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246657807 | ||||||
| chr1:246658099
|
T | A | 1 | a0008c0007t0003g0267 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1837-2100T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246658099 | ||||||
| chr1:246658204
|
T | C | 8 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0038others(5): Show | 8 | HG00733.hp1 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1837-1995T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246658204 | ||||||
| chr1:246658273
|
CCT | C | 25 | a0001c0001t0001g0011a0001c0001t0001g0059a0001c0001t0001g0167others(22): Show | 25 | HG00558.hp1 HG00621.hp2 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.1837-1922_1837-192 others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246658273 | |||||
| chr1:246658297
|
A | G | 90 | a0001c0001t0001g0025a0001c0001t0001g0135a0001c0001t0001g0290others(87): Show | 91 | HG00423.hp2 HG00733.hp1 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.1837-1902A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246658297 | ||||||
| chr1:246658465
|
CTTGTTGA others(3): Show |
C | 1 | a0006c0005t0023g0043 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1837-1731_1837-172 others(14): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246658465 | |||||
| chr1:246658472
|
A | AT | 21 | a0001c0001t0001g0025a0001c0001t0001g0059a0001c0001t0001g0060others(18): Show | 21 | HG01175.hp2 HG01978.hp2 HG02293.hp1 others(18): Show |
intron_variant | MODIFIER | c.1837-1717dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246658472 | |||||
| chr1:246658558
|
C | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0290 | 2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1837-1641C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246658558 | ||||||
| chr1:246658582
|
C | T | 1 | a0001c0001t0002g0310 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1837-1617C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246658582 | ||||||
| chr1:246658614
|
C | T | 1 | a0001c0001t0003g0220 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1837-1585C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246658614 | ||||||
| chr1:246658670
|
A | G | 1 | a0001c0001t0016g0136 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1837-1529A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246658670 | ||||||
| chr1:246658687
|
C | A | 1 | a0001c0001t0002g0083 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1837-1512C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246658687 | ||||||
| chr1:246658709
|
GGCCAGCA others(10): Show |
G | 7 | a0003c0003t0001g0037a0004c0004t0003g0119a0004c0004t0003g0184others(4): Show | 7 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1837-1474_1837-145 others(21): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246658709 | |||||
| chr1:246658721
|
ACTGATGC others(15): Show |
A | 54 | a0001c0001t0001g0170a0001c0001t0001g0304a0001c0001t0002g0183others(51): Show | 55 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.1837-1457_1837-143 others(26): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246658721 | |||||
| chr1:246658912
|
C | T | 1 | a0006c0005t0023g0043 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1837-1287C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246658912 | ||||||
| chr1:246658976
|
G | T | 7 | a0003c0003t0001g0037a0004c0004t0003g0119a0004c0004t0003g0184others(4): Show | 7 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1837-1223G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246658976 | ||||||
| chr1:246659004
|
TAGGC | T | 8 | a0001c0001t0001g0025a0001c0001t0001g0135a0001c0001t0004g0026others(5): Show | 8 | HG02486.hp1 HG02486.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1837-1191_1837-118 others(8): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246659004 | |||||
| chr1:246659151
|
G | A | 1 | a0003c0003t0001g0039 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1837-1048G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659151 | ||||||
| chr1:246659184
|
C | T | 1 | a0001c0012t0002g0278 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1837-1015C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659184 | ||||||
| chr1:246659203
|
G | A | 4 | a0001c0001t0003g0137a0001c0001t0003g0226a0001c0001t0003g0227others(1): Show | 4 | NA18985.hp2 NA18999.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1837-996G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659203 | ||||||
| chr1:246659247
|
G | C | 1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1837-952G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659247 | ||||||
| chr1:246659251
|
T | G | 1 | a0001c0001t0003g0294 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1837-948T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659251 | ||||||
| chr1:246659319
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1837-880G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659319 | ||||||
| chr1:246659320
|
T | C | 106 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0060others(103): Show | 107 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1837-879T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659320 | ||||||
| chr1:246659321
|
G | A | 3 | a0001c0001t0010g0229a0001c0001t0010g0230a0001c0001t0010g0286 | 3 | HG00558.hp2 HG02080.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1837-878G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659321 | ||||||
| chr1:246659322
|
C | T | 1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1837-877C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659322 | ||||||
| chr1:246659323
|
G | C | 3 | a0001c0001t0010g0229a0001c0001t0010g0230a0001c0001t0010g0286 | 3 | HG00558.hp2 HG02080.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1837-876G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659323 | ||||||
| chr1:246659333
|
A | G | 29 | a0001c0001t0003g0054a0001c0001t0003g0073a0001c0001t0003g0074others(26): Show | 29 | HG00733.hp1 HG00741.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.1837-866A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659333 | ||||||
| chr1:246659361
|
A | G | 20 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0016others(17): Show | 20 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1837-838A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659361 | ||||||
| chr1:246659365
|
C | A | 1 | a0002c0002t0001g0110 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1837-834C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659365 | ||||||
| chr1:246659369
|
C | T | 1 | a0002c0002t0001g0110 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1837-830C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659369 | ||||||
| chr1:246659370
|
A | G | 2 | a0001c0006t0001g0009a0002c0002t0001g0110 | 2 | HG02129.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1837-829A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659370 | ||||||
| chr1:246659376
|
C | T | 13 | a0001c0001t0001g0025a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG00140.hp1 HG01515.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.1837-823C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659376 | ||||||
| chr1:246659377
|
G | T | 14 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0016others(11): Show | 14 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1837-822G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659377 | ||||||
| chr1:246659390
|
C | G | 33 | a0001c0001t0001g0025a0001c0001t0001g0088a0001c0001t0001g0089others(30): Show | 33 | HG00140.hp1 HG00733.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.1837-809C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659390 | ||||||
| chr1:246659403
|
G | A | 2 | a0001c0001t0001g0060a0009c0008t0001g0161 | 2 | HG01978.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1837-796G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659403 | ||||||
| chr1:246659405
|
T | A | 24 | a0001c0001t0001g0011a0001c0001t0001g0088a0001c0001t0001g0089others(21): Show | 24 | HG00140.hp1 HG00558.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.1837-794T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659405 | ||||||
| chr1:246659405
|
T | C | 59 | a0001c0001t0001g0170a0001c0001t0001g0198a0001c0001t0001g0304others(56): Show | 60 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.1837-794T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659405 | ||||||
| chr1:246659409
|
T | A | 136 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0053others(133): Show | 136 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1837-790T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659409 | ||||||
| chr1:246659411
|
G | A | 17 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0169others(14): Show | 17 | HG00558.hp1 HG00621.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.1837-788G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659411 | ||||||
| chr1:246659421
|
C | T | 210 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(207): Show | 211 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.1837-778C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659421 | ||||||
| chr1:246659431
|
G | A | 4 | a0001c0001t0001g0219a0001c0001t0001g0299a0001c0001t0002g0195others(1): Show | 4 | HG02300.hp1 NA18951.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1837-768G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659431 | ||||||
| chr1:246659438
|
C | G | 2 | a0001c0001t0001g0219a0001c0001t0001g0299 | 2 | NA18951.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1837-761C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659438 | ||||||
| chr1:246659464
|
G | A | 4 | a0002c0002t0006g0030a0003c0003t0004g0034a0003c0003t0004g0035others(1): Show | 4 | HG01243.hp1 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1837-735G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659464 | ||||||
| chr1:246659467
|
T | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1837-732T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659467 | ||||||
| chr1:246659467
|
T | C | 1 | a0001c0001t0004g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1837-732T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659467 | ||||||
| chr1:246659527
|
G | A | 1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1837-672G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659527 | ||||||
| chr1:246659531
|
A | G | 1 | a0001c0006t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1837-668A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659531 | ||||||
| chr1:246659573
|
C | T | 1 | a0001c0001t0024g0269 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1837-626C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659573 | ||||||
| chr1:246659579
|
A | G | 1 | a0001c0001t0024g0269 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1837-620A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659579 | ||||||
| chr1:246659582
|
A | G | 61 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0059others(58): Show | 61 | HG00558.hp1 HG00621.hp2 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.1837-617A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659582 | ||||||
| chr1:246659589
|
T | C | 2 | a0001c0001t0001g0167a0001c0001t0001g0169 | 2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1837-610T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659589 | ||||||
| chr1:246659594
|
C | CA | 9 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(6): Show | 9 | HG00140.hp1 HG01515.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1837-591dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246659594 | |||||
| chr1:246659594
|
CA | C | 23 | a0001c0001t0001g0060a0001c0001t0001g0156a0001c0001t0001g0291others(20): Show | 23 | HG01175.hp2 HG01243.hp1 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.1837-591delA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246659594 | |||||
| chr1:246660011
|
G | A | 44 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0059others(41): Show | 44 | HG00558.hp1 HG00621.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.1837-188G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246660011 | ||||||
| chr1:246660445
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1972+111G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246660445 | ||||||
| chr1:246660447
|
C | G | 1 | a0004c0004t0021g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1972+113C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246660447 | ||||||
| chr1:246660496
|
C | T | 1 | a0006c0005t0023g0043 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1972+162C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246660496 | ||||||
| chr1:246660555
|
G | A | 94 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0059others(91): Show | 95 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.1972+221G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246660555 | ||||||
| chr1:246660632
|
G | A | 1 | a0001c0001t0003g0144 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1972+298G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246660632 | ||||||
| chr1:246660676
|
G | T | 30 | a0001c0001t0001g0060a0001c0001t0001g0156a0001c0001t0001g0291others(27): Show | 30 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.1972+342G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246660676 | ||||||
| chr1:246660783
|
A | C | 1 | a0004c0004t0021g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1972+449A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246660783 | ||||||
| chr1:246661021
|
T | G | 135 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0059others(132): Show | 136 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(133): Show |
intron_variant | MODIFIER | c.1972+687T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246661021 | ||||||
| chr1:246661319
|
T | C | 8 | a0002c0002t0001g0027a0003c0003t0001g0032a0003c0003t0001g0033others(5): Show | 8 | HG00733.hp1 HG00741.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1972+985T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246661319 | ||||||
| chr1:246661442
|
A | G | 1 | a0001c0001t0002g0077 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1972+1108A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246661442 | ||||||
| chr1:246661538
|
T | A | 300 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(297): Show | 301 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.1972+1204T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246661538 | ||||||
| chr1:246661618
|
A | G | 1 | a0001c0001t0002g0129 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1972+1284A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246661618 | ||||||
| chr1:246661752
|
T | TA | 4 | a0001c0001t0004g0157a0001c0001t0004g0158a0001c0001t0004g0159others(1): Show | 4 | HG01109.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1972+1422dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 246661752 | |||||
| chr1:246661888
|
C | G | 10 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0017others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1972+1554C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246661888 | ||||||
| chr1:246662031
|
C | T | 1 | a0006c0005t0023g0043 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1972+1697C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246662031 | ||||||
| chr1:246662118
|
A | G | 31 | a0001c0001t0001g0060a0001c0001t0001g0156a0001c0001t0001g0177others(28): Show | 31 | HG00735.hp1 HG01109.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.1972+1784A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246662118 | ||||||
| chr1:246662177
|
G | T | 3 | a0001c0001t0002g0172a0001c0001t0002g0175a0001c0001t0002g0183 | 3 | HG01891.hp1 HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1972+1843G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246662177 | ||||||
| chr1:246662540
|
C | G | 1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1972+2206C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246662540 | ||||||
| chr1:246662543
|
G | C | 128 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0059others(125): Show | 129 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(126): Show |
intron_variant | MODIFIER | c.1972+2209G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246662543 | ||||||
| chr1:246662545
|
C | T | 2 | a0001c0001t0003g0222a0006c0005t0023g0043 | 2 | HG03209.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1972+2211C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246662545 | ||||||
| chr1:246662681
|
G | A | 10 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0017others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1972+2347G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246662681 | ||||||
| chr1:246662877
|
C | T | 75 | a0001c0001t0001g0059a0001c0001t0001g0076a0001c0001t0001g0167others(72): Show | 76 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.1972+2543C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246662877 | ||||||
| chr1:246663109
|
T | G | 11 | a0001c0001t0004g0026a0001c0001t0004g0157a0001c0001t0004g0158others(8): Show | 11 | HG01109.hp2 HG01243.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1973-2591T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246663109 | ||||||
| chr1:246663111
|
C | T | 7 | a0003c0003t0001g0037a0004c0004t0003g0119a0004c0004t0003g0184others(4): Show | 7 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1973-2589C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246663111 | ||||||
| chr1:246663213
|
G | A | 12 | a0001c0001t0004g0007a0001c0001t0004g0016a0001c0001t0004g0042others(9): Show | 12 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1973-2487G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246663213 | ||||||
| chr1:246663234
|
T | G | 316 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(313): Show | 317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.1973-2466T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246663234 | ||||||
| chr1:246663270
|
T | C | 8 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0017others(5): Show | 8 | HG02647.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1973-2430T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246663270 | ||||||
| chr1:246663271
|
C | T | 4 | a0001c0001t0007g0062a0002c0002t0001g0141a0002c0002t0007g0142others(1): Show | 4 | HG02083.hp1 NA18612.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.1973-2429C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246663271 | ||||||
| chr1:246663272
|
G | A | 7 | a0003c0003t0001g0037a0004c0004t0003g0119a0004c0004t0003g0184others(4): Show | 7 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1973-2428G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246663272 | ||||||
| chr1:246663336
|
T | TA | 14 | a0001c0001t0004g0007a0001c0001t0004g0016a0001c0001t0004g0042others(11): Show | 14 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1973-2348dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 246663336 | |||||
| chr1:246663336
|
T | TAA | 7 | a0001c0001t0003g0082a0001c0001t0004g0026a0002c0002t0006g0030others(4): Show | 7 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1973-2349_1973-234 others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 246663336 | |||||
| chr1:246663365
|
C | T | 244 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(241): Show | 245 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.1973-2335C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246663365 | ||||||
| chr1:246663368
|
A | G | 3 | a0001c0001t0001g0217a0001c0001t0001g0254a0001c0001t0001g0301 | 3 | HG02015.hp2 NA18969.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1973-2332A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246663368 | ||||||
| chr1:246663740
|
C | CA | 11 | a0001c0001t0002g0310a0002c0002t0001g0122a0002c0002t0001g0151others(8): Show | 11 | HG01175.hp2 HG02451.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1973-1949dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 246663740 | |||||
| chr1:246663749
|
A | C | 1 | a0001c0001t0002g0049 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1973-1951A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246663749 | ||||||
| chr1:246663900
|
G | A | 135 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0059others(132): Show | 136 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(133): Show |
intron_variant | MODIFIER | c.1973-1800G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246663900 | ||||||
| chr1:246663929
|
T | C | 2 | a0001c0001t0002g0262a0001c0001t0002g0284 | 2 | HG02698.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1973-1771T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246663929 | ||||||
| chr1:246663937
|
T | C | 22 | a0001c0001t0004g0007a0001c0001t0004g0016a0001c0001t0004g0026others(19): Show | 22 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.1973-1763T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246663937 | ||||||
| chr1:246664254
|
A | G | 3 | a0002c0002t0001g0122a0002c0002t0001g0133a0002c0002t0001g0151 | 3 | HG01175.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1973-1446A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664254 | ||||||
| chr1:246664350
|
T | G | 2 | a0001c0001t0001g0253a0001c0001t0001g0309 | 2 | HG00408.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1973-1350T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664350 | ||||||
| chr1:246664375
|
G | A | 4 | a0001c0001t0004g0157a0001c0001t0004g0158a0001c0001t0004g0159others(1): Show | 4 | HG01109.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1973-1325G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664375 | ||||||
| chr1:246664431
|
C | CTT | 14 | a0001c0001t0001g0060a0001c0001t0001g0088a0001c0001t0001g0089others(11): Show | 14 | HG00140.hp1 HG01175.hp2 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.1973-1257_1973-125 others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 246664431 | |||||
| chr1:246664449
|
A | T | 1 | a0001c0001t0001g0303 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1973-1251A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664449 | ||||||
| chr1:246664496
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1973-1204A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664496 | ||||||
| chr1:246664503
|
T | G | 1 | a0001c0001t0001g0272 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1973-1197T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664503 | ||||||
| chr1:246664512
|
C | T | 1 | a0001c0001t0022g0085 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1973-1188C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664512 | ||||||
| chr1:246664527
|
T | C | 37 | a0001c0001t0001g0060a0001c0001t0001g0088a0001c0001t0001g0089others(34): Show | 37 | HG00140.hp1 HG01109.hp2 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.1973-1173T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664527 | ||||||
| chr1:246664551
|
T | C | 1 | a0001c0001t0003g0294 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1973-1149T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664551 | ||||||
| chr1:246664581
|
C | T | 1 | a0001c0001t0019g0106 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1973-1119C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664581 | ||||||
| chr1:246664583
|
C | T | 3 | a0001c0001t0009g0010a0001c0001t0009g0012a0001c0001t0009g0013 | 3 | HG02976.hp1 HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1973-1117C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664583 | ||||||
| chr1:246664600
|
A | G | 75 | a0001c0001t0001g0025a0001c0001t0001g0135a0001c0001t0001g0237others(72): Show | 76 | HG00738.hp2 HG00741.hp2 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.1973-1100A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664600 | ||||||
| chr1:246664616
|
C | T | 7 | a0001c0001t0001g0059a0001c0001t0001g0215a0001c0001t0001g0236others(4): Show | 7 | HG01109.hp1 HG01175.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1973-1084C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664616 | ||||||
| chr1:246664617
|
G | A | 33 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(30): Show | 33 | HG00140.hp1 HG00733.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1973-1083G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664617 | ||||||
| chr1:246664619
|
G | A | 6 | a0001c0001t0001g0059a0001c0001t0001g0215a0001c0001t0001g0236others(3): Show | 6 | HG01109.hp1 HG01175.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1973-1081G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664619 | ||||||
| chr1:246664628
|
G | A | 1 | a0002c0002t0007g0143 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1973-1072G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664628 | ||||||
| chr1:246664628
|
G | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0290 | 2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1973-1072G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664628 | ||||||
| chr1:246664632
|
C | T | 234 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(231): Show | 235 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.1973-1068C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664632 | ||||||
| chr1:246664633
|
A | G | 1 | a0002c0002t0007g0143 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1973-1067A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664633 | ||||||
| chr1:246664637
|
A | G | 17 | a0001c0001t0001g0025a0001c0001t0001g0088a0001c0001t0001g0089others(14): Show | 17 | HG00140.hp1 HG01175.hp2 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.1973-1063A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664637 | ||||||
| chr1:246664640
|
A | C | 1 | a0001c0001t0001g0274 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1973-1060A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664640 | ||||||
| chr1:246664643
|
G | A | 4 | a0001c0001t0003g0054a0001c0001t0003g0073a0001c0001t0003g0075others(1): Show | 4 | HG02071.hp1 HG02135.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.1973-1057G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664643 | ||||||
| chr1:246664647
|
C | G | 3 | a0001c0001t0001g0076a0001c0001t0001g0240a0001c0001t0001g0283 | 3 | HG01934.hp2 NA18945.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1973-1053C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664647 | ||||||
| chr1:246664647
|
C | T | 1 | a0001c0001t0003g0084 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1973-1053C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664647 | ||||||
| chr1:246664648
|
G | C | 26 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0305others(23): Show | 26 | HG00738.hp2 HG01109.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.1973-1052G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664648 | ||||||
| chr1:246664661
|
C | T | 62 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0088others(59): Show | 62 | HG00140.hp1 HG00733.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.1973-1039C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664661 | ||||||
| chr1:246664662
|
G | A | 1 | a0001c0001t0003g0084 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1973-1038G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664662 | ||||||
| chr1:246664669
|
G | A | 1 | a0001c0001t0003g0282 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1973-1031G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664669 | ||||||
| chr1:246664672
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0289a0001c0001t0001g0300 | 3 | HG02145.hp1 HG02258.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.1973-1028C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664672 | ||||||
| chr1:246664673
|
G | A | 3 | a0001c0001t0001g0307a0001c0001t0003g0084a0001c0001t0022g0085 | 3 | HG03239.hp2 HG04228.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1973-1027G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664673 | ||||||
| chr1:246664677
|
C | T | 164 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0052others(161): Show | 165 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1973-1023C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664677 | ||||||
| chr1:246664678
|
A | G | 234 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0025others(231): Show | 235 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.1973-1022A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664678 | ||||||
| chr1:246664716
|
A | G | 6 | a0001c0001t0001g0156a0001c0001t0001g0236a0001c0001t0001g0291others(3): Show | 6 | HG01255.hp1 HG01952.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1973-984A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664716 | ||||||
| chr1:246664718
|
A | G | 14 | a0001c0001t0001g0011a0001c0001t0001g0156a0001c0001t0001g0291others(11): Show | 14 | HG00733.hp1 HG00741.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.1973-982A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664718 | ||||||
| chr1:246664722
|
A | G | 3 | a0001c0001t0001g0156a0001c0001t0001g0291a0001c0001t0003g0065 | 3 | HG01255.hp1 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1973-978A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664722 | ||||||
| chr1:246664887
|
T | A | 2 | a0001c0001t0001g0271a0010c0010t0002g0028 | 2 | HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1973-813T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664887 | ||||||
| chr1:246664888
|
A | T | 2 | a0001c0001t0003g0047a0001c0001t0003g0048 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1973-812A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664888 | ||||||
| chr1:246664991
|
T | C | 14 | a0001c0001t0001g0060a0001c0001t0001g0088a0001c0001t0001g0089others(11): Show | 14 | HG00140.hp1 HG01175.hp2 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.1973-709T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664991 | ||||||
| chr1:246665087
|
G | A | 31 | a0001c0001t0004g0007a0001c0001t0004g0016a0001c0001t0004g0026others(28): Show | 31 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1973-613G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246665087 | ||||||
| chr1:246665105
|
C | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0169 | 2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1973-595C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246665105 | ||||||
| chr1:246665135
|
C | T | 3 | a0001c0001t0001g0296a0002c0002t0001g0112a0002c0002t0001g0149 | 3 | HG00621.hp1 NA18946.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.1973-565C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246665135 | ||||||
| chr1:246665246
|
G | GC | 14 | a0001c0001t0001g0060a0001c0001t0001g0088a0001c0001t0001g0089others(11): Show | 14 | HG00140.hp1 HG01175.hp2 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.1973-452dupC | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 246665246 | |||||
| chr1:246665396
|
A | T | 1 | a0002c0002t0001g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1973-304A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246665396 | ||||||
| chr1:246665588
|
C | T | 1 | a0001c0001t0002g0049 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1973-112C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246665588 | ||||||
| chr1:246665670
|
A | G | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1973-30A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246665670 |