Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 3781 |
|---|---|
| ensemblid | ENSG00000080709.17 |
| hgncid | 6291 |
| symbol | KCNN2 |
| name | potassium calcium-activated channel subfamily N member 2 |
| refseq_nuc | NM_021614.4 |
| refseq_prot | NP_067627.3 |
| ensembl_nuc | ENST00000673685.1 |
| ensembl_prot | ENSP00000501239.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 114362070 |
| end | 114496496 |
| strand | + |
| ver | v1.2 |
| region | chr5:114362070-114496496 |
| region5000 | chr5:114357070-114501496 |
| regionname0 | KCNN2_chr5_114362070_114496496 |
| regionname5000 | KCNN2_chr5_114357070_114501496 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 791 | 114 | 43 | 29 | 15 | 11 | 15 | 13 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0002 | 0/1 | 792 | 108 | 21 | 25 | 42 | 3 | 16 | 32 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0003 | 0/0 | 791 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0004 | 0/0 | 793 | 5 | 3 | 2 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0005 | 0/0 | 792 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0006 | 0/0 | 792 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0007 | 0/0 | 791 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0008 | 0/0 | 792 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0009 | 0/0 | 792 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0010 | 0/0 | 791 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0011 | 0/0 | 792 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 2376 | 105 | 37 | 28 | 14 | 10 | 15 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| c0002 | 0/1 | 2379 | 100 | 16 | 23 | 41 | 3 | 16 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| c0003 | 0/0 | 2376 | 6 | 6 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| c0004 | 0/0 | 2379 | 5 | 5 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| c0005 | 0/0 | 2379 | 4 | 3 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| c0006 | 0/0 | 2376 | 4 | 4 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| c0007 | 0/0 | 2379 | 4 | 4 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| c0008 | 0/0 | 2382 | 3 | 3 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| c0009 | 0/0 | 2376 | 2 | 2 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| c0010 | 0/0 | 2376 | 2 | 2 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| c0011 | 0/0 | 2379 | 2 | 1 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| c0012 | 0/0 | 2382 | 2 | 0 | 2 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| c0013 | 0/0 | 2379 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| c0014 | 0/0 | 2379 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| c0015 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| c0016 | 0/0 | 2379 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| c0017 | 0/0 | 2379 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| c0018 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| c0019 | 0/0 | 2376 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| c0020 | 0/0 | 2376 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| c0021 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| c0022 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| c0023 | 0/0 | 2379 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 385 | 248 | 88 | 56 | 57 | 14 | 31 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| t0002 | 0/0 | 385 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| t0003 | 0/0 | 385 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| 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 | 0 | 0 | 0 | 2 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0077 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0113 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2376 | 105 | 37 | 28 | 14 | 10 | 15 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0001c0006 | 0/0 | 2376 | 4 | 4 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0001c0015 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0001c0018 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0001c0019 | 0/0 | 2376 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0001c0020 | 0/0 | 2376 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0001c0021 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0002c0002 | 0/1 | 2379 | 100 | 16 | 23 | 41 | 3 | 16 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0002c0005 | 0/0 | 2379 | 4 | 3 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0002c0011 | 0/0 | 2379 | 2 | 1 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0002c0014 | 0/0 | 2379 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0002c0017 | 0/0 | 2379 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0003c0003 | 0/0 | 2376 | 6 | 6 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0003c0009 | 0/0 | 2376 | 2 | 2 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0004c0008 | 0/0 | 2382 | 3 | 3 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0004c0012 | 0/0 | 2382 | 2 | 0 | 2 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0005c0004 | 0/0 | 2379 | 5 | 5 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0006c0007 | 0/0 | 2379 | 4 | 4 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0007c0010 | 0/0 | 2376 | 2 | 2 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0008c0013 | 0/0 | 2379 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0009c0023 | 0/0 | 2379 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0010c0022 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0011c0016 | 0/0 | 2379 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2760 | 104 | 37 | 28 | 14 | 10 | 14 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0001c0001t0002 | 0/0 | 2760 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0001c0006t0001 | 0/0 | 2760 | 4 | 4 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0001c0015t0001 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0001c0018t0001 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0001c0019t0001 | 0/0 | 2760 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0001c0020t0001 | 0/0 | 2760 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0001c0021t0001 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0002c0002t0001 | 0/1 | 2763 | 100 | 16 | 23 | 41 | 3 | 16 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0002c0005t0001 | 0/0 | 2763 | 4 | 3 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0002c0011t0001 | 0/0 | 2763 | 2 | 1 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0002c0014t0001 | 0/0 | 2763 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0002c0017t0001 | 0/0 | 2763 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0003c0003t0001 | 0/0 | 2760 | 6 | 6 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0003c0009t0001 | 0/0 | 2760 | 2 | 2 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0004c0008t0001 | 0/0 | 2766 | 3 | 3 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0004c0012t0001 | 0/0 | 2766 | 2 | 0 | 2 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0005c0004t0001 | 0/0 | 2763 | 5 | 5 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0006c0007t0001 | 0/0 | 2763 | 4 | 4 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0007c0010t0001 | 0/0 | 2760 | 2 | 2 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0008c0013t0001 | 0/0 | 2763 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0009c0023t0001 | 0/0 | 2763 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0010c0022t0001 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| a0011c0016t0003 | 0/0 | 2763 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | copy fasta | chr5 | 114357070 | 114501496 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0077 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0006t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0006t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0006t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0006t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0015t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0018t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0019t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0020t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0021t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0113 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0005t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0005t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0005t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0005t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0011t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0011t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0014t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0017t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0003c0003t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0003c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0003c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0003c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0003c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0003c0003t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0003c0009t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0003c0009t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0004c0008t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0004c0008t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0004c0008t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0004c0012t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0004c0012t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0005c0004t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0005c0004t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0005c0004t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0005c0004t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0005c0004t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0006c0007t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0006c0007t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0006c0007t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0006c0007t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0007c0010t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0007c0010t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0008c0013t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0009c0023t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0010c0022t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0011c0016t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0208 | EUR | GBR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0141 | EUR | GBR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0235 | EUR | FIN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0206 | EUR | FIN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0242 | EAS | CHS | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0175 | EAS | CHS | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | CHS | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | CHS | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0139 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0114 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0138 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0186 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01070 | hp1 | a0004 | c0012 | t0001 | g0143 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0123 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0140 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0122 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0167 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0132 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0173 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0224 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01243 | hp1 | a0002 | c0011 | t0001 | g0241 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01243 | hp2 | a0002 | c0005 | t0001 | g0014 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0202 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01256 | hp2 | a0004 | c0012 | t0001 | g0142 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0203 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01261 | hp1 | a0001 | c0019 | t0001 | g0234 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0117 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0133 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0181 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0231 | EUR | IBS | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | IBS | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01516 | hp2 | a0001 | c0020 | t0001 | g0232 | EUR | IBS | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | IBS | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | IBS | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0225 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0156 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0111 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02040 | hp1 | a0001 | c0018 | t0001 | g0029 | EAS | KHV | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0166 | EAS | KHV | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02055 | hp1 | a0001 | c0006 | t0001 | g0095 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0209 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | KHV | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | KHV | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | KHV | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02145 | hp2 | a0001 | c0006 | t0001 | g0098 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0226 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0135 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0171 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0210 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0159 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0152 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02451 | hp1 | a0002 | c0011 | t0001 | g0239 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02451 | hp2 | a0002 | c0005 | t0001 | g0013 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | KHV | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | KHV | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02572 | hp1 | a0002 | c0014 | t0001 | g0017 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0118 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0201 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02622 | hp1 | a0006 | c0007 | t0001 | g0104 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02630 | hp1 | a0001 | c0021 | t0001 | g0220 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0207 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0238 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0130 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02809 | hp1 | a0003 | c0009 | t0001 | g0194 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02818 | hp1 | a0005 | c0004 | t0001 | g0149 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02886 | hp2 | a0008 | c0013 | t0001 | g0237 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02895 | hp1 | a0007 | c0010 | t0001 | g0191 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02895 | hp2 | a0001 | c0006 | t0001 | g0097 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02896 | hp1 | a0004 | c0008 | t0001 | g0012 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0127 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02897 | hp1 | a0007 | c0010 | t0001 | g0192 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02897 | hp2 | a0004 | c0008 | t0001 | g0011 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02922 | hp2 | a0003 | c0003 | t0001 | g0200 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02965 | hp2 | a0001 | c0015 | t0001 | g0219 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0236 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02976 | hp2 | a0002 | c0005 | t0001 | g0016 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0103 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0131 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03098 | hp1 | a0002 | c0005 | t0001 | g0015 | AFR | MSL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03098 | hp2 | a0006 | c0007 | t0001 | g0221 | AFR | MSL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0102 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03130 | hp2 | a0003 | c0003 | t0001 | g0197 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03139 | hp1 | a0010 | c0022 | t0001 | g0072 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0205 | AFR | MSL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03209 | hp2 | a0003 | c0003 | t0001 | g0198 | AFR | MSL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03225 | hp2 | a0005 | c0004 | t0001 | g0148 | AFR | MSL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | MSL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03486 | hp1 | a0003 | c0003 | t0001 | g0199 | AFR | MSL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0134 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0240 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | MSL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0204 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0110 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0112 | SAS | STU | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03704 | hp2 | a0009 | c0023 | t0001 | g0160 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0120 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0180 | SAS | BEB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0170 | SAS | BEB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | BEB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0119 | SAS | STU | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | STU | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0115 | SAS | STU | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0162 | SAS | STU | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | STU | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | STU | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0128 | SAS | STU | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | STU | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18522 | hp1 | a0006 | c0007 | t0001 | g0223 | AFR | YRI | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18522 | hp2 | a0003 | c0009 | t0001 | g0195 | AFR | YRI | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18906 | hp1 | a0001 | c0006 | t0001 | g0093 | AFR | YRI | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | YRI | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18999 | hp1 | a0002 | c0017 | t0001 | g0178 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | LWK | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | LWK | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19043 | hp2 | a0003 | c0003 | t0001 | g0196 | AFR | LWK | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19077 | hp2 | a0011 | c0016 | t0003 | g0177 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | YRI | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19240 | hp2 | a0005 | c0004 | t0001 | g0176 | AFR | YRI | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA20129 | hp1 | a0004 | c0008 | t0001 | g0010 | AFR | ASW | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA20129 | hp2 | a0003 | c0003 | t0001 | g0193 | AFR | ASW | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0229 | EUR | TSI | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | TSI | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | TSI | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0228 | EUR | TSI | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0137 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02486 | hp2 | a0005 | c0004 | t0001 | g0147 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02559 | hp2 | a0005 | c0004 | t0001 | g0146 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG06807 | hp1 | a0006 | c0007 | t0001 | g0222 | AFR | USA | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | USA | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | USA | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0116 | AFR | USA | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0113 | REF | REF | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0077 | REF | REF | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:114362339
|
T | A | 1 | a0008 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.200T>A | p.Leu67His | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/8 | 270/2760 | 200/2376 | 67/791 | chr5 | 114362339 | ||
| chr5:114362471
|
C | CCTG | 1 | a0004 | 5 | HG01070.hp1 HG01256.hp2 HG02896.hp1 others(2): Show |
disruptive_inframe_insertion | MODERATE | c.350_352dupGCT | p.Cys117dup | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/8 | 423/2760 | 353/2376 | 118/791 | INFO_REALIGN_3_PRIME | chr5 | 114362471 | |
| chr5:114362474
|
G | C | 1 | a0005 | 5 | HG02486.hp2 HG02559.hp2 HG02818.hp1 others(2): Show |
missense_variant | MODERATE | c.335G>C | p.Cys112Ser | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/8 | 405/2760 | 335/2376 | 112/791 | chr5 | 114362474 | ||
| chr5:114362567
|
A | C | 1 | a0009 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.428A>C | p.Tyr143Ser | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/8 | 498/2760 | 428/2376 | 143/791 | chr5 | 114362567 | ||
| chr5:114362625
|
C | G | 1 | a0010 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.486C>G | p.Ser162Arg | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/8 | 556/2760 | 486/2376 | 162/791 | chr5 | 114362625 | ||
| chr5:114362675
|
G | C | 2 | a0003a0007 | 10 | HG02809.hp1 HG02895.hp1 HG02897.hp1 others(7): Show |
missense_variant | MODERATE | c.536G>C | p.Gly179Ala | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/8 | 606/2760 | 536/2376 | 179/791 | chr5 | 114362675 | ||
| chr5:114362677
|
C | G | 1 | a0006 | 4 | HG02622.hp1 HG03098.hp2 HG06807.hp1 others(1): Show |
missense_variant | MODERATE | c.538C>G | p.Pro180Ala | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/8 | 608/2760 | 538/2376 | 180/791 | chr5 | 114362677 | ||
| chr5:114362704
|
C | T | 1 | a0007 | 2 | HG02895.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.565C>T | p.Pro189Ser | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/8 | 635/2760 | 565/2376 | 189/791 | chr5 | 114362704 | ||
| chr5:114362934
|
T | TGCC | 7 | a0002a0004a0005others(4): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
disruptive_inframe_insertion | MODERATE | c.807_809dupCGC | p.Ala270dup | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/8 | 880/2760 | 810/2376 | 270/791 | INFO_REALIGN_3_PRIME | chr5 | 114362934 | |
| chr5:114495971
|
T | A | 1 | a0011 | 1 | NA19077.hp2 | missense_variant | MODERATE | c.2165T>A | p.Leu722Gln | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 8/8 | 2235/2760 | 2165/2376 | 722/791 | chr5 | 114495971 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:114362439
|
G | A | 4 | a0001c0015a0002c0005a0002c0014others(1): Show | 9 | HG01243.hp2 HG02451.hp2 HG02572.hp1 others(6): Show |
synonymous_variant | LOW | c.300G>A | p.Arg100Arg | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/8 | 370/2760 | 300/2376 | 100/791 | chr5 | 114362439 | ||
| chr5:114362847
|
G | C | 12 | a0002c0002a0002c0005a0002c0011others(9): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
synonymous_variant | LOW | c.708G>C | p.Leu236Leu | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/8 | 778/2760 | 708/2376 | 236/791 | chr5 | 114362847 | ||
| chr5:114362964
|
C | G | 1 | a0001c0021 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.825C>G | p.Ala275Ala | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/8 | 895/2760 | 825/2376 | 275/791 | chr5 | 114362964 | ||
| chr5:114473092
|
A | G | 1 | a0008c0013 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.1818A>G | p.Ala606Ala | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/8 | 1888/2760 | 1818/2376 | 606/791 | chr5 | 114473092 | ||
| chr5:114473125
|
C | T | 1 | a0001c0020 | 1 | HG01516.hp2 | synonymous_variant | LOW | c.1851C>T | p.His617His | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/8 | 1921/2760 | 1851/2376 | 617/791 | chr5 | 114473125 | ||
| chr5:114493424
|
G | A | 5 | a0001c0006a0001c0015a0002c0011others(2): Show | 10 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
synonymous_variant | LOW | c.2040G>A | p.Glu680Glu | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/8 | 2110/2760 | 2040/2376 | 680/791 | chr5 | 114493424 | ||
| chr5:114495999
|
T | C | 1 | a0002c0017 | 1 | NA18999.hp1 | synonymous_variant | LOW | c.2193T>C | p.Gly731Gly | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 8/8 | 2263/2760 | 2193/2376 | 731/791 | chr5 | 114495999 | ||
| chr5:114496059
|
C | T | 1 | a0001c0019 | 1 | HG01261.hp1 | synonymous_variant | LOW | c.2253C>T | p.Phe751Phe | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 8/8 | 2323/2760 | 2253/2376 | 751/791 | chr5 | 114496059 | ||
| chr5:114496092
|
C | T | 1 | a0001c0018 | 1 | HG02040.hp1 | synonymous_variant | LOW | c.2286C>T | p.His762His | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 8/8 | 2356/2760 | 2286/2376 | 762/791 | chr5 | 114496092 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:114496223
|
A | T | 1 | a0011c0016t0003 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*41A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 8/8 | 41 | chr5 | 114496223 | |||||
| chr5:114496407
|
C | T | 1 | a0001c0001t0002 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*225C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 8/8 | 225 | chr5 | 114496407 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:114363418
|
G | C | 1 | a0002c0002t0001g0002 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1122+157G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/7 | chr5 | 114363418 | ||||||
| chr5:114363435
|
G | T | 1 | a0002c0002t0001g0249 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1122+174G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/7 | chr5 | 114363435 | ||||||
| chr5:114363503
|
C | T | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1122+242C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/7 | chr5 | 114363503 | ||||||
| chr5:114363586
|
A | G | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246 | 3 | NA18964.hp2 NA19074.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1123-320A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/7 | chr5 | 114363586 | ||||||
| chr5:114363642
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1123-264C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/7 | chr5 | 114363642 | ||||||
| chr5:114363675
|
C | T | 1 | a0002c0002t0001g0242 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1123-231C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/7 | chr5 | 114363675 | ||||||
| chr5:114363846
|
C | A | 1 | a0002c0002t0001g0003 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1123-60C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/7 | chr5 | 114363846 | ||||||
| chr5:114364088
|
C | G | 6 | a0002c0002t0001g0236a0002c0002t0001g0238a0002c0002t0001g0240others(3): Show | 6 | HG01243.hp1 HG02451.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1218+87C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114364088 | ||||||
| chr5:114364249
|
C | A | 1 | a0002c0002t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1218+248C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114364249 | ||||||
| chr5:114364507
|
C | T | 9 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0229others(6): Show | 9 | HG00280.hp1 HG01192.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1218+506C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114364507 | ||||||
| chr5:114364616
|
C | CT | 26 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(23): Show | 26 | HG00099.hp1 HG00280.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1218+629dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114364616 | |||||
| chr5:114364616
|
CT | C | 5 | a0001c0001t0001g0247a0001c0001t0001g0248a0002c0002t0001g0005others(2): Show | 5 | HG02922.hp1 HG03491.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1218+629delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114364616 | |||||
| chr5:114364685
|
A | G | 101 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(98): Show | 101 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1218+684A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114364685 | ||||||
| chr5:114364863
|
G | C | 10 | a0002c0002t0001g0110a0002c0002t0001g0111a0002c0002t0001g0112others(7): Show | 10 | HG00738.hp2 HG01192.hp1 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.1218+862G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114364863 | ||||||
| chr5:114364882
|
T | A | 1 | a0002c0002t0001g0117 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1218+881T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114364882 | ||||||
| chr5:114364896
|
GT | G | 11 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0118others(8): Show | 11 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.1218+906delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114364896 | |||||
| chr5:114365101
|
G | A | 29 | a0002c0002t0001g0118a0002c0002t0001g0119a0002c0002t0001g0120others(26): Show | 29 | HG00099.hp2 HG00438.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1218+1100G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114365101 | ||||||
| chr5:114365257
|
G | C | 1 | a0002c0002t0001g0145 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1218+1256G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114365257 | ||||||
| chr5:114365335
|
C | A | 4 | a0005c0004t0001g0146a0005c0004t0001g0147a0005c0004t0001g0148others(1): Show | 4 | HG02486.hp2 HG02559.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218+1334C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114365335 | ||||||
| chr5:114365559
|
G | A | 9 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0229others(6): Show | 9 | HG00280.hp1 HG01192.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1218+1558G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114365559 | ||||||
| chr5:114365934
|
A | G | 6 | a0002c0002t0001g0139a0002c0002t0001g0140a0002c0002t0001g0141others(3): Show | 6 | HG00099.hp2 HG00642.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.1218+1933A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114365934 | ||||||
| chr5:114366014
|
A | G | 1 | a0002c0002t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1218+2013A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366014 | ||||||
| chr5:114366172
|
A | G | 4 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(1): Show | 4 | HG00642.hp1 HG00738.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.1218+2171A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366172 | ||||||
| chr5:114366201
|
G | A | 1 | a0002c0002t0001g0150 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1218+2200G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366201 | ||||||
| chr5:114366205
|
A | G | 1 | a0002c0002t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1218+2204A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366205 | ||||||
| chr5:114366309
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1218+2308A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366309 | ||||||
| chr5:114366322
|
C | T | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1218+2321C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366322 | ||||||
| chr5:114366351
|
G | C | 1 | a0002c0002t0001g0151 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1218+2350G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366351 | ||||||
| chr5:114366361
|
C | A | 86 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(83): Show | 86 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1218+2360C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366361 | ||||||
| chr5:114366366
|
C | G | 5 | a0001c0021t0001g0220a0006c0007t0001g0104a0006c0007t0001g0221others(2): Show | 5 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1218+2365C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366366 | ||||||
| chr5:114366435
|
G | A | 68 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(65): Show | 69 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(66): Show |
intron_variant | MODIFIER | c.1218+2434G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366435 | ||||||
| chr5:114366537
|
C | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(191): Show | 195 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.1218+2536C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366537 | ||||||
| chr5:114366603
|
G | A | 1 | a0002c0002t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1218+2602G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366603 | ||||||
| chr5:114366649
|
A | G | 1 | a0002c0002t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1218+2648A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366649 | ||||||
| chr5:114366767
|
T | C | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1218+2766T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366767 | ||||||
| chr5:114366795
|
G | A | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1218+2794G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366795 | ||||||
| chr5:114366917
|
T | G | 1 | a0002c0002t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1218+2916T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366917 | ||||||
| chr5:114367111
|
C | T | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1218+3110C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114367111 | ||||||
| chr5:114367184
|
T | A | 1 | a0002c0002t0001g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1218+3183T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114367184 | ||||||
| chr5:114367357
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1218+3356C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114367357 | ||||||
| chr5:114367376
|
C | G | 1 | a0001c0015t0001g0219 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1218+3375C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114367376 | ||||||
| chr5:114367576
|
T | C | 133 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0094others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.1218+3575T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114367576 | ||||||
| chr5:114367650
|
A | AT | 13 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(10): Show | 13 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1218+3663dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114367650 | |||||
| chr5:114367650
|
A | T | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1218+3649A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114367650 | ||||||
| chr5:114367931
|
C | G | 34 | a0001c0021t0001g0220a0002c0002t0001g0004a0002c0002t0001g0008others(31): Show | 34 | HG00099.hp1 HG00280.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.1218+3930C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114367931 | ||||||
| chr5:114367968
|
AAC | A | 5 | a0002c0002t0001g0238a0002c0002t0001g0240a0002c0011t0001g0239others(2): Show | 5 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1218+3969_1218+397 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114367968 | |||||
| chr5:114368094
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1218+4093G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114368094 | ||||||
| chr5:114368270
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1218+4269A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114368270 | ||||||
| chr5:114368308
|
G | C | 13 | a0002c0002t0001g0110a0002c0002t0001g0111a0002c0002t0001g0112others(10): Show | 13 | HG00099.hp2 HG00642.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1218+4307G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114368308 | ||||||
| chr5:114368449
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1218+4448G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114368449 | ||||||
| chr5:114368494
|
G | T | 8 | a0002c0002t0001g0004a0002c0002t0001g0236a0002c0002t0001g0238others(5): Show | 8 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1218+4493G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114368494 | ||||||
| chr5:114368657
|
C | T | 4 | a0003c0003t0001g0197a0003c0003t0001g0198a0003c0003t0001g0199others(1): Show | 4 | HG02922.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1218+4656C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114368657 | ||||||
| chr5:114368815
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1218+4814A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114368815 | ||||||
| chr5:114368870
|
A | AT | 207 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(204): Show | 208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.1218+4878dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114368870 | |||||
| chr5:114369034
|
G | A | 68 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(65): Show | 69 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(66): Show |
intron_variant | MODIFIER | c.1218+5033G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114369034 | ||||||
| chr5:114369071
|
G | A | 1 | a0002c0002t0001g0002 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1218+5070G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114369071 | ||||||
| chr5:114369136
|
G | T | 2 | a0003c0003t0001g0196a0003c0009t0001g0195 | 2 | NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1218+5135G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114369136 | ||||||
| chr5:114369347
|
C | A | 1 | a0002c0002t0001g0154 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1218+5346C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114369347 | ||||||
| chr5:114369444
|
A | G | 11 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0094others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1218+5443A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114369444 | ||||||
| chr5:114369448
|
G | T | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1218+5447G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114369448 | ||||||
| chr5:114369498
|
C | T | 1 | a0002c0002t0001g0138 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1218+5497C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114369498 | ||||||
| chr5:114369772
|
T | G | 141 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0094others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1218+5771T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114369772 | ||||||
| chr5:114369820
|
A | G | 4 | a0003c0003t0001g0197a0003c0003t0001g0198a0003c0003t0001g0199others(1): Show | 4 | HG02922.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1218+5819A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114369820 | ||||||
| chr5:114369894
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1218+5893A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114369894 | ||||||
| chr5:114369986
|
G | A | 10 | a0003c0003t0001g0193a0003c0003t0001g0196a0003c0003t0001g0197others(7): Show | 10 | HG02809.hp1 HG02895.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.1218+5985G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114369986 | ||||||
| chr5:114370147
|
T | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0020 | 2 | NA19088.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1218+6146T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114370147 | ||||||
| chr5:114370237
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1218+6236C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114370237 | ||||||
| chr5:114370576
|
C | T | 1 | a0002c0002t0001g0150 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1218+6575C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114370576 | ||||||
| chr5:114370642
|
A | G | 2 | a0001c0001t0001g0217a0001c0001t0001g0218 | 2 | HG01074.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1218+6641A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114370642 | ||||||
| chr5:114370970
|
T | TAGAG | 141 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0094others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1218+6971_1218+697 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114370970 | |||||
| chr5:114371481
|
G | A | 10 | a0002c0002t0001g0201a0002c0002t0001g0202a0002c0002t0001g0203others(7): Show | 10 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.1218+7480G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114371481 | ||||||
| chr5:114371602
|
T | A | 131 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0094others(128): Show | 131 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.1218+7601T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114371602 | ||||||
| chr5:114371724
|
A | T | 2 | a0002c0002t0001g0209a0002c0002t0001g0210 | 2 | HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1218+7723A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114371724 | ||||||
| chr5:114371752
|
T | C | 1 | a0002c0002t0001g0008 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1218+7751T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114371752 | ||||||
| chr5:114371846
|
A | G | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1218+7845A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114371846 | ||||||
| chr5:114372144
|
A | G | 120 | a0001c0021t0001g0220a0002c0002t0001g0002a0002c0002t0001g0003others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.1218+8143A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114372144 | ||||||
| chr5:114372146
|
C | T | 6 | a0002c0002t0001g0238a0002c0002t0001g0240a0002c0011t0001g0239others(3): Show | 6 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1218+8145C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114372146 | ||||||
| chr5:114372180
|
G | A | 2 | a0002c0002t0001g0008a0002c0002t0001g0009 | 2 | HG02523.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1218+8179G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114372180 | ||||||
| chr5:114372203
|
C | A | 3 | a0004c0008t0001g0010a0004c0008t0001g0011a0004c0008t0001g0012 | 3 | HG02896.hp1 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1218+8202C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114372203 | ||||||
| chr5:114372206
|
G | T | 11 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0094others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1218+8205G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114372206 | ||||||
| chr5:114372419
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1218+8418G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114372419 | ||||||
| chr5:114372561
|
A | G | 1 | a0002c0002t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1218+8560A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114372561 | ||||||
| chr5:114372614
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1218+8613A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114372614 | ||||||
| chr5:114372752
|
C | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(191): Show | 195 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.1218+8751C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114372752 | ||||||
| chr5:114372957
|
A | T | 6 | a0002c0002t0001g0238a0002c0002t0001g0240a0002c0011t0001g0239others(3): Show | 6 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1218+8956A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114372957 | ||||||
| chr5:114373078
|
T | C | 1 | a0002c0002t0001g0151 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1218+9077T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114373078 | ||||||
| chr5:114373421
|
A | G | 7 | a0002c0002t0001g0236a0002c0002t0001g0238a0002c0002t0001g0240others(4): Show | 7 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1218+9420A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114373421 | ||||||
| chr5:114373450
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1218+9449G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114373450 | ||||||
| chr5:114373640
|
T | A | 1 | a0001c0001t0001g0021 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1218+9639T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114373640 | ||||||
| chr5:114373640
|
T | TATATATA others(38): Show |
1 | a0002c0002t0001g0155 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1218+9639_1218+964 others(49): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114373640 | ||||||
| chr5:114373640
|
T | TTA | 7 | a0001c0001t0001g0109a0002c0002t0001g0120a0002c0002t0001g0157others(4): Show | 7 | HG00099.hp1 HG01169.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1218+9656_1218+965 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATA | 5 | a0001c0001t0001g0018a0001c0001t0001g0022a0004c0008t0001g0010others(2): Show | 5 | HG01358.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1218+9654_1218+965 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATATA | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0002c0002t0001g0121 | 3 | NA19009.hp2 NA19088.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1218+9652_1218+965 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATATAT others(3): Show |
1 | a0002c0002t0001g0242 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1218+9648_1218+965 others(14): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATATAT others(7): Show |
1 | a0002c0002t0001g0110 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1218+9644_1218+965 others(18): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATATAT others(9): Show |
1 | a0002c0002t0001g0187 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1218+9642_1218+965 others(20): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATATAT others(11): Show |
8 | a0002c0002t0001g0004a0002c0002t0001g0122a0002c0002t0001g0236others(5): Show | 8 | HG01109.hp2 HG01243.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1218+9640_1218+965 others(22): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATATAT others(13): Show |
2 | a0002c0002t0001g0117a0008c0013t0001g0237 | 2 | HG01261.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(24): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATATAT others(15): Show |
5 | a0001c0001t0001g0023a0001c0001t0001g0247a0002c0002t0001g0123others(2): Show | 5 | HG01070.hp2 HG02559.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(26): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATATAT others(17): Show |
6 | a0001c0001t0001g0024a0001c0001t0001g0248a0002c0002t0001g0118others(3): Show | 6 | HG01192.hp1 HG01943.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(28): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATATAT others(19): Show |
2 | a0002c0002t0001g0125a0002c0002t0001g0158 | 2 | NA18959.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(30): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATATAT others(21): Show |
2 | a0002c0002t0001g0111a0002c0002t0001g0159 | 2 | HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(32): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATATAT others(23): Show |
1 | a0001c0001t0001g0025 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1218+9657_1218+965 others(34): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATATAT others(25): Show |
7 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(4): Show | 7 | HG01099.hp1 HG01978.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(36): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATATAT others(27): Show |
2 | a0002c0002t0001g0161a0009c0023t0001g0160 | 2 | HG03704.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(38): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATATAT others(29): Show |
2 | a0001c0001t0001g0055a0002c0002t0001g0145 | 2 | HG02109.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(40): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATATAT others(31): Show |
2 | a0001c0001t0001g0001a0005c0004t0001g0147 | 3 | HG02486.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(42): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATATAT others(33): Show |
6 | a0001c0001t0001g0031a0001c0001t0001g0244a0002c0002t0001g0152others(3): Show | 6 | HG01361.hp2 HG02300.hp2 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(44): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATATAT others(35): Show |
9 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(6): Show | 9 | HG01081.hp2 HG01257.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(46): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATATAT others(37): Show |
19 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0053others(16): Show | 19 | HG00558.hp2 HG00741.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(48): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATATAT others(39): Show |
14 | a0001c0001t0001g0037a0001c0001t0001g0058a0001c0001t0001g0059others(11): Show | 14 | HG00642.hp2 HG00738.hp2 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(50): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATATAT others(41): Show |
20 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(17): Show | 20 | HG01074.hp2 HG01169.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(52): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATATAT others(43): Show |
16 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(13): Show | 16 | HG00438.hp2 HG01192.hp2 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(54): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATATAT others(45): Show |
8 | a0001c0001t0001g0050a0002c0002t0001g0116a0002c0002t0001g0136others(5): Show | 8 | HG01070.hp1 HG01433.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(56): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATATAT others(47): Show |
6 | a0001c0019t0001g0234a0002c0002t0001g0141a0002c0002t0001g0144others(3): Show | 6 | HG00099.hp2 HG01261.hp1 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(58): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATATAT others(49): Show |
3 | a0001c0001t0001g0051a0002c0002t0001g0002a0002c0002t0001g0185 | 3 | HG02080.hp1 NA18942.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(60): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATATAT others(51): Show |
2 | a0001c0001t0001g0235a0002c0002t0001g0186 | 2 | HG00280.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(62): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATATAT others(39): Show |
1 | a0001c0001t0001g0063 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1218+9650_1218+965 others(50): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTATATAT others(43): Show |
1 | a0001c0001t0001g0064 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1218+9650_1218+965 others(54): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTTATATA others(24): Show |
1 | a0003c0003t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1218+9640_1218+964 others(35): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTTTATAT others(3): Show |
1 | a0003c0009t0001g0194 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1218+9640_1218+964 others(14): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTTTATAT others(19): Show |
1 | a0003c0003t0001g0197 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1218+9640_1218+964 others(30): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTTTATAT others(35): Show |
1 | a0003c0003t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1218+9640_1218+964 others(46): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTTTATAT others(37): Show |
1 | a0003c0003t0001g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1218+9640_1218+964 others(48): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTTTATAT others(39): Show |
1 | a0003c0003t0001g0200 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1218+9640_1218+964 others(50): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTTTATAT others(43): Show |
1 | a0003c0009t0001g0195 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1218+9640_1218+964 others(54): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373640
|
T | TTTTATAT others(45): Show |
1 | a0003c0003t0001g0196 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1218+9640_1218+964 others(56): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | |||||
| chr5:114373645
|
T | TATATATA others(33): Show |
1 | a0002c0002t0001g0008 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1218+9657_1218+965 others(44): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373645 | |||||
| chr5:114373645
|
T | TATATATA others(39): Show |
1 | a0002c0002t0001g0009 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1218+9657_1218+965 others(50): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373645 | |||||
| chr5:114373657
|
T | TATATATA others(3): Show |
10 | a0001c0001t0001g0091a0001c0001t0001g0094a0001c0001t0001g0096others(7): Show | 10 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(14): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373657 | |||||
| chr5:114373657
|
T | TATATATA others(29): Show |
1 | a0001c0018t0001g0029 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1218+9657_1218+965 others(40): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373657 | |||||
| chr5:114373657
|
T | TATATATA others(35): Show |
2 | a0001c0001t0001g0030a0001c0001t0001g0227 | 2 | HG01346.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(46): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373657 | |||||
| chr5:114373657
|
T | TATATATA others(39): Show |
1 | a0001c0001t0001g0052 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1218+9657_1218+965 others(50): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373657 | |||||
| chr5:114373657
|
T | TATATATA others(43): Show |
1 | a0001c0001t0001g0039 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1218+9657_1218+965 others(54): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373657 | |||||
| chr5:114373658
|
A | ATATATAT others(36): Show |
1 | a0001c0001t0001g0021 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1218+9657_1218+965 others(47): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114373658 | ||||||
| chr5:114373658
|
A | ATATATAT others(42): Show |
2 | a0002c0002t0001g0179a0002c0017t0001g0178 | 2 | NA18999.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(53): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114373658 | ||||||
| chr5:114373658
|
A | ATATATAT others(48): Show |
1 | a0002c0002t0001g0249 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1218+9657_1218+965 others(59): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114373658 | ||||||
| chr5:114373798
|
AT | A | 13 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0054others(10): Show | 13 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1218+9808delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373798 | |||||
| chr5:114374010
|
A | G | 1 | a0002c0002t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1218+10009A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114374010 | ||||||
| chr5:114374128
|
A | C | 1 | a0002c0002t0001g0207 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1218+10127A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114374128 | ||||||
| chr5:114374144
|
A | T | 3 | a0004c0008t0001g0010a0004c0008t0001g0011a0004c0008t0001g0012 | 3 | HG02896.hp1 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1218+10143A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114374144 | ||||||
| chr5:114374547
|
G | A | 1 | a0002c0002t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1218+10546G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114374547 | ||||||
| chr5:114374569
|
C | T | 11 | a0002c0002t0001g0004a0003c0003t0001g0193a0003c0003t0001g0196others(8): Show | 11 | HG02809.hp1 HG02895.hp1 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.1218+10568C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114374569 | ||||||
| chr5:114374661
|
C | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(87): Show | 91 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(88): Show |
intron_variant | MODIFIER | c.1218+10660C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114374661 | ||||||
| chr5:114374741
|
A | G | 2 | a0002c0002t0001g0139a0002c0002t0001g0140 | 2 | HG00642.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1218+10740A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114374741 | ||||||
| chr5:114374787
|
C | G | 1 | a0001c0001t0001g0034 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1218+10786C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114374787 | ||||||
| chr5:114374805
|
C | T | 1 | a0002c0002t0001g0151 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1218+10804C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114374805 | ||||||
| chr5:114374912
|
G | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(191): Show | 195 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.1218+10911G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114374912 | ||||||
| chr5:114374954
|
G | A | 11 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(8): Show | 11 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.1218+10953G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114374954 | ||||||
| chr5:114375064
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1218+11063T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114375064 | ||||||
| chr5:114375485
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1218+11484A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114375485 | ||||||
| chr5:114375692
|
G | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(104): Show | 108 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1218+11691G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114375692 | ||||||
| chr5:114375694
|
T | A | 1 | a0002c0002t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1218+11693T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114375694 | ||||||
| chr5:114375952
|
G | GTA | 7 | a0001c0001t0001g0065a0001c0001t0001g0069a0001c0001t0001g0070others(4): Show | 7 | HG01109.hp1 HG01358.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.1218+11975_1218+11 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | |||||
| chr5:114375952
|
G | GTATA | 6 | a0001c0001t0001g0067a0001c0001t0001g0068a0003c0003t0001g0197others(3): Show | 6 | HG01516.hp1 HG01517.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1218+11973_1218+11 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | |||||
| chr5:114375952
|
G | GTATATAT others(3): Show |
1 | a0002c0002t0001g0205 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1218+11967_1218+11 others(16): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | |||||
| chr5:114375952
|
G | GTATATAT others(5): Show |
2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1218+11965_1218+11 others(18): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | |||||
| chr5:114375952
|
G | GTATATAT others(7): Show |
1 | a0002c0011t0001g0241 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1218+11963_1218+11 others(20): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | |||||
| chr5:114375952
|
G | GTATATAT others(9): Show |
11 | a0001c0001t0001g0092a0002c0002t0001g0004a0002c0002t0001g0005others(8): Show | 11 | HG01070.hp1 HG01361.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.1218+11961_1218+11 others(22): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | |||||
| chr5:114375952
|
G | GTATATAT others(11): Show |
26 | a0001c0001t0001g0091a0001c0001t0001g0099a0002c0002t0001g0119others(23): Show | 26 | HG00741.hp1 HG01175.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.1218+11959_1218+11 others(24): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | |||||
| chr5:114375952
|
G | GTATATAT others(13): Show |
26 | a0001c0006t0001g0097a0001c0006t0001g0098a0002c0002t0001g0110others(23): Show | 26 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.1218+11957_1218+11 others(26): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | |||||
| chr5:114375952
|
G | GTATATAT others(15): Show |
18 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0111others(15): Show | 18 | HG00099.hp1 HG00642.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1218+11955_1218+11 others(28): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | |||||
| chr5:114375952
|
G | GTATATAT others(17): Show |
17 | a0001c0001t0001g0096a0002c0002t0001g0113a0002c0002t0001g0117others(14): Show | 17 | HG00741.hp2 HG01070.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.1218+11953_1218+11 others(30): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | |||||
| chr5:114375952
|
G | GTATATAT others(19): Show |
7 | a0001c0006t0001g0095a0002c0002t0001g0006a0002c0002t0001g0127others(4): Show | 7 | HG02055.hp1 HG02523.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1218+11976_1218+11 others(32): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | |||||
| chr5:114375952
|
G | GTATATAT others(21): Show |
3 | a0001c0001t0001g0094a0002c0002t0001g0151a0002c0002t0001g0166 | 3 | HG02040.hp2 HG02559.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1218+11976_1218+11 others(34): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | |||||
| chr5:114375952
|
G | GTATATAT others(23): Show |
2 | a0001c0006t0001g0093a0002c0002t0001g0165 | 2 | HG02080.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1218+11976_1218+11 others(36): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | |||||
| chr5:114375952
|
G | GTGTATAT others(11): Show |
1 | a0002c0002t0001g0206 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1218+11952_1218+11 others(24): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | |||||
| chr5:114375952
|
GTA | G | 27 | a0001c0001t0001g0034a0001c0001t0001g0054a0001c0001t0001g0055others(24): Show | 27 | HG01081.hp2 HG01243.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.1218+11975_1218+11 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | |||||
| chr5:114375952
|
GTATA | G | 63 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(60): Show | 64 | HG00280.hp1 HG01081.hp1 HG01099.hp1 others(61): Show |
intron_variant | MODIFIER | c.1218+11973_1218+11 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | |||||
| chr5:114375974
|
A | ATATATAT others(15): Show |
1 | a0005c0004t0001g0146 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1218+11976_1218+11 others(28): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375974 | |||||
| chr5:114375974
|
A | ATATATAT others(11): Show |
1 | a0002c0002t0001g0116 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1218+11976_1218+11 others(24): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375974 | |||||
| chr5:114376006
|
C | G | 1 | a0002c0002t0001g0207 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1218+12005C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376006 | ||||||
| chr5:114376090
|
A | G | 11 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0094others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1218+12089A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376090 | ||||||
| chr5:114376111
|
T | TAC | 18 | a0001c0001t0001g0082a0001c0021t0001g0220a0002c0002t0001g0008others(15): Show | 18 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.1218+12113_1218+12 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114376111 | |||||
| chr5:114376115
|
C | A | 1 | a0001c0001t0001g0021 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1218+12114C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376115 | ||||||
| chr5:114376188
|
T | C | 43 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0021others(40): Show | 44 | HG01081.hp2 HG01099.hp1 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.1218+12187T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376188 | ||||||
| chr5:114376194
|
G | A | 10 | a0003c0003t0001g0193a0003c0003t0001g0196a0003c0003t0001g0197others(7): Show | 10 | HG02809.hp1 HG02895.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.1218+12193G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376194 | ||||||
| chr5:114376258
|
G | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(63): Show | 67 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(64): Show |
intron_variant | MODIFIER | c.1218+12257G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376258 | ||||||
| chr5:114376267
|
T | C | 1 | a0002c0002t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1218+12266T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376267 | ||||||
| chr5:114376315
|
G | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(103): Show | 107 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1218+12314G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376315 | ||||||
| chr5:114376326
|
G | T | 68 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(65): Show | 69 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(66): Show |
intron_variant | MODIFIER | c.1218+12325G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376326 | ||||||
| chr5:114376454
|
C | A | 1 | a0002c0002t0001g0201 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1218+12453C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376454 | ||||||
| chr5:114376470
|
T | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(144): Show | 148 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.1218+12469T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376470 | ||||||
| chr5:114376475
|
A | G | 1 | a0002c0002t0001g0168 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1218+12474A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376475 | ||||||
| chr5:114376662
|
G | C | 57 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(54): Show | 57 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.1218+12661G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376662 | ||||||
| chr5:114376778
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1218+12777A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376778 | ||||||
| chr5:114376877
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(104): Show | 108 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1218+12876G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376877 | ||||||
| chr5:114377057
|
G | T | 23 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0083others(20): Show | 23 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.1218+13056G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114377057 | ||||||
| chr5:114377067
|
G | A | 5 | a0001c0021t0001g0220a0006c0007t0001g0104a0006c0007t0001g0221others(2): Show | 5 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1218+13066G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114377067 | ||||||
| chr5:114377085
|
A | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(87): Show | 91 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(88): Show |
intron_variant | MODIFIER | c.1218+13084A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114377085 | ||||||
| chr5:114377157
|
C | G | 1 | a0002c0005t0001g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1218+13156C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114377157 | ||||||
| chr5:114377434
|
C | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0021others(40): Show | 44 | HG01099.hp1 HG01175.hp2 HG01257.hp1 others(41): Show |
intron_variant | MODIFIER | c.1218+13433C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114377434 | ||||||
| chr5:114377584
|
G | A | 4 | a0003c0003t0001g0197a0003c0003t0001g0198a0003c0003t0001g0199others(1): Show | 4 | HG02922.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1218+13583G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114377584 | ||||||
| chr5:114377666
|
T | C | 3 | a0004c0008t0001g0010a0004c0008t0001g0011a0004c0008t0001g0012 | 3 | HG02896.hp1 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1218+13665T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114377666 | ||||||
| chr5:114377680
|
T | C | 46 | a0001c0001t0001g0066a0001c0001t0001g0082a0001c0001t0001g0083others(43): Show | 46 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.1218+13679T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114377680 | ||||||
| chr5:114377730
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1218+13729G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114377730 | ||||||
| chr5:114377730
|
G | C | 1 | a0002c0005t0001g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1218+13729G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114377730 | ||||||
| chr5:114377747
|
C | T | 1 | a0002c0002t0001g0120 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1218+13746C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114377747 | ||||||
| chr5:114377918
|
G | A | 1 | a0002c0002t0001g0166 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1218+13917G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114377918 | ||||||
| chr5:114378171
|
A | G | 18 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0102others(15): Show | 18 | HG01243.hp1 HG01243.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1218+14170A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114378171 | ||||||
| chr5:114378176
|
TA | T | 18 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0102others(15): Show | 18 | HG01243.hp1 HG01243.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1218+14183delA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114378176 | |||||
| chr5:114378209
|
C | T | 28 | a0001c0001t0001g0066a0001c0001t0001g0082a0001c0001t0001g0083others(25): Show | 28 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1218+14208C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114378209 | ||||||
| chr5:114378280
|
A | G | 7 | a0002c0002t0001g0236a0002c0002t0001g0238a0002c0002t0001g0240others(4): Show | 7 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1218+14279A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114378280 | ||||||
| chr5:114378372
|
G | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(76): Show | 80 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(77): Show |
intron_variant | MODIFIER | c.1218+14371G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114378372 | ||||||
| chr5:114378406
|
A | G | 1 | a0002c0002t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1218+14405A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114378406 | ||||||
| chr5:114378489
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1218+14488T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114378489 | ||||||
| chr5:114378542
|
C | T | 9 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0005t0001g0013others(6): Show | 9 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.1218+14541C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114378542 | ||||||
| chr5:114378544
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(74): Show | 78 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(75): Show |
intron_variant | MODIFIER | c.1218+14543G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114378544 | ||||||
| chr5:114378551
|
G | C | 1 | a0001c0001t0001g0044 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1218+14550G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114378551 | ||||||
| chr5:114378558
|
A | T | 1 | a0001c0001t0001g0053 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1218+14557A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114378558 | ||||||
| chr5:114378723
|
TAGTGTCA others(11): Show |
T | 6 | a0002c0002t0001g0238a0002c0002t0001g0240a0002c0011t0001g0239others(3): Show | 6 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1218+14725_1218+14 others(24): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114378723 | |||||
| chr5:114378756
|
T | C | 17 | a0002c0002t0001g0236a0002c0002t0001g0238a0002c0002t0001g0240others(14): Show | 17 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.1218+14755T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114378756 | ||||||
| chr5:114378902
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1218+14901G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114378902 | ||||||
| chr5:114379052
|
A | G | 10 | a0002c0002t0001g0201a0002c0002t0001g0202a0002c0002t0001g0203others(7): Show | 10 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.1218+15051A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379052 | ||||||
| chr5:114379066
|
C | A | 1 | a0002c0002t0001g0006 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1218+15065C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379066 | ||||||
| chr5:114379078
|
G | T | 29 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0082others(26): Show | 29 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.1218+15077G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379078 | ||||||
| chr5:114379095
|
A | T | 1 | a0001c0001t0001g0101 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1218+15094A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379095 | ||||||
| chr5:114379140
|
T | C | 1 | a0002c0002t0001g0115 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1218+15139T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379140 | ||||||
| chr5:114379296
|
T | G | 1 | a0001c0001t0001g0044 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1218+15295T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379296 | ||||||
| chr5:114379299
|
C | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0061 | 2 | HG01099.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1218+15298C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379299 | ||||||
| chr5:114379361
|
T | C | 1 | a0002c0002t0001g0173 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1218+15360T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379361 | ||||||
| chr5:114379422
|
A | AATATTAT others(25): Show |
2 | a0002c0002t0001g0115a0002c0002t0001g0150 | 2 | HG02132.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1218+15510_1218+15 others(38): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379422 | |||||
| chr5:114379422
|
AATATTAT others(25): Show |
A | 6 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0006t0001g0093others(3): Show | 6 | HG02055.hp1 HG02559.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1218+15510_1218+15 others(38): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379422 | |||||
| chr5:114379422
|
AATATTAT others(57): Show |
A | 16 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0054others(13): Show | 16 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.1218+15478_1218+15 others(70): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379422 | |||||
| chr5:114379451
|
G | T | 39 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0021others(36): Show | 40 | HG01099.hp1 HG01175.hp2 HG01257.hp1 others(37): Show |
intron_variant | MODIFIER | c.1218+15450G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379451 | ||||||
| chr5:114379477
|
TTTATAGA others(56): Show |
T | 10 | a0001c0001t0001g0069a0001c0001t0001g0229a0001c0001t0001g0230others(7): Show | 10 | HG00099.hp1 HG00280.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1218+15510_1218+15 others(69): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379477 | |||||
| chr5:114379477
|
TTTATAGA others(87): Show |
T | 7 | a0001c0001t0001g0025a0001c0001t0001g0049a0001c0001t0001g0090others(4): Show | 7 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1218+15511_1218+15 others(100): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379477 | |||||
| chr5:114379496
|
A | G | 11 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(8): Show | 11 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.1218+15495A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379496 | ||||||
| chr5:114379507
|
TATTTATA others(88): Show |
T | 3 | a0001c0001t0001g0039a0001c0001t0001g0052a0001c0018t0001g0029 | 3 | HG02040.hp1 NA19060.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1218+15507_1218+15 others(101): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379507 | ||||||
| chr5:114379508
|
AT | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0021others(85): Show | 89 | HG00280.hp2 HG01074.hp1 HG01081.hp2 others(86): Show |
intron_variant | MODIFIER | c.1218+15510delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379508 | |||||
| chr5:114379534
|
TTATATAT others(115): Show |
T | 8 | a0001c0001t0001g0026a0001c0001t0001g0091a0001c0001t0001g0092others(5): Show | 8 | HG01978.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1218+15542_1218+15 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379534 | |||||
| chr5:114379540
|
A | AT | 81 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0021others(78): Show | 82 | HG00280.hp2 HG01074.hp1 HG01081.hp2 others(79): Show |
intron_variant | MODIFIER | c.1218+15541dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379540 | |||||
| chr5:114379541
|
TTATAGAA others(23): Show |
T | 2 | a0001c0001t0001g0231a0001c0019t0001g0234 | 2 | HG01261.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1218+15542_1218+15 others(36): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379541 | |||||
| chr5:114379543
|
A | ATATAACA others(13): Show |
4 | a0003c0003t0001g0197a0003c0003t0001g0198a0003c0003t0001g0199others(1): Show | 4 | HG02922.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1218+15544_1218+15 others(26): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379543 | |||||
| chr5:114379543
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0021others(76): Show | 80 | HG00280.hp2 HG01074.hp1 HG01081.hp2 others(77): Show |
intron_variant | MODIFIER | c.1218+15542A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379543 | ||||||
| chr5:114379565
|
TTATATAT others(84): Show |
T | 83 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0021others(80): Show | 84 | HG00280.hp2 HG01074.hp1 HG01081.hp2 others(81): Show |
intron_variant | MODIFIER | c.1218+15573_1218+15 others(97): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379565 | |||||
| chr5:114379571
|
A | AT | 20 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0054others(17): Show | 20 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1218+15572dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379571 | |||||
| chr5:114379574
|
A | G | 22 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0054others(19): Show | 22 | HG01081.hp1 HG01099.hp2 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.1218+15573A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379574 | ||||||
| chr5:114379593
|
ATAT | A | 4 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(1): Show | 4 | HG01433.hp2 HG01993.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218+15596_1218+15 others(9): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379593 | |||||
| chr5:114379596
|
TTATATAT others(53): Show |
T | 1 | a0002c0002t0001g0208 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1218+15605_1218+15 others(66): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379596 | |||||
| chr5:114379601
|
TA | T | 4 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(1): Show | 4 | HG01433.hp2 HG01993.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218+15601delA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379601 | ||||||
| chr5:114379605
|
T | A | 11 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0049others(8): Show | 11 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1218+15604T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379605 | ||||||
| chr5:114379605
|
T | G | 4 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(1): Show | 4 | HG01433.hp2 HG01993.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218+15604T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379605 | ||||||
| chr5:114379605
|
T | TG | 39 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0057others(36): Show | 39 | HG00280.hp1 HG01081.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.1218+15604_1218+15 others(7): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379605 | ||||||
| chr5:114379605
|
T | TGTAGAAT others(23): Show |
1 | a0002c0002t0001g0009 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1218+15604_1218+15 others(36): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379605 | ||||||
| chr5:114379610
|
A | T | 1 | a0002c0002t0001g0126 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1218+15609A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379610 | ||||||
| chr5:114379624
|
ATAT | A | 9 | a0002c0002t0001g0102a0002c0002t0001g0103a0002c0005t0001g0013others(6): Show | 9 | HG01243.hp2 HG02451.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1218+15627_1218+15 others(9): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379624 | |||||
| chr5:114379625
|
TATTATAT others(24): Show |
T | 1 | a0001c0001t0001g0049 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1218+15625_1218+15 others(37): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379625 | ||||||
| chr5:114379637
|
G | A | 1 | a0002c0002t0001g0009 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1218+15636G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379637 | ||||||
| chr5:114379637
|
GTAGAATA others(22): Show |
G | 4 | a0002c0014t0001g0017a0007c0010t0001g0191a0007c0010t0001g0192others(1): Show | 4 | HG02572.hp1 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218+15659_1218+15 others(35): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379637 | |||||
| chr5:114379656
|
A | ATAT | 45 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0025others(42): Show | 45 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1218+15656_1218+15 others(9): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379656 | |||||
| chr5:114379656
|
A | ATATATAT others(89): Show |
1 | a0002c0002t0001g0008 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1218+15664_1218+15 others(102): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379656 | |||||
| chr5:114379656
|
A | ATATTATA others(28): Show |
3 | a0003c0003t0001g0193a0003c0003t0001g0196a0003c0009t0001g0195 | 3 | NA18522.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1218+15658_1218+15 others(41): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379656 | |||||
| chr5:114379666
|
A | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(124): Show | 128 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1218+15665A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379666 | ||||||
| chr5:114379698
|
A | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(124): Show | 128 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(125): Show |
intron_variant | MODIFIER | c.1218+15697A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379698 | ||||||
| chr5:114379730
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(112): Show | 116 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(113): Show |
intron_variant | MODIFIER | c.1218+15729A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379730 | ||||||
| chr5:114379748
|
CATATTAT others(27): Show |
C | 9 | a0002c0002t0001g0201a0002c0002t0001g0202a0002c0002t0001g0203others(6): Show | 9 | HG00280.hp2 HG01256.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1218+15752_1218+15 others(40): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379748 | |||||
| chr5:114379762
|
A | G | 14 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0091others(11): Show | 14 | HG02055.hp1 HG02145.hp2 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.1218+15761A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379762 | ||||||
| chr5:114379780
|
CAT | C | 48 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0082others(45): Show | 48 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.1218+15786_1218+15 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379780 | |||||
| chr5:114379781
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1218+15780A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379781 | ||||||
| chr5:114379882
|
G | A | 27 | a0002c0002t0001g0201a0002c0002t0001g0202a0002c0002t0001g0203others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.1218+15881G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379882 | ||||||
| chr5:114379897
|
G | T | 1 | a0002c0002t0001g0126 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1218+15896G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379897 | ||||||
| chr5:114379947
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1218+15946G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379947 | ||||||
| chr5:114379964
|
T | C | 3 | a0002c0002t0001g0144a0004c0012t0001g0142a0004c0012t0001g0143 | 3 | HG01070.hp1 HG01256.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1218+15963T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379964 | ||||||
| chr5:114380017
|
A | G | 10 | a0002c0002t0001g0201a0002c0002t0001g0202a0002c0002t0001g0203others(7): Show | 10 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.1218+16016A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114380017 | ||||||
| chr5:114380248
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1218+16247G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114380248 | ||||||
| chr5:114380373
|
T | C | 43 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0021others(40): Show | 44 | HG01081.hp2 HG01099.hp1 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.1218+16372T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114380373 | ||||||
| chr5:114380378
|
C | G | 26 | a0001c0001t0001g0059a0001c0001t0001g0062a0001c0001t0001g0066others(23): Show | 26 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1218+16377C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114380378 | ||||||
| chr5:114380461
|
G | C | 1 | a0011c0016t0003g0177 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1218+16460G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114380461 | ||||||
| chr5:114380785
|
G | T | 7 | a0002c0002t0001g0201a0002c0002t0001g0202a0002c0002t0001g0203others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1218+16784G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114380785 | ||||||
| chr5:114380807
|
T | C | 1 | a0011c0016t0003g0177 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1218+16806T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114380807 | ||||||
| chr5:114380835
|
G | A | 146 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(143): Show | 147 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1218+16834G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114380835 | ||||||
| chr5:114380991
|
G | A | 4 | a0002c0002t0001g0122a0002c0002t0001g0130a0002c0002t0001g0133others(1): Show | 4 | HG01109.hp2 HG01361.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1218+16990G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114380991 | ||||||
| chr5:114381030
|
G | T | 1 | a0001c0001t0001g0028 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1218+17029G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114381030 | ||||||
| chr5:114381044
|
C | G | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1218+17043C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114381044 | ||||||
| chr5:114381238
|
C | G | 1 | a0001c0001t0001g0101 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1218+17237C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114381238 | ||||||
| chr5:114381340
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1218+17339A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114381340 | ||||||
| chr5:114381560
|
C | A | 1 | a0011c0016t0003g0177 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1218+17559C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114381560 | ||||||
| chr5:114381564
|
T | C | 1 | a0011c0016t0003g0177 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1218+17563T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114381564 | ||||||
| chr5:114381591
|
G | T | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1218+17590G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114381591 | ||||||
| chr5:114381700
|
C | T | 2 | a0002c0002t0001g0102a0002c0002t0001g0103 | 2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1218+17699C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114381700 | ||||||
| chr5:114381735
|
G | A | 5 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0107others(2): Show | 5 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1218+17734G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114381735 | ||||||
| chr5:114381774
|
G | A | 9 | a0002c0002t0001g0004a0002c0002t0001g0008a0002c0002t0001g0009others(6): Show | 9 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.1218+17773G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114381774 | ||||||
| chr5:114382020
|
G | A | 20 | a0002c0002t0001g0236a0002c0002t0001g0238a0002c0002t0001g0240others(17): Show | 20 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.1218+18019G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114382020 | ||||||
| chr5:114382078
|
G | A | 1 | a0002c0002t0001g0157 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1218+18077G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114382078 | ||||||
| chr5:114382194
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1218+18193C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114382194 | ||||||
| chr5:114382445
|
G | C | 1 | a0002c0002t0001g0167 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1218+18444G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114382445 | ||||||
| chr5:114382631
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1218+18630C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114382631 | ||||||
| chr5:114382632
|
C | A | 1 | a0002c0002t0001g0133 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1218+18631C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114382632 | ||||||
| chr5:114382737
|
C | G | 5 | a0001c0021t0001g0220a0006c0007t0001g0104a0006c0007t0001g0221others(2): Show | 5 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1218+18736C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114382737 | ||||||
| chr5:114382760
|
G | A | 44 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0021others(41): Show | 45 | HG01099.hp1 HG01175.hp2 HG01257.hp1 others(42): Show |
intron_variant | MODIFIER | c.1218+18759G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114382760 | ||||||
| chr5:114382921
|
T | C | 7 | a0002c0002t0001g0201a0002c0002t0001g0202a0002c0002t0001g0203others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1218+18920T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114382921 | ||||||
| chr5:114383139
|
A | C | 1 | a0001c0001t0001g0090 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1218+19138A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383139 | ||||||
| chr5:114383235
|
A | G | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1218+19234A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383235 | ||||||
| chr5:114383250
|
G | A | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1218+19249G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383250 | ||||||
| chr5:114383290
|
G | A | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1218+19289G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383290 | ||||||
| chr5:114383302
|
G | T | 1 | a0001c0001t0001g0030 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1218+19301G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383302 | ||||||
| chr5:114383431
|
G | C | 1 | a0002c0002t0001g0133 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1218+19430G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383431 | ||||||
| chr5:114383434
|
G | A | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1218+19433G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383434 | ||||||
| chr5:114383448
|
T | G | 3 | a0001c0001t0001g0247a0001c0001t0001g0248a0003c0009t0001g0194 | 3 | HG02809.hp1 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1218+19447T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383448 | ||||||
| chr5:114383464
|
C | CT | 20 | a0001c0001t0001g0070a0001c0001t0001g0079a0001c0001t0001g0080others(17): Show | 20 | HG00438.hp1 HG01109.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.1218+19487dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114383464 | |||||
| chr5:114383464
|
CT | C | 71 | a0001c0001t0001g0066a0001c0001t0001g0083a0001c0001t0001g0084others(68): Show | 71 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.1218+19487delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114383464 | |||||
| chr5:114383464
|
CTT | C | 12 | a0001c0001t0001g0087a0001c0001t0001g0247a0001c0001t0001g0248others(9): Show | 12 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.1218+19486_1218+19 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114383464 | |||||
| chr5:114383464
|
CTTTTTTT others(5): Show |
C | 68 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(65): Show | 69 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(66): Show |
intron_variant | MODIFIER | c.1218+19476_1218+19 others(18): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114383464 | |||||
| chr5:114383594
|
A | C | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1218+19593A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383594 | ||||||
| chr5:114383615
|
G | C | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1218+19614G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383615 | ||||||
| chr5:114383641
|
T | G | 11 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(8): Show | 11 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.1218+19640T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383641 | ||||||
| chr5:114383654
|
G | A | 6 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0107others(3): Show | 6 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1218+19653G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383654 | ||||||
| chr5:114383940
|
T | C | 1 | a0002c0002t0001g0201 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1218+19939T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383940 | ||||||
| chr5:114383955
|
C | T | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0062 | 3 | HG02280.hp1 HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1218+19954C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383955 | ||||||
| chr5:114384045
|
A | G | 2 | a0002c0002t0001g0130a0002c0002t0001g0137 | 2 | HG02109.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1218+20044A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114384045 | ||||||
| chr5:114384255
|
C | T | 1 | a0002c0002t0001g0205 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1219-20183C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114384255 | ||||||
| chr5:114384504
|
G | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(127): Show | 131 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1219-19934G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114384504 | ||||||
| chr5:114384517
|
A | C | 1 | a0002c0002t0001g0071 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1219-19921A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114384517 | ||||||
| chr5:114384667
|
A | G | 1 | a0003c0003t0001g0197 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1219-19771A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114384667 | ||||||
| chr5:114384961
|
CTTAA | C | 9 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0229others(6): Show | 9 | HG00280.hp1 HG01192.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1219-19473_1219-19 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114384961 | |||||
| chr5:114385234
|
C | T | 15 | a0001c0001t0001g0082a0001c0021t0001g0220a0002c0002t0001g0004others(12): Show | 15 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.1219-19204C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385234 | ||||||
| chr5:114385244
|
T | C | 11 | a0001c0001t0001g0248a0003c0003t0001g0193a0003c0003t0001g0196others(8): Show | 11 | HG02809.hp1 HG02895.hp1 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.1219-19194T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385244 | ||||||
| chr5:114385310
|
T | C | 3 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215 | 3 | HG02886.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1219-19128T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385310 | ||||||
| chr5:114385501
|
C | T | 15 | a0001c0001t0001g0082a0001c0021t0001g0220a0002c0002t0001g0004others(12): Show | 15 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.1219-18937C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385501 | ||||||
| chr5:114385514
|
T | TGC | 9 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0231others(6): Show | 9 | HG01109.hp1 HG01192.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.1219-18919_1219-18 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385514 | |||||
| chr5:114385514
|
T | TGCGC | 3 | a0001c0001t0001g0028a0001c0001t0001g0050a0001c0015t0001g0219 | 3 | HG02965.hp2 HG03704.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1219-18921_1219-18 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385514 | |||||
| chr5:114385514
|
TGC | T | 4 | a0001c0001t0001g0057a0001c0001t0001g0061a0002c0005t0001g0014others(1): Show | 4 | HG01099.hp2 HG01243.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1219-18919_1219-18 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385514 | |||||
| chr5:114385514
|
TGCGC | T | 9 | a0001c0001t0001g0082a0001c0021t0001g0220a0002c0002t0001g0008others(6): Show | 9 | HG02523.hp1 HG02630.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.1219-18921_1219-18 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385514 | |||||
| chr5:114385515
|
GCGCGCAC others(7): Show |
G | 1 | a0006c0007t0001g0223 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1219-18921_1219-18 others(20): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385515 | |||||
| chr5:114385517
|
G | A | 2 | a0002c0002t0001g0004a0002c0005t0001g0013 | 2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1219-18921G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385517 | ||||||
| chr5:114385517
|
G | GCA | 9 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0054others(6): Show | 9 | HG01433.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1219-18920_1219-18 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385517 | |||||
| chr5:114385519
|
G | A | 16 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0054others(13): Show | 16 | HG01081.hp1 HG01243.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.1219-18919G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385519 | ||||||
| chr5:114385519
|
G | GCA | 10 | a0001c0001t0001g0066a0001c0001t0001g0084a0001c0001t0001g0085others(7): Show | 10 | HG00642.hp1 HG00738.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1219-18882_1219-18 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385519 | |||||
| chr5:114385519
|
G | GCACA | 9 | a0001c0001t0001g0076a0002c0002t0001g0201a0002c0002t0001g0202others(6): Show | 9 | HG00099.hp1 HG00280.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1219-18884_1219-18 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385519 | |||||
| chr5:114385519
|
G | GCACACA | 4 | a0001c0001t0001g0083a0002c0002t0001g0205a0002c0002t0001g0236others(1): Show | 4 | HG02886.hp2 HG02970.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1219-18886_1219-18 others(12): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385519 | |||||
| chr5:114385519
|
G | GCACACAC others(3): Show |
1 | a0002c0002t0001g0238 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1219-18890_1219-18 others(16): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385519 | |||||
| chr5:114385519
|
G | GCGCA | 39 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(36): Show | 39 | HG01099.hp1 HG01175.hp2 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.1219-18918_1219-18 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385519 | |||||
| chr5:114385519
|
G | GCGCACA | 4 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0215others(1): Show | 5 | HG02273.hp2 HG02886.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1219-18918_1219-18 others(12): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385519 | |||||
| chr5:114385519
|
G | GCGCACAC others(1): Show |
3 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0218 | 3 | HG01074.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1219-18918_1219-18 others(14): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385519 | |||||
| chr5:114385519
|
G | GCGCACAC others(3): Show |
4 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0216others(1): Show | 4 | HG02486.hp1 HG02615.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1219-18918_1219-18 others(16): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385519 | |||||
| chr5:114385519
|
GCA | G | 82 | a0001c0001t0001g0034a0001c0001t0001g0086a0001c0001t0001g0100others(79): Show | 82 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1219-18882_1219-18 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385519 | |||||
| chr5:114385519
|
GCACA | G | 4 | a0001c0001t0001g0247a0002c0002t0001g0002a0002c0002t0001g0167others(1): Show | 4 | HG01167.hp1 NA18906.hp2 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1219-18884_1219-18 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385519 | |||||
| chr5:114385521
|
A | G | 8 | a0001c0001t0001g0039a0001c0001t0001g0052a0001c0001t0001g0099others(5): Show | 8 | HG00280.hp1 HG00738.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1219-18917A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385521 | ||||||
| chr5:114385523
|
A | G | 10 | a0001c0001t0001g0034a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG01081.hp2 HG03139.hp1 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.1219-18915A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385523 | ||||||
| chr5:114385620
|
T | C | 1 | a0002c0002t0001g0120 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1219-18818T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385620 | ||||||
| chr5:114385654
|
C | G | 11 | a0001c0001t0001g0248a0003c0003t0001g0193a0003c0003t0001g0196others(8): Show | 11 | HG02809.hp1 HG02895.hp1 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.1219-18784C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385654 | ||||||
| chr5:114385691
|
C | G | 15 | a0001c0001t0001g0082a0001c0021t0001g0220a0002c0002t0001g0004others(12): Show | 15 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.1219-18747C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385691 | ||||||
| chr5:114385734
|
T | C | 15 | a0001c0001t0001g0082a0001c0021t0001g0220a0002c0002t0001g0004others(12): Show | 15 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.1219-18704T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385734 | ||||||
| chr5:114385741
|
T | C | 15 | a0001c0001t0001g0082a0001c0021t0001g0220a0002c0002t0001g0004others(12): Show | 15 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.1219-18697T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385741 | ||||||
| chr5:114385752
|
C | T | 33 | a0001c0001t0001g0066a0001c0001t0001g0083a0001c0001t0001g0084others(30): Show | 33 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.1219-18686C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385752 | ||||||
| chr5:114385825
|
G | GT | 10 | a0002c0002t0001g0123a0002c0002t0001g0127a0002c0002t0001g0131others(7): Show | 10 | HG00741.hp1 HG01070.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.1219-18603dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385825 | |||||
| chr5:114385929
|
A | T | 1 | a0001c0001t0001g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1219-18509A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385929 | ||||||
| chr5:114386014
|
T | TA | 15 | a0001c0001t0001g0082a0001c0021t0001g0220a0002c0002t0001g0004others(12): Show | 15 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.1219-18415dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114386014 | |||||
| chr5:114386015
|
A | G | 22 | a0001c0001t0001g0066a0001c0001t0001g0083a0001c0001t0001g0084others(19): Show | 22 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.1219-18423A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114386015 | ||||||
| chr5:114386098
|
C | T | 1 | a0002c0002t0001g0103 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1219-18340C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114386098 | ||||||
| chr5:114386181
|
T | TA | 19 | a0001c0001t0001g0070a0001c0001t0001g0073a0001c0001t0001g0082others(16): Show | 19 | HG01243.hp2 HG01981.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1219-18236dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114386181 | |||||
| chr5:114386181
|
TA | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(64): Show | 68 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(65): Show |
intron_variant | MODIFIER | c.1219-18236delA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114386181 | |||||
| chr5:114386195
|
A | G | 5 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(2): Show | 5 | HG01978.hp2 HG01981.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.1219-18243A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114386195 | ||||||
| chr5:114386392
|
G | GA | 15 | a0001c0001t0001g0082a0001c0021t0001g0220a0002c0002t0001g0004others(12): Show | 15 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.1219-18040dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114386392 | |||||
| chr5:114386401
|
A | G | 2 | a0007c0010t0001g0191a0007c0010t0001g0192 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1219-18037A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114386401 | ||||||
| chr5:114386402
|
T | G | 1 | a0001c0001t0001g0101 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1219-18036T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114386402 | ||||||
| chr5:114386660
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1219-17778G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114386660 | ||||||
| chr5:114386938
|
A | G | 4 | a0002c0002t0001g0122a0002c0002t0001g0130a0002c0002t0001g0133others(1): Show | 4 | HG01109.hp2 HG01361.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1219-17500A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114386938 | ||||||
| chr5:114387159
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1219-17279A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114387159 | ||||||
| chr5:114387238
|
A | T | 11 | a0001c0001t0001g0248a0003c0003t0001g0193a0003c0003t0001g0196others(8): Show | 11 | HG02809.hp1 HG02895.hp1 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.1219-17200A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114387238 | ||||||
| chr5:114387282
|
G | T | 9 | a0002c0002t0001g0004a0002c0002t0001g0008a0002c0002t0001g0009others(6): Show | 9 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.1219-17156G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114387282 | ||||||
| chr5:114387294
|
C | T | 27 | a0001c0001t0001g0066a0001c0001t0001g0083a0001c0001t0001g0084others(24): Show | 27 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1219-17144C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114387294 | ||||||
| chr5:114387302
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1219-17136T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114387302 | ||||||
| chr5:114387509
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1219-16929G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114387509 | ||||||
| chr5:114387533
|
TA | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(135): Show | 139 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1219-16896delA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114387533 | |||||
| chr5:114387743
|
C | G | 1 | a0002c0002t0001g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1219-16695C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114387743 | ||||||
| chr5:114387922
|
G | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(141): Show | 145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1219-16516G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114387922 | ||||||
| chr5:114388008
|
A | G | 4 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG01884.hp1 HG02572.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1219-16430A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114388008 | ||||||
| chr5:114388036
|
C | T | 7 | a0002c0002t0001g0201a0002c0002t0001g0202a0002c0002t0001g0203others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1219-16402C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114388036 | ||||||
| chr5:114388043
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1219-16395C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114388043 | ||||||
| chr5:114388127
|
A | G | 1 | a0002c0002t0001g0201 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1219-16311A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114388127 | ||||||
| chr5:114388134
|
G | A | 80 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(77): Show | 81 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(78): Show |
intron_variant | MODIFIER | c.1219-16304G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114388134 | ||||||
| chr5:114388187
|
G | A | 1 | a0002c0002t0001g0209 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1219-16251G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114388187 | ||||||
| chr5:114388249
|
C | T | 2 | a0001c0001t0001g0248a0003c0009t0001g0194 | 2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1219-16189C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114388249 | ||||||
| chr5:114388474
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1219-15964A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114388474 | ||||||
| chr5:114388632
|
G | A | 9 | a0002c0002t0001g0004a0002c0002t0001g0008a0002c0002t0001g0009others(6): Show | 9 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.1219-15806G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114388632 | ||||||
| chr5:114388700
|
A | T | 2 | a0001c0001t0001g0057a0001c0001t0001g0061 | 2 | HG01099.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1219-15738A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114388700 | ||||||
| chr5:114388725
|
A | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0062 | 2 | HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1219-15713A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114388725 | ||||||
| chr5:114388745
|
A | G | 1 | a0001c0001t0001g0228 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1219-15693A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114388745 | ||||||
| chr5:114388805
|
A | T | 4 | a0002c0005t0001g0013a0002c0005t0001g0014a0002c0005t0001g0015others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1219-15633A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114388805 | ||||||
| chr5:114388811
|
GT | G | 7 | a0002c0002t0001g0004a0002c0002t0001g0008a0002c0002t0001g0009others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.1219-15619delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114388811 | |||||
| chr5:114389140
|
A | G | 9 | a0002c0002t0001g0004a0002c0002t0001g0008a0002c0002t0001g0009others(6): Show | 9 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.1219-15298A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114389140 | ||||||
| chr5:114389217
|
G | T | 11 | a0001c0001t0001g0248a0003c0003t0001g0193a0003c0003t0001g0196others(8): Show | 11 | HG02809.hp1 HG02895.hp1 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.1219-15221G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114389217 | ||||||
| chr5:114389240
|
C | G | 1 | a0002c0002t0001g0124 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1219-15198C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114389240 | ||||||
| chr5:114389492
|
G | A | 9 | a0002c0002t0001g0004a0002c0002t0001g0008a0002c0002t0001g0009others(6): Show | 9 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.1219-14946G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114389492 | ||||||
| chr5:114389649
|
A | T | 11 | a0001c0001t0001g0248a0003c0003t0001g0193a0003c0003t0001g0196others(8): Show | 11 | HG02809.hp1 HG02895.hp1 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.1219-14789A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114389649 | ||||||
| chr5:114389692
|
A | G | 2 | a0002c0002t0001g0102a0002c0002t0001g0103 | 2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1219-14746A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114389692 | ||||||
| chr5:114389797
|
G | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(134): Show | 138 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1219-14641G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114389797 | ||||||
| chr5:114389974
|
A | G | 80 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(77): Show | 81 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(78): Show |
intron_variant | MODIFIER | c.1219-14464A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114389974 | ||||||
| chr5:114390013
|
C | G | 29 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0082others(26): Show | 29 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.1219-14425C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114390013 | ||||||
| chr5:114390177
|
A | G | 2 | a0002c0002t0001g0169a0002c0002t0001g0182 | 2 | HG02132.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1219-14261A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114390177 | ||||||
| chr5:114390213
|
G | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(76): Show | 80 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(77): Show |
intron_variant | MODIFIER | c.1219-14225G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114390213 | ||||||
| chr5:114390280
|
A | G | 4 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG01884.hp1 HG02572.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1219-14158A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114390280 | ||||||
| chr5:114390603
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1219-13835A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114390603 | ||||||
| chr5:114390705
|
A | C | 50 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0082others(47): Show | 50 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.1219-13733A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114390705 | ||||||
| chr5:114390842
|
G | A | 18 | a0001c0001t0001g0248a0002c0002t0001g0201a0002c0002t0001g0202others(15): Show | 18 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.1219-13596G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114390842 | ||||||
| chr5:114390907
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1219-13531G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114390907 | ||||||
| chr5:114391241
|
C | A | 14 | a0001c0021t0001g0220a0002c0002t0001g0004a0002c0002t0001g0008others(11): Show | 14 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.1219-13197C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114391241 | ||||||
| chr5:114391292
|
A | T | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1219-13146A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114391292 | ||||||
| chr5:114391352
|
T | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0021others(54): Show | 58 | HG01081.hp2 HG01099.hp1 HG01175.hp2 others(55): Show |
intron_variant | MODIFIER | c.1219-13086T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114391352 | ||||||
| chr5:114391415
|
C | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(128): Show | 132 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1219-13023C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114391415 | ||||||
| chr5:114391457
|
G | A | 5 | a0001c0021t0001g0220a0006c0007t0001g0104a0006c0007t0001g0221others(2): Show | 5 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1219-12981G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114391457 | ||||||
| chr5:114391488
|
C | G | 2 | a0002c0002t0001g0102a0002c0002t0001g0103 | 2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1219-12950C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114391488 | ||||||
| chr5:114391509
|
G | C | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0062 | 3 | HG02280.hp1 HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1219-12929G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114391509 | ||||||
| chr5:114391662
|
T | C | 1 | a0001c0001t0001g0039 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1219-12776T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114391662 | ||||||
| chr5:114391801
|
A | C | 8 | a0002c0002t0001g0129a0002c0002t0001g0157a0002c0002t0001g0158others(5): Show | 8 | HG02132.hp1 NA18959.hp1 NA18986.hp2 others(5): Show |
intron_variant | MODIFIER | c.1219-12637A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114391801 | ||||||
| chr5:114391937
|
T | C | 9 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(6): Show | 9 | HG01074.hp1 HG02486.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1219-12501T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114391937 | ||||||
| chr5:114391985
|
C | CT | 10 | a0002c0002t0001g0236a0002c0002t0001g0238a0002c0002t0001g0240others(7): Show | 10 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1219-12446dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114391985 | |||||
| chr5:114392442
|
C | G | 4 | a0003c0003t0001g0197a0003c0003t0001g0198a0003c0003t0001g0199others(1): Show | 4 | HG02922.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1219-11996C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114392442 | ||||||
| chr5:114392503
|
G | A | 1 | a0004c0012t0001g0143 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1219-11935G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114392503 | ||||||
| chr5:114392548
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1219-11890G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114392548 | ||||||
| chr5:114392669
|
C | T | 1 | a0002c0002t0001g0184 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1219-11769C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114392669 | ||||||
| chr5:114392706
|
T | A | 2 | a0002c0002t0001g0102a0002c0002t0001g0103 | 2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1219-11732T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114392706 | ||||||
| chr5:114392806
|
GT | G | 27 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0030others(24): Show | 27 | HG01081.hp1 HG01099.hp2 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.1219-11619delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114392806 | |||||
| chr5:114392806
|
GTT | G | 50 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0021others(47): Show | 51 | HG00280.hp1 HG01081.hp2 HG01099.hp1 others(48): Show |
intron_variant | MODIFIER | c.1219-11620_1219-11 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114392806 | |||||
| chr5:114393010
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1219-11428C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114393010 | ||||||
| chr5:114393340
|
T | A | 2 | a0007c0010t0001g0191a0007c0010t0001g0192 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1219-11098T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114393340 | ||||||
| chr5:114393410
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1219-11028G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114393410 | ||||||
| chr5:114393778
|
CT | C | 3 | a0004c0008t0001g0010a0004c0008t0001g0011a0004c0008t0001g0012 | 3 | HG02896.hp1 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1219-10656delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114393778 | |||||
| chr5:114393782
|
T | A | 127 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(124): Show | 128 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1219-10656T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114393782 | ||||||
| chr5:114393783
|
A | T | 1 | a0001c0001t0001g0065 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1219-10655A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114393783 | ||||||
| chr5:114393860
|
G | A | 1 | a0002c0002t0001g0236 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1219-10578G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114393860 | ||||||
| chr5:114393901
|
C | T | 10 | a0002c0002t0001g0236a0002c0002t0001g0238a0002c0002t0001g0240others(7): Show | 10 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1219-10537C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114393901 | ||||||
| chr5:114393927
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1219-10511A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114393927 | ||||||
| chr5:114393970
|
A | G | 14 | a0001c0021t0001g0220a0002c0002t0001g0004a0002c0002t0001g0008others(11): Show | 14 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.1219-10468A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114393970 | ||||||
| chr5:114393973
|
CAT | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(126): Show | 130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1219-10464_1219-10 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114393973 | ||||||
| chr5:114394005
|
T | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(75): Show | 79 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(76): Show |
intron_variant | MODIFIER | c.1219-10433T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114394005 | ||||||
| chr5:114394195
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1219-10243A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114394195 | ||||||
| chr5:114394202
|
A | G | 4 | a0003c0003t0001g0197a0003c0003t0001g0198a0003c0003t0001g0199others(1): Show | 4 | HG02922.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1219-10236A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114394202 | ||||||
| chr5:114394404
|
T | G | 1 | a0002c0002t0001g0180 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1219-10034T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114394404 | ||||||
| chr5:114394576
|
C | T | 11 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0094others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1219-9862C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114394576 | ||||||
| chr5:114394710
|
G | A | 67 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(64): Show | 68 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(65): Show |
intron_variant | MODIFIER | c.1219-9728G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114394710 | ||||||
| chr5:114395074
|
T | C | 2 | a0002c0002t0001g0126a0002c0002t0001g0158 | 2 | NA18959.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1219-9364T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395074 | ||||||
| chr5:114395272
|
C | T | 1 | a0002c0005t0001g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1219-9166C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395272 | ||||||
| chr5:114395311
|
A | G | 2 | a0002c0002t0001g0128a0002c0002t0001g0132 | 2 | HG01169.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1219-9127A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395311 | ||||||
| chr5:114395315
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1219-9123G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395315 | ||||||
| chr5:114395318
|
G | A | 1 | a0002c0002t0001g0168 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1219-9120G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395318 | ||||||
| chr5:114395322
|
T | C | 1 | a0002c0002t0001g0133 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1219-9116T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395322 | ||||||
| chr5:114395381
|
A | C | 68 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(65): Show | 69 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(66): Show |
intron_variant | MODIFIER | c.1219-9057A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395381 | ||||||
| chr5:114395430
|
A | T | 1 | a0001c0001t0001g0043 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1219-9008A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395430 | ||||||
| chr5:114395462
|
T | C | 5 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0107others(2): Show | 5 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1219-8976T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395462 | ||||||
| chr5:114395708
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1219-8730A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395708 | ||||||
| chr5:114395726
|
A | G | 42 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0082others(39): Show | 42 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.1219-8712A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395726 | ||||||
| chr5:114395822
|
C | G | 2 | a0001c0001t0001g0019a0001c0001t0001g0020 | 2 | NA19088.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1219-8616C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395822 | ||||||
| chr5:114395826
|
C | T | 68 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(65): Show | 69 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(66): Show |
intron_variant | MODIFIER | c.1219-8612C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395826 | ||||||
| chr5:114395877
|
C | T | 7 | a0002c0002t0001g0004a0002c0002t0001g0008a0002c0002t0001g0009others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.1219-8561C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395877 | ||||||
| chr5:114395959
|
T | C | 3 | a0002c0005t0001g0013a0002c0005t0001g0014a0002c0005t0001g0015 | 3 | HG01243.hp2 HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1219-8479T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395959 | ||||||
| chr5:114396054
|
A | G | 7 | a0002c0002t0001g0201a0002c0002t0001g0202a0002c0002t0001g0203others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1219-8384A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114396054 | ||||||
| chr5:114396096
|
A | C | 1 | a0002c0002t0001g0003 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1219-8342A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114396096 | ||||||
| chr5:114396124
|
A | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0021others(63): Show | 67 | HG00280.hp1 HG01081.hp2 HG01099.hp1 others(64): Show |
intron_variant | MODIFIER | c.1219-8314A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114396124 | ||||||
| chr5:114396141
|
G | T | 1 | a0002c0002t0001g0132 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1219-8297G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114396141 | ||||||
| chr5:114396142
|
C | A | 1 | a0001c0001t0001g0231 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1219-8296C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114396142 | ||||||
| chr5:114396157
|
CTCTT | C | 87 | a0001c0001t0001g0063a0002c0002t0001g0002a0002c0002t0001g0003others(84): Show | 87 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1219-8275_1219-827 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114396157 | |||||
| chr5:114396204
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1219-8234A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114396204 | ||||||
| chr5:114396313
|
C | G | 1 | a0001c0001t0001g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1219-8125C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114396313 | ||||||
| chr5:114396313
|
CTAAT | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(64): Show | 68 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(65): Show |
intron_variant | MODIFIER | c.1219-8121_1219-811 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114396313 | |||||
| chr5:114396490
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1219-7948G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114396490 | ||||||
| chr5:114396530
|
G | A | 1 | a0002c0005t0001g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1219-7908G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114396530 | ||||||
| chr5:114396551
|
CT | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(141): Show | 145 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.1219-7872delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114396551 | |||||
| chr5:114396688
|
A | G | 45 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0021others(42): Show | 46 | HG01099.hp1 HG01175.hp2 HG01257.hp1 others(43): Show |
intron_variant | MODIFIER | c.1219-7750A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114396688 | ||||||
| chr5:114396717
|
T | G | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1219-7721T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114396717 | ||||||
| chr5:114396830
|
C | T | 12 | a0001c0001t0001g0248a0002c0002t0001g0004a0003c0003t0001g0193others(9): Show | 12 | HG02809.hp1 HG02895.hp1 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.1219-7608C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114396830 | ||||||
| chr5:114396862
|
T | A | 1 | a0003c0003t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1219-7576T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114396862 | ||||||
| chr5:114397033
|
C | T | 11 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0094others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1219-7405C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114397033 | ||||||
| chr5:114397034
|
G | A | 10 | a0002c0002t0001g0236a0002c0002t0001g0238a0002c0002t0001g0240others(7): Show | 10 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1219-7404G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114397034 | ||||||
| chr5:114397084
|
A | G | 1 | a0002c0002t0001g0133 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1219-7354A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114397084 | ||||||
| chr5:114397114
|
C | A | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1219-7324C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114397114 | ||||||
| chr5:114397167
|
A | G | 10 | a0002c0002t0001g0236a0002c0002t0001g0238a0002c0002t0001g0240others(7): Show | 10 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1219-7271A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114397167 | ||||||
| chr5:114397412
|
G | T | 62 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(59): Show | 63 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(60): Show |
intron_variant | MODIFIER | c.1219-7026G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114397412 | ||||||
| chr5:114397542
|
A | G | 1 | a0001c0018t0001g0029 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1219-6896A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114397542 | ||||||
| chr5:114397548
|
G | A | 2 | a0001c0001t0001g0247a0002c0002t0001g0119 | 2 | HG04115.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1219-6890G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114397548 | ||||||
| chr5:114397634
|
C | T | 1 | a0002c0002t0001g0152 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1219-6804C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114397634 | ||||||
| chr5:114398039
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1219-6399C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114398039 | ||||||
| chr5:114398254
|
C | T | 1 | a0011c0016t0003g0177 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1219-6184C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114398254 | ||||||
| chr5:114398313
|
A | T | 1 | a0009c0023t0001g0160 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1219-6125A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114398313 | ||||||
| chr5:114398484
|
G | GT | 35 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0083others(32): Show | 35 | HG00738.hp1 HG01074.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.1219-5941dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114398484 | |||||
| chr5:114398484
|
G | GTT | 8 | a0001c0001t0001g0082a0001c0001t0001g0106a0001c0006t0001g0098others(5): Show | 8 | HG00642.hp1 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1219-5942_1219-594 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114398484 | |||||
| chr5:114398676
|
G | A | 1 | a0002c0002t0001g0201 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1219-5762G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114398676 | ||||||
| chr5:114398721
|
G | T | 58 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0082others(55): Show | 58 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.1219-5717G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114398721 | ||||||
| chr5:114398780
|
A | G | 58 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0082others(55): Show | 58 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.1219-5658A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114398780 | ||||||
| chr5:114398958
|
T | G | 1 | a0002c0002t0001g0206 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1219-5480T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114398958 | ||||||
| chr5:114398999
|
T | A | 1 | a0002c0002t0001g0134 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1219-5439T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114398999 | ||||||
| chr5:114399116
|
G | C | 1 | a0002c0002t0001g0141 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1219-5322G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399116 | ||||||
| chr5:114399367
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1219-5071T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399367 | ||||||
| chr5:114399394
|
T | G | 13 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0094others(10): Show | 13 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1219-5044T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399394 | ||||||
| chr5:114399431
|
C | T | 1 | a0002c0002t0001g0071 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1219-5007C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399431 | ||||||
| chr5:114399530
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1219-4908G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399530 | ||||||
| chr5:114399591
|
A | G | 4 | a0002c0002t0001g0236a0004c0008t0001g0010a0004c0008t0001g0011others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1219-4847A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399591 | ||||||
| chr5:114399616
|
A | G | 7 | a0002c0002t0001g0201a0002c0002t0001g0202a0002c0002t0001g0203others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1219-4822A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399616 | ||||||
| chr5:114399723
|
T | A | 47 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0082others(44): Show | 47 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1219-4715T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399723 | ||||||
| chr5:114399773
|
C | A | 1 | a0002c0002t0001g0187 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1219-4665C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399773 | ||||||
| chr5:114399833
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0037 | 2 | HG03195.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1219-4605G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399833 | ||||||
| chr5:114399847
|
C | T | 1 | a0002c0002t0001g0206 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1219-4591C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399847 | ||||||
| chr5:114399861
|
A | G | 1 | a0001c0001t0001g0023 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1219-4577A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399861 | ||||||
| chr5:114399929
|
T | G | 2 | a0001c0001t0001g0086a0001c0021t0001g0220 | 2 | HG01884.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1219-4509T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399929 | ||||||
| chr5:114399929
|
T | TTG | 7 | a0002c0002t0001g0004a0003c0003t0001g0193a0003c0003t0001g0196others(4): Show | 7 | HG02922.hp2 HG03209.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1219-4509_1219-450 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399929 | ||||||
| chr5:114399930
|
G | GT | 51 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0035others(48): Show | 51 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1219-4496dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114399930 | |||||
| chr5:114399930
|
G | T | 13 | a0001c0001t0001g0086a0001c0001t0001g0248a0001c0021t0001g0220others(10): Show | 13 | HG01884.hp1 HG02630.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.1219-4508G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399930 | ||||||
| chr5:114400081
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1219-4357T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114400081 | ||||||
| chr5:114400181
|
C | G | 1 | a0002c0002t0001g0207 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1219-4257C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114400181 | ||||||
| chr5:114400193
|
T | C | 2 | a0002c0002t0001g0102a0002c0002t0001g0103 | 2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1219-4245T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114400193 | ||||||
| chr5:114400310
|
A | G | 1 | a0002c0002t0001g0152 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1219-4128A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114400310 | ||||||
| chr5:114400350
|
C | T | 10 | a0002c0002t0001g0236a0002c0002t0001g0238a0002c0002t0001g0240others(7): Show | 10 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1219-4088C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114400350 | ||||||
| chr5:114400400
|
A | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(56): Show | 60 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(57): Show |
intron_variant | MODIFIER | c.1219-4038A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114400400 | ||||||
| chr5:114400442
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1219-3996C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114400442 | ||||||
| chr5:114400550
|
G | C | 8 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0102others(5): Show | 8 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.1219-3888G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114400550 | ||||||
| chr5:114400571
|
C | T | 1 | a0004c0012t0001g0142 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1219-3867C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114400571 | ||||||
| chr5:114400719
|
G | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(58): Show | 62 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(59): Show |
intron_variant | MODIFIER | c.1219-3719G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114400719 | ||||||
| chr5:114400768
|
C | A | 2 | a0002c0002t0001g0209a0002c0002t0001g0210 | 2 | HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1219-3670C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114400768 | ||||||
| chr5:114400899
|
T | C | 1 | a0002c0002t0001g0207 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1219-3539T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114400899 | ||||||
| chr5:114400969
|
CTA | C | 3 | a0001c0001t0001g0080a0002c0002t0001g0008a0002c0002t0001g0009 | 3 | HG02523.hp1 HG04204.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1219-3467_1219-346 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114400969 | |||||
| chr5:114400981
|
T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(134): Show | 138 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(135): Show |
intron_variant | MODIFIER | c.1219-3457T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114400981 | ||||||
| chr5:114401043
|
C | G | 1 | a0001c0001t0001g0053 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1219-3395C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114401043 | ||||||
| chr5:114401053
|
G | T | 3 | a0002c0005t0001g0013a0002c0005t0001g0014a0002c0005t0001g0015 | 3 | HG01243.hp2 HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1219-3385G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114401053 | ||||||
| chr5:114401302
|
C | G | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1219-3136C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114401302 | ||||||
| chr5:114401365
|
T | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(135): Show | 139 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(136): Show |
intron_variant | MODIFIER | c.1219-3073T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114401365 | ||||||
| chr5:114401453
|
C | G | 1 | a0001c0001t0001g0246 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1219-2985C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114401453 | ||||||
| chr5:114401464
|
G | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(58): Show | 62 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(59): Show |
intron_variant | MODIFIER | c.1219-2974G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114401464 | ||||||
| chr5:114401686
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1219-2752G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114401686 | ||||||
| chr5:114402302
|
G | T | 2 | a0001c0006t0001g0093a0001c0006t0001g0095 | 2 | HG02055.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1219-2136G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114402302 | ||||||
| chr5:114402335
|
G | T | 1 | a0002c0002t0001g0008 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1219-2103G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114402335 | ||||||
| chr5:114402402
|
G | C | 1 | a0002c0002t0001g0182 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1219-2036G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114402402 | ||||||
| chr5:114402403
|
G | T | 1 | a0001c0001t0001g0048 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1219-2035G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114402403 | ||||||
| chr5:114402502
|
A | G | 1 | a0002c0002t0001g0122 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1219-1936A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114402502 | ||||||
| chr5:114402570
|
TAAGG | T | 5 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0107others(2): Show | 5 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1219-1866_1219-186 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114402570 | |||||
| chr5:114402615
|
T | A | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1219-1823T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114402615 | ||||||
| chr5:114402764
|
G | C | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1219-1674G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114402764 | ||||||
| chr5:114402829
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1219-1609T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114402829 | ||||||
| chr5:114402977
|
A | T | 1 | a0001c0001t0001g0248 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1219-1461A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114402977 | ||||||
| chr5:114403017
|
G | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(67): Show | 71 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(68): Show |
intron_variant | MODIFIER | c.1219-1421G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114403017 | ||||||
| chr5:114403213
|
A | T | 4 | a0002c0005t0001g0013a0002c0005t0001g0014a0002c0005t0001g0015others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1219-1225A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114403213 | ||||||
| chr5:114403266
|
C | T | 2 | a0007c0010t0001g0191a0007c0010t0001g0192 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1219-1172C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114403266 | ||||||
| chr5:114403299
|
T | C | 1 | a0001c0001t0001g0019 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1219-1139T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114403299 | ||||||
| chr5:114403580
|
C | G | 6 | a0002c0002t0001g0238a0002c0002t0001g0240a0002c0011t0001g0239others(3): Show | 6 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1219-858C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114403580 | ||||||
| chr5:114403776
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1219-662C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114403776 | ||||||
| chr5:114404333
|
G | T | 1 | a0001c0001t0001g0065 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1219-105G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114404333 | ||||||
| chr5:114404940
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1637+84G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114404940 | ||||||
| chr5:114405269
|
G | A | 6 | a0001c0001t0001g0082a0001c0021t0001g0220a0006c0007t0001g0104others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1637+413G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114405269 | ||||||
| chr5:114405314
|
T | C | 13 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0054others(10): Show | 13 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1637+458T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114405314 | ||||||
| chr5:114405356
|
G | A | 1 | a0002c0002t0001g0133 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1637+500G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114405356 | ||||||
| chr5:114405532
|
T | C | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637+676T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114405532 | ||||||
| chr5:114405584
|
C | A | 1 | a0002c0002t0001g0207 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1637+728C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114405584 | ||||||
| chr5:114405632
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1637+776G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114405632 | ||||||
| chr5:114405716
|
GT | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(142): Show | 146 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1637+872delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114405716 | |||||
| chr5:114405773
|
C | T | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637+917C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114405773 | ||||||
| chr5:114405990
|
G | A | 8 | a0001c0001t0001g0034a0001c0001t0001g0227a0001c0001t0001g0229others(5): Show | 8 | HG00280.hp1 HG01081.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.1637+1134G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114405990 | ||||||
| chr5:114405996
|
C | A | 1 | a0002c0002t0001g0124 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1637+1140C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114405996 | ||||||
| chr5:114406000
|
G | A | 9 | a0001c0001t0001g0034a0001c0001t0001g0227a0001c0001t0001g0229others(6): Show | 9 | HG00280.hp1 HG01081.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.1637+1144G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114406000 | ||||||
| chr5:114406002
|
A | C | 1 | a0002c0002t0001g0009 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1637+1146A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114406002 | ||||||
| chr5:114406016
|
T | A | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637+1160T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114406016 | ||||||
| chr5:114406208
|
T | C | 14 | a0001c0001t0001g0082a0001c0021t0001g0220a0002c0002t0001g0008others(11): Show | 14 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.1637+1352T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114406208 | ||||||
| chr5:114406302
|
GCTAT | G | 14 | a0001c0001t0001g0082a0001c0021t0001g0220a0002c0002t0001g0008others(11): Show | 14 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.1637+1451_1637+145 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114406302 | |||||
| chr5:114406345
|
T | C | 3 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0045 | 3 | HG01358.hp2 HG03654.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1637+1489T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114406345 | ||||||
| chr5:114406390
|
A | G | 10 | a0002c0002t0001g0236a0002c0002t0001g0238a0002c0002t0001g0240others(7): Show | 10 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1637+1534A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114406390 | ||||||
| chr5:114406742
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1637+1886T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114406742 | ||||||
| chr5:114406860
|
AAG | A | 6 | a0002c0002t0001g0238a0002c0002t0001g0240a0002c0011t0001g0239others(3): Show | 6 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1637+2010_1637+201 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114406860 | |||||
| chr5:114406868
|
T | G | 1 | a0002c0002t0001g0124 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1637+2012T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114406868 | ||||||
| chr5:114406888
|
T | A | 12 | a0001c0001t0001g0248a0002c0002t0001g0004a0003c0003t0001g0193others(9): Show | 12 | HG02809.hp1 HG02895.hp1 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.1637+2032T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114406888 | ||||||
| chr5:114407056
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1637+2200G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114407056 | ||||||
| chr5:114407075
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1637+2219T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114407075 | ||||||
| chr5:114407083
|
C | CACAAGGA others(26): Show |
1 | a0002c0002t0001g0138 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1637+2239_1637+227 others(37): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114407083 | |||||
| chr5:114407127
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1637+2271A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114407127 | ||||||
| chr5:114407172
|
G | T | 60 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(57): Show | 61 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(58): Show |
intron_variant | MODIFIER | c.1637+2316G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114407172 | ||||||
| chr5:114407434
|
T | A | 1 | a0002c0002t0001g0209 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1637+2578T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114407434 | ||||||
| chr5:114407757
|
A | G | 14 | a0001c0001t0001g0082a0001c0021t0001g0220a0002c0002t0001g0008others(11): Show | 14 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.1637+2901A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114407757 | ||||||
| chr5:114407766
|
C | G | 1 | a0003c0003t0001g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1637+2910C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114407766 | ||||||
| chr5:114407787
|
A | G | 3 | a0002c0002t0001g0163a0002c0002t0001g0175a0002c0017t0001g0178 | 3 | HG00438.hp2 NA18999.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1637+2931A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114407787 | ||||||
| chr5:114407931
|
C | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(68): Show | 72 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(69): Show |
intron_variant | MODIFIER | c.1637+3075C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114407931 | ||||||
| chr5:114407932
|
G | A | 7 | a0002c0002t0001g0201a0002c0002t0001g0202a0002c0002t0001g0203others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637+3076G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114407932 | ||||||
| chr5:114407956
|
A | G | 58 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0021others(55): Show | 59 | HG00741.hp1 HG01070.hp2 HG01099.hp1 others(56): Show |
intron_variant | MODIFIER | c.1637+3100A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114407956 | ||||||
| chr5:114408016
|
C | G | 1 | a0006c0007t0001g0222 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1637+3160C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114408016 | ||||||
| chr5:114408180
|
A | C | 6 | a0002c0002t0001g0238a0002c0002t0001g0240a0002c0011t0001g0239others(3): Show | 6 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1637+3324A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114408180 | ||||||
| chr5:114408201
|
C | CT | 29 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0094others(26): Show | 29 | HG00099.hp1 HG00280.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1637+3360dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114408201 | |||||
| chr5:114408311
|
G | T | 7 | a0002c0002t0001g0201a0002c0002t0001g0202a0002c0002t0001g0203others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637+3455G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114408311 | ||||||
| chr5:114408410
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1637+3554G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114408410 | ||||||
| chr5:114408639
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1637+3783A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114408639 | ||||||
| chr5:114408758
|
A | C | 39 | a0001c0001t0001g0066a0001c0001t0001g0083a0001c0001t0001g0084others(36): Show | 39 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1637+3902A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114408758 | ||||||
| chr5:114408762
|
C | T | 2 | a0002c0002t0001g0102a0002c0002t0001g0103 | 2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1637+3906C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114408762 | ||||||
| chr5:114408851
|
C | T | 3 | a0002c0002t0001g0240a0002c0011t0001g0239a0002c0011t0001g0241 | 3 | HG01243.hp1 HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1637+3995C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114408851 | ||||||
| chr5:114408899
|
A | G | 1 | a0003c0003t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1637+4043A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114408899 | ||||||
| chr5:114409009
|
C | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0021others(45): Show | 49 | HG00741.hp1 HG01070.hp2 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.1637+4153C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114409009 | ||||||
| chr5:114409084
|
A | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0031 | 2 | HG01099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1637+4228A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114409084 | ||||||
| chr5:114409174
|
C | T | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637+4318C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114409174 | ||||||
| chr5:114409178
|
C | G | 1 | a0002c0002t0001g0207 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1637+4322C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114409178 | ||||||
| chr5:114409332
|
T | TA | 72 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(69): Show | 73 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.1637+4485dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114409332 | |||||
| chr5:114409715
|
T | TAGGAGCA others(3): Show |
2 | a0001c0006t0001g0093a0001c0006t0001g0095 | 2 | HG02055.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1637+4868_1637+486 others(14): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114409715 | |||||
| chr5:114409771
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1637+4915G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114409771 | ||||||
| chr5:114409832
|
T | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(71): Show | 75 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(72): Show |
intron_variant | MODIFIER | c.1637+4976T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114409832 | ||||||
| chr5:114409867
|
T | TTCTC | 2 | a0007c0010t0001g0191a0007c0010t0001g0192 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1637+5029_1637+503 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114409867 | |||||
| chr5:114409995
|
T | C | 1 | a0002c0002t0001g0236 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1637+5139T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114409995 | ||||||
| chr5:114410041
|
T | C | 125 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(122): Show | 126 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(123): Show |
intron_variant | MODIFIER | c.1637+5185T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114410041 | ||||||
| chr5:114410052
|
C | G | 1 | a0010c0022t0001g0072 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1637+5196C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114410052 | ||||||
| chr5:114410115
|
G | C | 1 | a0003c0003t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1637+5259G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114410115 | ||||||
| chr5:114410140
|
C | G | 146 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(143): Show | 147 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1637+5284C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114410140 | ||||||
| chr5:114410219
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1637+5363G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114410219 | ||||||
| chr5:114410281
|
G | A | 1 | a0005c0004t0001g0149 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1637+5425G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114410281 | ||||||
| chr5:114410287
|
A | G | 3 | a0002c0002t0001g0153a0002c0002t0001g0161a0002c0002t0001g0183 | 3 | NA19001.hp1 NA19001.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1637+5431A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114410287 | ||||||
| chr5:114410429
|
G | A | 7 | a0002c0002t0001g0201a0002c0002t0001g0202a0002c0002t0001g0203others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637+5573G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114410429 | ||||||
| chr5:114410483
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(135): Show | 139 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(136): Show |
intron_variant | MODIFIER | c.1637+5627A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114410483 | ||||||
| chr5:114410632
|
T | A | 10 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0040others(7): Show | 10 | HG01978.hp2 HG02080.hp1 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.1637+5776T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114410632 | ||||||
| chr5:114410894
|
A | G | 7 | a0002c0002t0001g0201a0002c0002t0001g0202a0002c0002t0001g0203others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637+6038A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114410894 | ||||||
| chr5:114410944
|
C | T | 1 | a0002c0002t0001g0117 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1637+6088C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114410944 | ||||||
| chr5:114411011
|
G | A | 5 | a0001c0021t0001g0220a0006c0007t0001g0104a0006c0007t0001g0221others(2): Show | 5 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1637+6155G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114411011 | ||||||
| chr5:114411251
|
T | G | 13 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0054others(10): Show | 13 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1637+6395T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114411251 | ||||||
| chr5:114411449
|
T | G | 148 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(145): Show | 149 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1637+6593T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114411449 | ||||||
| chr5:114411544
|
C | T | 5 | a0001c0021t0001g0220a0006c0007t0001g0104a0006c0007t0001g0221others(2): Show | 5 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1637+6688C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114411544 | ||||||
| chr5:114411545
|
C | A | 5 | a0001c0021t0001g0220a0006c0007t0001g0104a0006c0007t0001g0221others(2): Show | 5 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1637+6689C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114411545 | ||||||
| chr5:114411572
|
G | C | 13 | a0001c0021t0001g0220a0002c0002t0001g0008a0002c0002t0001g0009others(10): Show | 13 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.1637+6716G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114411572 | ||||||
| chr5:114411576
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1637+6720A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114411576 | ||||||
| chr5:114411671
|
A | AG | 8 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0064others(5): Show | 8 | HG01081.hp1 HG01081.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.1637+6820dupG | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114411671 | |||||
| chr5:114411954
|
T | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(145): Show | 149 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1637+7098T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114411954 | ||||||
| chr5:114412391
|
A | G | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1637+7535A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114412391 | ||||||
| chr5:114412438
|
A | ATAGAGT | 148 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(145): Show | 149 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1637+7583_1637+758 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114412438 | |||||
| chr5:114412523
|
A | G | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637+7667A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114412523 | ||||||
| chr5:114412685
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1637+7829G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114412685 | ||||||
| chr5:114412817
|
A | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0049 | 2 | HG01943.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1637+7961A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114412817 | ||||||
| chr5:114412874
|
C | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(129): Show | 133 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(130): Show |
intron_variant | MODIFIER | c.1637+8018C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114412874 | ||||||
| chr5:114412918
|
A | G | 1 | a0002c0002t0001g0158 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1637+8062A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114412918 | ||||||
| chr5:114413262
|
C | CTTGTTTT others(3): Show |
1 | a0002c0002t0001g0138 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1637+8419_1637+842 others(14): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114413262 | |||||
| chr5:114413311
|
T | A | 1 | a0002c0002t0001g0009 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1637+8455T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114413311 | ||||||
| chr5:114413346
|
A | G | 148 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(145): Show | 149 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1637+8490A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114413346 | ||||||
| chr5:114413348
|
AAT | A | 8 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0102others(5): Show | 8 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.1637+8493_1637+849 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114413348 | ||||||
| chr5:114413505
|
C | G | 6 | a0002c0002t0001g0117a0002c0002t0001g0152a0002c0002t0001g0159others(3): Show | 6 | HG00741.hp2 HG01261.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1637+8649C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114413505 | ||||||
| chr5:114413641
|
T | A | 1 | a0001c0001t0001g0032 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1637+8785T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114413641 | ||||||
| chr5:114413733
|
A | C | 1 | a0002c0002t0001g0129 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1637+8877A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114413733 | ||||||
| chr5:114413763
|
A | G | 71 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(68): Show | 72 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(69): Show |
intron_variant | MODIFIER | c.1637+8907A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114413763 | ||||||
| chr5:114413842
|
C | A | 1 | a0001c0001t0001g0023 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1637+8986C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114413842 | ||||||
| chr5:114413891
|
C | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(145): Show | 149 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1637+9035C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114413891 | ||||||
| chr5:114414042
|
T | C | 58 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0082others(55): Show | 58 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.1637+9186T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114414042 | ||||||
| chr5:114414249
|
T | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(136): Show | 140 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(137): Show |
intron_variant | MODIFIER | c.1637+9393T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114414249 | ||||||
| chr5:114414367
|
G | C | 2 | a0002c0002t0001g0155a0002c0002t0001g0164 | 2 | HG00558.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1637+9511G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114414367 | ||||||
| chr5:114414469
|
T | C | 2 | a0007c0010t0001g0191a0007c0010t0001g0192 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1637+9613T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114414469 | ||||||
| chr5:114414512
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1637+9656C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114414512 | ||||||
| chr5:114414513
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1637+9657G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114414513 | ||||||
| chr5:114414748
|
T | G | 72 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(69): Show | 73 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.1637+9892T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114414748 | ||||||
| chr5:114415128
|
A | G | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637+10272A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114415128 | ||||||
| chr5:114415328
|
C | G | 1 | a0002c0002t0001g0116 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1637+10472C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114415328 | ||||||
| chr5:114415424
|
C | CGT | 3 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215 | 3 | HG02886.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1637+10579_1637+10 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114415424 | |||||
| chr5:114415710
|
A | C | 17 | a0001c0001t0001g0082a0001c0001t0001g0212a0001c0021t0001g0220others(14): Show | 17 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.1637+10854A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114415710 | ||||||
| chr5:114415719
|
T | G | 2 | a0001c0001t0001g0019a0001c0001t0001g0020 | 2 | NA19088.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1637+10863T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114415719 | ||||||
| chr5:114415895
|
T | C | 2 | a0007c0010t0001g0191a0007c0010t0001g0192 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1637+11039T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114415895 | ||||||
| chr5:114416190
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1637+11334A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114416190 | ||||||
| chr5:114416395
|
C | T | 1 | a0002c0002t0001g0154 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1637+11539C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114416395 | ||||||
| chr5:114416420
|
T | G | 148 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(145): Show | 149 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1637+11564T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114416420 | ||||||
| chr5:114416663
|
G | A | 1 | a0003c0003t0001g0197 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1637+11807G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114416663 | ||||||
| chr5:114416827
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1637+11971A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114416827 | ||||||
| chr5:114417226
|
C | T | 1 | a0002c0002t0001g0124 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1637+12370C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114417226 | ||||||
| chr5:114417303
|
T | G | 7 | a0002c0002t0001g0236a0002c0002t0001g0238a0002c0002t0001g0240others(4): Show | 7 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637+12447T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114417303 | ||||||
| chr5:114417357
|
G | A | 1 | a0006c0007t0001g0223 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1637+12501G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114417357 | ||||||
| chr5:114417397
|
A | G | 1 | a0001c0015t0001g0219 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1637+12541A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114417397 | ||||||
| chr5:114417424
|
G | C | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637+12568G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114417424 | ||||||
| chr5:114417674
|
A | T | 15 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0102others(12): Show | 15 | HG00099.hp1 HG00280.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1637+12818A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114417674 | ||||||
| chr5:114417740
|
T | A | 2 | a0002c0002t0001g0102a0002c0002t0001g0103 | 2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1637+12884T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114417740 | ||||||
| chr5:114418027
|
A | G | 3 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0088 | 3 | HG01346.hp2 HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1637+13171A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114418027 | ||||||
| chr5:114418107
|
G | A | 1 | a0002c0002t0001g0124 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1637+13251G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114418107 | ||||||
| chr5:114418260
|
T | G | 1 | a0001c0001t0001g0022 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1637+13404T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114418260 | ||||||
| chr5:114418557
|
T | A | 1 | a0001c0001t0001g0053 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1637+13701T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114418557 | ||||||
| chr5:114418749
|
G | C | 1 | a0001c0001t0001g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1637+13893G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114418749 | ||||||
| chr5:114418772
|
A | G | 1 | a0002c0002t0001g0175 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1637+13916A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114418772 | ||||||
| chr5:114418775
|
T | G | 11 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(8): Show | 11 | HG01074.hp1 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1637+13919T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114418775 | ||||||
| chr5:114419007
|
C | T | 1 | a0003c0003t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1637+14151C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114419007 | ||||||
| chr5:114419044
|
G | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(58): Show | 62 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(59): Show |
intron_variant | MODIFIER | c.1637+14188G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114419044 | ||||||
| chr5:114419934
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1637+15078G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114419934 | ||||||
| chr5:114419940
|
A | G | 1 | a0002c0002t0001g0122 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1637+15084A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114419940 | ||||||
| chr5:114420100
|
T | C | 60 | a0001c0001t0001g0066a0001c0001t0001g0082a0001c0001t0001g0083others(57): Show | 60 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.1637+15244T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114420100 | ||||||
| chr5:114420167
|
C | T | 1 | a0002c0002t0001g0162 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1637+15311C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114420167 | ||||||
| chr5:114420236
|
C | T | 6 | a0001c0001t0001g0082a0001c0021t0001g0220a0006c0007t0001g0104others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1637+15380C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114420236 | ||||||
| chr5:114420262
|
T | C | 1 | a0002c0002t0001g0179 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1637+15406T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114420262 | ||||||
| chr5:114420270
|
C | G | 4 | a0002c0002t0001g0236a0002c0002t0001g0238a0002c0014t0001g0017others(1): Show | 4 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1637+15414C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114420270 | ||||||
| chr5:114420585
|
G | A | 9 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0102others(6): Show | 9 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.1637+15729G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114420585 | ||||||
| chr5:114420611
|
G | C | 1 | a0002c0002t0001g0208 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1637+15755G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114420611 | ||||||
| chr5:114420740
|
T | C | 1 | a0002c0002t0001g0114 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1637+15884T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114420740 | ||||||
| chr5:114420824
|
A | G | 1 | a0001c0001t0001g0228 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1637+15968A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114420824 | ||||||
| chr5:114420919
|
T | TAAAAATA others(315): Show |
1 | a0002c0002t0001g0123 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1637+16079_1637+16 others(328): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114420919 | |||||
| chr5:114420927
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1637+16071A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114420927 | ||||||
| chr5:114420977
|
C | T | 8 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0102others(5): Show | 8 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.1637+16121C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114420977 | ||||||
| chr5:114421101
|
A | G | 1 | a0002c0002t0001g0207 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1637+16245A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114421101 | ||||||
| chr5:114421108
|
G | A | 72 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(69): Show | 73 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.1637+16252G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114421108 | ||||||
| chr5:114421119
|
G | T | 35 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0083others(32): Show | 35 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.1637+16263G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114421119 | ||||||
| chr5:114421165
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1637+16309T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114421165 | ||||||
| chr5:114421169
|
A | G | 4 | a0002c0002t0001g0236a0002c0002t0001g0238a0002c0014t0001g0017others(1): Show | 4 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1637+16313A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114421169 | ||||||
| chr5:114421226
|
C | CA | 111 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(108): Show | 112 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(109): Show |
intron_variant | MODIFIER | c.1637+16380dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114421226 | |||||
| chr5:114421226
|
C | CAA | 11 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0094others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1637+16379_1637+16 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114421226 | |||||
| chr5:114421254
|
G | T | 3 | a0002c0002t0001g0165a0002c0002t0001g0166a0002c0002t0001g0167 | 3 | HG01167.hp1 HG02040.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.1637+16398G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114421254 | ||||||
| chr5:114421287
|
A | T | 44 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0082others(41): Show | 44 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.1637+16431A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114421287 | ||||||
| chr5:114421342
|
G | A | 91 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(88): Show | 92 | HG00099.hp1 HG00280.hp2 HG00741.hp1 others(89): Show |
intron_variant | MODIFIER | c.1637+16486G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114421342 | ||||||
| chr5:114421426
|
G | A | 4 | a0002c0002t0001g0236a0002c0002t0001g0238a0002c0014t0001g0017others(1): Show | 4 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1637+16570G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114421426 | ||||||
| chr5:114421666
|
A | G | 27 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0082others(24): Show | 27 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1637+16810A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114421666 | ||||||
| chr5:114421750
|
C | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | HG01081.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1637+16894C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114421750 | ||||||
| chr5:114421784
|
A | G | 6 | a0001c0001t0001g0082a0001c0021t0001g0220a0006c0007t0001g0104others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1637+16928A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114421784 | ||||||
| chr5:114422258
|
G | A | 1 | a0002c0002t0001g0158 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1637+17402G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114422258 | ||||||
| chr5:114422268
|
A | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(137): Show | 141 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(138): Show |
intron_variant | MODIFIER | c.1637+17412A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114422268 | ||||||
| chr5:114422298
|
C | A | 1 | a0001c0001t0001g0230 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1637+17442C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114422298 | ||||||
| chr5:114422366
|
C | A | 1 | a0001c0001t0001g0228 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1637+17510C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114422366 | ||||||
| chr5:114422410
|
A | G | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG01074.hp1 HG01243.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1637+17554A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114422410 | ||||||
| chr5:114422476
|
G | A | 3 | a0002c0002t0001g0238a0002c0014t0001g0017a0008c0013t0001g0237 | 3 | HG02572.hp1 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1637+17620G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114422476 | ||||||
| chr5:114422476
|
G | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(141): Show | 145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1637+17620G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114422476 | ||||||
| chr5:114422623
|
G | A | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637+17767G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114422623 | ||||||
| chr5:114422701
|
C | A | 8 | a0001c0001t0001g0227a0001c0001t0001g0229a0001c0001t0001g0230others(5): Show | 8 | HG00280.hp1 HG01192.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1637+17845C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114422701 | ||||||
| chr5:114422793
|
A | C | 7 | a0002c0002t0001g0201a0002c0002t0001g0202a0002c0002t0001g0203others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637+17937A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114422793 | ||||||
| chr5:114422915
|
G | A | 4 | a0002c0002t0001g0236a0002c0002t0001g0238a0002c0014t0001g0017others(1): Show | 4 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1637+18059G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114422915 | ||||||
| chr5:114423009
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1637+18153C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423009 | ||||||
| chr5:114423018
|
A | G | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637+18162A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423018 | ||||||
| chr5:114423028
|
A | G | 58 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0021others(55): Show | 59 | HG00741.hp1 HG01070.hp2 HG01099.hp1 others(56): Show |
intron_variant | MODIFIER | c.1637+18172A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423028 | ||||||
| chr5:114423100
|
T | C | 3 | a0002c0002t0001g0165a0002c0002t0001g0166a0002c0002t0001g0167 | 3 | HG01167.hp1 HG02040.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.1637+18244T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423100 | ||||||
| chr5:114423205
|
A | T | 1 | a0003c0003t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1637+18349A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423205 | ||||||
| chr5:114423275
|
G | T | 71 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(68): Show | 72 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(69): Show |
intron_variant | MODIFIER | c.1637+18419G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423275 | ||||||
| chr5:114423288
|
G | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(135): Show | 139 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(136): Show |
intron_variant | MODIFIER | c.1637+18432G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423288 | ||||||
| chr5:114423317
|
A | G | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG01074.hp1 HG01243.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1637+18461A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423317 | ||||||
| chr5:114423333
|
C | A | 4 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(1): Show | 4 | HG01981.hp1 HG02148.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1637+18477C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423333 | ||||||
| chr5:114423343
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1637+18487C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423343 | ||||||
| chr5:114423380
|
A | G | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637+18524A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423380 | ||||||
| chr5:114423400
|
G | A | 4 | a0002c0002t0001g0236a0002c0002t0001g0238a0002c0014t0001g0017others(1): Show | 4 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1637+18544G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423400 | ||||||
| chr5:114423618
|
G | A | 11 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0102others(8): Show | 11 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.1637+18762G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423618 | ||||||
| chr5:114423619
|
C | T | 11 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0102others(8): Show | 11 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.1637+18763C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423619 | ||||||
| chr5:114423738
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(135): Show | 139 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(136): Show |
intron_variant | MODIFIER | c.1637+18882G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423738 | ||||||
| chr5:114423932
|
C | A | 1 | a0002c0002t0001g0125 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1637+19076C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423932 | ||||||
| chr5:114423978
|
T | C | 9 | a0001c0001t0001g0082a0001c0021t0001g0220a0004c0008t0001g0010others(6): Show | 9 | HG02622.hp1 HG02630.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1637+19122T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423978 | ||||||
| chr5:114424003
|
A | C | 1 | a0002c0002t0001g0171 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1637+19147A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114424003 | ||||||
| chr5:114424006
|
C | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(79): Show | 83 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(80): Show |
intron_variant | MODIFIER | c.1637+19150C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114424006 | ||||||
| chr5:114424223
|
T | A | 6 | a0001c0001t0001g0082a0001c0021t0001g0220a0006c0007t0001g0104others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1637+19367T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114424223 | ||||||
| chr5:114425005
|
G | A | 1 | a0002c0002t0001g0207 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1637+20149G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114425005 | ||||||
| chr5:114425200
|
T | G | 20 | a0001c0021t0001g0220a0002c0002t0001g0008a0002c0002t0001g0009others(17): Show | 20 | HG00099.hp1 HG00280.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.1637+20344T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114425200 | ||||||
| chr5:114425303
|
T | C | 2 | a0002c0002t0001g0102a0002c0002t0001g0103 | 2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1637+20447T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114425303 | ||||||
| chr5:114425310
|
C | A | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637+20454C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114425310 | ||||||
| chr5:114425337
|
T | C | 4 | a0003c0003t0001g0197a0003c0003t0001g0198a0003c0003t0001g0199others(1): Show | 4 | HG02922.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1637+20481T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114425337 | ||||||
| chr5:114425581
|
C | T | 2 | a0002c0002t0001g0102a0002c0002t0001g0103 | 2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1637+20725C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114425581 | ||||||
| chr5:114425674
|
T | C | 7 | a0002c0002t0001g0201a0002c0002t0001g0202a0002c0002t0001g0203others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637+20818T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114425674 | ||||||
| chr5:114425974
|
G | C | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1637+21118G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114425974 | ||||||
| chr5:114426011
|
C | T | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637+21155C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114426011 | ||||||
| chr5:114426017
|
C | CA | 13 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(10): Show | 13 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.1637+21176dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114426017 | |||||
| chr5:114426017
|
CA | C | 18 | a0001c0001t0001g0068a0001c0001t0001g0090a0001c0001t0001g0231others(15): Show | 18 | HG00738.hp2 HG01109.hp1 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.1637+21176delA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114426017 | |||||
| chr5:114426160
|
C | CA | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG01074.hp1 HG01243.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1637+21314dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114426160 | |||||
| chr5:114426171
|
T | A | 5 | a0001c0021t0001g0220a0006c0007t0001g0104a0006c0007t0001g0221others(2): Show | 5 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1637+21315T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114426171 | ||||||
| chr5:114426223
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1637+21367A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114426223 | ||||||
| chr5:114426372
|
C | G | 9 | a0001c0001t0001g0034a0001c0001t0001g0227a0001c0001t0001g0229others(6): Show | 9 | HG00280.hp1 HG01081.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.1637+21516C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114426372 | ||||||
| chr5:114426426
|
C | T | 1 | a0002c0002t0001g0114 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1637+21570C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114426426 | ||||||
| chr5:114426943
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1637+22087C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114426943 | ||||||
| chr5:114427113
|
A | G | 102 | a0001c0001t0001g0065a0001c0001t0001g0067a0001c0001t0001g0068others(99): Show | 102 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1637+22257A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114427113 | ||||||
| chr5:114427159
|
T | C | 247 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(244): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1637+22303T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114427159 | ||||||
| chr5:114427381
|
G | A | 1 | a0002c0002t0001g0124 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1637+22525G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114427381 | ||||||
| chr5:114427481
|
C | T | 1 | a0003c0003t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1637+22625C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114427481 | ||||||
| chr5:114427541
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0031 | 2 | HG01099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1637+22685G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114427541 | ||||||
| chr5:114428017
|
A | G | 1 | a0002c0002t0001g0113 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1637+23161A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114428017 | ||||||
| chr5:114428077
|
AT | A | 3 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218 | 3 | HG01074.hp1 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1637+23224delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114428077 | |||||
| chr5:114428087
|
A | T | 1 | a0001c0001t0001g0045 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1637+23231A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114428087 | ||||||
| chr5:114428091
|
C | T | 8 | a0001c0001t0001g0227a0001c0001t0001g0229a0001c0001t0001g0230others(5): Show | 8 | HG00280.hp1 HG01192.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1637+23235C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114428091 | ||||||
| chr5:114428167
|
C | G | 2 | a0001c0001t0001g0217a0001c0001t0001g0218 | 2 | HG01074.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1637+23311C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114428167 | ||||||
| chr5:114428208
|
A | G | 5 | a0001c0021t0001g0220a0006c0007t0001g0104a0006c0007t0001g0221others(2): Show | 5 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1637+23352A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114428208 | ||||||
| chr5:114428411
|
C | T | 11 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0094others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1637+23555C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114428411 | ||||||
| chr5:114428445
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1637+23589T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114428445 | ||||||
| chr5:114428749
|
C | T | 11 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0094others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1637+23893C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114428749 | ||||||
| chr5:114428958
|
C | A | 2 | a0002c0002t0001g0102a0002c0002t0001g0103 | 2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1637+24102C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114428958 | ||||||
| chr5:114429263
|
C | A | 2 | a0005c0004t0001g0147a0005c0004t0001g0149 | 2 | HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1637+24407C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114429263 | ||||||
| chr5:114429285
|
A | G | 111 | a0001c0001t0001g0034a0001c0001t0001g0065a0001c0001t0001g0067others(108): Show | 111 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1637+24429A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114429285 | ||||||
| chr5:114429354
|
T | G | 33 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 34 | HG01099.hp1 HG01175.hp2 HG01358.hp2 others(31): Show |
intron_variant | MODIFIER | c.1637+24498T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114429354 | ||||||
| chr5:114429634
|
G | A | 13 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0054others(10): Show | 13 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1637+24778G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114429634 | ||||||
| chr5:114429818
|
C | CT | 81 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(78): Show | 81 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1637+24985dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114429818 | |||||
| chr5:114429818
|
C | CTT | 16 | a0001c0001t0001g0065a0001c0001t0001g0070a0001c0001t0001g0089others(13): Show | 16 | HG00099.hp2 HG00642.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.1637+24984_1637+24 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114429818 | |||||
| chr5:114429818
|
CT | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(75): Show | 79 | HG00741.hp1 HG01070.hp2 HG01074.hp1 others(76): Show |
intron_variant | MODIFIER | c.1637+24985delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114429818 | |||||
| chr5:114429818
|
CTT | C | 14 | a0001c0001t0001g0049a0001c0001t0001g0054a0001c0001t0001g0055others(11): Show | 14 | HG01433.hp2 HG01993.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1637+24984_1637+24 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114429818 | |||||
| chr5:114429990
|
TA | T | 9 | a0001c0001t0001g0034a0001c0001t0001g0227a0001c0001t0001g0229others(6): Show | 9 | HG00280.hp1 HG01081.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.1637+25135delA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114429990 | ||||||
| chr5:114430067
|
C | G | 1 | a0009c0023t0001g0160 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1637+25211C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114430067 | ||||||
| chr5:114430849
|
T | A | 102 | a0001c0001t0001g0065a0001c0001t0001g0067a0001c0001t0001g0068others(99): Show | 102 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1637+25993T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114430849 | ||||||
| chr5:114431129
|
C | G | 1 | a0001c0001t0001g0075 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1637+26273C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114431129 | ||||||
| chr5:114431130
|
G | A | 8 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0102others(5): Show | 8 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.1637+26274G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114431130 | ||||||
| chr5:114431162
|
T | A | 1 | a0001c0001t0001g0053 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1637+26306T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114431162 | ||||||
| chr5:114431293
|
T | A | 3 | a0004c0008t0001g0010a0004c0008t0001g0011a0004c0008t0001g0012 | 3 | HG02896.hp1 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1637+26437T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114431293 | ||||||
| chr5:114431383
|
T | A | 1 | a0002c0002t0001g0206 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1637+26527T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114431383 | ||||||
| chr5:114431402
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1637+26546A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114431402 | ||||||
| chr5:114431638
|
CT | C | 60 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(57): Show | 61 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(58): Show |
intron_variant | MODIFIER | c.1637+26783delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114431638 | ||||||
| chr5:114431886
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1637+27030T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114431886 | ||||||
| chr5:114432152
|
T | C | 2 | a0005c0004t0001g0147a0005c0004t0001g0149 | 2 | HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1637+27296T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432152 | ||||||
| chr5:114432295
|
A | G | 6 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0005t0001g0013others(3): Show | 6 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.1637+27439A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432295 | ||||||
| chr5:114432391
|
C | T | 3 | a0002c0002t0001g0145a0002c0002t0001g0155a0002c0002t0001g0164 | 3 | HG00558.hp1 HG02523.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1637+27535C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432391 | ||||||
| chr5:114432395
|
T | C | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246 | 3 | NA18964.hp2 NA19074.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1637+27539T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432395 | ||||||
| chr5:114432429
|
C | A | 1 | a0001c0001t0001g0021 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1637+27573C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432429 | ||||||
| chr5:114432433
|
G | A | 245 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1637+27577G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432433 | ||||||
| chr5:114432469
|
T | TA | 7 | a0002c0002t0001g0201a0002c0002t0001g0202a0002c0002t0001g0203others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637+27616dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114432469 | |||||
| chr5:114432514
|
G | A | 1 | a0001c0001t0001g0001 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1637+27658G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432514 | ||||||
| chr5:114432550
|
C | T | 101 | a0001c0001t0001g0065a0001c0001t0001g0067a0001c0001t0001g0068others(98): Show | 101 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1637+27694C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432550 | ||||||
| chr5:114432678
|
A | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(203): Show | 207 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(204): Show |
intron_variant | MODIFIER | c.1637+27822A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432678 | ||||||
| chr5:114432714
|
C | T | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637+27858C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432714 | ||||||
| chr5:114432741
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1637+27885G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432741 | ||||||
| chr5:114432765
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1637+27909G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432765 | ||||||
| chr5:114432767
|
G | A | 1 | a0002c0002t0001g0236 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1637+27911G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432767 | ||||||
| chr5:114432849
|
G | C | 1 | a0001c0001t0001g0101 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1637+27993G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432849 | ||||||
| chr5:114432916
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1637+28060C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432916 | ||||||
| chr5:114432922
|
G | A | 7 | a0002c0002t0001g0236a0002c0002t0001g0238a0002c0002t0001g0240others(4): Show | 7 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637+28066G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432922 | ||||||
| chr5:114432963
|
A | T | 102 | a0001c0001t0001g0065a0001c0001t0001g0067a0001c0001t0001g0068others(99): Show | 102 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1637+28107A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432963 | ||||||
| chr5:114433353
|
C | G | 1 | a0002c0002t0001g0224 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1637+28497C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114433353 | ||||||
| chr5:114433559
|
G | T | 1 | a0002c0002t0001g0150 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1637+28703G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114433559 | ||||||
| chr5:114433714
|
T | C | 1 | a0002c0002t0001g0071 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1637+28858T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114433714 | ||||||
| chr5:114433728
|
A | G | 13 | a0001c0021t0001g0220a0002c0002t0001g0008a0002c0002t0001g0009others(10): Show | 13 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.1637+28872A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114433728 | ||||||
| chr5:114433780
|
C | G | 1 | a0002c0002t0001g0207 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1637+28924C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114433780 | ||||||
| chr5:114433796
|
C | T | 7 | a0002c0002t0001g0201a0002c0002t0001g0202a0002c0002t0001g0203others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637+28940C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114433796 | ||||||
| chr5:114433809
|
C | G | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1637+28953C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114433809 | ||||||
| chr5:114433877
|
G | A | 46 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0021others(43): Show | 47 | HG00741.hp1 HG01070.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.1637+29021G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114433877 | ||||||
| chr5:114433884
|
C | A | 1 | a0001c0001t0001g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1637+29028C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114433884 | ||||||
| chr5:114433997
|
A | C | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1638-29052A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114433997 | ||||||
| chr5:114434119
|
T | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0021others(44): Show | 48 | HG00741.hp1 HG01070.hp2 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.1638-28930T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114434119 | ||||||
| chr5:114434138
|
G | T | 60 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(57): Show | 61 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(58): Show |
intron_variant | MODIFIER | c.1638-28911G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114434138 | ||||||
| chr5:114434180
|
A | AT | 118 | a0001c0001t0001g0034a0001c0001t0001g0065a0001c0001t0001g0067others(115): Show | 118 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.1638-28861dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114434180 | |||||
| chr5:114434230
|
A | AT | 13 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0054others(10): Show | 13 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1638-28810dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114434230 | |||||
| chr5:114434255
|
G | C | 102 | a0001c0001t0001g0065a0001c0001t0001g0067a0001c0001t0001g0068others(99): Show | 102 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1638-28794G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114434255 | ||||||
| chr5:114434346
|
A | G | 9 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0094others(6): Show | 9 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1638-28703A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114434346 | ||||||
| chr5:114434367
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1638-28682A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114434367 | ||||||
| chr5:114434453
|
A | G | 8 | a0001c0021t0001g0220a0004c0008t0001g0010a0004c0008t0001g0011others(5): Show | 8 | HG02622.hp1 HG02630.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1638-28596A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114434453 | ||||||
| chr5:114434575
|
A | G | 2 | a0001c0001t0001g0247a0002c0002t0001g0236 | 2 | HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1638-28474A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114434575 | ||||||
| chr5:114434585
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1638-28464G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114434585 | ||||||
| chr5:114434877
|
A | T | 2 | a0002c0002t0001g0119a0002c0002t0001g0132 | 2 | HG01169.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1638-28172A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114434877 | ||||||
| chr5:114434965
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0031 | 2 | HG01099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1638-28084G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114434965 | ||||||
| chr5:114435177
|
C | G | 5 | a0002c0002t0001g0007a0002c0002t0001g0187a0002c0002t0001g0188others(2): Show | 5 | NA18946.hp2 NA18962.hp1 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.1638-27872C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114435177 | ||||||
| chr5:114435431
|
G | A | 5 | a0002c0002t0001g0007a0002c0002t0001g0187a0002c0002t0001g0188others(2): Show | 5 | NA18946.hp2 NA18962.hp1 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.1638-27618G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114435431 | ||||||
| chr5:114435510
|
G | T | 1 | a0005c0004t0001g0149 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1638-27539G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114435510 | ||||||
| chr5:114435562
|
C | T | 244 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(241): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.1638-27487C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114435562 | ||||||
| chr5:114435641
|
A | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0066others(8): Show | 11 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1638-27408A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114435641 | ||||||
| chr5:114435726
|
A | G | 1 | a0002c0002t0001g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1638-27323A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114435726 | ||||||
| chr5:114435780
|
G | A | 2 | a0002c0002t0001g0102a0002c0002t0001g0103 | 2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1638-27269G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114435780 | ||||||
| chr5:114435837
|
A | G | 1 | a0002c0002t0001g0236 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1638-27212A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114435837 | ||||||
| chr5:114436081
|
T | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(239): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1638-26968T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114436081 | ||||||
| chr5:114436114
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0021others(206): Show | 210 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(207): Show |
intron_variant | MODIFIER | c.1638-26935A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114436114 | ||||||
| chr5:114436147
|
A | G | 1 | a0002c0002t0001g0006 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1638-26902A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114436147 | ||||||
| chr5:114436342
|
G | T | 3 | a0002c0002t0001g0240a0002c0011t0001g0239a0002c0011t0001g0241 | 3 | HG01243.hp1 HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1638-26707G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114436342 | ||||||
| chr5:114436413
|
C | T | 2 | a0002c0002t0001g0119a0002c0002t0001g0132 | 2 | HG01169.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1638-26636C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114436413 | ||||||
| chr5:114436584
|
C | T | 1 | a0002c0002t0001g0125 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1638-26465C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114436584 | ||||||
| chr5:114436606
|
C | T | 2 | a0002c0002t0001g0119a0002c0002t0001g0132 | 2 | HG01169.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1638-26443C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114436606 | ||||||
| chr5:114436635
|
A | G | 1 | a0003c0003t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1638-26414A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114436635 | ||||||
| chr5:114436774
|
A | G | 1 | a0002c0005t0001g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1638-26275A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114436774 | ||||||
| chr5:114436799
|
A | G | 2 | a0002c0002t0001g0119a0002c0002t0001g0132 | 2 | HG01169.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1638-26250A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114436799 | ||||||
| chr5:114437005
|
G | T | 1 | a0002c0002t0001g0009 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1638-26044G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114437005 | ||||||
| chr5:114437076
|
T | C | 1 | a0001c0001t0001g0023 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1638-25973T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114437076 | ||||||
| chr5:114437440
|
A | G | 1 | a0002c0005t0001g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1638-25609A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114437440 | ||||||
| chr5:114437769
|
A | G | 1 | a0002c0002t0001g0225 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1638-25280A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114437769 | ||||||
| chr5:114437931
|
G | A | 12 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(9): Show | 12 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.1638-25118G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114437931 | ||||||
| chr5:114438096
|
C | A | 12 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(9): Show | 12 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.1638-24953C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114438096 | ||||||
| chr5:114438216
|
G | A | 12 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(9): Show | 12 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.1638-24833G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114438216 | ||||||
| chr5:114438435
|
AAT | A | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0062 | 3 | HG02280.hp1 HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1638-24609_1638-24 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114438435 | |||||
| chr5:114438480
|
A | C | 12 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(9): Show | 12 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.1638-24569A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114438480 | ||||||
| chr5:114438819
|
C | T | 15 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(12): Show | 15 | HG01081.hp1 HG01099.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1638-24230C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114438819 | ||||||
| chr5:114438823
|
C | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0096 | 2 | HG02559.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1638-24226C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114438823 | ||||||
| chr5:114438936
|
G | A | 247 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(244): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1638-24113G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114438936 | ||||||
| chr5:114439043
|
T | A | 243 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(240): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1638-24006T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114439043 | ||||||
| chr5:114439075
|
A | T | 13 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0066others(10): Show | 13 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1638-23974A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114439075 | ||||||
| chr5:114439109
|
C | T | 10 | a0001c0001t0001g0227a0001c0001t0001g0229a0001c0001t0001g0230others(7): Show | 10 | HG00280.hp1 HG01192.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1638-23940C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114439109 | ||||||
| chr5:114439117
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1638-23932G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114439117 | ||||||
| chr5:114439220
|
A | C | 1 | a0002c0002t0001g0173 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1638-23829A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114439220 | ||||||
| chr5:114439372
|
C | CA | 13 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0066others(10): Show | 13 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1638-23676dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114439372 | |||||
| chr5:114439455
|
T | G | 1 | a0002c0005t0001g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1638-23594T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114439455 | ||||||
| chr5:114439516
|
A | T | 1 | a0011c0016t0003g0177 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1638-23533A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114439516 | ||||||
| chr5:114439633
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1638-23416G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114439633 | ||||||
| chr5:114439762
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1638-23287A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114439762 | ||||||
| chr5:114439812
|
G | C | 2 | a0002c0002t0001g0119a0002c0002t0001g0132 | 2 | HG01169.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1638-23237G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114439812 | ||||||
| chr5:114439918
|
A | G | 2 | a0003c0003t0001g0196a0003c0009t0001g0195 | 2 | NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1638-23131A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114439918 | ||||||
| chr5:114440113
|
G | C | 2 | a0002c0002t0001g0119a0002c0002t0001g0132 | 2 | HG01169.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1638-22936G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114440113 | ||||||
| chr5:114440173
|
C | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0021others(50): Show | 54 | HG00438.hp2 HG00558.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1638-22876C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114440173 | ||||||
| chr5:114440304
|
A | G | 3 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0047 | 3 | HG01257.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1638-22745A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114440304 | ||||||
| chr5:114440316
|
A | G | 11 | a0001c0001t0001g0227a0001c0001t0001g0229a0001c0001t0001g0230others(8): Show | 11 | HG00280.hp1 HG01192.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.1638-22733A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114440316 | ||||||
| chr5:114440612
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1638-22437T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114440612 | ||||||
| chr5:114440617
|
CAGGTGTG others(11): Show |
C | 1 | a0001c0001t0001g0030 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1638-22429_1638-22 others(24): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114440617 | |||||
| chr5:114440834
|
CAG | C | 120 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0033others(117): Show | 120 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1638-22214_1638-22 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114440834 | ||||||
| chr5:114440862
|
C | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1638-22187C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114440862 | ||||||
| chr5:114440871
|
A | G | 246 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1638-22178A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114440871 | ||||||
| chr5:114440895
|
A | C | 1 | a0002c0005t0001g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1638-22154A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114440895 | ||||||
| chr5:114440913
|
CT | C | 129 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(126): Show | 129 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1638-22128delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114440913 | |||||
| chr5:114440972
|
G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1638-22077G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114440972 | ||||||
| chr5:114441405
|
A | G | 1 | a0002c0002t0001g0224 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1638-21644A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114441405 | ||||||
| chr5:114441893
|
G | T | 4 | a0002c0002t0001g0004a0004c0008t0001g0010a0004c0008t0001g0011others(1): Show | 4 | HG02896.hp1 HG02897.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638-21156G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114441893 | ||||||
| chr5:114442186
|
C | T | 108 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0033others(105): Show | 108 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.1638-20863C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114442186 | ||||||
| chr5:114442247
|
C | CATAT | 10 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0082others(7): Show | 10 | HG01169.hp1 HG02523.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1638-20792_1638-20 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114442247 | |||||
| chr5:114442252
|
A | G | 1 | a0002c0002t0001g0205 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1638-20797A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114442252 | ||||||
| chr5:114442278
|
G | GTA | 16 | a0001c0001t0001g0039a0001c0001t0001g0108a0001c0001t0001g0211others(13): Show | 16 | HG00738.hp1 HG00738.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1638-20764_1638-20 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114442278 | |||||
| chr5:114442287
|
G | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1638-20762G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114442287 | ||||||
| chr5:114442289
|
G | T | 20 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0082others(17): Show | 20 | HG01169.hp1 HG02055.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.1638-20760G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114442289 | ||||||
| chr5:114442366
|
GTAGTGAT others(3): Show |
G | 15 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0091others(12): Show | 15 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1638-20682_1638-20 others(16): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114442366 | ||||||
| chr5:114442378
|
A | C | 15 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0091others(12): Show | 15 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1638-20671A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114442378 | ||||||
| chr5:114442974
|
G | GT | 111 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(108): Show | 111 | HG00280.hp1 HG00438.hp1 HG00642.hp1 others(108): Show |
intron_variant | MODIFIER | c.1638-20068dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114442974 | |||||
| chr5:114443161
|
C | T | 4 | a0001c0001t0001g0070a0001c0001t0002g0038a0002c0002t0001g0123others(1): Show | 4 | HG00741.hp1 HG01070.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1638-19888C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114443161 | ||||||
| chr5:114443162
|
G | A | 1 | a0010c0022t0001g0072 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1638-19887G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114443162 | ||||||
| chr5:114443461
|
T | G | 1 | a0001c0001t0001g0022 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1638-19588T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114443461 | ||||||
| chr5:114443504
|
T | C | 5 | a0002c0002t0001g0117a0002c0002t0001g0152a0002c0002t0001g0159others(2): Show | 5 | HG01261.hp2 HG01433.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.1638-19545T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114443504 | ||||||
| chr5:114443504
|
TGCCTTGC others(24): Show |
T | 1 | a0004c0008t0001g0011 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1638-19543_1638-19 others(37): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114443504 | |||||
| chr5:114443615
|
T | C | 17 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0091others(14): Show | 17 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1638-19434T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114443615 | ||||||
| chr5:114443724
|
G | A | 99 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0026others(96): Show | 99 | HG00099.hp2 HG00438.hp1 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.1638-19325G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114443724 | ||||||
| chr5:114443829
|
G | T | 1 | a0002c0002t0001g0111 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1638-19220G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114443829 | ||||||
| chr5:114443856
|
C | A | 239 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1638-19193C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114443856 | ||||||
| chr5:114443919
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1638-19130T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114443919 | ||||||
| chr5:114444083
|
G | T | 1 | a0001c0001t0001g0227 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1638-18966G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114444083 | ||||||
| chr5:114444348
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1638-18701G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114444348 | ||||||
| chr5:114444392
|
A | G | 2 | a0001c0001t0001g0057a0001c0001t0001g0089 | 2 | HG01099.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1638-18657A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114444392 | ||||||
| chr5:114444396
|
G | GA | 33 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0057others(30): Show | 33 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.1638-18645dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114444396 | |||||
| chr5:114444490
|
T | G | 100 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(97): Show | 100 | HG00099.hp2 HG00438.hp1 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.1638-18559T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114444490 | ||||||
| chr5:114444781
|
A | G | 3 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0109 | 3 | HG00642.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1638-18268A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114444781 | ||||||
| chr5:114444820
|
T | C | 1 | a0002c0002t0001g0006 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1638-18229T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114444820 | ||||||
| chr5:114445037
|
G | T | 1 | a0006c0007t0001g0222 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1638-18012G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114445037 | ||||||
| chr5:114445189
|
T | G | 6 | a0001c0001t0001g0018a0001c0001t0001g0084a0001c0001t0001g0085others(3): Show | 6 | HG00280.hp2 HG01358.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1638-17860T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114445189 | ||||||
| chr5:114445190
|
T | C | 6 | a0001c0001t0001g0018a0001c0001t0001g0084a0001c0001t0001g0085others(3): Show | 6 | HG00280.hp2 HG01358.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1638-17859T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114445190 | ||||||
| chr5:114445298
|
C | T | 4 | a0002c0002t0001g0004a0004c0008t0001g0010a0004c0008t0001g0011others(1): Show | 4 | HG02896.hp1 HG02897.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638-17751C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114445298 | ||||||
| chr5:114445312
|
G | A | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1638-17737G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114445312 | ||||||
| chr5:114445423
|
T | TA | 6 | a0001c0001t0001g0042a0002c0002t0001g0007a0002c0002t0001g0187others(3): Show | 6 | NA18942.hp2 NA18946.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.1638-17625dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114445423 | |||||
| chr5:114446124
|
C | G | 11 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(8): Show | 11 | HG01074.hp1 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1638-16925C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114446124 | ||||||
| chr5:114446406
|
C | G | 1 | a0003c0003t0001g0196 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1638-16643C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114446406 | ||||||
| chr5:114446700
|
A | T | 12 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0087others(9): Show | 12 | HG01169.hp1 HG01175.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1638-16349A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114446700 | ||||||
| chr5:114446835
|
G | A | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG01074.hp1 HG02486.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1638-16214G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114446835 | ||||||
| chr5:114446976
|
A | T | 1 | a0003c0003t0001g0196 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1638-16073A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114446976 | ||||||
| chr5:114447076
|
G | C | 149 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0020others(146): Show | 150 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.1638-15973G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114447076 | ||||||
| chr5:114447182
|
T | C | 1 | a0002c0002t0001g0071 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1638-15867T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114447182 | ||||||
| chr5:114447229
|
T | C | 5 | a0002c0005t0001g0013a0002c0005t0001g0014a0002c0005t0001g0015others(2): Show | 5 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1638-15820T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114447229 | ||||||
| chr5:114448271
|
A | G | 1 | a0002c0002t0001g0112 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1638-14778A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114448271 | ||||||
| chr5:114448292
|
T | C | 32 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0057others(29): Show | 32 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.1638-14757T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114448292 | ||||||
| chr5:114448399
|
C | A | 4 | a0002c0002t0001g0004a0004c0008t0001g0010a0004c0008t0001g0011others(1): Show | 4 | HG02896.hp1 HG02897.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638-14650C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114448399 | ||||||
| chr5:114448400
|
A | G | 1 | a0002c0002t0001g0175 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1638-14649A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114448400 | ||||||
| chr5:114448412
|
CTG | C | 4 | a0002c0002t0001g0004a0004c0008t0001g0010a0004c0008t0001g0011others(1): Show | 4 | HG02896.hp1 HG02897.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638-14633_1638-14 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114448412 | |||||
| chr5:114448525
|
G | A | 5 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0227others(2): Show | 5 | HG00280.hp2 HG02572.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.1638-14524G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114448525 | ||||||
| chr5:114448551
|
C | G | 4 | a0003c0003t0001g0197a0003c0003t0001g0198a0003c0003t0001g0199others(1): Show | 4 | HG02922.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1638-14498C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114448551 | ||||||
| chr5:114449061
|
A | C | 1 | a0002c0002t0001g0009 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1638-13988A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449061 | ||||||
| chr5:114449180
|
T | C | 24 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0074others(21): Show | 24 | HG01081.hp1 HG02055.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.1638-13869T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449180 | ||||||
| chr5:114449279
|
C | T | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG01074.hp1 HG02486.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1638-13770C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449279 | ||||||
| chr5:114449422
|
A | T | 4 | a0003c0003t0001g0197a0003c0003t0001g0198a0003c0003t0001g0199others(1): Show | 4 | HG02922.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1638-13627A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449422 | ||||||
| chr5:114449568
|
C | T | 1 | a0002c0002t0001g0208 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1638-13481C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449568 | ||||||
| chr5:114449825
|
C | T | 1 | a0002c0002t0001g0201 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1638-13224C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449825 | ||||||
| chr5:114449869
|
C | T | 1 | a0002c0002t0001g0236 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1638-13180C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449869 | ||||||
| chr5:114449879
|
T | TAC | 3 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0235 | 3 | HG00280.hp1 HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1638-13141_1638-13 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449879 | |||||
| chr5:114449879
|
T | TACAC | 9 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0227others(6): Show | 9 | HG00280.hp2 HG01081.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.1638-13143_1638-13 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449879 | |||||
| chr5:114449879
|
T | TACACAC | 4 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0231others(1): Show | 4 | HG01081.hp1 HG01515.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1638-13145_1638-13 others(12): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449879 | |||||
| chr5:114449879
|
T | TACACACA others(1): Show |
4 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0094others(1): Show | 4 | HG02559.hp1 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638-13147_1638-13 others(14): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449879 | |||||
| chr5:114449879
|
T | TACACACA others(3): Show |
7 | a0001c0001t0001g0092a0001c0001t0001g0100a0001c0006t0001g0093others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1638-13149_1638-13 others(16): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449879 | |||||
| chr5:114449879
|
T | TACACACA others(5): Show |
4 | a0001c0001t0001g0091a0001c0001t0001g0096a0002c0002t0001g0205others(1): Show | 4 | HG02615.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638-13151_1638-13 others(18): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449879 | |||||
| chr5:114449879
|
TACAC | T | 18 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0067others(15): Show | 18 | HG01099.hp2 HG01256.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1638-13143_1638-13 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449879 | |||||
| chr5:114449898
|
ACACACAC others(5): Show |
A | 1 | a0001c0001t0001g0018 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1638-13149_1638-13 others(18): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449898 | |||||
| chr5:114449900
|
ACACACAC others(3): Show |
A | 100 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0026others(97): Show | 100 | HG00099.hp2 HG00438.hp1 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.1638-13147_1638-13 others(16): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449900 | |||||
| chr5:114449902
|
ACACACAC others(1): Show |
A | 45 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(42): Show | 46 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1638-13145_1638-13 others(14): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449902 | |||||
| chr5:114449904
|
A | G | 4 | a0002c0002t0001g0004a0004c0008t0001g0010a0004c0008t0001g0011others(1): Show | 4 | HG02896.hp1 HG02897.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638-13145A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449904 | ||||||
| chr5:114449904
|
ACACACG | A | 3 | a0002c0002t0001g0145a0002c0002t0001g0155a0002c0002t0001g0164 | 3 | HG00558.hp1 HG02523.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1638-13143_1638-13 others(12): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449904 | |||||
| chr5:114449906
|
A | G | 5 | a0001c0021t0001g0220a0002c0002t0001g0004a0004c0008t0001g0010others(2): Show | 5 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1638-13143A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449906 | ||||||
| chr5:114449908
|
A | ACACACAC others(19): Show |
5 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0216others(2): Show | 5 | HG01074.hp1 HG03225.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1638-13140_1638-13 others(32): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | |||||
| chr5:114449908
|
A | ACACACAC others(21): Show |
2 | a0002c0011t0001g0239a0002c0011t0001g0241 | 2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1638-13140_1638-13 others(34): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | |||||
| chr5:114449908
|
A | ACACACAC others(17): Show |
1 | a0001c0001t0001g0217 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1638-13140_1638-13 others(30): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | |||||
| chr5:114449908
|
A | ACACACAC others(19): Show |
1 | a0001c0001t0001g0215 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1638-13140_1638-13 others(32): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | |||||
| chr5:114449908
|
A | ACACACAC others(13): Show |
1 | a0010c0022t0001g0072 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1638-13140_1638-13 others(26): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | |||||
| chr5:114449908
|
A | ACACACAC others(15): Show |
1 | a0001c0001t0001g0212 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1638-13140_1638-13 others(28): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | |||||
| chr5:114449908
|
A | ACACACAC others(17): Show |
3 | a0001c0001t0001g0211a0002c0002t0001g0119a0002c0002t0001g0132 | 3 | HG01169.hp1 HG02615.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1638-13140_1638-13 others(30): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | |||||
| chr5:114449908
|
A | ACACACAC others(11): Show |
3 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0082 | 3 | HG03139.hp2 HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1638-13140_1638-13 others(24): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | |||||
| chr5:114449908
|
A | ACACACAC others(13): Show |
1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1638-13140_1638-13 others(26): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | |||||
| chr5:114449908
|
A | ACACACAC others(11): Show |
1 | a0002c0002t0001g0128 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1638-13140_1638-13 others(24): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | |||||
| chr5:114449908
|
A | ACACACAC others(5): Show |
1 | a0001c0001t0001g0101 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1638-13140_1638-13 others(18): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | |||||
| chr5:114449908
|
A | ACACACAC others(9): Show |
1 | a0002c0002t0001g0003 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1638-13140_1638-13 others(22): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | |||||
| chr5:114449908
|
A | ACACACAC others(3): Show |
3 | a0001c0001t0001g0248a0007c0010t0001g0191a0007c0010t0001g0192 | 3 | HG02895.hp1 HG02897.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1638-13140_1638-13 others(16): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | |||||
| chr5:114449908
|
A | ACACACAC others(9): Show |
1 | a0002c0002t0001g0207 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1638-13140_1638-13 others(22): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | |||||
| chr5:114449908
|
A | ACACACAC others(11): Show |
1 | a0001c0001t0001g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1638-13140_1638-13 others(24): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | |||||
| chr5:114449908
|
A | ACACACAC others(1): Show |
5 | a0003c0003t0001g0193a0003c0003t0001g0197a0003c0003t0001g0198others(2): Show | 5 | HG02809.hp1 HG02922.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1638-13140_1638-13 others(14): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | |||||
| chr5:114449908
|
A | G | 23 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0067others(20): Show | 23 | HG01099.hp2 HG01256.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.1638-13141A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449908 | ||||||
| chr5:114449910
|
G | A | 5 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0227others(2): Show | 5 | HG00280.hp2 HG02572.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1638-13139G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449910 | ||||||
| chr5:114449912
|
G | A | 2 | a0002c0002t0001g0005a0002c0002t0001g0173 | 2 | HG01175.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1638-13137G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449912 | ||||||
| chr5:114449914
|
G | A | 3 | a0001c0001t0001g0217a0002c0002t0001g0005a0002c0002t0001g0173 | 3 | HG01175.hp1 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1638-13135G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449914 | ||||||
| chr5:114449916
|
G | A | 2 | a0002c0002t0001g0005a0002c0002t0001g0173 | 2 | HG01175.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1638-13133G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449916 | ||||||
| chr5:114449918
|
T | A | 2 | a0002c0002t0001g0005a0002c0002t0001g0173 | 2 | HG01175.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1638-13131T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449918 | ||||||
| chr5:114449920
|
G | A | 3 | a0001c0001t0001g0227a0002c0002t0001g0201a0002c0002t0001g0206 | 3 | HG00280.hp2 HG02602.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1638-13129G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449920 | ||||||
| chr5:114449923
|
T | C | 13 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0082others(10): Show | 13 | HG01169.hp1 HG01175.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.1638-13126T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449923 | ||||||
| chr5:114449925
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1638-13124C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449925 | ||||||
| chr5:114449927
|
C | T | 1 | a0002c0002t0001g0181 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1638-13122C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449927 | ||||||
| chr5:114449976
|
G | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(45): Show | 49 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1638-13073G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449976 | ||||||
| chr5:114449989
|
A | T | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1638-13060A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449989 | ||||||
| chr5:114449996
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1638-13053C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449996 | ||||||
| chr5:114450323
|
T | G | 3 | a0004c0008t0001g0010a0006c0007t0001g0222a0006c0007t0001g0223 | 3 | HG06807.hp1 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1638-12726T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114450323 | ||||||
| chr5:114450385
|
G | A | 1 | a0002c0002t0001g0071 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1638-12664G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114450385 | ||||||
| chr5:114450421
|
T | A | 1 | a0002c0002t0001g0006 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1638-12628T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114450421 | ||||||
| chr5:114450572
|
T | G | 1 | a0001c0001t0001g0018 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1638-12477T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114450572 | ||||||
| chr5:114450714
|
G | T | 1 | a0001c0001t0001g0056 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1638-12335G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114450714 | ||||||
| chr5:114450718
|
A | G | 17 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0091others(14): Show | 17 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1638-12331A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114450718 | ||||||
| chr5:114450791
|
C | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(45): Show | 49 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1638-12258C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114450791 | ||||||
| chr5:114450806
|
G | A | 3 | a0001c0001t0001g0063a0001c0001t0001g0064a0009c0023t0001g0160 | 3 | HG01081.hp1 HG02630.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1638-12243G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114450806 | ||||||
| chr5:114450819
|
C | G | 1 | a0003c0003t0001g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1638-12230C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114450819 | ||||||
| chr5:114451023
|
C | T | 1 | a0002c0002t0001g0164 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1638-12026C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451023 | ||||||
| chr5:114451040
|
G | A | 11 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(8): Show | 11 | HG01074.hp1 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1638-12009G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451040 | ||||||
| chr5:114451049
|
A | G | 1 | a0003c0003t0001g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1638-12000A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451049 | ||||||
| chr5:114451315
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1638-11734T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451315 | ||||||
| chr5:114451358
|
G | A | 1 | a0002c0002t0001g0006 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1638-11691G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451358 | ||||||
| chr5:114451568
|
T | C | 4 | a0002c0002t0001g0004a0004c0008t0001g0010a0004c0008t0001g0011others(1): Show | 4 | HG02896.hp1 HG02897.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638-11481T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451568 | ||||||
| chr5:114451598
|
A | G | 2 | a0002c0002t0001g0238a0002c0014t0001g0017 | 2 | HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1638-11451A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451598 | ||||||
| chr5:114451624
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1638-11425C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451624 | ||||||
| chr5:114451634
|
A | C | 21 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0091others(18): Show | 21 | HG02258.hp2 HG02559.hp1 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.1638-11415A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451634 | ||||||
| chr5:114451635
|
G | A | 1 | a0002c0002t0001g0007 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1638-11414G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451635 | ||||||
| chr5:114451663
|
A | G | 26 | a0001c0001t0001g0035a0001c0001t0001g0066a0001c0001t0001g0069others(23): Show | 26 | HG01169.hp1 HG02486.hp2 HG02723.hp1 others(23): Show |
intron_variant | MODIFIER | c.1638-11386A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451663 | ||||||
| chr5:114451671
|
C | T | 1 | a0003c0009t0001g0194 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1638-11378C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451671 | ||||||
| chr5:114451692
|
C | G | 2 | a0002c0002t0001g0209a0002c0002t0001g0210 | 2 | HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1638-11357C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451692 | ||||||
| chr5:114451693
|
A | G | 1 | a0002c0002t0001g0174 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1638-11356A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451693 | ||||||
| chr5:114451766
|
G | A | 7 | a0001c0001t0001g0211a0001c0001t0001g0213a0001c0001t0001g0214others(4): Show | 7 | HG01074.hp1 HG02615.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1638-11283G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451766 | ||||||
| chr5:114451820
|
C | A | 1 | a0002c0002t0001g0117 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1638-11229C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451820 | ||||||
| chr5:114451854
|
G | A | 2 | a0002c0002t0001g0209a0002c0002t0001g0210 | 2 | HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1638-11195G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451854 | ||||||
| chr5:114451912
|
A | G | 31 | a0001c0001t0001g0018a0001c0001t0001g0033a0001c0001t0001g0042others(28): Show | 31 | HG00438.hp1 HG00738.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.1638-11137A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451912 | ||||||
| chr5:114451915
|
A | G | 4 | a0006c0007t0001g0104a0006c0007t0001g0221a0006c0007t0001g0222others(1): Show | 4 | HG02622.hp1 HG03098.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638-11134A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451915 | ||||||
| chr5:114451942
|
G | T | 82 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0023others(79): Show | 82 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.1638-11107G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451942 | ||||||
| chr5:114451984
|
T | C | 14 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0091others(11): Show | 14 | HG02258.hp2 HG02559.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1638-11065T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451984 | ||||||
| chr5:114451994
|
C | CT | 18 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0091others(15): Show | 18 | HG02258.hp2 HG02559.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.1638-11052dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114451994 | |||||
| chr5:114452104
|
A | G | 4 | a0001c0001t0001g0230a0002c0002t0001g0134a0002c0002t0001g0173others(1): Show | 4 | HG01175.hp1 HG01192.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638-10945A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114452104 | ||||||
| chr5:114452218
|
G | T | 1 | a0001c0001t0001g0105 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1638-10831G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114452218 | ||||||
| chr5:114452233
|
G | A | 4 | a0002c0002t0001g0004a0004c0008t0001g0010a0004c0008t0001g0011others(1): Show | 4 | HG02896.hp1 HG02897.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638-10816G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114452233 | ||||||
| chr5:114452405
|
C | T | 1 | a0002c0002t0001g0006 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1638-10644C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114452405 | ||||||
| chr5:114452454
|
A | G | 3 | a0002c0002t0001g0114a0002c0002t0001g0156a0004c0012t0001g0142 | 3 | HG00738.hp2 HG01256.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1638-10595A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114452454 | ||||||
| chr5:114452626
|
T | G | 1 | a0002c0005t0001g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1638-10423T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114452626 | ||||||
| chr5:114452689
|
G | A | 1 | a0002c0002t0001g0158 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1638-10360G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114452689 | ||||||
| chr5:114452896
|
G | A | 74 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0023others(71): Show | 74 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1638-10153G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114452896 | ||||||
| chr5:114453034
|
A | C | 1 | a0001c0001t0001g0031 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1638-10015A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114453034 | ||||||
| chr5:114453047
|
C | A | 2 | a0001c0001t0001g0108a0002c0002t0001g0204 | 2 | HG00738.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1638-10002C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114453047 | ||||||
| chr5:114453058
|
C | T | 54 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0033others(51): Show | 54 | HG00099.hp2 HG00438.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1638-9991C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114453058 | ||||||
| chr5:114453252
|
C | A | 2 | a0002c0002t0001g0209a0002c0002t0001g0210 | 2 | HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1638-9797C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114453252 | ||||||
| chr5:114453283
|
T | G | 1 | a0002c0002t0001g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1638-9766T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114453283 | ||||||
| chr5:114453531
|
T | A | 1 | a0002c0005t0001g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1638-9518T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114453531 | ||||||
| chr5:114453916
|
A | G | 1 | a0002c0002t0001g0249 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1638-9133A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114453916 | ||||||
| chr5:114453973
|
G | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(220): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1638-9076G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114453973 | ||||||
| chr5:114454152
|
C | G | 1 | a0001c0001t0001g0037 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1638-8897C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114454152 | ||||||
| chr5:114454380
|
A | G | 3 | a0002c0002t0001g0240a0002c0011t0001g0239a0002c0011t0001g0241 | 3 | HG01243.hp1 HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1638-8669A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114454380 | ||||||
| chr5:114454693
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1638-8356G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114454693 | ||||||
| chr5:114454699
|
C | G | 1 | a0002c0002t0001g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1638-8350C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114454699 | ||||||
| chr5:114455065
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1638-7984C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114455065 | ||||||
| chr5:114455098
|
C | T | 1 | a0001c0001t0001g0032 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1638-7951C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114455098 | ||||||
| chr5:114455120
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1638-7929G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114455120 | ||||||
| chr5:114455239
|
G | A | 1 | a0002c0002t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1638-7810G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114455239 | ||||||
| chr5:114455348
|
A | G | 17 | a0001c0001t0001g0022a0001c0001t0001g0053a0001c0001t0001g0057others(14): Show | 17 | HG01099.hp2 HG01192.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.1638-7701A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114455348 | ||||||
| chr5:114455359
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1638-7690A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114455359 | ||||||
| chr5:114455365
|
C | G | 1 | a0001c0001t0001g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1638-7684C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114455365 | ||||||
| chr5:114455497
|
C | T | 7 | a0001c0001t0001g0023a0001c0001t0001g0024a0002c0002t0001g0008others(4): Show | 7 | HG00438.hp1 NA18986.hp1 NA19000.hp2 others(4): Show |
intron_variant | MODIFIER | c.1638-7552C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114455497 | ||||||
| chr5:114455498
|
G | A | 1 | a0002c0002t0001g0154 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1638-7551G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114455498 | ||||||
| chr5:114455594
|
A | G | 198 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(195): Show | 198 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1638-7455A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114455594 | ||||||
| chr5:114455933
|
G | A | 12 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0039others(9): Show | 12 | HG00099.hp2 HG00738.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.1638-7116G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114455933 | ||||||
| chr5:114456098
|
A | C | 1 | a0001c0001t0001g0105 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1638-6951A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114456098 | ||||||
| chr5:114456213
|
C | G | 9 | a0001c0001t0001g0099a0003c0003t0001g0193a0003c0003t0001g0197others(6): Show | 9 | HG02622.hp2 HG02809.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1638-6836C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114456213 | ||||||
| chr5:114456510
|
A | C | 38 | a0001c0001t0001g0022a0001c0001t0001g0053a0001c0001t0001g0057others(35): Show | 38 | HG01099.hp2 HG01192.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.1638-6539A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114456510 | ||||||
| chr5:114456679
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1638-6370C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114456679 | ||||||
| chr5:114456757
|
G | C | 2 | a0002c0002t0001g0238a0002c0014t0001g0017 | 2 | HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1638-6292G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114456757 | ||||||
| chr5:114456820
|
A | G | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0002c0002t0001g0008others(3): Show | 6 | NA18986.hp1 NA19000.hp2 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1638-6229A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114456820 | ||||||
| chr5:114456891
|
C | A | 196 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(193): Show | 196 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.1638-6158C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114456891 | ||||||
| chr5:114456927
|
G | C | 84 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(81): Show | 84 | HG00280.hp1 HG00558.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.1638-6122G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114456927 | ||||||
| chr5:114456988
|
A | G | 15 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0091others(12): Show | 15 | HG01243.hp2 HG02258.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1638-6061A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114456988 | ||||||
| chr5:114457249
|
C | G | 5 | a0001c0001t0001g0099a0003c0003t0001g0197a0003c0003t0001g0198others(2): Show | 5 | HG02622.hp2 HG02922.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1638-5800C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114457249 | ||||||
| chr5:114457375
|
C | G | 1 | a0001c0015t0001g0219 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1638-5674C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114457375 | ||||||
| chr5:114457589
|
A | G | 15 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0091others(12): Show | 15 | HG01243.hp2 HG02258.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1638-5460A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114457589 | ||||||
| chr5:114457635
|
T | G | 198 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(195): Show | 198 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1638-5414T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114457635 | ||||||
| chr5:114457675
|
C | G | 1 | a0001c0001t0001g0052 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1638-5374C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114457675 | ||||||
| chr5:114457915
|
G | C | 1 | a0001c0001t0001g0060 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1638-5134G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114457915 | ||||||
| chr5:114458226
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1638-4823C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114458226 | ||||||
| chr5:114458390
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1638-4659A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114458390 | ||||||
| chr5:114458396
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1638-4653C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114458396 | ||||||
| chr5:114458567
|
T | C | 4 | a0002c0002t0001g0103a0002c0005t0001g0016a0005c0004t0001g0147others(1): Show | 4 | HG02486.hp2 HG02818.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1638-4482T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114458567 | ||||||
| chr5:114458697
|
G | A | 197 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(194): Show | 197 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.1638-4352G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114458697 | ||||||
| chr5:114458941
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1638-4108G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114458941 | ||||||
| chr5:114458962
|
C | G | 46 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(43): Show | 46 | HG00558.hp1 HG00741.hp2 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.1638-4087C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114458962 | ||||||
| chr5:114459248
|
T | G | 8 | a0001c0001t0001g0099a0003c0003t0001g0197a0003c0003t0001g0198others(5): Show | 8 | HG02622.hp2 HG02809.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1638-3801T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114459248 | ||||||
| chr5:114459250
|
T | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0049 | 2 | HG01943.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1638-3799T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114459250 | ||||||
| chr5:114459595
|
T | C | 1 | a0001c0001t0001g0216 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1638-3454T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114459595 | ||||||
| chr5:114459734
|
T | G | 6 | a0001c0001t0001g0030a0001c0001t0001g0044a0001c0001t0001g0058others(3): Show | 6 | HG01346.hp1 HG02280.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.1638-3315T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114459734 | ||||||
| chr5:114459861
|
T | C | 63 | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0032others(60): Show | 63 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.1638-3188T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114459861 | ||||||
| chr5:114460169
|
A | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1638-2880A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114460169 | ||||||
| chr5:114460232
|
T | TTTTG | 3 | a0001c0001t0001g0065a0001c0001t0001g0067a0001c0001t0001g0068 | 3 | HG01358.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1638-2802_1638-279 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114460232 | |||||
| chr5:114460435
|
G | C | 2 | a0001c0001t0001g0019a0002c0002t0001g0182 | 2 | NA19060.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1638-2614G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114460435 | ||||||
| chr5:114460555
|
T | A | 192 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(189): Show | 192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.1638-2494T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114460555 | ||||||
| chr5:114460567
|
G | A | 1 | a0003c0003t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1638-2482G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114460567 | ||||||
| chr5:114460584
|
T | G | 1 | a0001c0001t0001g0083 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1638-2465T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114460584 | ||||||
| chr5:114460665
|
A | T | 113 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(110): Show | 113 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.1638-2384A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114460665 | ||||||
| chr5:114460763
|
T | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1638-2286T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114460763 | ||||||
| chr5:114460776
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1638-2273T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114460776 | ||||||
| chr5:114460806
|
A | G | 6 | a0001c0001t0001g0042a0002c0002t0001g0007a0002c0002t0001g0187others(3): Show | 6 | NA18942.hp2 NA18946.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.1638-2243A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114460806 | ||||||
| chr5:114460895
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1638-2154A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114460895 | ||||||
| chr5:114461218
|
A | G | 4 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(1): Show | 4 | NA18964.hp2 NA19009.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1638-1831A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114461218 | ||||||
| chr5:114461266
|
A | G | 1 | a0002c0002t0001g0126 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1638-1783A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114461266 | ||||||
| chr5:114461304
|
A | G | 1 | a0002c0002t0001g0249 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1638-1745A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114461304 | ||||||
| chr5:114461568
|
T | G | 1 | a0001c0001t0001g0035 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1638-1481T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114461568 | ||||||
| chr5:114461630
|
G | A | 1 | a0002c0002t0001g0151 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1638-1419G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114461630 | ||||||
| chr5:114461639
|
G | A | 222 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1638-1410G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114461639 | ||||||
| chr5:114461730
|
G | GA | 15 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0091others(12): Show | 15 | HG01243.hp2 HG02258.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1638-1306dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114461730 | |||||
| chr5:114461747
|
T | C | 68 | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0032others(65): Show | 68 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.1638-1302T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114461747 | ||||||
| chr5:114461847
|
C | G | 89 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0026others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1638-1202C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114461847 | ||||||
| chr5:114461907
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1638-1142C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114461907 | ||||||
| chr5:114461908
|
G | A | 91 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(88): Show | 91 | HG00280.hp1 HG00558.hp1 HG00741.hp2 others(88): Show |
intron_variant | MODIFIER | c.1638-1141G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114461908 | ||||||
| chr5:114462217
|
G | A | 44 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(41): Show | 44 | HG00558.hp1 HG00741.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.1638-832G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114462217 | ||||||
| chr5:114462319
|
G | T | 177 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(174): Show | 177 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.1638-730G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114462319 | ||||||
| chr5:114462424
|
A | C | 2 | a0001c0001t0001g0100a0005c0004t0001g0146 | 2 | HG02559.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1638-625A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114462424 | ||||||
| chr5:114462878
|
G | A | 1 | a0002c0002t0001g0179 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1638-171G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114462878 | ||||||
| chr5:114462945
|
A | G | 1 | a0002c0002t0001g0158 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1638-104A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114462945 | ||||||
| chr5:114463226
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1779+36C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114463226 | ||||||
| chr5:114463244
|
A | G | 15 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0091others(12): Show | 15 | HG01243.hp2 HG02258.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1779+54A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114463244 | ||||||
| chr5:114463289
|
C | T | 24 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(21): Show | 24 | HG01169.hp1 HG01358.hp1 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.1779+99C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114463289 | ||||||
| chr5:114463353
|
C | T | 24 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(21): Show | 24 | HG01169.hp1 HG01358.hp1 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.1779+163C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114463353 | ||||||
| chr5:114463706
|
G | A | 92 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(89): Show | 92 | HG00280.hp1 HG00558.hp1 HG00741.hp2 others(89): Show |
intron_variant | MODIFIER | c.1779+516G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114463706 | ||||||
| chr5:114463720
|
A | T | 10 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(7): Show | 10 | HG01074.hp1 HG02486.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1779+530A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114463720 | ||||||
| chr5:114463851
|
C | T | 4 | a0002c0002t0001g0004a0004c0008t0001g0010a0004c0008t0001g0011others(1): Show | 4 | HG02896.hp1 HG02897.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1779+661C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114463851 | ||||||
| chr5:114463881
|
A | C | 63 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(60): Show | 63 | HG00280.hp1 HG00558.hp1 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.1779+691A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114463881 | ||||||
| chr5:114464047
|
G | A | 92 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(89): Show | 92 | HG00280.hp1 HG00558.hp1 HG00741.hp2 others(89): Show |
intron_variant | MODIFIER | c.1779+857G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114464047 | ||||||
| chr5:114464367
|
A | G | 2 | a0002c0002t0001g0139a0002c0002t0001g0140 | 2 | HG00642.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1779+1177A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114464367 | ||||||
| chr5:114464467
|
G | A | 1 | a0005c0004t0001g0176 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1779+1277G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114464467 | ||||||
| chr5:114464627
|
G | A | 2 | a0002c0002t0001g0209a0002c0002t0001g0210 | 2 | HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1779+1437G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114464627 | ||||||
| chr5:114464713
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1779+1523A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114464713 | ||||||
| chr5:114464803
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1779+1613G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114464803 | ||||||
| chr5:114464809
|
T | TA | 6 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0089others(3): Show | 6 | HG02145.hp1 HG02293.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1779+1630dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 114464809 | |||||
| chr5:114464809
|
TA | T | 31 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0027others(28): Show | 32 | HG00099.hp1 HG00558.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.1779+1630delA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 114464809 | |||||
| chr5:114464822
|
G | A | 98 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(95): Show | 98 | HG00280.hp1 HG00558.hp1 HG00741.hp2 others(95): Show |
intron_variant | MODIFIER | c.1779+1632G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114464822 | ||||||
| chr5:114464837
|
CTGTT | C | 235 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(232): Show | 236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1779+1653_1779+165 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 114464837 | |||||
| chr5:114464858
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1779+1668A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114464858 | ||||||
| chr5:114465004
|
G | A | 1 | a0002c0005t0001g0015 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1779+1814G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465004 | ||||||
| chr5:114465141
|
A | G | 1 | a0002c0002t0001g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1779+1951A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465141 | ||||||
| chr5:114465162
|
G | A | 7 | a0001c0001t0001g0099a0003c0003t0001g0193a0003c0003t0001g0197others(4): Show | 7 | HG02622.hp2 HG02809.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1779+1972G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465162 | ||||||
| chr5:114465253
|
T | G | 1 | a0001c0018t0001g0029 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1779+2063T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465253 | ||||||
| chr5:114465333
|
C | G | 1 | a0010c0022t0001g0072 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1779+2143C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465333 | ||||||
| chr5:114465350
|
C | T | 1 | a0006c0007t0001g0104 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1779+2160C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465350 | ||||||
| chr5:114465381
|
G | A | 1 | a0002c0002t0001g0125 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1779+2191G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465381 | ||||||
| chr5:114465424
|
C | G | 1 | a0001c0001t0001g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1779+2234C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465424 | ||||||
| chr5:114465519
|
G | A | 2 | a0002c0002t0001g0209a0002c0002t0001g0210 | 2 | HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1779+2329G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465519 | ||||||
| chr5:114465544
|
G | A | 1 | a0002c0002t0001g0203 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1779+2354G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465544 | ||||||
| chr5:114465547
|
G | T | 108 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(105): Show | 108 | HG00280.hp1 HG00558.hp1 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1779+2357G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465547 | ||||||
| chr5:114465615
|
C | CA | 33 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0073others(30): Show | 33 | HG01099.hp2 HG01192.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.1779+2438dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 114465615 | |||||
| chr5:114465635
|
G | A | 15 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0091others(12): Show | 15 | HG01243.hp2 HG02258.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1779+2445G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465635 | ||||||
| chr5:114465726
|
A | G | 100 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0026others(97): Show | 100 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1779+2536A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465726 | ||||||
| chr5:114465934
|
G | A | 1 | a0002c0002t0001g0180 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1779+2744G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465934 | ||||||
| chr5:114465973
|
C | T | 2 | a0007c0010t0001g0191a0007c0010t0001g0192 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1779+2783C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465973 | ||||||
| chr5:114466058
|
TTACCAAG others(5): Show |
T | 1 | a0002c0002t0001g0179 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1779+2871_1779+288 others(16): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 114466058 | |||||
| chr5:114466115
|
T | G | 1 | a0002c0002t0001g0183 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1779+2925T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114466115 | ||||||
| chr5:114466165
|
A | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0078a0002c0002t0001g0208 | 3 | HG00099.hp1 HG01346.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1779+2975A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114466165 | ||||||
| chr5:114466175
|
C | T | 1 | a0002c0002t0001g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1779+2985C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114466175 | ||||||
| chr5:114466282
|
A | G | 18 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(15): Show | 18 | HG01169.hp1 HG01175.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.1779+3092A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114466282 | ||||||
| chr5:114466329
|
G | C | 1 | a0001c0001t0001g0060 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1779+3139G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114466329 | ||||||
| chr5:114466444
|
G | A | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1779+3254G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114466444 | ||||||
| chr5:114466474
|
A | AAT | 4 | a0001c0001t0001g0211a0002c0005t0001g0013a0002c0005t0001g0014others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1779+3302_1779+330 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 114466474 | |||||
| chr5:114466474
|
AAT | A | 179 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(176): Show | 179 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.1779+3302_1779+330 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 114466474 | |||||
| chr5:114466945
|
A | G | 182 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(179): Show | 182 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.1779+3755A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114466945 | ||||||
| chr5:114467013
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1779+3823G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114467013 | ||||||
| chr5:114467231
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1779+4041A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114467231 | ||||||
| chr5:114467443
|
T | G | 6 | a0001c0001t0001g0030a0001c0001t0001g0044a0001c0001t0001g0058others(3): Show | 6 | HG01346.hp1 HG02280.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.1779+4253T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114467443 | ||||||
| chr5:114467506
|
C | T | 181 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(178): Show | 181 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.1779+4316C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114467506 | ||||||
| chr5:114467563
|
T | C | 5 | a0001c0001t0001g0082a0006c0007t0001g0104a0006c0007t0001g0221others(2): Show | 5 | HG02622.hp1 HG03098.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1779+4373T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114467563 | ||||||
| chr5:114467747
|
A | G | 17 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(14): Show | 17 | HG01169.hp1 HG01175.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.1779+4557A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114467747 | ||||||
| chr5:114467882
|
C | A | 2 | a0002c0002t0001g0103a0002c0005t0001g0016 | 2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1779+4692C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114467882 | ||||||
| chr5:114467974
|
A | G | 3 | a0001c0001t0001g0057a0001c0001t0001g0089a0001c0001t0001g0228 | 3 | HG01099.hp2 HG02145.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1779+4784A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114467974 | ||||||
| chr5:114467984
|
C | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(223): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.1779+4794C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114467984 | ||||||
| chr5:114468092
|
T | G | 1 | a0002c0002t0001g0153 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1779+4902T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114468092 | ||||||
| chr5:114468124
|
T | C | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | HG01081.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1780-4930T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114468124 | ||||||
| chr5:114468152
|
G | A | 1 | a0001c0001t0001g0020 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1780-4902G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114468152 | ||||||
| chr5:114468377
|
C | G | 18 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(15): Show | 18 | HG01169.hp1 HG01175.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.1780-4677C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114468377 | ||||||
| chr5:114468443
|
A | T | 1 | a0003c0003t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1780-4611A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114468443 | ||||||
| chr5:114468482
|
C | T | 1 | a0002c0002t0001g0203 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1780-4572C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114468482 | ||||||
| chr5:114468789
|
G | A | 15 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0073others(12): Show | 15 | HG01099.hp2 HG01192.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.1780-4265G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114468789 | ||||||
| chr5:114468797
|
T | C | 4 | a0002c0002t0001g0103a0002c0005t0001g0016a0005c0004t0001g0147others(1): Show | 4 | HG02486.hp2 HG02818.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1780-4257T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114468797 | ||||||
| chr5:114468940
|
T | C | 1 | a0003c0003t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1780-4114T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114468940 | ||||||
| chr5:114469133
|
C | T | 1 | a0002c0002t0001g0162 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1780-3921C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114469133 | ||||||
| chr5:114469138
|
G | A | 1 | a0002c0002t0001g0103 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1780-3916G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114469138 | ||||||
| chr5:114469656
|
T | C | 1 | a0002c0005t0001g0013 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1780-3398T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114469656 | ||||||
| chr5:114469665
|
T | C | 64 | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0032others(61): Show | 64 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1780-3389T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114469665 | ||||||
| chr5:114469814
|
A | G | 16 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0085others(13): Show | 16 | HG01243.hp2 HG02258.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1780-3240A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114469814 | ||||||
| chr5:114469855
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1780-3199C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114469855 | ||||||
| chr5:114469977
|
T | A | 200 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(197): Show | 200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.1780-3077T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114469977 | ||||||
| chr5:114470299
|
G | A | 9 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(6): Show | 9 | HG01169.hp1 HG01358.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.1780-2755G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114470299 | ||||||
| chr5:114470487
|
TG | T | 4 | a0001c0001t0001g0243a0003c0003t0001g0198a0003c0003t0001g0199others(1): Show | 4 | HG02922.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1780-2565delG | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 114470487 | |||||
| chr5:114470590
|
C | T | 20 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0085others(17): Show | 20 | HG01243.hp2 HG02258.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.1780-2464C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114470590 | ||||||
| chr5:114470705
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1780-2349C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114470705 | ||||||
| chr5:114470894
|
T | C | 2 | a0001c0001t0001g0107a0001c0001t0001g0109 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1780-2160T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114470894 | ||||||
| chr5:114471109
|
T | C | 1 | a0001c0001t0001g0039 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1780-1945T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114471109 | ||||||
| chr5:114471131
|
C | T | 1 | a0001c0019t0001g0234 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1780-1923C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114471131 | ||||||
| chr5:114471256
|
T | C | 17 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(14): Show | 17 | HG01169.hp1 HG01175.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.1780-1798T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114471256 | ||||||
| chr5:114471330
|
CTT | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1780-1721_1780-172 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 114471330 | |||||
| chr5:114471531
|
A | G | 66 | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0032others(63): Show | 66 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1780-1523A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114471531 | ||||||
| chr5:114471655
|
C | T | 7 | a0001c0001t0001g0023a0001c0001t0001g0024a0002c0002t0001g0008others(4): Show | 7 | HG00438.hp1 NA18986.hp1 NA19000.hp2 others(4): Show |
intron_variant | MODIFIER | c.1780-1399C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114471655 | ||||||
| chr5:114471904
|
T | C | 2 | a0002c0011t0001g0239a0002c0011t0001g0241 | 2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1780-1150T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114471904 | ||||||
| chr5:114471928
|
T | G | 1 | a0001c0001t0001g0043 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1780-1126T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114471928 | ||||||
| chr5:114472047
|
A | G | 63 | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0032others(60): Show | 63 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1780-1007A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114472047 | ||||||
| chr5:114472214
|
C | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0045a0001c0001t0001g0078others(1): Show | 4 | HG00099.hp1 HG01346.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1780-840C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114472214 | ||||||
| chr5:114472239
|
TCTTTC | T | 63 | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0032others(60): Show | 63 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1780-814_1780-810d others(7): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114472239 | ||||||
| chr5:114472275
|
G | A | 5 | a0002c0002t0001g0103a0002c0002t0001g0238a0002c0005t0001g0016others(2): Show | 5 | HG02486.hp2 HG02723.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1780-779G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114472275 | ||||||
| chr5:114472332
|
C | G | 3 | a0001c0001t0001g0063a0001c0001t0001g0064a0009c0023t0001g0160 | 3 | HG01081.hp1 HG02630.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1780-722C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114472332 | ||||||
| chr5:114472334
|
T | C | 177 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(174): Show | 177 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.1780-720T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114472334 | ||||||
| chr5:114472353
|
A | G | 1 | a0003c0003t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1780-701A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114472353 | ||||||
| chr5:114472389
|
T | C | 1 | a0003c0003t0001g0196 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1780-665T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114472389 | ||||||
| chr5:114472395
|
A | ATGAAGAT others(26): Show |
1 | a0001c0001t0001g0230 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1780-657_1780-625d others(35): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 114472395 | |||||
| chr5:114472436
|
C | T | 203 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(200): Show | 203 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.1780-618C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114472436 | ||||||
| chr5:114472549
|
A | C | 203 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(200): Show | 203 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.1780-505A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114472549 | ||||||
| chr5:114472550
|
C | CTGA | 203 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(200): Show | 203 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.1780-503_1780-501d others(5): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 114472550 | |||||
| chr5:114472558
|
G | C | 1 | a0002c0002t0001g0183 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1780-496G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114472558 | ||||||
| chr5:114472667
|
A | G | 19 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0027others(16): Show | 20 | HG00099.hp1 HG01099.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.1780-387A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114472667 | ||||||
| chr5:114472739
|
G | A | 18 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0027others(15): Show | 19 | HG00099.hp1 HG01099.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.1780-315G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114472739 | ||||||
| chr5:114473678
|
G | T | 2 | a0002c0002t0001g0209a0002c0002t0001g0210 | 2 | HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1890+514G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114473678 | ||||||
| chr5:114473697
|
A | G | 1 | a0002c0002t0001g0187 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1890+533A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114473697 | ||||||
| chr5:114474108
|
A | C | 5 | a0001c0001t0001g0243a0003c0003t0001g0197a0003c0003t0001g0198others(2): Show | 5 | HG02922.hp2 HG03130.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1890+944A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114474108 | ||||||
| chr5:114474173
|
A | G | 2 | a0002c0002t0001g0003a0002c0002t0001g0203 | 2 | HG01257.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1890+1009A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114474173 | ||||||
| chr5:114474265
|
G | A | 13 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(10): Show | 13 | HG01081.hp1 HG02622.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1890+1101G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114474265 | ||||||
| chr5:114474361
|
T | C | 44 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0027others(41): Show | 45 | HG00099.hp1 HG00558.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.1890+1197T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114474361 | ||||||
| chr5:114474629
|
A | T | 1 | a0002c0002t0001g0158 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1890+1465A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114474629 | ||||||
| chr5:114474828
|
A | C | 1 | a0002c0002t0001g0153 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1890+1664A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114474828 | ||||||
| chr5:114474933
|
T | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1890+1769T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114474933 | ||||||
| chr5:114474937
|
C | T | 115 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(112): Show | 115 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.1890+1773C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114474937 | ||||||
| chr5:114475172
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1890+2008C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114475172 | ||||||
| chr5:114475347
|
C | G | 1 | a0002c0002t0001g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1890+2183C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114475347 | ||||||
| chr5:114475616
|
C | T | 4 | a0002c0002t0001g0004a0004c0008t0001g0010a0004c0008t0001g0011others(1): Show | 4 | HG02896.hp1 HG02897.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1890+2452C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114475616 | ||||||
| chr5:114475748
|
G | A | 1 | a0002c0002t0001g0111 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1890+2584G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114475748 | ||||||
| chr5:114476250
|
A | G | 63 | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0032others(60): Show | 63 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1890+3086A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114476250 | ||||||
| chr5:114476365
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1890+3201T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114476365 | ||||||
| chr5:114476442
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1890+3278T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114476442 | ||||||
| chr5:114476490
|
A | G | 1 | a0002c0002t0001g0150 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1890+3326A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114476490 | ||||||
| chr5:114476496
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0069 | 2 | HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1890+3332G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114476496 | ||||||
| chr5:114476695
|
A | C | 2 | a0002c0002t0001g0124a0002c0002t0001g0164 | 2 | NA19065.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1890+3531A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114476695 | ||||||
| chr5:114476753
|
C | G | 1 | a0002c0002t0001g0179 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1890+3589C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114476753 | ||||||
| chr5:114477002
|
T | TAATTCTA others(35): Show |
61 | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0032others(58): Show | 61 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.1890+3839_1890+388 others(46): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114477002 | |||||
| chr5:114477152
|
A | AT | 98 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(95): Show | 98 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.1890+3994dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114477152 | |||||
| chr5:114477250
|
G | A | 115 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(112): Show | 115 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.1890+4086G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114477250 | ||||||
| chr5:114477451
|
T | C | 179 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(176): Show | 179 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.1890+4287T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114477451 | ||||||
| chr5:114477524
|
G | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1890+4360G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114477524 | ||||||
| chr5:114477534
|
C | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 5 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1890+4370C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114477534 | ||||||
| chr5:114477636
|
A | G | 81 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(78): Show | 81 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1890+4472A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114477636 | ||||||
| chr5:114477821
|
A | T | 4 | a0001c0001t0001g0055a0001c0001t0001g0229a0002c0002t0001g0122others(1): Show | 4 | HG01109.hp2 HG02109.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1890+4657A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114477821 | ||||||
| chr5:114477898
|
C | G | 1 | a0001c0001t0001g0083 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1890+4734C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114477898 | ||||||
| chr5:114478030
|
A | G | 34 | a0001c0001t0001g0022a0001c0001t0001g0053a0001c0001t0001g0057others(31): Show | 34 | HG01099.hp2 HG01169.hp1 HG01175.hp1 others(31): Show |
intron_variant | MODIFIER | c.1890+4866A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114478030 | ||||||
| chr5:114478162
|
C | G | 2 | a0002c0002t0001g0124a0002c0002t0001g0164 | 2 | NA19065.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1890+4998C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114478162 | ||||||
| chr5:114478296
|
A | G | 1 | a0002c0002t0001g0071 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1890+5132A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114478296 | ||||||
| chr5:114478381
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1890+5217C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114478381 | ||||||
| chr5:114478459
|
A | C | 1 | a0002c0002t0001g0170 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1890+5295A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114478459 | ||||||
| chr5:114478567
|
C | G | 11 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(8): Show | 11 | HG01081.hp1 HG02622.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1890+5403C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114478567 | ||||||
| chr5:114478657
|
C | T | 11 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(8): Show | 11 | HG01081.hp1 HG02622.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1890+5493C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114478657 | ||||||
| chr5:114478747
|
C | G | 1 | a0001c0001t0001g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1890+5583C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114478747 | ||||||
| chr5:114478757
|
A | G | 64 | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0032others(61): Show | 64 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1890+5593A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114478757 | ||||||
| chr5:114478899
|
C | T | 1 | a0002c0002t0001g0208 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1890+5735C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114478899 | ||||||
| chr5:114478992
|
A | C | 1 | a0002c0002t0001g0167 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1890+5828A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114478992 | ||||||
| chr5:114479015
|
A | G | 11 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0230others(8): Show | 11 | HG00280.hp1 HG01081.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.1890+5851A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114479015 | ||||||
| chr5:114479046
|
CAATAGT | C | 6 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(3): Show | 6 | HG01074.hp1 HG02886.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1890+5885_1890+589 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114479046 | |||||
| chr5:114479084
|
A | ATTAAAAG others(68): Show |
7 | a0001c0001t0001g0023a0001c0001t0001g0024a0002c0002t0001g0008others(4): Show | 7 | HG00438.hp1 NA18986.hp1 NA19000.hp2 others(4): Show |
intron_variant | MODIFIER | c.1890+5921_1890+599 others(79): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114479084 | |||||
| chr5:114479226
|
T | TA | 190 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(187): Show | 190 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1890+6075dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114479226 | |||||
| chr5:114479226
|
T | TAA | 6 | a0001c0001t0001g0030a0001c0001t0001g0044a0001c0001t0001g0058others(3): Show | 6 | HG01346.hp1 HG02280.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.1890+6074_1890+607 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114479226 | |||||
| chr5:114479380
|
C | T | 178 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(175): Show | 178 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.1890+6216C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114479380 | ||||||
| chr5:114479388
|
A | G | 1 | a0002c0002t0001g0123 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1890+6224A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114479388 | ||||||
| chr5:114479763
|
G | A | 248 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(245): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.1890+6599G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114479763 | ||||||
| chr5:114479833
|
T | G | 64 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0026others(61): Show | 64 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1890+6669T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114479833 | ||||||
| chr5:114479859
|
A | G | 1 | a0001c0021t0001g0220 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1890+6695A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114479859 | ||||||
| chr5:114479926
|
C | A | 1 | a0001c0001t0001g0075 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1890+6762C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114479926 | ||||||
| chr5:114479976
|
A | C | 65 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0026others(62): Show | 65 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1890+6812A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114479976 | ||||||
| chr5:114480454
|
A | G | 64 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0026others(61): Show | 64 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1891-6596A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114480454 | ||||||
| chr5:114480513
|
C | G | 9 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(6): Show | 9 | HG01074.hp1 HG02486.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1891-6537C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114480513 | ||||||
| chr5:114480588
|
C | T | 1 | a0002c0002t0001g0126 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1891-6462C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114480588 | ||||||
| chr5:114480759
|
C | G | 7 | a0001c0001t0001g0099a0001c0001t0001g0243a0002c0002t0001g0240others(4): Show | 7 | HG02622.hp2 HG02922.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1891-6291C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114480759 | ||||||
| chr5:114480784
|
G | A | 2 | a0002c0002t0001g0134a0002c0002t0001g0224 | 2 | HG01192.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1891-6266G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114480784 | ||||||
| chr5:114480823
|
A | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0044 | 2 | HG01358.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1891-6227A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114480823 | ||||||
| chr5:114480829
|
A | G | 222 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1891-6221A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114480829 | ||||||
| chr5:114480864
|
C | A | 63 | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0032others(60): Show | 63 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1891-6186C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114480864 | ||||||
| chr5:114480867
|
C | T | 63 | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0032others(60): Show | 63 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1891-6183C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114480867 | ||||||
| chr5:114480885
|
C | G | 1 | a0003c0009t0001g0194 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1891-6165C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114480885 | ||||||
| chr5:114480930
|
G | A | 50 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(47): Show | 50 | HG00438.hp1 HG00558.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.1891-6120G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114480930 | ||||||
| chr5:114481189
|
T | A | 1 | a0003c0003t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1891-5861T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114481189 | ||||||
| chr5:114481213
|
G | A | 17 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0085others(14): Show | 17 | HG01243.hp2 HG02258.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1891-5837G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114481213 | ||||||
| chr5:114481353
|
A | G | 22 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0083others(19): Show | 22 | HG01243.hp2 HG02258.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.1891-5697A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114481353 | ||||||
| chr5:114481358
|
C | G | 13 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(10): Show | 13 | HG01081.hp1 HG02622.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1891-5692C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114481358 | ||||||
| chr5:114481673
|
C | T | 3 | a0001c0001t0001g0063a0001c0001t0001g0064a0009c0023t0001g0160 | 3 | HG01081.hp1 HG02630.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1891-5377C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114481673 | ||||||
| chr5:114481746
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1891-5304A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114481746 | ||||||
| chr5:114481883
|
C | A | 1 | a0001c0001t0001g0060 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1891-5167C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114481883 | ||||||
| chr5:114481971
|
G | A | 1 | a0002c0002t0001g0172 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1891-5079G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114481971 | ||||||
| chr5:114481988
|
C | G | 1 | a0001c0001t0001g0086 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1891-5062C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114481988 | ||||||
| chr5:114481994
|
T | C | 1 | a0005c0004t0001g0146 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1891-5056T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114481994 | ||||||
| chr5:114482006
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1891-5044T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114482006 | ||||||
| chr5:114482028
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1891-5022A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114482028 | ||||||
| chr5:114482568
|
T | C | 1 | a0010c0022t0001g0072 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1891-4482T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114482568 | ||||||
| chr5:114482726
|
G | T | 1 | a0002c0002t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1891-4324G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114482726 | ||||||
| chr5:114482823
|
T | C | 3 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0082 | 3 | HG03139.hp2 HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1891-4227T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114482823 | ||||||
| chr5:114482885
|
G | C | 1 | a0001c0001t0001g0034 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1891-4165G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114482885 | ||||||
| chr5:114482888
|
G | C | 63 | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0032others(60): Show | 63 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1891-4162G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114482888 | ||||||
| chr5:114482916
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1891-4134T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114482916 | ||||||
| chr5:114482946
|
G | C | 64 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0026others(61): Show | 64 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1891-4104G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114482946 | ||||||
| chr5:114483072
|
C | T | 1 | a0002c0002t0001g0179 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1891-3978C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114483072 | ||||||
| chr5:114483124
|
T | C | 1 | a0001c0001t0001g0037 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1891-3926T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114483124 | ||||||
| chr5:114483231
|
T | G | 1 | a0005c0004t0001g0146 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1891-3819T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114483231 | ||||||
| chr5:114483273
|
CT | C | 37 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0027others(34): Show | 38 | HG00099.hp1 HG00558.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1891-3758delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114483273 | |||||
| chr5:114483273
|
CTT | C | 194 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(191): Show | 194 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1891-3759_1891-375 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114483273 | |||||
| chr5:114483273
|
CTTT | C | 6 | a0001c0001t0001g0047a0001c0001t0001g0105a0001c0001t0001g0246others(3): Show | 6 | HG01517.hp2 HG02896.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1891-3760_1891-375 others(7): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114483273 | |||||
| chr5:114483335
|
C | T | 61 | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0032others(58): Show | 61 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.1891-3715C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114483335 | ||||||
| chr5:114483373
|
C | G | 16 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(13): Show | 16 | HG01169.hp1 HG01358.hp1 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.1891-3677C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114483373 | ||||||
| chr5:114483427
|
A | G | 4 | a0001c0001t0001g0085a0002c0005t0001g0013a0002c0005t0001g0014others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1891-3623A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114483427 | ||||||
| chr5:114483712
|
ACT | A | 4 | a0002c0002t0001g0004a0004c0008t0001g0010a0004c0008t0001g0011others(1): Show | 4 | HG02896.hp1 HG02897.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1891-3337_1891-333 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114483712 | ||||||
| chr5:114483713
|
C | CTG | 72 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(69): Show | 72 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1891-3307_1891-330 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114483713 | |||||
| chr5:114483713
|
C | CTGTG | 63 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0024others(60): Show | 64 | HG00099.hp1 HG00558.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1891-3309_1891-330 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114483713 | |||||
| chr5:114483713
|
C | CTGTGTG | 8 | a0001c0001t0001g0042a0001c0001t0001g0049a0001c0001t0001g0052others(5): Show | 8 | HG02523.hp1 HG02735.hp1 HG04199.hp1 others(5): Show |
intron_variant | MODIFIER | c.1891-3311_1891-330 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114483713 | |||||
| chr5:114483713
|
CTG | C | 18 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(15): Show | 18 | HG01081.hp1 HG01169.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.1891-3307_1891-330 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114483713 | |||||
| chr5:114483713
|
CTGTG | C | 9 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0096others(6): Show | 9 | HG02280.hp2 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1891-3309_1891-330 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114483713 | |||||
| chr5:114483713
|
CTGTGTG | C | 9 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0085others(6): Show | 9 | HG01243.hp2 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1891-3311_1891-330 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114483713 | |||||
| chr5:114483926
|
T | C | 1 | a0002c0002t0001g0208 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1891-3124T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114483926 | ||||||
| chr5:114483971
|
T | C | 1 | a0002c0002t0001g0184 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1891-3079T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114483971 | ||||||
| chr5:114484145
|
A | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0027others(42): Show | 46 | HG00099.hp1 HG00558.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.1891-2905A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114484145 | ||||||
| chr5:114484283
|
G | A | 1 | a0002c0002t0001g0205 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1891-2767G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114484283 | ||||||
| chr5:114484372
|
T | C | 1 | a0002c0002t0001g0168 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1891-2678T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114484372 | ||||||
| chr5:114484401
|
C | T | 6 | a0001c0001t0001g0030a0001c0001t0001g0044a0001c0001t0001g0058others(3): Show | 6 | HG01346.hp1 HG02280.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.1891-2649C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114484401 | ||||||
| chr5:114484633
|
G | A | 1 | a0002c0002t0001g0179 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1891-2417G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114484633 | ||||||
| chr5:114484755
|
G | T | 33 | a0001c0001t0001g0018a0001c0001t0001g0033a0001c0001t0001g0042others(30): Show | 33 | HG00438.hp1 HG00738.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1891-2295G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114484755 | ||||||
| chr5:114484775
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1891-2275A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114484775 | ||||||
| chr5:114484808
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1891-2242T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114484808 | ||||||
| chr5:114485133
|
G | A | 3 | a0001c0001t0001g0247a0002c0002t0001g0236a0008c0013t0001g0237 | 3 | HG02886.hp2 HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1891-1917G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114485133 | ||||||
| chr5:114485146
|
T | C | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246 | 3 | NA18964.hp2 NA19074.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1891-1904T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114485146 | ||||||
| chr5:114485148
|
G | A | 1 | a0002c0002t0001g0008 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1891-1902G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114485148 | ||||||
| chr5:114485264
|
G | C | 1 | a0001c0001t0001g0035 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1891-1786G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114485264 | ||||||
| chr5:114485298
|
G | A | 21 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0085others(18): Show | 21 | HG01243.hp2 HG02258.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.1891-1752G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114485298 | ||||||
| chr5:114485429
|
A | G | 1 | a0002c0002t0001g0225 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1891-1621A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114485429 | ||||||
| chr5:114485534
|
C | G | 4 | a0001c0001t0001g0085a0002c0005t0001g0013a0002c0005t0001g0014others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1891-1516C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114485534 | ||||||
| chr5:114485899
|
G | T | 2 | a0002c0002t0001g0002a0002c0002t0001g0185 | 2 | NA18942.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1891-1151G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114485899 | ||||||
| chr5:114485920
|
C | T | 2 | a0002c0002t0001g0119a0002c0002t0001g0132 | 2 | HG01169.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1891-1130C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114485920 | ||||||
| chr5:114486213
|
G | A | 21 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0085others(18): Show | 21 | HG01243.hp2 HG02258.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.1891-837G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114486213 | ||||||
| chr5:114486500
|
G | A | 61 | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0032others(58): Show | 61 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.1891-550G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114486500 | ||||||
| chr5:114486508
|
C | T | 177 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(174): Show | 177 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.1891-542C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114486508 | ||||||
| chr5:114486590
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1891-460A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114486590 | ||||||
| chr5:114486880
|
C | A | 9 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(6): Show | 9 | HG01074.hp1 HG02486.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1891-170C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114486880 | ||||||
| chr5:114487009
|
G | T | 1 | a0001c0001t0001g0020 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1891-41G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114487009 | ||||||
| chr5:114487038
|
T | C | 1 | a0002c0002t0001g0129 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1891-12T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114487038 | ||||||
| chr5:114487304
|
A | T | 1 | a0001c0001t0001g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2018+127A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114487304 | ||||||
| chr5:114487436
|
T | C | 4 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0109others(1): Show | 4 | HG00642.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.2018+259T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114487436 | ||||||
| chr5:114488045
|
A | G | 2 | a0001c0001t0001g0075a0005c0004t0001g0176 | 2 | HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2018+868A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114488045 | ||||||
| chr5:114488219
|
T | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(179): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.2018+1042T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114488219 | ||||||
| chr5:114488271
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2018+1094C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114488271 | ||||||
| chr5:114488279
|
G | A | 21 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0085others(18): Show | 21 | HG01243.hp2 HG02258.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.2018+1102G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114488279 | ||||||
| chr5:114488391
|
T | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(203): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.2018+1214T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114488391 | ||||||
| chr5:114488432
|
A | G | 45 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0027others(42): Show | 46 | HG00099.hp1 HG00558.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.2018+1255A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114488432 | ||||||
| chr5:114488457
|
A | C | 1 | a0002c0002t0001g0120 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2018+1280A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114488457 | ||||||
| chr5:114488476
|
G | C | 1 | a0002c0002t0001g0170 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2018+1299G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114488476 | ||||||
| chr5:114488737
|
G | C | 2 | a0001c0001t0001g0108a0002c0002t0001g0204 | 2 | HG00738.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.2018+1560G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114488737 | ||||||
| chr5:114488816
|
C | T | 2 | a0002c0002t0001g0136a0002c0002t0001g0249 | 2 | NA18964.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.2018+1639C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114488816 | ||||||
| chr5:114488823
|
A | G | 1 | a0002c0002t0001g0209 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2018+1646A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114488823 | ||||||
| chr5:114488910
|
A | G | 1 | a0002c0002t0001g0207 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2018+1733A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114488910 | ||||||
| chr5:114488940
|
C | T | 1 | a0002c0002t0001g0167 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2018+1763C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114488940 | ||||||
| chr5:114489052
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2018+1875T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114489052 | ||||||
| chr5:114489159
|
A | G | 23 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0083others(20): Show | 23 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.2018+1982A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114489159 | ||||||
| chr5:114489189
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2018+2012T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114489189 | ||||||
| chr5:114489267
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2018+2090C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114489267 | ||||||
| chr5:114489298
|
T | G | 17 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(14): Show | 17 | HG01169.hp1 HG01175.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.2018+2121T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114489298 | ||||||
| chr5:114489319
|
A | G | 23 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0083others(20): Show | 23 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.2018+2142A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114489319 | ||||||
| chr5:114489331
|
T | C | 1 | a0001c0001t0001g0246 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2018+2154T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114489331 | ||||||
| chr5:114489360
|
A | G | 1 | a0002c0002t0001g0112 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2018+2183A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114489360 | ||||||
| chr5:114489483
|
G | T | 1 | a0002c0002t0001g0113 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2018+2306G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114489483 | ||||||
| chr5:114489485
|
T | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.2018+2308T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114489485 | ||||||
| chr5:114489554
|
A | G | 2 | a0001c0001t0001g0084a0002c0002t0001g0173 | 2 | HG01175.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2018+2377A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114489554 | ||||||
| chr5:114489657
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2018+2480C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114489657 | ||||||
| chr5:114489789
|
C | A | 1 | a0001c0001t0001g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2018+2612C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114489789 | ||||||
| chr5:114489972
|
A | C | 1 | a0001c0001t0001g0060 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2018+2795A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114489972 | ||||||
| chr5:114490014
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2018+2837T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114490014 | ||||||
| chr5:114490114
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2018+2937G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114490114 | ||||||
| chr5:114490135
|
C | A | 248 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(245): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.2018+2958C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114490135 | ||||||
| chr5:114490935
|
T | C | 1 | a0002c0002t0001g0249 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2019-2468T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114490935 | ||||||
| chr5:114491042
|
A | G | 65 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0026others(62): Show | 65 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.2019-2361A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114491042 | ||||||
| chr5:114491423
|
C | G | 1 | a0002c0002t0001g0240 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2019-1980C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114491423 | ||||||
| chr5:114491509
|
CT | C | 217 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(214): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.2019-1878delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 114491509 | |||||
| chr5:114491509
|
CTT | C | 18 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0076others(15): Show | 18 | HG00280.hp1 HG01109.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.2019-1879_2019-187 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 114491509 | |||||
| chr5:114491525
|
T | A | 6 | a0001c0001t0001g0069a0001c0021t0001g0220a0002c0002t0001g0004others(3): Show | 6 | HG01361.hp1 HG02630.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2019-1878T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114491525 | ||||||
| chr5:114491532
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2019-1871A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114491532 | ||||||
| chr5:114491533
|
G | A | 2 | a0001c0001t0001g0069a0004c0008t0001g0012 | 2 | HG02896.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2019-1870G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114491533 | ||||||
| chr5:114491533
|
GA | G | 7 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0067others(4): Show | 7 | HG01081.hp1 HG01517.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.2019-1855delA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 114491533 | |||||
| chr5:114491534
|
A | G | 2 | a0002c0002t0001g0071a0004c0008t0001g0012 | 2 | HG02896.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.2019-1869A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114491534 | ||||||
| chr5:114491564
|
TAAAG | T | 3 | a0001c0001t0001g0063a0001c0001t0001g0064a0009c0023t0001g0160 | 3 | HG01081.hp1 HG02630.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2019-1837_2019-183 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 114491564 | |||||
| chr5:114491590
|
A | G | 22 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0083others(19): Show | 22 | HG01243.hp2 HG02258.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.2019-1813A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114491590 | ||||||
| chr5:114491680
|
C | T | 1 | a0002c0002t0001g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2019-1723C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114491680 | ||||||
| chr5:114492167
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2019-1236T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114492167 | ||||||
| chr5:114492525
|
T | TAA | 6 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(3): Show | 6 | HG01074.hp1 HG02886.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.2019-876_2019-875d others(4): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 114492525 | |||||
| chr5:114492769
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2019-634A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114492769 | ||||||
| chr5:114492802
|
T | C | 10 | a0001c0001t0001g0099a0001c0001t0001g0243a0002c0002t0001g0240others(7): Show | 10 | HG02622.hp2 HG02895.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.2019-601T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114492802 | ||||||
| chr5:114492886
|
G | GT | 47 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0027others(44): Show | 48 | HG00099.hp1 HG00558.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.2019-506dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 114492886 | |||||
| chr5:114492992
|
A | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(220): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.2019-411A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114492992 | ||||||
| chr5:114493224
|
T | C | 1 | a0002c0002t0001g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2019-179T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114493224 | ||||||
| chr5:114493510
|
T | C | 1 | a0002c0002t0001g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2088+38T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114493510 | ||||||
| chr5:114493551
|
A | C | 23 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0083others(20): Show | 23 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.2088+79A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114493551 | ||||||
| chr5:114493615
|
C | A | 4 | a0001c0001t0001g0055a0001c0001t0001g0229a0002c0002t0001g0122others(1): Show | 4 | HG01109.hp2 HG02109.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.2088+143C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114493615 | ||||||
| chr5:114493692
|
C | T | 1 | a0002c0002t0001g0135 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2088+220C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114493692 | ||||||
| chr5:114493705
|
A | C | 24 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0083others(21): Show | 24 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.2088+233A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114493705 | ||||||
| chr5:114493754
|
A | C | 1 | a0001c0001t0001g0027 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2088+282A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114493754 | ||||||
| chr5:114493783
|
C | T | 1 | a0002c0002t0001g0238 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2088+311C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114493783 | ||||||
| chr5:114494067
|
T | A | 1 | a0011c0016t0003g0177 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2088+595T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114494067 | ||||||
| chr5:114494172
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2088+700G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114494172 | ||||||
| chr5:114494196
|
A | G | 1 | a0002c0002t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2088+724A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114494196 | ||||||
| chr5:114494259
|
G | GT | 213 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.2088+796dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 114494259 | |||||
| chr5:114494259
|
G | GTT | 10 | a0001c0001t0001g0099a0001c0001t0001g0243a0002c0002t0001g0153others(7): Show | 10 | HG02622.hp2 HG02895.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.2088+795_2088+796d others(4): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 114494259 | |||||
| chr5:114494418
|
G | C | 6 | a0001c0001t0001g0030a0001c0001t0001g0044a0001c0001t0001g0058others(3): Show | 6 | HG01346.hp1 HG02280.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.2088+946G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114494418 | ||||||
| chr5:114494508
|
G | A | 22 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0027others(19): Show | 23 | HG00099.hp1 HG00558.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.2088+1036G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114494508 | ||||||
| chr5:114494702
|
A | T | 2 | a0001c0001t0001g0083a0002c0002t0001g0209 | 2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2089-1193A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114494702 | ||||||
| chr5:114494714
|
G | GGACT | 4 | a0002c0002t0001g0004a0004c0008t0001g0010a0004c0008t0001g0011others(1): Show | 4 | HG02896.hp1 HG02897.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089-1179_2089-117 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 114494714 | |||||
| chr5:114494879
|
A | T | 1 | a0011c0016t0003g0177 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2089-1016A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114494879 | ||||||
| chr5:114495105
|
A | T | 63 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(60): Show | 63 | HG00280.hp1 HG00558.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.2089-790A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114495105 | ||||||
| chr5:114495454
|
A | T | 1 | a0010c0022t0001g0072 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2089-441A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114495454 | ||||||
| chr5:114495466
|
C | T | 3 | a0001c0001t0001g0063a0001c0001t0001g0064a0009c0023t0001g0160 | 3 | HG01081.hp1 HG02630.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2089-429C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114495466 | ||||||
| chr5:114495707
|
A | T | 1 | a0011c0016t0003g0177 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2089-188A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114495707 |