Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 157855 |
|---|---|
| ensemblid | ENSG00000215262.8 |
| hgncid | 18867 |
| symbol | KCNU1 |
| name | potassium calcium-activated channel subfamily U member 1 |
| refseq_nuc | NM_001031836.3 |
| refseq_prot | NP_001027006.2 |
| ensembl_nuc | ENST00000399881.8 |
| ensembl_prot | ENSP00000382770.3 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 36784374 |
| end | 36936125 |
| strand | + |
| ver | v1.2 |
| region | chr8:36784374-36936125 |
| region5000 | chr8:36779374-36941125 |
| regionname0 | KCNU1_chr8_36784374_36936125 |
| regionname5000 | KCNU1_chr8_36779374_36941125 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1149 | 130 | 28 | 24 | 58 | 6 | 13 | 41 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0002 | 1/0 | 1149 | 95 | 23 | 17 | 46 | 3 | 5 | 35 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0003 | 0/0 | 1149 | 65 | 18 | 9 | 30 | 2 | 6 | 22 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0004 | 0/0 | 1149 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0005 | 0/0 | 1149 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0006 | 0/0 | 1149 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0007 | 0/0 | 1149 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| 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 | 3450 | 89 | 19 | 16 | 45 | 3 | 5 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| c0002 | 0/1 | 3450 | 83 | 22 | 22 | 24 | 6 | 8 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| c0003 | 0/0 | 3450 | 55 | 17 | 8 | 22 | 2 | 6 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| c0004 | 0/0 | 3450 | 38 | 0 | 1 | 34 | 0 | 3 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| c0005 | 0/0 | 3450 | 9 | 1 | 0 | 8 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| c0006 | 0/0 | 3450 | 5 | 5 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| c0007 | 0/0 | 3450 | 3 | 3 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| c0008 | 0/0 | 3450 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| c0009 | 0/0 | 3450 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| c0010 | 0/0 | 3450 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| c0011 | 0/0 | 3450 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| c0012 | 0/0 | 3450 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| c0013 | 0/0 | 3450 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| c0014 | 0/0 | 3450 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| c0015 | 0/0 | 3450 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| c0016 | 0/0 | 3450 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| c0017 | 0/0 | 3450 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| c0018 | 0/0 | 3450 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| c0019 | 0/0 | 3450 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| 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 | 243 | 293 | 70 | 50 | 135 | 12 | 24 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| t0002 | 0/0 | 243 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| 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 | 3 | 0 | 0 | 3 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0055 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0248 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/1 | 3450 | 83 | 22 | 22 | 24 | 6 | 8 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0001c0004 | 0/0 | 3450 | 38 | 0 | 1 | 34 | 0 | 3 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0001c0006 | 0/0 | 3450 | 5 | 5 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0001c0009 | 0/0 | 3450 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0001c0014 | 0/0 | 3450 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0001c0017 | 0/0 | 3450 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0001c0018 | 0/0 | 3450 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0002c0001 | 1/0 | 3450 | 89 | 19 | 16 | 45 | 3 | 5 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0002c0007 | 0/0 | 3450 | 3 | 3 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0002c0011 | 0/0 | 3450 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0002c0016 | 0/0 | 3450 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0002c0019 | 0/0 | 3450 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0003c0003 | 0/0 | 3450 | 55 | 17 | 8 | 22 | 2 | 6 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0003c0005 | 0/0 | 3450 | 9 | 1 | 0 | 8 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0003c0012 | 0/0 | 3450 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0004c0015 | 0/0 | 3450 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0005c0013 | 0/0 | 3450 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0006c0010 | 0/0 | 3450 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0007c0008 | 0/0 | 3450 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/1 | 3692 | 83 | 22 | 22 | 24 | 6 | 8 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0001c0004t0001 | 0/0 | 3692 | 37 | 0 | 1 | 33 | 0 | 3 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0001c0004t0002 | 0/0 | 3692 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0001c0006t0001 | 0/0 | 3692 | 5 | 5 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0001c0009t0001 | 0/0 | 3692 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0001c0014t0001 | 0/0 | 3692 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0001c0017t0001 | 0/0 | 3692 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0001c0018t0001 | 0/0 | 3692 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0002c0001t0001 | 1/0 | 3692 | 89 | 19 | 16 | 45 | 3 | 5 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0002c0007t0001 | 0/0 | 3692 | 3 | 3 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0002c0011t0001 | 0/0 | 3692 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0002c0016t0001 | 0/0 | 3692 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0002c0019t0001 | 0/0 | 3692 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0003c0003t0001 | 0/0 | 3692 | 55 | 17 | 8 | 22 | 2 | 6 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0003c0005t0001 | 0/0 | 3692 | 9 | 1 | 0 | 8 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0003c0012t0001 | 0/0 | 3692 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0004c0015t0001 | 0/0 | 3692 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0005c0013t0001 | 0/0 | 3692 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0006c0010t0001 | 0/0 | 3692 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| a0007c0008t0001 | 0/0 | 3692 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | copy fasta | chr8 | 36779374 | 36941125 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0248 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0006t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0006t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0006t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0006t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0006t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0009t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0014t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0017t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0018t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0055 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0007t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0007t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0007t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0011t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0016t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0019t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0005t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0005t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0005t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0005t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0005t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0005t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0005t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0005t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0005t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0012t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0004c0015t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0005c0013t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0006c0010t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0007c0008t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0003 | t0001 | g0076 | EUR | GBR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0049 | EUR | GBR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0251 | EUR | GBR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00140 | hp2 | a0003 | c0003 | t0001 | g0098 | EUR | GBR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00438 | hp1 | a0002 | c0001 | t0001 | g0129 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00544 | hp1 | a0002 | c0001 | t0001 | g0140 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00544 | hp2 | a0001 | c0004 | t0001 | g0216 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00558 | hp1 | a0002 | c0001 | t0001 | g0131 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00558 | hp2 | a0001 | c0004 | t0001 | g0200 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00597 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00597 | hp2 | a0002 | c0001 | t0001 | g0143 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00609 | hp1 | a0003 | c0003 | t0001 | g0089 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00609 | hp2 | a0002 | c0001 | t0001 | g0116 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00621 | hp1 | a0003 | c0005 | t0001 | g0210 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00621 | hp2 | a0004 | c0015 | t0001 | g0250 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00639 | hp1 | a0003 | c0003 | t0001 | g0097 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0258 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00673 | hp2 | a0002 | c0001 | t0001 | g0053 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0267 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00735 | hp2 | a0002 | c0001 | t0001 | g0036 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00738 | hp1 | a0002 | c0001 | t0001 | g0122 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0256 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01071 | hp1 | a0002 | c0001 | t0001 | g0120 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01071 | hp2 | a0003 | c0003 | t0001 | g0147 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01074 | hp2 | a0002 | c0001 | t0001 | g0029 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01081 | hp1 | a0002 | c0001 | t0001 | g0042 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0238 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01099 | hp1 | a0002 | c0001 | t0001 | g0025 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0246 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01109 | hp1 | a0002 | c0001 | t0001 | g0043 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01109 | hp2 | a0001 | c0009 | t0001 | g0169 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01167 | hp1 | a0003 | c0003 | t0001 | g0079 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0276 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01168 | hp1 | a0003 | c0003 | t0001 | g0084 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0269 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0237 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01169 | hp2 | a0003 | c0003 | t0001 | g0083 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01243 | hp1 | a0002 | c0001 | t0001 | g0179 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0266 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0274 | AMR | CLM | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01255 | hp2 | a0003 | c0012 | t0001 | g0099 | AMR | CLM | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0156 | AMR | CLM | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01257 | hp2 | a0002 | c0001 | t0001 | g0038 | AMR | CLM | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0155 | AMR | CLM | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01258 | hp2 | a0002 | c0001 | t0001 | g0031 | AMR | CLM | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0054 | AMR | CLM | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01358 | hp2 | a0001 | c0004 | t0001 | g0162 | AMR | CLM | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01433 | hp1 | a0002 | c0001 | t0001 | g0112 | AMR | CLM | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0264 | AMR | CLM | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0245 | AMR | CLM | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01496 | hp2 | a0003 | c0003 | t0001 | g0082 | AMR | CLM | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01515 | hp1 | a0002 | c0001 | t0001 | g0013 | EUR | IBS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0259 | EUR | IBS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01516 | hp1 | a0002 | c0001 | t0001 | g0056 | EUR | IBS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0003 | EUR | IBS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0003 | EUR | IBS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01517 | hp2 | a0002 | c0001 | t0001 | g0012 | EUR | IBS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0289 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01891 | hp2 | a0002 | c0001 | t0001 | g0021 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01928 | hp1 | a0002 | c0001 | t0001 | g0111 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0244 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01934 | hp1 | a0003 | c0003 | t0001 | g0081 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0275 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01978 | hp1 | a0002 | c0001 | t0001 | g0150 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0257 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01981 | hp1 | a0002 | c0001 | t0001 | g0105 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0247 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02004 | hp1 | a0003 | c0003 | t0001 | g0077 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02004 | hp2 | a0002 | c0001 | t0001 | g0037 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02015 | hp1 | a0001 | c0004 | t0001 | g0212 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02015 | hp2 | a0003 | c0003 | t0001 | g0063 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02027 | hp2 | a0003 | c0003 | t0001 | g0062 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0283 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0173 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02056 | hp1 | a0002 | c0001 | t0001 | g0149 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02056 | hp2 | a0001 | c0004 | t0001 | g0213 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02071 | hp1 | a0002 | c0001 | t0001 | g0114 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02074 | hp1 | a0003 | c0003 | t0001 | g0005 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02074 | hp2 | a0001 | c0004 | t0001 | g0190 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02080 | hp1 | a0001 | c0004 | t0001 | g0194 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02083 | hp1 | a0002 | c0001 | t0001 | g0117 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02083 | hp2 | a0003 | c0003 | t0001 | g0154 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02129 | hp1 | a0002 | c0001 | t0001 | g0148 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02129 | hp2 | a0001 | c0004 | t0001 | g0201 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02132 | hp1 | a0003 | c0003 | t0001 | g0232 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02132 | hp2 | a0002 | c0001 | t0001 | g0040 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02148 | hp1 | a0002 | c0019 | t0001 | g0152 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0261 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02165 | hp1 | a0005 | c0013 | t0001 | g0121 | EAS | CDX | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | CDX | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0172 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0281 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02258 | hp1 | a0003 | c0005 | t0001 | g0223 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02258 | hp2 | a0002 | c0001 | t0001 | g0071 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02280 | hp1 | a0002 | c0001 | t0001 | g0080 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02280 | hp2 | a0003 | c0003 | t0001 | g0006 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0277 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02293 | hp2 | a0002 | c0001 | t0001 | g0151 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02523 | hp2 | a0001 | c0004 | t0001 | g0211 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02615 | hp1 | a0001 | c0006 | t0001 | g0287 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02615 | hp2 | a0002 | c0007 | t0001 | g0046 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02630 | hp1 | a0003 | c0003 | t0001 | g0100 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0176 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02647 | hp1 | a0001 | c0018 | t0001 | g0180 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02647 | hp2 | a0002 | c0001 | t0001 | g0024 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02683 | hp1 | a0001 | c0014 | t0001 | g0233 | SAS | PJL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02683 | hp2 | a0003 | c0003 | t0001 | g0064 | SAS | PJL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02717 | hp1 | a0002 | c0001 | t0001 | g0010 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02717 | hp2 | a0007 | c0008 | t0001 | g0279 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02738 | hp1 | a0002 | c0001 | t0001 | g0107 | SAS | PJL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02738 | hp2 | a0001 | c0017 | t0001 | g0217 | SAS | PJL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02809 | hp1 | a0002 | c0001 | t0001 | g0085 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0187 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0278 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02818 | hp2 | a0001 | c0006 | t0001 | g0280 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02886 | hp1 | a0001 | c0006 | t0001 | g0171 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02886 | hp2 | a0002 | c0001 | t0001 | g0068 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0144 | AFR | ESN | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02922 | hp2 | a0002 | c0007 | t0001 | g0153 | AFR | ESN | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02965 | hp1 | a0003 | c0003 | t0001 | g0032 | AFR | ESN | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0158 | AFR | ESN | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03041 | hp1 | a0001 | c0006 | t0001 | g0170 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03041 | hp2 | a0003 | c0003 | t0001 | g0181 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03098 | hp1 | a0002 | c0001 | t0001 | g0027 | AFR | MSL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0282 | AFR | MSL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03130 | hp1 | a0002 | c0001 | t0001 | g0066 | AFR | ESN | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03130 | hp2 | a0003 | c0003 | t0001 | g0033 | AFR | ESN | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03139 | hp1 | a0003 | c0003 | t0001 | g0101 | AFR | ESN | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0174 | AFR | ESN | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03195 | hp1 | a0002 | c0011 | t0001 | g0072 | AFR | ESN | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0286 | AFR | ESN | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03225 | hp1 | a0002 | c0001 | t0001 | g0028 | AFR | MSL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03225 | hp2 | a0003 | c0003 | t0001 | g0035 | AFR | MSL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03239 | hp1 | a0003 | c0003 | t0001 | g0078 | SAS | PJL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0243 | SAS | PJL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03486 | hp1 | a0002 | c0001 | t0001 | g0103 | AFR | MSL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03486 | hp2 | a0003 | c0003 | t0001 | g0011 | AFR | MSL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03492 | hp1 | a0003 | c0003 | t0001 | g0087 | SAS | PJL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0271 | SAS | PJL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0290 | AFR | ESN | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03516 | hp2 | a0003 | c0003 | t0001 | g0284 | AFR | ESN | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0177 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03540 | hp2 | a0002 | c0001 | t0001 | g0004 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0157 | AFR | MSL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03579 | hp2 | a0003 | c0003 | t0001 | g0026 | AFR | MSL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03654 | hp1 | a0001 | c0004 | t0001 | g0221 | SAS | PJL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03654 | hp2 | a0002 | c0001 | t0001 | g0134 | SAS | PJL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0047 | SAS | PJL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03704 | hp2 | a0002 | c0001 | t0001 | g0125 | SAS | PJL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03834 | hp1 | a0003 | c0003 | t0001 | g0007 | SAS | BEB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03834 | hp2 | a0001 | c0004 | t0001 | g0219 | SAS | BEB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03927 | hp1 | a0001 | c0004 | t0001 | g0225 | SAS | BEB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0234 | SAS | BEB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG04115 | hp1 | a0003 | c0003 | t0001 | g0065 | SAS | STU | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0166 | SAS | STU | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0061 | SAS | BEB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG04184 | hp2 | a0002 | c0001 | t0001 | g0136 | SAS | BEB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0249 | SAS | STU | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG04228 | hp2 | a0003 | c0003 | t0001 | g0145 | SAS | STU | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18522 | hp1 | a0003 | c0003 | t0001 | g0034 | AFR | YRI | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18522 | hp2 | a0003 | c0003 | t0001 | g0182 | AFR | YRI | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | CHB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18612 | hp2 | a0003 | c0003 | t0001 | g0260 | EAS | CHB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0288 | AFR | YRI | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18906 | hp2 | a0003 | c0003 | t0001 | g0185 | AFR | YRI | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18942 | hp2 | a0002 | c0001 | t0001 | g0041 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18943 | hp1 | a0001 | c0004 | t0001 | g0227 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18943 | hp2 | a0002 | c0001 | t0001 | g0108 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18944 | hp1 | a0001 | c0004 | t0001 | g0160 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18944 | hp2 | a0002 | c0001 | t0001 | g0095 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18945 | hp1 | a0001 | c0004 | t0001 | g0207 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18945 | hp2 | a0002 | c0001 | t0001 | g0132 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18946 | hp1 | a0003 | c0003 | t0001 | g0092 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18947 | hp1 | a0001 | c0004 | t0001 | g0206 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18947 | hp2 | a0002 | c0001 | t0001 | g0110 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18948 | hp2 | a0002 | c0001 | t0001 | g0016 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18952 | hp1 | a0003 | c0003 | t0001 | g0074 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18952 | hp2 | a0002 | c0001 | t0001 | g0235 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18953 | hp1 | a0002 | c0001 | t0001 | g0019 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18953 | hp2 | a0003 | c0005 | t0001 | g0214 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18954 | hp1 | a0001 | c0004 | t0001 | g0208 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18954 | hp2 | a0003 | c0003 | t0001 | g0075 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18962 | hp1 | a0003 | c0003 | t0001 | g0086 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18962 | hp2 | a0001 | c0004 | t0001 | g0215 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18963 | hp1 | a0001 | c0004 | t0001 | g0198 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18963 | hp2 | a0003 | c0005 | t0001 | g0199 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18964 | hp1 | a0003 | c0003 | t0001 | g0093 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18964 | hp2 | a0002 | c0001 | t0001 | g0113 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18965 | hp1 | a0003 | c0003 | t0001 | g0104 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18965 | hp2 | a0001 | c0004 | t0002 | g0226 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18966 | hp2 | a0002 | c0001 | t0001 | g0127 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18967 | hp2 | a0002 | c0001 | t0001 | g0009 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18969 | hp1 | a0003 | c0003 | t0001 | g0137 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18969 | hp2 | a0002 | c0001 | t0001 | g0094 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18970 | hp2 | a0001 | c0004 | t0001 | g0168 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18972 | hp1 | a0002 | c0001 | t0001 | g0146 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18972 | hp2 | a0003 | c0003 | t0001 | g0231 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18975 | hp1 | a0001 | c0004 | t0001 | g0202 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18975 | hp2 | a0002 | c0001 | t0001 | g0126 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18978 | hp1 | a0002 | c0001 | t0001 | g0106 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18980 | hp1 | a0003 | c0005 | t0001 | g0197 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18982 | hp2 | a0003 | c0005 | t0001 | g0220 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18983 | hp1 | a0002 | c0001 | t0001 | g0115 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18983 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18984 | hp1 | a0001 | c0004 | t0001 | g0205 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18984 | hp2 | a0002 | c0001 | t0001 | g0059 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18985 | hp1 | a0002 | c0001 | t0001 | g0124 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18988 | hp2 | a0003 | c0005 | t0001 | g0196 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18989 | hp1 | a0002 | c0001 | t0001 | g0020 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18989 | hp2 | a0002 | c0001 | t0001 | g0060 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18994 | hp1 | a0001 | c0004 | t0001 | g0159 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18994 | hp2 | a0002 | c0001 | t0001 | g0130 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18995 | hp1 | a0001 | c0004 | t0001 | g0008 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18995 | hp2 | a0002 | c0001 | t0001 | g0015 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18998 | hp1 | a0002 | c0001 | t0001 | g0135 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18998 | hp2 | a0003 | c0003 | t0001 | g0091 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18999 | hp1 | a0002 | c0001 | t0001 | g0142 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18999 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19000 | hp1 | a0001 | c0004 | t0001 | g0228 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19000 | hp2 | a0003 | c0003 | t0001 | g0045 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19001 | hp1 | a0001 | c0004 | t0001 | g0195 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19001 | hp2 | a0002 | c0001 | t0001 | g0141 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19002 | hp1 | a0002 | c0001 | t0001 | g0096 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19002 | hp2 | a0003 | c0003 | t0001 | g0118 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19030 | hp1 | a0001 | c0006 | t0001 | g0178 | AFR | LWK | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19030 | hp2 | a0002 | c0001 | t0001 | g0070 | AFR | LWK | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19043 | hp1 | a0003 | c0003 | t0001 | g0023 | AFR | LWK | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19043 | hp2 | a0002 | c0001 | t0001 | g0183 | AFR | LWK | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19054 | hp1 | a0002 | c0001 | t0001 | g0128 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19054 | hp2 | a0001 | c0004 | t0001 | g0161 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19056 | hp2 | a0001 | c0004 | t0001 | g0209 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19066 | hp1 | a0003 | c0003 | t0001 | g0090 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19066 | hp2 | a0002 | c0001 | t0001 | g0119 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19070 | hp1 | a0002 | c0001 | t0001 | g0058 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19074 | hp1 | a0002 | c0001 | t0001 | g0133 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19074 | hp2 | a0001 | c0004 | t0001 | g0192 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19077 | hp1 | a0003 | c0005 | t0001 | g0189 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19081 | hp1 | a0002 | c0001 | t0001 | g0057 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19081 | hp2 | a0001 | c0004 | t0001 | g0203 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19082 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19082 | hp2 | a0001 | c0004 | t0001 | g0218 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19083 | hp1 | a0002 | c0001 | t0001 | g0138 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19083 | hp2 | a0001 | c0004 | t0001 | g0193 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19084 | hp1 | a0001 | c0004 | t0001 | g0191 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19084 | hp2 | a0003 | c0005 | t0001 | g0222 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19086 | hp2 | a0002 | c0001 | t0001 | g0030 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19087 | hp1 | a0002 | c0016 | t0001 | g0224 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19087 | hp2 | a0003 | c0003 | t0001 | g0017 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19088 | hp1 | a0001 | c0004 | t0001 | g0204 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19088 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19090 | hp2 | a0002 | c0001 | t0001 | g0139 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19240 | hp1 | a0002 | c0001 | t0001 | g0044 | AFR | YRI | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19240 | hp2 | a0002 | c0007 | t0001 | g0069 | AFR | YRI | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA20805 | hp1 | a0006 | c0010 | t0001 | g0022 | EUR | TSI | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0265 | EUR | TSI | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA20905 | hp1 | a0002 | c0001 | t0001 | g0039 | SAS | GIH | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0167 | SAS | GIH | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02109 | hp1 | a0003 | c0003 | t0001 | g0186 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02109 | hp2 | a0002 | c0001 | t0001 | g0052 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02486 | hp2 | a0002 | c0001 | t0001 | g0285 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02559 | hp1 | a0002 | c0001 | t0001 | g0184 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02559 | hp2 | a0003 | c0003 | t0001 | g0067 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG06807 | hp1 | a0003 | c0003 | t0001 | g0102 | AFR | USA | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0175 | AFR | USA | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA20300 | hp1 | a0002 | c0001 | t0001 | g0088 | AFR | USA | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0241 | AFR | USA | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0048 | AFR | LWK | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0188 | AFR | LWK | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0248 | REF | REF | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| homoSapiens_grch38 | hp1 | a0002 | c0001 | t0001 | g0055 | REF | REF | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:36840520
|
C | A | 1 | a0007 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.1576C>A | p.Leu526Met | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 15/27 | 1613/3692 | 1576/3450 | 526/1149 | chr8 | 36840520 | ||
| chr8:36840575
|
G | T | 1 | a0004 | 1 | HG00621.hp2 | missense_variant&splice_region_variant | MODERATE | c.1631G>T | p.Arg544Leu | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 15/27 | 1668/3692 | 1631/3450 | 544/1149 | chr8 | 36840575 | ||
| chr8:36909403
|
C | G | 1 | a0005 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.2199C>G | p.Asn733Lys | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/27 | 2236/3692 | 2199/3450 | 733/1149 | chr8 | 36909403 | ||
| chr8:36909506
|
T | C | 3 | a0001a0005a0007 | 132 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(129): Show |
missense_variant | MODERATE | c.2302T>C | p.Trp768Arg | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/27 | 2339/3692 | 2302/3450 | 768/1149 | chr8 | 36909506 | ||
| chr8:36930961
|
A | G | 1 | a0003 | 65 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(62): Show |
missense_variant | MODERATE | c.2747A>G | p.Asn916Ser | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 25/27 | 2784/3692 | 2747/3450 | 916/1149 | chr8 | 36930961 | ||
| chr8:36935751
|
C | T | 1 | a0006 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.3281C>T | p.Pro1094Leu | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 27/27 | 3318/3692 | 3281/3450 | 1094/1149 | chr8 | 36935751 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:36787356
|
C | T | 1 | a0002c0019 | 1 | HG02148.hp1 | synonymous_variant | LOW | c.246C>T | p.His82His | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/27 | 283/3692 | 246/3450 | 82/1149 | chr8 | 36787356 | ||
| chr8:36817716
|
C | T | 1 | a0001c0018 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.1062C>T | p.Arg354Arg | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/27 | 1099/3692 | 1062/3450 | 354/1149 | chr8 | 36817716 | ||
| chr8:36836876
|
C | T | 4 | a0001c0004a0001c0017a0002c0016others(1): Show | 49 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(46): Show |
synonymous_variant | LOW | c.1449C>T | p.Ile483Ile | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/27 | 1486/3692 | 1449/3450 | 483/1149 | chr8 | 36836876 | ||
| chr8:36864483
|
A | G | 2 | a0001c0014a0001c0017 | 2 | HG02683.hp1 HG02738.hp2 |
synonymous_variant | LOW | c.1971A>G | p.Val657Val | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/27 | 2008/3692 | 1971/3450 | 657/1149 | chr8 | 36864483 | ||
| chr8:36905708
|
G | A | 1 | a0001c0009 | 1 | HG01109.hp2 | splice_region_variant&synonymous_variant | LOW | c.2010G>A | p.Arg670Arg | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/27 | 2047/3692 | 2010/3450 | 670/1149 | chr8 | 36905708 | ||
| chr8:36922620
|
G | C | 2 | a0001c0006a0001c0018 | 6 | HG02615.hp1 HG02647.hp1 HG02818.hp2 others(3): Show |
synonymous_variant | LOW | c.2727G>C | p.Leu909Leu | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/27 | 2764/3692 | 2727/3450 | 909/1149 | chr8 | 36922620 | ||
| chr8:36931139
|
C | T | 1 | a0002c0007 | 3 | HG02615.hp2 HG02922.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.2925C>T | p.Asp975Asp | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 25/27 | 2962/3692 | 2925/3450 | 975/1149 | chr8 | 36931139 | ||
| chr8:36932931
|
C | G | 1 | a0002c0011 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.2943C>G | p.Thr981Thr | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 26/27 | 2980/3692 | 2943/3450 | 981/1149 | chr8 | 36932931 | ||
| chr8:36935659
|
A | G | 1 | a0003c0012 | 1 | HG01255.hp2 | synonymous_variant | LOW | c.3189A>G | p.Ser1063Ser | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 27/27 | 3226/3692 | 3189/3450 | 1063/1149 | chr8 | 36935659 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:36936016
|
C | T | 1 | a0001c0004t0002 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*96C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 27/27 | 96 | chr8 | 36936016 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:36784779
|
C | G | 6 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(3): Show | 6 | HG01891.hp1 HG02486.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.195+174C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36784779 | ||||||
| chr8:36784830
|
A | G | 1 | a0003c0003t0001g0284 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.195+225A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36784830 | ||||||
| chr8:36784918
|
C | G | 1 | a0001c0002t0001g0283 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.195+313C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36784918 | ||||||
| chr8:36784954
|
A | G | 138 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(135): Show | 141 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(138): Show |
intron_variant | MODIFIER | c.195+349A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36784954 | ||||||
| chr8:36784982
|
A | G | 6 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(3): Show | 6 | HG01891.hp1 HG02486.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.195+377A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36784982 | ||||||
| chr8:36784988
|
A | G | 138 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(135): Show | 141 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(138): Show |
intron_variant | MODIFIER | c.195+383A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36784988 | ||||||
| chr8:36785067
|
G | A | 2 | a0001c0002t0001g0155a0001c0002t0001g0156 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.195+462G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36785067 | ||||||
| chr8:36785107
|
A | G | 1 | a0003c0003t0001g0154 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.195+502A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36785107 | ||||||
| chr8:36785470
|
C | G | 2 | a0001c0002t0001g0281a0001c0002t0001g0282 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.195+865C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36785470 | ||||||
| chr8:36785607
|
T | C | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.195+1002T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36785607 | ||||||
| chr8:36786001
|
T | A | 1 | a0002c0001t0001g0004 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.196-1305T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36786001 | ||||||
| chr8:36786112
|
C | CA | 11 | a0001c0002t0001g0163a0001c0002t0001g0164a0001c0002t0001g0165others(8): Show | 11 | HG01358.hp2 HG02027.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.196-1179dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr8 | 36786112 | |||||
| chr8:36786217
|
A | T | 1 | a0002c0007t0001g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.196-1089A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36786217 | ||||||
| chr8:36786311
|
T | C | 2 | a0001c0002t0001g0166a0001c0002t0001g0167 | 2 | HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.196-995T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36786311 | ||||||
| chr8:36786386
|
T | C | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.196-920T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36786386 | ||||||
| chr8:36786616
|
A | G | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.196-690A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36786616 | ||||||
| chr8:36786756
|
C | T | 3 | a0002c0001t0001g0150a0002c0001t0001g0151a0002c0019t0001g0152 | 3 | HG01978.hp1 HG02148.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.196-550C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36786756 | ||||||
| chr8:36787142
|
C | T | 1 | a0001c0006t0001g0280 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.196-164C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36787142 | ||||||
| chr8:36787199
|
G | A | 1 | a0001c0004t0001g0168 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.196-107G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36787199 | ||||||
| chr8:36787462
|
T | G | 1 | a0001c0009t0001g0169 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.315+37T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36787462 | ||||||
| chr8:36787688
|
TATG | T | 30 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(27): Show | 30 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.315+266_315+268del others(3): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36787688 | |||||
| chr8:36787700
|
T | C | 1 | a0001c0002t0001g0283 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.315+275T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36787700 | ||||||
| chr8:36787740
|
C | T | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.315+315C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36787740 | ||||||
| chr8:36787841
|
A | G | 2 | a0002c0001t0001g0148a0002c0001t0001g0149 | 2 | HG02056.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.315+416A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36787841 | ||||||
| chr8:36787856
|
C | CTAAT | 139 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(136): Show | 142 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.315+434_315+437dup others(4): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36787856 | |||||
| chr8:36787958
|
A | G | 58 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(55): Show | 59 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.315+533A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36787958 | ||||||
| chr8:36788024
|
T | C | 47 | a0001c0004t0001g0001a0001c0004t0001g0008a0001c0004t0001g0159others(44): Show | 49 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.315+599T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36788024 | ||||||
| chr8:36788028
|
T | C | 4 | a0001c0002t0001g0229a0001c0002t0001g0230a0003c0003t0001g0231others(1): Show | 4 | HG00438.hp2 HG02132.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.315+603T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36788028 | ||||||
| chr8:36788544
|
T | C | 1 | a0001c0009t0001g0169 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.315+1119T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36788544 | ||||||
| chr8:36788674
|
A | C | 3 | a0002c0001t0001g0150a0002c0001t0001g0151a0002c0019t0001g0152 | 3 | HG01978.hp1 HG02148.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.315+1249A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36788674 | ||||||
| chr8:36788699
|
C | T | 139 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(136): Show | 142 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.315+1274C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36788699 | ||||||
| chr8:36788761
|
T | C | 60 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(57): Show | 61 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.315+1336T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36788761 | ||||||
| chr8:36789135
|
C | T | 1 | a0003c0003t0001g0147 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.315+1710C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36789135 | ||||||
| chr8:36789196
|
T | C | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.315+1771T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36789196 | ||||||
| chr8:36789271
|
G | A | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.315+1846G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36789271 | ||||||
| chr8:36789362
|
T | TA | 9 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(6): Show | 9 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.315+1948dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36789362 | |||||
| chr8:36789792
|
T | C | 62 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(59): Show | 63 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.315+2367T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36789792 | ||||||
| chr8:36789810
|
A | G | 1 | a0001c0002t0001g0278 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.315+2385A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36789810 | ||||||
| chr8:36789924
|
G | A | 2 | a0002c0001t0001g0010a0003c0003t0001g0011 | 2 | HG02717.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.315+2499G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36789924 | ||||||
| chr8:36790001
|
C | A | 27 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(24): Show | 27 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.315+2576C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36790001 | ||||||
| chr8:36790427
|
C | T | 1 | a0002c0001t0001g0146 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.315+3002C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36790427 | ||||||
| chr8:36790511
|
A | G | 62 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(59): Show | 63 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.315+3086A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36790511 | ||||||
| chr8:36790664
|
A | G | 27 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(24): Show | 27 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.315+3239A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36790664 | ||||||
| chr8:36790801
|
T | A | 1 | a0003c0003t0001g0005 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.315+3376T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36790801 | ||||||
| chr8:36790872
|
C | A | 2 | a0002c0001t0001g0012a0002c0001t0001g0013 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.315+3447C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36790872 | ||||||
| chr8:36790874
|
A | G | 1 | a0003c0003t0001g0145 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.315+3449A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36790874 | ||||||
| chr8:36790998
|
GA | G | 138 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(135): Show | 141 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(138): Show |
intron_variant | MODIFIER | c.315+3586delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36790998 | |||||
| chr8:36791036
|
G | A | 1 | a0001c0002t0001g0014 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.315+3611G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36791036 | ||||||
| chr8:36791352
|
G | A | 1 | a0002c0001t0001g0009 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.315+3927G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36791352 | ||||||
| chr8:36791526
|
C | A | 1 | a0002c0001t0001g0015 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.315+4101C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36791526 | ||||||
| chr8:36791527
|
T | G | 1 | a0002c0001t0001g0015 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.315+4102T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36791527 | ||||||
| chr8:36791569
|
TAGATAAA others(17): Show |
T | 1 | a0002c0001t0001g0016 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.315+4146_315+4169d others(26): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36791569 | |||||
| chr8:36791603
|
T | G | 139 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(136): Show | 142 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.315+4178T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36791603 | ||||||
| chr8:36791666
|
G | A | 5 | a0001c0002t0001g0018a0002c0001t0001g0016a0002c0001t0001g0019others(2): Show | 5 | NA18948.hp2 NA18953.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.315+4241G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36791666 | ||||||
| chr8:36791978
|
G | A | 2 | a0001c0002t0001g0281a0001c0002t0001g0282 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.315+4553G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36791978 | ||||||
| chr8:36792030
|
A | G | 1 | a0003c0003t0001g0011 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.315+4605A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36792030 | ||||||
| chr8:36792225
|
T | A | 2 | a0001c0002t0001g0281a0001c0002t0001g0282 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.315+4800T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36792225 | ||||||
| chr8:36792601
|
C | T | 48 | a0001c0002t0001g0144a0001c0004t0001g0001a0001c0004t0001g0008others(45): Show | 50 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.315+5176C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36792601 | ||||||
| chr8:36792881
|
G | T | 62 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(59): Show | 63 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.315+5456G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36792881 | ||||||
| chr8:36793093
|
C | T | 58 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(55): Show | 59 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.315+5668C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36793093 | ||||||
| chr8:36793100
|
A | T | 3 | a0001c0002t0001g0275a0001c0002t0001g0276a0001c0002t0001g0277 | 3 | HG01167.hp2 HG01934.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.315+5675A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36793100 | ||||||
| chr8:36793215
|
G | A | 1 | a0001c0002t0001g0283 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.315+5790G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36793215 | ||||||
| chr8:36793217
|
G | A | 1 | a0002c0001t0001g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.315+5792G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36793217 | ||||||
| chr8:36793338
|
G | C | 1 | a0006c0010t0001g0022 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.315+5913G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36793338 | ||||||
| chr8:36793457
|
C | T | 19 | a0001c0002t0001g0187a0001c0002t0001g0188a0001c0002t0001g0286others(16): Show | 19 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.315+6032C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36793457 | ||||||
| chr8:36793718
|
AGTTGTCC others(10): Show |
A | 3 | a0001c0006t0001g0178a0001c0018t0001g0180a0002c0001t0001g0179 | 3 | HG01243.hp1 HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.315+6297_315+6313d others(19): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36793718 | |||||
| chr8:36793725
|
C | T | 88 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(85): Show | 89 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.315+6300C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36793725 | ||||||
| chr8:36793883
|
G | A | 2 | a0002c0001t0001g0024a0003c0003t0001g0023 | 2 | HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.315+6458G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36793883 | ||||||
| chr8:36793920
|
G | A | 1 | a0001c0002t0001g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.315+6495G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36793920 | ||||||
| chr8:36793957
|
G | A | 1 | a0002c0001t0001g0025 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.315+6532G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36793957 | ||||||
| chr8:36793979
|
G | T | 46 | a0001c0002t0001g0109a0001c0002t0001g0123a0002c0001t0001g0009others(43): Show | 46 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.315+6554G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36793979 | ||||||
| chr8:36794040
|
C | T | 1 | a0001c0002t0001g0283 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.315+6615C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36794040 | ||||||
| chr8:36794055
|
C | CA | 41 | a0001c0002t0001g0109a0001c0004t0001g0001a0001c0004t0001g0159others(38): Show | 43 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.315+6652dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36794055 | |||||
| chr8:36794055
|
CA | C | 25 | a0001c0002t0001g0187a0001c0002t0001g0188a0001c0002t0001g0286others(22): Show | 25 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.315+6652delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36794055 | |||||
| chr8:36794055
|
CAA | C | 61 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0157others(58): Show | 62 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.315+6651_315+6652d others(4): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36794055 | |||||
| chr8:36794055
|
CAAA | C | 8 | a0001c0002t0001g0156a0001c0002t0001g0172a0001c0002t0001g0173others(5): Show | 8 | HG01257.hp1 HG02055.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.315+6650_315+6652d others(5): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36794055 | |||||
| chr8:36794270
|
G | T | 3 | a0003c0003t0001g0097a0003c0003t0001g0098a0003c0012t0001g0099 | 3 | HG00140.hp2 HG00639.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.315+6845G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36794270 | ||||||
| chr8:36794409
|
A | C | 89 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(86): Show | 90 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.315+6984A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36794409 | ||||||
| chr8:36794513
|
C | A | 6 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.315+7088C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36794513 | ||||||
| chr8:36794955
|
C | A | 139 | a0001c0002t0001g0003a0001c0002t0001g0144a0001c0002t0001g0155others(136): Show | 142 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.315+7530C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36794955 | ||||||
| chr8:36795224
|
C | T | 5 | a0001c0002t0001g0018a0002c0001t0001g0016a0002c0001t0001g0019others(2): Show | 5 | NA18948.hp2 NA18953.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.315+7799C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36795224 | ||||||
| chr8:36795455
|
C | T | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.315+8030C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36795455 | ||||||
| chr8:36795550
|
A | T | 87 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(84): Show | 88 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.315+8125A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36795550 | ||||||
| chr8:36795676
|
T | C | 1 | a0002c0001t0001g0016 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.315+8251T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36795676 | ||||||
| chr8:36795818
|
G | A | 1 | a0001c0002t0001g0283 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.316-8209G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36795818 | ||||||
| chr8:36795914
|
A | G | 1 | a0001c0002t0001g0274 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.316-8113A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36795914 | ||||||
| chr8:36795940
|
G | C | 1 | a0001c0002t0001g0234 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.316-8087G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36795940 | ||||||
| chr8:36796049
|
T | A | 3 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174 | 3 | HG02055.hp2 HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.316-7978T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796049 | ||||||
| chr8:36796086
|
G | T | 1 | a0002c0001t0001g0016 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.316-7941G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796086 | ||||||
| chr8:36796105
|
C | A | 90 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(87): Show | 91 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.316-7922C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796105 | ||||||
| chr8:36796131
|
T | C | 1 | a0002c0001t0001g0016 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.316-7896T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796131 | ||||||
| chr8:36796132
|
C | T | 1 | a0002c0001t0001g0016 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.316-7895C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796132 | ||||||
| chr8:36796133
|
T | C | 1 | a0002c0001t0001g0016 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.316-7894T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796133 | ||||||
| chr8:36796271
|
T | C | 1 | a0002c0001t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.316-7756T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796271 | ||||||
| chr8:36796285
|
C | T | 2 | a0001c0002t0001g0283a0002c0001t0001g0143 | 2 | HG00597.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.316-7742C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796285 | ||||||
| chr8:36796316
|
G | C | 89 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(86): Show | 90 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.316-7711G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796316 | ||||||
| chr8:36796337
|
C | T | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.316-7690C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796337 | ||||||
| chr8:36796384
|
A | G | 1 | a0001c0002t0001g0273 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.316-7643A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796384 | ||||||
| chr8:36796407
|
C | T | 87 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(84): Show | 88 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.316-7620C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796407 | ||||||
| chr8:36796533
|
T | C | 2 | a0001c0006t0001g0170a0001c0006t0001g0171 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.316-7494T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796533 | ||||||
| chr8:36796859
|
G | T | 1 | a0003c0003t0001g0104 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.316-7168G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796859 | ||||||
| chr8:36797250
|
T | C | 19 | a0001c0002t0001g0187a0001c0002t0001g0188a0001c0002t0001g0286others(16): Show | 19 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.316-6777T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36797250 | ||||||
| chr8:36797293
|
T | A | 1 | a0002c0001t0001g0235 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.316-6734T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36797293 | ||||||
| chr8:36797304
|
CT | C | 49 | a0001c0004t0001g0001a0001c0004t0001g0008a0001c0004t0001g0159others(46): Show | 51 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.316-6713delT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36797304 | |||||
| chr8:36797491
|
G | T | 1 | a0001c0002t0001g0283 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.316-6536G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36797491 | ||||||
| chr8:36797535
|
C | T | 1 | a0002c0001t0001g0096 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.316-6492C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36797535 | ||||||
| chr8:36797634
|
CT | C | 64 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(61): Show | 65 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.316-6380delT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36797634 | |||||
| chr8:36797737
|
C | G | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.316-6290C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36797737 | ||||||
| chr8:36797866
|
T | C | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.316-6161T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36797866 | ||||||
| chr8:36798015
|
T | C | 60 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(57): Show | 61 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.316-6012T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36798015 | ||||||
| chr8:36798089
|
C | G | 2 | a0001c0002t0001g0281a0001c0002t0001g0282 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.316-5938C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36798089 | ||||||
| chr8:36798201
|
G | A | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.316-5826G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36798201 | ||||||
| chr8:36798251
|
T | C | 8 | a0001c0002t0001g0187a0002c0001t0001g0183a0002c0001t0001g0184others(5): Show | 8 | HG02109.hp1 HG02559.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.316-5776T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36798251 | ||||||
| chr8:36798406
|
T | G | 58 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(55): Show | 59 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.316-5621T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36798406 | ||||||
| chr8:36798650
|
C | T | 6 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.316-5377C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36798650 | ||||||
| chr8:36798698
|
A | T | 39 | a0001c0004t0001g0001a0001c0004t0001g0008a0001c0004t0001g0168others(36): Show | 41 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.316-5329A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36798698 | ||||||
| chr8:36799100
|
C | G | 1 | a0001c0002t0001g0272 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.316-4927C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36799100 | ||||||
| chr8:36799147
|
C | A | 1 | a0002c0001t0001g0029 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.316-4880C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36799147 | ||||||
| chr8:36799258
|
A | G | 91 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(88): Show | 92 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.316-4769A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36799258 | ||||||
| chr8:36799484
|
C | T | 89 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(86): Show | 90 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.316-4543C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36799484 | ||||||
| chr8:36799510
|
G | C | 1 | a0001c0002t0001g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.316-4517G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36799510 | ||||||
| chr8:36799684
|
G | A | 1 | a0001c0002t0001g0236 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.316-4343G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36799684 | ||||||
| chr8:36799700
|
A | AT | 65 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(62): Show | 66 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.316-4314dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36799700 | |||||
| chr8:36799700
|
A | ATT | 25 | a0001c0002t0001g0165a0001c0002t0001g0187a0001c0002t0001g0188others(22): Show | 25 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.316-4315_316-4314d others(4): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36799700 | |||||
| chr8:36799793
|
G | A | 8 | a0001c0002t0001g0187a0002c0001t0001g0183a0002c0001t0001g0184others(5): Show | 8 | HG02109.hp1 HG02559.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.316-4234G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36799793 | ||||||
| chr8:36799860
|
T | C | 2 | a0001c0006t0001g0170a0001c0006t0001g0171 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.316-4167T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36799860 | ||||||
| chr8:36800005
|
C | T | 60 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(57): Show | 61 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.316-4022C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36800005 | ||||||
| chr8:36800310
|
G | C | 90 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(87): Show | 91 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.316-3717G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36800310 | ||||||
| chr8:36800554
|
G | A | 1 | a0002c0001t0001g0030 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.316-3473G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36800554 | ||||||
| chr8:36800636
|
A | C | 1 | a0002c0001t0001g0141 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.316-3391A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36800636 | ||||||
| chr8:36800872
|
G | A | 59 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(56): Show | 60 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.316-3155G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36800872 | ||||||
| chr8:36800872
|
G | T | 1 | a0001c0002t0001g0272 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.316-3155G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36800872 | ||||||
| chr8:36800918
|
A | G | 1 | a0002c0001t0001g0140 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.316-3109A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36800918 | ||||||
| chr8:36800934
|
G | T | 1 | a0001c0002t0001g0283 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.316-3093G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36800934 | ||||||
| chr8:36801137
|
C | G | 2 | a0001c0002t0001g0281a0001c0002t0001g0282 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.316-2890C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36801137 | ||||||
| chr8:36801396
|
C | T | 55 | a0001c0002t0001g0018a0001c0002t0001g0073a0002c0001t0001g0004others(52): Show | 56 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.316-2631C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36801396 | ||||||
| chr8:36801431
|
CT | C | 90 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(87): Show | 91 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.316-2586delT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36801431 | |||||
| chr8:36801433
|
T | C | 1 | a0002c0001t0001g0031 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.316-2594T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36801433 | ||||||
| chr8:36801483
|
T | G | 87 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(84): Show | 88 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.316-2544T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36801483 | ||||||
| chr8:36801491
|
G | A | 1 | a0003c0003t0001g0005 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.316-2536G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36801491 | ||||||
| chr8:36801510
|
T | C | 6 | a0003c0003t0001g0006a0003c0003t0001g0026a0003c0003t0001g0032others(3): Show | 6 | HG02280.hp2 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.316-2517T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36801510 | ||||||
| chr8:36801641
|
A | G | 1 | a0002c0001t0001g0139 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.316-2386A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36801641 | ||||||
| chr8:36801868
|
A | G | 140 | a0001c0002t0001g0003a0001c0002t0001g0144a0001c0002t0001g0155others(137): Show | 143 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.316-2159A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36801868 | ||||||
| chr8:36802048
|
G | T | 1 | a0001c0002t0001g0283 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.316-1979G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802048 | ||||||
| chr8:36802076
|
T | A | 1 | a0001c0002t0001g0283 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.316-1951T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802076 | ||||||
| chr8:36802087
|
G | C | 140 | a0001c0002t0001g0003a0001c0002t0001g0144a0001c0002t0001g0155others(137): Show | 143 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.316-1940G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802087 | ||||||
| chr8:36802090
|
A | C | 1 | a0001c0002t0001g0290 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.316-1937A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802090 | ||||||
| chr8:36802108
|
C | CA | 52 | a0001c0004t0001g0001a0001c0004t0001g0008a0001c0004t0001g0159others(49): Show | 54 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.316-1895dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36802108 | |||||
| chr8:36802108
|
CA | C | 13 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0175others(10): Show | 14 | HG00609.hp1 HG02055.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.316-1895delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36802108 | |||||
| chr8:36802108
|
CAA | C | 9 | a0001c0002t0001g0166a0001c0002t0001g0167a0001c0002t0001g0239others(6): Show | 9 | HG01934.hp2 HG02257.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.316-1896_316-1895d others(4): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36802108 | |||||
| chr8:36802108
|
CAAA | C | 71 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(68): Show | 72 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.316-1897_316-1895d others(5): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36802108 | |||||
| chr8:36802108
|
CAAAAAAA others(6): Show |
C | 4 | a0003c0003t0001g0097a0003c0003t0001g0098a0003c0003t0001g0147others(1): Show | 4 | HG00140.hp2 HG00639.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.316-1907_316-1895d others(15): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36802108 | |||||
| chr8:36802166
|
A | G | 8 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.316-1861A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802166 | ||||||
| chr8:36802167
|
C | A | 8 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.316-1860C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802167 | ||||||
| chr8:36802395
|
G | A | 140 | a0001c0002t0001g0003a0001c0002t0001g0144a0001c0002t0001g0155others(137): Show | 143 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.316-1632G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802395 | ||||||
| chr8:36802564
|
T | G | 2 | a0001c0002t0001g0281a0001c0002t0001g0282 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.316-1463T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802564 | ||||||
| chr8:36802580
|
A | C | 1 | a0003c0003t0001g0062 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.316-1447A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802580 | ||||||
| chr8:36802654
|
G | A | 3 | a0002c0001t0001g0066a0002c0001t0001g0068a0003c0003t0001g0067 | 3 | HG02559.hp2 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.316-1373G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802654 | ||||||
| chr8:36802664
|
G | C | 1 | a0001c0002t0001g0242 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.316-1363G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802664 | ||||||
| chr8:36802669
|
G | A | 140 | a0001c0002t0001g0003a0001c0002t0001g0144a0001c0002t0001g0155others(137): Show | 143 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.316-1358G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802669 | ||||||
| chr8:36802675
|
G | T | 4 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.316-1352G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802675 | ||||||
| chr8:36802771
|
T | A | 140 | a0001c0002t0001g0003a0001c0002t0001g0144a0001c0002t0001g0155others(137): Show | 143 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.316-1256T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802771 | ||||||
| chr8:36802804
|
A | C | 18 | a0001c0002t0001g0187a0001c0002t0001g0286a0001c0002t0001g0288others(15): Show | 18 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.316-1223A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802804 | ||||||
| chr8:36802952
|
G | A | 1 | a0002c0001t0001g0179 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.316-1075G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802952 | ||||||
| chr8:36803306
|
T | C | 1 | a0002c0001t0001g0025 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.316-721T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36803306 | ||||||
| chr8:36803439
|
C | T | 89 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(86): Show | 90 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.316-588C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36803439 | ||||||
| chr8:36803486
|
T | TA | 18 | a0001c0002t0001g0187a0001c0002t0001g0286a0001c0002t0001g0288others(15): Show | 18 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.316-533dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36803486 | |||||
| chr8:36803500
|
T | G | 2 | a0002c0001t0001g0148a0002c0001t0001g0149 | 2 | HG02056.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.316-527T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36803500 | ||||||
| chr8:36803754
|
A | T | 4 | a0002c0001t0001g0103a0003c0003t0001g0100a0003c0003t0001g0101others(1): Show | 4 | HG02630.hp1 HG03139.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.316-273A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36803754 | ||||||
| chr8:36803826
|
T | C | 7 | a0001c0002t0001g0155a0001c0002t0001g0156a0001c0002t0001g0243others(4): Show | 7 | HG01099.hp2 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.316-201T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36803826 | ||||||
| chr8:36803930
|
G | A | 1 | a0002c0001t0001g0037 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.316-97G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36803930 | ||||||
| chr8:36804168
|
A | C | 70 | a0001c0002t0001g0003a0001c0002t0001g0109a0001c0002t0001g0155others(67): Show | 71 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.377+80A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 3/26 | chr8 | 36804168 | ||||||
| chr8:36804191
|
A | G | 1 | a0001c0002t0001g0283 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.377+103A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 3/26 | chr8 | 36804191 | ||||||
| chr8:36804236
|
T | C | 1 | a0002c0001t0001g0025 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.377+148T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 3/26 | chr8 | 36804236 | ||||||
| chr8:36804453
|
C | T | 2 | a0001c0002t0001g0175a0001c0002t0001g0176 | 2 | HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377+365C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 3/26 | chr8 | 36804453 | ||||||
| chr8:36804662
|
T | C | 1 | a0001c0002t0001g0175 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.378-533T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 3/26 | chr8 | 36804662 | ||||||
| chr8:36804696
|
G | A | 4 | a0002c0001t0001g0070a0002c0001t0001g0071a0002c0007t0001g0069others(1): Show | 4 | HG02258.hp2 HG03195.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.378-499G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 3/26 | chr8 | 36804696 | ||||||
| chr8:36804869
|
T | A | 2 | a0001c0002t0001g0175a0001c0002t0001g0176 | 2 | HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.378-326T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 3/26 | chr8 | 36804869 | ||||||
| chr8:36804897
|
T | C | 140 | a0001c0002t0001g0003a0001c0002t0001g0073a0001c0002t0001g0144others(137): Show | 143 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.378-298T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 3/26 | chr8 | 36804897 | ||||||
| chr8:36804946
|
C | G | 1 | a0003c0003t0001g0231 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.378-249C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 3/26 | chr8 | 36804946 | ||||||
| chr8:36804994
|
G | T | 2 | a0002c0001t0001g0148a0002c0001t0001g0149 | 2 | HG02056.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.378-201G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 3/26 | chr8 | 36804994 | ||||||
| chr8:36805162
|
G | T | 92 | a0001c0002t0001g0003a0001c0002t0001g0073a0001c0002t0001g0155others(89): Show | 93 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.378-33G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 3/26 | chr8 | 36805162 | ||||||
| chr8:36805629
|
G | A | 2 | a0001c0002t0001g0281a0001c0002t0001g0282 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.468+344G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 4/26 | chr8 | 36805629 | ||||||
| chr8:36805661
|
A | C | 1 | a0001c0002t0001g0061 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.468+376A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 4/26 | chr8 | 36805661 | ||||||
| chr8:36805703
|
T | C | 1 | a0002c0001t0001g0038 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.468+418T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 4/26 | chr8 | 36805703 | ||||||
| chr8:36805997
|
C | T | 1 | a0002c0001t0001g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.469-272C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 4/26 | chr8 | 36805997 | ||||||
| chr8:36806000
|
C | T | 49 | a0001c0002t0001g0018a0002c0001t0001g0004a0002c0001t0001g0016others(46): Show | 50 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.469-269C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 4/26 | chr8 | 36806000 | ||||||
| chr8:36806089
|
C | T | 1 | a0001c0002t0001g0282 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.469-180C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 4/26 | chr8 | 36806089 | ||||||
| chr8:36806118
|
G | A | 24 | a0001c0002t0001g0061a0002c0001t0001g0010a0002c0001t0001g0021others(21): Show | 24 | HG00735.hp2 HG01081.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.469-151G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 4/26 | chr8 | 36806118 | ||||||
| chr8:36806553
|
A | C | 89 | a0001c0002t0001g0003a0001c0002t0001g0073a0001c0002t0001g0155others(86): Show | 90 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.580+173A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 5/26 | chr8 | 36806553 | ||||||
| chr8:36806695
|
A | G | 1 | a0002c0001t0001g0016 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.580+315A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 5/26 | chr8 | 36806695 | ||||||
| chr8:36806760
|
T | G | 140 | a0001c0002t0001g0003a0001c0002t0001g0073a0001c0002t0001g0144others(137): Show | 143 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.580+380T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 5/26 | chr8 | 36806760 | ||||||
| chr8:36807195
|
A | C | 66 | a0001c0002t0001g0003a0001c0002t0001g0073a0001c0002t0001g0155others(63): Show | 67 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.581-180A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 5/26 | chr8 | 36807195 | ||||||
| chr8:36807312
|
C | T | 1 | a0002c0001t0001g0112 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.581-63C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 5/26 | chr8 | 36807312 | ||||||
| chr8:36807316
|
G | A | 6 | a0001c0002t0001g0014a0001c0002t0001g0047a0001c0002t0001g0048others(3): Show | 6 | HG00099.hp2 HG01074.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.581-59G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 5/26 | chr8 | 36807316 | ||||||
| chr8:36807506
|
T | C | 2 | a0002c0001t0001g0105a0002c0001t0001g0111 | 2 | HG01928.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.656+56T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 6/26 | chr8 | 36807506 | ||||||
| chr8:36807729
|
C | CA | 50 | a0001c0002t0001g0144a0001c0002t0001g0188a0001c0004t0001g0001others(47): Show | 52 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.656+295dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr8 | 36807729 | |||||
| chr8:36807737
|
A | C | 1 | a0003c0003t0001g0154 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.656+287A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 6/26 | chr8 | 36807737 | ||||||
| chr8:36807791
|
A | G | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.656+341A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 6/26 | chr8 | 36807791 | ||||||
| chr8:36807813
|
T | TA | 89 | a0001c0002t0001g0003a0001c0002t0001g0073a0001c0002t0001g0155others(86): Show | 90 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.656+373dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr8 | 36807813 | |||||
| chr8:36807902
|
T | C | 89 | a0001c0002t0001g0003a0001c0002t0001g0073a0001c0002t0001g0155others(86): Show | 90 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.656+452T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 6/26 | chr8 | 36807902 | ||||||
| chr8:36808344
|
A | C | 140 | a0001c0002t0001g0003a0001c0002t0001g0073a0001c0002t0001g0144others(137): Show | 143 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.657-374A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 6/26 | chr8 | 36808344 | ||||||
| chr8:36808583
|
C | T | 2 | a0002c0001t0001g0010a0003c0003t0001g0011 | 2 | HG02717.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.657-135C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 6/26 | chr8 | 36808583 | ||||||
| chr8:36808665
|
G | A | 90 | a0001c0002t0001g0003a0001c0002t0001g0073a0001c0002t0001g0155others(87): Show | 91 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.657-53G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 6/26 | chr8 | 36808665 | ||||||
| chr8:36808800
|
A | G | 17 | a0001c0002t0001g0187a0001c0002t0001g0286a0001c0002t0001g0288others(14): Show | 17 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(14): Show |
splice_region_variant&intron_variant | LOW | c.732+7A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36808800 | ||||||
| chr8:36808811
|
A | G | 3 | a0003c0003t0001g0064a0003c0003t0001g0065a0003c0003t0001g0087 | 3 | HG02683.hp2 HG03492.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.732+18A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36808811 | ||||||
| chr8:36808883
|
T | C | 2 | a0002c0001t0001g0012a0002c0001t0001g0013 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.732+90T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36808883 | ||||||
| chr8:36809220
|
C | T | 3 | a0003c0003t0001g0097a0003c0003t0001g0098a0003c0012t0001g0099 | 3 | HG00140.hp2 HG00639.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.732+427C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36809220 | ||||||
| chr8:36809369
|
G | A | 89 | a0001c0002t0001g0003a0001c0002t0001g0073a0001c0002t0001g0155others(86): Show | 90 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.732+576G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36809369 | ||||||
| chr8:36809511
|
C | G | 138 | a0001c0002t0001g0003a0001c0002t0001g0073a0001c0002t0001g0144others(135): Show | 141 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(138): Show |
intron_variant | MODIFIER | c.732+718C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36809511 | ||||||
| chr8:36809725
|
G | C | 1 | a0002c0001t0001g0113 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.732+932G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36809725 | ||||||
| chr8:36809814
|
A | C | 1 | a0001c0002t0001g0283 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.732+1021A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36809814 | ||||||
| chr8:36809859
|
T | C | 2 | a0001c0002t0001g0175a0001c0002t0001g0176 | 2 | HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.732+1066T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36809859 | ||||||
| chr8:36809926
|
G | A | 2 | a0002c0001t0001g0114a0002c0001t0001g0115 | 2 | HG02071.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.732+1133G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36809926 | ||||||
| chr8:36810029
|
G | T | 1 | a0001c0002t0001g0283 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.732+1236G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36810029 | ||||||
| chr8:36810193
|
A | G | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.732+1400A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36810193 | ||||||
| chr8:36810250
|
C | CA | 144 | a0001c0002t0001g0003a0001c0002t0001g0073a0001c0002t0001g0144others(141): Show | 147 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(144): Show |
intron_variant | MODIFIER | c.732+1471dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr8 | 36810250 | |||||
| chr8:36810501
|
A | G | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.732+1708A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36810501 | ||||||
| chr8:36810768
|
A | C | 89 | a0001c0002t0001g0003a0001c0002t0001g0073a0001c0002t0001g0155others(86): Show | 90 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.732+1975A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36810768 | ||||||
| chr8:36810975
|
G | A | 1 | a0003c0003t0001g0097 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.732+2182G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36810975 | ||||||
| chr8:36811328
|
T | G | 9 | a0001c0002t0001g0061a0002c0001t0001g0030a0002c0001t0001g0036others(6): Show | 9 | HG00735.hp2 HG01081.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.732+2535T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36811328 | ||||||
| chr8:36811431
|
C | G | 2 | a0002c0001t0001g0103a0003c0003t0001g0102 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.732+2638C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36811431 | ||||||
| chr8:36811448
|
A | G | 1 | a0002c0007t0001g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.732+2655A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36811448 | ||||||
| chr8:36811813
|
A | C | 1 | a0002c0001t0001g0134 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.733-2394A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36811813 | ||||||
| chr8:36811829
|
G | A | 1 | a0002c0001t0001g0038 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.733-2378G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36811829 | ||||||
| chr8:36811865
|
G | A | 47 | a0001c0002t0001g0144a0001c0004t0001g0001a0001c0004t0001g0008others(44): Show | 49 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.733-2342G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36811865 | ||||||
| chr8:36812032
|
C | G | 17 | a0001c0002t0001g0187a0001c0002t0001g0286a0001c0002t0001g0288others(14): Show | 17 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.733-2175C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36812032 | ||||||
| chr8:36812074
|
C | A | 1 | a0002c0001t0001g0044 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.733-2133C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36812074 | ||||||
| chr8:36812177
|
C | G | 17 | a0001c0002t0001g0187a0001c0002t0001g0286a0001c0002t0001g0288others(14): Show | 17 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.733-2030C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36812177 | ||||||
| chr8:36812308
|
A | G | 59 | a0001c0002t0001g0003a0001c0002t0001g0073a0001c0002t0001g0155others(56): Show | 60 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.733-1899A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36812308 | ||||||
| chr8:36812378
|
C | CA | 26 | a0001c0002t0001g0187a0001c0002t0001g0283a0001c0002t0001g0286others(23): Show | 26 | HG00735.hp2 HG01358.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.733-1810dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr8 | 36812378 | |||||
| chr8:36812378
|
C | CAA | 49 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(46): Show | 51 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.733-1811_733-1810d others(4): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr8 | 36812378 | |||||
| chr8:36812378
|
CA | C | 74 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(71): Show | 75 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.733-1810delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr8 | 36812378 | |||||
| chr8:36812933
|
A | C | 59 | a0001c0002t0001g0003a0001c0002t0001g0073a0001c0002t0001g0155others(56): Show | 60 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.733-1274A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36812933 | ||||||
| chr8:36813012
|
G | A | 1 | a0001c0004t0001g0191 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.733-1195G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36813012 | ||||||
| chr8:36813273
|
T | C | 2 | a0001c0002t0001g0281a0001c0002t0001g0282 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.733-934T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36813273 | ||||||
| chr8:36813430
|
A | T | 1 | a0001c0002t0001g0050 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.733-777A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36813430 | ||||||
| chr8:36813503
|
A | G | 1 | a0001c0002t0001g0176 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.733-704A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36813503 | ||||||
| chr8:36813664
|
G | T | 1 | a0002c0001t0001g0103 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.733-543G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36813664 | ||||||
| chr8:36813670
|
T | TA | 76 | a0001c0002t0001g0003a0001c0002t0001g0155a0001c0002t0001g0156others(73): Show | 77 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.733-537_733-536ins others(1): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36813670 | ||||||
| chr8:36813670
|
T | TAA | 12 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(9): Show | 12 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.733-537_733-536ins others(2): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36813670 | ||||||
| chr8:36813671
|
T | A | 89 | a0001c0002t0001g0003a0001c0002t0001g0073a0001c0002t0001g0155others(86): Show | 90 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.733-536T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36813671 | ||||||
| chr8:36813855
|
C | T | 23 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(20): Show | 23 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.733-352C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36813855 | ||||||
| chr8:36813865
|
G | GA | 140 | a0001c0002t0001g0003a0001c0002t0001g0073a0001c0002t0001g0144others(137): Show | 143 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.733-342_733-341ins others(1): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36813865 | ||||||
| chr8:36813932
|
T | A | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.733-275T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36813932 | ||||||
| chr8:36813992
|
G | A | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.733-215G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36813992 | ||||||
| chr8:36814066
|
A | T | 1 | a0001c0006t0001g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.733-141A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36814066 | ||||||
| chr8:36814082
|
T | G | 1 | a0001c0002t0001g0283 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.733-125T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36814082 | ||||||
| chr8:36814483
|
A | G | 7 | a0002c0001t0001g0179a0003c0003t0001g0006a0003c0003t0001g0026others(4): Show | 7 | HG01243.hp1 HG02280.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.903+106A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 8/26 | chr8 | 36814483 | ||||||
| chr8:36814664
|
T | A | 1 | a0003c0003t0001g0063 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.903+287T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 8/26 | chr8 | 36814664 | ||||||
| chr8:36814671
|
A | G | 2 | a0003c0003t0001g0045a0003c0003t0001g0062 | 2 | HG02027.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.903+294A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 8/26 | chr8 | 36814671 | ||||||
| chr8:36814945
|
G | A | 1 | a0002c0001t0001g0116 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.903+568G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 8/26 | chr8 | 36814945 | ||||||
| chr8:36815007
|
T | G | 1 | a0001c0002t0001g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.904-589T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 8/26 | chr8 | 36815007 | ||||||
| chr8:36815075
|
A | C | 1 | a0001c0004t0001g0190 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.904-521A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 8/26 | chr8 | 36815075 | ||||||
| chr8:36815213
|
C | A | 3 | a0002c0001t0001g0044a0002c0007t0001g0046a0002c0007t0001g0153 | 3 | HG02615.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.904-383C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 8/26 | chr8 | 36815213 | ||||||
| chr8:36815563
|
G | A | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.904-33G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 8/26 | chr8 | 36815563 | ||||||
| chr8:36815701
|
T | A | 48 | a0001c0002t0001g0144a0001c0004t0001g0001a0001c0004t0001g0008others(45): Show | 50 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.995+14T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36815701 | ||||||
| chr8:36815761
|
A | G | 2 | a0001c0002t0001g0049a0001c0002t0001g0050 | 2 | HG00099.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.995+74A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36815761 | ||||||
| chr8:36815795
|
A | G | 1 | a0002c0001t0001g0060 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.995+108A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36815795 | ||||||
| chr8:36815842
|
A | T | 1 | a0003c0003t0001g0101 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.995+155A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36815842 | ||||||
| chr8:36816101
|
A | ATAAT | 142 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(139): Show | 145 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.995+416_995+419dup others(4): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr8 | 36816101 | |||||
| chr8:36816101
|
A | T | 2 | a0001c0002t0001g0187a0001c0002t0001g0283 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.995+414A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36816101 | ||||||
| chr8:36816234
|
T | A | 142 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(139): Show | 145 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.995+547T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36816234 | ||||||
| chr8:36816246
|
T | C | 48 | a0001c0002t0001g0144a0001c0004t0001g0001a0001c0004t0001g0008others(45): Show | 50 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.995+559T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36816246 | ||||||
| chr8:36816255
|
A | G | 92 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(89): Show | 93 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.995+568A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36816255 | ||||||
| chr8:36816262
|
A | G | 92 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(89): Show | 93 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.995+575A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36816262 | ||||||
| chr8:36816315
|
G | A | 8 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.995+628G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36816315 | ||||||
| chr8:36816452
|
C | T | 8 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.995+765C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36816452 | ||||||
| chr8:36816528
|
G | A | 1 | a0001c0002t0001g0047 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.995+841G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36816528 | ||||||
| chr8:36816644
|
AC | A | 92 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(89): Show | 93 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.995+958delC | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36816644 | ||||||
| chr8:36816649
|
A | T | 92 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(89): Show | 93 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.995+962A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36816649 | ||||||
| chr8:36816944
|
AAAC | A | 91 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(88): Show | 92 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.996-685_996-683del others(3): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr8 | 36816944 | |||||
| chr8:36817116
|
T | A | 2 | a0001c0004t0001g0192a0001c0004t0001g0215 | 2 | NA18962.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.996-534T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36817116 | ||||||
| chr8:36817128
|
G | A | 1 | a0001c0009t0001g0169 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.996-522G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36817128 | ||||||
| chr8:36817131
|
G | A | 1 | a0001c0002t0001g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.996-519G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36817131 | ||||||
| chr8:36817195
|
A | G | 2 | a0001c0002t0001g0187a0001c0002t0001g0283 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.996-455A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36817195 | ||||||
| chr8:36817274
|
C | T | 1 | a0003c0003t0001g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.996-376C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36817274 | ||||||
| chr8:36817289
|
C | T | 2 | a0001c0006t0001g0170a0001c0006t0001g0171 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.996-361C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36817289 | ||||||
| chr8:36817359
|
C | T | 1 | a0001c0004t0001g0190 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.996-291C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36817359 | ||||||
| chr8:36817376
|
T | G | 269 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0047others(266): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.996-274T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36817376 | ||||||
| chr8:36817385
|
G | A | 2 | a0002c0001t0001g0027a0002c0001t0001g0052 | 2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.996-265G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36817385 | ||||||
| chr8:36817499
|
C | CA | 13 | a0002c0001t0001g0027a0002c0001t0001g0039a0002c0001t0001g0052others(10): Show | 13 | HG00673.hp2 HG01243.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.996-125dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr8 | 36817499 | |||||
| chr8:36817499
|
C | CAAAAAA | 26 | a0001c0002t0001g0157a0001c0004t0001g0001a0001c0004t0001g0008others(23): Show | 28 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.996-130_996-125dup others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr8 | 36817499 | |||||
| chr8:36817499
|
C | CAAAAAAA | 15 | a0001c0002t0001g0187a0001c0002t0001g0283a0001c0004t0001g0160others(12): Show | 15 | HG00544.hp2 HG01358.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.996-131_996-125dup others(7): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr8 | 36817499 | |||||
| chr8:36817499
|
CA | C | 51 | a0001c0002t0001g0018a0001c0002t0001g0051a0001c0002t0001g0109others(48): Show | 51 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.996-125delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr8 | 36817499 | |||||
| chr8:36817499
|
CAAA | C | 24 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0249others(21): Show | 24 | HG01891.hp1 HG01934.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.996-127_996-125del others(3): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr8 | 36817499 | |||||
| chr8:36817499
|
CAAAA | C | 63 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(60): Show | 64 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.996-128_996-125del others(4): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr8 | 36817499 | |||||
| chr8:36817541
|
T | C | 1 | a0005c0013t0001g0121 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.996-109T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36817541 | ||||||
| chr8:36817579
|
T | C | 50 | a0001c0002t0001g0144a0001c0002t0001g0187a0001c0002t0001g0283others(47): Show | 52 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.996-71T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36817579 | ||||||
| chr8:36817632
|
C | T | 8 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.996-18C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36817632 | ||||||
| chr8:36817909
|
C | A | 1 | a0002c0001t0001g0122 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1106+149C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36817909 | ||||||
| chr8:36817997
|
G | A | 2 | a0001c0002t0001g0187a0001c0002t0001g0283 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1106+237G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36817997 | ||||||
| chr8:36818268
|
C | A | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1106+508C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36818268 | ||||||
| chr8:36818320
|
T | A | 1 | a0001c0004t0001g0200 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1106+560T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36818320 | ||||||
| chr8:36818367
|
CT | C | 16 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(13): Show | 16 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1106+610delT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 36818367 | |||||
| chr8:36818427
|
A | G | 1 | a0001c0002t0001g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1106+667A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36818427 | ||||||
| chr8:36818447
|
C | T | 1 | a0002c0001t0001g0122 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1106+687C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36818447 | ||||||
| chr8:36818644
|
C | T | 68 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(65): Show | 69 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1106+884C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36818644 | ||||||
| chr8:36818689
|
T | G | 3 | a0002c0001t0001g0024a0002c0001t0001g0088a0003c0003t0001g0023 | 3 | HG02647.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1106+929T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36818689 | ||||||
| chr8:36818856
|
A | G | 2 | a0001c0006t0001g0170a0001c0006t0001g0171 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1106+1096A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36818856 | ||||||
| chr8:36819964
|
T | C | 2 | a0002c0001t0001g0040a0002c0001t0001g0041 | 2 | HG02132.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1106+2204T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36819964 | ||||||
| chr8:36820064
|
A | G | 1 | a0002c0001t0001g0085 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1106+2304A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36820064 | ||||||
| chr8:36820116
|
T | C | 142 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(139): Show | 145 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.1106+2356T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36820116 | ||||||
| chr8:36820361
|
G | A | 9 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(6): Show | 9 | HG01891.hp1 HG02486.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1106+2601G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36820361 | ||||||
| chr8:36820484
|
C | T | 9 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(6): Show | 9 | HG01891.hp1 HG02486.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1106+2724C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36820484 | ||||||
| chr8:36820573
|
C | T | 1 | a0001c0002t0001g0272 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1106+2813C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36820573 | ||||||
| chr8:36820614
|
G | GA | 7 | a0002c0001t0001g0183a0002c0001t0001g0184a0003c0003t0001g0181others(4): Show | 7 | HG02109.hp1 HG02559.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1106+2867dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 36820614 | |||||
| chr8:36820614
|
GA | G | 50 | a0001c0002t0001g0270a0001c0004t0001g0001a0001c0004t0001g0008others(47): Show | 52 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1106+2867delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 36820614 | |||||
| chr8:36820816
|
G | A | 2 | a0003c0003t0001g0074a0003c0003t0001g0075 | 2 | NA18952.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1106+3056G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36820816 | ||||||
| chr8:36821103
|
T | G | 2 | a0002c0001t0001g0039a0006c0010t0001g0022 | 2 | NA20805.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1106+3343T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36821103 | ||||||
| chr8:36821186
|
A | G | 4 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1106+3426A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36821186 | ||||||
| chr8:36821322
|
G | A | 3 | a0002c0001t0001g0029a0002c0001t0001g0031a0002c0001t0001g0037 | 3 | HG01074.hp2 HG01258.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1106+3562G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36821322 | ||||||
| chr8:36821347
|
G | A | 2 | a0001c0002t0001g0187a0001c0002t0001g0283 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1106+3587G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36821347 | ||||||
| chr8:36821784
|
T | A | 1 | a0001c0002t0001g0248 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1106+4024T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36821784 | ||||||
| chr8:36821834
|
C | CTT | 144 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(141): Show | 147 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.1106+4075_1106+407 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 36821834 | |||||
| chr8:36821917
|
C | T | 16 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(13): Show | 16 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1106+4157C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36821917 | ||||||
| chr8:36821926
|
G | A | 2 | a0001c0006t0001g0170a0001c0006t0001g0171 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1106+4166G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36821926 | ||||||
| chr8:36822178
|
T | C | 1 | a0001c0002t0001g0177 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1106+4418T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36822178 | ||||||
| chr8:36822233
|
T | TGTATGTA others(26): Show |
4 | a0001c0002t0001g0229a0001c0002t0001g0230a0003c0003t0001g0231others(1): Show | 4 | HG00438.hp2 HG02132.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.1106+4482_1106+451 others(37): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 36822233 | |||||
| chr8:36822263
|
A | G | 1 | a0002c0001t0001g0134 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1106+4503A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36822263 | ||||||
| chr8:36822295
|
T | C | 143 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(140): Show | 146 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.1106+4535T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36822295 | ||||||
| chr8:36822840
|
C | A | 1 | a0002c0001t0001g0108 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1106+5080C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36822840 | ||||||
| chr8:36823046
|
G | A | 2 | a0001c0002t0001g0049a0001c0002t0001g0050 | 2 | HG00099.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1106+5286G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36823046 | ||||||
| chr8:36823211
|
C | T | 3 | a0002c0001t0001g0058a0002c0001t0001g0059a0002c0001t0001g0060 | 3 | NA18984.hp2 NA18989.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1106+5451C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36823211 | ||||||
| chr8:36823223
|
A | G | 16 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(13): Show | 16 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1106+5463A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36823223 | ||||||
| chr8:36823353
|
T | G | 1 | a0001c0009t0001g0169 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1106+5593T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36823353 | ||||||
| chr8:36823463
|
T | A | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1106+5703T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36823463 | ||||||
| chr8:36823835
|
C | A | 1 | a0001c0002t0001g0172 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1106+6075C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36823835 | ||||||
| chr8:36823836
|
C | CT | 42 | a0001c0002t0001g0144a0001c0004t0001g0001a0001c0004t0001g0008others(39): Show | 44 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.1106+6094dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 36823836 | |||||
| chr8:36823836
|
C | CTT | 8 | a0001c0004t0001g0159a0001c0004t0001g0160a0001c0004t0001g0161others(5): Show | 8 | HG01358.hp2 HG02258.hp1 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.1106+6093_1106+609 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 36823836 | |||||
| chr8:36823836
|
CT | C | 94 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(91): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.1106+6094delT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 36823836 | |||||
| chr8:36823838
|
T | C | 1 | a0001c0002t0001g0172 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1106+6078T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36823838 | ||||||
| chr8:36823922
|
C | T | 1 | a0003c0003t0001g0065 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1106+6162C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36823922 | ||||||
| chr8:36824000
|
A | G | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1106+6240A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36824000 | ||||||
| chr8:36824084
|
G | A | 1 | a0001c0004t0001g0162 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1106+6324G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36824084 | ||||||
| chr8:36824247
|
G | A | 1 | a0002c0001t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1106+6487G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36824247 | ||||||
| chr8:36824363
|
G | A | 3 | a0001c0002t0001g0157a0001c0002t0001g0158a0003c0003t0001g0182 | 3 | HG02965.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1106+6603G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36824363 | ||||||
| chr8:36824528
|
G | T | 6 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1106+6768G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36824528 | ||||||
| chr8:36824665
|
A | G | 2 | a0002c0001t0001g0132a0002c0001t0001g0133 | 2 | NA18945.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1106+6905A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36824665 | ||||||
| chr8:36824716
|
C | G | 50 | a0001c0002t0001g0144a0001c0002t0001g0187a0001c0002t0001g0283others(47): Show | 52 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1106+6956C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36824716 | ||||||
| chr8:36824739
|
T | A | 16 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(13): Show | 16 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1106+6979T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36824739 | ||||||
| chr8:36824819
|
T | C | 2 | a0002c0001t0001g0103a0003c0003t0001g0102 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1106+7059T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36824819 | ||||||
| chr8:36824941
|
T | C | 1 | a0002c0001t0001g0031 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1106+7181T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36824941 | ||||||
| chr8:36824966
|
G | A | 1 | a0001c0009t0001g0169 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1106+7206G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36824966 | ||||||
| chr8:36824979
|
T | C | 1 | a0002c0001t0001g0095 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1106+7219T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36824979 | ||||||
| chr8:36825031
|
G | T | 2 | a0001c0002t0001g0014a0002c0001t0001g0028 | 2 | HG01074.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1106+7271G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36825031 | ||||||
| chr8:36825035
|
G | A | 48 | a0001c0002t0001g0144a0001c0004t0001g0001a0001c0004t0001g0008others(45): Show | 50 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1106+7275G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36825035 | ||||||
| chr8:36825071
|
C | G | 2 | a0001c0002t0001g0238a0001c0002t0001g0267 | 2 | HG00735.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1106+7311C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36825071 | ||||||
| chr8:36825153
|
A | C | 1 | a0001c0002t0001g0270 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1106+7393A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36825153 | ||||||
| chr8:36825504
|
C | T | 8 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1106+7744C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36825504 | ||||||
| chr8:36825516
|
A | ATTG | 50 | a0001c0002t0001g0144a0001c0002t0001g0187a0001c0002t0001g0283others(47): Show | 52 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1106+7758_1106+775 others(7): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 36825516 | |||||
| chr8:36825559
|
A | G | 1 | a0001c0002t0001g0266 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1106+7799A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36825559 | ||||||
| chr8:36825692
|
A | G | 3 | a0003c0003t0001g0077a0003c0003t0001g0081a0003c0003t0001g0082 | 3 | HG01496.hp2 HG01934.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1107-7862A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36825692 | ||||||
| chr8:36825960
|
T | C | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1107-7594T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36825960 | ||||||
| chr8:36826262
|
C | T | 144 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(141): Show | 147 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.1107-7292C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36826262 | ||||||
| chr8:36826266
|
G | C | 144 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(141): Show | 147 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.1107-7288G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36826266 | ||||||
| chr8:36826271
|
C | G | 144 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(141): Show | 147 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.1107-7283C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36826271 | ||||||
| chr8:36826272
|
T | C | 144 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(141): Show | 147 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.1107-7282T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36826272 | ||||||
| chr8:36826473
|
G | C | 1 | a0003c0003t0001g0089 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1107-7081G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36826473 | ||||||
| chr8:36826501
|
C | T | 2 | a0001c0002t0001g0187a0001c0002t0001g0283 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1107-7053C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36826501 | ||||||
| chr8:36826718
|
T | A | 4 | a0002c0001t0001g0029a0002c0001t0001g0031a0002c0001t0001g0037others(1): Show | 4 | HG01074.hp2 HG01258.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1107-6836T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36826718 | ||||||
| chr8:36826719
|
A | T | 1 | a0006c0010t0001g0022 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1107-6835A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36826719 | ||||||
| chr8:36826727
|
T | G | 1 | a0001c0002t0001g0123 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1107-6827T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36826727 | ||||||
| chr8:36826934
|
G | A | 6 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1107-6620G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36826934 | ||||||
| chr8:36826975
|
C | T | 1 | a0001c0002t0001g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1107-6579C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36826975 | ||||||
| chr8:36827152
|
G | A | 1 | a0001c0002t0001g0229 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1107-6402G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36827152 | ||||||
| chr8:36827274
|
T | C | 1 | a0002c0001t0001g0151 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1107-6280T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36827274 | ||||||
| chr8:36827531
|
T | C | 39 | a0001c0004t0001g0001a0001c0004t0001g0008a0001c0004t0001g0168others(36): Show | 41 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.1107-6023T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36827531 | ||||||
| chr8:36827838
|
A | T | 50 | a0001c0002t0001g0144a0001c0002t0001g0187a0001c0002t0001g0283others(47): Show | 52 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1107-5716A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36827838 | ||||||
| chr8:36827843
|
A | T | 144 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(141): Show | 147 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.1107-5711A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36827843 | ||||||
| chr8:36827983
|
A | C | 48 | a0001c0002t0001g0144a0001c0004t0001g0001a0001c0004t0001g0008others(45): Show | 50 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1107-5571A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36827983 | ||||||
| chr8:36828566
|
G | A | 6 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1107-4988G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36828566 | ||||||
| chr8:36828618
|
T | C | 2 | a0001c0006t0001g0170a0001c0006t0001g0171 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1107-4936T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36828618 | ||||||
| chr8:36828636
|
C | T | 1 | a0003c0003t0001g0186 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1107-4918C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36828636 | ||||||
| chr8:36828780
|
G | A | 6 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1107-4774G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36828780 | ||||||
| chr8:36828825
|
G | T | 45 | a0001c0002t0001g0051a0001c0002t0001g0109a0001c0002t0001g0123others(42): Show | 45 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1107-4729G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36828825 | ||||||
| chr8:36828858
|
T | C | 1 | a0004c0015t0001g0250 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1107-4696T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36828858 | ||||||
| chr8:36829146
|
G | A | 50 | a0001c0002t0001g0144a0001c0002t0001g0187a0001c0002t0001g0283others(47): Show | 52 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1107-4408G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36829146 | ||||||
| chr8:36829348
|
T | A | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1107-4206T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36829348 | ||||||
| chr8:36829397
|
T | C | 8 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1107-4157T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36829397 | ||||||
| chr8:36829405
|
G | A | 1 | a0001c0017t0001g0217 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1107-4149G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36829405 | ||||||
| chr8:36829486
|
A | G | 1 | a0001c0002t0001g0281 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1107-4068A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36829486 | ||||||
| chr8:36829499
|
T | A | 16 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(13): Show | 16 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1107-4055T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36829499 | ||||||
| chr8:36829572
|
A | AT | 49 | a0001c0002t0001g0144a0001c0004t0001g0001a0001c0004t0001g0008others(46): Show | 51 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.1107-3973dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 36829572 | |||||
| chr8:36829738
|
T | C | 1 | a0002c0001t0001g0117 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1107-3816T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36829738 | ||||||
| chr8:36829775
|
G | T | 2 | a0001c0002t0001g0187a0001c0002t0001g0283 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1107-3779G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36829775 | ||||||
| chr8:36829800
|
T | A | 2 | a0001c0002t0001g0281a0001c0002t0001g0282 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1107-3754T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36829800 | ||||||
| chr8:36829890
|
T | C | 2 | a0001c0002t0001g0238a0001c0002t0001g0267 | 2 | HG00735.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1107-3664T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36829890 | ||||||
| chr8:36829962
|
A | G | 45 | a0001c0002t0001g0051a0001c0002t0001g0109a0001c0002t0001g0123others(42): Show | 45 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1107-3592A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36829962 | ||||||
| chr8:36830142
|
T | G | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1107-3412T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36830142 | ||||||
| chr8:36830443
|
C | A | 1 | a0002c0001t0001g0004 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1107-3111C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36830443 | ||||||
| chr8:36830443
|
C | T | 2 | a0001c0002t0001g0187a0001c0002t0001g0283 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1107-3111C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36830443 | ||||||
| chr8:36830444
|
G | A | 1 | a0001c0002t0001g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1107-3110G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36830444 | ||||||
| chr8:36830496
|
C | T | 3 | a0003c0003t0001g0077a0003c0003t0001g0081a0003c0003t0001g0082 | 3 | HG01496.hp2 HG01934.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1107-3058C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36830496 | ||||||
| chr8:36830529
|
T | C | 3 | a0002c0001t0001g0024a0002c0001t0001g0088a0003c0003t0001g0023 | 3 | HG02647.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1107-3025T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36830529 | ||||||
| chr8:36830601
|
G | T | 48 | a0001c0002t0001g0144a0001c0004t0001g0001a0001c0004t0001g0008others(45): Show | 50 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1107-2953G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36830601 | ||||||
| chr8:36830631
|
G | A | 16 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(13): Show | 16 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1107-2923G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36830631 | ||||||
| chr8:36830755
|
T | A | 1 | a0002c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1107-2799T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36830755 | ||||||
| chr8:36830755
|
T | G | 68 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(65): Show | 69 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1107-2799T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36830755 | ||||||
| chr8:36830891
|
G | A | 6 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1107-2663G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36830891 | ||||||
| chr8:36831028
|
G | A | 1 | a0001c0017t0001g0217 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1107-2526G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831028 | ||||||
| chr8:36831056
|
A | G | 63 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(60): Show | 64 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1107-2498A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831056 | ||||||
| chr8:36831207
|
C | T | 6 | a0003c0003t0001g0006a0003c0003t0001g0026a0003c0003t0001g0032others(3): Show | 6 | HG02280.hp2 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1107-2347C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831207 | ||||||
| chr8:36831297
|
T | G | 1 | a0001c0002t0001g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1107-2257T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831297 | ||||||
| chr8:36831306
|
T | C | 1 | a0001c0002t0001g0175 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1107-2248T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831306 | ||||||
| chr8:36831329
|
G | A | 2 | a0001c0002t0001g0047a0001c0002t0001g0048 | 2 | HG03704.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1107-2225G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831329 | ||||||
| chr8:36831350
|
G | C | 1 | a0003c0003t0001g0005 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1107-2204G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831350 | ||||||
| chr8:36831513
|
T | C | 1 | a0003c0005t0001g0223 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1107-2041T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831513 | ||||||
| chr8:36831520
|
C | T | 1 | a0001c0002t0001g0265 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1107-2034C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831520 | ||||||
| chr8:36831585
|
T | C | 1 | a0003c0003t0001g0101 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1107-1969T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831585 | ||||||
| chr8:36831586
|
G | A | 1 | a0003c0003t0001g0101 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1107-1968G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831586 | ||||||
| chr8:36831663
|
T | A | 1 | a0001c0002t0001g0242 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1107-1891T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831663 | ||||||
| chr8:36831683
|
T | C | 1 | a0001c0002t0001g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1107-1871T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831683 | ||||||
| chr8:36831734
|
C | A | 1 | a0001c0002t0001g0230 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1107-1820C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831734 | ||||||
| chr8:36831875
|
G | A | 1 | a0001c0004t0001g0211 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1107-1679G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831875 | ||||||
| chr8:36831917
|
G | A | 146 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(143): Show | 149 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.1107-1637G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831917 | ||||||
| chr8:36831973
|
A | C | 1 | a0001c0002t0001g0281 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1107-1581A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831973 | ||||||
| chr8:36832036
|
G | A | 2 | a0001c0002t0001g0281a0001c0002t0001g0282 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1107-1518G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36832036 | ||||||
| chr8:36832311
|
C | T | 48 | a0001c0002t0001g0144a0001c0004t0001g0001a0001c0004t0001g0008others(45): Show | 50 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1107-1243C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36832311 | ||||||
| chr8:36832805
|
C | T | 128 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(125): Show | 131 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.1107-749C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36832805 | ||||||
| chr8:36832868
|
A | G | 37 | a0001c0004t0001g0001a0001c0004t0001g0008a0001c0004t0001g0168others(34): Show | 39 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.1107-686A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36832868 | ||||||
| chr8:36832878
|
G | C | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1107-676G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36832878 | ||||||
| chr8:36832896
|
G | T | 1 | a0003c0003t0001g0147 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1107-658G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36832896 | ||||||
| chr8:36833082
|
C | G | 1 | a0002c0001t0001g0059 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1107-472C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36833082 | ||||||
| chr8:36833131
|
T | G | 8 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1107-423T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36833131 | ||||||
| chr8:36833314
|
A | T | 2 | a0002c0001t0001g0024a0003c0003t0001g0023 | 2 | HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1107-240A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36833314 | ||||||
| chr8:36833403
|
A | G | 1 | a0003c0003t0001g0017 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1107-151A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36833403 | ||||||
| chr8:36833671
|
C | T | 144 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(141): Show | 147 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.1212+12C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 11/26 | chr8 | 36833671 | ||||||
| chr8:36833873
|
A | G | 3 | a0001c0004t0001g0159a0001c0004t0001g0160a0001c0004t0001g0161 | 3 | NA18944.hp1 NA18994.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1212+214A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 11/26 | chr8 | 36833873 | ||||||
| chr8:36833965
|
C | A | 48 | a0001c0002t0001g0144a0001c0004t0001g0001a0001c0004t0001g0008others(45): Show | 50 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1212+306C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 11/26 | chr8 | 36833965 | ||||||
| chr8:36834041
|
A | G | 1 | a0006c0010t0001g0022 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1212+382A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 11/26 | chr8 | 36834041 | ||||||
| chr8:36834082
|
A | G | 2 | a0001c0002t0001g0187a0001c0002t0001g0283 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1212+423A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 11/26 | chr8 | 36834082 | ||||||
| chr8:36834123
|
C | T | 6 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1212+464C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 11/26 | chr8 | 36834123 | ||||||
| chr8:36834293
|
C | G | 2 | a0001c0002t0001g0238a0001c0002t0001g0267 | 2 | HG00735.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1213-493C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 11/26 | chr8 | 36834293 | ||||||
| chr8:36834548
|
T | A | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1213-238T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 11/26 | chr8 | 36834548 | ||||||
| chr8:36834601
|
C | T | 3 | a0002c0001t0001g0132a0002c0001t0001g0133a0002c0001t0001g0141 | 3 | NA18945.hp2 NA19001.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1213-185C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 11/26 | chr8 | 36834601 | ||||||
| chr8:36834898
|
G | T | 1 | a0001c0002t0001g0177 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1295+30G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 12/26 | chr8 | 36834898 | ||||||
| chr8:36834997
|
G | A | 2 | a0001c0002t0001g0166a0001c0002t0001g0167 | 2 | HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1295+129G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 12/26 | chr8 | 36834997 | ||||||
| chr8:36835121
|
C | T | 1 | a0001c0002t0001g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1295+253C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 12/26 | chr8 | 36835121 | ||||||
| chr8:36835205
|
T | C | 1 | a0001c0002t0001g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1295+337T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 12/26 | chr8 | 36835205 | ||||||
| chr8:36835274
|
G | A | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1295+406G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 12/26 | chr8 | 36835274 | ||||||
| chr8:36835282
|
A | T | 5 | a0002c0001t0001g0070a0002c0001t0001g0071a0002c0001t0001g0080others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1295+414A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 12/26 | chr8 | 36835282 | ||||||
| chr8:36835348
|
C | CTTTTCT | 47 | a0001c0002t0001g0144a0001c0004t0001g0001a0001c0004t0001g0008others(44): Show | 49 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1295+484_1295+485i others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr8 | 36835348 | |||||
| chr8:36835576
|
G | C | 6 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(3): Show | 6 | HG01891.hp1 HG02486.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1295+708G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 12/26 | chr8 | 36835576 | ||||||
| chr8:36835631
|
C | T | 4 | a0001c0002t0001g0237a0001c0002t0001g0264a0001c0002t0001g0269others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.1296-665C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 12/26 | chr8 | 36835631 | ||||||
| chr8:36835664
|
A | T | 1 | a0001c0002t0001g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1296-632A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 12/26 | chr8 | 36835664 | ||||||
| chr8:36835706
|
T | A | 48 | a0001c0002t0001g0144a0001c0004t0001g0001a0001c0004t0001g0008others(45): Show | 50 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1296-590T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 12/26 | chr8 | 36835706 | ||||||
| chr8:36835954
|
C | A | 1 | a0002c0007t0001g0069 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1296-342C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 12/26 | chr8 | 36835954 | ||||||
| chr8:36835976
|
T | A | 68 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(65): Show | 69 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1296-320T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 12/26 | chr8 | 36835976 | ||||||
| chr8:36836440
|
G | T | 1 | a0002c0001t0001g0179 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1365+75G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 13/26 | chr8 | 36836440 | ||||||
| chr8:36836660
|
C | A | 1 | a0001c0004t0001g0225 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1366-133C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 13/26 | chr8 | 36836660 | ||||||
| chr8:36836962
|
C | A | 52 | a0001c0002t0001g0144a0001c0002t0001g0157a0001c0002t0001g0158others(49): Show | 54 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.1518+17C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36836962 | ||||||
| chr8:36837433
|
C | A | 2 | a0001c0002t0001g0014a0002c0001t0001g0028 | 2 | HG01074.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1518+488C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36837433 | ||||||
| chr8:36837466
|
C | T | 8 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1518+521C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36837466 | ||||||
| chr8:36837563
|
G | A | 8 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1518+618G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36837563 | ||||||
| chr8:36837590
|
T | G | 1 | a0001c0002t0001g0175 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1518+645T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36837590 | ||||||
| chr8:36837639
|
C | T | 1 | a0002c0001t0001g0057 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1518+694C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36837639 | ||||||
| chr8:36837852
|
A | C | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1518+907A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36837852 | ||||||
| chr8:36837867
|
A | G | 68 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(65): Show | 69 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1518+922A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36837867 | ||||||
| chr8:36837900
|
G | A | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1518+955G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36837900 | ||||||
| chr8:36837905
|
TTCCTC | T | 68 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(65): Show | 69 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1518+962_1518+966d others(7): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr8 | 36837905 | |||||
| chr8:36837931
|
C | T | 1 | a0003c0003t0001g0104 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1518+986C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36837931 | ||||||
| chr8:36838116
|
G | C | 2 | a0001c0002t0001g0187a0001c0002t0001g0283 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1518+1171G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36838116 | ||||||
| chr8:36838180
|
G | A | 6 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1518+1235G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36838180 | ||||||
| chr8:36838218
|
G | A | 1 | a0002c0001t0001g0124 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1518+1273G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36838218 | ||||||
| chr8:36838304
|
T | C | 4 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1518+1359T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36838304 | ||||||
| chr8:36838325
|
A | T | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1518+1380A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36838325 | ||||||
| chr8:36838538
|
T | C | 1 | a0001c0002t0001g0172 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1518+1593T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36838538 | ||||||
| chr8:36838636
|
G | T | 2 | a0001c0006t0001g0170a0001c0006t0001g0171 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1518+1691G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36838636 | ||||||
| chr8:36838675
|
C | T | 6 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1518+1730C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36838675 | ||||||
| chr8:36839058
|
T | G | 1 | a0002c0001t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1519-1405T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36839058 | ||||||
| chr8:36839101
|
C | G | 2 | a0001c0002t0001g0262a0001c0002t0001g0263 | 2 | HG02523.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1519-1362C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36839101 | ||||||
| chr8:36839125
|
C | T | 2 | a0002c0001t0001g0024a0003c0003t0001g0023 | 2 | HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1519-1338C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36839125 | ||||||
| chr8:36839135
|
A | G | 1 | a0001c0002t0001g0261 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1519-1328A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36839135 | ||||||
| chr8:36839353
|
C | A | 68 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(65): Show | 69 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1519-1110C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36839353 | ||||||
| chr8:36839473
|
G | A | 16 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(13): Show | 16 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1519-990G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36839473 | ||||||
| chr8:36839639
|
C | T | 1 | a0003c0003t0001g0097 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1519-824C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36839639 | ||||||
| chr8:36839761
|
G | T | 51 | a0001c0002t0001g0018a0002c0001t0001g0004a0002c0001t0001g0016others(48): Show | 52 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.1519-702G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36839761 | ||||||
| chr8:36839788
|
A | C | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1519-675A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36839788 | ||||||
| chr8:36839885
|
G | C | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1519-578G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36839885 | ||||||
| chr8:36840266
|
T | C | 3 | a0001c0002t0001g0275a0001c0002t0001g0276a0001c0002t0001g0277 | 3 | HG01167.hp2 HG01934.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1519-197T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36840266 | ||||||
| chr8:36840652
|
A | G | 1 | a0002c0016t0001g0224 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1631+77A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 15/26 | chr8 | 36840652 | ||||||
| chr8:36840671
|
A | C | 1 | a0001c0004t0001g0209 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1631+96A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 15/26 | chr8 | 36840671 | ||||||
| chr8:36840687
|
G | A | 4 | a0002c0001t0001g0105a0002c0001t0001g0111a0002c0001t0001g0134others(1): Show | 4 | HG01928.hp1 HG01981.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.1631+112G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 15/26 | chr8 | 36840687 | ||||||
| chr8:36840915
|
C | T | 1 | a0002c0001t0001g0116 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1632-17C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 15/26 | chr8 | 36840915 | ||||||
| chr8:36841034
|
G | GT | 69 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(66): Show | 70 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.1703+53dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 36841034 | |||||
| chr8:36841034
|
G | T | 1 | a0002c0001t0001g0015 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1703+31G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36841034 | ||||||
| chr8:36841034
|
GT | G | 20 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(17): Show | 20 | HG01081.hp1 HG01891.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1703+53delT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 36841034 | |||||
| chr8:36841053
|
TTTTC | T | 43 | a0001c0002t0001g0144a0001c0004t0001g0001a0001c0004t0001g0159others(40): Show | 45 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.1703+51_1703+54del others(4): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36841053 | ||||||
| chr8:36841055
|
TTC | T | 9 | a0001c0002t0001g0157a0001c0002t0001g0158a0001c0002t0001g0172others(6): Show | 9 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1703+53_1703+54del others(2): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36841055 | ||||||
| chr8:36841057
|
C | T | 1 | a0001c0004t0001g0008 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1703+54C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36841057 | ||||||
| chr8:36841236
|
C | T | 47 | a0001c0004t0001g0001a0001c0004t0001g0008a0001c0004t0001g0159others(44): Show | 49 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1703+233C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36841236 | ||||||
| chr8:36841467
|
G | A | 68 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(65): Show | 69 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1703+464G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36841467 | ||||||
| chr8:36841785
|
T | C | 4 | a0002c0001t0001g0070a0002c0001t0001g0071a0002c0007t0001g0069others(1): Show | 4 | HG02258.hp2 HG03195.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1703+782T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36841785 | ||||||
| chr8:36841910
|
A | C | 16 | a0001c0002t0001g0123a0002c0001t0001g0015a0002c0001t0001g0108others(13): Show | 16 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(13): Show |
intron_variant | MODIFIER | c.1703+907A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36841910 | ||||||
| chr8:36841978
|
T | TA | 68 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(65): Show | 69 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1703+985dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 36841978 | |||||
| chr8:36841978
|
TA | T | 10 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(7): Show | 10 | HG00735.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1703+985delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 36841978 | |||||
| chr8:36842045
|
G | C | 1 | a0001c0002t0001g0166 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1703+1042G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36842045 | ||||||
| chr8:36842207
|
A | G | 7 | a0002c0001t0001g0183a0002c0001t0001g0184a0003c0003t0001g0181others(4): Show | 7 | HG02109.hp1 HG02559.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1703+1204A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36842207 | ||||||
| chr8:36842369
|
A | T | 10 | a0001c0002t0001g0157a0001c0002t0001g0158a0001c0002t0001g0172others(7): Show | 10 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1703+1366A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36842369 | ||||||
| chr8:36842430
|
C | G | 2 | a0001c0004t0001g0191a0001c0004t0001g0198 | 2 | NA18963.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1703+1427C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36842430 | ||||||
| chr8:36842637
|
C | T | 3 | a0002c0001t0001g0066a0002c0001t0001g0068a0003c0003t0001g0067 | 3 | HG02559.hp2 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1703+1634C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36842637 | ||||||
| chr8:36842688
|
G | C | 2 | a0001c0006t0001g0170a0001c0006t0001g0171 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1703+1685G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36842688 | ||||||
| chr8:36843112
|
G | A | 1 | a0002c0001t0001g0127 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1703+2109G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36843112 | ||||||
| chr8:36843278
|
G | A | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1703+2275G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36843278 | ||||||
| chr8:36843356
|
T | C | 2 | a0001c0002t0001g0175a0001c0002t0001g0176 | 2 | HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1704-2224T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36843356 | ||||||
| chr8:36843360
|
C | A | 1 | a0001c0002t0001g0157 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1704-2220C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36843360 | ||||||
| chr8:36843387
|
C | A | 58 | a0001c0002t0001g0144a0001c0002t0001g0157a0001c0002t0001g0158others(55): Show | 60 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1704-2193C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36843387 | ||||||
| chr8:36843562
|
T | C | 1 | a0001c0002t0001g0051 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1704-2018T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36843562 | ||||||
| chr8:36843638
|
T | A | 1 | a0001c0002t0001g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1704-1942T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36843638 | ||||||
| chr8:36843818
|
C | T | 1 | a0002c0001t0001g0037 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1704-1762C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36843818 | ||||||
| chr8:36844067
|
C | A | 1 | a0001c0002t0001g0176 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1704-1513C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36844067 | ||||||
| chr8:36844080
|
A | T | 1 | a0001c0002t0001g0003 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1704-1500A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36844080 | ||||||
| chr8:36844087
|
T | C | 127 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(124): Show | 130 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.1704-1493T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36844087 | ||||||
| chr8:36844268
|
T | C | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1704-1312T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36844268 | ||||||
| chr8:36844374
|
C | G | 2 | a0001c0002t0001g0187a0001c0002t0001g0283 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1704-1206C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36844374 | ||||||
| chr8:36844376
|
G | A | 2 | a0001c0002t0001g0187a0001c0002t0001g0283 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1704-1204G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36844376 | ||||||
| chr8:36844390
|
C | CA | 14 | a0001c0002t0001g0157a0001c0002t0001g0158a0001c0002t0001g0172others(11): Show | 14 | HG02055.hp1 HG02055.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.1704-1180dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 36844390 | |||||
| chr8:36844394
|
A | AC | 48 | a0001c0002t0001g0144a0001c0004t0001g0001a0001c0004t0001g0008others(45): Show | 50 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1704-1186_1704-118 others(5): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36844394 | ||||||
| chr8:36844396
|
A | AT | 68 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(65): Show | 69 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1704-1184_1704-118 others(5): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36844396 | ||||||
| chr8:36844402
|
G | T | 1 | a0002c0001t0001g0107 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1704-1178G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36844402 | ||||||
| chr8:36844521
|
A | G | 2 | a0001c0002t0001g0187a0001c0002t0001g0283 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1704-1059A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36844521 | ||||||
| chr8:36845038
|
C | T | 16 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(13): Show | 16 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1704-542C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36845038 | ||||||
| chr8:36845092
|
G | A | 16 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(13): Show | 16 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1704-488G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36845092 | ||||||
| chr8:36845093
|
C | G | 68 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(65): Show | 69 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1704-487C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36845093 | ||||||
| chr8:36845401
|
TCAAA | T | 7 | a0001c0004t0001g0159a0001c0004t0001g0160a0001c0004t0001g0161others(4): Show | 7 | HG01358.hp2 HG02258.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.1704-174_1704-171d others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 36845401 | |||||
| chr8:36845505
|
T | G | 16 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(13): Show | 16 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1704-75T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36845505 | ||||||
| chr8:36846137
|
A | T | 9 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(6): Show | 9 | HG01891.hp1 HG02486.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1891+238A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36846137 | ||||||
| chr8:36846169
|
G | A | 5 | a0001c0004t0001g0001a0001c0004t0001g0200a0001c0004t0001g0202others(2): Show | 7 | HG00558.hp2 HG00597.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.1891+270G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36846169 | ||||||
| chr8:36846326
|
C | G | 4 | a0001c0002t0001g0188a0001c0002t0001g0281a0001c0002t0001g0282others(1): Show | 4 | HG01109.hp2 HG02257.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1891+427C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36846326 | ||||||
| chr8:36846405
|
T | G | 2 | a0002c0001t0001g0105a0002c0001t0001g0111 | 2 | HG01928.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1891+506T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36846405 | ||||||
| chr8:36846524
|
T | C | 284 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(281): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1891+625T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36846524 | ||||||
| chr8:36846532
|
G | A | 1 | a0003c0003t0001g0186 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1891+633G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36846532 | ||||||
| chr8:36846671
|
G | A | 7 | a0002c0001t0001g0183a0002c0001t0001g0184a0003c0003t0001g0181others(4): Show | 7 | HG02109.hp1 HG02559.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1891+772G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36846671 | ||||||
| chr8:36846764
|
G | A | 1 | a0001c0004t0001g0162 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1891+865G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36846764 | ||||||
| chr8:36846788
|
G | GA | 16 | a0001c0002t0001g0051a0001c0002t0001g0259a0001c0006t0001g0178others(13): Show | 16 | HG01496.hp2 HG01515.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1891+907dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36846788 | |||||
| chr8:36846788
|
G | GAA | 112 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(109): Show | 115 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.1891+906_1891+907d others(4): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36846788 | |||||
| chr8:36846788
|
G | GAAA | 8 | a0001c0002t0001g0173a0001c0002t0001g0187a0001c0002t0001g0283others(5): Show | 8 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1891+905_1891+907d others(5): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36846788 | |||||
| chr8:36846811
|
G | A | 3 | a0002c0001t0001g0103a0003c0003t0001g0101a0003c0003t0001g0102 | 3 | HG03139.hp1 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1891+912G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36846811 | ||||||
| chr8:36846877
|
A | T | 2 | a0001c0006t0001g0170a0001c0006t0001g0171 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1891+978A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36846877 | ||||||
| chr8:36846927
|
G | A | 4 | a0001c0002t0001g0109a0002c0001t0001g0094a0002c0001t0001g0135others(1): Show | 4 | NA18612.hp1 NA18969.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1891+1028G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36846927 | ||||||
| chr8:36847299
|
A | G | 1 | a0002c0001t0001g0040 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1891+1400A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36847299 | ||||||
| chr8:36847355
|
T | G | 2 | a0002c0001t0001g0148a0002c0001t0001g0149 | 2 | HG02056.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1891+1456T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36847355 | ||||||
| chr8:36847379
|
C | A | 1 | a0001c0002t0001g0251 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1891+1480C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36847379 | ||||||
| chr8:36847776
|
C | T | 1 | a0001c0002t0001g0003 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1891+1877C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36847776 | ||||||
| chr8:36847791
|
A | G | 1 | a0001c0002t0001g0271 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1891+1892A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36847791 | ||||||
| chr8:36847881
|
T | A | 1 | a0003c0003t0001g0082 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1891+1982T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36847881 | ||||||
| chr8:36848165
|
C | A | 1 | a0001c0009t0001g0169 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1891+2266C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36848165 | ||||||
| chr8:36848173
|
T | A | 1 | a0001c0002t0001g0177 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1891+2274T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36848173 | ||||||
| chr8:36848254
|
G | A | 7 | a0002c0001t0001g0183a0002c0001t0001g0184a0003c0003t0001g0181others(4): Show | 7 | HG02109.hp1 HG02559.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1891+2355G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36848254 | ||||||
| chr8:36848817
|
A | C | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1891+2918A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36848817 | ||||||
| chr8:36849040
|
T | C | 1 | a0001c0002t0001g0265 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1891+3141T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36849040 | ||||||
| chr8:36849132
|
A | G | 2 | a0002c0001t0001g0148a0002c0001t0001g0149 | 2 | HG02056.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1891+3233A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36849132 | ||||||
| chr8:36849182
|
A | T | 135 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(132): Show | 138 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1891+3283A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36849182 | ||||||
| chr8:36849265
|
T | C | 2 | a0001c0002t0001g0187a0001c0002t0001g0283 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1891+3366T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36849265 | ||||||
| chr8:36849418
|
G | A | 10 | a0002c0001t0001g0103a0003c0003t0001g0006a0003c0003t0001g0026others(7): Show | 10 | HG02280.hp2 HG02630.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1891+3519G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36849418 | ||||||
| chr8:36849698
|
A | G | 1 | a0001c0004t0001g0216 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1891+3799A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36849698 | ||||||
| chr8:36849791
|
G | A | 1 | a0001c0002t0001g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1891+3892G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36849791 | ||||||
| chr8:36849905
|
A | G | 1 | a0001c0002t0001g0261 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1891+4006A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36849905 | ||||||
| chr8:36849925
|
C | T | 3 | a0002c0001t0001g0024a0002c0001t0001g0088a0003c0003t0001g0023 | 3 | HG02647.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1891+4026C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36849925 | ||||||
| chr8:36850123
|
A | G | 2 | a0002c0001t0001g0027a0002c0001t0001g0052 | 2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1891+4224A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36850123 | ||||||
| chr8:36850133
|
A | T | 1 | a0001c0004t0001g0202 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1891+4234A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36850133 | ||||||
| chr8:36850159
|
G | T | 48 | a0001c0002t0001g0109a0001c0002t0001g0123a0001c0002t0001g0172others(45): Show | 50 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1891+4260G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36850159 | ||||||
| chr8:36850403
|
C | T | 136 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(133): Show | 139 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.1891+4504C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36850403 | ||||||
| chr8:36850455
|
C | CT | 122 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(119): Show | 125 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.1891+4570dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36850455 | |||||
| chr8:36850536
|
A | G | 1 | a0002c0001t0001g0179 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1891+4637A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36850536 | ||||||
| chr8:36850590
|
G | T | 2 | a0001c0002t0001g0276a0001c0002t0001g0277 | 2 | HG01167.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1891+4691G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36850590 | ||||||
| chr8:36850672
|
T | G | 136 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(133): Show | 139 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.1891+4773T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36850672 | ||||||
| chr8:36850737
|
A | G | 1 | a0001c0002t0001g0281 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1891+4838A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36850737 | ||||||
| chr8:36851368
|
T | TTCCCTTC others(4): Show |
1 | a0002c0001t0001g0114 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1891+5472_1891+548 others(15): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36851368 | |||||
| chr8:36851373
|
T | TTC | 27 | a0001c0002t0001g0049a0001c0002t0001g0050a0001c0002t0001g0054others(24): Show | 27 | HG00099.hp2 HG00438.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1891+5486_1891+548 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36851373 | |||||
| chr8:36851373
|
T | TTCTC | 20 | a0001c0002t0001g0109a0001c0002t0001g0123a0001c0002t0001g0173others(17): Show | 20 | HG00673.hp1 HG01243.hp2 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.1891+5484_1891+548 others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36851373 | |||||
| chr8:36851373
|
T | TTCTCTC | 35 | a0001c0002t0001g0051a0001c0002t0001g0061a0001c0002t0001g0073others(32): Show | 37 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.1891+5482_1891+548 others(10): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36851373 | |||||
| chr8:36851373
|
T | TTCTCTCT others(1): Show |
12 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0163others(9): Show | 13 | HG01169.hp1 HG01358.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.1891+5480_1891+548 others(12): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36851373 | |||||
| chr8:36851373
|
T | TTCTCTCT others(3): Show |
6 | a0001c0002t0001g0236a0001c0002t0001g0264a0001c0002t0001g0265others(3): Show | 6 | HG01433.hp2 HG02080.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1891+5478_1891+548 others(14): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36851373 | |||||
| chr8:36851373
|
T | TTCTCTCT others(5): Show |
1 | a0001c0002t0001g0274 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1891+5476_1891+548 others(16): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36851373 | |||||
| chr8:36851381
|
CTCTCTA | C | 3 | a0001c0002t0001g0014a0001c0002t0001g0175a0001c0002t0001g0177 | 3 | HG01074.hp1 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1891+5488_1891+549 others(10): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36851381 | |||||
| chr8:36851385
|
CTA | C | 4 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0229others(1): Show | 4 | HG01109.hp2 HG02165.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1891+5488_1891+548 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36851385 | |||||
| chr8:36851387
|
A | ATC | 8 | a0001c0002t0001g0144a0002c0001t0001g0027a0002c0001t0001g0052others(5): Show | 8 | HG02004.hp1 HG02109.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.1891+5512_1891+551 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36851387 | |||||
| chr8:36851387
|
A | ATCTC | 8 | a0002c0001t0001g0183a0002c0001t0001g0184a0003c0003t0001g0181others(5): Show | 8 | HG02109.hp1 HG02559.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1891+5510_1891+551 others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36851387 | |||||
| chr8:36851387
|
A | C | 114 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0049others(111): Show | 117 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.1891+5488A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36851387 | ||||||
| chr8:36851387
|
A | G | 4 | a0002c0001t0001g0094a0002c0001t0001g0135a0002c0001t0001g0136others(1): Show | 4 | HG04184.hp2 NA18969.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1891+5488A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36851387 | ||||||
| chr8:36851469
|
A | G | 2 | a0001c0002t0001g0165a0001c0002t0001g0255 | 2 | NA19086.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1891+5570A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36851469 | ||||||
| chr8:36851493
|
G | C | 134 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(131): Show | 137 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.1891+5594G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36851493 | ||||||
| chr8:36851587
|
G | A | 1 | a0003c0005t0001g0214 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1891+5688G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36851587 | ||||||
| chr8:36851656
|
T | C | 122 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(119): Show | 125 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.1891+5757T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36851656 | ||||||
| chr8:36852112
|
G | A | 1 | a0001c0002t0001g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1891+6213G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36852112 | ||||||
| chr8:36852423
|
A | G | 2 | a0001c0002t0001g0187a0001c0002t0001g0283 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1891+6524A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36852423 | ||||||
| chr8:36852492
|
G | A | 1 | a0002c0001t0001g0125 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1891+6593G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36852492 | ||||||
| chr8:36852623
|
A | G | 66 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.1891+6724A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36852623 | ||||||
| chr8:36852700
|
T | C | 2 | a0002c0001t0001g0012a0002c0001t0001g0013 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1891+6801T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36852700 | ||||||
| chr8:36852849
|
T | A | 1 | a0002c0001t0001g0116 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1891+6950T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36852849 | ||||||
| chr8:36853112
|
G | A | 1 | a0006c0010t0001g0022 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1891+7213G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36853112 | ||||||
| chr8:36853516
|
A | G | 3 | a0001c0006t0001g0178a0001c0006t0001g0280a0001c0018t0001g0180 | 3 | HG02647.hp1 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1891+7617A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36853516 | ||||||
| chr8:36853714
|
C | A | 1 | a0002c0001t0001g0119 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1891+7815C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36853714 | ||||||
| chr8:36853865
|
C | T | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1891+7966C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36853865 | ||||||
| chr8:36854025
|
C | T | 3 | a0001c0006t0001g0178a0001c0006t0001g0280a0001c0018t0001g0180 | 3 | HG02647.hp1 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1891+8126C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36854025 | ||||||
| chr8:36854114
|
G | A | 122 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(119): Show | 125 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.1891+8215G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36854114 | ||||||
| chr8:36854139
|
T | A | 1 | a0001c0002t0001g0272 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1891+8240T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36854139 | ||||||
| chr8:36854139
|
T | G | 121 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(118): Show | 124 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.1891+8240T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36854139 | ||||||
| chr8:36854289
|
T | C | 1 | a0001c0009t0001g0169 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1891+8390T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36854289 | ||||||
| chr8:36854377
|
G | A | 2 | a0002c0001t0001g0235a0004c0015t0001g0250 | 2 | HG00621.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1891+8478G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36854377 | ||||||
| chr8:36854390
|
G | T | 1 | a0002c0001t0001g0114 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1891+8491G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36854390 | ||||||
| chr8:36854472
|
C | CT | 131 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(128): Show | 134 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.1891+8587dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36854472 | |||||
| chr8:36854501
|
G | C | 1 | a0001c0002t0001g0251 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1891+8602G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36854501 | ||||||
| chr8:36854922
|
C | G | 1 | a0001c0002t0001g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1891+9023C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36854922 | ||||||
| chr8:36854994
|
T | C | 1 | a0001c0002t0001g0248 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1891+9095T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36854994 | ||||||
| chr8:36855024
|
C | A | 2 | a0001c0002t0001g0187a0001c0002t0001g0283 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1891+9125C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36855024 | ||||||
| chr8:36855344
|
C | T | 3 | a0002c0001t0001g0105a0002c0001t0001g0111a0002c0001t0001g0134 | 3 | HG01928.hp1 HG01981.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1892-9060C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36855344 | ||||||
| chr8:36855421
|
G | A | 1 | a0003c0003t0001g0026 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1892-8983G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36855421 | ||||||
| chr8:36855563
|
T | C | 2 | a0001c0002t0001g0187a0001c0002t0001g0283 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1892-8841T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36855563 | ||||||
| chr8:36855629
|
G | A | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1892-8775G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36855629 | ||||||
| chr8:36855646
|
G | C | 1 | a0001c0002t0001g0166 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1892-8758G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36855646 | ||||||
| chr8:36855652
|
G | A | 2 | a0001c0004t0001g0212a0001c0004t0001g0219 | 2 | HG02015.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1892-8752G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36855652 | ||||||
| chr8:36855739
|
C | T | 1 | a0002c0001t0001g0085 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1892-8665C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36855739 | ||||||
| chr8:36855740
|
G | A | 1 | a0002c0001t0001g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1892-8664G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36855740 | ||||||
| chr8:36855841
|
T | A | 2 | a0001c0002t0001g0187a0001c0002t0001g0283 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1892-8563T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36855841 | ||||||
| chr8:36856073
|
A | C | 7 | a0001c0002t0001g0155a0001c0002t0001g0156a0001c0002t0001g0244others(4): Show | 7 | HG01099.hp2 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1892-8331A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36856073 | ||||||
| chr8:36856159
|
T | G | 2 | a0001c0006t0001g0170a0001c0006t0001g0171 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1892-8245T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36856159 | ||||||
| chr8:36856467
|
T | G | 1 | a0002c0001t0001g0132 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1892-7937T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36856467 | ||||||
| chr8:36856595
|
AT | A | 133 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(130): Show | 136 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.1892-7805delT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36856595 | |||||
| chr8:36856751
|
C | A | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1892-7653C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36856751 | ||||||
| chr8:36856801
|
C | T | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1892-7603C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36856801 | ||||||
| chr8:36856947
|
G | A | 7 | a0002c0001t0001g0183a0002c0001t0001g0184a0003c0003t0001g0181others(4): Show | 7 | HG02109.hp1 HG02559.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1892-7457G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36856947 | ||||||
| chr8:36856991
|
C | T | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1892-7413C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36856991 | ||||||
| chr8:36857307
|
C | G | 1 | a0002c0001t0001g0110 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1892-7097C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36857307 | ||||||
| chr8:36857398
|
G | C | 1 | a0002c0001t0001g0179 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1892-7006G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36857398 | ||||||
| chr8:36857632
|
G | GT | 121 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(118): Show | 124 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.1892-6765dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36857632 | |||||
| chr8:36857722
|
T | C | 1 | a0001c0002t0001g0268 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1892-6682T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36857722 | ||||||
| chr8:36857775
|
A | AGCTGGGA others(128): Show |
1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1892-6601_1892-660 others(139): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36857775 | |||||
| chr8:36857804
|
T | C | 133 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(130): Show | 136 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.1892-6600T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36857804 | ||||||
| chr8:36857939
|
C | G | 2 | a0001c0002t0001g0281a0001c0002t0001g0282 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1892-6465C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36857939 | ||||||
| chr8:36858176
|
C | CA | 129 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(126): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.1892-6205dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36858176 | |||||
| chr8:36858176
|
C | CAA | 51 | a0001c0002t0001g0061a0001c0002t0001g0123a0001c0002t0001g0144others(48): Show | 51 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.1892-6206_1892-620 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36858176 | |||||
| chr8:36858176
|
C | CAAA | 7 | a0001c0002t0001g0281a0001c0006t0001g0178a0001c0006t0001g0280others(4): Show | 7 | HG00438.hp1 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1892-6207_1892-620 others(7): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36858176 | |||||
| chr8:36858205
|
C | T | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1892-6199C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36858205 | ||||||
| chr8:36858240
|
A | C | 136 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(133): Show | 139 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.1892-6164A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36858240 | ||||||
| chr8:36858295
|
A | T | 120 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(117): Show | 123 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.1892-6109A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36858295 | ||||||
| chr8:36858673
|
C | T | 2 | a0001c0002t0001g0187a0001c0002t0001g0283 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1892-5731C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36858673 | ||||||
| chr8:36858853
|
A | G | 1 | a0002c0001t0001g0110 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1892-5551A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36858853 | ||||||
| chr8:36858889
|
C | T | 2 | a0001c0002t0001g0187a0001c0002t0001g0283 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1892-5515C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36858889 | ||||||
| chr8:36859078
|
C | A | 2 | a0003c0003t0001g0079a0003c0003t0001g0083 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1892-5326C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36859078 | ||||||
| chr8:36859345
|
T | A | 122 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(119): Show | 125 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.1892-5059T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36859345 | ||||||
| chr8:36859441
|
C | T | 121 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(118): Show | 124 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.1892-4963C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36859441 | ||||||
| chr8:36859449
|
T | C | 7 | a0003c0003t0001g0002a0003c0003t0001g0089a0003c0003t0001g0090others(4): Show | 8 | HG00609.hp1 NA18946.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.1892-4955T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36859449 | ||||||
| chr8:36859451
|
C | T | 1 | a0001c0002t0001g0261 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1892-4953C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36859451 | ||||||
| chr8:36859454
|
A | T | 1 | a0001c0002t0001g0236 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1892-4950A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36859454 | ||||||
| chr8:36859484
|
C | A | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1892-4920C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36859484 | ||||||
| chr8:36859553
|
C | T | 1 | a0003c0003t0001g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1892-4851C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36859553 | ||||||
| chr8:36859614
|
G | A | 1 | a0001c0002t0001g0174 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1892-4790G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36859614 | ||||||
| chr8:36859767
|
T | C | 7 | a0002c0001t0001g0183a0002c0001t0001g0184a0003c0003t0001g0181others(4): Show | 7 | HG02109.hp1 HG02559.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1892-4637T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36859767 | ||||||
| chr8:36859821
|
C | T | 3 | a0001c0002t0001g0014a0001c0002t0001g0175a0001c0002t0001g0176 | 3 | HG01074.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1892-4583C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36859821 | ||||||
| chr8:36859888
|
A | G | 4 | a0002c0001t0001g0094a0002c0001t0001g0135a0002c0001t0001g0136others(1): Show | 4 | HG04184.hp2 NA18969.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1892-4516A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36859888 | ||||||
| chr8:36860081
|
A | AT | 133 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(130): Show | 136 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.1892-4315dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36860081 | |||||
| chr8:36860108
|
C | G | 2 | a0002c0001t0001g0027a0002c0001t0001g0052 | 2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1892-4296C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36860108 | ||||||
| chr8:36860306
|
T | C | 1 | a0001c0002t0001g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1892-4098T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36860306 | ||||||
| chr8:36860429
|
T | A | 1 | a0001c0002t0001g0236 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1892-3975T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36860429 | ||||||
| chr8:36860481
|
A | G | 8 | a0003c0003t0001g0002a0003c0003t0001g0084a0003c0003t0001g0089others(5): Show | 9 | HG00609.hp1 HG01168.hp1 NA18946.hp1 others(6): Show |
intron_variant | MODIFIER | c.1892-3923A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36860481 | ||||||
| chr8:36860485
|
G | A | 2 | a0001c0006t0001g0170a0001c0006t0001g0171 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1892-3919G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36860485 | ||||||
| chr8:36860598
|
G | A | 3 | a0001c0006t0001g0178a0001c0006t0001g0280a0001c0018t0001g0180 | 3 | HG02647.hp1 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1892-3806G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36860598 | ||||||
| chr8:36860655
|
A | C | 1 | a0001c0009t0001g0169 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1892-3749A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36860655 | ||||||
| chr8:36860659
|
C | T | 8 | a0002c0001t0001g0113a0002c0001t0001g0119a0002c0001t0001g0130others(5): Show | 8 | HG00544.hp1 HG00558.hp1 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.1892-3745C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36860659 | ||||||
| chr8:36860911
|
C | CT | 6 | a0001c0002t0001g0144a0001c0006t0001g0178a0001c0006t0001g0280others(3): Show | 6 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1892-3479dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36860911 | |||||
| chr8:36860974
|
A | G | 1 | a0002c0001t0001g0053 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1892-3430A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36860974 | ||||||
| chr8:36861035
|
T | A | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1892-3369T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36861035 | ||||||
| chr8:36861101
|
C | A | 129 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(126): Show | 132 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.1892-3303C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36861101 | ||||||
| chr8:36861102
|
T | C | 2 | a0001c0002t0001g0187a0001c0002t0001g0283 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1892-3302T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36861102 | ||||||
| chr8:36861179
|
T | C | 9 | a0002c0001t0001g0016a0002c0001t0001g0019a0002c0001t0001g0020others(6): Show | 9 | HG01258.hp2 HG02004.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1892-3225T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36861179 | ||||||
| chr8:36861235
|
G | A | 125 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0047others(122): Show | 128 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.1892-3169G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36861235 | ||||||
| chr8:36861484
|
A | G | 126 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(123): Show | 129 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.1892-2920A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36861484 | ||||||
| chr8:36861509
|
G | A | 1 | a0003c0005t0001g0223 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1892-2895G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36861509 | ||||||
| chr8:36861669
|
A | G | 1 | a0003c0003t0001g0260 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1892-2735A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36861669 | ||||||
| chr8:36861704
|
G | A | 11 | a0001c0002t0001g0073a0001c0002t0001g0163a0001c0002t0001g0164others(8): Show | 11 | HG02027.hp1 HG02071.hp2 NA18942.hp1 others(8): Show |
intron_variant | MODIFIER | c.1892-2700G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36861704 | ||||||
| chr8:36862141
|
G | A | 1 | a0001c0002t0001g0268 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1892-2263G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36862141 | ||||||
| chr8:36862915
|
G | A | 1 | a0001c0002t0001g0054 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1892-1489G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36862915 | ||||||
| chr8:36863044
|
T | G | 1 | a0001c0004t0001g0162 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1892-1360T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36863044 | ||||||
| chr8:36863093
|
A | G | 1 | a0002c0001t0001g0052 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1892-1311A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36863093 | ||||||
| chr8:36863233
|
A | G | 7 | a0003c0003t0001g0002a0003c0003t0001g0089a0003c0003t0001g0090others(4): Show | 8 | HG00609.hp1 NA18946.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.1892-1171A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36863233 | ||||||
| chr8:36863683
|
T | G | 3 | a0001c0006t0001g0178a0001c0006t0001g0280a0001c0018t0001g0180 | 3 | HG02647.hp1 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1892-721T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36863683 | ||||||
| chr8:36863773
|
T | C | 2 | a0002c0016t0001g0224a0003c0005t0001g0222 | 2 | NA19084.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1892-631T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36863773 | ||||||
| chr8:36863931
|
C | T | 3 | a0001c0006t0001g0178a0001c0006t0001g0280a0001c0018t0001g0180 | 3 | HG02647.hp1 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1892-473C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36863931 | ||||||
| chr8:36864194
|
A | G | 1 | a0001c0004t0001g0204 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1892-210A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36864194 | ||||||
| chr8:36864529
|
C | T | 1 | a0002c0001t0001g0107 | 1 | HG02738.hp1 | splice_region_variant&intron_variant | LOW | c.2009+8C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36864529 | ||||||
| chr8:36864649
|
A | G | 1 | a0001c0002t0001g0247 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2009+128A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36864649 | ||||||
| chr8:36864753
|
T | C | 1 | a0001c0002t0001g0051 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2009+232T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36864753 | ||||||
| chr8:36865013
|
G | T | 1 | a0002c0001t0001g0141 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2009+492G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36865013 | ||||||
| chr8:36865024
|
G | A | 119 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(116): Show | 122 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.2009+503G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36865024 | ||||||
| chr8:36865365
|
A | G | 1 | a0002c0001t0001g0015 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2009+844A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36865365 | ||||||
| chr8:36865558
|
G | A | 2 | a0001c0002t0001g0187a0001c0002t0001g0283 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2009+1037G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36865558 | ||||||
| chr8:36865610
|
TA | T | 11 | a0001c0002t0001g0258a0001c0006t0001g0178a0001c0006t0001g0280others(8): Show | 11 | HG00639.hp1 HG00639.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.2009+1105delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36865610 | |||||
| chr8:36865610
|
TAA | T | 119 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(116): Show | 122 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.2009+1104_2009+110 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36865610 | |||||
| chr8:36865773
|
C | CA | 10 | a0001c0002t0001g0144a0001c0002t0001g0290a0001c0006t0001g0178others(7): Show | 10 | HG01081.hp1 HG01109.hp1 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.2009+1277dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36865773 | |||||
| chr8:36865773
|
CA | C | 9 | a0001c0002t0001g0283a0001c0006t0001g0287a0002c0001t0001g0009others(6): Show | 9 | HG00639.hp1 HG02004.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2009+1277delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36865773 | |||||
| chr8:36865773
|
CAAAAA | C | 107 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(104): Show | 110 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.2009+1273_2009+127 others(9): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36865773 | |||||
| chr8:36865773
|
CAAAAAA | C | 6 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0001g0243others(3): Show | 6 | HG01515.hp2 HG01978.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.2009+1272_2009+127 others(10): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36865773 | |||||
| chr8:36866114
|
C | CTTA | 4 | a0001c0002t0001g0144a0001c0006t0001g0178a0001c0006t0001g0280others(1): Show | 4 | HG02647.hp1 HG02818.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2009+1599_2009+160 others(7): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36866114 | |||||
| chr8:36866142
|
G | A | 1 | a0003c0003t0001g0231 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2009+1621G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36866142 | ||||||
| chr8:36866346
|
A | G | 3 | a0002c0001t0001g0044a0002c0007t0001g0046a0002c0007t0001g0153 | 3 | HG02615.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2009+1825A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36866346 | ||||||
| chr8:36866425
|
C | T | 1 | a0001c0002t0001g0251 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2009+1904C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36866425 | ||||||
| chr8:36866652
|
T | C | 1 | a0001c0002t0001g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2009+2131T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36866652 | ||||||
| chr8:36866678
|
A | G | 4 | a0001c0002t0001g0144a0001c0006t0001g0178a0001c0006t0001g0280others(1): Show | 4 | HG02647.hp1 HG02818.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2009+2157A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36866678 | ||||||
| chr8:36866709
|
T | C | 1 | a0001c0002t0001g0014 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2009+2188T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36866709 | ||||||
| chr8:36866801
|
G | A | 126 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(123): Show | 129 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.2009+2280G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36866801 | ||||||
| chr8:36867011
|
G | A | 2 | a0002c0001t0001g0027a0002c0001t0001g0052 | 2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2009+2490G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36867011 | ||||||
| chr8:36867136
|
T | C | 3 | a0001c0002t0001g0229a0001c0002t0001g0230a0003c0003t0001g0231 | 3 | HG00438.hp2 HG02165.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.2009+2615T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36867136 | ||||||
| chr8:36867154
|
A | C | 1 | a0003c0003t0001g0034 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2009+2633A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36867154 | ||||||
| chr8:36867239
|
G | T | 6 | a0002c0001t0001g0016a0002c0001t0001g0019a0002c0001t0001g0020others(3): Show | 6 | HG01258.hp2 HG02004.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.2009+2718G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36867239 | ||||||
| chr8:36867286
|
C | G | 1 | a0002c0001t0001g0115 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2009+2765C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36867286 | ||||||
| chr8:36867307
|
T | C | 44 | a0002c0001t0001g0009a0002c0001t0001g0012a0002c0001t0001g0013others(41): Show | 44 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.2009+2786T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36867307 | ||||||
| chr8:36867507
|
T | C | 2 | a0001c0006t0001g0178a0001c0018t0001g0180 | 2 | HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2009+2986T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36867507 | ||||||
| chr8:36867613
|
A | C | 126 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(123): Show | 129 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.2009+3092A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36867613 | ||||||
| chr8:36867645
|
G | T | 1 | a0001c0002t0001g0177 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2009+3124G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36867645 | ||||||
| chr8:36867722
|
A | G | 4 | a0001c0002t0001g0241a0001c0002t0001g0257a0001c0002t0001g0258others(1): Show | 4 | HG00639.hp2 HG01978.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2009+3201A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36867722 | ||||||
| chr8:36868118
|
G | C | 2 | a0001c0002t0001g0187a0001c0002t0001g0283 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2009+3597G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36868118 | ||||||
| chr8:36868296
|
C | A | 1 | a0002c0001t0001g0037 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2009+3775C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36868296 | ||||||
| chr8:36868445
|
T | C | 1 | a0002c0001t0001g0057 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2009+3924T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36868445 | ||||||
| chr8:36868635
|
A | G | 1 | a0002c0001t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2009+4114A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36868635 | ||||||
| chr8:36868756
|
A | T | 1 | a0001c0004t0001g0193 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2009+4235A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36868756 | ||||||
| chr8:36868803
|
C | T | 3 | a0001c0002t0001g0249a0001c0002t0001g0264a0001c0002t0001g0274 | 3 | HG01255.hp1 HG01433.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2009+4282C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36868803 | ||||||
| chr8:36869249
|
G | A | 1 | a0001c0002t0001g0256 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2009+4728G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36869249 | ||||||
| chr8:36869605
|
T | G | 4 | a0003c0003t0001g0006a0003c0003t0001g0026a0003c0003t0001g0032others(1): Show | 4 | HG02280.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2009+5084T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36869605 | ||||||
| chr8:36869643
|
A | G | 1 | a0001c0018t0001g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2009+5122A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36869643 | ||||||
| chr8:36869855
|
G | A | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2009+5334G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36869855 | ||||||
| chr8:36870011
|
A | C | 126 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(123): Show | 129 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.2009+5490A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36870011 | ||||||
| chr8:36870038
|
C | A | 5 | a0001c0002t0001g0144a0001c0006t0001g0178a0001c0006t0001g0280others(2): Show | 5 | HG02647.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2009+5517C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36870038 | ||||||
| chr8:36870045
|
G | A | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2009+5524G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36870045 | ||||||
| chr8:36870090
|
C | T | 2 | a0001c0002t0001g0187a0001c0002t0001g0283 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2009+5569C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36870090 | ||||||
| chr8:36870330
|
C | T | 126 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(123): Show | 129 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.2009+5809C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36870330 | ||||||
| chr8:36870342
|
G | A | 1 | a0001c0004t0001g0213 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2009+5821G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36870342 | ||||||
| chr8:36870376
|
C | G | 3 | a0002c0001t0001g0044a0002c0007t0001g0046a0002c0007t0001g0153 | 3 | HG02615.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2009+5855C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36870376 | ||||||
| chr8:36870576
|
G | T | 7 | a0003c0005t0001g0189a0003c0005t0001g0196a0003c0005t0001g0197others(4): Show | 7 | HG00621.hp1 NA18953.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.2009+6055G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36870576 | ||||||
| chr8:36870738
|
G | A | 1 | a0002c0001t0001g0052 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2009+6217G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36870738 | ||||||
| chr8:36870996
|
G | A | 1 | a0003c0003t0001g0065 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2009+6475G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36870996 | ||||||
| chr8:36871038
|
G | A | 1 | a0001c0002t0001g0281 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2009+6517G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36871038 | ||||||
| chr8:36871081
|
T | C | 1 | a0001c0002t0001g0014 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2009+6560T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36871081 | ||||||
| chr8:36871126
|
A | C | 1 | a0002c0001t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2009+6605A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36871126 | ||||||
| chr8:36871390
|
C | CAT | 112 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0047others(109): Show | 114 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.2009+6885_2009+688 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36871390 | |||||
| chr8:36871390
|
C | CATAT | 3 | a0001c0002t0001g0177a0001c0002t0001g0281a0001c0002t0001g0282 | 3 | HG02257.hp2 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2009+6883_2009+688 others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36871390 | |||||
| chr8:36871406
|
T | TAC | 3 | a0001c0006t0001g0178a0001c0006t0001g0280a0001c0018t0001g0180 | 3 | HG02647.hp1 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2009+6887_2009+688 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36871406 | |||||
| chr8:36871408
|
C | T | 5 | a0001c0002t0001g0003a0001c0002t0001g0165a0001c0002t0001g0255others(2): Show | 6 | HG01167.hp2 HG01516.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.2009+6887C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36871408 | ||||||
| chr8:36871410
|
T | TACATAG | 5 | a0001c0002t0001g0003a0001c0002t0001g0165a0001c0002t0001g0255others(2): Show | 6 | HG01167.hp2 HG01516.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.2009+6890_2009+689 others(10): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36871410 | |||||
| chr8:36871410
|
T | TAG | 60 | a0001c0002t0001g0018a0001c0002t0001g0047a0001c0002t0001g0048others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.2009+6904_2009+690 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36871410 | |||||
| chr8:36871580
|
G | A | 1 | a0001c0002t0001g0051 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2009+7059G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36871580 | ||||||
| chr8:36871771
|
C | T | 1 | a0001c0002t0001g0259 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2009+7250C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36871771 | ||||||
| chr8:36871929
|
C | G | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2009+7408C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36871929 | ||||||
| chr8:36872076
|
T | C | 119 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(116): Show | 122 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.2009+7555T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36872076 | ||||||
| chr8:36872198
|
A | G | 119 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(116): Show | 122 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.2009+7677A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36872198 | ||||||
| chr8:36872205
|
C | A | 1 | a0002c0001t0001g0136 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2009+7684C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36872205 | ||||||
| chr8:36872291
|
G | A | 44 | a0002c0001t0001g0009a0002c0001t0001g0012a0002c0001t0001g0013others(41): Show | 44 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.2009+7770G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36872291 | ||||||
| chr8:36872338
|
T | C | 9 | a0001c0002t0001g0155a0001c0002t0001g0156a0001c0002t0001g0243others(6): Show | 9 | HG01099.hp2 HG01257.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2009+7817T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36872338 | ||||||
| chr8:36872422
|
C | T | 16 | a0002c0001t0001g0015a0002c0001t0001g0108a0002c0001t0001g0110others(13): Show | 16 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(13): Show |
intron_variant | MODIFIER | c.2009+7901C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36872422 | ||||||
| chr8:36872496
|
T | C | 2 | a0001c0002t0001g0187a0001c0002t0001g0283 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2009+7975T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36872496 | ||||||
| chr8:36872512
|
A | G | 1 | a0003c0003t0001g0026 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2009+7991A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36872512 | ||||||
| chr8:36873066
|
C | T | 3 | a0001c0002t0001g0286a0001c0002t0001g0289a0001c0006t0001g0287 | 3 | HG01891.hp1 HG02615.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2009+8545C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36873066 | ||||||
| chr8:36873098
|
C | A | 170 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(167): Show | 173 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.2009+8577C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36873098 | ||||||
| chr8:36873109
|
A | G | 5 | a0001c0002t0001g0144a0001c0006t0001g0178a0001c0006t0001g0280others(2): Show | 5 | HG02647.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2009+8588A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36873109 | ||||||
| chr8:36873274
|
C | T | 1 | a0001c0002t0001g0014 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2009+8753C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36873274 | ||||||
| chr8:36873339
|
C | T | 1 | a0001c0002t0001g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2009+8818C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36873339 | ||||||
| chr8:36873373
|
A | G | 1 | a0001c0002t0001g0281 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2009+8852A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36873373 | ||||||
| chr8:36873486
|
T | C | 1 | a0003c0003t0001g0087 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2009+8965T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36873486 | ||||||
| chr8:36873561
|
A | G | 1 | a0001c0002t0001g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2009+9040A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36873561 | ||||||
| chr8:36873600
|
A | G | 1 | a0002c0001t0001g0125 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2009+9079A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36873600 | ||||||
| chr8:36873721
|
G | A | 3 | a0002c0016t0001g0224a0003c0005t0001g0222a0003c0005t0001g0223 | 3 | HG02258.hp1 NA19084.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.2009+9200G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36873721 | ||||||
| chr8:36873807
|
A | G | 1 | a0001c0002t0001g0274 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2009+9286A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36873807 | ||||||
| chr8:36874108
|
C | G | 1 | a0003c0003t0001g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2009+9587C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36874108 | ||||||
| chr8:36874224
|
G | A | 2 | a0002c0001t0001g0112a0002c0001t0001g0122 | 2 | HG00738.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.2009+9703G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36874224 | ||||||
| chr8:36874337
|
C | A | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2009+9816C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36874337 | ||||||
| chr8:36874378
|
C | T | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2009+9857C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36874378 | ||||||
| chr8:36874571
|
T | C | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2009+10050T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36874571 | ||||||
| chr8:36874684
|
A | T | 1 | a0002c0001t0001g0127 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2009+10163A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36874684 | ||||||
| chr8:36874724
|
T | C | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2009+10203T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36874724 | ||||||
| chr8:36875013
|
C | A | 1 | a0001c0002t0001g0073 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2009+10492C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36875013 | ||||||
| chr8:36875040
|
A | C | 1 | a0002c0001t0001g0285 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2009+10519A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36875040 | ||||||
| chr8:36875482
|
A | G | 1 | a0002c0001t0001g0148 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2009+10961A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36875482 | ||||||
| chr8:36875637
|
A | G | 1 | a0003c0003t0001g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2009+11116A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36875637 | ||||||
| chr8:36875911
|
T | C | 3 | a0001c0002t0001g0242a0001c0002t0001g0252a0001c0002t0001g0270 | 3 | NA18942.hp1 NA18948.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.2009+11390T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36875911 | ||||||
| chr8:36875930
|
G | A | 2 | a0003c0005t0001g0189a0003c0005t0001g0197 | 2 | NA18980.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.2009+11409G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36875930 | ||||||
| chr8:36876178
|
C | T | 2 | a0001c0002t0001g0281a0001c0002t0001g0282 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2009+11657C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36876178 | ||||||
| chr8:36876185
|
C | T | 1 | a0003c0003t0001g0081 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2009+11664C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36876185 | ||||||
| chr8:36876202
|
T | C | 1 | a0001c0002t0001g0253 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2009+11681T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36876202 | ||||||
| chr8:36876341
|
C | A | 3 | a0003c0003t0001g0006a0003c0003t0001g0032a0003c0003t0001g0033 | 3 | HG02280.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2009+11820C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36876341 | ||||||
| chr8:36876630
|
G | A | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2009+12109G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36876630 | ||||||
| chr8:36876845
|
T | C | 1 | a0003c0003t0001g0074 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2009+12324T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36876845 | ||||||
| chr8:36876848
|
G | A | 4 | a0001c0002t0001g0144a0001c0006t0001g0178a0001c0006t0001g0280others(1): Show | 4 | HG02647.hp1 HG02818.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2009+12327G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36876848 | ||||||
| chr8:36877036
|
CTT | C | 3 | a0001c0002t0001g0281a0001c0002t0001g0282a0001c0009t0001g0169 | 3 | HG01109.hp2 HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2009+12518_2009+12 others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36877036 | |||||
| chr8:36877089
|
C | T | 2 | a0002c0001t0001g0148a0002c0001t0001g0149 | 2 | HG02056.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.2009+12568C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36877089 | ||||||
| chr8:36877101
|
T | C | 1 | a0003c0003t0001g0154 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2009+12580T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36877101 | ||||||
| chr8:36877145
|
A | G | 1 | a0003c0005t0001g0196 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2009+12624A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36877145 | ||||||
| chr8:36877305
|
G | GT | 6 | a0001c0002t0001g0061a0001c0002t0001g0187a0001c0002t0001g0283others(3): Show | 6 | HG01074.hp2 HG02055.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2009+12798dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36877305 | |||||
| chr8:36877337
|
T | C | 1 | a0001c0002t0001g0266 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2009+12816T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36877337 | ||||||
| chr8:36877347
|
G | T | 3 | a0001c0006t0001g0178a0001c0006t0001g0280a0001c0018t0001g0180 | 3 | HG02647.hp1 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2009+12826G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36877347 | ||||||
| chr8:36877410
|
C | G | 2 | a0001c0006t0001g0170a0001c0006t0001g0171 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2009+12889C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36877410 | ||||||
| chr8:36877448
|
G | A | 117 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(114): Show | 120 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.2009+12927G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36877448 | ||||||
| chr8:36877719
|
T | C | 126 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(123): Show | 129 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.2009+13198T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36877719 | ||||||
| chr8:36877845
|
C | T | 1 | a0001c0002t0001g0263 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2009+13324C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36877845 | ||||||
| chr8:36878096
|
T | C | 45 | a0001c0002t0001g0109a0001c0002t0001g0123a0001c0002t0001g0172others(42): Show | 47 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.2009+13575T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36878096 | ||||||
| chr8:36878128
|
A | G | 1 | a0001c0006t0001g0280 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2009+13607A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36878128 | ||||||
| chr8:36878420
|
C | G | 1 | a0003c0003t0001g0033 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2009+13899C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36878420 | ||||||
| chr8:36878436
|
A | C | 1 | a0003c0003t0001g0145 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2009+13915A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36878436 | ||||||
| chr8:36878484
|
C | T | 2 | a0001c0002t0001g0049a0001c0002t0001g0050 | 2 | HG00099.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2009+13963C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36878484 | ||||||
| chr8:36878583
|
G | A | 4 | a0002c0001t0001g0016a0002c0001t0001g0019a0002c0001t0001g0020others(1): Show | 4 | NA18948.hp2 NA18953.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.2009+14062G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36878583 | ||||||
| chr8:36878716
|
T | C | 2 | a0001c0004t0001g0190a0001c0004t0001g0218 | 2 | HG02074.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2009+14195T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36878716 | ||||||
| chr8:36878892
|
C | A | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2009+14371C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36878892 | ||||||
| chr8:36879138
|
C | T | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2009+14617C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36879138 | ||||||
| chr8:36879191
|
A | ATG | 16 | a0001c0002t0001g0144a0002c0001t0001g0039a0002c0001t0001g0042others(13): Show | 16 | HG00621.hp1 HG01071.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.2009+14690_2009+14 others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879191 | |||||
| chr8:36879191
|
A | G | 1 | a0001c0002t0001g0266 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2009+14670A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36879191 | ||||||
| chr8:36879203
|
G | A | 2 | a0003c0003t0001g0011a0003c0003t0001g0102 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2009+14682G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36879203 | ||||||
| chr8:36879207
|
G | GTATATAT others(5): Show |
1 | a0001c0002t0001g0230 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2009+14687_2009+14 others(18): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879207 | |||||
| chr8:36879209
|
G | A | 1 | a0001c0002t0001g0230 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2009+14688G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36879209 | ||||||
| chr8:36879209
|
G | GTATATA | 3 | a0001c0002t0001g0249a0001c0004t0001g0209a0001c0006t0001g0171 | 3 | HG02886.hp1 HG04228.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2009+14689_2009+14 others(12): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879209 | |||||
| chr8:36879209
|
G | GTATATAT others(1): Show |
10 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(7): Show | 10 | HG01255.hp1 HG01433.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.2009+14689_2009+14 others(14): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879209 | |||||
| chr8:36879209
|
G | GTATATAT others(3): Show |
25 | a0001c0002t0001g0047a0001c0002t0001g0049a0001c0002t0001g0165others(22): Show | 25 | HG00099.hp2 HG01167.hp2 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.2009+14689_2009+14 others(16): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879209 | |||||
| chr8:36879209
|
G | GTATATAT others(5): Show |
23 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0155others(20): Show | 24 | HG00735.hp1 HG01081.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.2009+14689_2009+14 others(18): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879209 | |||||
| chr8:36879209
|
G | GTATATAT others(7): Show |
28 | a0001c0002t0001g0050a0001c0002t0001g0061a0001c0002t0001g0109others(25): Show | 30 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.2009+14689_2009+14 others(20): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879209 | |||||
| chr8:36879209
|
G | GTATATAT others(9): Show |
9 | a0001c0002t0001g0051a0001c0002t0001g0054a0001c0002t0001g0244others(6): Show | 9 | HG01099.hp2 HG01243.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.2009+14689_2009+14 others(22): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879209 | |||||
| chr8:36879209
|
G | GTATATAT others(11): Show |
4 | a0001c0002t0001g0014a0001c0002t0001g0251a0001c0004t0001g0202others(1): Show | 4 | HG00140.hp1 HG01074.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.2009+14689_2009+14 others(24): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879209 | |||||
| chr8:36879209
|
GTGTATAT others(3): Show |
G | 2 | a0001c0002t0001g0187a0001c0002t0001g0283 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2009+14690_2009+14 others(16): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879209 | |||||
| chr8:36879211
|
G | A | 108 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(105): Show | 111 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.2009+14690G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36879211 | ||||||
| chr8:36879211
|
G | GTA | 76 | a0002c0001t0001g0009a0002c0001t0001g0015a0002c0001t0001g0016others(73): Show | 76 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.2009+14717_2009+14 others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879211 | |||||
| chr8:36879211
|
G | GTATA | 21 | a0002c0001t0001g0004a0002c0001t0001g0012a0002c0001t0001g0013others(18): Show | 21 | HG00558.hp1 HG00738.hp1 HG01515.hp1 others(18): Show |
intron_variant | MODIFIER | c.2009+14715_2009+14 others(10): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879211 | |||||
| chr8:36879211
|
G | GTATATA | 8 | a0002c0001t0001g0070a0002c0001t0001g0071a0002c0001t0001g0127others(5): Show | 8 | HG02015.hp2 HG02258.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.2009+14713_2009+14 others(12): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879211 | |||||
| chr8:36879211
|
G | GTATATAT others(1): Show |
3 | a0001c0002t0001g0073a0002c0001t0001g0179a0003c0003t0001g0154 | 3 | HG01243.hp1 HG02083.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.2009+14711_2009+14 others(14): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879211 | |||||
| chr8:36879211
|
G | GTATATAT others(3): Show |
2 | a0001c0002t0001g0241a0002c0001t0001g0080 | 2 | HG02280.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2009+14709_2009+14 others(16): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879211 | |||||
| chr8:36879211
|
G | GTATATAT others(5): Show |
4 | a0001c0002t0001g0048a0001c0002t0001g0163a0001c0002t0001g0164others(1): Show | 4 | HG01109.hp2 HG02027.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.2009+14707_2009+14 others(18): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879211 | |||||
| chr8:36879211
|
G | GTATATAT others(7): Show |
4 | a0001c0002t0001g0188a0001c0002t0001g0247a0001c0002t0001g0253others(1): Show | 4 | HG01981.hp2 HG02257.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.2009+14705_2009+14 others(20): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879211 | |||||
| chr8:36879211
|
G | GTATATAT others(9): Show |
1 | a0001c0002t0001g0282 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2009+14703_2009+14 others(22): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879211 | |||||
| chr8:36879211
|
G | GTGTA | 4 | a0001c0002t0001g0157a0001c0002t0001g0158a0003c0003t0001g0101others(1): Show | 4 | HG02965.hp2 HG03139.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2009+14691_2009+14 others(10): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879211 | |||||
| chr8:36879211
|
GTA | G | 12 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(9): Show | 12 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2009+14717_2009+14 others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879211 | |||||
| chr8:36879213
|
A | G | 1 | a0003c0005t0001g0214 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2009+14692A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36879213 | ||||||
| chr8:36879215
|
A | G | 4 | a0001c0002t0001g0286a0001c0002t0001g0289a0001c0002t0001g0290others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2009+14694A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36879215 | ||||||
| chr8:36879238
|
T | C | 5 | a0001c0002t0001g0144a0001c0002t0001g0187a0001c0002t0001g0283others(2): Show | 5 | HG02055.hp1 HG02683.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2009+14717T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36879238 | ||||||
| chr8:36879238
|
T | TAC | 3 | a0002c0001t0001g0148a0002c0001t0001g0149a0003c0003t0001g0065 | 3 | HG02056.hp1 HG02129.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.2009+14725_2009+14 others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879238 | |||||
| chr8:36879326
|
A | T | 5 | a0001c0002t0001g0144a0001c0006t0001g0178a0001c0006t0001g0280others(2): Show | 5 | HG02647.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2009+14805A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36879326 | ||||||
| chr8:36879823
|
C | G | 3 | a0002c0001t0001g0150a0002c0001t0001g0151a0002c0019t0001g0152 | 3 | HG01978.hp1 HG02148.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.2009+15302C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36879823 | ||||||
| chr8:36879974
|
G | A | 1 | a0001c0004t0001g0225 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2009+15453G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36879974 | ||||||
| chr8:36880450
|
A | T | 2 | a0001c0002t0001g0240a0001c0002t0001g0254 | 2 | NA18980.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.2009+15929A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36880450 | ||||||
| chr8:36880458
|
C | T | 3 | a0002c0001t0001g0058a0002c0001t0001g0059a0002c0001t0001g0060 | 3 | NA18984.hp2 NA18989.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.2009+15937C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36880458 | ||||||
| chr8:36880485
|
G | A | 1 | a0003c0003t0001g0062 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2009+15964G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36880485 | ||||||
| chr8:36880493
|
G | A | 5 | a0002c0001t0001g0070a0002c0001t0001g0071a0002c0001t0001g0080others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2009+15972G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36880493 | ||||||
| chr8:36880688
|
C | T | 44 | a0002c0001t0001g0009a0002c0001t0001g0012a0002c0001t0001g0013others(41): Show | 44 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.2009+16167C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36880688 | ||||||
| chr8:36880784
|
C | T | 3 | a0003c0003t0001g0006a0003c0003t0001g0032a0003c0003t0001g0033 | 3 | HG02280.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2009+16263C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36880784 | ||||||
| chr8:36881033
|
C | G | 1 | a0001c0004t0001g0218 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2009+16512C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36881033 | ||||||
| chr8:36881135
|
G | A | 1 | a0001c0002t0001g0177 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2009+16614G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36881135 | ||||||
| chr8:36881246
|
G | A | 2 | a0001c0006t0001g0170a0001c0006t0001g0171 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2009+16725G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36881246 | ||||||
| chr8:36881361
|
T | C | 1 | a0001c0004t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2009+16840T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36881361 | ||||||
| chr8:36881408
|
G | A | 1 | a0003c0003t0001g0181 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2009+16887G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36881408 | ||||||
| chr8:36881504
|
C | T | 1 | a0003c0003t0001g0185 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2009+16983C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36881504 | ||||||
| chr8:36881668
|
T | C | 1 | a0001c0002t0001g0164 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2009+17147T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36881668 | ||||||
| chr8:36881768
|
C | G | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2009+17247C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36881768 | ||||||
| chr8:36881796
|
T | TCA | 27 | a0001c0002t0001g0187a0001c0002t0001g0283a0002c0001t0001g0037others(24): Show | 28 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.2009+17322_2009+17 others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36881796 | |||||
| chr8:36881796
|
T | TCACA | 14 | a0003c0003t0001g0005a0003c0003t0001g0045a0003c0003t0001g0064others(11): Show | 14 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.2009+17320_2009+17 others(10): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36881796 | |||||
| chr8:36881796
|
T | TCACACA | 7 | a0003c0003t0001g0062a0003c0003t0001g0081a0003c0003t0001g0082others(4): Show | 7 | HG00140.hp2 HG00639.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.2009+17318_2009+17 others(12): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36881796 | |||||
| chr8:36881796
|
TCA | T | 22 | a0001c0002t0001g0144a0002c0001t0001g0016a0002c0001t0001g0019others(19): Show | 22 | HG00621.hp2 HG01516.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.2009+17322_2009+17 others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36881796 | |||||
| chr8:36881796
|
TCACA | T | 72 | a0001c0002t0001g0047a0001c0002t0001g0288a0001c0002t0001g0289others(69): Show | 72 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.2009+17320_2009+17 others(10): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36881796 | |||||
| chr8:36881796
|
TCACACA | T | 18 | a0001c0002t0001g0123a0001c0002t0001g0188a0001c0002t0001g0257others(15): Show | 18 | HG00544.hp2 HG00673.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.2009+17318_2009+17 others(12): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36881796 | |||||
| chr8:36881796
|
TCACACAC others(1): Show |
T | 44 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(41): Show | 46 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.2009+17316_2009+17 others(14): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36881796 | |||||
| chr8:36881796
|
TCACACAC others(3): Show |
T | 71 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(68): Show | 72 | HG00140.hp1 HG00438.hp2 HG01074.hp1 others(69): Show |
intron_variant | MODIFIER | c.2009+17314_2009+17 others(16): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36881796 | |||||
| chr8:36881796
|
TCACACAC others(5): Show |
T | 2 | a0001c0002t0001g0051a0001c0002t0001g0252 | 2 | NA18948.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.2009+17312_2009+17 others(18): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36881796 | |||||
| chr8:36881932
|
C | A | 1 | a0001c0002t0001g0268 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2009+17411C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36881932 | ||||||
| chr8:36882027
|
G | T | 4 | a0001c0002t0001g0144a0001c0006t0001g0178a0001c0006t0001g0280others(1): Show | 4 | HG02647.hp1 HG02818.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2009+17506G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36882027 | ||||||
| chr8:36882086
|
A | T | 3 | a0001c0006t0001g0178a0001c0006t0001g0280a0001c0018t0001g0180 | 3 | HG02647.hp1 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2009+17565A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36882086 | ||||||
| chr8:36882500
|
G | A | 2 | a0001c0002t0001g0187a0001c0002t0001g0283 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2009+17979G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36882500 | ||||||
| chr8:36882532
|
G | A | 1 | a0001c0002t0001g0248 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2009+18011G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36882532 | ||||||
| chr8:36882687
|
G | A | 1 | a0001c0002t0001g0249 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2009+18166G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36882687 | ||||||
| chr8:36882771
|
T | C | 1 | a0001c0002t0001g0234 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2009+18250T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36882771 | ||||||
| chr8:36883278
|
G | A | 1 | a0001c0002t0001g0176 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2009+18757G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36883278 | ||||||
| chr8:36883469
|
G | T | 1 | a0001c0004t0001g0190 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2009+18948G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36883469 | ||||||
| chr8:36883544
|
A | T | 2 | a0002c0001t0001g0148a0002c0001t0001g0149 | 2 | HG02056.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.2009+19023A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36883544 | ||||||
| chr8:36884041
|
C | T | 125 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(122): Show | 128 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.2009+19520C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36884041 | ||||||
| chr8:36884104
|
G | A | 1 | a0001c0002t0001g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2009+19583G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36884104 | ||||||
| chr8:36884188
|
AG | A | 55 | a0001c0002t0001g0109a0001c0002t0001g0123a0001c0002t0001g0157others(52): Show | 57 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.2009+19669delG | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36884188 | |||||
| chr8:36884361
|
G | C | 1 | a0003c0003t0001g0065 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2009+19840G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36884361 | ||||||
| chr8:36884402
|
G | A | 1 | a0002c0001t0001g0106 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2009+19881G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36884402 | ||||||
| chr8:36884411
|
G | A | 2 | a0001c0002t0001g0187a0001c0002t0001g0283 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2009+19890G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36884411 | ||||||
| chr8:36884463
|
C | T | 2 | a0001c0004t0001g0191a0001c0004t0001g0198 | 2 | NA18963.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2009+19942C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36884463 | ||||||
| chr8:36884464
|
G | A | 1 | a0001c0002t0001g0281 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2009+19943G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36884464 | ||||||
| chr8:36884472
|
A | G | 1 | a0001c0002t0001g0261 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2009+19951A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36884472 | ||||||
| chr8:36884697
|
C | G | 1 | a0001c0002t0001g0234 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2009+20176C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36884697 | ||||||
| chr8:36884765
|
A | T | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2009+20244A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36884765 | ||||||
| chr8:36884771
|
A | T | 4 | a0001c0002t0001g0144a0001c0006t0001g0178a0001c0006t0001g0280others(1): Show | 4 | HG02647.hp1 HG02818.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2009+20250A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36884771 | ||||||
| chr8:36884773
|
C | A | 1 | a0001c0002t0001g0258 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2009+20252C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36884773 | ||||||
| chr8:36884777
|
A | G | 1 | a0001c0002t0001g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2009+20256A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36884777 | ||||||
| chr8:36885014
|
C | T | 1 | a0001c0004t0001g0162 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2009+20493C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36885014 | ||||||
| chr8:36885197
|
A | G | 2 | a0001c0006t0001g0170a0001c0006t0001g0171 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2010-20511A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36885197 | ||||||
| chr8:36885242
|
A | G | 1 | a0003c0003t0001g0034 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2010-20466A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36885242 | ||||||
| chr8:36885272
|
T | A | 121 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(118): Show | 124 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.2010-20436T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36885272 | ||||||
| chr8:36885305
|
A | G | 1 | a0003c0003t0001g0104 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2010-20403A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36885305 | ||||||
| chr8:36885336
|
C | G | 1 | a0001c0002t0001g0229 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2010-20372C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36885336 | ||||||
| chr8:36885587
|
G | A | 11 | a0001c0002t0001g0073a0001c0002t0001g0163a0001c0002t0001g0164others(8): Show | 11 | HG02027.hp1 HG02071.hp2 NA18942.hp1 others(8): Show |
intron_variant | MODIFIER | c.2010-20121G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36885587 | ||||||
| chr8:36885640
|
A | G | 1 | a0002c0001t0001g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2010-20068A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36885640 | ||||||
| chr8:36885702
|
A | G | 47 | a0001c0002t0001g0109a0001c0002t0001g0123a0001c0002t0001g0172others(44): Show | 49 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.2010-20006A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36885702 | ||||||
| chr8:36886011
|
C | A | 2 | a0001c0004t0001g0162a0001c0004t0001g0221 | 2 | HG01358.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2010-19697C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36886011 | ||||||
| chr8:36886015
|
G | A | 2 | a0001c0004t0001g0162a0001c0004t0001g0221 | 2 | HG01358.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2010-19693G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36886015 | ||||||
| chr8:36886135
|
G | C | 5 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(2): Show | 5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-19573G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36886135 | ||||||
| chr8:36886377
|
T | C | 1 | a0001c0009t0001g0169 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2010-19331T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36886377 | ||||||
| chr8:36886499
|
A | C | 129 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(126): Show | 132 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.2010-19209A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36886499 | ||||||
| chr8:36886509
|
G | T | 1 | a0002c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2010-19199G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36886509 | ||||||
| chr8:36886555
|
G | A | 1 | a0003c0003t0001g0084 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2010-19153G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36886555 | ||||||
| chr8:36886615
|
T | G | 1 | a0002c0001t0001g0134 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2010-19093T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36886615 | ||||||
| chr8:36886684
|
T | A | 1 | a0002c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2010-19024T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36886684 | ||||||
| chr8:36886962
|
G | A | 2 | a0002c0001t0001g0148a0002c0001t0001g0149 | 2 | HG02056.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.2010-18746G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36886962 | ||||||
| chr8:36886981
|
T | G | 1 | a0003c0005t0001g0220 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2010-18727T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36886981 | ||||||
| chr8:36887159
|
T | C | 1 | a0002c0001t0001g0285 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2010-18549T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36887159 | ||||||
| chr8:36887232
|
C | T | 3 | a0001c0002t0001g0187a0001c0002t0001g0188a0001c0002t0001g0283 | 3 | HG02055.hp1 HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2010-18476C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36887232 | ||||||
| chr8:36887413
|
G | A | 1 | a0001c0009t0001g0169 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2010-18295G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36887413 | ||||||
| chr8:36887415
|
A | G | 1 | a0003c0003t0001g0145 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2010-18293A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36887415 | ||||||
| chr8:36887442
|
G | GT | 63 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(60): Show | 64 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.2010-18257dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36887442 | |||||
| chr8:36887452
|
G | GT | 57 | a0001c0002t0001g0109a0001c0002t0001g0123a0001c0002t0001g0172others(54): Show | 59 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.2010-18239dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36887452 | |||||
| chr8:36887452
|
G | GTT | 12 | a0001c0002t0001g0282a0001c0004t0001g0159a0001c0004t0001g0191others(9): Show | 12 | HG00544.hp2 HG01168.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.2010-18240_2010-18 others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36887452 | |||||
| chr8:36887452
|
G | T | 13 | a0001c0002t0001g0049a0001c0002t0001g0073a0001c0002t0001g0164others(10): Show | 13 | HG00099.hp2 HG01243.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.2010-18256G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36887452 | ||||||
| chr8:36887453
|
T | G | 6 | a0001c0002t0001g0049a0001c0006t0001g0170a0001c0006t0001g0171others(3): Show | 6 | HG00099.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2010-18255T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36887453 | ||||||
| chr8:36887459
|
T | G | 16 | a0003c0003t0001g0007a0003c0003t0001g0064a0003c0003t0001g0065others(13): Show | 16 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.2010-18249T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36887459 | ||||||
| chr8:36887548
|
G | C | 2 | a0003c0003t0001g0181a0003c0003t0001g0182 | 2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2010-18160G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36887548 | ||||||
| chr8:36887567
|
C | T | 2 | a0001c0006t0001g0178a0001c0018t0001g0180 | 2 | HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2010-18141C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36887567 | ||||||
| chr8:36887568
|
G | A | 5 | a0001c0006t0001g0170a0001c0006t0001g0171a0001c0006t0001g0178others(2): Show | 5 | HG02647.hp1 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2010-18140G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36887568 | ||||||
| chr8:36887618
|
A | T | 7 | a0001c0002t0001g0144a0001c0006t0001g0170a0001c0006t0001g0171others(4): Show | 7 | HG02647.hp1 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2010-18090A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36887618 | ||||||
| chr8:36887709
|
T | C | 46 | a0001c0002t0001g0109a0001c0002t0001g0123a0001c0002t0001g0172others(43): Show | 48 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2010-17999T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36887709 | ||||||
| chr8:36887960
|
G | A | 46 | a0001c0002t0001g0109a0001c0002t0001g0123a0001c0002t0001g0172others(43): Show | 48 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2010-17748G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36887960 | ||||||
| chr8:36888146
|
G | A | 129 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(126): Show | 132 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.2010-17562G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36888146 | ||||||
| chr8:36888221
|
A | G | 5 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(2): Show | 5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-17487A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36888221 | ||||||
| chr8:36888304
|
G | T | 1 | a0002c0001t0001g0122 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2010-17404G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36888304 | ||||||
| chr8:36888339
|
A | G | 1 | a0001c0002t0001g0014 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2010-17369A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36888339 | ||||||
| chr8:36888417
|
C | T | 1 | a0002c0001t0001g0096 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2010-17291C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36888417 | ||||||
| chr8:36888504
|
G | A | 5 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(2): Show | 5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-17204G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36888504 | ||||||
| chr8:36888559
|
G | A | 1 | a0001c0002t0001g0289 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2010-17149G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36888559 | ||||||
| chr8:36889022
|
G | A | 1 | a0003c0005t0001g0220 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2010-16686G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36889022 | ||||||
| chr8:36889122
|
A | G | 1 | a0002c0001t0001g0285 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2010-16586A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36889122 | ||||||
| chr8:36889243
|
G | A | 1 | a0001c0002t0001g0177 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2010-16465G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36889243 | ||||||
| chr8:36889319
|
G | T | 1 | a0002c0001t0001g0025 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2010-16389G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36889319 | ||||||
| chr8:36889404
|
T | G | 2 | a0002c0001t0001g0012a0002c0001t0001g0013 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2010-16304T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36889404 | ||||||
| chr8:36889419
|
C | A | 7 | a0001c0002t0001g0144a0001c0006t0001g0170a0001c0006t0001g0171others(4): Show | 7 | HG02647.hp1 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2010-16289C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36889419 | ||||||
| chr8:36889430
|
T | A | 117 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(114): Show | 120 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.2010-16278T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36889430 | ||||||
| chr8:36889464
|
C | T | 1 | a0002c0001t0001g0148 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2010-16244C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36889464 | ||||||
| chr8:36889902
|
C | G | 2 | a0001c0006t0001g0178a0001c0018t0001g0180 | 2 | HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2010-15806C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36889902 | ||||||
| chr8:36890183
|
G | A | 3 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174 | 3 | HG02055.hp2 HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2010-15525G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36890183 | ||||||
| chr8:36890231
|
A | G | 2 | a0002c0001t0001g0012a0002c0001t0001g0013 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2010-15477A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36890231 | ||||||
| chr8:36890551
|
A | G | 1 | a0001c0002t0001g0241 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2010-15157A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36890551 | ||||||
| chr8:36890686
|
A | G | 4 | a0002c0001t0001g0053a0002c0001t0001g0058a0002c0001t0001g0059others(1): Show | 4 | HG00673.hp2 NA18984.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.2010-15022A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36890686 | ||||||
| chr8:36890970
|
T | A | 1 | a0001c0002t0001g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2010-14738T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36890970 | ||||||
| chr8:36891021
|
T | C | 10 | a0003c0003t0001g0006a0003c0003t0001g0011a0003c0003t0001g0026others(7): Show | 10 | HG02280.hp2 HG02630.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.2010-14687T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36891021 | ||||||
| chr8:36891177
|
C | A | 2 | a0001c0002t0001g0144a0007c0008t0001g0279 | 2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2010-14531C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36891177 | ||||||
| chr8:36891395
|
C | T | 5 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(2): Show | 5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-14313C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36891395 | ||||||
| chr8:36891412
|
A | C | 2 | a0003c0003t0001g0023a0003c0003t0001g0067 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2010-14296A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36891412 | ||||||
| chr8:36891499
|
G | C | 1 | a0001c0002t0001g0014 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2010-14209G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36891499 | ||||||
| chr8:36891688
|
G | A | 1 | a0001c0002t0001g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2010-14020G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36891688 | ||||||
| chr8:36891772
|
A | G | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2010-13936A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36891772 | ||||||
| chr8:36892036
|
A | G | 7 | a0001c0002t0001g0144a0001c0006t0001g0170a0001c0006t0001g0171others(4): Show | 7 | HG02647.hp1 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2010-13672A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36892036 | ||||||
| chr8:36892236
|
C | A | 1 | a0002c0001t0001g0124 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2010-13472C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36892236 | ||||||
| chr8:36892336
|
A | T | 1 | a0002c0001t0001g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2010-13372A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36892336 | ||||||
| chr8:36892449
|
A | G | 1 | a0002c0001t0001g0140 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2010-13259A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36892449 | ||||||
| chr8:36892492
|
C | A | 1 | a0002c0001t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2010-13216C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36892492 | ||||||
| chr8:36892596
|
C | G | 5 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(2): Show | 5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-13112C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36892596 | ||||||
| chr8:36892631
|
C | T | 5 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(2): Show | 5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-13077C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36892631 | ||||||
| chr8:36893070
|
T | C | 5 | a0001c0006t0001g0170a0001c0006t0001g0171a0001c0006t0001g0178others(2): Show | 5 | HG02647.hp1 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2010-12638T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36893070 | ||||||
| chr8:36893118
|
T | C | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2010-12590T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36893118 | ||||||
| chr8:36893143
|
T | TTG | 8 | a0001c0002t0001g0230a0001c0002t0001g0281a0001c0002t0001g0282others(5): Show | 8 | HG00438.hp2 HG02257.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2010-12565_2010-12 others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36893143 | ||||||
| chr8:36893144
|
G | GT | 121 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(118): Show | 124 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.2010-12554dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36893144 | |||||
| chr8:36893144
|
G | T | 8 | a0001c0002t0001g0230a0001c0002t0001g0281a0001c0002t0001g0282others(5): Show | 8 | HG00438.hp2 HG02257.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2010-12564G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36893144 | ||||||
| chr8:36893262
|
C | G | 3 | a0003c0003t0001g0011a0003c0003t0001g0101a0003c0003t0001g0102 | 3 | HG03139.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2010-12446C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36893262 | ||||||
| chr8:36893266
|
A | T | 1 | a0003c0003t0001g0231 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2010-12442A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36893266 | ||||||
| chr8:36893327
|
C | CT | 10 | a0001c0002t0001g0163a0001c0002t0001g0164a0001c0002t0001g0177others(7): Show | 10 | HG02027.hp1 HG02071.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2010-12369dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36893327 | |||||
| chr8:36893327
|
CT | C | 11 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.2010-12369delT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36893327 | |||||
| chr8:36893341
|
C | T | 7 | a0003c0003t0001g0002a0003c0003t0001g0089a0003c0003t0001g0090others(4): Show | 8 | HG00609.hp1 NA18946.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.2010-12367C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36893341 | ||||||
| chr8:36893342
|
G | A | 1 | a0001c0002t0001g0266 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2010-12366G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36893342 | ||||||
| chr8:36893396
|
A | G | 3 | a0002c0001t0001g0004a0002c0001t0001g0068a0002c0001t0001g0184 | 3 | HG02559.hp1 HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2010-12312A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36893396 | ||||||
| chr8:36893885
|
T | G | 117 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(114): Show | 120 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.2010-11823T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36893885 | ||||||
| chr8:36894048
|
C | T | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2010-11660C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36894048 | ||||||
| chr8:36894348
|
T | C | 129 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(126): Show | 132 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.2010-11360T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36894348 | ||||||
| chr8:36894445
|
T | C | 129 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(126): Show | 132 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.2010-11263T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36894445 | ||||||
| chr8:36894478
|
T | G | 5 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(2): Show | 5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-11230T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36894478 | ||||||
| chr8:36894480
|
G | A | 117 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(114): Show | 120 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.2010-11228G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36894480 | ||||||
| chr8:36894814
|
A | G | 6 | a0003c0003t0001g0007a0003c0003t0001g0076a0003c0003t0001g0078others(3): Show | 6 | HG00099.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.2010-10894A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36894814 | ||||||
| chr8:36895001
|
A | T | 1 | a0001c0002t0001g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2010-10707A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36895001 | ||||||
| chr8:36895039
|
A | G | 1 | a0002c0001t0001g0037 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2010-10669A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36895039 | ||||||
| chr8:36895046
|
T | C | 129 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(126): Show | 132 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.2010-10662T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36895046 | ||||||
| chr8:36895089
|
AT | A | 5 | a0003c0003t0001g0002a0003c0003t0001g0090a0003c0003t0001g0092others(2): Show | 6 | NA18946.hp1 NA18969.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.2010-10607delT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36895089 | |||||
| chr8:36895223
|
C | T | 1 | a0002c0001t0001g0140 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2010-10485C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36895223 | ||||||
| chr8:36895325
|
C | T | 5 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(2): Show | 5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-10383C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36895325 | ||||||
| chr8:36895457
|
C | T | 5 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(2): Show | 5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-10251C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36895457 | ||||||
| chr8:36895673
|
T | G | 1 | a0002c0001t0001g0039 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2010-10035T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36895673 | ||||||
| chr8:36896034
|
T | C | 1 | a0001c0002t0001g0263 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2010-9674T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36896034 | ||||||
| chr8:36896111
|
A | AT | 115 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(112): Show | 118 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.2010-9590dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36896111 | |||||
| chr8:36896342
|
C | T | 1 | a0001c0018t0001g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2010-9366C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36896342 | ||||||
| chr8:36896580
|
G | A | 1 | a0002c0001t0001g0036 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2010-9128G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36896580 | ||||||
| chr8:36896586
|
C | T | 117 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(114): Show | 120 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.2010-9122C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36896586 | ||||||
| chr8:36896595
|
A | G | 1 | a0001c0004t0001g0209 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2010-9113A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36896595 | ||||||
| chr8:36896612
|
T | G | 129 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(126): Show | 132 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.2010-9096T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36896612 | ||||||
| chr8:36896623
|
A | T | 5 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(2): Show | 5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-9085A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36896623 | ||||||
| chr8:36896636
|
G | A | 1 | a0001c0002t0001g0054 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2010-9072G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36896636 | ||||||
| chr8:36896646
|
A | G | 2 | a0001c0002t0001g0281a0001c0002t0001g0282 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2010-9062A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36896646 | ||||||
| chr8:36896667
|
G | C | 3 | a0001c0004t0001g0227a0001c0004t0001g0228a0001c0004t0002g0226 | 3 | NA18943.hp1 NA18965.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.2010-9041G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36896667 | ||||||
| chr8:36896813
|
A | T | 2 | a0001c0002t0001g0281a0001c0002t0001g0282 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2010-8895A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36896813 | ||||||
| chr8:36897256
|
C | T | 117 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(114): Show | 120 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.2010-8452C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36897256 | ||||||
| chr8:36897331
|
CTT | C | 5 | a0001c0006t0001g0170a0001c0006t0001g0171a0001c0006t0001g0178others(2): Show | 5 | HG02647.hp1 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2010-8372_2010-837 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36897331 | |||||
| chr8:36897454
|
G | C | 1 | a0001c0002t0001g0230 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2010-8254G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36897454 | ||||||
| chr8:36897887
|
T | C | 129 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(126): Show | 132 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.2010-7821T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36897887 | ||||||
| chr8:36898201
|
C | T | 1 | a0002c0001t0001g0114 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2010-7507C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36898201 | ||||||
| chr8:36898241
|
C | T | 6 | a0003c0003t0001g0007a0003c0003t0001g0076a0003c0003t0001g0078others(3): Show | 6 | HG00099.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.2010-7467C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36898241 | ||||||
| chr8:36898270
|
T | C | 129 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(126): Show | 132 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.2010-7438T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36898270 | ||||||
| chr8:36898315
|
C | CAT | 12 | a0001c0002t0001g0144a0001c0002t0001g0286a0001c0002t0001g0288others(9): Show | 12 | HG01891.hp1 HG02615.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.2010-7393_2010-739 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36898315 | ||||||
| chr8:36898578
|
GA | G | 8 | a0001c0002t0001g0144a0001c0004t0001g0195a0001c0006t0001g0170others(5): Show | 8 | HG02647.hp1 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.2010-7120delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36898578 | |||||
| chr8:36898980
|
A | G | 9 | a0001c0002t0001g0155a0001c0002t0001g0156a0001c0002t0001g0243others(6): Show | 9 | HG01099.hp2 HG01257.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2010-6728A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36898980 | ||||||
| chr8:36899288
|
G | A | 1 | a0003c0003t0001g0034 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2010-6420G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36899288 | ||||||
| chr8:36899288
|
GA | G | 129 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(126): Show | 132 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.2010-6410delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36899288 | |||||
| chr8:36899328
|
A | T | 3 | a0002c0001t0001g0004a0002c0001t0001g0068a0002c0001t0001g0184 | 3 | HG02559.hp1 HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2010-6380A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36899328 | ||||||
| chr8:36899427
|
AAC | A | 5 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(2): Show | 5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-6277_2010-627 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36899427 | |||||
| chr8:36899543
|
T | C | 21 | a0002c0001t0001g0009a0002c0001t0001g0015a0002c0001t0001g0094others(18): Show | 21 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.2010-6165T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36899543 | ||||||
| chr8:36900159
|
GAC | G | 129 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(126): Show | 132 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.2010-5545_2010-554 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36900159 | |||||
| chr8:36900227
|
G | A | 1 | a0001c0004t0001g0160 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2010-5481G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36900227 | ||||||
| chr8:36900275
|
G | A | 3 | a0001c0002t0001g0237a0001c0002t0001g0259a0001c0002t0001g0269 | 3 | HG01168.hp2 HG01169.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.2010-5433G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36900275 | ||||||
| chr8:36900421
|
AG | A | 112 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(109): Show | 115 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.2010-5286delG | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36900421 | ||||||
| chr8:36900456
|
G | A | 1 | a0003c0003t0001g0063 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2010-5252G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36900456 | ||||||
| chr8:36900666
|
A | G | 1 | a0001c0002t0001g0265 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2010-5042A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36900666 | ||||||
| chr8:36900927
|
G | T | 1 | a0002c0001t0001g0134 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2010-4781G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36900927 | ||||||
| chr8:36900928
|
C | T | 1 | a0002c0001t0001g0134 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2010-4780C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36900928 | ||||||
| chr8:36901081
|
G | A | 129 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(126): Show | 132 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.2010-4627G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36901081 | ||||||
| chr8:36901196
|
A | C | 5 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(2): Show | 5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-4512A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36901196 | ||||||
| chr8:36901240
|
C | G | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2010-4468C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36901240 | ||||||
| chr8:36901266
|
T | C | 1 | a0002c0001t0001g0126 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2010-4442T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36901266 | ||||||
| chr8:36901428
|
C | T | 47 | a0003c0003t0001g0002a0003c0003t0001g0005a0003c0003t0001g0007others(44): Show | 48 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.2010-4280C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36901428 | ||||||
| chr8:36901596
|
C | T | 3 | a0001c0004t0001g0159a0001c0004t0001g0160a0001c0004t0001g0161 | 3 | NA18944.hp1 NA18994.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.2010-4112C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36901596 | ||||||
| chr8:36901808
|
C | T | 1 | a0001c0004t0001g0162 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2010-3900C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36901808 | ||||||
| chr8:36902025
|
T | C | 1 | a0002c0001t0001g0140 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2010-3683T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36902025 | ||||||
| chr8:36902044
|
A | G | 2 | a0001c0002t0001g0281a0001c0002t0001g0282 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2010-3664A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36902044 | ||||||
| chr8:36902068
|
C | T | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2010-3640C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36902068 | ||||||
| chr8:36902280
|
T | C | 1 | a0001c0002t0001g0281 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2010-3428T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36902280 | ||||||
| chr8:36902337
|
G | A | 2 | a0002c0001t0001g0148a0002c0001t0001g0149 | 2 | HG02056.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.2010-3371G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36902337 | ||||||
| chr8:36902385
|
C | A | 2 | a0001c0002t0001g0144a0007c0008t0001g0279 | 2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2010-3323C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36902385 | ||||||
| chr8:36902442
|
G | A | 1 | a0001c0002t0001g0123 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2010-3266G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36902442 | ||||||
| chr8:36902523
|
G | A | 1 | a0003c0005t0001g0196 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2010-3185G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36902523 | ||||||
| chr8:36902540
|
A | C | 1 | a0002c0001t0001g0010 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2010-3168A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36902540 | ||||||
| chr8:36902861
|
G | T | 2 | a0001c0002t0001g0144a0007c0008t0001g0279 | 2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2010-2847G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36902861 | ||||||
| chr8:36902882
|
T | G | 117 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(114): Show | 120 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.2010-2826T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36902882 | ||||||
| chr8:36902892
|
A | G | 8 | a0002c0001t0001g0106a0002c0001t0001g0114a0002c0001t0001g0115others(5): Show | 8 | HG00597.hp2 HG00609.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2010-2816A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36902892 | ||||||
| chr8:36903352
|
C | A | 2 | a0001c0006t0001g0170a0001c0006t0001g0171 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2010-2356C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36903352 | ||||||
| chr8:36903399
|
A | G | 1 | a0002c0001t0001g0124 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2010-2309A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36903399 | ||||||
| chr8:36903466
|
C | T | 117 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(114): Show | 120 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.2010-2242C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36903466 | ||||||
| chr8:36903632
|
T | A | 129 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(126): Show | 132 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.2010-2076T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36903632 | ||||||
| chr8:36903667
|
G | T | 1 | a0001c0004t0001g0168 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2010-2041G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36903667 | ||||||
| chr8:36903802
|
TGGAAGGG others(8): Show |
T | 1 | a0001c0002t0001g0255 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2010-1904_2010-189 others(19): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36903802 | |||||
| chr8:36903814
|
C | A | 1 | a0002c0001t0001g0057 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2010-1894C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36903814 | ||||||
| chr8:36904094
|
C | T | 5 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(2): Show | 5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-1614C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904094 | ||||||
| chr8:36904288
|
C | G | 2 | a0001c0002t0001g0262a0001c0002t0001g0263 | 2 | HG02523.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.2010-1420C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904288 | ||||||
| chr8:36904318
|
G | C | 1 | a0003c0003t0001g0082 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2010-1390G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904318 | ||||||
| chr8:36904344
|
C | G | 5 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(2): Show | 5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-1364C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904344 | ||||||
| chr8:36904555
|
G | A | 3 | a0001c0002t0001g0187a0001c0002t0001g0188a0001c0002t0001g0283 | 3 | HG02055.hp1 HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2010-1153G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904555 | ||||||
| chr8:36904571
|
C | T | 5 | a0001c0006t0001g0170a0001c0006t0001g0171a0001c0006t0001g0178others(2): Show | 5 | HG02647.hp1 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2010-1137C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904571 | ||||||
| chr8:36904584
|
G | A | 1 | a0002c0001t0001g0015 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2010-1124G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904584 | ||||||
| chr8:36904614
|
A | G | 1 | a0002c0001t0001g0016 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2010-1094A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904614 | ||||||
| chr8:36904620
|
T | C | 129 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(126): Show | 132 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.2010-1088T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904620 | ||||||
| chr8:36904736
|
G | C | 1 | a0002c0011t0001g0072 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2010-972G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904736 | ||||||
| chr8:36904761
|
T | C | 5 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(2): Show | 5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-947T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904761 | ||||||
| chr8:36904799
|
C | G | 2 | a0003c0003t0001g0017a0003c0005t0001g0222 | 2 | NA19084.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.2010-909C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904799 | ||||||
| chr8:36904891
|
T | C | 117 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(114): Show | 120 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.2010-817T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904891 | ||||||
| chr8:36904954
|
C | T | 129 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(126): Show | 132 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.2010-754C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904954 | ||||||
| chr8:36904987
|
G | T | 1 | a0003c0003t0001g0154 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2010-721G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904987 | ||||||
| chr8:36905015
|
C | G | 2 | a0001c0002t0001g0144a0007c0008t0001g0279 | 2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2010-693C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36905015 | ||||||
| chr8:36905073
|
A | G | 1 | a0001c0004t0001g0209 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2010-635A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36905073 | ||||||
| chr8:36905091
|
G | A | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2010-617G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36905091 | ||||||
| chr8:36905190
|
A | G | 1 | a0002c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2010-518A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36905190 | ||||||
| chr8:36905460
|
C | CA | 241 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(238): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.2010-233dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36905460 | |||||
| chr8:36905460
|
C | CAA | 10 | a0001c0002t0001g0251a0001c0004t0001g0193a0002c0001t0001g0031others(7): Show | 10 | HG00140.hp1 HG01258.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.2010-234_2010-233d others(4): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36905460 | |||||
| chr8:36905561
|
T | G | 1 | a0002c0001t0001g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2010-147T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36905561 | ||||||
| chr8:36905693
|
A | G | 1 | a0003c0003t0001g0284 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2010-15A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36905693 | ||||||
| chr8:36906181
|
C | CT | 28 | a0001c0002t0001g0286a0002c0001t0001g0025a0002c0001t0001g0027others(25): Show | 28 | HG00673.hp2 HG00735.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.2106+391dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr8 | 36906181 | |||||
| chr8:36906181
|
C | CTT | 245 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(242): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.2106+390_2106+391d others(4): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr8 | 36906181 | |||||
| chr8:36906181
|
C | CTTT | 6 | a0001c0002t0001g0073a0001c0002t0001g0163a0001c0002t0001g0164others(3): Show | 6 | HG00544.hp1 HG01517.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.2106+389_2106+391d others(5): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr8 | 36906181 | |||||
| chr8:36906248
|
T | C | 1 | a0001c0006t0001g0171 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2106+444T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36906248 | ||||||
| chr8:36906312
|
A | G | 5 | a0001c0006t0001g0170a0001c0006t0001g0171a0001c0006t0001g0178others(2): Show | 5 | HG02647.hp1 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2106+508A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36906312 | ||||||
| chr8:36906452
|
T | G | 1 | a0002c0001t0001g0059 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2106+648T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36906452 | ||||||
| chr8:36906571
|
C | T | 5 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(2): Show | 5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2106+767C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36906571 | ||||||
| chr8:36906600
|
T | A | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2106+796T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36906600 | ||||||
| chr8:36906872
|
C | T | 2 | a0001c0002t0001g0144a0007c0008t0001g0279 | 2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2106+1068C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36906872 | ||||||
| chr8:36906996
|
T | C | 4 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2106+1192T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36906996 | ||||||
| chr8:36907417
|
A | G | 58 | a0001c0002t0001g0109a0001c0002t0001g0123a0001c0002t0001g0144others(55): Show | 60 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.2106+1613A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36907417 | ||||||
| chr8:36907564
|
A | G | 1 | a0001c0002t0001g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2107-1747A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36907564 | ||||||
| chr8:36907626
|
G | A | 1 | a0002c0001t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2107-1685G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36907626 | ||||||
| chr8:36907982
|
G | T | 1 | a0001c0002t0001g0262 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2107-1329G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36907982 | ||||||
| chr8:36908032
|
G | A | 1 | a0001c0002t0001g0047 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2107-1279G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36908032 | ||||||
| chr8:36908073
|
C | A | 3 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174 | 3 | HG02055.hp2 HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2107-1238C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36908073 | ||||||
| chr8:36908131
|
T | A | 1 | a0001c0002t0001g0255 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2107-1180T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36908131 | ||||||
| chr8:36908178
|
A | C | 1 | a0001c0002t0001g0255 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2107-1133A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36908178 | ||||||
| chr8:36908265
|
A | G | 6 | a0003c0003t0001g0007a0003c0003t0001g0076a0003c0003t0001g0078others(3): Show | 6 | HG00099.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.2107-1046A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36908265 | ||||||
| chr8:36908273
|
T | C | 1 | a0003c0003t0001g0102 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2107-1038T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36908273 | ||||||
| chr8:36908558
|
A | G | 1 | a0001c0014t0001g0233 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2107-753A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36908558 | ||||||
| chr8:36908569
|
A | C | 129 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(126): Show | 132 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.2107-742A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36908569 | ||||||
| chr8:36908755
|
A | G | 5 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(2): Show | 5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2107-556A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36908755 | ||||||
| chr8:36908756
|
T | C | 2 | a0003c0003t0001g0079a0003c0003t0001g0083 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2107-555T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36908756 | ||||||
| chr8:36908799
|
T | TA | 5 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(2): Show | 5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2107-507dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr8 | 36908799 | |||||
| chr8:36908834
|
T | C | 1 | a0002c0001t0001g0122 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2107-477T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36908834 | ||||||
| chr8:36909152
|
A | T | 1 | a0001c0002t0001g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2107-159A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36909152 | ||||||
| chr8:36909178
|
A | G | 1 | a0001c0002t0001g0266 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2107-133A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36909178 | ||||||
| chr8:36909260
|
A | T | 2 | a0001c0002t0001g0236a0001c0002t0001g0273 | 2 | NA18966.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.2107-51A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36909260 | ||||||
| chr8:36909545
|
A | T | 1 | a0001c0002t0001g0255 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2331+10A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/26 | chr8 | 36909545 | ||||||
| chr8:36909567
|
A | G | 60 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0047others(57): Show | 61 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.2331+32A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/26 | chr8 | 36909567 | ||||||
| chr8:36909627
|
C | G | 129 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(126): Show | 132 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.2331+92C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/26 | chr8 | 36909627 | ||||||
| chr8:36909707
|
T | A | 1 | a0001c0002t0001g0255 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2331+172T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/26 | chr8 | 36909707 | ||||||
| chr8:36909734
|
G | A | 1 | a0001c0002t0001g0229 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2331+199G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/26 | chr8 | 36909734 | ||||||
| chr8:36909901
|
T | C | 2 | a0001c0002t0001g0229a0001c0002t0001g0230 | 2 | HG00438.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.2331+366T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/26 | chr8 | 36909901 | ||||||
| chr8:36910169
|
C | T | 3 | a0003c0003t0001g0064a0003c0003t0001g0065a0003c0003t0001g0087 | 3 | HG02683.hp2 HG03492.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.2331+634C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/26 | chr8 | 36910169 | ||||||
| chr8:36910345
|
G | A | 3 | a0001c0006t0001g0178a0001c0006t0001g0287a0001c0018t0001g0180 | 3 | HG02615.hp1 HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2332-585G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/26 | chr8 | 36910345 | ||||||
| chr8:36910618
|
G | C | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2332-312G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/26 | chr8 | 36910618 | ||||||
| chr8:36910643
|
C | T | 1 | a0006c0010t0001g0022 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2332-287C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/26 | chr8 | 36910643 | ||||||
| chr8:36910717
|
G | A | 1 | a0001c0002t0001g0246 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2332-213G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/26 | chr8 | 36910717 | ||||||
| chr8:36910734
|
G | T | 129 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(126): Show | 132 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.2332-196G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/26 | chr8 | 36910734 | ||||||
| chr8:36910896
|
G | A | 7 | a0003c0003t0001g0023a0003c0003t0001g0067a0003c0003t0001g0181others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.2332-34G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/26 | chr8 | 36910896 | ||||||
| chr8:36911156
|
G | A | 1 | a0002c0001t0001g0057 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2521+37G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36911156 | ||||||
| chr8:36911425
|
C | T | 1 | a0002c0001t0001g0126 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2521+306C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36911425 | ||||||
| chr8:36911469
|
G | C | 3 | a0001c0002t0001g0237a0001c0002t0001g0259a0001c0002t0001g0269 | 3 | HG01168.hp2 HG01169.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.2521+350G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36911469 | ||||||
| chr8:36911540
|
T | G | 1 | a0001c0006t0001g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2521+421T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36911540 | ||||||
| chr8:36911541
|
G | C | 4 | a0001c0002t0001g0018a0001c0002t0001g0239a0001c0002t0001g0240others(1): Show | 4 | NA18978.hp2 NA18980.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.2521+422G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36911541 | ||||||
| chr8:36911564
|
C | G | 1 | a0003c0003t0001g0186 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2521+445C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36911564 | ||||||
| chr8:36912192
|
G | A | 2 | a0001c0002t0001g0144a0007c0008t0001g0279 | 2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2521+1073G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36912192 | ||||||
| chr8:36912228
|
G | A | 1 | a0002c0001t0001g0030 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2521+1109G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36912228 | ||||||
| chr8:36912359
|
A | G | 7 | a0001c0002t0001g0155a0001c0002t0001g0156a0001c0002t0001g0244others(4): Show | 7 | HG01099.hp2 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2521+1240A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36912359 | ||||||
| chr8:36912371
|
T | C | 68 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(65): Show | 69 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.2521+1252T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36912371 | ||||||
| chr8:36912501
|
C | T | 46 | a0001c0002t0001g0109a0001c0002t0001g0123a0001c0002t0001g0172others(43): Show | 48 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2521+1382C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36912501 | ||||||
| chr8:36912682
|
G | A | 4 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(1): Show | 4 | HG01891.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2521+1563G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36912682 | ||||||
| chr8:36912697
|
C | T | 1 | a0002c0001t0001g0058 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2521+1578C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36912697 | ||||||
| chr8:36912700
|
G | A | 68 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(65): Show | 69 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.2521+1581G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36912700 | ||||||
| chr8:36912738
|
G | A | 4 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(1): Show | 4 | HG01891.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2521+1619G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36912738 | ||||||
| chr8:36912836
|
C | T | 1 | a0003c0003t0001g0082 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2521+1717C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36912836 | ||||||
| chr8:36912840
|
C | T | 197 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(194): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2521+1721C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36912840 | ||||||
| chr8:36912860
|
C | T | 1 | a0003c0003t0001g0154 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2521+1741C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36912860 | ||||||
| chr8:36912861
|
G | A | 2 | a0002c0001t0001g0031a0002c0001t0001g0037 | 2 | HG01258.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.2521+1742G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36912861 | ||||||
| chr8:36912953
|
C | CA | 34 | a0001c0002t0001g0288a0001c0002t0001g0289a0001c0004t0001g0213others(31): Show | 34 | HG00438.hp1 HG00544.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.2521+1860dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr8 | 36912953 | |||||
| chr8:36912953
|
CA | C | 140 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(137): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.2521+1860delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr8 | 36912953 | |||||
| chr8:36913072
|
G | T | 1 | a0002c0001t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2521+1953G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36913072 | ||||||
| chr8:36913114
|
C | T | 1 | a0003c0003t0001g0063 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2521+1995C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36913114 | ||||||
| chr8:36913134
|
G | A | 1 | a0001c0002t0001g0109 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2521+2015G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36913134 | ||||||
| chr8:36913175
|
G | T | 46 | a0001c0002t0001g0109a0001c0002t0001g0123a0001c0002t0001g0172others(43): Show | 48 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2521+2056G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36913175 | ||||||
| chr8:36913185
|
C | T | 64 | a0003c0003t0001g0002a0003c0003t0001g0005a0003c0003t0001g0006others(61): Show | 65 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.2521+2066C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36913185 | ||||||
| chr8:36913465
|
G | A | 4 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(1): Show | 4 | HG01891.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2521+2346G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36913465 | ||||||
| chr8:36913509
|
C | T | 1 | a0001c0002t0001g0014 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2521+2390C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36913509 | ||||||
| chr8:36913599
|
C | T | 6 | a0002c0001t0001g0024a0002c0001t0001g0031a0002c0001t0001g0037others(3): Show | 6 | HG01258.hp2 HG02004.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2521+2480C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36913599 | ||||||
| chr8:36913600
|
A | AT | 13 | a0002c0001t0001g0009a0002c0001t0001g0021a0002c0001t0001g0105others(10): Show | 13 | HG00438.hp1 HG01891.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.2521+2500dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr8 | 36913600 | |||||
| chr8:36913600
|
AT | A | 77 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(74): Show | 78 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.2521+2500delT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr8 | 36913600 | |||||
| chr8:36913847
|
T | C | 197 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(194): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2521+2728T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36913847 | ||||||
| chr8:36913853
|
G | A | 1 | a0002c0001t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2521+2734G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36913853 | ||||||
| chr8:36913891
|
A | G | 197 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(194): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2521+2772A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36913891 | ||||||
| chr8:36914153
|
A | G | 1 | a0001c0002t0001g0166 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2521+3034A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36914153 | ||||||
| chr8:36914261
|
G | C | 68 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(65): Show | 69 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.2521+3142G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36914261 | ||||||
| chr8:36914446
|
A | G | 5 | a0003c0003t0001g0006a0003c0003t0001g0026a0003c0003t0001g0032others(2): Show | 5 | HG02280.hp2 HG02965.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2521+3327A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36914446 | ||||||
| chr8:36914452
|
C | T | 2 | a0002c0001t0001g0010a0002c0001t0001g0103 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2521+3333C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36914452 | ||||||
| chr8:36914589
|
A | G | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2521+3470A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36914589 | ||||||
| chr8:36914605
|
T | G | 2 | a0001c0002t0001g0155a0001c0002t0001g0156 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2521+3486T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36914605 | ||||||
| chr8:36914694
|
G | A | 1 | a0002c0001t0001g0115 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2521+3575G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36914694 | ||||||
| chr8:36914751
|
G | A | 121 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(118): Show | 124 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.2521+3632G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36914751 | ||||||
| chr8:36914840
|
C | A | 197 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(194): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2521+3721C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36914840 | ||||||
| chr8:36914940
|
C | T | 4 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(1): Show | 4 | HG01891.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2521+3821C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36914940 | ||||||
| chr8:36914960
|
G | A | 1 | a0002c0001t0001g0085 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2521+3841G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36914960 | ||||||
| chr8:36915013
|
A | C | 1 | a0002c0001t0001g0053 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2522-3810A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36915013 | ||||||
| chr8:36915043
|
G | A | 2 | a0001c0002t0001g0144a0007c0008t0001g0279 | 2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2522-3780G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36915043 | ||||||
| chr8:36915050
|
G | A | 64 | a0003c0003t0001g0002a0003c0003t0001g0005a0003c0003t0001g0006others(61): Show | 65 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.2522-3773G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36915050 | ||||||
| chr8:36915082
|
T | C | 7 | a0003c0005t0001g0189a0003c0005t0001g0196a0003c0005t0001g0197others(4): Show | 7 | HG00621.hp1 NA18953.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.2522-3741T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36915082 | ||||||
| chr8:36915561
|
T | C | 3 | a0001c0002t0001g0237a0001c0002t0001g0259a0001c0002t0001g0269 | 3 | HG01168.hp2 HG01169.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.2522-3262T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36915561 | ||||||
| chr8:36915748
|
C | A | 1 | a0002c0001t0001g0140 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2522-3075C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36915748 | ||||||
| chr8:36915919
|
T | C | 1 | a0001c0002t0001g0051 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2522-2904T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36915919 | ||||||
| chr8:36915971
|
G | A | 64 | a0003c0003t0001g0002a0003c0003t0001g0005a0003c0003t0001g0006others(61): Show | 65 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.2522-2852G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36915971 | ||||||
| chr8:36916353
|
AGAAG | A | 4 | a0001c0002t0001g0241a0001c0002t0001g0257a0001c0002t0001g0258others(1): Show | 4 | HG00639.hp2 HG01978.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2522-2453_2522-245 others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr8 | 36916353 | |||||
| chr8:36916703
|
G | A | 1 | a0003c0003t0001g0067 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2522-2120G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36916703 | ||||||
| chr8:36916860
|
A | G | 4 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(1): Show | 4 | HG01891.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2522-1963A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36916860 | ||||||
| chr8:36916957
|
G | C | 1 | a0001c0002t0001g0282 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2522-1866G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36916957 | ||||||
| chr8:36916969
|
C | T | 1 | a0001c0002t0001g0018 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2522-1854C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36916969 | ||||||
| chr8:36917017
|
C | T | 1 | a0001c0002t0001g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2522-1806C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36917017 | ||||||
| chr8:36917156
|
A | C | 41 | a0002c0001t0001g0009a0002c0001t0001g0012a0002c0001t0001g0013others(38): Show | 41 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2522-1667A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36917156 | ||||||
| chr8:36917354
|
C | CT | 61 | a0002c0001t0001g0138a0003c0003t0001g0002a0003c0003t0001g0005others(58): Show | 62 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.2522-1456dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr8 | 36917354 | |||||
| chr8:36917354
|
CT | C | 14 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(11): Show | 14 | HG01891.hp1 HG02132.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.2522-1456delT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr8 | 36917354 | |||||
| chr8:36917356
|
T | C | 15 | a0002c0001t0001g0015a0002c0001t0001g0108a0002c0001t0001g0110others(12): Show | 15 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(12): Show |
intron_variant | MODIFIER | c.2522-1467T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36917356 | ||||||
| chr8:36917357
|
T | C | 1 | a0002c0001t0001g0141 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2522-1466T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36917357 | ||||||
| chr8:36917517
|
A | AT | 188 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(185): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.2522-1294dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr8 | 36917517 | |||||
| chr8:36917566
|
G | T | 121 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(118): Show | 124 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.2522-1257G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36917566 | ||||||
| chr8:36917840
|
A | G | 41 | a0002c0001t0001g0009a0002c0001t0001g0012a0002c0001t0001g0013others(38): Show | 41 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2522-983A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36917840 | ||||||
| chr8:36917957
|
G | A | 7 | a0003c0003t0001g0023a0003c0003t0001g0067a0003c0003t0001g0181others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.2522-866G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36917957 | ||||||
| chr8:36918102
|
T | C | 1 | a0003c0003t0001g0067 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2522-721T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36918102 | ||||||
| chr8:36918209
|
C | G | 1 | a0001c0002t0001g0176 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2522-614C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36918209 | ||||||
| chr8:36918591
|
C | G | 64 | a0003c0003t0001g0002a0003c0003t0001g0005a0003c0003t0001g0006others(61): Show | 65 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.2522-232C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36918591 | ||||||
| chr8:36918664
|
A | G | 64 | a0003c0003t0001g0002a0003c0003t0001g0005a0003c0003t0001g0006others(61): Show | 65 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.2522-159A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36918664 | ||||||
| chr8:36918718
|
A | C | 2 | a0001c0002t0001g0264a0001c0002t0001g0274 | 2 | HG01255.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.2522-105A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36918718 | ||||||
| chr8:36918749
|
T | G | 197 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(194): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2522-74T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36918749 | ||||||
| chr8:36918756
|
T | G | 8 | a0001c0002t0001g0144a0001c0006t0001g0170a0001c0006t0001g0171others(5): Show | 8 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2522-67T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36918756 | ||||||
| chr8:36918815
|
C | T | 4 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(1): Show | 4 | HG01891.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.2522-8C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36918815 | ||||||
| chr8:36919296
|
G | T | 4 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(1): Show | 4 | HG01891.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2596+399G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36919296 | ||||||
| chr8:36919332
|
G | A | 4 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(1): Show | 4 | HG01891.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2596+435G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36919332 | ||||||
| chr8:36919379
|
C | G | 1 | a0002c0001t0001g0110 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2596+482C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36919379 | ||||||
| chr8:36919428
|
C | CA | 30 | a0001c0002t0001g0018a0001c0002t0001g0144a0001c0002t0001g0239others(27): Show | 30 | HG00735.hp2 HG01099.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.2596+549dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr8 | 36919428 | |||||
| chr8:36919428
|
C | CAA | 51 | a0001c0002t0001g0003a0001c0002t0001g0047a0001c0002t0001g0048others(48): Show | 52 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.2596+548_2596+549d others(4): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr8 | 36919428 | |||||
| chr8:36919428
|
C | CAAA | 55 | a0001c0002t0001g0014a0001c0002t0001g0051a0001c0002t0001g0054others(52): Show | 57 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.2596+547_2596+549d others(5): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr8 | 36919428 | |||||
| chr8:36919428
|
C | CAAAA | 7 | a0001c0004t0001g0191a0001c0004t0001g0194a0001c0004t0001g0218others(4): Show | 7 | HG02080.hp1 HG02738.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.2596+546_2596+549d others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr8 | 36919428 | |||||
| chr8:36919428
|
CA | C | 68 | a0002c0001t0001g0004a0002c0001t0001g0044a0002c0001t0001g0053others(65): Show | 69 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.2596+549delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr8 | 36919428 | |||||
| chr8:36919605
|
C | T | 121 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(118): Show | 124 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.2596+708C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36919605 | ||||||
| chr8:36919960
|
C | T | 1 | a0002c0001t0001g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2596+1063C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36919960 | ||||||
| chr8:36920091
|
A | G | 1 | a0002c0001t0001g0125 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2596+1194A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36920091 | ||||||
| chr8:36920498
|
T | C | 121 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(118): Show | 124 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.2596+1601T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36920498 | ||||||
| chr8:36920548
|
CTTG | C | 72 | a0001c0002t0001g0144a0001c0006t0001g0170a0001c0006t0001g0171others(69): Show | 73 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.2596+1656_2596+165 others(7): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr8 | 36920548 | |||||
| chr8:36920730
|
G | A | 1 | a0002c0001t0001g0151 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2597-1760G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36920730 | ||||||
| chr8:36920801
|
G | A | 72 | a0001c0002t0001g0144a0001c0006t0001g0170a0001c0006t0001g0171others(69): Show | 73 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.2597-1689G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36920801 | ||||||
| chr8:36920889
|
A | G | 5 | a0003c0003t0001g0006a0003c0003t0001g0026a0003c0003t0001g0032others(2): Show | 5 | HG02280.hp2 HG02965.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2597-1601A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36920889 | ||||||
| chr8:36920914
|
C | A | 1 | a0001c0002t0001g0176 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2597-1576C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36920914 | ||||||
| chr8:36921060
|
C | T | 8 | a0001c0002t0001g0123a0001c0004t0001g0168a0001c0004t0001g0192others(5): Show | 8 | HG00673.hp1 HG02080.hp1 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.2597-1430C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36921060 | ||||||
| chr8:36921142
|
A | G | 1 | a0002c0001t0001g0040 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2597-1348A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36921142 | ||||||
| chr8:36921261
|
C | T | 1 | a0002c0001t0001g0134 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2597-1229C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36921261 | ||||||
| chr8:36921395
|
T | A | 118 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(115): Show | 121 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.2597-1095T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36921395 | ||||||
| chr8:36921485
|
C | G | 1 | a0001c0004t0001g0221 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2597-1005C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36921485 | ||||||
| chr8:36921596
|
T | C | 1 | a0001c0002t0001g0003 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2597-894T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36921596 | ||||||
| chr8:36921647
|
C | T | 1 | a0002c0001t0001g0085 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2597-843C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36921647 | ||||||
| chr8:36921659
|
GA | G | 247 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(244): Show | 251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.2597-810delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr8 | 36921659 | |||||
| chr8:36921659
|
GAA | G | 17 | a0001c0002t0001g0157a0001c0002t0001g0158a0001c0002t0001g0259others(14): Show | 17 | HG00099.hp1 HG00735.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.2597-811_2597-810d others(4): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr8 | 36921659 | |||||
| chr8:36921659
|
GAAAAAAA others(3): Show |
G | 1 | a0003c0003t0001g0005 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2597-819_2597-810d others(12): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr8 | 36921659 | |||||
| chr8:36921808
|
G | A | 1 | a0002c0001t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2597-682G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36921808 | ||||||
| chr8:36922172
|
C | T | 1 | a0001c0002t0001g0177 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2597-318C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36922172 | ||||||
| chr8:36922284
|
A | G | 1 | a0002c0001t0001g0130 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2597-206A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36922284 | ||||||
| chr8:36922330
|
GA | G | 77 | a0001c0002t0001g0144a0001c0002t0001g0264a0001c0002t0001g0286others(74): Show | 78 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.2597-150delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr8 | 36922330 | |||||
| chr8:36922421
|
G | T | 40 | a0001c0002t0001g0109a0001c0002t0001g0123a0001c0004t0001g0001others(37): Show | 42 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.2597-69G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36922421 | ||||||
| chr8:36922432
|
ACTT | A | 6 | a0001c0006t0001g0170a0001c0006t0001g0171a0001c0006t0001g0178others(3): Show | 6 | HG02615.hp1 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2597-54_2597-52del others(3): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr8 | 36922432 | |||||
| chr8:36922691
|
A | G | 197 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(194): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2736+62A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36922691 | ||||||
| chr8:36922768
|
C | T | 1 | a0001c0004t0001g0201 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2736+139C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36922768 | ||||||
| chr8:36923142
|
T | A | 1 | a0001c0002t0001g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2736+513T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36923142 | ||||||
| chr8:36923228
|
A | G | 1 | a0002c0016t0001g0224 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2736+599A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36923228 | ||||||
| chr8:36923408
|
A | G | 1 | a0002c0001t0001g0036 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2736+779A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36923408 | ||||||
| chr8:36923462
|
G | T | 1 | a0001c0002t0001g0248 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2736+833G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36923462 | ||||||
| chr8:36923527
|
G | C | 1 | a0002c0001t0001g0134 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2736+898G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36923527 | ||||||
| chr8:36923844
|
G | A | 2 | a0001c0002t0001g0144a0007c0008t0001g0279 | 2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2736+1215G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36923844 | ||||||
| chr8:36923979
|
T | C | 1 | a0002c0001t0001g0039 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2736+1350T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36923979 | ||||||
| chr8:36923986
|
G | A | 121 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(118): Show | 124 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.2736+1357G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36923986 | ||||||
| chr8:36924017
|
G | T | 1 | a0001c0002t0001g0003 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2736+1388G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36924017 | ||||||
| chr8:36924031
|
A | G | 1 | a0001c0002t0001g0048 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2736+1402A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36924031 | ||||||
| chr8:36924655
|
G | T | 2 | a0001c0002t0001g0144a0007c0008t0001g0279 | 2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2736+2026G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36924655 | ||||||
| chr8:36924896
|
T | C | 6 | a0002c0001t0001g0024a0002c0001t0001g0031a0002c0001t0001g0037others(3): Show | 6 | HG01258.hp2 HG02004.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2736+2267T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36924896 | ||||||
| chr8:36925114
|
T | A | 1 | a0007c0008t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2736+2485T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36925114 | ||||||
| chr8:36925259
|
C | T | 1 | a0001c0002t0001g0176 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2736+2630C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36925259 | ||||||
| chr8:36925354
|
G | A | 6 | a0001c0006t0001g0170a0001c0006t0001g0171a0001c0006t0001g0178others(3): Show | 6 | HG02615.hp1 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2736+2725G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36925354 | ||||||
| chr8:36925675
|
C | T | 4 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(1): Show | 4 | HG01891.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2736+3046C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36925675 | ||||||
| chr8:36926009
|
A | G | 197 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(194): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2736+3380A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36926009 | ||||||
| chr8:36926291
|
C | A | 2 | a0001c0002t0001g0238a0001c0002t0001g0267 | 2 | HG00735.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.2736+3662C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36926291 | ||||||
| chr8:36926297
|
G | C | 1 | a0001c0002t0001g0252 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2736+3668G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36926297 | ||||||
| chr8:36926501
|
A | T | 1 | a0002c0001t0001g0116 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2736+3872A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36926501 | ||||||
| chr8:36926622
|
C | T | 44 | a0001c0002t0001g0109a0001c0002t0001g0123a0001c0002t0001g0172others(41): Show | 46 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.2736+3993C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36926622 | ||||||
| chr8:36926825
|
C | T | 1 | a0002c0001t0001g0029 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2737-4126C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36926825 | ||||||
| chr8:36926840
|
T | C | 2 | a0001c0002t0001g0229a0001c0002t0001g0230 | 2 | HG00438.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.2737-4111T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36926840 | ||||||
| chr8:36926878
|
G | A | 1 | a0002c0016t0001g0224 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2737-4073G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36926878 | ||||||
| chr8:36926890
|
G | A | 1 | a0003c0003t0001g0101 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2737-4061G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36926890 | ||||||
| chr8:36926891
|
G | A | 1 | a0002c0001t0001g0029 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2737-4060G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36926891 | ||||||
| chr8:36927002
|
C | T | 2 | a0001c0002t0001g0144a0007c0008t0001g0279 | 2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2737-3949C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36927002 | ||||||
| chr8:36927338
|
T | C | 3 | a0001c0002t0001g0187a0001c0002t0001g0188a0001c0002t0001g0283 | 3 | HG02055.hp1 HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2737-3613T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36927338 | ||||||
| chr8:36927350
|
T | C | 1 | a0001c0002t0001g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2737-3601T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36927350 | ||||||
| chr8:36927457
|
A | T | 1 | a0002c0001t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2737-3494A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36927457 | ||||||
| chr8:36927545
|
G | T | 1 | a0003c0003t0001g0084 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2737-3406G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36927545 | ||||||
| chr8:36927792
|
A | T | 2 | a0001c0002t0001g0144a0007c0008t0001g0279 | 2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2737-3159A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36927792 | ||||||
| chr8:36927857
|
G | T | 1 | a0001c0004t0001g0218 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2737-3094G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36927857 | ||||||
| chr8:36927942
|
G | C | 1 | a0001c0002t0001g0251 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2737-3009G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36927942 | ||||||
| chr8:36927966
|
C | T | 1 | a0001c0017t0001g0217 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2737-2985C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36927966 | ||||||
| chr8:36927986
|
A | G | 197 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(194): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2737-2965A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36927986 | ||||||
| chr8:36928097
|
C | T | 1 | a0002c0001t0001g0126 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2737-2854C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36928097 | ||||||
| chr8:36928647
|
G | A | 2 | a0001c0002t0001g0276a0001c0002t0001g0277 | 2 | HG01167.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.2737-2304G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36928647 | ||||||
| chr8:36928649
|
C | G | 2 | a0002c0001t0001g0027a0002c0001t0001g0052 | 2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2737-2302C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36928649 | ||||||
| chr8:36928716
|
C | T | 288 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(285): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.2737-2235C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36928716 | ||||||
| chr8:36928760
|
C | G | 288 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(285): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.2737-2191C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36928760 | ||||||
| chr8:36928861
|
C | A | 66 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0047others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.2737-2090C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36928861 | ||||||
| chr8:36928878
|
C | T | 193 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(190): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.2737-2073C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36928878 | ||||||
| chr8:36928884
|
C | G | 1 | a0002c0001t0001g0112 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2737-2067C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36928884 | ||||||
| chr8:36928942
|
T | C | 2 | a0003c0003t0001g0097a0003c0003t0001g0098 | 2 | HG00140.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.2737-2009T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36928942 | ||||||
| chr8:36929260
|
T | C | 4 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(1): Show | 4 | HG01891.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2737-1691T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36929260 | ||||||
| chr8:36929303
|
G | A | 1 | a0003c0003t0001g0260 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2737-1648G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36929303 | ||||||
| chr8:36929387
|
CA | C | 17 | a0001c0002t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(14): Show | 17 | HG01515.hp1 HG01516.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2737-1544delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr8 | 36929387 | |||||
| chr8:36929387
|
CAA | C | 64 | a0001c0002t0001g0051a0001c0004t0001g0227a0001c0004t0001g0228others(61): Show | 65 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.2737-1545_2737-154 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr8 | 36929387 | |||||
| chr8:36929387
|
CAAA | C | 120 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(117): Show | 123 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.2737-1546_2737-154 others(7): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr8 | 36929387 | |||||
| chr8:36929429
|
A | AC | 42 | a0001c0002t0001g0109a0001c0002t0001g0123a0001c0002t0001g0157others(39): Show | 44 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.2737-1522_2737-152 others(5): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36929429 | ||||||
| chr8:36929435
|
A | AG | 73 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(70): Show | 74 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.2737-1516_2737-151 others(5): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36929435 | ||||||
| chr8:36929435
|
A | C | 2 | a0003c0003t0001g0086a0003c0003t0001g0118 | 2 | NA18962.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.2737-1516A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36929435 | ||||||
| chr8:36929435
|
A | G | 42 | a0001c0002t0001g0109a0001c0002t0001g0123a0001c0002t0001g0157others(39): Show | 44 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.2737-1516A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36929435 | ||||||
| chr8:36929635
|
T | C | 2 | a0001c0002t0001g0014a0001c0002t0001g0175 | 2 | HG01074.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2737-1316T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36929635 | ||||||
| chr8:36929772
|
A | G | 197 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(194): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2737-1179A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36929772 | ||||||
| chr8:36930219
|
T | TG | 5 | a0003c0005t0001g0189a0003c0005t0001g0196a0003c0005t0001g0197others(2): Show | 5 | HG00621.hp1 NA18980.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.2737-731dupG | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr8 | 36930219 | |||||
| chr8:36930382
|
T | A | 1 | a0001c0002t0001g0187 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2737-569T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36930382 | ||||||
| chr8:36930473
|
A | T | 1 | a0001c0004t0001g0216 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2737-478A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36930473 | ||||||
| chr8:36930498
|
C | T | 197 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(194): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2737-453C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36930498 | ||||||
| chr8:36930866
|
C | T | 3 | a0003c0003t0001g0017a0003c0005t0001g0222a0003c0005t0001g0223 | 3 | HG02258.hp1 NA19084.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.2737-85C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36930866 | ||||||
| chr8:36930873
|
A | T | 1 | a0003c0003t0001g0147 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2737-78A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36930873 | ||||||
| chr8:36930887
|
T | G | 2 | a0001c0002t0001g0144a0007c0008t0001g0279 | 2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2737-64T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36930887 | ||||||
| chr8:36930889
|
C | A | 2 | a0001c0002t0001g0144a0007c0008t0001g0279 | 2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2737-62C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36930889 | ||||||
| chr8:36930891
|
C | T | 2 | a0001c0002t0001g0144a0007c0008t0001g0279 | 2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2737-60C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36930891 | ||||||
| chr8:36930938
|
C | G | 2 | a0002c0001t0001g0148a0002c0001t0001g0149 | 2 | HG02056.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.2737-13C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36930938 | ||||||
| chr8:36931175
|
T | C | 197 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(194): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2931+30T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 25/26 | chr8 | 36931175 | ||||||
| chr8:36931418
|
A | G | 2 | a0001c0002t0001g0229a0001c0002t0001g0230 | 2 | HG00438.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.2931+273A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 25/26 | chr8 | 36931418 | ||||||
| chr8:36931798
|
T | C | 1 | a0003c0003t0001g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2931+653T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 25/26 | chr8 | 36931798 | ||||||
| chr8:36931805
|
T | C | 1 | a0002c0001t0001g0096 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2931+660T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 25/26 | chr8 | 36931805 | ||||||
| chr8:36932073
|
A | G | 197 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(194): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2932-847A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 25/26 | chr8 | 36932073 | ||||||
| chr8:36932108
|
G | A | 6 | a0001c0006t0001g0170a0001c0006t0001g0171a0001c0006t0001g0178others(3): Show | 6 | HG02615.hp1 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2932-812G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 25/26 | chr8 | 36932108 | ||||||
| chr8:36932215
|
C | T | 64 | a0003c0003t0001g0002a0003c0003t0001g0005a0003c0003t0001g0006others(61): Show | 65 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.2932-705C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 25/26 | chr8 | 36932215 | ||||||
| chr8:36932518
|
G | A | 6 | a0001c0006t0001g0170a0001c0006t0001g0171a0001c0006t0001g0178others(3): Show | 6 | HG02615.hp1 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2932-402G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 25/26 | chr8 | 36932518 | ||||||
| chr8:36932665
|
CA | C | 10 | a0002c0001t0001g0030a0002c0001t0001g0036a0002c0001t0001g0039others(7): Show | 10 | HG00621.hp2 HG00735.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.2932-254delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 25/26 | chr8 | 36932665 | ||||||
| chr8:36932821
|
G | A | 64 | a0003c0003t0001g0002a0003c0003t0001g0005a0003c0003t0001g0006others(61): Show | 65 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.2932-99G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 25/26 | chr8 | 36932821 | ||||||
| chr8:36932914
|
C | T | 1 | a0003c0003t0001g0231 | 1 | NA18972.hp2 | splice_region_variant&intron_variant | LOW | c.2932-6C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 25/26 | chr8 | 36932914 | ||||||
| chr8:36933202
|
G | A | 1 | a0003c0003t0001g0231 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.3044+170G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 26/26 | chr8 | 36933202 | ||||||
| chr8:36933252
|
G | A | 6 | a0001c0006t0001g0170a0001c0006t0001g0171a0001c0006t0001g0178others(3): Show | 6 | HG02615.hp1 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.3044+220G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 26/26 | chr8 | 36933252 | ||||||
| chr8:36933617
|
A | G | 3 | a0002c0007t0001g0046a0002c0007t0001g0069a0002c0007t0001g0153 | 3 | HG02615.hp2 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3044+585A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 26/26 | chr8 | 36933617 | ||||||
| chr8:36933699
|
G | A | 1 | a0001c0002t0001g0176 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3044+667G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 26/26 | chr8 | 36933699 | ||||||
| chr8:36934446
|
T | C | 1 | a0001c0002t0001g0281 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3045-1069T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 26/26 | chr8 | 36934446 | ||||||
| chr8:36934525
|
G | A | 197 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(194): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.3045-990G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 26/26 | chr8 | 36934525 | ||||||
| chr8:36934614
|
T | C | 16 | a0002c0001t0001g0015a0002c0001t0001g0108a0002c0001t0001g0110others(13): Show | 16 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(13): Show |
intron_variant | MODIFIER | c.3045-901T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 26/26 | chr8 | 36934614 | ||||||
| chr8:36934745
|
A | G | 1 | a0002c0001t0001g0066 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3045-770A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 26/26 | chr8 | 36934745 | ||||||
| chr8:36934903
|
G | A | 197 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0018others(194): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.3045-612G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 26/26 | chr8 | 36934903 | ||||||
| chr8:36935098
|
G | A | 2 | a0002c0001t0001g0010a0002c0001t0001g0103 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3045-417G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 26/26 | chr8 | 36935098 | ||||||
| chr8:36935173
|
A | G | 6 | a0001c0002t0001g0144a0001c0002t0001g0286a0001c0002t0001g0288others(3): Show | 6 | HG01891.hp1 HG02717.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3045-342A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 26/26 | chr8 | 36935173 |