| geneid | 57582 |
|---|---|
| ensemblid | ENSG00000107147.14 |
| hgncid | 18865 |
| symbol | KCNT1 |
| name | potassium sodium-activated channel subfamily T member 1 |
| refseq_nuc | NM_020822.3 |
| refseq_prot | NP_065873.2 |
| ensembl_nuc | ENST00000371757.7 |
| ensembl_prot | ENSP00000360822.2 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 135702185 |
| end | 135795502 |
| strand | + |
| ver | v1.2 |
| region | chr9:135702185-135795502 |
| region5000 | chr9:135697185-135800502 |
| regionname0 | KCNT1_chr9_135702185_135795502 |
| regionname5000 | KCNT1_chr9_135697185_135800502 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1235 | 264 | 83 | 55 | 83 | 12 | 29 | 49 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0002 | 0/0 | 1235 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0003 | 0/0 | 1235 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0004 | 0/0 | 1235 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0005 | 0/0 | 1235 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0006 | 0/0 | 1235 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0007 | 0/0 | 1235 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0008 | 0/0 | 1235 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 3708 | 101 | 18 | 34 | 26 | 6 | 16 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| c0002 | 0/0 | 3708 | 58 | 21 | 6 | 21 | 1 | 9 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| c0003 | 1/0 | 3708 | 50 | 17 | 7 | 18 | 4 | 3 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| c0004 | 0/0 | 3708 | 29 | 12 | 6 | 11 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| c0005 | 0/0 | 3708 | 5 | 0 | 0 | 5 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| c0006 | 0/0 | 3708 | 4 | 3 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| c0007 | 0/0 | 3708 | 2 | 0 | 0 | 2 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| c0008 | 0/0 | 3708 | 2 | 0 | 2 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| c0009 | 0/0 | 3708 | 2 | 2 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| c0010 | 0/0 | 3708 | 2 | 2 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| c0011 | 0/0 | 3708 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| c0012 | 0/0 | 3708 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| c0013 | 0/0 | 3708 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| c0014 | 0/0 | 3708 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| c0015 | 0/0 | 3708 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| c0016 | 0/0 | 3708 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| c0017 | 0/0 | 3708 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| c0018 | 0/0 | 3708 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| c0019 | 0/0 | 3708 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| c0020 | 0/0 | 3708 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| c0021 | 0/0 | 3708 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| c0022 | 0/0 | 3708 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| c0023 | 0/0 | 3708 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| c0024 | 0/0 | 3708 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| c0025 | 0/0 | 3708 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| c0026 | 0/0 | 3708 | 1 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| c0027 | 0/0 | 3708 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| 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 | 3416 | 147 | 25 | 40 | 54 | 7 | 19 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0002 | 0/0 | 3417 | 35 | 9 | 6 | 18 | 2 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0003 | 0/0 | 3419 | 13 | 0 | 2 | 0 | 2 | 9 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0004 | 0/0 | 3416 | 9 | 7 | 1 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0005 | 0/0 | 3419 | 7 | 4 | 3 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0006 | 0/0 | 3417 | 5 | 5 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0007 | 0/0 | 3417 | 5 | 5 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0008 | 0/0 | 3420 | 4 | 4 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0009 | 0/0 | 3421 | 4 | 4 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0010 | 0/0 | 3417 | 3 | 3 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0011 | 0/0 | 3416 | 2 | 0 | 0 | 2 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0012 | 0/0 | 3416 | 2 | 0 | 0 | 2 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0013 | 0/0 | 3416 | 2 | 2 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0014 | 0/0 | 3433 | 2 | 2 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0015 | 0/0 | 3416 | 2 | 0 | 2 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0016 | 0/0 | 3419 | 2 | 0 | 0 | 1 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0017 | 0/0 | 3421 | 2 | 2 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0018 | 0/0 | 3416 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0019 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0020 | 0/0 | 3416 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0021 | 0/0 | 3416 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0022 | 0/0 | 3417 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0023 | 0/0 | 3417 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0024 | 0/0 | 3416 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0025 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0026 | 0/0 | 3416 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0027 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0028 | 0/0 | 3416 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0029 | 0/0 | 3417 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0030 | 0/0 | 3417 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0031 | 0/0 | 3416 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0032 | 0/0 | 3416 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0033 | 0/0 | 3416 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0034 | 0/0 | 3416 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0035 | 0/0 | 3416 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0036 | 0/0 | 3417 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0037 | 0/0 | 3416 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0038 | 0/0 | 3419 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0039 | 0/0 | 3416 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0040 | 0/0 | 3419 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0041 | 0/0 | 3416 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0042 | 0/0 | 3416 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| t0043 | 0/0 | 3416 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0024 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0122 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3708 | 101 | 18 | 34 | 26 | 6 | 16 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0002 | 0/0 | 3708 | 58 | 21 | 6 | 21 | 1 | 9 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0003 | 1/0 | 3708 | 50 | 17 | 7 | 18 | 4 | 3 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0004 | 0/0 | 3708 | 29 | 12 | 6 | 11 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0005 | 0/0 | 3708 | 5 | 0 | 0 | 5 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0006 | 0/0 | 3708 | 4 | 3 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0007 | 0/0 | 3708 | 2 | 0 | 0 | 2 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0009 | 0/0 | 3708 | 2 | 2 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0010 | 0/0 | 3708 | 2 | 2 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0013 | 0/0 | 3708 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0014 | 0/0 | 3708 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0015 | 0/0 | 3708 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0016 | 0/0 | 3708 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0019 | 0/0 | 3708 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0020 | 0/0 | 3708 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0022 | 0/0 | 3708 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0024 | 0/0 | 3708 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0025 | 0/0 | 3708 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0026 | 0/0 | 3708 | 1 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0027 | 0/0 | 3708 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0002c0008 | 0/0 | 3708 | 2 | 0 | 2 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0003c0011 | 0/0 | 3708 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0004c0017 | 0/0 | 3708 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0005c0021 | 0/0 | 3708 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0006c0018 | 0/0 | 3708 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0007c0023 | 0/0 | 3708 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0008c0012 | 0/0 | 3708 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 7123 | 55 | 7 | 27 | 9 | 4 | 7 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0001t0002 | 0/0 | 7124 | 17 | 2 | 2 | 12 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0001t0003 | 0/0 | 7126 | 7 | 0 | 0 | 0 | 1 | 6 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0001t0005 | 0/0 | 7126 | 3 | 1 | 2 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0001t0007 | 0/0 | 7124 | 4 | 4 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0001t0008 | 0/0 | 7127 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0001t0011 | 0/0 | 7123 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0001t0013 | 0/0 | 7123 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0001t0015 | 0/0 | 7123 | 2 | 0 | 2 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0001t0016 | 0/0 | 7126 | 2 | 0 | 0 | 1 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0001t0022 | 0/0 | 7124 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0001t0026 | 0/0 | 7123 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0001t0027 | 0/0 | 7127 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0001t0028 | 0/0 | 7123 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0001t0038 | 0/0 | 7126 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0001t0039 | 0/0 | 7123 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0001t0042 | 0/0 | 7123 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0001t0043 | 0/0 | 7123 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0002t0001 | 0/0 | 7123 | 31 | 7 | 2 | 15 | 0 | 7 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0002t0002 | 0/0 | 7124 | 8 | 5 | 1 | 2 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0002t0003 | 0/0 | 7126 | 2 | 0 | 1 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0002t0004 | 0/0 | 7123 | 2 | 1 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0002t0005 | 0/0 | 7126 | 4 | 3 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0002t0006 | 0/0 | 7124 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0002t0008 | 0/0 | 7127 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0002t0009 | 0/0 | 7128 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0002t0011 | 0/0 | 7123 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0002t0025 | 0/0 | 7139 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0002t0029 | 0/0 | 7124 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0002t0032 | 0/0 | 7123 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0002t0033 | 0/0 | 7123 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0002t0034 | 0/0 | 7123 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0002t0035 | 0/0 | 7123 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0002t0040 | 0/0 | 7126 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0003t0001 | 1/0 | 7123 | 32 | 7 | 5 | 14 | 2 | 3 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0003t0002 | 0/0 | 7124 | 7 | 2 | 1 | 3 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0003t0003 | 0/0 | 7126 | 2 | 0 | 1 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0003t0006 | 0/0 | 7124 | 2 | 2 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0003t0008 | 0/0 | 7127 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0003t0009 | 0/0 | 7128 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0003t0010 | 0/0 | 7124 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0003t0013 | 0/0 | 7123 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0003t0021 | 0/0 | 7123 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0003t0031 | 0/0 | 7123 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0003t0041 | 0/0 | 7123 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0004t0001 | 0/0 | 7123 | 11 | 1 | 2 | 8 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0004t0002 | 0/0 | 7124 | 3 | 0 | 2 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0004t0004 | 0/0 | 7123 | 6 | 5 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0004t0006 | 0/0 | 7124 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0004t0007 | 0/0 | 7124 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0004t0008 | 0/0 | 7127 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0004t0012 | 0/0 | 7123 | 2 | 0 | 0 | 2 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0004t0014 | 0/0 | 7140 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0004t0020 | 0/0 | 7123 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0004t0030 | 0/0 | 7124 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0004t0037 | 0/0 | 7123 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0005t0001 | 0/0 | 7123 | 5 | 0 | 0 | 5 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0006t0009 | 0/0 | 7128 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0006t0010 | 0/0 | 7124 | 2 | 2 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0006t0036 | 0/0 | 7124 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0007t0001 | 0/0 | 7123 | 2 | 0 | 0 | 2 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0009t0006 | 0/0 | 7124 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0009t0018 | 0/0 | 7123 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0010t0001 | 0/0 | 7123 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0010t0014 | 0/0 | 7140 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0013t0024 | 0/0 | 7123 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0014t0017 | 0/0 | 7128 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0015t0001 | 0/0 | 7123 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0016t0019 | 0/0 | 7127 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0019t0003 | 0/0 | 7126 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0020t0017 | 0/0 | 7128 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0022t0001 | 0/0 | 7123 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0024t0023 | 0/0 | 7124 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0025t0001 | 0/0 | 7123 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0026t0001 | 0/0 | 7123 | 1 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0001c0027t0009 | 0/0 | 7128 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0002c0008t0001 | 0/0 | 7123 | 2 | 0 | 2 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0003c0011t0001 | 0/0 | 7123 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0004c0017t0004 | 0/0 | 7123 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0005c0021t0001 | 0/0 | 7123 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0006c0018t0001 | 0/0 | 7123 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0007c0023t0001 | 0/0 | 7123 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| a0008c0012t0003 | 0/0 | 7126 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | copy fasta | chr9 | 135697185 | 135800502 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0122 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0005g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0005g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0007g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0007g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0008g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0011g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0013g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0015g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0015g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0016g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0016g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0022g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0026g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0027g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0028g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0038g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0039g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0042g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0001t0043g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0004g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0005g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0008g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0011g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0025g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0029g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0032g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0033g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0034g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0035g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0002t0040g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0024 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0009g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0010g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0013g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0021g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0031g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0003t0041g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0007g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0008g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0012g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0012g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0014g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0020g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0030g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0004t0037g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0005t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0005t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0005t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0005t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0005t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0006t0009g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0006t0010g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0006t0010g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0006t0036g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0007t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0007t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0009t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0009t0018g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0010t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0010t0014g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0013t0024g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0014t0017g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0015t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0016t0019g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0019t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0020t0017g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0022t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0024t0023g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0025t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0026t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0001c0027t0009g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0002c0008t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0002c0008t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0003c0011t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0004c0017t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0005c0021t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0006c0018t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0007c0023t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| a0008c0012t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0003 | g0059 | EUR | GBR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG00099 | hp2 | a0001 | c0026 | t0001 | g0051 | EUR | GBR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG00140 | hp1 | a0001 | c0002 | t0004 | g0137 | EUR | GBR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG00140 | hp2 | a0001 | c0003 | t0001 | g0069 | EUR | GBR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0248 | EUR | FIN | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | FIN | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | FIN | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | FIN | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | CHS | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG00423 | hp2 | a0001 | c0007 | t0001 | g0155 | EAS | CHS | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | CHS | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG00438 | hp2 | a0001 | c0003 | t0001 | g0082 | EAS | CHS | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | CHS | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG00609 | hp1 | a0001 | c0001 | t0022 | g0193 | EAS | CHS | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG00609 | hp2 | a0001 | c0004 | t0012 | g0225 | EAS | CHS | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG00642 | hp2 | a0001 | c0001 | t0015 | g0104 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG00741 | hp2 | a0001 | c0004 | t0004 | g0025 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01070 | hp2 | a0001 | c0003 | t0002 | g0101 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01074 | hp1 | a0001 | c0004 | t0001 | g0005 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01074 | hp2 | a0002 | c0008 | t0001 | g0170 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0175 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01099 | hp1 | a0001 | c0004 | t0037 | g0004 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0173 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01109 | hp1 | a0001 | c0006 | t0036 | g0009 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01109 | hp2 | a0001 | c0002 | t0032 | g0200 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01167 | hp1 | a0002 | c0008 | t0001 | g0171 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01167 | hp2 | a0001 | c0002 | t0005 | g0220 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01168 | hp2 | a0001 | c0004 | t0001 | g0092 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0064 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01175 | hp2 | a0001 | c0003 | t0001 | g0084 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01192 | hp1 | a0001 | c0001 | t0015 | g0103 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01192 | hp2 | a0001 | c0004 | t0002 | g0147 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0131 | AMR | CLM | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01346 | hp2 | a0001 | c0003 | t0003 | g0058 | AMR | CLM | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01358 | hp2 | a0001 | c0002 | t0003 | g0120 | AMR | CLM | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01361 | hp2 | a0001 | c0003 | t0001 | g0066 | AMR | CLM | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01433 | hp1 | a0001 | c0022 | t0001 | g0070 | AMR | CLM | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01433 | hp2 | a0006 | c0018 | t0001 | g0061 | AMR | CLM | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01496 | hp2 | a0001 | c0004 | t0002 | g0045 | AMR | CLM | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0073 | EUR | IBS | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0065 | EUR | IBS | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01884 | hp1 | a0001 | c0002 | t0006 | g0054 | AFR | ACB | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0172 | AFR | ACB | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01891 | hp1 | a0001 | c0002 | t0040 | g0160 | AFR | ACB | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01891 | hp2 | a0001 | c0002 | t0005 | g0081 | AFR | ACB | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01943 | hp1 | a0001 | c0003 | t0001 | g0144 | AMR | PEL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0037 | AMR | PEL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01978 | hp2 | a0001 | c0001 | t0043 | g0197 | AMR | PEL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0231 | AMR | PEL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0264 | AMR | PEL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | KHV | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02015 | hp2 | a0001 | c0004 | t0001 | g0209 | EAS | KHV | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02027 | hp1 | a0001 | c0003 | t0002 | g0199 | EAS | KHV | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02040 | hp1 | a0001 | c0003 | t0001 | g0091 | EAS | KHV | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | KHV | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02055 | hp1 | a0001 | c0006 | t0010 | g0010 | AFR | ACB | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02055 | hp2 | a0001 | c0010 | t0001 | g0158 | AFR | ACB | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02056 | hp1 | a0001 | c0004 | t0001 | g0135 | EAS | KHV | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | KHV | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02071 | hp1 | a0001 | c0003 | t0002 | g0192 | EAS | KHV | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02071 | hp2 | a0001 | c0003 | t0002 | g0236 | EAS | KHV | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | KHV | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0228 | EAS | KHV | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02080 | hp1 | a0001 | c0002 | t0034 | g0179 | EAS | KHV | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | KHV | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | KHV | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02129 | hp2 | a0001 | c0005 | t0001 | g0261 | EAS | KHV | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02135 | hp2 | a0001 | c0005 | t0001 | g0217 | EAS | KHV | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0086 | AFR | ACB | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0107 | AFR | ACB | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | CDX | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0262 | EAS | CDX | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CDX | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02165 | hp2 | a0001 | c0003 | t0001 | g0163 | EAS | CDX | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0028 | AFR | ACB | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0145 | AFR | ACB | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02258 | hp2 | a0001 | c0003 | t0002 | g0153 | AFR | ACB | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0260 | AFR | ACB | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02280 | hp2 | a0001 | c0004 | t0008 | g0203 | AFR | ACB | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02451 | hp1 | a0001 | c0020 | t0017 | g0001 | AFR | ACB | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02451 | hp2 | a0001 | c0013 | t0024 | g0046 | AFR | ACB | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02572 | hp1 | a0001 | c0006 | t0010 | g0011 | AFR | GWD | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02572 | hp2 | a0001 | c0004 | t0006 | g0110 | AFR | GWD | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02602 | hp1 | a0001 | c0001 | t0016 | g0102 | SAS | PJL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0245 | SAS | PJL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02615 | hp1 | a0001 | c0003 | t0009 | g0177 | AFR | GWD | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | GWD | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0114 | AFR | GWD | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0022 | AFR | GWD | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0174 | AFR | GWD | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0021 | AFR | GWD | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0267 | AFR | GWD | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02647 | hp2 | a0001 | c0006 | t0009 | g0012 | AFR | GWD | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02698 | hp1 | a0005 | c0021 | t0001 | g0246 | SAS | PJL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02717 | hp2 | a0001 | c0004 | t0004 | g0258 | AFR | GWD | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02723 | hp1 | a0001 | c0004 | t0030 | g0146 | AFR | GWD | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0030 | AFR | GWD | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0243 | SAS | PJL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02809 | hp1 | a0001 | c0003 | t0002 | g0027 | AFR | GWD | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02809 | hp2 | a0001 | c0001 | t0013 | g0176 | AFR | GWD | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02886 | hp1 | a0001 | c0003 | t0021 | g0259 | AFR | GWD | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02886 | hp2 | a0001 | c0015 | t0001 | g0271 | AFR | GWD | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02897 | hp2 | a0001 | c0009 | t0018 | g0162 | AFR | GWD | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02922 | hp1 | a0001 | c0002 | t0005 | g0079 | AFR | ESN | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0008 | AFR | ESN | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0272 | AFR | ESN | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0071 | AFR | ESN | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02976 | hp1 | a0001 | c0003 | t0031 | g0269 | AFR | ESN | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02976 | hp2 | a0001 | c0004 | t0001 | g0007 | AFR | ESN | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0096 | SAS | PJL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0227 | SAS | PJL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0151 | AFR | GWD | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03041 | hp2 | a0001 | c0014 | t0017 | g0212 | AFR | GWD | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03098 | hp1 | a0001 | c0004 | t0004 | g0255 | AFR | MSL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03098 | hp2 | a0001 | c0004 | t0014 | g0002 | AFR | MSL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03130 | hp1 | a0001 | c0003 | t0010 | g0148 | AFR | ESN | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0029 | AFR | ESN | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0094 | AFR | ESN | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0115 | AFR | ESN | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03195 | hp1 | a0001 | c0009 | t0006 | g0159 | AFR | ESN | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0080 | AFR | ESN | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03209 | hp1 | a0001 | c0003 | t0013 | g0068 | AFR | MSL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0150 | AFR | MSL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03225 | hp1 | a0001 | c0004 | t0004 | g0256 | AFR | MSL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03225 | hp2 | a0001 | c0004 | t0020 | g0215 | AFR | MSL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0164 | AFR | MSL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03453 | hp2 | a0001 | c0002 | t0004 | g0257 | AFR | MSL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03486 | hp1 | a0001 | c0001 | t0039 | g0156 | AFR | MSL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03486 | hp2 | a0001 | c0010 | t0014 | g0161 | AFR | MSL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03492 | hp1 | a0007 | c0023 | t0001 | g0017 | SAS | PJL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03492 | hp2 | a0001 | c0001 | t0038 | g0100 | SAS | PJL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03516 | hp1 | a0001 | c0002 | t0025 | g0149 | AFR | ESN | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03516 | hp2 | a0001 | c0002 | t0008 | g0026 | AFR | ESN | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0154 | AFR | GWD | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03540 | hp2 | a0004 | c0017 | t0004 | g0223 | AFR | GWD | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | MSL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03579 | hp2 | a0001 | c0002 | t0005 | g0270 | AFR | MSL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0121 | SAS | PJL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03669 | hp1 | a0001 | c0019 | t0003 | g0089 | SAS | PJL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03669 | hp2 | a0001 | c0003 | t0001 | g0108 | SAS | PJL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0218 | SAS | STU | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03688 | hp2 | a0001 | c0003 | t0001 | g0018 | SAS | STU | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03704 | hp1 | a0001 | c0002 | t0033 | g0139 | SAS | PJL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0229 | SAS | PJL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0168 | SAS | BEB | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0087 | SAS | BEB | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0090 | SAS | BEB | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0222 | SAS | STU | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | STU | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG04199 | hp1 | a0001 | c0001 | t0028 | g0077 | SAS | STU | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG04199 | hp2 | a0008 | c0012 | t0003 | g0241 | SAS | STU | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0244 | SAS | STU | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0016 | SAS | STU | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0184 | SAS | STU | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | STU | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18522 | hp1 | a0001 | c0003 | t0006 | g0023 | AFR | YRI | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18522 | hp2 | a0001 | c0003 | t0008 | g0043 | AFR | YRI | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18612 | hp1 | a0001 | c0004 | t0012 | g0226 | EAS | CHB | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18612 | hp2 | a0001 | c0001 | t0016 | g0254 | EAS | CHB | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | CHB | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18747 | hp2 | a0001 | c0004 | t0001 | g0263 | EAS | CHB | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | YRI | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0219 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18947 | hp1 | a0001 | c0007 | t0001 | g0232 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18948 | hp2 | a0001 | c0003 | t0001 | g0126 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18959 | hp1 | a0001 | c0003 | t0001 | g0178 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18962 | hp2 | a0001 | c0003 | t0001 | g0253 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18964 | hp2 | a0001 | c0003 | t0001 | g0127 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18966 | hp2 | a0001 | c0001 | t0026 | g0123 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18969 | hp2 | a0001 | c0004 | t0002 | g0125 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18970 | hp1 | a0001 | c0003 | t0001 | g0180 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18971 | hp1 | a0001 | c0004 | t0001 | g0134 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18971 | hp2 | a0001 | c0002 | t0029 | g0182 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18983 | hp1 | a0001 | c0004 | t0001 | g0133 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18983 | hp2 | a0001 | c0003 | t0041 | g0093 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18990 | hp1 | a0001 | c0003 | t0001 | g0210 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19000 | hp2 | a0001 | c0004 | t0001 | g0187 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19005 | hp1 | a0001 | c0003 | t0001 | g0034 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19005 | hp2 | a0003 | c0011 | t0001 | g0044 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19007 | hp1 | a0001 | c0005 | t0001 | g0208 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19007 | hp2 | a0001 | c0002 | t0011 | g0083 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19009 | hp2 | a0001 | c0003 | t0001 | g0040 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19011 | hp1 | a0001 | c0003 | t0001 | g0035 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19012 | hp1 | a0001 | c0005 | t0001 | g0207 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19012 | hp2 | a0001 | c0003 | t0001 | g0252 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19043 | hp1 | a0001 | c0004 | t0007 | g0006 | AFR | LWK | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19043 | hp2 | a0001 | c0024 | t0023 | g0048 | AFR | LWK | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19065 | hp1 | a0001 | c0003 | t0001 | g0036 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19065 | hp2 | a0001 | c0004 | t0001 | g0195 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19068 | hp2 | a0001 | c0002 | t0035 | g0109 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19074 | hp1 | a0001 | c0005 | t0001 | g0240 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19074 | hp2 | a0001 | c0001 | t0042 | g0265 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19082 | hp2 | a0001 | c0001 | t0011 | g0032 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19088 | hp2 | a0001 | c0004 | t0001 | g0130 | EAS | JPT | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19240 | hp1 | a0001 | c0025 | t0001 | g0113 | AFR | YRI | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA19240 | hp2 | a0001 | c0003 | t0006 | g0117 | AFR | YRI | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0181 | EUR | TSI | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA20752 | hp2 | a0001 | c0003 | t0002 | g0247 | EUR | TSI | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | GIH | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA20905 | hp2 | a0001 | c0002 | t0003 | g0105 | SAS | GIH | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02486 | hp1 | a0001 | c0002 | t0009 | g0047 | AFR | ACB | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03471 | hp1 | a0001 | c0027 | t0009 | g0268 | AFR | MSL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG03471 | hp2 | a0001 | c0004 | t0004 | g0003 | AFR | MSL | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG06807 | hp1 | a0001 | c0016 | t0019 | g0116 | AFR | USA | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| HG06807 | hp2 | a0001 | c0004 | t0004 | g0224 | AFR | USA | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | USA | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| NA20300 | hp2 | a0001 | c0001 | t0027 | g0157 | AFR | USA | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0122 | REF | REF | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0024 | REF | REF | KCNT1_chr9_135697185_135800502 | KCNT1 | chr9 | 135697185 | 135800502 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:135702317
|
G | C | 1 | a0003 | 1 | NA19005.hp2 | missense_variant | MODERATE | c.59G>C | p.Gly20Ala | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/31 | 133/7123 | 59/3708 | 20/1235 | chr9 | 135702317 | ||
| chr9:135768871
|
G | A | 1 | a0008 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.1444G>A | p.Ala482Thr | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/31 | 1518/7123 | 1444/3708 | 482/1235 | chr9 | 135768871 | ||
| chr9:135771027
|
C | T | 1 | a0007 | 1 | HG03492.hp1 | missense_variant | MODERATE | c.1940C>T | p.Ala647Val | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 18/31 | 2014/7123 | 1940/3708 | 647/1235 | chr9 | 135771027 | ||
| chr9:135772757
|
C | T | 1 | a0004 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.2051C>T | p.Thr684Met | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/31 | 2125/7123 | 2051/3708 | 684/1235 | chr9 | 135772757 | ||
| chr9:135772916
|
C | T | 1 | a0002 | 2 | HG01074.hp2 HG01167.hp1 |
missense_variant | MODERATE | c.2210C>T | p.Thr737Met | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/31 | 2284/7123 | 2210/3708 | 737/1235 | chr9 | 135772916 | ||
| chr9:135786407
|
G | A | 1 | a0006 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.3388G>A | p.Ala1130Thr | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/31 | 3462/7123 | 3388/3708 | 1130/1235 | chr9 | 135786407 | ||
| chr9:135786456
|
G | A | 1 | a0005 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.3437G>A | p.Arg1146His | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/31 | 3511/7123 | 3437/3708 | 1146/1235 | chr9 | 135786456 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:135702288
|
G | A | 1 | a0003c0011 | 1 | NA19005.hp2 | synonymous_variant | LOW | c.30G>A | p.Pro10Pro | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/31 | 104/7123 | 30/3708 | 10/1235 | chr9 | 135702288 | ||
| chr9:135702357
|
A | G | 1 | a0001c0027 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.99A>G | p.Gln33Gln | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/31 | 173/7123 | 99/3708 | 33/1235 | chr9 | 135702357 | ||
| chr9:135757333
|
C | G | 1 | a0001c0026 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.711C>G | p.Pro237Pro | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 9/31 | 785/7123 | 711/3708 | 237/1235 | chr9 | 135757333 | ||
| chr9:135759802
|
A | G | 4 | a0001c0009a0001c0010a0001c0024others(1): Show | 6 | HG02055.hp2 HG02897.hp2 HG03195.hp1 others(3): Show |
synonymous_variant | LOW | c.978A>G | p.Pro326Pro | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/31 | 1052/7123 | 978/3708 | 326/1235 | chr9 | 135759802 | ||
| chr9:135765051
|
C | G | 1 | a0001c0006 | 4 | HG01109.hp1 HG02055.hp1 HG02572.hp1 others(1): Show |
synonymous_variant | LOW | c.1056C>G | p.Leu352Leu | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 12/31 | 1130/7123 | 1056/3708 | 352/1235 | chr9 | 135765051 | ||
| chr9:135770427
|
G | A | 11 | a0001c0002a0001c0004a0001c0007others(8): Show | 98 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(95): Show |
synonymous_variant | LOW | c.1749G>A | p.Ala583Ala | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 17/31 | 1823/7123 | 1749/3708 | 583/1235 | chr9 | 135770427 | ||
| chr9:135772920
|
G | A | 1 | a0001c0013 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.2214G>A | p.Pro738Pro | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/31 | 2288/7123 | 2214/3708 | 738/1235 | chr9 | 135772920 | ||
| chr9:135777364
|
C | T | 1 | a0001c0022 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.2376C>T | p.Asp792Asp | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 21/31 | 2450/7123 | 2376/3708 | 792/1235 | chr9 | 135777364 | ||
| chr9:135777415
|
G | A | 15 | a0001c0001a0001c0002a0001c0007others(12): Show | 176 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(173): Show |
synonymous_variant | LOW | c.2427G>A | p.Thr809Thr | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 21/31 | 2501/7123 | 2427/3708 | 809/1235 | chr9 | 135777415 | ||
| chr9:135778712
|
C | T | 1 | a0001c0007 | 2 | HG00423.hp2 NA18947.hp1 |
synonymous_variant | LOW | c.2619C>T | p.Gly873Gly | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/31 | 2693/7123 | 2619/3708 | 873/1235 | chr9 | 135778712 | ||
| chr9:135784074
|
C | T | 2 | a0001c0014a0001c0020 | 2 | HG02451.hp1 HG03041.hp2 |
synonymous_variant | LOW | c.2892C>T | p.Phe964Phe | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 25/31 | 2966/7123 | 2892/3708 | 964/1235 | chr9 | 135784074 | ||
| chr9:135786331
|
G | A | 1 | a0001c0015 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.3312G>A | p.Leu1104Leu | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/31 | 3386/7123 | 3312/3708 | 1104/1235 | chr9 | 135786331 | ||
| chr9:135786409
|
G | A | 1 | a0001c0005 | 5 | HG02129.hp2 HG02135.hp2 NA19007.hp1 others(2): Show |
synonymous_variant | LOW | c.3390G>A | p.Ala1130Ala | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/31 | 3464/7123 | 3390/3708 | 1130/1235 | chr9 | 135786409 | ||
| chr9:135791852
|
C | T | 1 | a0001c0019 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.3558C>T | p.Pro1186Pro | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 30/31 | 3632/7123 | 3558/3708 | 1186/1235 | chr9 | 135791852 | ||
| chr9:135792059
|
C | T | 1 | a0001c0016 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.3606C>T | p.Asp1202Asp | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 3680/7123 | 3606/3708 | 1202/1235 | chr9 | 135792059 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:135702232
|
C | G | 1 | a0001c0001t0043 | 1 | HG01978.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-27C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/31 | chr9 | 135702232 | ||||||
| chr9:135702243
|
C | T | 1 | a0001c0001t0042 | 1 | NA19074.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-16C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/31 | chr9 | 135702243 | ||||||
| chr9:135792220
|
G | T | 2 | a0001c0001t0007a0001c0004t0007 | 5 | HG02257.hp1 HG02723.hp2 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*59G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 59 | chr9 | 135792220 | |||||
| chr9:135792224
|
G | A | 5 | a0001c0002t0006a0001c0003t0006a0001c0004t0006others(2): Show | 6 | HG01884.hp1 HG02572.hp2 HG02897.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*63G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 63 | chr9 | 135792224 | |||||
| chr9:135792269
|
T | A | 2 | a0001c0001t0011a0001c0002t0011 | 2 | NA19007.hp2 NA19082.hp2 |
3_prime_UTR_variant | MODIFIER | c.*108T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 108 | chr9 | 135792269 | |||||
| chr9:135792315
|
C | A | 1 | a0001c0016t0019 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*154C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 154 | chr9 | 135792315 | |||||
| chr9:135792391
|
T | C | 1 | a0001c0004t0012 | 2 | HG00609.hp2 NA18612.hp1 |
3_prime_UTR_variant | MODIFIER | c.*230T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 230 | chr9 | 135792391 | |||||
| chr9:135792472
|
C | T | 1 | a0001c0003t0041 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*311C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 311 | chr9 | 135792472 | |||||
| chr9:135792473
|
G | A | 1 | a0001c0004t0020 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*312G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 312 | chr9 | 135792473 | |||||
| chr9:135792561
|
G | A | 1 | a0001c0003t0021 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*400G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 400 | chr9 | 135792561 | |||||
| chr9:135792593
|
C | T | 6 | a0001c0002t0009a0001c0003t0009a0001c0006t0009others(3): Show | 6 | HG02451.hp1 HG02486.hp1 HG02615.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*432C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 432 | chr9 | 135792593 | |||||
| chr9:135792608
|
A | G | 21 | a0001c0001t0003a0001c0001t0005a0001c0001t0016others(18): Show | 41 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*447A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 447 | chr9 | 135792608 | |||||
| chr9:135792614
|
G | A | 2 | a0001c0001t0011a0001c0002t0011 | 2 | NA19007.hp2 NA19082.hp2 |
3_prime_UTR_variant | MODIFIER | c.*453G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 453 | chr9 | 135792614 | |||||
| chr9:135792677
|
G | A | 1 | a0001c0001t0038 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*516G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 516 | chr9 | 135792677 | |||||
| chr9:135792685
|
G | C | 1 | a0001c0001t0022 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*524G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 524 | chr9 | 135792685 | |||||
| chr9:135792713
|
G | GAAGT | 6 | a0001c0002t0009a0001c0003t0009a0001c0006t0009others(3): Show | 6 | HG02451.hp1 HG02486.hp1 HG02615.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*553_*556dupAAGT | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 557 | INFO_REALIGN_3_PRIME | chr9 | 135792713 | ||||
| chr9:135792745
|
C | T | 1 | a0001c0001t0015 | 2 | HG00642.hp2 HG01192.hp1 |
3_prime_UTR_variant | MODIFIER | c.*584C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 584 | chr9 | 135792745 | |||||
| chr9:135792784
|
G | A | 1 | a0001c0001t0016 | 2 | HG02602.hp1 NA18612.hp2 |
3_prime_UTR_variant | MODIFIER | c.*623G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 623 | chr9 | 135792784 | |||||
| chr9:135792792
|
C | T | 1 | a0001c0004t0037 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*631C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 631 | chr9 | 135792792 | |||||
| chr9:135792823
|
C | T | 4 | a0001c0003t0010a0001c0004t0037a0001c0006t0010others(1): Show | 5 | HG01099.hp1 HG01109.hp1 HG02055.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*662C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 662 | chr9 | 135792823 | |||||
| chr9:135793095
|
G | A | 1 | a0001c0024t0023 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*934G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 934 | chr9 | 135793095 | |||||
| chr9:135793448
|
C | G | 1 | a0001c0002t0035 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1287C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 1287 | chr9 | 135793448 | |||||
| chr9:135793468
|
C | T | 1 | a0001c0002t0034 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1307C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 1307 | chr9 | 135793468 | |||||
| chr9:135793617
|
G | A | 7 | a0001c0001t0003a0001c0001t0038a0001c0001t0039others(4): Show | 15 | HG00099.hp1 HG01346.hp2 HG01358.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1456G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 1456 | chr9 | 135793617 | |||||
| chr9:135793628
|
C | T | 1 | a0001c0002t0033 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1467C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 1467 | chr9 | 135793628 | |||||
| chr9:135793812
|
A | G | 7 | a0001c0001t0003a0001c0001t0038a0001c0001t0039others(4): Show | 15 | HG00099.hp1 HG01346.hp2 HG01358.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1651A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 1651 | chr9 | 135793812 | |||||
| chr9:135793851
|
G | T | 10 | a0001c0001t0003a0001c0001t0005a0001c0001t0038others(7): Show | 23 | HG00099.hp1 HG01081.hp2 HG01106.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1690G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 1690 | chr9 | 135793851 | |||||
| chr9:135793907
|
C | T | 1 | a0001c0002t0032 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1746C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 1746 | chr9 | 135793907 | |||||
| chr9:135793912
|
C | G | 1 | a0001c0003t0031 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1751C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 1751 | chr9 | 135793912 | |||||
| chr9:135793927
|
C | T | 1 | a0001c0001t0016 | 2 | HG02602.hp1 NA18612.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1766C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 1766 | chr9 | 135793927 | |||||
| chr9:135793933
|
C | T | 1 | a0001c0004t0030 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1772C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 1772 | chr9 | 135793933 | |||||
| chr9:135793950
|
A | ACCCCGCC others(9): Show |
3 | a0001c0002t0025a0001c0004t0014a0001c0010t0014 | 3 | HG03098.hp2 HG03486.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1793_*1808dupCGCC others(12): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 1809 | INFO_REALIGN_3_PRIME | chr9 | 135793950 | ||||
| chr9:135793954
|
C | T | 2 | a0001c0014t0017a0001c0020t0017 | 2 | HG02451.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1793C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 1793 | chr9 | 135793954 | |||||
| chr9:135793960
|
G | T | 10 | a0001c0001t0003a0001c0001t0005a0001c0001t0038others(7): Show | 23 | HG00099.hp1 HG01081.hp2 HG01106.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1799G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 1799 | chr9 | 135793960 | |||||
| chr9:135793966
|
G | A | 6 | a0001c0001t0013a0001c0001t0016a0001c0003t0013others(3): Show | 7 | HG01099.hp1 HG02451.hp2 HG02602.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1805G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 1805 | chr9 | 135793966 | |||||
| chr9:135793974
|
G | T | 2 | a0001c0014t0017a0001c0020t0017 | 2 | HG02451.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1813G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 1813 | chr9 | 135793974 | |||||
| chr9:135794042
|
G | A | 10 | a0001c0001t0003a0001c0001t0005a0001c0001t0038others(7): Show | 23 | HG00099.hp1 HG01081.hp2 HG01106.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1881G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 1881 | chr9 | 135794042 | |||||
| chr9:135794043
|
G | C | 6 | a0001c0002t0009a0001c0003t0009a0001c0006t0009others(3): Show | 6 | HG02451.hp1 HG02486.hp1 HG02615.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1882G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 1882 | chr9 | 135794043 | |||||
| chr9:135794073
|
A | G | 18 | a0001c0001t0003a0001c0001t0005a0001c0001t0013others(15): Show | 33 | HG00099.hp1 HG01081.hp2 HG01099.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1912A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 1912 | chr9 | 135794073 | |||||
| chr9:135794183
|
G | A | 1 | a0001c0001t0026 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2022G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 2022 | chr9 | 135794183 | |||||
| chr9:135794210
|
T | C | 10 | a0001c0001t0003a0001c0001t0005a0001c0001t0038others(7): Show | 23 | HG00099.hp1 HG01081.hp2 HG01106.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2049T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 2049 | chr9 | 135794210 | |||||
| chr9:135794319
|
C | T | 14 | a0001c0001t0003a0001c0001t0005a0001c0001t0013others(11): Show | 28 | HG00099.hp1 HG01081.hp2 HG01099.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2158C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 2158 | chr9 | 135794319 | |||||
| chr9:135794446
|
A | AATC | 6 | a0001c0001t0008a0001c0001t0027a0001c0002t0008others(3): Show | 6 | HG02280.hp2 HG02922.hp2 HG03516.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2286_*2288dupATC | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 2289 | INFO_REALIGN_3_PRIME | chr9 | 135794446 | ||||
| chr9:135794574
|
G | A | 1 | a0001c0001t0028 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2413G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 2413 | chr9 | 135794574 | |||||
| chr9:135794610
|
C | T | 4 | a0001c0002t0006a0001c0003t0006a0001c0004t0006others(1): Show | 5 | HG01884.hp1 HG02572.hp2 HG03195.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2449C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 2449 | chr9 | 135794610 | |||||
| chr9:135794725
|
A | C | 46 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(43): Show | 96 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*2564A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 2564 | chr9 | 135794725 | |||||
| chr9:135794842
|
A | C | 1 | a0001c0001t0016 | 2 | HG02602.hp1 NA18612.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2681A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 2681 | chr9 | 135794842 | |||||
| chr9:135795242
|
C | A | 4 | a0001c0001t0008a0001c0002t0008a0001c0003t0008others(1): Show | 4 | HG02280.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3081C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 3081 | chr9 | 135795242 | |||||
| chr9:135795246
|
G | A | 10 | a0001c0001t0003a0001c0001t0005a0001c0001t0038others(7): Show | 23 | HG00099.hp1 HG01081.hp2 HG01106.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3085G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 3085 | chr9 | 135795246 | |||||
| chr9:135795264
|
C | A | 11 | a0001c0001t0008a0001c0001t0027a0001c0002t0006others(8): Show | 12 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3103C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 3103 | chr9 | 135795264 | |||||
| chr9:135795284
|
C | CA | 31 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(28): Show | 67 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*3134dupA | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 3135 | INFO_REALIGN_3_PRIME | chr9 | 135795284 | ||||
| chr9:135795295
|
A | AAAT | 10 | a0001c0001t0003a0001c0001t0005a0001c0001t0016others(7): Show | 24 | HG00099.hp1 HG01081.hp2 HG01106.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3134_*3135insAAT | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 3135 | chr9 | 135795295 | |||||
| chr9:135795409
|
A | G | 1 | a0001c0009t0018 | 1 | HG02897.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3248A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 31/31 | 3248 | chr9 | 135795409 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:135702406
|
C | T | 3 | a0001c0002t0005g0270a0001c0003t0001g0272a0001c0015t0001g0271 | 3 | HG02886.hp2 HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.110+38C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135702406 | ||||||
| chr9:135702418
|
A | G | 1 | a0001c0003t0031g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.110+50A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135702418 | ||||||
| chr9:135702420
|
A | AC | 223 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.110+57dupC | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr9 | 135702420 | |||||
| chr9:135702433
|
C | T | 1 | a0001c0027t0009g0268 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.110+65C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135702433 | ||||||
| chr9:135702445
|
C | T | 4 | a0001c0003t0001g0267a0001c0003t0008g0043a0001c0004t0002g0045others(1): Show | 4 | HG01496.hp2 HG02647.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.110+77C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135702445 | ||||||
| chr9:135702514
|
C | T | 1 | a0001c0001t0002g0266 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.110+146C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135702514 | ||||||
| chr9:135702522
|
G | A | 3 | a0001c0002t0009g0047a0001c0013t0024g0046a0001c0024t0023g0048 | 3 | HG02451.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.110+154G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135702522 | ||||||
| chr9:135702590
|
A | G | 15 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0002g0039others(12): Show | 15 | HG01081.hp1 HG01943.hp2 HG02004.hp1 others(12): Show |
intron_variant | MODIFIER | c.110+222A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135702590 | ||||||
| chr9:135702651
|
C | T | 1 | a0001c0004t0002g0045 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.110+283C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135702651 | ||||||
| chr9:135702977
|
C | T | 1 | a0001c0005t0001g0261 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.110+609C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135702977 | ||||||
| chr9:135703060
|
C | T | 1 | a0001c0003t0001g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.110+692C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135703060 | ||||||
| chr9:135703061
|
G | A | 1 | a0001c0001t0002g0049 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.110+693G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135703061 | ||||||
| chr9:135703087
|
G | A | 14 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0002g0039others(11): Show | 14 | HG01081.hp1 HG01943.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+719G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135703087 | ||||||
| chr9:135703102
|
G | A | 124 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.110+734G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135703102 | ||||||
| chr9:135703122
|
C | T | 210 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.110+754C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135703122 | ||||||
| chr9:135703165
|
C | T | 1 | a0001c0003t0021g0259 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.110+797C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135703165 | ||||||
| chr9:135703173
|
C | T | 1 | a0003c0011t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.110+805C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135703173 | ||||||
| chr9:135703338
|
G | A | 1 | a0001c0002t0001g0050 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.110+970G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135703338 | ||||||
| chr9:135703383
|
TGAG | T | 3 | a0001c0001t0001g0169a0002c0008t0001g0170a0002c0008t0001g0171 | 3 | HG01074.hp2 HG01167.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.110+1020_110+1022d others(5): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr9 | 135703383 | |||||
| chr9:135703431
|
C | G | 1 | a0001c0001t0003g0168 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.110+1063C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135703431 | ||||||
| chr9:135703447
|
T | C | 1 | a0001c0002t0001g0172 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.110+1079T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135703447 | ||||||
| chr9:135703558
|
C | T | 4 | a0001c0002t0004g0257a0001c0004t0004g0255a0001c0004t0004g0256others(1): Show | 4 | HG02717.hp2 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.110+1190C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135703558 | ||||||
| chr9:135703595
|
A | G | 246 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0042others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.110+1227A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135703595 | ||||||
| chr9:135703656
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.110+1288C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135703656 | ||||||
| chr9:135703771
|
C | T | 1 | a0001c0001t0016g0254 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.110+1403C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135703771 | ||||||
| chr9:135703796
|
G | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.110+1428G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135703796 | ||||||
| chr9:135703824
|
C | T | 4 | a0001c0001t0001g0031a0001c0001t0007g0028a0001c0001t0007g0029others(1): Show | 4 | HG02257.hp1 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.110+1456C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135703824 | ||||||
| chr9:135703911
|
C | T | 5 | a0001c0001t0001g0031a0001c0001t0007g0028a0001c0001t0007g0029others(2): Show | 5 | HG02257.hp1 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.110+1543C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135703911 | ||||||
| chr9:135704076
|
G | C | 3 | a0001c0002t0005g0270a0001c0003t0001g0272a0001c0015t0001g0271 | 3 | HG02886.hp2 HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.110+1708G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135704076 | ||||||
| chr9:135704139
|
C | T | 1 | a0001c0003t0001g0163 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.110+1771C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135704139 | ||||||
| chr9:135704187
|
G | A | 1 | a0003c0011t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.110+1819G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135704187 | ||||||
| chr9:135704288
|
A | G | 14 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0002g0039others(11): Show | 14 | HG01081.hp1 HG01943.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+1920A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135704288 | ||||||
| chr9:135704403
|
G | A | 220 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.110+2035G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135704403 | ||||||
| chr9:135704604
|
G | T | 2 | a0001c0003t0001g0252a0001c0003t0001g0253 | 2 | NA18962.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.110+2236G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135704604 | ||||||
| chr9:135704641
|
C | T | 1 | a0001c0003t0002g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.110+2273C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135704641 | ||||||
| chr9:135704689
|
G | T | 1 | a0001c0003t0031g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.110+2321G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135704689 | ||||||
| chr9:135704842
|
T | A | 2 | a0001c0002t0034g0179a0001c0003t0001g0178 | 2 | HG02080.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.110+2474T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135704842 | ||||||
| chr9:135704861
|
G | A | 10 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG01081.hp2 HG01106.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.110+2493G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135704861 | ||||||
| chr9:135704875
|
G | A | 3 | a0001c0003t0001g0164a0001c0003t0008g0043a0001c0004t0002g0045 | 3 | HG01496.hp2 HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.110+2507G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135704875 | ||||||
| chr9:135704922
|
G | A | 1 | a0001c0003t0031g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.110+2554G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135704922 | ||||||
| chr9:135705045
|
G | C | 1 | a0001c0026t0001g0051 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.110+2677G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135705045 | ||||||
| chr9:135705128
|
G | A | 223 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.110+2760G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135705128 | ||||||
| chr9:135705557
|
A | G | 14 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0002g0039others(11): Show | 14 | HG01081.hp1 HG01943.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+3189A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135705557 | ||||||
| chr9:135705600
|
G | A | 237 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0042others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.110+3232G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135705600 | ||||||
| chr9:135705613
|
G | A | 3 | a0001c0001t0001g0169a0002c0008t0001g0170a0002c0008t0001g0171 | 3 | HG01074.hp2 HG01167.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.110+3245G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135705613 | ||||||
| chr9:135705773
|
C | T | 2 | a0001c0004t0004g0003a0001c0004t0014g0002 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.110+3405C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135705773 | ||||||
| chr9:135705785
|
A | C | 5 | a0001c0002t0040g0160a0001c0009t0006g0159a0001c0009t0018g0162others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.110+3417A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135705785 | ||||||
| chr9:135705827
|
G | A | 1 | a0001c0003t0002g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.110+3459G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135705827 | ||||||
| chr9:135705895
|
C | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.110+3527C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135705895 | ||||||
| chr9:135705982
|
A | C | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.110+3614A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135705982 | ||||||
| chr9:135706011
|
G | A | 1 | a0001c0003t0001g0180 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.110+3643G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135706011 | ||||||
| chr9:135706014
|
C | A | 10 | a0001c0001t0027g0157a0001c0001t0039g0156a0001c0002t0040g0160others(7): Show | 10 | HG01496.hp2 HG01891.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.110+3646C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135706014 | ||||||
| chr9:135706160
|
G | A | 203 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.110+3792G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135706160 | ||||||
| chr9:135706214
|
T | C | 250 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0042others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.110+3846T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135706214 | ||||||
| chr9:135706215
|
G | A | 4 | a0001c0003t0001g0164a0001c0003t0008g0043a0001c0003t0031g0269others(1): Show | 4 | HG01496.hp2 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.110+3847G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135706215 | ||||||
| chr9:135706280
|
C | T | 1 | a0001c0001t0002g0049 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.110+3912C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135706280 | ||||||
| chr9:135706395
|
G | A | 2 | a0001c0001t0003g0181a0001c0004t0014g0002 | 2 | HG03098.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.110+4027G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135706395 | ||||||
| chr9:135706447
|
G | A | 1 | a0001c0003t0002g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.110+4079G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135706447 | ||||||
| chr9:135706468
|
G | C | 1 | a0001c0013t0024g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.110+4100G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135706468 | ||||||
| chr9:135706516
|
C | T | 3 | a0001c0002t0005g0270a0001c0003t0001g0272a0001c0015t0001g0271 | 3 | HG02886.hp2 HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.110+4148C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135706516 | ||||||
| chr9:135706554
|
G | A | 1 | a0001c0003t0031g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.110+4186G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135706554 | ||||||
| chr9:135706629
|
A | G | 7 | a0001c0001t0027g0157a0001c0001t0039g0156a0001c0002t0040g0160others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.110+4261A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135706629 | ||||||
| chr9:135706694
|
C | T | 14 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0002g0039others(11): Show | 14 | HG01081.hp1 HG01943.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+4326C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135706694 | ||||||
| chr9:135706703
|
T | G | 2 | a0001c0003t0002g0027a0003c0011t0001g0044 | 2 | HG02809.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.110+4335T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135706703 | ||||||
| chr9:135706783
|
T | A | 2 | a0001c0002t0009g0047a0001c0013t0024g0046 | 2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.110+4415T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135706783 | ||||||
| chr9:135706833
|
C | T | 1 | a0001c0007t0001g0155 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.110+4465C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135706833 | ||||||
| chr9:135706839
|
T | C | 11 | a0001c0001t0008g0008a0001c0002t0001g0013a0001c0002t0001g0014others(8): Show | 11 | HG01074.hp1 HG01099.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.110+4471T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135706839 | ||||||
| chr9:135706922
|
A | G | 7 | a0001c0001t0002g0152a0001c0002t0001g0154a0001c0002t0002g0150others(4): Show | 7 | HG02258.hp2 HG03041.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.110+4554A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135706922 | ||||||
| chr9:135707023
|
G | C | 14 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0002g0039others(11): Show | 14 | HG01081.hp1 HG01943.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+4655G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135707023 | ||||||
| chr9:135707045
|
G | A | 61 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.110+4677G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135707045 | ||||||
| chr9:135707055
|
C | T | 7 | a0001c0001t0027g0157a0001c0001t0039g0156a0001c0002t0040g0160others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.110+4687C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135707055 | ||||||
| chr9:135707114
|
T | C | 2 | a0001c0002t0009g0047a0001c0013t0024g0046 | 2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.110+4746T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135707114 | ||||||
| chr9:135707147
|
A | G | 14 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0002g0039others(11): Show | 14 | HG01081.hp1 HG01943.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+4779A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135707147 | ||||||
| chr9:135707162
|
C | T | 1 | a0001c0001t0016g0102 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.110+4794C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135707162 | ||||||
| chr9:135707163
|
G | A | 1 | a0003c0011t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.110+4795G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135707163 | ||||||
| chr9:135707317
|
C | T | 19 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0002g0039others(16): Show | 19 | HG01081.hp1 HG01943.hp2 HG02004.hp1 others(16): Show |
intron_variant | MODIFIER | c.110+4949C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135707317 | ||||||
| chr9:135707429
|
A | T | 1 | a0001c0004t0004g0025 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.110+5061A>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135707429 | ||||||
| chr9:135707472
|
C | T | 1 | a0001c0003t0002g0101 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.110+5104C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135707472 | ||||||
| chr9:135707489
|
G | A | 1 | a0001c0004t0037g0004 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.110+5121G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135707489 | ||||||
| chr9:135707615
|
G | C | 2 | a0001c0001t0015g0103a0001c0001t0015g0104 | 2 | HG00642.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.110+5247G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135707615 | ||||||
| chr9:135707627
|
C | A | 1 | a0001c0002t0006g0054 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.110+5259C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135707627 | ||||||
| chr9:135707628
|
A | G | 1 | a0001c0004t0002g0147 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.110+5260A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135707628 | ||||||
| chr9:135707691
|
A | G | 3 | a0001c0001t0001g0169a0002c0008t0001g0170a0002c0008t0001g0171 | 3 | HG01074.hp2 HG01167.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.110+5323A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135707691 | ||||||
| chr9:135707692
|
G | C | 3 | a0001c0001t0001g0169a0002c0008t0001g0170a0002c0008t0001g0171 | 3 | HG01074.hp2 HG01167.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.110+5324G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135707692 | ||||||
| chr9:135707794
|
C | T | 1 | a0001c0001t0038g0100 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.110+5426C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135707794 | ||||||
| chr9:135707799
|
C | T | 218 | a0001c0001t0001g0031a0001c0001t0001g0052a0001c0001t0001g0053others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.110+5431C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135707799 | ||||||
| chr9:135707835
|
G | A | 1 | a0001c0002t0003g0105 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.110+5467G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135707835 | ||||||
| chr9:135707879
|
C | G | 1 | a0001c0027t0009g0268 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.110+5511C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135707879 | ||||||
| chr9:135707937
|
G | A | 1 | a0003c0011t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.110+5569G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135707937 | ||||||
| chr9:135708008
|
G | A | 203 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.110+5640G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135708008 | ||||||
| chr9:135708032
|
C | T | 249 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0042others(246): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.110+5664C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135708032 | ||||||
| chr9:135708046
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.110+5678G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135708046 | ||||||
| chr9:135708105
|
A | T | 19 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0002g0039others(16): Show | 19 | HG01081.hp1 HG01943.hp2 HG02004.hp1 others(16): Show |
intron_variant | MODIFIER | c.110+5737A>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135708105 | ||||||
| chr9:135708122
|
A | G | 30 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0002g0039others(27): Show | 30 | HG01081.hp1 HG01496.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.110+5754A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135708122 | ||||||
| chr9:135708192
|
A | G | 1 | a0001c0003t0002g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.110+5824A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135708192 | ||||||
| chr9:135708216
|
A | C | 1 | a0001c0004t0030g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.110+5848A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135708216 | ||||||
| chr9:135708336
|
C | T | 1 | a0001c0003t0001g0180 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.110+5968C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135708336 | ||||||
| chr9:135708387
|
A | G | 3 | a0001c0003t0001g0164a0001c0003t0008g0043a0001c0004t0002g0045 | 3 | HG01496.hp2 HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.110+6019A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135708387 | ||||||
| chr9:135708399
|
A | G | 2 | a0001c0004t0004g0003a0001c0004t0014g0002 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.110+6031A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135708399 | ||||||
| chr9:135708496
|
G | T | 1 | a0001c0003t0001g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.111-6081G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135708496 | ||||||
| chr9:135708553
|
T | G | 1 | a0001c0002t0029g0182 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.111-6024T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135708553 | ||||||
| chr9:135708851
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.111-5726A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135708851 | ||||||
| chr9:135708979
|
A | G | 1 | a0003c0011t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.111-5598A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135708979 | ||||||
| chr9:135709035
|
G | A | 1 | a0001c0002t0002g0107 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.111-5542G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135709035 | ||||||
| chr9:135709044
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.111-5533G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135709044 | ||||||
| chr9:135709135
|
T | C | 14 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0002g0039others(11): Show | 14 | HG01081.hp1 HG01943.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.111-5442T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135709135 | ||||||
| chr9:135709155
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG01168.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.111-5422G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135709155 | ||||||
| chr9:135709238
|
A | C | 13 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0002g0039others(10): Show | 13 | HG01081.hp1 HG01943.hp2 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.111-5339A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135709238 | ||||||
| chr9:135709282
|
C | T | 1 | a0001c0009t0018g0162 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.111-5295C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135709282 | ||||||
| chr9:135709348
|
C | T | 1 | a0001c0003t0001g0272 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.111-5229C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135709348 | ||||||
| chr9:135709388
|
C | A | 3 | a0001c0002t0005g0270a0001c0003t0001g0272a0001c0015t0001g0271 | 3 | HG02886.hp2 HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.111-5189C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135709388 | ||||||
| chr9:135709504
|
C | T | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.111-5073C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135709504 | ||||||
| chr9:135709539
|
AC | A | 19 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0002g0039others(16): Show | 19 | HG01081.hp1 HG01943.hp2 HG02004.hp1 others(16): Show |
intron_variant | MODIFIER | c.111-5032delC | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr9 | 135709539 | |||||
| chr9:135709573
|
G | A | 2 | a0001c0003t0008g0043a0001c0004t0002g0045 | 2 | HG01496.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.111-5004G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135709573 | ||||||
| chr9:135709615
|
G | C | 1 | a0001c0003t0001g0108 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.111-4962G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135709615 | ||||||
| chr9:135709952
|
A | G | 220 | a0001c0001t0001g0031a0001c0001t0001g0052a0001c0001t0001g0053others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.111-4625A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135709952 | ||||||
| chr9:135710017
|
C | T | 248 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0042others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.111-4560C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135710017 | ||||||
| chr9:135710078
|
C | T | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.111-4499C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135710078 | ||||||
| chr9:135710190
|
G | A | 1 | a0001c0003t0001g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.111-4387G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135710190 | ||||||
| chr9:135710207
|
C | T | 1 | a0001c0001t0002g0266 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.111-4370C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135710207 | ||||||
| chr9:135710349
|
C | T | 1 | a0001c0002t0002g0145 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.111-4228C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135710349 | ||||||
| chr9:135710382
|
C | T | 218 | a0001c0001t0001g0031a0001c0001t0001g0052a0001c0001t0001g0053others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.111-4195C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135710382 | ||||||
| chr9:135710553
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.111-4024G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135710553 | ||||||
| chr9:135710685
|
G | A | 1 | a0001c0002t0001g0184 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.111-3892G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135710685 | ||||||
| chr9:135710821
|
G | A | 237 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0042others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.111-3756G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135710821 | ||||||
| chr9:135710894
|
G | A | 1 | a0001c0003t0031g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.111-3683G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135710894 | ||||||
| chr9:135711004
|
A | G | 257 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0042others(254): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.111-3573A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135711004 | ||||||
| chr9:135711150
|
G | A | 1 | a0001c0002t0035g0109 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.111-3427G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135711150 | ||||||
| chr9:135711200
|
A | G | 10 | a0001c0001t0027g0157a0001c0001t0039g0156a0001c0002t0040g0160others(7): Show | 10 | HG01496.hp2 HG01891.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.111-3377A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135711200 | ||||||
| chr9:135711338
|
A | G | 1 | a0001c0003t0009g0177 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.111-3239A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135711338 | ||||||
| chr9:135711373
|
A | G | 240 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0042others(237): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.111-3204A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135711373 | ||||||
| chr9:135711542
|
G | A | 1 | a0001c0003t0002g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.111-3035G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135711542 | ||||||
| chr9:135711590
|
G | A | 3 | a0001c0002t0005g0270a0001c0003t0001g0272a0001c0015t0001g0271 | 3 | HG02886.hp2 HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.111-2987G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135711590 | ||||||
| chr9:135711641
|
A | G | 1 | a0001c0003t0001g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.111-2936A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135711641 | ||||||
| chr9:135711654
|
C | T | 1 | a0001c0004t0004g0258 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.111-2923C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135711654 | ||||||
| chr9:135711695
|
C | T | 3 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0002g0251 | 3 | HG02027.hp2 HG02165.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.111-2882C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135711695 | ||||||
| chr9:135711742
|
C | G | 10 | a0001c0001t0027g0157a0001c0001t0039g0156a0001c0002t0040g0160others(7): Show | 10 | HG01496.hp2 HG01891.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.111-2835C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135711742 | ||||||
| chr9:135711782
|
C | T | 10 | a0001c0001t0027g0157a0001c0001t0039g0156a0001c0002t0040g0160others(7): Show | 10 | HG01496.hp2 HG01891.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.111-2795C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135711782 | ||||||
| chr9:135711792
|
C | T | 1 | a0001c0003t0001g0272 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.111-2785C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135711792 | ||||||
| chr9:135711793
|
G | A | 219 | a0001c0001t0001g0031a0001c0001t0001g0052a0001c0001t0001g0053others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.111-2784G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135711793 | ||||||
| chr9:135711803
|
G | C | 1 | a0001c0024t0023g0048 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.111-2774G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135711803 | ||||||
| chr9:135711848
|
G | C | 219 | a0001c0001t0001g0031a0001c0001t0001g0052a0001c0001t0001g0053others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.111-2729G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135711848 | ||||||
| chr9:135711894
|
C | T | 144 | a0001c0001t0001g0106a0001c0001t0001g0111a0001c0001t0001g0112others(141): Show | 144 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.111-2683C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135711894 | ||||||
| chr9:135712008
|
C | T | 47 | a0001c0001t0001g0106a0001c0001t0001g0118a0001c0001t0001g0119others(44): Show | 47 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(44): Show |
intron_variant | MODIFIER | c.111-2569C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135712008 | ||||||
| chr9:135712057
|
G | C | 15 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0002g0039others(12): Show | 15 | HG01081.hp1 HG01943.hp2 HG02004.hp1 others(12): Show |
intron_variant | MODIFIER | c.111-2520G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135712057 | ||||||
| chr9:135712126
|
C | T | 6 | a0001c0001t0001g0242a0001c0001t0003g0243a0001c0001t0003g0245others(3): Show | 6 | HG02602.hp2 HG02698.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.111-2451C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135712126 | ||||||
| chr9:135712127
|
G | A | 1 | a0003c0011t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.111-2450G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135712127 | ||||||
| chr9:135712188
|
C | T | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.111-2389C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135712188 | ||||||
| chr9:135712746
|
G | A | 52 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0186others(49): Show | 52 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.111-1831G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135712746 | ||||||
| chr9:135712856
|
G | A | 247 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0042others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.111-1721G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135712856 | ||||||
| chr9:135713076
|
G | A | 2 | a0001c0003t0031g0269a0003c0011t0001g0044 | 2 | HG02976.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.111-1501G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135713076 | ||||||
| chr9:135713090
|
C | T | 12 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0002g0039others(9): Show | 12 | HG01081.hp1 HG01943.hp2 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.111-1487C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135713090 | ||||||
| chr9:135713101
|
C | G | 220 | a0001c0001t0001g0031a0001c0001t0001g0052a0001c0001t0001g0053others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.111-1476C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135713101 | ||||||
| chr9:135713212
|
G | T | 3 | a0001c0001t0001g0169a0002c0008t0001g0170a0002c0008t0001g0171 | 3 | HG01074.hp2 HG01167.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.111-1365G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135713212 | ||||||
| chr9:135713260
|
T | C | 1 | a0001c0002t0001g0213 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.111-1317T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135713260 | ||||||
| chr9:135713346
|
C | A | 104 | a0001c0001t0001g0106a0001c0001t0001g0111a0001c0001t0001g0112others(101): Show | 104 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.111-1231C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135713346 | ||||||
| chr9:135713376
|
G | A | 4 | a0001c0001t0001g0031a0001c0001t0007g0028a0001c0001t0007g0029others(1): Show | 4 | HG02257.hp1 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-1201G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135713376 | ||||||
| chr9:135713403
|
A | T | 1 | a0001c0001t0001g0097 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.111-1174A>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135713403 | ||||||
| chr9:135713421
|
C | A | 1 | a0001c0001t0001g0118 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.111-1156C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135713421 | ||||||
| chr9:135713504
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.111-1073G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135713504 | ||||||
| chr9:135713516
|
G | A | 3 | a0001c0001t0001g0057a0001c0003t0003g0058a0001c0003t0003g0059 | 3 | HG00099.hp1 HG00741.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.111-1061G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135713516 | ||||||
| chr9:135713860
|
A | T | 2 | a0001c0003t0008g0043a0001c0004t0002g0045 | 2 | HG01496.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.111-717A>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135713860 | ||||||
| chr9:135713896
|
C | A | 20 | a0001c0001t0001g0031a0001c0001t0007g0028a0001c0001t0007g0029others(17): Show | 20 | HG01496.hp2 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.111-681C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135713896 | ||||||
| chr9:135713913
|
C | G | 1 | a0003c0011t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.111-664C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135713913 | ||||||
| chr9:135713979
|
C | G | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.111-598C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135713979 | ||||||
| chr9:135714042
|
G | A | 1 | a0001c0026t0001g0051 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.111-535G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135714042 | ||||||
| chr9:135714069
|
C | T | 1 | a0003c0011t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.111-508C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135714069 | ||||||
| chr9:135714078
|
C | T | 165 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.111-499C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135714078 | ||||||
| chr9:135714084
|
G | T | 2 | a0001c0001t0001g0095a0001c0002t0001g0096 | 2 | HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.111-493G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135714084 | ||||||
| chr9:135714140
|
C | G | 1 | a0001c0014t0017g0212 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.111-437C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135714140 | ||||||
| chr9:135714175
|
G | C | 13 | a0001c0001t0027g0157a0001c0001t0039g0156a0001c0002t0008g0026others(10): Show | 13 | HG01496.hp2 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.111-402G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135714175 | ||||||
| chr9:135714306
|
T | C | 1 | a0001c0003t0001g0272 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.111-271T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135714306 | ||||||
| chr9:135714314
|
T | G | 48 | a0001c0001t0001g0183a0001c0001t0001g0216a0001c0001t0001g0221others(45): Show | 48 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.111-263T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135714314 | ||||||
| chr9:135714337
|
G | A | 1 | a0001c0002t0006g0054 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.111-240G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135714337 | ||||||
| chr9:135714364
|
C | T | 1 | a0001c0002t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.111-213C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135714364 | ||||||
| chr9:135714407
|
G | GC | 7 | a0001c0001t0001g0060a0001c0001t0001g0249a0001c0001t0002g0266others(4): Show | 7 | HG00438.hp1 HG00738.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-165dupC | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr9 | 135714407 | |||||
| chr9:135714481
|
G | C | 6 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0175others(3): Show | 6 | HG01081.hp2 HG01106.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.111-96G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135714481 | ||||||
| chr9:135714550
|
C | T | 2 | a0001c0002t0001g0211a0001c0003t0001g0210 | 2 | NA18948.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.111-27C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 1/30 | chr9 | 135714550 | ||||||
| chr9:135714735
|
C | CGG | 78 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0031others(75): Show | 78 | HG00544.hp1 HG00609.hp2 HG00741.hp2 others(75): Show |
intron_variant | MODIFIER | c.254+18_254+19dupGG | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135714735 | |||||
| chr9:135714740
|
T | C | 79 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0031others(76): Show | 79 | HG00544.hp1 HG00609.hp2 HG00741.hp2 others(76): Show |
intron_variant | MODIFIER | c.254+20T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135714740 | ||||||
| chr9:135714761
|
C | T | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+41C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135714761 | ||||||
| chr9:135714785
|
G | A | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+65G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135714785 | ||||||
| chr9:135714857
|
G | C | 1 | a0001c0001t0001g0119 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.254+137G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135714857 | ||||||
| chr9:135714876
|
G | A | 1 | a0001c0002t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.254+156G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135714876 | ||||||
| chr9:135714973
|
G | A | 1 | a0001c0001t0002g0098 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.254+253G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135714973 | ||||||
| chr9:135715020
|
C | A | 1 | a0001c0001t0001g0015 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.254+300C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135715020 | ||||||
| chr9:135715092
|
C | T | 1 | a0001c0024t0023g0048 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.254+372C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135715092 | ||||||
| chr9:135715157
|
G | A | 7 | a0001c0001t0027g0157a0001c0001t0039g0156a0001c0002t0040g0160others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.254+437G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135715157 | ||||||
| chr9:135715253
|
G | A | 1 | a0001c0003t0002g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.254+533G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135715253 | ||||||
| chr9:135715426
|
C | T | 1 | a0001c0003t0041g0093 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.254+706C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135715426 | ||||||
| chr9:135715532
|
G | A | 2 | a0001c0002t0008g0026a0003c0011t0001g0044 | 2 | HG03516.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.254+812G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135715532 | ||||||
| chr9:135715533
|
G | A | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+813G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135715533 | ||||||
| chr9:135715550
|
A | AGGGCTCC others(16): Show |
187 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0042others(184): Show | 187 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.254+837_254+859dup others(23): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135715550 | |||||
| chr9:135715578
|
T | TCCGTCAC others(16): Show |
2 | a0001c0002t0008g0026a0003c0011t0001g0044 | 2 | HG03516.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.254+859_254+860ins others(23): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135715578 | |||||
| chr9:135715621
|
C | A | 12 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0002g0039others(9): Show | 12 | HG01081.hp1 HG01943.hp2 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.254+901C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135715621 | ||||||
| chr9:135715705
|
A | T | 122 | a0001c0001t0001g0031a0001c0001t0001g0106a0001c0001t0001g0111others(119): Show | 122 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.254+985A>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135715705 | ||||||
| chr9:135715850
|
T | C | 3 | a0001c0003t0001g0164a0001c0003t0008g0043a0001c0004t0002g0045 | 3 | HG01496.hp2 HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.254+1130T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135715850 | ||||||
| chr9:135716109
|
C | T | 1 | a0001c0004t0001g0092 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.254+1389C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135716109 | ||||||
| chr9:135716234
|
A | G | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+1514A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135716234 | ||||||
| chr9:135716368
|
C | T | 5 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0003t0001g0091others(2): Show | 5 | HG01257.hp1 HG01258.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.254+1648C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135716368 | ||||||
| chr9:135716390
|
T | G | 12 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0002g0039others(9): Show | 12 | HG01081.hp1 HG01943.hp2 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.254+1670T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135716390 | ||||||
| chr9:135716433
|
C | T | 1 | a0001c0001t0001g0031 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.254+1713C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135716433 | ||||||
| chr9:135716511
|
A | C | 122 | a0001c0001t0001g0031a0001c0001t0001g0106a0001c0001t0001g0111others(119): Show | 122 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.254+1791A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135716511 | ||||||
| chr9:135716541
|
G | A | 1 | a0001c0002t0001g0235 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.254+1821G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135716541 | ||||||
| chr9:135716671
|
G | T | 2 | a0001c0002t0008g0026a0003c0011t0001g0044 | 2 | HG03516.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.254+1951G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135716671 | ||||||
| chr9:135716716
|
C | T | 47 | a0001c0001t0001g0031a0001c0001t0001g0183a0001c0001t0001g0221others(44): Show | 47 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.254+1996C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135716716 | ||||||
| chr9:135716745
|
G | A | 102 | a0001c0001t0001g0106a0001c0001t0001g0111a0001c0001t0001g0112others(99): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.254+2025G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135716745 | ||||||
| chr9:135716901
|
G | A | 43 | a0001c0001t0001g0183a0001c0001t0001g0221a0001c0001t0001g0230others(40): Show | 43 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.254+2181G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135716901 | ||||||
| chr9:135717006
|
G | T | 267 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0038others(264): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.254+2286G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135717006 | ||||||
| chr9:135717014
|
C | T | 55 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0183others(52): Show | 55 | HG00544.hp1 HG00609.hp2 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.254+2294C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135717014 | ||||||
| chr9:135717048
|
T | G | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+2328T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135717048 | ||||||
| chr9:135717094
|
T | C | 1 | a0001c0002t0002g0021 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.254+2374T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135717094 | ||||||
| chr9:135717097
|
A | G | 1 | a0001c0001t0002g0143 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.254+2377A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135717097 | ||||||
| chr9:135717104
|
GGGAGGGA others(37): Show |
G | 1 | a0001c0001t0042g0265 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.254+2427_254+2470d others(46): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135717104 | |||||
| chr9:135717126
|
G | C | 1 | a0001c0001t0001g0214 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.254+2406G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135717126 | ||||||
| chr9:135717442
|
G | A | 2 | a0001c0001t0001g0062a0006c0018t0001g0061 | 2 | HG00323.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.254+2722G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135717442 | ||||||
| chr9:135717475
|
G | A | 1 | a0001c0003t0021g0259 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.254+2755G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135717475 | ||||||
| chr9:135717617
|
G | A | 3 | a0001c0002t0005g0270a0001c0003t0001g0272a0001c0015t0001g0271 | 3 | HG02886.hp2 HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.254+2897G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135717617 | ||||||
| chr9:135717631
|
G | A | 101 | a0001c0001t0001g0106a0001c0001t0001g0111a0001c0001t0001g0112others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.254+2911G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135717631 | ||||||
| chr9:135717636
|
A | G | 2 | a0001c0005t0001g0207a0001c0005t0001g0208 | 2 | NA19007.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.254+2916A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135717636 | ||||||
| chr9:135717668
|
C | T | 15 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0002g0039others(12): Show | 15 | HG01081.hp1 HG01943.hp2 HG02004.hp1 others(12): Show |
intron_variant | MODIFIER | c.254+2948C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135717668 | ||||||
| chr9:135718010
|
G | A | 3 | a0001c0002t0008g0026a0001c0004t0004g0003a0001c0004t0014g0002 | 3 | HG03098.hp2 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.254+3290G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135718010 | ||||||
| chr9:135718182
|
C | T | 117 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(114): Show | 117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.254+3462C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135718182 | ||||||
| chr9:135718221
|
C | G | 1 | a0001c0003t0001g0018 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.254+3501C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135718221 | ||||||
| chr9:135718256
|
G | A | 1 | a0001c0003t0002g0101 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.254+3536G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135718256 | ||||||
| chr9:135718340
|
A | G | 197 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0052others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.254+3620A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135718340 | ||||||
| chr9:135718413
|
A | G | 184 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0052others(181): Show | 184 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.254+3693A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135718413 | ||||||
| chr9:135718496
|
C | A | 5 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0065others(2): Show | 5 | HG00738.hp2 HG01099.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.254+3776C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135718496 | ||||||
| chr9:135718519
|
G | C | 148 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0052others(145): Show | 148 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.254+3799G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135718519 | ||||||
| chr9:135718719
|
G | A | 12 | a0001c0001t0001g0038a0001c0001t0002g0039a0001c0001t0011g0032others(9): Show | 12 | HG01081.hp1 HG01943.hp2 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.254+3999G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135718719 | ||||||
| chr9:135718752
|
C | T | 1 | a0001c0001t0027g0157 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.254+4032C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135718752 | ||||||
| chr9:135718906
|
G | A | 2 | a0001c0001t0001g0167a0001c0004t0001g0092 | 2 | HG01168.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.254+4186G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135718906 | ||||||
| chr9:135718937
|
A | AC | 4 | a0001c0001t0001g0106a0001c0001t0002g0188a0001c0004t0004g0255others(1): Show | 4 | HG01978.hp1 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.254+4219dupC | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135718937 | |||||
| chr9:135718940
|
G | A | 1 | a0001c0003t0002g0247 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.254+4220G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135718940 | ||||||
| chr9:135719070
|
C | T | 1 | a0001c0002t0001g0206 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.254+4350C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135719070 | ||||||
| chr9:135719104
|
C | G | 13 | a0001c0001t0001g0038a0001c0001t0002g0039a0001c0001t0011g0032others(10): Show | 13 | HG01081.hp1 HG01943.hp2 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.254+4384C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135719104 | ||||||
| chr9:135719229
|
C | T | 1 | a0001c0002t0002g0021 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.254+4509C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135719229 | ||||||
| chr9:135719255
|
G | C | 1 | a0001c0003t0001g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.254+4535G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135719255 | ||||||
| chr9:135719293
|
G | A | 46 | a0001c0001t0001g0057a0001c0001t0001g0060a0001c0001t0001g0063others(43): Show | 46 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.254+4573G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135719293 | ||||||
| chr9:135719423
|
G | A | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+4703G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135719423 | ||||||
| chr9:135719517
|
A | G | 1 | a0001c0001t0016g0254 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.254+4797A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135719517 | ||||||
| chr9:135719555
|
C | T | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+4835C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135719555 | ||||||
| chr9:135719691
|
T | C | 189 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0052others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.254+4971T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135719691 | ||||||
| chr9:135719847
|
G | C | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+5127G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135719847 | ||||||
| chr9:135720281
|
C | A | 46 | a0001c0001t0001g0057a0001c0001t0001g0060a0001c0001t0001g0063others(43): Show | 46 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.254+5561C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135720281 | ||||||
| chr9:135720333
|
C | T | 1 | a0001c0001t0038g0100 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.254+5613C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135720333 | ||||||
| chr9:135720341
|
T | A | 1 | a0001c0004t0002g0045 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.254+5621T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135720341 | ||||||
| chr9:135720342
|
C | A | 1 | a0001c0004t0002g0045 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.254+5622C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135720342 | ||||||
| chr9:135720367
|
T | G | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+5647T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135720367 | ||||||
| chr9:135720391
|
CG | C | 151 | a0001c0001t0001g0042a0001c0001t0001g0052a0001c0001t0001g0053others(148): Show | 151 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.254+5675delG | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135720391 | |||||
| chr9:135720404
|
T | C | 1 | a0001c0004t0006g0110 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.254+5684T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135720404 | ||||||
| chr9:135720410
|
C | T | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+5690C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135720410 | ||||||
| chr9:135720421
|
G | A | 1 | a0001c0004t0001g0092 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.254+5701G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135720421 | ||||||
| chr9:135720438
|
C | T | 1 | a0001c0002t0001g0205 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.254+5718C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135720438 | ||||||
| chr9:135720456
|
C | T | 10 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG01081.hp2 HG01106.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.254+5736C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135720456 | ||||||
| chr9:135720457
|
G | A | 1 | a0001c0027t0009g0268 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.254+5737G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135720457 | ||||||
| chr9:135720541
|
T | A | 140 | a0001c0001t0001g0042a0001c0001t0001g0052a0001c0001t0001g0053others(137): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.254+5821T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135720541 | ||||||
| chr9:135720586
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.254+5866G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135720586 | ||||||
| chr9:135720648
|
G | C | 12 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0175others(9): Show | 12 | HG01081.hp2 HG01106.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.254+5928G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135720648 | ||||||
| chr9:135720665
|
C | T | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+5945C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135720665 | ||||||
| chr9:135720819
|
C | T | 1 | a0003c0011t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.254+6099C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135720819 | ||||||
| chr9:135720849
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.254+6129C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135720849 | ||||||
| chr9:135720991
|
C | T | 3 | a0001c0002t0008g0026a0001c0027t0009g0268a0003c0011t0001g0044 | 3 | HG03471.hp1 HG03516.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.254+6271C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135720991 | ||||||
| chr9:135721238
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.254+6518G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721238 | ||||||
| chr9:135721266
|
A | AGGGAAAC others(21): Show |
1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+6550_254+6577d others(30): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135721266 | |||||
| chr9:135721336
|
G | A | 1 | a0001c0003t0008g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.254+6616G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721336 | ||||||
| chr9:135721365
|
A | G | 155 | a0001c0001t0001g0042a0001c0001t0001g0052a0001c0001t0001g0053others(152): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.254+6645A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721365 | ||||||
| chr9:135721492
|
A | T | 1 | a0001c0001t0003g0245 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.254+6772A>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721492 | ||||||
| chr9:135721499
|
T | A | 1 | a0001c0001t0003g0245 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.254+6779T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721499 | ||||||
| chr9:135721506
|
C | A | 1 | a0001c0001t0003g0245 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.254+6786C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721506 | ||||||
| chr9:135721507
|
A | G | 1 | a0001c0001t0003g0245 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.254+6787A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721507 | ||||||
| chr9:135721529
|
C | T | 3 | a0001c0001t0002g0039a0001c0001t0011g0032a0001c0003t0001g0040 | 3 | NA19009.hp2 NA19068.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.254+6809C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721529 | ||||||
| chr9:135721542
|
C | T | 3 | a0001c0002t0008g0026a0001c0027t0009g0268a0003c0011t0001g0044 | 3 | HG03471.hp1 HG03516.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.254+6822C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721542 | ||||||
| chr9:135721564
|
C | G | 1 | a0001c0001t0003g0245 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.254+6844C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721564 | ||||||
| chr9:135721573
|
A | G | 1 | a0001c0001t0003g0245 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.254+6853A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721573 | ||||||
| chr9:135721577
|
T | A | 1 | a0001c0001t0003g0245 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.254+6857T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721577 | ||||||
| chr9:135721578
|
C | G | 1 | a0001c0001t0003g0245 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.254+6858C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721578 | ||||||
| chr9:135721581
|
G | C | 1 | a0001c0001t0003g0245 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.254+6861G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721581 | ||||||
| chr9:135721584
|
C | A | 1 | a0001c0001t0003g0245 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.254+6864C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721584 | ||||||
| chr9:135721594
|
T | C | 1 | a0001c0001t0003g0245 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.254+6874T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721594 | ||||||
| chr9:135721596
|
T | A | 1 | a0001c0001t0003g0245 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.254+6876T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721596 | ||||||
| chr9:135721616
|
T | A | 1 | a0001c0001t0003g0245 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.254+6896T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721616 | ||||||
| chr9:135721731
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.254+7011G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721731 | ||||||
| chr9:135721808
|
G | T | 1 | a0003c0011t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.254+7088G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721808 | ||||||
| chr9:135721833
|
T | G | 1 | a0001c0001t0003g0245 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.254+7113T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721833 | ||||||
| chr9:135721835
|
T | G | 1 | a0001c0001t0003g0245 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.254+7115T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721835 | ||||||
| chr9:135721838
|
C | CGCACCAG others(4): Show |
1 | a0001c0001t0003g0245 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.254+7118_254+7119i others(13): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721838 | ||||||
| chr9:135721885
|
C | A | 1 | a0001c0001t0003g0245 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.254+7165C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721885 | ||||||
| chr9:135721904
|
G | T | 1 | a0001c0001t0003g0245 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.254+7184G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721904 | ||||||
| chr9:135721962
|
C | T | 2 | a0001c0001t0001g0095a0001c0002t0001g0096 | 2 | HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.254+7242C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721962 | ||||||
| chr9:135721965
|
C | T | 1 | a0001c0001t0003g0245 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.254+7245C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721965 | ||||||
| chr9:135721970
|
C | T | 47 | a0001c0001t0001g0057a0001c0001t0001g0060a0001c0001t0001g0063others(44): Show | 47 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.254+7250C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135721970 | ||||||
| chr9:135722319
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.254+7599G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135722319 | ||||||
| chr9:135722435
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.254+7715G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135722435 | ||||||
| chr9:135722515
|
G | A | 1 | a0001c0003t0001g0022 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.254+7795G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135722515 | ||||||
| chr9:135722664
|
C | T | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.254+7944C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135722664 | ||||||
| chr9:135722668
|
G | A | 1 | a0001c0001t0003g0222 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.254+7948G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135722668 | ||||||
| chr9:135722715
|
G | A | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+7995G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135722715 | ||||||
| chr9:135722727
|
C | T | 1 | a0001c0024t0023g0048 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.254+8007C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135722727 | ||||||
| chr9:135722733
|
C | T | 1 | a0001c0001t0002g0020 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.254+8013C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135722733 | ||||||
| chr9:135722788
|
C | T | 1 | a0001c0003t0031g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.254+8068C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135722788 | ||||||
| chr9:135722952
|
G | C | 1 | a0003c0011t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.254+8232G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135722952 | ||||||
| chr9:135722966
|
G | A | 47 | a0001c0001t0001g0057a0001c0001t0001g0060a0001c0001t0001g0063others(44): Show | 47 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.254+8246G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135722966 | ||||||
| chr9:135723145
|
G | A | 49 | a0001c0001t0001g0038a0001c0001t0001g0183a0001c0001t0001g0221others(46): Show | 49 | HG00544.hp1 HG00609.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.254+8425G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135723145 | ||||||
| chr9:135723159
|
G | A | 252 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0052others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.254+8439G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135723159 | ||||||
| chr9:135723175
|
A | G | 1 | a0001c0001t0013g0176 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.254+8455A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135723175 | ||||||
| chr9:135723256
|
T | G | 1 | a0001c0002t0001g0050 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.254+8536T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135723256 | ||||||
| chr9:135723298
|
G | C | 1 | a0001c0003t0001g0248 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.254+8578G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135723298 | ||||||
| chr9:135723461
|
A | G | 3 | a0001c0002t0001g0014a0001c0002t0008g0026a0001c0027t0009g0268 | 3 | HG02717.hp1 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.254+8741A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135723461 | ||||||
| chr9:135723508
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.254+8788G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135723508 | ||||||
| chr9:135723516
|
G | T | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+8796G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135723516 | ||||||
| chr9:135723551
|
C | T | 2 | a0001c0002t0005g0270a0001c0015t0001g0271 | 2 | HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.254+8831C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135723551 | ||||||
| chr9:135723552
|
G | A | 2 | a0001c0001t0027g0157a0001c0001t0039g0156 | 2 | HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.254+8832G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135723552 | ||||||
| chr9:135723576
|
G | A | 1 | a0001c0001t0003g0168 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.254+8856G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135723576 | ||||||
| chr9:135723594
|
G | A | 12 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0175others(9): Show | 12 | HG01081.hp2 HG01106.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.254+8874G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135723594 | ||||||
| chr9:135723672
|
C | T | 1 | a0001c0002t0001g0244 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.254+8952C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135723672 | ||||||
| chr9:135723680
|
G | A | 1 | a0001c0027t0009g0268 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.254+8960G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135723680 | ||||||
| chr9:135723706
|
G | A | 1 | a0001c0027t0009g0268 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.254+8986G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135723706 | ||||||
| chr9:135723859
|
C | G | 2 | a0001c0003t0001g0151a0001c0003t0010g0148 | 2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.254+9139C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135723859 | ||||||
| chr9:135723915
|
C | T | 1 | a0001c0027t0009g0268 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.254+9195C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135723915 | ||||||
| chr9:135723929
|
G | A | 10 | a0001c0001t0002g0039a0001c0001t0011g0032a0001c0002t0001g0185others(7): Show | 10 | HG01943.hp2 HG02004.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.254+9209G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135723929 | ||||||
| chr9:135723933
|
C | T | 12 | a0001c0001t0001g0019a0001c0001t0002g0020a0001c0001t0008g0008others(9): Show | 12 | HG01074.hp1 HG01099.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.254+9213C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135723933 | ||||||
| chr9:135723987
|
G | A | 1 | a0001c0001t0007g0028 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.254+9267G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135723987 | ||||||
| chr9:135724060
|
C | T | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+9340C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135724060 | ||||||
| chr9:135724120
|
A | G | 181 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0052others(178): Show | 181 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.254+9400A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135724120 | ||||||
| chr9:135724134
|
G | A | 1 | a0001c0003t0013g0068 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.254+9414G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135724134 | ||||||
| chr9:135724144
|
G | C | 1 | a0001c0001t0002g0098 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.254+9424G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135724144 | ||||||
| chr9:135724212
|
T | C | 45 | a0001c0001t0001g0183a0001c0001t0001g0216a0001c0001t0001g0221others(42): Show | 45 | HG00544.hp1 HG00609.hp2 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.254+9492T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135724212 | ||||||
| chr9:135724326
|
C | G | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+9606C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135724326 | ||||||
| chr9:135724474
|
G | C | 1 | a0001c0002t0005g0220 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.254+9754G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135724474 | ||||||
| chr9:135724512
|
A | G | 1 | a0001c0020t0017g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.254+9792A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135724512 | ||||||
| chr9:135724677
|
G | T | 2 | a0001c0001t0001g0186a0001c0004t0001g0187 | 2 | NA18964.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.254+9957G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135724677 | ||||||
| chr9:135724683
|
A | C | 1 | a0001c0027t0009g0268 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.254+9963A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135724683 | ||||||
| chr9:135724757
|
G | T | 3 | a0001c0002t0001g0213a0001c0002t0034g0179a0001c0003t0001g0178 | 3 | HG02080.hp1 NA18959.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.254+10037G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135724757 | ||||||
| chr9:135724762
|
G | A | 1 | a0001c0003t0010g0148 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.254+10042G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135724762 | ||||||
| chr9:135724785
|
G | A | 1 | a0001c0003t0008g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.254+10065G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135724785 | ||||||
| chr9:135724815
|
C | T | 1 | a0001c0024t0023g0048 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.254+10095C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135724815 | ||||||
| chr9:135724837
|
G | A | 1 | a0001c0013t0024g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.254+10117G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135724837 | ||||||
| chr9:135724878
|
C | A | 12 | a0001c0001t0001g0214a0001c0001t0005g0173a0001c0001t0005g0174others(9): Show | 12 | HG01081.hp2 HG01106.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.254+10158C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135724878 | ||||||
| chr9:135724893
|
G | A | 11 | a0001c0001t0001g0216a0001c0001t0001g0238a0001c0001t0002g0098others(8): Show | 11 | HG02071.hp2 NA18747.hp1 NA18945.hp2 others(8): Show |
intron_variant | MODIFIER | c.254+10173G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135724893 | ||||||
| chr9:135724930
|
A | T | 1 | a0001c0001t0001g0204 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.254+10210A>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135724930 | ||||||
| chr9:135725008
|
G | A | 2 | a0001c0001t0001g0042a0001c0002t0001g0041 | 2 | HG02129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.254+10288G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135725008 | ||||||
| chr9:135725050
|
C | T | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+10330C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135725050 | ||||||
| chr9:135725051
|
G | T | 1 | a0001c0001t0002g0142 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.254+10331G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135725051 | ||||||
| chr9:135725144
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.254+10424G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135725144 | ||||||
| chr9:135725160
|
C | T | 1 | a0001c0010t0014g0161 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.254+10440C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135725160 | ||||||
| chr9:135725161
|
G | A | 37 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(34): Show | 37 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.254+10441G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135725161 | ||||||
| chr9:135725171
|
G | A | 37 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(34): Show | 37 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.254+10451G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135725171 | ||||||
| chr9:135725188
|
CG | C | 38 | a0001c0001t0001g0019a0001c0001t0001g0183a0001c0001t0001g0214others(35): Show | 38 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.254+10475delG | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135725188 | |||||
| chr9:135725190
|
G | A | 34 | a0001c0001t0001g0183a0001c0001t0001g0221a0001c0001t0001g0230others(31): Show | 34 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.254+10470G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135725190 | ||||||
| chr9:135725276
|
C | G | 2 | a0001c0003t0001g0267a0001c0003t0008g0043 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.254+10556C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135725276 | ||||||
| chr9:135725444
|
G | A | 2 | a0001c0002t0009g0047a0001c0013t0024g0046 | 2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.254+10724G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135725444 | ||||||
| chr9:135725454
|
G | C | 141 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0052others(138): Show | 141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.254+10734G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135725454 | ||||||
| chr9:135725457
|
T | C | 116 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0057others(113): Show | 116 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.254+10737T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135725457 | ||||||
| chr9:135725464
|
A | G | 3 | a0001c0003t0001g0267a0001c0003t0008g0043a0001c0024t0023g0048 | 3 | HG02647.hp1 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.254+10744A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135725464 | ||||||
| chr9:135725655
|
G | C | 59 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0057others(56): Show | 59 | HG00099.hp1 HG00423.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.254+10935G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135725655 | ||||||
| chr9:135725690
|
C | G | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+10970C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135725690 | ||||||
| chr9:135725740
|
T | C | 1 | a0001c0003t0001g0082 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.254+11020T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135725740 | ||||||
| chr9:135725769
|
C | T | 76 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0057others(73): Show | 76 | HG00099.hp1 HG00423.hp2 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.254+11049C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135725769 | ||||||
| chr9:135725842
|
G | A | 2 | a0001c0002t0009g0047a0001c0013t0024g0046 | 2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.254+11122G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135725842 | ||||||
| chr9:135725845
|
T | A | 1 | a0001c0003t0001g0069 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.254+11125T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135725845 | ||||||
| chr9:135725957
|
G | A | 1 | a0001c0024t0023g0048 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.254+11237G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135725957 | ||||||
| chr9:135725977
|
C | T | 36 | a0001c0001t0001g0183a0001c0001t0001g0221a0001c0001t0001g0230others(33): Show | 36 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.254+11257C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135725977 | ||||||
| chr9:135725987
|
C | G | 2 | a0001c0001t0001g0202a0001c0001t0001g0214 | 2 | HG01243.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.254+11267C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135725987 | ||||||
| chr9:135726048
|
A | G | 2 | a0001c0002t0001g0121a0001c0002t0003g0120 | 2 | HG01358.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.254+11328A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726048 | ||||||
| chr9:135726230
|
C | G | 1 | a0001c0003t0001g0272 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.254+11510C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726230 | ||||||
| chr9:135726295
|
G | A | 2 | a0001c0003t0001g0267a0001c0003t0008g0043 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.254+11575G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726295 | ||||||
| chr9:135726309
|
G | A | 2 | a0001c0003t0001g0267a0001c0003t0008g0043 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.254+11589G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726309 | ||||||
| chr9:135726318
|
G | C | 2 | a0001c0003t0001g0267a0001c0003t0008g0043 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.254+11598G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726318 | ||||||
| chr9:135726399
|
T | A | 1 | a0001c0020t0017g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.254+11679T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726399 | ||||||
| chr9:135726469
|
A | AC | 8 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0002g0078others(5): Show | 8 | HG01243.hp2 HG01361.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.254+11754dupC | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135726469 | |||||
| chr9:135726475
|
A | AC | 4 | a0001c0001t0001g0057a0001c0001t0001g0191a0001c0003t0002g0236others(1): Show | 4 | HG00741.hp1 HG02071.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.254+11759dupC | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135726475 | |||||
| chr9:135726567
|
A | G | 1 | a0001c0003t0001g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.254+11847A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726567 | ||||||
| chr9:135726610
|
G | A | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+11890G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726610 | ||||||
| chr9:135726654
|
T | A | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+11934T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726654 | ||||||
| chr9:135726663
|
C | T | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+11943C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726663 | ||||||
| chr9:135726669
|
A | C | 2 | a0001c0001t0001g0233a0001c0002t0001g0189 | 2 | HG02015.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.254+11949A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726669 | ||||||
| chr9:135726724
|
T | C | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12004T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726724 | ||||||
| chr9:135726729
|
A | C | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12009A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726729 | ||||||
| chr9:135726733
|
T | TTCCCTCC others(5): Show |
1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+12032_254+1204 others(16): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135726733 | |||||
| chr9:135726736
|
C | T | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12016C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726736 | ||||||
| chr9:135726751
|
CCCTCTCT others(15): Show |
C | 38 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(35): Show | 38 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.254+12040_254+1206 others(26): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135726751 | |||||
| chr9:135726752
|
C | T | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12032C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726752 | ||||||
| chr9:135726760
|
C | T | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12040C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726760 | ||||||
| chr9:135726777
|
C | T | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12057C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726777 | ||||||
| chr9:135726784
|
C | T | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12064C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726784 | ||||||
| chr9:135726785
|
G | C | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12065G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726785 | ||||||
| chr9:135726786
|
T | G | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12066T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726786 | ||||||
| chr9:135726789
|
T | C | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12069T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726789 | ||||||
| chr9:135726795
|
T | C | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12075T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726795 | ||||||
| chr9:135726795
|
TTC | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.254+12088_254+1208 others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135726795 | |||||
| chr9:135726800
|
T | C | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12080T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726800 | ||||||
| chr9:135726817
|
T | C | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12097T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726817 | ||||||
| chr9:135726819
|
C | G | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12099C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726819 | ||||||
| chr9:135726821
|
C | A | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12101C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726821 | ||||||
| chr9:135726822
|
A | T | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12102A>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726822 | ||||||
| chr9:135726824
|
T | C | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12104T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726824 | ||||||
| chr9:135726830
|
ACTCTCTC others(5): Show |
A | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+12121_254+1213 others(16): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135726830 | |||||
| chr9:135726838
|
C | A | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12118C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726838 | ||||||
| chr9:135726841
|
G | C | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12121G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726841 | ||||||
| chr9:135726860
|
CCTCT | C | 31 | a0001c0001t0001g0183a0001c0001t0001g0221a0001c0001t0001g0230others(28): Show | 31 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.254+12145_254+1214 others(8): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135726860 | |||||
| chr9:135726878
|
T | TCTCTCTC others(1): Show |
5 | a0001c0001t0001g0015a0001c0001t0003g0016a0001c0003t0001g0018others(2): Show | 5 | HG02735.hp2 HG03453.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.254+12171_254+1217 others(12): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135726878 | |||||
| chr9:135726892
|
T | C | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12172T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726892 | ||||||
| chr9:135726894
|
C | CCT | 37 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(34): Show | 37 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.254+12177_254+1217 others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135726894 | |||||
| chr9:135726894
|
C | T | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12174C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726894 | ||||||
| chr9:135726909
|
C | CTCTCTCT others(9): Show |
3 | a0001c0003t0001g0267a0001c0003t0008g0043a0001c0007t0001g0232 | 3 | HG02647.hp1 NA18522.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.254+12203_254+1220 others(20): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135726909 | |||||
| chr9:135726918
|
C | T | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12198C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726918 | ||||||
| chr9:135726922
|
T | C | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12202T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726922 | ||||||
| chr9:135726923
|
C | CCA | 35 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(32): Show | 35 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.254+12203_254+1220 others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726923 | ||||||
| chr9:135726929
|
C | T | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12209C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726929 | ||||||
| chr9:135726930
|
T | C | 2 | a0001c0001t0026g0123a0001c0002t0001g0206 | 2 | NA18966.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.254+12210T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726930 | ||||||
| chr9:135726932
|
C | CCTCTCTC others(61): Show |
35 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(32): Show | 35 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.254+12215_254+1221 others(72): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135726932 | |||||
| chr9:135726933
|
C | T | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12213C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726933 | ||||||
| chr9:135726936
|
C | G | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12216C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726936 | ||||||
| chr9:135726940
|
T | TCTCTCCC others(53): Show |
1 | a0001c0004t0001g0092 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.254+12221_254+1222 others(64): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135726940 | |||||
| chr9:135726942
|
C | CCTCTCTT others(19): Show |
2 | a0001c0001t0002g0188a0001c0002t0001g0201 | 2 | NA18962.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.254+12239_254+1224 others(30): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135726942 | |||||
| chr9:135726942
|
C | CCTCTCTT others(28): Show |
1 | a0001c0001t0002g0039 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.254+12239_254+1224 others(39): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135726942 | |||||
| chr9:135726942
|
C | CCTCTCTT others(27): Show |
210 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0038others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.254+12239_254+1224 others(38): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135726942 | |||||
| chr9:135726942
|
C | CCTCTCTT others(85): Show |
1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+12239_254+1224 others(96): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135726942 | |||||
| chr9:135726942
|
C | T | 1 | a0001c0004t0001g0092 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.254+12222C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726942 | ||||||
| chr9:135726944
|
T | G | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12224T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726944 | ||||||
| chr9:135726950
|
T | C | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12230T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726950 | ||||||
| chr9:135726953
|
C | G | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12233C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726953 | ||||||
| chr9:135726959
|
C | CTCTCTCC others(26): Show |
2 | a0001c0001t0001g0067a0001c0002t0035g0109 | 2 | HG01070.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.254+12239_254+1224 others(37): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726959 | ||||||
| chr9:135726960
|
C | T | 5 | a0001c0001t0001g0166a0001c0002t0001g0189a0001c0003t0001g0267others(2): Show | 5 | HG01257.hp1 HG02015.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.254+12240C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726960 | ||||||
| chr9:135726965
|
C | CCCTCTCT others(26): Show |
1 | a0001c0001t0001g0166 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.254+12252_254+1225 others(37): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135726965 | |||||
| chr9:135726966
|
C | T | 3 | a0001c0003t0001g0267a0001c0003t0008g0043a0001c0007t0001g0232 | 3 | HG02647.hp1 NA18522.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.254+12246C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726966 | ||||||
| chr9:135726970
|
T | C | 3 | a0001c0003t0001g0267a0001c0003t0008g0043a0001c0007t0001g0232 | 3 | HG02647.hp1 NA18522.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.254+12250T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726970 | ||||||
| chr9:135726973
|
T | C | 3 | a0001c0003t0001g0267a0001c0003t0008g0043a0001c0007t0001g0232 | 3 | HG02647.hp1 NA18522.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.254+12253T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726973 | ||||||
| chr9:135726974
|
T | G | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12254T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726974 | ||||||
| chr9:135726976
|
C | T | 3 | a0001c0003t0001g0267a0001c0003t0008g0043a0001c0007t0001g0232 | 3 | HG02647.hp1 NA18522.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.254+12256C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726976 | ||||||
| chr9:135726978
|
A | C | 2 | a0001c0003t0001g0267a0001c0003t0008g0043 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.254+12258A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726978 | ||||||
| chr9:135726978
|
A | T | 1 | a0001c0007t0001g0232 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.254+12258A>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726978 | ||||||
| chr9:135726979
|
T | C | 2 | a0001c0003t0001g0267a0001c0003t0008g0043 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.254+12259T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726979 | ||||||
| chr9:135726982
|
T | C | 1 | a0001c0007t0001g0232 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.254+12262T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726982 | ||||||
| chr9:135726984
|
T | A | 1 | a0001c0007t0001g0232 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.254+12264T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726984 | ||||||
| chr9:135726984
|
T | C | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12264T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726984 | ||||||
| chr9:135726985
|
C | T | 1 | a0001c0007t0001g0232 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.254+12265C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726985 | ||||||
| chr9:135726986
|
T | G | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12266T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726986 | ||||||
| chr9:135726987
|
C | T | 2 | a0001c0003t0001g0267a0001c0003t0008g0043 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.254+12267C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726987 | ||||||
| chr9:135726990
|
C | T | 40 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0111others(37): Show | 40 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.254+12270C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726990 | ||||||
| chr9:135726992
|
T | A | 2 | a0001c0003t0001g0267a0001c0003t0008g0043 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.254+12272T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726992 | ||||||
| chr9:135726992
|
T | TCC | 40 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0111others(37): Show | 40 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.254+12273_254+1227 others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135726992 | |||||
| chr9:135726993
|
C | T | 2 | a0001c0003t0001g0267a0001c0003t0008g0043 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.254+12273C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726993 | ||||||
| chr9:135726998
|
C | T | 40 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0111others(37): Show | 40 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.254+12278C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135726998 | ||||||
| chr9:135727000
|
T | C | 41 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0111others(38): Show | 41 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.254+12280T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727000 | ||||||
| chr9:135727005
|
C | G | 5 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0111others(2): Show | 5 | HG01168.hp1 HG01257.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.254+12285C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727005 | ||||||
| chr9:135727018
|
C | T | 40 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0111others(37): Show | 40 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.254+12298C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727018 | ||||||
| chr9:135727020
|
T | C | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12300T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727020 | ||||||
| chr9:135727034
|
C | T | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12314C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727034 | ||||||
| chr9:135727035
|
C | G | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12315C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727035 | ||||||
| chr9:135727036
|
A | T | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12316A>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727036 | ||||||
| chr9:135727040
|
T | C | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12320T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727040 | ||||||
| chr9:135727042
|
T | A | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12322T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727042 | ||||||
| chr9:135727046
|
T | TCTCC | 40 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0111others(37): Show | 40 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.254+12329_254+1233 others(8): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727046 | |||||
| chr9:135727052
|
C | CAT | 5 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0111others(2): Show | 5 | HG01168.hp1 HG01257.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.254+12332_254+1233 others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727052 | ||||||
| chr9:135727054
|
T | TCC | 35 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(32): Show | 35 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.254+12335_254+1233 others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727054 | |||||
| chr9:135727065
|
G | C | 44 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0111others(41): Show | 44 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.254+12345G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727065 | ||||||
| chr9:135727067
|
T | C | 35 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(32): Show | 35 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.254+12347T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727067 | ||||||
| chr9:135727067
|
T | G | 6 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0111others(3): Show | 6 | HG01168.hp1 HG01257.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.254+12347T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727067 | ||||||
| chr9:135727068
|
T | C | 40 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0111others(37): Show | 40 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.254+12348T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727068 | ||||||
| chr9:135727069
|
C | A | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12349C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727069 | ||||||
| chr9:135727070
|
C | T | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12350C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727070 | ||||||
| chr9:135727072
|
A | C | 41 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0111others(38): Show | 41 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.254+12352A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727072 | ||||||
| chr9:135727073
|
T | A | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12353T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727073 | ||||||
| chr9:135727075
|
C | T | 40 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0111others(37): Show | 40 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.254+12355C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727075 | ||||||
| chr9:135727078
|
T | TCCCCC | 40 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0111others(37): Show | 40 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.254+12359_254+1236 others(9): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727078 | |||||
| chr9:135727086
|
T | TCC | 40 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0111others(37): Show | 40 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.254+12367_254+1236 others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727086 | |||||
| chr9:135727086
|
T | TCTCTTTC others(67): Show |
2 | a0001c0001t0002g0039a0001c0003t0002g0236 | 2 | HG02071.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.254+12370_254+1237 others(78): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727086 | |||||
| chr9:135727086
|
T | TCTCTTTC others(66): Show |
220 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0031others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.254+12370_254+1237 others(77): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727086 | |||||
| chr9:135727086
|
T | TCTCTTTC others(67): Show |
1 | a0001c0004t0004g0025 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.254+12370_254+1237 others(78): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727086 | |||||
| chr9:135727086
|
T | TCTCTTTC others(65): Show |
3 | a0001c0001t0001g0067a0001c0001t0001g0204a0001c0002t0035g0109 | 3 | HG01070.hp1 NA18945.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.254+12370_254+1237 others(76): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727086 | |||||
| chr9:135727086
|
T | TCTCTTTC others(67): Show |
1 | a0001c0007t0001g0232 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.254+12370_254+1237 others(78): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727086 | |||||
| chr9:135727086
|
T | TCTCTTTC others(66): Show |
2 | a0001c0003t0001g0267a0001c0003t0008g0043 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.254+12370_254+1237 others(77): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727086 | |||||
| chr9:135727086
|
T | TCTCTTTC others(68): Show |
1 | a0001c0001t0002g0188 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.254+12370_254+1237 others(79): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727086 | |||||
| chr9:135727091
|
C | G | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12371C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727091 | ||||||
| chr9:135727092
|
T | C | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12372T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727092 | ||||||
| chr9:135727097
|
C | A | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12377C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727097 | ||||||
| chr9:135727099
|
T | A | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12379T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727099 | ||||||
| chr9:135727100
|
T | C | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12380T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727100 | ||||||
| chr9:135727101
|
C | T | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12381C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727101 | ||||||
| chr9:135727105
|
T | C | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12385T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727105 | ||||||
| chr9:135727106
|
T | C | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12386T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727106 | ||||||
| chr9:135727110
|
T | TC | 38 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(35): Show | 38 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.254+12394dupC | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727110 | |||||
| chr9:135727113
|
C | A | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12393C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727113 | ||||||
| chr9:135727114
|
C | G | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12394C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727114 | ||||||
| chr9:135727117
|
T | G | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12397T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727117 | ||||||
| chr9:135727119
|
C | T | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12399C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727119 | ||||||
| chr9:135727125
|
T | TCTGCTGA others(4): Show |
1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12406_254+1240 others(15): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727125 | |||||
| chr9:135727127
|
C | CCTCTCTC others(13): Show |
37 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(34): Show | 37 | HG00544.hp1 HG00609.hp2 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.254+12418_254+1241 others(24): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727127 | |||||
| chr9:135727130
|
C | T | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12410C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727130 | ||||||
| chr9:135727136
|
C | T | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12416C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727136 | ||||||
| chr9:135727137
|
T | C | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12417T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727137 | ||||||
| chr9:135727139
|
C | T | 1 | a0001c0001t0005g0175 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.254+12419C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727139 | ||||||
| chr9:135727143
|
T | TACCTCTC others(12): Show |
1 | a0001c0001t0005g0175 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.254+12423_254+1242 others(23): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727143 | ||||||
| chr9:135727144
|
T | C | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12424T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727144 | ||||||
| chr9:135727145
|
C | T | 1 | a0001c0001t0005g0175 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.254+12425C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727145 | ||||||
| chr9:135727147
|
T | C | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12427T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727147 | ||||||
| chr9:135727149
|
T | TCGAACCA others(51): Show |
1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12430_254+1243 others(62): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727149 | |||||
| chr9:135727151
|
T | TC | 78 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0038others(75): Show | 78 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.254+12438dupC | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727151 | |||||
| chr9:135727157
|
C | CCCTCCCT others(6): Show |
1 | a0001c0001t0013g0176 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.254+12438_254+1243 others(17): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727157 | |||||
| chr9:135727157
|
C | CCTCCCTC others(5): Show |
33 | a0001c0001t0001g0183a0001c0001t0001g0221a0001c0001t0001g0230others(30): Show | 33 | HG00544.hp1 HG00609.hp2 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.254+12444_254+1244 others(16): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727157 | |||||
| chr9:135727157
|
C | CTCCCTCT others(4): Show |
1 | a0001c0002t0005g0220 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.254+12437_254+1243 others(15): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727157 | ||||||
| chr9:135727158
|
C | G | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+12438C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727158 | ||||||
| chr9:135727159
|
T | C | 3 | a0001c0002t0001g0189a0001c0002t0040g0160a0001c0003t0001g0252 | 3 | HG01891.hp1 HG02015.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.254+12439T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727159 | ||||||
| chr9:135727160
|
C | T | 1 | a0001c0002t0040g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.254+12440C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727160 | ||||||
| chr9:135727163
|
TC | T | 12 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(9): Show | 12 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(9): Show |
intron_variant | MODIFIER | c.254+12449delC | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727163 | |||||
| chr9:135727164
|
C | CTCCCTCT others(4): Show |
1 | a0001c0001t0005g0175 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.254+12444_254+1244 others(15): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727164 | ||||||
| chr9:135727169
|
CT | C | 3 | a0001c0003t0001g0069a0001c0003t0001g0248a0001c0003t0002g0247 | 3 | HG00140.hp2 HG00280.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.254+12452delT | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727169 | |||||
| chr9:135727184
|
T | C | 38 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(35): Show | 38 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.254+12464T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727184 | ||||||
| chr9:135727195
|
TTC | T | 2 | a0001c0001t0001g0085a0001c0003t0001g0035 | 2 | HG00733.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.254+12484_254+1248 others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727195 | |||||
| chr9:135727203
|
C | T | 39 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(36): Show | 39 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.254+12483C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727203 | ||||||
| chr9:135727212
|
C | T | 1 | a0001c0001t0002g0039 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.254+12492C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727212 | ||||||
| chr9:135727212
|
CCT | C | 38 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(35): Show | 38 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.254+12505_254+1250 others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727212 | |||||
| chr9:135727214
|
T | C | 1 | a0001c0001t0002g0039 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.254+12494T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727214 | ||||||
| chr9:135727233
|
TTC | T | 142 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0052others(139): Show | 142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.254+12520_254+1252 others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727233 | |||||
| chr9:135727240
|
T | TCC | 35 | a0001c0001t0001g0183a0001c0001t0001g0221a0001c0001t0001g0230others(32): Show | 35 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.254+12524_254+1252 others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727240 | |||||
| chr9:135727246
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.254+12526T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727246 | ||||||
| chr9:135727248
|
T | A | 1 | a0001c0003t0008g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.254+12528T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727248 | ||||||
| chr9:135727260
|
T | G | 1 | a0001c0004t0001g0092 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.254+12540T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727260 | ||||||
| chr9:135727292
|
CCT | C | 36 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(33): Show | 36 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.254+12573_254+1257 others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727292 | ||||||
| chr9:135727298
|
CCT | C | 38 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(35): Show | 38 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.254+12583_254+1258 others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727298 | |||||
| chr9:135727301
|
C | T | 36 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(33): Show | 36 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.254+12581C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727301 | ||||||
| chr9:135727324
|
CCT | C | 5 | a0001c0001t0001g0216a0001c0002t0001g0185a0001c0003t0001g0035others(2): Show | 5 | HG01943.hp2 HG02056.hp2 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.254+12610_254+1261 others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727324 | |||||
| chr9:135727369
|
C | T | 4 | a0001c0003t0001g0022a0001c0003t0006g0023a0001c0004t0004g0025others(1): Show | 4 | HG00741.hp2 HG02572.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.254+12649C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727369 | ||||||
| chr9:135727372
|
C | CCTCTCCC others(3): Show |
1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+12670_254+1267 others(14): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727372 | |||||
| chr9:135727390
|
T | TCTCTCTC others(3): Show |
1 | a0001c0003t0002g0153 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.254+12680_254+1268 others(14): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727390 | |||||
| chr9:135727396
|
TC | T | 3 | a0001c0001t0001g0166a0001c0002t0035g0109a0001c0009t0018g0162 | 3 | HG01257.hp1 HG02897.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.254+12679delC | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727396 | |||||
| chr9:135727408
|
C | CCT | 37 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(34): Show | 37 | HG00544.hp1 HG00609.hp2 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.254+12693_254+1269 others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727408 | |||||
| chr9:135727426
|
T | C | 1 | a0001c0002t0002g0145 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.254+12706T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727426 | ||||||
| chr9:135727437
|
C | CCT | 49 | a0001c0001t0001g0038a0001c0001t0001g0057a0001c0001t0001g0060others(46): Show | 49 | HG00099.hp1 HG00423.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.254+12734_254+1273 others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135727437 | |||||
| chr9:135727460
|
C | G | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.254+12740C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727460 | ||||||
| chr9:135727470
|
CT | C | 19 | a0001c0001t0001g0216a0001c0001t0002g0039a0001c0001t0011g0032others(16): Show | 19 | HG01891.hp1 HG01943.hp2 HG02004.hp1 others(16): Show |
intron_variant | MODIFIER | c.254+12751delT | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727470 | ||||||
| chr9:135727570
|
G | A | 1 | a0001c0004t0002g0125 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.254+12850G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727570 | ||||||
| chr9:135727620
|
T | C | 39 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(36): Show | 39 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.254+12900T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727620 | ||||||
| chr9:135727663
|
G | A | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+12943G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727663 | ||||||
| chr9:135727697
|
A | G | 112 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0057others(109): Show | 112 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.254+12977A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727697 | ||||||
| chr9:135727802
|
T | C | 37 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(34): Show | 37 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.254+13082T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727802 | ||||||
| chr9:135727846
|
T | C | 2 | a0001c0001t0001g0214a0003c0011t0001g0044 | 2 | HG02895.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.254+13126T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727846 | ||||||
| chr9:135727881
|
GCTGTGCA others(6): Show |
G | 1 | a0001c0004t0004g0025 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.254+13162_254+1317 others(17): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727881 | ||||||
| chr9:135727965
|
C | T | 1 | a0003c0011t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.254+13245C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135727965 | ||||||
| chr9:135728016
|
C | T | 3 | a0001c0003t0001g0267a0001c0003t0008g0043a0001c0013t0024g0046 | 3 | HG02451.hp2 HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.254+13296C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135728016 | ||||||
| chr9:135728129
|
C | T | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+13409C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135728129 | ||||||
| chr9:135728179
|
C | T | 259 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0038others(256): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.254+13459C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135728179 | ||||||
| chr9:135728222
|
T | A | 1 | a0001c0001t0002g0188 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.254+13502T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135728222 | ||||||
| chr9:135728275
|
G | T | 1 | a0001c0004t0001g0092 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.254+13555G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135728275 | ||||||
| chr9:135728282
|
G | A | 2 | a0001c0003t0001g0267a0001c0003t0008g0043 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.254+13562G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135728282 | ||||||
| chr9:135728318
|
C | T | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.254+13598C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135728318 | ||||||
| chr9:135728460
|
G | A | 1 | a0001c0007t0001g0232 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.254+13740G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135728460 | ||||||
| chr9:135728479
|
G | A | 7 | a0001c0001t0001g0204a0001c0001t0001g0250a0001c0002t0001g0211others(4): Show | 7 | HG02165.hp1 NA18945.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.254+13759G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135728479 | ||||||
| chr9:135728547
|
C | T | 2 | a0001c0002t0009g0047a0001c0013t0024g0046 | 2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.254+13827C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135728547 | ||||||
| chr9:135728683
|
G | A | 36 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(33): Show | 36 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.254+13963G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135728683 | ||||||
| chr9:135728740
|
G | A | 2 | a0001c0003t0001g0267a0001c0003t0008g0043 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.254+14020G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135728740 | ||||||
| chr9:135728836
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0003g0181 | 2 | HG02486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.254+14116C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135728836 | ||||||
| chr9:135728900
|
C | A | 1 | a0001c0026t0001g0051 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.254+14180C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135728900 | ||||||
| chr9:135728903
|
G | A | 1 | a0001c0003t0008g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.254+14183G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135728903 | ||||||
| chr9:135729045
|
A | G | 37 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(34): Show | 37 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.254+14325A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135729045 | ||||||
| chr9:135729217
|
G | A | 1 | a0001c0010t0014g0161 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.254+14497G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135729217 | ||||||
| chr9:135729280
|
T | C | 38 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(35): Show | 38 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.254+14560T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135729280 | ||||||
| chr9:135729298
|
G | A | 35 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(32): Show | 35 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.254+14578G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135729298 | ||||||
| chr9:135729307
|
T | C | 116 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0057others(113): Show | 116 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.254+14587T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135729307 | ||||||
| chr9:135729436
|
T | C | 5 | a0001c0001t0001g0015a0001c0001t0003g0016a0001c0003t0001g0018others(2): Show | 5 | HG02735.hp2 HG03453.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.254+14716T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135729436 | ||||||
| chr9:135729601
|
G | A | 34 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(31): Show | 34 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.254+14881G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135729601 | ||||||
| chr9:135729813
|
G | A | 2 | a0001c0004t0004g0224a0004c0017t0004g0223 | 2 | HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.254+15093G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135729813 | ||||||
| chr9:135729890
|
C | T | 1 | a0001c0003t0003g0059 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.254+15170C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135729890 | ||||||
| chr9:135729897
|
T | A | 1 | a0001c0001t0001g0214 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.254+15177T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135729897 | ||||||
| chr9:135729933
|
C | T | 6 | a0001c0001t0027g0157a0001c0002t0040g0160a0001c0009t0006g0159others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.254+15213C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135729933 | ||||||
| chr9:135729934
|
G | A | 141 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0052others(138): Show | 141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.254+15214G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135729934 | ||||||
| chr9:135729968
|
C | A | 1 | a0001c0004t0002g0147 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.254+15248C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135729968 | ||||||
| chr9:135730038
|
C | T | 2 | a0001c0003t0001g0267a0001c0003t0008g0043 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.254+15318C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135730038 | ||||||
| chr9:135730051
|
C | T | 1 | a0001c0002t0035g0109 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.254+15331C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135730051 | ||||||
| chr9:135730139
|
C | T | 1 | a0001c0004t0002g0147 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.254+15419C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135730139 | ||||||
| chr9:135730151
|
T | C | 1 | a0001c0003t0008g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.254+15431T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135730151 | ||||||
| chr9:135730344
|
A | ACTATGTA others(29): Show |
1 | a0001c0003t0001g0127 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.254+15625_254+1566 others(40): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135730344 | |||||
| chr9:135730479
|
G | T | 1 | a0001c0003t0002g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.254+15759G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135730479 | ||||||
| chr9:135730613
|
C | G | 1 | a0001c0003t0001g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.254+15893C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135730613 | ||||||
| chr9:135730727
|
T | C | 1 | a0001c0001t0022g0193 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.254+16007T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135730727 | ||||||
| chr9:135730811
|
C | A | 2 | a0001c0003t0001g0267a0001c0003t0008g0043 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.254+16091C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135730811 | ||||||
| chr9:135730990
|
T | A | 1 | a0001c0003t0008g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.254+16270T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135730990 | ||||||
| chr9:135730990
|
T | TA | 43 | a0001c0001t0001g0031a0001c0001t0001g0055a0001c0001t0001g0056others(40): Show | 43 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.254+16293dupA | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135730990 | |||||
| chr9:135730990
|
T | TAA | 19 | a0001c0001t0001g0085a0001c0001t0002g0188a0001c0001t0007g0028others(16): Show | 19 | HG00733.hp2 HG01891.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.254+16292_254+1629 others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135730990 | |||||
| chr9:135730990
|
T | TAAA | 39 | a0001c0001t0001g0038a0001c0001t0001g0057a0001c0001t0001g0060others(36): Show | 39 | HG00099.hp1 HG00423.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.254+16291_254+1629 others(7): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135730990 | |||||
| chr9:135730990
|
T | TAAAA | 11 | a0001c0001t0001g0063a0001c0001t0001g0088a0001c0001t0001g0099others(8): Show | 11 | HG01099.hp2 HG01257.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.254+16290_254+1629 others(8): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135730990 | |||||
| chr9:135730990
|
T | TAAAAAAA others(5): Show |
1 | a0001c0001t0001g0214 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.254+16282_254+1629 others(16): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135730990 | |||||
| chr9:135730990
|
T | TAAAAAAA others(21): Show |
1 | a0003c0011t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.254+16293_254+1629 others(32): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135730990 | |||||
| chr9:135730990
|
T | TGAAAAAA others(1): Show |
15 | a0001c0001t0001g0230a0001c0001t0003g0222a0001c0001t0005g0174others(12): Show | 15 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.254+16270_254+1627 others(12): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135730990 | ||||||
| chr9:135730990
|
T | TGAAAAAA others(2): Show |
13 | a0001c0001t0001g0183a0001c0001t0001g0221a0001c0001t0001g0233others(10): Show | 13 | HG01106.hp2 HG01358.hp1 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.254+16270_254+1627 others(13): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135730990 | ||||||
| chr9:135730990
|
T | TGAAAAAA others(3): Show |
2 | a0001c0002t0002g0219a0001c0004t0012g0225 | 2 | HG00609.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.254+16270_254+1627 others(14): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135730990 | ||||||
| chr9:135730990
|
TA | T | 14 | a0001c0001t0001g0019a0001c0001t0015g0103a0001c0002t0001g0185others(11): Show | 14 | HG01192.hp1 HG01192.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.254+16293delA | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135730990 | |||||
| chr9:135730990
|
TAAAAAAA others(3): Show |
T | 1 | a0001c0002t0001g0172 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.254+16284_254+1629 others(14): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135730990 | |||||
| chr9:135730996
|
A | G | 1 | a0001c0013t0024g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.254+16276A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135730996 | ||||||
| chr9:135731150
|
C | T | 1 | a0001c0004t0020g0215 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.254+16430C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731150 | ||||||
| chr9:135731212
|
T | A | 1 | a0001c0002t0011g0083 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.254+16492T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731212 | ||||||
| chr9:135731276
|
C | T | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+16556C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731276 | ||||||
| chr9:135731277
|
G | A | 1 | a0001c0003t0002g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.254+16557G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731277 | ||||||
| chr9:135731284
|
G | A | 1 | a0001c0003t0001g0035 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.254+16564G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731284 | ||||||
| chr9:135731323
|
C | G | 1 | a0001c0003t0002g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.254+16603C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731323 | ||||||
| chr9:135731481
|
C | T | 1 | a0001c0003t0001g0036 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.254+16761C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731481 | ||||||
| chr9:135731492
|
C | G | 1 | a0001c0003t0002g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.254+16772C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731492 | ||||||
| chr9:135731492
|
C | T | 1 | a0001c0003t0001g0108 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.254+16772C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731492 | ||||||
| chr9:135731594
|
G | A | 1 | a0001c0001t0002g0143 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.254+16874G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731594 | ||||||
| chr9:135731614
|
G | A | 35 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(32): Show | 35 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.254+16894G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731614 | ||||||
| chr9:135731661
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.254+16941C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731661 | ||||||
| chr9:135731694
|
C | A | 1 | a0001c0002t0001g0201 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.254+16974C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731694 | ||||||
| chr9:135731695
|
A | T | 1 | a0001c0002t0001g0201 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.254+16975A>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731695 | ||||||
| chr9:135731803
|
T | C | 1 | a0001c0003t0001g0084 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.254+17083T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731803 | ||||||
| chr9:135731834
|
G | C | 1 | a0001c0002t0001g0213 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.254+17114G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731834 | ||||||
| chr9:135731835
|
C | G | 1 | a0001c0002t0001g0213 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.254+17115C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731835 | ||||||
| chr9:135731840
|
G | A | 38 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(35): Show | 38 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.254+17120G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731840 | ||||||
| chr9:135731847
|
A | G | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+17127A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731847 | ||||||
| chr9:135731857
|
A | G | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+17137A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731857 | ||||||
| chr9:135731901
|
C | T | 1 | a0003c0011t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.254+17181C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731901 | ||||||
| chr9:135731957
|
C | T | 1 | a0001c0003t0001g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.254+17237C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731957 | ||||||
| chr9:135731957
|
CGTGTATA others(4): Show |
C | 1 | a0001c0002t0001g0213 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.254+17238_254+1724 others(15): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731957 | ||||||
| chr9:135731959
|
T | G | 1 | a0001c0002t0011g0083 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.254+17239T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731959 | ||||||
| chr9:135731960
|
G | GTA | 3 | a0001c0001t0001g0088a0001c0001t0001g0099a0001c0001t0001g0234 | 3 | HG01258.hp2 HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.254+17271_254+1727 others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731960 | |||||
| chr9:135731960
|
G | GTATA | 3 | a0001c0001t0001g0063a0001c0001t0002g0020a0001c0001t0002g0237 | 3 | HG01099.hp2 NA18906.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.254+17269_254+1727 others(8): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731960 | |||||
| chr9:135731960
|
G | GTATATAT others(1): Show |
3 | a0001c0001t0001g0015a0001c0003t0001g0108a0006c0018t0001g0061 | 3 | HG01433.hp2 HG02735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.254+17265_254+1727 others(12): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731960 | |||||
| chr9:135731960
|
G | GTATATAT others(3): Show |
6 | a0001c0001t0001g0062a0001c0001t0002g0239a0001c0001t0027g0157others(3): Show | 6 | HG00323.hp1 HG01361.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.254+17263_254+1727 others(14): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731960 | |||||
| chr9:135731960
|
G | GTATATAT others(5): Show |
4 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0003g0016others(1): Show | 4 | HG00738.hp2 HG01515.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.254+17261_254+1727 others(16): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731960 | |||||
| chr9:135731960
|
G | GTATATAT others(7): Show |
1 | a0001c0004t0001g0263 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.254+17259_254+1727 others(18): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731960 | |||||
| chr9:135731960
|
G | GTATATAT others(9): Show |
2 | a0001c0001t0001g0238a0001c0001t0003g0218 | 2 | HG03688.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.254+17257_254+1727 others(20): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731960 | |||||
| chr9:135731960
|
GTATA | G | 4 | a0001c0002t0008g0026a0001c0002t0009g0047a0001c0013t0024g0046others(1): Show | 4 | HG02451.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.254+17269_254+1727 others(8): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731960 | |||||
| chr9:135731960
|
GTATATAT others(1): Show |
G | 30 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(27): Show | 30 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.254+17265_254+1727 others(12): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731960 | |||||
| chr9:135731961
|
T | G | 1 | a0001c0002t0011g0083 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.254+17241T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731961 | ||||||
| chr9:135731962
|
A | T | 1 | a0001c0002t0011g0083 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.254+17242A>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731962 | ||||||
| chr9:135731963
|
T | G | 1 | a0001c0002t0011g0083 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.254+17243T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731963 | ||||||
| chr9:135731969
|
T | TGAGTATG others(7): Show |
1 | a0001c0002t0011g0083 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.254+17249_254+1725 others(18): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731969 | ||||||
| chr9:135731970
|
A | G | 1 | a0001c0002t0001g0213 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.254+17250A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731970 | ||||||
| chr9:135731979
|
T | G | 1 | a0001c0003t0008g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.254+17259T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731979 | ||||||
| chr9:135731981
|
T | A | 1 | a0001c0004t0001g0092 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.254+17261T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731981 | ||||||
| chr9:135731981
|
T | G | 3 | a0001c0002t0008g0026a0001c0003t0008g0043a0003c0011t0001g0044 | 3 | HG03516.hp2 NA18522.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.254+17261T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731981 | ||||||
| chr9:135731981
|
TATATATA others(7): Show |
T | 1 | a0001c0004t0007g0006 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.254+17263_254+1727 others(18): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731981 | |||||
| chr9:135731981
|
TATATATA others(9): Show |
T | 1 | a0001c0002t0006g0054 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.254+17263_254+1727 others(20): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731981 | |||||
| chr9:135731983
|
T | G | 15 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00609.hp2 HG01081.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.254+17263T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731983 | ||||||
| chr9:135731983
|
TATATATA others(5): Show |
T | 1 | a0001c0002t0001g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.254+17265_254+1727 others(16): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731983 | |||||
| chr9:135731985
|
T | G | 32 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0230others(29): Show | 32 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.254+17265T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731985 | ||||||
| chr9:135731985
|
T | TAGAGAGA others(1): Show |
3 | a0001c0003t0003g0059a0001c0003t0006g0023a0001c0004t0004g0255 | 3 | HG00099.hp1 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.254+17266_254+1726 others(12): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731985 | |||||
| chr9:135731985
|
T | TAGAGAGA others(3): Show |
1 | a0001c0003t0001g0035 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.254+17266_254+1726 others(14): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731985 | |||||
| chr9:135731985
|
T | TAGAGAGA others(9): Show |
1 | a0001c0025t0001g0113 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.254+17266_254+1726 others(20): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731985 | |||||
| chr9:135731985
|
TATATATA others(5): Show |
T | 2 | a0001c0004t0001g0005a0001c0004t0001g0007 | 2 | HG01074.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.254+17267_254+1727 others(16): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731985 | |||||
| chr9:135731985
|
TATATATA others(7): Show |
T | 1 | a0001c0004t0002g0045 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.254+17267_254+1728 others(18): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731985 | |||||
| chr9:135731987
|
T | G | 50 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0183others(47): Show | 50 | HG00099.hp1 HG00544.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.254+17267T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731987 | ||||||
| chr9:135731987
|
T | TAGAGAGA others(7): Show |
1 | a0001c0004t0008g0203 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.254+17268_254+1726 others(18): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731987 | |||||
| chr9:135731987
|
T | TAGAGAGA others(9): Show |
1 | a0001c0001t0002g0039 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.254+17268_254+1726 others(20): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731987 | |||||
| chr9:135731987
|
TATATAGA others(3): Show |
T | 1 | a0001c0003t0001g0064 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.254+17269_254+1727 others(14): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731987 | |||||
| chr9:135731987
|
TATATAGA others(7): Show |
T | 1 | a0001c0024t0023g0048 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.254+17269_254+1728 others(18): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731987 | |||||
| chr9:135731987
|
TATATAGA others(9): Show |
T | 2 | a0001c0002t0001g0154a0001c0004t0037g0004 | 2 | HG01099.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.254+17269_254+1728 others(20): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731987 | |||||
| chr9:135731989
|
T | G | 56 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0183others(53): Show | 56 | HG00099.hp1 HG00544.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.254+17269T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731989 | ||||||
| chr9:135731989
|
T | TAGAGAGA others(7): Show |
1 | a0001c0002t0002g0114 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.254+17270_254+1727 others(18): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731989 | |||||
| chr9:135731989
|
T | TAGAGAGA others(11): Show |
1 | a0001c0003t0001g0037 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.254+17270_254+1727 others(22): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731989 | |||||
| chr9:135731989
|
TATAGAGA others(5): Show |
T | 1 | a0001c0001t0008g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.254+17271_254+1728 others(16): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731989 | |||||
| chr9:135731991
|
T | G | 68 | a0001c0001t0001g0141a0001c0001t0001g0165a0001c0001t0001g0166others(65): Show | 68 | HG00099.hp1 HG00544.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.254+17271T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731991 | ||||||
| chr9:135731991
|
T | TAGAGAGA others(3): Show |
1 | a0001c0002t0001g0264 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.254+17312_254+1732 others(14): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TAGAGAGA others(5): Show |
1 | a0001c0002t0002g0021 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.254+17310_254+1732 others(16): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TAGAGAGA others(7): Show |
1 | a0001c0004t0004g0025 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.254+17308_254+1732 others(18): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TAGAGAGA others(9): Show |
1 | a0001c0001t0016g0254 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.254+17306_254+1732 others(20): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TAGAGAGA others(11): Show |
1 | a0001c0001t0001g0190 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.254+17304_254+1732 others(22): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TAGAGAGA others(15): Show |
1 | a0001c0001t0001g0111 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.254+17300_254+1732 others(26): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATAGAGA others(3): Show |
3 | a0001c0001t0001g0038a0001c0001t0002g0266a0001c0009t0006g0159 | 3 | HG00438.hp1 HG01081.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.254+17272_254+1727 others(14): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATAGAGA others(5): Show |
5 | a0001c0001t0001g0122a0001c0001t0002g0049a0001c0003t0001g0036others(2): Show | 5 | HG00733.hp1 HG01346.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.254+17272_254+1727 others(16): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATAGAGA others(7): Show |
5 | a0001c0001t0001g0074a0001c0001t0002g0098a0001c0002t0002g0107others(2): Show | 5 | HG00423.hp2 HG02055.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.254+17272_254+1727 others(18): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATAGAGA others(11): Show |
1 | a0001c0004t0001g0195 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.254+17272_254+1727 others(22): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATAGAGA others(13): Show |
1 | a0001c0003t0010g0148 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(24): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATAGAGA others(15): Show |
3 | a0001c0001t0002g0196a0001c0001t0043g0197a0001c0005t0001g0207 | 3 | HG01978.hp2 HG02155.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.254+17272_254+1727 others(26): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATAGAGA others(17): Show |
2 | a0001c0002t0035g0109a0001c0003t0002g0192 | 2 | HG02071.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.254+17272_254+1727 others(28): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATAGAGA others(19): Show |
4 | a0001c0001t0001g0204a0001c0003t0002g0247a0001c0004t0001g0133others(1): Show | 4 | HG03225.hp2 NA18945.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.254+17272_254+1727 others(30): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATAGAGA others(21): Show |
2 | a0001c0003t0001g0210a0001c0004t0002g0125 | 2 | NA18969.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.254+17272_254+1727 others(32): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATAGAGA others(25): Show |
1 | a0001c0026t0001g0051 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.254+17272_254+1727 others(36): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATAGAGA others(27): Show |
3 | a0001c0001t0001g0132a0001c0002t0001g0205a0001c0003t0001g0082 | 3 | HG00438.hp2 HG01496.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.254+17272_254+1727 others(38): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATAGA others(5): Show |
1 | a0001c0003t0002g0101 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.254+17272_254+1727 others(16): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATAGA others(7): Show |
4 | a0001c0001t0001g0057a0001c0001t0001g0191a0001c0001t0003g0245others(1): Show | 4 | HG00741.hp1 HG02602.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.254+17272_254+1727 others(18): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATAGA others(9): Show |
1 | a0001c0001t0001g0242 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(20): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATAGA others(13): Show |
1 | a0001c0002t0001g0244 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(24): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATAGA others(15): Show |
1 | a0001c0001t0001g0250 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(26): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATAGA others(17): Show |
4 | a0001c0001t0003g0168a0001c0001t0007g0029a0001c0002t0001g0115others(1): Show | 4 | HG03130.hp2 HG03139.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.254+17272_254+1727 others(28): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATAGA others(19): Show |
4 | a0001c0001t0001g0053a0001c0002t0001g0172a0001c0003t0001g0022others(1): Show | 4 | HG00280.hp2 HG01884.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.254+17272_254+1727 others(30): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATAGA others(21): Show |
3 | a0001c0001t0001g0052a0001c0003t0001g0248a0001c0005t0001g0208 | 3 | HG00280.hp1 HG00323.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.254+17272_254+1727 others(32): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATAGA others(23): Show |
1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(34): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATAGA others(31): Show |
3 | a0001c0001t0001g0106a0001c0001t0007g0028a0001c0004t0001g0134 | 3 | HG01978.hp1 HG02257.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.254+17272_254+1727 others(42): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATAGA others(22): Show |
1 | a0001c0002t0025g0149 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(33): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATAGA others(31): Show |
1 | a0001c0004t0030g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(42): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(3): Show |
1 | a0001c0003t0002g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(14): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(5): Show |
2 | a0001c0003t0001g0253a0001c0004t0004g0003 | 2 | HG03471.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.254+17272_254+1727 others(16): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(7): Show |
2 | a0001c0002t0001g0235a0001c0002t0001g0262 | 2 | HG02155.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.254+17272_254+1727 others(18): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(11): Show |
2 | a0001c0001t0003g0243a0001c0003t0006g0117 | 2 | HG02735.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.254+17272_254+1727 others(22): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(17): Show |
3 | a0001c0001t0001g0167a0001c0001t0002g0198a0001c0002t0001g0138 | 3 | HG00544.hp2 HG02486.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.254+17272_254+1727 others(28): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(19): Show |
2 | a0001c0001t0001g0202a0001c0003t0001g0127 | 2 | HG01243.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.254+17272_254+1727 others(30): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(21): Show |
4 | a0001c0001t0026g0123a0001c0002t0002g0150a0001c0002t0004g0137others(1): Show | 4 | HG00140.hp1 HG03209.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.254+17272_254+1727 others(32): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(23): Show |
1 | a0001c0003t0001g0034 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(34): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(25): Show |
4 | a0001c0001t0001g0136a0001c0001t0007g0030a0001c0002t0003g0105others(1): Show | 4 | HG00738.hp1 HG02723.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.254+17272_254+1727 others(36): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(27): Show |
1 | a0001c0001t0002g0143 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.254+17272_254+1727 others(38): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(29): Show |
1 | a0001c0002t0001g0050 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.254+17272_254+1727 others(40): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(37): Show |
1 | a0001c0004t0001g0135 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(48): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(3): Show |
1 | a0001c0002t0040g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(14): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(5): Show |
1 | a0001c0003t0031g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(16): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(7): Show |
2 | a0001c0004t0004g0258a0002c0008t0001g0171 | 2 | HG01167.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.254+17272_254+1727 others(18): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(9): Show |
3 | a0001c0001t0001g0216a0001c0003t0001g0252a0001c0003t0041g0093 | 3 | NA18983.hp2 NA19011.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.254+17272_254+1727 others(20): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(11): Show |
3 | a0001c0002t0004g0257a0001c0022t0001g0070a0002c0008t0001g0170 | 3 | HG01074.hp2 HG01433.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.254+17272_254+1727 others(22): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(17): Show |
1 | a0001c0003t0002g0199 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(28): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(19): Show |
2 | a0001c0001t0002g0152a0001c0004t0006g0110 | 2 | HG02572.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.254+17272_254+1727 others(30): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(21): Show |
2 | a0001c0002t0001g0041a0001c0006t0036g0009 | 2 | HG01109.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.254+17272_254+1727 others(32): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(23): Show |
2 | a0001c0001t0001g0031a0001c0001t0002g0142 | 2 | HG02074.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.254+17272_254+1727 others(34): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(29): Show |
1 | a0001c0001t0039g0156 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(40): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(33): Show |
1 | a0001c0003t0001g0151 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(44): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(5): Show |
1 | a0001c0004t0001g0209 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.254+17272_254+1727 others(16): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(9): Show |
1 | a0001c0004t0014g0002 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.254+17272_254+1727 others(20): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(11): Show |
1 | a0001c0002t0001g0096 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(22): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(15): Show |
2 | a0001c0002t0001g0206a0001c0004t0001g0187 | 2 | NA18966.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.254+17272_254+1727 others(26): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(21): Show |
1 | a0001c0027t0009g0268 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(32): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(23): Show |
3 | a0001c0001t0022g0193a0001c0002t0001g0124a0001c0002t0005g0079 | 3 | HG00423.hp1 HG00609.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.254+17272_254+1727 others(34): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(27): Show |
2 | a0001c0001t0001g0119a0001c0006t0009g0012 | 2 | HG00642.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.254+17272_254+1727 others(38): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(33): Show |
1 | a0001c0001t0002g0251 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(44): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(7): Show |
1 | a0001c0001t0002g0078 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.254+17272_254+1727 others(18): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(15): Show |
1 | a0001c0001t0001g0042 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(26): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(19): Show |
1 | a0001c0003t0001g0080 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.254+17272_254+1727 others(30): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(23): Show |
1 | a0001c0001t0003g0181 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(34): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(25): Show |
1 | a0001c0001t0001g0118 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(36): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(27): Show |
2 | a0001c0001t0001g0055a0001c0001t0001g0129 | 2 | HG01257.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.254+17272_254+1727 others(38): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(9): Show |
2 | a0001c0001t0028g0077a0007c0023t0001g0017 | 2 | HG03492.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.254+17272_254+1727 others(20): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(19): Show |
1 | a0001c0002t0001g0201 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(30): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(25): Show |
1 | a0001c0002t0005g0081 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.254+17272_254+1727 others(36): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(11): Show |
1 | a0001c0002t0001g0140 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(22): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(17): Show |
1 | a0001c0001t0002g0075 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.254+17272_254+1727 others(28): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(21): Show |
2 | a0001c0001t0001g0085a0001c0002t0032g0200 | 2 | HG00733.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.254+17272_254+1727 others(32): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(31): Show |
1 | a0001c0001t0001g0056 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(42): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(33): Show |
1 | a0001c0001t0038g0100 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.254+17272_254+1727 others(44): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(35): Show |
1 | a0001c0001t0001g0097 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(46): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(37): Show |
1 | a0001c0002t0033g0139 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(48): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(39): Show |
1 | a0001c0001t0001g0249 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.254+17272_254+1727 others(50): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(13): Show |
1 | a0001c0003t0001g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(24): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(15): Show |
1 | a0001c0001t0001g0095 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.254+17272_254+1727 others(26): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(19): Show |
1 | a0001c0002t0001g0086 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.254+17272_254+1727 others(30): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
T | TATATATA others(19): Show |
1 | a0001c0002t0001g0087 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.254+17272_254+1727 others(30): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731991
|
TAGAGAGA others(7): Show |
T | 1 | a0001c0002t0001g0014 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.254+17308_254+1732 others(18): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731991 | |||||
| chr9:135731993
|
G | T | 18 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0060others(15): Show | 18 | HG00323.hp1 HG00738.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.254+17273G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731993 | ||||||
| chr9:135731995
|
G | T | 16 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0060others(13): Show | 16 | HG00738.hp2 HG01981.hp1 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.254+17275G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731995 | ||||||
| chr9:135731997
|
G | T | 13 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0060others(10): Show | 13 | HG00738.hp2 HG01070.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.254+17277G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731997 | ||||||
| chr9:135731998
|
A | AGAGAGAG others(14): Show |
1 | a0001c0005t0001g0240 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.254+17279_254+1729 others(25): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135731998 | |||||
| chr9:135731999
|
G | T | 12 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0067others(9): Show | 12 | HG01070.hp1 HG01981.hp1 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.254+17279G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135731999 | ||||||
| chr9:135732000
|
A | AGAGAGAG others(14): Show |
1 | a0001c0001t0001g0112 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.254+17281_254+1730 others(25): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135732000 | |||||
| chr9:135732001
|
G | T | 7 | a0001c0001t0001g0015a0001c0001t0001g0099a0001c0001t0001g0169others(4): Show | 7 | HG01993.hp1 HG02004.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.254+17281G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135732001 | ||||||
| chr9:135732003
|
G | T | 5 | a0001c0001t0001g0015a0001c0001t0001g0169a0001c0001t0002g0237others(2): Show | 5 | HG01993.hp1 HG02735.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.254+17283G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135732003 | ||||||
| chr9:135732004
|
A | AGAGAAGA others(3): Show |
1 | a0001c0002t0011g0083 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.254+17288_254+1728 others(14): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135732004 | |||||
| chr9:135732005
|
G | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0169a0001c0001t0002g0237others(1): Show | 4 | HG01993.hp1 HG02735.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.254+17285G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135732005 | ||||||
| chr9:135732006
|
A | G | 36 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(33): Show | 36 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.254+17286A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135732006 | ||||||
| chr9:135732007
|
G | T | 1 | a0001c0001t0001g0015 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.254+17287G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135732007 | ||||||
| chr9:135732010
|
A | G | 38 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(35): Show | 38 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.254+17290A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135732010 | ||||||
| chr9:135732012
|
A | AGAGAGAG others(11): Show |
1 | a0001c0003t0001g0040 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.254+17309_254+1731 others(22): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135732012 | |||||
| chr9:135732013
|
G | GAGAGAGA others(18): Show |
1 | a0001c0004t0001g0092 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.254+17294_254+1731 others(29): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135732013 | |||||
| chr9:135732020
|
A | AGAGAGAG others(17): Show |
1 | a0001c0006t0010g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.254+17321_254+1732 others(28): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135732020 | |||||
| chr9:135732020
|
A | AGAGAGAG others(5): Show |
1 | a0001c0006t0010g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.254+17311_254+1731 others(16): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135732020 | |||||
| chr9:135732020
|
A | G | 2 | a0001c0001t0039g0156a0001c0006t0009g0012 | 2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.254+17300A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135732020 | ||||||
| chr9:135732022
|
A | G | 1 | a0001c0004t0030g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.254+17302A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135732022 | ||||||
| chr9:135732024
|
A | AGAGAGAG others(30): Show |
1 | a0001c0004t0001g0130 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.254+17321_254+1732 others(41): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135732024 | |||||
| chr9:135732024
|
A | AGAGAGAG others(25): Show |
1 | a0001c0001t0042g0265 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.254+17321_254+1732 others(36): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135732024 | |||||
| chr9:135732024
|
A | AGAGAGAG others(26): Show |
1 | a0001c0003t0001g0069 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.254+17321_254+1732 others(37): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135732024 | |||||
| chr9:135732024
|
A | AGAGAGAG others(23): Show |
1 | a0001c0001t0015g0104 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.254+17321_254+1732 others(34): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135732024 | |||||
| chr9:135732024
|
A | AGAGAGAG others(19): Show |
2 | a0001c0001t0015g0103a0001c0002t0002g0131 | 2 | HG01192.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.254+17321_254+1732 others(30): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135732024 | |||||
| chr9:135732024
|
A | AGAGAGAG others(17): Show |
4 | a0001c0001t0001g0194a0001c0001t0002g0188a0001c0003t0001g0180others(1): Show | 4 | HG01952.hp2 HG02886.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.254+17321_254+1732 others(28): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135732024 | |||||
| chr9:135732024
|
A | AGAGAGAG others(15): Show |
1 | a0001c0003t0002g0153 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.254+17321_254+1732 others(26): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135732024 | |||||
| chr9:135732024
|
A | AGAGAGAG others(13): Show |
2 | a0001c0001t0001g0128a0001c0005t0001g0261 | 2 | HG01952.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.254+17321_254+1732 others(24): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135732024 | |||||
| chr9:135732024
|
A | AGAGAGAG others(9): Show |
1 | a0001c0005t0001g0217 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.254+17319_254+1732 others(20): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135732024 | |||||
| chr9:135732024
|
A | AGGAGAGG others(28): Show |
1 | a0001c0001t0001g0141 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.254+17305_254+1730 others(39): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135732024 | |||||
| chr9:135732024
|
A | G | 115 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0052others(112): Show | 115 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.254+17304A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135732024 | ||||||
| chr9:135732026
|
A | G | 39 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(36): Show | 39 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.254+17306A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135732026 | ||||||
| chr9:135732040
|
A | G | 1 | a0001c0024t0023g0048 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.254+17320A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135732040 | ||||||
| chr9:135732041
|
G | GA | 4 | a0001c0002t0005g0079a0001c0003t0002g0101a0001c0003t0031g0269others(1): Show | 4 | HG01070.hp2 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.254+17321_254+1732 others(5): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135732041 | ||||||
| chr9:135732041
|
G | GAGAGAGA others(6): Show |
1 | a0001c0002t0001g0185 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.254+17321_254+1732 others(17): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135732041 | ||||||
| chr9:135732042
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0003g0243 | 2 | HG02735.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.254+17322G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135732042 | ||||||
| chr9:135732119
|
C | T | 1 | a0001c0002t0001g0041 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.254+17399C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135732119 | ||||||
| chr9:135732120
|
G | A | 2 | a0001c0003t0001g0267a0001c0003t0008g0043 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.254+17400G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135732120 | ||||||
| chr9:135732176
|
G | A | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254+17456G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135732176 | ||||||
| chr9:135732308
|
C | G | 34 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(31): Show | 34 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.254+17588C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135732308 | ||||||
| chr9:135732344
|
C | T | 11 | a0001c0001t0001g0216a0001c0001t0002g0039a0001c0001t0011g0032others(8): Show | 11 | HG01943.hp2 HG02004.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.254+17624C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135732344 | ||||||
| chr9:135732384
|
G | T | 1 | a0001c0002t0003g0105 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.254+17664G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135732384 | ||||||
| chr9:135732435
|
C | T | 1 | a0001c0002t0033g0139 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.255-17663C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135732435 | ||||||
| chr9:135732453
|
G | A | 35 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(32): Show | 35 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.255-17645G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135732453 | ||||||
| chr9:135732511
|
C | G | 11 | a0001c0001t0001g0216a0001c0001t0002g0039a0001c0001t0011g0032others(8): Show | 11 | HG01943.hp2 HG02004.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.255-17587C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135732511 | ||||||
| chr9:135732645
|
C | G | 3 | a0001c0002t0008g0026a0001c0003t0001g0267a0001c0003t0008g0043 | 3 | HG02647.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.255-17453C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135732645 | ||||||
| chr9:135732724
|
G | T | 1 | a0001c0001t0001g0057 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.255-17374G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135732724 | ||||||
| chr9:135732750
|
A | ATC | 10 | a0001c0001t0002g0266a0001c0002t0001g0185a0001c0002t0009g0047others(7): Show | 10 | HG00438.hp1 HG02056.hp2 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.255-17323_255-1732 others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135732750 | |||||
| chr9:135732750
|
A | ATCTC | 118 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0052others(115): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.255-17325_255-1732 others(8): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135732750 | |||||
| chr9:135732750
|
A | ATCTCTC | 7 | a0001c0001t0001g0122a0001c0001t0001g0128a0001c0001t0001g0191others(4): Show | 7 | HG00140.hp1 HG01243.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.255-17327_255-1732 others(10): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135732750 | |||||
| chr9:135732750
|
ATC | A | 4 | a0001c0001t0001g0214a0001c0002t0008g0026a0001c0003t0001g0267others(1): Show | 4 | HG02647.hp1 HG02895.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.255-17323_255-1732 others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135732750 | |||||
| chr9:135732750
|
ATCTC | A | 3 | a0001c0002t0001g0213a0001c0004t0004g0003a0001c0004t0014g0002 | 3 | HG03098.hp2 HG03471.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.255-17325_255-1732 others(8): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135732750 | |||||
| chr9:135732750
|
ATCTCTC | A | 70 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0057others(67): Show | 70 | HG00099.hp1 HG00423.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.255-17327_255-1732 others(10): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135732750 | |||||
| chr9:135732796
|
T | C | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255-17302T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135732796 | ||||||
| chr9:135732839
|
G | A | 1 | a0001c0001t0002g0266 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.255-17259G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135732839 | ||||||
| chr9:135733037
|
C | T | 2 | a0001c0001t0002g0266a0001c0003t0002g0192 | 2 | HG00438.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.255-17061C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733037 | ||||||
| chr9:135733038
|
G | A | 4 | a0001c0002t0004g0257a0001c0002t0005g0079a0001c0002t0005g0081others(1): Show | 4 | HG01891.hp2 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.255-17060G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733038 | ||||||
| chr9:135733111
|
G | A | 2 | a0001c0004t0004g0003a0001c0004t0014g0002 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.255-16987G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733111 | ||||||
| chr9:135733256
|
GC | G | 3 | a0001c0001t0001g0141a0001c0003t0001g0253a0001c0004t0001g0092 | 3 | HG01168.hp2 HG01361.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.255-16838delC | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733256 | |||||
| chr9:135733274
|
C | T | 1 | a0001c0003t0001g0253 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.255-16824C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733274 | ||||||
| chr9:135733295
|
C | T | 1 | a0001c0010t0014g0161 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.255-16803C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733295 | ||||||
| chr9:135733301
|
C | T | 34 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(31): Show | 34 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.255-16797C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733301 | ||||||
| chr9:135733304
|
C | G | 2 | a0001c0003t0001g0267a0001c0003t0008g0043 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.255-16794C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733304 | ||||||
| chr9:135733319
|
A | T | 2 | a0001c0003t0001g0267a0001c0003t0008g0043 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.255-16779A>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733319 | ||||||
| chr9:135733320
|
G | T | 2 | a0001c0003t0001g0267a0001c0003t0008g0043 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.255-16778G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733320 | ||||||
| chr9:135733323
|
C | T | 2 | a0001c0003t0001g0267a0001c0003t0008g0043 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.255-16775C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733323 | ||||||
| chr9:135733334
|
A | ACAACTGC others(27): Show |
1 | a0001c0003t0008g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.255-16762_255-1676 others(38): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733334 | |||||
| chr9:135733337
|
C | A | 2 | a0001c0003t0001g0267a0001c0003t0008g0043 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.255-16761C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733337 | ||||||
| chr9:135733344
|
T | C | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255-16754T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733344 | ||||||
| chr9:135733347
|
C | T | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255-16751C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733347 | ||||||
| chr9:135733350
|
C | A | 30 | a0001c0001t0001g0183a0001c0001t0001g0221a0001c0001t0001g0230others(27): Show | 30 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.255-16748C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733350 | ||||||
| chr9:135733357
|
C | T | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255-16741C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733357 | ||||||
| chr9:135733358
|
A | G | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255-16740A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733358 | ||||||
| chr9:135733367
|
T | C | 1 | a0001c0003t0008g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.255-16731T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733367 | ||||||
| chr9:135733368
|
T | C | 1 | a0001c0003t0008g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.255-16730T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733368 | ||||||
| chr9:135733369
|
C | T | 1 | a0001c0003t0008g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.255-16729C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733369 | ||||||
| chr9:135733370
|
A | C | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255-16728A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733370 | ||||||
| chr9:135733370
|
A | G | 1 | a0001c0003t0008g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.255-16728A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733370 | ||||||
| chr9:135733371
|
T | C | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255-16727T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733371 | ||||||
| chr9:135733373
|
C | A | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255-16725C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733373 | ||||||
| chr9:135733376
|
G | C | 1 | a0001c0003t0008g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.255-16722G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733376 | ||||||
| chr9:135733380
|
C | T | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255-16718C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733380 | ||||||
| chr9:135733385
|
A | C | 2 | a0001c0003t0001g0267a0001c0003t0008g0043 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.255-16713A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733385 | ||||||
| chr9:135733396
|
T | C | 2 | a0001c0003t0001g0267a0001c0003t0008g0043 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.255-16702T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733396 | ||||||
| chr9:135733406
|
T | C | 1 | a0001c0003t0008g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.255-16692T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733406 | ||||||
| chr9:135733407
|
G | A | 1 | a0001c0003t0008g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.255-16691G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733407 | ||||||
| chr9:135733408
|
C | T | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255-16690C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733408 | ||||||
| chr9:135733413
|
G | C | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255-16685G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733413 | ||||||
| chr9:135733419
|
A | C | 1 | a0001c0003t0008g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.255-16679A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733419 | ||||||
| chr9:135733426
|
T | C | 1 | a0001c0003t0008g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.255-16672T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733426 | ||||||
| chr9:135733433
|
T | TGCCCCCA others(17): Show |
1 | a0001c0003t0008g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.255-16653_255-1663 others(28): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733433 | |||||
| chr9:135733433
|
T | TGCCCCCA others(100): Show |
1 | a0001c0004t0004g0025 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.255-16654_255-1665 others(111): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733433 | |||||
| chr9:135733433
|
T | TGCCCCCA others(89): Show |
1 | a0001c0003t0031g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.255-16654_255-1665 others(100): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733433 | |||||
| chr9:135733433
|
T | TGCCCCCA others(77): Show |
1 | a0001c0003t0003g0058 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.255-16654_255-1665 others(88): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733433 | |||||
| chr9:135733433
|
T | TGCCCCCA others(89): Show |
4 | a0001c0001t0001g0112a0001c0001t0002g0266a0001c0002t0004g0137others(1): Show | 4 | HG00140.hp1 HG00438.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.255-16654_255-1665 others(100): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733433 | |||||
| chr9:135733433
|
T | TGCCCCCA others(90): Show |
1 | a0001c0006t0010g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.255-16654_255-1665 others(101): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733433 | |||||
| chr9:135733433
|
T | TGCCCCCA others(101): Show |
122 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0042others(119): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.255-16654_255-1665 others(112): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733433 | |||||
| chr9:135733433
|
T | TGCCCCCA others(102): Show |
1 | a0001c0003t0001g0034 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.255-16654_255-1665 others(113): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733433 | |||||
| chr9:135733433
|
T | TGCCCCCA others(90): Show |
1 | a0001c0002t0025g0149 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.255-16654_255-1665 others(101): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733433 | |||||
| chr9:135733433
|
T | TGCCCCCA others(100): Show |
1 | a0001c0003t0001g0127 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.255-16654_255-1665 others(111): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733433 | |||||
| chr9:135733433
|
T | TGCCCCCA others(100): Show |
1 | a0001c0004t0020g0215 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.255-16654_255-1665 others(111): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733433 | |||||
| chr9:135733433
|
T | TGCCCCCA others(102): Show |
1 | a0001c0003t0001g0084 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.255-16654_255-1665 others(113): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733433 | |||||
| chr9:135733433
|
T | TGCCCCCA others(102): Show |
2 | a0001c0001t0002g0198a0001c0004t0006g0110 | 2 | HG00544.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.255-16654_255-1665 others(113): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733433 | |||||
| chr9:135733433
|
T | TGCCCCCA others(101): Show |
1 | a0001c0015t0001g0271 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.255-16654_255-1665 others(112): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733433 | |||||
| chr9:135733433
|
T | TGCCCCCA others(77): Show |
46 | a0001c0001t0001g0038a0001c0001t0001g0060a0001c0001t0001g0065others(43): Show | 46 | HG00423.hp2 HG00738.hp2 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.255-16654_255-1665 others(88): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733433 | |||||
| chr9:135733433
|
T | TGCCCCCA others(89): Show |
31 | a0001c0001t0001g0015a0001c0001t0001g0063a0001c0001t0001g0067others(28): Show | 31 | HG00099.hp1 HG00733.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.255-16654_255-1665 others(100): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733433 | |||||
| chr9:135733433
|
T | TGCCCCCA others(101): Show |
42 | a0001c0001t0001g0183a0001c0001t0001g0214a0001c0001t0001g0221others(39): Show | 42 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.255-16654_255-1665 others(112): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733433 | |||||
| chr9:135733433
|
T | TGCCCCCA others(113): Show |
2 | a0001c0002t0009g0047a0001c0003t0001g0260 | 2 | HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.255-16654_255-1665 others(124): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733433 | |||||
| chr9:135733433
|
T | TGCCCCCA others(93): Show |
1 | a0001c0002t0001g0121 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.255-16654_255-1665 others(104): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733433 | |||||
| chr9:135733433
|
T | TGCCCCCA others(93): Show |
1 | a0001c0001t0001g0057 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.255-16654_255-1665 others(104): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733433 | |||||
| chr9:135733433
|
T | TGCCCCCA others(77): Show |
1 | a0001c0003t0002g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.255-16654_255-1665 others(88): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733433 | |||||
| chr9:135733433
|
T | TGCCCCCC others(90): Show |
1 | a0001c0001t0001g0141 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.255-16659_255-1665 others(101): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733433 | |||||
| chr9:135733433
|
T | TGCCCCCC others(102): Show |
1 | a0008c0012t0003g0241 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.255-16659_255-1665 others(113): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733433 | |||||
| chr9:135733434
|
G | GCCCCCAC others(102): Show |
1 | a0001c0001t0001g0097 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.255-16654_255-1665 others(113): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733434 | |||||
| chr9:135733440
|
A | ACACCTGC others(102): Show |
1 | a0001c0002t0011g0083 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.255-16654_255-1665 others(113): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733440 | |||||
| chr9:135733442
|
A | ACCTGCCC others(78): Show |
1 | a0001c0003t0001g0253 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.255-16654_255-1665 others(89): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733442 | |||||
| chr9:135733445
|
C | T | 3 | a0001c0001t0001g0097a0001c0002t0008g0026a0001c0009t0018g0162 | 3 | HG02135.hp1 HG02897.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.255-16653C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733445 | ||||||
| chr9:135733446
|
G | GCCCCTGT others(5): Show |
1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.255-16648_255-1664 others(16): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733446 | |||||
| chr9:135733446
|
G | GCCCCTGT others(89): Show |
1 | a0001c0009t0018g0162 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.255-16648_255-1664 others(100): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733446 | |||||
| chr9:135733457
|
C | CGCCCCCA others(5): Show |
13 | a0001c0001t0001g0216a0001c0001t0002g0039a0001c0001t0011g0032others(10): Show | 13 | HG01943.hp2 HG02004.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.255-16629_255-1661 others(16): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733457 | |||||
| chr9:135733457
|
C | T | 168 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0052others(165): Show | 168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.255-16641C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733457 | ||||||
| chr9:135733458
|
G | GCCCCCAC others(6): Show |
1 | a0001c0001t0002g0266 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.255-16635_255-1662 others(17): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733458 | |||||
| chr9:135733459
|
C | CCCCCACA others(4): Show |
1 | a0001c0001t0001g0112 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.255-16634_255-1662 others(15): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733459 | |||||
| chr9:135733469
|
T | C | 40 | a0001c0001t0001g0038a0001c0001t0001g0060a0001c0001t0001g0065others(37): Show | 40 | HG00423.hp2 HG00738.hp2 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.255-16629T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733469 | ||||||
| chr9:135733469
|
T | TGCCCCCA others(17): Show |
1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.255-16613_255-1661 others(28): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733469 | |||||
| chr9:135733474
|
CCACACCC others(5): Show |
C | 28 | a0001c0001t0001g0057a0001c0001t0001g0063a0001c0001t0001g0067others(25): Show | 28 | HG00099.hp1 HG00733.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.255-16612_255-1660 others(16): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733474 | |||||
| chr9:135733481
|
C | T | 45 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0060others(42): Show | 45 | HG00423.hp2 HG00738.hp2 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.255-16617C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733481 | ||||||
| chr9:135733486
|
T | C | 47 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0060others(44): Show | 47 | HG00423.hp2 HG00738.hp2 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.255-16612T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733486 | ||||||
| chr9:135733494
|
G | GC | 6 | a0001c0001t0001g0191a0001c0002t0001g0086a0001c0002t0033g0139others(3): Show | 6 | HG01433.hp2 HG02056.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.255-16599dupC | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733494 | |||||
| chr9:135733494
|
GC | G | 32 | a0001c0001t0001g0183a0001c0001t0001g0221a0001c0001t0001g0230others(29): Show | 32 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.255-16599delC | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733494 | |||||
| chr9:135733495
|
C | CCCTCACA others(4): Show |
2 | a0001c0002t0001g0121a0001c0002t0009g0047 | 2 | HG02486.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.255-16601_255-1660 others(15): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733495 | |||||
| chr9:135733529
|
GC | G | 33 | a0001c0001t0001g0183a0001c0001t0001g0221a0001c0001t0001g0230others(30): Show | 33 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.255-16563delC | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135733529 | |||||
| chr9:135733540
|
C | A | 32 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0194others(29): Show | 32 | HG00438.hp1 HG00544.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.255-16558C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733540 | ||||||
| chr9:135733547
|
T | C | 2 | a0001c0002t0008g0026a0001c0003t0001g0267 | 2 | HG02647.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.255-16551T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733547 | ||||||
| chr9:135733564
|
C | G | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255-16534C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733564 | ||||||
| chr9:135733641
|
C | CACACTCT others(8): Show |
1 | a0001c0001t0001g0112 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.255-16457_255-1645 others(19): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733641 | ||||||
| chr9:135733646
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.255-16452C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733646 | ||||||
| chr9:135733648
|
C | A | 1 | a0001c0001t0001g0112 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.255-16450C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733648 | ||||||
| chr9:135733649
|
T | G | 1 | a0001c0001t0001g0112 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.255-16449T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733649 | ||||||
| chr9:135733740
|
C | G | 1 | a0001c0004t0004g0025 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.255-16358C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733740 | ||||||
| chr9:135733750
|
G | T | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255-16348G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733750 | ||||||
| chr9:135733755
|
G | T | 2 | a0001c0004t0004g0256a0001c0004t0004g0258 | 2 | HG02717.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.255-16343G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733755 | ||||||
| chr9:135733794
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.255-16304C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733794 | ||||||
| chr9:135733846
|
A | C | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.255-16252A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733846 | ||||||
| chr9:135733896
|
C | T | 1 | a0001c0003t0031g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.255-16202C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135733896 | ||||||
| chr9:135734067
|
A | G | 130 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0057others(127): Show | 130 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.255-16031A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135734067 | ||||||
| chr9:135734166
|
T | G | 1 | a0001c0024t0023g0048 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.255-15932T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135734166 | ||||||
| chr9:135734256
|
G | T | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255-15842G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135734256 | ||||||
| chr9:135734270
|
C | T | 1 | a0001c0002t0001g0172 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.255-15828C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135734270 | ||||||
| chr9:135734303
|
C | T | 11 | a0001c0001t0001g0216a0001c0001t0002g0039a0001c0001t0011g0032others(8): Show | 11 | HG01943.hp2 HG02004.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.255-15795C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135734303 | ||||||
| chr9:135734315
|
C | T | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255-15783C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135734315 | ||||||
| chr9:135734370
|
G | T | 1 | a0001c0003t0001g0127 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.255-15728G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135734370 | ||||||
| chr9:135734409
|
A | G | 33 | a0001c0001t0001g0183a0001c0001t0001g0221a0001c0001t0001g0230others(30): Show | 33 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.255-15689A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135734409 | ||||||
| chr9:135734672
|
A | C | 33 | a0001c0001t0001g0183a0001c0001t0001g0221a0001c0001t0001g0230others(30): Show | 33 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.255-15426A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135734672 | ||||||
| chr9:135734699
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.255-15399C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135734699 | ||||||
| chr9:135734700
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.255-15398G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135734700 | ||||||
| chr9:135734704
|
C | T | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255-15394C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135734704 | ||||||
| chr9:135734708
|
T | TG | 3 | a0001c0003t0001g0253a0001c0004t0001g0187a0001c0004t0002g0045 | 3 | HG01496.hp2 NA18962.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.255-15387dupG | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135734708 | |||||
| chr9:135734717
|
G | A | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255-15381G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135734717 | ||||||
| chr9:135734732
|
G | A | 1 | a0001c0003t0002g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.255-15366G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135734732 | ||||||
| chr9:135734770
|
G | A | 1 | a0001c0001t0001g0031 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.255-15328G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135734770 | ||||||
| chr9:135734799
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.255-15299C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135734799 | ||||||
| chr9:135734897
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.255-15201C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135734897 | ||||||
| chr9:135734964
|
C | T | 2 | a0001c0002t0002g0150a0001c0002t0025g0149 | 2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.255-15134C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135734964 | ||||||
| chr9:135735026
|
C | T | 1 | a0001c0001t0016g0254 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.255-15072C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135735026 | ||||||
| chr9:135735141
|
T | G | 1 | a0001c0001t0001g0057 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.255-14957T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135735141 | ||||||
| chr9:135735159
|
C | T | 7 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0175others(4): Show | 7 | HG01081.hp2 HG01106.hp2 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.255-14939C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135735159 | ||||||
| chr9:135735209
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.255-14889C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135735209 | ||||||
| chr9:135735211
|
G | C | 2 | a0001c0001t0011g0032a0001c0003t0001g0040 | 2 | NA19009.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.255-14887G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135735211 | ||||||
| chr9:135735238
|
C | G | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255-14860C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135735238 | ||||||
| chr9:135735247
|
C | T | 4 | a0001c0001t0001g0015a0001c0001t0003g0016a0001c0003t0001g0018others(1): Show | 4 | HG02735.hp2 HG03492.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.255-14851C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135735247 | ||||||
| chr9:135735248
|
G | A | 1 | a0003c0011t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.255-14850G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135735248 | ||||||
| chr9:135735257
|
G | A | 2 | a0001c0001t0001g0186a0001c0004t0001g0187 | 2 | NA18964.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.255-14841G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135735257 | ||||||
| chr9:135735365
|
C | T | 1 | a0001c0003t0002g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.255-14733C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135735365 | ||||||
| chr9:135735411
|
C | T | 1 | a0001c0003t0008g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.255-14687C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135735411 | ||||||
| chr9:135735499
|
G | A | 5 | a0001c0001t0027g0157a0001c0009t0006g0159a0001c0009t0018g0162others(2): Show | 5 | HG02055.hp2 HG02897.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.255-14599G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135735499 | ||||||
| chr9:135735589
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0242 | 2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.255-14509G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135735589 | ||||||
| chr9:135735701
|
GGAAGAAA others(7): Show |
G | 1 | a0001c0003t0001g0127 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.255-14396_255-1438 others(18): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135735701 | ||||||
| chr9:135735740
|
A | G | 1 | a0003c0011t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.255-14358A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135735740 | ||||||
| chr9:135735769
|
G | A | 1 | a0001c0003t0006g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.255-14329G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135735769 | ||||||
| chr9:135735807
|
G | A | 2 | a0001c0001t0002g0152a0001c0003t0002g0153 | 2 | HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.255-14291G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135735807 | ||||||
| chr9:135735832
|
C | T | 4 | a0001c0001t0001g0221a0001c0001t0001g0233a0001c0002t0001g0184others(1): Show | 4 | HG03017.hp2 HG03654.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.255-14266C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135735832 | ||||||
| chr9:135735865
|
G | A | 1 | a0001c0003t0001g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.255-14233G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135735865 | ||||||
| chr9:135735877
|
C | T | 1 | a0001c0003t0002g0236 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.255-14221C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135735877 | ||||||
| chr9:135736126
|
C | G | 2 | a0001c0002t0002g0114a0001c0002t0002g0145 | 2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.255-13972C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135736126 | ||||||
| chr9:135736279
|
C | T | 1 | a0001c0003t0001g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.255-13819C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135736279 | ||||||
| chr9:135736499
|
C | G | 32 | a0001c0001t0001g0190a0001c0001t0001g0194a0001c0001t0001g0202others(29): Show | 32 | HG00438.hp1 HG00544.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.255-13599C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135736499 | ||||||
| chr9:135736507
|
C | T | 87 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0057others(84): Show | 87 | HG00099.hp1 HG00423.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.255-13591C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135736507 | ||||||
| chr9:135736586
|
C | G | 1 | a0001c0004t0004g0003 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.255-13512C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135736586 | ||||||
| chr9:135736616
|
C | A | 1 | a0001c0001t0039g0156 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.255-13482C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135736616 | ||||||
| chr9:135736626
|
C | T | 1 | a0001c0003t0008g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.255-13472C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135736626 | ||||||
| chr9:135736683
|
G | A | 4 | a0001c0009t0006g0159a0001c0009t0018g0162a0001c0010t0001g0158others(1): Show | 4 | HG02055.hp2 HG02897.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.255-13415G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135736683 | ||||||
| chr9:135736698
|
C | T | 1 | a0001c0001t0002g0098 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.255-13400C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135736698 | ||||||
| chr9:135736713
|
C | T | 2 | a0001c0003t0001g0267a0001c0003t0008g0043 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.255-13385C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135736713 | ||||||
| chr9:135736891
|
G | C | 2 | a0001c0002t0001g0138a0001c0002t0001g0206 | 2 | NA18966.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.255-13207G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135736891 | ||||||
| chr9:135736914
|
C | T | 1 | a0001c0002t0001g0154 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.255-13184C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135736914 | ||||||
| chr9:135736919
|
C | T | 10 | a0001c0001t0008g0008a0001c0002t0001g0013a0001c0002t0001g0014others(7): Show | 10 | HG01074.hp1 HG01099.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.255-13179C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135736919 | ||||||
| chr9:135736929
|
C | T | 1 | a0001c0004t0002g0147 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.255-13169C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135736929 | ||||||
| chr9:135736970
|
G | A | 221 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0038others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.255-13128G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135736970 | ||||||
| chr9:135737105
|
C | T | 4 | a0001c0003t0001g0022a0001c0003t0006g0023a0001c0004t0004g0025others(1): Show | 4 | HG00741.hp2 HG02572.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.255-12993C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135737105 | ||||||
| chr9:135737148
|
G | A | 1 | a0001c0003t0002g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.255-12950G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135737148 | ||||||
| chr9:135737182
|
C | T | 1 | a0001c0003t0021g0259 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.255-12916C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135737182 | ||||||
| chr9:135737207
|
T | C | 1 | a0001c0027t0009g0268 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.255-12891T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135737207 | ||||||
| chr9:135737475
|
G | C | 1 | a0001c0003t0009g0177 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.255-12623G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135737475 | ||||||
| chr9:135737521
|
C | T | 4 | a0001c0009t0006g0159a0001c0009t0018g0162a0001c0010t0001g0158others(1): Show | 4 | HG02055.hp2 HG02897.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.255-12577C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135737521 | ||||||
| chr9:135737578
|
A | G | 1 | a0001c0003t0008g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.255-12520A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135737578 | ||||||
| chr9:135737619
|
TGGGGAGA others(6): Show |
T | 4 | a0001c0001t0001g0015a0001c0001t0003g0016a0001c0003t0001g0018others(1): Show | 4 | HG02735.hp2 HG03492.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.255-12474_255-1246 others(17): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135737619 | |||||
| chr9:135737633
|
G | GGGGCCTT others(3): Show |
1 | a0001c0001t0001g0057 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.255-12462_255-1245 others(14): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135737633 | |||||
| chr9:135737756
|
C | T | 1 | a0001c0003t0001g0151 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.255-12342C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135737756 | ||||||
| chr9:135737814
|
C | G | 130 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0052others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.255-12284C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135737814 | ||||||
| chr9:135737826
|
G | T | 1 | a0001c0002t0001g0231 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.255-12272G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135737826 | ||||||
| chr9:135737899
|
T | G | 1 | a0001c0001t0003g0222 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.255-12199T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135737899 | ||||||
| chr9:135737994
|
C | T | 1 | a0001c0027t0009g0268 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.255-12104C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135737994 | ||||||
| chr9:135737995
|
G | A | 3 | a0001c0001t0001g0204a0001c0003t0001g0126a0001c0003t0001g0210 | 3 | NA18945.hp1 NA18948.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.255-12103G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135737995 | ||||||
| chr9:135738126
|
G | A | 1 | a0001c0003t0001g0040 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.255-11972G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135738126 | ||||||
| chr9:135738229
|
C | A | 5 | a0001c0001t0001g0015a0001c0001t0003g0016a0001c0003t0001g0018others(2): Show | 5 | HG02735.hp2 HG03492.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.255-11869C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135738229 | ||||||
| chr9:135738229
|
C | T | 1 | a0001c0002t0001g0050 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.255-11869C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135738229 | ||||||
| chr9:135738230
|
G | A | 20 | a0001c0001t0001g0216a0001c0001t0002g0039a0001c0001t0011g0032others(17): Show | 20 | HG01192.hp2 HG01943.hp2 HG02004.hp1 others(17): Show |
intron_variant | MODIFIER | c.255-11868G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135738230 | ||||||
| chr9:135738260
|
C | T | 7 | a0001c0001t0001g0230a0001c0002t0001g0213a0001c0002t0002g0228others(4): Show | 7 | HG00544.hp1 HG00609.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.255-11838C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135738260 | ||||||
| chr9:135738363
|
C | A | 1 | a0001c0020t0017g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.255-11735C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135738363 | ||||||
| chr9:135738597
|
A | C | 268 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0038others(265): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.255-11501A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135738597 | ||||||
| chr9:135738770
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.255-11328G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135738770 | ||||||
| chr9:135738813
|
G | A | 1 | a0001c0002t0003g0105 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.255-11285G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135738813 | ||||||
| chr9:135738947
|
G | A | 3 | a0001c0002t0001g0213a0001c0002t0002g0228a0001c0007t0001g0232 | 3 | HG02074.hp2 NA18947.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.255-11151G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135738947 | ||||||
| chr9:135739001
|
T | C | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255-11097T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135739001 | ||||||
| chr9:135739464
|
A | G | 1 | a0003c0011t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.255-10634A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135739464 | ||||||
| chr9:135739532
|
C | T | 1 | a0001c0003t0008g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.255-10566C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135739532 | ||||||
| chr9:135739553
|
G | A | 2 | a0001c0003t0008g0043a0003c0011t0001g0044 | 2 | NA18522.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.255-10545G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135739553 | ||||||
| chr9:135739564
|
C | T | 1 | a0003c0011t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.255-10534C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135739564 | ||||||
| chr9:135739596
|
G | A | 2 | a0001c0002t0011g0083a0001c0003t0001g0082 | 2 | HG00438.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.255-10502G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135739596 | ||||||
| chr9:135739600
|
C | T | 1 | a0003c0011t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.255-10498C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135739600 | ||||||
| chr9:135739691
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.255-10407G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135739691 | ||||||
| chr9:135739728
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.255-10370C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135739728 | ||||||
| chr9:135739808
|
C | T | 99 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0052others(96): Show | 99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.255-10290C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135739808 | ||||||
| chr9:135739840
|
C | G | 3 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0004t0037g0004 | 3 | HG01099.hp1 HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.255-10258C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135739840 | ||||||
| chr9:135739861
|
G | T | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255-10237G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135739861 | ||||||
| chr9:135740145
|
T | G | 36 | a0001c0001t0001g0183a0001c0001t0001g0221a0001c0001t0001g0230others(33): Show | 36 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.255-9953T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135740145 | ||||||
| chr9:135740189
|
A | G | 1 | a0001c0004t0001g0092 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.255-9909A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135740189 | ||||||
| chr9:135740284
|
A | C | 36 | a0001c0001t0001g0183a0001c0001t0001g0221a0001c0001t0001g0230others(33): Show | 36 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.255-9814A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135740284 | ||||||
| chr9:135740557
|
A | G | 37 | a0001c0001t0001g0183a0001c0001t0001g0221a0001c0001t0001g0230others(34): Show | 37 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.255-9541A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135740557 | ||||||
| chr9:135740628
|
C | A | 1 | a0001c0001t0007g0029 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.255-9470C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135740628 | ||||||
| chr9:135740672
|
G | A | 1 | a0001c0003t0001g0040 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.255-9426G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135740672 | ||||||
| chr9:135740695
|
G | A | 3 | a0001c0001t0001g0141a0001c0001t0015g0103a0001c0001t0015g0104 | 3 | HG00642.hp2 HG01192.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.255-9403G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135740695 | ||||||
| chr9:135740844
|
TCCTGGAC others(73): Show |
T | 1 | a0003c0011t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.255-9249_255-9170d others(82): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135740844 | |||||
| chr9:135740884
|
G | A | 32 | a0001c0001t0001g0183a0001c0001t0001g0221a0001c0001t0001g0230others(29): Show | 32 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.255-9214G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135740884 | ||||||
| chr9:135740957
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.255-9141G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135740957 | ||||||
| chr9:135740976
|
G | C | 1 | a0001c0003t0013g0068 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.255-9122G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135740976 | ||||||
| chr9:135741129
|
G | A | 2 | a0001c0003t0001g0252a0001c0003t0001g0253 | 2 | NA18962.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.255-8969G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135741129 | ||||||
| chr9:135741218
|
C | T | 1 | a0001c0004t0002g0147 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.255-8880C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135741218 | ||||||
| chr9:135741234
|
C | G | 1 | a0001c0001t0001g0202 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.255-8864C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135741234 | ||||||
| chr9:135741268
|
C | T | 1 | a0001c0003t0031g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.255-8830C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135741268 | ||||||
| chr9:135741279
|
A | C | 1 | a0001c0001t0002g0143 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.255-8819A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135741279 | ||||||
| chr9:135741321
|
G | T | 2 | a0001c0003t0001g0267a0003c0011t0001g0044 | 2 | HG02647.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.255-8777G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135741321 | ||||||
| chr9:135741553
|
G | A | 1 | a0001c0003t0013g0068 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.255-8545G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135741553 | ||||||
| chr9:135741561
|
C | T | 99 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0052others(96): Show | 99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.255-8537C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135741561 | ||||||
| chr9:135741580
|
G | A | 2 | a0001c0002t0001g0184a0001c0003t0001g0084 | 2 | HG01175.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.255-8518G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135741580 | ||||||
| chr9:135741693
|
C | T | 2 | a0001c0002t0001g0087a0001c0002t0032g0200 | 2 | HG01109.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.255-8405C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135741693 | ||||||
| chr9:135741698
|
A | G | 36 | a0001c0001t0001g0183a0001c0001t0001g0221a0001c0001t0001g0230others(33): Show | 36 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.255-8400A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135741698 | ||||||
| chr9:135741714
|
A | G | 36 | a0001c0001t0001g0183a0001c0001t0001g0221a0001c0001t0001g0230others(33): Show | 36 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.255-8384A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135741714 | ||||||
| chr9:135741777
|
T | C | 36 | a0001c0001t0001g0183a0001c0001t0001g0221a0001c0001t0001g0230others(33): Show | 36 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.255-8321T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135741777 | ||||||
| chr9:135741811
|
A | G | 1 | a0001c0003t0002g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.255-8287A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135741811 | ||||||
| chr9:135741859
|
C | T | 11 | a0001c0001t0001g0216a0001c0001t0002g0039a0001c0001t0011g0032others(8): Show | 11 | HG01943.hp2 HG02004.hp1 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.255-8239C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135741859 | ||||||
| chr9:135741915
|
G | C | 2 | a0001c0004t0012g0225a0001c0004t0012g0226 | 2 | HG00609.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.255-8183G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135741915 | ||||||
| chr9:135741956
|
T | C | 271 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0031others(268): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.255-8142T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135741956 | ||||||
| chr9:135742265
|
G | A | 1 | a0001c0001t0003g0181 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.255-7833G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135742265 | ||||||
| chr9:135742294
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.255-7804G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135742294 | ||||||
| chr9:135742403
|
G | A | 2 | a0001c0002t0001g0087a0001c0002t0032g0200 | 2 | HG01109.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.255-7695G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135742403 | ||||||
| chr9:135742470
|
G | A | 4 | a0001c0001t0001g0136a0001c0002t0001g0013a0001c0002t0001g0014others(1): Show | 4 | HG00738.hp1 HG01099.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.255-7628G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135742470 | ||||||
| chr9:135742477
|
T | C | 239 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0038others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.255-7621T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135742477 | ||||||
| chr9:135742584
|
C | G | 6 | a0001c0001t0027g0157a0001c0009t0006g0159a0001c0009t0018g0162others(3): Show | 6 | HG02055.hp2 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.255-7514C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135742584 | ||||||
| chr9:135742587
|
G | T | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255-7511G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135742587 | ||||||
| chr9:135742607
|
C | G | 1 | a0001c0003t0001g0127 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.255-7491C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135742607 | ||||||
| chr9:135742608
|
CCCCCAG | C | 100 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0057others(97): Show | 100 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.255-7489_255-7484d others(8): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135742608 | ||||||
| chr9:135742737
|
C | G | 36 | a0001c0001t0001g0183a0001c0001t0001g0221a0001c0001t0001g0230others(33): Show | 36 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.255-7361C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135742737 | ||||||
| chr9:135743119
|
G | T | 101 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0052others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.255-6979G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135743119 | ||||||
| chr9:135743184
|
G | A | 21 | a0001c0001t0001g0183a0001c0001t0001g0221a0001c0001t0001g0230others(18): Show | 21 | HG00544.hp1 HG00609.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.255-6914G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135743184 | ||||||
| chr9:135743208
|
C | G | 1 | a0001c0004t0001g0187 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.255-6890C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135743208 | ||||||
| chr9:135743239
|
G | A | 5 | a0001c0001t0002g0188a0001c0001t0002g0237a0001c0002t0001g0185others(2): Show | 5 | HG02015.hp1 HG02056.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.255-6859G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135743239 | ||||||
| chr9:135743330
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.255-6768C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135743330 | ||||||
| chr9:135743590
|
C | T | 2 | a0001c0024t0023g0048a0001c0027t0009g0268 | 2 | HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.255-6508C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135743590 | ||||||
| chr9:135743633
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.255-6465G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135743633 | ||||||
| chr9:135743661
|
G | A | 3 | a0001c0001t0001g0216a0001c0003t0001g0035a0001c0003t0001g0037 | 3 | HG01943.hp2 NA19011.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.255-6437G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135743661 | ||||||
| chr9:135743727
|
C | T | 1 | a0001c0013t0024g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.255-6371C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135743727 | ||||||
| chr9:135743742
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.255-6356C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135743742 | ||||||
| chr9:135743764
|
G | A | 32 | a0001c0001t0001g0183a0001c0001t0001g0221a0001c0001t0001g0230others(29): Show | 32 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.255-6334G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135743764 | ||||||
| chr9:135743865
|
C | A | 2 | a0001c0001t0026g0123a0001c0001t0042g0265 | 2 | NA18966.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.255-6233C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135743865 | ||||||
| chr9:135743874
|
C | T | 1 | a0001c0027t0009g0268 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.255-6224C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135743874 | ||||||
| chr9:135743909
|
C | T | 1 | a0001c0002t0001g0096 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.255-6189C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135743909 | ||||||
| chr9:135743910
|
G | A | 34 | a0001c0001t0001g0183a0001c0001t0001g0221a0001c0001t0001g0230others(31): Show | 34 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.255-6188G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135743910 | ||||||
| chr9:135744055
|
G | A | 12 | a0001c0001t0001g0216a0001c0001t0002g0039a0001c0001t0011g0032others(9): Show | 12 | HG01943.hp2 HG02004.hp1 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.255-6043G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135744055 | ||||||
| chr9:135744086
|
C | T | 34 | a0001c0001t0001g0183a0001c0001t0001g0221a0001c0001t0001g0230others(31): Show | 34 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.255-6012C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135744086 | ||||||
| chr9:135744087
|
G | A | 2 | a0001c0003t0002g0027a0001c0003t0008g0043 | 2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.255-6011G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135744087 | ||||||
| chr9:135744355
|
C | T | 6 | a0001c0001t0027g0157a0001c0009t0006g0159a0001c0009t0018g0162others(3): Show | 6 | HG02055.hp2 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.255-5743C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135744355 | ||||||
| chr9:135744600
|
C | T | 2 | a0001c0003t0021g0259a0003c0011t0001g0044 | 2 | HG02886.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.255-5498C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135744600 | ||||||
| chr9:135744944
|
A | T | 1 | a0001c0002t0001g0124 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.255-5154A>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135744944 | ||||||
| chr9:135744967
|
G | A | 3 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0003t0001g0066 | 3 | HG00738.hp2 HG01361.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.255-5131G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135744967 | ||||||
| chr9:135744989
|
T | C | 1 | a0001c0001t0005g0175 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.255-5109T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135744989 | ||||||
| chr9:135745000
|
G | A | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255-5098G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135745000 | ||||||
| chr9:135745043
|
G | C | 1 | a0001c0027t0009g0268 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.255-5055G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135745043 | ||||||
| chr9:135745123
|
G | A | 2 | a0002c0008t0001g0170a0002c0008t0001g0171 | 2 | HG01074.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.255-4975G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135745123 | ||||||
| chr9:135745209
|
C | T | 1 | a0001c0003t0002g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.255-4889C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135745209 | ||||||
| chr9:135745233
|
G | A | 1 | a0001c0003t0002g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.255-4865G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135745233 | ||||||
| chr9:135745290
|
T | G | 1 | a0001c0002t0003g0105 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.255-4808T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135745290 | ||||||
| chr9:135745291
|
C | G | 1 | a0001c0002t0003g0105 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.255-4807C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135745291 | ||||||
| chr9:135745293
|
T | A | 1 | a0001c0002t0003g0105 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.255-4805T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135745293 | ||||||
| chr9:135745295
|
T | A | 1 | a0001c0026t0001g0051 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.255-4803T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135745295 | ||||||
| chr9:135745297
|
C | T | 1 | a0001c0002t0003g0105 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.255-4801C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135745297 | ||||||
| chr9:135745319
|
G | C | 6 | a0001c0001t0001g0230a0001c0002t0001g0213a0001c0002t0002g0228others(3): Show | 6 | HG00544.hp1 HG00609.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.255-4779G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135745319 | ||||||
| chr9:135745382
|
G | A | 2 | a0001c0001t0002g0020a0001c0002t0001g0121 | 2 | HG03654.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.255-4716G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135745382 | ||||||
| chr9:135745387
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0242 | 2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.255-4711C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135745387 | ||||||
| chr9:135745473
|
G | A | 6 | a0001c0001t0027g0157a0001c0009t0006g0159a0001c0009t0018g0162others(3): Show | 6 | HG02055.hp2 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.255-4625G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135745473 | ||||||
| chr9:135745534
|
C | A | 1 | a0001c0002t0035g0109 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.255-4564C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135745534 | ||||||
| chr9:135745535
|
G | C | 1 | a0001c0002t0035g0109 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.255-4563G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135745535 | ||||||
| chr9:135745558
|
C | A | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255-4540C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135745558 | ||||||
| chr9:135745577
|
G | A | 6 | a0001c0001t0027g0157a0001c0009t0006g0159a0001c0009t0018g0162others(3): Show | 6 | HG02055.hp2 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.255-4521G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135745577 | ||||||
| chr9:135745595
|
G | C | 35 | a0001c0001t0001g0015a0001c0001t0001g0190a0001c0001t0001g0194others(32): Show | 35 | HG00438.hp1 HG00544.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.255-4503G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135745595 | ||||||
| chr9:135745684
|
A | G | 7 | a0001c0001t0027g0157a0001c0009t0006g0159a0001c0009t0018g0162others(4): Show | 7 | HG02055.hp2 HG02897.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.255-4414A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135745684 | ||||||
| chr9:135745686
|
G | C | 7 | a0001c0001t0027g0157a0001c0009t0006g0159a0001c0009t0018g0162others(4): Show | 7 | HG02055.hp2 HG02897.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.255-4412G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135745686 | ||||||
| chr9:135745817
|
C | A | 1 | a0001c0003t0001g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.255-4281C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135745817 | ||||||
| chr9:135745869
|
C | T | 1 | a0001c0004t0001g0187 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.255-4229C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135745869 | ||||||
| chr9:135745870
|
G | A | 1 | a0003c0011t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.255-4228G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135745870 | ||||||
| chr9:135745910
|
A | G | 1 | a0003c0011t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.255-4188A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135745910 | ||||||
| chr9:135745969
|
C | T | 4 | a0001c0002t0009g0047a0001c0013t0024g0046a0001c0024t0023g0048others(1): Show | 4 | HG02451.hp2 HG02486.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.255-4129C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135745969 | ||||||
| chr9:135746026
|
C | A | 1 | a0003c0011t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.255-4072C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135746026 | ||||||
| chr9:135746027
|
G | A | 1 | a0001c0024t0023g0048 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.255-4071G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135746027 | ||||||
| chr9:135746031
|
C | T | 36 | a0001c0001t0001g0015a0001c0001t0001g0190a0001c0001t0001g0194others(33): Show | 36 | HG00438.hp1 HG00544.hp2 HG01952.hp2 others(33): Show |
intron_variant | MODIFIER | c.255-4067C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135746031 | ||||||
| chr9:135746052
|
G | T | 1 | a0003c0011t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.255-4046G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135746052 | ||||||
| chr9:135746108
|
T | G | 1 | a0001c0001t0001g0183 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.255-3990T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135746108 | ||||||
| chr9:135746410
|
G | A | 2 | a0001c0004t0004g0003a0001c0004t0014g0002 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.255-3688G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135746410 | ||||||
| chr9:135746427
|
G | T | 1 | a0001c0004t0001g0135 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.255-3671G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135746427 | ||||||
| chr9:135746436
|
G | A | 1 | a0001c0014t0017g0212 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.255-3662G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135746436 | ||||||
| chr9:135746536
|
C | T | 41 | a0001c0001t0001g0183a0001c0001t0001g0221a0001c0001t0001g0230others(38): Show | 41 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.255-3562C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135746536 | ||||||
| chr9:135746537
|
T | G | 1 | a0001c0003t0001g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.255-3561T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135746537 | ||||||
| chr9:135746592
|
G | A | 2 | a0001c0024t0023g0048a0001c0027t0009g0268 | 2 | HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.255-3506G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135746592 | ||||||
| chr9:135746626
|
C | G | 1 | a0001c0003t0002g0101 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.255-3472C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135746626 | ||||||
| chr9:135746627
|
C | G | 1 | a0001c0020t0017g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.255-3471C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135746627 | ||||||
| chr9:135746652
|
C | A | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255-3446C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135746652 | ||||||
| chr9:135746652
|
C | T | 1 | a0001c0001t0008g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.255-3446C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135746652 | ||||||
| chr9:135746687
|
G | A | 1 | a0001c0027t0009g0268 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.255-3411G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135746687 | ||||||
| chr9:135746714
|
C | T | 38 | a0001c0001t0001g0183a0001c0001t0001g0221a0001c0001t0001g0230others(35): Show | 38 | HG00544.hp1 HG00609.hp2 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.255-3384C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135746714 | ||||||
| chr9:135746790
|
G | A | 12 | a0001c0001t0001g0216a0001c0001t0002g0039a0001c0001t0011g0032others(9): Show | 12 | HG01943.hp2 HG02004.hp1 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.255-3308G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135746790 | ||||||
| chr9:135746957
|
C | T | 1 | a0001c0001t0002g0237 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.255-3141C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135746957 | ||||||
| chr9:135747003
|
G | A | 2 | a0002c0008t0001g0170a0002c0008t0001g0171 | 2 | HG01074.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.255-3095G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135747003 | ||||||
| chr9:135747018
|
G | A | 5 | a0001c0009t0006g0159a0001c0009t0018g0162a0001c0010t0001g0158others(2): Show | 5 | HG02055.hp2 HG02897.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.255-3080G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135747018 | ||||||
| chr9:135747272
|
C | T | 164 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0052others(161): Show | 164 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.255-2826C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135747272 | ||||||
| chr9:135747326
|
G | A | 2 | a0001c0001t0002g0266a0001c0003t0002g0192 | 2 | HG00438.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.255-2772G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135747326 | ||||||
| chr9:135747431
|
G | A | 260 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0038others(257): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.255-2667G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135747431 | ||||||
| chr9:135747448
|
G | GC | 43 | a0001c0001t0001g0015a0001c0001t0001g0095a0001c0001t0001g0190others(40): Show | 43 | HG00438.hp1 HG00544.hp2 HG01952.hp2 others(40): Show |
intron_variant | MODIFIER | c.255-2645dupC | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135747448 | |||||
| chr9:135747480
|
C | G | 1 | a0001c0003t0002g0199 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.255-2618C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135747480 | ||||||
| chr9:135747570
|
C | A | 5 | a0001c0002t0009g0047a0001c0004t0004g0003a0001c0004t0014g0002others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.255-2528C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135747570 | ||||||
| chr9:135747585
|
C | G | 19 | a0001c0001t0001g0183a0001c0001t0001g0230a0001c0001t0003g0222others(16): Show | 19 | HG00544.hp1 HG00609.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.255-2513C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135747585 | ||||||
| chr9:135747600
|
T | C | 45 | a0001c0001t0001g0015a0001c0001t0001g0095a0001c0001t0001g0190others(42): Show | 45 | HG00438.hp1 HG00544.hp2 HG01952.hp2 others(42): Show |
intron_variant | MODIFIER | c.255-2498T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135747600 | ||||||
| chr9:135747623
|
A | G | 110 | a0001c0001t0001g0031a0001c0001t0001g0057a0001c0001t0001g0060others(107): Show | 110 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.255-2475A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135747623 | ||||||
| chr9:135747764
|
G | A | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255-2334G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135747764 | ||||||
| chr9:135747783
|
C | A | 2 | a0001c0001t0001g0183a0001c0002t0001g0231 | 2 | HG01358.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.255-2315C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135747783 | ||||||
| chr9:135747823
|
G | A | 1 | a0001c0003t0031g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.255-2275G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135747823 | ||||||
| chr9:135747966
|
G | A | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255-2132G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135747966 | ||||||
| chr9:135748028
|
A | G | 259 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0038others(256): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.255-2070A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135748028 | ||||||
| chr9:135748044
|
C | T | 1 | a0005c0021t0001g0246 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.255-2054C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135748044 | ||||||
| chr9:135748121
|
C | T | 1 | a0001c0004t0002g0045 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.255-1977C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135748121 | ||||||
| chr9:135748162
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.255-1936G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135748162 | ||||||
| chr9:135748229
|
C | T | 130 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0042others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.255-1869C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135748229 | ||||||
| chr9:135748230
|
G | A | 22 | a0001c0001t0001g0183a0001c0001t0001g0230a0001c0001t0003g0222others(19): Show | 22 | HG00544.hp1 HG00609.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.255-1868G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135748230 | ||||||
| chr9:135748321
|
C | G | 119 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0042others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.255-1777C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135748321 | ||||||
| chr9:135748321
|
C | T | 1 | a0001c0005t0001g0217 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.255-1777C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135748321 | ||||||
| chr9:135748423
|
C | T | 1 | a0001c0001t0002g0098 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.255-1675C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135748423 | ||||||
| chr9:135748427
|
C | T | 79 | a0001c0001t0001g0015a0001c0001t0001g0095a0001c0001t0001g0183others(76): Show | 79 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.255-1671C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135748427 | ||||||
| chr9:135748452
|
A | T | 1 | a0001c0002t0001g0184 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.255-1646A>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135748452 | ||||||
| chr9:135748627
|
G | C | 40 | a0001c0001t0001g0183a0001c0001t0001g0230a0001c0001t0003g0222others(37): Show | 40 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.255-1471G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135748627 | ||||||
| chr9:135748727
|
G | A | 129 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0042others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.255-1371G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135748727 | ||||||
| chr9:135748762
|
G | A | 11 | a0001c0001t0008g0008a0001c0002t0001g0013a0001c0002t0001g0014others(8): Show | 11 | HG01074.hp1 HG01099.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.255-1336G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135748762 | ||||||
| chr9:135748772
|
G | T | 1 | a0001c0001t0001g0031 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.255-1326G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135748772 | ||||||
| chr9:135748942
|
G | GC | 52 | a0001c0001t0001g0183a0001c0001t0001g0230a0001c0001t0003g0222others(49): Show | 52 | HG00544.hp1 HG00609.hp2 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.255-1156_255-1155i others(3): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135748942 | ||||||
| chr9:135749157
|
C | A | 6 | a0001c0001t0027g0157a0001c0009t0006g0159a0001c0009t0018g0162others(3): Show | 6 | HG02055.hp2 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.255-941C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135749157 | ||||||
| chr9:135749332
|
C | T | 46 | a0001c0001t0001g0015a0001c0001t0001g0095a0001c0001t0001g0190others(43): Show | 46 | HG00438.hp1 HG00544.hp2 HG01952.hp2 others(43): Show |
intron_variant | MODIFIER | c.255-766C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135749332 | ||||||
| chr9:135749354
|
T | C | 10 | a0001c0001t0039g0156a0001c0002t0001g0115a0001c0002t0008g0026others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.255-744T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135749354 | ||||||
| chr9:135749370
|
G | A | 1 | a0001c0003t0041g0093 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.255-728G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135749370 | ||||||
| chr9:135749499
|
G | A | 6 | a0001c0001t0027g0157a0001c0009t0006g0159a0001c0009t0018g0162others(3): Show | 6 | HG02055.hp2 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.255-599G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135749499 | ||||||
| chr9:135749619
|
A | G | 31 | a0001c0001t0001g0183a0001c0001t0001g0230a0001c0001t0003g0222others(28): Show | 31 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.255-479A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135749619 | ||||||
| chr9:135749681
|
C | T | 3 | a0001c0002t0002g0107a0001c0002t0002g0114a0001c0002t0002g0145 | 3 | HG02145.hp2 HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.255-417C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135749681 | ||||||
| chr9:135749693
|
A | C | 1 | a0001c0001t0022g0193 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.255-405A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135749693 | ||||||
| chr9:135749704
|
T | C | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255-394T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135749704 | ||||||
| chr9:135749743
|
A | G | 34 | a0001c0001t0001g0190a0001c0001t0001g0194a0001c0001t0001g0204others(31): Show | 34 | HG00438.hp1 HG00544.hp2 HG01952.hp2 others(31): Show |
intron_variant | MODIFIER | c.255-355A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135749743 | ||||||
| chr9:135749769
|
CG | C | 9 | a0001c0001t0011g0032a0001c0002t0001g0086a0001c0002t0001g0087others(6): Show | 9 | HG01109.hp2 HG02004.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.255-327delG | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr9 | 135749769 | |||||
| chr9:135749790
|
G | C | 31 | a0001c0001t0001g0183a0001c0001t0001g0230a0001c0001t0003g0222others(28): Show | 31 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.255-308G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135749790 | ||||||
| chr9:135749803
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.255-295C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135749803 | ||||||
| chr9:135749804
|
G | A | 28 | a0001c0001t0001g0183a0001c0001t0001g0230a0001c0001t0003g0222others(25): Show | 28 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.255-294G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135749804 | ||||||
| chr9:135749815
|
C | T | 2 | a0001c0002t0001g0115a0001c0003t0006g0117 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.255-283C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135749815 | ||||||
| chr9:135749825
|
C | A | 2 | a0001c0003t0031g0269a0001c0020t0017g0001 | 2 | HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.255-273C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135749825 | ||||||
| chr9:135749826
|
G | A | 1 | a0001c0001t0028g0077 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.255-272G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135749826 | ||||||
| chr9:135749858
|
G | A | 2 | a0001c0004t0004g0224a0004c0017t0004g0223 | 2 | HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.255-240G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135749858 | ||||||
| chr9:135749931
|
A | G | 1 | a0003c0011t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.255-167A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135749931 | ||||||
| chr9:135749934
|
A | G | 47 | a0001c0001t0001g0183a0001c0001t0001g0230a0001c0001t0003g0222others(44): Show | 47 | HG00544.hp1 HG00609.hp2 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.255-164A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135749934 | ||||||
| chr9:135749958
|
G | C | 1 | a0001c0027t0009g0268 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.255-140G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 2/30 | chr9 | 135749958 | ||||||
| chr9:135750314
|
G | A | 43 | a0001c0001t0001g0015a0001c0001t0001g0095a0001c0001t0001g0097others(40): Show | 43 | HG00438.hp1 HG00544.hp2 HG01952.hp2 others(40): Show |
intron_variant | MODIFIER | c.334+137G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 3/30 | chr9 | 135750314 | ||||||
| chr9:135750330
|
G | A | 6 | a0001c0001t0027g0157a0001c0009t0006g0159a0001c0009t0018g0162others(3): Show | 6 | HG02055.hp2 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.334+153G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 3/30 | chr9 | 135750330 | ||||||
| chr9:135750372
|
C | T | 46 | a0001c0001t0001g0015a0001c0001t0001g0095a0001c0001t0001g0190others(43): Show | 46 | HG00438.hp1 HG00544.hp2 HG01952.hp2 others(43): Show |
intron_variant | MODIFIER | c.334+195C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 3/30 | chr9 | 135750372 | ||||||
| chr9:135750408
|
G | C | 30 | a0001c0001t0001g0183a0001c0001t0001g0230a0001c0001t0003g0222others(27): Show | 30 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.334+231G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 3/30 | chr9 | 135750408 | ||||||
| chr9:135750418
|
T | C | 30 | a0001c0001t0001g0183a0001c0001t0001g0230a0001c0001t0003g0222others(27): Show | 30 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.334+241T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 3/30 | chr9 | 135750418 | ||||||
| chr9:135750506
|
G | T | 1 | a0001c0003t0002g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.334+329G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 3/30 | chr9 | 135750506 | ||||||
| chr9:135750705
|
C | T | 3 | a0001c0001t0001g0076a0001c0001t0001g0088a0001c0001t0001g0099 | 3 | HG01981.hp1 HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.335-237C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 3/30 | chr9 | 135750705 | ||||||
| chr9:135750759
|
A | G | 4 | a0001c0001t0005g0175a0001c0001t0013g0176a0001c0002t0005g0220others(1): Show | 4 | HG01081.hp2 HG01167.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.335-183A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 3/30 | chr9 | 135750759 | ||||||
| chr9:135750926
|
G | A | 2 | a0001c0002t0001g0138a0001c0002t0001g0206 | 2 | NA18966.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.335-16G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 3/30 | chr9 | 135750926 | ||||||
| chr9:135751066
|
C | A | 148 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0031others(145): Show | 148 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.434+25C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135751066 | ||||||
| chr9:135751260
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.434+219G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135751260 | ||||||
| chr9:135751291
|
C | T | 2 | a0001c0004t0004g0003a0001c0004t0014g0002 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.434+250C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135751291 | ||||||
| chr9:135751310
|
G | A | 8 | a0001c0001t0027g0157a0001c0003t0031g0269a0001c0009t0006g0159others(5): Show | 8 | HG02055.hp2 HG02897.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.434+269G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135751310 | ||||||
| chr9:135751363
|
C | T | 104 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0052others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.434+322C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135751363 | ||||||
| chr9:135751410
|
G | T | 104 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0052others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.434+369G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135751410 | ||||||
| chr9:135751441
|
C | G | 46 | a0001c0001t0001g0015a0001c0001t0001g0095a0001c0001t0001g0190others(43): Show | 46 | HG00438.hp1 HG00544.hp2 HG01952.hp2 others(43): Show |
intron_variant | MODIFIER | c.434+400C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135751441 | ||||||
| chr9:135751487
|
C | T | 6 | a0001c0001t0027g0157a0001c0009t0006g0159a0001c0009t0018g0162others(3): Show | 6 | HG02055.hp2 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.434+446C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135751487 | ||||||
| chr9:135751548
|
G | A | 6 | a0001c0001t0027g0157a0001c0009t0006g0159a0001c0009t0018g0162others(3): Show | 6 | HG02055.hp2 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.434+507G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135751548 | ||||||
| chr9:135751567
|
C | T | 1 | a0001c0004t0001g0209 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.434+526C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135751567 | ||||||
| chr9:135751585
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.434+544G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135751585 | ||||||
| chr9:135751586
|
G | A | 6 | a0001c0001t0027g0157a0001c0009t0006g0159a0001c0009t0018g0162others(3): Show | 6 | HG02055.hp2 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.434+545G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135751586 | ||||||
| chr9:135751640
|
G | C | 9 | a0001c0001t0008g0008a0001c0002t0001g0013a0001c0002t0001g0014others(6): Show | 9 | HG01074.hp1 HG01099.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.434+599G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135751640 | ||||||
| chr9:135751678
|
C | G | 47 | a0001c0001t0001g0019a0001c0001t0001g0052a0001c0001t0001g0053others(44): Show | 47 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.434+637C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135751678 | ||||||
| chr9:135751700
|
G | C | 1 | a0001c0004t0006g0110 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.434+659G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135751700 | ||||||
| chr9:135751762
|
G | C | 3 | a0001c0003t0001g0267a0001c0024t0023g0048a0001c0027t0009g0268 | 3 | HG02647.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.434+721G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135751762 | ||||||
| chr9:135751780
|
G | A | 1 | a0001c0003t0001g0272 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.434+739G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135751780 | ||||||
| chr9:135751802
|
G | A | 4 | a0001c0001t0005g0175a0001c0001t0013g0176a0001c0002t0005g0220others(1): Show | 4 | HG01081.hp2 HG01167.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.434+761G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135751802 | ||||||
| chr9:135751829
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.434+788G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135751829 | ||||||
| chr9:135751837
|
T | C | 144 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0052others(141): Show | 144 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.434+796T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135751837 | ||||||
| chr9:135751841
|
C | G | 1 | a0001c0024t0023g0048 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.434+800C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135751841 | ||||||
| chr9:135752015
|
G | A | 1 | a0001c0004t0002g0147 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.434+974G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135752015 | ||||||
| chr9:135752040
|
T | A | 5 | a0001c0001t0002g0142a0001c0001t0002g0188a0001c0002t0001g0185others(2): Show | 5 | HG02015.hp1 HG02056.hp2 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.434+999T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135752040 | ||||||
| chr9:135752074
|
G | A | 58 | a0001c0001t0001g0019a0001c0001t0001g0052a0001c0001t0001g0053others(55): Show | 58 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.434+1033G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135752074 | ||||||
| chr9:135752161
|
C | T | 1 | a0001c0001t0028g0077 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.434+1120C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135752161 | ||||||
| chr9:135752201
|
G | A | 9 | a0001c0001t0008g0008a0001c0002t0001g0013a0001c0002t0001g0014others(6): Show | 9 | HG01074.hp1 HG01099.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.434+1160G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135752201 | ||||||
| chr9:135752231
|
G | A | 1 | a0003c0011t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.434+1190G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135752231 | ||||||
| chr9:135752305
|
G | A | 2 | a0001c0003t0001g0267a0001c0027t0009g0268 | 2 | HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.434+1264G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135752305 | ||||||
| chr9:135752357
|
T | C | 143 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0052others(140): Show | 143 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.434+1316T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135752357 | ||||||
| chr9:135752619
|
G | A | 46 | a0001c0001t0001g0015a0001c0001t0001g0095a0001c0001t0001g0190others(43): Show | 46 | HG00438.hp1 HG00544.hp2 HG01952.hp2 others(43): Show |
intron_variant | MODIFIER | c.435-1318G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135752619 | ||||||
| chr9:135752625
|
T | TGATGGAT others(1): Show |
3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0062 | 3 | HG00280.hp2 HG00323.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.435-1305_435-1298d others(10): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr9 | 135752625 | |||||
| chr9:135752629
|
G | A | 46 | a0001c0001t0001g0015a0001c0001t0001g0095a0001c0001t0001g0190others(43): Show | 46 | HG00438.hp1 HG00544.hp2 HG01952.hp2 others(43): Show |
intron_variant | MODIFIER | c.435-1308G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135752629 | ||||||
| chr9:135752636
|
TGGACGGA others(5): Show |
T | 6 | a0001c0001t0027g0157a0001c0009t0006g0159a0001c0009t0018g0162others(3): Show | 6 | HG02055.hp2 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.435-1297_435-1286d others(14): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr9 | 135752636 | |||||
| chr9:135752641
|
G | A | 2 | a0001c0002t0001g0013a0001c0002t0001g0014 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.435-1296G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135752641 | ||||||
| chr9:135752652
|
T | A | 1 | a0001c0002t0035g0109 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.435-1285T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135752652 | ||||||
| chr9:135752664
|
TGGAGTGG others(6): Show |
T | 9 | a0001c0001t0011g0032a0001c0002t0001g0086a0001c0002t0001g0087others(6): Show | 9 | HG01109.hp2 HG02004.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.435-1269_435-1257d others(15): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr9 | 135752664 | |||||
| chr9:135752771
|
A | C | 1 | a0001c0002t0035g0109 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.435-1166A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135752771 | ||||||
| chr9:135752778
|
G | A | 1 | a0001c0003t0008g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.435-1159G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135752778 | ||||||
| chr9:135752780
|
TGATG | T | 4 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0003g0105others(1): Show | 4 | HG00280.hp2 HG00323.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.435-1136_435-1133d others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr9 | 135752780 | |||||
| chr9:135752941
|
A | G | 1 | a0001c0003t0001g0082 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.435-996A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135752941 | ||||||
| chr9:135752949
|
G | A | 2 | a0001c0009t0006g0159a0001c0009t0018g0162 | 2 | HG02897.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.435-988G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135752949 | ||||||
| chr9:135752983
|
T | G | 1 | a0001c0003t0001g0082 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.435-954T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135752983 | ||||||
| chr9:135752986
|
T | A | 1 | a0001c0003t0001g0082 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.435-951T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135752986 | ||||||
| chr9:135752991
|
G | T | 1 | a0001c0003t0001g0082 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.435-946G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135752991 | ||||||
| chr9:135753014
|
AGGGATGG others(56): Show |
A | 1 | a0001c0003t0001g0082 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.435-922_435-860del others(63): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135753014 | ||||||
| chr9:135753035
|
TGAG | T | 9 | a0001c0001t0008g0008a0001c0002t0001g0013a0001c0002t0001g0014others(6): Show | 9 | HG01074.hp1 HG01099.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.435-901_435-899del others(3): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135753035 | ||||||
| chr9:135753077
|
G | GATGAGTG others(13): Show |
58 | a0001c0001t0001g0019a0001c0001t0001g0052a0001c0001t0001g0053others(55): Show | 58 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.435-841_435-822dup others(20): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr9 | 135753077 | |||||
| chr9:135753151
|
G | A | 46 | a0001c0001t0001g0015a0001c0001t0001g0095a0001c0001t0001g0190others(43): Show | 46 | HG00438.hp1 HG00544.hp2 HG01952.hp2 others(43): Show |
intron_variant | MODIFIER | c.435-786G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135753151 | ||||||
| chr9:135753220
|
C | T | 2 | a0001c0004t0004g0003a0001c0004t0014g0002 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.435-717C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135753220 | ||||||
| chr9:135753261
|
A | G | 9 | a0001c0001t0002g0266a0001c0003t0001g0126a0001c0003t0001g0127others(6): Show | 9 | HG00438.hp1 HG02071.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.435-676A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135753261 | ||||||
| chr9:135753356
|
A | G | 59 | a0001c0001t0001g0019a0001c0001t0001g0052a0001c0001t0001g0053others(56): Show | 59 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.435-581A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135753356 | ||||||
| chr9:135753525
|
C | A | 1 | a0001c0015t0001g0271 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.435-412C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135753525 | ||||||
| chr9:135753680
|
G | C | 58 | a0001c0001t0001g0019a0001c0001t0001g0052a0001c0001t0001g0053others(55): Show | 58 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.435-257G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135753680 | ||||||
| chr9:135753870
|
C | T | 56 | a0001c0001t0001g0019a0001c0001t0001g0052a0001c0001t0001g0053others(53): Show | 56 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.435-67C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 4/30 | chr9 | 135753870 | ||||||
| chr9:135754002
|
ACACTCCA others(57): Show |
A | 1 | a0001c0001t0016g0102 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.491+88_491+151delA others(63): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr9 | 135754002 | |||||
| chr9:135754028
|
C | T | 1 | a0001c0002t0002g0219 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.491+35C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 5/30 | chr9 | 135754028 | ||||||
| chr9:135754238
|
C | G | 1 | a0001c0001t0001g0067 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.491+245C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 5/30 | chr9 | 135754238 | ||||||
| chr9:135754419
|
G | T | 144 | a0001c0001t0001g0019a0001c0001t0001g0052a0001c0001t0001g0053others(141): Show | 144 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.491+426G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 5/30 | chr9 | 135754419 | ||||||
| chr9:135754445
|
T | C | 1 | a0003c0011t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.491+452T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 5/30 | chr9 | 135754445 | ||||||
| chr9:135754472
|
C | T | 50 | a0001c0001t0001g0019a0001c0001t0001g0052a0001c0001t0001g0053others(47): Show | 50 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.491+479C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 5/30 | chr9 | 135754472 | ||||||
| chr9:135754551
|
G | A | 27 | a0001c0001t0001g0183a0001c0001t0001g0230a0001c0001t0003g0222others(24): Show | 27 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.491+558G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 5/30 | chr9 | 135754551 | ||||||
| chr9:135754959
|
A | G | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.492-162A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 5/30 | chr9 | 135754959 | ||||||
| chr9:135755004
|
A | G | 1 | a0001c0002t0001g0121 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.492-117A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 5/30 | chr9 | 135755004 | ||||||
| chr9:135755027
|
A | G | 27 | a0001c0001t0001g0183a0001c0001t0001g0230a0001c0001t0003g0222others(24): Show | 27 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.492-94A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 5/30 | chr9 | 135755027 | ||||||
| chr9:135755035
|
C | T | 57 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(54): Show | 57 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.492-86C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 5/30 | chr9 | 135755035 | ||||||
| chr9:135755208
|
T | G | 6 | a0001c0001t0027g0157a0001c0009t0006g0159a0001c0009t0018g0162others(3): Show | 6 | HG02055.hp2 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.540+39T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 6/30 | chr9 | 135755208 | ||||||
| chr9:135755260
|
C | T | 1 | a0001c0005t0001g0240 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.540+91C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 6/30 | chr9 | 135755260 | ||||||
| chr9:135755282
|
C | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.540+113C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 6/30 | chr9 | 135755282 | ||||||
| chr9:135755432
|
G | A | 1 | a0001c0002t0002g0219 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.540+263G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 6/30 | chr9 | 135755432 | ||||||
| chr9:135755649
|
G | A | 55 | a0001c0001t0001g0015a0001c0001t0001g0095a0001c0001t0001g0190others(52): Show | 55 | HG00438.hp1 HG00544.hp2 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.540+480G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 6/30 | chr9 | 135755649 | ||||||
| chr9:135755778
|
G | A | 112 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0052others(109): Show | 112 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.540+609G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 6/30 | chr9 | 135755778 | ||||||
| chr9:135755796
|
TCAGGCTC others(21): Show |
T | 2 | a0001c0013t0024g0046a0001c0027t0009g0268 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.540+654_540+681del others(28): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr9 | 135755796 | |||||
| chr9:135755847
|
C | A | 4 | a0001c0002t0002g0021a0001c0002t0002g0107a0001c0002t0002g0114others(1): Show | 4 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+678C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 6/30 | chr9 | 135755847 | ||||||
| chr9:135756220
|
G | A | 22 | a0001c0001t0001g0183a0001c0001t0001g0230a0001c0001t0003g0222others(19): Show | 22 | HG00544.hp1 HG00609.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.541-653G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 6/30 | chr9 | 135756220 | ||||||
| chr9:135756243
|
C | T | 3 | a0001c0003t0001g0267a0001c0024t0023g0048a0001c0027t0009g0268 | 3 | HG02647.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.541-630C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 6/30 | chr9 | 135756243 | ||||||
| chr9:135756318
|
T | C | 56 | a0001c0001t0001g0015a0001c0001t0001g0095a0001c0001t0001g0190others(53): Show | 56 | HG00438.hp1 HG00544.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.541-555T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 6/30 | chr9 | 135756318 | ||||||
| chr9:135756598
|
G | A | 11 | a0001c0001t0008g0008a0001c0002t0001g0013a0001c0002t0001g0014others(8): Show | 11 | HG01074.hp1 HG01099.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.541-275G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 6/30 | chr9 | 135756598 | ||||||
| chr9:135756648
|
C | T | 27 | a0001c0001t0001g0183a0001c0001t0001g0230a0001c0001t0003g0222others(24): Show | 27 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.541-225C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 6/30 | chr9 | 135756648 | ||||||
| chr9:135756686
|
C | T | 10 | a0001c0001t0008g0008a0001c0002t0001g0013a0001c0002t0001g0014others(7): Show | 10 | HG01074.hp1 HG01099.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.541-187C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 6/30 | chr9 | 135756686 | ||||||
| chr9:135756739
|
A | G | 1 | a0001c0001t0016g0254 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.541-134A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 6/30 | chr9 | 135756739 | ||||||
| chr9:135756967
|
GTCCCCAC others(2): Show |
G | 32 | a0001c0001t0001g0183a0001c0001t0001g0230a0001c0001t0003g0218others(29): Show | 32 | HG00544.hp1 HG00609.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.600+51_600+59delCC others(7): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr9 | 135756967 | |||||
| chr9:135756983
|
C | G | 112 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0052others(109): Show | 112 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.600+51C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 7/30 | chr9 | 135756983 | ||||||
| chr9:135756991
|
A | C | 111 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0052others(108): Show | 111 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.600+59A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 7/30 | chr9 | 135756991 | ||||||
| chr9:135756992
|
G | A | 111 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0052others(108): Show | 111 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.600+60G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 7/30 | chr9 | 135756992 | ||||||
| chr9:135757003
|
C | CCTCTCCC others(1): Show |
111 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0052others(108): Show | 111 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.600+71_600+72insCT others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 7/30 | chr9 | 135757003 | ||||||
| chr9:135757005
|
C | CCCCCACC others(11): Show |
32 | a0001c0001t0001g0183a0001c0001t0001g0230a0001c0001t0003g0218others(29): Show | 32 | HG00544.hp1 HG00609.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.600+86_600+87insCA others(16): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr9 | 135757005 | |||||
| chr9:135757005
|
C | CT | 111 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0052others(108): Show | 111 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.600+73_600+74insT | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 7/30 | chr9 | 135757005 | ||||||
| chr9:135757477
|
C | T | 1 | a0001c0003t0009g0177 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.759+96C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 9/30 | chr9 | 135757477 | ||||||
| chr9:135757857
|
C | A | 47 | a0001c0001t0001g0019a0001c0001t0001g0052a0001c0001t0001g0053others(44): Show | 47 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.759+476C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 9/30 | chr9 | 135757857 | ||||||
| chr9:135758052
|
A | AGGCTGCC others(81): Show |
50 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0072others(47): Show | 50 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(47): Show |
intron_variant | MODIFIER | c.760-354_760-353ins others(88): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr9 | 135758052 | |||||
| chr9:135758057
|
G | GC | 141 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0052others(138): Show | 141 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.760-354dupC | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr9 | 135758057 | |||||
| chr9:135758069
|
C | T | 63 | a0001c0001t0001g0015a0001c0001t0001g0095a0001c0001t0001g0190others(60): Show | 63 | HG00438.hp1 HG00544.hp2 HG01109.hp2 others(60): Show |
intron_variant | MODIFIER | c.760-345C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 9/30 | chr9 | 135758069 | ||||||
| chr9:135758094
|
C | T | 2 | a0001c0001t0002g0196a0001c0003t0002g0199 | 2 | HG02027.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.760-320C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 9/30 | chr9 | 135758094 | ||||||
| chr9:135758120
|
G | A | 3 | a0001c0002t0009g0047a0001c0004t0002g0147a0001c0013t0024g0046 | 3 | HG01192.hp2 HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.760-294G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 9/30 | chr9 | 135758120 | ||||||
| chr9:135758160
|
C | T | 1 | a0001c0004t0002g0045 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.760-254C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 9/30 | chr9 | 135758160 | ||||||
| chr9:135758167
|
A | ACAGGTGT others(85): Show |
15 | a0001c0001t0001g0038a0001c0001t0001g0106a0001c0001t0001g0118others(12): Show | 15 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.760-156_760-155ins others(92): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr9 | 135758167 | |||||
| chr9:135758183
|
G | GCAGGCTG others(85): Show |
1 | a0001c0002t0003g0120 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.760-156_760-155ins others(92): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr9 | 135758183 | |||||
| chr9:135758195
|
G | A | 1 | a0001c0003t0031g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.760-219G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 9/30 | chr9 | 135758195 | ||||||
| chr9:135758229
|
G | A | 1 | a0001c0003t0031g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.760-185G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 9/30 | chr9 | 135758229 | ||||||
| chr9:135758241
|
A | G | 1 | a0001c0003t0031g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.760-173A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 9/30 | chr9 | 135758241 | ||||||
| chr9:135758259
|
A | G | 1 | a0001c0003t0031g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.760-155A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 9/30 | chr9 | 135758259 | ||||||
| chr9:135758275
|
A | ACAGGCTG others(85): Show |
76 | a0001c0001t0001g0015a0001c0001t0001g0095a0001c0001t0001g0183others(73): Show | 76 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.760-98_760-97insAG others(90): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr9 | 135758275 | |||||
| chr9:135758275
|
A | ACAGGCTG others(361): Show |
1 | a0001c0002t0001g0231 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.760-98_760-97insAG others(366): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr9 | 135758275 | |||||
| chr9:135758275
|
A | ACAGGCTG others(85): Show |
10 | a0001c0001t0011g0032a0001c0002t0001g0086a0001c0002t0001g0087others(7): Show | 10 | HG01109.hp2 HG02004.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.760-98_760-97insAG others(90): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr9 | 135758275 | |||||
| chr9:135758275
|
A | G | 12 | a0001c0001t0001g0214a0001c0002t0003g0120a0001c0002t0004g0257others(9): Show | 12 | HG01358.hp2 HG01891.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.760-139A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 9/30 | chr9 | 135758275 | ||||||
| chr9:135758276
|
C | CAGGCTGC others(85): Show |
45 | a0001c0001t0001g0019a0001c0001t0001g0052a0001c0001t0001g0053others(42): Show | 45 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.760-110_760-109ins others(92): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr9 | 135758276 | |||||
| chr9:135758276
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.760-138C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 9/30 | chr9 | 135758276 | ||||||
| chr9:135758299
|
C | CGAGACGC others(39): Show |
1 | a0001c0027t0009g0268 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.760-98_760-97insAG others(44): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr9 | 135758299 | |||||
| chr9:135758331
|
C | T | 1 | a0001c0003t0031g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.760-83C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 9/30 | chr9 | 135758331 | ||||||
| chr9:135758367
|
C | T | 3 | a0001c0001t0001g0167a0001c0001t0003g0181a0001c0002t0001g0124 | 3 | HG00423.hp1 HG02486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.760-47C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 9/30 | chr9 | 135758367 | ||||||
| chr9:135758544
|
G | A | 1 | a0001c0002t0001g0115 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.854+36G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 10/30 | chr9 | 135758544 | ||||||
| chr9:135758574
|
G | A | 1 | a0001c0001t0001g0242 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.854+66G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 10/30 | chr9 | 135758574 | ||||||
| chr9:135758577
|
C | G | 1 | a0001c0003t0008g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.854+69C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 10/30 | chr9 | 135758577 | ||||||
| chr9:135758690
|
C | T | 1 | a0001c0002t0005g0081 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.854+182C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 10/30 | chr9 | 135758690 | ||||||
| chr9:135758810
|
G | A | 8 | a0001c0004t0002g0045a0001c0004t0004g0003a0001c0004t0014g0002others(5): Show | 8 | HG01496.hp2 HG02055.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.854+302G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 10/30 | chr9 | 135758810 | ||||||
| chr9:135758860
|
G | C | 1 | a0001c0003t0001g0022 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.854+352G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 10/30 | chr9 | 135758860 | ||||||
| chr9:135758890
|
G | A | 1 | a0001c0002t0001g0262 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.854+382G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 10/30 | chr9 | 135758890 | ||||||
| chr9:135758910
|
ATGCCCAC others(2): Show |
A | 15 | a0001c0001t0001g0038a0001c0001t0001g0106a0001c0001t0001g0118others(12): Show | 15 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.854+410_854+418del others(9): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 10/30 | INFO_REALIGN_3_PRIME | chr9 | 135758910 | |||||
| chr9:135759080
|
C | T | 1 | a0001c0016t0019g0116 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.854+572C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 10/30 | chr9 | 135759080 | ||||||
| chr9:135759226
|
G | A | 1 | a0001c0003t0031g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.855-453G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 10/30 | chr9 | 135759226 | ||||||
| chr9:135759249
|
G | A | 43 | a0001c0001t0001g0015a0001c0001t0001g0042a0001c0001t0001g0095others(40): Show | 43 | HG00438.hp1 HG00544.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.855-430G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 10/30 | chr9 | 135759249 | ||||||
| chr9:135759372
|
C | T | 1 | a0001c0003t0001g0126 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.855-307C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 10/30 | chr9 | 135759372 | ||||||
| chr9:135759396
|
AG | A | 19 | a0001c0001t0001g0230a0001c0001t0003g0222a0001c0002t0001g0121others(16): Show | 19 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.855-280delG | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 10/30 | INFO_REALIGN_3_PRIME | chr9 | 135759396 | |||||
| chr9:135759419
|
G | A | 1 | a0001c0003t0001g0272 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.855-260G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 10/30 | chr9 | 135759419 | ||||||
| chr9:135759636
|
A | G | 54 | a0001c0001t0001g0015a0001c0001t0001g0042a0001c0001t0001g0095others(51): Show | 54 | HG00438.hp1 HG00544.hp2 HG01099.hp1 others(51): Show |
intron_variant | MODIFIER | c.855-43A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 10/30 | chr9 | 135759636 | ||||||
| chr9:135759880
|
C | A | 1 | a0001c0002t0002g0228 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1035+21C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135759880 | ||||||
| chr9:135759891
|
A | T | 2 | a0001c0002t0005g0079a0001c0002t0040g0160 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1035+32A>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135759891 | ||||||
| chr9:135760020
|
C | G | 1 | a0001c0002t0001g0115 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1035+161C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135760020 | ||||||
| chr9:135760151
|
C | T | 46 | a0001c0001t0001g0015a0001c0001t0001g0042a0001c0001t0001g0095others(43): Show | 46 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.1035+292C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135760151 | ||||||
| chr9:135760182
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1035+323C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135760182 | ||||||
| chr9:135760257
|
C | T | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1035+398C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135760257 | ||||||
| chr9:135760288
|
C | T | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1035+429C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135760288 | ||||||
| chr9:135760313
|
A | G | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1035+454A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135760313 | ||||||
| chr9:135760457
|
G | A | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1035+598G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135760457 | ||||||
| chr9:135760533
|
C | T | 1 | a0001c0020t0017g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1035+674C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135760533 | ||||||
| chr9:135760612
|
T | C | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1035+753T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135760612 | ||||||
| chr9:135760664
|
C | A | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1035+805C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135760664 | ||||||
| chr9:135760710
|
C | T | 3 | a0001c0001t0002g0188a0001c0002t0001g0185a0001c0002t0001g0189 | 3 | HG02015.hp1 HG02056.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1035+851C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135760710 | ||||||
| chr9:135760802
|
C | G | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1035+943C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135760802 | ||||||
| chr9:135760806
|
C | T | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1035+947C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135760806 | ||||||
| chr9:135760809
|
G | A | 1 | a0001c0003t0002g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1035+950G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135760809 | ||||||
| chr9:135760840
|
G | A | 45 | a0001c0001t0001g0015a0001c0001t0001g0042a0001c0001t0001g0095others(42): Show | 45 | HG00438.hp1 HG00544.hp2 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.1035+981G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135760840 | ||||||
| chr9:135760882
|
C | T | 17 | a0001c0001t0003g0222a0001c0002t0001g0121a0001c0002t0001g0184others(14): Show | 17 | HG00140.hp1 HG00609.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.1035+1023C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135760882 | ||||||
| chr9:135760889
|
CTTCCCCC others(3): Show |
C | 1 | a0001c0003t0001g0040 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1035+1034_1035+104 others(14): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr9 | 135760889 | |||||
| chr9:135760979
|
C | T | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1035+1120C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135760979 | ||||||
| chr9:135761027
|
A | AT | 85 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0042others(82): Show | 85 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1035+1180dupT | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr9 | 135761027 | |||||
| chr9:135761039
|
T | TA | 12 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0154others(9): Show | 12 | HG00741.hp2 HG01074.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.1035+1183dupA | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr9 | 135761039 | |||||
| chr9:135761087
|
C | T | 1 | a0001c0003t0001g0022 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1035+1228C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135761087 | ||||||
| chr9:135761105
|
C | T | 1 | a0001c0003t0001g0037 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1035+1246C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135761105 | ||||||
| chr9:135761147
|
C | T | 1 | a0001c0002t0006g0054 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1035+1288C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135761147 | ||||||
| chr9:135761225
|
C | T | 1 | a0001c0001t0002g0142 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1035+1366C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135761225 | ||||||
| chr9:135761323
|
G | A | 1 | a0001c0003t0001g0180 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1035+1464G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135761323 | ||||||
| chr9:135761357
|
C | G | 1 | a0001c0003t0001g0022 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1035+1498C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135761357 | ||||||
| chr9:135761435
|
G | C | 1 | a0001c0002t0009g0047 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1035+1576G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135761435 | ||||||
| chr9:135761446
|
G | T | 1 | a0001c0019t0003g0089 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1035+1587G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135761446 | ||||||
| chr9:135761482
|
C | T | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1035+1623C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135761482 | ||||||
| chr9:135761618
|
C | T | 1 | a0001c0001t0005g0174 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1035+1759C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135761618 | ||||||
| chr9:135761634
|
G | A | 1 | a0001c0003t0002g0236 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1035+1775G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135761634 | ||||||
| chr9:135761645
|
G | A | 1 | a0001c0016t0019g0116 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1035+1786G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135761645 | ||||||
| chr9:135761645
|
G | T | 46 | a0001c0001t0001g0019a0001c0001t0001g0052a0001c0001t0001g0053others(43): Show | 46 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.1035+1786G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135761645 | ||||||
| chr9:135761662
|
A | G | 104 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0042others(101): Show | 104 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1035+1803A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135761662 | ||||||
| chr9:135761666
|
C | T | 35 | a0001c0001t0001g0038a0001c0001t0001g0057a0001c0001t0001g0072others(32): Show | 35 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.1035+1807C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135761666 | ||||||
| chr9:135761667
|
G | A | 3 | a0001c0004t0004g0025a0001c0004t0004g0224a0004c0017t0004g0223 | 3 | HG00741.hp2 HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1035+1808G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135761667 | ||||||
| chr9:135761806
|
A | G | 77 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(74): Show | 77 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1035+1947A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135761806 | ||||||
| chr9:135761857
|
G | A | 1 | a0001c0003t0002g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1035+1998G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135761857 | ||||||
| chr9:135761913
|
C | T | 1 | a0001c0026t0001g0051 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1035+2054C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135761913 | ||||||
| chr9:135762013
|
G | A | 1 | a0001c0001t0043g0197 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1035+2154G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135762013 | ||||||
| chr9:135762054
|
G | A | 1 | a0001c0003t0002g0199 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1035+2195G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135762054 | ||||||
| chr9:135762066
|
C | T | 1 | a0001c0002t0001g0154 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1035+2207C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135762066 | ||||||
| chr9:135762080
|
G | A | 1 | a0001c0003t0001g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1035+2221G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135762080 | ||||||
| chr9:135762311
|
C | T | 68 | a0001c0001t0001g0141a0001c0001t0001g0169a0001c0001t0001g0214others(65): Show | 68 | HG00140.hp1 HG00609.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.1035+2452C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135762311 | ||||||
| chr9:135762314
|
C | T | 9 | a0001c0002t0001g0086a0001c0002t0001g0087a0001c0002t0001g0244others(6): Show | 9 | HG01109.hp2 HG02004.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1035+2455C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135762314 | ||||||
| chr9:135762434
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1035+2575G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135762434 | ||||||
| chr9:135762460
|
A | C | 47 | a0001c0001t0027g0157a0001c0002t0001g0086a0001c0002t0001g0087others(44): Show | 47 | HG00140.hp1 HG00609.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.1036-2571A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135762460 | ||||||
| chr9:135762468
|
C | A | 70 | a0001c0001t0001g0042a0001c0001t0001g0052a0001c0001t0001g0053others(67): Show | 70 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.1036-2563C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135762468 | ||||||
| chr9:135762514
|
G | A | 1 | a0001c0002t0001g0229 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1036-2517G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135762514 | ||||||
| chr9:135762525
|
A | G | 11 | a0001c0001t0001g0202a0001c0001t0039g0156a0001c0002t0001g0013others(8): Show | 11 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.1036-2506A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135762525 | ||||||
| chr9:135762545
|
C | T | 4 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0002g0049others(1): Show | 4 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.1036-2486C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135762545 | ||||||
| chr9:135762573
|
C | G | 1 | a0001c0002t0003g0120 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1036-2458C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135762573 | ||||||
| chr9:135762577
|
G | A | 7 | a0001c0002t0001g0086a0001c0002t0001g0087a0001c0002t0001g0244others(4): Show | 7 | HG01109.hp2 HG02004.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1036-2454G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135762577 | ||||||
| chr9:135762642
|
C | T | 29 | a0001c0001t0001g0019a0001c0001t0001g0038a0001c0001t0001g0057others(26): Show | 29 | HG00099.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1036-2389C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135762642 | ||||||
| chr9:135762773
|
A | G | 7 | a0001c0002t0005g0220a0001c0002t0006g0054a0001c0004t0004g0025others(4): Show | 7 | HG00741.hp2 HG01167.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1036-2258A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135762773 | ||||||
| chr9:135762927
|
C | A | 1 | a0001c0001t0002g0098 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1036-2104C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135762927 | ||||||
| chr9:135762927
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0003g0181 | 2 | HG02486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1036-2104C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135762927 | ||||||
| chr9:135763077
|
C | T | 1 | a0001c0013t0024g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1036-1954C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135763077 | ||||||
| chr9:135763244
|
A | ATGACTGG others(14): Show |
46 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(43): Show | 46 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.1036-1767_1036-176 others(25): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr9 | 135763244 | |||||
| chr9:135763274
|
G | A | 1 | a0001c0002t0001g0184 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1036-1757G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135763274 | ||||||
| chr9:135763285
|
T | C | 108 | a0001c0001t0001g0019a0001c0001t0001g0052a0001c0001t0001g0053others(105): Show | 108 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1036-1746T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135763285 | ||||||
| chr9:135763286
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1036-1745G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135763286 | ||||||
| chr9:135763475
|
G | A | 7 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0003t0002g0027others(4): Show | 7 | HG01106.hp2 HG01109.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1036-1556G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135763475 | ||||||
| chr9:135763489
|
G | A | 9 | a0001c0002t0001g0172a0001c0002t0002g0021a0001c0002t0002g0107others(6): Show | 9 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1036-1542G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135763489 | ||||||
| chr9:135763645
|
G | A | 72 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0042others(69): Show | 72 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.1036-1386G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135763645 | ||||||
| chr9:135763716
|
T | G | 8 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0154others(5): Show | 8 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1036-1315T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135763716 | ||||||
| chr9:135763814
|
G | A | 25 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(22): Show | 25 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.1036-1217G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135763814 | ||||||
| chr9:135763826
|
T | G | 44 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1036-1205T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135763826 | ||||||
| chr9:135763836
|
C | T | 1 | a0001c0002t0025g0149 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1036-1195C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135763836 | ||||||
| chr9:135763840
|
G | A | 1 | a0001c0004t0001g0209 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1036-1191G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135763840 | ||||||
| chr9:135763857
|
G | C | 1 | a0001c0002t0001g0087 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1036-1174G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135763857 | ||||||
| chr9:135763977
|
C | T | 7 | a0001c0002t0001g0086a0001c0002t0001g0087a0001c0002t0001g0244others(4): Show | 7 | HG01109.hp2 HG02004.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1036-1054C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135763977 | ||||||
| chr9:135764049
|
G | A | 2 | a0001c0002t0005g0079a0001c0002t0040g0160 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1036-982G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764049 | ||||||
| chr9:135764080
|
C | A | 44 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1036-951C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764080 | ||||||
| chr9:135764133
|
C | T | 7 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0003t0002g0027others(4): Show | 7 | HG01106.hp2 HG01109.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1036-898C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764133 | ||||||
| chr9:135764162
|
C | G | 1 | a0001c0003t0001g0034 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1036-869C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764162 | ||||||
| chr9:135764165
|
G | A | 2 | a0001c0010t0001g0158a0001c0010t0014g0161 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1036-866G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764165 | ||||||
| chr9:135764205
|
C | T | 1 | a0001c0002t0001g0201 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1036-826C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764205 | ||||||
| chr9:135764217
|
A | G | 1 | a0001c0002t0001g0086 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1036-814A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764217 | ||||||
| chr9:135764293
|
AAAAAAT | A | 25 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(22): Show | 25 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.1036-727_1036-722d others(8): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr9 | 135764293 | |||||
| chr9:135764313
|
G | C | 8 | a0001c0002t0001g0172a0001c0002t0002g0021a0001c0002t0002g0107others(5): Show | 8 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1036-718G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764313 | ||||||
| chr9:135764318
|
T | G | 44 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1036-713T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764318 | ||||||
| chr9:135764330
|
T | C | 44 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1036-701T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764330 | ||||||
| chr9:135764350
|
C | T | 7 | a0001c0002t0001g0050a0001c0002t0001g0185a0001c0002t0001g0189others(4): Show | 7 | HG00423.hp2 HG02015.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036-681C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764350 | ||||||
| chr9:135764422
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1036-609G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764422 | ||||||
| chr9:135764450
|
C | A | 44 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1036-581C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764450 | ||||||
| chr9:135764452
|
T | C | 5 | a0001c0003t0002g0027a0001c0006t0009g0012a0001c0006t0010g0010others(2): Show | 5 | HG01109.hp1 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1036-579T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764452 | ||||||
| chr9:135764505
|
C | T | 1 | a0001c0001t0003g0218 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1036-526C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764505 | ||||||
| chr9:135764522
|
G | A | 1 | a0001c0003t0006g0023 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1036-509G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764522 | ||||||
| chr9:135764588
|
G | A | 44 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1036-443G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764588 | ||||||
| chr9:135764691
|
C | T | 1 | a0001c0001t0028g0077 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1036-340C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764691 | ||||||
| chr9:135764788
|
G | A | 3 | a0001c0001t0001g0015a0001c0003t0001g0018a0007c0023t0001g0017 | 3 | HG02735.hp2 HG03492.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1036-243G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764788 | ||||||
| chr9:135764798
|
C | T | 44 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1036-233C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764798 | ||||||
| chr9:135764824
|
C | T | 44 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1036-207C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764824 | ||||||
| chr9:135764825
|
G | A | 40 | a0001c0002t0001g0094a0001c0002t0001g0121a0001c0002t0001g0184others(37): Show | 40 | HG00140.hp1 HG00609.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.1036-206G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764825 | ||||||
| chr9:135764826
|
G | T | 9 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0154others(6): Show | 9 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.1036-205G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764826 | ||||||
| chr9:135764861
|
A | G | 25 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(22): Show | 25 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.1036-170A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764861 | ||||||
| chr9:135764863
|
C | G | 3 | a0001c0001t0001g0202a0001c0001t0039g0156a0001c0003t0001g0267 | 3 | HG01243.hp1 HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1036-168C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764863 | ||||||
| chr9:135764871
|
G | T | 8 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0154others(5): Show | 8 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1036-160G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764871 | ||||||
| chr9:135764937
|
T | C | 44 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1036-94T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764937 | ||||||
| chr9:135764992
|
A | G | 44 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1036-39A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135764992 | ||||||
| chr9:135765016
|
G | A | 9 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0154others(6): Show | 9 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.1036-15G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 11/30 | chr9 | 135765016 | ||||||
| chr9:135765207
|
T | G | 44 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1200+12T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 12/30 | chr9 | 135765207 | ||||||
| chr9:135765263
|
A | G | 8 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0154others(5): Show | 8 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1200+68A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 12/30 | chr9 | 135765263 | ||||||
| chr9:135765289
|
C | A | 2 | a0001c0003t0008g0043a0001c0020t0017g0001 | 2 | HG02451.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1200+94C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 12/30 | chr9 | 135765289 | ||||||
| chr9:135765325
|
T | C | 44 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1200+130T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 12/30 | chr9 | 135765325 | ||||||
| chr9:135765340
|
G | A | 1 | a0001c0002t0004g0257 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1200+145G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 12/30 | chr9 | 135765340 | ||||||
| chr9:135765349
|
CGCCATCC others(13): Show |
C | 84 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(81): Show | 84 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1200+177_1200+196d others(22): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 12/30 | INFO_REALIGN_3_PRIME | chr9 | 135765349 | |||||
| chr9:135765472
|
G | T | 1 | a0001c0020t0017g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1201-152G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 12/30 | chr9 | 135765472 | ||||||
| chr9:135765515
|
T | C | 2 | a0001c0004t0001g0005a0001c0004t0001g0007 | 2 | HG01074.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1201-109T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 12/30 | chr9 | 135765515 | ||||||
| chr9:135765569
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1201-55G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 12/30 | chr9 | 135765569 | ||||||
| chr9:135765575
|
G | T | 1 | a0001c0002t0001g0115 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1201-49G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 12/30 | chr9 | 135765575 | ||||||
| chr9:135765577
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1201-47G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 12/30 | chr9 | 135765577 | ||||||
| chr9:135765593
|
C | T | 1 | a0001c0001t0003g0222 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1201-31C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 12/30 | chr9 | 135765593 | ||||||
| chr9:135765789
|
A | G | 44 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1337+29A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135765789 | ||||||
| chr9:135765798
|
C | T | 1 | a0001c0003t0001g0126 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1337+38C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135765798 | ||||||
| chr9:135765841
|
G | A | 44 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1337+81G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135765841 | ||||||
| chr9:135765873
|
C | A | 1 | a0001c0004t0002g0125 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1337+113C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135765873 | ||||||
| chr9:135765881
|
A | C | 25 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(22): Show | 25 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.1337+121A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135765881 | ||||||
| chr9:135765931
|
G | A | 1 | a0001c0013t0024g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1337+171G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135765931 | ||||||
| chr9:135765958
|
T | C | 7 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0003t0002g0027others(4): Show | 7 | HG01106.hp2 HG01109.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1337+198T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135765958 | ||||||
| chr9:135766056
|
AGGGTGGA others(7): Show |
A | 42 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(39): Show | 42 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1337+310_1337+323d others(16): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135766056 | |||||
| chr9:135766174
|
G | A | 1 | a0001c0003t0001g0040 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1337+414G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135766174 | ||||||
| chr9:135766177
|
C | T | 44 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1337+417C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135766177 | ||||||
| chr9:135766238
|
AGGGTGGA others(21): Show |
A | 1 | a0001c0001t0038g0100 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1337+491_1337+518d others(30): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135766238 | |||||
| chr9:135766322
|
G | T | 44 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1337+562G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135766322 | ||||||
| chr9:135766358
|
T | C | 44 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1337+598T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135766358 | ||||||
| chr9:135766400
|
C | T | 1 | a0001c0003t0001g0272 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1337+640C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135766400 | ||||||
| chr9:135766414
|
C | A | 1 | a0001c0001t0001g0042 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1337+654C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135766414 | ||||||
| chr9:135766495
|
G | A | 8 | a0001c0002t0001g0172a0001c0002t0002g0021a0001c0002t0002g0107others(5): Show | 8 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1337+735G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135766495 | ||||||
| chr9:135766537
|
ATCTGGGG others(7): Show |
A | 10 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0003t0002g0027others(7): Show | 10 | HG01106.hp2 HG01109.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1337+789_1337+802d others(16): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135766537 | |||||
| chr9:135766570
|
TGGTGGAC others(7): Show |
T | 7 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0003t0002g0027others(4): Show | 7 | HG01106.hp2 HG01109.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1337+819_1337+832d others(16): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135766570 | |||||
| chr9:135766662
|
T | C | 44 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1337+902T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135766662 | ||||||
| chr9:135766663
|
G | A | 44 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1337+903G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135766663 | ||||||
| chr9:135766665
|
C | T | 1 | a0001c0014t0017g0212 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1337+905C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135766665 | ||||||
| chr9:135766687
|
T | C | 44 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1337+927T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135766687 | ||||||
| chr9:135766718
|
C | T | 19 | a0001c0001t0001g0019a0001c0001t0001g0057a0001c0001t0001g0122others(16): Show | 19 | HG00099.hp1 HG00741.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1337+958C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135766718 | ||||||
| chr9:135766816
|
G | A | 3 | a0001c0004t0002g0147a0001c0010t0001g0158a0001c0010t0014g0161 | 3 | HG01192.hp2 HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1337+1056G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135766816 | ||||||
| chr9:135767009
|
C | T | 3 | a0001c0003t0001g0126a0001c0003t0001g0180a0001c0003t0001g0210 | 3 | NA18948.hp2 NA18970.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1337+1249C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135767009 | ||||||
| chr9:135767032
|
G | A | 7 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0003t0002g0027others(4): Show | 7 | HG01106.hp2 HG01109.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1337+1272G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135767032 | ||||||
| chr9:135767092
|
C | CTGAATGT others(6): Show |
1 | a0001c0001t0011g0032 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1337+1333_1337+134 others(17): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135767092 | |||||
| chr9:135767094
|
G | A | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1337+1334G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135767094 | ||||||
| chr9:135767119
|
T | G | 44 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1337+1359T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135767119 | ||||||
| chr9:135767225
|
C | T | 1 | a0001c0003t0001g0248 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1338-1385C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135767225 | ||||||
| chr9:135767302
|
G | A | 55 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0042others(52): Show | 55 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.1338-1308G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135767302 | ||||||
| chr9:135767418
|
TAGAC | T | 40 | a0001c0002t0001g0094a0001c0002t0001g0121a0001c0002t0001g0184others(37): Show | 40 | HG00140.hp1 HG00609.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.1338-1189_1338-118 others(8): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135767418 | |||||
| chr9:135767439
|
T | G | 1 | a0001c0001t0001g0038 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1338-1171T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135767439 | ||||||
| chr9:135767440
|
A | G | 44 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1338-1170A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135767440 | ||||||
| chr9:135767481
|
G | A | 55 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0042others(52): Show | 55 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.1338-1129G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135767481 | ||||||
| chr9:135767554
|
G | A | 44 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1338-1056G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135767554 | ||||||
| chr9:135767685
|
C | T | 1 | a0001c0003t0002g0101 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1338-925C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135767685 | ||||||
| chr9:135767716
|
C | G | 44 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1338-894C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135767716 | ||||||
| chr9:135767801
|
C | T | 1 | a0001c0013t0024g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1338-809C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135767801 | ||||||
| chr9:135767855
|
C | A | 3 | a0001c0002t0009g0047a0001c0004t0004g0003a0001c0004t0014g0002 | 3 | HG02486.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1338-755C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135767855 | ||||||
| chr9:135767961
|
GC | G | 9 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0154others(6): Show | 9 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.1338-644delC | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135767961 | |||||
| chr9:135767988
|
A | G | 3 | a0001c0003t0001g0126a0001c0003t0001g0180a0001c0003t0001g0210 | 3 | NA18948.hp2 NA18970.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1338-622A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135767988 | ||||||
| chr9:135767992
|
G | A | 3 | a0001c0003t0001g0126a0001c0003t0001g0180a0001c0003t0001g0210 | 3 | NA18948.hp2 NA18970.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1338-618G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135767992 | ||||||
| chr9:135768001
|
G | A | 5 | a0001c0003t0001g0080a0001c0003t0001g0164a0001c0003t0001g0260others(2): Show | 5 | HG02280.hp1 HG02886.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1338-609G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768001 | ||||||
| chr9:135768049
|
CAG | C | 25 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(22): Show | 25 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.1338-560_1338-559d others(4): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768049 | ||||||
| chr9:135768054
|
G | A | 4 | a0001c0002t0009g0047a0001c0004t0004g0003a0001c0004t0014g0002others(1): Show | 4 | HG02486.hp1 HG03098.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1338-556G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768054 | ||||||
| chr9:135768082
|
C | T | 1 | a0001c0019t0003g0089 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1338-528C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768082 | ||||||
| chr9:135768108
|
G | A | 10 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0003t0002g0027others(7): Show | 10 | HG01106.hp2 HG01109.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1338-502G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768108 | ||||||
| chr9:135768138
|
G | A | 1 | a0001c0002t0032g0200 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1338-472G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768138 | ||||||
| chr9:135768145
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1338-465G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768145 | ||||||
| chr9:135768185
|
G | A | 2 | a0001c0002t0001g0094a0001c0002t0005g0270 | 2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1338-425G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768185 | ||||||
| chr9:135768238
|
T | TGTGGGGG others(1): Show |
3 | a0001c0001t0001g0216a0001c0005t0001g0261a0003c0011t0001g0044 | 3 | HG02129.hp2 NA19005.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1338-371_1338-370i others(10): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768238 | |||||
| chr9:135768238
|
T | TGTGGGGG others(2): Show |
4 | a0001c0003t0001g0127a0001c0003t0001g0180a0001c0003t0001g0210others(1): Show | 4 | HG02135.hp2 NA18964.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1338-371_1338-370i others(11): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768238 | |||||
| chr9:135768240
|
C | CG | 29 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(26): Show | 29 | HG00140.hp2 HG01074.hp1 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.1338-353dupG | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768240 | |||||
| chr9:135768240
|
C | CGG | 22 | a0001c0001t0001g0136a0001c0001t0002g0098a0001c0001t0002g0152others(19): Show | 22 | HG00423.hp2 HG00738.hp1 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.1338-354_1338-353d others(4): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768240 | |||||
| chr9:135768240
|
C | CGGG | 33 | a0001c0001t0001g0038a0001c0001t0001g0060a0001c0001t0001g0063others(30): Show | 33 | HG00423.hp1 HG00438.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1338-355_1338-353d others(5): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768240 | |||||
| chr9:135768240
|
C | CGGGG | 17 | a0001c0001t0001g0065a0001c0001t0001g0119a0001c0001t0001g0230others(14): Show | 17 | HG00544.hp1 HG00642.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.1338-356_1338-353d others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768240 | |||||
| chr9:135768240
|
C | CGGGGGGG others(3): Show |
5 | a0001c0001t0001g0042a0001c0001t0001g0204a0001c0001t0002g0198others(2): Show | 5 | HG00544.hp2 HG02451.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.1338-362_1338-353d others(12): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768240 | |||||
| chr9:135768240
|
C | CGGGGGGG others(4): Show |
1 | a0001c0001t0027g0157 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1338-363_1338-353d others(13): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768240 | |||||
| chr9:135768240
|
C | CGGGGGGG others(6): Show |
1 | a0001c0022t0001g0070 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1338-365_1338-353d others(15): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768240 | |||||
| chr9:135768240
|
C | CGGGGGGG others(8): Show |
1 | a0001c0001t0002g0196 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1338-367_1338-353d others(17): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768240 | |||||
| chr9:135768240
|
C | G | 9 | a0001c0001t0001g0216a0001c0003t0001g0126a0001c0003t0001g0127others(6): Show | 9 | HG02129.hp2 HG02135.hp2 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.1338-370C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768240 | ||||||
| chr9:135768240
|
CG | C | 23 | a0001c0002t0001g0087a0001c0002t0001g0094a0001c0002t0001g0184others(20): Show | 23 | HG00140.hp1 HG00609.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1338-353delG | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768240 | |||||
| chr9:135768244
|
GGGGGGGG others(21): Show |
G | 13 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0055others(10): Show | 13 | HG00280.hp2 HG00733.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.1338-357_1338-330d others(30): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768244 | |||||
| chr9:135768245
|
GGGGGGGG others(20): Show |
G | 15 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0062others(12): Show | 15 | HG00323.hp1 HG00323.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.1338-356_1338-330d others(29): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768245 | |||||
| chr9:135768246
|
GGGGGGGG others(19): Show |
G | 10 | a0001c0001t0001g0141a0001c0001t0001g0167a0001c0001t0001g0169others(7): Show | 10 | HG00642.hp2 HG01361.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.1338-355_1338-330d others(28): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768246 | |||||
| chr9:135768247
|
GGGGGGGG others(18): Show |
G | 1 | a0001c0001t0003g0218 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1338-354_1338-330d others(27): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768247 | |||||
| chr9:135768248
|
G | A | 3 | a0001c0002t0004g0257a0001c0002t0005g0079a0001c0002t0040g0160 | 3 | HG01891.hp1 HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1338-362G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768248 | ||||||
| chr9:135768249
|
GGGGGGGG others(16): Show |
G | 3 | a0001c0001t0001g0057a0001c0003t0003g0058a0001c0003t0003g0059 | 3 | HG00099.hp1 HG00741.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1338-349_1338-327d others(25): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768249 | |||||
| chr9:135768253
|
G | A | 1 | a0001c0002t0001g0087 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1338-357G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768253 | ||||||
| chr9:135768254
|
GGGGCACT others(11): Show |
G | 1 | a0001c0001t0001g0015 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1338-352_1338-335d others(20): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768254 | |||||
| chr9:135768255
|
GGGCACTG others(7): Show |
G | 1 | a0001c0004t0004g0003 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1338-352_1338-339d others(16): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768255 | |||||
| chr9:135768255
|
GGGCACTG others(10): Show |
G | 1 | a0001c0003t0001g0018 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1338-352_1338-336d others(19): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768255 | |||||
| chr9:135768256
|
GGCACTGG others(9): Show |
G | 2 | a0001c0004t0014g0002a0007c0023t0001g0017 | 2 | HG03098.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1338-352_1338-337d others(18): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768256 | |||||
| chr9:135768257
|
GCACTGGG others(5): Show |
G | 1 | a0001c0001t0002g0039 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1338-352_1338-341d others(14): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768257 | ||||||
| chr9:135768257
|
GCACTGGG others(8): Show |
G | 1 | a0001c0002t0009g0047 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1338-352_1338-338d others(17): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768257 | ||||||
| chr9:135768269
|
C | CG | 54 | a0001c0001t0001g0074a0001c0001t0001g0186a0001c0001t0001g0204others(51): Show | 54 | HG00099.hp2 HG01109.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1338-339dupG | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768269 | |||||
| chr9:135768269
|
C | CGG | 20 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0072others(17): Show | 20 | HG00438.hp1 HG00544.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.1338-340_1338-339d others(4): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768269 | |||||
| chr9:135768269
|
C | CGGG | 4 | a0001c0001t0007g0028a0001c0001t0007g0071a0001c0004t0004g0025others(1): Show | 4 | HG00741.hp2 HG02257.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1338-339_1338-338i others(5): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768269 | |||||
| chr9:135768272
|
T | G | 131 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0072others(128): Show | 131 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1338-338T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768272 | ||||||
| chr9:135768273
|
G | T | 1 | a0001c0003t0006g0023 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1338-337G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768273 | ||||||
| chr9:135768276
|
G | A | 1 | a0001c0004t0001g0135 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1338-334G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768276 | ||||||
| chr9:135768276
|
G | C | 19 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0002t0001g0013others(16): Show | 19 | HG01074.hp1 HG01099.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.1338-334G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768276 | ||||||
| chr9:135768277
|
G | A | 1 | a0001c0004t0002g0147 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1338-333G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768277 | ||||||
| chr9:135768284
|
A | T | 25 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(22): Show | 25 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.1338-326A>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768284 | ||||||
| chr9:135768287
|
G | A | 3 | a0001c0004t0002g0147a0001c0010t0001g0158a0001c0010t0014g0161 | 3 | HG01192.hp2 HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1338-323G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768287 | ||||||
| chr9:135768344
|
T | TG | 20 | a0001c0001t0001g0063a0001c0001t0001g0234a0001c0001t0001g0238others(17): Show | 20 | HG00438.hp2 HG01070.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.1338-252dupG | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768344 | |||||
| chr9:135768344
|
T | TGG | 19 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0106others(16): Show | 19 | HG00609.hp1 HG00642.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1338-253_1338-252d others(4): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768344 | |||||
| chr9:135768344
|
T | TGGC | 30 | a0001c0001t0001g0019a0001c0001t0001g0052a0001c0001t0001g0053others(27): Show | 30 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1338-264_1338-263i others(5): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768344 | |||||
| chr9:135768344
|
T | TGGCG | 46 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(43): Show | 46 | HG00099.hp2 HG00438.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.1338-264_1338-263i others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768344 | |||||
| chr9:135768344
|
T | TGGCGG | 22 | a0001c0001t0001g0015a0001c0001t0001g0042a0001c0001t0001g0169others(19): Show | 22 | HG00544.hp2 HG01433.hp1 HG01978.hp2 others(19): Show |
intron_variant | MODIFIER | c.1338-264_1338-263i others(7): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768344 | |||||
| chr9:135768344
|
T | TGGCGGG | 17 | a0001c0001t0001g0031a0001c0001t0001g0204a0001c0001t0001g0250others(14): Show | 17 | HG00642.hp2 HG01192.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.1338-264_1338-263i others(8): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768344 | |||||
| chr9:135768344
|
T | TGGCGGGG others(4): Show |
2 | a0001c0001t0002g0039a0001c0001t0027g0157 | 2 | NA19068.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1338-264_1338-263i others(13): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768344 | |||||
| chr9:135768344
|
T | TGGG | 19 | a0001c0001t0001g0038a0001c0001t0001g0136a0001c0001t0001g0165others(16): Show | 19 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(16): Show |
intron_variant | MODIFIER | c.1338-254_1338-252d others(5): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768344 | |||||
| chr9:135768345
|
G | GGC | 30 | a0001c0001t0001g0067a0001c0001t0001g0085a0001c0001t0005g0173others(27): Show | 30 | HG00140.hp1 HG00733.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1338-264_1338-263i others(4): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768345 | |||||
| chr9:135768346
|
G | GC | 15 | a0001c0002t0005g0220a0001c0002t0006g0054a0001c0003t0001g0151others(12): Show | 15 | HG00741.hp2 HG01109.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1338-264_1338-263i others(3): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768346 | ||||||
| chr9:135768347
|
G | C | 2 | a0001c0010t0001g0158a0001c0010t0014g0161 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1338-263G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768347 | ||||||
| chr9:135768349
|
G | T | 1 | a0001c0013t0024g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1338-261G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768349 | ||||||
| chr9:135768354
|
G | C | 1 | a0001c0001t0001g0204 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1338-256G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768354 | ||||||
| chr9:135768391
|
G | A | 46 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(43): Show | 46 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.1338-219G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768391 | ||||||
| chr9:135768422
|
T | TCCCGCCT others(9): Show |
14 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0002t0001g0172others(11): Show | 14 | HG01106.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1338-171_1338-156d others(18): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768422 | |||||
| chr9:135768422
|
T | TCCCGCCT others(25): Show |
1 | a0001c0006t0010g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1338-187_1338-156d others(34): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr9 | 135768422 | |||||
| chr9:135768426
|
G | A | 1 | a0001c0002t0001g0264 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1338-184G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768426 | ||||||
| chr9:135768441
|
C | T | 2 | a0001c0003t0008g0043a0001c0020t0017g0001 | 2 | HG02451.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1338-169C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768441 | ||||||
| chr9:135768442
|
G | A | 14 | a0001c0001t0001g0238a0001c0001t0002g0098a0001c0001t0002g0237others(11): Show | 14 | HG00438.hp2 HG01943.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1338-168G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768442 | ||||||
| chr9:135768455
|
T | C | 2 | a0001c0004t0004g0003a0001c0004t0014g0002 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1338-155T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768455 | ||||||
| chr9:135768554
|
G | A | 7 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0003t0002g0027others(4): Show | 7 | HG01106.hp2 HG01109.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1338-56G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 13/30 | chr9 | 135768554 | ||||||
| chr9:135768702
|
G | A | 34 | a0001c0002t0001g0094a0001c0002t0001g0121a0001c0002t0001g0205others(31): Show | 34 | HG00140.hp1 HG00609.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.1401+29G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 14/30 | chr9 | 135768702 | ||||||
| chr9:135768728
|
C | CG | 7 | a0001c0001t0001g0097a0001c0001t0001g0249a0001c0001t0002g0039others(4): Show | 7 | HG00544.hp2 HG01433.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.1401+60dupG | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr9 | 135768728 | |||||
| chr9:135768729
|
G | A | 1 | a0001c0004t0004g0256 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1401+56G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 14/30 | chr9 | 135768729 | ||||||
| chr9:135768765
|
C | T | 17 | a0001c0002t0001g0086a0001c0002t0001g0087a0001c0002t0001g0172others(14): Show | 17 | HG01109.hp2 HG01884.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.1402-64C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 14/30 | chr9 | 135768765 | ||||||
| chr9:135768795
|
C | A | 1 | a0001c0002t0009g0047 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1402-34C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 14/30 | chr9 | 135768795 | ||||||
| chr9:135769017
|
C | T | 1 | a0001c0002t0001g0231 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1510+80C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769017 | ||||||
| chr9:135769023
|
G | A | 1 | a0001c0002t0001g0096 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1510+86G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769023 | ||||||
| chr9:135769033
|
A | G | 35 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(32): Show | 35 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.1510+96A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769033 | ||||||
| chr9:135769059
|
A | ACGCATGT others(73): Show |
1 | a0001c0003t0006g0023 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1510+125_1510+126i others(82): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr9 | 135769059 | |||||
| chr9:135769100
|
T | C | 35 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(32): Show | 35 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.1510+163T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769100 | ||||||
| chr9:135769103
|
GTGTGCAC others(33): Show |
G | 38 | a0001c0002t0001g0094a0001c0002t0001g0121a0001c0002t0001g0184others(35): Show | 38 | HG00140.hp1 HG00609.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.1510+183_1510+222d others(42): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr9 | 135769103 | |||||
| chr9:135769120
|
T | A | 35 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(32): Show | 35 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.1510+183T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769120 | ||||||
| chr9:135769120
|
TCGGTGCG others(33): Show |
T | 31 | a0001c0001t0001g0019a0001c0001t0001g0057a0001c0001t0001g0122others(28): Show | 31 | HG00099.hp1 HG00741.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.1510+206_1510+245d others(42): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr9 | 135769120 | |||||
| chr9:135769121
|
C | A | 1 | a0001c0003t0002g0101 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1510+184C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769121 | ||||||
| chr9:135769134
|
G | A | 1 | a0001c0003t0001g0144 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1510+197G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769134 | ||||||
| chr9:135769139
|
G | A | 1 | a0001c0003t0006g0023 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1510+202G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769139 | ||||||
| chr9:135769139
|
G | GCGCGTGT others(73): Show |
32 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(29): Show | 32 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.1510+205_1510+206i others(82): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr9 | 135769139 | |||||
| chr9:135769143
|
A | G | 35 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(32): Show | 35 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.1510+206A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769143 | ||||||
| chr9:135769162
|
G | A | 1 | a0001c0015t0001g0271 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1510+225G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769162 | ||||||
| chr9:135769167
|
G | A | 1 | a0001c0015t0001g0271 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1510+230G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769167 | ||||||
| chr9:135769181
|
G | A | 1 | a0001c0015t0001g0271 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1510+244G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769181 | ||||||
| chr9:135769188
|
C | CACACGTG others(73): Show |
1 | a0001c0001t0001g0056 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1510+264_1510+265i others(82): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr9 | 135769188 | |||||
| chr9:135769188
|
C | T | 23 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(20): Show | 23 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.1510+251C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769188 | ||||||
| chr9:135769196
|
G | T | 1 | a0001c0015t0001g0271 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1510+259G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769196 | ||||||
| chr9:135769200
|
A | T | 1 | a0001c0015t0001g0271 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1510+263A>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769200 | ||||||
| chr9:135769202
|
A | G | 38 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(35): Show | 38 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.1510+265A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769202 | ||||||
| chr9:135769206
|
C | T | 1 | a0001c0015t0001g0271 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1510+269C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769206 | ||||||
| chr9:135769207
|
A | G | 14 | a0001c0001t0001g0214a0001c0002t0001g0086a0001c0002t0001g0087others(11): Show | 14 | HG01109.hp2 HG01192.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.1510+270A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769207 | ||||||
| chr9:135769220
|
C | T | 1 | a0001c0015t0001g0271 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1510+283C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769220 | ||||||
| chr9:135769221
|
A | G | 1 | a0001c0015t0001g0271 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1510+284A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769221 | ||||||
| chr9:135769230
|
C | T | 1 | a0001c0015t0001g0271 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1510+293C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769230 | ||||||
| chr9:135769234
|
T | G | 1 | a0001c0015t0001g0271 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1510+297T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769234 | ||||||
| chr9:135769238
|
T | A | 1 | a0001c0015t0001g0271 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1510+301T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769238 | ||||||
| chr9:135769239
|
C | T | 1 | a0001c0015t0001g0271 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1510+302C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769239 | ||||||
| chr9:135769240
|
G | A | 1 | a0001c0003t0001g0272 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1510+303G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769240 | ||||||
| chr9:135769244
|
T | C | 35 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(32): Show | 35 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.1510+307T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769244 | ||||||
| chr9:135769258
|
C | T | 35 | a0001c0002t0001g0094a0001c0002t0001g0121a0001c0002t0001g0184others(32): Show | 35 | HG00140.hp1 HG00609.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1510+321C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769258 | ||||||
| chr9:135769818
|
C | T | 1 | a0001c0002t0001g0244 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1511-129C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769818 | ||||||
| chr9:135769832
|
G | A | 1 | a0001c0003t0001g0272 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1511-115G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 15/30 | chr9 | 135769832 | ||||||
| chr9:135770073
|
C | T | 1 | a0001c0024t0023g0048 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1619+18C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 16/30 | chr9 | 135770073 | ||||||
| chr9:135770093
|
C | T | 8 | a0001c0002t0001g0172a0001c0002t0002g0021a0001c0002t0002g0107others(5): Show | 8 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1619+38C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 16/30 | chr9 | 135770093 | ||||||
| chr9:135770100
|
G | A | 1 | a0001c0024t0023g0048 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1619+45G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 16/30 | chr9 | 135770100 | ||||||
| chr9:135770168
|
G | A | 2 | a0001c0004t0002g0147a0001c0013t0024g0046 | 2 | HG01192.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1619+113G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 16/30 | chr9 | 135770168 | ||||||
| chr9:135770237
|
C | T | 1 | a0001c0003t0001g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1620-61C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 16/30 | chr9 | 135770237 | ||||||
| chr9:135770238
|
G | A | 1 | a0001c0001t0003g0181 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1620-60G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 16/30 | chr9 | 135770238 | ||||||
| chr9:135770253
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1620-45C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 16/30 | chr9 | 135770253 | ||||||
| chr9:135770281
|
C | T | 1 | a0001c0027t0009g0268 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1620-17C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 16/30 | chr9 | 135770281 | ||||||
| chr9:135770463
|
A | G | 202 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0031others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.1769+16A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 17/30 | chr9 | 135770463 | ||||||
| chr9:135770514
|
T | G | 25 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(22): Show | 25 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.1769+67T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 17/30 | chr9 | 135770514 | ||||||
| chr9:135770545
|
G | A | 8 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0154others(5): Show | 8 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1769+98G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 17/30 | chr9 | 135770545 | ||||||
| chr9:135770619
|
G | T | 142 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0031others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.1769+172G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 17/30 | chr9 | 135770619 | ||||||
| chr9:135770637
|
C | T | 1 | a0001c0001t0038g0100 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1769+190C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 17/30 | chr9 | 135770637 | ||||||
| chr9:135770741
|
C | A | 3 | a0001c0001t0001g0202a0001c0001t0039g0156a0001c0003t0001g0267 | 3 | HG01243.hp1 HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1770-116C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 17/30 | chr9 | 135770741 | ||||||
| chr9:135770815
|
G | A | 141 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0031others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.1770-42G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 17/30 | chr9 | 135770815 | ||||||
| chr9:135771116
|
G | A | 27 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(24): Show | 27 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.2008+21G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 18/30 | chr9 | 135771116 | ||||||
| chr9:135771143
|
G | A | 1 | a0001c0004t0002g0147 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2008+48G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 18/30 | chr9 | 135771143 | ||||||
| chr9:135771156
|
G | A | 1 | a0001c0003t0001g0272 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2008+61G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 18/30 | chr9 | 135771156 | ||||||
| chr9:135771209
|
T | C | 8 | a0001c0002t0001g0172a0001c0002t0002g0021a0001c0002t0002g0107others(5): Show | 8 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2008+114T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 18/30 | chr9 | 135771209 | ||||||
| chr9:135771210
|
G | A | 138 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0031others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.2008+115G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 18/30 | chr9 | 135771210 | ||||||
| chr9:135771290
|
G | A | 1 | a0001c0004t0002g0045 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2008+195G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 18/30 | chr9 | 135771290 | ||||||
| chr9:135771310
|
G | A | 140 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0031others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.2008+215G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 18/30 | chr9 | 135771310 | ||||||
| chr9:135771333
|
A | G | 141 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0031others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.2008+238A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 18/30 | chr9 | 135771333 | ||||||
| chr9:135771621
|
C | T | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2008+526C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 18/30 | chr9 | 135771621 | ||||||
| chr9:135771809
|
A | AGGGCCAG others(34): Show |
2 | a0001c0003t0013g0068a0001c0003t0031g0269 | 2 | HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2008+722_2008+762d others(43): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr9 | 135771809 | |||||
| chr9:135771851
|
G | A | 77 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0031others(74): Show | 77 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.2008+756G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 18/30 | chr9 | 135771851 | ||||||
| chr9:135771897
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2008+802A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 18/30 | chr9 | 135771897 | ||||||
| chr9:135771950
|
G | T | 164 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0031others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.2009-765G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 18/30 | chr9 | 135771950 | ||||||
| chr9:135772029
|
T | C | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2009-686T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 18/30 | chr9 | 135772029 | ||||||
| chr9:135772064
|
C | T | 3 | a0001c0002t0009g0047a0001c0004t0004g0003a0001c0004t0014g0002 | 3 | HG02486.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2009-651C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 18/30 | chr9 | 135772064 | ||||||
| chr9:135772099
|
G | A | 27 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(24): Show | 27 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.2009-616G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 18/30 | chr9 | 135772099 | ||||||
| chr9:135772244
|
C | G | 1 | a0001c0001t0022g0193 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2009-471C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 18/30 | chr9 | 135772244 | ||||||
| chr9:135772493
|
G | A | 25 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(22): Show | 25 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.2009-222G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 18/30 | chr9 | 135772493 | ||||||
| chr9:135772509
|
G | A | 8 | a0001c0002t0001g0172a0001c0002t0002g0021a0001c0002t0002g0107others(5): Show | 8 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2009-206G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 18/30 | chr9 | 135772509 | ||||||
| chr9:135772676
|
G | A | 8 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0154others(5): Show | 8 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.2009-39G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 18/30 | chr9 | 135772676 | ||||||
| chr9:135772993
|
G | A | 1 | a0001c0001t0003g0016 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2243+44G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135772993 | ||||||
| chr9:135773005
|
G | A | 49 | a0001c0001t0001g0183a0001c0002t0001g0013a0001c0002t0001g0014others(46): Show | 49 | HG00140.hp1 HG00609.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.2243+56G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135773005 | ||||||
| chr9:135773077
|
A | G | 5 | a0001c0002t0005g0220a0001c0002t0006g0054a0001c0004t0006g0110others(2): Show | 5 | HG01167.hp2 HG01884.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2243+128A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135773077 | ||||||
| chr9:135773121
|
C | T | 8 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0154others(5): Show | 8 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.2243+172C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135773121 | ||||||
| chr9:135773127
|
G | A | 159 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0031others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.2243+178G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135773127 | ||||||
| chr9:135773179
|
G | A | 7 | a0001c0002t0001g0086a0001c0002t0001g0087a0001c0002t0001g0244others(4): Show | 7 | HG01109.hp2 HG02004.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2243+230G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135773179 | ||||||
| chr9:135773212
|
G | A | 1 | a0001c0002t0008g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2243+263G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135773212 | ||||||
| chr9:135773226
|
A | T | 36 | a0001c0001t0001g0183a0001c0002t0001g0094a0001c0002t0001g0121others(33): Show | 36 | HG00140.hp1 HG00609.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.2243+277A>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135773226 | ||||||
| chr9:135773277
|
G | A | 8 | a0001c0002t0001g0041a0001c0002t0001g0213a0001c0002t0002g0131others(5): Show | 8 | HG01346.hp1 HG02056.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.2243+328G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135773277 | ||||||
| chr9:135773287
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2243+338G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135773287 | ||||||
| chr9:135773297
|
C | T | 35 | a0001c0001t0001g0183a0001c0002t0001g0094a0001c0002t0001g0121others(32): Show | 35 | HG00140.hp1 HG00609.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.2243+348C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135773297 | ||||||
| chr9:135773621
|
T | C | 1 | a0001c0009t0006g0159 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2243+672T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135773621 | ||||||
| chr9:135773777
|
A | G | 269 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0031others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.2243+828A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135773777 | ||||||
| chr9:135773919
|
C | T | 7 | a0001c0002t0001g0172a0001c0002t0002g0021a0001c0002t0002g0107others(4): Show | 7 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2243+970C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135773919 | ||||||
| chr9:135773944
|
T | C | 49 | a0001c0001t0001g0183a0001c0002t0001g0013a0001c0002t0001g0014others(46): Show | 49 | HG00140.hp1 HG00609.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.2243+995T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135773944 | ||||||
| chr9:135773946
|
C | A | 2 | a0001c0004t0002g0147a0001c0013t0024g0046 | 2 | HG01192.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2243+997C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135773946 | ||||||
| chr9:135774034
|
G | GGT | 24 | a0001c0001t0001g0019a0001c0001t0001g0057a0001c0001t0001g0095others(21): Show | 24 | HG00099.hp1 HG00741.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.2243+1097_2243+109 others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr9 | 135774034 | |||||
| chr9:135774103
|
CGT | C | 50 | a0001c0001t0001g0183a0001c0002t0001g0013a0001c0002t0001g0014others(47): Show | 50 | HG00140.hp1 HG00609.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.2243+1159_2243+116 others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr9 | 135774103 | |||||
| chr9:135774117
|
G | A | 1 | a0001c0001t0003g0016 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2243+1168G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135774117 | ||||||
| chr9:135774214
|
G | A | 39 | a0001c0001t0001g0183a0001c0002t0001g0094a0001c0002t0001g0121others(36): Show | 39 | HG00140.hp1 HG00609.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.2244-1096G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135774214 | ||||||
| chr9:135774246
|
CGTGTGTG others(2): Show |
C | 10 | a0001c0002t0001g0172a0001c0002t0002g0021a0001c0002t0002g0107others(7): Show | 10 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2244-1052_2244-104 others(13): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr9 | 135774246 | |||||
| chr9:135774247
|
G | A | 8 | a0001c0002t0001g0086a0001c0002t0001g0087a0001c0002t0001g0244others(5): Show | 8 | HG01109.hp2 HG02004.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.2244-1063G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135774247 | ||||||
| chr9:135774253
|
GGTGTGTG others(11): Show |
G | 6 | a0001c0002t0001g0086a0001c0002t0001g0087a0001c0002t0001g0262others(3): Show | 6 | HG01109.hp2 HG02004.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.2244-1043_2244-102 others(22): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr9 | 135774253 | |||||
| chr9:135774259
|
TGTGGTGT others(14): Show |
T | 1 | a0001c0002t0001g0244 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2244-1047_2244-102 others(25): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr9 | 135774259 | |||||
| chr9:135774287
|
T | G | 1 | a0001c0002t0002g0131 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2244-1023T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135774287 | ||||||
| chr9:135774293
|
T | G | 5 | a0001c0003t0002g0027a0001c0006t0009g0012a0001c0006t0010g0010others(2): Show | 5 | HG01109.hp1 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2244-1017T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135774293 | ||||||
| chr9:135774294
|
G | T | 5 | a0001c0003t0002g0027a0001c0006t0009g0012a0001c0006t0010g0010others(2): Show | 5 | HG01109.hp1 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2244-1016G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135774294 | ||||||
| chr9:135774319
|
T | C | 2 | a0001c0002t0002g0150a0001c0002t0025g0149 | 2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2244-991T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135774319 | ||||||
| chr9:135774416
|
GTGTC | G | 54 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0072others(51): Show | 54 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.2244-890_2244-887d others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr9 | 135774416 | |||||
| chr9:135774429
|
GTGTGGTG others(4): Show |
G | 54 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0072others(51): Show | 54 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.2244-865_2244-855d others(13): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr9 | 135774429 | |||||
| chr9:135774470
|
G | A | 70 | a0001c0001t0001g0042a0001c0001t0001g0183a0001c0001t0001g0186others(67): Show | 70 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.2244-840G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135774470 | ||||||
| chr9:135774478
|
C | T | 10 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0154others(7): Show | 10 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.2244-832C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135774478 | ||||||
| chr9:135774479
|
G | A | 9 | a0001c0001t0001g0216a0001c0003t0001g0126a0001c0003t0001g0127others(6): Show | 9 | HG02129.hp2 HG02135.hp2 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.2244-831G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135774479 | ||||||
| chr9:135774585
|
C | T | 3 | a0001c0002t0001g0041a0001c0002t0001g0213a0001c0004t0001g0135 | 3 | HG02056.hp1 HG02129.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.2244-725C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135774585 | ||||||
| chr9:135774587
|
A | G | 13 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0154others(10): Show | 13 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.2244-723A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135774587 | ||||||
| chr9:135774614
|
ATGTTGTG others(12): Show |
A | 1 | a0001c0003t0001g0248 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2244-684_2244-666d others(21): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr9 | 135774614 | |||||
| chr9:135774626
|
G | A | 2 | a0001c0004t0002g0147a0001c0013t0024g0046 | 2 | HG01192.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2244-684G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135774626 | ||||||
| chr9:135774663
|
G | A | 1 | a0001c0002t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2244-647G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135774663 | ||||||
| chr9:135774673
|
C | T | 46 | a0001c0001t0001g0031a0001c0001t0001g0072a0001c0001t0001g0074others(43): Show | 46 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.2244-637C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135774673 | ||||||
| chr9:135774697
|
A | G | 13 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0154others(10): Show | 13 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.2244-613A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135774697 | ||||||
| chr9:135774802
|
T | C | 3 | a0001c0003t0001g0069a0001c0003t0001g0248a0001c0003t0002g0247 | 3 | HG00140.hp2 HG00280.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2244-508T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135774802 | ||||||
| chr9:135774830
|
G | A | 2 | a0001c0004t0002g0147a0001c0013t0024g0046 | 2 | HG01192.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2244-480G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135774830 | ||||||
| chr9:135774852
|
CT | C | 8 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0154others(5): Show | 8 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.2244-456delT | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr9 | 135774852 | |||||
| chr9:135774854
|
T | C | 193 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0031others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.2244-456T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135774854 | ||||||
| chr9:135774983
|
C | T | 13 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0154others(10): Show | 13 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.2244-327C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135774983 | ||||||
| chr9:135775001
|
T | C | 13 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0154others(10): Show | 13 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.2244-309T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135775001 | ||||||
| chr9:135775080
|
G | A | 1 | a0001c0003t0003g0059 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2244-230G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135775080 | ||||||
| chr9:135775093
|
T | C | 13 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0154others(10): Show | 13 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.2244-217T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135775093 | ||||||
| chr9:135775126
|
G | A | 13 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0154others(10): Show | 13 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.2244-184G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135775126 | ||||||
| chr9:135775160
|
C | A | 2 | a0001c0003t0001g0164a0001c0025t0001g0113 | 2 | HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2244-150C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135775160 | ||||||
| chr9:135775165
|
C | T | 1 | a0001c0003t0021g0259 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2244-145C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135775165 | ||||||
| chr9:135775220
|
G | A | 2 | a0001c0003t0001g0180a0001c0003t0001g0210 | 2 | NA18970.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.2244-90G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 19/30 | chr9 | 135775220 | ||||||
| chr9:135775468
|
C | T | 1 | a0001c0001t0008g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2349+53C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135775468 | ||||||
| chr9:135775474
|
T | C | 13 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0154others(10): Show | 13 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.2349+59T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135775474 | ||||||
| chr9:135775563
|
A | G | 13 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0154others(10): Show | 13 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.2349+148A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135775563 | ||||||
| chr9:135775591
|
G | A | 2 | a0001c0001t0005g0173a0001c0001t0005g0174 | 2 | HG01106.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2349+176G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135775591 | ||||||
| chr9:135775684
|
C | T | 3 | a0001c0003t0008g0043a0001c0020t0017g0001a0001c0024t0023g0048 | 3 | HG02451.hp1 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2349+269C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135775684 | ||||||
| chr9:135775716
|
G | A | 17 | a0001c0001t0001g0019a0001c0001t0001g0122a0001c0001t0001g0128others(14): Show | 17 | HG01243.hp1 HG01952.hp1 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.2349+301G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135775716 | ||||||
| chr9:135775734
|
C | A | 3 | a0001c0003t0008g0043a0001c0020t0017g0001a0001c0024t0023g0048 | 3 | HG02451.hp1 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2349+319C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135775734 | ||||||
| chr9:135775740
|
C | CA | 13 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0154others(10): Show | 13 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.2349+325_2349+326i others(3): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135775740 | ||||||
| chr9:135775741
|
G | T | 13 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0154others(10): Show | 13 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.2349+326G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135775741 | ||||||
| chr9:135775750
|
G | A | 1 | a0001c0003t0031g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2349+335G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135775750 | ||||||
| chr9:135775757
|
AGGACAGG others(18): Show |
A | 1 | a0001c0001t0001g0221 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2349+344_2349+368d others(27): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr9 | 135775757 | |||||
| chr9:135775821
|
G | A | 13 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0154others(10): Show | 13 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.2349+406G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135775821 | ||||||
| chr9:135775826
|
G | A | 2 | a0001c0002t0001g0185a0001c0002t0001g0189 | 2 | HG02015.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.2349+411G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135775826 | ||||||
| chr9:135775861
|
C | G | 13 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0154others(10): Show | 13 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.2349+446C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135775861 | ||||||
| chr9:135775894
|
A | T | 2 | a0001c0004t0020g0215a0001c0016t0019g0116 | 2 | HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2349+479A>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135775894 | ||||||
| chr9:135775905
|
G | A | 1 | a0001c0003t0001g0034 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2349+490G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135775905 | ||||||
| chr9:135775971
|
AC | A | 3 | a0001c0002t0009g0047a0001c0004t0004g0003a0001c0004t0014g0002 | 3 | HG02486.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2349+558delC | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr9 | 135775971 | |||||
| chr9:135775999
|
C | T | 3 | a0001c0002t0009g0047a0001c0004t0004g0003a0001c0004t0014g0002 | 3 | HG02486.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2349+584C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135775999 | ||||||
| chr9:135776000
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2349+585G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135776000 | ||||||
| chr9:135776183
|
C | T | 3 | a0001c0002t0009g0047a0001c0004t0004g0003a0001c0004t0014g0002 | 3 | HG02486.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2349+768C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135776183 | ||||||
| chr9:135776227
|
A | G | 202 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0031others(199): Show | 202 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.2349+812A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135776227 | ||||||
| chr9:135776355
|
T | C | 3 | a0001c0002t0009g0047a0001c0004t0004g0003a0001c0004t0014g0002 | 3 | HG02486.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2349+940T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135776355 | ||||||
| chr9:135776385
|
G | A | 10 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0154others(7): Show | 10 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.2350-953G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135776385 | ||||||
| chr9:135776425
|
TTTTA | T | 4 | a0001c0002t0001g0086a0001c0002t0001g0087a0001c0002t0032g0200others(1): Show | 4 | HG01109.hp2 HG02145.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2350-897_2350-894d others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr9 | 135776425 | |||||
| chr9:135776434
|
T | G | 3 | a0001c0002t0009g0047a0001c0004t0004g0003a0001c0004t0014g0002 | 3 | HG02486.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2350-904T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135776434 | ||||||
| chr9:135776441
|
A | AT | 3 | a0001c0001t0011g0032a0001c0002t0001g0013a0001c0002t0001g0014 | 3 | HG02615.hp2 HG02717.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.2350-891dupT | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr9 | 135776441 | |||||
| chr9:135776445
|
T | A | 2 | a0001c0004t0002g0147a0001c0013t0024g0046 | 2 | HG01192.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2350-893T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135776445 | ||||||
| chr9:135776673
|
A | G | 3 | a0001c0002t0009g0047a0001c0004t0004g0003a0001c0004t0014g0002 | 3 | HG02486.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2350-665A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135776673 | ||||||
| chr9:135776698
|
A | G | 3 | a0001c0002t0009g0047a0001c0004t0004g0003a0001c0004t0014g0002 | 3 | HG02486.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2350-640A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135776698 | ||||||
| chr9:135776777
|
A | G | 3 | a0001c0002t0009g0047a0001c0004t0004g0003a0001c0004t0014g0002 | 3 | HG02486.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2350-561A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135776777 | ||||||
| chr9:135776836
|
C | G | 8 | a0001c0001t0022g0193a0001c0002t0001g0086a0001c0002t0001g0087others(5): Show | 8 | HG00609.hp1 HG01109.hp2 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.2350-502C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135776836 | ||||||
| chr9:135776987
|
G | A | 7 | a0001c0002t0001g0086a0001c0002t0001g0087a0001c0002t0001g0244others(4): Show | 7 | HG01109.hp2 HG02004.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2350-351G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135776987 | ||||||
| chr9:135777080
|
C | G | 1 | a0001c0001t0001g0095 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2350-258C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135777080 | ||||||
| chr9:135777140
|
C | T | 1 | a0001c0002t0032g0200 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2350-198C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135777140 | ||||||
| chr9:135777181
|
T | TC | 11 | a0001c0001t0022g0193a0001c0002t0001g0086a0001c0002t0001g0262others(8): Show | 11 | HG00609.hp1 HG01074.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2350-153dupC | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr9 | 135777181 | |||||
| chr9:135777229
|
A | G | 7 | a0001c0002t0001g0172a0001c0002t0002g0021a0001c0002t0002g0114others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2350-109A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135777229 | ||||||
| chr9:135777282
|
T | C | 1 | a0001c0001t0016g0254 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2350-56T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135777282 | ||||||
| chr9:135777282
|
T | G | 2 | a0001c0001t0001g0249a0001c0001t0002g0251 | 2 | HG02027.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2350-56T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | chr9 | 135777282 | ||||||
| chr9:135777297
|
ACAGCCCT others(5): Show |
A | 6 | a0001c0003t0001g0151a0001c0004t0002g0147a0001c0004t0004g0003others(3): Show | 6 | HG01192.hp2 HG02717.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2350-24_2350-13del others(12): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr9 | 135777297 | |||||
| chr9:135777546
|
C | T | 2 | a0001c0003t0001g0180a0001c0003t0001g0210 | 2 | NA18970.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.2522+36C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 21/30 | chr9 | 135777546 | ||||||
| chr9:135777613
|
G | A | 2 | a0001c0001t0001g0194a0001c0001t0043g0197 | 2 | HG01952.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.2522+103G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 21/30 | chr9 | 135777613 | ||||||
| chr9:135777685
|
C | CCTCCTGC others(22): Show |
1 | a0001c0004t0002g0147 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2522+200_2522+228d others(31): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr9 | 135777685 | |||||
| chr9:135777685
|
CCTCCTGC others(22): Show |
C | 2 | a0001c0001t0016g0102a0001c0001t0016g0254 | 2 | HG02602.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.2522+200_2522+228d others(31): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr9 | 135777685 | |||||
| chr9:135777710
|
A | C | 1 | a0001c0001t0001g0202 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2522+200A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 21/30 | chr9 | 135777710 | ||||||
| chr9:135777710
|
ACCCACTC others(22): Show |
A | 6 | a0001c0002t0006g0054a0001c0003t0006g0023a0001c0003t0006g0117others(3): Show | 6 | HG01884.hp1 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.2522+205_2522+233d others(31): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr9 | 135777710 | |||||
| chr9:135777891
|
C | T | 1 | a0001c0024t0023g0048 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2522+381C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 21/30 | chr9 | 135777891 | ||||||
| chr9:135777985
|
A | ATGCTCTC others(10): Show |
91 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0095others(88): Show | 91 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.2523-425_2523-424i others(19): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr9 | 135777985 | |||||
| chr9:135778041
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2523-383T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 21/30 | chr9 | 135778041 | ||||||
| chr9:135778130
|
C | A | 73 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0242others(70): Show | 73 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.2523-294C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 21/30 | chr9 | 135778130 | ||||||
| chr9:135778301
|
C | T | 6 | a0001c0002t0006g0054a0001c0003t0006g0023a0001c0003t0006g0117others(3): Show | 6 | HG01884.hp1 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.2523-123C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 21/30 | chr9 | 135778301 | ||||||
| chr9:135778306
|
C | T | 1 | a0001c0013t0024g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2523-118C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 21/30 | chr9 | 135778306 | ||||||
| chr9:135778325
|
C | A | 2 | a0001c0002t0005g0081a0001c0015t0001g0271 | 2 | HG01891.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2523-99C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 21/30 | chr9 | 135778325 | ||||||
| chr9:135778605
|
C | G | 12 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0175others(9): Show | 12 | HG00741.hp2 HG01081.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.2595-83C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 22/30 | chr9 | 135778605 | ||||||
| chr9:135778831
|
A | G | 6 | a0001c0002t0006g0054a0001c0003t0006g0023a0001c0003t0006g0117others(3): Show | 6 | HG01884.hp1 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.2729+9A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | chr9 | 135778831 | ||||||
| chr9:135778853
|
A | G | 82 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0095others(79): Show | 82 | HG00438.hp1 HG00544.hp2 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.2729+31A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | chr9 | 135778853 | ||||||
| chr9:135778856
|
A | ACCCCACA others(29): Show |
4 | a0001c0001t0002g0078a0002c0008t0001g0170a0002c0008t0001g0171others(1): Show | 4 | HG01074.hp2 HG01167.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.2729+108_2729+143d others(38): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | INFO_REALIGN_3_PRIME | chr9 | 135778856 | |||||
| chr9:135778856
|
A | ACCCCACA others(65): Show |
8 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0175others(5): Show | 8 | HG01081.hp2 HG01106.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.2729+72_2729+143du others(73): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | INFO_REALIGN_3_PRIME | chr9 | 135778856 | |||||
| chr9:135778856
|
ACCCCACA others(29): Show |
A | 17 | a0001c0001t0008g0008a0001c0001t0027g0157a0001c0002t0005g0081others(14): Show | 17 | HG01346.hp2 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.2729+108_2729+143d others(38): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | INFO_REALIGN_3_PRIME | chr9 | 135778856 | |||||
| chr9:135778858
|
C | CCCACAGC others(101): Show |
1 | a0001c0004t0004g0256 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2729+80_2729+187du others(109): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | INFO_REALIGN_3_PRIME | chr9 | 135778858 | |||||
| chr9:135778871
|
C | A | 3 | a0001c0002t0009g0047a0001c0004t0002g0147a0001c0027t0009g0268 | 3 | HG01192.hp2 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2729+49C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | chr9 | 135778871 | ||||||
| chr9:135778883
|
G | A | 1 | a0001c0001t0016g0254 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2729+61G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | chr9 | 135778883 | ||||||
| chr9:135778894
|
C | CCCACAGC others(101): Show |
1 | a0001c0001t0001g0099 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2729+143_2729+144i others(110): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | INFO_REALIGN_3_PRIME | chr9 | 135778894 | |||||
| chr9:135778894
|
C | CCCACAGC others(65): Show |
2 | a0001c0001t0001g0076a0001c0001t0001g0088 | 2 | HG01981.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.2729+116_2729+187d others(74): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | INFO_REALIGN_3_PRIME | chr9 | 135778894 | |||||
| chr9:135778909
|
A | C | 1 | a0001c0001t0001g0221 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2729+87A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | chr9 | 135778909 | ||||||
| chr9:135778910
|
C | A | 1 | a0001c0001t0001g0221 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2729+88C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | chr9 | 135778910 | ||||||
| chr9:135778911
|
G | A | 2 | a0001c0014t0017g0212a0001c0020t0017g0001 | 2 | HG02451.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2729+89G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | chr9 | 135778911 | ||||||
| chr9:135778911
|
G | C | 1 | a0001c0001t0001g0221 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2729+89G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | chr9 | 135778911 | ||||||
| chr9:135778919
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2729+97G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | chr9 | 135778919 | ||||||
| chr9:135778934
|
C | T | 1 | a0001c0001t0039g0156 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2729+112C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | chr9 | 135778934 | ||||||
| chr9:135778955
|
G | A | 2 | a0001c0002t0009g0047a0001c0027t0009g0268 | 2 | HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2729+133G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | chr9 | 135778955 | ||||||
| chr9:135778966
|
G | C | 9 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0095others(6): Show | 9 | HG02155.hp2 HG02698.hp2 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2729+144G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | chr9 | 135778966 | ||||||
| chr9:135778966
|
G | GCCACAGC others(29): Show |
1 | a0001c0003t0001g0066 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2729+152_2729+187d others(38): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | INFO_REALIGN_3_PRIME | chr9 | 135778966 | |||||
| chr9:135779002
|
C | G | 1 | a0001c0001t0039g0156 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2729+180C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | chr9 | 135779002 | ||||||
| chr9:135779010
|
T | C | 1 | a0001c0001t0039g0156 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2729+188T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | chr9 | 135779010 | ||||||
| chr9:135779012
|
T | C | 1 | a0001c0001t0039g0156 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2729+190T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | chr9 | 135779012 | ||||||
| chr9:135779019
|
A | G | 9 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0095others(6): Show | 9 | HG02155.hp2 HG02698.hp2 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2729+197A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | chr9 | 135779019 | ||||||
| chr9:135779020
|
A | G | 9 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0095others(6): Show | 9 | HG02155.hp2 HG02698.hp2 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2729+198A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | chr9 | 135779020 | ||||||
| chr9:135779025
|
C | T | 9 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0095others(6): Show | 9 | HG02155.hp2 HG02698.hp2 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2729+203C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | chr9 | 135779025 | ||||||
| chr9:135779027
|
A | G | 9 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0095others(6): Show | 9 | HG02155.hp2 HG02698.hp2 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2729+205A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | chr9 | 135779027 | ||||||
| chr9:135779034
|
A | G | 9 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0095others(6): Show | 9 | HG02155.hp2 HG02698.hp2 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2729+212A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | chr9 | 135779034 | ||||||
| chr9:135779112
|
A | C | 2 | a0001c0003t0009g0177a0001c0006t0009g0012 | 2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2730-247A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | chr9 | 135779112 | ||||||
| chr9:135779186
|
GTGGGACC others(60): Show |
G | 14 | a0001c0001t0008g0008a0001c0001t0027g0157a0001c0002t0005g0081others(11): Show | 14 | HG01884.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.2730-164_2730-98de others(68): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | INFO_REALIGN_3_PRIME | chr9 | 135779186 | |||||
| chr9:135779334
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2730-25G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 23/30 | chr9 | 135779334 | ||||||
| chr9:135779524
|
G | C | 1 | a0001c0006t0009g0012 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2841+54G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135779524 | ||||||
| chr9:135779579
|
G | T | 27 | a0001c0001t0001g0204a0001c0001t0001g0249a0001c0001t0001g0250others(24): Show | 27 | HG00438.hp1 HG00544.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.2841+109G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135779579 | ||||||
| chr9:135779581
|
C | G | 1 | a0001c0003t0001g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2841+111C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135779581 | ||||||
| chr9:135779602
|
A | G | 3 | a0001c0003t0001g0267a0001c0003t0013g0068a0001c0003t0031g0269 | 3 | HG02647.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2841+132A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135779602 | ||||||
| chr9:135779682
|
G | A | 11 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0175others(8): Show | 11 | HG01081.hp2 HG01106.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.2841+212G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135779682 | ||||||
| chr9:135779720
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2841+250C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135779720 | ||||||
| chr9:135779779
|
G | A | 1 | a0001c0002t0001g0121 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2841+309G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135779779 | ||||||
| chr9:135779805
|
G | A | 4 | a0001c0003t0001g0151a0001c0004t0004g0256a0001c0004t0004g0258others(1): Show | 4 | HG02717.hp2 HG02723.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2841+335G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135779805 | ||||||
| chr9:135779824
|
G | T | 1 | a0001c0002t0005g0081 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2841+354G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135779824 | ||||||
| chr9:135779866
|
C | T | 40 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0095others(37): Show | 40 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.2841+396C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135779866 | ||||||
| chr9:135779873
|
G | A | 12 | a0001c0001t0001g0242a0001c0001t0003g0016a0001c0001t0003g0168others(9): Show | 12 | HG02602.hp2 HG02735.hp1 HG03492.hp2 others(9): Show |
intron_variant | MODIFIER | c.2841+403G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135779873 | ||||||
| chr9:135779934
|
C | G | 5 | a0001c0003t0010g0148a0001c0004t0037g0004a0001c0006t0010g0010others(2): Show | 5 | HG01099.hp1 HG01109.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.2841+464C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135779934 | ||||||
| chr9:135780050
|
G | A | 3 | a0001c0002t0009g0047a0001c0004t0002g0147a0001c0027t0009g0268 | 3 | HG01192.hp2 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2841+580G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135780050 | ||||||
| chr9:135780103
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2841+633G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135780103 | ||||||
| chr9:135780114
|
G | A | 8 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0175others(5): Show | 8 | HG01081.hp2 HG01106.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.2841+644G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135780114 | ||||||
| chr9:135780247
|
T | TCAG | 71 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0095others(68): Show | 71 | HG00438.hp1 HG00544.hp2 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.2841+783_2841+785d others(5): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | INFO_REALIGN_3_PRIME | chr9 | 135780247 | |||||
| chr9:135780259
|
C | T | 79 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0095others(76): Show | 79 | HG00438.hp1 HG00544.hp2 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.2841+789C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135780259 | ||||||
| chr9:135780269
|
T | C | 1 | a0001c0003t0002g0236 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2841+799T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135780269 | ||||||
| chr9:135780270
|
A | C | 20 | a0001c0001t0001g0202a0001c0001t0001g0242a0001c0001t0003g0016others(17): Show | 20 | HG00099.hp1 HG01243.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.2841+800A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135780270 | ||||||
| chr9:135780358
|
A | G | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2841+888A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135780358 | ||||||
| chr9:135780362
|
T | C | 1 | a0001c0003t0002g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2841+892T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135780362 | ||||||
| chr9:135780395
|
C | T | 4 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0074others(1): Show | 4 | HG00099.hp2 HG01099.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.2841+925C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135780395 | ||||||
| chr9:135780411
|
C | T | 15 | a0001c0001t0001g0242a0001c0001t0003g0016a0001c0001t0003g0168others(12): Show | 15 | HG00099.hp1 HG01346.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.2841+941C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135780411 | ||||||
| chr9:135780560
|
C | T | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2841+1090C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135780560 | ||||||
| chr9:135780623
|
C | T | 8 | a0001c0001t0008g0008a0001c0001t0027g0157a0001c0002t0005g0081others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2841+1153C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135780623 | ||||||
| chr9:135780624
|
G | A | 1 | a0001c0003t0001g0144 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2841+1154G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135780624 | ||||||
| chr9:135780681
|
C | T | 5 | a0001c0003t0010g0148a0001c0004t0037g0004a0001c0006t0010g0010others(2): Show | 5 | HG01099.hp1 HG01109.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.2841+1211C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135780681 | ||||||
| chr9:135780696
|
C | T | 1 | a0001c0002t0002g0131 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2841+1226C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135780696 | ||||||
| chr9:135780732
|
G | A | 2 | a0001c0009t0006g0159a0001c0009t0018g0162 | 2 | HG02897.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2841+1262G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135780732 | ||||||
| chr9:135780806
|
G | A | 94 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0095others(91): Show | 94 | HG00438.hp1 HG00544.hp2 HG00733.hp1 others(91): Show |
intron_variant | MODIFIER | c.2841+1336G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135780806 | ||||||
| chr9:135780843
|
C | T | 1 | a0001c0001t0016g0254 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2841+1373C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135780843 | ||||||
| chr9:135780885
|
C | G | 15 | a0001c0001t0001g0242a0001c0001t0003g0016a0001c0001t0003g0168others(12): Show | 15 | HG00099.hp1 HG01346.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.2841+1415C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135780885 | ||||||
| chr9:135780931
|
C | T | 1 | a0001c0003t0002g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2841+1461C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135780931 | ||||||
| chr9:135780986
|
A | C | 2 | a0001c0003t0013g0068a0001c0003t0031g0269 | 2 | HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2841+1516A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135780986 | ||||||
| chr9:135780988
|
G | C | 1 | a0007c0023t0001g0017 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2841+1518G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135780988 | ||||||
| chr9:135780991
|
C | A | 1 | a0001c0004t0004g0025 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2841+1521C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135780991 | ||||||
| chr9:135780998
|
A | G | 72 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0095others(69): Show | 72 | HG00099.hp1 HG01081.hp2 HG01099.hp1 others(69): Show |
intron_variant | MODIFIER | c.2841+1528A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135780998 | ||||||
| chr9:135781013
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2841+1543G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135781013 | ||||||
| chr9:135781034
|
C | T | 1 | a0001c0002t0009g0047 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2841+1564C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135781034 | ||||||
| chr9:135781117
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2841+1647C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135781117 | ||||||
| chr9:135781227
|
C | T | 1 | a0006c0018t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2841+1757C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135781227 | ||||||
| chr9:135781228
|
G | A | 47 | a0001c0001t0001g0204a0001c0001t0001g0249a0001c0001t0001g0250others(44): Show | 47 | HG00438.hp1 HG00544.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.2841+1758G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135781228 | ||||||
| chr9:135781336
|
G | A | 6 | a0001c0002t0006g0054a0001c0003t0006g0023a0001c0003t0006g0117others(3): Show | 6 | HG01884.hp1 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.2841+1866G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135781336 | ||||||
| chr9:135781370
|
C | A | 1 | a0001c0001t0039g0156 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2841+1900C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135781370 | ||||||
| chr9:135781388
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2841+1918G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135781388 | ||||||
| chr9:135781456
|
C | G | 15 | a0001c0001t0001g0242a0001c0001t0003g0016a0001c0001t0003g0168others(12): Show | 15 | HG00099.hp1 HG01346.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.2841+1986C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135781456 | ||||||
| chr9:135781471
|
T | C | 26 | a0001c0001t0001g0242a0001c0001t0003g0016a0001c0001t0003g0168others(23): Show | 26 | HG00099.hp1 HG01192.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.2841+2001T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135781471 | ||||||
| chr9:135781639
|
T | TA | 96 | a0001c0001t0001g0019a0001c0001t0001g0038a0001c0001t0001g0042others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.2841+2184dupA | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | INFO_REALIGN_3_PRIME | chr9 | 135781639 | |||||
| chr9:135781639
|
T | TAA | 13 | a0001c0001t0001g0097a0001c0001t0001g0186a0001c0001t0001g0230others(10): Show | 13 | HG00140.hp2 HG00544.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.2841+2183_2841+218 others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | INFO_REALIGN_3_PRIME | chr9 | 135781639 | |||||
| chr9:135781639
|
TA | T | 7 | a0001c0001t0001g0015a0001c0001t0001g0112a0001c0001t0001g0214others(4): Show | 7 | HG01884.hp1 HG02015.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.2841+2184delA | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | INFO_REALIGN_3_PRIME | chr9 | 135781639 | |||||
| chr9:135781784
|
C | T | 15 | a0001c0001t0008g0008a0001c0001t0027g0157a0001c0002t0005g0081others(12): Show | 15 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2842-2240C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135781784 | ||||||
| chr9:135781936
|
G | A | 3 | a0001c0001t0001g0194a0001c0001t0043g0197a0001c0002t0001g0264 | 3 | HG01952.hp2 HG01978.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.2842-2088G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135781936 | ||||||
| chr9:135782195
|
C | T | 2 | a0001c0002t0005g0081a0001c0015t0001g0271 | 2 | HG01891.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2842-1829C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135782195 | ||||||
| chr9:135782203
|
C | CA | 5 | a0001c0001t0001g0221a0001c0002t0002g0150a0001c0002t0025g0149others(2): Show | 5 | HG03098.hp2 HG03209.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2842-1813dupA | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | INFO_REALIGN_3_PRIME | chr9 | 135782203 | |||||
| chr9:135782212
|
C | A | 1 | a0001c0001t0039g0156 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2842-1812C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135782212 | ||||||
| chr9:135782247
|
G | C | 1 | a0001c0004t0014g0002 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2842-1777G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135782247 | ||||||
| chr9:135782287
|
C | T | 16 | a0001c0001t0001g0242a0001c0001t0003g0016a0001c0001t0003g0168others(13): Show | 16 | HG00099.hp1 HG01346.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.2842-1737C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135782287 | ||||||
| chr9:135782288
|
A | G | 26 | a0001c0001t0001g0202a0001c0001t0001g0242a0001c0001t0003g0016others(23): Show | 26 | HG00099.hp1 HG01099.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.2842-1736A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135782288 | ||||||
| chr9:135782396
|
C | T | 1 | a0001c0001t0007g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2842-1628C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135782396 | ||||||
| chr9:135782484
|
G | A | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2842-1540G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135782484 | ||||||
| chr9:135782582
|
C | G | 15 | a0001c0001t0001g0242a0001c0001t0003g0016a0001c0001t0003g0168others(12): Show | 15 | HG00099.hp1 HG01346.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.2842-1442C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135782582 | ||||||
| chr9:135782583
|
C | T | 1 | a0001c0004t0002g0147 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2842-1441C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135782583 | ||||||
| chr9:135782673
|
GTCTC | G | 5 | a0001c0003t0010g0148a0001c0004t0037g0004a0001c0006t0010g0010others(2): Show | 5 | HG01099.hp1 HG01109.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.2842-1345_2842-134 others(8): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | INFO_REALIGN_3_PRIME | chr9 | 135782673 | |||||
| chr9:135782754
|
C | G | 1 | a0001c0001t0001g0202 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2842-1270C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135782754 | ||||||
| chr9:135782879
|
G | A | 1 | a0001c0001t0002g0049 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2842-1145G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135782879 | ||||||
| chr9:135782914
|
C | G | 1 | a0001c0004t0020g0215 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2842-1110C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135782914 | ||||||
| chr9:135782966
|
C | T | 15 | a0001c0001t0001g0242a0001c0001t0003g0016a0001c0001t0003g0168others(12): Show | 15 | HG00099.hp1 HG01346.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.2842-1058C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135782966 | ||||||
| chr9:135782990
|
G | A | 1 | a0001c0003t0001g0108 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2842-1034G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135782990 | ||||||
| chr9:135782990
|
G | C | 1 | a0001c0004t0004g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2842-1034G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135782990 | ||||||
| chr9:135783028
|
G | A | 6 | a0001c0003t0001g0151a0001c0004t0004g0255a0001c0004t0004g0256others(3): Show | 6 | HG02717.hp2 HG02723.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2842-996G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135783028 | ||||||
| chr9:135783042
|
G | A | 5 | a0001c0005t0001g0207a0001c0005t0001g0208a0001c0005t0001g0217others(2): Show | 5 | HG02129.hp2 HG02135.hp2 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.2842-982G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135783042 | ||||||
| chr9:135783151
|
G | A | 1 | a0001c0003t0002g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2842-873G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135783151 | ||||||
| chr9:135783169
|
G | A | 5 | a0001c0003t0010g0148a0001c0004t0037g0004a0001c0006t0010g0010others(2): Show | 5 | HG01099.hp1 HG01109.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.2842-855G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135783169 | ||||||
| chr9:135783209
|
C | T | 15 | a0001c0001t0001g0242a0001c0001t0003g0016a0001c0001t0003g0168others(12): Show | 15 | HG00099.hp1 HG01346.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.2842-815C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135783209 | ||||||
| chr9:135783259
|
G | T | 4 | a0001c0003t0009g0177a0001c0006t0009g0012a0001c0014t0017g0212others(1): Show | 4 | HG02451.hp1 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2842-765G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135783259 | ||||||
| chr9:135783341
|
A | G | 18 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0175others(15): Show | 18 | HG01081.hp2 HG01099.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.2842-683A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135783341 | ||||||
| chr9:135783401
|
CCAGA | C | 16 | a0001c0001t0001g0074a0001c0001t0001g0242a0001c0001t0003g0016others(13): Show | 16 | HG00099.hp1 HG01346.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.2842-622_2842-619d others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135783401 | ||||||
| chr9:135783406
|
G | T | 16 | a0001c0001t0001g0074a0001c0001t0001g0242a0001c0001t0003g0016others(13): Show | 16 | HG00099.hp1 HG01346.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.2842-618G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135783406 | ||||||
| chr9:135783411
|
C | T | 16 | a0001c0001t0001g0074a0001c0001t0001g0242a0001c0001t0003g0016others(13): Show | 16 | HG00099.hp1 HG01346.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.2842-613C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135783411 | ||||||
| chr9:135783570
|
A | G | 76 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0074others(73): Show | 76 | HG00099.hp1 HG01081.hp2 HG01099.hp1 others(73): Show |
intron_variant | MODIFIER | c.2842-454A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135783570 | ||||||
| chr9:135783643
|
G | A | 3 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0003t0001g0091 | 3 | HG02040.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2842-381G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135783643 | ||||||
| chr9:135783670
|
G | A | 1 | a0001c0003t0001g0084 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2842-354G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135783670 | ||||||
| chr9:135783705
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2842-319G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135783705 | ||||||
| chr9:135783738
|
C | A | 2 | a0001c0001t0016g0102a0001c0001t0016g0254 | 2 | HG02602.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.2842-286C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135783738 | ||||||
| chr9:135783739
|
C | A | 2 | a0001c0001t0016g0102a0001c0001t0016g0254 | 2 | HG02602.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.2842-285C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135783739 | ||||||
| chr9:135783767
|
C | T | 1 | a0005c0021t0001g0246 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2842-257C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135783767 | ||||||
| chr9:135783944
|
C | G | 41 | a0001c0001t0001g0074a0001c0001t0001g0095a0001c0001t0001g0204others(38): Show | 41 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.2842-80C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135783944 | ||||||
| chr9:135783955
|
A | C | 62 | a0001c0001t0001g0074a0001c0001t0001g0095a0001c0001t0001g0204others(59): Show | 62 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.2842-69A>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135783955 | ||||||
| chr9:135784009
|
C | T | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2842-15C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 24/30 | chr9 | 135784009 | ||||||
| chr9:135784131
|
C | T | 6 | a0001c0003t0001g0267a0001c0003t0010g0148a0001c0004t0037g0004others(3): Show | 6 | HG01099.hp1 HG01109.hp1 HG02055.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.2943+6C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 25/30 | chr9 | 135784131 | ||||||
| chr9:135784392
|
C | CTG | 4 | a0001c0003t0009g0177a0001c0006t0009g0012a0001c0014t0017g0212others(1): Show | 4 | HG02451.hp1 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2944-133_2944-132d others(4): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 25/30 | INFO_REALIGN_3_PRIME | chr9 | 135784392 | |||||
| chr9:135784482
|
G | GCTCC | 51 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0060others(48): Show | 51 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(48): Show |
splice_region_variant&intron_variant | LOW | c.2944-10_2944-7dupC others(3): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 25/30 | INFO_REALIGN_3_PRIME | chr9 | 135784482 | |||||
| chr9:135784482
|
G | GCTCCCTC others(1): Show |
14 | a0001c0001t0001g0057a0001c0001t0026g0123a0001c0001t0038g0100others(11): Show | 14 | HG00099.hp1 HG00280.hp1 HG00741.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.2944-14_2944-7dupC others(7): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 25/30 | INFO_REALIGN_3_PRIME | chr9 | 135784482 | |||||
| chr9:135784482
|
G | GCTCCCTC others(5): Show |
3 | a0001c0002t0006g0054a0001c0004t0012g0226a0001c0004t0014g0002 | 3 | HG01884.hp1 HG03098.hp2 NA18612.hp1 |
splice_region_variant&intron_variant | LOW | c.2944-18_2944-7dupC others(11): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 25/30 | INFO_REALIGN_3_PRIME | chr9 | 135784482 | |||||
| chr9:135784482
|
G | GCTCCCTC others(9): Show |
2 | a0001c0003t0001g0272a0001c0026t0001g0051 | 2 | HG00099.hp2 HG02965.hp1 |
splice_region_variant&intron_variant | LOW | c.2944-22_2944-7dupC others(15): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 25/30 | INFO_REALIGN_3_PRIME | chr9 | 135784482 | |||||
| chr9:135784482
|
G | GCTCCCTC others(13): Show |
1 | a0001c0002t0005g0220 | 1 | HG01167.hp2 | splice_region_variant&intron_variant | LOW | c.2944-26_2944-7dupC others(19): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 25/30 | INFO_REALIGN_3_PRIME | chr9 | 135784482 | |||||
| chr9:135784482
|
G | GCTCCCTC others(17): Show |
1 | a0001c0001t0001g0234 | 1 | HG01258.hp2 | splice_region_variant&intron_variant | LOW | c.2944-30_2944-7dupC others(23): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 25/30 | INFO_REALIGN_3_PRIME | chr9 | 135784482 | |||||
| chr9:135784482
|
G | GCTCCCTC others(29): Show |
1 | a0001c0002t0035g0109 | 1 | NA19068.hp2 | splice_region_variant&intron_variant | LOW | c.2944-42_2944-7dupC others(35): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 25/30 | INFO_REALIGN_3_PRIME | chr9 | 135784482 | |||||
| chr9:135784482
|
GCTCC | G | 62 | a0001c0001t0001g0038a0001c0001t0001g0056a0001c0001t0001g0062others(59): Show | 62 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(59): Show |
splice_region_variant&intron_variant | LOW | c.2944-10_2944-7delC others(3): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 25/30 | INFO_REALIGN_3_PRIME | chr9 | 135784482 | |||||
| chr9:135784482
|
GCTCCCTC others(1): Show |
G | 55 | a0001c0001t0001g0031a0001c0001t0001g0055a0001c0001t0001g0074others(52): Show | 55 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(52): Show |
splice_region_variant&intron_variant | LOW | c.2944-14_2944-7delC others(7): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 25/30 | INFO_REALIGN_3_PRIME | chr9 | 135784482 | |||||
| chr9:135784482
|
GCTCCCTC others(5): Show |
G | 31 | a0001c0001t0001g0085a0001c0001t0001g0111a0001c0001t0001g0112others(28): Show | 31 | HG00544.hp1 HG00642.hp2 HG00733.hp2 others(28): Show |
splice_region_variant&intron_variant | LOW | c.2944-18_2944-7delC others(11): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 25/30 | INFO_REALIGN_3_PRIME | chr9 | 135784482 | |||||
| chr9:135784482
|
GCTCCCTC others(13): Show |
G | 10 | a0001c0001t0001g0119a0001c0001t0001g0136a0001c0001t0016g0102others(7): Show | 10 | HG00642.hp1 HG00738.hp1 HG01074.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.2944-26_2944-7delC others(19): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 25/30 | INFO_REALIGN_3_PRIME | chr9 | 135784482 | |||||
| chr9:135784482
|
GCTCCCTC others(17): Show |
G | 1 | a0001c0010t0001g0158 | 1 | HG02055.hp2 | splice_region_variant&intron_variant | LOW | c.2944-30_2944-7delC others(23): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 25/30 | INFO_REALIGN_3_PRIME | chr9 | 135784482 | |||||
| chr9:135784482
|
GCTCCCTC others(21): Show |
G | 10 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0095others(7): Show | 10 | HG01109.hp2 HG02145.hp1 HG02155.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.2944-34_2944-7delC others(27): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 25/30 | INFO_REALIGN_3_PRIME | chr9 | 135784482 | |||||
| chr9:135784525
|
C | T | 1 | a0001c0001t0002g0142 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2944-10C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 25/30 | chr9 | 135784525 | ||||||
| chr9:135784671
|
G | T | 1 | a0001c0001t0001g0076 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3027+53G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 26/30 | chr9 | 135784671 | ||||||
| chr9:135784747
|
T | G | 2 | a0001c0001t0005g0173a0001c0001t0005g0174 | 2 | HG01106.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.3028-14T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 26/30 | chr9 | 135784747 | ||||||
| chr9:135785125
|
C | T | 1 | a0001c0009t0006g0159 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3157-185C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 27/30 | chr9 | 135785125 | ||||||
| chr9:135785302
|
C | T | 2 | a0001c0002t0009g0047a0001c0027t0009g0268 | 2 | HG02486.hp1 HG03471.hp1 |
splice_region_variant&intron_variant | LOW | c.3157-8C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 27/30 | chr9 | 135785302 | ||||||
| chr9:135785397
|
A | T | 11 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0175others(8): Show | 11 | HG01081.hp2 HG01106.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.3177+67A>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 28/30 | chr9 | 135785397 | ||||||
| chr9:135785409
|
CCCCA | C | 9 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0175others(6): Show | 9 | HG01081.hp2 HG01106.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.3177+97_3177+100de others(5): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 28/30 | INFO_REALIGN_3_PRIME | chr9 | 135785409 | |||||
| chr9:135785458
|
C | T | 1 | a0001c0004t0007g0006 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3177+128C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 28/30 | chr9 | 135785458 | ||||||
| chr9:135785459
|
G | A | 2 | a0002c0008t0001g0170a0002c0008t0001g0171 | 2 | HG01074.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.3177+129G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 28/30 | chr9 | 135785459 | ||||||
| chr9:135785652
|
C | T | 1 | a0001c0004t0004g0258 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3177+322C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 28/30 | chr9 | 135785652 | ||||||
| chr9:135785691
|
A | G | 51 | a0001c0001t0001g0074a0001c0001t0001g0204a0001c0001t0001g0242others(48): Show | 51 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.3177+361A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 28/30 | chr9 | 135785691 | ||||||
| chr9:135785692
|
T | A | 51 | a0001c0001t0001g0074a0001c0001t0001g0204a0001c0001t0001g0242others(48): Show | 51 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.3177+362T>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 28/30 | chr9 | 135785692 | ||||||
| chr9:135785818
|
C | G | 1 | a0001c0001t0001g0088 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.3178-379C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 28/30 | chr9 | 135785818 | ||||||
| chr9:135785840
|
G | A | 1 | a0001c0022t0001g0070 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3178-357G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 28/30 | chr9 | 135785840 | ||||||
| chr9:135785845
|
G | C | 5 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0122others(2): Show | 5 | HG00099.hp2 HG01099.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.3178-352G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 28/30 | chr9 | 135785845 | ||||||
| chr9:135785911
|
C | T | 1 | a0001c0002t0001g0264 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3178-286C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 28/30 | chr9 | 135785911 | ||||||
| chr9:135786085
|
C | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0095others(8): Show | 11 | HG01109.hp2 HG02145.hp1 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.3178-112C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 28/30 | chr9 | 135786085 | ||||||
| chr9:135786170
|
CGCCCT | C | 97 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0074others(94): Show | 97 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(94): Show |
splice_region_variant&intron_variant | LOW | c.3178-7_3178-3delTG others(3): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 28/30 | INFO_REALIGN_3_PRIME | chr9 | 135786170 | |||||
| chr9:135786537
|
G | A | 9 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0175others(6): Show | 9 | HG01081.hp2 HG01106.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.3502+16G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135786537 | ||||||
| chr9:135786637
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3502+116T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135786637 | ||||||
| chr9:135786701
|
C | T | 1 | a0001c0002t0001g0140 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.3502+180C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135786701 | ||||||
| chr9:135786821
|
G | A | 1 | a0001c0001t0013g0176 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3502+300G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135786821 | ||||||
| chr9:135786902
|
C | T | 1 | a0001c0003t0001g0036 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.3502+381C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135786902 | ||||||
| chr9:135786929
|
G | A | 2 | a0001c0003t0013g0068a0001c0003t0031g0269 | 2 | HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3502+408G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135786929 | ||||||
| chr9:135787108
|
T | C | 99 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0074others(96): Show | 99 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.3502+587T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135787108 | ||||||
| chr9:135787148
|
A | G | 1 | a0001c0001t0016g0102 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3502+627A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135787148 | ||||||
| chr9:135787280
|
G | A | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3502+759G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135787280 | ||||||
| chr9:135787298
|
T | G | 2 | a0001c0002t0009g0047a0001c0027t0009g0268 | 2 | HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3502+777T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135787298 | ||||||
| chr9:135787302
|
G | A | 2 | a0001c0001t0001g0038a0001c0004t0007g0006 | 2 | HG01081.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3502+781G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135787302 | ||||||
| chr9:135787340
|
C | G | 27 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0074others(24): Show | 27 | HG00099.hp1 HG01109.hp2 HG01346.hp2 others(24): Show |
intron_variant | MODIFIER | c.3502+819C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135787340 | ||||||
| chr9:135787388
|
G | A | 6 | a0001c0001t0011g0032a0001c0002t0001g0124a0001c0002t0011g0083others(3): Show | 6 | HG00423.hp1 NA18971.hp2 NA19005.hp1 others(3): Show |
intron_variant | MODIFIER | c.3502+867G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135787388 | ||||||
| chr9:135787573
|
C | T | 1 | a0001c0002t0002g0145 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3502+1052C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135787573 | ||||||
| chr9:135787626
|
C | T | 21 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0175others(18): Show | 21 | HG01081.hp2 HG01106.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.3502+1105C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135787626 | ||||||
| chr9:135787655
|
G | A | 1 | a0001c0001t0028g0077 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3502+1134G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135787655 | ||||||
| chr9:135787728
|
G | A | 1 | a0001c0002t0001g0262 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3502+1207G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135787728 | ||||||
| chr9:135787754
|
A | G | 2 | a0001c0001t0015g0103a0001c0001t0015g0104 | 2 | HG00642.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.3502+1233A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135787754 | ||||||
| chr9:135787761
|
C | T | 50 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0074others(47): Show | 50 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.3502+1240C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135787761 | ||||||
| chr9:135787768
|
G | A | 7 | a0001c0001t0016g0102a0001c0001t0016g0254a0001c0003t0010g0148others(4): Show | 7 | HG01099.hp1 HG01109.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.3502+1247G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135787768 | ||||||
| chr9:135787836
|
T | C | 1 | a0001c0003t0001g0144 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3502+1315T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135787836 | ||||||
| chr9:135787913
|
C | T | 1 | a0001c0003t0001g0036 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.3502+1392C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135787913 | ||||||
| chr9:135787967
|
G | A | 1 | a0001c0001t0016g0102 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3502+1446G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135787967 | ||||||
| chr9:135787984
|
C | T | 2 | a0001c0003t0001g0180a0001c0003t0001g0210 | 2 | NA18970.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.3502+1463C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135787984 | ||||||
| chr9:135788016
|
C | T | 2 | a0001c0001t0016g0102a0001c0001t0016g0254 | 2 | HG02602.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.3502+1495C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135788016 | ||||||
| chr9:135788017
|
A | G | 68 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0074others(65): Show | 68 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.3502+1496A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135788017 | ||||||
| chr9:135788024
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3502+1503C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135788024 | ||||||
| chr9:135788049
|
T | C | 100 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0074others(97): Show | 100 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.3502+1528T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135788049 | ||||||
| chr9:135788065
|
C | G | 91 | a0001c0001t0001g0038a0001c0001t0001g0053a0001c0001t0001g0062others(88): Show | 91 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.3502+1544C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135788065 | ||||||
| chr9:135788067
|
T | C | 1 | a0001c0002t0033g0139 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3502+1546T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135788067 | ||||||
| chr9:135788193
|
G | A | 21 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0175others(18): Show | 21 | HG01081.hp2 HG01099.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.3502+1672G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135788193 | ||||||
| chr9:135788220
|
C | T | 1 | a0001c0003t0008g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3502+1699C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135788220 | ||||||
| chr9:135788332
|
G | C | 1 | a0001c0001t0001g0042 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3502+1811G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135788332 | ||||||
| chr9:135788370
|
C | T | 1 | a0001c0002t0002g0219 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.3502+1849C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135788370 | ||||||
| chr9:135788388
|
G | A | 1 | a0001c0004t0004g0003 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3502+1867G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135788388 | ||||||
| chr9:135788409
|
C | T | 2 | a0001c0001t0001g0186a0001c0001t0002g0239 | 2 | NA18747.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.3502+1888C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135788409 | ||||||
| chr9:135788494
|
T | G | 175 | a0001c0001t0001g0019a0001c0001t0001g0038a0001c0001t0001g0042others(172): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.3502+1973T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135788494 | ||||||
| chr9:135788624
|
C | T | 4 | a0001c0003t0009g0177a0001c0006t0009g0012a0001c0014t0017g0212others(1): Show | 4 | HG02451.hp1 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.3502+2103C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135788624 | ||||||
| chr9:135788742
|
G | A | 1 | a0001c0003t0013g0068 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3502+2221G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135788742 | ||||||
| chr9:135788775
|
C | T | 4 | a0001c0003t0009g0177a0001c0006t0009g0012a0001c0014t0017g0212others(1): Show | 4 | HG02451.hp1 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.3502+2254C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135788775 | ||||||
| chr9:135788836
|
G | T | 1 | a0001c0001t0001g0060 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3502+2315G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135788836 | ||||||
| chr9:135789055
|
T | C | 98 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0074others(95): Show | 98 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.3502+2534T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135789055 | ||||||
| chr9:135789100
|
C | T | 3 | a0001c0003t0002g0027a0001c0003t0013g0068a0001c0003t0031g0269 | 3 | HG02809.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3502+2579C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135789100 | ||||||
| chr9:135789176
|
G | A | 2 | a0001c0004t0001g0005a0001c0004t0001g0007 | 2 | HG01074.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3503-2621G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135789176 | ||||||
| chr9:135789177
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3503-2620C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135789177 | ||||||
| chr9:135789228
|
C | T | 1 | a0001c0001t0039g0156 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3503-2569C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135789228 | ||||||
| chr9:135789260
|
C | T | 1 | a0001c0003t0001g0272 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3503-2537C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135789260 | ||||||
| chr9:135789403
|
C | T | 1 | a0001c0001t0002g0020 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3503-2394C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135789403 | ||||||
| chr9:135789582
|
C | T | 1 | a0001c0002t0005g0081 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3503-2215C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135789582 | ||||||
| chr9:135789583
|
G | A | 27 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0095others(24): Show | 27 | HG00099.hp1 HG01109.hp2 HG01346.hp2 others(24): Show |
intron_variant | MODIFIER | c.3503-2214G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135789583 | ||||||
| chr9:135789817
|
C | T | 5 | a0001c0003t0010g0148a0001c0004t0037g0004a0001c0006t0010g0010others(2): Show | 5 | HG01099.hp1 HG01109.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.3503-1980C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135789817 | ||||||
| chr9:135790077
|
C | T | 2 | a0001c0001t0016g0102a0001c0001t0016g0254 | 2 | HG02602.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.3503-1720C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135790077 | ||||||
| chr9:135790178
|
C | T | 1 | a0001c0004t0002g0147 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3503-1619C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135790178 | ||||||
| chr9:135790282
|
G | A | 2 | a0001c0001t0016g0102a0001c0001t0016g0254 | 2 | HG02602.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.3503-1515G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135790282 | ||||||
| chr9:135790339
|
C | T | 1 | a0001c0002t0005g0220 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3503-1458C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135790339 | ||||||
| chr9:135790531
|
C | G | 1 | a0001c0004t0001g0187 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.3503-1266C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135790531 | ||||||
| chr9:135790531
|
C | T | 1 | a0001c0019t0003g0089 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3503-1266C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135790531 | ||||||
| chr9:135790711
|
CAG | C | 3 | a0001c0002t0025g0149a0001c0004t0014g0002a0001c0010t0014g0161 | 3 | HG03098.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3503-1081_3503-108 others(6): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | INFO_REALIGN_3_PRIME | chr9 | 135790711 | |||||
| chr9:135790739
|
G | A | 2 | a0001c0003t0009g0177a0001c0006t0009g0012 | 2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.3503-1058G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135790739 | ||||||
| chr9:135790812
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3503-985A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135790812 | ||||||
| chr9:135790814
|
G | C | 1 | a0001c0001t0001g0057 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3503-983G>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135790814 | ||||||
| chr9:135790828
|
C | A | 1 | a0001c0003t0031g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3503-969C>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135790828 | ||||||
| chr9:135790905
|
C | T | 4 | a0001c0002t0001g0033a0001c0002t0001g0140a0001c0002t0001g0211others(1): Show | 4 | NA18947.hp2 NA18948.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.3503-892C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135790905 | ||||||
| chr9:135791020
|
C | G | 1 | a0001c0003t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3503-777C>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135791020 | ||||||
| chr9:135791154
|
G | A | 5 | a0001c0001t0001g0106a0001c0001t0001g0129a0001c0003t0001g0035others(2): Show | 5 | HG01943.hp2 HG01978.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.3503-643G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135791154 | ||||||
| chr9:135791167
|
C | T | 1 | a0001c0003t0003g0059 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3503-630C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135791167 | ||||||
| chr9:135791248
|
G | T | 40 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0095others(37): Show | 40 | HG00099.hp1 HG01099.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.3503-549G>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135791248 | ||||||
| chr9:135791278
|
T | G | 3 | a0001c0001t0001g0076a0001c0001t0001g0088a0001c0001t0001g0099 | 3 | HG01981.hp1 HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.3503-519T>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135791278 | ||||||
| chr9:135791381
|
CTGCAGGT others(3): Show |
C | 1 | a0001c0002t0002g0228 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3503-406_3503-397d others(12): Show |
KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | INFO_REALIGN_3_PRIME | chr9 | 135791381 | |||||
| chr9:135791438
|
G | A | 12 | a0001c0001t0008g0008a0001c0001t0027g0157a0001c0002t0006g0054others(9): Show | 12 | HG01192.hp2 HG01884.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.3503-359G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135791438 | ||||||
| chr9:135791442
|
C | T | 4 | a0001c0002t0002g0021a0001c0002t0002g0107a0001c0002t0002g0114others(1): Show | 4 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.3503-355C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135791442 | ||||||
| chr9:135791460
|
G | A | 1 | a0001c0002t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3503-337G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135791460 | ||||||
| chr9:135791486
|
T | C | 1 | a0001c0001t0013g0176 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3503-311T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135791486 | ||||||
| chr9:135791696
|
A | G | 1 | a0001c0003t0001g0272 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3503-101A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135791696 | ||||||
| chr9:135791729
|
T | C | 47 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0095others(44): Show | 47 | HG00099.hp1 HG01099.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.3503-68T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135791729 | ||||||
| chr9:135791730
|
G | A | 3 | a0001c0001t0003g0016a0001c0001t0003g0222a0001c0002t0001g0184 | 3 | HG04115.hp1 HG04204.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.3503-67G>A | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135791730 | ||||||
| chr9:135791754
|
C | T | 1 | a0001c0003t0001g0064 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3503-43C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 29/30 | chr9 | 135791754 | ||||||
| chr9:135791910
|
A | AC | 18 | a0001c0001t0016g0102a0001c0001t0016g0254a0001c0001t0027g0157others(15): Show | 18 | HG01884.hp1 HG02572.hp2 HG02602.hp1 others(15): Show |
intron_variant | MODIFIER | c.3587+36dupC | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr9 | 135791910 | |||||
| chr9:135791944
|
T | C | 24 | a0001c0001t0001g0056a0001c0001t0001g0191a0001c0001t0003g0016others(21): Show | 24 | HG00099.hp1 HG01168.hp1 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.3587+63T>C | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 30/30 | chr9 | 135791944 | ||||||
| chr9:135791952
|
C | T | 19 | a0001c0001t0003g0016a0001c0001t0003g0168a0001c0001t0003g0181others(16): Show | 19 | HG00099.hp1 HG01346.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.3587+71C>T | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 30/30 | chr9 | 135791952 | ||||||
| chr9:135791990
|
A | G | 2 | a0001c0001t0016g0102a0001c0001t0016g0254 | 2 | HG02602.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.3588-51A>G | KCNT1 | ENSG00000107147.14 | transcript | ENST00000371757.7 | protein_coding | 30/30 | chr9 | 135791990 |