| geneid | 286 |
|---|---|
| ensemblid | ENSG00000029534.22 |
| hgncid | 492 |
| symbol | ANK1 |
| name | ankyrin 1 |
| refseq_nuc | NM_000037.4 |
| refseq_prot | NP_000028.3 |
| ensembl_nuc | ENST00000289734.13 |
| ensembl_prot | ENSP00000289734.8 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 41653225 |
| end | 41797622 |
| strand | - |
| ver | v1.2 |
| region | chr8:41653225-41797622 |
| region5000 | chr8:41648225-41802622 |
| regionname0 | ANK1_chr8_41653225_41797622 |
| regionname5000 | ANK1_chr8_41648225_41802622 |
| 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 | 1880 | 233 | 58 | 46 | 84 | 12 | 31 | 61 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0002 | 0/0 | 1880 | 12 | 10 | 2 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0003 | 0/0 | 1880 | 10 | 3 | 1 | 3 | 0 | 3 | 3 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0004 | 0/0 | 1880 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0005 | 0/0 | 1880 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0006 | 0/0 | 1880 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0007 | 0/0 | 1880 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0008 | 0/0 | 1880 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0009 | 0/0 | 1880 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0010 | 0/0 | 1880 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0011 | 0/0 | 1880 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0012 | 0/0 | 1880 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0013 | 0/0 | 1880 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0014 | 0/0 | 1880 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0015 | 0/0 | 492 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0016 | 0/0 | 1880 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| 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 | 0/0 | 5643 | 45 | 7 | 6 | 26 | 2 | 4 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0002 | 0/0 | 5643 | 38 | 4 | 11 | 12 | 4 | 7 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0003 | 0/1 | 5643 | 27 | 1 | 8 | 7 | 2 | 8 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0004 | 0/0 | 5643 | 24 | 1 | 3 | 13 | 0 | 7 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0005 | 1/0 | 5643 | 24 | 12 | 5 | 6 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0006 | 0/0 | 5643 | 12 | 12 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0007 | 0/0 | 5643 | 8 | 7 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0008 | 0/0 | 5643 | 7 | 0 | 0 | 5 | 2 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0009 | 0/0 | 5643 | 7 | 0 | 5 | 0 | 1 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0010 | 0/0 | 5643 | 6 | 0 | 0 | 6 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0011 | 0/0 | 5643 | 5 | 5 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0012 | 0/0 | 5643 | 5 | 3 | 1 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0013 | 0/0 | 5643 | 4 | 4 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0014 | 0/0 | 5643 | 4 | 0 | 1 | 0 | 0 | 3 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0015 | 0/0 | 5643 | 3 | 0 | 0 | 3 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0016 | 0/0 | 5643 | 3 | 2 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0017 | 0/0 | 5643 | 3 | 3 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0018 | 0/0 | 5643 | 3 | 1 | 0 | 2 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0019 | 0/0 | 5643 | 3 | 0 | 1 | 2 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0020 | 0/0 | 5643 | 3 | 3 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0021 | 0/0 | 5643 | 2 | 2 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0022 | 0/0 | 5643 | 2 | 0 | 2 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0023 | 0/0 | 5643 | 2 | 2 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0024 | 0/0 | 5643 | 2 | 2 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0025 | 0/0 | 5643 | 2 | 0 | 0 | 0 | 0 | 2 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0026 | 0/0 | 5643 | 2 | 0 | 0 | 2 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0027 | 0/0 | 5643 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0028 | 0/0 | 5643 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0029 | 0/0 | 5643 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0030 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0031 | 0/0 | 5643 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0032 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0033 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0034 | 0/0 | 5643 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0035 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0036 | 0/0 | 5643 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0037 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0038 | 0/0 | 5643 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0039 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0040 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0041 | 0/0 | 5643 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0042 | 0/0 | 5643 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0043 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0044 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0045 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0046 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0047 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0048 | 0/0 | 5643 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0049 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0050 | 0/0 | 5643 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0051 | 0/0 | 5643 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0052 | 0/0 | 5643 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0053 | 0/0 | 5663 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0054 | 0/0 | 5643 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0055 | 0/0 | 5643 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0056 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0057 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| c0058 | 0/0 | 5643 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2641 | 103 | 28 | 24 | 35 | 5 | 10 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0002 | 0/0 | 2648 | 98 | 18 | 21 | 41 | 4 | 14 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0003 | 0/0 | 2633 | 20 | 8 | 0 | 9 | 1 | 2 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0004 | 1/0 | 2650 | 8 | 7 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0005 | 0/0 | 2637 | 6 | 6 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0006 | 0/0 | 2641 | 5 | 4 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0007 | 0/0 | 2652 | 4 | 3 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0008 | 0/0 | 2636 | 4 | 0 | 1 | 0 | 0 | 3 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0009 | 0/0 | 2637 | 3 | 1 | 1 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0010 | 0/0 | 2654 | 2 | 2 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0011 | 0/0 | 2652 | 2 | 0 | 0 | 0 | 0 | 2 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0012 | 0/0 | 2643 | 2 | 0 | 2 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0013 | 0/0 | 2641 | 2 | 0 | 2 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0014 | 0/0 | 2640 | 2 | 0 | 0 | 0 | 1 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0015 | 0/0 | 2647 | 2 | 0 | 0 | 1 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0016 | 0/0 | 2652 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0017 | 0/0 | 2651 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0018 | 0/0 | 2639 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0019 | 0/0 | 2641 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0020 | 0/0 | 2641 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0021 | 0/0 | 2649 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0022 | 0/0 | 2650 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0023 | 0/0 | 2648 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0024 | 0/0 | 2648 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0025 | 0/0 | 2634 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0026 | 0/0 | 2634 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0027 | 0/0 | 2641 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0028 | 0/0 | 2641 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0029 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| t0030 | 0/0 | 2633 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0072 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0207 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| 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 | 0/0 | 5643 | 45 | 7 | 6 | 26 | 2 | 4 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0002 | 0/0 | 5643 | 38 | 4 | 11 | 12 | 4 | 7 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0003 | 0/1 | 5643 | 27 | 1 | 8 | 7 | 2 | 8 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0004 | 0/0 | 5643 | 24 | 1 | 3 | 13 | 0 | 7 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0005 | 1/0 | 5643 | 24 | 12 | 5 | 6 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0006 | 0/0 | 5643 | 12 | 12 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0008 | 0/0 | 5643 | 7 | 0 | 0 | 5 | 2 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0009 | 0/0 | 5643 | 7 | 0 | 5 | 0 | 1 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0010 | 0/0 | 5643 | 6 | 0 | 0 | 6 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0012 | 0/0 | 5643 | 5 | 3 | 1 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0013 | 0/0 | 5643 | 4 | 4 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0016 | 0/0 | 5643 | 3 | 2 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0017 | 0/0 | 5643 | 3 | 3 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0018 | 0/0 | 5643 | 3 | 1 | 0 | 2 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0019 | 0/0 | 5643 | 3 | 0 | 1 | 2 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0022 | 0/0 | 5643 | 2 | 0 | 2 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0023 | 0/0 | 5643 | 2 | 2 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0025 | 0/0 | 5643 | 2 | 0 | 0 | 0 | 0 | 2 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0026 | 0/0 | 5643 | 2 | 0 | 0 | 2 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0028 | 0/0 | 5643 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0029 | 0/0 | 5643 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0030 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0032 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0034 | 0/0 | 5643 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0037 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0038 | 0/0 | 5643 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0040 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0046 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0051 | 0/0 | 5643 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0052 | 0/0 | 5643 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0054 | 0/0 | 5643 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0056 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0058 | 0/0 | 5643 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0002c0007 | 0/0 | 5643 | 8 | 7 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0002c0039 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0002c0042 | 0/0 | 5643 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0002c0043 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0002c0057 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0003c0014 | 0/0 | 5643 | 4 | 0 | 1 | 0 | 0 | 3 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0003c0015 | 0/0 | 5643 | 3 | 0 | 0 | 3 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0003c0024 | 0/0 | 5643 | 2 | 2 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0003c0049 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0004c0011 | 0/0 | 5643 | 5 | 5 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0004c0020 | 0/0 | 5643 | 3 | 3 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0004c0044 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0005c0021 | 0/0 | 5643 | 2 | 2 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0005c0035 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0006c0031 | 0/0 | 5643 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0007c0033 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0008c0050 | 0/0 | 5643 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0009c0047 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0010c0048 | 0/0 | 5643 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0011c0036 | 0/0 | 5643 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0012c0045 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0013c0041 | 0/0 | 5643 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0014c0055 | 0/0 | 5643 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0015c0053 | 0/0 | 5663 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0016c0027 | 0/0 | 5643 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8283 | 12 | 0 | 0 | 12 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0001t0002 | 0/0 | 8290 | 31 | 7 | 5 | 13 | 2 | 4 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0001t0013 | 0/0 | 8283 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0001t0023 | 0/0 | 8290 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0002t0001 | 0/0 | 8283 | 27 | 3 | 9 | 9 | 2 | 4 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0002t0002 | 0/0 | 8290 | 4 | 0 | 0 | 3 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0002t0003 | 0/0 | 8275 | 3 | 0 | 0 | 0 | 1 | 2 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0002t0009 | 0/0 | 8279 | 2 | 1 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0002t0012 | 0/0 | 8285 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0002t0014 | 0/0 | 8282 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0003t0001 | 0/1 | 8283 | 21 | 0 | 8 | 5 | 2 | 5 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0003t0002 | 0/0 | 8290 | 3 | 1 | 0 | 1 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0003t0009 | 0/0 | 8279 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0003t0014 | 0/0 | 8282 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0003t0019 | 0/0 | 8283 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0004t0001 | 0/0 | 8283 | 2 | 1 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0004t0002 | 0/0 | 8290 | 21 | 0 | 3 | 12 | 0 | 6 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0004t0024 | 0/0 | 8290 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0005t0001 | 0/0 | 8283 | 8 | 1 | 3 | 4 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0005t0002 | 0/0 | 8290 | 3 | 1 | 1 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0005t0003 | 0/0 | 8275 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0005t0004 | 1/0 | 8292 | 7 | 6 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0005t0010 | 0/0 | 8296 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0005t0013 | 0/0 | 8283 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0005t0020 | 0/0 | 8283 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0005t0028 | 0/0 | 8283 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0005t0029 | 0/0 | 8282 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0006t0001 | 0/0 | 8283 | 7 | 7 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0006t0003 | 0/0 | 8275 | 3 | 3 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0006t0005 | 0/0 | 8279 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0006t0018 | 0/0 | 8281 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0008t0002 | 0/0 | 8290 | 6 | 0 | 0 | 5 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0008t0015 | 0/0 | 8289 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0009t0002 | 0/0 | 8290 | 7 | 0 | 5 | 0 | 1 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0010t0002 | 0/0 | 8290 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0010t0003 | 0/0 | 8275 | 5 | 0 | 0 | 5 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0012t0001 | 0/0 | 8283 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0012t0005 | 0/0 | 8279 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0012t0006 | 0/0 | 8283 | 2 | 2 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0012t0015 | 0/0 | 8289 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0013t0001 | 0/0 | 8283 | 2 | 2 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0013t0006 | 0/0 | 8283 | 2 | 2 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0016t0002 | 0/0 | 8290 | 3 | 2 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0017t0005 | 0/0 | 8279 | 3 | 3 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0018t0001 | 0/0 | 8283 | 2 | 0 | 0 | 2 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0018t0026 | 0/0 | 8276 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0019t0002 | 0/0 | 8290 | 3 | 0 | 1 | 2 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0022t0002 | 0/0 | 8290 | 2 | 0 | 2 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0023t0001 | 0/0 | 8283 | 2 | 2 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0025t0011 | 0/0 | 8294 | 2 | 0 | 0 | 0 | 0 | 2 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0026t0001 | 0/0 | 8283 | 2 | 0 | 0 | 2 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0028t0003 | 0/0 | 8275 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0029t0001 | 0/0 | 8283 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0030t0017 | 0/0 | 8293 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0032t0003 | 0/0 | 8275 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0034t0002 | 0/0 | 8290 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0037t0003 | 0/0 | 8275 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0038t0002 | 0/0 | 8290 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0040t0001 | 0/0 | 8283 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0046t0030 | 0/0 | 8275 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0051t0008 | 0/0 | 8278 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0052t0001 | 0/0 | 8283 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0054t0001 | 0/0 | 8283 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0056t0003 | 0/0 | 8275 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0001c0058t0022 | 0/0 | 8292 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0002c0007t0001 | 0/0 | 8283 | 2 | 2 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0002c0007t0007 | 0/0 | 8294 | 4 | 3 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0002c0007t0021 | 0/0 | 8291 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0002c0007t0027 | 0/0 | 8283 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0002c0039t0010 | 0/0 | 8296 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0002c0042t0016 | 0/0 | 8294 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0002c0043t0002 | 0/0 | 8290 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0002c0057t0005 | 0/0 | 8279 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0003c0014t0002 | 0/0 | 8290 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0003c0014t0008 | 0/0 | 8278 | 3 | 0 | 0 | 0 | 0 | 3 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0003c0015t0003 | 0/0 | 8275 | 3 | 0 | 0 | 3 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0003c0024t0001 | 0/0 | 8283 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0003c0024t0003 | 0/0 | 8275 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0003c0049t0001 | 0/0 | 8283 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0004c0011t0001 | 0/0 | 8283 | 2 | 2 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0004c0011t0002 | 0/0 | 8290 | 3 | 3 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0004c0020t0001 | 0/0 | 8283 | 3 | 3 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0004c0044t0004 | 0/0 | 8292 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0005c0021t0002 | 0/0 | 8290 | 2 | 2 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0005c0035t0001 | 0/0 | 8283 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0006c0031t0002 | 0/0 | 8290 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0007c0033t0001 | 0/0 | 8283 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0008c0050t0001 | 0/0 | 8283 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0009c0047t0002 | 0/0 | 8290 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0010c0048t0001 | 0/0 | 8283 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0011c0036t0002 | 0/0 | 8290 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0012c0045t0025 | 0/0 | 8276 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0013c0041t0012 | 0/0 | 8285 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0014c0055t0006 | 0/0 | 8283 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0015c0053t0002 | 0/0 | 8310 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| a0016c0027t0002 | 0/0 | 8290 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | copy fasta | chr8 | 41648225 | 41802622 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0013g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0001t0023g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0009g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0009g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0012g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0002t0014g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0003t0001g0072 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0003t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0003t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0003t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0003t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0003t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0003t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0003t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0003t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0003t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0003t0009g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0003t0014g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0003t0019g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0004t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0004t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0004t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0004t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0004t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0004t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0004t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0004t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0004t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0004t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0004t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0004t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0004t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0004t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0004t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0004t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0004t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0004t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0004t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0004t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0004t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0004t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0004t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0004t0024g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0005t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0005t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0005t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0005t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0005t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0005t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0005t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0005t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0005t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0005t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0005t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0005t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0005t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0005t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0005t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0005t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0005t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0005t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0005t0004g0207 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0005t0010g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0005t0013g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0005t0020g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0005t0028g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0005t0029g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0006t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0006t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0006t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0006t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0006t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0006t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0006t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0006t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0006t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0006t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0006t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0006t0018g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0008t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0008t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0008t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0008t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0008t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0008t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0008t0015g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0009t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0009t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0009t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0009t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0009t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0009t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0009t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0010t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0010t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0010t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0010t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0010t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0010t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0012t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0012t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0012t0006g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0012t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0012t0015g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0013t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0013t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0013t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0013t0006g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0016t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0016t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0016t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0017t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0017t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0017t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0018t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0018t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0018t0026g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0019t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0019t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0019t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0022t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0022t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0023t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0023t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0025t0011g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0026t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0026t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0028t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0029t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0030t0017g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0032t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0034t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0037t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0038t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0040t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0046t0030g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0051t0008g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0052t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0054t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0056t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0001c0058t0022g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0002c0007t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0002c0007t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0002c0007t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0002c0007t0007g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0002c0007t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0002c0007t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0002c0007t0021g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0002c0007t0027g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0002c0039t0010g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0002c0042t0016g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0002c0043t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0002c0057t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0003c0014t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0003c0014t0008g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0003c0014t0008g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0003c0014t0008g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0003c0015t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0003c0015t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0003c0015t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0003c0024t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0003c0024t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0003c0049t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0004c0011t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0004c0011t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0004c0011t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0004c0011t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0004c0011t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0004c0020t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0004c0020t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0004c0020t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0004c0044t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0005c0021t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0005c0021t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0005c0035t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0006c0031t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0007c0033t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0008c0050t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0009c0047t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0010c0048t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0011c0036t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0012c0045t0025g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0013c0041t0012g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0014c0055t0006g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0015c0053t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| a0016c0027t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0171 | EUR | GBR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0062 | EUR | GBR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0071 | EUR | GBR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0121 | EUR | GBR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0078 | EUR | FIN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG00323 | hp2 | a0001 | c0052 | t0001 | g0235 | EUR | FIN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | CHS | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG00408 | hp2 | a0001 | c0005 | t0002 | g0190 | EAS | CHS | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG00423 | hp1 | a0011 | c0036 | t0002 | g0076 | EAS | CHS | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG00423 | hp2 | a0001 | c0004 | t0002 | g0211 | EAS | CHS | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG00438 | hp1 | a0001 | c0026 | t0001 | g0167 | EAS | CHS | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG00438 | hp2 | a0001 | c0008 | t0002 | g0198 | EAS | CHS | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG00639 | hp1 | a0003 | c0014 | t0002 | g0209 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG00639 | hp2 | a0001 | c0009 | t0002 | g0061 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0134 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG00733 | hp2 | a0001 | c0022 | t0002 | g0232 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0183 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG00738 | hp1 | a0001 | c0051 | t0008 | g0274 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG00738 | hp2 | a0001 | c0009 | t0002 | g0046 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG00741 | hp1 | a0001 | c0054 | t0001 | g0131 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0144 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01069 | hp1 | a0001 | c0004 | t0002 | g0126 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01070 | hp1 | a0001 | c0009 | t0002 | g0082 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01070 | hp2 | a0001 | c0005 | t0013 | g0004 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01071 | hp1 | a0001 | c0001 | t0013 | g0091 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01071 | hp2 | a0001 | c0005 | t0002 | g0003 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01081 | hp1 | a0001 | c0009 | t0002 | g0047 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0140 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01099 | hp2 | a0001 | c0003 | t0001 | g0142 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01106 | hp1 | a0001 | c0009 | t0002 | g0052 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01106 | hp2 | a0014 | c0055 | t0006 | g0012 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01167 | hp1 | a0002 | c0042 | t0016 | g0045 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0143 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01168 | hp1 | a0001 | c0004 | t0002 | g0224 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0172 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01175 | hp1 | a0016 | c0027 | t0002 | g0054 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0150 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0181 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01192 | hp2 | a0001 | c0016 | t0002 | g0007 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01243 | hp1 | a0001 | c0019 | t0002 | g0164 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01243 | hp2 | a0002 | c0007 | t0007 | g0023 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01255 | hp1 | a0001 | c0003 | t0001 | g0060 | AMR | CLM | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0127 | AMR | CLM | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01258 | hp1 | a0001 | c0038 | t0002 | g0200 | AMR | CLM | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0136 | AMR | CLM | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01261 | hp1 | a0001 | c0002 | t0012 | g0022 | AMR | CLM | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01261 | hp2 | a0001 | c0005 | t0001 | g0083 | AMR | CLM | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | CLM | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01496 | hp2 | a0001 | c0003 | t0001 | g0093 | AMR | CLM | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01515 | hp1 | a0001 | c0008 | t0002 | g0194 | EUR | IBS | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01515 | hp2 | a0001 | c0002 | t0014 | g0129 | EUR | IBS | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0128 | EUR | IBS | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01517 | hp2 | a0001 | c0008 | t0015 | g0196 | EUR | IBS | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01891 | hp1 | a0002 | c0057 | t0005 | g0269 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01891 | hp2 | a0001 | c0023 | t0001 | g0276 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01928 | hp1 | a0008 | c0050 | t0001 | g0153 | AMR | PEL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01928 | hp2 | a0001 | c0012 | t0001 | g0138 | AMR | PEL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01934 | hp1 | a0001 | c0003 | t0001 | g0064 | AMR | PEL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0141 | AMR | PEL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | PEL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01952 | hp2 | a0010 | c0048 | t0001 | g0182 | AMR | PEL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01975 | hp1 | a0001 | c0005 | t0001 | g0257 | AMR | PEL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01975 | hp2 | a0001 | c0002 | t0009 | g0130 | AMR | PEL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01978 | hp1 | a0001 | c0004 | t0002 | g0066 | AMR | PEL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01978 | hp2 | a0001 | c0003 | t0001 | g0139 | AMR | PEL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0135 | AMR | PEL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02004 | hp2 | a0001 | c0022 | t0002 | g0231 | AMR | PEL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02015 | hp2 | a0001 | c0008 | t0002 | g0218 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0227 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02040 | hp2 | a0001 | c0003 | t0001 | g0049 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02071 | hp1 | a0001 | c0005 | t0001 | g0238 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02071 | hp2 | a0001 | c0010 | t0002 | g0056 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02074 | hp1 | a0001 | c0028 | t0003 | g0053 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02074 | hp2 | a0001 | c0010 | t0003 | g0189 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02080 | hp1 | a0001 | c0010 | t0003 | g0002 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02080 | hp2 | a0001 | c0004 | t0002 | g0212 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02083 | hp1 | a0001 | c0004 | t0002 | g0244 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02145 | hp1 | a0001 | c0006 | t0001 | g0264 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0050 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02258 | hp1 | a0002 | c0007 | t0007 | g0025 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02280 | hp1 | a0005 | c0021 | t0002 | g0133 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02280 | hp2 | a0001 | c0005 | t0003 | g0032 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02451 | hp1 | a0001 | c0018 | t0026 | g0113 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02451 | hp2 | a0002 | c0007 | t0021 | g0118 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02572 | hp1 | a0001 | c0017 | t0005 | g0116 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02572 | hp2 | a0004 | c0020 | t0001 | g0033 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02602 | hp1 | a0001 | c0004 | t0002 | g0271 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02602 | hp2 | a0001 | c0003 | t0002 | g0199 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02622 | hp1 | a0001 | c0012 | t0006 | g0099 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02622 | hp2 | a0001 | c0006 | t0001 | g0267 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02630 | hp1 | a0001 | c0006 | t0001 | g0100 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02630 | hp2 | a0004 | c0020 | t0001 | g0036 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02647 | hp1 | a0001 | c0056 | t0003 | g0026 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02647 | hp2 | a0001 | c0016 | t0002 | g0006 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0151 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02683 | hp2 | a0001 | c0004 | t0002 | g0154 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02698 | hp1 | a0001 | c0004 | t0002 | g0195 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0048 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02717 | hp1 | a0001 | c0037 | t0003 | g0233 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02717 | hp2 | a0001 | c0005 | t0002 | g0010 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02723 | hp1 | a0002 | c0043 | t0002 | g0044 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02723 | hp2 | a0001 | c0046 | t0030 | g0277 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02735 | hp1 | a0001 | c0003 | t0001 | g0073 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0092 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02809 | hp1 | a0001 | c0012 | t0005 | g0103 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02809 | hp2 | a0004 | c0011 | t0001 | g0186 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02818 | hp1 | a0001 | c0005 | t0004 | g0086 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02818 | hp2 | a0003 | c0024 | t0003 | g0102 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02886 | hp1 | a0001 | c0005 | t0004 | g0011 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02886 | hp2 | a0002 | c0007 | t0001 | g0040 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02895 | hp1 | a0007 | c0033 | t0001 | g0108 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02895 | hp2 | a0001 | c0005 | t0029 | g0111 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02897 | hp1 | a0001 | c0005 | t0004 | g0030 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02897 | hp2 | a0001 | c0005 | t0028 | g0112 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02922 | hp1 | a0001 | c0005 | t0004 | g0043 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02922 | hp2 | a0001 | c0016 | t0002 | g0008 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02965 | hp1 | a0001 | c0002 | t0009 | g0098 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02965 | hp2 | a0001 | c0005 | t0004 | g0029 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02970 | hp1 | a0001 | c0005 | t0004 | g0042 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02970 | hp2 | a0001 | c0013 | t0001 | g0037 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02976 | hp1 | a0001 | c0013 | t0001 | g0027 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02976 | hp2 | a0003 | c0024 | t0001 | g0273 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03017 | hp1 | a0001 | c0003 | t0014 | g0065 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03041 | hp1 | a0001 | c0006 | t0003 | g0005 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03041 | hp2 | a0004 | c0020 | t0001 | g0034 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03098 | hp1 | a0001 | c0013 | t0006 | g0124 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03098 | hp2 | a0001 | c0012 | t0006 | g0085 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03130 | hp1 | a0001 | c0006 | t0001 | g0266 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03130 | hp2 | a0001 | c0017 | t0005 | g0120 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03139 | hp1 | a0002 | c0007 | t0001 | g0038 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03139 | hp2 | a0001 | c0005 | t0010 | g0019 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03195 | hp1 | a0003 | c0049 | t0001 | g0104 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03195 | hp2 | a0004 | c0011 | t0002 | g0096 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03209 | hp1 | a0001 | c0006 | t0001 | g0268 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03225 | hp1 | a0002 | c0039 | t0010 | g0018 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03225 | hp2 | a0001 | c0004 | t0001 | g0109 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03239 | hp1 | a0003 | c0014 | t0008 | g0203 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03239 | hp2 | a0001 | c0009 | t0002 | g0059 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03453 | hp1 | a0001 | c0006 | t0003 | g0013 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03453 | hp2 | a0001 | c0006 | t0001 | g0039 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03486 | hp1 | a0002 | c0007 | t0027 | g0035 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03486 | hp2 | a0009 | c0047 | t0002 | g0016 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03490 | hp1 | a0001 | c0002 | t0003 | g0080 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03490 | hp2 | a0003 | c0014 | t0008 | g0095 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03491 | hp1 | a0001 | c0003 | t0001 | g0237 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03491 | hp2 | a0001 | c0025 | t0011 | g0001 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03492 | hp1 | a0001 | c0025 | t0011 | g0001 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03492 | hp2 | a0003 | c0014 | t0008 | g0094 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03516 | hp1 | a0001 | c0040 | t0001 | g0087 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0088 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03540 | hp2 | a0002 | c0007 | t0007 | g0021 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03579 | hp1 | a0001 | c0017 | t0005 | g0119 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03688 | hp1 | a0001 | c0004 | t0002 | g0074 | SAS | STU | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03688 | hp2 | a0001 | c0003 | t0001 | g0058 | SAS | STU | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0184 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03704 | hp2 | a0001 | c0003 | t0009 | g0170 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03710 | hp1 | a0001 | c0004 | t0001 | g0159 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03710 | hp2 | a0001 | c0058 | t0022 | g0089 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03834 | hp1 | a0001 | c0004 | t0002 | g0251 | SAS | BEB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03834 | hp2 | a0001 | c0002 | t0003 | g0146 | SAS | BEB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03942 | hp1 | a0001 | c0003 | t0001 | g0169 | SAS | BEB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0265 | SAS | BEB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | STU | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0180 | SAS | STU | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG04228 | hp1 | a0001 | c0003 | t0001 | g0057 | SAS | STU | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0122 | SAS | STU | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18522 | hp1 | a0001 | c0006 | t0001 | g0017 | AFR | YRI | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18522 | hp2 | a0004 | c0044 | t0004 | g0041 | AFR | YRI | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18612 | hp1 | a0001 | c0019 | t0002 | g0239 | EAS | CHB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | CHB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18747 | hp2 | a0001 | c0004 | t0024 | g0210 | EAS | CHB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18950 | hp1 | a0001 | c0004 | t0002 | g0219 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18950 | hp2 | a0003 | c0015 | t0003 | g0250 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18960 | hp1 | a0001 | c0019 | t0002 | g0145 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18967 | hp2 | a0001 | c0004 | t0002 | g0193 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18969 | hp1 | a0001 | c0003 | t0001 | g0158 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18969 | hp2 | a0001 | c0012 | t0015 | g0240 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18973 | hp1 | a0001 | c0008 | t0002 | g0252 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18973 | hp2 | a0001 | c0003 | t0001 | g0261 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18979 | hp1 | a0001 | c0010 | t0003 | g0114 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18980 | hp1 | a0001 | c0010 | t0003 | g0236 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18981 | hp2 | a0001 | c0003 | t0001 | g0177 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18986 | hp1 | a0006 | c0031 | t0002 | g0255 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18988 | hp1 | a0001 | c0003 | t0019 | g0068 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18992 | hp1 | a0001 | c0005 | t0001 | g0055 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18992 | hp2 | a0001 | c0008 | t0002 | g0246 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18998 | hp2 | a0001 | c0018 | t0001 | g0156 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18999 | hp1 | a0001 | c0004 | t0002 | g0215 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19004 | hp1 | a0001 | c0005 | t0001 | g0228 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19004 | hp2 | a0001 | c0003 | t0002 | g0163 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19007 | hp2 | a0001 | c0004 | t0002 | g0149 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19010 | hp1 | a0003 | c0015 | t0003 | g0137 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19010 | hp2 | a0001 | c0004 | t0002 | g0249 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19012 | hp2 | a0001 | c0010 | t0003 | g0270 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19043 | hp1 | a0012 | c0045 | t0025 | g0188 | AFR | LWK | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19043 | hp2 | a0001 | c0030 | t0017 | g0051 | AFR | LWK | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19056 | hp2 | a0001 | c0004 | t0002 | g0258 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19057 | hp1 | a0001 | c0026 | t0001 | g0165 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19057 | hp2 | a0001 | c0004 | t0002 | g0243 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19063 | hp1 | a0001 | c0004 | t0002 | g0247 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19066 | hp2 | a0001 | c0029 | t0001 | g0253 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19067 | hp1 | a0001 | c0018 | t0001 | g0147 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19068 | hp1 | a0003 | c0015 | t0003 | g0220 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19068 | hp2 | a0001 | c0005 | t0020 | g0179 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19076 | hp1 | a0015 | c0053 | t0002 | g0263 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19079 | hp2 | a0001 | c0005 | t0001 | g0229 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19084 | hp1 | a0001 | c0001 | t0023 | g0081 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19084 | hp2 | a0001 | c0004 | t0002 | g0259 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19087 | hp2 | a0001 | c0008 | t0002 | g0213 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19091 | hp2 | a0001 | c0003 | t0001 | g0221 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19240 | hp1 | a0004 | c0011 | t0002 | g0084 | AFR | YRI | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA19240 | hp2 | a0005 | c0035 | t0001 | g0132 | AFR | YRI | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA20129 | hp1 | a0001 | c0005 | t0001 | g0101 | AFR | ASW | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | ASW | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA20752 | hp1 | a0001 | c0009 | t0002 | g0069 | EUR | TSI | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA20752 | hp2 | a0001 | c0002 | t0003 | g0079 | EUR | TSI | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA20905 | hp1 | a0001 | c0034 | t0002 | g0157 | SAS | GIH | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA20905 | hp2 | a0001 | c0004 | t0002 | g0070 | SAS | GIH | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01123 | hp1 | a0001 | c0005 | t0001 | g0256 | AMR | CLM | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG01123 | hp2 | a0013 | c0041 | t0012 | g0174 | AMR | CLM | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02109 | hp2 | a0001 | c0006 | t0005 | g0015 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0201 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02486 | hp2 | a0001 | c0003 | t0002 | g0067 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02559 | hp1 | a0004 | c0011 | t0002 | g0097 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG02559 | hp2 | a0005 | c0021 | t0002 | g0115 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03471 | hp1 | a0001 | c0013 | t0006 | g0123 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG03471 | hp2 | a0004 | c0011 | t0001 | g0187 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG06807 | hp1 | a0001 | c0006 | t0018 | g0117 | AFR | USA | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0185 | AFR | USA | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA20300 | hp1 | a0001 | c0023 | t0001 | g0275 | AFR | USA | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA20300 | hp2 | a0001 | c0006 | t0003 | g0014 | AFR | USA | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA21309 | hp1 | a0002 | c0007 | t0007 | g0028 | AFR | LWK | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| NA21309 | hp2 | a0001 | c0032 | t0003 | g0105 | AFR | LWK | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0072 | REF | REF | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| homoSapiens_grch38 | hp1 | a0001 | c0005 | t0004 | g0207 | REF | REF | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:41684589
|
G | A | 1 | a0012 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.4492C>T | p.Arg1498Trp | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/43 | 4576/8292 | 4492/5643 | 1498/1880 | chr8 | 41684589 | ||
| chr8:41686157
|
G | A | 1 | a0013 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.4385C>T | p.Ala1462Val | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/43 | 4469/8292 | 4385/5643 | 1462/1880 | chr8 | 41686157 | ||
| chr8:41690485
|
T | C | 2 | a0002a0014 | 13 | HG01106.hp2 HG01167.hp1 HG01243.hp2 others(10): Show |
missense_variant | MODERATE | c.3973A>G | p.Met1325Val | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 32/43 | 4057/8292 | 3973/5643 | 1325/1880 | chr8 | 41690485 | ||
| chr8:41692838
|
A | G | 1 | a0011 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.3668T>C | p.Val1223Ala | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/43 | 3752/8292 | 3668/5643 | 1223/1880 | chr8 | 41692838 | ||
| chr8:41693954
|
G | A | 1 | a0008 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.3476C>T | p.Pro1159Leu | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/43 | 3560/8292 | 3476/5643 | 1159/1880 | chr8 | 41693954 | ||
| chr8:41694695
|
G | A | 2 | a0004a0007 | 10 | HG02559.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
missense_variant | MODERATE | c.3224C>T | p.Thr1075Ile | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 28/43 | 3308/8292 | 3224/5643 | 1075/1880 | chr8 | 41694695 | ||
| chr8:41696493
|
C | T | 1 | a0014 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.2830G>A | p.Ala944Thr | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/43 | 2914/8292 | 2830/5643 | 944/1880 | chr8 | 41696493 | ||
| chr8:41699467
|
G | A | 1 | a0010 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.2543C>T | p.Pro848Leu | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/43 | 2627/8292 | 2543/5643 | 848/1880 | chr8 | 41699467 | ||
| chr8:41699515
|
C | T | 2 | a0005a0007 | 4 | HG02280.hp1 HG02559.hp2 HG02895.hp1 others(1): Show |
missense_variant | MODERATE | c.2495G>A | p.Arg832Gln | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/43 | 2579/8292 | 2495/5643 | 832/1880 | chr8 | 41699515 | ||
| chr8:41704438
|
T | C | 1 | a0009 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.2132A>G | p.Tyr711Cys | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 19/43 | 2216/8292 | 2132/5643 | 711/1880 | chr8 | 41704438 | ||
| chr8:41708920
|
C | T | 2 | a0003a0008 | 11 | HG00639.hp1 HG01928.hp1 HG02818.hp2 others(8): Show |
missense_variant | MODERATE | c.1856G>A | p.Arg619His | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/43 | 1940/8292 | 1856/5643 | 619/1880 | chr8 | 41708920 | ||
| chr8:41715771
|
T | G | 1 | a0007 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.1483A>C | p.Asn495His | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 14/43 | 1567/8292 | 1483/5643 | 495/1880 | chr8 | 41715771 | ||
| chr8:41717010
|
G | GTGCCCGG others(13): Show |
1 | a0015 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.1327_1346dupATGGCA others(14): Show |
p.His449fs | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 13/43 | 1430/8292 | 1346/5643 | 449/1880 | chr8 | 41717010 | ||
| chr8:41719771
|
C | T | 1 | a0016 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.997G>A | p.Asp333Asn | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/43 | 1081/8292 | 997/5643 | 333/1880 | chr8 | 41719771 | ||
| chr8:41724473
|
C | T | 1 | a0006 | 1 | NA18986.hp1 | missense_variant | MODERATE | c.694G>A | p.Val232Ile | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/43 | 778/8292 | 694/5643 | 232/1880 | chr8 | 41724473 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:41668396
|
C | T | 14 | a0001c0004a0001c0009a0001c0016others(11): Show | 55 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(52): Show |
synonymous_variant | LOW | c.5265G>A | p.Val1755Val | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/43 | 5349/8292 | 5265/5643 | 1755/1880 | chr8 | 41668396 | ||
| chr8:41684575
|
G | A | 1 | a0013c0041 | 1 | HG01123.hp2 | synonymous_variant | LOW | c.4506C>T | p.Arg1502Arg | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/43 | 4590/8292 | 4506/5643 | 1502/1880 | chr8 | 41684575 | ||
| chr8:41690230
|
G | A | 21 | a0001c0006a0001c0010a0001c0013others(18): Show | 58 | HG01106.hp2 HG01123.hp2 HG01167.hp1 others(55): Show |
synonymous_variant | LOW | c.4101C>T | p.Ala1367Ala | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/43 | 4185/8292 | 4101/5643 | 1367/1880 | chr8 | 41690230 | ||
| chr8:41690323
|
C | T | 1 | a0001c0022 | 2 | HG00733.hp2 HG02004.hp2 |
synonymous_variant | LOW | c.4008G>A | p.Pro1336Pro | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/43 | 4092/8292 | 4008/5643 | 1336/1880 | chr8 | 41690323 | ||
| chr8:41692693
|
C | T | 2 | a0001c0037a0003c0024 | 3 | HG02717.hp1 HG02818.hp2 HG02976.hp2 |
synonymous_variant | LOW | c.3813G>A | p.Glu1271Glu | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/43 | 3897/8292 | 3813/5643 | 1271/1880 | chr8 | 41692693 | ||
| chr8:41693944
|
G | A | 6 | a0001c0013a0003c0049a0004c0011others(3): Show | 15 | HG02559.hp1 HG02572.hp2 HG02630.hp2 others(12): Show |
synonymous_variant | LOW | c.3486C>T | p.Ser1162Ser | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/43 | 3570/8292 | 3486/5643 | 1162/1880 | chr8 | 41693944 | ||
| chr8:41695253
|
G | A | 1 | a0012c0045 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.3039C>T | p.Asn1013Asn | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 27/43 | 3123/8292 | 3039/5643 | 1013/1880 | chr8 | 41695253 | ||
| chr8:41695259
|
G | A | 1 | a0001c0023 | 2 | HG01891.hp2 NA20300.hp1 |
synonymous_variant | LOW | c.3033C>T | p.Ser1011Ser | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 27/43 | 3117/8292 | 3033/5643 | 1011/1880 | chr8 | 41695259 | ||
| chr8:41695322
|
G | A | 1 | a0001c0017 | 3 | HG02572.hp1 HG03130.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.2970C>T | p.Ile990Ile | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 27/43 | 3054/8292 | 2970/5643 | 990/1880 | chr8 | 41695322 | ||
| chr8:41696410
|
C | G | 15 | a0001c0001a0001c0003a0001c0009others(12): Show | 97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
synonymous_variant | LOW | c.2913G>C | p.Leu971Leu | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/43 | 2997/8292 | 2913/5643 | 971/1880 | chr8 | 41696410 | ||
| chr8:41696563
|
G | A | 1 | a0001c0029 | 1 | NA19066.hp2 | synonymous_variant | LOW | c.2760C>T | p.Asp920Asp | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/43 | 2844/8292 | 2760/5643 | 920/1880 | chr8 | 41696563 | ||
| chr8:41698091
|
G | A | 1 | a0001c0046 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.2589C>T | p.Pro863Pro | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/43 | 2673/8292 | 2589/5643 | 863/1880 | chr8 | 41698091 | ||
| chr8:41701608
|
C | T | 1 | a0001c0051 | 1 | HG00738.hp1 | synonymous_variant | LOW | c.2403G>A | p.Lys801Lys | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/43 | 2487/8292 | 2403/5643 | 801/1880 | chr8 | 41701608 | ||
| chr8:41702091
|
G | A | 6 | a0001c0003a0001c0009a0001c0018others(3): Show | 40 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(37): Show |
synonymous_variant | LOW | c.2349C>T | p.Thr783Thr | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 21/43 | 2433/8292 | 2349/5643 | 783/1880 | chr8 | 41702091 | ||
| chr8:41704125
|
G | C | 2 | a0001c0010a0004c0011 | 11 | HG02071.hp2 HG02074.hp2 HG02080.hp1 others(8): Show |
synonymous_variant | LOW | c.2211C>G | p.Pro737Pro | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/43 | 2295/8292 | 2211/5643 | 737/1880 | chr8 | 41704125 | ||
| chr8:41706167
|
G | A | 6 | a0001c0003a0001c0009a0001c0018others(3): Show | 40 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(37): Show |
synonymous_variant | LOW | c.2073C>T | p.Gly691Gly | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/43 | 2157/8292 | 2073/5643 | 691/1880 | chr8 | 41706167 | ||
| chr8:41708808
|
C | T | 1 | a0001c0054 | 1 | HG00741.hp1 | synonymous_variant | LOW | c.1968G>A | p.Ser656Ser | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/43 | 2052/8292 | 1968/5643 | 656/1880 | chr8 | 41708808 | ||
| chr8:41714174
|
G | T | 1 | a0001c0034 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.1782C>A | p.Ser594Ser | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/43 | 1866/8292 | 1782/5643 | 594/1880 | chr8 | 41714174 | ||
| chr8:41715787
|
C | T | 1 | a0007c0033 | 1 | HG02895.hp1 | synonymous_variant | LOW | c.1467G>A | p.Leu489Leu | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 14/43 | 1551/8292 | 1467/5643 | 489/1880 | chr8 | 41715787 | ||
| chr8:41717037
|
C | T | 2 | a0001c0013a0001c0032 | 5 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(2): Show |
synonymous_variant | LOW | c.1320G>A | p.Pro440Pro | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 13/43 | 1404/8292 | 1320/5643 | 440/1880 | chr8 | 41717037 | ||
| chr8:41724492
|
G | A | 1 | a0001c0026 | 2 | HG00438.hp1 NA19057.hp1 |
synonymous_variant | LOW | c.675C>T | p.Leu225Leu | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/43 | 759/8292 | 675/5643 | 225/1880 | chr8 | 41724492 | ||
| chr8:41725776
|
C | T | 6 | a0001c0004a0001c0008a0001c0028others(3): Show | 35 | HG00423.hp2 HG00438.hp2 HG01069.hp1 others(32): Show |
synonymous_variant | LOW | c.597G>A | p.Pro199Pro | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/43 | 681/8292 | 597/5643 | 199/1880 | chr8 | 41725776 | ||
| chr8:41725884
|
G | A | 1 | a0003c0024 | 2 | HG02818.hp2 HG02976.hp2 |
synonymous_variant | LOW | c.489C>T | p.Leu163Leu | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/43 | 573/8292 | 489/5643 | 163/1880 | chr8 | 41725884 | ||
| chr8:41725923
|
T | C | 5 | a0001c0051a0001c0052a0003c0014others(2): Show | 8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
synonymous_variant | LOW | c.450A>G | p.Val150Val | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/43 | 534/8292 | 450/5643 | 150/1880 | chr8 | 41725923 | ||
| chr8:41727920
|
G | A | 13 | a0001c0002a0001c0012a0001c0019others(10): Show | 67 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(64): Show |
synonymous_variant | LOW | c.315C>T | p.Asn105Asn | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 4/43 | 399/8292 | 315/5643 | 105/1880 | chr8 | 41727920 | ||
| chr8:41727998
|
G | A | 1 | a0001c0058 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.237C>T | p.Asn79Asn | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 4/43 | 321/8292 | 237/5643 | 79/1880 | chr8 | 41727998 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:41653618
|
G | T | 1 | a0001c0005t0020 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2172C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 7848 | chr8 | 41653618 | |||||
| chr8:41653638
|
A | C | 94 | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(91): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*2152T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 7828 | chr8 | 41653638 | |||||
| chr8:41653667
|
C | A | 2 | a0001c0001t0013a0001c0005t0013 | 2 | HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2123G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 7799 | chr8 | 41653667 | |||||
| chr8:41653768
|
C | T | 2 | a0002c0007t0007a0002c0042t0016 | 5 | HG01167.hp1 HG01243.hp2 HG02258.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2022G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 7698 | chr8 | 41653768 | |||||
| chr8:41653891
|
C | T | 6 | a0001c0005t0010a0001c0025t0011a0001c0030t0017others(3): Show | 10 | HG01167.hp1 HG01243.hp2 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1899G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 7575 | chr8 | 41653891 | |||||
| chr8:41654122
|
C | T | 1 | a0001c0004t0024 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1668G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 7344 | chr8 | 41654122 | |||||
| chr8:41654123
|
A | T | 1 | a0001c0001t0023 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1667T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 7343 | chr8 | 41654123 | |||||
| chr8:41654181
|
G | C | 6 | a0001c0005t0010a0001c0025t0011a0001c0030t0017others(3): Show | 10 | HG01167.hp1 HG01243.hp2 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1609C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 7285 | chr8 | 41654181 | |||||
| chr8:41654388
|
C | A | 1 | a0001c0018t0026 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1402G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 7078 | chr8 | 41654388 | |||||
| chr8:41654933
|
G | T | 1 | a0001c0003t0019 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*857C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6533 | chr8 | 41654933 | |||||
| chr8:41654969
|
G | A | 1 | a0002c0007t0021 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*821C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6497 | chr8 | 41654969 | |||||
| chr8:41655016
|
T | C | 3 | a0001c0012t0006a0001c0013t0006a0014c0055t0006 | 5 | HG01106.hp2 HG02622.hp1 HG03098.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*774A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6450 | chr8 | 41655016 | |||||
| chr8:41655026
|
CAGAG | C | 5 | a0001c0006t0005a0001c0006t0018a0001c0012t0005others(2): Show | 7 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*760_*763delCTCT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6436 | chr8 | 41655026 | |||||
| chr8:41655062
|
CACAGCAG others(7): Show |
C | 60 | a0001c0001t0001a0001c0001t0013a0001c0002t0001others(57): Show | 156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*714_*727delATAGAC others(8): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6390 | chr8 | 41655062 | |||||
| chr8:41655129
|
G | GGT | 4 | a0001c0025t0011a0001c0030t0017a0002c0007t0007others(1): Show | 8 | HG01167.hp1 HG01243.hp2 HG02258.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*659_*660dupAC | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6336 | chr8 | 41655129 | |||||
| chr8:41655129
|
G | GGTGT | 42 | a0001c0001t0001a0001c0001t0013a0001c0002t0001others(39): Show | 125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*657_*660dupACAC | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6336 | chr8 | 41655129 | |||||
| chr8:41655129
|
G | GGTGTGT | 3 | a0001c0002t0012a0001c0006t0018a0013c0041t0012 | 3 | HG01123.hp2 HG01261.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*655_*660dupACACAC | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6336 | chr8 | 41655129 | |||||
| chr8:41655129
|
GGT | G | 40 | a0001c0001t0002a0001c0001t0023a0001c0002t0002others(37): Show | 126 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*659_*660delAC | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6335 | chr8 | 41655129 | |||||
| chr8:41655171
|
G | A | 1 | a0002c0042t0016 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*619C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6295 | chr8 | 41655171 | |||||
| chr8:41655305
|
C | CT | 48 | a0001c0001t0001a0001c0001t0013a0001c0002t0001others(45): Show | 136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*484dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6160 | chr8 | 41655305 | |||||
| chr8:41655305
|
CT | C | 13 | a0001c0002t0003a0001c0005t0003a0001c0006t0003others(10): Show | 23 | HG01517.hp2 HG02074.hp1 HG02074.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*484delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6160 | chr8 | 41655305 | |||||
| chr8:41655358
|
T | C | 1 | a0002c0007t0027 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*432A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6108 | chr8 | 41655358 | |||||
| chr8:41655404
|
AC | A | 6 | a0001c0005t0010a0001c0025t0011a0001c0030t0017others(3): Show | 10 | HG01167.hp1 HG01243.hp2 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*385delG | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6061 | chr8 | 41655404 | |||||
| chr8:41655552
|
A | G | 6 | a0001c0005t0010a0001c0025t0011a0001c0030t0017others(3): Show | 10 | HG01167.hp1 HG01243.hp2 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*238T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 5914 | chr8 | 41655552 | |||||
| chr8:41655674
|
G | A | 2 | a0001c0005t0028a0001c0005t0029 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*116C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 5792 | chr8 | 41655674 | |||||
| chr8:41797603
|
G | A | 1 | a0001c0046t0030 | 1 | HG02723.hp2 | 5_prime_UTR_variant | MODIFIER | c.-65C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/43 | 65 | chr8 | 41797603 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:41655932
|
G | A | 1 | a0001c0018t0026g0113 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.*37-179C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41655932 | ||||||
| chr8:41655934
|
C | T | 17 | a0001c0002t0003g0079a0001c0002t0003g0080a0001c0002t0003g0146others(14): Show | 17 | HG02074.hp1 HG02280.hp2 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.*37-181G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41655934 | ||||||
| chr8:41656012
|
T | C | 165 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(162): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.*37-259A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41656012 | ||||||
| chr8:41656020
|
T | C | 9 | a0001c0005t0010g0019a0001c0025t0011g0001a0001c0030t0017g0051others(6): Show | 10 | HG01167.hp1 HG01243.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.*37-267A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41656020 | ||||||
| chr8:41656100
|
C | T | 2 | a0001c0037t0003g0233a0003c0024t0003g0102 | 2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.*37-347G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41656100 | ||||||
| chr8:41656277
|
G | C | 10 | a0001c0002t0009g0098a0001c0005t0010g0019a0001c0025t0011g0001others(7): Show | 11 | HG01167.hp1 HG01243.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.*37-524C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41656277 | ||||||
| chr8:41656290
|
T | C | 165 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(162): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.*37-537A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41656290 | ||||||
| chr8:41656532
|
C | A | 2 | a0001c0001t0002g0151a0001c0001t0002g0152 | 2 | HG01952.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.*37-779G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41656532 | ||||||
| chr8:41656596
|
C | T | 1 | a0001c0016t0002g0007 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.*37-843G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41656596 | ||||||
| chr8:41656646
|
G | A | 1 | a0001c0006t0001g0267 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.*37-893C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41656646 | ||||||
| chr8:41656721
|
G | A | 1 | a0009c0047t0002g0016 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.*37-968C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41656721 | ||||||
| chr8:41656743
|
A | G | 1 | a0012c0045t0025g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.*37-990T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41656743 | ||||||
| chr8:41656778
|
G | C | 45 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0162others(42): Show | 45 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.*37-1025C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41656778 | ||||||
| chr8:41657239
|
G | A | 9 | a0001c0005t0010g0019a0001c0025t0011g0001a0001c0030t0017g0051others(6): Show | 10 | HG01167.hp1 HG01243.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.*37-1486C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41657239 | ||||||
| chr8:41657369
|
G | A | 166 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(163): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.*37-1616C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41657369 | ||||||
| chr8:41657380
|
A | G | 1 | a0001c0018t0026g0113 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.*37-1627T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41657380 | ||||||
| chr8:41657496
|
T | G | 18 | a0001c0001t0013g0091a0001c0002t0009g0098a0001c0005t0010g0019others(15): Show | 19 | HG01070.hp2 HG01071.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.*37-1743A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41657496 | ||||||
| chr8:41657571
|
C | A | 1 | a0001c0010t0003g0236 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.*37-1818G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41657571 | ||||||
| chr8:41657611
|
A | G | 165 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(162): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.*37-1858T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41657611 | ||||||
| chr8:41657769
|
G | C | 1 | a0001c0001t0001g0245 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.*37-2016C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41657769 | ||||||
| chr8:41658012
|
A | G | 165 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(162): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.*37-2259T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658012 | ||||||
| chr8:41658106
|
A | G | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG00140.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.*37-2353T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658106 | ||||||
| chr8:41658263
|
C | T | 1 | a0001c0006t0003g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.*37-2510G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658263 | ||||||
| chr8:41658298
|
G | A | 21 | a0001c0002t0003g0079a0001c0002t0003g0080a0001c0002t0003g0146others(18): Show | 21 | HG02074.hp1 HG02074.hp2 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.*37-2545C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658298 | ||||||
| chr8:41658427
|
C | T | 4 | a0001c0010t0003g0002a0001c0010t0003g0114a0001c0010t0003g0189others(1): Show | 4 | HG02074.hp2 HG02080.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.*37-2674G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658427 | ||||||
| chr8:41658474
|
G | A | 164 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(161): Show | 165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.*37-2721C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658474 | ||||||
| chr8:41658662
|
G | A | 1 | a0001c0002t0001g0202 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.*36+2768C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658662 | ||||||
| chr8:41658750
|
A | C | 3 | a0002c0007t0027g0035a0004c0011t0001g0186a0004c0011t0001g0187 | 3 | HG02809.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.*36+2680T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658750 | ||||||
| chr8:41658845
|
A | G | 2 | a0001c0037t0003g0233a0003c0024t0003g0102 | 2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.*36+2585T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658845 | ||||||
| chr8:41658897
|
T | TATAA | 76 | a0001c0001t0001g0148a0001c0001t0001g0162a0001c0001t0001g0191others(73): Show | 76 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.*36+2529_*36+2532d others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658897 | ||||||
| chr8:41658897
|
T | TATAAATA others(1): Show |
4 | a0001c0001t0002g0009a0001c0002t0001g0048a0001c0004t0002g0154others(1): Show | 4 | HG02083.hp1 HG02683.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.*36+2525_*36+2532d others(10): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658897 | ||||||
| chr8:41658897
|
TATAA | T | 20 | a0001c0001t0002g0151a0001c0002t0001g0183a0001c0002t0001g0265others(17): Show | 20 | HG00735.hp2 HG02074.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.*36+2529_*36+2532d others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658897 | ||||||
| chr8:41658897
|
TATAAATA others(5): Show |
T | 8 | a0001c0001t0002g0020a0001c0001t0002g0077a0001c0001t0002g0234others(5): Show | 8 | HG02258.hp2 HG02559.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.*36+2521_*36+2532d others(14): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658897 | ||||||
| chr8:41658897
|
TATAAATA others(9): Show |
T | 86 | a0001c0001t0001g0160a0001c0001t0001g0214a0001c0001t0001g0226others(83): Show | 87 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.*36+2517_*36+2532d others(18): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658897 | ||||||
| chr8:41658911
|
TAAATAAA others(4): Show |
T | 1 | a0001c0003t0001g0058 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.*36+2508_*36+2518d others(13): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658911 | ||||||
| chr8:41658966
|
T | C | 88 | a0001c0001t0001g0160a0001c0001t0001g0214a0001c0001t0001g0226others(85): Show | 89 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.*36+2464A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658966 | ||||||
| chr8:41658970
|
C | T | 2 | a0001c0019t0002g0145a0015c0053t0002g0263 | 2 | NA18960.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.*36+2460G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658970 | ||||||
| chr8:41659062
|
A | G | 183 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(180): Show | 184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.*36+2368T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659062 | ||||||
| chr8:41659065
|
C | T | 1 | a0001c0002t0012g0022 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.*36+2365G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659065 | ||||||
| chr8:41659081
|
C | T | 3 | a0001c0008t0002g0194a0001c0008t0015g0196a0005c0021t0002g0115 | 3 | HG01515.hp1 HG01517.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.*36+2349G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659081 | ||||||
| chr8:41659134
|
G | A | 1 | a0001c0005t0010g0019 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.*36+2296C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659134 | ||||||
| chr8:41659154
|
G | C | 2 | a0001c0001t0002g0151a0001c0001t0002g0152 | 2 | HG01952.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.*36+2276C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659154 | ||||||
| chr8:41659184
|
T | G | 1 | a0001c0003t0001g0139 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.*36+2246A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659184 | ||||||
| chr8:41659221
|
C | T | 6 | a0001c0006t0005g0015a0001c0006t0018g0117a0001c0012t0005g0103others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.*36+2209G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659221 | ||||||
| chr8:41659271
|
A | G | 60 | a0001c0001t0002g0009a0001c0001t0002g0024a0001c0001t0002g0063others(57): Show | 60 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.*36+2159T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659271 | ||||||
| chr8:41659376
|
G | T | 276 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(273): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.*36+2054C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659376 | ||||||
| chr8:41659396
|
C | T | 105 | a0001c0001t0001g0148a0001c0001t0001g0162a0001c0001t0001g0191others(102): Show | 106 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(103): Show |
intron_variant | MODIFIER | c.*36+2034G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659396 | ||||||
| chr8:41659422
|
G | A | 1 | a0002c0007t0027g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.*36+2008C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659422 | ||||||
| chr8:41659468
|
T | C | 23 | a0001c0003t0001g0158a0001c0004t0001g0159a0001c0005t0001g0101others(20): Show | 23 | HG01167.hp1 HG01891.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.*36+1962A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659468 | ||||||
| chr8:41659472
|
G | A | 64 | a0001c0001t0001g0155a0001c0001t0001g0223a0001c0001t0002g0009others(61): Show | 64 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.*36+1958C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659472 | ||||||
| chr8:41659539
|
T | C | 1 | a0001c0037t0003g0233 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.*36+1891A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659539 | ||||||
| chr8:41659545
|
T | C | 14 | a0001c0001t0002g0020a0001c0002t0009g0098a0001c0005t0002g0010others(11): Show | 14 | HG00738.hp1 HG01106.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.*36+1885A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659545 | ||||||
| chr8:41659576
|
C | T | 1 | a0002c0007t0007g0023 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.*36+1854G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659576 | ||||||
| chr8:41659667
|
G | A | 2 | a0003c0014t0008g0094a0003c0014t0008g0095 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.*36+1763C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659667 | ||||||
| chr8:41659813
|
G | A | 1 | a0003c0014t0008g0203 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.*36+1617C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659813 | ||||||
| chr8:41660155
|
C | G | 1 | a0001c0004t0002g0243 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.*36+1275G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41660155 | ||||||
| chr8:41660341
|
G | A | 72 | a0001c0001t0002g0009a0001c0001t0002g0020a0001c0001t0002g0024others(69): Show | 72 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.*36+1089C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41660341 | ||||||
| chr8:41660342
|
G | T | 3 | a0001c0002t0001g0166a0001c0002t0001g0173a0001c0002t0001g0178 | 3 | NA18972.hp2 NA18986.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.*36+1088C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41660342 | ||||||
| chr8:41660437
|
C | T | 2 | a0001c0001t0013g0091a0001c0005t0013g0004 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.*36+993G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41660437 | ||||||
| chr8:41660463
|
G | A | 1 | a0001c0005t0003g0032 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.*36+967C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41660463 | ||||||
| chr8:41660586
|
G | A | 1 | a0001c0003t0002g0199 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.*36+844C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41660586 | ||||||
| chr8:41660690
|
C | T | 4 | a0001c0010t0003g0002a0001c0010t0003g0114a0001c0010t0003g0189others(1): Show | 4 | HG02074.hp2 HG02080.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.*36+740G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41660690 | ||||||
| chr8:41661062
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.*36+368C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41661062 | ||||||
| chr8:41661137
|
A | T | 1 | a0001c0003t0001g0221 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.*36+293T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41661137 | ||||||
| chr8:41661197
|
C | T | 19 | a0001c0004t0001g0109a0001c0005t0001g0101a0001c0006t0001g0100others(16): Show | 19 | HG01891.hp2 HG02109.hp2 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.*36+233G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41661197 | ||||||
| chr8:41661307
|
C | T | 1 | a0001c0008t0002g0198 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.*36+123G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41661307 | ||||||
| chr8:41661354
|
G | C | 42 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0162others(39): Show | 42 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.*36+76C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41661354 | ||||||
| chr8:41661725
|
T | G | 1 | a0001c0003t0001g0062 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.5544+151A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 41/42 | chr8 | 41661725 | ||||||
| chr8:41661730
|
T | C | 219 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.5544+146A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 41/42 | chr8 | 41661730 | ||||||
| chr8:41661731
|
G | A | 3 | a0001c0002t0009g0098a0001c0005t0010g0019a0009c0047t0002g0016 | 3 | HG02965.hp1 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.5544+145C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 41/42 | chr8 | 41661731 | ||||||
| chr8:41661797
|
G | A | 2 | a0001c0005t0028g0112a0001c0005t0029g0111 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.5544+79C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 41/42 | chr8 | 41661797 | ||||||
| chr8:41661830
|
C | T | 2 | a0001c0037t0003g0233a0003c0024t0003g0102 | 2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.5544+46G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 41/42 | chr8 | 41661830 | ||||||
| chr8:41661944
|
A | G | 213 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
splice_region_variant&intron_variant | LOW | c.5479-3T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41661944 | ||||||
| chr8:41661986
|
C | T | 4 | a0001c0010t0003g0002a0001c0010t0003g0114a0001c0010t0003g0189others(1): Show | 4 | HG02074.hp2 HG02080.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.5479-45G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41661986 | ||||||
| chr8:41662033
|
G | A | 3 | a0001c0002t0009g0098a0001c0005t0010g0019a0009c0047t0002g0016 | 3 | HG02965.hp1 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.5479-92C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41662033 | ||||||
| chr8:41662118
|
G | A | 2 | a0001c0002t0001g0128a0001c0002t0014g0129 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.5479-177C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41662118 | ||||||
| chr8:41662242
|
G | C | 1 | a0001c0002t0009g0098 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.5479-301C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41662242 | ||||||
| chr8:41662256
|
C | CA | 69 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0162others(66): Show | 69 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.5479-316dupT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41662256 | ||||||
| chr8:41662426
|
T | C | 42 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0162others(39): Show | 42 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.5479-485A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41662426 | ||||||
| chr8:41662490
|
C | G | 1 | a0001c0001t0002g0075 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.5479-549G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41662490 | ||||||
| chr8:41662494
|
C | G | 1 | a0001c0001t0002g0088 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5479-553G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41662494 | ||||||
| chr8:41662553
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.5479-612G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41662553 | ||||||
| chr8:41662746
|
G | A | 3 | a0001c0002t0009g0098a0001c0005t0010g0019a0009c0047t0002g0016 | 3 | HG02965.hp1 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.5479-805C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41662746 | ||||||
| chr8:41662775
|
G | A | 1 | a0003c0014t0002g0209 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5479-834C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41662775 | ||||||
| chr8:41663098
|
G | C | 3 | a0001c0002t0009g0098a0001c0005t0010g0019a0009c0047t0002g0016 | 3 | HG02965.hp1 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.5478+561C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663098 | ||||||
| chr8:41663098
|
G | GTCTC | 7 | a0001c0006t0001g0017a0001c0006t0001g0039a0001c0006t0001g0264others(4): Show | 7 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.5478+557_5478+560d others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663098 | ||||||
| chr8:41663098
|
G | GTCTCTC | 73 | a0001c0001t0002g0009a0001c0001t0002g0020a0001c0001t0002g0024others(70): Show | 73 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.5478+555_5478+560d others(8): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663098 | ||||||
| chr8:41663098
|
G | GTCTCTCT others(1): Show |
3 | a0001c0003t0001g0058a0001c0037t0003g0233a0003c0024t0001g0273 | 3 | HG02717.hp1 HG02976.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.5478+553_5478+560d others(10): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663098 | ||||||
| chr8:41663100
|
C | G | 13 | a0001c0005t0001g0101a0001c0006t0001g0100a0001c0013t0006g0123others(10): Show | 13 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.5478+559G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663100 | ||||||
| chr8:41663110
|
C | CTGTGTGT others(1): Show |
3 | a0001c0002t0009g0098a0001c0005t0010g0019a0009c0047t0002g0016 | 3 | HG02965.hp1 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.5478+548_5478+549i others(10): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663110 | ||||||
| chr8:41663112
|
C | CTGTGTGT others(1): Show |
8 | a0001c0006t0003g0005a0001c0006t0003g0013a0001c0006t0003g0014others(5): Show | 8 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.5478+546_5478+547i others(10): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663112 | ||||||
| chr8:41663112
|
C | CTGTGTGT others(3): Show |
1 | a0001c0006t0018g0117 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5478+546_5478+547i others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663112 | ||||||
| chr8:41663112
|
C | G | 3 | a0001c0002t0009g0098a0001c0005t0010g0019a0009c0047t0002g0016 | 3 | HG02965.hp1 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.5478+547G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663112 | ||||||
| chr8:41663114
|
C | CTCTCTCT others(3): Show |
1 | a0003c0024t0003g0102 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.5478+544_5478+545i others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663114 | ||||||
| chr8:41663114
|
C | CTCTCTG | 47 | a0001c0001t0001g0160a0001c0001t0001g0214a0001c0001t0001g0226others(44): Show | 47 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.5478+544_5478+545i others(8): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663114 | ||||||
| chr8:41663114
|
C | CTCTCTGT others(1): Show |
3 | a0001c0001t0001g0245a0001c0003t0001g0261a0001c0003t0014g0065 | 3 | HG03017.hp1 NA18973.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.5478+544_5478+545i others(10): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663114 | ||||||
| chr8:41663114
|
C | CTCTCTGT others(3): Show |
1 | a0001c0005t0001g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.5478+544_5478+545i others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663114 | ||||||
| chr8:41663114
|
C | CTCTGTG | 7 | a0001c0001t0001g0242a0004c0011t0001g0186a0004c0011t0001g0187others(4): Show | 7 | HG02015.hp1 HG02572.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.5478+544_5478+545i others(8): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663114 | ||||||
| chr8:41663114
|
C | CTCTGTGT others(3): Show |
3 | a0001c0013t0006g0123a0001c0013t0006g0124a0012c0045t0025g0188 | 3 | HG03098.hp1 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.5478+544_5478+545i others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663114 | ||||||
| chr8:41663114
|
C | CTCTGTGT others(5): Show |
1 | a0001c0006t0001g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5478+544_5478+545i others(14): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663114 | ||||||
| chr8:41663114
|
C | CTG | 10 | a0002c0007t0001g0038a0002c0007t0001g0040a0002c0007t0007g0021others(7): Show | 10 | HG01167.hp1 HG01243.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.5478+543_5478+544d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663114 | ||||||
| chr8:41663114
|
C | CTGTG | 42 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0162others(39): Show | 42 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.5478+541_5478+544d others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663114 | ||||||
| chr8:41663114
|
C | CTGTGTGT others(3): Show |
4 | a0001c0018t0026g0113a0001c0023t0001g0275a0001c0023t0001g0276others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.5478+535_5478+544d others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663114 | ||||||
| chr8:41663114
|
C | G | 19 | a0001c0002t0001g0184a0001c0002t0009g0098a0001c0004t0002g0070others(16): Show | 19 | HG01192.hp2 HG01258.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.5478+545G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663114 | ||||||
| chr8:41663114
|
CTG | C | 2 | a0001c0025t0011g0001a0001c0030t0017g0051 | 3 | HG03491.hp2 HG03492.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.5478+543_5478+544d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663114 | ||||||
| chr8:41663116
|
G | C | 7 | a0001c0006t0001g0017a0001c0006t0001g0039a0001c0006t0001g0264others(4): Show | 7 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.5478+543C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663116 | ||||||
| chr8:41663142
|
A | G | 3 | a0002c0007t0001g0038a0002c0007t0001g0040a0002c0007t0027g0035 | 3 | HG02886.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.5478+517T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663142 | ||||||
| chr8:41663156
|
T | A | 2 | a0001c0003t0001g0169a0001c0003t0001g0237 | 2 | HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.5478+503A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663156 | ||||||
| chr8:41663435
|
C | T | 1 | a0001c0005t0010g0019 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5478+224G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663435 | ||||||
| chr8:41663842
|
A | G | 1 | a0001c0002t0002g0227 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5395-100T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41663842 | ||||||
| chr8:41663951
|
C | G | 137 | a0001c0001t0001g0160a0001c0001t0001g0214a0001c0001t0001g0226others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.5395-209G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41663951 | ||||||
| chr8:41663955
|
C | T | 6 | a0001c0005t0001g0101a0001c0006t0001g0100a0001c0013t0006g0123others(3): Show | 6 | HG02630.hp1 HG03098.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.5395-213G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41663955 | ||||||
| chr8:41663956
|
G | A | 1 | a0001c0005t0002g0010 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.5395-214C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41663956 | ||||||
| chr8:41664145
|
T | C | 140 | a0001c0001t0001g0160a0001c0001t0001g0214a0001c0001t0001g0226others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.5395-403A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41664145 | ||||||
| chr8:41664165
|
G | A | 2 | a0001c0001t0013g0091a0001c0005t0013g0004 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.5395-423C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41664165 | ||||||
| chr8:41664195
|
C | T | 1 | a0014c0055t0006g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.5395-453G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41664195 | ||||||
| chr8:41664244
|
G | C | 3 | a0001c0003t0001g0060a0001c0003t0001g0062a0001c0003t0001g0073 | 3 | HG00099.hp2 HG01255.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.5395-502C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41664244 | ||||||
| chr8:41664424
|
A | G | 42 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0162others(39): Show | 42 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.5395-682T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41664424 | ||||||
| chr8:41664462
|
T | G | 1 | a0001c0005t0010g0019 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5395-720A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41664462 | ||||||
| chr8:41664498
|
AAAGAG | A | 40 | a0001c0004t0001g0109a0001c0004t0001g0159a0001c0004t0002g0066others(37): Show | 40 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.5395-761_5395-757d others(7): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41664498 | ||||||
| chr8:41664672
|
C | T | 9 | a0001c0006t0003g0005a0001c0006t0003g0013a0001c0006t0003g0014others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.5395-930G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41664672 | ||||||
| chr8:41664687
|
T | G | 2 | a0001c0013t0006g0123a0001c0013t0006g0124 | 2 | HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.5395-945A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41664687 | ||||||
| chr8:41664694
|
C | G | 2 | a0001c0001t0001g0162a0001c0001t0001g0191 | 2 | NA18948.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.5395-952G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41664694 | ||||||
| chr8:41664698
|
C | T | 1 | a0001c0003t0001g0158 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.5395-956G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41664698 | ||||||
| chr8:41664708
|
C | G | 1 | a0001c0046t0030g0277 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5395-966G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41664708 | ||||||
| chr8:41664889
|
G | C | 9 | a0001c0006t0003g0005a0001c0006t0003g0013a0001c0006t0003g0014others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.5395-1147C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41664889 | ||||||
| chr8:41665028
|
G | A | 4 | a0001c0010t0003g0002a0001c0010t0003g0114a0001c0010t0003g0189others(1): Show | 4 | HG02074.hp2 HG02080.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.5395-1286C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41665028 | ||||||
| chr8:41665231
|
G | A | 9 | a0001c0006t0003g0005a0001c0006t0003g0013a0001c0006t0003g0014others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.5395-1489C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41665231 | ||||||
| chr8:41665322
|
T | C | 1 | a0001c0026t0001g0167 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5395-1580A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41665322 | ||||||
| chr8:41665325
|
C | T | 4 | a0001c0010t0003g0002a0001c0010t0003g0114a0001c0010t0003g0189others(1): Show | 4 | HG02074.hp2 HG02080.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.5395-1583G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41665325 | ||||||
| chr8:41665342
|
G | T | 2 | a0001c0002t0001g0144a0001c0002t0001g0181 | 2 | HG00741.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.5395-1600C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41665342 | ||||||
| chr8:41665473
|
A | G | 214 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.5395-1731T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41665473 | ||||||
| chr8:41665562
|
A | G | 1 | a0001c0003t0001g0140 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.5395-1820T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41665562 | ||||||
| chr8:41665610
|
G | A | 3 | a0001c0004t0001g0159a0001c0004t0002g0070a0001c0004t0002g0154 | 3 | HG02683.hp2 HG03710.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.5395-1868C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41665610 | ||||||
| chr8:41665645
|
C | A | 42 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0162others(39): Show | 42 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.5395-1903G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41665645 | ||||||
| chr8:41665816
|
C | T | 2 | a0001c0023t0001g0275a0001c0023t0001g0276 | 2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.5395-2074G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41665816 | ||||||
| chr8:41665840
|
A | G | 53 | a0001c0004t0001g0109a0001c0004t0001g0159a0001c0004t0002g0066others(50): Show | 54 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.5395-2098T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41665840 | ||||||
| chr8:41665918
|
C | T | 2 | a0001c0018t0026g0113a0002c0057t0005g0269 | 2 | HG01891.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.5395-2176G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41665918 | ||||||
| chr8:41666149
|
C | T | 2 | a0001c0001t0002g0216a0006c0031t0002g0255 | 2 | NA18986.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.5394+2118G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41666149 | ||||||
| chr8:41666150
|
G | A | 1 | a0001c0002t0001g0181 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5394+2117C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41666150 | ||||||
| chr8:41666170
|
C | T | 2 | a0001c0001t0002g0216a0006c0031t0002g0255 | 2 | NA18986.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.5394+2097G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41666170 | ||||||
| chr8:41666227
|
G | A | 57 | a0001c0002t0009g0098a0001c0004t0001g0109a0001c0004t0001g0159others(54): Show | 58 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.5394+2040C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41666227 | ||||||
| chr8:41666241
|
CT | C | 54 | a0001c0004t0001g0109a0001c0004t0001g0159a0001c0004t0002g0066others(51): Show | 55 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.5394+2025delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41666241 | ||||||
| chr8:41666257
|
G | A | 5 | a0001c0010t0003g0270a0001c0028t0003g0053a0003c0015t0003g0137others(2): Show | 5 | HG02074.hp1 NA18950.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.5394+2010C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41666257 | ||||||
| chr8:41666323
|
G | A | 3 | a0001c0002t0009g0098a0001c0005t0010g0019a0009c0047t0002g0016 | 3 | HG02965.hp1 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.5394+1944C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41666323 | ||||||
| chr8:41666769
|
A | G | 194 | a0001c0001t0001g0160a0001c0001t0001g0214a0001c0001t0001g0226others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.5394+1498T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41666769 | ||||||
| chr8:41666872
|
G | A | 1 | a0001c0004t0002g0271 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5394+1395C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41666872 | ||||||
| chr8:41666907
|
A | G | 54 | a0001c0004t0001g0109a0001c0004t0001g0159a0001c0004t0002g0066others(51): Show | 55 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.5394+1360T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41666907 | ||||||
| chr8:41666965
|
T | G | 2 | a0001c0018t0026g0113a0002c0057t0005g0269 | 2 | HG01891.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.5394+1302A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41666965 | ||||||
| chr8:41666987
|
A | G | 54 | a0001c0004t0001g0109a0001c0004t0001g0159a0001c0004t0002g0066others(51): Show | 55 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.5394+1280T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41666987 | ||||||
| chr8:41667018
|
C | T | 5 | a0001c0010t0003g0270a0001c0028t0003g0053a0003c0015t0003g0137others(2): Show | 5 | HG02074.hp1 NA18950.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.5394+1249G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41667018 | ||||||
| chr8:41667170
|
C | T | 53 | a0001c0004t0001g0109a0001c0004t0001g0159a0001c0004t0002g0066others(50): Show | 54 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.5394+1097G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41667170 | ||||||
| chr8:41667171
|
G | A | 5 | a0001c0010t0003g0270a0001c0028t0003g0053a0003c0015t0003g0137others(2): Show | 5 | HG02074.hp1 NA18950.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.5394+1096C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41667171 | ||||||
| chr8:41667290
|
G | C | 194 | a0001c0001t0001g0160a0001c0001t0001g0214a0001c0001t0001g0226others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.5394+977C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41667290 | ||||||
| chr8:41667332
|
A | T | 1 | a0001c0003t0002g0163 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.5394+935T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41667332 | ||||||
| chr8:41667381
|
A | G | 54 | a0001c0004t0001g0109a0001c0004t0001g0159a0001c0004t0002g0066others(51): Show | 55 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.5394+886T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41667381 | ||||||
| chr8:41667659
|
C | T | 5 | a0001c0001t0002g0024a0001c0001t0002g0125a0001c0012t0005g0103others(2): Show | 5 | HG02109.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.5394+608G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41667659 | ||||||
| chr8:41667825
|
G | A | 3 | a0002c0007t0001g0038a0002c0007t0001g0040a0002c0007t0027g0035 | 3 | HG02886.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.5394+442C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41667825 | ||||||
| chr8:41667838
|
G | A | 42 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0162others(39): Show | 42 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.5394+429C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41667838 | ||||||
| chr8:41667866
|
G | A | 4 | a0001c0010t0003g0002a0001c0010t0003g0114a0001c0010t0003g0189others(1): Show | 4 | HG02074.hp2 HG02080.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.5394+401C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41667866 | ||||||
| chr8:41667869
|
A | T | 137 | a0001c0001t0001g0160a0001c0001t0001g0214a0001c0001t0001g0226others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.5394+398T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41667869 | ||||||
| chr8:41667982
|
G | C | 192 | a0001c0001t0001g0160a0001c0001t0001g0214a0001c0001t0001g0226others(189): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.5394+285C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41667982 | ||||||
| chr8:41668070
|
C | T | 77 | a0001c0001t0002g0009a0001c0001t0002g0020a0001c0001t0002g0024others(74): Show | 77 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.5394+197G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41668070 | ||||||
| chr8:41668121
|
T | C | 1 | a0001c0004t0002g0211 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.5394+146A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41668121 | ||||||
| chr8:41668245
|
G | A | 10 | a0001c0003t0001g0158a0001c0006t0003g0005a0001c0006t0003g0013others(7): Show | 10 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.5394+22C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41668245 | ||||||
| chr8:41668246
|
C | T | 1 | a0001c0012t0005g0103 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.5394+21G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41668246 | ||||||
| chr8:41668256
|
C | T | 1 | a0001c0001t0002g0110 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.5394+11G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41668256 | ||||||
| chr8:41668711
|
G | T | 42 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0162others(39): Show | 42 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.5097-147C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41668711 | ||||||
| chr8:41668880
|
G | C | 9 | a0001c0006t0003g0005a0001c0006t0003g0013a0001c0006t0003g0014others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.5097-316C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41668880 | ||||||
| chr8:41669009
|
G | A | 135 | a0001c0001t0001g0160a0001c0001t0001g0214a0001c0001t0001g0226others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.5097-445C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41669009 | ||||||
| chr8:41669057
|
C | T | 1 | a0001c0001t0002g0088 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5097-493G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41669057 | ||||||
| chr8:41669058
|
G | A | 1 | a0001c0004t0002g0126 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.5097-494C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41669058 | ||||||
| chr8:41669123
|
CG | C | 9 | a0001c0006t0003g0005a0001c0006t0003g0013a0001c0006t0003g0014others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.5097-560delC | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41669123 | ||||||
| chr8:41669188
|
T | C | 2 | a0001c0005t0001g0101a0001c0006t0001g0100 | 2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.5097-624A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41669188 | ||||||
| chr8:41669267
|
T | G | 42 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0162others(39): Show | 42 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.5097-703A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41669267 | ||||||
| chr8:41669445
|
C | A | 2 | a0001c0003t0001g0169a0001c0003t0001g0237 | 2 | HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.5097-881G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41669445 | ||||||
| chr8:41669453
|
C | G | 8 | a0001c0023t0001g0275a0001c0023t0001g0276a0004c0011t0001g0186others(5): Show | 8 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.5097-889G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41669453 | ||||||
| chr8:41669737
|
C | T | 5 | a0001c0010t0003g0270a0001c0028t0003g0053a0003c0015t0003g0137others(2): Show | 5 | HG02074.hp1 NA18950.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.5097-1173G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41669737 | ||||||
| chr8:41669786
|
C | T | 1 | a0001c0037t0003g0233 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.5097-1222G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41669786 | ||||||
| chr8:41669902
|
C | T | 1 | a0001c0004t0002g0066 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.5097-1338G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41669902 | ||||||
| chr8:41670059
|
C | T | 1 | a0001c0003t0001g0261 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.5097-1495G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41670059 | ||||||
| chr8:41670067
|
C | T | 2 | a0001c0004t0002g0212a0001c0004t0024g0210 | 2 | HG02080.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.5097-1503G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41670067 | ||||||
| chr8:41670113
|
C | T | 5 | a0001c0010t0003g0270a0001c0028t0003g0053a0003c0015t0003g0137others(2): Show | 5 | HG02074.hp1 NA18950.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.5097-1549G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41670113 | ||||||
| chr8:41670178
|
G | T | 2 | a0004c0020t0001g0036a0007c0033t0001g0108 | 2 | HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.5097-1614C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41670178 | ||||||
| chr8:41670483
|
G | A | 1 | a0001c0004t0002g0074 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.5096+1871C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41670483 | ||||||
| chr8:41670486
|
C | G | 3 | a0001c0002t0001g0135a0001c0003t0001g0141a0001c0003t0009g0170 | 3 | HG01934.hp2 HG02004.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.5096+1868G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41670486 | ||||||
| chr8:41670660
|
G | T | 57 | a0001c0002t0009g0098a0001c0004t0001g0109a0001c0004t0001g0159others(54): Show | 58 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.5096+1694C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41670660 | ||||||
| chr8:41670710
|
G | C | 54 | a0001c0004t0001g0109a0001c0004t0001g0159a0001c0004t0002g0066others(51): Show | 55 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.5096+1644C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41670710 | ||||||
| chr8:41671035
|
T | C | 4 | a0001c0010t0003g0002a0001c0010t0003g0114a0001c0010t0003g0189others(1): Show | 4 | HG02074.hp2 HG02080.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.5096+1319A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41671035 | ||||||
| chr8:41671090
|
C | T | 3 | a0001c0004t0001g0109a0001c0018t0026g0113a0002c0057t0005g0269 | 3 | HG01891.hp1 HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.5096+1264G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41671090 | ||||||
| chr8:41671161
|
G | A | 1 | a0001c0003t0009g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.5096+1193C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41671161 | ||||||
| chr8:41671617
|
C | CCTCCCGG others(86): Show |
50 | a0001c0004t0001g0109a0001c0004t0001g0159a0001c0004t0002g0066others(47): Show | 51 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.5096+736_5096+737i others(95): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41671617 | ||||||
| chr8:41671654
|
A | G | 4 | a0002c0007t0007g0021a0002c0007t0007g0025a0002c0007t0007g0028others(1): Show | 4 | HG01167.hp1 HG02258.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.5096+700T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41671654 | ||||||
| chr8:41671657
|
ACCCCGAT others(24): Show |
A | 1 | a0001c0018t0026g0113 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5096+666_5096+696d others(33): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41671657 | ||||||
| chr8:41671715
|
C | T | 1 | a0009c0047t0002g0016 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5096+639G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41671715 | ||||||
| chr8:41671827
|
GTGAGTCC others(50): Show |
G | 2 | a0001c0018t0026g0113a0002c0057t0005g0269 | 2 | HG01891.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.5096+470_5096+526d others(59): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41671827 | ||||||
| chr8:41671877
|
G | A | 1 | a0001c0002t0001g0168 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.5096+477C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41671877 | ||||||
| chr8:41672242
|
A | C | 9 | a0001c0006t0003g0005a0001c0006t0003g0013a0001c0006t0003g0014others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.5096+112T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41672242 | ||||||
| chr8:41672243
|
G | T | 9 | a0001c0006t0003g0005a0001c0006t0003g0013a0001c0006t0003g0014others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.5096+111C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41672243 | ||||||
| chr8:41672244
|
A | AATTGCAC others(8): Show |
9 | a0001c0006t0003g0005a0001c0006t0003g0013a0001c0006t0003g0014others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.5096+109_5096+110i others(17): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41672244 | ||||||
| chr8:41672271
|
C | T | 4 | a0001c0051t0008g0274a0003c0014t0008g0094a0003c0014t0008g0095others(1): Show | 4 | HG00738.hp1 HG03239.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.5096+83G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41672271 | ||||||
| chr8:41672338
|
A | G | 267 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(264): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.5096+16T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41672338 | ||||||
| chr8:41672964
|
C | G | 254 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(251): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.4538-52G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41672964 | ||||||
| chr8:41672971
|
C | T | 3 | a0001c0002t0009g0098a0001c0005t0010g0019a0009c0047t0002g0016 | 3 | HG02965.hp1 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4538-59G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41672971 | ||||||
| chr8:41672980
|
CCACGCAC others(3): Show |
C | 1 | a0001c0004t0002g0066 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.4538-78_4538-69del others(10): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41672980 | ||||||
| chr8:41673014
|
G | A | 4 | a0001c0016t0002g0006a0001c0016t0002g0007a0001c0016t0002g0008others(1): Show | 4 | HG01192.hp2 HG01258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.4538-102C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41673014 | ||||||
| chr8:41673048
|
G | A | 1 | a0001c0003t0001g0057 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4538-136C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41673048 | ||||||
| chr8:41673099
|
G | T | 3 | a0001c0002t0009g0098a0001c0005t0010g0019a0009c0047t0002g0016 | 3 | HG02965.hp1 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4538-187C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41673099 | ||||||
| chr8:41673485
|
T | C | 136 | a0001c0001t0001g0160a0001c0001t0001g0214a0001c0001t0001g0226others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.4538-573A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41673485 | ||||||
| chr8:41673556
|
T | C | 251 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(248): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.4538-644A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41673556 | ||||||
| chr8:41673618
|
A | T | 1 | a0001c0001t0002g0175 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4538-706T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41673618 | ||||||
| chr8:41673721
|
T | C | 140 | a0001c0001t0001g0160a0001c0001t0001g0214a0001c0001t0001g0226others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.4538-809A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41673721 | ||||||
| chr8:41673733
|
G | C | 1 | a0012c0045t0025g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4538-821C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41673733 | ||||||
| chr8:41673960
|
C | T | 42 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0162others(39): Show | 42 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.4538-1048G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41673960 | ||||||
| chr8:41673968
|
C | T | 4 | a0001c0010t0003g0002a0001c0010t0003g0114a0001c0010t0003g0189others(1): Show | 4 | HG02074.hp2 HG02080.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.4538-1056G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41673968 | ||||||
| chr8:41673997
|
A | G | 2 | a0001c0018t0026g0113a0002c0057t0005g0269 | 2 | HG01891.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.4538-1085T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41673997 | ||||||
| chr8:41674098
|
C | T | 42 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0162others(39): Show | 42 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.4538-1186G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41674098 | ||||||
| chr8:41674115
|
C | CCCTCAGC others(12): Show |
2 | a0001c0002t0001g0184a0001c0004t0002g0224 | 2 | HG01168.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.4538-1222_4538-120 others(23): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41674115 | ||||||
| chr8:41674195
|
A | G | 1 | a0001c0004t0002g0219 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.4538-1283T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41674195 | ||||||
| chr8:41674324
|
C | A | 1 | a0001c0005t0001g0229 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.4538-1412G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41674324 | ||||||
| chr8:41674597
|
T | C | 1 | a0001c0004t0002g0126 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.4538-1685A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41674597 | ||||||
| chr8:41674615
|
A | T | 9 | a0001c0006t0003g0005a0001c0006t0003g0013a0001c0006t0003g0014others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.4538-1703T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41674615 | ||||||
| chr8:41674674
|
C | T | 3 | a0001c0002t0009g0098a0001c0005t0010g0019a0009c0047t0002g0016 | 3 | HG02965.hp1 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4538-1762G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41674674 | ||||||
| chr8:41674738
|
C | G | 9 | a0001c0006t0003g0005a0001c0006t0003g0013a0001c0006t0003g0014others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.4538-1826G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41674738 | ||||||
| chr8:41674824
|
T | G | 1 | a0001c0005t0010g0019 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4538-1912A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41674824 | ||||||
| chr8:41675073
|
T | C | 1 | a0005c0021t0002g0115 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4538-2161A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41675073 | ||||||
| chr8:41675129
|
T | C | 194 | a0001c0001t0001g0148a0001c0001t0001g0160a0001c0001t0001g0214others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.4538-2217A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41675129 | ||||||
| chr8:41675151
|
T | C | 2 | a0001c0019t0002g0145a0015c0053t0002g0263 | 2 | NA18960.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.4538-2239A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41675151 | ||||||
| chr8:41675245
|
C | T | 7 | a0001c0006t0001g0017a0001c0006t0001g0039a0001c0006t0001g0264others(4): Show | 7 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.4538-2333G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41675245 | ||||||
| chr8:41675253
|
C | T | 9 | a0001c0010t0003g0002a0001c0010t0003g0114a0001c0010t0003g0189others(6): Show | 9 | HG02074.hp1 HG02074.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.4538-2341G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41675253 | ||||||
| chr8:41675260
|
C | G | 1 | a0001c0016t0002g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4538-2348G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41675260 | ||||||
| chr8:41675682
|
C | A | 54 | a0001c0004t0001g0109a0001c0004t0001g0159a0001c0004t0002g0066others(51): Show | 54 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.4538-2770G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41675682 | ||||||
| chr8:41675683
|
T | C | 194 | a0001c0001t0001g0148a0001c0001t0001g0160a0001c0001t0001g0214others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.4538-2771A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41675683 | ||||||
| chr8:41675727
|
C | A | 1 | a0001c0001t0002g0254 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.4538-2815G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41675727 | ||||||
| chr8:41675879
|
C | T | 195 | a0001c0001t0001g0148a0001c0001t0001g0160a0001c0001t0001g0214others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.4538-2967G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41675879 | ||||||
| chr8:41675995
|
C | T | 1 | a0001c0004t0002g0074 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4538-3083G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41675995 | ||||||
| chr8:41675996
|
A | G | 54 | a0001c0004t0001g0109a0001c0004t0001g0159a0001c0004t0002g0066others(51): Show | 54 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.4538-3084T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41675996 | ||||||
| chr8:41676248
|
T | C | 11 | a0001c0040t0001g0087a0002c0007t0001g0038a0002c0007t0001g0040others(8): Show | 11 | HG01167.hp1 HG01243.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.4538-3336A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41676248 | ||||||
| chr8:41676329
|
A | T | 194 | a0001c0001t0001g0148a0001c0001t0001g0160a0001c0001t0001g0214others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.4538-3417T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41676329 | ||||||
| chr8:41676550
|
T | C | 54 | a0001c0004t0001g0109a0001c0004t0001g0159a0001c0004t0002g0066others(51): Show | 54 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.4538-3638A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41676550 | ||||||
| chr8:41676668
|
G | A | 1 | a0001c0013t0006g0123 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4538-3756C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41676668 | ||||||
| chr8:41676900
|
C | T | 1 | a0001c0005t0010g0019 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4538-3988G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41676900 | ||||||
| chr8:41676939
|
A | G | 140 | a0001c0001t0001g0148a0001c0001t0001g0160a0001c0001t0001g0214others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.4538-4027T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41676939 | ||||||
| chr8:41676966
|
C | T | 9 | a0001c0010t0003g0002a0001c0010t0003g0114a0001c0010t0003g0189others(6): Show | 9 | HG02074.hp1 HG02074.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.4538-4054G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41676966 | ||||||
| chr8:41676967
|
A | G | 213 | a0001c0001t0001g0148a0001c0001t0001g0160a0001c0001t0001g0214others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.4538-4055T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41676967 | ||||||
| chr8:41677092
|
G | A | 2 | a0001c0013t0006g0123a0001c0013t0006g0124 | 2 | HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4538-4180C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41677092 | ||||||
| chr8:41677584
|
C | T | 256 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(253): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.4538-4672G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41677584 | ||||||
| chr8:41677594
|
G | GT | 100 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0001t0001g0191others(97): Show | 101 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.4538-4683dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41677594 | ||||||
| chr8:41677594
|
G | GTT | 6 | a0001c0002t0001g0168a0001c0030t0017g0051a0002c0007t0001g0038others(3): Show | 6 | HG02451.hp2 HG02886.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.4538-4684_4538-468 others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41677594 | ||||||
| chr8:41677665
|
C | T | 1 | a0001c0002t0001g0168 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.4538-4753G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41677665 | ||||||
| chr8:41677693
|
G | A | 5 | a0001c0010t0003g0270a0001c0028t0003g0053a0003c0015t0003g0137others(2): Show | 5 | HG02074.hp1 NA18950.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.4538-4781C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41677693 | ||||||
| chr8:41677885
|
T | C | 194 | a0001c0001t0001g0148a0001c0001t0001g0160a0001c0001t0001g0214others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.4538-4973A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41677885 | ||||||
| chr8:41677922
|
T | G | 140 | a0001c0001t0001g0148a0001c0001t0001g0160a0001c0001t0001g0214others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.4538-5010A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41677922 | ||||||
| chr8:41678130
|
T | C | 1 | a0001c0001t0002g0088 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4538-5218A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41678130 | ||||||
| chr8:41678152
|
T | A | 1 | a0001c0028t0003g0053 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.4538-5240A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41678152 | ||||||
| chr8:41678229
|
C | T | 2 | a0001c0012t0006g0085a0001c0012t0006g0099 | 2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4538-5317G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41678229 | ||||||
| chr8:41678242
|
G | A | 1 | a0001c0003t0001g0049 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4538-5330C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41678242 | ||||||
| chr8:41678368
|
C | T | 43 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0001t0001g0191others(40): Show | 44 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.4538-5456G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41678368 | ||||||
| chr8:41678774
|
T | C | 3 | a0001c0001t0001g0214a0001c0001t0001g0245a0001c0001t0001g0262 | 3 | NA19002.hp2 NA19005.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.4537+5770A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41678774 | ||||||
| chr8:41679304
|
T | C | 267 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(264): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.4537+5240A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679304 | ||||||
| chr8:41679558
|
C | CT | 13 | a0001c0001t0001g0217a0001c0001t0002g0078a0001c0001t0002g0208others(10): Show | 13 | HG00323.hp1 HG00408.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.4537+4985dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679558 | ||||||
| chr8:41679558
|
C | CTT | 115 | a0001c0001t0001g0148a0001c0001t0001g0160a0001c0001t0001g0214others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.4537+4984_4537+498 others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679558 | ||||||
| chr8:41679558
|
C | CTTT | 13 | a0001c0002t0001g0135a0001c0003t0001g0058a0001c0003t0001g0141others(10): Show | 13 | HG00438.hp1 HG01891.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.4537+4983_4537+498 others(7): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679558 | ||||||
| chr8:41679558
|
CT | C | 54 | a0001c0001t0002g0241a0001c0002t0001g0143a0001c0004t0001g0109others(51): Show | 54 | HG00423.hp2 HG00639.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.4537+4985delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679558 | ||||||
| chr8:41679586
|
A | G | 195 | a0001c0001t0001g0148a0001c0001t0001g0160a0001c0001t0001g0214others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.4537+4958T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679586 | ||||||
| chr8:41679610
|
G | T | 1 | a0001c0010t0003g0236 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.4537+4934C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679610 | ||||||
| chr8:41679636
|
C | T | 1 | a0001c0004t0001g0159 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4537+4908G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679636 | ||||||
| chr8:41679656
|
G | A | 1 | a0001c0005t0010g0019 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4537+4888C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679656 | ||||||
| chr8:41679665
|
C | T | 5 | a0001c0010t0003g0270a0001c0028t0003g0053a0003c0015t0003g0137others(2): Show | 5 | HG02074.hp1 NA18950.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.4537+4879G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679665 | ||||||
| chr8:41679708
|
G | A | 4 | a0001c0037t0003g0233a0003c0024t0001g0273a0003c0024t0003g0102others(1): Show | 4 | HG02559.hp2 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.4537+4836C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679708 | ||||||
| chr8:41679723
|
A | C | 256 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(253): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.4537+4821T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679723 | ||||||
| chr8:41679800
|
G | A | 54 | a0001c0001t0002g0241a0001c0004t0001g0109a0001c0004t0001g0159others(51): Show | 54 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.4537+4744C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679800 | ||||||
| chr8:41679956
|
T | C | 1 | a0004c0011t0001g0186 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4537+4588A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679956 | ||||||
| chr8:41679958
|
T | G | 1 | a0014c0055t0006g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4537+4586A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679958 | ||||||
| chr8:41680097
|
G | C | 9 | a0001c0006t0003g0005a0001c0006t0003g0013a0001c0006t0003g0014others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.4537+4447C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41680097 | ||||||
| chr8:41680285
|
G | A | 8 | a0001c0003t0001g0064a0001c0003t0001g0136a0001c0003t0001g0139others(5): Show | 8 | HG01081.hp2 HG01099.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.4537+4259C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41680285 | ||||||
| chr8:41680392
|
C | T | 52 | a0001c0001t0001g0160a0001c0001t0001g0214a0001c0001t0001g0226others(49): Show | 52 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.4537+4152G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41680392 | ||||||
| chr8:41680421
|
G | A | 2 | a0001c0026t0001g0165a0001c0029t0001g0253 | 2 | NA19057.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.4537+4123C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41680421 | ||||||
| chr8:41680431
|
C | T | 1 | a0014c0055t0006g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4537+4113G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41680431 | ||||||
| chr8:41680520
|
G | T | 5 | a0001c0010t0003g0270a0001c0028t0003g0053a0003c0015t0003g0137others(2): Show | 5 | HG02074.hp1 NA18950.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.4537+4024C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41680520 | ||||||
| chr8:41680565
|
CA | C | 87 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0001t0001g0191others(84): Show | 88 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.4537+3978delT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41680565 | ||||||
| chr8:41680565
|
CAA | C | 55 | a0001c0001t0001g0148a0001c0001t0001g0217a0001c0001t0002g0063others(52): Show | 55 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.4537+3977_4537+397 others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41680565 | ||||||
| chr8:41680749
|
G | A | 3 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0008t0002g0252 | 3 | HG01952.hp1 HG02683.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.4537+3795C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41680749 | ||||||
| chr8:41680768
|
A | G | 191 | a0001c0001t0001g0148a0001c0001t0001g0160a0001c0001t0001g0214others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.4537+3776T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41680768 | ||||||
| chr8:41681096
|
G | A | 1 | a0001c0003t0001g0049 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4537+3448C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41681096 | ||||||
| chr8:41681180
|
C | T | 1 | a0001c0005t0010g0019 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4537+3364G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41681180 | ||||||
| chr8:41681330
|
C | A | 1 | a0001c0030t0017g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4537+3214G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41681330 | ||||||
| chr8:41681330
|
C | T | 1 | a0001c0016t0002g0006 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4537+3214G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41681330 | ||||||
| chr8:41681353
|
T | C | 45 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0001t0001g0191others(42): Show | 46 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.4537+3191A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41681353 | ||||||
| chr8:41681404
|
A | G | 10 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0016t0002g0006others(7): Show | 10 | HG00738.hp1 HG02559.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.4537+3140T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41681404 | ||||||
| chr8:41681678
|
C | T | 5 | a0001c0006t0005g0015a0001c0006t0018g0117a0001c0017t0005g0116others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.4537+2866G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41681678 | ||||||
| chr8:41681679
|
A | G | 5 | a0001c0006t0005g0015a0001c0006t0018g0117a0001c0017t0005g0116others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.4537+2865T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41681679 | ||||||
| chr8:41681681
|
G | GCTGGTTG others(4): Show |
5 | a0001c0006t0005g0015a0001c0006t0018g0117a0001c0017t0005g0116others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.4537+2862_4537+286 others(15): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41681681 | ||||||
| chr8:41681689
|
G | A | 1 | a0001c0003t0001g0049 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4537+2855C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41681689 | ||||||
| chr8:41682079
|
C | T | 1 | a0001c0012t0001g0138 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.4537+2465G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41682079 | ||||||
| chr8:41682266
|
G | A | 7 | a0001c0006t0001g0017a0001c0006t0001g0039a0001c0006t0001g0264others(4): Show | 7 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.4537+2278C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41682266 | ||||||
| chr8:41682380
|
C | G | 1 | a0012c0045t0025g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4537+2164G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41682380 | ||||||
| chr8:41682410
|
C | T | 2 | a0001c0008t0002g0198a0001c0008t0002g0218 | 2 | HG00438.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.4537+2134G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41682410 | ||||||
| chr8:41682452
|
G | A | 15 | a0001c0006t0001g0100a0001c0028t0003g0053a0003c0015t0003g0137others(12): Show | 15 | HG02074.hp1 HG02559.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.4537+2092C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41682452 | ||||||
| chr8:41682553
|
C | A | 3 | a0001c0037t0003g0233a0003c0024t0001g0273a0003c0024t0003g0102 | 3 | HG02717.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4537+1991G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41682553 | ||||||
| chr8:41682557
|
C | A | 1 | a0001c0006t0001g0268 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4537+1987G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41682557 | ||||||
| chr8:41682578
|
C | T | 5 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0001t0001g0191others(2): Show | 5 | NA18948.hp2 NA18979.hp2 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.4537+1966G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41682578 | ||||||
| chr8:41682674
|
G | A | 15 | a0001c0006t0001g0100a0001c0028t0003g0053a0003c0015t0003g0137others(12): Show | 15 | HG02074.hp1 HG02559.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.4537+1870C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41682674 | ||||||
| chr8:41682869
|
C | T | 64 | a0001c0002t0001g0031a0001c0002t0001g0048a0001c0002t0001g0050others(61): Show | 65 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.4537+1675G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41682869 | ||||||
| chr8:41682917
|
T | C | 2 | a0001c0005t0001g0101a0005c0035t0001g0132 | 2 | NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.4537+1627A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41682917 | ||||||
| chr8:41683031
|
C | CACGGACA others(13): Show |
15 | a0001c0006t0001g0100a0001c0028t0003g0053a0003c0015t0003g0137others(12): Show | 15 | HG02074.hp1 HG02559.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.4537+1493_4537+151 others(24): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683031 | ||||||
| chr8:41683097
|
C | A | 1 | a0001c0008t0002g0213 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.4537+1447G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683097 | ||||||
| chr8:41683098
|
G | A | 2 | a0001c0023t0001g0275a0001c0023t0001g0276 | 2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4537+1446C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683098 | ||||||
| chr8:41683103
|
C | T | 2 | a0001c0001t0002g0020a0002c0043t0002g0044 | 2 | HG02723.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4537+1441G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683103 | ||||||
| chr8:41683104
|
A | G | 1 | a0013c0041t0012g0174 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4537+1440T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683104 | ||||||
| chr8:41683115
|
TACGC | T | 8 | a0001c0006t0001g0017a0001c0006t0001g0039a0001c0006t0001g0264others(5): Show | 8 | HG02145.hp1 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.4537+1425_4537+142 others(8): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683115 | ||||||
| chr8:41683211
|
C | T | 1 | a0014c0055t0006g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4537+1333G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683211 | ||||||
| chr8:41683226
|
GGACAGTG others(2): Show |
G | 4 | a0001c0028t0003g0053a0003c0015t0003g0137a0003c0015t0003g0220others(1): Show | 4 | HG02074.hp1 NA18950.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.4537+1309_4537+131 others(13): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683226 | ||||||
| chr8:41683253
|
GCACGATA others(1276): Show |
G | 1 | a0001c0002t0002g0227 | 1 | HG02040.hp1 | splice_region_variant&intron_variant | LOW | c.4537+8_4537+1290de others(1): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683253 | ||||||
| chr8:41683282
|
G | A | 4 | a0001c0028t0003g0053a0003c0015t0003g0137a0003c0015t0003g0220others(1): Show | 4 | HG02074.hp1 NA18950.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.4537+1262C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683282 | ||||||
| chr8:41683292
|
G | C | 5 | a0001c0051t0008g0274a0003c0014t0002g0209a0003c0014t0008g0094others(2): Show | 5 | HG00639.hp1 HG00738.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.4537+1252C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683292 | ||||||
| chr8:41683310
|
T | C | 1 | a0013c0041t0012g0174 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4537+1234A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683310 | ||||||
| chr8:41683366
|
G | A | 53 | a0001c0001t0001g0160a0001c0001t0001g0214a0001c0001t0001g0262others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.4537+1178C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683366 | ||||||
| chr8:41683437
|
C | T | 1 | a0001c0010t0002g0056 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.4537+1107G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683437 | ||||||
| chr8:41683455
|
G | A | 3 | a0001c0037t0003g0233a0003c0024t0001g0273a0003c0024t0003g0102 | 3 | HG02717.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4537+1089C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683455 | ||||||
| chr8:41683531
|
C | T | 134 | a0001c0001t0001g0160a0001c0001t0001g0214a0001c0001t0001g0262others(131): Show | 135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.4537+1013G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683531 | ||||||
| chr8:41683768
|
C | T | 1 | a0001c0002t0003g0079 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.4537+776G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683768 | ||||||
| chr8:41683802
|
G | A | 2 | a0001c0005t0028g0112a0001c0005t0029g0111 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4537+742C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683802 | ||||||
| chr8:41684121
|
A | G | 1 | a0001c0005t0001g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4537+423T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41684121 | ||||||
| chr8:41684150
|
C | T | 1 | a0003c0014t0002g0209 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.4537+394G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41684150 | ||||||
| chr8:41684223
|
A | G | 262 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(259): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.4537+321T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41684223 | ||||||
| chr8:41684229
|
C | T | 1 | a0002c0007t0007g0021 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4537+315G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41684229 | ||||||
| chr8:41684328
|
G | A | 3 | a0001c0037t0003g0233a0003c0024t0001g0273a0003c0024t0003g0102 | 3 | HG02717.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4537+216C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41684328 | ||||||
| chr8:41684345
|
G | A | 4 | a0001c0006t0003g0005a0001c0006t0003g0013a0001c0006t0003g0014others(1): Show | 4 | HG02647.hp1 HG03041.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.4537+199C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41684345 | ||||||
| chr8:41684443
|
C | T | 1 | a0001c0004t0002g0195 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.4537+101G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41684443 | ||||||
| chr8:41684460
|
C | T | 2 | a0001c0002t0001g0184a0001c0002t0001g0185 | 2 | HG03704.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.4537+84G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41684460 | ||||||
| chr8:41684735
|
C | T | 1 | a0001c0002t0001g0127 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4391-45G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41684735 | ||||||
| chr8:41684739
|
G | A | 16 | a0001c0006t0001g0100a0001c0028t0003g0053a0003c0015t0003g0137others(13): Show | 16 | HG02074.hp1 HG02559.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.4391-49C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41684739 | ||||||
| chr8:41684810
|
G | A | 3 | a0001c0002t0009g0098a0001c0046t0030g0277a0009c0047t0002g0016 | 3 | HG02723.hp2 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4391-120C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41684810 | ||||||
| chr8:41684937
|
A | T | 4 | a0001c0006t0003g0005a0001c0006t0003g0013a0001c0006t0003g0014others(1): Show | 4 | HG02647.hp1 HG03041.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.4391-247T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41684937 | ||||||
| chr8:41684942
|
A | T | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.4391-252T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41684942 | ||||||
| chr8:41685025
|
C | T | 140 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0001t0002g0088others(137): Show | 141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.4391-335G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41685025 | ||||||
| chr8:41685054
|
G | A | 1 | a0001c0003t0019g0068 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.4391-364C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41685054 | ||||||
| chr8:41685086
|
G | A | 1 | a0001c0005t0010g0019 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4391-396C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41685086 | ||||||
| chr8:41685149
|
G | A | 1 | a0001c0040t0001g0087 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4391-459C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41685149 | ||||||
| chr8:41685398
|
A | G | 1 | a0001c0046t0030g0277 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4391-708T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41685398 | ||||||
| chr8:41685456
|
C | T | 5 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(2): Show | 5 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.4390+696G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41685456 | ||||||
| chr8:41685632
|
C | G | 2 | a0001c0002t0001g0184a0001c0002t0001g0185 | 2 | HG03704.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.4390+520G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41685632 | ||||||
| chr8:41685645
|
AT | A | 140 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0001t0002g0088others(137): Show | 141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.4390+506delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41685645 | ||||||
| chr8:41685670
|
T | G | 1 | a0003c0015t0003g0250 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.4390+482A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41685670 | ||||||
| chr8:41685823
|
C | A | 6 | a0001c0006t0001g0017a0001c0006t0001g0039a0001c0006t0001g0264others(3): Show | 6 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.4390+329G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41685823 | ||||||
| chr8:41685944
|
G | C | 1 | a0001c0002t0002g0180 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4390+208C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41685944 | ||||||
| chr8:41686355
|
C | T | 1 | a0001c0004t0002g0215 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.4259-72G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41686355 | ||||||
| chr8:41686424
|
G | A | 3 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0005t0001g0256 | 3 | HG01123.hp1 HG01952.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.4259-141C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41686424 | ||||||
| chr8:41686812
|
A | G | 29 | a0001c0006t0001g0017a0001c0006t0001g0039a0001c0006t0001g0264others(26): Show | 29 | HG01106.hp2 HG01123.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.4259-529T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41686812 | ||||||
| chr8:41686967
|
C | T | 2 | a0001c0002t0009g0098a0009c0047t0002g0016 | 2 | HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4259-684G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41686967 | ||||||
| chr8:41686974
|
ACACT | A | 6 | a0001c0010t0002g0056a0001c0010t0003g0002a0001c0010t0003g0114others(3): Show | 6 | HG02071.hp2 HG02074.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.4259-695_4259-692d others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41686974 | ||||||
| chr8:41687236
|
C | T | 5 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(2): Show | 5 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.4258+920G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41687236 | ||||||
| chr8:41687340
|
G | A | 1 | a0001c0001t0002g0175 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4258+816C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41687340 | ||||||
| chr8:41687456
|
C | A | 1 | a0003c0049t0001g0104 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4258+700G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41687456 | ||||||
| chr8:41687474
|
C | T | 4 | a0001c0028t0003g0053a0003c0015t0003g0137a0003c0015t0003g0220others(1): Show | 4 | HG02074.hp1 NA18950.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.4258+682G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41687474 | ||||||
| chr8:41687558
|
C | G | 93 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0001t0002g0088others(90): Show | 94 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.4258+598G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41687558 | ||||||
| chr8:41687585
|
C | T | 27 | a0001c0006t0001g0039a0001c0006t0001g0264a0001c0006t0001g0266others(24): Show | 27 | HG01106.hp2 HG01167.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.4258+571G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41687585 | ||||||
| chr8:41687677
|
T | C | 2 | a0001c0023t0001g0275a0001c0023t0001g0276 | 2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4258+479A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41687677 | ||||||
| chr8:41687740
|
T | C | 2 | a0001c0002t0001g0031a0001c0002t0012g0022 | 2 | HG01261.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4258+416A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41687740 | ||||||
| chr8:41687765
|
G | A | 1 | a0002c0007t0007g0023 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4258+391C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41687765 | ||||||
| chr8:41687987
|
G | A | 1 | a0001c0019t0002g0164 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4258+169C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41687987 | ||||||
| chr8:41687995
|
A | G | 1 | a0001c0005t0001g0256 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.4258+161T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41687995 | ||||||
| chr8:41687998
|
G | T | 1 | a0013c0041t0012g0174 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4258+158C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41687998 | ||||||
| chr8:41688123
|
A | G | 32 | a0001c0006t0001g0100a0001c0006t0003g0005a0001c0006t0003g0013others(29): Show | 32 | HG02074.hp1 HG02109.hp2 HG02559.hp1 others(29): Show |
intron_variant | MODIFIER | c.4258+33T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41688123 | ||||||
| chr8:41688297
|
G | A | 1 | a0001c0012t0005g0103 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4184-67C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 34/42 | chr8 | 41688297 | ||||||
| chr8:41688614
|
G | T | 1 | a0001c0002t0001g0048 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4105-25C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41688614 | ||||||
| chr8:41688675
|
G | A | 1 | a0001c0002t0001g0248 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.4105-86C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41688675 | ||||||
| chr8:41688735
|
A | G | 4 | a0001c0002t0009g0098a0001c0005t0010g0019a0001c0046t0030g0277others(1): Show | 4 | HG02723.hp2 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.4105-146T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41688735 | ||||||
| chr8:41688782
|
G | A | 1 | a0001c0004t0002g0193 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.4105-193C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41688782 | ||||||
| chr8:41688814
|
G | A | 1 | a0001c0001t0002g0161 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4105-225C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41688814 | ||||||
| chr8:41688876
|
G | A | 9 | a0001c0006t0001g0017a0001c0006t0001g0039a0001c0006t0001g0264others(6): Show | 9 | HG02145.hp1 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.4105-287C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41688876 | ||||||
| chr8:41688908
|
C | A | 20 | a0001c0006t0001g0100a0001c0013t0001g0027a0001c0013t0001g0037others(17): Show | 20 | HG02074.hp1 HG02559.hp1 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.4105-319G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41688908 | ||||||
| chr8:41688966
|
A | G | 262 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(259): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.4105-377T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41688966 | ||||||
| chr8:41688983
|
A | G | 1 | a0001c0010t0003g0270 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.4105-394T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41688983 | ||||||
| chr8:41688994
|
T | C | 1 | a0013c0041t0012g0174 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4105-405A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41688994 | ||||||
| chr8:41689138
|
G | A | 20 | a0001c0006t0001g0100a0001c0013t0001g0027a0001c0013t0001g0037others(17): Show | 20 | HG02074.hp1 HG02559.hp1 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.4105-549C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689138 | ||||||
| chr8:41689195
|
TC | T | 20 | a0001c0006t0001g0100a0001c0013t0001g0027a0001c0013t0001g0037others(17): Show | 20 | HG02074.hp1 HG02559.hp1 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.4105-607delG | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689195 | ||||||
| chr8:41689216
|
C | T | 3 | a0001c0002t0001g0135a0001c0003t0009g0170a0001c0012t0001g0138 | 3 | HG01928.hp2 HG02004.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.4105-627G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689216 | ||||||
| chr8:41689217
|
G | A | 1 | a0001c0058t0022g0089 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4105-628C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689217 | ||||||
| chr8:41689221
|
T | C | 5 | a0001c0001t0002g0024a0001c0001t0002g0125a0001c0012t0005g0103others(2): Show | 5 | HG02109.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.4105-632A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689221 | ||||||
| chr8:41689251
|
G | A | 2 | a0001c0004t0002g0212a0001c0004t0024g0210 | 2 | HG02080.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.4105-662C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689251 | ||||||
| chr8:41689296
|
A | AT | 125 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0001t0002g0088others(122): Show | 126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.4105-708dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689296 | ||||||
| chr8:41689302
|
T | A | 20 | a0001c0006t0001g0100a0001c0013t0001g0027a0001c0013t0001g0037others(17): Show | 20 | HG02074.hp1 HG02559.hp1 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.4105-713A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689302 | ||||||
| chr8:41689403
|
C | T | 9 | a0001c0006t0003g0005a0001c0006t0003g0013a0001c0006t0003g0014others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.4105-814G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689403 | ||||||
| chr8:41689420
|
G | A | 2 | a0001c0005t0001g0101a0005c0035t0001g0132 | 2 | NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.4104+807C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689420 | ||||||
| chr8:41689541
|
A | G | 2 | a0001c0023t0001g0275a0001c0023t0001g0276 | 2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4104+686T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689541 | ||||||
| chr8:41689601
|
G | C | 6 | a0001c0010t0002g0056a0001c0010t0003g0002a0001c0010t0003g0114others(3): Show | 6 | HG02071.hp2 HG02074.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.4104+626C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689601 | ||||||
| chr8:41689615
|
G | C | 3 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0005t0001g0256 | 3 | HG01123.hp1 HG01952.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.4104+612C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689615 | ||||||
| chr8:41689666
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.4104+561T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689666 | ||||||
| chr8:41689868
|
A | G | 58 | a0001c0006t0001g0017a0001c0006t0001g0039a0001c0006t0001g0100others(55): Show | 58 | HG01106.hp2 HG01123.hp2 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.4104+359T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689868 | ||||||
| chr8:41689937
|
C | A | 1 | a0006c0031t0002g0255 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.4104+290G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689937 | ||||||
| chr8:41690035
|
C | A | 3 | a0001c0037t0003g0233a0003c0024t0001g0273a0003c0024t0003g0102 | 3 | HG02717.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4104+192G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41690035 | ||||||
| chr8:41690056
|
A | G | 58 | a0001c0006t0001g0017a0001c0006t0001g0039a0001c0006t0001g0100others(55): Show | 58 | HG01106.hp2 HG01123.hp2 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.4104+171T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41690056 | ||||||
| chr8:41690142
|
G | A | 39 | a0001c0002t0001g0031a0001c0002t0001g0048a0001c0002t0001g0050others(36): Show | 40 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.4104+85C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41690142 | ||||||
| chr8:41690160
|
G | T | 3 | a0001c0040t0001g0087a0005c0021t0002g0115a0005c0021t0002g0133 | 3 | HG02280.hp1 HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.4104+67C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41690160 | ||||||
| chr8:41690165
|
T | C | 58 | a0001c0006t0001g0017a0001c0006t0001g0039a0001c0006t0001g0100others(55): Show | 58 | HG01106.hp2 HG01123.hp2 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.4104+62A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41690165 | ||||||
| chr8:41690689
|
C | T | 58 | a0001c0006t0001g0017a0001c0006t0001g0039a0001c0006t0001g0100others(55): Show | 58 | HG01106.hp2 HG01123.hp2 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.3859-90G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41690689 | ||||||
| chr8:41690691
|
C | T | 58 | a0001c0006t0001g0017a0001c0006t0001g0039a0001c0006t0001g0100others(55): Show | 58 | HG01106.hp2 HG01123.hp2 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.3859-92G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41690691 | ||||||
| chr8:41690780
|
T | C | 1 | a0001c0002t0001g0144 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3859-181A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41690780 | ||||||
| chr8:41690794
|
C | T | 58 | a0001c0006t0001g0017a0001c0006t0001g0039a0001c0006t0001g0100others(55): Show | 58 | HG01106.hp2 HG01123.hp2 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.3859-195G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41690794 | ||||||
| chr8:41690908
|
A | AAAC | 5 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(2): Show | 5 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3859-312_3859-310d others(5): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41690908 | ||||||
| chr8:41690917
|
C | T | 53 | a0001c0006t0001g0017a0001c0006t0001g0039a0001c0006t0001g0100others(50): Show | 53 | HG01106.hp2 HG01123.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.3859-318G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41690917 | ||||||
| chr8:41691011
|
T | G | 1 | a0001c0038t0002g0200 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.3859-412A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691011 | ||||||
| chr8:41691070
|
A | T | 61 | a0001c0006t0001g0017a0001c0006t0001g0039a0001c0006t0001g0100others(58): Show | 61 | HG01106.hp2 HG01123.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.3859-471T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691070 | ||||||
| chr8:41691077
|
C | T | 58 | a0001c0006t0001g0017a0001c0006t0001g0039a0001c0006t0001g0100others(55): Show | 58 | HG01106.hp2 HG01123.hp2 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.3859-478G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691077 | ||||||
| chr8:41691282
|
C | G | 29 | a0001c0006t0001g0100a0001c0006t0003g0005a0001c0006t0003g0013others(26): Show | 29 | HG02074.hp1 HG02109.hp2 HG02559.hp1 others(26): Show |
intron_variant | MODIFIER | c.3859-683G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691282 | ||||||
| chr8:41691339
|
T | C | 1 | a0001c0005t0001g0083 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3859-740A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691339 | ||||||
| chr8:41691368
|
G | C | 1 | a0001c0005t0010g0019 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3859-769C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691368 | ||||||
| chr8:41691393
|
A | T | 30 | a0001c0006t0001g0100a0001c0006t0003g0005a0001c0006t0003g0013others(27): Show | 30 | HG01123.hp2 HG02074.hp1 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.3859-794T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691393 | ||||||
| chr8:41691440
|
C | G | 5 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(2): Show | 5 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3859-841G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691440 | ||||||
| chr8:41691498
|
G | A | 2 | a0001c0001t0002g0216a0006c0031t0002g0255 | 2 | NA18986.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.3859-899C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691498 | ||||||
| chr8:41691595
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3859-996C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691595 | ||||||
| chr8:41691676
|
T | C | 30 | a0001c0006t0001g0100a0001c0006t0003g0005a0001c0006t0003g0013others(27): Show | 30 | HG01123.hp2 HG02074.hp1 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.3858+972A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691676 | ||||||
| chr8:41691893
|
C | T | 6 | a0001c0010t0002g0056a0001c0010t0003g0002a0001c0010t0003g0114others(3): Show | 6 | HG02071.hp2 HG02074.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.3858+755G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691893 | ||||||
| chr8:41691931
|
G | A | 1 | a0001c0001t0002g0009 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3858+717C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691931 | ||||||
| chr8:41691973
|
G | A | 1 | a0013c0041t0012g0174 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3858+675C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691973 | ||||||
| chr8:41692059
|
CT | C | 34 | a0001c0001t0001g0262a0001c0002t0001g0143a0001c0002t0003g0080others(31): Show | 34 | HG01070.hp2 HG01106.hp2 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.3858+588delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41692059 | ||||||
| chr8:41692081
|
G | C | 1 | a0001c0001t0002g0075 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3858+567C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41692081 | ||||||
| chr8:41692097
|
C | T | 6 | a0001c0010t0002g0056a0001c0010t0003g0002a0001c0010t0003g0114others(3): Show | 6 | HG02071.hp2 HG02074.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.3858+551G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41692097 | ||||||
| chr8:41692119
|
C | T | 19 | a0001c0010t0002g0056a0001c0010t0003g0002a0001c0010t0003g0114others(16): Show | 19 | HG01106.hp2 HG01167.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.3858+529G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41692119 | ||||||
| chr8:41692167
|
C | T | 5 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(2): Show | 5 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3858+481G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41692167 | ||||||
| chr8:41692300
|
G | A | 29 | a0001c0006t0001g0100a0001c0006t0003g0005a0001c0006t0003g0013others(26): Show | 29 | HG02074.hp1 HG02109.hp2 HG02559.hp1 others(26): Show |
intron_variant | MODIFIER | c.3858+348C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41692300 | ||||||
| chr8:41692344
|
A | G | 1 | a0001c0009t0002g0069 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3858+304T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41692344 | ||||||
| chr8:41692353
|
G | A | 21 | a0001c0006t0003g0005a0001c0006t0003g0013a0001c0006t0003g0014others(18): Show | 21 | HG02074.hp1 HG02109.hp2 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.3858+295C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41692353 | ||||||
| chr8:41692377
|
C | T | 1 | a0014c0055t0006g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3858+271G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41692377 | ||||||
| chr8:41692500
|
T | C | 4 | a0001c0006t0005g0015a0001c0006t0018g0117a0001c0017t0005g0116others(1): Show | 4 | HG02109.hp2 HG02572.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3858+148A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41692500 | ||||||
| chr8:41692562
|
C | T | 1 | a0012c0045t0025g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3858+86G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41692562 | ||||||
| chr8:41692580
|
T | C | 11 | a0001c0006t0001g0100a0004c0011t0001g0186a0004c0011t0001g0187others(8): Show | 11 | HG02559.hp1 HG02572.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.3858+68A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41692580 | ||||||
| chr8:41692948
|
GC | G | 28 | a0001c0006t0001g0017a0001c0006t0001g0039a0001c0006t0001g0264others(25): Show | 28 | HG01106.hp2 HG01167.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.3630-73delG | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 30/42 | chr8 | 41692948 | ||||||
| chr8:41692992
|
C | T | 7 | a0001c0010t0002g0056a0001c0010t0003g0002a0001c0010t0003g0114others(4): Show | 7 | HG01243.hp2 HG02071.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.3629+113G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 30/42 | chr8 | 41692992 | ||||||
| chr8:41693265
|
A | C | 1 | a0001c0001t0001g0242 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3533-64T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693265 | ||||||
| chr8:41693269
|
C | T | 9 | a0001c0006t0003g0005a0001c0006t0003g0013a0001c0006t0003g0014others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.3533-68G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693269 | ||||||
| chr8:41693417
|
CTTTTTTT others(2): Show |
C | 7 | a0001c0002t0001g0166a0001c0002t0001g0197a0001c0025t0011g0001others(4): Show | 8 | HG01123.hp2 HG02818.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.3533-225_3533-217d others(11): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693417 | ||||||
| chr8:41693417
|
CTTTTTTT others(3): Show |
C | 37 | a0001c0002t0001g0031a0001c0002t0001g0048a0001c0002t0001g0050others(34): Show | 37 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.3533-226_3533-217d others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693417 | ||||||
| chr8:41693417
|
CTTTTTTT others(4): Show |
C | 74 | a0001c0001t0002g0020a0001c0001t0002g0161a0001c0001t0002g0176others(71): Show | 74 | HG00140.hp1 HG00423.hp1 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.3533-227_3533-217d others(13): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693417 | ||||||
| chr8:41693417
|
CTTTTTTT others(5): Show |
C | 140 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.3533-228_3533-217d others(14): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693417 | ||||||
| chr8:41693417
|
CTTTTTTT others(6): Show |
C | 4 | a0001c0003t0001g0158a0001c0004t0002g0259a0001c0005t0013g0004others(1): Show | 4 | HG01070.hp2 NA18969.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.3533-229_3533-217d others(15): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693417 | ||||||
| chr8:41693491
|
G | A | 1 | a0005c0035t0001g0132 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3533-290C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693491 | ||||||
| chr8:41693645
|
G | A | 9 | a0001c0006t0003g0005a0001c0006t0003g0013a0001c0006t0003g0014others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.3532+253C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693645 | ||||||
| chr8:41693766
|
A | T | 9 | a0001c0006t0003g0005a0001c0006t0003g0013a0001c0006t0003g0014others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.3532+132T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693766 | ||||||
| chr8:41693767
|
G | C | 9 | a0001c0006t0003g0005a0001c0006t0003g0013a0001c0006t0003g0014others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.3532+131C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693767 | ||||||
| chr8:41693769
|
ACCTC | A | 9 | a0001c0006t0003g0005a0001c0006t0003g0013a0001c0006t0003g0014others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.3532+125_3532+128d others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693769 | ||||||
| chr8:41693780
|
G | A | 6 | a0001c0002t0009g0098a0001c0005t0010g0019a0001c0018t0026g0113others(3): Show | 6 | HG02451.hp1 HG02723.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.3532+118C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693780 | ||||||
| chr8:41693853
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3532+45G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693853 | ||||||
| chr8:41693885
|
G | T | 1 | a0001c0005t0003g0032 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3532+13C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693885 | ||||||
| chr8:41694163
|
A | G | 7 | a0001c0003t0001g0064a0001c0003t0001g0136a0001c0003t0001g0139others(4): Show | 7 | HG01081.hp2 HG01099.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.3328-61T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 28/42 | chr8 | 41694163 | ||||||
| chr8:41694202
|
G | A | 7 | a0001c0002t0001g0185a0001c0002t0009g0098a0001c0005t0010g0019others(4): Show | 7 | HG02451.hp1 HG02723.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3328-100C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 28/42 | chr8 | 41694202 | ||||||
| chr8:41694210
|
G | A | 19 | a0001c0006t0001g0017a0001c0006t0001g0039a0001c0006t0001g0264others(16): Show | 19 | HG01106.hp2 HG01167.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.3328-108C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 28/42 | chr8 | 41694210 | ||||||
| chr8:41694305
|
A | G | 1 | a0001c0003t0001g0177 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3328-203T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 28/42 | chr8 | 41694305 | ||||||
| chr8:41694372
|
G | A | 1 | a0001c0003t0001g0049 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3327+220C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 28/42 | chr8 | 41694372 | ||||||
| chr8:41694528
|
T | C | 5 | a0001c0051t0008g0274a0003c0014t0002g0209a0003c0014t0008g0094others(2): Show | 5 | HG00639.hp1 HG00738.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.3327+64A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 28/42 | chr8 | 41694528 | ||||||
| chr8:41694571
|
G | C | 15 | a0001c0006t0001g0100a0001c0028t0003g0053a0003c0015t0003g0137others(12): Show | 15 | HG02074.hp1 HG02559.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.3327+21C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 28/42 | chr8 | 41694571 | ||||||
| chr8:41694925
|
G | A | 16 | a0001c0006t0001g0017a0001c0006t0001g0039a0001c0006t0001g0264others(13): Show | 16 | HG02145.hp1 HG02559.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.3116-122C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 27/42 | chr8 | 41694925 | ||||||
| chr8:41695004
|
C | T | 1 | a0001c0002t0001g0050 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3115+173G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 27/42 | chr8 | 41695004 | ||||||
| chr8:41695026
|
C | T | 1 | a0001c0004t0002g0215 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3115+151G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 27/42 | chr8 | 41695026 | ||||||
| chr8:41695070
|
T | C | 1 | a0001c0004t0002g0215 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3115+107A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 27/42 | chr8 | 41695070 | ||||||
| chr8:41695168
|
C | T | 2 | a0001c0005t0010g0019a0009c0047t0002g0016 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3115+9G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 27/42 | chr8 | 41695168 | ||||||
| chr8:41695595
|
G | A | 2 | a0001c0004t0002g0195a0001c0004t0002g0271 | 2 | HG02602.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.2961-264C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41695595 | ||||||
| chr8:41695715
|
A | G | 5 | a0003c0014t0002g0209a0003c0014t0008g0094a0003c0014t0008g0095others(2): Show | 5 | HG00639.hp1 HG01123.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.2961-384T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41695715 | ||||||
| chr8:41695720
|
C | T | 2 | a0001c0018t0026g0113a0012c0045t0025g0188 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2961-389G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41695720 | ||||||
| chr8:41695726
|
C | T | 1 | a0001c0002t0001g0150 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2961-395G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41695726 | ||||||
| chr8:41695762
|
C | T | 7 | a0001c0005t0002g0003a0001c0005t0003g0032a0001c0005t0013g0004others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.2961-431G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41695762 | ||||||
| chr8:41695764
|
C | T | 1 | a0001c0005t0002g0010 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2961-433G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41695764 | ||||||
| chr8:41695828
|
A | T | 180 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.2961-497T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41695828 | ||||||
| chr8:41695906
|
T | C | 1 | a0001c0046t0030g0277 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2960+457A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41695906 | ||||||
| chr8:41695940
|
C | T | 5 | a0001c0002t0001g0166a0003c0015t0003g0137a0003c0015t0003g0220others(2): Show | 5 | HG03195.hp1 NA18950.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.2960+423G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41695940 | ||||||
| chr8:41695951
|
G | GC | 36 | a0001c0004t0001g0109a0001c0004t0001g0159a0001c0004t0002g0066others(33): Show | 36 | HG00423.hp2 HG00438.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.2960+411dupG | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41695951 | ||||||
| chr8:41696170
|
G | A | 6 | a0001c0006t0001g0017a0001c0006t0001g0039a0001c0006t0001g0264others(3): Show | 6 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2960+193C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41696170 | ||||||
| chr8:41696179
|
C | T | 1 | a0001c0002t0009g0130 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2960+184G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41696179 | ||||||
| chr8:41696307
|
C | T | 1 | a0001c0006t0001g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2960+56G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41696307 | ||||||
| chr8:41696317
|
G | A | 93 | a0001c0002t0001g0031a0001c0002t0001g0048a0001c0002t0001g0050others(90): Show | 94 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.2960+46C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41696317 | ||||||
| chr8:41696666
|
C | T | 1 | a0005c0035t0001g0132 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2735+10G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 25/42 | chr8 | 41696666 | ||||||
| chr8:41696862
|
C | A | 1 | a0001c0006t0001g0266 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2638-89G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41696862 | ||||||
| chr8:41696930
|
C | G | 2 | a0001c0005t0028g0112a0001c0005t0029g0111 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2638-157G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41696930 | ||||||
| chr8:41697084
|
GC | G | 233 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(230): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.2638-312delG | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697084 | ||||||
| chr8:41697230
|
T | C | 234 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.2638-457A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697230 | ||||||
| chr8:41697290
|
G | A | 1 | a0001c0010t0002g0056 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2638-517C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697290 | ||||||
| chr8:41697293
|
A | G | 268 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(265): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.2638-520T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697293 | ||||||
| chr8:41697318
|
C | T | 1 | a0001c0046t0030g0277 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2638-545G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697318 | ||||||
| chr8:41697333
|
G | C | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2638-560C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697333 | ||||||
| chr8:41697392
|
A | G | 240 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(237): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.2638-619T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697392 | ||||||
| chr8:41697463
|
A | G | 141 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.2637+580T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697463 | ||||||
| chr8:41697559
|
C | T | 91 | a0001c0002t0001g0031a0001c0002t0001g0048a0001c0002t0001g0050others(88): Show | 92 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.2637+484G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697559 | ||||||
| chr8:41697562
|
C | A | 18 | a0001c0002t0009g0098a0001c0012t0005g0103a0001c0012t0006g0085others(15): Show | 18 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.2637+481G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697562 | ||||||
| chr8:41697632
|
C | T | 1 | a0001c0013t0001g0037 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2637+411G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697632 | ||||||
| chr8:41697648
|
G | A | 1 | a0002c0057t0005g0269 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2637+395C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697648 | ||||||
| chr8:41697847
|
T | C | 1 | a0001c0046t0030g0277 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2637+196A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697847 | ||||||
| chr8:41697848
|
T | C | 103 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(100): Show | 103 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.2637+195A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697848 | ||||||
| chr8:41697855
|
G | A | 102 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(99): Show | 102 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.2637+188C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697855 | ||||||
| chr8:41697896
|
G | A | 2 | a0001c0005t0028g0112a0001c0005t0029g0111 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2637+147C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697896 | ||||||
| chr8:41697955
|
T | C | 113 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(110): Show | 114 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.2637+88A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697955 | ||||||
| chr8:41697971
|
C | T | 1 | a0004c0044t0004g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2637+72G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697971 | ||||||
| chr8:41698218
|
C | T | 10 | a0003c0014t0002g0209a0003c0014t0008g0094a0003c0014t0008g0095others(7): Show | 10 | HG00639.hp1 HG02818.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.2559-97G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698218 | ||||||
| chr8:41698222
|
A | G | 199 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(196): Show | 200 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.2559-101T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698222 | ||||||
| chr8:41698286
|
A | G | 34 | a0001c0002t0009g0098a0001c0005t0010g0019a0001c0005t0028g0112others(31): Show | 34 | HG00639.hp1 HG01106.hp2 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.2559-165T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698286 | ||||||
| chr8:41698292
|
C | T | 16 | a0001c0002t0009g0098a0001c0006t0001g0267a0001c0012t0005g0103others(13): Show | 16 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.2559-171G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698292 | ||||||
| chr8:41698388
|
C | G | 1 | a0001c0004t0002g0247 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2559-267G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698388 | ||||||
| chr8:41698407
|
T | G | 2 | a0001c0005t0010g0019a0009c0047t0002g0016 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2559-286A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698407 | ||||||
| chr8:41698417
|
T | C | 1 | a0001c0004t0002g0271 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2559-296A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698417 | ||||||
| chr8:41698436
|
C | T | 192 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(189): Show | 193 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.2559-315G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698436 | ||||||
| chr8:41698587
|
T | C | 1 | a0002c0007t0007g0025 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2559-466A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698587 | ||||||
| chr8:41698600
|
C | T | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2559-479G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698600 | ||||||
| chr8:41698680
|
T | C | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2559-559A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698680 | ||||||
| chr8:41698697
|
G | A | 1 | a0001c0013t0001g0037 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2559-576C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698697 | ||||||
| chr8:41698757
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0223 | 2 | NA18988.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.2559-636C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698757 | ||||||
| chr8:41698801
|
A | AT | 65 | a0001c0003t0001g0049a0001c0003t0001g0057a0001c0003t0001g0058others(62): Show | 65 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.2558+650dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698801 | ||||||
| chr8:41698801
|
A | T | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2558+651T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698801 | ||||||
| chr8:41698887
|
C | T | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2558+565G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698887 | ||||||
| chr8:41698962
|
A | ATTTTT | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2558+485_2558+489d others(7): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698962 | ||||||
| chr8:41699091
|
A | G | 77 | a0001c0003t0001g0049a0001c0003t0001g0057a0001c0003t0001g0058others(74): Show | 77 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.2558+361T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41699091 | ||||||
| chr8:41699185
|
G | A | 3 | a0005c0021t0002g0115a0005c0021t0002g0133a0005c0035t0001g0132 | 3 | HG02280.hp1 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2558+267C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41699185 | ||||||
| chr8:41699218
|
G | A | 1 | a0004c0044t0004g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2558+234C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41699218 | ||||||
| chr8:41699233
|
G | A | 4 | a0001c0006t0018g0117a0001c0017t0005g0116a0001c0017t0005g0119others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2558+219C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41699233 | ||||||
| chr8:41699255
|
C | T | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2558+197G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41699255 | ||||||
| chr8:41699274
|
G | A | 1 | a0001c0005t0002g0010 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2558+178C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41699274 | ||||||
| chr8:41699324
|
C | T | 12 | a0001c0005t0010g0019a0003c0014t0002g0209a0003c0014t0008g0094others(9): Show | 12 | HG00639.hp1 HG02818.hp2 HG02976.hp2 others(9): Show |
intron_variant | MODIFIER | c.2558+128G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41699324 | ||||||
| chr8:41699336
|
C | T | 1 | a0001c0005t0003g0032 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2558+116G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41699336 | ||||||
| chr8:41699368
|
T | C | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2558+84A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41699368 | ||||||
| chr8:41699578
|
G | A | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2462-30C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41699578 | ||||||
| chr8:41699583
|
A | G | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2462-35T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41699583 | ||||||
| chr8:41699631
|
G | A | 1 | a0001c0003t0001g0093 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2462-83C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41699631 | ||||||
| chr8:41699946
|
G | A | 18 | a0001c0002t0009g0098a0001c0012t0005g0103a0001c0012t0006g0085others(15): Show | 18 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.2462-398C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41699946 | ||||||
| chr8:41700000
|
T | C | 80 | a0001c0003t0001g0049a0001c0003t0001g0057a0001c0003t0001g0058others(77): Show | 80 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.2462-452A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41700000 | ||||||
| chr8:41700096
|
C | T | 1 | a0001c0001t0023g0081 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2462-548G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41700096 | ||||||
| chr8:41700364
|
C | G | 1 | a0014c0055t0006g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2462-816G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41700364 | ||||||
| chr8:41700519
|
A | G | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2462-971T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41700519 | ||||||
| chr8:41700577
|
C | A | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2461+973G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41700577 | ||||||
| chr8:41700648
|
T | C | 2 | a0001c0005t0028g0112a0001c0005t0029g0111 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2461+902A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41700648 | ||||||
| chr8:41700741
|
T | C | 3 | a0002c0007t0007g0021a0002c0007t0007g0025a0002c0007t0007g0028 | 3 | HG02258.hp1 HG03540.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2461+809A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41700741 | ||||||
| chr8:41700751
|
T | G | 114 | a0001c0002t0009g0098a0001c0003t0001g0049a0001c0003t0001g0057others(111): Show | 114 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.2461+799A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41700751 | ||||||
| chr8:41700814
|
G | T | 3 | a0003c0015t0003g0137a0003c0015t0003g0220a0003c0015t0003g0250 | 3 | NA18950.hp2 NA19010.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.2461+736C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41700814 | ||||||
| chr8:41700942
|
A | C | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2461+608T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41700942 | ||||||
| chr8:41700943
|
T | A | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2461+607A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41700943 | ||||||
| chr8:41700958
|
G | A | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2461+592C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41700958 | ||||||
| chr8:41701168
|
T | A | 10 | a0003c0014t0002g0209a0003c0014t0008g0094a0003c0014t0008g0095others(7): Show | 10 | HG00639.hp1 HG02818.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.2461+382A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41701168 | ||||||
| chr8:41701264
|
C | T | 4 | a0001c0005t0001g0228a0001c0005t0001g0238a0001c0005t0002g0190others(1): Show | 4 | HG00408.hp2 HG02071.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.2461+286G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41701264 | ||||||
| chr8:41701284
|
C | T | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2461+266G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41701284 | ||||||
| chr8:41701380
|
T | G | 115 | a0001c0002t0001g0168a0001c0002t0009g0098a0001c0003t0001g0049others(112): Show | 115 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.2461+170A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41701380 | ||||||
| chr8:41701436
|
T | C | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2461+114A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41701436 | ||||||
| chr8:41701664
|
C | T | 5 | a0004c0011t0001g0186a0004c0011t0001g0187a0004c0011t0002g0084others(2): Show | 5 | HG02559.hp1 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2389-42G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 21/42 | chr8 | 41701664 | ||||||
| chr8:41701666
|
CA | C | 12 | a0001c0005t0010g0019a0003c0014t0002g0209a0003c0014t0008g0094others(9): Show | 12 | HG00639.hp1 HG02818.hp2 HG02976.hp2 others(9): Show |
intron_variant | MODIFIER | c.2389-45delT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 21/42 | chr8 | 41701666 | ||||||
| chr8:41701766
|
C | G | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2389-144G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 21/42 | chr8 | 41701766 | ||||||
| chr8:41701841
|
C | G | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2388+211G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 21/42 | chr8 | 41701841 | ||||||
| chr8:41701874
|
C | T | 1 | a0012c0045t0025g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2388+178G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 21/42 | chr8 | 41701874 | ||||||
| chr8:41701914
|
C | T | 1 | a0001c0038t0002g0200 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2388+138G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 21/42 | chr8 | 41701914 | ||||||
| chr8:41701952
|
C | G | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2388+100G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 21/42 | chr8 | 41701952 | ||||||
| chr8:41701962
|
G | C | 1 | a0002c0039t0010g0018 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2388+90C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 21/42 | chr8 | 41701962 | ||||||
| chr8:41702164
|
G | A | 5 | a0004c0011t0001g0186a0004c0011t0001g0187a0004c0011t0002g0084others(2): Show | 5 | HG02559.hp1 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2296-20C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41702164 | ||||||
| chr8:41702179
|
G | T | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2296-35C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41702179 | ||||||
| chr8:41702251
|
C | T | 1 | a0001c0001t0002g0092 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2296-107G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41702251 | ||||||
| chr8:41702409
|
C | T | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2296-265G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41702409 | ||||||
| chr8:41702825
|
T | TTG | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2296-683_2296-682d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41702825 | ||||||
| chr8:41702881
|
G | A | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2296-737C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41702881 | ||||||
| chr8:41702986
|
A | AT | 15 | a0001c0003t0001g0141a0001c0005t0002g0010a0001c0005t0010g0019others(12): Show | 15 | HG00639.hp1 HG01934.hp2 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.2296-843dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41702986 | ||||||
| chr8:41702986
|
A | ATT | 5 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(2): Show | 5 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2296-844_2296-843d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41702986 | ||||||
| chr8:41703022
|
T | C | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2296-878A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703022 | ||||||
| chr8:41703204
|
A | G | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2295+837T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703204 | ||||||
| chr8:41703251
|
T | G | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2295+790A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703251 | ||||||
| chr8:41703383
|
CAT | C | 8 | a0001c0005t0028g0112a0001c0005t0029g0111a0001c0013t0001g0027others(5): Show | 8 | HG02895.hp2 HG02897.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.2295+656_2295+657d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703383 | ||||||
| chr8:41703400
|
A | ATGTGTGT others(1): Show |
4 | a0001c0006t0018g0117a0001c0017t0005g0116a0001c0017t0005g0119others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2295+633_2295+640d others(10): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703400 | ||||||
| chr8:41703400
|
A | G | 1 | a0001c0002t0002g0227 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2295+641T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703400 | ||||||
| chr8:41703420
|
G | A | 2 | a0001c0005t0010g0019a0009c0047t0002g0016 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2295+621C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703420 | ||||||
| chr8:41703420
|
G | GTA | 18 | a0001c0002t0009g0098a0001c0012t0005g0103a0001c0012t0006g0085others(15): Show | 18 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.2295+620_2295+621i others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703420 | ||||||
| chr8:41703420
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0160 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2295+620_2295+621i others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703420 | ||||||
| chr8:41703420
|
G | GTATATAT others(5): Show |
1 | a0001c0012t0001g0138 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2295+620_2295+621i others(14): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703420 | ||||||
| chr8:41703422
|
G | A | 16 | a0001c0001t0001g0160a0001c0001t0002g0208a0001c0005t0002g0010others(13): Show | 16 | HG01928.hp2 HG02109.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.2295+619C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | ||||||
| chr8:41703422
|
G | GTATATAT others(3): Show |
5 | a0001c0001t0002g0241a0001c0004t0002g0247a0001c0005t0003g0032others(2): Show | 5 | HG02280.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2295+609_2295+618d others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | ||||||
| chr8:41703422
|
G | GTATATAT others(5): Show |
1 | a0001c0022t0002g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2295+607_2295+618d others(14): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | ||||||
| chr8:41703422
|
G | GTATATAT others(7): Show |
8 | a0001c0001t0001g0217a0001c0001t0002g0063a0001c0001t0002g0152others(5): Show | 8 | HG00099.hp1 HG00735.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.2295+605_2295+618d others(16): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | ||||||
| chr8:41703422
|
G | GTATATAT others(9): Show |
3 | a0001c0001t0002g0020a0001c0001t0002g0216a0001c0034t0002g0157 | 3 | HG03516.hp2 NA19087.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2295+603_2295+618d others(18): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | ||||||
| chr8:41703422
|
G | GTATATAT others(11): Show |
1 | a0001c0001t0002g0222 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2295+601_2295+618d others(20): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | ||||||
| chr8:41703422
|
G | GTATATAT others(13): Show |
1 | a0001c0001t0002g0234 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2295+599_2295+618d others(22): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | ||||||
| chr8:41703422
|
G | GTGTATAT others(3): Show |
3 | a0001c0004t0002g0271a0001c0029t0001g0253a0013c0041t0012g0174 | 3 | HG01123.hp2 HG02602.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.2295+618_2295+619i others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | ||||||
| chr8:41703422
|
G | GTGTATAT others(5): Show |
1 | a0001c0028t0003g0053 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2295+618_2295+619i others(14): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | ||||||
| chr8:41703422
|
G | GTGTATAT others(19): Show |
1 | a0001c0001t0001g0148 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2295+618_2295+619i others(28): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | ||||||
| chr8:41703422
|
G | GTGTGTAT others(1): Show |
6 | a0001c0002t0001g0168a0001c0002t0003g0079a0001c0002t0003g0080others(3): Show | 6 | HG01192.hp2 HG02723.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.2295+618_2295+619i others(10): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | ||||||
| chr8:41703422
|
G | GTGTGTAT others(3): Show |
26 | a0001c0002t0001g0031a0001c0002t0001g0048a0001c0002t0001g0050others(23): Show | 27 | HG00140.hp2 HG00408.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.2295+618_2295+619i others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | ||||||
| chr8:41703422
|
G | GTGTGTAT others(5): Show |
10 | a0001c0002t0001g0127a0001c0002t0001g0134a0001c0002t0009g0130others(7): Show | 10 | HG00733.hp1 HG00741.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.2295+618_2295+619i others(14): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | ||||||
| chr8:41703422
|
G | GTGTGTAT others(9): Show |
3 | a0001c0002t0001g0135a0001c0019t0002g0239a0001c0026t0001g0167 | 3 | HG00438.hp1 HG02004.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.2295+618_2295+619i others(18): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | ||||||
| chr8:41703422
|
G | GTGTGTGT others(3): Show |
1 | a0001c0002t0002g0227 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2295+618_2295+619i others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | ||||||
| chr8:41703422
|
G | GTGTGTGT others(5): Show |
2 | a0001c0002t0002g0180a0001c0002t0002g0192 | 2 | HG04115.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.2295+618_2295+619i others(14): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | ||||||
| chr8:41703422
|
GTA | G | 8 | a0001c0005t0004g0030a0001c0005t0004g0042a0001c0005t0004g0043others(5): Show | 8 | HG01167.hp1 HG01891.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.2295+617_2295+618d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | ||||||
| chr8:41703422
|
GTATA | G | 11 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0001t0001g0214others(8): Show | 11 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(8): Show |
intron_variant | MODIFIER | c.2295+615_2295+618d others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | ||||||
| chr8:41703422
|
GTATATA | G | 9 | a0001c0001t0001g0191a0001c0001t0001g0226a0001c0005t0001g0055others(6): Show | 9 | HG01123.hp1 HG02071.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.2295+613_2295+618d others(8): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | ||||||
| chr8:41703422
|
GTATATAT others(9): Show |
G | 1 | a0001c0001t0002g0110 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2295+603_2295+618d others(18): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | ||||||
| chr8:41703424
|
A | G | 49 | a0001c0001t0001g0242a0001c0002t0001g0144a0001c0002t0001g0185others(46): Show | 49 | HG00423.hp2 HG00438.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.2295+617T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703424 | ||||||
| chr8:41703426
|
A | G | 12 | a0001c0002t0001g0185a0001c0010t0002g0056a0001c0010t0003g0002others(9): Show | 12 | HG00738.hp1 HG02071.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.2295+615T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703426 | ||||||
| chr8:41703428
|
A | G | 2 | a0001c0001t0002g0077a0001c0005t0002g0190 | 2 | HG00408.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.2295+613T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703428 | ||||||
| chr8:41703446
|
A | T | 1 | a0001c0005t0002g0010 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2295+595T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703446 | ||||||
| chr8:41703447
|
TATA | T | 8 | a0001c0003t0001g0064a0001c0003t0001g0136a0001c0003t0001g0139others(5): Show | 8 | HG01081.hp2 HG01099.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.2295+591_2295+593d others(5): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703447 | ||||||
| chr8:41703448
|
A | ATTT | 5 | a0001c0005t0010g0019a0003c0015t0003g0137a0003c0015t0003g0220others(2): Show | 5 | HG03139.hp2 HG03195.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.2295+592_2295+593i others(5): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703448 | ||||||
| chr8:41703448
|
A | T | 4 | a0001c0005t0002g0010a0001c0013t0001g0027a0001c0013t0001g0037others(1): Show | 4 | HG02572.hp1 HG02717.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2295+593T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703448 | ||||||
| chr8:41703448
|
ATAT | A | 8 | a0001c0001t0002g0161a0001c0003t0001g0058a0001c0003t0001g0169others(5): Show | 8 | HG00738.hp1 HG02965.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.2295+590_2295+592d others(5): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703448 | ||||||
| chr8:41703450
|
A | AT | 7 | a0001c0002t0001g0166a0001c0002t0001g0173a0001c0002t0001g0183others(4): Show | 8 | HG00438.hp1 HG00735.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.2295+590dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
A | ATATATAT others(4): Show |
12 | a0001c0004t0002g0126a0001c0004t0002g0149a0001c0004t0002g0195others(9): Show | 12 | HG00438.hp2 HG01069.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.2295+590_2295+591i others(13): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
A | ATATATAT others(6): Show |
5 | a0001c0001t0002g0254a0001c0004t0002g0249a0001c0004t0002g0251others(2): Show | 5 | HG02717.hp1 HG03834.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.2295+590_2295+591i others(15): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
A | ATATATAT others(8): Show |
2 | a0001c0001t0002g0009a0001c0008t0002g0213 | 2 | HG03209.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.2295+590_2295+591i others(17): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0002g0024 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2295+590_2295+591i others(19): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
A | ATATATAT others(35): Show |
1 | a0002c0007t0007g0023 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2295+590_2295+591i others(44): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0002g0125 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2295+590_2295+591i others(28): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
A | ATATATAT others(27): Show |
1 | a0002c0007t0007g0025 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2295+590_2295+591i others(36): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
A | ATATATAT others(23): Show |
1 | a0002c0057t0005g0269 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2295+590_2295+591i others(32): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
A | ATATATAT others(26): Show |
1 | a0002c0007t0001g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2295+590_2295+591i others(35): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
A | ATATATAT others(19): Show |
1 | a0002c0007t0021g0118 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2295+590_2295+591i others(28): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
A | ATATATAT others(22): Show |
1 | a0002c0007t0001g0040 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2295+590_2295+591i others(31): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
A | ATATATAT others(9): Show |
5 | a0001c0001t0002g0090a0001c0001t0002g0176a0001c0001t0013g0091others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.2295+590_2295+591i others(18): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
A | ATATATAT others(19): Show |
1 | a0001c0012t0005g0103 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2295+590_2295+591i others(28): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
A | ATATATAT others(20): Show |
2 | a0001c0002t0009g0098a0004c0020t0001g0034 | 2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2295+590_2295+591i others(29): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
A | ATATATAT others(21): Show |
1 | a0004c0020t0001g0033 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2295+590_2295+591i others(30): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
A | ATATATAT others(22): Show |
1 | a0002c0007t0027g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2295+590_2295+591i others(31): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
A | ATATATAT others(17): Show |
2 | a0001c0012t0006g0085a0001c0012t0006g0099 | 2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2295+590_2295+591i others(26): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
A | ATATATAT others(18): Show |
1 | a0004c0020t0001g0036 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2295+590_2295+591i others(27): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0088 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2295+590_2295+591i others(15): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
A | ATATATAT others(16): Show |
1 | a0014c0055t0006g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2295+590_2295+591i others(25): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
A | ATATATAT others(19): Show |
1 | a0002c0007t0007g0021 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2295+590_2295+591i others(28): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
A | ATATATAT others(4): Show |
3 | a0001c0004t0002g0244a0001c0008t0002g0194a0001c0008t0015g0196 | 3 | HG01515.hp1 HG01517.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.2295+590_2295+591i others(13): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
A | ATATATAT others(16): Show |
1 | a0001c0056t0003g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2295+590_2295+591i others(25): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
A | ATATATAT others(4): Show |
1 | a0001c0004t0002g0193 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2295+590_2295+591i others(13): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
A | ATATATAT others(15): Show |
1 | a0002c0007t0007g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2295+590_2295+591i others(24): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
A | T | 24 | a0001c0001t0001g0148a0001c0002t0001g0178a0001c0005t0001g0055others(21): Show | 24 | HG01123.hp1 HG01123.hp2 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.2295+591T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
AT | A | 10 | a0001c0001t0002g0201a0001c0002t0001g0150a0001c0005t0004g0011others(7): Show | 10 | HG01175.hp2 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.2295+590delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703450
|
ATTT | A | 25 | a0001c0001t0002g0272a0001c0003t0001g0057a0001c0003t0001g0060others(22): Show | 25 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.2295+588_2295+590d others(5): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | ||||||
| chr8:41703451
|
T | TA | 32 | a0001c0002t0001g0031a0001c0002t0001g0048a0001c0002t0001g0050others(29): Show | 32 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.2295+589_2295+590i others(3): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703451 | ||||||
| chr8:41703451
|
T | TATA | 4 | a0003c0014t0008g0094a0004c0011t0002g0084a0004c0011t0002g0096others(1): Show | 4 | HG02559.hp1 HG03195.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.2295+589_2295+590i others(5): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703451 | ||||||
| chr8:41703451
|
T | TATATATA others(4): Show |
5 | a0001c0002t0001g0144a0001c0004t0001g0109a0001c0004t0001g0159others(2): Show | 5 | HG00741.hp2 HG01243.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2295+589_2295+590i others(13): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703451 | ||||||
| chr8:41703451
|
T | TATATATA others(6): Show |
4 | a0001c0001t0002g0151a0001c0001t0002g0205a0001c0001t0002g0260others(1): Show | 4 | HG02683.hp1 NA18612.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.2295+589_2295+590i others(15): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703451 | ||||||
| chr8:41703451
|
T | TATATATA others(10): Show |
2 | a0001c0001t0001g0242a0001c0004t0002g0224 | 2 | HG01168.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.2295+589_2295+590i others(19): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703451 | ||||||
| chr8:41703452
|
T | A | 9 | a0001c0001t0001g0160a0001c0001t0002g0208a0001c0002t0001g0168others(6): Show | 9 | HG01928.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2295+589A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703452 | ||||||
| chr8:41703453
|
T | A | 14 | a0001c0002t0001g0121a0001c0003t0001g0049a0001c0004t0002g0154others(11): Show | 14 | HG00140.hp2 HG02040.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.2295+588A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703453 | ||||||
| chr8:41703454
|
T | A | 3 | a0001c0005t0003g0032a0004c0011t0001g0186a0004c0011t0001g0187 | 3 | HG02280.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2295+587A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703454 | ||||||
| chr8:41703455
|
T | A | 3 | a0001c0001t0002g0272a0001c0003t0001g0062a0001c0003t0001g0158 | 3 | HG00099.hp2 NA18969.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.2295+586A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703455 | ||||||
| chr8:41703471
|
C | G | 63 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(60): Show | 63 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.2295+570G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703471 | ||||||
| chr8:41703545
|
G | A | 1 | a0001c0005t0001g0257 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2295+496C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703545 | ||||||
| chr8:41703663
|
T | A | 110 | a0001c0002t0009g0098a0001c0003t0001g0049a0001c0003t0001g0057others(107): Show | 110 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.2295+378A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703663 | ||||||
| chr8:41703865
|
G | A | 50 | a0001c0002t0001g0031a0001c0002t0001g0048a0001c0002t0001g0050others(47): Show | 51 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.2295+176C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703865 | ||||||
| chr8:41703869
|
A | C | 1 | a0001c0010t0003g0189 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2295+172T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703869 | ||||||
| chr8:41703928
|
C | A | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2295+113G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703928 | ||||||
| chr8:41703967
|
C | T | 1 | a0001c0034t0002g0157 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2295+74G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703967 | ||||||
| chr8:41704268
|
A | C | 1 | a0001c0032t0003g0105 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2196+106T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 19/42 | chr8 | 41704268 | ||||||
| chr8:41704511
|
G | C | 4 | a0001c0006t0018g0117a0001c0017t0005g0116a0001c0017t0005g0119others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2098-39C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41704511 | ||||||
| chr8:41704563
|
C | T | 1 | a0013c0041t0012g0174 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2098-91G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41704563 | ||||||
| chr8:41704723
|
G | A | 6 | a0001c0010t0002g0056a0001c0010t0003g0002a0001c0010t0003g0114others(3): Show | 6 | HG02071.hp2 HG02074.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.2098-251C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41704723 | ||||||
| chr8:41704744
|
G | A | 1 | a0007c0033t0001g0108 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2098-272C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41704744 | ||||||
| chr8:41704849
|
A | T | 10 | a0001c0005t0004g0042a0001c0013t0001g0027a0001c0013t0001g0037others(7): Show | 10 | HG02280.hp1 HG02559.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.2098-377T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41704849 | ||||||
| chr8:41705034
|
G | T | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2098-562C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41705034 | ||||||
| chr8:41705049
|
T | C | 1 | a0001c0001t0002g0110 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2098-577A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41705049 | ||||||
| chr8:41705170
|
G | A | 2 | a0001c0001t0002g0151a0001c0001t0002g0152 | 2 | HG01952.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2098-698C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41705170 | ||||||
| chr8:41705198
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0223 | 2 | NA18988.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.2098-726C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41705198 | ||||||
| chr8:41705210
|
C | T | 18 | a0001c0002t0009g0098a0001c0012t0005g0103a0001c0012t0006g0085others(15): Show | 18 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.2098-738G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41705210 | ||||||
| chr8:41705211
|
C | T | 1 | a0007c0033t0001g0108 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2098-739G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41705211 | ||||||
| chr8:41705381
|
C | T | 3 | a0003c0015t0003g0137a0003c0015t0003g0220a0003c0015t0003g0250 | 3 | NA18950.hp2 NA19010.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.2097+762G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41705381 | ||||||
| chr8:41705731
|
G | A | 13 | a0001c0005t0001g0101a0001c0005t0003g0032a0001c0006t0001g0017others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.2097+412C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41705731 | ||||||
| chr8:41705841
|
T | G | 12 | a0001c0005t0010g0019a0003c0014t0002g0209a0003c0014t0008g0094others(9): Show | 12 | HG00639.hp1 HG02818.hp2 HG02976.hp2 others(9): Show |
intron_variant | MODIFIER | c.2097+302A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41705841 | ||||||
| chr8:41706258
|
G | A | 2 | a0001c0005t0028g0112a0001c0005t0029g0111 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1999-17C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41706258 | ||||||
| chr8:41706273
|
T | G | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1999-32A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41706273 | ||||||
| chr8:41706665
|
C | A | 3 | a0001c0001t0002g0020a0001c0001t0002g0234a0001c0037t0003g0233 | 3 | HG02258.hp2 HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1999-424G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41706665 | ||||||
| chr8:41706665
|
C | T | 1 | a0002c0007t0007g0023 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1999-424G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41706665 | ||||||
| chr8:41706909
|
G | A | 40 | a0001c0003t0001g0049a0001c0003t0001g0057a0001c0003t0001g0058others(37): Show | 40 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.1999-668C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41706909 | ||||||
| chr8:41707013
|
T | C | 80 | a0001c0003t0001g0049a0001c0003t0001g0057a0001c0003t0001g0058others(77): Show | 80 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.1999-772A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41707013 | ||||||
| chr8:41707145
|
C | T | 40 | a0001c0003t0001g0049a0001c0003t0001g0057a0001c0003t0001g0058others(37): Show | 40 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.1999-904G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41707145 | ||||||
| chr8:41707179
|
G | A | 1 | a0001c0005t0002g0010 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1999-938C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41707179 | ||||||
| chr8:41707270
|
C | T | 3 | a0001c0001t0001g0160a0001c0001t0002g0208a0001c0012t0001g0138 | 3 | HG01928.hp2 NA18747.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1999-1029G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41707270 | ||||||
| chr8:41707336
|
G | A | 1 | a0001c0002t0001g0048 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1999-1095C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41707336 | ||||||
| chr8:41707425
|
C | T | 1 | a0007c0033t0001g0108 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1999-1184G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41707425 | ||||||
| chr8:41707464
|
C | G | 1 | a0001c0046t0030g0277 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1999-1223G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41707464 | ||||||
| chr8:41707488
|
C | A | 13 | a0001c0005t0001g0101a0001c0005t0003g0032a0001c0006t0001g0017others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1999-1247G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41707488 | ||||||
| chr8:41707629
|
G | A | 1 | a0001c0003t0001g0049 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1998+1149C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41707629 | ||||||
| chr8:41707824
|
T | C | 63 | a0001c0003t0001g0049a0001c0003t0001g0057a0001c0003t0001g0058others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.1998+954A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41707824 | ||||||
| chr8:41707945
|
C | T | 7 | a0001c0005t0001g0101a0001c0005t0003g0032a0001c0006t0003g0005others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1998+833G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41707945 | ||||||
| chr8:41708051
|
G | A | 1 | a0001c0001t0002g0230 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1998+727C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708051 | ||||||
| chr8:41708063
|
C | T | 1 | a0002c0039t0010g0018 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1998+715G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708063 | ||||||
| chr8:41708064
|
G | A | 46 | a0001c0002t0001g0031a0001c0002t0001g0048a0001c0002t0001g0050others(43): Show | 47 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.1998+714C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708064 | ||||||
| chr8:41708214
|
CT | C | 20 | a0001c0001t0002g0107a0001c0002t0009g0098a0001c0003t0002g0199others(17): Show | 20 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1998+563delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708214 | ||||||
| chr8:41708223
|
T | G | 1 | a0001c0005t0002g0010 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1998+555A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708223 | ||||||
| chr8:41708260
|
T | C | 1 | a0002c0007t0021g0118 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1998+518A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708260 | ||||||
| chr8:41708281
|
T | C | 2 | a0001c0023t0001g0275a0001c0023t0001g0276 | 2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1998+497A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708281 | ||||||
| chr8:41708313
|
G | A | 1 | a0001c0010t0002g0056 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1998+465C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708313 | ||||||
| chr8:41708376
|
A | G | 1 | a0001c0006t0001g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1998+402T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708376 | ||||||
| chr8:41708439
|
G | A | 1 | a0002c0007t0021g0118 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1998+339C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708439 | ||||||
| chr8:41708464
|
G | A | 1 | a0003c0049t0001g0104 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1998+314C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708464 | ||||||
| chr8:41708511
|
T | C | 1 | a0012c0045t0025g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1998+267A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708511 | ||||||
| chr8:41708524
|
G | A | 1 | a0001c0001t0002g0009 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1998+254C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708524 | ||||||
| chr8:41708645
|
T | C | 1 | a0001c0001t0002g0125 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1998+133A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708645 | ||||||
| chr8:41708737
|
T | A | 1 | a0002c0039t0010g0018 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1998+41A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708737 | ||||||
| chr8:41708761
|
G | A | 1 | a0001c0012t0005g0103 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1998+17C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708761 | ||||||
| chr8:41709025
|
A | T | 3 | a0001c0016t0002g0006a0001c0016t0002g0007a0001c0016t0002g0008 | 3 | HG01192.hp2 HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1801-50T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41709025 | ||||||
| chr8:41709093
|
G | A | 9 | a0001c0006t0001g0017a0001c0006t0001g0039a0001c0006t0001g0264others(6): Show | 9 | HG02145.hp1 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1801-118C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41709093 | ||||||
| chr8:41709117
|
T | TAAAC | 247 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(244): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1801-146_1801-143d others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41709117 | ||||||
| chr8:41709117
|
T | TAAACAAA others(1): Show |
18 | a0001c0002t0009g0098a0001c0012t0005g0103a0001c0012t0006g0085others(15): Show | 18 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1801-150_1801-143d others(10): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41709117 | ||||||
| chr8:41709401
|
C | T | 40 | a0001c0003t0001g0049a0001c0003t0001g0057a0001c0003t0001g0058others(37): Show | 40 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.1801-426G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41709401 | ||||||
| chr8:41709564
|
A | T | 1 | a0001c0006t0001g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1801-589T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41709564 | ||||||
| chr8:41710113
|
C | T | 1 | a0001c0002t0003g0146 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1801-1138G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41710113 | ||||||
| chr8:41710131
|
G | T | 1 | a0001c0002t0009g0098 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1801-1156C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41710131 | ||||||
| chr8:41710132
|
C | CA | 76 | a0001c0002t0001g0031a0001c0002t0001g0048a0001c0002t0001g0050others(73): Show | 77 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1801-1158dupT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41710132 | ||||||
| chr8:41710134
|
T | G | 76 | a0001c0002t0001g0031a0001c0002t0001g0048a0001c0002t0001g0050others(73): Show | 77 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1801-1159A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41710134 | ||||||
| chr8:41710152
|
C | T | 2 | a0001c0019t0002g0145a0015c0053t0002g0263 | 2 | NA18960.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1801-1177G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41710152 | ||||||
| chr8:41710353
|
C | T | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1801-1378G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41710353 | ||||||
| chr8:41710577
|
T | G | 1 | a0002c0007t0007g0023 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1801-1602A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41710577 | ||||||
| chr8:41710632
|
G | A | 11 | a0003c0014t0002g0209a0003c0014t0008g0094a0003c0014t0008g0095others(8): Show | 11 | HG00639.hp1 HG01928.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1801-1657C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41710632 | ||||||
| chr8:41710640
|
C | T | 58 | a0001c0002t0001g0031a0001c0002t0001g0048a0001c0002t0001g0050others(55): Show | 59 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.1801-1665G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41710640 | ||||||
| chr8:41710657
|
C | G | 1 | a0001c0017t0005g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1801-1682G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41710657 | ||||||
| chr8:41711185
|
C | T | 1 | a0004c0044t0004g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1801-2210G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41711185 | ||||||
| chr8:41711721
|
A | G | 2 | a0001c0013t0001g0027a0001c0013t0001g0037 | 2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1800+2435T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41711721 | ||||||
| chr8:41711795
|
A | G | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1800+2361T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41711795 | ||||||
| chr8:41711844
|
C | A | 1 | a0001c0046t0030g0277 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1800+2312G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41711844 | ||||||
| chr8:41711844
|
C | T | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1800+2312G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41711844 | ||||||
| chr8:41711845
|
G | A | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1800+2311C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41711845 | ||||||
| chr8:41711856
|
G | A | 35 | a0001c0002t0009g0098a0001c0005t0010g0019a0001c0006t0018g0117others(32): Show | 35 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.1800+2300C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41711856 | ||||||
| chr8:41711870
|
G | T | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1800+2286C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41711870 | ||||||
| chr8:41711931
|
C | CT | 8 | a0001c0001t0001g0155a0001c0001t0001g0223a0001c0013t0001g0027others(5): Show | 8 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.1800+2224dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41711931 | ||||||
| chr8:41711931
|
CT | C | 49 | a0001c0001t0002g0204a0001c0003t0001g0049a0001c0003t0001g0057others(46): Show | 49 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.1800+2224delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41711931 | ||||||
| chr8:41712083
|
C | G | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1800+2073G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41712083 | ||||||
| chr8:41712221
|
G | C | 41 | a0001c0003t0001g0049a0001c0003t0001g0057a0001c0003t0001g0058others(38): Show | 41 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.1800+1935C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41712221 | ||||||
| chr8:41712294
|
C | T | 1 | a0002c0039t0010g0018 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1800+1862G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41712294 | ||||||
| chr8:41712326
|
G | A | 18 | a0001c0002t0009g0098a0001c0012t0005g0103a0001c0012t0006g0085others(15): Show | 18 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1800+1830C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41712326 | ||||||
| chr8:41712455
|
G | A | 6 | a0001c0006t0001g0017a0001c0006t0001g0039a0001c0006t0001g0264others(3): Show | 6 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1800+1701C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41712455 | ||||||
| chr8:41712457
|
A | G | 6 | a0001c0009t0002g0046a0001c0009t0002g0047a0001c0009t0002g0052others(3): Show | 6 | HG00738.hp2 HG01070.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.1800+1699T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41712457 | ||||||
| chr8:41712486
|
A | C | 1 | a0001c0001t0002g0234 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1800+1670T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41712486 | ||||||
| chr8:41712533
|
A | T | 2 | a0004c0020t0001g0033a0004c0020t0001g0034 | 2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1800+1623T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41712533 | ||||||
| chr8:41712547
|
T | C | 2 | a0001c0001t0001g0155a0001c0001t0001g0223 | 2 | NA18988.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1800+1609A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41712547 | ||||||
| chr8:41712629
|
C | T | 2 | a0001c0005t0010g0019a0009c0047t0002g0016 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1800+1527G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41712629 | ||||||
| chr8:41712904
|
A | C | 1 | a0002c0007t0007g0023 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1800+1252T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41712904 | ||||||
| chr8:41713062
|
G | A | 1 | a0001c0046t0030g0277 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1800+1094C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713062 | ||||||
| chr8:41713064
|
C | T | 1 | a0001c0004t0002g0066 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1800+1092G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713064 | ||||||
| chr8:41713171
|
C | T | 1 | a0013c0041t0012g0174 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1800+985G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713171 | ||||||
| chr8:41713223
|
C | T | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1800+933G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713223 | ||||||
| chr8:41713285
|
G | A | 4 | a0001c0006t0018g0117a0001c0017t0005g0116a0001c0017t0005g0119others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1800+871C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713285 | ||||||
| chr8:41713303
|
T | C | 1 | a0002c0039t0010g0018 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1800+853A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713303 | ||||||
| chr8:41713310
|
C | G | 30 | a0001c0002t0009g0098a0001c0005t0002g0010a0001c0005t0010g0019others(27): Show | 30 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1800+846G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713310 | ||||||
| chr8:41713310
|
C | T | 6 | a0001c0006t0001g0017a0001c0006t0001g0039a0001c0006t0001g0264others(3): Show | 6 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1800+846G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713310 | ||||||
| chr8:41713327
|
G | C | 30 | a0001c0002t0009g0098a0001c0005t0002g0010a0001c0005t0010g0019others(27): Show | 30 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1800+829C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713327 | ||||||
| chr8:41713364
|
C | T | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1800+792G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713364 | ||||||
| chr8:41713365
|
A | G | 36 | a0001c0002t0009g0098a0001c0005t0002g0010a0001c0005t0010g0019others(33): Show | 36 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1800+791T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713365 | ||||||
| chr8:41713421
|
C | T | 29 | a0001c0002t0009g0098a0001c0005t0010g0019a0001c0006t0018g0117others(26): Show | 29 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.1800+735G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713421 | ||||||
| chr8:41713508
|
C | T | 2 | a0001c0046t0030g0277a0004c0020t0001g0036 | 2 | HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1800+648G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713508 | ||||||
| chr8:41713715
|
T | C | 105 | a0001c0001t0001g0162a0001c0001t0001g0191a0001c0001t0001g0245others(102): Show | 106 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1800+441A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713715 | ||||||
| chr8:41713873
|
G | A | 1 | a0013c0041t0012g0174 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1800+283C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713873 | ||||||
| chr8:41713915
|
C | T | 102 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(99): Show | 102 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.1800+241G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713915 | ||||||
| chr8:41714284
|
C | G | 12 | a0001c0051t0008g0274a0003c0014t0002g0209a0003c0014t0008g0094others(9): Show | 12 | HG00639.hp1 HG00738.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.1702-30G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 15/42 | chr8 | 41714284 | ||||||
| chr8:41714308
|
C | G | 40 | a0001c0003t0001g0049a0001c0003t0001g0057a0001c0003t0001g0058others(37): Show | 40 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.1702-54G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 15/42 | chr8 | 41714308 | ||||||
| chr8:41714387
|
T | G | 36 | a0001c0002t0009g0098a0001c0005t0002g0010a0001c0005t0010g0019others(33): Show | 36 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1702-133A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 15/42 | chr8 | 41714387 | ||||||
| chr8:41714445
|
A | T | 40 | a0001c0003t0001g0049a0001c0003t0001g0057a0001c0003t0001g0058others(37): Show | 40 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.1702-191T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 15/42 | chr8 | 41714445 | ||||||
| chr8:41714447
|
G | A | 1 | a0001c0006t0001g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1702-193C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 15/42 | chr8 | 41714447 | ||||||
| chr8:41714583
|
G | A | 1 | a0001c0005t0002g0010 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1702-329C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 15/42 | chr8 | 41714583 | ||||||
| chr8:41714595
|
T | C | 6 | a0001c0013t0001g0027a0001c0013t0001g0037a0001c0013t0006g0123others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1702-341A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 15/42 | chr8 | 41714595 | ||||||
| chr8:41714678
|
A | G | 1 | a0003c0024t0003g0102 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1701+298T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 15/42 | chr8 | 41714678 | ||||||
| chr8:41714839
|
A | G | 2 | a0001c0005t0002g0010a0001c0005t0004g0029 | 2 | HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1701+137T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 15/42 | chr8 | 41714839 | ||||||
| chr8:41714867
|
A | G | 38 | a0001c0002t0009g0098a0001c0005t0002g0010a0001c0005t0004g0029others(35): Show | 38 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(35): Show |
intron_variant | MODIFIER | c.1701+109T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 15/42 | chr8 | 41714867 | ||||||
| chr8:41715222
|
C | T | 2 | a0001c0009t0002g0046a0001c0009t0002g0047 | 2 | HG00738.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1603-148G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 14/42 | chr8 | 41715222 | ||||||
| chr8:41715970
|
G | A | 63 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(60): Show | 63 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.1405-121C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 13/42 | chr8 | 41715970 | ||||||
| chr8:41716021
|
C | T | 1 | a0001c0005t0001g0238 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1405-172G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 13/42 | chr8 | 41716021 | ||||||
| chr8:41716039
|
C | T | 20 | a0001c0002t0009g0098a0001c0005t0010g0019a0001c0012t0005g0103others(17): Show | 20 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1405-190G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 13/42 | chr8 | 41716039 | ||||||
| chr8:41716164
|
T | G | 154 | a0001c0002t0001g0031a0001c0002t0001g0048a0001c0002t0001g0050others(151): Show | 155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1405-315A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 13/42 | chr8 | 41716164 | ||||||
| chr8:41716195
|
A | C | 1 | a0001c0001t0001g0148 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1405-346T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 13/42 | chr8 | 41716195 | ||||||
| chr8:41716355
|
C | T | 1 | a0001c0004t0002g0243 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1405-506G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 13/42 | chr8 | 41716355 | ||||||
| chr8:41716504
|
G | A | 18 | a0001c0002t0009g0098a0001c0012t0005g0103a0001c0012t0006g0085others(15): Show | 18 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1404+449C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 13/42 | chr8 | 41716504 | ||||||
| chr8:41716570
|
G | A | 4 | a0003c0015t0003g0137a0003c0015t0003g0220a0003c0015t0003g0250others(1): Show | 4 | HG03195.hp1 NA18950.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.1404+383C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 13/42 | chr8 | 41716570 | ||||||
| chr8:41716772
|
C | T | 267 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(264): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1404+181G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 13/42 | chr8 | 41716772 | ||||||
| chr8:41716914
|
C | T | 18 | a0001c0002t0009g0098a0001c0012t0005g0103a0001c0012t0006g0085others(15): Show | 18 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1404+39G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 13/42 | chr8 | 41716914 | ||||||
| chr8:41717092
|
G | C | 1 | a0001c0006t0018g0117 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1306-41C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 12/42 | chr8 | 41717092 | ||||||
| chr8:41717218
|
A | C | 275 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(272): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.1306-167T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 12/42 | chr8 | 41717218 | ||||||
| chr8:41717378
|
C | T | 1 | a0001c0001t0002g0009 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1305+226G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 12/42 | chr8 | 41717378 | ||||||
| chr8:41717580
|
G | A | 2 | a0001c0005t0010g0019a0009c0047t0002g0016 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1305+24C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 12/42 | chr8 | 41717580 | ||||||
| chr8:41717761
|
A | G | 2 | a0001c0005t0028g0112a0001c0005t0029g0111 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1207-59T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 11/42 | chr8 | 41717761 | ||||||
| chr8:41717865
|
T | C | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1207-163A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 11/42 | chr8 | 41717865 | ||||||
| chr8:41717902
|
A | C | 65 | a0001c0002t0001g0031a0001c0002t0001g0048a0001c0002t0001g0050others(62): Show | 66 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1207-200T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 11/42 | chr8 | 41717902 | ||||||
| chr8:41717902
|
A | G | 1 | a0001c0001t0002g0020 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1207-200T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 11/42 | chr8 | 41717902 | ||||||
| chr8:41717921
|
G | A | 98 | a0001c0002t0001g0031a0001c0002t0001g0048a0001c0002t0001g0050others(95): Show | 99 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1206+185C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 11/42 | chr8 | 41717921 | ||||||
| chr8:41718231
|
CA | C | 10 | a0001c0051t0008g0274a0003c0014t0002g0209a0003c0014t0008g0094others(7): Show | 10 | HG00639.hp1 HG00738.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.1108-28delT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718231 | ||||||
| chr8:41718262
|
C | T | 1 | a0001c0010t0003g0114 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1108-58G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718262 | ||||||
| chr8:41718263
|
G | A | 1 | a0001c0046t0030g0277 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1108-59C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718263 | ||||||
| chr8:41718326
|
T | C | 5 | a0004c0011t0001g0186a0004c0011t0001g0187a0004c0011t0002g0084others(2): Show | 5 | HG02559.hp1 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1108-122A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718326 | ||||||
| chr8:41718583
|
T | C | 1 | a0002c0007t0001g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1108-379A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718583 | ||||||
| chr8:41718616
|
T | G | 1 | a0001c0006t0001g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1108-412A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718616 | ||||||
| chr8:41718684
|
T | C | 1 | a0001c0003t0001g0177 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1108-480A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718684 | ||||||
| chr8:41718718
|
C | T | 2 | a0001c0001t0002g0204a0001c0001t0002g0260 | 2 | NA18948.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1108-514G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718718 | ||||||
| chr8:41718731
|
T | G | 6 | a0001c0005t0001g0101a0001c0006t0003g0005a0001c0006t0003g0013others(3): Show | 6 | HG02109.hp2 HG03041.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1108-527A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718731 | ||||||
| chr8:41718736
|
G | A | 2 | a0001c0022t0002g0231a0001c0022t0002g0232 | 2 | HG00733.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1108-532C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718736 | ||||||
| chr8:41718766
|
T | C | 2 | a0001c0005t0002g0010a0001c0005t0004g0029 | 2 | HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1108-562A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718766 | ||||||
| chr8:41718846
|
G | A | 1 | a0001c0001t0001g0160 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1108-642C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718846 | ||||||
| chr8:41718907
|
G | A | 39 | a0001c0003t0001g0049a0001c0003t0001g0057a0001c0003t0001g0058others(36): Show | 39 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.1108-703C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718907 | ||||||
| chr8:41718942
|
G | A | 2 | a0001c0005t0002g0010a0001c0005t0004g0029 | 2 | HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1107+719C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718942 | ||||||
| chr8:41719010
|
A | G | 73 | a0001c0002t0001g0031a0001c0002t0001g0048a0001c0002t0001g0050others(70): Show | 74 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1107+651T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41719010 | ||||||
| chr8:41719078
|
A | G | 1 | a0007c0033t0001g0108 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1107+583T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41719078 | ||||||
| chr8:41719101
|
G | T | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1107+560C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41719101 | ||||||
| chr8:41719228
|
A | G | 66 | a0001c0002t0001g0031a0001c0002t0001g0048a0001c0002t0001g0050others(63): Show | 67 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1107+433T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41719228 | ||||||
| chr8:41719338
|
T | A | 64 | a0001c0002t0001g0031a0001c0002t0001g0048a0001c0002t0001g0050others(61): Show | 65 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1107+323A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41719338 | ||||||
| chr8:41719397
|
G | A | 2 | a0001c0008t0002g0198a0001c0008t0002g0218 | 2 | HG00438.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.1107+264C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41719397 | ||||||
| chr8:41719425
|
C | T | 4 | a0001c0005t0001g0055a0001c0005t0001g0229a0001c0005t0001g0256others(1): Show | 4 | HG01123.hp1 HG01975.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.1107+236G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41719425 | ||||||
| chr8:41719496
|
A | G | 154 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0002t0001g0031others(151): Show | 155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1107+165T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41719496 | ||||||
| chr8:41719503
|
C | T | 3 | a0001c0016t0002g0006a0001c0016t0002g0007a0001c0016t0002g0008 | 3 | HG01192.hp2 HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1107+158G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41719503 | ||||||
| chr8:41719603
|
C | G | 37 | a0001c0002t0009g0098a0001c0006t0001g0017a0001c0006t0001g0264others(34): Show | 37 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.1107+58G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41719603 | ||||||
| chr8:41719977
|
T | C | 8 | a0001c0051t0008g0274a0001c0052t0001g0235a0003c0014t0002g0209others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.910-119A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41719977 | ||||||
| chr8:41720005
|
C | T | 8 | a0001c0051t0008g0274a0001c0052t0001g0235a0003c0014t0002g0209others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.910-147G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41720005 | ||||||
| chr8:41720016
|
C | T | 1 | a0003c0015t0003g0220 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.910-158G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41720016 | ||||||
| chr8:41720165
|
C | T | 7 | a0001c0005t0001g0101a0001c0005t0003g0032a0001c0006t0003g0005others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.910-307G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41720165 | ||||||
| chr8:41720214
|
C | T | 155 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0002t0001g0031others(152): Show | 156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.910-356G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41720214 | ||||||
| chr8:41720224
|
T | C | 267 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(264): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.910-366A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41720224 | ||||||
| chr8:41720232
|
C | T | 50 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0003t0001g0049others(47): Show | 50 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.910-374G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41720232 | ||||||
| chr8:41720351
|
G | A | 1 | a0001c0005t0001g0229 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.910-493C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41720351 | ||||||
| chr8:41720510
|
T | C | 8 | a0001c0051t0008g0274a0001c0052t0001g0235a0003c0014t0002g0209others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.910-652A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41720510 | ||||||
| chr8:41720719
|
G | A | 1 | a0001c0001t0002g0107 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.910-861C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41720719 | ||||||
| chr8:41720846
|
G | A | 8 | a0001c0051t0008g0274a0001c0052t0001g0235a0003c0014t0002g0209others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.910-988C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41720846 | ||||||
| chr8:41721203
|
A | C | 2 | a0001c0005t0002g0010a0001c0005t0004g0029 | 2 | HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.910-1345T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721203 | ||||||
| chr8:41721230
|
C | G | 35 | a0001c0004t0001g0109a0001c0004t0001g0159a0001c0004t0002g0066others(32): Show | 35 | HG00423.hp2 HG00438.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.910-1372G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721230 | ||||||
| chr8:41721322
|
C | T | 2 | a0001c0001t0002g0090a0001c0001t0013g0091 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.910-1464G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721322 | ||||||
| chr8:41721395
|
C | T | 1 | a0005c0035t0001g0132 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.910-1537G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721395 | ||||||
| chr8:41721407
|
C | A | 8 | a0001c0051t0008g0274a0001c0052t0001g0235a0003c0014t0002g0209others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.910-1549G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721407 | ||||||
| chr8:41721410
|
A | G | 38 | a0001c0004t0001g0109a0001c0004t0001g0159a0001c0004t0002g0066others(35): Show | 38 | HG00423.hp2 HG00438.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.910-1552T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721410 | ||||||
| chr8:41721569
|
A | G | 1 | a0001c0004t0001g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.909+1556T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721569 | ||||||
| chr8:41721608
|
G | A | 2 | a0001c0005t0010g0019a0009c0047t0002g0016 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.909+1517C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721608 | ||||||
| chr8:41721656
|
C | CA | 16 | a0001c0001t0001g0162a0001c0001t0002g0075a0001c0001t0002g0125others(13): Show | 16 | HG01175.hp1 HG01891.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.909+1468dupT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721656 | ||||||
| chr8:41721656
|
C | CAAAAAAA others(3): Show |
1 | a0003c0014t0008g0094 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.909+1459_909+1468d others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721656 | ||||||
| chr8:41721656
|
CA | C | 24 | a0001c0001t0001g0223a0001c0004t0002g0126a0001c0004t0024g0210others(21): Show | 24 | HG00438.hp2 HG01069.hp1 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.909+1468delT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721656 | ||||||
| chr8:41721656
|
CAAAAAAA others(5): Show |
C | 65 | a0001c0002t0001g0031a0001c0002t0001g0048a0001c0002t0001g0050others(62): Show | 66 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.909+1457_909+1468d others(14): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721656 | ||||||
| chr8:41721656
|
CAAAAAAA others(6): Show |
C | 2 | a0013c0041t0012g0174a0015c0053t0002g0263 | 2 | HG01123.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.909+1456_909+1468d others(15): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721656 | ||||||
| chr8:41721656
|
CAAAAAAA others(7): Show |
C | 9 | a0001c0001t0001g0262a0001c0003t0001g0158a0001c0006t0001g0039others(6): Show | 9 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.909+1455_909+1468d others(16): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721656 | ||||||
| chr8:41721656
|
CAAAAAAA others(8): Show |
C | 50 | a0001c0001t0001g0214a0001c0003t0001g0049a0001c0003t0001g0057others(47): Show | 50 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.909+1454_909+1468d others(17): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721656 | ||||||
| chr8:41721726
|
T | C | 8 | a0001c0006t0001g0017a0001c0006t0001g0264a0001c0006t0001g0266others(5): Show | 8 | HG02145.hp1 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.909+1399A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721726 | ||||||
| chr8:41721735
|
G | A | 8 | a0001c0051t0008g0274a0001c0052t0001g0235a0003c0014t0002g0209others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.909+1390C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721735 | ||||||
| chr8:41721880
|
A | G | 8 | a0001c0051t0008g0274a0001c0052t0001g0235a0003c0014t0002g0209others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.909+1245T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721880 | ||||||
| chr8:41721973
|
A | G | 1 | a0013c0041t0012g0174 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.909+1152T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721973 | ||||||
| chr8:41722089
|
T | A | 5 | a0004c0011t0001g0186a0004c0011t0001g0187a0004c0011t0002g0084others(2): Show | 5 | HG02559.hp1 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.909+1036A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41722089 | ||||||
| chr8:41722182
|
C | T | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.909+943G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41722182 | ||||||
| chr8:41722288
|
T | C | 1 | a0001c0005t0004g0011 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.909+837A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41722288 | ||||||
| chr8:41722308
|
C | T | 4 | a0001c0006t0018g0117a0001c0017t0005g0116a0001c0017t0005g0119others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+817G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41722308 | ||||||
| chr8:41722485
|
C | G | 2 | a0001c0005t0002g0010a0001c0005t0004g0029 | 2 | HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.909+640G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41722485 | ||||||
| chr8:41722628
|
G | A | 8 | a0001c0051t0008g0274a0001c0052t0001g0235a0003c0014t0002g0209others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.909+497C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41722628 | ||||||
| chr8:41722637
|
T | C | 8 | a0001c0051t0008g0274a0001c0052t0001g0235a0003c0014t0002g0209others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.909+488A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41722637 | ||||||
| chr8:41722667
|
C | T | 1 | a0001c0004t0002g0271 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.909+458G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41722667 | ||||||
| chr8:41722877
|
C | A | 1 | a0013c0041t0012g0174 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.909+248G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41722877 | ||||||
| chr8:41722942
|
C | G | 1 | a0001c0046t0030g0277 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.909+183G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41722942 | ||||||
| chr8:41723078
|
C | A | 1 | a0001c0001t0002g0222 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.909+47G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41723078 | ||||||
| chr8:41723089
|
T | C | 102 | a0001c0002t0001g0031a0001c0002t0001g0048a0001c0002t0001g0050others(99): Show | 103 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.909+36A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41723089 | ||||||
| chr8:41723118
|
T | C | 8 | a0001c0051t0008g0274a0001c0052t0001g0235a0003c0014t0002g0209others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.909+7A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41723118 | ||||||
| chr8:41723388
|
G | A | 41 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0003t0001g0049others(38): Show | 41 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.810+147C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 8/42 | chr8 | 41723388 | ||||||
| chr8:41723662
|
C | A | 1 | a0001c0009t0002g0069 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.712-29G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723662 | ||||||
| chr8:41723665
|
G | A | 5 | a0001c0010t0003g0002a0001c0010t0003g0114a0001c0010t0003g0189others(2): Show | 5 | HG02074.hp2 HG02080.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.712-32C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723665 | ||||||
| chr8:41723769
|
T | C | 165 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0002t0001g0031others(162): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.712-136A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723769 | ||||||
| chr8:41723778
|
T | TA | 7 | a0001c0052t0001g0235a0003c0014t0002g0209a0003c0014t0008g0094others(4): Show | 7 | HG00323.hp2 HG00639.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.712-146_712-145ins others(1): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723778 | ||||||
| chr8:41723781
|
T | A | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.712-148A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723781 | ||||||
| chr8:41723785
|
A | T | 7 | a0001c0052t0001g0235a0003c0014t0002g0209a0003c0014t0008g0094others(4): Show | 7 | HG00323.hp2 HG00639.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.712-152T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723785 | ||||||
| chr8:41723789
|
T | A | 1 | a0001c0001t0002g0092 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.712-156A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723789 | ||||||
| chr8:41723792
|
A | AT | 10 | a0001c0001t0002g0152a0001c0005t0010g0019a0001c0052t0001g0235others(7): Show | 10 | HG00323.hp2 HG00639.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.712-160dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723792 | ||||||
| chr8:41723792
|
A | T | 1 | a0014c0055t0006g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.712-159T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723792 | ||||||
| chr8:41723796
|
T | A | 5 | a0001c0006t0018g0117a0001c0017t0005g0116a0001c0017t0005g0119others(2): Show | 5 | HG00738.hp1 HG02572.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.712-163A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723796 | ||||||
| chr8:41723799
|
T | A | 11 | a0001c0003t0001g0060a0001c0003t0001g0062a0001c0003t0001g0073others(8): Show | 11 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.712-166A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723799 | ||||||
| chr8:41723812
|
C | T | 6 | a0001c0005t0001g0101a0001c0006t0003g0005a0001c0006t0003g0013others(3): Show | 6 | HG02109.hp2 HG03041.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.712-179G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723812 | ||||||
| chr8:41723829
|
G | T | 2 | a0001c0005t0010g0019a0009c0047t0002g0016 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.712-196C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723829 | ||||||
| chr8:41723883
|
G | A | 1 | a0013c0041t0012g0174 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.712-250C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723883 | ||||||
| chr8:41723887
|
T | C | 1 | a0001c0046t0030g0277 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.712-254A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723887 | ||||||
| chr8:41723938
|
C | A | 19 | a0001c0005t0002g0010a0001c0005t0004g0029a0001c0006t0018g0117others(16): Show | 19 | HG02071.hp2 HG02074.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.712-305G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723938 | ||||||
| chr8:41723951
|
G | A | 8 | a0001c0051t0008g0274a0001c0052t0001g0235a0003c0014t0002g0209others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.712-318C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723951 | ||||||
| chr8:41724021
|
C | G | 1 | a0001c0001t0002g0208 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.712-388G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41724021 | ||||||
| chr8:41724031
|
G | A | 1 | a0001c0001t0002g0272 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.712-398C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41724031 | ||||||
| chr8:41724039
|
C | T | 8 | a0001c0051t0008g0274a0001c0052t0001g0235a0003c0014t0002g0209others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.712-406G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41724039 | ||||||
| chr8:41724040
|
G | A | 2 | a0001c0005t0002g0010a0001c0005t0004g0029 | 2 | HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.712-407C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41724040 | ||||||
| chr8:41724080
|
G | A | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.711+376C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41724080 | ||||||
| chr8:41724081
|
C | A | 3 | a0001c0003t0001g0062a0001c0003t0001g0073a0001c0009t0002g0061 | 3 | HG00099.hp2 HG00639.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.711+375G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41724081 | ||||||
| chr8:41724092
|
A | G | 1 | a0001c0012t0001g0138 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.711+364T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41724092 | ||||||
| chr8:41724187
|
G | C | 2 | a0001c0026t0001g0165a0001c0026t0001g0167 | 2 | HG00438.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.711+269C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41724187 | ||||||
| chr8:41724200
|
A | T | 8 | a0001c0051t0008g0274a0001c0052t0001g0235a0003c0014t0002g0209others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.711+256T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41724200 | ||||||
| chr8:41724289
|
T | C | 11 | a0001c0010t0002g0056a0001c0010t0003g0002a0001c0010t0003g0114others(8): Show | 11 | HG02071.hp2 HG02074.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.711+167A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41724289 | ||||||
| chr8:41724423
|
C | T | 3 | a0001c0002t0003g0146a0001c0005t0001g0101a0001c0040t0001g0087 | 3 | HG03516.hp1 HG03834.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.711+33G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41724423 | ||||||
| chr8:41724576
|
G | A | 2 | a0001c0013t0001g0027a0001c0013t0001g0037 | 2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.613-22C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41724576 | ||||||
| chr8:41724644
|
C | A | 3 | a0004c0011t0002g0084a0004c0011t0002g0096a0004c0011t0002g0097 | 3 | HG02559.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.613-90G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41724644 | ||||||
| chr8:41724722
|
A | C | 1 | a0001c0004t0001g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.613-168T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41724722 | ||||||
| chr8:41724796
|
C | T | 1 | a0013c0041t0012g0174 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.613-242G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41724796 | ||||||
| chr8:41724844
|
T | G | 1 | a0001c0056t0003g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.613-290A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41724844 | ||||||
| chr8:41724892
|
G | T | 2 | a0001c0004t0002g0215a0001c0028t0003g0053 | 2 | HG02074.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.613-338C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41724892 | ||||||
| chr8:41724983
|
C | T | 4 | a0001c0006t0018g0117a0001c0017t0005g0116a0001c0017t0005g0119others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-429G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41724983 | ||||||
| chr8:41725023
|
C | A | 1 | a0001c0001t0002g0234 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.613-469G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41725023 | ||||||
| chr8:41725031
|
A | T | 2 | a0001c0003t0001g0064a0002c0057t0005g0269 | 2 | HG01891.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.613-477T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41725031 | ||||||
| chr8:41725352
|
G | A | 1 | a0003c0015t0003g0137 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.612+409C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41725352 | ||||||
| chr8:41725409
|
C | T | 1 | a0001c0010t0003g0002 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.612+352G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41725409 | ||||||
| chr8:41725451
|
G | C | 1 | a0001c0002t0001g0135 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.612+310C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41725451 | ||||||
| chr8:41725513
|
T | G | 1 | a0001c0004t0002g0066 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.612+248A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41725513 | ||||||
| chr8:41725684
|
G | A | 7 | a0001c0052t0001g0235a0003c0014t0002g0209a0003c0014t0008g0094others(4): Show | 7 | HG00323.hp2 HG00639.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.612+77C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41725684 | ||||||
| chr8:41725697
|
C | T | 8 | a0001c0051t0008g0274a0001c0052t0001g0235a0003c0014t0002g0209others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.612+64G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41725697 | ||||||
| chr8:41725743
|
C | G | 19 | a0001c0002t0009g0098a0001c0012t0005g0103a0001c0012t0006g0085others(16): Show | 19 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.612+18G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41725743 | ||||||
| chr8:41726029
|
C | T | 2 | a0001c0009t0002g0046a0001c0009t0002g0047 | 2 | HG00738.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.427-83G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41726029 | ||||||
| chr8:41726037
|
C | G | 1 | a0001c0006t0001g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.427-91G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41726037 | ||||||
| chr8:41726108
|
C | A | 1 | a0001c0009t0002g0069 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.427-162G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41726108 | ||||||
| chr8:41726180
|
T | C | 1 | a0001c0005t0001g0055 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.427-234A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41726180 | ||||||
| chr8:41726196
|
T | C | 8 | a0001c0051t0008g0274a0001c0052t0001g0235a0003c0014t0002g0209others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.427-250A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41726196 | ||||||
| chr8:41726372
|
A | C | 1 | a0001c0006t0003g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.427-426T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41726372 | ||||||
| chr8:41726399
|
T | A | 8 | a0001c0003t0001g0158a0001c0006t0001g0039a0001c0013t0001g0027others(5): Show | 8 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.427-453A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41726399 | ||||||
| chr8:41726548
|
C | A | 1 | a0001c0005t0001g0238 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.427-602G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41726548 | ||||||
| chr8:41726678
|
C | T | 3 | a0001c0016t0002g0006a0001c0016t0002g0007a0001c0016t0002g0008 | 3 | HG01192.hp2 HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.426+572G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41726678 | ||||||
| chr8:41726686
|
C | T | 1 | a0004c0044t0004g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.426+564G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41726686 | ||||||
| chr8:41726723
|
T | C | 18 | a0001c0002t0009g0098a0001c0012t0005g0103a0001c0012t0006g0085others(15): Show | 18 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.426+527A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41726723 | ||||||
| chr8:41726923
|
C | T | 11 | a0001c0010t0002g0056a0001c0010t0003g0002a0001c0010t0003g0114others(8): Show | 11 | HG02071.hp2 HG02074.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.426+327G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41726923 | ||||||
| chr8:41727046
|
G | A | 1 | a0001c0003t0001g0136 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.426+204C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41727046 | ||||||
| chr8:41727055
|
C | T | 1 | a0001c0058t0022g0089 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.426+195G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41727055 | ||||||
| chr8:41727124
|
C | T | 1 | a0001c0001t0002g0024 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.426+126G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41727124 | ||||||
| chr8:41727618
|
C | A | 2 | a0001c0005t0028g0112a0001c0005t0029g0111 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.328-270G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 4/42 | chr8 | 41727618 | ||||||
| chr8:41727677
|
C | T | 3 | a0001c0002t0001g0166a0001c0002t0001g0173a0001c0002t0001g0178 | 3 | NA18972.hp2 NA18986.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.327+231G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 4/42 | chr8 | 41727677 | ||||||
| chr8:41727820
|
C | T | 2 | a0001c0002t0001g0248a0001c0019t0002g0239 | 2 | NA18612.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.327+88G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 4/42 | chr8 | 41727820 | ||||||
| chr8:41727839
|
G | A | 2 | a0001c0005t0002g0003a0001c0005t0013g0004 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.327+69C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 4/42 | chr8 | 41727839 | ||||||
| chr8:41727866
|
T | G | 47 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0003t0001g0049others(44): Show | 47 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.327+42A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 4/42 | chr8 | 41727866 | ||||||
| chr8:41727905
|
T | C | 1 | a0001c0046t0030g0277 | 1 | HG02723.hp2 | splice_region_variant&intron_variant | LOW | c.327+3A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 4/42 | chr8 | 41727905 | ||||||
| chr8:41728053
|
C | T | 150 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0002t0001g0031others(147): Show | 151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.229-47G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728053 | ||||||
| chr8:41728059
|
G | A | 41 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0003t0001g0049others(38): Show | 41 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.229-53C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728059 | ||||||
| chr8:41728061
|
G | A | 8 | a0001c0051t0008g0274a0001c0052t0001g0235a0003c0014t0002g0209others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.229-55C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728061 | ||||||
| chr8:41728115
|
A | G | 1 | a0001c0001t0002g0272 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.229-109T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728115 | ||||||
| chr8:41728319
|
G | A | 1 | a0003c0015t0003g0220 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.229-313C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728319 | ||||||
| chr8:41728349
|
C | T | 2 | a0001c0003t0001g0060a0001c0003t0002g0067 | 2 | HG01255.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.229-343G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728349 | ||||||
| chr8:41728377
|
C | T | 2 | a0001c0001t0002g0204a0001c0001t0002g0260 | 2 | NA18948.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.229-371G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728377 | ||||||
| chr8:41728442
|
A | T | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.229-436T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728442 | ||||||
| chr8:41728462
|
C | T | 1 | a0001c0003t0001g0057 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.229-456G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728462 | ||||||
| chr8:41728471
|
C | A | 2 | a0001c0005t0028g0112a0001c0005t0029g0111 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.229-465G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728471 | ||||||
| chr8:41728680
|
C | A | 1 | a0005c0021t0002g0115 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.229-674G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728680 | ||||||
| chr8:41728838
|
G | A | 124 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0002t0001g0031others(121): Show | 125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.229-832C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728838 | ||||||
| chr8:41728874
|
C | G | 7 | a0001c0002t0009g0098a0002c0007t0001g0038a0002c0007t0001g0040others(4): Show | 7 | HG02572.hp2 HG02630.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.229-868G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728874 | ||||||
| chr8:41728963
|
G | C | 2 | a0001c0004t0002g0211a0001c0004t0002g0219 | 2 | HG00423.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.229-957C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728963 | ||||||
| chr8:41729000
|
G | A | 1 | a0012c0045t0025g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.229-994C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41729000 | ||||||
| chr8:41729002
|
C | A | 1 | a0012c0045t0025g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.229-996G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41729002 | ||||||
| chr8:41729132
|
G | A | 1 | a0001c0001t0002g0171 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.229-1126C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41729132 | ||||||
| chr8:41729159
|
G | A | 1 | a0002c0057t0005g0269 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.229-1153C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41729159 | ||||||
| chr8:41729177
|
A | G | 3 | a0001c0002t0001g0197a0001c0002t0001g0206a0001c0002t0001g0225 | 3 | HG00408.hp1 HG02129.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.229-1171T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41729177 | ||||||
| chr8:41729232
|
T | C | 56 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0003t0001g0049others(53): Show | 56 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.229-1226A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41729232 | ||||||
| chr8:41729255
|
A | G | 56 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0003t0001g0049others(53): Show | 56 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.229-1249T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41729255 | ||||||
| chr8:41729304
|
G | T | 41 | a0001c0003t0001g0158a0001c0005t0002g0010a0001c0005t0004g0029others(38): Show | 41 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.229-1298C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41729304 | ||||||
| chr8:41729311
|
T | C | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.229-1305A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41729311 | ||||||
| chr8:41729334
|
A | C | 1 | a0001c0004t0002g0215 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.229-1328T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41729334 | ||||||
| chr8:41729910
|
T | C | 3 | a0001c0005t0028g0112a0001c0005t0029g0111a0013c0041t0012g0174 | 3 | HG01123.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.229-1904A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41729910 | ||||||
| chr8:41730208
|
G | A | 133 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0002t0001g0031others(130): Show | 134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.229-2202C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41730208 | ||||||
| chr8:41730288
|
T | A | 1 | a0001c0001t0002g0201 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.229-2282A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41730288 | ||||||
| chr8:41730326
|
T | C | 6 | a0001c0006t0018g0117a0001c0017t0005g0116a0001c0017t0005g0119others(3): Show | 6 | HG02572.hp1 HG02818.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.229-2320A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41730326 | ||||||
| chr8:41730450
|
T | C | 41 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0003t0001g0049others(38): Show | 41 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.229-2444A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41730450 | ||||||
| chr8:41730451
|
C | CT | 86 | a0001c0001t0002g0024a0001c0001t0002g0075a0001c0002t0001g0031others(83): Show | 87 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.229-2446dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41730451 | ||||||
| chr8:41730598
|
T | TCCATTGG others(3): Show |
3 | a0001c0001t0002g0020a0001c0001t0002g0234a0001c0037t0003g0233 | 3 | HG02258.hp2 HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.229-2593_229-2592i others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41730598 | ||||||
| chr8:41730668
|
A | G | 135 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0001t0002g0024others(132): Show | 136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.229-2662T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41730668 | ||||||
| chr8:41730749
|
C | T | 42 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0003t0001g0049others(39): Show | 42 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.229-2743G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41730749 | ||||||
| chr8:41730880
|
C | T | 3 | a0001c0005t0028g0112a0001c0005t0029g0111a0013c0041t0012g0174 | 3 | HG01123.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.229-2874G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41730880 | ||||||
| chr8:41731157
|
C | T | 7 | a0001c0052t0001g0235a0003c0014t0002g0209a0003c0014t0008g0094others(4): Show | 7 | HG00323.hp2 HG00639.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.228+2814G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41731157 | ||||||
| chr8:41731201
|
T | G | 1 | a0001c0002t0012g0022 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.228+2770A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41731201 | ||||||
| chr8:41731346
|
T | C | 2 | a0001c0003t0001g0062a0001c0009t0002g0061 | 2 | HG00099.hp2 HG00639.hp2 |
intron_variant | MODIFIER | c.228+2625A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41731346 | ||||||
| chr8:41731526
|
T | G | 2 | a0001c0001t0002g0009a0001c0001t0002g0125 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.228+2445A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41731526 | ||||||
| chr8:41731580
|
CT | C | 14 | a0001c0005t0004g0030a0001c0005t0004g0086a0001c0006t0018g0117others(11): Show | 14 | HG01517.hp2 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.228+2390delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41731580 | ||||||
| chr8:41731753
|
G | C | 1 | a0004c0044t0004g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.228+2218C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41731753 | ||||||
| chr8:41731779
|
G | A | 1 | a0001c0003t0001g0073 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.228+2192C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41731779 | ||||||
| chr8:41731805
|
C | T | 1 | a0007c0033t0001g0108 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.228+2166G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41731805 | ||||||
| chr8:41731817
|
G | A | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.228+2154C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41731817 | ||||||
| chr8:41731908
|
C | T | 1 | a0001c0058t0022g0089 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.228+2063G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41731908 | ||||||
| chr8:41731950
|
C | T | 2 | a0001c0003t0001g0169a0001c0003t0009g0170 | 2 | HG03704.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.228+2021G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41731950 | ||||||
| chr8:41731963
|
G | A | 1 | a0001c0001t0002g0205 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.228+2008C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41731963 | ||||||
| chr8:41732210
|
C | T | 11 | a0001c0001t0002g0234a0001c0003t0001g0158a0001c0005t0002g0010others(8): Show | 11 | HG02258.hp2 HG02717.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.228+1761G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41732210 | ||||||
| chr8:41732227
|
C | A | 5 | a0001c0006t0001g0017a0001c0006t0001g0264a0001c0006t0001g0266others(2): Show | 5 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.228+1744G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41732227 | ||||||
| chr8:41732453
|
C | A | 2 | a0001c0001t0002g0204a0001c0001t0002g0260 | 2 | NA18948.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.228+1518G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41732453 | ||||||
| chr8:41732522
|
C | T | 1 | a0001c0017t0005g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.228+1449G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41732522 | ||||||
| chr8:41732527
|
C | T | 2 | a0002c0039t0010g0018a0003c0049t0001g0104 | 2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.228+1444G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41732527 | ||||||
| chr8:41732554
|
A | G | 1 | a0001c0017t0005g0119 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.228+1417T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41732554 | ||||||
| chr8:41732569
|
C | T | 3 | a0001c0002t0001g0144a0001c0002t0001g0181a0001c0025t0011g0001 | 4 | HG00741.hp2 HG01192.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.228+1402G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41732569 | ||||||
| chr8:41732610
|
G | A | 7 | a0001c0002t0009g0098a0001c0056t0003g0026a0002c0007t0007g0021others(4): Show | 7 | HG01106.hp2 HG01243.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.228+1361C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41732610 | ||||||
| chr8:41732631
|
T | G | 1 | a0001c0003t0009g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.228+1340A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41732631 | ||||||
| chr8:41732632
|
C | T | 2 | a0001c0003t0001g0060a0001c0003t0002g0067 | 2 | HG01255.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.228+1339G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41732632 | ||||||
| chr8:41732820
|
C | T | 2 | a0001c0051t0008g0274a0002c0043t0002g0044 | 2 | HG00738.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.228+1151G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41732820 | ||||||
| chr8:41733028
|
G | A | 1 | a0002c0057t0005g0269 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.228+943C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41733028 | ||||||
| chr8:41733029
|
C | T | 39 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0003t0001g0049others(36): Show | 39 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.228+942G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41733029 | ||||||
| chr8:41733162
|
G | C | 6 | a0001c0005t0003g0032a0001c0006t0003g0005a0001c0006t0003g0013others(3): Show | 6 | HG02109.hp2 HG02280.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.228+809C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41733162 | ||||||
| chr8:41733228
|
C | T | 1 | a0002c0007t0007g0023 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.228+743G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41733228 | ||||||
| chr8:41733282
|
G | A | 1 | a0001c0003t0001g0136 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.228+689C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41733282 | ||||||
| chr8:41733473
|
G | A | 2 | a0001c0022t0002g0231a0001c0022t0002g0232 | 2 | HG00733.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.228+498C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41733473 | ||||||
| chr8:41733540
|
T | C | 14 | a0001c0001t0002g0024a0001c0005t0001g0101a0001c0005t0010g0019others(11): Show | 14 | HG02109.hp1 HG02572.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.228+431A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41733540 | ||||||
| chr8:41733712
|
G | C | 2 | a0001c0002t0001g0183a0001c0002t0001g0265 | 2 | HG00735.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.228+259C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41733712 | ||||||
| chr8:41733756
|
G | A | 39 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0003t0001g0049others(36): Show | 39 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.228+215C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41733756 | ||||||
| chr8:41733838
|
C | G | 1 | a0001c0003t0001g0158 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.228+133G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41733838 | ||||||
| chr8:41734125
|
C | T | 37 | a0001c0004t0001g0109a0001c0004t0001g0159a0001c0004t0002g0066others(34): Show | 37 | HG00423.hp2 HG00438.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.130-56G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41734125 | ||||||
| chr8:41734247
|
C | T | 4 | a0001c0003t0001g0158a0001c0013t0006g0123a0001c0013t0006g0124others(1): Show | 4 | HG03098.hp1 HG03471.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-178G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41734247 | ||||||
| chr8:41734389
|
C | CTTAATTA others(4): Show |
1 | a0001c0001t0001g0262 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.130-331_130-321dup others(11): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41734389 | ||||||
| chr8:41734733
|
G | GA | 6 | a0001c0005t0003g0032a0001c0006t0003g0005a0001c0006t0003g0013others(3): Show | 6 | HG02109.hp2 HG02280.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.130-665dupT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41734733 | ||||||
| chr8:41734761
|
G | C | 1 | a0004c0044t0004g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.130-692C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41734761 | ||||||
| chr8:41734996
|
AAAAC | A | 5 | a0001c0006t0001g0017a0001c0006t0001g0264a0001c0006t0001g0266others(2): Show | 5 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.130-931_130-928del others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41734996 | ||||||
| chr8:41735102
|
T | C | 55 | a0001c0001t0002g0110a0001c0002t0001g0031a0001c0002t0001g0048others(52): Show | 56 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.130-1033A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735102 | ||||||
| chr8:41735153
|
T | A | 1 | a0004c0044t0004g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.130-1084A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735153 | ||||||
| chr8:41735265
|
T | C | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.130-1196A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735265 | ||||||
| chr8:41735303
|
C | A | 1 | a0001c0016t0002g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.130-1234G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735303 | ||||||
| chr8:41735410
|
T | G | 1 | a0001c0017t0005g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.130-1341A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735410 | ||||||
| chr8:41735420
|
C | T | 6 | a0002c0007t0001g0038a0002c0007t0001g0040a0002c0007t0027g0035others(3): Show | 6 | HG02572.hp2 HG02630.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.130-1351G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735420 | ||||||
| chr8:41735455
|
C | T | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.130-1386G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735455 | ||||||
| chr8:41735611
|
C | G | 2 | a0001c0046t0030g0277a0002c0007t0021g0118 | 2 | HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.130-1542G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735611 | ||||||
| chr8:41735705
|
C | T | 166 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(163): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.130-1636G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735705 | ||||||
| chr8:41735791
|
G | A | 9 | a0001c0003t0001g0093a0001c0052t0001g0235a0002c0039t0010g0018others(6): Show | 9 | HG00323.hp2 HG00639.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.130-1722C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735791 | ||||||
| chr8:41735861
|
G | A | 4 | a0001c0003t0001g0158a0001c0013t0006g0123a0001c0013t0006g0124others(1): Show | 4 | HG03098.hp1 HG03471.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-1792C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735861 | ||||||
| chr8:41735863
|
G | A | 3 | a0001c0002t0001g0166a0001c0002t0001g0173a0001c0002t0001g0178 | 3 | NA18972.hp2 NA18986.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.130-1794C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735863 | ||||||
| chr8:41735915
|
AC | A | 4 | a0001c0003t0001g0158a0001c0013t0006g0123a0001c0013t0006g0124others(1): Show | 4 | HG03098.hp1 HG03471.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-1847delG | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735915 | ||||||
| chr8:41735959
|
A | AG | 276 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(273): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.130-1891dupC | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735959 | ||||||
| chr8:41735973
|
G | T | 1 | a0001c0003t0001g0049 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.130-1904C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735973 | ||||||
| chr8:41735999
|
C | T | 2 | a0001c0002t0001g0128a0001c0002t0014g0129 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.130-1930G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735999 | ||||||
| chr8:41736108
|
T | C | 1 | a0003c0024t0003g0102 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.130-2039A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41736108 | ||||||
| chr8:41736265
|
A | G | 6 | a0001c0005t0003g0032a0001c0006t0003g0005a0001c0006t0003g0013others(3): Show | 6 | HG02109.hp2 HG02280.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.130-2196T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41736265 | ||||||
| chr8:41736284
|
C | T | 39 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0003t0001g0049others(36): Show | 39 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.130-2215G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41736284 | ||||||
| chr8:41736410
|
G | T | 1 | a0001c0003t0001g0221 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.130-2341C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41736410 | ||||||
| chr8:41736436
|
G | A | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.130-2367C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41736436 | ||||||
| chr8:41736519
|
T | C | 10 | a0001c0006t0001g0017a0001c0006t0001g0264a0001c0006t0001g0266others(7): Show | 10 | HG02145.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.130-2450A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41736519 | ||||||
| chr8:41736526
|
A | T | 53 | a0001c0002t0001g0031a0001c0002t0001g0048a0001c0002t0001g0050others(50): Show | 54 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.130-2457T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41736526 | ||||||
| chr8:41736634
|
C | T | 24 | a0001c0001t0002g0024a0001c0002t0009g0098a0001c0012t0005g0103others(21): Show | 24 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.130-2565G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41736634 | ||||||
| chr8:41736665
|
T | C | 2 | a0001c0004t0002g0251a0001c0008t0002g0252 | 2 | HG03834.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.130-2596A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41736665 | ||||||
| chr8:41736741
|
G | A | 1 | a0001c0003t0001g0169 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.130-2672C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41736741 | ||||||
| chr8:41736780
|
A | G | 6 | a0001c0006t0001g0100a0001c0006t0018g0117a0001c0017t0005g0116others(3): Show | 6 | HG02572.hp1 HG02630.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.130-2711T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41736780 | ||||||
| chr8:41737110
|
A | G | 98 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0002t0001g0031others(95): Show | 99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.130-3041T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41737110 | ||||||
| chr8:41737253
|
C | G | 43 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0003t0001g0049others(40): Show | 43 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.130-3184G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41737253 | ||||||
| chr8:41737507
|
G | A | 1 | a0003c0049t0001g0104 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.130-3438C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41737507 | ||||||
| chr8:41737567
|
C | T | 1 | a0003c0015t0003g0220 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.130-3498G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41737567 | ||||||
| chr8:41737644
|
C | T | 1 | a0001c0003t0001g0158 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.130-3575G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41737644 | ||||||
| chr8:41737687
|
C | T | 7 | a0001c0006t0001g0017a0001c0006t0001g0100a0001c0006t0018g0117others(4): Show | 7 | HG02572.hp1 HG02630.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.130-3618G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41737687 | ||||||
| chr8:41737773
|
G | T | 1 | a0001c0001t0001g0262 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.130-3704C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41737773 | ||||||
| chr8:41737817
|
T | C | 30 | a0001c0001t0002g0024a0001c0002t0009g0098a0001c0005t0003g0032others(27): Show | 30 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.130-3748A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41737817 | ||||||
| chr8:41737879
|
G | A | 1 | a0001c0004t0002g0249 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.130-3810C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41737879 | ||||||
| chr8:41738010
|
C | T | 1 | a0001c0003t0001g0073 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.130-3941G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41738010 | ||||||
| chr8:41738077
|
CAGAAG | C | 6 | a0001c0010t0002g0056a0001c0010t0003g0002a0001c0010t0003g0114others(3): Show | 6 | HG02071.hp2 HG02074.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.130-4013_130-4009d others(7): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41738077 | ||||||
| chr8:41738095
|
T | C | 147 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(144): Show | 148 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.130-4026A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41738095 | ||||||
| chr8:41738202
|
T | TGTATCTG others(1): Show |
134 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(131): Show | 135 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.130-4134_130-4133i others(10): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41738202 | ||||||
| chr8:41738205
|
T | C | 1 | a0007c0033t0001g0108 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.130-4136A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41738205 | ||||||
| chr8:41738236
|
T | C | 1 | a0001c0040t0001g0087 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.130-4167A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41738236 | ||||||
| chr8:41738258
|
C | T | 1 | a0001c0003t0019g0068 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.130-4189G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41738258 | ||||||
| chr8:41738415
|
G | A | 2 | a0001c0002t0001g0128a0001c0002t0014g0129 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.130-4346C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41738415 | ||||||
| chr8:41738645
|
T | A | 7 | a0001c0006t0001g0264a0001c0006t0001g0266a0001c0006t0001g0267others(4): Show | 7 | HG02145.hp1 HG02280.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.130-4576A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41738645 | ||||||
| chr8:41738902
|
A | G | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.130-4833T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41738902 | ||||||
| chr8:41738962
|
A | G | 3 | a0005c0021t0002g0115a0005c0021t0002g0133a0005c0035t0001g0132 | 3 | HG02280.hp1 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.130-4893T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41738962 | ||||||
| chr8:41739199
|
G | T | 35 | a0001c0004t0001g0109a0001c0004t0001g0159a0001c0004t0002g0070others(32): Show | 35 | HG00423.hp2 HG01168.hp1 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.130-5130C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739199 | ||||||
| chr8:41739215
|
C | T | 5 | a0001c0056t0003g0026a0002c0007t0007g0021a0002c0007t0007g0025others(2): Show | 5 | HG01106.hp2 HG02258.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.130-5146G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739215 | ||||||
| chr8:41739260
|
T | A | 1 | a0003c0024t0001g0273 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.130-5191A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739260 | ||||||
| chr8:41739325
|
T | C | 6 | a0001c0010t0002g0056a0001c0010t0003g0002a0001c0010t0003g0114others(3): Show | 6 | HG02071.hp2 HG02074.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.130-5256A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739325 | ||||||
| chr8:41739509
|
G | GTTTTTTT others(9): Show |
1 | a0001c0003t0019g0068 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.130-5456_130-5441d others(18): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739509 | ||||||
| chr8:41739521
|
CT | C | 211 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(208): Show | 212 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.130-5453delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739521 | ||||||
| chr8:41739521
|
CTT | C | 5 | a0001c0001t0001g0162a0001c0001t0001g0242a0001c0005t0001g0101others(2): Show | 5 | HG02015.hp1 HG02630.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.130-5454_130-5453d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739521 | ||||||
| chr8:41739522
|
T | TTTTTTTT others(7): Show |
4 | a0001c0009t0002g0046a0001c0009t0002g0047a0001c0009t0002g0052others(1): Show | 4 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-5454_130-5453i others(16): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739522 | ||||||
| chr8:41739522
|
T | TTTTTTTT others(8): Show |
34 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0003t0001g0049others(31): Show | 34 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.130-5454_130-5453i others(17): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739522 | ||||||
| chr8:41739523
|
T | TTTTTTTT others(7): Show |
1 | a0001c0003t0002g0067 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.130-5455_130-5454i others(16): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739523 | ||||||
| chr8:41739614
|
T | C | 134 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(131): Show | 135 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.130-5545A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739614 | ||||||
| chr8:41739616
|
C | T | 1 | a0001c0005t0010g0019 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.130-5547G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739616 | ||||||
| chr8:41739764
|
G | A | 6 | a0001c0001t0001g0242a0001c0001t0002g0176a0001c0001t0002g0204others(3): Show | 6 | HG02015.hp1 HG04115.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.130-5695C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739764 | ||||||
| chr8:41739770
|
C | T | 1 | a0001c0009t0002g0059 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.130-5701G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739770 | ||||||
| chr8:41740050
|
C | T | 4 | a0001c0006t0003g0005a0001c0006t0003g0013a0001c0006t0003g0014others(1): Show | 4 | HG02109.hp2 HG03041.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-5981G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41740050 | ||||||
| chr8:41740162
|
A | AT | 93 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0001t0002g0024others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.130-6094dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41740162 | ||||||
| chr8:41740162
|
AT | A | 130 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(127): Show | 131 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.130-6094delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41740162 | ||||||
| chr8:41740306
|
G | A | 40 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0003t0001g0049others(37): Show | 40 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.130-6237C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41740306 | ||||||
| chr8:41740334
|
G | C | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.130-6265C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41740334 | ||||||
| chr8:41740335
|
C | T | 234 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.130-6266G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41740335 | ||||||
| chr8:41740368
|
C | T | 3 | a0001c0005t0004g0029a0001c0013t0001g0027a0001c0013t0001g0037 | 3 | HG02965.hp2 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.130-6299G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41740368 | ||||||
| chr8:41740385
|
C | G | 2 | a0001c0002t0003g0079a0001c0002t0003g0080 | 2 | HG03490.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.130-6316G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41740385 | ||||||
| chr8:41740402
|
T | C | 48 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0003t0001g0049others(45): Show | 48 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.130-6333A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41740402 | ||||||
| chr8:41740455
|
CA | C | 74 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(71): Show | 74 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.130-6387delT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41740455 | ||||||
| chr8:41740749
|
T | C | 1 | a0001c0026t0001g0167 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.130-6680A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41740749 | ||||||
| chr8:41741202
|
G | A | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.130-7133C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41741202 | ||||||
| chr8:41741494
|
C | A | 132 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(129): Show | 133 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.130-7425G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41741494 | ||||||
| chr8:41741579
|
G | GA | 133 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(130): Show | 134 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.130-7511dupT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41741579 | ||||||
| chr8:41741617
|
C | T | 6 | a0001c0010t0002g0056a0001c0010t0003g0002a0001c0010t0003g0114others(3): Show | 6 | HG02071.hp2 HG02074.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.130-7548G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41741617 | ||||||
| chr8:41741637
|
C | T | 3 | a0001c0046t0030g0277a0002c0007t0021g0118a0006c0031t0002g0255 | 3 | HG02451.hp2 HG02723.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.130-7568G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41741637 | ||||||
| chr8:41741663
|
C | T | 1 | a0001c0004t0002g0154 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.130-7594G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41741663 | ||||||
| chr8:41741721
|
C | T | 1 | a0001c0056t0003g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.130-7652G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41741721 | ||||||
| chr8:41741825
|
A | C | 6 | a0001c0005t0003g0032a0001c0006t0003g0005a0001c0006t0003g0013others(3): Show | 6 | HG02109.hp2 HG02280.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.130-7756T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41741825 | ||||||
| chr8:41741899
|
T | C | 234 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.130-7830A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41741899 | ||||||
| chr8:41741963
|
C | G | 38 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0003t0001g0049others(35): Show | 38 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.130-7894G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41741963 | ||||||
| chr8:41742042
|
G | A | 86 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0001t0002g0024others(83): Show | 86 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.130-7973C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41742042 | ||||||
| chr8:41742167
|
T | C | 1 | a0001c0001t0001g0245 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.130-8098A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41742167 | ||||||
| chr8:41742282
|
G | A | 1 | a0001c0002t0001g0121 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.130-8213C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41742282 | ||||||
| chr8:41742507
|
C | T | 2 | a0001c0003t0001g0093a0008c0050t0001g0153 | 2 | HG01496.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.130-8438G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41742507 | ||||||
| chr8:41742591
|
C | T | 3 | a0001c0005t0004g0029a0001c0013t0001g0027a0001c0013t0001g0037 | 3 | HG02965.hp2 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.130-8522G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41742591 | ||||||
| chr8:41742607
|
T | G | 50 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0003t0001g0049others(47): Show | 50 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.130-8538A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41742607 | ||||||
| chr8:41742609
|
G | A | 3 | a0001c0005t0004g0029a0001c0013t0001g0027a0001c0013t0001g0037 | 3 | HG02965.hp2 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.130-8540C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41742609 | ||||||
| chr8:41742749
|
G | A | 1 | a0001c0004t0002g0070 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.130-8680C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41742749 | ||||||
| chr8:41742839
|
C | G | 4 | a0001c0005t0002g0010a0001c0005t0010g0019a0002c0039t0010g0018others(1): Show | 4 | HG02717.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-8770G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41742839 | ||||||
| chr8:41743037
|
G | C | 234 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.130-8968C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41743037 | ||||||
| chr8:41743130
|
G | A | 148 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(145): Show | 149 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.130-9061C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41743130 | ||||||
| chr8:41743178
|
C | G | 55 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0003t0001g0049others(52): Show | 55 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.130-9109G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41743178 | ||||||
| chr8:41743303
|
G | A | 1 | a0012c0045t0025g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.130-9234C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41743303 | ||||||
| chr8:41743588
|
G | A | 1 | a0001c0001t0002g0092 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.130-9519C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41743588 | ||||||
| chr8:41743809
|
CAT | C | 55 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0003t0001g0049others(52): Show | 55 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.130-9742_130-9741d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41743809 | ||||||
| chr8:41743914
|
G | A | 2 | a0001c0046t0030g0277a0002c0007t0021g0118 | 2 | HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.130-9845C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41743914 | ||||||
| chr8:41744006
|
T | C | 133 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(130): Show | 134 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.130-9937A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744006 | ||||||
| chr8:41744167
|
C | T | 133 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(130): Show | 134 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.130-10098G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744167 | ||||||
| chr8:41744363
|
A | G | 3 | a0001c0005t0004g0029a0001c0013t0001g0027a0001c0013t0001g0037 | 3 | HG02965.hp2 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.130-10294T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744363 | ||||||
| chr8:41744536
|
C | CT | 74 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0002t0009g0098others(71): Show | 74 | HG00140.hp1 HG00738.hp2 HG01070.hp1 others(71): Show |
intron_variant | MODIFIER | c.130-10468dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744536 | ||||||
| chr8:41744536
|
C | CTT | 8 | a0001c0001t0002g0024a0001c0003t0001g0139a0001c0003t0002g0067others(5): Show | 8 | HG01978.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.130-10469_130-1046 others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744536 | ||||||
| chr8:41744536
|
CTT | C | 129 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(126): Show | 130 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.130-10469_130-1046 others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744536 | ||||||
| chr8:41744543
|
T | C | 2 | a0003c0049t0001g0104a0007c0033t0001g0108 | 2 | HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.130-10474A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744543 | ||||||
| chr8:41744597
|
T | C | 234 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.130-10528A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744597 | ||||||
| chr8:41744663
|
A | G | 1 | a0001c0002t0001g0168 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.130-10594T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744663 | ||||||
| chr8:41744684
|
G | A | 3 | a0001c0004t0002g0251a0001c0008t0002g0252a0003c0015t0003g0220 | 3 | HG03834.hp1 NA18973.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.130-10615C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744684 | ||||||
| chr8:41744691
|
C | T | 4 | a0001c0003t0001g0158a0001c0013t0006g0123a0001c0013t0006g0124others(1): Show | 4 | HG03098.hp1 HG03471.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-10622G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744691 | ||||||
| chr8:41744825
|
G | A | 4 | a0001c0006t0001g0264a0001c0006t0001g0266a0001c0006t0001g0267others(1): Show | 4 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-10756C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744825 | ||||||
| chr8:41744827
|
G | A | 1 | a0001c0013t0006g0123 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.130-10758C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744827 | ||||||
| chr8:41744839
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.130-10770G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744839 | ||||||
| chr8:41744874
|
T | C | 138 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(135): Show | 139 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.130-10805A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744874 | ||||||
| chr8:41744982
|
G | A | 7 | a0001c0005t0004g0030a0001c0006t0001g0017a0001c0006t0001g0100others(4): Show | 7 | HG02572.hp1 HG02630.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.130-10913C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744982 | ||||||
| chr8:41745047
|
A | G | 1 | a0001c0001t0001g0148 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.130-10978T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41745047 | ||||||
| chr8:41745091
|
AACAG | A | 135 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(132): Show | 136 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.130-11026_130-1102 others(8): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41745091 | ||||||
| chr8:41745150
|
G | A | 60 | a0001c0002t0001g0031a0001c0002t0001g0048a0001c0002t0001g0050others(57): Show | 61 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.130-11081C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41745150 | ||||||
| chr8:41745257
|
A | T | 60 | a0001c0002t0001g0031a0001c0002t0001g0048a0001c0002t0001g0050others(57): Show | 61 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.130-11188T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41745257 | ||||||
| chr8:41745455
|
C | T | 1 | a0001c0003t0001g0261 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.130-11386G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41745455 | ||||||
| chr8:41745489
|
A | T | 2 | a0001c0002t0001g0048a0001c0002t0001g0143 | 2 | HG01167.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.130-11420T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41745489 | ||||||
| chr8:41745895
|
G | T | 233 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(230): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.130-11826C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41745895 | ||||||
| chr8:41746028
|
G | A | 1 | a0001c0032t0003g0105 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.130-11959C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41746028 | ||||||
| chr8:41746155
|
C | G | 76 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(73): Show | 76 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.129+11881G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41746155 | ||||||
| chr8:41746705
|
C | G | 1 | a0003c0024t0003g0102 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.129+11331G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41746705 | ||||||
| chr8:41746851
|
G | A | 4 | a0001c0005t0002g0010a0001c0005t0010g0019a0002c0039t0010g0018others(1): Show | 4 | HG02717.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+11185C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41746851 | ||||||
| chr8:41746868
|
T | TA | 75 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0162others(72): Show | 75 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.129+11167dupT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41746868 | ||||||
| chr8:41746868
|
TA | T | 19 | a0001c0001t0002g0024a0001c0002t0003g0146a0001c0003t0001g0158others(16): Show | 19 | HG00639.hp2 HG01243.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.129+11167delT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41746868 | ||||||
| chr8:41747022
|
G | A | 1 | a0004c0044t0004g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.129+11014C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41747022 | ||||||
| chr8:41747220
|
T | A | 6 | a0001c0005t0003g0032a0001c0006t0003g0005a0001c0006t0003g0013others(3): Show | 6 | HG00738.hp1 HG02109.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+10816A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41747220 | ||||||
| chr8:41747542
|
T | C | 2 | a0001c0005t0004g0030a0002c0007t0021g0118 | 2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.129+10494A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41747542 | ||||||
| chr8:41747630
|
C | T | 5 | a0001c0005t0002g0010a0001c0005t0010g0019a0001c0046t0030g0277others(2): Show | 5 | HG02717.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.129+10406G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41747630 | ||||||
| chr8:41747748
|
C | T | 1 | a0001c0005t0004g0029 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.129+10288G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41747748 | ||||||
| chr8:41747769
|
G | A | 1 | a0001c0002t0009g0130 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.129+10267C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41747769 | ||||||
| chr8:41748053
|
C | A | 1 | a0001c0010t0003g0114 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.129+9983G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748053 | ||||||
| chr8:41748090
|
C | T | 1 | a0001c0003t0002g0199 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.129+9946G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748090 | ||||||
| chr8:41748114
|
T | A | 4 | a0001c0006t0001g0264a0001c0006t0001g0266a0001c0006t0001g0267others(1): Show | 4 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+9922A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748114 | ||||||
| chr8:41748119
|
G | C | 111 | a0001c0001t0001g0162a0001c0001t0001g0214a0001c0001t0001g0262others(108): Show | 112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.129+9917C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748119 | ||||||
| chr8:41748201
|
A | G | 5 | a0001c0010t0002g0056a0001c0010t0003g0114a0001c0010t0003g0189others(2): Show | 5 | HG02071.hp2 HG02074.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+9835T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748201 | ||||||
| chr8:41748312
|
C | T | 2 | a0001c0023t0001g0275a0001c0023t0001g0276 | 2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.129+9724G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748312 | ||||||
| chr8:41748435
|
T | A | 1 | a0002c0007t0007g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.129+9601A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748435 | ||||||
| chr8:41748461
|
C | T | 73 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(70): Show | 73 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.129+9575G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748461 | ||||||
| chr8:41748709
|
G | A | 7 | a0001c0006t0003g0005a0001c0006t0003g0013a0001c0006t0003g0014others(4): Show | 7 | HG01891.hp2 HG02109.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.129+9327C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748709 | ||||||
| chr8:41748771
|
T | C | 4 | a0001c0005t0001g0055a0001c0005t0001g0229a0001c0005t0001g0256others(1): Show | 4 | HG01123.hp1 HG01975.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+9265A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748771 | ||||||
| chr8:41748791
|
T | C | 5 | a0001c0005t0004g0030a0001c0005t0010g0019a0001c0006t0001g0017others(2): Show | 5 | HG02451.hp2 HG02897.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.129+9245A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748791 | ||||||
| chr8:41748801
|
T | C | 1 | a0001c0001t0002g0161 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.129+9235A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748801 | ||||||
| chr8:41748802
|
A | G | 1 | a0001c0001t0002g0161 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.129+9234T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748802 | ||||||
| chr8:41748818
|
G | A | 1 | a0001c0003t0014g0065 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.129+9218C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748818 | ||||||
| chr8:41748831
|
C | G | 1 | a0001c0003t0014g0065 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.129+9205G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748831 | ||||||
| chr8:41748832
|
A | G | 46 | a0001c0001t0002g0024a0001c0002t0009g0098a0001c0003t0014g0065others(43): Show | 46 | HG01106.hp2 HG01192.hp2 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.129+9204T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748832 | ||||||
| chr8:41748842
|
C | T | 1 | a0001c0003t0014g0065 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.129+9194G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748842 | ||||||
| chr8:41748843
|
A | G | 1 | a0001c0003t0014g0065 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.129+9193T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748843 | ||||||
| chr8:41748852
|
A | G | 3 | a0001c0002t0001g0197a0001c0002t0001g0206a0001c0002t0001g0225 | 3 | HG00408.hp1 HG02129.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.129+9184T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748852 | ||||||
| chr8:41748859
|
T | C | 2 | a0003c0024t0001g0273a0003c0049t0001g0104 | 2 | HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.129+9177A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748859 | ||||||
| chr8:41748903
|
C | T | 4 | a0001c0005t0002g0010a0001c0005t0010g0019a0002c0039t0010g0018others(1): Show | 4 | HG02717.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+9133G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748903 | ||||||
| chr8:41748952
|
A | G | 15 | a0001c0002t0001g0121a0001c0002t0001g0122a0001c0002t0001g0127others(12): Show | 15 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.129+9084T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748952 | ||||||
| chr8:41748959
|
T | C | 1 | a0001c0006t0001g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.129+9077A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748959 | ||||||
| chr8:41749000
|
C | A | 5 | a0001c0006t0003g0005a0001c0006t0003g0013a0001c0006t0003g0014others(2): Show | 5 | HG02109.hp2 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+9036G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749000 | ||||||
| chr8:41749022
|
A | G | 1 | a0012c0045t0025g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.129+9014T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749022 | ||||||
| chr8:41749034
|
C | CA | 63 | a0001c0001t0001g0162a0001c0001t0002g0024a0001c0002t0001g0031others(60): Show | 64 | HG00408.hp1 HG00438.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.129+9001dupT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749034 | ||||||
| chr8:41749034
|
C | CAA | 6 | a0001c0002t0003g0079a0001c0002t0003g0080a0001c0018t0001g0147others(3): Show | 6 | HG02895.hp1 HG03195.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.129+9000_129+9001d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749034 | ||||||
| chr8:41749226
|
A | G | 7 | a0001c0005t0002g0010a0001c0005t0004g0030a0001c0005t0010g0019others(4): Show | 7 | HG02451.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.129+8810T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749226 | ||||||
| chr8:41749295
|
C | CT | 32 | a0001c0001t0002g0176a0001c0001t0002g0222a0001c0002t0001g0121others(29): Show | 32 | HG00140.hp2 HG00438.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.129+8740dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749295 | ||||||
| chr8:41749295
|
C | CTTT | 27 | a0001c0003t0001g0049a0001c0003t0001g0057a0001c0003t0001g0058others(24): Show | 27 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.129+8738_129+8740d others(5): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749295 | ||||||
| chr8:41749295
|
CT | C | 44 | a0001c0001t0001g0155a0001c0001t0001g0191a0001c0001t0001g0214others(41): Show | 44 | HG00423.hp2 HG01168.hp1 HG01175.hp1 others(41): Show |
intron_variant | MODIFIER | c.129+8740delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749295 | ||||||
| chr8:41749390
|
C | T | 20 | a0001c0001t0002g0024a0001c0002t0009g0098a0001c0013t0001g0027others(17): Show | 20 | HG01106.hp2 HG01243.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.129+8646G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749390 | ||||||
| chr8:41749437
|
G | A | 2 | a0001c0005t0004g0030a0002c0007t0021g0118 | 2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.129+8599C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749437 | ||||||
| chr8:41749449
|
C | G | 2 | a0001c0005t0004g0030a0002c0007t0021g0118 | 2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.129+8587G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749449 | ||||||
| chr8:41749567
|
GA | G | 276 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(273): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.129+8468delT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749567 | ||||||
| chr8:41749631
|
A | G | 2 | a0001c0002t0001g0183a0001c0002t0001g0184 | 2 | HG00735.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.129+8405T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749631 | ||||||
| chr8:41749670
|
T | C | 2 | a0001c0005t0004g0030a0002c0007t0021g0118 | 2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.129+8366A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749670 | ||||||
| chr8:41749761
|
C | T | 61 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0002t0001g0031others(58): Show | 62 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.129+8275G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749761 | ||||||
| chr8:41749855
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.129+8181C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749855 | ||||||
| chr8:41749960
|
C | T | 11 | a0001c0006t0001g0100a0001c0006t0001g0264a0001c0006t0001g0266others(8): Show | 11 | HG02145.hp1 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.129+8076G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749960 | ||||||
| chr8:41750072
|
G | A | 1 | a0001c0006t0001g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.129+7964C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750072 | ||||||
| chr8:41750174
|
C | T | 268 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(265): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.129+7862G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750174 | ||||||
| chr8:41750197
|
G | A | 108 | a0001c0001t0001g0148a0001c0001t0001g0160a0001c0001t0001g0223others(105): Show | 108 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.129+7839C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750197 | ||||||
| chr8:41750339
|
G | A | 1 | a0001c0003t0001g0057 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.129+7697C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750339 | ||||||
| chr8:41750350
|
C | A | 1 | a0012c0045t0025g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.129+7686G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750350 | ||||||
| chr8:41750393
|
C | T | 33 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(30): Show | 33 | HG00423.hp2 HG01168.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.129+7643G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750393 | ||||||
| chr8:41750495
|
G | C | 11 | a0001c0006t0001g0100a0001c0006t0001g0264a0001c0006t0001g0266others(8): Show | 11 | HG02145.hp1 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.129+7541C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750495 | ||||||
| chr8:41750515
|
T | G | 1 | a0001c0006t0001g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.129+7521A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750515 | ||||||
| chr8:41750558
|
A | G | 11 | a0001c0006t0001g0100a0001c0006t0001g0264a0001c0006t0001g0266others(8): Show | 11 | HG02145.hp1 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.129+7478T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750558 | ||||||
| chr8:41750565
|
CT | C | 76 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0001t0002g0216others(73): Show | 77 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.129+7470delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750565 | ||||||
| chr8:41750646
|
C | G | 240 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(237): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.129+7390G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750646 | ||||||
| chr8:41750841
|
C | T | 269 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.129+7195G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750841 | ||||||
| chr8:41750847
|
A | G | 269 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.129+7189T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750847 | ||||||
| chr8:41750848
|
G | C | 11 | a0001c0006t0001g0100a0001c0006t0001g0264a0001c0006t0001g0266others(8): Show | 11 | HG02145.hp1 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.129+7188C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750848 | ||||||
| chr8:41750909
|
A | G | 1 | a0001c0001t0002g0152 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.129+7127T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750909 | ||||||
| chr8:41751306
|
G | A | 1 | a0001c0001t0002g0171 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.129+6730C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41751306 | ||||||
| chr8:41751333
|
T | C | 1 | a0001c0003t0002g0199 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.129+6703A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41751333 | ||||||
| chr8:41751348
|
T | C | 275 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(272): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.129+6688A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41751348 | ||||||
| chr8:41751385
|
C | T | 1 | a0002c0057t0005g0269 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.129+6651G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41751385 | ||||||
| chr8:41751582
|
G | T | 5 | a0001c0005t0002g0010a0001c0005t0010g0019a0002c0039t0010g0018others(2): Show | 5 | HG02717.hp2 HG02818.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.129+6454C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41751582 | ||||||
| chr8:41751792
|
C | T | 1 | a0001c0006t0001g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.129+6244G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41751792 | ||||||
| chr8:41752050
|
G | A | 20 | a0001c0001t0002g0024a0001c0002t0009g0098a0001c0013t0001g0027others(17): Show | 20 | HG01106.hp2 HG01243.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.129+5986C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752050 | ||||||
| chr8:41752105
|
C | T | 106 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0002t0001g0031others(103): Show | 107 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.129+5931G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752105 | ||||||
| chr8:41752325
|
G | A | 106 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0002t0001g0031others(103): Show | 107 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.129+5711C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752325 | ||||||
| chr8:41752398
|
C | T | 1 | a0001c0009t0002g0052 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.129+5638G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752398 | ||||||
| chr8:41752399
|
G | A | 1 | a0001c0038t0002g0200 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.129+5637C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752399 | ||||||
| chr8:41752444
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.129+5592T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752444 | ||||||
| chr8:41752596
|
C | T | 106 | a0001c0001t0001g0148a0001c0001t0001g0160a0001c0001t0001g0217others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.129+5440G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752596 | ||||||
| chr8:41752655
|
C | T | 14 | a0001c0006t0001g0100a0001c0006t0001g0264a0001c0006t0001g0266others(11): Show | 14 | HG02145.hp1 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.129+5381G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752655 | ||||||
| chr8:41752716
|
G | A | 107 | a0001c0001t0001g0148a0001c0001t0001g0160a0001c0001t0001g0217others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.129+5320C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752716 | ||||||
| chr8:41752748
|
C | T | 1 | a0001c0003t0002g0199 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.129+5288G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752748 | ||||||
| chr8:41752798
|
G | GC | 69 | a0001c0001t0001g0155a0001c0001t0002g0092a0001c0001t0002g0151others(66): Show | 70 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.129+5237dupG | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752798 | ||||||
| chr8:41752798
|
G | GCC | 89 | a0001c0001t0001g0148a0001c0001t0001g0160a0001c0001t0001g0217others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.129+5236_129+5237d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752798 | ||||||
| chr8:41752798
|
G | GCCC | 21 | a0001c0001t0002g0009a0001c0001t0002g0078a0001c0001t0002g0176others(18): Show | 21 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(18): Show |
intron_variant | MODIFIER | c.129+5235_129+5237d others(5): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752798 | ||||||
| chr8:41752816
|
G | A | 2 | a0001c0003t0001g0064a0001c0003t0014g0065 | 2 | HG01934.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.129+5220C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752816 | ||||||
| chr8:41752827
|
C | T | 14 | a0001c0001t0001g0155a0001c0002t0001g0121a0001c0002t0001g0122others(11): Show | 14 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.129+5209G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752827 | ||||||
| chr8:41752828
|
G | A | 107 | a0001c0001t0001g0148a0001c0001t0001g0160a0001c0001t0001g0217others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.129+5208C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752828 | ||||||
| chr8:41752925
|
C | T | 42 | a0001c0001t0001g0162a0001c0002t0001g0031a0001c0002t0001g0048others(39): Show | 43 | HG00408.hp1 HG00438.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.129+5111G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752925 | ||||||
| chr8:41752972
|
A | G | 1 | a0003c0024t0003g0102 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.129+5064T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752972 | ||||||
| chr8:41752976
|
A | C | 59 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0002t0001g0031others(56): Show | 60 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.129+5060T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752976 | ||||||
| chr8:41752991
|
G | A | 214 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(211): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.129+5045C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752991 | ||||||
| chr8:41753060
|
C | CT | 27 | a0001c0003t0001g0049a0001c0003t0001g0057a0001c0003t0001g0058others(24): Show | 27 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.129+4975dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753060 | ||||||
| chr8:41753060
|
CT | C | 80 | a0001c0001t0001g0155a0001c0001t0001g0160a0001c0001t0002g0024others(77): Show | 81 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.129+4975delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753060 | ||||||
| chr8:41753125
|
C | T | 106 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0002t0001g0031others(103): Show | 107 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.129+4911G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753125 | ||||||
| chr8:41753173
|
T | C | 20 | a0001c0001t0002g0024a0001c0002t0009g0098a0001c0013t0001g0027others(17): Show | 20 | HG01106.hp2 HG01243.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.129+4863A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753173 | ||||||
| chr8:41753317
|
C | T | 1 | a0002c0039t0010g0018 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.129+4719G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753317 | ||||||
| chr8:41753318
|
G | A | 14 | a0001c0006t0001g0100a0001c0006t0001g0264a0001c0006t0001g0266others(11): Show | 14 | HG02145.hp1 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.129+4718C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753318 | ||||||
| chr8:41753345
|
T | C | 214 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(211): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.129+4691A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753345 | ||||||
| chr8:41753362
|
G | A | 7 | a0001c0013t0001g0037a0002c0007t0001g0038a0002c0007t0001g0040others(4): Show | 7 | HG02572.hp2 HG02630.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.129+4674C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753362 | ||||||
| chr8:41753424
|
G | C | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.129+4612C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753424 | ||||||
| chr8:41753451
|
G | A | 106 | a0001c0001t0001g0148a0001c0001t0001g0160a0001c0001t0001g0223others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.129+4585C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753451 | ||||||
| chr8:41753520
|
C | G | 1 | a0001c0058t0022g0089 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.129+4516G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753520 | ||||||
| chr8:41753774
|
G | GCC | 106 | a0001c0001t0001g0148a0001c0001t0001g0160a0001c0001t0001g0223others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.129+4260_129+4261d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753774 | ||||||
| chr8:41753857
|
T | C | 106 | a0001c0001t0001g0148a0001c0001t0001g0160a0001c0001t0001g0223others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.129+4179A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753857 | ||||||
| chr8:41753966
|
C | T | 1 | a0001c0032t0003g0105 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.129+4070G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753966 | ||||||
| chr8:41754030
|
T | C | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.129+4006A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41754030 | ||||||
| chr8:41754227
|
A | G | 214 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(211): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.129+3809T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41754227 | ||||||
| chr8:41754276
|
C | T | 214 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(211): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.129+3760G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41754276 | ||||||
| chr8:41754288
|
C | T | 2 | a0001c0009t0002g0069a0001c0009t0002g0082 | 2 | HG01070.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.129+3748G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41754288 | ||||||
| chr8:41754542
|
A | G | 1 | a0001c0005t0004g0030 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.129+3494T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41754542 | ||||||
| chr8:41754737
|
C | T | 107 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0001t0001g0217others(104): Show | 108 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.129+3299G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41754737 | ||||||
| chr8:41754969
|
C | T | 106 | a0001c0001t0001g0148a0001c0001t0001g0160a0001c0001t0001g0223others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.129+3067G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41754969 | ||||||
| chr8:41755033
|
T | C | 214 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(211): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.129+3003A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755033 | ||||||
| chr8:41755069
|
C | A | 17 | a0001c0001t0001g0155a0001c0002t0001g0121a0001c0002t0001g0122others(14): Show | 17 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.129+2967G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755069 | ||||||
| chr8:41755146
|
G | A | 1 | a0001c0003t0001g0064 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.129+2890C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755146 | ||||||
| chr8:41755219
|
C | T | 1 | a0001c0002t0001g0197 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.129+2817G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755219 | ||||||
| chr8:41755272
|
C | T | 3 | a0001c0032t0003g0105a0003c0049t0001g0104a0007c0033t0001g0108 | 3 | HG02895.hp1 HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.129+2764G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755272 | ||||||
| chr8:41755294
|
C | T | 1 | a0001c0005t0001g0238 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.129+2742G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755294 | ||||||
| chr8:41755297
|
A | C | 1 | a0001c0005t0003g0032 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.129+2739T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755297 | ||||||
| chr8:41755305
|
A | G | 33 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(30): Show | 33 | HG00423.hp2 HG01168.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.129+2731T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755305 | ||||||
| chr8:41755542
|
T | G | 66 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0001t0001g0217others(63): Show | 67 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.129+2494A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755542 | ||||||
| chr8:41755551
|
G | A | 33 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(30): Show | 33 | HG00423.hp2 HG01168.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.129+2485C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755551 | ||||||
| chr8:41755627
|
G | A | 14 | a0001c0006t0001g0100a0001c0006t0001g0264a0001c0006t0001g0266others(11): Show | 14 | HG02145.hp1 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.129+2409C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755627 | ||||||
| chr8:41755664
|
G | C | 1 | a0001c0005t0003g0032 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.129+2372C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755664 | ||||||
| chr8:41755684
|
C | T | 33 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(30): Show | 33 | HG00423.hp2 HG01168.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.129+2352G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755684 | ||||||
| chr8:41755822
|
A | G | 21 | a0001c0001t0002g0024a0001c0002t0009g0098a0001c0013t0001g0027others(18): Show | 21 | HG01106.hp2 HG01243.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.129+2214T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755822 | ||||||
| chr8:41755885
|
C | T | 14 | a0001c0006t0001g0100a0001c0006t0001g0264a0001c0006t0001g0266others(11): Show | 14 | HG02145.hp1 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.129+2151G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755885 | ||||||
| chr8:41755903
|
A | T | 2 | a0001c0005t0004g0030a0002c0007t0021g0118 | 2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.129+2133T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755903 | ||||||
| chr8:41755978
|
T | C | 109 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0001t0001g0217others(106): Show | 110 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.129+2058A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755978 | ||||||
| chr8:41755980
|
A | G | 1 | a0001c0009t0002g0082 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.129+2056T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755980 | ||||||
| chr8:41756070
|
A | G | 1 | a0001c0003t0001g0261 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.129+1966T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756070 | ||||||
| chr8:41756128
|
ATTTATTT others(10): Show |
A | 2 | a0001c0005t0002g0003a0001c0005t0013g0004 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.129+1891_129+1907d others(19): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756128 | ||||||
| chr8:41756231
|
C | T | 33 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(30): Show | 33 | HG00423.hp2 HG01168.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.129+1805G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756231 | ||||||
| chr8:41756365
|
C | T | 3 | a0001c0032t0003g0105a0003c0049t0001g0104a0007c0033t0001g0108 | 3 | HG02895.hp1 HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.129+1671G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756365 | ||||||
| chr8:41756379
|
C | T | 2 | a0001c0001t0001g0214a0001c0001t0001g0262 | 2 | NA19002.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.129+1657G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756379 | ||||||
| chr8:41756435
|
C | T | 4 | a0001c0013t0001g0027a0002c0007t0007g0021a0002c0007t0007g0025others(1): Show | 4 | HG02258.hp1 HG02976.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+1601G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756435 | ||||||
| chr8:41756670
|
T | G | 1 | a0001c0002t0001g0265 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.129+1366A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756670 | ||||||
| chr8:41756683
|
T | C | 35 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(32): Show | 35 | HG00140.hp1 HG00423.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.129+1353A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756683 | ||||||
| chr8:41756738
|
G | A | 67 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0001t0001g0217others(64): Show | 68 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.129+1298C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756738 | ||||||
| chr8:41756740
|
A | C | 28 | a0001c0003t0001g0049a0001c0003t0001g0057a0001c0003t0001g0058others(25): Show | 28 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.129+1296T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756740 | ||||||
| chr8:41756769
|
G | C | 67 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0001t0001g0217others(64): Show | 68 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.129+1267C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756769 | ||||||
| chr8:41756811
|
T | C | 1 | a0001c0002t0002g0180 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.129+1225A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756811 | ||||||
| chr8:41756859
|
G | A | 16 | a0001c0006t0001g0017a0001c0006t0001g0100a0001c0006t0001g0264others(13): Show | 16 | HG00738.hp1 HG02145.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.129+1177C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756859 | ||||||
| chr8:41756985
|
G | A | 84 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0001t0001g0217others(81): Show | 85 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.129+1051C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756985 | ||||||
| chr8:41757049
|
G | A | 111 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0001t0001g0217others(108): Show | 112 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.129+987C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41757049 | ||||||
| chr8:41757197
|
C | T | 36 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(33): Show | 36 | HG00140.hp1 HG00423.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.129+839G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41757197 | ||||||
| chr8:41757321
|
G | A | 1 | a0001c0004t0002g0154 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.129+715C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41757321 | ||||||
| chr8:41757402
|
G | T | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.129+634C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41757402 | ||||||
| chr8:41757541
|
A | G | 1 | a0001c0006t0001g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.129+495T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41757541 | ||||||
| chr8:41757562
|
C | T | 1 | a0006c0031t0002g0255 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.129+474G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41757562 | ||||||
| chr8:41757620
|
G | A | 79 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.129+416C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41757620 | ||||||
| chr8:41757648
|
G | A | 1 | a0003c0024t0001g0273 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.129+388C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41757648 | ||||||
| chr8:41757911
|
G | A | 270 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(267): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.129+125C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41757911 | ||||||
| chr8:41758220
|
C | T | 1 | a0001c0003t0001g0057 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.28-83G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41758220 | ||||||
| chr8:41758221
|
A | G | 1 | a0001c0002t0001g0248 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.28-84T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41758221 | ||||||
| chr8:41758288
|
G | T | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-151C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41758288 | ||||||
| chr8:41758333
|
G | T | 1 | a0002c0039t0010g0018 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.28-196C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41758333 | ||||||
| chr8:41758685
|
A | G | 1 | a0001c0001t0001g0148 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.28-548T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41758685 | ||||||
| chr8:41758839
|
G | A | 2 | a0001c0005t0004g0030a0002c0007t0021g0118 | 2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.28-702C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41758839 | ||||||
| chr8:41758960
|
G | A | 78 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(75): Show | 78 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.28-823C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41758960 | ||||||
| chr8:41758983
|
G | A | 36 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(33): Show | 36 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.28-846C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41758983 | ||||||
| chr8:41759010
|
C | G | 78 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(75): Show | 78 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.28-873G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759010 | ||||||
| chr8:41759058
|
C | G | 1 | a0001c0006t0001g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.28-921G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759058 | ||||||
| chr8:41759157
|
G | A | 2 | a0001c0013t0006g0123a0001c0013t0006g0124 | 2 | HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.28-1020C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759157 | ||||||
| chr8:41759195
|
A | G | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-1058T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759195 | ||||||
| chr8:41759291
|
A | G | 2 | a0001c0003t0001g0064a0001c0003t0014g0065 | 2 | HG01934.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.28-1154T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759291 | ||||||
| chr8:41759361
|
C | A | 78 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(75): Show | 78 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.28-1224G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759361 | ||||||
| chr8:41759431
|
G | A | 60 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0001t0001g0217others(57): Show | 61 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.28-1294C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759431 | ||||||
| chr8:41759431
|
G | C | 1 | a0001c0006t0001g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.28-1294C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759431 | ||||||
| chr8:41759443
|
T | C | 1 | a0001c0016t0002g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.28-1306A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759443 | ||||||
| chr8:41759506
|
A | AAAACAAA others(1): Show |
27 | a0001c0003t0001g0049a0001c0003t0001g0057a0001c0003t0001g0058others(24): Show | 27 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.28-1377_28-1370dup others(8): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759506 | ||||||
| chr8:41759506
|
A | AAAACAAA others(5): Show |
51 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(48): Show | 51 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.28-1381_28-1370dup others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759506 | ||||||
| chr8:41759547
|
G | A | 1 | a0001c0013t0006g0123 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.28-1410C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759547 | ||||||
| chr8:41759674
|
T | A | 268 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(265): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.28-1537A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759674 | ||||||
| chr8:41759986
|
G | A | 1 | a0001c0006t0003g0013 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.28-1849C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759986 | ||||||
| chr8:41760017
|
C | T | 27 | a0001c0003t0001g0049a0001c0003t0001g0057a0001c0003t0001g0058others(24): Show | 27 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.28-1880G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41760017 | ||||||
| chr8:41760039
|
A | G | 4 | a0001c0005t0002g0010a0001c0005t0010g0019a0002c0039t0010g0018others(1): Show | 4 | HG02717.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-1902T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41760039 | ||||||
| chr8:41760202
|
C | T | 14 | a0001c0006t0001g0100a0001c0006t0001g0264a0001c0006t0001g0266others(11): Show | 14 | HG02145.hp1 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.28-2065G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41760202 | ||||||
| chr8:41760309
|
C | T | 79 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.28-2172G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41760309 | ||||||
| chr8:41760433
|
T | C | 4 | a0001c0006t0001g0264a0001c0006t0001g0266a0001c0006t0001g0267others(1): Show | 4 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-2296A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41760433 | ||||||
| chr8:41760505
|
G | A | 2 | a0001c0005t0004g0030a0002c0007t0021g0118 | 2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.28-2368C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41760505 | ||||||
| chr8:41760573
|
C | T | 1 | a0001c0001t0002g0254 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.28-2436G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41760573 | ||||||
| chr8:41760659
|
G | A | 1 | a0013c0041t0012g0174 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.28-2522C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41760659 | ||||||
| chr8:41760695
|
G | A | 36 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(33): Show | 36 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.28-2558C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41760695 | ||||||
| chr8:41760977
|
TGAA | T | 60 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0001t0001g0217others(57): Show | 61 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.28-2843_28-2841del others(3): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41760977 | ||||||
| chr8:41760998
|
A | G | 2 | a0001c0005t0004g0030a0002c0007t0021g0118 | 2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.28-2861T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41760998 | ||||||
| chr8:41761123
|
G | GCA | 14 | a0001c0001t0002g0020a0001c0001t0002g0234a0001c0005t0001g0055others(11): Show | 14 | HG01891.hp2 HG02258.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.28-2988_28-2987dup others(2): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761123 | ||||||
| chr8:41761123
|
GCA | G | 64 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(61): Show | 64 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.28-2988_28-2987del others(2): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761123 | ||||||
| chr8:41761142
|
CAT | C | 16 | a0001c0005t0004g0030a0001c0006t0001g0100a0001c0006t0001g0264others(13): Show | 16 | HG02145.hp1 HG02451.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.28-3007_28-3006del others(2): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761142 | ||||||
| chr8:41761172
|
TGCACACA others(11): Show |
T | 36 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(33): Show | 36 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.28-3053_28-3036del others(18): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761172 | ||||||
| chr8:41761205
|
TCA | T | 146 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0001t0001g0191others(143): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.28-3070_28-3069del others(2): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761205 | ||||||
| chr8:41761300
|
C | T | 36 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(33): Show | 36 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.28-3163G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761300 | ||||||
| chr8:41761303
|
A | C | 2 | a0001c0005t0004g0030a0002c0007t0021g0118 | 2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.28-3166T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761303 | ||||||
| chr8:41761308
|
C | T | 1 | a0001c0046t0030g0277 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.28-3171G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761308 | ||||||
| chr8:41761335
|
C | A | 79 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.28-3198G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761335 | ||||||
| chr8:41761371
|
G | GCA | 146 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(143): Show | 147 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.28-3236_28-3235dup others(2): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761371 | ||||||
| chr8:41761371
|
GCA | G | 35 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(32): Show | 35 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.28-3236_28-3235del others(2): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761371 | ||||||
| chr8:41761371
|
GCACA | G | 43 | a0001c0003t0001g0049a0001c0003t0001g0057a0001c0003t0001g0058others(40): Show | 43 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.28-3238_28-3235del others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761371 | ||||||
| chr8:41761373
|
A | G | 5 | a0001c0005t0002g0010a0001c0005t0010g0019a0002c0039t0010g0018others(2): Show | 5 | HG02717.hp2 HG02818.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-3236T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761373 | ||||||
| chr8:41761390
|
T | C | 1 | a0001c0032t0003g0105 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.28-3253A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761390 | ||||||
| chr8:41761402
|
C | T | 79 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.28-3265G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761402 | ||||||
| chr8:41761439
|
A | C | 1 | a0001c0032t0003g0105 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.28-3302T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761439 | ||||||
| chr8:41761488
|
C | T | 1 | a0001c0002t0002g0180 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.28-3351G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761488 | ||||||
| chr8:41761518
|
C | T | 2 | a0001c0005t0004g0030a0002c0007t0021g0118 | 2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.28-3381G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761518 | ||||||
| chr8:41761637
|
C | T | 6 | a0001c0009t0002g0046a0001c0009t0002g0047a0001c0009t0002g0052others(3): Show | 6 | HG00738.hp2 HG01070.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-3500G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761637 | ||||||
| chr8:41761653
|
CTCATGCA others(7): Show |
C | 1 | a0001c0001t0001g0262 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.28-3530_28-3517del others(14): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761653 | ||||||
| chr8:41761855
|
G | A | 1 | a0001c0005t0020g0179 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.28-3718C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761855 | ||||||
| chr8:41762020
|
G | A | 36 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(33): Show | 36 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.28-3883C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41762020 | ||||||
| chr8:41762038
|
T | C | 1 | a0001c0003t0001g0057 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.28-3901A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41762038 | ||||||
| chr8:41762044
|
A | C | 5 | a0001c0005t0002g0010a0001c0005t0010g0019a0002c0039t0010g0018others(2): Show | 5 | HG02717.hp2 HG02818.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-3907T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41762044 | ||||||
| chr8:41762195
|
A | G | 138 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0001t0001g0191others(135): Show | 139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.28-4058T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41762195 | ||||||
| chr8:41762250
|
A | G | 5 | a0001c0005t0002g0010a0001c0005t0010g0019a0002c0039t0010g0018others(2): Show | 5 | HG02717.hp2 HG02818.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-4113T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41762250 | ||||||
| chr8:41762510
|
T | C | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-4373A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41762510 | ||||||
| chr8:41762541
|
G | A | 5 | a0001c0005t0002g0010a0001c0005t0010g0019a0002c0039t0010g0018others(2): Show | 5 | HG02717.hp2 HG02818.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-4404C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41762541 | ||||||
| chr8:41762594
|
A | G | 27 | a0001c0003t0001g0049a0001c0003t0001g0057a0001c0003t0001g0058others(24): Show | 27 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.28-4457T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41762594 | ||||||
| chr8:41762654
|
A | G | 14 | a0001c0006t0001g0100a0001c0006t0001g0264a0001c0006t0001g0266others(11): Show | 14 | HG02145.hp1 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.28-4517T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41762654 | ||||||
| chr8:41762667
|
G | A | 1 | a0001c0009t0002g0069 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.28-4530C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41762667 | ||||||
| chr8:41762672
|
G | C | 1 | a0001c0002t0001g0122 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.28-4535C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41762672 | ||||||
| chr8:41763093
|
G | A | 1 | a0001c0004t0002g0074 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.28-4956C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763093 | ||||||
| chr8:41763120
|
G | A | 2 | a0001c0005t0004g0030a0002c0007t0021g0118 | 2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.28-4983C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763120 | ||||||
| chr8:41763193
|
G | A | 36 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(33): Show | 36 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.28-5056C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763193 | ||||||
| chr8:41763213
|
C | CA | 6 | a0001c0001t0002g0171a0001c0003t0001g0237a0001c0003t0002g0199others(3): Show | 6 | HG00099.hp1 HG01123.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-5077dupT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763213 | ||||||
| chr8:41763213
|
C | CAA | 131 | a0001c0001t0001g0148a0001c0001t0001g0160a0001c0001t0001g0223others(128): Show | 131 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.28-5078_28-5077dup others(2): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763213 | ||||||
| chr8:41763213
|
C | CAAA | 53 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0001t0001g0217others(50): Show | 54 | HG00408.hp1 HG00438.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.28-5079_28-5077dup others(3): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763213 | ||||||
| chr8:41763564
|
C | A | 1 | a0001c0032t0003g0105 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.28-5427G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763564 | ||||||
| chr8:41763627
|
A | G | 25 | a0001c0003t0001g0049a0001c0003t0001g0057a0001c0003t0001g0058others(22): Show | 25 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.28-5490T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763627 | ||||||
| chr8:41763657
|
T | C | 7 | a0001c0005t0002g0010a0001c0005t0004g0030a0001c0005t0010g0019others(4): Show | 7 | HG02451.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.28-5520A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763657 | ||||||
| chr8:41763678
|
A | G | 2 | a0001c0005t0004g0030a0002c0007t0021g0118 | 2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.28-5541T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763678 | ||||||
| chr8:41763805
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.28-5668G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763805 | ||||||
| chr8:41763806
|
G | A | 36 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(33): Show | 36 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.28-5669C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763806 | ||||||
| chr8:41763858
|
C | A | 36 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(33): Show | 36 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.28-5721G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763858 | ||||||
| chr8:41763869
|
C | T | 78 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0002g0063others(75): Show | 78 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.28-5732G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763869 | ||||||
| chr8:41763881
|
C | CT | 9 | a0001c0003t0001g0062a0001c0003t0001g0064a0001c0003t0002g0067others(6): Show | 9 | HG00099.hp2 HG00639.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.28-5745dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763881 | ||||||
| chr8:41763881
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0010t0003g0189 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.28-5757_28-5745del others(13): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763881 | ||||||
| chr8:41763884
|
TTTTTC | T | 32 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0002g0063others(29): Show | 32 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.28-5752_28-5748del others(5): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763884 | ||||||
| chr8:41763886
|
TTTC | T | 12 | a0001c0002t0009g0098a0001c0006t0001g0100a0001c0006t0001g0264others(9): Show | 12 | HG02145.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.28-5752_28-5750del others(3): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763886 | ||||||
| chr8:41763889
|
C | CT | 110 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(107): Show | 110 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.28-5753dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763889 | ||||||
| chr8:41763889
|
C | CTT | 16 | a0001c0001t0002g0077a0001c0001t0002g0176a0001c0001t0002g0241others(13): Show | 16 | HG00423.hp1 HG01123.hp2 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.28-5754_28-5753dup others(2): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763889 | ||||||
| chr8:41763889
|
C | CTTT | 6 | a0001c0001t0002g0009a0001c0001t0002g0075a0001c0001t0002g0222others(3): Show | 6 | HG02071.hp1 HG03209.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-5755_28-5753dup others(3): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763889 | ||||||
| chr8:41763889
|
C | T | 25 | a0001c0003t0001g0057a0001c0003t0001g0058a0001c0003t0001g0062others(22): Show | 25 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.28-5752G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763889 | ||||||
| chr8:41763889
|
CT | C | 37 | a0001c0001t0001g0162a0001c0001t0001g0217a0001c0002t0001g0048others(34): Show | 38 | HG00408.hp1 HG00438.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.28-5753delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763889 | ||||||
| chr8:41763889
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0046t0030g0277 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.28-5765_28-5753del others(13): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763889 | ||||||
| chr8:41763917
|
G | T | 276 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(273): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.28-5780C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763917 | ||||||
| chr8:41763983
|
G | C | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-5846C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763983 | ||||||
| chr8:41764040
|
A | G | 3 | a0001c0016t0002g0006a0001c0016t0002g0007a0001c0016t0002g0008 | 3 | HG01192.hp2 HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.28-5903T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41764040 | ||||||
| chr8:41764110
|
G | A | 78 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(75): Show | 78 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.28-5973C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41764110 | ||||||
| chr8:41764167
|
AT | A | 147 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0001t0001g0191others(144): Show | 148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.28-6031delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41764167 | ||||||
| chr8:41764286
|
C | T | 36 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(33): Show | 36 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.28-6149G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41764286 | ||||||
| chr8:41764385
|
C | T | 78 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(75): Show | 78 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.28-6248G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41764385 | ||||||
| chr8:41764512
|
G | A | 1 | a0001c0005t0003g0032 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.28-6375C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41764512 | ||||||
| chr8:41764589
|
C | T | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-6452G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41764589 | ||||||
| chr8:41764606
|
G | A | 1 | a0001c0002t0001g0181 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.28-6469C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41764606 | ||||||
| chr8:41764684
|
T | C | 1 | a0001c0006t0001g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.28-6547A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41764684 | ||||||
| chr8:41764719
|
G | A | 2 | a0001c0023t0001g0275a0001c0023t0001g0276 | 2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.28-6582C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41764719 | ||||||
| chr8:41764722
|
C | T | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-6585G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41764722 | ||||||
| chr8:41764869
|
A | G | 2 | a0001c0005t0001g0101a0001c0040t0001g0087 | 2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.28-6732T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41764869 | ||||||
| chr8:41765103
|
C | T | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-6966G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765103 | ||||||
| chr8:41765159
|
C | T | 15 | a0001c0002t0009g0098a0001c0006t0001g0100a0001c0006t0001g0264others(12): Show | 15 | HG02145.hp1 HG02559.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.28-7022G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765159 | ||||||
| chr8:41765173
|
C | CCTTT | 54 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(51): Show | 54 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.28-7040_28-7037dup others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765173 | ||||||
| chr8:41765173
|
CCTTT | C | 28 | a0001c0003t0001g0049a0001c0003t0001g0057a0001c0003t0001g0058others(25): Show | 28 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.28-7040_28-7037del others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765173 | ||||||
| chr8:41765243
|
A | G | 1 | a0001c0003t0002g0199 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.28-7106T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765243 | ||||||
| chr8:41765266
|
C | T | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-7129G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765266 | ||||||
| chr8:41765411
|
T | TA | 146 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0162others(143): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.28-7275dupT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765411 | ||||||
| chr8:41765431
|
G | A | 26 | a0001c0003t0001g0049a0001c0003t0001g0057a0001c0003t0001g0058others(23): Show | 26 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.28-7294C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765431 | ||||||
| chr8:41765483
|
G | A | 99 | a0001c0001t0001g0160a0001c0001t0001g0223a0001c0001t0001g0226others(96): Show | 99 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.28-7346C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765483 | ||||||
| chr8:41765528
|
T | C | 270 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(267): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.28-7391A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765528 | ||||||
| chr8:41765531
|
G | A | 2 | a0001c0001t0002g0075a0001c0001t0002g0077 | 2 | NA19007.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.28-7394C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765531 | ||||||
| chr8:41765533
|
C | T | 5 | a0001c0005t0002g0010a0001c0005t0010g0019a0002c0039t0010g0018others(2): Show | 5 | HG02717.hp2 HG02818.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-7396G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765533 | ||||||
| chr8:41765639
|
G | A | 1 | a0007c0033t0001g0108 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.28-7502C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765639 | ||||||
| chr8:41765845
|
C | T | 1 | a0001c0038t0002g0200 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.28-7708G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765845 | ||||||
| chr8:41766020
|
C | T | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-7883G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41766020 | ||||||
| chr8:41766084
|
G | A | 47 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(44): Show | 47 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.28-7947C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41766084 | ||||||
| chr8:41766331
|
G | A | 3 | a0001c0001t0002g0088a0001c0001t0002g0090a0001c0001t0013g0091 | 3 | HG01069.hp2 HG01071.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.28-8194C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41766331 | ||||||
| chr8:41766429
|
C | T | 1 | a0001c0016t0002g0006 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.28-8292G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41766429 | ||||||
| chr8:41766566
|
A | T | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-8429T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41766566 | ||||||
| chr8:41766587
|
C | T | 63 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0162others(60): Show | 64 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.28-8450G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41766587 | ||||||
| chr8:41766672
|
C | T | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-8535G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41766672 | ||||||
| chr8:41766807
|
A | T | 1 | a0001c0003t0001g0158 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.28-8670T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41766807 | ||||||
| chr8:41767015
|
G | A | 1 | a0012c0045t0025g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.28-8878C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41767015 | ||||||
| chr8:41767184
|
C | G | 1 | a0001c0003t0001g0058 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.28-9047G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41767184 | ||||||
| chr8:41767271
|
C | G | 1 | a0001c0001t0002g0110 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.28-9134G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41767271 | ||||||
| chr8:41767290
|
G | A | 4 | a0001c0006t0001g0264a0001c0006t0001g0266a0001c0006t0001g0267others(1): Show | 4 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-9153C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41767290 | ||||||
| chr8:41767310
|
G | C | 1 | a0001c0001t0001g0262 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.28-9173C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41767310 | ||||||
| chr8:41767312
|
C | G | 1 | a0001c0001t0001g0262 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.28-9175G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41767312 | ||||||
| chr8:41767381
|
C | G | 2 | a0001c0005t0001g0101a0001c0040t0001g0087 | 2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.28-9244G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41767381 | ||||||
| chr8:41767415
|
C | G | 1 | a0001c0038t0002g0200 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.28-9278G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41767415 | ||||||
| chr8:41767423
|
C | T | 2 | a0001c0003t0001g0064a0001c0003t0014g0065 | 2 | HG01934.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.28-9286G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41767423 | ||||||
| chr8:41767473
|
G | A | 45 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(42): Show | 45 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.28-9336C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41767473 | ||||||
| chr8:41767665
|
G | A | 1 | a0001c0003t0001g0057 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.28-9528C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41767665 | ||||||
| chr8:41767666
|
C | A | 2 | a0001c0002t0001g0048a0001c0002t0001g0143 | 2 | HG01167.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.28-9529G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41767666 | ||||||
| chr8:41767883
|
A | G | 46 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(43): Show | 46 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.28-9746T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41767883 | ||||||
| chr8:41768186
|
A | T | 46 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(43): Show | 46 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.28-10049T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41768186 | ||||||
| chr8:41768269
|
G | A | 1 | a0001c0001t0002g0107 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.28-10132C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41768269 | ||||||
| chr8:41768375
|
G | T | 1 | a0007c0033t0001g0108 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.28-10238C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41768375 | ||||||
| chr8:41768430
|
C | G | 270 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(267): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.28-10293G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41768430 | ||||||
| chr8:41768549
|
G | T | 11 | a0001c0002t0009g0098a0001c0006t0001g0100a0001c0006t0018g0117others(8): Show | 11 | HG02559.hp1 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-10412C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41768549 | ||||||
| chr8:41768629
|
C | A | 44 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0002g0063others(41): Show | 44 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.28-10492G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41768629 | ||||||
| chr8:41768629
|
C | G | 1 | a0001c0001t0001g0262 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.28-10492G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41768629 | ||||||
| chr8:41768800
|
CA | C | 211 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(208): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.28-10664delT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41768800 | ||||||
| chr8:41768800
|
CAA | C | 15 | a0001c0002t0009g0098a0001c0003t0001g0049a0001c0003t0001g0237others(12): Show | 15 | HG02040.hp2 HG02451.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.28-10665_28-10664d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41768800 | ||||||
| chr8:41768800
|
CAAAA | C | 32 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(29): Show | 32 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.28-10667_28-10664d others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41768800 | ||||||
| chr8:41768844
|
G | A | 4 | a0001c0010t0002g0056a0001c0010t0003g0114a0001c0010t0003g0189others(1): Show | 4 | HG02071.hp2 HG02074.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-10707C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41768844 | ||||||
| chr8:41768936
|
G | A | 2 | a0001c0004t0002g0070a0001c0004t0002g0154 | 2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.28-10799C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41768936 | ||||||
| chr8:41769054
|
CAG | C | 35 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(32): Show | 35 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.28-10919_28-10918d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769054 | ||||||
| chr8:41769169
|
A | T | 11 | a0001c0002t0009g0098a0001c0006t0001g0100a0001c0006t0018g0117others(8): Show | 11 | HG02559.hp1 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-11032T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769169 | ||||||
| chr8:41769349
|
G | A | 3 | a0001c0001t0002g0171a0001c0003t0001g0169a0001c0003t0009g0170 | 3 | HG00099.hp1 HG03704.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.28-11212C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769349 | ||||||
| chr8:41769436
|
T | C | 6 | a0001c0001t0002g0175a0001c0001t0002g0230a0001c0003t0001g0237others(3): Show | 6 | HG00639.hp1 HG00733.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-11299A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769436 | ||||||
| chr8:41769523
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.28-11386G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769523 | ||||||
| chr8:41769540
|
T | A | 1 | a0012c0045t0025g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.28-11403A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769540 | ||||||
| chr8:41769567
|
G | A | 2 | a0001c0005t0001g0101a0001c0040t0001g0087 | 2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.28-11430C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769567 | ||||||
| chr8:41769797
|
G | C | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-11660C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769797 | ||||||
| chr8:41769867
|
A | T | 6 | a0001c0001t0002g0075a0001c0005t0002g0010a0001c0005t0010g0019others(3): Show | 6 | HG02717.hp2 HG02818.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-11730T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769867 | ||||||
| chr8:41769967
|
TTTC | T | 43 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0002g0063others(40): Show | 43 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.28-11833_28-11831d others(5): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769967 | ||||||
| chr8:41769977
|
C | CT | 110 | a0001c0001t0001g0160a0001c0001t0001g0223a0001c0001t0001g0226others(107): Show | 110 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.28-11841dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769977 | ||||||
| chr8:41769977
|
C | CTT | 10 | a0001c0001t0023g0081a0001c0002t0001g0197a0001c0003t0001g0177others(7): Show | 10 | HG01106.hp2 HG02109.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.28-11842_28-11841d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769977 | ||||||
| chr8:41769977
|
CT | C | 6 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0185others(3): Show | 6 | HG01081.hp1 HG01168.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-11841delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769977 | ||||||
| chr8:41769977
|
CTT | C | 24 | a0001c0001t0001g0214a0001c0001t0002g0260a0001c0004t0002g0070others(21): Show | 24 | HG00423.hp2 HG01168.hp1 HG01515.hp1 others(21): Show |
intron_variant | MODIFIER | c.28-11842_28-11841d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769977 | ||||||
| chr8:41769977
|
CTTT | C | 9 | a0001c0001t0001g0191a0001c0001t0002g0063a0001c0002t0001g0265others(6): Show | 9 | HG00140.hp1 HG00735.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.28-11843_28-11841d others(5): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769977 | ||||||
| chr8:41769997
|
T | A | 1 | a0001c0001t0001g0262 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.28-11860A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769997 | ||||||
| chr8:41770027
|
G | C | 32 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(29): Show | 32 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.28-11890C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41770027 | ||||||
| chr8:41770131
|
A | G | 242 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(239): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.28-11994T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41770131 | ||||||
| chr8:41770258
|
C | T | 1 | a0001c0017t0005g0119 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.28-12121G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41770258 | ||||||
| chr8:41770620
|
T | C | 11 | a0001c0002t0009g0098a0001c0006t0001g0100a0001c0006t0018g0117others(8): Show | 11 | HG02559.hp1 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-12483A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41770620 | ||||||
| chr8:41770743
|
G | T | 1 | a0005c0035t0001g0132 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.28-12606C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41770743 | ||||||
| chr8:41770892
|
C | A | 4 | a0001c0006t0001g0264a0001c0006t0001g0266a0001c0006t0001g0267others(1): Show | 4 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-12755G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41770892 | ||||||
| chr8:41771132
|
A | G | 101 | a0001c0001t0001g0160a0001c0001t0001g0223a0001c0001t0001g0226others(98): Show | 101 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.28-12995T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41771132 | ||||||
| chr8:41771277
|
A | G | 1 | a0001c0008t0002g0246 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.28-13140T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41771277 | ||||||
| chr8:41771345
|
A | T | 8 | a0001c0001t0002g0208a0001c0003t0001g0136a0001c0003t0001g0139others(5): Show | 8 | HG01081.hp2 HG01099.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.28-13208T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41771345 | ||||||
| chr8:41771409
|
C | T | 1 | a0001c0019t0002g0239 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.28-13272G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41771409 | ||||||
| chr8:41771481
|
C | T | 45 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(42): Show | 45 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.28-13344G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41771481 | ||||||
| chr8:41771682
|
A | T | 1 | a0001c0017t0005g0116 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.28-13545T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41771682 | ||||||
| chr8:41771721
|
G | A | 1 | a0001c0006t0001g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.28-13584C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41771721 | ||||||
| chr8:41771767
|
G | A | 1 | a0001c0008t0002g0213 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.28-13630C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41771767 | ||||||
| chr8:41771815
|
G | A | 40 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(37): Show | 40 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.28-13678C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41771815 | ||||||
| chr8:41771828
|
T | G | 1 | a0001c0005t0001g0055 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.28-13691A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41771828 | ||||||
| chr8:41771951
|
C | T | 1 | a0001c0008t0002g0246 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.28-13814G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41771951 | ||||||
| chr8:41771975
|
G | C | 3 | a0001c0052t0001g0235a0003c0014t0008g0094a0003c0014t0008g0095 | 3 | HG00323.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.28-13838C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41771975 | ||||||
| chr8:41772010
|
C | A | 2 | a0001c0005t0004g0030a0002c0007t0021g0118 | 2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.28-13873G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772010 | ||||||
| chr8:41772143
|
G | A | 4 | a0001c0002t0001g0031a0001c0002t0012g0022a0001c0005t0004g0030others(1): Show | 4 | HG01261.hp1 HG02451.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-14006C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772143 | ||||||
| chr8:41772144
|
C | T | 1 | a0001c0003t0001g0158 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.28-14007G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772144 | ||||||
| chr8:41772156
|
C | T | 34 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(31): Show | 34 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.28-14019G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772156 | ||||||
| chr8:41772317
|
G | A | 34 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0262others(31): Show | 34 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.28-14180C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772317 | ||||||
| chr8:41772367
|
G | A | 1 | a0013c0041t0012g0174 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.28-14230C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772367 | ||||||
| chr8:41772453
|
G | A | 6 | a0001c0009t0002g0046a0001c0009t0002g0047a0001c0009t0002g0052others(3): Show | 6 | HG00738.hp2 HG01070.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-14316C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772453 | ||||||
| chr8:41772498
|
G | A | 9 | a0001c0002t0001g0121a0001c0002t0001g0127a0001c0002t0001g0128others(6): Show | 9 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.28-14361C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772498 | ||||||
| chr8:41772565
|
T | C | 242 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(239): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.28-14428A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772565 | ||||||
| chr8:41772655
|
A | G | 4 | a0001c0006t0001g0264a0001c0006t0001g0266a0001c0006t0001g0267others(1): Show | 4 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-14518T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772655 | ||||||
| chr8:41772706
|
T | A | 1 | a0001c0040t0001g0087 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.28-14569A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772706 | ||||||
| chr8:41772715
|
G | A | 1 | a0001c0002t0003g0146 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.28-14578C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772715 | ||||||
| chr8:41772813
|
A | G | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-14676T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772813 | ||||||
| chr8:41772838
|
C | G | 1 | a0001c0001t0002g0088 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.28-14701G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772838 | ||||||
| chr8:41772887
|
G | A | 111 | a0001c0001t0001g0226a0001c0001t0001g0242a0001c0001t0001g0245others(108): Show | 111 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.28-14750C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772887 | ||||||
| chr8:41772929
|
G | A | 112 | a0001c0001t0001g0226a0001c0001t0001g0242a0001c0001t0001g0245others(109): Show | 112 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.28-14792C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772929 | ||||||
| chr8:41773055
|
AC | A | 9 | a0001c0002t0001g0121a0001c0002t0001g0127a0001c0002t0001g0128others(6): Show | 9 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.28-14919delG | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773055 | ||||||
| chr8:41773056
|
C | G | 24 | a0001c0001t0002g0024a0001c0005t0001g0101a0001c0006t0001g0264others(21): Show | 24 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.28-14919G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773056 | ||||||
| chr8:41773059
|
C | A | 1 | a0016c0027t0002g0054 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.28-14922G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773059 | ||||||
| chr8:41773103
|
G | A | 1 | a0001c0005t0001g0257 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.28-14966C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773103 | ||||||
| chr8:41773184
|
G | A | 15 | a0001c0001t0002g0024a0001c0013t0001g0027a0001c0013t0001g0037others(12): Show | 15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.28-15047C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773184 | ||||||
| chr8:41773226
|
C | T | 4 | a0001c0009t0002g0046a0001c0009t0002g0047a0001c0009t0002g0052others(1): Show | 4 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-15089G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773226 | ||||||
| chr8:41773326
|
G | A | 1 | a0001c0003t0001g0093 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.28-15189C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773326 | ||||||
| chr8:41773414
|
G | T | 119 | a0001c0001t0001g0155a0001c0001t0001g0191a0001c0001t0001g0214others(116): Show | 119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.28-15277C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773414 | ||||||
| chr8:41773494
|
T | A | 1 | a0001c0046t0030g0277 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.28-15357A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773494 | ||||||
| chr8:41773555
|
G | A | 8 | a0001c0001t0002g0208a0001c0003t0001g0136a0001c0003t0001g0139others(5): Show | 8 | HG01081.hp2 HG01099.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.28-15418C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773555 | ||||||
| chr8:41773603
|
C | A | 269 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.28-15466G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773603 | ||||||
| chr8:41773627
|
A | T | 1 | a0002c0007t0001g0040 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.28-15490T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773627 | ||||||
| chr8:41773724
|
C | T | 7 | a0001c0002t0009g0098a0001c0005t0004g0029a0001c0012t0006g0085others(4): Show | 7 | HG02559.hp1 HG02622.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.28-15587G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773724 | ||||||
| chr8:41773786
|
A | G | 4 | a0001c0003t0001g0064a0001c0003t0014g0065a0003c0014t0008g0094others(1): Show | 4 | HG01934.hp1 HG03017.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-15649T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773786 | ||||||
| chr8:41773862
|
G | A | 1 | a0002c0039t0010g0018 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.28-15725C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773862 | ||||||
| chr8:41773963
|
A | C | 25 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0001t0002g0204others(22): Show | 25 | HG01070.hp2 HG01071.hp2 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.28-15826T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773963 | ||||||
| chr8:41773965
|
C | T | 4 | a0001c0004t0002g0195a0001c0004t0002g0271a0001c0008t0002g0194others(1): Show | 4 | HG01515.hp1 HG01517.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-15828G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773965 | ||||||
| chr8:41774040
|
CAGAATTC others(4): Show |
C | 127 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(124): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.28-15914_28-15904d others(13): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774040 | ||||||
| chr8:41774107
|
C | T | 16 | a0001c0001t0002g0024a0001c0006t0001g0039a0001c0013t0001g0027others(13): Show | 16 | HG01243.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.28-15970G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774107 | ||||||
| chr8:41774115
|
C | T | 117 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(114): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.28-15978G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774115 | ||||||
| chr8:41774227
|
T | C | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-16090A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774227 | ||||||
| chr8:41774244
|
T | C | 49 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(46): Show | 50 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.28-16107A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774244 | ||||||
| chr8:41774270
|
G | C | 119 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(116): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.28-16133C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774270 | ||||||
| chr8:41774315
|
G | A | 99 | a0001c0001t0002g0009a0001c0001t0002g0024a0001c0001t0002g0063others(96): Show | 99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.28-16178C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774315 | ||||||
| chr8:41774348
|
T | C | 1 | a0001c0010t0003g0236 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.28-16211A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774348 | ||||||
| chr8:41774379
|
A | G | 5 | a0001c0001t0002g0020a0001c0005t0002g0010a0001c0005t0010g0019others(2): Show | 5 | HG02717.hp2 HG03139.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-16242T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774379 | ||||||
| chr8:41774412
|
A | C | 54 | a0001c0001t0002g0024a0001c0001t0002g0063a0001c0001t0002g0110others(51): Show | 54 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.28-16275T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774412 | ||||||
| chr8:41774712
|
C | T | 91 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0217others(88): Show | 91 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.28-16575G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774712 | ||||||
| chr8:41774737
|
G | A | 1 | a0001c0003t0001g0237 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.28-16600C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774737 | ||||||
| chr8:41774760
|
C | A | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-16623G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774760 | ||||||
| chr8:41774894
|
C | T | 1 | a0014c0055t0006g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.28-16757G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774894 | ||||||
| chr8:41774913
|
C | T | 1 | a0001c0002t0003g0146 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.28-16776G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774913 | ||||||
| chr8:41774967
|
G | A | 257 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(254): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.28-16830C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774967 | ||||||
| chr8:41775061
|
CT | C | 51 | a0001c0001t0002g0024a0001c0001t0002g0063a0001c0001t0002g0110others(48): Show | 51 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.28-16925delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41775061 | ||||||
| chr8:41775164
|
C | T | 1 | a0001c0010t0003g0002 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.28-17027G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41775164 | ||||||
| chr8:41775228
|
A | G | 264 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(261): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.28-17091T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41775228 | ||||||
| chr8:41775255
|
G | A | 5 | a0001c0002t0003g0079a0001c0002t0003g0080a0001c0010t0002g0056others(2): Show | 5 | HG02071.hp2 HG02074.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-17118C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41775255 | ||||||
| chr8:41775334
|
C | T | 3 | a0001c0023t0001g0275a0001c0023t0001g0276a0003c0024t0001g0273 | 3 | HG01891.hp2 HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.28-17197G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41775334 | ||||||
| chr8:41775802
|
G | A | 50 | a0001c0001t0002g0024a0001c0001t0002g0063a0001c0001t0002g0110others(47): Show | 50 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.28-17665C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41775802 | ||||||
| chr8:41775937
|
A | T | 1 | a0006c0031t0002g0255 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.28-17800T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41775937 | ||||||
| chr8:41775980
|
C | A | 50 | a0001c0001t0002g0024a0001c0001t0002g0063a0001c0001t0002g0110others(47): Show | 50 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.28-17843G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41775980 | ||||||
| chr8:41776004
|
C | A | 3 | a0001c0003t0001g0177a0001c0005t0020g0179a0003c0015t0003g0137 | 3 | NA18981.hp2 NA19010.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.28-17867G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41776004 | ||||||
| chr8:41776089
|
G | T | 1 | a0006c0031t0002g0255 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.28-17952C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41776089 | ||||||
| chr8:41776090
|
T | G | 1 | a0006c0031t0002g0255 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.28-17953A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41776090 | ||||||
| chr8:41776092
|
G | T | 1 | a0006c0031t0002g0255 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.28-17955C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41776092 | ||||||
| chr8:41776339
|
G | A | 91 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0217others(88): Show | 91 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.28-18202C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41776339 | ||||||
| chr8:41776501
|
A | G | 4 | a0001c0012t0005g0103a0001c0046t0030g0277a0003c0024t0003g0102others(1): Show | 4 | HG02723.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-18364T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41776501 | ||||||
| chr8:41776836
|
G | A | 4 | a0001c0002t0003g0079a0001c0002t0003g0080a0001c0010t0002g0056others(1): Show | 4 | HG02071.hp2 HG02074.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-18699C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41776836 | ||||||
| chr8:41776873
|
G | A | 1 | a0001c0002t0001g0122 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.28-18736C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41776873 | ||||||
| chr8:41776962
|
C | T | 2 | a0001c0002t0001g0031a0001c0002t0012g0022 | 2 | HG01261.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.28-18825G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41776962 | ||||||
| chr8:41777238
|
G | C | 4 | a0001c0013t0001g0027a0002c0007t0007g0021a0002c0007t0007g0025others(1): Show | 4 | HG02258.hp1 HG02976.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-19101C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41777238 | ||||||
| chr8:41777275
|
G | A | 8 | a0001c0004t0001g0109a0001c0005t0004g0029a0001c0005t0004g0030others(5): Show | 8 | HG02630.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.28-19138C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41777275 | ||||||
| chr8:41777303
|
A | G | 1 | a0001c0004t0001g0159 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.28-19166T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41777303 | ||||||
| chr8:41777377
|
C | T | 10 | a0001c0001t0002g0009a0001c0001t0002g0020a0001c0005t0002g0010others(7): Show | 10 | HG01106.hp2 HG02109.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.28-19240G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41777377 | ||||||
| chr8:41777406
|
C | T | 3 | a0001c0010t0002g0056a0001c0010t0003g0114a0001c0010t0003g0189 | 3 | HG02071.hp2 HG02074.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.28-19269G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41777406 | ||||||
| chr8:41777497
|
C | T | 10 | a0001c0002t0001g0121a0001c0002t0001g0122a0001c0002t0001g0127others(7): Show | 10 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.28-19360G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41777497 | ||||||
| chr8:41777515
|
T | C | 165 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(162): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.28-19378A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41777515 | ||||||
| chr8:41777609
|
T | A | 55 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(52): Show | 56 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.28-19472A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41777609 | ||||||
| chr8:41777611
|
A | C | 55 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(52): Show | 56 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.28-19474T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41777611 | ||||||
| chr8:41777611
|
AAAAC | A | 4 | a0001c0001t0002g0201a0001c0005t0001g0238a0001c0010t0003g0002others(1): Show | 4 | HG00738.hp1 HG02071.hp1 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-19478_28-19475d others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41777611 | ||||||
| chr8:41777778
|
G | A | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-19641C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41777778 | ||||||
| chr8:41777818
|
A | C | 2 | a0001c0001t0001g0155a0001c0003t0001g0158 | 2 | NA18969.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.28-19681T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41777818 | ||||||
| chr8:41778063
|
G | C | 1 | a0001c0004t0002g0271 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.27+19449C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41778063 | ||||||
| chr8:41778269
|
G | T | 1 | a0001c0001t0002g0241 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.27+19243C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41778269 | ||||||
| chr8:41778484
|
T | A | 30 | a0001c0001t0002g0063a0001c0001t0002g0110a0001c0001t0023g0081others(27): Show | 30 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.27+19028A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41778484 | ||||||
| chr8:41778493
|
A | G | 65 | a0001c0001t0002g0024a0001c0001t0002g0063a0001c0001t0002g0110others(62): Show | 65 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.27+19019T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41778493 | ||||||
| chr8:41778546
|
C | T | 3 | a0001c0012t0005g0103a0001c0046t0030g0277a0003c0024t0003g0102 | 3 | HG02723.hp2 HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.27+18966G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41778546 | ||||||
| chr8:41778553
|
C | T | 46 | a0001c0001t0002g0024a0001c0001t0002g0063a0001c0001t0002g0110others(43): Show | 46 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.27+18959G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41778553 | ||||||
| chr8:41778636
|
G | A | 16 | a0001c0001t0002g0024a0001c0006t0001g0039a0001c0013t0001g0027others(13): Show | 16 | HG01243.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.27+18876C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41778636 | ||||||
| chr8:41778733
|
T | C | 101 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0217others(98): Show | 101 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.27+18779A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41778733 | ||||||
| chr8:41778886
|
G | T | 46 | a0001c0001t0002g0024a0001c0001t0002g0063a0001c0001t0002g0110others(43): Show | 46 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.27+18626C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41778886 | ||||||
| chr8:41778921
|
G | C | 1 | a0001c0002t0001g0144 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.27+18591C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41778921 | ||||||
| chr8:41779081
|
G | A | 1 | a0001c0019t0002g0145 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.27+18431C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41779081 | ||||||
| chr8:41779358
|
C | G | 1 | a0001c0003t0001g0058 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.27+18154G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41779358 | ||||||
| chr8:41779398
|
C | T | 16 | a0001c0001t0002g0024a0001c0006t0001g0039a0001c0013t0001g0027others(13): Show | 16 | HG01243.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.27+18114G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41779398 | ||||||
| chr8:41779628
|
A | C | 1 | a0001c0046t0030g0277 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.27+17884T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41779628 | ||||||
| chr8:41779637
|
AT | A | 47 | a0001c0001t0002g0024a0001c0001t0002g0063a0001c0001t0002g0110others(44): Show | 47 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.27+17874delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41779637 | ||||||
| chr8:41779684
|
C | A | 2 | a0001c0005t0001g0101a0001c0040t0001g0087 | 2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.27+17828G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41779684 | ||||||
| chr8:41779720
|
G | A | 3 | a0001c0005t0028g0112a0001c0005t0029g0111a0001c0006t0003g0005 | 3 | HG02895.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.27+17792C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41779720 | ||||||
| chr8:41779806
|
G | A | 30 | a0001c0001t0002g0063a0001c0001t0002g0110a0001c0001t0023g0081others(27): Show | 30 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.27+17706C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41779806 | ||||||
| chr8:41779842
|
C | T | 46 | a0001c0001t0002g0024a0001c0001t0002g0063a0001c0001t0002g0110others(43): Show | 46 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.27+17670G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41779842 | ||||||
| chr8:41779854
|
G | C | 30 | a0001c0001t0002g0063a0001c0001t0002g0110a0001c0001t0023g0081others(27): Show | 30 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.27+17658C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41779854 | ||||||
| chr8:41779968
|
G | A | 30 | a0001c0001t0002g0063a0001c0001t0002g0110a0001c0001t0023g0081others(27): Show | 30 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.27+17544C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41779968 | ||||||
| chr8:41780068
|
A | G | 1 | a0002c0039t0010g0018 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.27+17444T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41780068 | ||||||
| chr8:41780154
|
G | A | 5 | a0001c0001t0002g0020a0001c0005t0002g0010a0001c0005t0010g0019others(2): Show | 5 | HG02717.hp2 HG03139.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+17358C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41780154 | ||||||
| chr8:41780287
|
C | T | 1 | a0001c0010t0003g0002 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+17225G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41780287 | ||||||
| chr8:41780376
|
T | C | 4 | a0001c0006t0003g0013a0001c0006t0003g0014a0001c0006t0005g0015others(1): Show | 4 | HG01106.hp2 HG02109.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+17136A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41780376 | ||||||
| chr8:41780476
|
C | T | 3 | a0001c0023t0001g0275a0001c0023t0001g0276a0003c0024t0001g0273 | 3 | HG01891.hp2 HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.27+17036G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41780476 | ||||||
| chr8:41780573
|
T | C | 3 | a0001c0023t0001g0275a0001c0023t0001g0276a0003c0024t0001g0273 | 3 | HG01891.hp2 HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.27+16939A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41780573 | ||||||
| chr8:41780620
|
T | C | 262 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(259): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.27+16892A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41780620 | ||||||
| chr8:41780648
|
T | C | 1 | a0001c0002t0001g0181 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.27+16864A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41780648 | ||||||
| chr8:41780713
|
C | T | 48 | a0001c0001t0002g0024a0001c0001t0002g0063a0001c0001t0002g0110others(45): Show | 48 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.27+16799G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41780713 | ||||||
| chr8:41780727
|
C | T | 4 | a0001c0012t0005g0103a0001c0046t0030g0277a0003c0024t0003g0102others(1): Show | 4 | HG02723.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+16785G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41780727 | ||||||
| chr8:41781240
|
C | G | 2 | a0001c0005t0001g0101a0001c0040t0001g0087 | 2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.27+16272G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41781240 | ||||||
| chr8:41781455
|
C | T | 65 | a0001c0001t0002g0024a0001c0001t0002g0063a0001c0001t0002g0088others(62): Show | 65 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.27+16057G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41781455 | ||||||
| chr8:41781722
|
G | A | 62 | a0001c0001t0002g0024a0001c0001t0002g0063a0001c0001t0002g0088others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.27+15790C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41781722 | ||||||
| chr8:41781730
|
G | A | 3 | a0001c0002t0001g0202a0001c0012t0015g0240a0001c0019t0002g0239 | 3 | NA18612.hp1 NA18969.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.27+15782C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41781730 | ||||||
| chr8:41781748
|
C | A | 88 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0217others(85): Show | 88 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.27+15764G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41781748 | ||||||
| chr8:41781857
|
G | T | 1 | a0002c0007t0007g0025 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.27+15655C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41781857 | ||||||
| chr8:41782242
|
A | G | 1 | a0001c0010t0003g0002 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+15270T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41782242 | ||||||
| chr8:41782248
|
G | A | 6 | a0001c0001t0001g0242a0001c0001t0001g0245a0001c0001t0002g0241others(3): Show | 6 | HG02015.hp1 HG02083.hp1 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.27+15264C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41782248 | ||||||
| chr8:41782257
|
C | T | 1 | a0001c0001t0002g0063 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.27+15255G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41782257 | ||||||
| chr8:41782324
|
G | A | 1 | a0001c0003t0001g0049 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.27+15188C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41782324 | ||||||
| chr8:41782572
|
C | T | 4 | a0001c0001t0002g0063a0001c0002t0001g0048a0001c0030t0017g0051others(1): Show | 4 | HG00735.hp1 HG02698.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+14940G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41782572 | ||||||
| chr8:41782607
|
C | T | 45 | a0001c0001t0002g0063a0001c0001t0002g0075a0001c0001t0002g0077others(42): Show | 45 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.27+14905G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41782607 | ||||||
| chr8:41782628
|
G | C | 7 | a0001c0002t0001g0248a0001c0004t0002g0247a0001c0004t0002g0249others(4): Show | 7 | NA18950.hp2 NA18979.hp1 NA18992.hp2 others(4): Show |
intron_variant | MODIFIER | c.27+14884C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41782628 | ||||||
| chr8:41782651
|
G | A | 6 | a0001c0002t0001g0248a0001c0004t0002g0247a0001c0004t0002g0249others(3): Show | 6 | NA18950.hp2 NA18992.hp2 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+14861C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41782651 | ||||||
| chr8:41782755
|
C | G | 5 | a0001c0002t0003g0079a0001c0002t0003g0080a0001c0010t0002g0056others(2): Show | 5 | HG02071.hp2 HG02074.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+14757G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41782755 | ||||||
| chr8:41782794
|
C | T | 4 | a0001c0005t0028g0112a0001c0005t0029g0111a0001c0006t0003g0005others(1): Show | 4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+14718G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41782794 | ||||||
| chr8:41782803
|
A | G | 11 | a0001c0001t0002g0009a0001c0001t0002g0020a0001c0005t0002g0010others(8): Show | 11 | HG01106.hp2 HG02109.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.27+14709T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41782803 | ||||||
| chr8:41783057
|
C | T | 1 | a0001c0002t0002g0180 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.27+14455G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41783057 | ||||||
| chr8:41783128
|
G | C | 79 | a0001c0001t0002g0024a0001c0001t0002g0063a0001c0001t0002g0075others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.27+14384C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41783128 | ||||||
| chr8:41783139
|
G | A | 46 | a0001c0001t0002g0063a0001c0001t0002g0075a0001c0001t0002g0077others(43): Show | 46 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.27+14373C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41783139 | ||||||
| chr8:41783388
|
C | T | 201 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(198): Show | 202 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.27+14124G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41783388 | ||||||
| chr8:41783401
|
G | A | 1 | a0001c0003t0001g0060 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.27+14111C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41783401 | ||||||
| chr8:41783557
|
C | T | 55 | a0001c0001t0002g0063a0001c0001t0002g0075a0001c0001t0002g0077others(52): Show | 55 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.27+13955G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41783557 | ||||||
| chr8:41783617
|
GGAGACT | G | 122 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0217others(119): Show | 122 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.27+13889_27+13894d others(8): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41783617 | ||||||
| chr8:41783633
|
T | C | 34 | a0001c0001t0002g0063a0001c0001t0002g0075a0001c0001t0002g0077others(31): Show | 34 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.27+13879A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41783633 | ||||||
| chr8:41783821
|
G | A | 1 | a0003c0049t0001g0104 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.27+13691C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41783821 | ||||||
| chr8:41783875
|
C | T | 50 | a0001c0001t0002g0063a0001c0001t0002g0075a0001c0001t0002g0077others(47): Show | 50 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.27+13637G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41783875 | ||||||
| chr8:41783891
|
C | T | 7 | a0001c0003t0001g0136a0001c0003t0001g0139a0001c0003t0001g0140others(4): Show | 7 | HG01081.hp2 HG01099.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.27+13621G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41783891 | ||||||
| chr8:41784039
|
C | T | 31 | a0001c0001t0002g0107a0001c0001t0002g0125a0001c0002t0001g0121others(28): Show | 31 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.27+13473G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41784039 | ||||||
| chr8:41784057
|
C | CA | 36 | a0001c0001t0001g0191a0001c0001t0002g0107a0001c0001t0002g0125others(33): Show | 36 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.27+13454dupT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41784057 | ||||||
| chr8:41784057
|
CAA | C | 132 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(129): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.27+13453_27+13454d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41784057 | ||||||
| chr8:41784106
|
G | A | 76 | a0001c0001t0002g0024a0001c0001t0002g0063a0001c0001t0002g0075others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.27+13406C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41784106 | ||||||
| chr8:41784232
|
C | T | 6 | a0001c0001t0002g0009a0001c0001t0002g0020a0001c0005t0002g0010others(3): Show | 6 | HG02717.hp2 HG03139.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+13280G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41784232 | ||||||
| chr8:41784239
|
A | G | 21 | a0001c0001t0002g0125a0001c0002t0001g0121a0001c0002t0001g0122others(18): Show | 21 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.27+13273T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41784239 | ||||||
| chr8:41784252
|
C | G | 1 | a0001c0032t0003g0105 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.27+13260G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41784252 | ||||||
| chr8:41784416
|
T | C | 51 | a0001c0001t0002g0063a0001c0001t0002g0075a0001c0001t0002g0077others(48): Show | 51 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.27+13096A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41784416 | ||||||
| chr8:41784444
|
T | C | 1 | a0006c0031t0002g0255 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.27+13068A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41784444 | ||||||
| chr8:41784598
|
T | A | 135 | a0001c0001t0002g0009a0001c0001t0002g0020a0001c0001t0002g0024others(132): Show | 135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.27+12914A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41784598 | ||||||
| chr8:41784646
|
C | G | 21 | a0001c0001t0002g0125a0001c0002t0001g0121a0001c0002t0001g0122others(18): Show | 21 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.27+12866G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41784646 | ||||||
| chr8:41784978
|
C | T | 1 | a0001c0001t0002g0009 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.27+12534G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41784978 | ||||||
| chr8:41785020
|
C | G | 5 | a0001c0006t0018g0117a0001c0017t0005g0116a0001c0017t0005g0119others(2): Show | 5 | HG02451.hp2 HG02572.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+12492G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41785020 | ||||||
| chr8:41785124
|
G | C | 1 | a0002c0007t0001g0040 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.27+12388C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41785124 | ||||||
| chr8:41785202
|
T | C | 11 | a0001c0002t0009g0098a0001c0005t0004g0042a0001c0005t0004g0043others(8): Show | 11 | HG01167.hp1 HG02559.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.27+12310A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41785202 | ||||||
| chr8:41785220
|
G | A | 2 | a0001c0005t0001g0256a0001c0005t0001g0257 | 2 | HG01123.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.27+12292C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41785220 | ||||||
| chr8:41785253
|
G | A | 1 | a0001c0002t0001g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.27+12259C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41785253 | ||||||
| chr8:41785368
|
A | G | 56 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(53): Show | 57 | HG00099.hp1 HG00438.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.27+12144T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41785368 | ||||||
| chr8:41785610
|
C | T | 1 | a0001c0002t0012g0022 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.27+11902G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41785610 | ||||||
| chr8:41785727
|
C | T | 1 | a0001c0002t0003g0079 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.27+11785G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41785727 | ||||||
| chr8:41785843
|
G | A | 1 | a0001c0005t0020g0179 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.27+11669C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41785843 | ||||||
| chr8:41785939
|
G | C | 193 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(190): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.27+11573C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41785939 | ||||||
| chr8:41785993
|
C | T | 134 | a0001c0001t0002g0009a0001c0001t0002g0020a0001c0001t0002g0024others(131): Show | 134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.27+11519G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41785993 | ||||||
| chr8:41786018
|
C | T | 20 | a0001c0001t0002g0024a0001c0002t0001g0031a0001c0002t0012g0022others(17): Show | 20 | HG01243.hp2 HG01261.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.27+11494G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41786018 | ||||||
| chr8:41786080
|
A | G | 1 | a0001c0010t0003g0002 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+11432T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41786080 | ||||||
| chr8:41786154
|
C | T | 1 | a0001c0010t0003g0002 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+11358G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41786154 | ||||||
| chr8:41786304
|
T | C | 1 | a0001c0010t0003g0002 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+11208A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41786304 | ||||||
| chr8:41786310
|
CT | C | 6 | a0001c0001t0002g0125a0001c0006t0018g0117a0001c0017t0005g0116others(3): Show | 6 | HG02451.hp2 HG02572.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+11201delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41786310 | ||||||
| chr8:41786591
|
A | G | 1 | a0001c0002t0001g0206 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.27+10921T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41786591 | ||||||
| chr8:41786609
|
C | T | 2 | a0001c0003t0001g0062a0001c0009t0002g0061 | 2 | HG00099.hp2 HG00639.hp2 |
intron_variant | MODIFIER | c.27+10903G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41786609 | ||||||
| chr8:41786748
|
A | T | 192 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(189): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.27+10764T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41786748 | ||||||
| chr8:41786980
|
C | T | 5 | a0001c0005t0004g0011a0001c0006t0003g0013a0001c0006t0003g0014others(2): Show | 5 | HG01106.hp2 HG02109.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+10532G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41786980 | ||||||
| chr8:41787059
|
T | A | 1 | a0001c0002t0002g0180 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.27+10453A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41787059 | ||||||
| chr8:41787074
|
G | A | 9 | a0001c0001t0002g0107a0001c0002t0002g0106a0001c0004t0001g0109others(6): Show | 9 | HG01192.hp2 HG02647.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.27+10438C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41787074 | ||||||
| chr8:41787149
|
CTGGCCTG others(17): Show |
C | 1 | a0001c0002t0001g0181 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.27+10339_27+10362d others(26): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41787149 | ||||||
| chr8:41787343
|
T | C | 192 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(189): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.27+10169A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41787343 | ||||||
| chr8:41787344
|
G | C | 3 | a0001c0010t0002g0056a0001c0010t0003g0114a0001c0010t0003g0189 | 3 | HG02071.hp2 HG02074.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.27+10168C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41787344 | ||||||
| chr8:41787360
|
A | T | 2 | a0001c0001t0002g0204a0001c0001t0002g0205 | 2 | NA18612.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.27+10152T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41787360 | ||||||
| chr8:41787556
|
A | G | 194 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.27+9956T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41787556 | ||||||
| chr8:41787600
|
C | T | 1 | a0001c0002t0003g0146 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.27+9912G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41787600 | ||||||
| chr8:41788047
|
C | T | 192 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(189): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.27+9465G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41788047 | ||||||
| chr8:41788176
|
G | A | 1 | a0001c0001t0002g0024 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.27+9336C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41788176 | ||||||
| chr8:41788192
|
C | T | 194 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.27+9320G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41788192 | ||||||
| chr8:41788227
|
C | T | 1 | a0012c0045t0025g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.27+9285G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41788227 | ||||||
| chr8:41788487
|
C | T | 2 | a0001c0001t0002g0024a0002c0007t0007g0023 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.27+9025G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41788487 | ||||||
| chr8:41788503
|
A | G | 100 | a0001c0001t0002g0024a0001c0001t0002g0063a0001c0001t0002g0075others(97): Show | 100 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.27+9009T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41788503 | ||||||
| chr8:41788845
|
A | G | 1 | a0001c0010t0003g0002 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+8667T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41788845 | ||||||
| chr8:41789132
|
C | T | 1 | a0001c0001t0002g0009 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.27+8380G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789132 | ||||||
| chr8:41789165
|
A | C | 110 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(107): Show | 111 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.27+8347T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789165 | ||||||
| chr8:41789222
|
G | A | 36 | a0001c0001t0002g0063a0001c0001t0002g0075a0001c0001t0002g0077others(33): Show | 36 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.27+8290C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789222 | ||||||
| chr8:41789243
|
T | C | 2 | a0001c0001t0002g0020a0001c0005t0010g0019 | 2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.27+8269A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789243 | ||||||
| chr8:41789281
|
T | C | 2 | a0001c0004t0001g0109a0007c0033t0001g0108 | 2 | HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.27+8231A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789281 | ||||||
| chr8:41789394
|
G | C | 2 | a0001c0010t0003g0114a0001c0010t0003g0189 | 2 | HG02074.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.27+8118C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789394 | ||||||
| chr8:41789413
|
G | A | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.27+8099C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789413 | ||||||
| chr8:41789426
|
G | A | 2 | a0001c0002t0001g0031a0001c0002t0012g0022 | 2 | HG01261.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.27+8086C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789426 | ||||||
| chr8:41789437
|
A | G | 2 | a0001c0010t0003g0114a0001c0010t0003g0189 | 2 | HG02074.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.27+8075T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789437 | ||||||
| chr8:41789479
|
T | G | 193 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(190): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.27+8033A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789479 | ||||||
| chr8:41789503
|
C | T | 1 | a0003c0049t0001g0104 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.27+8009G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789503 | ||||||
| chr8:41789596
|
C | T | 22 | a0001c0001t0002g0024a0001c0002t0001g0031a0001c0002t0012g0022others(19): Show | 22 | HG01243.hp2 HG01261.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.27+7916G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789596 | ||||||
| chr8:41789663
|
G | A | 4 | a0001c0006t0001g0266a0001c0006t0001g0267a0001c0006t0001g0268others(1): Show | 4 | HG01891.hp1 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+7849C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789663 | ||||||
| chr8:41789826
|
G | A | 1 | a0001c0006t0001g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.27+7686C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789826 | ||||||
| chr8:41789845
|
A | G | 13 | a0001c0001t0002g0107a0001c0002t0002g0106a0001c0004t0001g0109others(10): Show | 13 | HG01192.hp2 HG02145.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.27+7667T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789845 | ||||||
| chr8:41789930
|
C | G | 1 | a0001c0009t0002g0059 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.27+7582G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789930 | ||||||
| chr8:41789975
|
A | C | 194 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.27+7537T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789975 | ||||||
| chr8:41790042
|
G | A | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.27+7470C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41790042 | ||||||
| chr8:41790215
|
C | T | 3 | a0001c0012t0005g0103a0001c0046t0030g0277a0003c0024t0003g0102 | 3 | HG02723.hp2 HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.27+7297G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41790215 | ||||||
| chr8:41790259
|
G | A | 195 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.27+7253C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41790259 | ||||||
| chr8:41790468
|
GTCACTAT others(15): Show |
G | 1 | a0001c0001t0001g0155 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.27+7022_27+7043del others(22): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41790468 | ||||||
| chr8:41790495
|
G | T | 1 | a0001c0001t0001g0155 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.27+7017C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41790495 | ||||||
| chr8:41790605
|
G | A | 11 | a0001c0001t0002g0009a0001c0001t0002g0020a0001c0005t0002g0010others(8): Show | 11 | HG01106.hp2 HG02109.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.27+6907C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41790605 | ||||||
| chr8:41790662
|
C | T | 1 | a0001c0005t0001g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.27+6850G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41790662 | ||||||
| chr8:41790663
|
G | A | 41 | a0001c0001t0002g0009a0001c0001t0002g0020a0001c0001t0002g0125others(38): Show | 41 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.27+6849C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41790663 | ||||||
| chr8:41790756
|
C | T | 1 | a0003c0014t0008g0203 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.27+6756G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41790756 | ||||||
| chr8:41790840
|
G | A | 93 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(90): Show | 94 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.27+6672C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41790840 | ||||||
| chr8:41791050
|
G | T | 2 | a0001c0003t0001g0057a0001c0003t0001g0058 | 2 | HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.27+6462C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791050 | ||||||
| chr8:41791126
|
C | T | 5 | a0001c0005t0004g0011a0001c0006t0003g0013a0001c0006t0003g0014others(2): Show | 5 | HG01106.hp2 HG02109.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+6386G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791126 | ||||||
| chr8:41791194
|
G | GT | 18 | a0001c0001t0002g0201a0001c0001t0002g0272a0001c0002t0001g0048others(15): Show | 18 | HG00408.hp2 HG00438.hp2 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.27+6317dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791194 | ||||||
| chr8:41791194
|
GT | G | 71 | a0001c0001t0001g0148a0001c0001t0001g0262a0001c0001t0002g0063others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.27+6317delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791194 | ||||||
| chr8:41791194
|
GTT | G | 87 | a0001c0001t0001g0155a0001c0001t0001g0160a0001c0001t0001g0162others(84): Show | 88 | HG00099.hp1 HG00438.hp1 HG00735.hp2 others(85): Show |
intron_variant | MODIFIER | c.27+6316_27+6317del others(2): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791194 | ||||||
| chr8:41791194
|
GTTTTTTT others(4): Show |
G | 1 | a0015c0053t0002g0263 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.27+6307_27+6317del others(11): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791194 | ||||||
| chr8:41791209
|
T | G | 2 | a0001c0002t0001g0134a0001c0002t0001g0135 | 2 | HG00733.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.27+6303A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791209 | ||||||
| chr8:41791254
|
C | A | 30 | a0001c0001t0002g0125a0001c0002t0001g0121a0001c0002t0001g0122others(27): Show | 30 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.27+6258G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791254 | ||||||
| chr8:41791447
|
C | CT | 7 | a0001c0001t0001g0191a0001c0001t0002g0009a0001c0006t0018g0117others(4): Show | 7 | HG02451.hp2 HG02572.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.27+6064dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791447 | ||||||
| chr8:41791447
|
CT | C | 5 | a0001c0009t0002g0082a0001c0010t0003g0002a0001c0023t0001g0275others(2): Show | 5 | HG00738.hp1 HG01070.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+6064delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791447 | ||||||
| chr8:41791573
|
A | G | 2 | a0001c0009t0002g0046a0001c0009t0002g0047 | 2 | HG00738.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.27+5939T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791573 | ||||||
| chr8:41791634
|
C | T | 12 | a0001c0001t0002g0009a0001c0001t0002g0020a0001c0005t0002g0010others(9): Show | 12 | HG01106.hp2 HG02109.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.27+5878G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791634 | ||||||
| chr8:41791768
|
C | T | 39 | a0001c0001t0002g0063a0001c0001t0002g0075a0001c0001t0002g0077others(36): Show | 39 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.27+5744G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791768 | ||||||
| chr8:41791916
|
T | TG | 194 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.27+5595dupC | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791916 | ||||||
| chr8:41791921
|
T | G | 196 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(193): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.27+5591A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791921 | ||||||
| chr8:41791986
|
A | G | 3 | a0001c0023t0001g0275a0001c0023t0001g0276a0001c0051t0008g0274 | 3 | HG00738.hp1 HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.27+5526T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791986 | ||||||
| chr8:41792052
|
C | T | 2 | a0001c0023t0001g0275a0001c0023t0001g0276 | 2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.27+5460G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41792052 | ||||||
| chr8:41792254
|
G | A | 1 | a0001c0010t0003g0002 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+5258C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41792254 | ||||||
| chr8:41792324
|
T | G | 4 | a0001c0010t0003g0002a0001c0023t0001g0275a0001c0023t0001g0276others(1): Show | 4 | HG00738.hp1 HG01891.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+5188A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41792324 | ||||||
| chr8:41792445
|
C | A | 1 | a0001c0010t0003g0002 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+5067G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41792445 | ||||||
| chr8:41792455
|
G | C | 1 | a0001c0010t0003g0002 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+5057C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41792455 | ||||||
| chr8:41792534
|
C | T | 1 | a0005c0021t0002g0115 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.27+4978G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41792534 | ||||||
| chr8:41792854
|
C | T | 1 | a0001c0010t0003g0002 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+4658G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41792854 | ||||||
| chr8:41792957
|
A | G | 1 | a0001c0006t0003g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.27+4555T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41792957 | ||||||
| chr8:41793104
|
C | T | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.27+4408G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41793104 | ||||||
| chr8:41793169
|
G | C | 1 | a0003c0024t0001g0273 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.27+4343C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41793169 | ||||||
| chr8:41793187
|
G | C | 1 | a0001c0002t0001g0265 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.27+4325C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41793187 | ||||||
| chr8:41793238
|
C | T | 20 | a0001c0001t0002g0024a0001c0002t0001g0031a0001c0002t0012g0022others(17): Show | 20 | HG01243.hp2 HG01261.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.27+4274G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41793238 | ||||||
| chr8:41793394
|
T | TA | 10 | a0001c0006t0001g0039a0001c0010t0003g0002a0001c0013t0001g0037others(7): Show | 10 | HG02080.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.27+4117dupT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41793394 | ||||||
| chr8:41793436
|
C | G | 1 | a0001c0010t0003g0002 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+4076G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41793436 | ||||||
| chr8:41793782
|
A | T | 1 | a0001c0010t0003g0002 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+3730T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41793782 | ||||||
| chr8:41793897
|
GA | G | 4 | a0001c0005t0004g0042a0001c0005t0004g0043a0002c0042t0016g0045others(1): Show | 4 | HG01167.hp1 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+3614delT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41793897 | ||||||
| chr8:41793950
|
T | C | 96 | a0001c0001t0002g0024a0001c0001t0002g0063a0001c0001t0002g0075others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.27+3562A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41793950 | ||||||
| chr8:41793950
|
T | G | 4 | a0001c0006t0001g0266a0001c0006t0001g0267a0001c0006t0001g0268others(1): Show | 4 | HG01891.hp1 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+3562A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41793950 | ||||||
| chr8:41793996
|
C | A | 9 | a0001c0001t0002g0107a0001c0002t0002g0106a0001c0004t0001g0109others(6): Show | 9 | HG01192.hp2 HG02647.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.27+3516G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41793996 | ||||||
| chr8:41794083
|
C | T | 2 | a0001c0023t0001g0275a0001c0023t0001g0276 | 2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.27+3429G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41794083 | ||||||
| chr8:41794208
|
A | G | 23 | a0001c0001t0002g0024a0001c0002t0001g0031a0001c0002t0012g0022others(20): Show | 23 | HG01243.hp2 HG01261.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.27+3304T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41794208 | ||||||
| chr8:41794494
|
C | T | 3 | a0001c0023t0001g0275a0001c0023t0001g0276a0001c0051t0008g0274 | 3 | HG00738.hp1 HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.27+3018G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41794494 | ||||||
| chr8:41794689
|
T | C | 1 | a0001c0001t0002g0110 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.27+2823A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41794689 | ||||||
| chr8:41794783
|
C | T | 23 | a0001c0001t0002g0024a0001c0002t0001g0031a0001c0002t0012g0022others(20): Show | 23 | HG01243.hp2 HG01261.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.27+2729G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41794783 | ||||||
| chr8:41794865
|
T | C | 1 | a0001c0010t0003g0002 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+2647A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41794865 | ||||||
| chr8:41794931
|
C | G | 6 | a0001c0003t0001g0136a0001c0003t0001g0139a0001c0003t0001g0140others(3): Show | 6 | HG01081.hp2 HG01099.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+2581G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41794931 | ||||||
| chr8:41794948
|
C | T | 12 | a0001c0001t0002g0009a0001c0001t0002g0020a0001c0005t0002g0010others(9): Show | 12 | HG01106.hp2 HG02109.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.27+2564G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41794948 | ||||||
| chr8:41794965
|
A | G | 1 | a0001c0005t0002g0190 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.27+2547T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41794965 | ||||||
| chr8:41795047
|
A | G | 1 | a0001c0010t0003g0002 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+2465T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795047 | ||||||
| chr8:41795051
|
C | T | 1 | a0001c0010t0003g0002 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+2461G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795051 | ||||||
| chr8:41795069
|
T | C | 1 | a0001c0010t0003g0002 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+2443A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795069 | ||||||
| chr8:41795130
|
G | T | 1 | a0001c0010t0003g0002 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+2382C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795130 | ||||||
| chr8:41795131
|
C | T | 3 | a0001c0016t0002g0006a0001c0016t0002g0007a0001c0016t0002g0008 | 3 | HG01192.hp2 HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.27+2381G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795131 | ||||||
| chr8:41795202
|
G | T | 3 | a0001c0023t0001g0275a0001c0023t0001g0276a0001c0051t0008g0274 | 3 | HG00738.hp1 HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.27+2310C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795202 | ||||||
| chr8:41795214
|
G | A | 1 | a0001c0010t0003g0002 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+2298C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795214 | ||||||
| chr8:41795215
|
T | C | 3 | a0001c0023t0001g0275a0001c0023t0001g0276a0001c0051t0008g0274 | 3 | HG00738.hp1 HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.27+2297A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795215 | ||||||
| chr8:41795250
|
C | A | 1 | a0001c0004t0002g0271 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.27+2262G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795250 | ||||||
| chr8:41795284
|
G | A | 28 | a0001c0001t0002g0125a0001c0002t0001g0121a0001c0002t0001g0122others(25): Show | 28 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.27+2228C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795284 | ||||||
| chr8:41795284
|
G | T | 3 | a0001c0023t0001g0275a0001c0023t0001g0276a0001c0051t0008g0274 | 3 | HG00738.hp1 HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.27+2228C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795284 | ||||||
| chr8:41795288
|
G | A | 1 | a0001c0010t0003g0002 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+2224C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795288 | ||||||
| chr8:41795311
|
G | A | 3 | a0001c0023t0001g0275a0001c0023t0001g0276a0001c0051t0008g0274 | 3 | HG00738.hp1 HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.27+2201C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795311 | ||||||
| chr8:41795361
|
T | G | 21 | a0001c0001t0002g0125a0001c0002t0001g0121a0001c0002t0001g0122others(18): Show | 21 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.27+2151A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795361 | ||||||
| chr8:41795548
|
A | G | 1 | a0001c0051t0008g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.27+1964T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795548 | ||||||
| chr8:41795572
|
C | T | 4 | a0001c0010t0003g0002a0001c0023t0001g0275a0001c0023t0001g0276others(1): Show | 4 | HG00738.hp1 HG01891.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+1940G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795572 | ||||||
| chr8:41795646
|
G | A | 1 | a0001c0010t0003g0002 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+1866C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795646 | ||||||
| chr8:41795678
|
A | G | 1 | a0003c0015t0003g0137 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.27+1834T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795678 | ||||||
| chr8:41795738
|
C | T | 1 | a0001c0003t0001g0136 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.27+1774G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795738 | ||||||
| chr8:41795748
|
G | A | 3 | a0001c0002t0001g0183a0001c0002t0001g0184a0001c0002t0001g0185 | 3 | HG00735.hp2 HG03704.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.27+1764C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795748 | ||||||
| chr8:41795953
|
T | G | 4 | a0001c0010t0003g0002a0001c0023t0001g0275a0001c0023t0001g0276others(1): Show | 4 | HG00738.hp1 HG01891.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+1559A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795953 | ||||||
| chr8:41796022
|
T | G | 53 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(50): Show | 54 | HG00099.hp1 HG00438.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.27+1490A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41796022 | ||||||
| chr8:41796073
|
T | C | 2 | a0001c0023t0001g0275a0001c0023t0001g0276 | 2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.27+1439A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41796073 | ||||||
| chr8:41796297
|
G | C | 2 | a0001c0023t0001g0275a0001c0023t0001g0276 | 2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.27+1215C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41796297 | ||||||
| chr8:41796549
|
G | GA | 6 | a0001c0001t0002g0272a0001c0010t0003g0189a0003c0024t0001g0273others(3): Show | 6 | HG02074.hp2 HG02809.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+962dupT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41796549 | ||||||
| chr8:41796686
|
C | T | 1 | a0001c0006t0003g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.27+826G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41796686 | ||||||
| chr8:41796940
|
C | T | 194 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0160others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.27+572G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41796940 | ||||||
| chr8:41796956
|
C | T | 1 | a0001c0010t0003g0002 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+556G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41796956 | ||||||
| chr8:41796957
|
C | T | 2 | a0001c0005t0002g0003a0001c0005t0013g0004 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.27+555G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41796957 | ||||||
| chr8:41796979
|
A | G | 1 | a0001c0010t0003g0002 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+533T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41796979 | ||||||
| chr8:41796998
|
T | C | 4 | a0001c0010t0003g0002a0001c0023t0001g0275a0001c0023t0001g0276others(1): Show | 4 | HG00738.hp1 HG01891.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+514A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41796998 | ||||||
| chr8:41796999
|
A | C | 4 | a0001c0010t0003g0002a0001c0023t0001g0275a0001c0023t0001g0276others(1): Show | 4 | HG00738.hp1 HG01891.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+513T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41796999 | ||||||
| chr8:41797079
|
T | G | 1 | a0003c0024t0001g0273 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.27+433A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41797079 | ||||||
| chr8:41797235
|
G | C | 3 | a0001c0023t0001g0275a0001c0023t0001g0276a0001c0051t0008g0274 | 3 | HG00738.hp1 HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.27+277C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41797235 |