| geneid | 22848 |
|---|---|
| ensemblid | ENSG00000115977.21 |
| hgncid | 19679 |
| symbol | AAK1 |
| name | AP2 associated kinase 1 |
| refseq_nuc | NM_014911.5 |
| refseq_prot | NP_055726.4 |
| ensembl_nuc | ENST00000409085.9 |
| ensembl_prot | ENSP00000386456.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 69457997 |
| end | 69643739 |
| strand | - |
| ver | v1.2 |
| region | chr2:69457997-69643739 |
| region5000 | chr2:69452997-69648739 |
| regionname0 | AAK1_chr2_69457997_69643739 |
| regionname5000 | AAK1_chr2_69452997_69648739 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 961 | 184 | 61 | 27 | 78 | 3 | 14 | 59 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002 | 0/0 | 960 | 96 | 16 | 20 | 49 | 3 | 8 | 39 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0003 | 0/0 | 960 | 4 | 2 | 2 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0004 | 0/0 | 961 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0005 | 0/0 | 961 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0006 | 0/0 | 960 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0007 | 0/0 | 961 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0008 | 1/0 | 961 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0009 | 0/0 | 960 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0010 | 0/0 | 961 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2886 | 127 | 31 | 24 | 63 | 1 | 7 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| c0002 | 0/0 | 2883 | 83 | 5 | 20 | 48 | 3 | 7 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| c0003 | 0/0 | 2886 | 19 | 5 | 0 | 11 | 0 | 3 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| c0004 | 0/0 | 2886 | 15 | 7 | 1 | 2 | 2 | 3 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| c0005 | 0/0 | 2883 | 9 | 8 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| c0006 | 0/0 | 2886 | 7 | 6 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| c0007 | 0/0 | 2886 | 5 | 5 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| c0008 | 0/0 | 2886 | 4 | 0 | 1 | 2 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| c0009 | 0/0 | 2886 | 3 | 3 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| c0010 | 0/0 | 2886 | 3 | 0 | 3 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| c0011 | 0/0 | 2886 | 3 | 3 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| c0012 | 0/0 | 2886 | 2 | 2 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| c0013 | 0/0 | 2886 | 2 | 2 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| c0014 | 0/0 | 2883 | 2 | 2 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| c0015 | 0/0 | 2883 | 2 | 0 | 0 | 2 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| c0016 | 0/0 | 2883 | 2 | 2 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| c0017 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| c0018 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| c0019 | 0/0 | 2883 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| c0020 | 0/0 | 2883 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| c0021 | 0/0 | 2883 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| c0022 | 1/0 | 2886 | 1 | 0 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| c0023 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| c0024 | 0/0 | 2883 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| c0025 | 0/0 | 2883 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| c0026 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 18273 | 15 | 0 | 3 | 10 | 1 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0002 | 0/0 | 18271 | 14 | 3 | 0 | 9 | 0 | 2 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0003 | 0/0 | 18274 | 13 | 0 | 6 | 6 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0004 | 0/0 | 18276 | 13 | 1 | 0 | 11 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0005 | 0/0 | 18277 | 12 | 0 | 0 | 12 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0006 | 0/0 | 18273 | 11 | 0 | 11 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0007 | 0/0 | 18272 | 10 | 1 | 2 | 7 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0008 | 0/0 | 18272 | 9 | 5 | 0 | 2 | 0 | 2 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0009 | 0/0 | 18271 | 6 | 1 | 1 | 4 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0010 | 0/0 | 18275 | 6 | 1 | 4 | 0 | 1 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0011 | 0/0 | 18276 | 6 | 0 | 0 | 6 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0012 | 0/0 | 18279 | 5 | 0 | 0 | 4 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0013 | 0/0 | 18272 | 5 | 0 | 1 | 4 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0014 | 0/0 | 18279 | 4 | 3 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0015 | 0/0 | 18274 | 3 | 1 | 0 | 1 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0016 | 0/0 | 18275 | 3 | 2 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0017 | 0/0 | 18276 | 3 | 3 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0018 | 0/0 | 18270 | 3 | 3 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0019 | 0/0 | 18275 | 3 | 0 | 1 | 2 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0020 | 0/0 | 18273 | 3 | 0 | 0 | 3 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0021 | 0/0 | 18272 | 3 | 2 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0022 | 0/0 | 18273 | 2 | 1 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0023 | 0/0 | 18274 | 2 | 0 | 1 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0024 | 0/0 | 18272 | 2 | 0 | 0 | 2 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0025 | 0/0 | 18276 | 2 | 2 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0026 | 0/0 | 18279 | 2 | 2 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0027 | 0/0 | 18271 | 2 | 1 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0028 | 0/0 | 18270 | 2 | 2 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0029 | 0/0 | 18272 | 2 | 2 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0030 | 0/0 | 18278 | 2 | 0 | 0 | 2 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0031 | 0/0 | 18270 | 2 | 0 | 1 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0032 | 0/0 | 18270 | 2 | 0 | 0 | 2 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0033 | 0/0 | 18277 | 2 | 0 | 0 | 2 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0034 | 0/0 | 18273 | 2 | 1 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0035 | 0/0 | 18273 | 2 | 2 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0036 | 0/0 | 18273 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0037 | 0/0 | 18274 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0038 | 0/0 | 18274 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0039 | 0/0 | 18273 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0040 | 0/0 | 18273 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0041 | 0/0 | 18272 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0042 | 0/0 | 18272 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0043 | 0/0 | 18283 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0044 | 0/0 | 18273 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0045 | 0/0 | 18272 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0046 | 0/0 | 18279 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0047 | 0/0 | 18273 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0048 | 0/0 | 18276 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0049 | 0/0 | 18273 | 1 | 0 | 0 | 0 | 1 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0050 | 0/0 | 18276 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0051 | 0/0 | 18273 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0052 | 0/0 | 18273 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0053 | 0/0 | 18274 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0054 | 0/0 | 18273 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0055 | 0/0 | 18273 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0056 | 0/1 | 18276 | 1 | 0 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0057 | 0/0 | 18272 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0058 | 0/0 | 18271 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0059 | 0/0 | 18272 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0060 | 0/0 | 18273 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0061 | 0/0 | 18273 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0062 | 0/0 | 18273 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0063 | 0/0 | 18273 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0064 | 0/0 | 18272 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0065 | 0/0 | 18277 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0066 | 0/0 | 18276 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0067 | 0/0 | 18276 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0068 | 0/0 | 18275 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0069 | 0/0 | 18276 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0070 | 0/0 | 18270 | 1 | 0 | 0 | 0 | 1 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0071 | 0/0 | 18243 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0072 | 0/0 | 18242 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0073 | 0/0 | 18269 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0074 | 0/0 | 18275 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0075 | 0/0 | 18275 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0076 | 0/0 | 18275 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0077 | 0/0 | 18270 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0078 | 0/0 | 18274 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0079 | 0/0 | 18273 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0080 | 0/0 | 18279 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0081 | 0/0 | 18279 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0082 | 0/0 | 18276 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0083 | 0/0 | 18276 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0084 | 0/0 | 18281 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0085 | 0/0 | 18273 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0086 | 0/0 | 18271 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0087 | 0/0 | 18271 | 1 | 0 | 0 | 0 | 1 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0088 | 0/0 | 18271 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0089 | 0/0 | 18275 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0090 | 0/0 | 18271 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0091 | 0/0 | 18270 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0092 | 0/0 | 18271 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0093 | 0/0 | 18271 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0094 | 1/0 | 18272 | 1 | 0 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0095 | 0/0 | 18273 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0096 | 0/0 | 18271 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0097 | 0/0 | 18272 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0098 | 0/0 | 18241 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0099 | 0/0 | 18270 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0100 | 0/0 | 18269 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0101 | 0/0 | 18274 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0102 | 0/0 | 18274 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0103 | 0/0 | 18276 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0104 | 0/0 | 18281 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0105 | 0/0 | 18270 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0106 | 0/0 | 18279 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0107 | 0/0 | 18276 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0108 | 0/0 | 18275 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0109 | 0/0 | 18272 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0110 | 0/0 | 18271 | 1 | 0 | 0 | 0 | 1 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0111 | 0/0 | 18271 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0112 | 0/0 | 18274 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0113 | 0/0 | 18270 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0114 | 0/0 | 18271 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0115 | 0/0 | 18275 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0116 | 0/0 | 18274 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0117 | 0/0 | 18274 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0118 | 0/0 | 18274 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0119 | 0/0 | 18274 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0120 | 0/0 | 18277 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0121 | 0/0 | 18276 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0122 | 0/0 | 18274 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0123 | 0/0 | 18276 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0124 | 0/0 | 18272 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0125 | 0/0 | 18274 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0126 | 0/0 | 18274 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0127 | 0/0 | 18277 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0128 | 0/0 | 18274 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0129 | 0/0 | 18273 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0130 | 0/0 | 18273 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0131 | 0/0 | 18274 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0132 | 0/0 | 18275 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0133 | 0/0 | 18277 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0134 | 0/0 | 18279 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0135 | 0/0 | 18277 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0136 | 0/0 | 18273 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0137 | 0/0 | 18279 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0138 | 0/0 | 18272 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0139 | 0/0 | 18278 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0140 | 0/0 | 18276 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0141 | 0/0 | 18278 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0142 | 0/0 | 18279 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0143 | 0/0 | 18276 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0144 | 0/0 | 18274 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0145 | 0/0 | 18273 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0146 | 0/0 | 18276 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0147 | 0/0 | 18272 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0148 | 0/0 | 18278 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0149 | 0/0 | 18272 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0150 | 0/0 | 18273 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0151 | 0/0 | 18272 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0152 | 0/0 | 18280 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0153 | 0/0 | 18277 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0154 | 0/0 | 18273 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| t0155 | 0/0 | 18273 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0058 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0133 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2886 | 127 | 31 | 24 | 63 | 1 | 7 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0003 | 0/0 | 2886 | 19 | 5 | 0 | 11 | 0 | 3 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0004 | 0/0 | 2886 | 15 | 7 | 1 | 2 | 2 | 3 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0006 | 0/0 | 2886 | 7 | 6 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0007 | 0/0 | 2886 | 5 | 5 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0008 | 0/0 | 2886 | 4 | 0 | 1 | 2 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0009 | 0/0 | 2886 | 3 | 3 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0011 | 0/0 | 2886 | 3 | 3 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0026 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002 | 0/0 | 2883 | 83 | 5 | 20 | 48 | 3 | 7 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0005 | 0/0 | 2883 | 9 | 8 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0016 | 0/0 | 2883 | 2 | 2 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0019 | 0/0 | 2883 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0024 | 0/0 | 2883 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0003c0014 | 0/0 | 2883 | 2 | 2 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0003c0020 | 0/0 | 2883 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0003c0021 | 0/0 | 2883 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0004c0012 | 0/0 | 2886 | 2 | 2 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0004c0013 | 0/0 | 2886 | 2 | 2 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0005c0010 | 0/0 | 2886 | 3 | 0 | 3 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0006c0015 | 0/0 | 2883 | 2 | 0 | 0 | 2 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0007c0017 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0007c0018 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0008c0022 | 1/0 | 2886 | 1 | 0 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0009c0025 | 0/0 | 2883 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0010c0023 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 21156 | 12 | 3 | 0 | 8 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0004 | 0/0 | 21161 | 13 | 1 | 0 | 11 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0006 | 0/0 | 21158 | 11 | 0 | 11 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0007 | 0/0 | 21157 | 8 | 1 | 1 | 6 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0008 | 0/0 | 21157 | 6 | 3 | 0 | 2 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0009 | 0/0 | 21156 | 5 | 1 | 1 | 3 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0011 | 0/0 | 21161 | 6 | 0 | 0 | 6 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0013 | 0/0 | 21157 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0014 | 0/0 | 21164 | 3 | 2 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0020 | 0/0 | 21158 | 3 | 0 | 0 | 3 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0021 | 0/0 | 21157 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0022 | 0/0 | 21158 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0024 | 0/0 | 21157 | 2 | 0 | 0 | 2 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0027 | 0/0 | 21156 | 2 | 1 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0031 | 0/0 | 21155 | 2 | 0 | 1 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0032 | 0/0 | 21155 | 2 | 0 | 0 | 2 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0034 | 0/0 | 21158 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0037 | 0/0 | 21159 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0045 | 0/0 | 21157 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0056 | 0/1 | 21161 | 1 | 0 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0057 | 0/0 | 21157 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0058 | 0/0 | 21156 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0063 | 0/0 | 21158 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0073 | 0/0 | 21154 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0074 | 0/0 | 21160 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0075 | 0/0 | 21160 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0076 | 0/0 | 21160 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0077 | 0/0 | 21155 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0078 | 0/0 | 21159 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0083 | 0/0 | 21161 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0086 | 0/0 | 21156 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0087 | 0/0 | 21156 | 1 | 0 | 0 | 0 | 1 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0088 | 0/0 | 21156 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0089 | 0/0 | 21160 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0090 | 0/0 | 21156 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0091 | 0/0 | 21155 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0092 | 0/0 | 21156 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0093 | 0/0 | 21156 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0095 | 0/0 | 21158 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0096 | 0/0 | 21156 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0099 | 0/0 | 21155 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0101 | 0/0 | 21159 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0102 | 0/0 | 21159 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0104 | 0/0 | 21166 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0105 | 0/0 | 21155 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0112 | 0/0 | 21159 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0113 | 0/0 | 21155 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0114 | 0/0 | 21156 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0116 | 0/0 | 21159 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0117 | 0/0 | 21159 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0118 | 0/0 | 21159 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0119 | 0/0 | 21159 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0120 | 0/0 | 21162 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0121 | 0/0 | 21161 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0124 | 0/0 | 21157 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0126 | 0/0 | 21159 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0136 | 0/0 | 21158 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0137 | 0/0 | 21164 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0138 | 0/0 | 21157 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0139 | 0/0 | 21163 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0140 | 0/0 | 21161 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0143 | 0/0 | 21161 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0144 | 0/0 | 21159 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0147 | 0/0 | 21157 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0001t0149 | 0/0 | 21157 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0003t0012 | 0/0 | 21164 | 5 | 0 | 0 | 4 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0003t0022 | 0/0 | 21158 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0003t0026 | 0/0 | 21164 | 2 | 2 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0003t0030 | 0/0 | 21163 | 2 | 0 | 0 | 2 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0003t0046 | 0/0 | 21164 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0003t0064 | 0/0 | 21157 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0003t0080 | 0/0 | 21164 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0003t0081 | 0/0 | 21164 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0003t0082 | 0/0 | 21161 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0003t0106 | 0/0 | 21164 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0003t0108 | 0/0 | 21160 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0003t0109 | 0/0 | 21157 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0003t0142 | 0/0 | 21164 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0004t0002 | 0/0 | 21156 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0004t0010 | 0/0 | 21160 | 3 | 1 | 1 | 0 | 1 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0004t0014 | 0/0 | 21164 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0004t0017 | 0/0 | 21161 | 3 | 3 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0004t0067 | 0/0 | 21161 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0004t0068 | 0/0 | 21160 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0004t0070 | 0/0 | 21155 | 1 | 0 | 0 | 0 | 1 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0004t0071 | 0/0 | 21128 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0004t0072 | 0/0 | 21127 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0004t0146 | 0/0 | 21161 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0004t0153 | 0/0 | 21162 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0006t0016 | 0/0 | 21160 | 3 | 2 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0006t0028 | 0/0 | 21155 | 2 | 2 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0006t0041 | 0/0 | 21157 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0006t0042 | 0/0 | 21157 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0007t0021 | 0/0 | 21157 | 2 | 2 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0007t0034 | 0/0 | 21158 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0007t0035 | 0/0 | 21158 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0007t0148 | 0/0 | 21163 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0008t0069 | 0/0 | 21161 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0008t0097 | 0/0 | 21157 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0008t0098 | 0/0 | 21126 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0008t0135 | 0/0 | 21162 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0009t0035 | 0/0 | 21158 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0009t0125 | 0/0 | 21159 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0009t0141 | 0/0 | 21163 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0011t0029 | 0/0 | 21157 | 2 | 2 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0011t0079 | 0/0 | 21158 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0001c0026t0152 | 0/0 | 21165 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0001 | 0/0 | 21155 | 14 | 0 | 3 | 9 | 1 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0003 | 0/0 | 21156 | 12 | 0 | 6 | 5 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0005 | 0/0 | 21159 | 12 | 0 | 0 | 12 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0007 | 0/0 | 21154 | 2 | 0 | 1 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0008 | 0/0 | 21154 | 2 | 1 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0013 | 0/0 | 21154 | 3 | 0 | 1 | 2 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0015 | 0/0 | 21156 | 3 | 1 | 0 | 1 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0019 | 0/0 | 21157 | 3 | 0 | 1 | 2 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0023 | 0/0 | 21156 | 2 | 0 | 1 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0033 | 0/0 | 21159 | 2 | 0 | 0 | 2 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0038 | 0/0 | 21156 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0039 | 0/0 | 21155 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0044 | 0/0 | 21155 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0047 | 0/0 | 21155 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0048 | 0/0 | 21158 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0049 | 0/0 | 21155 | 1 | 0 | 0 | 0 | 1 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0050 | 0/0 | 21158 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0051 | 0/0 | 21155 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0052 | 0/0 | 21155 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0053 | 0/0 | 21156 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0054 | 0/0 | 21155 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0055 | 0/0 | 21155 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0059 | 0/0 | 21154 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0062 | 0/0 | 21155 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0085 | 0/0 | 21155 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0110 | 0/0 | 21153 | 1 | 0 | 0 | 0 | 1 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0111 | 0/0 | 21153 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0115 | 0/0 | 21157 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0127 | 0/0 | 21159 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0128 | 0/0 | 21156 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0129 | 0/0 | 21155 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0130 | 0/0 | 21155 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0131 | 0/0 | 21156 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0132 | 0/0 | 21157 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0133 | 0/0 | 21159 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0145 | 0/0 | 21155 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0154 | 0/0 | 21155 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0002t0155 | 0/0 | 21155 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0005t0009 | 0/0 | 21153 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0005t0018 | 0/0 | 21152 | 3 | 3 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0005t0040 | 0/0 | 21155 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0005t0100 | 0/0 | 21151 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0005t0122 | 0/0 | 21156 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0005t0123 | 0/0 | 21158 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0005t0150 | 0/0 | 21155 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0016t0103 | 0/0 | 21158 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0016t0134 | 0/0 | 21161 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0019t0065 | 0/0 | 21159 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0002c0024t0060 | 0/0 | 21155 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0003c0014t0025 | 0/0 | 21158 | 2 | 2 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0003c0020t0084 | 0/0 | 21163 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0003c0021t0151 | 0/0 | 21154 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0004c0012t0036 | 0/0 | 21158 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0004c0012t0061 | 0/0 | 21158 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0004c0013t0043 | 0/0 | 21168 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0004c0013t0107 | 0/0 | 21161 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0005c0010t0010 | 0/0 | 21160 | 3 | 0 | 3 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0006c0015t0001 | 0/0 | 21155 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0006c0015t0013 | 0/0 | 21154 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0007c0017t0066 | 0/0 | 21161 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0007c0018t0002 | 0/0 | 21156 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0008c0022t0094 | 1/0 | 21157 | 1 | 0 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0009c0025t0003 | 0/0 | 21156 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| a0010c0023t0008 | 0/0 | 21157 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | copy fasta | chr2 | 69452997 | 69648739 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0006g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0006g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0006g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0006g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0006g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0006g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0006g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0006g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0006g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0006g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0006g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0007g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0007g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0007g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0007g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0007g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0007g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0007g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0007g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0008g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0008g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0008g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0008g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0008g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0009g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0009g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0009g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0009g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0009g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0011g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0011g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0011g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0011g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0011g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0011g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0013g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0014g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0014g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0014g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0020g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0020g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0020g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0021g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0022g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0024g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0024g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0027g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0027g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0031g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0031g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0032g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0032g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0034g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0037g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0045g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0056g0058 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0057g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0058g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0063g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0073g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0074g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0075g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0076g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0077g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0078g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0083g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0086g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0087g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0088g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0089g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0090g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0091g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0092g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0093g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0095g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0096g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0099g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0101g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0102g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0104g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0105g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0112g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0113g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0114g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0116g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0117g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0118g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0119g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0120g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0121g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0124g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0126g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0136g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0137g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0138g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0139g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0140g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0143g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0144g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0147g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0001t0149g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0003t0012g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0003t0012g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0003t0012g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0003t0012g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0003t0012g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0003t0022g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0003t0026g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0003t0026g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0003t0030g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0003t0030g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0003t0046g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0003t0064g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0003t0080g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0003t0081g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0003t0082g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0003t0106g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0003t0108g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0003t0109g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0003t0142g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0004t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0004t0010g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0004t0010g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0004t0010g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0004t0014g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0004t0017g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0004t0017g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0004t0017g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0004t0067g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0004t0068g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0004t0070g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0004t0071g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0004t0072g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0004t0146g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0004t0153g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0006t0016g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0006t0016g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0006t0016g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0006t0028g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0006t0028g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0006t0041g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0006t0042g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0007t0021g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0007t0021g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0007t0034g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0007t0035g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0007t0148g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0008t0069g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0008t0097g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0008t0098g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0008t0135g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0009t0035g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0009t0125g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0009t0141g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0011t0029g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0011t0029g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0011t0079g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0001c0026t0152g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0005g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0005g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0005g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0005g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0005g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0005g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0005g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0007g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0007g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0008g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0008g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0013g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0013g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0013g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0015g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0015g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0015g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0019g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0019g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0019g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0023g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0023g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0033g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0033g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0038g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0039g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0044g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0047g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0048g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0049g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0050g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0051g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0052g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0053g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0054g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0055g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0059g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0062g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0085g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0110g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0111g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0115g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0127g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0128g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0129g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0130g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0131g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0132g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0133g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0145g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0154g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0002t0155g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0005t0009g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0005t0018g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0005t0018g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0005t0018g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0005t0040g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0005t0100g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0005t0122g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0005t0123g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0005t0150g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0016t0103g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0016t0134g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0019t0065g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0002c0024t0060g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0003c0014t0025g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0003c0014t0025g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0003c0020t0084g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0003c0021t0151g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0004c0012t0036g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0004c0012t0061g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0004c0013t0043g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0004c0013t0107g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0005c0010t0010g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0005c0010t0010g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0005c0010t0010g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0006c0015t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0006c0015t0013g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0007c0017t0066g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0007c0018t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0008c0022t0094g0133 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0009c0025t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| a0010c0023t0008g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0110 | g0177 | EUR | GBR | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG00099 | hp2 | a0001 | c0004 | t0070 | g0071 | EUR | GBR | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0040 | EUR | GBR | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG00140 | hp2 | a0001 | c0001 | t0087 | g0135 | EUR | GBR | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG00323 | hp1 | a0001 | c0004 | t0010 | g0148 | EUR | FIN | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG00323 | hp2 | a0002 | c0002 | t0049 | g0047 | EUR | FIN | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | CHS | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG00408 | hp2 | a0001 | c0001 | t0022 | g0011 | EAS | CHS | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG00438 | hp1 | a0002 | c0002 | t0005 | g0235 | EAS | CHS | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | CHS | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0221 | EAS | CHS | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | CHS | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG00558 | hp1 | a0001 | c0008 | t0098 | g0140 | EAS | CHS | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG00558 | hp2 | a0006 | c0015 | t0001 | g0024 | EAS | CHS | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | CHS | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0254 | EAS | CHS | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG00735 | hp1 | a0002 | c0002 | t0003 | g0263 | AMR | PUR | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG00735 | hp2 | a0001 | c0006 | t0016 | g0289 | AMR | PUR | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG00738 | hp1 | a0002 | c0002 | t0003 | g0251 | AMR | PUR | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG00738 | hp2 | a0001 | c0001 | t0031 | g0174 | AMR | PUR | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01074 | hp1 | a0002 | c0002 | t0023 | g0026 | AMR | PUR | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01074 | hp2 | a0001 | c0008 | t0097 | g0131 | AMR | PUR | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01099 | hp1 | a0002 | c0002 | t0019 | g0115 | AMR | PUR | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01099 | hp2 | a0002 | c0002 | t0145 | g0275 | AMR | PUR | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01106 | hp1 | a0005 | c0010 | t0010 | g0153 | AMR | PUR | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01106 | hp2 | a0002 | c0002 | t0003 | g0246 | AMR | PUR | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01167 | hp1 | a0001 | c0001 | t0078 | g0055 | AMR | PUR | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01167 | hp2 | a0001 | c0001 | t0027 | g0128 | AMR | PUR | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01175 | hp1 | a0002 | c0002 | t0130 | g0243 | AMR | PUR | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01175 | hp2 | a0001 | c0004 | t0010 | g0127 | AMR | PUR | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01192 | hp1 | a0001 | c0001 | t0095 | g0136 | AMR | PUR | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0057 | AMR | PUR | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01243 | hp1 | a0001 | c0001 | t0014 | g0060 | AMR | PUR | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01243 | hp2 | a0001 | c0001 | t0140 | g0269 | AMR | PUR | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01255 | hp1 | a0001 | c0001 | t0007 | g0081 | AMR | CLM | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01255 | hp2 | a0002 | c0002 | t0053 | g0056 | AMR | CLM | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01257 | hp1 | a0001 | c0001 | t0147 | g0274 | AMR | CLM | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01257 | hp2 | a0001 | c0001 | t0009 | g0147 | AMR | CLM | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01258 | hp1 | a0001 | c0001 | t0006 | g0207 | AMR | CLM | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01258 | hp2 | a0002 | c0002 | t0013 | g0144 | AMR | CLM | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01358 | hp1 | a0002 | c0002 | t0007 | g0068 | AMR | CLM | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01358 | hp2 | a0001 | c0001 | t0006 | g0223 | AMR | CLM | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01361 | hp1 | a0001 | c0001 | t0092 | g0164 | AMR | CLM | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01361 | hp2 | a0002 | c0002 | t0115 | g0180 | AMR | CLM | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01433 | hp1 | a0003 | c0020 | t0084 | g0105 | AMR | CLM | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01433 | hp2 | a0002 | c0002 | t0044 | g0041 | AMR | CLM | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | ACB | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01884 | hp2 | a0001 | c0006 | t0042 | g0007 | AFR | ACB | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01891 | hp1 | a0001 | c0001 | t0027 | g0145 | AFR | ACB | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01891 | hp2 | a0003 | c0014 | t0025 | g0286 | AFR | ACB | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01928 | hp1 | a0001 | c0001 | t0006 | g0222 | AMR | PEL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01928 | hp2 | a0003 | c0021 | t0151 | g0282 | AMR | PEL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01934 | hp1 | a0002 | c0002 | t0127 | g0249 | AMR | PEL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01934 | hp2 | a0001 | c0001 | t0006 | g0217 | AMR | PEL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01943 | hp1 | a0002 | c0002 | t0003 | g0227 | AMR | PEL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01943 | hp2 | a0001 | c0001 | t0136 | g0212 | AMR | PEL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01952 | hp1 | a0001 | c0001 | t0006 | g0225 | AMR | PEL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01952 | hp2 | a0005 | c0010 | t0010 | g0142 | AMR | PEL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01975 | hp1 | a0001 | c0001 | t0006 | g0213 | AMR | PEL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01975 | hp2 | a0002 | c0002 | t0003 | g0244 | AMR | PEL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0043 | AMR | PEL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01978 | hp2 | a0001 | c0001 | t0006 | g0204 | AMR | PEL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01981 | hp1 | a0005 | c0010 | t0010 | g0123 | AMR | PEL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG01981 | hp2 | a0001 | c0001 | t0006 | g0218 | AMR | PEL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02004 | hp1 | a0001 | c0001 | t0006 | g0220 | AMR | PEL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02004 | hp2 | a0002 | c0002 | t0128 | g0237 | AMR | PEL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02015 | hp1 | a0001 | c0001 | t0011 | g0197 | EAS | KHV | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02015 | hp2 | a0001 | c0001 | t0007 | g0089 | EAS | KHV | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02040 | hp1 | a0001 | c0001 | t0024 | g0090 | EAS | KHV | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02040 | hp2 | a0001 | c0008 | t0135 | g0262 | EAS | KHV | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02056 | hp1 | a0001 | c0001 | t0009 | g0124 | EAS | KHV | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | KHV | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02074 | hp1 | a0009 | c0025 | t0003 | g0260 | EAS | KHV | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02074 | hp2 | a0001 | c0003 | t0106 | g0141 | EAS | KHV | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02080 | hp1 | a0001 | c0001 | t0007 | g0099 | EAS | KHV | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | KHV | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0264 | EAS | KHV | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02083 | hp2 | a0002 | c0002 | t0003 | g0199 | EAS | KHV | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02132 | hp1 | a0001 | c0001 | t0074 | g0048 | EAS | KHV | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02132 | hp2 | a0007 | c0017 | t0066 | g0076 | EAS | KHV | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02135 | hp1 | a0001 | c0001 | t0008 | g0082 | EAS | KHV | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02135 | hp2 | a0002 | c0002 | t0003 | g0203 | EAS | KHV | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02145 | hp1 | a0002 | c0002 | t0015 | g0003 | AFR | ACB | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02145 | hp2 | a0001 | c0004 | t0068 | g0079 | AFR | ACB | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0028 | AMR | PEL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02148 | hp2 | a0001 | c0001 | t0006 | g0224 | AMR | PEL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02165 | hp1 | a0002 | c0002 | t0005 | g0248 | EAS | CDX | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02165 | hp2 | a0001 | c0001 | t0032 | g0175 | EAS | CDX | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02257 | hp1 | a0001 | c0001 | t0008 | g0012 | AFR | ACB | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02257 | hp2 | a0002 | c0019 | t0065 | g0062 | AFR | ACB | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02280 | hp1 | a0001 | c0001 | t0124 | g0188 | AFR | ACB | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02280 | hp2 | a0001 | c0009 | t0125 | g0179 | AFR | ACB | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02293 | hp1 | a0002 | c0002 | t0003 | g0245 | AMR | PEL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02293 | hp2 | a0001 | c0001 | t0006 | g0205 | AMR | PEL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02300 | hp1 | a0001 | c0001 | t0093 | g0121 | AMR | PEL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02300 | hp2 | a0001 | c0001 | t0119 | g0181 | AMR | PEL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02451 | hp1 | a0001 | c0003 | t0026 | g0015 | AFR | ACB | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02451 | hp2 | a0001 | c0001 | t0073 | g0052 | AFR | ACB | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02572 | hp1 | a0002 | c0005 | t0040 | g0006 | AFR | GWD | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02572 | hp2 | a0004 | c0013 | t0043 | g0284 | AFR | GWD | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02602 | hp1 | a0001 | c0003 | t0012 | g0088 | SAS | PJL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02602 | hp2 | a0002 | c0002 | t0003 | g0215 | SAS | PJL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02622 | hp1 | a0002 | c0005 | t0018 | g0104 | AFR | GWD | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02622 | hp2 | a0001 | c0003 | t0026 | g0014 | AFR | GWD | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02630 | hp1 | a0001 | c0006 | t0016 | g0017 | AFR | GWD | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02630 | hp2 | a0001 | c0004 | t0010 | g0156 | AFR | GWD | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02698 | hp1 | a0002 | c0002 | t0054 | g0030 | SAS | PJL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02698 | hp2 | a0001 | c0008 | t0069 | g0102 | SAS | PJL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02717 | hp1 | a0002 | c0002 | t0059 | g0032 | AFR | GWD | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02717 | hp2 | a0001 | c0001 | t0063 | g0288 | AFR | GWD | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02723 | hp1 | a0001 | c0004 | t0017 | g0078 | AFR | GWD | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02723 | hp2 | a0001 | c0001 | t0121 | g0186 | AFR | GWD | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0261 | SAS | PJL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02738 | hp2 | a0002 | c0002 | t0008 | g0070 | SAS | PJL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02809 | hp1 | a0002 | c0002 | t0052 | g0023 | AFR | GWD | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02809 | hp2 | a0001 | c0007 | t0021 | g0276 | AFR | GWD | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02818 | hp1 | a0001 | c0006 | t0028 | g0126 | AFR | GWD | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02818 | hp2 | a0001 | c0001 | t0037 | g0009 | AFR | GWD | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02895 | hp1 | a0002 | c0002 | t0111 | g0173 | AFR | GWD | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02895 | hp2 | a0002 | c0016 | t0134 | g0272 | AFR | GWD | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02896 | hp1 | a0001 | c0007 | t0021 | g0279 | AFR | GWD | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02896 | hp2 | a0002 | c0005 | t0100 | g0116 | AFR | GWD | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02922 | hp1 | a0001 | c0009 | t0035 | g0190 | AFR | ESN | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02922 | hp2 | a0001 | c0001 | t0105 | g0108 | AFR | ESN | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02965 | hp1 | a0001 | c0011 | t0029 | g0293 | AFR | ESN | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02965 | hp2 | a0004 | c0013 | t0107 | g0107 | AFR | ESN | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02970 | hp1 | a0001 | c0004 | t0014 | g0063 | AFR | ESN | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02970 | hp2 | a0001 | c0001 | t0104 | g0292 | AFR | ESN | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0160 | AFR | ESN | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02976 | hp2 | a0001 | c0007 | t0148 | g0277 | AFR | ESN | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03041 | hp2 | a0001 | c0004 | t0017 | g0073 | AFR | GWD | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0084 | AFR | MSL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03098 | hp2 | a0002 | c0005 | t0150 | g0281 | AFR | MSL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03139 | hp1 | a0001 | c0001 | t0077 | g0072 | AFR | ESN | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03139 | hp2 | a0002 | c0002 | t0008 | g0050 | AFR | ESN | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03195 | hp1 | a0001 | c0003 | t0081 | g0080 | AFR | ESN | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03195 | hp2 | a0001 | c0001 | t0096 | g0162 | AFR | ESN | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03209 | hp1 | a0001 | c0001 | t0120 | g0187 | AFR | MSL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03209 | hp2 | a0001 | c0001 | t0057 | g0291 | AFR | MSL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03225 | hp1 | a0003 | c0014 | t0025 | g0285 | AFR | MSL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0065 | AFR | MSL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03453 | hp1 | a0001 | c0006 | t0016 | g0061 | AFR | MSL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03453 | hp2 | a0001 | c0001 | t0116 | g0185 | AFR | MSL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03486 | hp1 | a0002 | c0005 | t0018 | g0103 | AFR | MSL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03486 | hp2 | a0002 | c0005 | t0123 | g0183 | AFR | MSL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03491 | hp1 | a0001 | c0004 | t0146 | g0273 | SAS | PJL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03491 | hp2 | a0001 | c0004 | t0002 | g0137 | SAS | PJL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03516 | hp1 | a0001 | c0001 | t0118 | g0184 | AFR | ESN | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03516 | hp2 | a0001 | c0001 | t0099 | g0161 | AFR | ESN | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03540 | hp1 | a0010 | c0023 | t0008 | g0083 | AFR | GWD | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03540 | hp2 | a0001 | c0004 | t0017 | g0075 | AFR | GWD | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03579 | hp1 | a0002 | c0005 | t0122 | g0182 | AFR | MSL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03579 | hp2 | a0002 | c0016 | t0103 | g0106 | AFR | MSL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03654 | hp1 | a0001 | c0004 | t0153 | g0296 | SAS | PJL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03654 | hp2 | a0001 | c0001 | t0008 | g0022 | SAS | PJL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03669 | hp1 | a0002 | c0002 | t0015 | g0002 | SAS | PJL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03710 | hp1 | a0002 | c0024 | t0060 | g0031 | SAS | PJL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03710 | hp2 | a0001 | c0001 | t0144 | g0232 | SAS | PJL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03831 | hp1 | a0002 | c0002 | t0047 | g0053 | SAS | BEB | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03831 | hp2 | a0001 | c0001 | t0113 | g0178 | SAS | BEB | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0051 | SAS | STU | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG04115 | hp2 | a0001 | c0001 | t0021 | g0278 | SAS | STU | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG04199 | hp1 | a0001 | c0003 | t0142 | g0214 | SAS | STU | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG04199 | hp2 | a0002 | c0002 | t0039 | g0004 | SAS | STU | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG04228 | hp1 | a0001 | c0001 | t0139 | g0231 | SAS | STU | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG04228 | hp2 | a0001 | c0003 | t0046 | g0100 | SAS | STU | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18612 | hp1 | a0001 | c0003 | t0108 | g0138 | EAS | CHB | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18612 | hp2 | a0002 | c0002 | t0055 | g0021 | EAS | CHB | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18747 | hp1 | a0001 | c0001 | t0149 | g0280 | EAS | CHB | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18747 | hp2 | a0002 | c0002 | t0013 | g0112 | EAS | CHB | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18906 | hp1 | a0001 | c0001 | t0091 | g0117 | AFR | YRI | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18906 | hp2 | a0001 | c0001 | t0014 | g0059 | AFR | YRI | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18939 | hp1 | a0001 | c0003 | t0109 | g0166 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18939 | hp2 | a0002 | c0002 | t0005 | g0252 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18943 | hp1 | a0001 | c0001 | t0011 | g0201 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18943 | hp2 | a0002 | c0002 | t0133 | g0210 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18945 | hp1 | a0002 | c0002 | t0062 | g0054 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18945 | hp2 | a0001 | c0001 | t0126 | g0219 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18946 | hp1 | a0001 | c0001 | t0007 | g0049 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18948 | hp1 | a0002 | c0002 | t0129 | g0241 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18948 | hp2 | a0001 | c0001 | t0009 | g0129 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18950 | hp1 | a0002 | c0002 | t0005 | g0239 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18950 | hp2 | a0001 | c0004 | t0071 | g0074 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18953 | hp1 | a0002 | c0002 | t0005 | g0253 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0268 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18956 | hp1 | a0001 | c0001 | t0020 | g0208 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18956 | hp2 | a0002 | c0002 | t0051 | g0045 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18960 | hp1 | a0001 | c0001 | t0114 | g0171 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18960 | hp2 | a0002 | c0002 | t0003 | g0238 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18961 | hp1 | a0002 | c0002 | t0005 | g0240 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18961 | hp2 | a0001 | c0003 | t0030 | g0168 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18963 | hp1 | a0002 | c0002 | t0131 | g0211 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18963 | hp2 | a0001 | c0001 | t0020 | g0202 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18966 | hp1 | a0002 | c0002 | t0023 | g0036 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18966 | hp2 | a0001 | c0003 | t0012 | g0096 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18967 | hp1 | a0002 | c0002 | t0013 | g0110 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18968 | hp1 | a0001 | c0001 | t0058 | g0092 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18968 | hp2 | a0002 | c0002 | t0038 | g0001 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18969 | hp1 | a0002 | c0002 | t0005 | g0226 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18969 | hp2 | a0001 | c0003 | t0030 | g0169 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18970 | hp1 | a0002 | c0002 | t0155 | g0298 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18970 | hp2 | a0001 | c0001 | t0090 | g0119 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18973 | hp1 | a0001 | c0001 | t0076 | g0037 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18973 | hp2 | a0001 | c0003 | t0080 | g0094 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18977 | hp1 | a0001 | c0001 | t0007 | g0086 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18977 | hp2 | a0002 | c0002 | t0005 | g0230 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18980 | hp1 | a0001 | c0001 | t0011 | g0195 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18980 | hp2 | a0001 | c0003 | t0012 | g0097 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18983 | hp2 | a0001 | c0001 | t0086 | g0167 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18992 | hp1 | a0001 | c0001 | t0143 | g0198 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18992 | hp2 | a0002 | c0002 | t0085 | g0109 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18993 | hp1 | a0001 | c0001 | t0112 | g0170 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18993 | hp2 | a0002 | c0002 | t0015 | g0005 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18994 | hp1 | a0001 | c0001 | t0008 | g0069 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18994 | hp2 | a0002 | c0002 | t0033 | g0200 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19002 | hp1 | a0001 | c0003 | t0082 | g0098 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19002 | hp2 | a0001 | c0001 | t0011 | g0196 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19004 | hp1 | a0001 | c0004 | t0072 | g0093 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19004 | hp2 | a0001 | c0003 | t0012 | g0091 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19005 | hp2 | a0002 | c0002 | t0154 | g0297 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19006 | hp1 | a0002 | c0002 | t0132 | g0236 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19006 | hp2 | a0007 | c0018 | t0002 | g0165 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19007 | hp1 | a0002 | c0002 | t0033 | g0255 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19007 | hp2 | a0001 | c0001 | t0089 | g0122 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19009 | hp2 | a0002 | c0002 | t0005 | g0234 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19010 | hp1 | a0001 | c0001 | t0011 | g0192 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19010 | hp2 | a0002 | c0002 | t0005 | g0229 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19011 | hp1 | a0001 | c0001 | t0007 | g0101 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19011 | hp2 | a0001 | c0001 | t0020 | g0193 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19030 | hp1 | a0001 | c0003 | t0022 | g0010 | AFR | LWK | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19030 | hp2 | a0001 | c0006 | t0041 | g0008 | AFR | LWK | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19043 | hp1 | a0001 | c0001 | t0008 | g0013 | AFR | LWK | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19043 | hp2 | a0001 | c0007 | t0034 | g0270 | AFR | LWK | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19055 | hp1 | a0001 | c0001 | t0138 | g0209 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19055 | hp2 | a0002 | c0002 | t0048 | g0039 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19056 | hp2 | a0002 | c0005 | t0009 | g0163 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19058 | hp1 | a0001 | c0001 | t0009 | g0139 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19058 | hp2 | a0002 | c0002 | t0005 | g0228 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19060 | hp1 | a0002 | c0002 | t0003 | g0250 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0206 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19062 | hp1 | a0001 | c0001 | t0007 | g0027 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19062 | hp2 | a0001 | c0001 | t0013 | g0151 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19063 | hp2 | a0001 | c0001 | t0102 | g0113 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19065 | hp1 | a0002 | c0002 | t0007 | g0018 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19065 | hp2 | a0001 | c0003 | t0012 | g0095 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19066 | hp1 | a0002 | c0002 | t0005 | g0256 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19066 | hp2 | a0001 | c0001 | t0075 | g0020 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19068 | hp1 | a0001 | c0001 | t0034 | g0267 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19068 | hp2 | a0001 | c0001 | t0101 | g0118 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19074 | hp2 | a0002 | c0002 | t0050 | g0035 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19077 | hp1 | a0006 | c0015 | t0013 | g0111 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19077 | hp2 | a0001 | c0001 | t0032 | g0172 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19078 | hp1 | a0002 | c0002 | t0019 | g0159 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19078 | hp2 | a0001 | c0001 | t0004 | g0258 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19079 | hp1 | a0001 | c0001 | t0137 | g0247 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19079 | hp2 | a0002 | c0002 | t0019 | g0143 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19080 | hp1 | a0001 | c0001 | t0031 | g0176 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0265 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19084 | hp2 | a0002 | c0002 | t0003 | g0242 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19088 | hp2 | a0001 | c0001 | t0024 | g0087 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19090 | hp2 | a0001 | c0001 | t0011 | g0194 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19240 | hp1 | a0001 | c0004 | t0067 | g0077 | AFR | YRI | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA19240 | hp2 | a0001 | c0009 | t0141 | g0191 | AFR | YRI | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | ASW | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA20129 | hp2 | a0001 | c0003 | t0064 | g0085 | AFR | ASW | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02109 | hp1 | a0001 | c0001 | t0045 | g0287 | AFR | ACB | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02109 | hp2 | a0004 | c0012 | t0061 | g0067 | AFR | ACB | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02486 | hp1 | a0001 | c0011 | t0079 | g0290 | AFR | ACB | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02486 | hp2 | a0001 | c0001 | t0088 | g0146 | AFR | ACB | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02559 | hp1 | a0001 | c0011 | t0029 | g0294 | AFR | ACB | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG02559 | hp2 | a0002 | c0005 | t0018 | g0064 | AFR | ACB | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03471 | hp1 | a0001 | c0001 | t0117 | g0189 | AFR | MSL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG03471 | hp2 | a0004 | c0012 | t0036 | g0283 | AFR | MSL | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG06807 | hp1 | a0001 | c0026 | t0152 | g0295 | AFR | USA | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| HG06807 | hp2 | a0001 | c0007 | t0035 | g0271 | AFR | USA | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA20300 | hp1 | a0001 | c0006 | t0028 | g0134 | AFR | USA | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0259 | AFR | USA | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA21309 | hp1 | a0001 | c0001 | t0083 | g0016 | AFR | LWK | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| NA21309 | hp2 | a0001 | c0001 | t0014 | g0066 | AFR | LWK | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0056 | g0058 | REF | REF | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| homoSapiens_grch38 | hp1 | a0008 | c0022 | t0094 | g0133 | REF | REF | AAK1_chr2_69452997_69648739 | AAK1 | chr2 | 69452997 | 69648739 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:69496038
|
G | C | 1 | a0009 | 1 | HG02074.hp1 | missense_variant | MODERATE | c.2312C>G | p.Pro771Arg | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/22 | 2711/21157 | 2312/2886 | 771/961 | chr2 | 69496038 | ||
| chr2:69496053
|
A | G | 1 | a0006 | 2 | HG00558.hp2 NA19077.hp1 |
missense_variant | MODERATE | c.2297T>C | p.Val766Ala | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/22 | 2696/21157 | 2297/2886 | 766/961 | chr2 | 69496053 | ||
| chr2:69509429
|
A | G | 1 | a0005 | 3 | HG01106.hp1 HG01952.hp2 HG01981.hp1 |
missense_variant | MODERATE | c.1808T>C | p.Val603Ala | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 14/22 | 2207/21157 | 1808/2886 | 603/961 | chr2 | 69509429 | ||
| chr2:69514503
|
C | T | 1 | a0010 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.1744G>A | p.Ala582Thr | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/22 | 2143/21157 | 1744/2886 | 582/961 | chr2 | 69514503 | ||
| chr2:69514621
|
CTGT | C | 4 | a0002a0003a0006others(1): Show | 103 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(100): Show |
disruptive_inframe_deletion | MODERATE | c.1623_1625delACA | p.Gln542del | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/22 | 2024/21157 | 1623/2886 | 541/961 | chr2 | 69514621 | ||
| chr2:69514722
|
T | G | 9 | a0001a0002a0003others(6): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
missense_variant | MODERATE | c.1525A>C | p.Lys509Gln | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/22 | 1924/21157 | 1525/2886 | 509/961 | chr2 | 69514722 | ||
| chr2:69519010
|
C | G | 2 | a0003a0004 | 8 | HG01433.hp1 HG01891.hp2 HG01928.hp2 others(5): Show |
missense_variant | MODERATE | c.1441G>C | p.Ala481Pro | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/22 | 1840/21157 | 1441/2886 | 481/961 | chr2 | 69519010 | ||
| chr2:69544478
|
C | T | 1 | a0007 | 2 | HG02132.hp2 NA19006.hp2 |
missense_variant | MODERATE | c.349G>A | p.Gly117Ser | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 4/22 | 748/21157 | 349/2886 | 117/961 | chr2 | 69544478 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:69482787
|
A | G | 8 | a0001c0004a0001c0006a0001c0008others(5): Show | 35 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(32): Show |
synonymous_variant | LOW | c.2391T>C | p.Ser797Ser | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 18/22 | 2790/21157 | 2391/2886 | 797/961 | chr2 | 69482787 | ||
| chr2:69496028
|
G | A | 1 | a0001c0011 | 3 | HG02486.hp1 HG02559.hp1 HG02965.hp1 |
synonymous_variant | LOW | c.2322C>T | p.Ser774Ser | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/22 | 2721/21157 | 2322/2886 | 774/961 | chr2 | 69496028 | ||
| chr2:69507428
|
A | C | 1 | a0004c0012 | 2 | HG02109.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.2157T>G | p.Leu719Leu | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 15/22 | 2556/21157 | 2157/2886 | 719/961 | chr2 | 69507428 | ||
| chr2:69514477
|
C | T | 5 | a0002c0002a0002c0024a0003c0020others(2): Show | 88 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(85): Show |
synonymous_variant | LOW | c.1770G>A | p.Glu590Glu | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/22 | 2169/21157 | 1770/2886 | 590/961 | chr2 | 69514477 | ||
| chr2:69514507
|
A | G | 1 | a0002c0024 | 1 | HG03710.hp1 | synonymous_variant | LOW | c.1740T>C | p.Ala580Ala | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/22 | 2139/21157 | 1740/2886 | 580/961 | chr2 | 69514507 | ||
| chr2:69514669
|
C | T | 5 | a0001c0003a0001c0004a0001c0008others(2): Show | 42 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(39): Show |
synonymous_variant | LOW | c.1578G>A | p.Gln526Gln | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/22 | 1977/21157 | 1578/2886 | 526/961 | chr2 | 69514669 | ||
| chr2:69519164
|
C | T | 4 | a0001c0003a0001c0004a0002c0019others(1): Show | 36 | HG00099.hp2 HG00323.hp1 HG01175.hp2 others(33): Show |
synonymous_variant | LOW | c.1287G>A | p.Pro429Pro | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/22 | 1686/21157 | 1287/2886 | 429/961 | chr2 | 69519164 | ||
| chr2:69530024
|
G | A | 1 | a0001c0007 | 5 | HG02809.hp2 HG02896.hp1 HG02976.hp2 others(2): Show |
synonymous_variant | LOW | c.855C>T | p.Asp285Asp | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/22 | 1254/21157 | 855/2886 | 285/961 | chr2 | 69530024 | ||
| chr2:69542649
|
G | A | 1 | a0001c0026 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.408C>T | p.Asn136Asn | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/22 | 807/21157 | 408/2886 | 136/961 | chr2 | 69542649 | ||
| chr2:69642987
|
G | T | 1 | a0001c0009 | 3 | HG02280.hp2 HG02922.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.54C>A | p.Ser18Ser | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/22 | 453/21157 | 54/2886 | 18/961 | chr2 | 69642987 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:69458000
|
C | T | 1 | a0002c0002t0128 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*17869G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 17869 | chr2 | 69458000 | |||||
| chr2:69458196
|
G | A | 4 | a0001c0006t0028a0001c0006t0041a0001c0006t0042others(1): Show | 5 | HG01884.hp2 HG02818.hp1 HG03471.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*17673C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 17673 | chr2 | 69458196 | |||||
| chr2:69458218
|
C | G | 2 | a0001c0003t0026a0001c0003t0081 | 3 | HG02451.hp1 HG02622.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*17651G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 17651 | chr2 | 69458218 | |||||
| chr2:69458308
|
TCTC | T | 4 | a0001c0001t0083a0001c0001t0105a0001c0009t0141others(1): Show | 4 | HG02922.hp2 HG02965.hp2 NA19240.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*17558_*17560delGA others(1): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 17558 | chr2 | 69458308 | |||||
| chr2:69458681
|
A | G | 1 | a0002c0002t0047 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*17188T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 17188 | chr2 | 69458681 | |||||
| chr2:69458707
|
G | GCA | 12 | a0001c0001t0073a0001c0001t0078a0001c0001t0099others(9): Show | 16 | HG00735.hp2 HG01167.hp1 HG02257.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*17160_*17161dupTG | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 17161 | chr2 | 69458707 | |||||
| chr2:69458707
|
G | GCACA | 16 | a0001c0001t0056a0001c0004t0010a0001c0004t0017others(13): Show | 23 | HG00323.hp1 HG00558.hp1 HG01074.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*17158_*17161dupTG others(2): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 17161 | chr2 | 69458707 | |||||
| chr2:69458941
|
A | G | 2 | a0001c0011t0029a0001c0011t0079 | 3 | HG02486.hp1 HG02559.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*16928T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 16928 | chr2 | 69458941 | |||||
| chr2:69458945
|
A | G | 1 | a0001c0001t0073 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*16924T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 16924 | chr2 | 69458945 | |||||
| chr2:69459138
|
C | A | 2 | a0001c0011t0029a0001c0011t0079 | 3 | HG02486.hp1 HG02559.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*16731G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 16731 | chr2 | 69459138 | |||||
| chr2:69459154
|
A | G | 124 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(121): Show | 208 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(205): Show |
3_prime_UTR_variant | MODIFIER | c.*16715T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 16715 | chr2 | 69459154 | |||||
| chr2:69459212
|
C | T | 3 | a0001c0001t0121a0001c0011t0029a0001c0011t0079 | 4 | HG02486.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*16657G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 16657 | chr2 | 69459212 | |||||
| chr2:69459375
|
C | T | 2 | a0002c0002t0052a0002c0002t0110 | 2 | HG00099.hp1 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*16494G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 16494 | chr2 | 69459375 | |||||
| chr2:69459490
|
A | T | 2 | a0002c0002t0131a0002c0002t0132 | 2 | NA18963.hp1 NA19006.hp1 |
3_prime_UTR_variant | MODIFIER | c.*16379T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 16379 | chr2 | 69459490 | |||||
| chr2:69459565
|
A | G | 13 | a0001c0001t0004a0001c0001t0011a0001c0001t0020others(10): Show | 32 | HG00544.hp1 HG00597.hp2 HG02015.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*16304T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 16304 | chr2 | 69459565 | |||||
| chr2:69459600
|
G | C | 1 | a0001c0004t0068 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*16269C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 16269 | chr2 | 69459600 | |||||
| chr2:69459869
|
C | T | 1 | a0001c0004t0070 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*16000G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 16000 | chr2 | 69459869 | |||||
| chr2:69460092
|
C | T | 47 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(44): Show | 93 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*15777G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 15777 | chr2 | 69460092 | |||||
| chr2:69460113
|
A | G | 4 | a0001c0006t0028a0001c0006t0041a0001c0006t0042others(1): Show | 5 | HG01884.hp2 HG02818.hp1 HG03471.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*15756T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 15756 | chr2 | 69460113 | |||||
| chr2:69460122
|
G | A | 4 | a0001c0001t0073a0001c0001t0099a0002c0005t0018others(1): Show | 6 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*15747C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 15747 | chr2 | 69460122 | |||||
| chr2:69460188
|
T | A | 1 | a0001c0001t0121 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*15681A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 15681 | chr2 | 69460188 | |||||
| chr2:69460243
|
A | C | 18 | a0001c0001t0004a0001c0001t0011a0001c0001t0020others(15): Show | 37 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*15626T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 15626 | chr2 | 69460243 | |||||
| chr2:69460340
|
ATATAT | A | 4 | a0001c0001t0073a0001c0001t0099a0002c0005t0018others(1): Show | 6 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*15524_*15528delAT others(3): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 15524 | chr2 | 69460340 | |||||
| chr2:69460454
|
A | G | 25 | a0001c0001t0004a0001c0001t0011a0001c0001t0020others(22): Show | 46 | HG00544.hp1 HG00597.hp2 HG01167.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*15415T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 15415 | chr2 | 69460454 | |||||
| chr2:69460594
|
A | G | 126 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(123): Show | 210 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*15275T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 15275 | chr2 | 69460594 | |||||
| chr2:69460599
|
C | G | 125 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(122): Show | 209 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*15270G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 15270 | chr2 | 69460599 | |||||
| chr2:69460823
|
T | C | 1 | a0001c0001t0140 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*15046A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 15046 | chr2 | 69460823 | |||||
| chr2:69461047
|
T | C | 1 | a0001c0009t0141 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14822A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 14822 | chr2 | 69461047 | |||||
| chr2:69461109
|
T | C | 4 | a0001c0006t0028a0001c0006t0041a0001c0006t0042others(1): Show | 5 | HG01884.hp2 HG02818.hp1 HG03471.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*14760A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 14760 | chr2 | 69461109 | |||||
| chr2:69461374
|
T | C | 29 | a0001c0001t0004a0001c0001t0011a0001c0001t0020others(26): Show | 51 | HG00544.hp1 HG00597.hp2 HG01167.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*14495A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 14495 | chr2 | 69461374 | |||||
| chr2:69461401
|
T | C | 1 | a0003c0021t0151 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14468A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 14468 | chr2 | 69461401 | |||||
| chr2:69461434
|
C | T | 1 | a0001c0001t0027 | 2 | HG01167.hp2 HG01891.hp1 |
3_prime_UTR_variant | MODIFIER | c.*14435G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 14435 | chr2 | 69461434 | |||||
| chr2:69461499
|
C | CA | 36 | a0001c0001t0095a0001c0001t0099a0001c0001t0104others(33): Show | 47 | HG00323.hp1 HG00558.hp1 HG01074.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*14369dupT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 14369 | chr2 | 69461499 | |||||
| chr2:69461499
|
CA | C | 7 | a0001c0001t0045a0001c0001t0091a0002c0002t0130others(4): Show | 7 | HG01175.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*14369delT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 14369 | chr2 | 69461499 | |||||
| chr2:69461517
|
T | C | 17 | a0001c0004t0010a0001c0004t0017a0001c0004t0067others(14): Show | 24 | HG00323.hp1 HG00558.hp1 HG01074.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*14352A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 14352 | chr2 | 69461517 | |||||
| chr2:69461595
|
A | AT | 6 | a0001c0001t0121a0001c0004t0071a0001c0026t0152others(3): Show | 7 | HG01074.hp1 HG02723.hp2 HG02895.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*14273dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 14273 | chr2 | 69461595 | |||||
| chr2:69461595
|
AT | A | 21 | a0001c0001t0004a0001c0001t0011a0001c0001t0020others(18): Show | 40 | HG00544.hp1 HG00597.hp2 HG01167.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*14273delA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 14273 | chr2 | 69461595 | |||||
| chr2:69461595
|
ATT | A | 7 | a0001c0001t0073a0001c0006t0028a0001c0006t0041others(4): Show | 10 | HG01884.hp2 HG02451.hp2 HG02559.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*14272_*14273delAA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 14272 | chr2 | 69461595 | |||||
| chr2:69461708
|
C | T | 1 | a0001c0001t0045 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14161G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 14161 | chr2 | 69461708 | |||||
| chr2:69461804
|
C | A | 1 | a0002c0002t0054 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14065G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 14065 | chr2 | 69461804 | |||||
| chr2:69461856
|
T | G | 1 | a0001c0001t0078 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14013A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 14013 | chr2 | 69461856 | |||||
| chr2:69461871
|
C | T | 1 | a0001c0001t0092 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13998G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 13998 | chr2 | 69461871 | |||||
| chr2:69461872
|
G | A | 2 | a0001c0001t0057a0001c0001t0117 | 2 | HG03209.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*13997C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 13997 | chr2 | 69461872 | |||||
| chr2:69462116
|
AAT | A | 4 | a0001c0001t0073a0001c0001t0099a0002c0005t0018others(1): Show | 6 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*13751_*13752delAT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 13751 | chr2 | 69462116 | |||||
| chr2:69462160
|
T | C | 1 | a0001c0001t0078 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13709A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 13709 | chr2 | 69462160 | |||||
| chr2:69462187
|
T | G | 125 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(122): Show | 209 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*13682A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 13682 | chr2 | 69462187 | |||||
| chr2:69462296
|
G | A | 1 | a0002c0002t0127 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13573C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 13573 | chr2 | 69462296 | |||||
| chr2:69462296
|
G | C | 125 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(122): Show | 209 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*13573C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 13573 | chr2 | 69462296 | |||||
| chr2:69462366
|
A | G | 1 | a0001c0011t0079 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13503T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 13503 | chr2 | 69462366 | |||||
| chr2:69462376
|
T | A | 3 | a0001c0001t0078a0002c0019t0065a0003c0020t0084 | 3 | HG01167.hp1 HG01433.hp1 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*13493A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 13493 | chr2 | 69462376 | |||||
| chr2:69462377
|
A | T | 34 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(31): Show | 67 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*13492T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 13492 | chr2 | 69462377 | |||||
| chr2:69462408
|
C | T | 1 | a0002c0002t0051 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*13461G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 13461 | chr2 | 69462408 | |||||
| chr2:69462468
|
C | T | 1 | a0004c0012t0061 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*13401G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 13401 | chr2 | 69462468 | |||||
| chr2:69462503
|
A | AC | 18 | a0001c0004t0010a0001c0004t0017a0001c0004t0067others(15): Show | 25 | HG00323.hp1 HG00558.hp1 HG01074.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*13365dupG | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 13365 | chr2 | 69462503 | |||||
| chr2:69462541
|
C | T | 6 | a0001c0001t0073a0001c0001t0099a0001c0001t0104others(3): Show | 8 | HG02451.hp2 HG02559.hp2 HG02572.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*13328G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 13328 | chr2 | 69462541 | |||||
| chr2:69462565
|
G | C | 1 | a0003c0021t0151 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*13304C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 13304 | chr2 | 69462565 | |||||
| chr2:69462572
|
G | A | 1 | a0001c0026t0152 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13297C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 13297 | chr2 | 69462572 | |||||
| chr2:69462652
|
A | T | 1 | a0001c0001t0078 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13217T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 13217 | chr2 | 69462652 | |||||
| chr2:69462676
|
GA | G | 48 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(45): Show | 92 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*13192delT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 13192 | chr2 | 69462676 | |||||
| chr2:69462693
|
T | A | 2 | a0002c0016t0134a0002c0019t0065 | 2 | HG02257.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*13176A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 13176 | chr2 | 69462693 | |||||
| chr2:69462719
|
C | G | 4 | a0001c0001t0073a0001c0001t0099a0002c0005t0018others(1): Show | 6 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*13150G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 13150 | chr2 | 69462719 | |||||
| chr2:69462812
|
A | G | 1 | a0001c0004t0067 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13057T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 13057 | chr2 | 69462812 | |||||
| chr2:69462855
|
C | T | 1 | a0001c0001t0121 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*13014G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 13014 | chr2 | 69462855 | |||||
| chr2:69463055
|
A | G | 125 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(122): Show | 209 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*12814T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 12814 | chr2 | 69463055 | |||||
| chr2:69463065
|
A | G | 1 | a0001c0001t0078 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12804T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 12804 | chr2 | 69463065 | |||||
| chr2:69463125
|
C | T | 1 | a0001c0001t0078 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12744G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 12744 | chr2 | 69463125 | |||||
| chr2:69463252
|
T | C | 24 | a0001c0001t0004a0001c0001t0011a0001c0001t0020others(21): Show | 45 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*12617A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 12617 | chr2 | 69463252 | |||||
| chr2:69463542
|
C | T | 1 | a0003c0021t0151 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12327G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 12327 | chr2 | 69463542 | |||||
| chr2:69463543
|
G | A | 2 | a0001c0001t0076a0001c0001t0102 | 2 | NA18973.hp1 NA19063.hp2 |
3_prime_UTR_variant | MODIFIER | c.*12326C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 12326 | chr2 | 69463543 | |||||
| chr2:69463604
|
C | T | 1 | a0002c0002t0128 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12265G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 12265 | chr2 | 69463604 | |||||
| chr2:69463612
|
A | C | 1 | a0001c0006t0041 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12257T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 12257 | chr2 | 69463612 | |||||
| chr2:69463615
|
G | A | 1 | a0001c0001t0092 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12254C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 12254 | chr2 | 69463615 | |||||
| chr2:69463668
|
C | T | 1 | a0001c0001t0078 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12201G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 12201 | chr2 | 69463668 | |||||
| chr2:69463713
|
A | T | 18 | a0001c0001t0004a0001c0001t0011a0001c0001t0020others(15): Show | 37 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*12156T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 12156 | chr2 | 69463713 | |||||
| chr2:69463758
|
A | T | 1 | a0001c0001t0119 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12111T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 12111 | chr2 | 69463758 | |||||
| chr2:69463805
|
C | G | 1 | a0001c0006t0016 | 3 | HG00735.hp2 HG02630.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*12064G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 12064 | chr2 | 69463805 | |||||
| chr2:69463856
|
C | A | 2 | a0001c0001t0104a0004c0013t0043 | 2 | HG02572.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*12013G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 12013 | chr2 | 69463856 | |||||
| chr2:69463888
|
T | C | 1 | a0002c0002t0145 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11981A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 11981 | chr2 | 69463888 | |||||
| chr2:69463897
|
T | C | 33 | a0001c0001t0004a0001c0001t0011a0001c0001t0020others(30): Show | 55 | HG00544.hp1 HG00597.hp2 HG01167.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*11972A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 11972 | chr2 | 69463897 | |||||
| chr2:69463923
|
T | C | 1 | a0002c0002t0059 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11946A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 11946 | chr2 | 69463923 | |||||
| chr2:69464194
|
A | AAAC | 26 | a0001c0001t0004a0001c0001t0011a0001c0001t0073others(23): Show | 59 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*11672_*11674dupGT others(1): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 11674 | chr2 | 69464194 | |||||
| chr2:69464194
|
A | AAACAAC | 16 | a0001c0001t0014a0001c0001t0083a0001c0001t0137others(13): Show | 24 | HG01243.hp1 HG02074.hp2 HG02451.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*11669_*11674dupGT others(4): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 11674 | chr2 | 69464194 | |||||
| chr2:69464194
|
A | AAACAACA others(2): Show |
3 | a0001c0001t0104a0003c0020t0084a0004c0013t0043 | 3 | HG01433.hp1 HG02572.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11666_*11674dupGT others(7): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 11674 | chr2 | 69464194 | |||||
| chr2:69464194
|
AAAC | A | 3 | a0001c0001t0077a0001c0001t0124a0001c0008t0097 | 3 | HG01074.hp2 HG02280.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*11672_*11674delGT others(1): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 11672 | chr2 | 69464194 | |||||
| chr2:69464211
|
AC | A | 7 | a0001c0001t0121a0001c0006t0028a0001c0006t0041others(4): Show | 9 | HG01884.hp2 HG02486.hp1 HG02559.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*11657delG | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 11657 | chr2 | 69464211 | |||||
| chr2:69464230
|
C | A | 39 | a0001c0001t0004a0001c0001t0011a0001c0001t0020others(36): Show | 62 | HG00544.hp1 HG00597.hp2 HG01167.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*11639G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 11639 | chr2 | 69464230 | |||||
| chr2:69464356
|
G | A | 1 | a0001c0001t0121 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11513C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 11513 | chr2 | 69464356 | |||||
| chr2:69464470
|
C | A | 48 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(45): Show | 92 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*11399G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 11399 | chr2 | 69464470 | |||||
| chr2:69464513
|
G | A | 1 | a0002c0002t0033 | 2 | NA18994.hp2 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*11356C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 11356 | chr2 | 69464513 | |||||
| chr2:69464528
|
A | G | 1 | a0001c0001t0120 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11341T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 11341 | chr2 | 69464528 | |||||
| chr2:69464644
|
ACACACGT others(27): Show |
A | 3 | a0001c0004t0071a0001c0004t0072a0001c0008t0098 | 3 | HG00558.hp1 NA18950.hp2 NA19004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*11191_*11224delAG others(32): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 11191 | chr2 | 69464644 | |||||
| chr2:69464681
|
C | T | 4 | a0001c0004t0017a0001c0004t0067a0001c0004t0068others(1): Show | 7 | HG01891.hp2 HG02145.hp2 HG02723.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*11188G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 11188 | chr2 | 69464681 | |||||
| chr2:69464809
|
G | A | 1 | a0001c0001t0093 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11060C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 11060 | chr2 | 69464809 | |||||
| chr2:69465034
|
G | A | 12 | a0001c0001t0004a0001c0001t0011a0001c0001t0020others(9): Show | 31 | HG00544.hp1 HG00597.hp2 HG02015.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*10835C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 10835 | chr2 | 69465034 | |||||
| chr2:69465118
|
G | C | 1 | a0003c0021t0151 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10751C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 10751 | chr2 | 69465118 | |||||
| chr2:69465124
|
C | T | 4 | a0001c0001t0078a0001c0001t0090a0001c0001t0104others(1): Show | 4 | HG01167.hp1 HG02572.hp2 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*10745G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 10745 | chr2 | 69465124 | |||||
| chr2:69465125
|
G | A | 18 | a0001c0001t0004a0001c0001t0011a0001c0001t0020others(15): Show | 37 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*10744C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 10744 | chr2 | 69465125 | |||||
| chr2:69465164
|
T | A | 2 | a0001c0001t0104a0004c0013t0043 | 2 | HG02572.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10705A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 10705 | chr2 | 69465164 | |||||
| chr2:69465256
|
C | T | 1 | a0001c0001t0113 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10613G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 10613 | chr2 | 69465256 | |||||
| chr2:69465391
|
T | C | 20 | a0001c0001t0004a0001c0001t0011a0001c0001t0020others(17): Show | 41 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*10478A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 10478 | chr2 | 69465391 | |||||
| chr2:69465608
|
T | A | 2 | a0002c0002t0038a0002c0002t0055 | 2 | NA18612.hp2 NA18968.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10261A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 10261 | chr2 | 69465608 | |||||
| chr2:69465874
|
C | T | 43 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(40): Show | 77 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*9995G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 9995 | chr2 | 69465874 | |||||
| chr2:69465944
|
T | C | 1 | a0001c0001t0063 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9925A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 9925 | chr2 | 69465944 | |||||
| chr2:69466032
|
A | G | 4 | a0001c0006t0028a0001c0006t0041a0001c0006t0042others(1): Show | 5 | HG01884.hp2 HG02818.hp1 HG03471.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*9837T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 9837 | chr2 | 69466032 | |||||
| chr2:69466265
|
G | T | 3 | a0001c0001t0078a0001c0001t0104a0004c0013t0043 | 3 | HG01167.hp1 HG02572.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9604C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 9604 | chr2 | 69466265 | |||||
| chr2:69466571
|
A | G | 2 | a0001c0011t0029a0001c0011t0079 | 3 | HG02486.hp1 HG02559.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9298T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 9298 | chr2 | 69466571 | |||||
| chr2:69466610
|
T | C | 1 | a0001c0003t0026 | 2 | HG02451.hp1 HG02622.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9259A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 9259 | chr2 | 69466610 | |||||
| chr2:69466615
|
T | C | 18 | a0001c0004t0010a0001c0004t0017a0001c0004t0067others(15): Show | 25 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*9254A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 9254 | chr2 | 69466615 | |||||
| chr2:69466714
|
C | T | 4 | a0001c0001t0073a0001c0001t0099a0002c0005t0018others(1): Show | 6 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*9155G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 9155 | chr2 | 69466714 | |||||
| chr2:69467027
|
G | T | 1 | a0001c0001t0126 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8842C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 8842 | chr2 | 69467027 | |||||
| chr2:69467061
|
T | A | 3 | a0001c0001t0011a0001c0001t0143a0001c0001t0149 | 8 | HG02015.hp1 NA18747.hp1 NA18943.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*8808A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 8808 | chr2 | 69467061 | |||||
| chr2:69467067
|
A | G | 4 | a0001c0006t0028a0001c0006t0041a0001c0006t0042others(1): Show | 5 | HG01884.hp2 HG02818.hp1 HG03471.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8802T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 8802 | chr2 | 69467067 | |||||
| chr2:69467150
|
C | T | 4 | a0001c0006t0028a0001c0006t0041a0001c0006t0042others(1): Show | 5 | HG01884.hp2 HG02818.hp1 HG03471.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8719G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 8719 | chr2 | 69467150 | |||||
| chr2:69467575
|
G | C | 2 | a0001c0007t0148a0003c0020t0084 | 2 | HG01433.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8294C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 8294 | chr2 | 69467575 | |||||
| chr2:69467601
|
A | C | 23 | a0001c0001t0004a0001c0001t0006a0001c0001t0011others(20): Show | 52 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*8268T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 8268 | chr2 | 69467601 | |||||
| chr2:69467958
|
A | G | 1 | a0001c0001t0136 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7911T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 7911 | chr2 | 69467958 | |||||
| chr2:69468052
|
C | T | 1 | a0001c0001t0088 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7817G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 7817 | chr2 | 69468052 | |||||
| chr2:69468276
|
T | C | 21 | a0001c0001t0004a0001c0001t0006a0001c0001t0011others(18): Show | 50 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*7593A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 7593 | chr2 | 69468276 | |||||
| chr2:69468303
|
G | A | 16 | a0001c0001t0083a0001c0001t0105a0001c0003t0012others(13): Show | 22 | HG02074.hp2 HG02280.hp2 HG02451.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*7566C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 7566 | chr2 | 69468303 | |||||
| chr2:69468504
|
T | A | 16 | a0001c0001t0083a0001c0001t0105a0001c0003t0012others(13): Show | 22 | HG02074.hp2 HG02280.hp2 HG02451.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*7365A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 7365 | chr2 | 69468504 | |||||
| chr2:69468507
|
T | G | 1 | a0001c0001t0139 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7362A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 7362 | chr2 | 69468507 | |||||
| chr2:69468582
|
C | A | 7 | a0001c0001t0078a0001c0001t0104a0001c0006t0028others(4): Show | 8 | HG01167.hp1 HG01884.hp2 HG02572.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7287G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 7287 | chr2 | 69468582 | |||||
| chr2:69468702
|
G | T | 1 | a0001c0001t0074 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7167C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 7167 | chr2 | 69468702 | |||||
| chr2:69468736
|
G | A | 11 | a0001c0003t0012a0001c0003t0026a0001c0003t0030others(8): Show | 17 | HG02074.hp2 HG02451.hp1 HG02602.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*7133C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 7133 | chr2 | 69468736 | |||||
| chr2:69468761
|
C | T | 6 | a0001c0001t0104a0001c0006t0028a0001c0006t0041others(3): Show | 7 | HG01884.hp2 HG02572.hp2 HG02818.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7108G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 7108 | chr2 | 69468761 | |||||
| chr2:69468792
|
C | T | 1 | a0001c0001t0087 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7077G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 7077 | chr2 | 69468792 | |||||
| chr2:69468869
|
G | A | 127 | a0001c0001t0004a0001c0001t0006a0001c0001t0011others(124): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*7000C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 7000 | chr2 | 69468869 | |||||
| chr2:69469300
|
C | T | 17 | a0001c0001t0045a0001c0001t0077a0001c0001t0078others(14): Show | 19 | HG01167.hp1 HG01884.hp2 HG02109.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*6569G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 6569 | chr2 | 69469300 | |||||
| chr2:69469516
|
T | C | 1 | a0001c0001t0096 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6353A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 6353 | chr2 | 69469516 | |||||
| chr2:69469559
|
C | T | 1 | a0001c0001t0078 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6310G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 6310 | chr2 | 69469559 | |||||
| chr2:69469756
|
C | T | 1 | a0001c0001t0037 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6113G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 6113 | chr2 | 69469756 | |||||
| chr2:69470194
|
C | T | 1 | a0001c0026t0152 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5675G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 5675 | chr2 | 69470194 | |||||
| chr2:69470284
|
C | T | 17 | a0001c0001t0045a0001c0001t0077a0001c0001t0078others(14): Show | 19 | HG01167.hp1 HG01884.hp2 HG02109.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*5585G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 5585 | chr2 | 69470284 | |||||
| chr2:69470338
|
G | T | 1 | a0001c0003t0109 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5531C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 5531 | chr2 | 69470338 | |||||
| chr2:69470347
|
T | C | 1 | a0001c0003t0109 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5522A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 5522 | chr2 | 69470347 | |||||
| chr2:69470489
|
C | T | 2 | a0002c0002t0049a0002c0024t0060 | 2 | HG00323.hp2 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5380G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 5380 | chr2 | 69470489 | |||||
| chr2:69470581
|
C | T | 2 | a0001c0001t0104a0004c0013t0043 | 2 | HG02572.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5288G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 5288 | chr2 | 69470581 | |||||
| chr2:69470639
|
G | A | 10 | a0001c0001t0045a0001c0001t0077a0001c0001t0121others(7): Show | 11 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5230C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 5230 | chr2 | 69470639 | |||||
| chr2:69470655
|
C | T | 17 | a0001c0001t0045a0001c0001t0077a0001c0001t0078others(14): Show | 19 | HG01167.hp1 HG01884.hp2 HG02109.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*5214G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 5214 | chr2 | 69470655 | |||||
| chr2:69470960
|
T | C | 16 | a0001c0001t0083a0001c0001t0105a0001c0003t0012others(13): Show | 22 | HG02074.hp2 HG02280.hp2 HG02451.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4909A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 4909 | chr2 | 69470960 | |||||
| chr2:69471026
|
G | A | 127 | a0001c0001t0004a0001c0001t0006a0001c0001t0011others(124): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*4843C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 4843 | chr2 | 69471026 | |||||
| chr2:69471196
|
G | A | 1 | a0001c0001t0118 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4673C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 4673 | chr2 | 69471196 | |||||
| chr2:69471326
|
T | C | 8 | a0001c0001t0045a0001c0001t0077a0001c0001t0124others(5): Show | 8 | HG02109.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4543A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 4543 | chr2 | 69471326 | |||||
| chr2:69471339
|
T | C | 1 | a0003c0021t0151 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4530A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 4530 | chr2 | 69471339 | |||||
| chr2:69471577
|
T | C | 4 | a0001c0001t0073a0001c0001t0099a0002c0005t0018others(1): Show | 6 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4292A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 4292 | chr2 | 69471577 | |||||
| chr2:69471583
|
C | A | 3 | a0001c0001t0121a0001c0011t0029a0001c0011t0079 | 4 | HG02486.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4286G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 4286 | chr2 | 69471583 | |||||
| chr2:69471640
|
A | T | 46 | a0001c0001t0004a0001c0001t0006a0001c0001t0011others(43): Show | 81 | HG00544.hp1 HG00597.hp2 HG01167.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*4229T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 4229 | chr2 | 69471640 | |||||
| chr2:69471679
|
T | C | 1 | a0001c0001t0124 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4190A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 4190 | chr2 | 69471679 | |||||
| chr2:69471682
|
C | G | 1 | a0003c0021t0151 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4187G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 4187 | chr2 | 69471682 | |||||
| chr2:69471831
|
G | C | 1 | a0001c0003t0064 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4038C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 4038 | chr2 | 69471831 | |||||
| chr2:69471887
|
A | G | 2 | a0001c0008t0135a0007c0017t0066 | 2 | HG02040.hp2 HG02132.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3982T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 3982 | chr2 | 69471887 | |||||
| chr2:69471936
|
C | T | 1 | a0001c0001t0077 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3933G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 3933 | chr2 | 69471936 | |||||
| chr2:69471972
|
T | A | 19 | a0001c0004t0010a0001c0004t0017a0001c0004t0067others(16): Show | 28 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*3897A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 3897 | chr2 | 69471972 | |||||
| chr2:69472004
|
G | A | 1 | a0001c0003t0106 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3865C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 3865 | chr2 | 69472004 | |||||
| chr2:69472308
|
T | C | 1 | a0004c0013t0107 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3561A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 3561 | chr2 | 69472308 | |||||
| chr2:69472385
|
C | T | 1 | a0003c0014t0025 | 2 | HG01891.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3484G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 3484 | chr2 | 69472385 | |||||
| chr2:69472609
|
C | T | 1 | a0002c0002t0048 | 1 | NA19055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3260G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 3260 | chr2 | 69472609 | |||||
| chr2:69472795
|
ATCT | A | 16 | a0001c0004t0010a0001c0004t0017a0001c0004t0067others(13): Show | 23 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3071_*3073delAGA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 3071 | chr2 | 69472795 | |||||
| chr2:69473141
|
G | A | 8 | a0001c0001t0045a0001c0001t0077a0001c0001t0124others(5): Show | 8 | HG02109.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2728C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 2728 | chr2 | 69473141 | |||||
| chr2:69473262
|
G | A | 2 | a0001c0011t0029a0001c0011t0079 | 3 | HG02486.hp1 HG02559.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2607C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 2607 | chr2 | 69473262 | |||||
| chr2:69473357
|
T | C | 3 | a0001c0001t0078a0001c0001t0104a0004c0013t0043 | 3 | HG01167.hp1 HG02572.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2512A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 2512 | chr2 | 69473357 | |||||
| chr2:69473409
|
G | A | 1 | a0002c0005t0100 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2460C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 2460 | chr2 | 69473409 | |||||
| chr2:69473448
|
T | C | 1 | a0002c0002t0133 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2421A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 2421 | chr2 | 69473448 | |||||
| chr2:69473467
|
G | A | 1 | a0002c0002t0039 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2402C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 2402 | chr2 | 69473467 | |||||
| chr2:69473516
|
A | G | 4 | a0001c0001t0073a0001c0001t0099a0002c0005t0018others(1): Show | 6 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2353T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 2353 | chr2 | 69473516 | |||||
| chr2:69473552
|
A | G | 2 | a0001c0001t0024a0001c0001t0086 | 3 | HG02040.hp1 NA18983.hp2 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2317T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 2317 | chr2 | 69473552 | |||||
| chr2:69473879
|
G | T | 1 | a0001c0001t0078 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1990C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 1990 | chr2 | 69473879 | |||||
| chr2:69474112
|
T | A | 1 | a0001c0001t0140 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1757A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 1757 | chr2 | 69474112 | |||||
| chr2:69474253
|
T | G | 8 | a0001c0001t0045a0001c0001t0077a0001c0001t0124others(5): Show | 8 | HG02109.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1616A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 1616 | chr2 | 69474253 | |||||
| chr2:69474320
|
C | T | 6 | a0001c0006t0028a0001c0006t0041a0001c0006t0042others(3): Show | 8 | HG01884.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1549G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 1549 | chr2 | 69474320 | |||||
| chr2:69474540
|
T | A | 1 | a0001c0001t0078 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1329A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 1329 | chr2 | 69474540 | |||||
| chr2:69474622
|
G | A | 47 | a0001c0001t0004a0001c0001t0006a0001c0001t0011others(44): Show | 82 | HG00544.hp1 HG00597.hp2 HG01167.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1247C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 1247 | chr2 | 69474622 | |||||
| chr2:69474962
|
C | A | 8 | a0001c0001t0104a0001c0006t0028a0001c0006t0041others(5): Show | 10 | HG01884.hp2 HG02486.hp1 HG02559.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*907G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 907 | chr2 | 69474962 | |||||
| chr2:69475054
|
C | A | 16 | a0001c0001t0083a0001c0001t0105a0001c0003t0012others(13): Show | 22 | HG02074.hp2 HG02280.hp2 HG02451.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*815G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 815 | chr2 | 69475054 | |||||
| chr2:69475097
|
A | G | 1 | a0002c0002t0047 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*772T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 772 | chr2 | 69475097 | |||||
| chr2:69475102
|
T | G | 1 | a0003c0021t0151 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*767A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 767 | chr2 | 69475102 | |||||
| chr2:69475170
|
G | A | 3 | a0001c0003t0082a0001c0003t0108a0001c0003t0109 | 3 | NA18612.hp1 NA18939.hp1 NA19002.hp1 |
3_prime_UTR_variant | MODIFIER | c.*699C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 699 | chr2 | 69475170 | |||||
| chr2:69475383
|
T | C | 1 | a0001c0001t0083 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*486A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 486 | chr2 | 69475383 | |||||
| chr2:69475496
|
C | T | 41 | a0001c0001t0013a0001c0001t0037a0001c0001t0126others(38): Show | 84 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*373G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 373 | chr2 | 69475496 | |||||
| chr2:69475781
|
T | A | 1 | a0001c0001t0143 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*88A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 88 | chr2 | 69475781 | |||||
| chr2:69475782
|
A | T | 2 | a0001c0001t0045a0001c0003t0046 | 2 | HG02109.hp1 HG04228.hp2 |
3_prime_UTR_variant | MODIFIER | c.*87T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 87 | chr2 | 69475782 | |||||
| chr2:69475804
|
C | T | 1 | a0002c0002t0044 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*65G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 65 | chr2 | 69475804 | |||||
| chr2:69475828
|
G | A | 1 | a0001c0001t0144 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*41C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 22/22 | 41 | chr2 | 69475828 | |||||
| chr2:69643049
|
T | C | 1 | a0003c0020t0084 | 1 | HG01433.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-9A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/22 | chr2 | 69643049 | ||||||
| chr2:69643085
|
A | AT | 67 | a0001c0001t0007a0001c0001t0008a0001c0001t0014others(64): Show | 111 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(108): Show |
5_prime_UTR_variant | MODIFIER | c.-46dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/22 | 46 | chr2 | 69643085 | |||||
| chr2:69643085
|
A | ATT | 42 | a0001c0001t0004a0001c0001t0006a0001c0001t0011others(39): Show | 96 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(93): Show |
5_prime_UTR_variant | MODIFIER | c.-47_-46dupAA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/22 | 46 | chr2 | 69643085 | |||||
| chr2:69643085
|
A | ATTT | 12 | a0001c0001t0116a0001c0001t0117a0001c0001t0118others(9): Show | 12 | HG01361.hp2 HG02280.hp1 HG02280.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-48_-46dupAAA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/22 | 46 | chr2 | 69643085 | |||||
| chr2:69643085
|
AT | A | 7 | a0001c0001t0031a0001c0001t0032a0001c0001t0112others(4): Show | 9 | HG00099.hp1 HG00738.hp2 HG02165.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-46delA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/22 | 46 | chr2 | 69643085 | |||||
| chr2:69643169
|
C | A | 52 | a0001c0001t0004a0001c0001t0006a0001c0001t0011others(49): Show | 105 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(102): Show |
5_prime_UTR_variant | MODIFIER | c.-129G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/22 | 129 | chr2 | 69643169 | |||||
| chr2:69643659
|
G | A | 1 | a0001c0026t0152 | 1 | HG06807.hp1 | 5_prime_UTR_variant | MODIFIER | c.-319C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 1/22 | 619 | chr2 | 69643659 | |||||
| chr2:69643663
|
G | A | 1 | a0001c0004t0153 | 1 | HG03654.hp1 | 5_prime_UTR_variant | MODIFIER | c.-323C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 1/22 | 623 | chr2 | 69643663 | |||||
| chr2:69643680
|
G | C | 2 | a0002c0002t0154a0002c0002t0155 | 2 | NA18970.hp1 NA19005.hp2 |
5_prime_UTR_variant | MODIFIER | c.-340C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 1/22 | 640 | chr2 | 69643680 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:69476011
|
G | A | 1 | a0001c0001t0086g0167 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2792-48C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 21/21 | chr2 | 69476011 | ||||||
| chr2:69476068
|
A | C | 1 | a0001c0001t0121g0186 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2792-105T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 21/21 | chr2 | 69476068 | ||||||
| chr2:69476077
|
C | A | 1 | a0001c0004t0010g0148 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2792-114G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 21/21 | chr2 | 69476077 | ||||||
| chr2:69476116
|
T | G | 1 | a0001c0001t0078g0055 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2792-153A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 21/21 | chr2 | 69476116 | ||||||
| chr2:69476386
|
C | T | 1 | a0002c0016t0134g0272 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2792-423G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 21/21 | chr2 | 69476386 | ||||||
| chr2:69476397
|
A | T | 1 | a0001c0001t0007g0065 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2792-434T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 21/21 | chr2 | 69476397 | ||||||
| chr2:69476546
|
T | C | 1 | a0001c0001t0116g0185 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2791+334A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 21/21 | chr2 | 69476546 | ||||||
| chr2:69476659
|
G | C | 24 | a0001c0004t0002g0137a0001c0004t0010g0127a0001c0004t0010g0148others(21): Show | 24 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.2791+221C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 21/21 | chr2 | 69476659 | ||||||
| chr2:69476696
|
C | T | 5 | a0001c0006t0028g0126a0001c0006t0028g0134a0001c0006t0041g0008others(2): Show | 5 | HG01884.hp2 HG02818.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2791+184G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 21/21 | chr2 | 69476696 | ||||||
| chr2:69477105
|
T | C | 5 | a0001c0001t0045g0287a0002c0005t0040g0006a0002c0005t0122g0182others(2): Show | 5 | HG02109.hp1 HG02572.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2681-115A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 20/21 | chr2 | 69477105 | ||||||
| chr2:69477161
|
GAT | G | 3 | a0001c0001t0002g0150a0001c0001t0002g0157a0007c0018t0002g0165 | 3 | HG00597.hp1 NA19006.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.2681-173_2681-172d others(4): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 20/21 | chr2 | 69477161 | ||||||
| chr2:69477204
|
T | TA | 221 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.2681-215dupT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 20/21 | chr2 | 69477204 | ||||||
| chr2:69477221
|
G | A | 5 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(2): Show | 5 | HG01243.hp1 HG02970.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.2681-231C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 20/21 | chr2 | 69477221 | ||||||
| chr2:69477285
|
T | C | 49 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(46): Show | 49 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(46): Show |
intron_variant | MODIFIER | c.2681-295A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 20/21 | chr2 | 69477285 | ||||||
| chr2:69477482
|
G | A | 29 | a0001c0004t0002g0137a0001c0004t0010g0127a0001c0004t0010g0148others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.2681-492C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 20/21 | chr2 | 69477482 | ||||||
| chr2:69477809
|
A | G | 91 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(88): Show | 91 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.2681-819T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 20/21 | chr2 | 69477809 | ||||||
| chr2:69477838
|
G | T | 67 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(64): Show | 67 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.2681-848C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 20/21 | chr2 | 69477838 | ||||||
| chr2:69478154
|
C | T | 29 | a0001c0004t0002g0137a0001c0004t0010g0127a0001c0004t0010g0148others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.2680+797G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 20/21 | chr2 | 69478154 | ||||||
| chr2:69478466
|
T | G | 56 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(53): Show | 56 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(53): Show |
intron_variant | MODIFIER | c.2680+485A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 20/21 | chr2 | 69478466 | ||||||
| chr2:69478545
|
G | A | 88 | a0001c0001t0013g0151a0001c0001t0126g0219a0001c0001t0144g0232others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.2680+406C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 20/21 | chr2 | 69478545 | ||||||
| chr2:69478583
|
G | A | 4 | a0002c0016t0134g0272a0002c0019t0065g0062a0003c0014t0025g0285others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2680+368C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 20/21 | chr2 | 69478583 | ||||||
| chr2:69478754
|
G | A | 22 | a0001c0004t0002g0137a0001c0004t0010g0127a0001c0004t0010g0148others(19): Show | 22 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.2680+197C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 20/21 | chr2 | 69478754 | ||||||
| chr2:69478757
|
C | T | 4 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(1): Show | 4 | HG01243.hp1 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2680+194G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 20/21 | chr2 | 69478757 | ||||||
| chr2:69478758
|
G | A | 1 | a0001c0003t0012g0097 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2680+193C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 20/21 | chr2 | 69478758 | ||||||
| chr2:69478860
|
T | A | 52 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(49): Show | 52 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.2680+91A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 20/21 | chr2 | 69478860 | ||||||
| chr2:69479337
|
T | C | 4 | a0001c0001t0020g0193a0001c0001t0020g0202a0001c0001t0020g0208others(1): Show | 4 | NA18956.hp1 NA18963.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.2570-276A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 19/21 | chr2 | 69479337 | ||||||
| chr2:69479360
|
A | C | 1 | a0001c0001t0140g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2570-299T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 19/21 | chr2 | 69479360 | ||||||
| chr2:69479364
|
C | A | 4 | a0001c0001t0144g0232a0002c0002t0001g0019a0002c0002t0013g0110others(1): Show | 4 | HG03710.hp2 NA18954.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.2570-303G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 19/21 | chr2 | 69479364 | ||||||
| chr2:69479424
|
G | A | 1 | a0001c0001t0124g0188 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2570-363C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 19/21 | chr2 | 69479424 | ||||||
| chr2:69479434
|
T | A | 4 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(1): Show | 4 | HG01243.hp1 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2570-373A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 19/21 | chr2 | 69479434 | ||||||
| chr2:69479442
|
T | C | 52 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(49): Show | 52 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.2570-381A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 19/21 | chr2 | 69479442 | ||||||
| chr2:69479578
|
C | A | 8 | a0001c0001t0037g0009a0001c0001t0045g0287a0001c0001t0077g0072others(5): Show | 8 | HG02109.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2570-517G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 19/21 | chr2 | 69479578 | ||||||
| chr2:69479848
|
T | G | 1 | a0001c0001t0008g0022 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2570-787A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 19/21 | chr2 | 69479848 | ||||||
| chr2:69479944
|
G | A | 1 | a0002c0002t0005g0226 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2570-883C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 19/21 | chr2 | 69479944 | ||||||
| chr2:69480038
|
A | G | 1 | a0001c0001t0002g0125 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2569+822T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 19/21 | chr2 | 69480038 | ||||||
| chr2:69480046
|
C | T | 3 | a0001c0011t0029g0293a0001c0011t0029g0294a0001c0011t0079g0290 | 3 | HG02486.hp1 HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2569+814G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 19/21 | chr2 | 69480046 | ||||||
| chr2:69480250
|
G | A | 3 | a0002c0002t0001g0040a0002c0002t0001g0057a0002c0002t0044g0041 | 3 | HG00140.hp1 HG01192.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.2569+610C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 19/21 | chr2 | 69480250 | ||||||
| chr2:69480260
|
C | CA | 13 | a0001c0001t0002g0154a0001c0001t0063g0288a0001c0006t0016g0017others(10): Show | 13 | HG00735.hp2 HG02040.hp2 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.2569+599dupT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 19/21 | chr2 | 69480260 | ||||||
| chr2:69480260
|
CA | C | 14 | a0001c0001t0037g0009a0001c0001t0045g0287a0001c0001t0077g0072others(11): Show | 14 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.2569+599delT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 19/21 | chr2 | 69480260 | ||||||
| chr2:69480261
|
A | C | 52 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(49): Show | 52 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.2569+599T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 19/21 | chr2 | 69480261 | ||||||
| chr2:69480539
|
C | T | 1 | a0004c0013t0107g0107 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2569+321G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 19/21 | chr2 | 69480539 | ||||||
| chr2:69480545
|
A | G | 84 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(81): Show | 84 | HG00544.hp1 HG00597.hp2 HG01167.hp1 others(81): Show |
intron_variant | MODIFIER | c.2569+315T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 19/21 | chr2 | 69480545 | ||||||
| chr2:69480620
|
A | G | 52 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(49): Show | 52 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.2569+240T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 19/21 | chr2 | 69480620 | ||||||
| chr2:69480629
|
C | G | 1 | a0001c0001t0007g0081 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2569+231G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 19/21 | chr2 | 69480629 | ||||||
| chr2:69480792
|
G | A | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2569+68C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 19/21 | chr2 | 69480792 | ||||||
| chr2:69480853
|
G | C | 1 | a0001c0001t0011g0194 | 1 | NA19090.hp2 | splice_region_variant&intron_variant | LOW | c.2569+7C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 19/21 | chr2 | 69480853 | ||||||
| chr2:69481037
|
A | C | 1 | a0002c0002t0005g0240 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2468-76T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 18/21 | chr2 | 69481037 | ||||||
| chr2:69481235
|
T | C | 54 | a0001c0001t0105g0108a0001c0003t0012g0088a0001c0003t0012g0091others(51): Show | 54 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.2468-274A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 18/21 | chr2 | 69481235 | ||||||
| chr2:69481511
|
G | A | 1 | a0001c0004t0067g0077 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2468-550C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 18/21 | chr2 | 69481511 | ||||||
| chr2:69481864
|
G | A | 1 | a0004c0012t0061g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2467+847C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 18/21 | chr2 | 69481864 | ||||||
| chr2:69481947
|
A | T | 35 | a0001c0004t0002g0137a0001c0004t0010g0127a0001c0004t0010g0148others(32): Show | 35 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.2467+764T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 18/21 | chr2 | 69481947 | ||||||
| chr2:69481973
|
C | T | 2 | a0001c0001t0056g0058a0001c0001t0093g0121 | 2 | HG02300.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2467+738G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 18/21 | chr2 | 69481973 | ||||||
| chr2:69482083
|
G | T | 1 | a0001c0001t0011g0194 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2467+628C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 18/21 | chr2 | 69482083 | ||||||
| chr2:69482194
|
A | T | 1 | a0001c0001t0063g0288 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2467+517T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 18/21 | chr2 | 69482194 | ||||||
| chr2:69482378
|
C | G | 1 | a0001c0001t0124g0188 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2467+333G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 18/21 | chr2 | 69482378 | ||||||
| chr2:69482532
|
G | A | 12 | a0001c0001t0007g0049a0001c0001t0008g0069a0001c0001t0008g0082others(9): Show | 12 | HG02056.hp1 HG02135.hp1 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.2467+179C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 18/21 | chr2 | 69482532 | ||||||
| chr2:69482642
|
G | C | 6 | a0001c0001t0063g0288a0001c0001t0121g0186a0001c0011t0029g0293others(3): Show | 6 | HG02486.hp1 HG02559.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2467+69C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 18/21 | chr2 | 69482642 | ||||||
| chr2:69482678
|
G | A | 4 | a0002c0005t0018g0064a0002c0005t0018g0103a0002c0005t0018g0104others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2467+33C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 18/21 | chr2 | 69482678 | ||||||
| chr2:69482895
|
A | G | 1 | a0001c0001t0093g0121 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2366-83T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69482895 | ||||||
| chr2:69482926
|
G | A | 66 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(63): Show | 66 | HG00544.hp1 HG00597.hp2 HG01167.hp1 others(63): Show |
intron_variant | MODIFIER | c.2366-114C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69482926 | ||||||
| chr2:69483057
|
T | C | 1 | a0009c0025t0003g0260 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2366-245A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69483057 | ||||||
| chr2:69483102
|
G | A | 1 | a0002c0002t0053g0056 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2366-290C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69483102 | ||||||
| chr2:69483111
|
A | C | 4 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(1): Show | 4 | HG01243.hp1 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2366-299T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69483111 | ||||||
| chr2:69483143
|
A | G | 4 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(1): Show | 4 | HG01243.hp1 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2366-331T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69483143 | ||||||
| chr2:69483212
|
C | T | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2366-400G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69483212 | ||||||
| chr2:69483252
|
A | G | 1 | a0001c0004t0014g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2366-440T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69483252 | ||||||
| chr2:69483493
|
T | A | 8 | a0001c0001t0037g0009a0001c0001t0045g0287a0001c0001t0077g0072others(5): Show | 8 | HG02109.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2366-681A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69483493 | ||||||
| chr2:69483518
|
T | A | 1 | a0001c0001t0045g0287 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2366-706A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69483518 | ||||||
| chr2:69483538
|
G | A | 1 | a0002c0002t0001g0042 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2366-726C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69483538 | ||||||
| chr2:69483693
|
T | C | 4 | a0002c0005t0018g0064a0002c0005t0018g0103a0002c0005t0018g0104others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2366-881A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69483693 | ||||||
| chr2:69483742
|
T | C | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2366-930A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69483742 | ||||||
| chr2:69483744
|
G | C | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2366-932C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69483744 | ||||||
| chr2:69484416
|
T | C | 1 | a0001c0001t0006g0222 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2366-1604A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69484416 | ||||||
| chr2:69484429
|
C | T | 1 | a0001c0001t0063g0288 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2366-1617G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69484429 | ||||||
| chr2:69484465
|
C | G | 1 | a0001c0008t0069g0102 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2366-1653G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69484465 | ||||||
| chr2:69484504
|
G | C | 4 | a0001c0011t0029g0293a0001c0011t0029g0294a0001c0011t0079g0290others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2366-1692C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69484504 | ||||||
| chr2:69484588
|
T | C | 9 | a0001c0001t0037g0009a0001c0001t0045g0287a0001c0001t0077g0072others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2366-1776A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69484588 | ||||||
| chr2:69484614
|
G | C | 2 | a0001c0006t0028g0126a0001c0006t0028g0134 | 2 | HG02818.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2366-1802C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69484614 | ||||||
| chr2:69484651
|
G | A | 1 | a0002c0002t0001g0051 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2366-1839C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69484651 | ||||||
| chr2:69484672
|
T | C | 1 | a0001c0004t0010g0127 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2366-1860A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69484672 | ||||||
| chr2:69484674
|
G | T | 1 | a0001c0004t0070g0071 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2366-1862C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69484674 | ||||||
| chr2:69484717
|
A | G | 1 | a0003c0020t0084g0105 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2366-1905T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69484717 | ||||||
| chr2:69484736
|
G | A | 7 | a0001c0001t0008g0084a0001c0001t0009g0160a0001c0001t0091g0117others(4): Show | 7 | HG02922.hp1 HG02976.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.2366-1924C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69484736 | ||||||
| chr2:69484743
|
C | T | 3 | a0001c0001t0078g0055a0004c0013t0043g0284a0004c0013t0107g0107 | 3 | HG01167.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2366-1931G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69484743 | ||||||
| chr2:69484788
|
T | C | 1 | a0001c0003t0026g0014 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2366-1976A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69484788 | ||||||
| chr2:69484869
|
A | C | 9 | a0001c0001t0037g0009a0001c0001t0045g0287a0001c0001t0077g0072others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2366-2057T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69484869 | ||||||
| chr2:69484877
|
A | T | 4 | a0001c0001t0073g0052a0002c0002t0013g0110a0002c0002t0051g0045others(1): Show | 4 | HG02451.hp2 NA18956.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.2366-2065T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69484877 | ||||||
| chr2:69484880
|
T | A | 62 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(59): Show | 62 | HG00544.hp1 HG00597.hp2 HG01243.hp1 others(59): Show |
intron_variant | MODIFIER | c.2366-2068A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69484880 | ||||||
| chr2:69484883
|
T | A | 1 | a0001c0001t0011g0196 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2366-2071A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69484883 | ||||||
| chr2:69484980
|
G | A | 4 | a0001c0001t0020g0193a0001c0001t0020g0202a0001c0001t0020g0208others(1): Show | 4 | NA18956.hp1 NA18963.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.2366-2168C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69484980 | ||||||
| chr2:69485105
|
G | A | 4 | a0002c0005t0018g0064a0002c0005t0018g0103a0002c0005t0018g0104others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2366-2293C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69485105 | ||||||
| chr2:69485548
|
C | T | 1 | a0002c0002t0001g0044 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2366-2736G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69485548 | ||||||
| chr2:69485645
|
T | C | 1 | a0009c0025t0003g0260 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2366-2833A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69485645 | ||||||
| chr2:69485659
|
CT | C | 7 | a0001c0011t0029g0293a0001c0011t0029g0294a0001c0011t0079g0290others(4): Show | 7 | HG02486.hp1 HG02559.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2366-2848delA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69485659 | ||||||
| chr2:69485735
|
CT | C | 223 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.2366-2924delA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69485735 | ||||||
| chr2:69485911
|
G | A | 1 | a0004c0013t0107g0107 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2366-3099C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69485911 | ||||||
| chr2:69485928
|
G | A | 2 | a0001c0006t0028g0126a0001c0006t0028g0134 | 2 | HG02818.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2366-3116C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69485928 | ||||||
| chr2:69485958
|
C | CT | 59 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(56): Show | 59 | HG00544.hp1 HG00597.hp2 HG01192.hp1 others(56): Show |
intron_variant | MODIFIER | c.2366-3147dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69485958 | ||||||
| chr2:69486097
|
G | A | 2 | a0002c0002t0001g0029a0002c0002t0001g0034 | 2 | HG00544.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.2366-3285C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69486097 | ||||||
| chr2:69486113
|
C | T | 71 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(68): Show | 71 | HG00544.hp1 HG00597.hp2 HG01167.hp1 others(68): Show |
intron_variant | MODIFIER | c.2366-3301G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69486113 | ||||||
| chr2:69486116
|
G | A | 1 | a0004c0012t0036g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2366-3304C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69486116 | ||||||
| chr2:69486135
|
T | C | 1 | a0001c0001t0113g0178 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2366-3323A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69486135 | ||||||
| chr2:69486333
|
C | T | 1 | a0002c0005t0018g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2366-3521G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69486333 | ||||||
| chr2:69486370
|
G | T | 11 | a0001c0001t0037g0009a0001c0001t0045g0287a0001c0001t0077g0072others(8): Show | 11 | HG01167.hp1 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2366-3558C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69486370 | ||||||
| chr2:69486375
|
A | C | 1 | a0001c0001t0006g0224 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2366-3563T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69486375 | ||||||
| chr2:69486463
|
A | C | 2 | a0002c0005t0018g0103a0002c0005t0018g0104 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2366-3651T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69486463 | ||||||
| chr2:69486603
|
G | A | 56 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(53): Show | 56 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(53): Show |
intron_variant | MODIFIER | c.2366-3791C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69486603 | ||||||
| chr2:69486721
|
G | A | 1 | a0002c0002t0039g0004 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2366-3909C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69486721 | ||||||
| chr2:69486886
|
A | G | 1 | a0001c0026t0152g0295 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2366-4074T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69486886 | ||||||
| chr2:69486910
|
C | T | 4 | a0001c0011t0029g0293a0001c0011t0029g0294a0001c0011t0079g0290others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2366-4098G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69486910 | ||||||
| chr2:69487151
|
G | A | 1 | a0001c0001t0073g0052 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2366-4339C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69487151 | ||||||
| chr2:69487379
|
G | C | 2 | a0001c0003t0022g0010a0001c0003t0064g0085 | 2 | NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2366-4567C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69487379 | ||||||
| chr2:69487471
|
C | T | 1 | a0001c0008t0097g0131 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2366-4659G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69487471 | ||||||
| chr2:69487585
|
C | T | 86 | a0001c0001t0013g0151a0001c0001t0144g0232a0002c0002t0001g0019others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.2366-4773G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69487585 | ||||||
| chr2:69487710
|
T | A | 4 | a0001c0011t0029g0293a0001c0011t0029g0294a0001c0011t0079g0290others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2366-4898A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69487710 | ||||||
| chr2:69487787
|
C | CT | 6 | a0001c0001t0073g0052a0001c0006t0016g0289a0002c0002t0001g0046others(3): Show | 6 | HG00438.hp1 HG00735.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.2366-4976dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69487787 | ||||||
| chr2:69487787
|
CT | C | 66 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(63): Show | 66 | HG00544.hp1 HG00597.hp2 HG01243.hp1 others(63): Show |
intron_variant | MODIFIER | c.2366-4976delA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69487787 | ||||||
| chr2:69487794
|
T | C | 1 | a0002c0002t0055g0021 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2366-4982A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69487794 | ||||||
| chr2:69487798
|
T | C | 25 | a0001c0001t0105g0108a0001c0003t0012g0088a0001c0003t0012g0091others(22): Show | 25 | HG02074.hp2 HG02280.hp2 HG02451.hp1 others(22): Show |
intron_variant | MODIFIER | c.2366-4986A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69487798 | ||||||
| chr2:69487804
|
T | C | 1 | a0002c0002t0007g0018 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2366-4992A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69487804 | ||||||
| chr2:69487897
|
C | T | 1 | a0004c0012t0061g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2366-5085G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69487897 | ||||||
| chr2:69487908
|
G | A | 52 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(49): Show | 52 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.2366-5096C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69487908 | ||||||
| chr2:69487915
|
G | A | 4 | a0002c0005t0018g0064a0002c0005t0018g0103a0002c0005t0018g0104others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2366-5103C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69487915 | ||||||
| chr2:69487930
|
T | C | 1 | a0001c0001t0104g0292 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2366-5118A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69487930 | ||||||
| chr2:69488029
|
G | A | 1 | a0004c0013t0043g0284 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2366-5217C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69488029 | ||||||
| chr2:69488124
|
C | T | 4 | a0001c0011t0029g0293a0001c0011t0029g0294a0001c0011t0079g0290others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2366-5312G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69488124 | ||||||
| chr2:69488149
|
C | CGT | 13 | a0001c0001t0002g0114a0001c0001t0002g0120a0001c0001t0007g0081others(10): Show | 13 | HG01175.hp2 HG01255.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.2366-5339_2366-533 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69488149 | ||||||
| chr2:69488149
|
C | CGTGT | 8 | a0001c0001t0027g0128a0001c0001t0027g0145a0002c0002t0001g0019others(5): Show | 8 | HG01167.hp2 HG01891.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2366-5341_2366-533 others(8): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69488149 | ||||||
| chr2:69488149
|
C | CGTGTGT | 77 | a0001c0001t0144g0232a0002c0002t0001g0025a0002c0002t0001g0028others(74): Show | 77 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.2366-5343_2366-533 others(10): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69488149 | ||||||
| chr2:69488149
|
C | CGTGTGTG others(1): Show |
10 | a0001c0001t0013g0151a0001c0001t0149g0280a0002c0002t0001g0040others(7): Show | 10 | HG00140.hp1 HG01175.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.2366-5345_2366-533 others(12): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69488149 | ||||||
| chr2:69488149
|
C | CGTGTGTG others(3): Show |
7 | a0001c0001t0076g0037a0001c0001t0078g0055a0001c0001t0102g0113others(4): Show | 7 | HG01167.hp1 HG02145.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2366-5347_2366-533 others(14): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69488149 | ||||||
| chr2:69488149
|
C | CGTGTGTG others(5): Show |
39 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(36): Show | 39 | HG00544.hp1 HG00597.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.2366-5349_2366-533 others(16): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69488149 | ||||||
| chr2:69488149
|
C | CGTGTGTG others(7): Show |
14 | a0001c0001t0006g0217a0001c0001t0011g0197a0001c0001t0020g0202others(11): Show | 14 | HG01934.hp2 HG02015.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.2366-5351_2366-533 others(18): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69488149 | ||||||
| chr2:69488149
|
C | CGTGTGTG others(9): Show |
6 | a0001c0001t0006g0213a0001c0001t0063g0288a0001c0001t0137g0247others(3): Show | 6 | HG01975.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2366-5353_2366-533 others(20): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69488149 | ||||||
| chr2:69488149
|
C | CGTGTGTG others(11): Show |
4 | a0001c0001t0004g0233a0001c0001t0124g0188a0001c0001t0140g0269others(1): Show | 4 | HG01243.hp2 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.2366-5355_2366-533 others(22): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69488149 | ||||||
| chr2:69488149
|
CGT | C | 22 | a0001c0001t0105g0108a0001c0001t0117g0189a0001c0003t0012g0088others(19): Show | 22 | HG02074.hp2 HG02451.hp1 HG02602.hp1 others(19): Show |
intron_variant | MODIFIER | c.2366-5339_2366-533 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69488149 | ||||||
| chr2:69488179
|
T | TGTGTGTG others(6): Show |
1 | a0001c0001t0147g0274 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2366-5368_2366-536 others(17): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69488179 | ||||||
| chr2:69488179
|
T | TGTGTGTG others(10): Show |
1 | a0002c0005t0018g0103 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2366-5368_2366-536 others(21): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69488179 | ||||||
| chr2:69488194
|
C | T | 4 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(1): Show | 4 | HG01243.hp1 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2366-5382G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69488194 | ||||||
| chr2:69488327
|
T | C | 4 | a0001c0007t0021g0276a0001c0007t0021g0279a0001c0007t0034g0270others(1): Show | 4 | HG02809.hp2 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2366-5515A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69488327 | ||||||
| chr2:69488346
|
TAG | T | 3 | a0001c0003t0012g0096a0001c0003t0030g0168a0001c0003t0080g0094 | 3 | NA18961.hp2 NA18966.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.2366-5536_2366-553 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69488346 | ||||||
| chr2:69488379
|
T | C | 1 | a0002c0002t0050g0035 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2366-5567A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69488379 | ||||||
| chr2:69488713
|
T | C | 224 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(221): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.2366-5901A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69488713 | ||||||
| chr2:69488911
|
A | G | 18 | a0001c0001t0037g0009a0001c0001t0045g0287a0001c0001t0077g0072others(15): Show | 18 | HG01167.hp1 HG01884.hp2 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2366-6099T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69488911 | ||||||
| chr2:69489012
|
C | CT | 87 | a0001c0001t0013g0151a0001c0001t0144g0232a0002c0002t0001g0019others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.2366-6201dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69489012 | ||||||
| chr2:69489038
|
G | A | 1 | a0001c0001t0078g0055 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2366-6226C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69489038 | ||||||
| chr2:69489191
|
C | T | 24 | a0001c0001t0105g0108a0001c0003t0012g0088a0001c0003t0012g0091others(21): Show | 24 | HG02074.hp2 HG02451.hp1 HG02602.hp1 others(21): Show |
intron_variant | MODIFIER | c.2366-6379G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69489191 | ||||||
| chr2:69489193
|
G | C | 5 | a0001c0001t0037g0009a0001c0001t0045g0287a0001c0001t0077g0072others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2366-6381C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69489193 | ||||||
| chr2:69489287
|
C | T | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2366-6475G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69489287 | ||||||
| chr2:69489324
|
G | T | 4 | a0001c0007t0021g0276a0001c0007t0021g0279a0001c0007t0034g0270others(1): Show | 4 | HG02809.hp2 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2366-6512C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69489324 | ||||||
| chr2:69489395
|
A | G | 11 | a0001c0001t0037g0009a0001c0001t0045g0287a0001c0001t0077g0072others(8): Show | 11 | HG01884.hp2 HG01928.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.2366-6583T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69489395 | ||||||
| chr2:69489450
|
C | CA | 75 | a0001c0001t0002g0132a0001c0001t0006g0223a0001c0001t0014g0059others(72): Show | 75 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2365+6534dupT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69489450 | ||||||
| chr2:69489450
|
C | CAA | 135 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(132): Show | 135 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.2365+6533_2365+653 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69489450 | ||||||
| chr2:69489564
|
G | A | 2 | a0001c0008t0135g0262a0007c0017t0066g0076 | 2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.2365+6421C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69489564 | ||||||
| chr2:69489573
|
C | G | 18 | a0001c0001t0037g0009a0001c0001t0045g0287a0001c0001t0077g0072others(15): Show | 18 | HG01167.hp1 HG01884.hp2 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2365+6412G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69489573 | ||||||
| chr2:69489620
|
C | T | 1 | a0001c0004t0017g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2365+6365G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69489620 | ||||||
| chr2:69489783
|
G | T | 7 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(4): Show | 7 | HG00735.hp2 HG01243.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2365+6202C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69489783 | ||||||
| chr2:69489799
|
T | C | 1 | a0001c0004t0067g0077 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2365+6186A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69489799 | ||||||
| chr2:69489904
|
T | C | 1 | a0001c0004t0010g0156 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2365+6081A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69489904 | ||||||
| chr2:69490053
|
T | G | 73 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(70): Show | 73 | HG00544.hp1 HG00597.hp2 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.2365+5932A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69490053 | ||||||
| chr2:69490250
|
T | C | 73 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(70): Show | 73 | HG00544.hp1 HG00597.hp2 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.2365+5735A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69490250 | ||||||
| chr2:69490253
|
T | C | 54 | a0001c0001t0105g0108a0001c0003t0012g0088a0001c0003t0012g0091others(51): Show | 54 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.2365+5732A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69490253 | ||||||
| chr2:69490324
|
T | C | 1 | a0001c0008t0135g0262 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2365+5661A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69490324 | ||||||
| chr2:69490390
|
C | T | 4 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(1): Show | 4 | HG01243.hp1 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2365+5595G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69490390 | ||||||
| chr2:69490590
|
C | T | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2365+5395G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69490590 | ||||||
| chr2:69490738
|
T | C | 3 | a0001c0011t0029g0293a0001c0011t0029g0294a0001c0011t0079g0290 | 3 | HG02486.hp1 HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2365+5247A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69490738 | ||||||
| chr2:69490917
|
G | A | 1 | a0002c0002t0015g0005 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2365+5068C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69490917 | ||||||
| chr2:69490923
|
C | CCA | 101 | a0001c0001t0002g0132a0001c0001t0002g0150a0001c0001t0002g0157others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.2365+5060_2365+506 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69490923 | ||||||
| chr2:69490923
|
C | CCACA | 6 | a0001c0011t0029g0293a0001c0011t0029g0294a0001c0011t0079g0290others(3): Show | 6 | HG02056.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2365+5058_2365+506 others(8): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69490923 | ||||||
| chr2:69490923
|
C | CCACACAC others(1): Show |
6 | a0001c0001t0140g0269a0001c0006t0016g0017a0001c0006t0016g0061others(3): Show | 6 | HG01243.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2365+5054_2365+506 others(12): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69490923 | ||||||
| chr2:69490923
|
C | CCACACAC others(3): Show |
9 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(6): Show | 9 | HG01167.hp1 HG01243.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2365+5052_2365+506 others(14): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69490923 | ||||||
| chr2:69490923
|
C | CCACACAC others(5): Show |
48 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(45): Show | 48 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(45): Show |
intron_variant | MODIFIER | c.2365+5050_2365+506 others(16): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69490923 | ||||||
| chr2:69490923
|
C | CCACACAC others(9): Show |
1 | a0001c0001t0063g0288 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2365+5046_2365+506 others(20): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69490923 | ||||||
| chr2:69490928
|
C | CACACACA others(6): Show |
1 | a0001c0001t0004g0257 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2365+5044_2365+505 others(17): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69490928 | ||||||
| chr2:69490986
|
A | G | 80 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(77): Show | 80 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.2365+4999T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69490986 | ||||||
| chr2:69491034
|
C | T | 1 | a0001c0001t0021g0278 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2365+4951G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69491034 | ||||||
| chr2:69491114
|
A | AT | 6 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(3): Show | 6 | HG01243.hp1 HG02630.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2365+4870dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69491114 | ||||||
| chr2:69491146
|
C | T | 1 | a0002c0002t0003g0251 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2365+4839G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69491146 | ||||||
| chr2:69491191
|
C | T | 1 | a0003c0020t0084g0105 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2365+4794G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69491191 | ||||||
| chr2:69491780
|
G | A | 2 | a0001c0001t0004g0206a0001c0001t0004g0233 | 2 | NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2365+4205C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69491780 | ||||||
| chr2:69491822
|
A | G | 14 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(11): Show | 14 | HG00735.hp2 HG01167.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.2365+4163T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69491822 | ||||||
| chr2:69492045
|
A | C | 222 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.2365+3940T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69492045 | ||||||
| chr2:69492136
|
C | T | 71 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(68): Show | 71 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.2365+3849G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69492136 | ||||||
| chr2:69492187
|
G | A | 1 | a0001c0001t0011g0195 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2365+3798C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69492187 | ||||||
| chr2:69492220
|
C | CT | 11 | a0001c0001t0004g0257a0001c0001t0037g0009a0001c0001t0045g0287others(8): Show | 11 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2365+3764dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69492220 | ||||||
| chr2:69492372
|
C | A | 88 | a0001c0001t0013g0151a0001c0001t0144g0232a0002c0002t0001g0019others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.2365+3613G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69492372 | ||||||
| chr2:69492504
|
G | A | 3 | a0001c0001t0006g0207a0001c0001t0006g0223a0001c0001t0147g0274 | 3 | HG01257.hp1 HG01258.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.2365+3481C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69492504 | ||||||
| chr2:69492518
|
C | CT | 34 | a0001c0001t0002g0132a0001c0001t0021g0278a0001c0001t0105g0108others(31): Show | 34 | HG00438.hp2 HG01891.hp2 HG01975.hp2 others(31): Show |
intron_variant | MODIFIER | c.2365+3466dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69492518 | ||||||
| chr2:69492518
|
C | CTT | 88 | a0001c0001t0144g0232a0001c0004t0002g0137a0001c0004t0010g0127others(85): Show | 88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.2365+3465_2365+346 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69492518 | ||||||
| chr2:69492518
|
C | CTTT | 22 | a0001c0001t0013g0151a0001c0004t0010g0156a0001c0004t0072g0093others(19): Show | 22 | HG00738.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.2365+3464_2365+346 others(7): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69492518 | ||||||
| chr2:69492518
|
C | CTTTTTT | 10 | a0001c0001t0037g0009a0001c0001t0045g0287a0001c0001t0077g0072others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2365+3461_2365+346 others(10): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69492518 | ||||||
| chr2:69492518
|
C | CTTTTTTT | 46 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0254others(43): Show | 46 | HG00597.hp2 HG00735.hp2 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.2365+3460_2365+346 others(11): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69492518 | ||||||
| chr2:69492518
|
C | CTTTTTTT others(1): Show |
18 | a0001c0001t0004g0221a0001c0001t0004g0233a0001c0001t0004g0258others(15): Show | 18 | HG00544.hp1 HG01167.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.2365+3459_2365+346 others(12): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69492518 | ||||||
| chr2:69492518
|
C | CTTTTTTT others(3): Show |
1 | a0004c0013t0043g0284 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2365+3457_2365+346 others(14): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69492518 | ||||||
| chr2:69492518
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0014g0060 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2365+3456_2365+346 others(15): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69492518 | ||||||
| chr2:69492616
|
G | A | 4 | a0001c0001t0002g0114a0001c0001t0002g0120a0001c0001t0027g0128others(1): Show | 4 | HG01167.hp2 HG01884.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.2365+3369C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69492616 | ||||||
| chr2:69492724
|
G | A | 224 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(221): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.2365+3261C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69492724 | ||||||
| chr2:69492876
|
C | T | 3 | a0001c0004t0017g0073a0001c0004t0017g0075a0001c0004t0067g0077 | 3 | HG03041.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2365+3109G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69492876 | ||||||
| chr2:69492880
|
A | T | 1 | a0002c0002t0110g0177 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2365+3105T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69492880 | ||||||
| chr2:69492890
|
T | C | 297 | a0001c0001t0002g0114a0001c0001t0002g0120a0001c0001t0002g0125others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.2365+3095A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69492890 | ||||||
| chr2:69492979
|
G | C | 1 | a0003c0020t0084g0105 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2365+3006C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69492979 | ||||||
| chr2:69493002
|
C | T | 1 | a0001c0004t0070g0071 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2365+2983G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493002 | ||||||
| chr2:69493036
|
G | C | 3 | a0001c0011t0029g0293a0001c0011t0029g0294a0001c0011t0079g0290 | 3 | HG02486.hp1 HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2365+2949C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493036 | ||||||
| chr2:69493050
|
C | T | 1 | a0001c0003t0082g0098 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2365+2935G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493050 | ||||||
| chr2:69493155
|
T | A | 1 | a0002c0002t0131g0211 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2365+2830A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493155 | ||||||
| chr2:69493158
|
C | CAAAA | 32 | a0001c0001t0013g0151a0002c0002t0003g0199a0002c0002t0003g0203others(29): Show | 32 | HG00438.hp1 HG00735.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.2365+2823_2365+282 others(8): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAA | 7 | a0001c0004t0014g0063a0002c0002t0003g0245a0002c0002t0005g0239others(4): Show | 7 | HG01175.hp1 HG02293.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2365+2822_2365+282 others(9): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(3): Show |
5 | a0001c0001t0140g0269a0001c0006t0016g0017a0001c0006t0016g0061others(2): Show | 5 | HG00735.hp2 HG01243.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2365+2817_2365+282 others(14): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(4): Show |
6 | a0001c0001t0078g0055a0001c0007t0021g0279a0001c0007t0034g0270others(3): Show | 6 | HG01167.hp1 HG01433.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2365+2816_2365+282 others(15): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(5): Show |
2 | a0001c0007t0021g0276a0002c0002t0131g0211 | 2 | HG02809.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.2365+2815_2365+282 others(16): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(6): Show |
1 | a0002c0002t0132g0236 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2365+2814_2365+282 others(17): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(8): Show |
2 | a0002c0002t0023g0026a0004c0012t0036g0283 | 2 | HG01074.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2365+2812_2365+282 others(19): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(9): Show |
3 | a0002c0002t0001g0042a0002c0002t0001g0044a0002c0002t0013g0112 | 3 | NA18747.hp2 NA18955.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2365+2811_2365+282 others(20): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(10): Show |
14 | a0001c0001t0004g0216a0001c0001t0004g0233a0001c0001t0004g0264others(11): Show | 14 | HG01934.hp2 HG01943.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.2365+2810_2365+282 others(21): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(11): Show |
21 | a0001c0001t0004g0221a0001c0001t0004g0254a0001c0001t0004g0259others(18): Show | 21 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.2365+2809_2365+282 others(22): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(12): Show |
22 | a0001c0001t0004g0257a0001c0001t0004g0258a0001c0001t0004g0265others(19): Show | 22 | HG01358.hp2 HG01975.hp1 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.2365+2808_2365+282 others(23): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(13): Show |
20 | a0001c0001t0004g0206a0001c0001t0006g0207a0001c0001t0006g0222others(17): Show | 20 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(17): Show |
intron_variant | MODIFIER | c.2365+2826_2365+282 others(24): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(14): Show |
16 | a0001c0001t0083g0016a0001c0001t0144g0232a0001c0004t0010g0148others(13): Show | 16 | HG00323.hp1 HG00558.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.2365+2826_2365+282 others(25): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(15): Show |
8 | a0001c0003t0012g0096a0001c0003t0030g0169a0001c0003t0080g0094others(5): Show | 8 | HG02132.hp2 HG02895.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.2365+2826_2365+282 others(26): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(16): Show |
17 | a0001c0001t0124g0188a0001c0003t0012g0088a0001c0003t0012g0091others(14): Show | 17 | HG01175.hp2 HG02280.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.2365+2826_2365+282 others(27): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(17): Show |
4 | a0001c0003t0026g0014a0002c0005t0123g0183a0002c0005t0150g0281others(1): Show | 4 | HG02622.hp2 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2365+2826_2365+282 others(28): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(18): Show |
3 | a0001c0003t0106g0141a0001c0006t0028g0126a0002c0016t0103g0106 | 3 | HG02074.hp2 HG02818.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2365+2826_2365+282 others(29): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(19): Show |
3 | a0001c0001t0139g0231a0001c0004t0153g0296a0002c0002t0049g0047 | 3 | HG00323.hp2 HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2365+2826_2365+282 others(30): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(20): Show |
1 | a0002c0002t0015g0005 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2365+2826_2365+282 others(31): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(22): Show |
4 | a0001c0003t0026g0015a0001c0006t0041g0008a0002c0002t0019g0115others(1): Show | 4 | HG01099.hp1 HG01099.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.2365+2826_2365+282 others(33): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(23): Show |
2 | a0002c0002t0001g0038a0002c0002t0015g0002 | 2 | HG03669.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.2365+2826_2365+282 others(34): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(25): Show |
1 | a0003c0020t0084g0105 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2365+2826_2365+282 others(36): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(27): Show |
1 | a0002c0002t0001g0028 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2365+2826_2365+282 others(38): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(29): Show |
2 | a0001c0003t0081g0080a0001c0006t0028g0134 | 2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2365+2826_2365+282 others(40): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(30): Show |
1 | a0002c0002t0001g0040 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2365+2826_2365+282 others(41): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(31): Show |
1 | a0002c0002t0001g0043 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2365+2826_2365+282 others(42): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(32): Show |
4 | a0002c0002t0001g0057a0002c0002t0008g0050a0002c0002t0115g0180others(1): Show | 4 | HG01192.hp2 HG01361.hp2 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.2365+2826_2365+282 others(43): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(34): Show |
1 | a0002c0002t0015g0003 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2365+2826_2365+282 others(45): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(38): Show |
1 | a0002c0002t0013g0144 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2365+2826_2365+282 others(49): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
C | CAAAAAAA others(39): Show |
1 | a0002c0002t0001g0051 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2365+2826_2365+282 others(50): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493158
|
CAAAAAAA others(3): Show |
C | 4 | a0002c0005t0018g0064a0002c0005t0018g0103a0002c0005t0018g0104others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2365+2817_2365+282 others(14): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493158 | ||||||
| chr2:69493258
|
C | T | 3 | a0001c0011t0029g0293a0001c0011t0029g0294a0001c0011t0079g0290 | 3 | HG02486.hp1 HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2365+2727G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493258 | ||||||
| chr2:69493303
|
G | A | 56 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(53): Show | 56 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(53): Show |
intron_variant | MODIFIER | c.2365+2682C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493303 | ||||||
| chr2:69493328
|
G | C | 53 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(50): Show | 53 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.2365+2657C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493328 | ||||||
| chr2:69493491
|
G | A | 3 | a0001c0011t0029g0293a0001c0011t0029g0294a0001c0011t0079g0290 | 3 | HG02486.hp1 HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2365+2494C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493491 | ||||||
| chr2:69493564
|
G | A | 1 | a0001c0001t0007g0049 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2365+2421C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493564 | ||||||
| chr2:69493605
|
C | T | 51 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(48): Show | 51 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.2365+2380G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493605 | ||||||
| chr2:69493788
|
G | A | 58 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(55): Show | 58 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(55): Show |
intron_variant | MODIFIER | c.2365+2197C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493788 | ||||||
| chr2:69493808
|
C | T | 3 | a0001c0001t0078g0055a0004c0013t0043g0284a0004c0013t0107g0107 | 3 | HG01167.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2365+2177G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493808 | ||||||
| chr2:69493849
|
C | T | 2 | a0002c0002t0001g0040a0002c0002t0044g0041 | 2 | HG00140.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.2365+2136G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493849 | ||||||
| chr2:69493851
|
A | C | 1 | a0002c0016t0103g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2365+2134T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69493851 | ||||||
| chr2:69494160
|
C | G | 4 | a0002c0005t0018g0064a0002c0005t0018g0103a0002c0005t0018g0104others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2365+1825G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69494160 | ||||||
| chr2:69494208
|
G | A | 1 | a0002c0002t0044g0041 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2365+1777C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69494208 | ||||||
| chr2:69494234
|
G | A | 1 | a0001c0001t0020g0193 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2365+1751C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69494234 | ||||||
| chr2:69494527
|
G | A | 7 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(4): Show | 7 | HG00735.hp2 HG01243.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2365+1458C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69494527 | ||||||
| chr2:69494916
|
A | C | 10 | a0001c0001t0007g0049a0001c0001t0008g0069a0001c0001t0008g0082others(7): Show | 10 | HG02056.hp1 HG02135.hp1 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.2365+1069T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69494916 | ||||||
| chr2:69494983
|
G | A | 215 | a0001c0001t0002g0132a0001c0001t0004g0206a0001c0001t0004g0216others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.2365+1002C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69494983 | ||||||
| chr2:69495172
|
A | G | 1 | a0001c0001t0021g0278 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2365+813T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69495172 | ||||||
| chr2:69495186
|
G | A | 1 | a0002c0002t0007g0018 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2365+799C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69495186 | ||||||
| chr2:69495255
|
C | T | 17 | a0001c0003t0012g0088a0001c0003t0012g0091a0001c0003t0012g0095others(14): Show | 17 | HG02074.hp2 HG02451.hp1 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.2365+730G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69495255 | ||||||
| chr2:69495484
|
T | C | 22 | a0001c0004t0002g0137a0001c0004t0010g0127a0001c0004t0010g0148others(19): Show | 22 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.2365+501A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69495484 | ||||||
| chr2:69495756
|
G | A | 1 | a0001c0003t0046g0100 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2365+229C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69495756 | ||||||
| chr2:69495928
|
A | G | 1 | a0001c0004t0017g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2365+57T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 17/21 | chr2 | 69495928 | ||||||
| chr2:69496091
|
G | T | 7 | a0001c0001t0105g0108a0001c0007t0021g0276a0001c0007t0021g0279others(4): Show | 7 | HG02809.hp2 HG02896.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.2270-11C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69496091 | ||||||
| chr2:69496097
|
G | A | 1 | a0001c0001t0063g0288 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2270-17C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69496097 | ||||||
| chr2:69496273
|
G | GT | 34 | a0001c0001t0002g0125a0001c0001t0002g0132a0001c0001t0002g0149others(31): Show | 34 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.2270-194dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69496273 | ||||||
| chr2:69496273
|
G | GTT | 9 | a0001c0001t0063g0288a0001c0001t0105g0108a0001c0001t0140g0269others(6): Show | 9 | HG01243.hp2 HG02717.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2270-195_2270-194d others(4): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69496273 | ||||||
| chr2:69496273
|
G | GTTT | 45 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(42): Show | 45 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(42): Show |
intron_variant | MODIFIER | c.2270-196_2270-194d others(5): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69496273 | ||||||
| chr2:69496273
|
G | GTTTT | 6 | a0001c0001t0004g0261a0001c0001t0006g0204a0001c0001t0006g0223others(3): Show | 6 | HG01358.hp2 HG01978.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.2270-197_2270-194d others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69496273 | ||||||
| chr2:69496307
|
G | A | 5 | a0002c0005t0018g0064a0002c0005t0018g0103a0002c0005t0018g0104others(2): Show | 5 | HG01928.hp2 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2270-227C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69496307 | ||||||
| chr2:69496330
|
T | C | 5 | a0002c0005t0040g0006a0002c0005t0122g0182a0002c0005t0123g0183others(2): Show | 5 | HG02572.hp1 HG02895.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2270-250A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69496330 | ||||||
| chr2:69496359
|
G | A | 20 | a0001c0003t0012g0088a0001c0003t0012g0091a0001c0003t0012g0095others(17): Show | 20 | HG02074.hp2 HG02451.hp1 HG02602.hp1 others(17): Show |
intron_variant | MODIFIER | c.2270-279C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69496359 | ||||||
| chr2:69496362
|
T | TC | 140 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(137): Show | 140 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.2270-283dupG | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69496362 | ||||||
| chr2:69496409
|
G | A | 1 | a0002c0002t0003g0238 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2270-329C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69496409 | ||||||
| chr2:69496469
|
G | C | 1 | a0004c0013t0043g0284 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2270-389C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69496469 | ||||||
| chr2:69496578
|
C | T | 140 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(137): Show | 140 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.2270-498G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69496578 | ||||||
| chr2:69496615
|
G | T | 1 | a0002c0002t0110g0177 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2270-535C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69496615 | ||||||
| chr2:69496763
|
G | A | 1 | a0001c0001t0090g0119 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2270-683C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69496763 | ||||||
| chr2:69497080
|
G | A | 7 | a0001c0001t0105g0108a0001c0007t0021g0276a0001c0007t0021g0279others(4): Show | 7 | HG02809.hp2 HG02896.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.2270-1000C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69497080 | ||||||
| chr2:69497234
|
TAGTA | T | 140 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(137): Show | 140 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.2270-1158_2270-115 others(8): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69497234 | ||||||
| chr2:69497239
|
G | C | 140 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(137): Show | 140 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.2270-1159C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69497239 | ||||||
| chr2:69497294
|
T | A | 1 | a0001c0001t0002g0150 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2270-1214A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69497294 | ||||||
| chr2:69497295
|
C | CT | 79 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(76): Show | 79 | HG00544.hp1 HG00735.hp2 HG01257.hp1 others(76): Show |
intron_variant | MODIFIER | c.2270-1216dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69497295 | ||||||
| chr2:69497295
|
C | CTT | 50 | a0001c0001t0004g0233a0001c0001t0004g0254a0001c0001t0011g0201others(47): Show | 50 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2270-1217_2270-121 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69497295 | ||||||
| chr2:69497295
|
C | CTTT | 7 | a0001c0001t0120g0187a0001c0001t0138g0209a0001c0004t0067g0077others(4): Show | 7 | HG00099.hp2 HG02559.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2270-1218_2270-121 others(7): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69497295 | ||||||
| chr2:69497295
|
CT | C | 11 | a0001c0001t0002g0120a0001c0001t0009g0139a0001c0001t0057g0291others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2270-1216delA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69497295 | ||||||
| chr2:69497374
|
C | T | 1 | a0002c0002t0003g0238 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2270-1294G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69497374 | ||||||
| chr2:69497517
|
C | G | 140 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(137): Show | 140 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.2270-1437G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69497517 | ||||||
| chr2:69497574
|
A | G | 5 | a0001c0001t0037g0009a0001c0001t0077g0072a0001c0001t0124g0188others(2): Show | 5 | HG02280.hp1 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2270-1494T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69497574 | ||||||
| chr2:69497851
|
G | A | 1 | a0004c0012t0061g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2270-1771C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69497851 | ||||||
| chr2:69497917
|
T | C | 1 | a0001c0001t0006g0225 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2270-1837A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69497917 | ||||||
| chr2:69497986
|
C | T | 1 | a0001c0004t0010g0156 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2270-1906G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69497986 | ||||||
| chr2:69498121
|
T | C | 3 | a0001c0001t0007g0027a0001c0001t0007g0086a0001c0001t0007g0099 | 3 | HG02080.hp1 NA18977.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.2270-2041A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69498121 | ||||||
| chr2:69498277
|
A | G | 4 | a0002c0005t0018g0064a0002c0005t0018g0103a0002c0005t0018g0104others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2270-2197T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69498277 | ||||||
| chr2:69498465
|
C | T | 1 | a0002c0002t0115g0180 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2270-2385G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69498465 | ||||||
| chr2:69498481
|
G | A | 1 | a0001c0004t0014g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2270-2401C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69498481 | ||||||
| chr2:69498773
|
G | A | 1 | a0001c0003t0142g0214 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2270-2693C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69498773 | ||||||
| chr2:69498786
|
A | C | 1 | a0001c0001t0004g0221 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2270-2706T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69498786 | ||||||
| chr2:69498850
|
G | C | 22 | a0001c0004t0002g0137a0001c0004t0010g0127a0001c0004t0010g0148others(19): Show | 22 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.2270-2770C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69498850 | ||||||
| chr2:69498857
|
G | T | 1 | a0001c0001t0007g0065 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2270-2777C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69498857 | ||||||
| chr2:69498908
|
T | C | 228 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(225): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.2270-2828A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69498908 | ||||||
| chr2:69498929
|
T | C | 90 | a0001c0001t0007g0049a0001c0001t0008g0069a0001c0001t0013g0151others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.2270-2849A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69498929 | ||||||
| chr2:69499022
|
T | C | 92 | a0001c0001t0007g0049a0001c0001t0008g0069a0001c0001t0013g0151others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.2270-2942A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69499022 | ||||||
| chr2:69499565
|
C | T | 2 | a0003c0014t0025g0285a0003c0014t0025g0286 | 2 | HG01891.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2270-3485G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69499565 | ||||||
| chr2:69499690
|
A | C | 2 | a0002c0005t0018g0103a0002c0005t0018g0104 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2270-3610T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69499690 | ||||||
| chr2:69499702
|
T | A | 87 | a0002c0002t0001g0019a0002c0002t0001g0025a0002c0002t0001g0028others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.2270-3622A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69499702 | ||||||
| chr2:69499726
|
C | T | 9 | a0001c0001t0105g0108a0001c0007t0021g0276a0001c0007t0021g0279others(6): Show | 9 | HG02280.hp2 HG02809.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.2270-3646G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69499726 | ||||||
| chr2:69500181
|
T | G | 1 | a0001c0004t0010g0156 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2270-4101A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500181 | ||||||
| chr2:69500215
|
A | G | 1 | a0001c0001t0083g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2270-4135T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500215 | ||||||
| chr2:69500502
|
C | T | 1 | a0001c0001t0149g0280 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2270-4422G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500502 | ||||||
| chr2:69500664
|
A | AAT | 8 | a0001c0001t0002g0157a0001c0001t0002g0158a0001c0001t0007g0027others(5): Show | 8 | HG01167.hp2 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.2270-4586_2270-458 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500664 | ||||||
| chr2:69500664
|
A | AATAAATA others(11): Show |
1 | a0002c0002t0019g0143 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2270-4585_2270-458 others(22): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500664 | ||||||
| chr2:69500664
|
A | AATAT | 4 | a0001c0001t0002g0149a0001c0001t0008g0082a0001c0001t0009g0129others(1): Show | 4 | HG02135.hp1 HG03540.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.2270-4588_2270-458 others(8): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500664 | ||||||
| chr2:69500664
|
A | AATATACA others(9): Show |
1 | a0001c0004t0067g0077 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2270-4585_2270-458 others(20): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500664 | ||||||
| chr2:69500664
|
A | AATATAT | 6 | a0001c0001t0008g0069a0001c0001t0009g0124a0001c0001t0032g0175others(3): Show | 6 | HG02056.hp1 HG02148.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.2270-4590_2270-458 others(10): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500664 | ||||||
| chr2:69500664
|
A | AATATATA others(1): Show |
3 | a0001c0001t0113g0178a0002c0002t0001g0040a0007c0018t0002g0165 | 3 | HG00140.hp1 HG03831.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.2270-4592_2270-458 others(12): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500664 | ||||||
| chr2:69500664
|
A | AATATATA others(3): Show |
9 | a0001c0001t0002g0150a0001c0004t0017g0078a0002c0002t0003g0203others(6): Show | 9 | HG00597.hp1 HG00735.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.2270-4594_2270-458 others(14): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500664 | ||||||
| chr2:69500664
|
A | AATATATA others(5): Show |
9 | a0002c0002t0001g0034a0002c0002t0001g0046a0002c0002t0001g0057others(6): Show | 9 | HG00099.hp1 HG00544.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.2270-4596_2270-458 others(16): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500664 | ||||||
| chr2:69500664
|
A | AATATATA others(7): Show |
17 | a0001c0006t0028g0126a0002c0002t0001g0025a0002c0002t0001g0033others(14): Show | 17 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(14): Show |
intron_variant | MODIFIER | c.2270-4598_2270-458 others(18): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500664 | ||||||
| chr2:69500664
|
A | AATATATA others(9): Show |
2 | a0001c0001t0034g0267a0002c0002t0003g0242 | 2 | NA19068.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.2270-4600_2270-458 others(20): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500664 | ||||||
| chr2:69500664
|
A | AATATATA others(11): Show |
3 | a0001c0001t0007g0049a0002c0002t0003g0199a0006c0015t0001g0024 | 3 | HG00558.hp2 HG02083.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.2270-4602_2270-458 others(22): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500664 | ||||||
| chr2:69500664
|
A | AATATATA others(13): Show |
3 | a0001c0001t0007g0065a0001c0001t0031g0176a0002c0002t0008g0050 | 3 | HG03139.hp2 HG03225.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.2270-4604_2270-458 others(24): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500664 | ||||||
| chr2:69500664
|
A | AATATATA others(15): Show |
2 | a0001c0004t0017g0073a0002c0002t0003g0238 | 2 | HG03041.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.2270-4606_2270-458 others(26): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500664 | ||||||
| chr2:69500664
|
A | AATATATA others(17): Show |
1 | a0009c0025t0003g0260 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2270-4608_2270-458 others(28): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500664 | ||||||
| chr2:69500664
|
AAT | A | 17 | a0001c0001t0004g0216a0001c0001t0004g0259a0001c0001t0004g0261others(14): Show | 17 | HG01928.hp1 HG02083.hp1 HG02132.hp1 others(14): Show |
intron_variant | MODIFIER | c.2270-4586_2270-458 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500664 | ||||||
| chr2:69500664
|
AATAT | A | 17 | a0001c0001t0004g0254a0001c0001t0011g0192a0001c0001t0011g0194others(14): Show | 17 | HG00597.hp2 HG01433.hp1 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.2270-4588_2270-458 others(8): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500664 | ||||||
| chr2:69500664
|
AATATAT | A | 9 | a0001c0001t0007g0086a0001c0001t0007g0099a0001c0001t0045g0287others(6): Show | 9 | HG02080.hp1 HG02109.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2270-4590_2270-458 others(10): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500664 | ||||||
| chr2:69500664
|
AATATATA others(1): Show |
A | 4 | a0001c0001t0007g0101a0001c0001t0022g0011a0001c0001t0037g0009others(1): Show | 4 | HG00408.hp2 HG02818.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2270-4592_2270-458 others(12): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500664 | ||||||
| chr2:69500664
|
AATATATA others(3): Show |
A | 3 | a0001c0001t0007g0089a0001c0001t0008g0022a0001c0001t0063g0288 | 3 | HG02015.hp2 HG02717.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2270-4594_2270-458 others(14): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500664 | ||||||
| chr2:69500668
|
T | A | 2 | a0002c0002t0005g0256a0002c0002t0019g0159 | 2 | NA19066.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.2270-4588A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500668 | ||||||
| chr2:69500684
|
T | C | 2 | a0001c0001t0006g0205a0001c0001t0006g0224 | 2 | HG02148.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.2270-4604A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500684 | ||||||
| chr2:69500686
|
T | C | 23 | a0001c0001t0004g0206a0001c0001t0004g0221a0001c0001t0004g0233others(20): Show | 23 | HG00544.hp1 HG01257.hp1 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.2270-4606A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500686 | ||||||
| chr2:69500688
|
T | C | 37 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(34): Show | 37 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(34): Show |
intron_variant | MODIFIER | c.2270-4608A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500688 | ||||||
| chr2:69500688
|
TATATATA others(13): Show |
T | 2 | a0001c0001t0120g0187a0003c0021t0151g0282 | 2 | HG01928.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2270-4628_2270-460 others(24): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500688 | ||||||
| chr2:69500689
|
A | ATATATAT others(15): Show |
1 | a0001c0006t0016g0061 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2270-4610_2270-460 others(26): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500689 | ||||||
| chr2:69500690
|
T | C | 44 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(41): Show | 44 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(41): Show |
intron_variant | MODIFIER | c.2270-4610A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500690 | ||||||
| chr2:69500690
|
TATATATA others(7): Show |
T | 1 | a0002c0005t0018g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2270-4624_2270-461 others(18): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500690 | ||||||
| chr2:69500690
|
TATATATA others(9): Show |
T | 4 | a0002c0005t0018g0103a0002c0005t0018g0104a0002c0005t0100g0116others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2270-4626_2270-461 others(20): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500690 | ||||||
| chr2:69500691
|
A | G | 1 | a0001c0006t0016g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2270-4611T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500691 | ||||||
| chr2:69500692
|
T | C | 54 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(51): Show | 54 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(51): Show |
intron_variant | MODIFIER | c.2270-4612A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500692 | ||||||
| chr2:69500694
|
T | C | 57 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(54): Show | 57 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(54): Show |
intron_variant | MODIFIER | c.2270-4614A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500694 | ||||||
| chr2:69500696
|
T | C | 66 | a0001c0001t0002g0132a0001c0001t0004g0206a0001c0001t0004g0216others(63): Show | 66 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.2270-4616A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500696 | ||||||
| chr2:69500696
|
T | TAC | 4 | a0001c0003t0108g0138a0001c0011t0029g0293a0001c0011t0029g0294others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2270-4617_2270-461 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500696 | ||||||
| chr2:69500696
|
T | TACACAC | 3 | a0001c0001t0078g0055a0001c0003t0022g0010a0001c0009t0125g0179 | 3 | HG01167.hp1 HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2270-4617_2270-461 others(10): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500696 | ||||||
| chr2:69500698
|
T | C | 83 | a0001c0001t0002g0130a0001c0001t0002g0152a0001c0001t0004g0206others(80): Show | 83 | HG00544.hp1 HG00597.hp2 HG01167.hp1 others(80): Show |
intron_variant | MODIFIER | c.2270-4618A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TAC | 9 | a0001c0001t0002g0114a0001c0001t0002g0120a0001c0001t0021g0278others(6): Show | 9 | HG00099.hp2 HG01884.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2270-4620_2270-461 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TACAC | 7 | a0001c0003t0082g0098a0001c0003t0109g0166a0001c0004t0146g0273others(4): Show | 7 | HG02809.hp2 HG02896.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.2270-4622_2270-461 others(8): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TACACAC | 3 | a0001c0003t0012g0097a0001c0003t0030g0169a0001c0003t0064g0085 | 3 | NA18969.hp2 NA18980.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2270-4624_2270-461 others(10): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TAGACACA others(5): Show |
1 | a0001c0001t0014g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2270-4619_2270-461 others(16): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TATAC | 7 | a0001c0001t0002g0154a0001c0001t0009g0139a0001c0001t0027g0145others(4): Show | 7 | HG00558.hp1 HG01891.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2270-4619_2270-461 others(8): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TATACAC | 12 | a0001c0001t0105g0108a0001c0003t0012g0091a0001c0003t0012g0095others(9): Show | 12 | HG00323.hp1 HG01106.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.2270-4619_2270-461 others(10): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TATACACA others(5): Show |
1 | a0001c0006t0016g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2270-4619_2270-461 others(16): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TATATAC | 5 | a0001c0001t0073g0052a0001c0004t0072g0093a0001c0008t0097g0131others(2): Show | 5 | HG01074.hp2 HG02040.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.2270-4619_2270-461 others(10): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TATATACA others(1): Show |
6 | a0001c0004t0010g0127a0001c0007t0148g0277a0002c0002t0001g0051others(3): Show | 6 | HG01175.hp2 HG01891.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.2270-4619_2270-461 others(12): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TATATACA others(3): Show |
4 | a0001c0001t0014g0060a0001c0001t0014g0066a0001c0003t0081g0080others(1): Show | 4 | HG01243.hp1 HG03195.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2270-4619_2270-461 others(14): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TATATACA others(7): Show |
1 | a0001c0003t0142g0214 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2270-4619_2270-461 others(18): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TATATATA others(3): Show |
1 | a0001c0004t0153g0296 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2270-4619_2270-461 others(14): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TATATATA others(9): Show |
1 | a0002c0005t0122g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2270-4619_2270-461 others(20): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TATATATA others(11): Show |
1 | a0002c0016t0134g0272 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2270-4619_2270-461 others(22): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TATATATA others(3): Show |
3 | a0001c0004t0014g0063a0001c0006t0028g0134a0001c0006t0042g0007 | 3 | HG01884.hp2 HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2270-4619_2270-461 others(14): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TATATATA others(5): Show |
5 | a0001c0003t0012g0088a0001c0003t0026g0015a0002c0002t0003g0251others(2): Show | 5 | HG00738.hp1 HG01099.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2270-4619_2270-461 others(16): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TATATATA others(7): Show |
1 | a0002c0002t0005g0248 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2270-4619_2270-461 others(18): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TATATATA others(9): Show |
1 | a0002c0002t0003g0245 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2270-4619_2270-461 others(20): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TATATATA others(15): Show |
2 | a0002c0005t0123g0183a0002c0005t0150g0281 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2270-4619_2270-461 others(26): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TATATATA others(5): Show |
11 | a0002c0002t0001g0029a0002c0002t0003g0227a0002c0002t0003g0246others(8): Show | 11 | HG01099.hp2 HG01106.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.2270-4619_2270-461 others(16): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TATATATA others(7): Show |
4 | a0001c0001t0007g0081a0002c0002t0048g0039a0002c0002t0111g0173others(1): Show | 4 | HG01255.hp1 HG02895.hp1 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.2270-4619_2270-461 others(18): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TATATATA others(7): Show |
9 | a0001c0006t0041g0008a0002c0002t0001g0044a0002c0002t0005g0240others(6): Show | 9 | HG01175.hp1 NA18961.hp1 NA18970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2270-4619_2270-461 others(18): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TATATATA others(9): Show |
1 | a0002c0002t0033g0200 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2270-4619_2270-461 others(20): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TATATATA others(9): Show |
8 | a0002c0002t0001g0019a0002c0002t0001g0038a0002c0002t0003g0215others(5): Show | 8 | HG01934.hp1 HG01975.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.2270-4619_2270-461 others(20): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TATATATA others(13): Show |
1 | a0002c0002t0005g0230 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2270-4619_2270-461 others(24): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TATATATA others(23): Show |
1 | a0002c0005t0040g0006 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2270-4619_2270-461 others(34): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TATATATA others(15): Show |
1 | a0002c0002t0131g0211 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2270-4619_2270-461 others(26): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TATATATA others(17): Show |
2 | a0002c0002t0005g0256a0002c0002t0019g0159 | 2 | NA19066.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.2270-4619_2270-461 others(28): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TATATATA others(17): Show |
1 | a0002c0002t0051g0045 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2270-4619_2270-461 others(28): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TATATATA others(19): Show |
1 | a0002c0002t0015g0003 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2270-4619_2270-461 others(30): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500698
|
T | TATATATA others(13): Show |
1 | a0001c0006t0016g0289 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2270-4619_2270-461 others(24): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500698 | ||||||
| chr2:69500700
|
C | T | 14 | a0001c0001t0002g0150a0001c0001t0007g0065a0001c0001t0008g0012others(11): Show | 14 | HG00140.hp1 HG00597.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.2270-4620G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500700 | ||||||
| chr2:69500702
|
C | T | 2 | a0001c0001t0008g0012a0001c0001t0008g0013 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2270-4622G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69500702 | ||||||
| chr2:69501020
|
C | T | 96 | a0002c0002t0001g0019a0002c0002t0001g0025a0002c0002t0001g0028others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.2269+4549G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69501020 | ||||||
| chr2:69501023
|
A | G | 230 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(227): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.2269+4546T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69501023 | ||||||
| chr2:69501120
|
A | C | 1 | a0001c0003t0012g0088 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2269+4449T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69501120 | ||||||
| chr2:69501344
|
C | T | 1 | a0001c0001t0037g0009 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2269+4225G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69501344 | ||||||
| chr2:69501383
|
A | AT | 7 | a0001c0004t0070g0071a0001c0006t0016g0017a0001c0006t0016g0061others(4): Show | 7 | HG00099.hp2 HG00735.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2269+4185dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69501383 | ||||||
| chr2:69501696
|
C | T | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2269+3873G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69501696 | ||||||
| chr2:69501720
|
C | T | 60 | a0001c0003t0012g0088a0001c0003t0012g0091a0001c0003t0012g0095others(57): Show | 60 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2269+3849G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69501720 | ||||||
| chr2:69502061
|
T | C | 1 | a0002c0002t0003g0238 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2269+3508A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69502061 | ||||||
| chr2:69502181
|
T | A | 5 | a0002c0005t0018g0064a0002c0005t0018g0103a0002c0005t0018g0104others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2269+3388A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69502181 | ||||||
| chr2:69502618
|
T | C | 2 | a0002c0002t0131g0211a0002c0002t0132g0236 | 2 | NA18963.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.2269+2951A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69502618 | ||||||
| chr2:69503018
|
G | A | 2 | a0002c0005t0018g0103a0002c0005t0018g0104 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2269+2551C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69503018 | ||||||
| chr2:69503535
|
T | C | 4 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(1): Show | 4 | HG01243.hp1 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2269+2034A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69503535 | ||||||
| chr2:69503734
|
TG | T | 3 | a0001c0011t0029g0293a0001c0011t0029g0294a0001c0011t0079g0290 | 3 | HG02486.hp1 HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2269+1834delC | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69503734 | ||||||
| chr2:69503790
|
G | C | 1 | a0002c0002t0005g0248 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2269+1779C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69503790 | ||||||
| chr2:69503810
|
C | T | 60 | a0001c0003t0012g0088a0001c0003t0012g0091a0001c0003t0012g0095others(57): Show | 60 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2269+1759G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69503810 | ||||||
| chr2:69503824
|
T | A | 1 | a0002c0002t0019g0115 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2269+1745A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69503824 | ||||||
| chr2:69503953
|
C | T | 4 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(1): Show | 4 | HG01243.hp1 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2269+1616G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69503953 | ||||||
| chr2:69503998
|
T | TA | 97 | a0001c0001t0088g0146a0002c0002t0001g0019a0002c0002t0001g0025others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.2269+1570dupT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69503998 | ||||||
| chr2:69503998
|
TA | T | 88 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(85): Show | 88 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.2269+1570delT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69503998 | ||||||
| chr2:69504277
|
G | C | 1 | a0002c0002t0019g0115 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2269+1292C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69504277 | ||||||
| chr2:69504351
|
CTG | C | 4 | a0001c0001t0004g0264a0001c0001t0004g0265a0001c0001t0004g0266others(1): Show | 4 | HG02083.hp1 NA18954.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.2269+1216_2269+121 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69504351 | ||||||
| chr2:69504397
|
C | CA | 15 | a0001c0001t0002g0157a0001c0001t0007g0027a0001c0001t0007g0049others(12): Show | 15 | HG02056.hp1 HG02135.hp1 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.2269+1171dupT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69504397 | ||||||
| chr2:69504397
|
C | CAA | 9 | a0001c0001t0105g0108a0001c0007t0021g0276a0001c0007t0021g0279others(6): Show | 9 | HG02280.hp2 HG02809.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.2269+1170_2269+117 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69504397 | ||||||
| chr2:69504397
|
CA | C | 156 | a0001c0001t0002g0120a0001c0001t0014g0059a0001c0001t0014g0060others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.2269+1171delT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69504397 | ||||||
| chr2:69504397
|
CAA | C | 54 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(51): Show | 54 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.2269+1170_2269+117 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69504397 | ||||||
| chr2:69504429
|
T | C | 1 | a0001c0026t0152g0295 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2269+1140A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69504429 | ||||||
| chr2:69504434
|
G | A | 1 | a0001c0001t0140g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2269+1135C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69504434 | ||||||
| chr2:69504711
|
G | C | 1 | a0001c0001t0063g0288 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2269+858C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69504711 | ||||||
| chr2:69504929
|
A | G | 1 | a0001c0006t0016g0061 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2269+640T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69504929 | ||||||
| chr2:69505122
|
T | C | 96 | a0002c0002t0001g0019a0002c0002t0001g0025a0002c0002t0001g0028others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.2269+447A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69505122 | ||||||
| chr2:69505124
|
C | T | 1 | a0003c0020t0084g0105 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2269+445G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69505124 | ||||||
| chr2:69505127
|
A | G | 50 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(47): Show | 50 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(47): Show |
intron_variant | MODIFIER | c.2269+442T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69505127 | ||||||
| chr2:69505129
|
A | G | 1 | a0001c0001t0004g0221 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2269+440T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69505129 | ||||||
| chr2:69505131
|
ACACC | A | 3 | a0001c0001t0063g0288a0001c0009t0125g0179a0001c0009t0141g0191 | 3 | HG02280.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2269+434_2269+437d others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69505131 | ||||||
| chr2:69505133
|
ACC | A | 61 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(58): Show | 61 | HG00544.hp1 HG00597.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.2269+434_2269+435d others(4): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69505133 | ||||||
| chr2:69505135
|
C | A | 7 | a0001c0001t0006g0225a0001c0001t0014g0059a0001c0001t0014g0060others(4): Show | 7 | HG01243.hp1 HG01952.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2269+434G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69505135 | ||||||
| chr2:69505135
|
CCA | C | 148 | a0001c0003t0012g0088a0001c0003t0012g0091a0001c0003t0012g0095others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.2269+432_2269+433d others(4): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69505135 | ||||||
| chr2:69505135
|
CCACA | C | 7 | a0001c0003t0082g0098a0001c0003t0108g0138a0001c0003t0109g0166others(4): Show | 7 | HG01928.hp2 HG02109.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.2269+430_2269+433d others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69505135 | ||||||
| chr2:69505394
|
T | C | 1 | a0001c0001t0056g0058 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2269+175A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69505394 | ||||||
| chr2:69505532
|
C | G | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2269+37G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 16/21 | chr2 | 69505532 | ||||||
| chr2:69505719
|
G | A | 1 | a0002c0002t0005g0229 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2165-46C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 15/21 | chr2 | 69505719 | ||||||
| chr2:69505776
|
A | T | 1 | a0001c0001t0119g0181 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2165-103T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 15/21 | chr2 | 69505776 | ||||||
| chr2:69506164
|
G | A | 1 | a0002c0024t0060g0031 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2165-491C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 15/21 | chr2 | 69506164 | ||||||
| chr2:69506354
|
G | C | 4 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(1): Show | 4 | HG01243.hp1 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2165-681C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 15/21 | chr2 | 69506354 | ||||||
| chr2:69506640
|
G | A | 1 | a0001c0001t0078g0055 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2164+781C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 15/21 | chr2 | 69506640 | ||||||
| chr2:69506776
|
T | A | 4 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(1): Show | 4 | HG01243.hp1 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2164+645A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 15/21 | chr2 | 69506776 | ||||||
| chr2:69506868
|
C | CTG | 9 | a0001c0001t0002g0125a0001c0001t0007g0081a0001c0001t0113g0178others(6): Show | 9 | HG01255.hp1 HG01433.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.2164+551_2164+552d others(4): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 15/21 | chr2 | 69506868 | ||||||
| chr2:69506868
|
C | CTGTG | 6 | a0001c0004t0017g0075a0001c0006t0016g0017a0001c0006t0016g0061others(3): Show | 6 | HG00735.hp2 HG01928.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2164+549_2164+552d others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 15/21 | chr2 | 69506868 | ||||||
| chr2:69506868
|
C | CTGTGTG | 109 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(106): Show | 109 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.2164+547_2164+552d others(8): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 15/21 | chr2 | 69506868 | ||||||
| chr2:69506868
|
C | CTGTGTGT others(1): Show |
17 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0037g0009others(14): Show | 17 | HG00323.hp1 HG01074.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2164+545_2164+552d others(10): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 15/21 | chr2 | 69506868 | ||||||
| chr2:69506868
|
C | CTGTGTGT others(3): Show |
4 | a0001c0001t0014g0066a0001c0001t0077g0072a0001c0001t0144g0232others(1): Show | 4 | HG02572.hp2 HG03139.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.2164+543_2164+552d others(12): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 15/21 | chr2 | 69506868 | ||||||
| chr2:69506868
|
C | CTGTGTGT others(5): Show |
1 | a0001c0001t0124g0188 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2164+541_2164+552d others(14): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 15/21 | chr2 | 69506868 | ||||||
| chr2:69506868
|
CTGTG | C | 87 | a0002c0002t0001g0019a0002c0002t0001g0025a0002c0002t0001g0028others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.2164+549_2164+552d others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 15/21 | chr2 | 69506868 | ||||||
| chr2:69506928
|
C | T | 7 | a0001c0001t0037g0009a0001c0001t0045g0287a0001c0001t0077g0072others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2164+493G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 15/21 | chr2 | 69506928 | ||||||
| chr2:69507112
|
C | A | 1 | a0001c0004t0017g0073 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2164+309G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 15/21 | chr2 | 69507112 | ||||||
| chr2:69507340
|
C | T | 1 | a0001c0001t0008g0022 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2164+81G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 15/21 | chr2 | 69507340 | ||||||
| chr2:69507613
|
T | C | 1 | a0001c0026t0152g0295 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2007-35A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 14/21 | chr2 | 69507613 | ||||||
| chr2:69507663
|
A | G | 2 | a0004c0012t0036g0283a0004c0012t0061g0067 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2007-85T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 14/21 | chr2 | 69507663 | ||||||
| chr2:69507707
|
A | AT | 9 | a0001c0001t0007g0086a0002c0005t0040g0006a0002c0005t0122g0182others(6): Show | 9 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2007-130dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 14/21 | chr2 | 69507707 | ||||||
| chr2:69507707
|
AT | A | 19 | a0001c0001t0037g0009a0001c0001t0077g0072a0001c0001t0105g0108others(16): Show | 19 | HG00735.hp2 HG02109.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.2007-130delA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 14/21 | chr2 | 69507707 | ||||||
| chr2:69507793
|
G | A | 1 | a0002c0002t0047g0053 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2007-215C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 14/21 | chr2 | 69507793 | ||||||
| chr2:69507806
|
A | C | 1 | a0001c0001t0113g0178 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2007-228T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 14/21 | chr2 | 69507806 | ||||||
| chr2:69507986
|
C | T | 54 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(51): Show | 54 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.2007-408G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 14/21 | chr2 | 69507986 | ||||||
| chr2:69508021
|
A | G | 1 | a0001c0001t0002g0152 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2007-443T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 14/21 | chr2 | 69508021 | ||||||
| chr2:69508097
|
T | C | 4 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(1): Show | 4 | HG01243.hp1 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2007-519A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 14/21 | chr2 | 69508097 | ||||||
| chr2:69508549
|
A | G | 1 | a0003c0020t0084g0105 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2006+682T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 14/21 | chr2 | 69508549 | ||||||
| chr2:69508611
|
C | A | 88 | a0002c0002t0001g0019a0002c0002t0001g0025a0002c0002t0001g0028others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.2006+620G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 14/21 | chr2 | 69508611 | ||||||
| chr2:69508620
|
G | A | 88 | a0002c0002t0001g0019a0002c0002t0001g0025a0002c0002t0001g0028others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.2006+611C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 14/21 | chr2 | 69508620 | ||||||
| chr2:69508804
|
A | G | 2 | a0004c0012t0036g0283a0004c0012t0061g0067 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2006+427T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 14/21 | chr2 | 69508804 | ||||||
| chr2:69508914
|
C | T | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2006+317G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 14/21 | chr2 | 69508914 | ||||||
| chr2:69509655
|
T | A | 3 | a0001c0001t0020g0202a0001c0001t0020g0208a0001c0001t0138g0209 | 3 | NA18956.hp1 NA18963.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.1777-195A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69509655 | ||||||
| chr2:69509841
|
T | C | 5 | a0002c0005t0018g0064a0002c0005t0018g0103a0002c0005t0018g0104others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1777-381A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69509841 | ||||||
| chr2:69509922
|
A | G | 1 | a0001c0001t0006g0222 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1777-462T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69509922 | ||||||
| chr2:69510034
|
G | A | 1 | a0001c0001t0105g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1777-574C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69510034 | ||||||
| chr2:69510071
|
T | C | 1 | a0001c0001t0009g0124 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1777-611A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69510071 | ||||||
| chr2:69510247
|
C | T | 102 | a0002c0002t0001g0019a0002c0002t0001g0025a0002c0002t0001g0028others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.1777-787G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69510247 | ||||||
| chr2:69510816
|
G | A | 88 | a0002c0002t0001g0019a0002c0002t0001g0025a0002c0002t0001g0028others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1777-1356C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69510816 | ||||||
| chr2:69510842
|
G | T | 1 | a0001c0001t0087g0135 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1777-1382C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69510842 | ||||||
| chr2:69510961
|
C | T | 88 | a0002c0002t0001g0019a0002c0002t0001g0025a0002c0002t0001g0028others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1777-1501G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69510961 | ||||||
| chr2:69511380
|
A | T | 1 | a0001c0001t0078g0055 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1777-1920T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69511380 | ||||||
| chr2:69511479
|
C | T | 1 | a0001c0001t0021g0278 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1777-2019G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69511479 | ||||||
| chr2:69511498
|
T | C | 1 | a0001c0001t0121g0186 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1777-2038A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69511498 | ||||||
| chr2:69511641
|
T | C | 2 | a0004c0012t0036g0283a0004c0012t0061g0067 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1777-2181A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69511641 | ||||||
| chr2:69511658
|
T | C | 107 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(104): Show | 107 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.1777-2198A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69511658 | ||||||
| chr2:69511857
|
A | G | 4 | a0001c0006t0028g0126a0001c0006t0028g0134a0001c0006t0041g0008others(1): Show | 4 | HG01884.hp2 HG02818.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1777-2397T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69511857 | ||||||
| chr2:69511900
|
A | G | 5 | a0002c0005t0018g0064a0002c0005t0018g0103a0002c0005t0018g0104others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1777-2440T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69511900 | ||||||
| chr2:69511988
|
G | C | 1 | a0001c0004t0017g0073 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1776+2483C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69511988 | ||||||
| chr2:69512033
|
A | G | 58 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(55): Show | 58 | HG00544.hp1 HG00597.hp2 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.1776+2438T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69512033 | ||||||
| chr2:69512039
|
A | T | 1 | a0001c0003t0026g0015 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1776+2432T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69512039 | ||||||
| chr2:69512287
|
A | G | 8 | a0002c0005t0040g0006a0002c0005t0122g0182a0002c0005t0123g0183others(5): Show | 8 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1776+2184T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69512287 | ||||||
| chr2:69512543
|
C | T | 104 | a0002c0002t0001g0019a0002c0002t0001g0025a0002c0002t0001g0028others(101): Show | 104 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1776+1928G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69512543 | ||||||
| chr2:69512582
|
C | T | 41 | a0001c0003t0012g0088a0001c0003t0012g0091a0001c0003t0012g0095others(38): Show | 41 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1776+1889G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69512582 | ||||||
| chr2:69512596
|
T | C | 1 | a0001c0001t0056g0058 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1776+1875A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69512596 | ||||||
| chr2:69512610
|
AG | A | 88 | a0002c0002t0001g0019a0002c0002t0001g0025a0002c0002t0001g0028others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1776+1860delC | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69512610 | ||||||
| chr2:69512690
|
C | T | 1 | a0001c0001t0124g0188 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1776+1781G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69512690 | ||||||
| chr2:69512725
|
A | G | 1 | a0001c0004t0017g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1776+1746T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69512725 | ||||||
| chr2:69512805
|
C | T | 2 | a0001c0004t0070g0071a0001c0008t0097g0131 | 2 | HG00099.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1776+1666G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69512805 | ||||||
| chr2:69512959
|
C | T | 211 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1776+1512G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69512959 | ||||||
| chr2:69513095
|
G | C | 104 | a0002c0002t0001g0019a0002c0002t0001g0025a0002c0002t0001g0028others(101): Show | 104 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1776+1376C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69513095 | ||||||
| chr2:69513147
|
T | G | 102 | a0002c0002t0001g0019a0002c0002t0001g0025a0002c0002t0001g0028others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.1776+1324A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69513147 | ||||||
| chr2:69513191
|
A | G | 1 | a0003c0020t0084g0105 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1776+1280T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69513191 | ||||||
| chr2:69513234
|
C | T | 8 | a0002c0005t0040g0006a0002c0005t0122g0182a0002c0005t0123g0183others(5): Show | 8 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1776+1237G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69513234 | ||||||
| chr2:69513260
|
T | C | 1 | a0002c0002t0001g0057 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1776+1211A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69513260 | ||||||
| chr2:69513279
|
T | C | 8 | a0002c0005t0040g0006a0002c0005t0122g0182a0002c0005t0123g0183others(5): Show | 8 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1776+1192A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69513279 | ||||||
| chr2:69513477
|
G | A | 1 | a0004c0013t0107g0107 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1776+994C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69513477 | ||||||
| chr2:69513516
|
G | A | 9 | a0001c0001t0105g0108a0001c0007t0021g0276a0001c0007t0021g0279others(6): Show | 9 | HG02280.hp2 HG02809.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1776+955C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69513516 | ||||||
| chr2:69513575
|
G | A | 2 | a0004c0012t0036g0283a0004c0012t0061g0067 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1776+896C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69513575 | ||||||
| chr2:69513633
|
C | T | 104 | a0002c0002t0001g0019a0002c0002t0001g0025a0002c0002t0001g0028others(101): Show | 104 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1776+838G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69513633 | ||||||
| chr2:69513845
|
C | T | 1 | a0004c0012t0036g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1776+626G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69513845 | ||||||
| chr2:69514072
|
A | C | 1 | a0002c0002t0054g0030 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1776+399T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69514072 | ||||||
| chr2:69514144
|
C | T | 1 | a0002c0002t0003g0251 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1776+327G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69514144 | ||||||
| chr2:69514334
|
G | A | 2 | a0001c0001t0078g0055a0004c0013t0107g0107 | 2 | HG01167.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1776+137C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 13/21 | chr2 | 69514334 | ||||||
| chr2:69514935
|
T | A | 102 | a0002c0002t0001g0019a0002c0002t0001g0025a0002c0002t0001g0028others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.1498-186A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69514935 | ||||||
| chr2:69514958
|
C | A | 8 | a0002c0002t0003g0227a0002c0002t0003g0244a0002c0002t0003g0245others(5): Show | 8 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.1498-209G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69514958 | ||||||
| chr2:69515150
|
T | C | 1 | a0002c0002t0059g0032 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1498-401A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69515150 | ||||||
| chr2:69515352
|
T | C | 228 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(225): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1498-603A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69515352 | ||||||
| chr2:69515436
|
C | T | 9 | a0001c0001t0105g0108a0001c0007t0021g0276a0001c0007t0021g0279others(6): Show | 9 | HG02280.hp2 HG02809.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1498-687G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69515436 | ||||||
| chr2:69515457
|
C | G | 4 | a0002c0005t0040g0006a0002c0005t0122g0182a0002c0005t0123g0183others(1): Show | 4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1498-708G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69515457 | ||||||
| chr2:69515541
|
G | A | 1 | a0001c0001t0073g0052 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1498-792C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69515541 | ||||||
| chr2:69515580
|
C | T | 1 | a0004c0013t0107g0107 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1498-831G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69515580 | ||||||
| chr2:69515592
|
A | G | 249 | a0001c0001t0002g0114a0001c0001t0002g0120a0001c0001t0004g0206others(246): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1498-843T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69515592 | ||||||
| chr2:69515729
|
C | T | 1 | a0001c0001t0007g0081 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1498-980G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69515729 | ||||||
| chr2:69515739
|
T | C | 1 | a0001c0004t0014g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1498-990A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69515739 | ||||||
| chr2:69515750
|
G | A | 9 | a0001c0001t0105g0108a0001c0007t0021g0276a0001c0007t0021g0279others(6): Show | 9 | HG02280.hp2 HG02809.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1498-1001C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69515750 | ||||||
| chr2:69515792
|
T | C | 56 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(53): Show | 56 | HG00544.hp1 HG00597.hp2 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.1498-1043A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69515792 | ||||||
| chr2:69515838
|
C | CA | 14 | a0002c0005t0018g0064a0002c0005t0018g0103a0002c0005t0018g0104others(11): Show | 14 | HG01891.hp2 HG01928.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1498-1090dupT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69515838 | ||||||
| chr2:69515838
|
CA | C | 91 | a0001c0004t0067g0077a0001c0026t0152g0295a0002c0002t0001g0019others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1498-1090delT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69515838 | ||||||
| chr2:69515857
|
C | A | 42 | a0001c0003t0012g0088a0001c0003t0012g0091a0001c0003t0012g0095others(39): Show | 42 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1498-1108G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69515857 | ||||||
| chr2:69515939
|
T | C | 1 | a0001c0004t0153g0296 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1498-1190A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69515939 | ||||||
| chr2:69516134
|
T | A | 228 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(225): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1498-1385A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69516134 | ||||||
| chr2:69516153
|
T | C | 1 | a0001c0004t0067g0077 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1498-1404A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69516153 | ||||||
| chr2:69516262
|
C | T | 5 | a0001c0001t0008g0082a0001c0001t0009g0124a0001c0001t0009g0129others(2): Show | 5 | HG02056.hp1 HG02135.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.1498-1513G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69516262 | ||||||
| chr2:69516314
|
G | GA | 11 | a0001c0006t0016g0017a0001c0006t0016g0061a0001c0006t0016g0289others(8): Show | 11 | HG00735.hp2 HG01884.hp2 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.1498-1566dupT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69516314 | ||||||
| chr2:69516314
|
GA | G | 6 | a0002c0005t0018g0064a0002c0005t0018g0103a0002c0005t0018g0104others(3): Show | 6 | HG02559.hp2 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1498-1566delT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69516314 | ||||||
| chr2:69516328
|
C | A | 1 | a0001c0006t0016g0061 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1498-1579G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69516328 | ||||||
| chr2:69516390
|
T | C | 3 | a0002c0002t0015g0003a0002c0002t0049g0047a0002c0024t0060g0031 | 3 | HG00323.hp2 HG02145.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1498-1641A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69516390 | ||||||
| chr2:69516446
|
G | C | 1 | a0001c0001t0104g0292 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1498-1697C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69516446 | ||||||
| chr2:69517001
|
T | C | 1 | a0001c0001t0024g0090 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1497+1953A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69517001 | ||||||
| chr2:69517096
|
T | C | 61 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(58): Show | 61 | HG00544.hp1 HG00597.hp2 HG01243.hp1 others(58): Show |
intron_variant | MODIFIER | c.1497+1858A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69517096 | ||||||
| chr2:69517449
|
C | T | 1 | a0001c0003t0012g0088 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1497+1505G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69517449 | ||||||
| chr2:69517495
|
C | T | 3 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066 | 3 | HG01243.hp1 NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1497+1459G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69517495 | ||||||
| chr2:69517525
|
G | GCTCCCTG others(317): Show |
2 | a0001c0008t0069g0102a0005c0010t0010g0142 | 2 | HG01952.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1497+1428_1497+142 others(328): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69517525 | ||||||
| chr2:69517525
|
G | GCTCCCTG others(318): Show |
1 | a0005c0010t0010g0153 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1497+1428_1497+142 others(329): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69517525 | ||||||
| chr2:69517525
|
G | GCTCCCTG others(319): Show |
1 | a0005c0010t0010g0123 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1497+1428_1497+142 others(330): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69517525 | ||||||
| chr2:69517525
|
G | GCTCCCTG others(327): Show |
1 | a0001c0001t0088g0146 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1497+1428_1497+142 others(338): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69517525 | ||||||
| chr2:69517668
|
C | T | 219 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1497+1286G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69517668 | ||||||
| chr2:69517882
|
T | G | 1 | a0001c0001t0078g0055 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1497+1072A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69517882 | ||||||
| chr2:69517963
|
C | T | 2 | a0002c0002t0001g0029a0002c0002t0001g0034 | 2 | HG00544.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.1497+991G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69517963 | ||||||
| chr2:69518000
|
T | C | 1 | a0002c0005t0100g0116 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1497+954A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69518000 | ||||||
| chr2:69518031
|
A | G | 2 | a0004c0013t0043g0284a0004c0013t0107g0107 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1497+923T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69518031 | ||||||
| chr2:69518105
|
G | C | 1 | a0001c0003t0106g0141 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1497+849C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69518105 | ||||||
| chr2:69518136
|
T | C | 1 | a0001c0001t0113g0178 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1497+818A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69518136 | ||||||
| chr2:69518177
|
T | C | 2 | a0003c0014t0025g0285a0003c0014t0025g0286 | 2 | HG01891.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1497+777A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69518177 | ||||||
| chr2:69518213
|
T | C | 104 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(101): Show | 104 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.1497+741A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69518213 | ||||||
| chr2:69518258
|
C | T | 3 | a0001c0001t0002g0149a0001c0001t0002g0154a0001c0001t0034g0267 | 3 | NA18967.hp2 NA19063.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1497+696G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69518258 | ||||||
| chr2:69518278
|
A | G | 1 | a0001c0001t0113g0178 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1497+676T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69518278 | ||||||
| chr2:69518357
|
G | A | 1 | a0001c0001t0113g0178 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1497+597C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69518357 | ||||||
| chr2:69518383
|
A | G | 1 | a0002c0002t0145g0275 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1497+571T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69518383 | ||||||
| chr2:69518419
|
T | TG | 48 | a0001c0001t0002g0130a0001c0001t0004g0261a0001c0001t0008g0084others(45): Show | 48 | HG00099.hp2 HG00323.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.1497+534_1497+535i others(3): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69518419 | ||||||
| chr2:69518420
|
T | G | 244 | a0001c0001t0002g0114a0001c0001t0002g0120a0001c0001t0002g0125others(241): Show | 244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.1497+534A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69518420 | ||||||
| chr2:69518427
|
T | G | 4 | a0003c0014t0025g0285a0003c0014t0025g0286a0003c0020t0084g0105others(1): Show | 4 | HG01433.hp1 HG01891.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.1497+527A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69518427 | ||||||
| chr2:69518449
|
T | C | 101 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(98): Show | 101 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.1497+505A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69518449 | ||||||
| chr2:69518481
|
A | G | 223 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.1497+473T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69518481 | ||||||
| chr2:69518659
|
C | A | 4 | a0002c0005t0040g0006a0002c0005t0122g0182a0002c0005t0123g0183others(1): Show | 4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1497+295G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 12/21 | chr2 | 69518659 | ||||||
| chr2:69519358
|
T | C | 1 | a0002c0002t0019g0159 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1211-118A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 11/21 | chr2 | 69519358 | ||||||
| chr2:69519389
|
T | A | 1 | a0002c0002t0015g0002 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1211-149A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 11/21 | chr2 | 69519389 | ||||||
| chr2:69519620
|
C | T | 2 | a0004c0013t0043g0284a0004c0013t0107g0107 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1211-380G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 11/21 | chr2 | 69519620 | ||||||
| chr2:69519669
|
A | G | 1 | a0002c0002t0003g0227 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1211-429T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 11/21 | chr2 | 69519669 | ||||||
| chr2:69519710
|
C | T | 2 | a0004c0013t0043g0284a0004c0013t0107g0107 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1211-470G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 11/21 | chr2 | 69519710 | ||||||
| chr2:69519783
|
G | A | 1 | a0004c0013t0043g0284 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1211-543C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 11/21 | chr2 | 69519783 | ||||||
| chr2:69520001
|
C | T | 2 | a0003c0014t0025g0285a0003c0014t0025g0286 | 2 | HG01891.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1211-761G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 11/21 | chr2 | 69520001 | ||||||
| chr2:69520162
|
C | G | 1 | a0001c0001t0126g0219 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1210+672G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 11/21 | chr2 | 69520162 | ||||||
| chr2:69520207
|
T | C | 1 | a0001c0001t0063g0288 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1210+627A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 11/21 | chr2 | 69520207 | ||||||
| chr2:69520237
|
A | T | 1 | a0001c0001t0063g0288 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1210+597T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 11/21 | chr2 | 69520237 | ||||||
| chr2:69520358
|
C | CT | 54 | a0001c0001t0004g0261a0001c0001t0008g0084a0001c0001t0009g0160others(51): Show | 54 | HG00099.hp2 HG00323.hp1 HG01175.hp2 others(51): Show |
intron_variant | MODIFIER | c.1210+475dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 11/21 | chr2 | 69520358 | ||||||
| chr2:69520358
|
C | CTT | 9 | a0001c0001t0078g0055a0001c0003t0012g0096a0001c0003t0022g0010others(6): Show | 9 | HG01167.hp1 HG03041.hp2 HG03540.hp2 others(6): Show |
intron_variant | MODIFIER | c.1210+474_1210+475d others(4): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 11/21 | chr2 | 69520358 | ||||||
| chr2:69520478
|
C | G | 2 | a0004c0013t0043g0284a0004c0013t0107g0107 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1210+356G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 11/21 | chr2 | 69520478 | ||||||
| chr2:69520522
|
C | T | 2 | a0001c0001t0045g0287a0001c0001t0124g0188 | 2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1210+312G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 11/21 | chr2 | 69520522 | ||||||
| chr2:69520627
|
A | G | 3 | a0004c0012t0036g0283a0004c0012t0061g0067a0005c0010t0010g0153 | 3 | HG01106.hp1 HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1210+207T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 11/21 | chr2 | 69520627 | ||||||
| chr2:69520685
|
G | C | 220 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.1210+149C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 11/21 | chr2 | 69520685 | ||||||
| chr2:69520685
|
G | T | 1 | a0001c0001t0004g0264 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1210+149C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 11/21 | chr2 | 69520685 | ||||||
| chr2:69520789
|
A | G | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1210+45T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 11/21 | chr2 | 69520789 | ||||||
| chr2:69521007
|
A | G | 1 | a0003c0020t0084g0105 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1056-19T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69521007 | ||||||
| chr2:69521256
|
A | T | 3 | a0001c0001t0002g0149a0001c0001t0002g0154a0001c0001t0034g0267 | 3 | NA18967.hp2 NA19063.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1056-268T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69521256 | ||||||
| chr2:69521280
|
A | G | 1 | a0004c0013t0043g0284 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1056-292T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69521280 | ||||||
| chr2:69521328
|
C | T | 1 | a0001c0001t0073g0052 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1056-340G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69521328 | ||||||
| chr2:69521455
|
C | G | 2 | a0004c0013t0043g0284a0004c0013t0107g0107 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1056-467G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69521455 | ||||||
| chr2:69521497
|
C | A | 4 | a0003c0014t0025g0285a0003c0014t0025g0286a0003c0020t0084g0105others(1): Show | 4 | HG01433.hp1 HG01891.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.1056-509G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69521497 | ||||||
| chr2:69521799
|
T | C | 2 | a0004c0013t0043g0284a0004c0013t0107g0107 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1056-811A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69521799 | ||||||
| chr2:69521843
|
C | A | 1 | a0002c0002t0053g0056 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1056-855G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69521843 | ||||||
| chr2:69521915
|
A | G | 2 | a0001c0001t0074g0048a0001c0008t0135g0262 | 2 | HG02040.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1056-927T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69521915 | ||||||
| chr2:69521996
|
C | T | 5 | a0001c0001t0037g0009a0001c0001t0045g0287a0001c0001t0077g0072others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1056-1008G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69521996 | ||||||
| chr2:69522131
|
G | C | 2 | a0004c0013t0043g0284a0004c0013t0107g0107 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1056-1143C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69522131 | ||||||
| chr2:69522142
|
C | A | 1 | a0001c0001t0045g0287 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1056-1154G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69522142 | ||||||
| chr2:69522168
|
G | A | 2 | a0002c0002t0049g0047a0002c0024t0060g0031 | 2 | HG00323.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1056-1180C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69522168 | ||||||
| chr2:69522204
|
G | T | 3 | a0001c0004t0017g0073a0001c0004t0017g0075a0001c0004t0067g0077 | 3 | HG03041.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1056-1216C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69522204 | ||||||
| chr2:69522367
|
C | T | 1 | a0003c0020t0084g0105 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1056-1379G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69522367 | ||||||
| chr2:69522443
|
A | G | 1 | a0003c0014t0025g0286 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1056-1455T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69522443 | ||||||
| chr2:69522461
|
G | A | 1 | a0001c0001t0004g0261 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1056-1473C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69522461 | ||||||
| chr2:69522629
|
C | T | 2 | a0002c0002t0131g0211a0002c0002t0132g0236 | 2 | NA18963.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1056-1641G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69522629 | ||||||
| chr2:69522638
|
T | G | 2 | a0001c0001t0011g0194a0001c0001t0011g0196 | 2 | NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1056-1650A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69522638 | ||||||
| chr2:69522660
|
C | T | 1 | a0001c0001t0101g0118 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1056-1672G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69522660 | ||||||
| chr2:69522674
|
C | T | 3 | a0003c0014t0025g0285a0003c0014t0025g0286a0003c0021t0151g0282 | 3 | HG01891.hp2 HG01928.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1056-1686G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69522674 | ||||||
| chr2:69522773
|
C | T | 1 | a0001c0026t0152g0295 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1056-1785G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69522773 | ||||||
| chr2:69522803
|
C | CA | 50 | a0001c0001t0002g0155a0001c0001t0014g0059a0001c0001t0014g0060others(47): Show | 50 | HG00099.hp2 HG00323.hp1 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.1056-1816dupT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69522803 | ||||||
| chr2:69522855
|
C | T | 1 | a0002c0002t0005g0229 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1056-1867G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69522855 | ||||||
| chr2:69522859
|
C | T | 2 | a0004c0013t0043g0284a0004c0013t0107g0107 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1056-1871G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69522859 | ||||||
| chr2:69522893
|
T | G | 4 | a0002c0005t0018g0064a0002c0005t0018g0103a0002c0005t0018g0104others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1056-1905A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69522893 | ||||||
| chr2:69522955
|
C | T | 8 | a0003c0014t0025g0285a0003c0014t0025g0286a0003c0020t0084g0105others(5): Show | 8 | HG01433.hp1 HG01891.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.1056-1967G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69522955 | ||||||
| chr2:69522981
|
C | T | 144 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.1056-1993G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69522981 | ||||||
| chr2:69522995
|
G | C | 2 | a0001c0001t0057g0291a0001c0001t0117g0189 | 2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1056-2007C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69522995 | ||||||
| chr2:69522998
|
T | C | 4 | a0003c0014t0025g0285a0003c0014t0025g0286a0003c0020t0084g0105others(1): Show | 4 | HG01433.hp1 HG01891.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.1056-2010A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69522998 | ||||||
| chr2:69523223
|
G | C | 49 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(46): Show | 49 | HG00099.hp2 HG00323.hp1 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.1055+1810C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69523223 | ||||||
| chr2:69523316
|
T | C | 2 | a0004c0013t0043g0284a0004c0013t0107g0107 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1055+1717A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69523316 | ||||||
| chr2:69523400
|
CTTTAGAG others(3): Show |
C | 1 | a0001c0001t0124g0188 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1055+1623_1055+163 others(14): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69523400 | ||||||
| chr2:69523412
|
A | C | 1 | a0001c0001t0124g0188 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1055+1621T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69523412 | ||||||
| chr2:69523414
|
CTAAAATA others(3): Show |
C | 1 | a0001c0001t0124g0188 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1055+1609_1055+161 others(14): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69523414 | ||||||
| chr2:69523425
|
T | C | 1 | a0001c0001t0124g0188 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1055+1608A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69523425 | ||||||
| chr2:69523647
|
G | A | 3 | a0001c0001t0045g0287a0004c0013t0043g0284a0004c0013t0107g0107 | 3 | HG02109.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1055+1386C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69523647 | ||||||
| chr2:69523743
|
T | C | 4 | a0003c0014t0025g0285a0003c0014t0025g0286a0003c0020t0084g0105others(1): Show | 4 | HG01433.hp1 HG01891.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.1055+1290A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69523743 | ||||||
| chr2:69524012
|
A | G | 1 | a0001c0001t0014g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1055+1021T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69524012 | ||||||
| chr2:69524019
|
T | A | 52 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(49): Show | 52 | HG00099.hp2 HG00323.hp1 HG01167.hp1 others(49): Show |
intron_variant | MODIFIER | c.1055+1014A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69524019 | ||||||
| chr2:69524071
|
C | T | 219 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1055+962G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69524071 | ||||||
| chr2:69524255
|
T | A | 2 | a0004c0012t0036g0283a0004c0012t0061g0067 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1055+778A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69524255 | ||||||
| chr2:69524366
|
C | T | 1 | a0001c0001t0078g0055 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1055+667G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69524366 | ||||||
| chr2:69524412
|
T | TTTTTG | 5 | a0001c0001t0002g0132a0001c0001t0045g0287a0001c0008t0098g0140others(2): Show | 5 | HG00438.hp2 HG00558.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1055+616_1055+620d others(7): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69524412 | ||||||
| chr2:69524412
|
T | TTTTTGTT others(8): Show |
1 | a0001c0001t0073g0052 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1055+606_1055+620d others(17): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69524412 | ||||||
| chr2:69524412
|
TTTTTG | T | 209 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(206): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1055+616_1055+620d others(7): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69524412 | ||||||
| chr2:69524412
|
TTTTTGTT others(3): Show |
T | 3 | a0001c0003t0108g0138a0004c0012t0036g0283a0004c0012t0061g0067 | 3 | HG02109.hp2 HG03471.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1055+611_1055+620d others(12): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69524412 | ||||||
| chr2:69524617
|
T | TAG | 297 | a0001c0001t0002g0114a0001c0001t0002g0120a0001c0001t0002g0125others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.1055+414_1055+415d others(4): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69524617 | ||||||
| chr2:69524652
|
T | C | 2 | a0001c0001t0105g0108a0001c0026t0152g0295 | 2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1055+381A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69524652 | ||||||
| chr2:69524675
|
T | C | 52 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(49): Show | 52 | HG00099.hp2 HG00323.hp1 HG01167.hp1 others(49): Show |
intron_variant | MODIFIER | c.1055+358A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69524675 | ||||||
| chr2:69524713
|
G | T | 3 | a0001c0001t0045g0287a0004c0013t0043g0284a0004c0013t0107g0107 | 3 | HG02109.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1055+320C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69524713 | ||||||
| chr2:69524724
|
C | T | 4 | a0001c0001t0037g0009a0001c0001t0077g0072a0001c0001t0078g0055others(1): Show | 4 | HG01167.hp1 HG02280.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1055+309G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69524724 | ||||||
| chr2:69524863
|
CTT | C | 3 | a0001c0001t0045g0287a0004c0013t0043g0284a0004c0013t0107g0107 | 3 | HG02109.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1055+168_1055+169d others(4): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 10/21 | chr2 | 69524863 | ||||||
| chr2:69525319
|
T | C | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.976-207A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 9/21 | chr2 | 69525319 | ||||||
| chr2:69525522
|
C | T | 6 | a0003c0014t0025g0285a0003c0014t0025g0286a0003c0020t0084g0105others(3): Show | 6 | HG01433.hp1 HG01891.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.976-410G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 9/21 | chr2 | 69525522 | ||||||
| chr2:69525677
|
C | G | 3 | a0001c0001t0009g0160a0001c0001t0096g0162a0001c0001t0099g0161 | 3 | HG02976.hp1 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.976-565G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 9/21 | chr2 | 69525677 | ||||||
| chr2:69525709
|
T | A | 1 | a0002c0002t0015g0005 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.976-597A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 9/21 | chr2 | 69525709 | ||||||
| chr2:69525751
|
G | A | 1 | a0003c0020t0084g0105 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.976-639C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 9/21 | chr2 | 69525751 | ||||||
| chr2:69526032
|
A | G | 1 | a0001c0007t0035g0271 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.976-920T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 9/21 | chr2 | 69526032 | ||||||
| chr2:69526033
|
C | T | 1 | a0001c0001t0078g0055 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.976-921G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 9/21 | chr2 | 69526033 | ||||||
| chr2:69526099
|
T | C | 1 | a0002c0002t0008g0050 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.976-987A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 9/21 | chr2 | 69526099 | ||||||
| chr2:69526109
|
G | A | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.976-997C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 9/21 | chr2 | 69526109 | ||||||
| chr2:69526162
|
G | A | 1 | a0002c0002t0007g0068 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.976-1050C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 9/21 | chr2 | 69526162 | ||||||
| chr2:69526191
|
C | T | 3 | a0001c0001t0045g0287a0004c0013t0043g0284a0004c0013t0107g0107 | 3 | HG02109.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.975+1025G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 9/21 | chr2 | 69526191 | ||||||
| chr2:69526343
|
A | G | 1 | a0001c0011t0029g0293 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.975+873T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 9/21 | chr2 | 69526343 | ||||||
| chr2:69527042
|
T | C | 4 | a0001c0001t0020g0193a0001c0001t0020g0202a0001c0001t0020g0208others(1): Show | 4 | NA18956.hp1 NA18963.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.975+174A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 9/21 | chr2 | 69527042 | ||||||
| chr2:69527345
|
A | C | 1 | a0002c0002t0127g0249 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.872-26T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/21 | chr2 | 69527345 | ||||||
| chr2:69527393
|
C | T | 1 | a0001c0001t0004g0254 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.872-74G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/21 | chr2 | 69527393 | ||||||
| chr2:69527433
|
T | C | 11 | a0002c0002t0001g0019a0002c0002t0001g0040a0002c0002t0001g0057others(8): Show | 11 | HG00140.hp1 HG01074.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.872-114A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/21 | chr2 | 69527433 | ||||||
| chr2:69527659
|
T | C | 1 | a0002c0005t0040g0006 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.872-340A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/21 | chr2 | 69527659 | ||||||
| chr2:69527686
|
G | A | 15 | a0001c0001t0007g0049a0001c0001t0031g0176a0001c0007t0021g0276others(12): Show | 15 | HG02280.hp2 HG02572.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.872-367C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/21 | chr2 | 69527686 | ||||||
| chr2:69528012
|
T | A | 1 | a0001c0001t0002g0158 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.872-693A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/21 | chr2 | 69528012 | ||||||
| chr2:69528080
|
G | A | 5 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(2): Show | 5 | HG01243.hp1 HG01243.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.872-761C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/21 | chr2 | 69528080 | ||||||
| chr2:69528126
|
A | G | 2 | a0004c0012t0036g0283a0004c0012t0061g0067 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.872-807T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/21 | chr2 | 69528126 | ||||||
| chr2:69528553
|
C | T | 1 | a0001c0001t0009g0129 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.872-1234G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/21 | chr2 | 69528553 | ||||||
| chr2:69528594
|
C | T | 1 | a0001c0001t0140g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.872-1275G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/21 | chr2 | 69528594 | ||||||
| chr2:69528706
|
C | T | 1 | a0001c0001t0149g0280 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.871+1302G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/21 | chr2 | 69528706 | ||||||
| chr2:69528770
|
T | C | 6 | a0003c0014t0025g0285a0003c0014t0025g0286a0003c0020t0084g0105others(3): Show | 6 | HG01433.hp1 HG01891.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.871+1238A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/21 | chr2 | 69528770 | ||||||
| chr2:69528883
|
C | T | 2 | a0001c0004t0014g0063a0002c0019t0065g0062 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.871+1125G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/21 | chr2 | 69528883 | ||||||
| chr2:69528896
|
C | T | 2 | a0004c0012t0036g0283a0004c0012t0061g0067 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.871+1112G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/21 | chr2 | 69528896 | ||||||
| chr2:69528960
|
TA | T | 84 | a0002c0002t0001g0019a0002c0002t0001g0025a0002c0002t0001g0028others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.871+1047delT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/21 | chr2 | 69528960 | ||||||
| chr2:69529144
|
C | T | 1 | a0002c0002t0019g0115 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.871+864G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/21 | chr2 | 69529144 | ||||||
| chr2:69529254
|
G | C | 1 | a0002c0002t0062g0054 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.871+754C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/21 | chr2 | 69529254 | ||||||
| chr2:69529312
|
A | T | 2 | a0003c0014t0025g0285a0003c0014t0025g0286 | 2 | HG01891.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.871+696T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/21 | chr2 | 69529312 | ||||||
| chr2:69529376
|
T | C | 3 | a0001c0011t0029g0293a0001c0011t0029g0294a0001c0011t0079g0290 | 3 | HG02486.hp1 HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.871+632A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/21 | chr2 | 69529376 | ||||||
| chr2:69529400
|
C | CT | 47 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(44): Show | 47 | HG00099.hp2 HG00323.hp1 HG01175.hp2 others(44): Show |
intron_variant | MODIFIER | c.871+607dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/21 | chr2 | 69529400 | ||||||
| chr2:69529401
|
T | C | 1 | a0001c0001t0020g0193 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.871+607A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/21 | chr2 | 69529401 | ||||||
| chr2:69529583
|
C | T | 54 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(51): Show | 54 | HG00099.hp2 HG00323.hp1 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.871+425G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/21 | chr2 | 69529583 | ||||||
| chr2:69529606
|
C | G | 53 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.871+402G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/21 | chr2 | 69529606 | ||||||
| chr2:69529670
|
G | T | 1 | a0003c0020t0084g0105 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.871+338C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/21 | chr2 | 69529670 | ||||||
| chr2:69529754
|
T | C | 1 | a0002c0002t0005g0226 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.871+254A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/21 | chr2 | 69529754 | ||||||
| chr2:69529865
|
G | A | 2 | a0002c0002t0003g0250a0002c0002t0019g0143 | 2 | NA19060.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.871+143C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/21 | chr2 | 69529865 | ||||||
| chr2:69529903
|
C | T | 1 | a0001c0001t0104g0292 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.871+105G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 8/21 | chr2 | 69529903 | ||||||
| chr2:69530159
|
A | G | 53 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(50): Show | 53 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(50): Show |
intron_variant | MODIFIER | c.739-19T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 7/21 | chr2 | 69530159 | ||||||
| chr2:69530424
|
C | A | 1 | a0002c0002t0008g0050 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.738+201G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 7/21 | chr2 | 69530424 | ||||||
| chr2:69530547
|
C | T | 2 | a0001c0001t0008g0084a0010c0023t0008g0083 | 2 | HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.738+78G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 7/21 | chr2 | 69530547 | ||||||
| chr2:69530808
|
T | G | 4 | a0002c0005t0018g0064a0002c0005t0018g0103a0002c0005t0018g0104others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-102A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 6/21 | chr2 | 69530808 | ||||||
| chr2:69530874
|
C | A | 2 | a0001c0001t0006g0213a0001c0001t0006g0218 | 2 | HG01975.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.657-168G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 6/21 | chr2 | 69530874 | ||||||
| chr2:69531173
|
T | C | 3 | a0001c0011t0029g0293a0001c0011t0029g0294a0001c0011t0079g0290 | 3 | HG02486.hp1 HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.657-467A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 6/21 | chr2 | 69531173 | ||||||
| chr2:69531308
|
T | C | 2 | a0002c0002t0005g0230a0002c0002t0005g0248 | 2 | HG02165.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.657-602A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 6/21 | chr2 | 69531308 | ||||||
| chr2:69531315
|
C | T | 45 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(42): Show | 45 | HG00099.hp2 HG00323.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.657-609G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 6/21 | chr2 | 69531315 | ||||||
| chr2:69531344
|
G | A | 4 | a0001c0001t0045g0287a0002c0016t0103g0106a0004c0013t0043g0284others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-638C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 6/21 | chr2 | 69531344 | ||||||
| chr2:69531388
|
A | G | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.656+653T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 6/21 | chr2 | 69531388 | ||||||
| chr2:69531451
|
A | T | 1 | a0001c0001t0078g0055 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.656+590T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 6/21 | chr2 | 69531451 | ||||||
| chr2:69531732
|
C | T | 51 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(48): Show | 51 | HG00099.hp2 HG00323.hp1 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.656+309G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 6/21 | chr2 | 69531732 | ||||||
| chr2:69531795
|
C | T | 147 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(144): Show | 147 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.656+246G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 6/21 | chr2 | 69531795 | ||||||
| chr2:69531802
|
C | A | 2 | a0001c0006t0016g0017a0001c0006t0016g0289 | 2 | HG00735.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.656+239G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 6/21 | chr2 | 69531802 | ||||||
| chr2:69531825
|
C | A | 3 | a0001c0011t0029g0293a0001c0011t0029g0294a0001c0011t0079g0290 | 3 | HG02486.hp1 HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.656+216G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 6/21 | chr2 | 69531825 | ||||||
| chr2:69531857
|
C | T | 51 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(48): Show | 51 | HG00099.hp2 HG00323.hp1 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.656+184G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 6/21 | chr2 | 69531857 | ||||||
| chr2:69532283
|
G | A | 221 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.535-121C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69532283 | ||||||
| chr2:69532297
|
C | T | 2 | a0004c0012t0036g0283a0004c0012t0061g0067 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.535-135G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69532297 | ||||||
| chr2:69532373
|
A | C | 56 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(53): Show | 56 | HG00099.hp2 HG00323.hp1 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.535-211T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69532373 | ||||||
| chr2:69532915
|
C | A | 34 | a0001c0003t0012g0088a0001c0003t0012g0091a0001c0003t0012g0095others(31): Show | 34 | HG00099.hp2 HG00323.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.535-753G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69532915 | ||||||
| chr2:69532960
|
A | T | 1 | a0001c0001t0008g0012 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.535-798T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69532960 | ||||||
| chr2:69533352
|
G | A | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.535-1190C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69533352 | ||||||
| chr2:69533425
|
A | G | 4 | a0001c0001t0045g0287a0002c0016t0103g0106a0004c0013t0043g0284others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-1263T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69533425 | ||||||
| chr2:69533710
|
C | T | 51 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(48): Show | 51 | HG00099.hp2 HG00323.hp1 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.535-1548G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69533710 | ||||||
| chr2:69533810
|
C | T | 1 | a0005c0010t0010g0153 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.535-1648G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69533810 | ||||||
| chr2:69533849
|
T | C | 1 | a0001c0001t0011g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.535-1687A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69533849 | ||||||
| chr2:69533902
|
C | T | 4 | a0003c0020t0084g0105a0003c0021t0151g0282a0004c0012t0036g0283others(1): Show | 4 | HG01433.hp1 HG01928.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-1740G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69533902 | ||||||
| chr2:69534033
|
G | A | 2 | a0003c0020t0084g0105a0003c0021t0151g0282 | 2 | HG01433.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.535-1871C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69534033 | ||||||
| chr2:69534046
|
A | G | 3 | a0001c0001t0037g0009a0001c0001t0077g0072a0001c0001t0124g0188 | 3 | HG02280.hp1 HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.535-1884T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69534046 | ||||||
| chr2:69534071
|
A | G | 2 | a0002c0002t0001g0040a0002c0002t0044g0041 | 2 | HG00140.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.535-1909T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69534071 | ||||||
| chr2:69534150
|
C | T | 2 | a0004c0012t0036g0283a0004c0012t0061g0067 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.535-1988G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69534150 | ||||||
| chr2:69534201
|
C | T | 17 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(14): Show | 17 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.535-2039G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69534201 | ||||||
| chr2:69534315
|
G | A | 4 | a0001c0006t0028g0126a0001c0006t0028g0134a0001c0006t0041g0008others(1): Show | 4 | HG01884.hp2 HG02818.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-2153C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69534315 | ||||||
| chr2:69534546
|
C | A | 1 | a0001c0001t0137g0247 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.535-2384G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69534546 | ||||||
| chr2:69534588
|
C | T | 1 | a0002c0002t0013g0144 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.535-2426G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69534588 | ||||||
| chr2:69534628
|
T | A | 4 | a0001c0006t0028g0126a0001c0006t0028g0134a0001c0006t0041g0008others(1): Show | 4 | HG01884.hp2 HG02818.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-2466A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69534628 | ||||||
| chr2:69534697
|
C | A | 219 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.535-2535G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69534697 | ||||||
| chr2:69534997
|
C | T | 1 | a0001c0001t0002g0155 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.535-2835G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69534997 | ||||||
| chr2:69535012
|
C | T | 1 | a0001c0001t0140g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.535-2850G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69535012 | ||||||
| chr2:69535023
|
C | A | 4 | a0002c0005t0040g0006a0002c0005t0122g0182a0002c0005t0123g0183others(1): Show | 4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-2861G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69535023 | ||||||
| chr2:69535095
|
T | C | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.535-2933A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69535095 | ||||||
| chr2:69535109
|
T | C | 21 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(18): Show | 21 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.535-2947A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69535109 | ||||||
| chr2:69535157
|
G | C | 1 | a0003c0020t0084g0105 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.535-2995C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69535157 | ||||||
| chr2:69535236
|
C | G | 1 | a0003c0020t0084g0105 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.535-3074G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69535236 | ||||||
| chr2:69535259
|
C | T | 22 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(19): Show | 22 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.535-3097G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69535259 | ||||||
| chr2:69535376
|
A | G | 2 | a0001c0001t0105g0108a0001c0026t0152g0295 | 2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.535-3214T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69535376 | ||||||
| chr2:69535406
|
CA | C | 84 | a0002c0002t0001g0019a0002c0002t0001g0025a0002c0002t0001g0028others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.535-3245delT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69535406 | ||||||
| chr2:69535426
|
A | C | 1 | a0001c0001t0095g0136 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.535-3264T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69535426 | ||||||
| chr2:69535983
|
C | T | 1 | a0002c0002t0133g0210 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.535-3821G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69535983 | ||||||
| chr2:69536095
|
T | G | 1 | a0001c0003t0106g0141 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.535-3933A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69536095 | ||||||
| chr2:69536100
|
G | A | 1 | a0001c0001t0083g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.535-3938C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69536100 | ||||||
| chr2:69536153
|
C | T | 2 | a0004c0012t0036g0283a0004c0012t0061g0067 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.535-3991G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69536153 | ||||||
| chr2:69536202
|
C | T | 1 | a0001c0001t0056g0058 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.535-4040G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69536202 | ||||||
| chr2:69536255
|
A | G | 5 | a0001c0001t0037g0009a0001c0001t0077g0072a0001c0001t0078g0055others(2): Show | 5 | HG01167.hp1 HG02280.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.535-4093T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69536255 | ||||||
| chr2:69536408
|
CT | C | 7 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(4): Show | 7 | HG01243.hp1 HG01243.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.535-4247delA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69536408 | ||||||
| chr2:69536454
|
G | T | 2 | a0001c0006t0041g0008a0001c0006t0042g0007 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.535-4292C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69536454 | ||||||
| chr2:69536491
|
C | G | 1 | a0002c0002t0023g0026 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.535-4329G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69536491 | ||||||
| chr2:69536608
|
C | T | 5 | a0001c0001t0037g0009a0001c0001t0077g0072a0001c0001t0078g0055others(2): Show | 5 | HG01167.hp1 HG02280.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.535-4446G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69536608 | ||||||
| chr2:69536793
|
TTCAG | T | 3 | a0002c0002t0001g0040a0002c0002t0001g0057a0002c0002t0044g0041 | 3 | HG00140.hp1 HG01192.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.535-4635_535-4632d others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69536793 | ||||||
| chr2:69536931
|
G | A | 8 | a0001c0001t0007g0065a0001c0001t0008g0012a0001c0001t0008g0013others(5): Show | 8 | HG02257.hp1 HG02723.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.535-4769C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69536931 | ||||||
| chr2:69536951
|
T | C | 15 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(12): Show | 15 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.535-4789A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69536951 | ||||||
| chr2:69536955
|
A | G | 3 | a0001c0011t0029g0293a0001c0011t0029g0294a0001c0011t0079g0290 | 3 | HG02486.hp1 HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.535-4793T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69536955 | ||||||
| chr2:69537114
|
C | T | 1 | a0001c0001t0095g0136 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.535-4952G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69537114 | ||||||
| chr2:69537169
|
C | T | 8 | a0001c0001t0063g0288a0001c0001t0078g0055a0001c0001t0105g0108others(5): Show | 8 | HG01167.hp1 HG01243.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.535-5007G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69537169 | ||||||
| chr2:69537473
|
C | T | 3 | a0001c0001t0063g0288a0001c0026t0152g0295a0002c0005t0009g0163 | 3 | HG02717.hp2 HG06807.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.534+5050G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69537473 | ||||||
| chr2:69537542
|
G | A | 10 | a0001c0001t0045g0287a0001c0001t0063g0288a0001c0001t0105g0108others(7): Show | 10 | HG01928.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.534+4981C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69537542 | ||||||
| chr2:69537599
|
T | C | 8 | a0001c0001t0078g0055a0001c0001t0124g0188a0001c0003t0081g0080others(5): Show | 8 | HG01167.hp1 HG01928.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.534+4924A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69537599 | ||||||
| chr2:69537739
|
G | A | 15 | a0001c0001t0045g0287a0001c0001t0063g0288a0001c0001t0078g0055others(12): Show | 15 | HG01167.hp1 HG01243.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.534+4784C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69537739 | ||||||
| chr2:69537763
|
C | T | 3 | a0001c0004t0014g0063a0002c0016t0134g0272a0002c0019t0065g0062 | 3 | HG02257.hp2 HG02895.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.534+4760G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69537763 | ||||||
| chr2:69537991
|
T | C | 1 | a0002c0002t0111g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.534+4532A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69537991 | ||||||
| chr2:69538051
|
G | A | 33 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0014g0059others(30): Show | 33 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.534+4472C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69538051 | ||||||
| chr2:69538089
|
T | A | 32 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0014g0059others(29): Show | 32 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.534+4434A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69538089 | ||||||
| chr2:69538350
|
G | A | 56 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(53): Show | 56 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(53): Show |
intron_variant | MODIFIER | c.534+4173C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69538350 | ||||||
| chr2:69538508
|
C | T | 5 | a0001c0001t0045g0287a0001c0001t0105g0108a0001c0026t0152g0295others(2): Show | 5 | HG02109.hp1 HG02572.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.534+4015G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69538508 | ||||||
| chr2:69538549
|
T | C | 1 | a0004c0012t0036g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.534+3974A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69538549 | ||||||
| chr2:69538711
|
G | A | 9 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0045g0287others(6): Show | 9 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.534+3812C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69538711 | ||||||
| chr2:69538743
|
G | A | 1 | a0001c0001t0034g0267 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.534+3780C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69538743 | ||||||
| chr2:69538750
|
C | T | 4 | a0001c0001t0004g0258a0001c0001t0091g0117a0002c0002t0005g0256others(1): Show | 4 | NA18906.hp1 NA19066.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.534+3773G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69538750 | ||||||
| chr2:69538856
|
T | C | 83 | a0001c0001t0004g0258a0001c0001t0056g0058a0002c0002t0001g0019others(80): Show | 83 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.534+3667A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69538856 | ||||||
| chr2:69539003
|
C | G | 23 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(20): Show | 23 | HG01167.hp1 HG01243.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.534+3520G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69539003 | ||||||
| chr2:69539158
|
A | C | 1 | a0002c0002t0047g0053 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.534+3365T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69539158 | ||||||
| chr2:69539175
|
G | T | 180 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.534+3348C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69539175 | ||||||
| chr2:69539176
|
A | T | 180 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.534+3347T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69539176 | ||||||
| chr2:69539245
|
G | A | 9 | a0002c0002t0003g0227a0002c0002t0003g0244a0002c0002t0003g0245others(6): Show | 9 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.534+3278C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69539245 | ||||||
| chr2:69539273
|
T | C | 32 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0014g0059others(29): Show | 32 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.534+3250A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69539273 | ||||||
| chr2:69539313
|
TC | T | 5 | a0001c0001t0002g0114a0001c0001t0002g0120a0001c0001t0027g0128others(2): Show | 5 | HG01167.hp2 HG01884.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.534+3209delG | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69539313 | ||||||
| chr2:69539397
|
A | T | 16 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(13): Show | 16 | HG01243.hp1 HG02280.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.534+3126T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69539397 | ||||||
| chr2:69539398
|
C | A | 16 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(13): Show | 16 | HG01243.hp1 HG02280.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.534+3125G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69539398 | ||||||
| chr2:69539416
|
CG | C | 32 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0014g0059others(29): Show | 32 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.534+3106delC | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69539416 | ||||||
| chr2:69539897
|
C | T | 86 | a0001c0001t0004g0258a0001c0001t0056g0058a0002c0002t0001g0019others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.534+2626G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69539897 | ||||||
| chr2:69539930
|
T | C | 1 | a0001c0001t0092g0164 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.534+2593A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69539930 | ||||||
| chr2:69540041
|
C | T | 9 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0045g0287others(6): Show | 9 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.534+2482G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69540041 | ||||||
| chr2:69540090
|
T | C | 1 | a0002c0016t0103g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.534+2433A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69540090 | ||||||
| chr2:69540115
|
A | C | 220 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.534+2408T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69540115 | ||||||
| chr2:69540121
|
C | CT | 21 | a0001c0001t0004g0261a0001c0001t0008g0013a0001c0001t0009g0129others(18): Show | 21 | HG00099.hp1 HG01243.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.534+2401dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69540121 | ||||||
| chr2:69540121
|
C | CTT | 23 | a0001c0001t0008g0012a0001c0001t0014g0059a0001c0001t0014g0060others(20): Show | 23 | HG01167.hp1 HG01243.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.534+2400_534+2401d others(4): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69540121 | ||||||
| chr2:69540242
|
C | T | 2 | a0001c0001t0118g0184a0001c0001t0121g0186 | 2 | HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.534+2281G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69540242 | ||||||
| chr2:69540243
|
G | T | 35 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0014g0059others(32): Show | 35 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.534+2280C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69540243 | ||||||
| chr2:69540413
|
G | A | 1 | a0003c0020t0084g0105 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.534+2110C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69540413 | ||||||
| chr2:69540417
|
G | A | 2 | a0001c0006t0041g0008a0001c0006t0042g0007 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.534+2106C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69540417 | ||||||
| chr2:69540462
|
C | T | 1 | a0002c0002t0019g0143 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.534+2061G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69540462 | ||||||
| chr2:69540646
|
T | C | 1 | a0001c0003t0064g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.534+1877A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69540646 | ||||||
| chr2:69540653
|
T | C | 1 | a0001c0006t0016g0061 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.534+1870A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69540653 | ||||||
| chr2:69540671
|
A | G | 219 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.534+1852T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69540671 | ||||||
| chr2:69540785
|
A | G | 3 | a0002c0005t0040g0006a0002c0005t0123g0183a0002c0005t0150g0281 | 3 | HG02572.hp1 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.534+1738T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69540785 | ||||||
| chr2:69540949
|
A | G | 2 | a0001c0007t0035g0271a0001c0007t0148g0277 | 2 | HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.534+1574T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69540949 | ||||||
| chr2:69540960
|
G | A | 32 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0014g0059others(29): Show | 32 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.534+1563C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69540960 | ||||||
| chr2:69541104
|
C | G | 220 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.534+1419G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69541104 | ||||||
| chr2:69541227
|
C | CT | 22 | a0001c0001t0002g0130a0001c0001t0002g0154a0001c0001t0002g0155others(19): Show | 22 | HG00544.hp1 HG01433.hp1 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.534+1295dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69541227 | ||||||
| chr2:69541227
|
CTTT | C | 7 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0063g0288others(4): Show | 7 | HG01243.hp2 HG02257.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.534+1293_534+1295d others(5): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69541227 | ||||||
| chr2:69541227
|
CTTTT | C | 23 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(20): Show | 23 | HG01167.hp1 HG01243.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.534+1292_534+1295d others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69541227 | ||||||
| chr2:69541377
|
T | C | 19 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(16): Show | 19 | HG01167.hp1 HG01243.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.534+1146A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69541377 | ||||||
| chr2:69541414
|
T | C | 9 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0045g0287others(6): Show | 9 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.534+1109A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69541414 | ||||||
| chr2:69541471
|
A | T | 2 | a0001c0004t0014g0063a0002c0019t0065g0062 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.534+1052T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69541471 | ||||||
| chr2:69541704
|
G | C | 9 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0045g0287others(6): Show | 9 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.534+819C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69541704 | ||||||
| chr2:69541724
|
G | A | 9 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0045g0287others(6): Show | 9 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.534+799C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69541724 | ||||||
| chr2:69541755
|
C | A | 1 | a0002c0002t0005g0252 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.534+768G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69541755 | ||||||
| chr2:69541825
|
C | T | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.534+698G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69541825 | ||||||
| chr2:69541826
|
G | A | 1 | a0001c0006t0016g0061 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.534+697C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69541826 | ||||||
| chr2:69541878
|
T | C | 1 | a0002c0002t0155g0298 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.534+645A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69541878 | ||||||
| chr2:69542162
|
T | G | 1 | a0001c0001t0006g0223 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.534+361A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69542162 | ||||||
| chr2:69542235
|
C | T | 5 | a0001c0007t0021g0276a0001c0007t0021g0279a0001c0007t0034g0270others(2): Show | 5 | HG02809.hp2 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.534+288G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69542235 | ||||||
| chr2:69542385
|
C | G | 16 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(13): Show | 16 | HG01243.hp1 HG02280.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.534+138G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 5/21 | chr2 | 69542385 | ||||||
| chr2:69542731
|
G | A | 19 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(16): Show | 19 | HG01167.hp1 HG01243.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.392-66C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 4/21 | chr2 | 69542731 | ||||||
| chr2:69542839
|
T | C | 2 | a0002c0002t0005g0253a0002c0002t0145g0275 | 2 | HG01099.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.392-174A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 4/21 | chr2 | 69542839 | ||||||
| chr2:69542845
|
A | G | 5 | a0001c0006t0028g0126a0001c0006t0028g0134a0001c0006t0041g0008others(2): Show | 5 | HG01433.hp1 HG01884.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.392-180T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 4/21 | chr2 | 69542845 | ||||||
| chr2:69542989
|
G | A | 1 | a0001c0004t0146g0273 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.392-324C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 4/21 | chr2 | 69542989 | ||||||
| chr2:69543003
|
A | G | 3 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0063g0288 | 3 | HG02257.hp1 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.392-338T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 4/21 | chr2 | 69543003 | ||||||
| chr2:69543043
|
C | T | 1 | a0001c0006t0016g0061 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.392-378G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 4/21 | chr2 | 69543043 | ||||||
| chr2:69543061
|
C | G | 2 | a0001c0001t0008g0012a0001c0001t0008g0013 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.392-396G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 4/21 | chr2 | 69543061 | ||||||
| chr2:69543255
|
T | C | 1 | a0001c0001t0002g0155 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.392-590A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 4/21 | chr2 | 69543255 | ||||||
| chr2:69543467
|
G | A | 4 | a0001c0004t0014g0063a0002c0016t0103g0106a0002c0019t0065g0062others(1): Show | 4 | HG01928.hp2 HG02257.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.392-802C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 4/21 | chr2 | 69543467 | ||||||
| chr2:69543524
|
C | T | 1 | a0001c0001t0024g0087 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.392-859G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 4/21 | chr2 | 69543524 | ||||||
| chr2:69543558
|
C | A | 1 | a0002c0002t0005g0253 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.391+878G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 4/21 | chr2 | 69543558 | ||||||
| chr2:69543610
|
G | T | 1 | a0001c0009t0141g0191 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.391+826C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 4/21 | chr2 | 69543610 | ||||||
| chr2:69543702
|
G | A | 20 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(17): Show | 20 | HG01167.hp1 HG01243.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.391+734C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 4/21 | chr2 | 69543702 | ||||||
| chr2:69544026
|
C | T | 1 | a0001c0001t0045g0287 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.391+410G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 4/21 | chr2 | 69544026 | ||||||
| chr2:69544199
|
T | G | 1 | a0001c0001t0074g0048 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.391+237A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 4/21 | chr2 | 69544199 | ||||||
| chr2:69544265
|
C | A | 4 | a0001c0001t0020g0193a0001c0001t0020g0202a0001c0001t0020g0208others(1): Show | 4 | NA18956.hp1 NA18963.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+171G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 4/21 | chr2 | 69544265 | ||||||
| chr2:69544266
|
G | A | 29 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0014g0059others(26): Show | 29 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.391+170C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 4/21 | chr2 | 69544266 | ||||||
| chr2:69544332
|
A | T | 2 | a0001c0001t0078g0055a0001c0003t0081g0080 | 2 | HG01167.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.391+104T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 4/21 | chr2 | 69544332 | ||||||
| chr2:69544352
|
C | T | 208 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.391+84G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 4/21 | chr2 | 69544352 | ||||||
| chr2:69544893
|
G | A | 8 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0045g0287others(5): Show | 8 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.283-349C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69544893 | ||||||
| chr2:69545171
|
T | G | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.283-627A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69545171 | ||||||
| chr2:69545236
|
T | C | 1 | a0001c0001t0007g0089 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.283-692A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69545236 | ||||||
| chr2:69545607
|
A | C | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.283-1063T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69545607 | ||||||
| chr2:69545690
|
T | C | 1 | a0002c0002t0115g0180 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.283-1146A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69545690 | ||||||
| chr2:69545783
|
T | C | 1 | a0001c0001t0024g0087 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.283-1239A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69545783 | ||||||
| chr2:69545794
|
G | A | 11 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0045g0287others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.283-1250C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69545794 | ||||||
| chr2:69545953
|
G | A | 31 | a0001c0001t0037g0009a0001c0001t0077g0072a0001c0003t0012g0088others(28): Show | 31 | HG00099.hp2 HG01175.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.283-1409C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69545953 | ||||||
| chr2:69546098
|
C | CT | 18 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0045g0287others(15): Show | 18 | HG01243.hp2 HG01433.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.283-1555dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69546098 | ||||||
| chr2:69546110
|
C | T | 125 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(122): Show | 125 | HG00099.hp2 HG00544.hp1 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.283-1566G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69546110 | ||||||
| chr2:69546148
|
A | C | 7 | a0001c0006t0028g0126a0001c0006t0028g0134a0001c0006t0041g0008others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.283-1604T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69546148 | ||||||
| chr2:69546641
|
C | G | 204 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.283-2097G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69546641 | ||||||
| chr2:69546725
|
C | A | 8 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0045g0287others(5): Show | 8 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.283-2181G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69546725 | ||||||
| chr2:69547050
|
G | GA | 31 | a0001c0001t0037g0009a0001c0001t0077g0072a0001c0003t0012g0088others(28): Show | 31 | HG00099.hp2 HG01175.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.283-2507dupT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69547050 | ||||||
| chr2:69547109
|
C | T | 2 | a0004c0012t0036g0283a0004c0012t0061g0067 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.283-2565G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69547109 | ||||||
| chr2:69547177
|
G | A | 2 | a0001c0001t0045g0287a0004c0013t0043g0284 | 2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.283-2633C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69547177 | ||||||
| chr2:69547220
|
T | C | 2 | a0001c0006t0016g0017a0001c0006t0016g0289 | 2 | HG00735.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.283-2676A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69547220 | ||||||
| chr2:69547221
|
A | G | 3 | a0001c0011t0029g0293a0001c0011t0029g0294a0001c0011t0079g0290 | 3 | HG02486.hp1 HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.283-2677T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69547221 | ||||||
| chr2:69547338
|
A | G | 2 | a0001c0004t0014g0063a0002c0019t0065g0062 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.283-2794T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69547338 | ||||||
| chr2:69547370
|
G | A | 1 | a0001c0001t0056g0058 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.283-2826C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69547370 | ||||||
| chr2:69547430
|
C | T | 1 | a0001c0003t0142g0214 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.283-2886G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69547430 | ||||||
| chr2:69547645
|
T | C | 2 | a0004c0012t0036g0283a0004c0012t0061g0067 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.283-3101A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69547645 | ||||||
| chr2:69547794
|
T | C | 1 | a0004c0012t0061g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.283-3250A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69547794 | ||||||
| chr2:69547919
|
T | C | 1 | a0001c0001t0009g0129 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.283-3375A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69547919 | ||||||
| chr2:69547972
|
C | A | 211 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.283-3428G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69547972 | ||||||
| chr2:69548212
|
G | A | 5 | a0001c0001t0008g0022a0002c0002t0003g0199a0002c0002t0003g0238others(2): Show | 5 | HG02083.hp2 HG03654.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-3668C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69548212 | ||||||
| chr2:69548328
|
G | GA | 212 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.283-3785dupT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69548328 | ||||||
| chr2:69548341
|
T | C | 204 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.283-3797A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69548341 | ||||||
| chr2:69548401
|
C | T | 8 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0045g0287others(5): Show | 8 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.283-3857G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69548401 | ||||||
| chr2:69548467
|
TTTC | T | 4 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0105g0108others(1): Show | 4 | HG02257.hp1 HG02922.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-3926_283-3924d others(5): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69548467 | ||||||
| chr2:69548549
|
C | T | 1 | a0001c0006t0016g0061 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.283-4005G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69548549 | ||||||
| chr2:69548552
|
CTT | C | 17 | a0001c0003t0012g0088a0001c0003t0012g0095a0001c0003t0012g0096others(14): Show | 17 | HG02451.hp1 HG02602.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.283-4010_283-4009d others(4): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69548552 | ||||||
| chr2:69548561
|
TTTTC | T | 4 | a0001c0006t0028g0126a0001c0006t0028g0134a0001c0006t0041g0008others(1): Show | 4 | HG01884.hp2 HG02818.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-4021_283-4018d others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69548561 | ||||||
| chr2:69548690
|
T | C | 219 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.283-4146A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69548690 | ||||||
| chr2:69548691
|
G | A | 1 | a0002c0002t0062g0054 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.283-4147C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69548691 | ||||||
| chr2:69548824
|
C | T | 2 | a0001c0001t0008g0012a0001c0001t0008g0013 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.283-4280G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69548824 | ||||||
| chr2:69548838
|
C | T | 2 | a0001c0001t0008g0012a0001c0001t0008g0013 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.283-4294G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69548838 | ||||||
| chr2:69548839
|
G | T | 3 | a0001c0004t0017g0073a0001c0004t0017g0075a0001c0004t0067g0077 | 3 | HG03041.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.283-4295C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69548839 | ||||||
| chr2:69548972
|
G | A | 8 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0045g0287others(5): Show | 8 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.283-4428C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69548972 | ||||||
| chr2:69549262
|
G | A | 2 | a0004c0012t0036g0283a0004c0012t0061g0067 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.283-4718C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69549262 | ||||||
| chr2:69549508
|
T | C | 6 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0045g0287others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-4964A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69549508 | ||||||
| chr2:69549598
|
C | T | 178 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.283-5054G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69549598 | ||||||
| chr2:69549698
|
C | T | 8 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0045g0287others(5): Show | 8 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.283-5154G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69549698 | ||||||
| chr2:69549795
|
A | G | 2 | a0002c0016t0103g0106a0004c0013t0107g0107 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.283-5251T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69549795 | ||||||
| chr2:69549933
|
C | A | 203 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.283-5389G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69549933 | ||||||
| chr2:69550034
|
G | A | 20 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(17): Show | 20 | HG01167.hp1 HG01243.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.283-5490C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69550034 | ||||||
| chr2:69550140
|
T | A | 1 | a0002c0002t0047g0053 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.283-5596A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69550140 | ||||||
| chr2:69550245
|
T | C | 3 | a0001c0011t0029g0293a0001c0011t0029g0294a0001c0011t0079g0290 | 3 | HG02486.hp1 HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.283-5701A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69550245 | ||||||
| chr2:69550298
|
C | G | 1 | a0001c0006t0016g0061 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.283-5754G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69550298 | ||||||
| chr2:69550300
|
G | A | 2 | a0002c0016t0103g0106a0004c0013t0107g0107 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.283-5756C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69550300 | ||||||
| chr2:69550356
|
G | T | 7 | a0001c0006t0028g0126a0001c0006t0028g0134a0001c0006t0041g0008others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.283-5812C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69550356 | ||||||
| chr2:69550366
|
G | A | 1 | a0001c0001t0011g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.283-5822C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69550366 | ||||||
| chr2:69550373
|
C | T | 7 | a0001c0006t0028g0126a0001c0006t0028g0134a0001c0006t0041g0008others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.283-5829G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69550373 | ||||||
| chr2:69550419
|
C | G | 3 | a0001c0011t0029g0293a0001c0011t0029g0294a0001c0011t0079g0290 | 3 | HG02486.hp1 HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.283-5875G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69550419 | ||||||
| chr2:69550535
|
C | T | 20 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(17): Show | 20 | HG01167.hp1 HG01243.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.283-5991G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69550535 | ||||||
| chr2:69550733
|
A | G | 1 | a0001c0003t0046g0100 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.282+6127T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69550733 | ||||||
| chr2:69550751
|
G | C | 2 | a0002c0016t0103g0106a0004c0013t0107g0107 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.282+6109C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69550751 | ||||||
| chr2:69550795
|
T | C | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.282+6065A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69550795 | ||||||
| chr2:69550861
|
C | A | 4 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0105g0108others(1): Show | 4 | HG02257.hp1 HG02922.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.282+5999G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69550861 | ||||||
| chr2:69550934
|
G | A | 1 | a0002c0002t0008g0070 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.282+5926C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69550934 | ||||||
| chr2:69550936
|
G | A | 2 | a0001c0004t0014g0063a0002c0019t0065g0062 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.282+5924C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69550936 | ||||||
| chr2:69550972
|
A | G | 2 | a0001c0001t0027g0128a0001c0001t0027g0145 | 2 | HG01167.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.282+5888T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69550972 | ||||||
| chr2:69551089
|
T | C | 1 | a0001c0004t0017g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.282+5771A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69551089 | ||||||
| chr2:69551108
|
A | C | 4 | a0001c0001t0002g0130a0001c0001t0002g0155a0001c0001t0090g0119others(1): Show | 4 | NA18953.hp2 NA18955.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.282+5752T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69551108 | ||||||
| chr2:69551274
|
A | C | 2 | a0001c0003t0026g0014a0001c0003t0026g0015 | 2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.282+5586T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69551274 | ||||||
| chr2:69551289
|
T | C | 1 | a0004c0012t0036g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.282+5571A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69551289 | ||||||
| chr2:69551294
|
T | C | 1 | a0005c0010t0010g0123 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.282+5566A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69551294 | ||||||
| chr2:69551426
|
C | T | 85 | a0001c0001t0004g0258a0001c0001t0007g0065a0001c0001t0056g0058others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.282+5434G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69551426 | ||||||
| chr2:69551560
|
T | C | 17 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(14): Show | 17 | HG01243.hp1 HG02280.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.282+5300A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69551560 | ||||||
| chr2:69551591
|
A | C | 1 | a0004c0013t0043g0284 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.282+5269T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69551591 | ||||||
| chr2:69551911
|
G | A | 7 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0105g0108others(4): Show | 7 | HG02257.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.282+4949C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69551911 | ||||||
| chr2:69552081
|
T | C | 1 | a0002c0002t0003g0203 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.282+4779A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69552081 | ||||||
| chr2:69552152
|
A | T | 2 | a0002c0016t0103g0106a0004c0013t0107g0107 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.282+4708T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69552152 | ||||||
| chr2:69552209
|
G | A | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.282+4651C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69552209 | ||||||
| chr2:69552263
|
G | T | 1 | a0002c0002t0059g0032 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.282+4597C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69552263 | ||||||
| chr2:69552339
|
T | C | 2 | a0001c0001t0063g0288a0001c0001t0140g0269 | 2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.282+4521A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69552339 | ||||||
| chr2:69552523
|
C | G | 1 | a0004c0012t0061g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.282+4337G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69552523 | ||||||
| chr2:69552555
|
T | C | 1 | a0002c0002t0051g0045 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.282+4305A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69552555 | ||||||
| chr2:69552580
|
G | A | 10 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0045g0287others(7): Show | 10 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.282+4280C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69552580 | ||||||
| chr2:69552831
|
C | A | 218 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.282+4029G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69552831 | ||||||
| chr2:69553034
|
A | G | 1 | a0004c0012t0036g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.282+3826T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69553034 | ||||||
| chr2:69553086
|
A | G | 2 | a0001c0004t0014g0063a0002c0019t0065g0062 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.282+3774T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69553086 | ||||||
| chr2:69553210
|
A | G | 2 | a0001c0001t0057g0291a0001c0001t0117g0189 | 2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.282+3650T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69553210 | ||||||
| chr2:69553272
|
C | G | 11 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0045g0287others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.282+3588G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69553272 | ||||||
| chr2:69553366
|
C | T | 1 | a0001c0001t0063g0288 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.282+3494G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69553366 | ||||||
| chr2:69553428
|
T | C | 1 | a0001c0004t0067g0077 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.282+3432A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69553428 | ||||||
| chr2:69553437
|
G | GT | 17 | a0001c0001t0002g0149a0001c0001t0007g0101a0001c0001t0008g0069others(14): Show | 17 | HG01192.hp1 HG01981.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.282+3422dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69553437 | ||||||
| chr2:69553437
|
G | GTT | 12 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0045g0287others(9): Show | 12 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.282+3421_282+3422d others(4): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69553437 | ||||||
| chr2:69553437
|
G | GTTT | 9 | a0001c0006t0028g0126a0001c0006t0028g0134a0001c0009t0035g0190others(6): Show | 9 | HG01433.hp1 HG02280.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.282+3420_282+3422d others(5): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69553437 | ||||||
| chr2:69553437
|
G | GTTTT | 16 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(13): Show | 16 | HG01167.hp1 HG01243.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.282+3419_282+3422d others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69553437 | ||||||
| chr2:69553437
|
GT | G | 29 | a0001c0001t0004g0206a0001c0001t0004g0261a0001c0001t0004g0265others(26): Show | 29 | HG00544.hp2 HG01175.hp1 HG01928.hp2 others(26): Show |
intron_variant | MODIFIER | c.282+3422delA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69553437 | ||||||
| chr2:69553437
|
GTT | G | 148 | a0001c0001t0004g0216a0001c0001t0004g0221a0001c0001t0004g0233others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.282+3421_282+3422d others(4): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69553437 | ||||||
| chr2:69553437
|
GTTTTTTT others(7): Show |
G | 2 | a0001c0004t0017g0073a0005c0010t0010g0153 | 2 | HG01106.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.282+3409_282+3422d others(16): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69553437 | ||||||
| chr2:69553505
|
G | A | 175 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(172): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.282+3355C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69553505 | ||||||
| chr2:69553630
|
C | T | 218 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.282+3230G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69553630 | ||||||
| chr2:69553700
|
C | A | 1 | a0002c0002t0050g0035 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.282+3160G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69553700 | ||||||
| chr2:69553741
|
C | T | 7 | a0001c0006t0028g0126a0001c0006t0028g0134a0001c0006t0041g0008others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.282+3119G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69553741 | ||||||
| chr2:69553756
|
C | CA | 20 | a0001c0001t0014g0059a0001c0001t0014g0060a0001c0001t0014g0066others(17): Show | 20 | HG01167.hp1 HG01243.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.282+3103dupT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69553756 | ||||||
| chr2:69553872
|
G | A | 5 | a0001c0001t0007g0065a0002c0005t0018g0064a0002c0005t0018g0103others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.282+2988C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69553872 | ||||||
| chr2:69553914
|
GA | G | 8 | a0001c0001t0140g0269a0001c0006t0028g0126a0001c0006t0028g0134others(5): Show | 8 | HG01243.hp2 HG01433.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.282+2945delT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69553914 | ||||||
| chr2:69554069
|
T | A | 11 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0045g0287others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.282+2791A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69554069 | ||||||
| chr2:69554398
|
C | A | 218 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.282+2462G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69554398 | ||||||
| chr2:69554486
|
A | G | 1 | a0001c0004t0002g0137 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.282+2374T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69554486 | ||||||
| chr2:69554606
|
G | C | 2 | a0004c0012t0036g0283a0004c0012t0061g0067 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.282+2254C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69554606 | ||||||
| chr2:69554818
|
C | T | 1 | a0005c0010t0010g0123 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.282+2042G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69554818 | ||||||
| chr2:69554864
|
C | T | 9 | a0002c0002t0001g0029a0002c0002t0001g0034a0002c0002t0001g0042others(6): Show | 9 | HG00544.hp2 HG02080.hp2 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.282+1996G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69554864 | ||||||
| chr2:69554865
|
C | A | 7 | a0001c0006t0028g0126a0001c0006t0028g0134a0001c0006t0041g0008others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.282+1995G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69554865 | ||||||
| chr2:69554865
|
C | G | 224 | a0001c0001t0002g0114a0001c0001t0002g0120a0001c0001t0004g0206others(221): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.282+1995G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69554865 | ||||||
| chr2:69554878
|
C | T | 1 | a0001c0001t0021g0278 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.282+1982G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69554878 | ||||||
| chr2:69554986
|
C | T | 2 | a0001c0006t0016g0017a0001c0006t0016g0289 | 2 | HG00735.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.282+1874G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69554986 | ||||||
| chr2:69555178
|
C | A | 1 | a0001c0001t0021g0278 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.282+1682G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69555178 | ||||||
| chr2:69555241
|
G | A | 7 | a0001c0003t0012g0095a0001c0003t0012g0096a0001c0003t0012g0097others(4): Show | 7 | NA18961.hp2 NA18966.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.282+1619C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69555241 | ||||||
| chr2:69555275
|
G | T | 2 | a0001c0004t0014g0063a0002c0019t0065g0062 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.282+1585C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69555275 | ||||||
| chr2:69555398
|
G | A | 2 | a0001c0006t0016g0017a0001c0006t0016g0289 | 2 | HG00735.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.282+1462C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69555398 | ||||||
| chr2:69555549
|
G | A | 1 | a0001c0001t0087g0135 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.282+1311C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69555549 | ||||||
| chr2:69555550
|
C | T | 1 | a0001c0001t0087g0135 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.282+1310G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69555550 | ||||||
| chr2:69556046
|
CTCTT | C | 8 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0045g0287others(5): Show | 8 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.282+810_282+813del others(4): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69556046 | ||||||
| chr2:69556242
|
T | C | 2 | a0001c0004t0014g0063a0002c0019t0065g0062 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.282+618A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69556242 | ||||||
| chr2:69556598
|
A | G | 1 | a0002c0002t0001g0033 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.282+262T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69556598 | ||||||
| chr2:69556663
|
G | GCTC | 220 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.282+196_282+197ins others(3): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 3/21 | chr2 | 69556663 | ||||||
| chr2:69557015
|
T | C | 1 | a0002c0002t0005g0235 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.164-37A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69557015 | ||||||
| chr2:69557123
|
C | T | 83 | a0001c0001t0004g0258a0001c0001t0007g0049a0001c0001t0056g0058others(80): Show | 83 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.164-145G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69557123 | ||||||
| chr2:69557146
|
T | C | 220 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.164-168A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69557146 | ||||||
| chr2:69557225
|
T | C | 15 | a0001c0003t0012g0088a0001c0003t0012g0095a0001c0003t0012g0096others(12): Show | 15 | HG02451.hp1 HG02602.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.164-247A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69557225 | ||||||
| chr2:69557301
|
C | CG | 11 | a0001c0001t0004g0261a0001c0001t0006g0204a0001c0001t0006g0218others(8): Show | 11 | HG01175.hp2 HG01978.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.164-324_164-323ins others(1): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69557301 | ||||||
| chr2:69557301
|
C | CT | 6 | a0001c0001t0056g0058a0001c0004t0017g0073a0001c0004t0017g0075others(3): Show | 6 | HG02145.hp2 HG02723.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-324dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69557301 | ||||||
| chr2:69557301
|
CT | C | 34 | a0001c0001t0002g0155a0001c0001t0008g0012a0001c0001t0008g0013others(31): Show | 34 | HG01243.hp1 HG01243.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.164-324delA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69557301 | ||||||
| chr2:69557301
|
CTT | C | 7 | a0001c0006t0028g0126a0001c0006t0028g0134a0001c0006t0041g0008others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-325_164-324del others(2): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69557301 | ||||||
| chr2:69557302
|
T | G | 45 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(42): Show | 45 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(42): Show |
intron_variant | MODIFIER | c.164-324A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69557302 | ||||||
| chr2:69557378
|
T | C | 12 | a0001c0001t0007g0027a0001c0001t0007g0086a0001c0001t0007g0089others(9): Show | 12 | HG00408.hp2 HG02015.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.164-400A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69557378 | ||||||
| chr2:69557386
|
T | C | 7 | a0001c0006t0028g0126a0001c0006t0028g0134a0001c0006t0041g0008others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-408A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69557386 | ||||||
| chr2:69557405
|
G | A | 11 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0045g0287others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.164-427C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69557405 | ||||||
| chr2:69557444
|
G | A | 7 | a0001c0006t0028g0126a0001c0006t0028g0134a0001c0006t0041g0008others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-466C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69557444 | ||||||
| chr2:69557514
|
G | A | 11 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0045g0287others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.164-536C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69557514 | ||||||
| chr2:69557753
|
C | T | 1 | a0002c0002t0015g0005 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.164-775G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69557753 | ||||||
| chr2:69557859
|
A | T | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.164-881T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69557859 | ||||||
| chr2:69557937
|
G | A | 2 | a0002c0002t0038g0001a0002c0002t0055g0021 | 2 | NA18612.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.164-959C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69557937 | ||||||
| chr2:69558049
|
C | T | 7 | a0001c0006t0028g0126a0001c0006t0028g0134a0001c0006t0041g0008others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-1071G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69558049 | ||||||
| chr2:69558163
|
C | T | 7 | a0001c0006t0028g0126a0001c0006t0028g0134a0001c0006t0041g0008others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-1185G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69558163 | ||||||
| chr2:69558212
|
C | T | 2 | a0001c0001t0057g0291a0001c0001t0117g0189 | 2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.164-1234G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69558212 | ||||||
| chr2:69558222
|
T | C | 1 | a0001c0001t0032g0172 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.164-1244A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69558222 | ||||||
| chr2:69558281
|
T | C | 7 | a0001c0006t0028g0126a0001c0006t0028g0134a0001c0006t0041g0008others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-1303A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69558281 | ||||||
| chr2:69558331
|
C | T | 22 | a0001c0001t0004g0258a0002c0002t0003g0250a0002c0002t0005g0226others(19): Show | 22 | HG00438.hp1 HG01099.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.164-1353G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69558331 | ||||||
| chr2:69558339
|
C | CA | 205 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.164-1362dupT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69558339 | ||||||
| chr2:69558339
|
C | CAA | 9 | a0001c0001t0063g0288a0001c0001t0140g0269a0001c0003t0022g0010others(6): Show | 9 | HG01243.hp2 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.164-1363_164-1362d others(4): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69558339 | ||||||
| chr2:69558339
|
CA | C | 8 | a0001c0001t0027g0128a0001c0006t0028g0126a0001c0006t0028g0134others(5): Show | 8 | HG01167.hp2 HG01433.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.164-1362delT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69558339 | ||||||
| chr2:69558555
|
C | T | 202 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.164-1577G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69558555 | ||||||
| chr2:69558713
|
T | A | 7 | a0001c0006t0028g0126a0001c0006t0028g0134a0001c0006t0041g0008others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-1735A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69558713 | ||||||
| chr2:69558739
|
T | C | 220 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.164-1761A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69558739 | ||||||
| chr2:69558890
|
C | T | 1 | a0001c0001t0073g0052 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.164-1912G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69558890 | ||||||
| chr2:69559036
|
A | AT | 220 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.164-2059dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69559036 | ||||||
| chr2:69559056
|
G | A | 125 | a0001c0001t0004g0258a0001c0001t0007g0049a0001c0001t0007g0065others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.164-2078C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69559056 | ||||||
| chr2:69559249
|
A | ATC | 6 | a0001c0001t0011g0195a0001c0001t0101g0118a0001c0006t0028g0126others(3): Show | 6 | HG01433.hp1 HG01884.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.164-2273_164-2272d others(4): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69559249 | ||||||
| chr2:69559262
|
T | A | 4 | a0001c0001t0002g0125a0001c0001t0013g0151a0001c0001t0057g0291others(1): Show | 4 | HG03209.hp2 HG03471.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-2284A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69559262 | ||||||
| chr2:69559262
|
T | TCA | 4 | a0001c0001t0002g0130a0001c0001t0002g0155a0001c0001t0027g0128others(1): Show | 4 | HG01167.hp2 HG01975.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-2286_164-2285d others(4): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69559262 | ||||||
| chr2:69559262
|
T | TCACA | 3 | a0001c0001t0008g0069a0001c0001t0089g0122a0001c0001t0112g0170 | 3 | NA18993.hp1 NA18994.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.164-2288_164-2285d others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69559262 | ||||||
| chr2:69559262
|
TCA | T | 13 | a0001c0001t0002g0132a0001c0001t0092g0164a0001c0001t0105g0108others(10): Show | 13 | HG00438.hp2 HG00558.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.164-2286_164-2285d others(4): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69559262 | ||||||
| chr2:69559262
|
TCACA | T | 11 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0056g0058others(8): Show | 11 | HG00323.hp1 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.164-2288_164-2285d others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69559262 | ||||||
| chr2:69559264
|
A | T | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG01167.hp1 others(83): Show |
intron_variant | MODIFIER | c.164-2286T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69559264 | ||||||
| chr2:69559266
|
A | T | 72 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(69): Show | 72 | HG00544.hp1 HG00597.hp2 HG01175.hp2 others(69): Show |
intron_variant | MODIFIER | c.164-2288T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69559266 | ||||||
| chr2:69559268
|
A | T | 11 | a0001c0001t0004g0261a0001c0001t0008g0012a0001c0001t0008g0013others(8): Show | 11 | HG02257.hp1 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.164-2290T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69559268 | ||||||
| chr2:69559270
|
A | T | 5 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0011t0029g0293others(2): Show | 5 | HG02257.hp1 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-2292T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69559270 | ||||||
| chr2:69559284
|
ACACACAC others(9): Show |
A | 1 | a0002c0002t0005g0229 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.164-2322_164-2307d others(18): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69559284 | ||||||
| chr2:69559294
|
ACACACT | A | 28 | a0001c0001t0037g0009a0001c0001t0077g0072a0001c0003t0012g0088others(25): Show | 28 | HG00099.hp2 HG01891.hp2 HG02132.hp2 others(25): Show |
intron_variant | MODIFIER | c.164-2322_164-2317d others(8): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69559294 | ||||||
| chr2:69559296
|
A | T | 1 | a0004c0012t0036g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.164-2318T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69559296 | ||||||
| chr2:69559296
|
ACACT | A | 81 | a0001c0001t0007g0049a0001c0001t0007g0065a0001c0001t0014g0059others(78): Show | 81 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.164-2322_164-2319d others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69559296 | ||||||
| chr2:69559298
|
A | T | 14 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0045g0287others(11): Show | 14 | HG01433.hp1 HG02109.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.164-2320T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69559298 | ||||||
| chr2:69559298
|
ACT | A | 7 | a0001c0001t0063g0288a0001c0006t0016g0017a0001c0006t0016g0289others(4): Show | 7 | HG00140.hp1 HG00735.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.164-2322_164-2321d others(4): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69559298 | ||||||
| chr2:69559300
|
T | A | 78 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(75): Show | 78 | HG00544.hp1 HG00597.hp2 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.164-2322A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69559300 | ||||||
| chr2:69559304
|
T | A | 1 | a0001c0001t0004g0266 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.164-2326A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69559304 | ||||||
| chr2:69559716
|
T | G | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.164-2738A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69559716 | ||||||
| chr2:69560007
|
C | G | 4 | a0001c0003t0022g0010a0001c0003t0064g0085a0002c0016t0103g0106others(1): Show | 4 | HG02965.hp2 HG03579.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-3029G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69560007 | ||||||
| chr2:69560136
|
C | G | 4 | a0001c0001t0009g0147a0001c0001t0031g0174a0001c0001t0095g0136others(1): Show | 4 | HG00738.hp2 HG01074.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-3158G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69560136 | ||||||
| chr2:69560265
|
C | G | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.164-3287G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69560265 | ||||||
| chr2:69560269
|
C | G | 7 | a0001c0006t0028g0126a0001c0006t0028g0134a0001c0006t0041g0008others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-3291G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69560269 | ||||||
| chr2:69560327
|
G | T | 1 | a0001c0006t0042g0007 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.164-3349C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69560327 | ||||||
| chr2:69560374
|
T | C | 1 | a0001c0004t0071g0074 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.164-3396A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69560374 | ||||||
| chr2:69560491
|
G | C | 15 | a0001c0003t0012g0088a0001c0003t0012g0095a0001c0003t0012g0096others(12): Show | 15 | HG02451.hp1 HG02602.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.164-3513C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69560491 | ||||||
| chr2:69560569
|
C | G | 1 | a0001c0001t0143g0198 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.164-3591G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69560569 | ||||||
| chr2:69560672
|
C | T | 1 | a0001c0003t0142g0214 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.164-3694G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69560672 | ||||||
| chr2:69560840
|
G | T | 3 | a0001c0001t0027g0128a0001c0001t0027g0145a0001c0004t0010g0156 | 3 | HG01167.hp2 HG01891.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.164-3862C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69560840 | ||||||
| chr2:69560874
|
G | T | 7 | a0001c0006t0028g0126a0001c0006t0028g0134a0001c0006t0041g0008others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-3896C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69560874 | ||||||
| chr2:69560949
|
T | C | 221 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.164-3971A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69560949 | ||||||
| chr2:69560980
|
G | A | 1 | a0001c0006t0016g0289 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.164-4002C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69560980 | ||||||
| chr2:69560988
|
G | GT | 28 | a0001c0001t0037g0009a0001c0001t0077g0072a0001c0003t0012g0088others(25): Show | 28 | HG00099.hp2 HG01891.hp2 HG02132.hp2 others(25): Show |
intron_variant | MODIFIER | c.164-4011dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69560988 | ||||||
| chr2:69561122
|
C | T | 7 | a0001c0006t0028g0126a0001c0006t0028g0134a0001c0006t0041g0008others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-4144G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69561122 | ||||||
| chr2:69561151
|
T | G | 207 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.164-4173A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69561151 | ||||||
| chr2:69561325
|
C | T | 1 | a0002c0002t0115g0180 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.164-4347G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69561325 | ||||||
| chr2:69561332
|
G | A | 59 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(56): Show | 59 | HG00544.hp1 HG00597.hp2 HG01175.hp2 others(56): Show |
intron_variant | MODIFIER | c.164-4354C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69561332 | ||||||
| chr2:69561365
|
A | G | 14 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0105g0108others(11): Show | 14 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.164-4387T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69561365 | ||||||
| chr2:69561465
|
C | T | 117 | a0001c0001t0004g0258a0001c0001t0007g0049a0001c0001t0007g0065others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.164-4487G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69561465 | ||||||
| chr2:69561472
|
C | G | 8 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0105g0108others(5): Show | 8 | HG01433.hp1 HG02257.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-4494G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69561472 | ||||||
| chr2:69561667
|
A | G | 1 | a0002c0002t0133g0210 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.164-4689T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69561667 | ||||||
| chr2:69561675
|
G | A | 12 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0105g0108others(9): Show | 12 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.164-4697C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69561675 | ||||||
| chr2:69562121
|
T | C | 11 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0105g0108others(8): Show | 11 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.164-5143A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69562121 | ||||||
| chr2:69562122
|
G | A | 1 | a0004c0012t0061g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.164-5144C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69562122 | ||||||
| chr2:69562193
|
G | A | 11 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0105g0108others(8): Show | 11 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.164-5215C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69562193 | ||||||
| chr2:69562269
|
T | C | 1 | a0001c0003t0026g0014 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.164-5291A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69562269 | ||||||
| chr2:69562334
|
T | C | 4 | a0002c0016t0103g0106a0004c0012t0036g0283a0004c0012t0061g0067others(1): Show | 4 | HG02109.hp2 HG02965.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-5356A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69562334 | ||||||
| chr2:69562542
|
C | A | 1 | a0001c0001t0058g0092 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.164-5564G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69562542 | ||||||
| chr2:69562656
|
T | C | 1 | a0002c0002t0005g0235 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.164-5678A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69562656 | ||||||
| chr2:69562658
|
G | A | 1 | a0001c0001t0006g0217 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.164-5680C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69562658 | ||||||
| chr2:69562688
|
A | G | 1 | a0002c0002t0001g0051 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.164-5710T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69562688 | ||||||
| chr2:69562767
|
G | A | 1 | a0001c0026t0152g0295 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-5789C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69562767 | ||||||
| chr2:69562847
|
A | G | 9 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0063g0288others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-5869T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69562847 | ||||||
| chr2:69562869
|
G | A | 1 | a0002c0002t0132g0236 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.164-5891C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69562869 | ||||||
| chr2:69562896
|
A | C | 1 | a0001c0001t0009g0147 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.164-5918T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69562896 | ||||||
| chr2:69562901
|
A | G | 82 | a0001c0001t0002g0130a0001c0001t0004g0258a0001c0001t0007g0049others(79): Show | 82 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.164-5923T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69562901 | ||||||
| chr2:69562995
|
T | C | 1 | a0001c0001t0006g0204 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.164-6017A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69562995 | ||||||
| chr2:69563003
|
A | G | 42 | a0001c0001t0014g0059a0001c0001t0037g0009a0001c0001t0077g0072others(39): Show | 42 | HG00099.hp2 HG01433.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.164-6025T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69563003 | ||||||
| chr2:69563284
|
A | G | 41 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0037g0009others(38): Show | 41 | HG00099.hp2 HG01884.hp2 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.164-6306T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69563284 | ||||||
| chr2:69563348
|
A | G | 1 | a0002c0002t0013g0144 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.164-6370T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69563348 | ||||||
| chr2:69563488
|
C | T | 1 | a0001c0004t0017g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.164-6510G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69563488 | ||||||
| chr2:69563587
|
A | G | 1 | a0001c0006t0016g0289 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.164-6609T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69563587 | ||||||
| chr2:69563640
|
C | T | 2 | a0002c0002t0001g0051a0002c0002t0052g0023 | 2 | HG02809.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.164-6662G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69563640 | ||||||
| chr2:69563732
|
T | C | 9 | a0002c0002t0001g0029a0002c0002t0001g0034a0002c0002t0001g0042others(6): Show | 9 | HG00544.hp2 HG02080.hp2 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-6754A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69563732 | ||||||
| chr2:69563965
|
A | G | 9 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0063g0288others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-6987T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69563965 | ||||||
| chr2:69564106
|
T | C | 9 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0063g0288others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-7128A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69564106 | ||||||
| chr2:69564286
|
A | T | 2 | a0001c0006t0041g0008a0001c0006t0042g0007 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.164-7308T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69564286 | ||||||
| chr2:69564597
|
A | G | 9 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0063g0288others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-7619T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69564597 | ||||||
| chr2:69564600
|
A | C | 9 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0063g0288others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-7622T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69564600 | ||||||
| chr2:69564763
|
C | T | 8 | a0001c0001t0011g0192a0001c0001t0011g0194a0001c0001t0011g0195others(5): Show | 8 | HG02015.hp1 NA18747.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-7785G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69564763 | ||||||
| chr2:69564770
|
C | T | 124 | a0001c0001t0004g0258a0001c0001t0007g0049a0001c0001t0007g0065others(121): Show | 124 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.164-7792G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69564770 | ||||||
| chr2:69565078
|
T | C | 1 | a0004c0012t0061g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.164-8100A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69565078 | ||||||
| chr2:69565717
|
T | C | 11 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0063g0288others(8): Show | 11 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.164-8739A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69565717 | ||||||
| chr2:69565718
|
G | A | 4 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0063g0288others(1): Show | 4 | HG02257.hp1 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-8740C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69565718 | ||||||
| chr2:69565719
|
G | A | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.164-8741C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69565719 | ||||||
| chr2:69565766
|
G | A | 1 | a0003c0020t0084g0105 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.164-8788C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69565766 | ||||||
| chr2:69565822
|
T | C | 2 | a0003c0014t0025g0285a0003c0014t0025g0286 | 2 | HG01891.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.164-8844A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69565822 | ||||||
| chr2:69565828
|
CACTATTC others(87): Show |
C | 1 | a0002c0002t0003g0199 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.164-8944_164-8851d others(96): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69565828 | ||||||
| chr2:69566052
|
G | A | 56 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(53): Show | 56 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(53): Show |
intron_variant | MODIFIER | c.164-9074C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69566052 | ||||||
| chr2:69566186
|
T | C | 1 | a0001c0001t0140g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.164-9208A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69566186 | ||||||
| chr2:69566301
|
T | C | 1 | a0002c0002t0005g0240 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.164-9323A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69566301 | ||||||
| chr2:69566486
|
C | A | 1 | a0002c0002t0131g0211 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.164-9508G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69566486 | ||||||
| chr2:69566516
|
T | A | 1 | a0003c0020t0084g0105 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.164-9538A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69566516 | ||||||
| chr2:69566778
|
T | C | 1 | a0002c0002t0001g0033 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.164-9800A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69566778 | ||||||
| chr2:69566860
|
G | A | 2 | a0001c0006t0041g0008a0001c0006t0042g0007 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.164-9882C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69566860 | ||||||
| chr2:69566919
|
A | G | 5 | a0001c0006t0016g0017a0001c0006t0016g0289a0001c0011t0029g0293others(2): Show | 5 | HG00735.hp2 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-9941T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69566919 | ||||||
| chr2:69567123
|
C | T | 5 | a0001c0004t0014g0063a0002c0016t0103g0106a0002c0019t0065g0062others(2): Show | 5 | HG02109.hp2 HG02257.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-10145G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69567123 | ||||||
| chr2:69567196
|
C | T | 1 | a0002c0002t0023g0036 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.164-10218G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69567196 | ||||||
| chr2:69567204
|
C | T | 1 | a0001c0003t0064g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.164-10226G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69567204 | ||||||
| chr2:69567218
|
A | G | 127 | a0001c0001t0004g0258a0001c0001t0007g0049a0001c0001t0007g0065others(124): Show | 127 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.164-10240T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69567218 | ||||||
| chr2:69567365
|
G | C | 1 | a0001c0008t0097g0131 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.164-10387C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69567365 | ||||||
| chr2:69567435
|
C | A | 5 | a0001c0004t0014g0063a0002c0016t0103g0106a0002c0019t0065g0062others(2): Show | 5 | HG02109.hp2 HG02257.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-10457G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69567435 | ||||||
| chr2:69567523
|
T | C | 1 | a0002c0002t0003g0227 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.164-10545A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69567523 | ||||||
| chr2:69567550
|
G | A | 2 | a0001c0006t0041g0008a0001c0006t0042g0007 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.164-10572C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69567550 | ||||||
| chr2:69567570
|
A | T | 2 | a0001c0006t0041g0008a0001c0006t0042g0007 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.164-10592T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69567570 | ||||||
| chr2:69567590
|
A | G | 4 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0063g0288others(1): Show | 4 | HG02257.hp1 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-10612T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69567590 | ||||||
| chr2:69567789
|
G | A | 5 | a0001c0004t0014g0063a0002c0016t0103g0106a0002c0019t0065g0062others(2): Show | 5 | HG02109.hp2 HG02257.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-10811C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69567789 | ||||||
| chr2:69567851
|
C | T | 58 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(55): Show | 58 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(55): Show |
intron_variant | MODIFIER | c.164-10873G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69567851 | ||||||
| chr2:69567855
|
T | G | 1 | a0001c0001t0140g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.164-10877A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69567855 | ||||||
| chr2:69568006
|
C | T | 2 | a0001c0006t0041g0008a0001c0006t0042g0007 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.164-11028G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69568006 | ||||||
| chr2:69568007
|
G | A | 3 | a0001c0004t0014g0063a0002c0019t0065g0062a0004c0012t0061g0067 | 3 | HG02109.hp2 HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.164-11029C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69568007 | ||||||
| chr2:69568069
|
A | G | 4 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0063g0288others(1): Show | 4 | HG02257.hp1 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-11091T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69568069 | ||||||
| chr2:69568164
|
T | C | 9 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0063g0288others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-11186A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69568164 | ||||||
| chr2:69568346
|
C | T | 1 | a0002c0016t0134g0272 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.164-11368G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69568346 | ||||||
| chr2:69568360
|
G | T | 3 | a0001c0004t0014g0063a0002c0019t0065g0062a0004c0012t0061g0067 | 3 | HG02109.hp2 HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.164-11382C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69568360 | ||||||
| chr2:69568425
|
C | CT | 6 | a0001c0001t0004g0261a0001c0006t0041g0008a0001c0006t0042g0007others(3): Show | 6 | HG01175.hp1 HG01884.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.164-11448dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69568425 | ||||||
| chr2:69568425
|
CT | C | 33 | a0001c0001t0004g0206a0001c0001t0004g0268a0001c0001t0009g0147others(30): Show | 33 | HG01074.hp2 HG01257.hp2 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.164-11448delA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69568425 | ||||||
| chr2:69568425
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0027g0145 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.164-11457_164-1144 others(14): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69568425 | ||||||
| chr2:69568696
|
T | C | 4 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0063g0288others(1): Show | 4 | HG02257.hp1 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-11718A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69568696 | ||||||
| chr2:69568754
|
T | A | 4 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0117g0189others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-11776A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69568754 | ||||||
| chr2:69568893
|
G | T | 56 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(53): Show | 56 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(53): Show |
intron_variant | MODIFIER | c.164-11915C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69568893 | ||||||
| chr2:69568894
|
G | A | 15 | a0001c0001t0014g0060a0001c0001t0014g0066a0001c0001t0021g0278others(12): Show | 15 | HG01243.hp1 HG02280.hp2 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.164-11916C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69568894 | ||||||
| chr2:69569092
|
G | C | 184 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(181): Show | 184 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.164-12114C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69569092 | ||||||
| chr2:69569127
|
G | A | 187 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.164-12149C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69569127 | ||||||
| chr2:69569158
|
C | T | 1 | a0002c0002t0003g0215 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.164-12180G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69569158 | ||||||
| chr2:69569197
|
T | C | 2 | a0002c0002t0131g0211a0002c0002t0132g0236 | 2 | NA18963.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.164-12219A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69569197 | ||||||
| chr2:69569214
|
G | A | 183 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(180): Show | 183 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.164-12236C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69569214 | ||||||
| chr2:69569265
|
A | C | 1 | a0001c0004t0002g0137 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.164-12287T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69569265 | ||||||
| chr2:69569672
|
G | A | 1 | a0001c0001t0140g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.164-12694C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69569672 | ||||||
| chr2:69569740
|
T | C | 188 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.164-12762A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69569740 | ||||||
| chr2:69569876
|
G | A | 1 | a0001c0001t0002g0152 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.164-12898C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69569876 | ||||||
| chr2:69569876
|
G | T | 97 | a0001c0001t0004g0258a0001c0001t0007g0049a0001c0001t0007g0065others(94): Show | 97 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.164-12898C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69569876 | ||||||
| chr2:69569903
|
G | A | 1 | a0006c0015t0001g0024 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.164-12925C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69569903 | ||||||
| chr2:69570505
|
C | T | 1 | a0001c0001t0126g0219 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.164-13527G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69570505 | ||||||
| chr2:69570597
|
G | A | 68 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(65): Show | 68 | HG00544.hp1 HG00597.hp2 HG01243.hp1 others(65): Show |
intron_variant | MODIFIER | c.164-13619C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69570597 | ||||||
| chr2:69570633
|
A | C | 1 | a0001c0003t0012g0097 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.164-13655T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69570633 | ||||||
| chr2:69570713
|
T | C | 1 | a0002c0002t0001g0043 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.164-13735A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69570713 | ||||||
| chr2:69570797
|
T | G | 7 | a0001c0001t0007g0065a0001c0001t0073g0052a0001c0006t0016g0061others(4): Show | 7 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.164-13819A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69570797 | ||||||
| chr2:69570901
|
C | T | 13 | a0002c0002t0003g0199a0002c0002t0003g0203a0002c0002t0003g0227others(10): Show | 13 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.164-13923G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69570901 | ||||||
| chr2:69570953
|
T | TC | 114 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(111): Show | 114 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(111): Show |
intron_variant | MODIFIER | c.164-13976_164-1397 others(5): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69570953 | ||||||
| chr2:69570955
|
T | A | 114 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(111): Show | 114 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(111): Show |
intron_variant | MODIFIER | c.164-13977A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69570955 | ||||||
| chr2:69571114
|
T | G | 2 | a0001c0004t0014g0063a0002c0019t0065g0062 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.164-14136A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69571114 | ||||||
| chr2:69571117
|
T | A | 1 | a0001c0001t0027g0145 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.164-14139A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69571117 | ||||||
| chr2:69571211
|
C | T | 1 | a0002c0005t0009g0163 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.164-14233G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69571211 | ||||||
| chr2:69571516
|
T | C | 8 | a0001c0001t0021g0278a0001c0007t0021g0276a0001c0007t0021g0279others(5): Show | 8 | HG02280.hp2 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-14538A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69571516 | ||||||
| chr2:69571812
|
T | C | 1 | a0001c0001t0008g0022 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.164-14834A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69571812 | ||||||
| chr2:69571838
|
C | G | 1 | a0001c0001t0034g0267 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.164-14860G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69571838 | ||||||
| chr2:69572238
|
G | A | 7 | a0001c0001t0007g0065a0001c0001t0073g0052a0001c0006t0016g0061others(4): Show | 7 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.164-15260C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69572238 | ||||||
| chr2:69572311
|
T | A | 4 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0063g0288others(1): Show | 4 | HG02257.hp1 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-15333A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69572311 | ||||||
| chr2:69572600
|
C | T | 1 | a0001c0001t0014g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.164-15622G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69572600 | ||||||
| chr2:69572613
|
C | T | 9 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(6): Show | 9 | HG01243.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-15635G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69572613 | ||||||
| chr2:69572620
|
T | TA | 59 | a0001c0001t0002g0154a0001c0001t0004g0216a0001c0001t0004g0221others(56): Show | 59 | HG00544.hp1 HG00597.hp2 HG01175.hp2 others(56): Show |
intron_variant | MODIFIER | c.164-15643dupT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69572620 | ||||||
| chr2:69572620
|
TA | T | 90 | a0001c0001t0002g0120a0001c0001t0002g0152a0001c0001t0002g0155others(87): Show | 90 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.164-15643delT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69572620 | ||||||
| chr2:69572620
|
TAA | T | 8 | a0001c0003t0081g0080a0001c0007t0021g0276a0001c0007t0021g0279others(5): Show | 8 | HG02698.hp1 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-15644_164-1564 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69572620 | ||||||
| chr2:69572643
|
A | G | 1 | a0004c0012t0036g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.164-15665T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69572643 | ||||||
| chr2:69572680
|
G | C | 1 | a0004c0012t0036g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.164-15702C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69572680 | ||||||
| chr2:69572714
|
G | C | 1 | a0001c0001t0002g0155 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.164-15736C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69572714 | ||||||
| chr2:69572834
|
C | T | 25 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0003t0012g0088others(22): Show | 25 | HG00735.hp2 HG01433.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.164-15856G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69572834 | ||||||
| chr2:69572839
|
G | A | 106 | a0001c0001t0007g0027a0001c0001t0007g0049a0001c0001t0007g0081others(103): Show | 106 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.164-15861C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69572839 | ||||||
| chr2:69572982
|
A | G | 115 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(112): Show | 115 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(112): Show |
intron_variant | MODIFIER | c.164-16004T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69572982 | ||||||
| chr2:69573126
|
C | A | 1 | a0001c0001t0021g0278 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.164-16148G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69573126 | ||||||
| chr2:69573250
|
C | T | 7 | a0001c0001t0007g0065a0001c0001t0073g0052a0001c0006t0016g0061others(4): Show | 7 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.164-16272G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69573250 | ||||||
| chr2:69573425
|
C | T | 7 | a0001c0003t0012g0095a0001c0003t0012g0096a0001c0003t0012g0097others(4): Show | 7 | NA18961.hp2 NA18966.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-16447G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69573425 | ||||||
| chr2:69573447
|
T | C | 70 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(67): Show | 70 | HG00544.hp1 HG00597.hp2 HG01243.hp1 others(67): Show |
intron_variant | MODIFIER | c.164-16469A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69573447 | ||||||
| chr2:69573492
|
G | A | 70 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(67): Show | 70 | HG00544.hp1 HG00597.hp2 HG01243.hp1 others(67): Show |
intron_variant | MODIFIER | c.164-16514C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69573492 | ||||||
| chr2:69573508
|
C | G | 4 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0063g0288others(1): Show | 4 | HG02257.hp1 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-16530G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69573508 | ||||||
| chr2:69573553
|
G | T | 12 | a0001c0003t0012g0088a0001c0003t0012g0095a0001c0003t0012g0096others(9): Show | 12 | HG02451.hp1 HG02602.hp1 HG04228.hp2 others(9): Show |
intron_variant | MODIFIER | c.164-16575C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69573553 | ||||||
| chr2:69573581
|
C | T | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.164-16603G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69573581 | ||||||
| chr2:69573633
|
C | G | 1 | a0001c0001t0083g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.164-16655G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69573633 | ||||||
| chr2:69573640
|
T | C | 220 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(217): Show | 220 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.164-16662A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69573640 | ||||||
| chr2:69573666
|
T | C | 1 | a0001c0001t0014g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.164-16688A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69573666 | ||||||
| chr2:69573777
|
A | T | 1 | a0002c0002t0003g0203 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.164-16799T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69573777 | ||||||
| chr2:69573994
|
CAAAATA | C | 70 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(67): Show | 70 | HG00544.hp1 HG00597.hp2 HG01243.hp1 others(67): Show |
intron_variant | MODIFIER | c.164-17022_164-1701 others(10): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69573994 | ||||||
| chr2:69574073
|
A | G | 9 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(6): Show | 9 | HG01243.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-17095T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69574073 | ||||||
| chr2:69574303
|
G | A | 1 | a0002c0002t0003g0246 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.164-17325C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69574303 | ||||||
| chr2:69574377
|
C | CA | 15 | a0001c0001t0004g0268a0001c0001t0006g0218a0001c0001t0008g0084others(12): Show | 15 | HG00735.hp2 HG01981.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.164-17400dupT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69574377 | ||||||
| chr2:69574377
|
C | CAA | 65 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(62): Show | 65 | HG00544.hp1 HG00597.hp2 HG01243.hp1 others(62): Show |
intron_variant | MODIFIER | c.164-17401_164-1740 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69574377 | ||||||
| chr2:69574377
|
CA | C | 105 | a0001c0001t0002g0149a0001c0001t0002g0158a0001c0001t0007g0081others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.164-17400delT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69574377 | ||||||
| chr2:69574377
|
CAA | C | 13 | a0001c0001t0007g0027a0001c0001t0007g0049a0001c0001t0078g0055others(10): Show | 13 | HG00323.hp2 HG00738.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.164-17401_164-1740 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69574377 | ||||||
| chr2:69574400
|
G | A | 1 | a0001c0001t0011g0194 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.164-17422C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69574400 | ||||||
| chr2:69574482
|
G | T | 2 | a0001c0004t0014g0063a0002c0019t0065g0062 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.164-17504C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69574482 | ||||||
| chr2:69574610
|
T | G | 9 | a0001c0001t0007g0065a0001c0001t0014g0059a0001c0001t0045g0287others(6): Show | 9 | HG02109.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-17632A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69574610 | ||||||
| chr2:69574619
|
T | TA | 7 | a0001c0001t0007g0065a0001c0001t0073g0052a0001c0006t0016g0061others(4): Show | 7 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.164-17642dupT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69574619 | ||||||
| chr2:69574689
|
C | T | 1 | a0001c0001t0113g0178 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.164-17711G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69574689 | ||||||
| chr2:69574746
|
G | A | 1 | a0004c0012t0061g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.164-17768C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69574746 | ||||||
| chr2:69574960
|
C | T | 1 | a0001c0001t0140g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.164-17982G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69574960 | ||||||
| chr2:69574974
|
C | T | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.164-17996G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69574974 | ||||||
| chr2:69575003
|
G | A | 1 | a0001c0001t0144g0232 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.164-18025C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69575003 | ||||||
| chr2:69575019
|
A | AC | 68 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(65): Show | 68 | HG00544.hp1 HG00597.hp2 HG01243.hp1 others(65): Show |
intron_variant | MODIFIER | c.164-18042dupG | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69575019 | ||||||
| chr2:69575020
|
C | CA | 11 | a0001c0001t0007g0086a0001c0001t0009g0124a0001c0001t0092g0164others(8): Show | 11 | HG01243.hp2 HG01361.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.164-18043dupT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69575020 | ||||||
| chr2:69575020
|
CA | C | 6 | a0001c0001t0009g0147a0001c0001t0031g0174a0001c0001t0095g0136others(3): Show | 6 | HG00099.hp2 HG00738.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-18043delT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69575020 | ||||||
| chr2:69575204
|
G | C | 1 | a0001c0001t0114g0171 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.164-18226C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69575204 | ||||||
| chr2:69575308
|
ACCAGGG | A | 106 | a0001c0001t0007g0027a0001c0001t0007g0049a0001c0001t0007g0081others(103): Show | 106 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.164-18336_164-1833 others(10): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69575308 | ||||||
| chr2:69575381
|
T | A | 224 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(221): Show | 224 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.164-18403A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69575381 | ||||||
| chr2:69575464
|
A | AT | 24 | a0001c0001t0002g0130a0001c0001t0002g0149a0001c0001t0002g0154others(21): Show | 24 | HG01175.hp1 HG01175.hp2 HG01952.hp1 others(21): Show |
intron_variant | MODIFIER | c.164-18487dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69575464 | ||||||
| chr2:69575464
|
AT | A | 9 | a0001c0001t0091g0117a0001c0001t0093g0121a0001c0001t0101g0118others(6): Show | 9 | HG01943.hp2 HG02300.hp1 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-18487delA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69575464 | ||||||
| chr2:69575465
|
T | A | 2 | a0002c0016t0103g0106a0004c0013t0107g0107 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.164-18487A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69575465 | ||||||
| chr2:69575493
|
G | C | 1 | a0001c0003t0022g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.164-18515C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69575493 | ||||||
| chr2:69575501
|
C | T | 70 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(67): Show | 70 | HG00544.hp1 HG00597.hp2 HG01243.hp1 others(67): Show |
intron_variant | MODIFIER | c.164-18523G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69575501 | ||||||
| chr2:69575555
|
C | T | 7 | a0001c0001t0007g0065a0001c0001t0073g0052a0001c0006t0016g0061others(4): Show | 7 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.164-18577G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69575555 | ||||||
| chr2:69575605
|
A | G | 8 | a0001c0001t0021g0278a0001c0007t0021g0276a0001c0007t0021g0279others(5): Show | 8 | HG02280.hp2 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-18627T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69575605 | ||||||
| chr2:69575612
|
G | A | 1 | a0001c0001t0014g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.164-18634C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69575612 | ||||||
| chr2:69575714
|
C | A | 1 | a0002c0002t0015g0003 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.164-18736G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69575714 | ||||||
| chr2:69575715
|
G | A | 1 | a0003c0020t0084g0105 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.164-18737C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69575715 | ||||||
| chr2:69576184
|
A | G | 9 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066others(6): Show | 9 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-19206T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69576184 | ||||||
| chr2:69576331
|
GT | G | 11 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0006t0041g0008others(8): Show | 11 | HG01243.hp2 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.164-19354delA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69576331 | ||||||
| chr2:69576412
|
G | C | 1 | a0001c0001t0139g0231 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.164-19434C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69576412 | ||||||
| chr2:69576518
|
C | T | 87 | a0001c0001t0007g0027a0001c0001t0007g0049a0001c0001t0008g0022others(84): Show | 87 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.164-19540G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69576518 | ||||||
| chr2:69576560
|
C | T | 2 | a0001c0001t0090g0119a0001c0001t0114g0171 | 2 | NA18960.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.164-19582G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69576560 | ||||||
| chr2:69576582
|
G | C | 1 | a0002c0002t0001g0051 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.164-19604C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69576582 | ||||||
| chr2:69576665
|
A | G | 9 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(6): Show | 9 | HG01243.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-19687T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69576665 | ||||||
| chr2:69576930
|
C | A | 1 | a0001c0001t0140g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.164-19952G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69576930 | ||||||
| chr2:69576961
|
C | A | 9 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066others(6): Show | 9 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-19983G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69576961 | ||||||
| chr2:69577124
|
G | A | 2 | a0002c0002t0049g0047a0002c0024t0060g0031 | 2 | HG00323.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.164-20146C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69577124 | ||||||
| chr2:69577349
|
G | A | 1 | a0005c0010t0010g0142 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.164-20371C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69577349 | ||||||
| chr2:69577362
|
T | G | 16 | a0001c0003t0012g0088a0001c0003t0012g0095a0001c0003t0012g0096others(13): Show | 16 | HG01433.hp1 HG02451.hp1 HG02602.hp1 others(13): Show |
intron_variant | MODIFIER | c.164-20384A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69577362 | ||||||
| chr2:69577399
|
G | A | 1 | a0004c0012t0036g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.164-20421C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69577399 | ||||||
| chr2:69577409
|
G | A | 62 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(59): Show | 62 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(59): Show |
intron_variant | MODIFIER | c.164-20431C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69577409 | ||||||
| chr2:69577468
|
G | A | 1 | a0001c0006t0016g0289 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.164-20490C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69577468 | ||||||
| chr2:69577706
|
G | T | 9 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(6): Show | 9 | HG01243.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-20728C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69577706 | ||||||
| chr2:69577797
|
G | T | 62 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(59): Show | 62 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(59): Show |
intron_variant | MODIFIER | c.164-20819C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69577797 | ||||||
| chr2:69577805
|
C | T | 1 | a0002c0002t0005g0234 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.164-20827G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69577805 | ||||||
| chr2:69577992
|
A | C | 1 | a0001c0004t0071g0074 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.164-21014T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69577992 | ||||||
| chr2:69578117
|
G | A | 2 | a0001c0001t0004g0258a0002c0002t0005g0256 | 2 | NA19066.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.164-21139C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69578117 | ||||||
| chr2:69578209
|
C | T | 1 | a0001c0004t0068g0079 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.164-21231G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69578209 | ||||||
| chr2:69578347
|
A | C | 1 | a0001c0001t0140g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.164-21369T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69578347 | ||||||
| chr2:69578500
|
T | C | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.164-21522A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69578500 | ||||||
| chr2:69578618
|
C | T | 2 | a0001c0001t0089g0122a0001c0001t0112g0170 | 2 | NA18993.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.164-21640G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69578618 | ||||||
| chr2:69578699
|
C | A | 5 | a0001c0001t0117g0189a0002c0005t0122g0182a0002c0005t0123g0183others(2): Show | 5 | HG02895.hp2 HG03098.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-21721G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69578699 | ||||||
| chr2:69578804
|
CT | C | 6 | a0001c0001t0024g0090a0001c0001t0138g0209a0002c0002t0003g0244others(3): Show | 6 | HG01928.hp2 HG01975.hp2 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.164-21827delA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69578804 | ||||||
| chr2:69578827
|
G | A | 1 | a0001c0001t0140g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.164-21849C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69578827 | ||||||
| chr2:69578838
|
C | T | 1 | a0001c0001t0092g0164 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.164-21860G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69578838 | ||||||
| chr2:69579515
|
G | A | 1 | a0001c0001t0014g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.164-22537C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69579515 | ||||||
| chr2:69579661
|
C | A | 1 | a0001c0001t0008g0022 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.164-22683G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69579661 | ||||||
| chr2:69579702
|
G | A | 1 | a0004c0012t0036g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.164-22724C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69579702 | ||||||
| chr2:69579791
|
T | C | 1 | a0002c0002t0111g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.164-22813A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69579791 | ||||||
| chr2:69579844
|
T | C | 1 | a0002c0002t0039g0004 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.164-22866A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69579844 | ||||||
| chr2:69580095
|
T | G | 1 | a0001c0001t0087g0135 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.164-23117A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69580095 | ||||||
| chr2:69580269
|
C | T | 1 | a0001c0001t0140g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.164-23291G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69580269 | ||||||
| chr2:69580378
|
T | G | 62 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(59): Show | 62 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(59): Show |
intron_variant | MODIFIER | c.164-23400A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69580378 | ||||||
| chr2:69580411
|
T | C | 1 | a0001c0003t0082g0098 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.164-23433A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69580411 | ||||||
| chr2:69580478
|
A | T | 2 | a0001c0006t0041g0008a0001c0006t0042g0007 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.164-23500T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69580478 | ||||||
| chr2:69580528
|
A | G | 9 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(6): Show | 9 | HG01243.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-23550T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69580528 | ||||||
| chr2:69580603
|
G | A | 8 | a0001c0001t0021g0278a0001c0007t0021g0276a0001c0007t0021g0279others(5): Show | 8 | HG02280.hp2 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-23625C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69580603 | ||||||
| chr2:69580634
|
G | A | 1 | a0001c0001t0140g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.164-23656C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69580634 | ||||||
| chr2:69580793
|
A | G | 10 | a0002c0002t0003g0199a0002c0002t0003g0227a0002c0002t0003g0238others(7): Show | 10 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.164-23815T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69580793 | ||||||
| chr2:69580995
|
CT | C | 82 | a0001c0001t0002g0125a0001c0001t0004g0206a0001c0001t0004g0216others(79): Show | 82 | HG00099.hp2 HG00544.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.164-24018delA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69580995 | ||||||
| chr2:69581008
|
T | C | 225 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(222): Show | 225 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.164-24030A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69581008 | ||||||
| chr2:69581137
|
G | A | 2 | a0001c0001t0095g0136a0002c0002t0131g0211 | 2 | HG01192.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.164-24159C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69581137 | ||||||
| chr2:69581176
|
C | T | 1 | a0001c0001t0021g0278 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.164-24198G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69581176 | ||||||
| chr2:69581376
|
G | T | 1 | a0002c0002t0005g0253 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.164-24398C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69581376 | ||||||
| chr2:69581451
|
T | C | 1 | a0002c0002t0015g0002 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.164-24473A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69581451 | ||||||
| chr2:69581506
|
C | T | 2 | a0002c0002t0013g0110a0002c0002t0085g0109 | 2 | NA18967.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.164-24528G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69581506 | ||||||
| chr2:69581548
|
C | T | 1 | a0002c0002t0131g0211 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.164-24570G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69581548 | ||||||
| chr2:69581584
|
G | A | 1 | a0001c0001t0008g0013 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.164-24606C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69581584 | ||||||
| chr2:69581666
|
T | C | 4 | a0001c0001t0014g0059a0001c0006t0041g0008a0001c0006t0042g0007others(1): Show | 4 | HG01884.hp2 NA18906.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-24688A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69581666 | ||||||
| chr2:69581736
|
G | A | 2 | a0002c0016t0103g0106a0004c0013t0107g0107 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.164-24758C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69581736 | ||||||
| chr2:69581781
|
G | A | 221 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(218): Show | 221 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.164-24803C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69581781 | ||||||
| chr2:69581797
|
C | A | 1 | a0002c0002t0053g0056 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.164-24819G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69581797 | ||||||
| chr2:69581797
|
C | T | 4 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0104g0292others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-24819G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69581797 | ||||||
| chr2:69581979
|
T | C | 1 | a0001c0006t0016g0061 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.164-25001A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69581979 | ||||||
| chr2:69581979
|
TA | T | 6 | a0001c0007t0021g0276a0001c0007t0021g0279a0001c0007t0034g0270others(3): Show | 6 | HG02809.hp2 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-25002delT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69581979 | ||||||
| chr2:69582000
|
T | C | 9 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(6): Show | 9 | HG01243.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-25022A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69582000 | ||||||
| chr2:69582293
|
T | C | 9 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(6): Show | 9 | HG01243.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-25315A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69582293 | ||||||
| chr2:69582325
|
C | T | 2 | a0001c0001t0089g0122a0001c0001t0112g0170 | 2 | NA18993.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.164-25347G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69582325 | ||||||
| chr2:69582362
|
C | T | 1 | a0002c0002t0111g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.164-25384G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69582362 | ||||||
| chr2:69582373
|
GCGTGTGT others(5): Show |
G | 9 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(6): Show | 9 | HG01243.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-25407_164-2539 others(16): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69582373 | ||||||
| chr2:69582385
|
ACGTGTGT others(5): Show |
A | 1 | a0004c0012t0036g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.164-25419_164-2540 others(16): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69582385 | ||||||
| chr2:69582396
|
T | C | 1 | a0001c0008t0098g0140 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.164-25418A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69582396 | ||||||
| chr2:69582411
|
G | A | 2 | a0001c0006t0041g0008a0001c0006t0042g0007 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.164-25433C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69582411 | ||||||
| chr2:69582454
|
C | T | 1 | a0001c0001t0140g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.164-25476G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69582454 | ||||||
| chr2:69582625
|
T | A | 4 | a0001c0001t0014g0059a0001c0006t0041g0008a0001c0006t0042g0007others(1): Show | 4 | HG01884.hp2 NA18906.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-25647A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69582625 | ||||||
| chr2:69582648
|
G | A | 7 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066others(4): Show | 7 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-25670C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69582648 | ||||||
| chr2:69582649
|
CT | C | 3 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066 | 3 | HG01243.hp1 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.164-25672delA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69582649 | ||||||
| chr2:69582979
|
A | G | 4 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0063g0288others(1): Show | 4 | HG02257.hp1 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-26001T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69582979 | ||||||
| chr2:69583089
|
C | A | 8 | a0001c0001t0021g0278a0001c0007t0021g0276a0001c0007t0021g0279others(5): Show | 8 | HG02280.hp2 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-26111G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69583089 | ||||||
| chr2:69583130
|
C | T | 1 | a0002c0002t0003g0199 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.164-26152G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69583130 | ||||||
| chr2:69583454
|
T | C | 2 | a0001c0001t0014g0059a0001c0009t0141g0191 | 2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.164-26476A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69583454 | ||||||
| chr2:69583480
|
G | A | 1 | a0001c0001t0093g0121 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.164-26502C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69583480 | ||||||
| chr2:69583481
|
C | G | 1 | a0001c0001t0093g0121 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.164-26503G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69583481 | ||||||
| chr2:69583692
|
T | C | 1 | a0001c0001t0007g0101 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.164-26714A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69583692 | ||||||
| chr2:69583729
|
A | T | 8 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0104g0292others(5): Show | 8 | HG00735.hp2 HG02109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-26751T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69583729 | ||||||
| chr2:69583837
|
AT | A | 62 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(59): Show | 62 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(59): Show |
intron_variant | MODIFIER | c.164-26860delA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69583837 | ||||||
| chr2:69584343
|
T | C | 33 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(30): Show | 33 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(30): Show |
intron_variant | MODIFIER | c.164-27365A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69584343 | ||||||
| chr2:69584715
|
C | T | 1 | a0001c0001t0073g0052 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.164-27737G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69584715 | ||||||
| chr2:69584858
|
A | G | 227 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(224): Show | 227 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.164-27880T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69584858 | ||||||
| chr2:69584937
|
C | T | 128 | a0001c0001t0007g0027a0001c0001t0007g0049a0001c0001t0007g0081others(125): Show | 128 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.164-27959G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69584937 | ||||||
| chr2:69585016
|
G | T | 1 | a0001c0004t0010g0148 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.164-28038C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69585016 | ||||||
| chr2:69585047
|
C | A | 1 | a0001c0001t0088g0146 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.164-28069G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69585047 | ||||||
| chr2:69585145
|
C | T | 227 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(224): Show | 227 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.164-28167G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69585145 | ||||||
| chr2:69585292
|
C | T | 3 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0063g0288 | 3 | HG02257.hp1 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.164-28314G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69585292 | ||||||
| chr2:69585464
|
G | C | 1 | a0001c0001t0004g0261 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.164-28486C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69585464 | ||||||
| chr2:69585612
|
C | T | 4 | a0001c0003t0012g0096a0001c0003t0012g0097a0001c0003t0030g0168others(1): Show | 4 | NA18961.hp2 NA18966.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-28634G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69585612 | ||||||
| chr2:69585615
|
C | T | 5 | a0001c0007t0021g0276a0001c0007t0021g0279a0001c0007t0034g0270others(2): Show | 5 | HG02809.hp2 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-28637G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69585615 | ||||||
| chr2:69585617
|
T | C | 3 | a0001c0011t0029g0293a0001c0011t0029g0294a0001c0011t0079g0290 | 3 | HG02486.hp1 HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.164-28639A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69585617 | ||||||
| chr2:69585933
|
T | G | 87 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(84): Show | 87 | HG00544.hp1 HG00597.hp2 HG01243.hp1 others(84): Show |
intron_variant | MODIFIER | c.164-28955A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69585933 | ||||||
| chr2:69586008
|
G | A | 1 | a0001c0006t0028g0134 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.164-29030C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69586008 | ||||||
| chr2:69586102
|
G | A | 8 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0104g0292others(5): Show | 8 | HG00735.hp2 HG02109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-29124C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69586102 | ||||||
| chr2:69586213
|
A | C | 89 | a0001c0001t0007g0027a0001c0001t0007g0049a0001c0001t0008g0022others(86): Show | 89 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.164-29235T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69586213 | ||||||
| chr2:69586326
|
T | C | 18 | a0001c0001t0007g0081a0001c0001t0037g0009a0001c0001t0077g0072others(15): Show | 18 | HG00099.hp2 HG01255.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.164-29348A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69586326 | ||||||
| chr2:69586380
|
A | G | 130 | a0001c0001t0007g0027a0001c0001t0007g0049a0001c0001t0007g0081others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.164-29402T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69586380 | ||||||
| chr2:69586436
|
G | A | 62 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(59): Show | 62 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(59): Show |
intron_variant | MODIFIER | c.164-29458C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69586436 | ||||||
| chr2:69586490
|
C | T | 1 | a0001c0001t0004g0233 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.164-29512G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69586490 | ||||||
| chr2:69586581
|
G | T | 224 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(221): Show | 224 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.164-29603C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69586581 | ||||||
| chr2:69586694
|
G | A | 1 | a0001c0006t0028g0126 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.164-29716C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69586694 | ||||||
| chr2:69586876
|
C | T | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.164-29898G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69586876 | ||||||
| chr2:69586935
|
T | G | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.164-29957A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69586935 | ||||||
| chr2:69587076
|
C | T | 1 | a0002c0002t0001g0040 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.164-30098G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69587076 | ||||||
| chr2:69587079
|
T | A | 1 | a0001c0001t0102g0113 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.164-30101A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69587079 | ||||||
| chr2:69587087
|
A | T | 2 | a0002c0016t0103g0106a0004c0013t0107g0107 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.164-30109T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69587087 | ||||||
| chr2:69587172
|
C | T | 1 | a0002c0002t0013g0144 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.164-30194G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69587172 | ||||||
| chr2:69587207
|
C | G | 6 | a0001c0001t0021g0278a0001c0007t0021g0276a0001c0007t0021g0279others(3): Show | 6 | HG02809.hp2 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-30229G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69587207 | ||||||
| chr2:69587330
|
CAT | C | 12 | a0001c0001t0014g0059a0001c0001t0021g0278a0001c0006t0041g0008others(9): Show | 12 | HG01884.hp2 HG02280.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.164-30354_164-3035 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69587330 | ||||||
| chr2:69587336
|
C | T | 1 | a0002c0002t0001g0046 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.164-30358G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69587336 | ||||||
| chr2:69587340
|
C | T | 1 | a0001c0001t0139g0231 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.164-30362G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69587340 | ||||||
| chr2:69587360
|
TATGCGTG others(23): Show |
T | 1 | a0001c0001t0139g0231 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.164-30412_164-3038 others(34): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69587360 | ||||||
| chr2:69587362
|
T | C | 12 | a0001c0001t0014g0059a0001c0001t0021g0278a0001c0006t0041g0008others(9): Show | 12 | HG01884.hp2 HG02280.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.164-30384A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69587362 | ||||||
| chr2:69587364
|
C | T | 13 | a0001c0001t0014g0059a0001c0001t0021g0278a0001c0001t0032g0172others(10): Show | 13 | HG01884.hp2 HG02280.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.164-30386G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69587364 | ||||||
| chr2:69587382
|
TAC | T | 222 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(219): Show | 222 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.164-30406_164-3040 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69587382 | ||||||
| chr2:69587384
|
C | T | 1 | a0002c0002t0023g0036 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.164-30406G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69587384 | ||||||
| chr2:69587390
|
C | T | 223 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(220): Show | 223 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.164-30412G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69587390 | ||||||
| chr2:69587437
|
A | G | 9 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(6): Show | 9 | HG01243.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-30459T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69587437 | ||||||
| chr2:69587461
|
G | GTATA | 3 | a0001c0001t0045g0287a0001c0001t0057g0291a0004c0013t0043g0284 | 3 | HG02109.hp1 HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.164-30487_164-3048 others(8): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69587461 | ||||||
| chr2:69587461
|
GTA | G | 5 | a0001c0001t0014g0059a0001c0006t0016g0289a0001c0006t0041g0008others(2): Show | 5 | HG00735.hp2 HG01884.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-30485_164-3048 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69587461 | ||||||
| chr2:69587463
|
A | G | 1 | a0001c0001t0011g0201 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.164-30485T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69587463 | ||||||
| chr2:69587473
|
A | AT | 42 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(39): Show | 42 | HG00544.hp1 HG01257.hp1 HG01258.hp1 others(39): Show |
intron_variant | MODIFIER | c.164-30496dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69587473 | ||||||
| chr2:69587473
|
A | T | 1 | a0001c0001t0004g0259 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.164-30495T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69587473 | ||||||
| chr2:69587475
|
A | AT | 19 | a0001c0001t0004g0254a0001c0001t0006g0205a0001c0001t0020g0193others(16): Show | 19 | HG00597.hp2 HG01192.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.164-30498dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69587475 | ||||||
| chr2:69587475
|
A | ATT | 6 | a0001c0007t0021g0276a0001c0007t0021g0279a0001c0007t0034g0270others(3): Show | 6 | HG02280.hp2 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.164-30498_164-3049 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69587475 | ||||||
| chr2:69587475
|
A | T | 63 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(60): Show | 63 | HG00408.hp1 HG00544.hp1 HG01257.hp1 others(60): Show |
intron_variant | MODIFIER | c.164-30497T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69587475 | ||||||
| chr2:69587477
|
A | T | 191 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(188): Show | 191 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.164-30499T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69587477 | ||||||
| chr2:69587552
|
G | A | 1 | a0001c0001t0140g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.164-30574C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69587552 | ||||||
| chr2:69587878
|
T | C | 128 | a0001c0001t0007g0027a0001c0001t0007g0049a0001c0001t0007g0081others(125): Show | 128 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.164-30900A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69587878 | ||||||
| chr2:69587910
|
G | C | 4 | a0001c0001t0014g0059a0001c0006t0041g0008a0001c0006t0042g0007others(1): Show | 4 | HG01884.hp2 NA18906.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-30932C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69587910 | ||||||
| chr2:69588101
|
T | C | 1 | a0004c0012t0036g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.164-31123A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69588101 | ||||||
| chr2:69588136
|
T | C | 4 | a0001c0001t0014g0059a0001c0006t0041g0008a0001c0006t0042g0007others(1): Show | 4 | HG01884.hp2 NA18906.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-31158A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69588136 | ||||||
| chr2:69588411
|
G | A | 9 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(6): Show | 9 | HG01243.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-31433C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69588411 | ||||||
| chr2:69588486
|
T | C | 1 | a0003c0020t0084g0105 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.164-31508A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69588486 | ||||||
| chr2:69588517
|
A | G | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG01243.hp1 others(83): Show |
intron_variant | MODIFIER | c.164-31539T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69588517 | ||||||
| chr2:69588647
|
T | C | 62 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(59): Show | 62 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(59): Show |
intron_variant | MODIFIER | c.164-31669A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69588647 | ||||||
| chr2:69588820
|
A | G | 9 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066others(6): Show | 9 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-31842T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69588820 | ||||||
| chr2:69588897
|
T | C | 1 | a0001c0001t0140g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.164-31919A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69588897 | ||||||
| chr2:69588913
|
AAAAAGGC others(14): Show |
A | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.164-31956_164-3193 others(25): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69588913 | ||||||
| chr2:69589088
|
G | T | 1 | a0001c0001t0031g0176 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.164-32110C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69589088 | ||||||
| chr2:69589095
|
G | T | 62 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(59): Show | 62 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(59): Show |
intron_variant | MODIFIER | c.164-32117C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69589095 | ||||||
| chr2:69589325
|
CAG | C | 63 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(60): Show | 63 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(60): Show |
intron_variant | MODIFIER | c.164-32349_164-3234 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69589325 | ||||||
| chr2:69589336
|
G | C | 1 | a0002c0002t0005g0230 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.164-32358C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69589336 | ||||||
| chr2:69589341
|
A | G | 8 | a0001c0001t0021g0278a0001c0007t0021g0276a0001c0007t0021g0279others(5): Show | 8 | HG02280.hp2 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-32363T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69589341 | ||||||
| chr2:69589390
|
G | A | 8 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0104g0292others(5): Show | 8 | HG00735.hp2 HG02109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-32412C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69589390 | ||||||
| chr2:69589475
|
G | A | 8 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0104g0292others(5): Show | 8 | HG00735.hp2 HG02109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-32497C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69589475 | ||||||
| chr2:69589506
|
C | T | 2 | a0002c0002t0013g0110a0002c0002t0085g0109 | 2 | NA18967.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.164-32528G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69589506 | ||||||
| chr2:69589566
|
G | A | 2 | a0001c0001t0076g0037a0001c0001t0102g0113 | 2 | NA18973.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.164-32588C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69589566 | ||||||
| chr2:69589664
|
G | A | 1 | a0001c0001t0002g0152 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.164-32686C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69589664 | ||||||
| chr2:69589708
|
C | CA | 17 | a0001c0001t0002g0149a0001c0001t0002g0154a0001c0001t0002g0157others(14): Show | 17 | HG01952.hp2 HG02145.hp2 HG02148.hp1 others(14): Show |
intron_variant | MODIFIER | c.164-32731dupT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69589708 | ||||||
| chr2:69589722
|
A | G | 2 | a0001c0006t0041g0008a0001c0006t0042g0007 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.164-32744T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69589722 | ||||||
| chr2:69589726
|
A | G | 67 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(64): Show | 67 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(64): Show |
intron_variant | MODIFIER | c.164-32748T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69589726 | ||||||
| chr2:69589757
|
G | A | 1 | a0002c0002t0001g0025 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.164-32779C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69589757 | ||||||
| chr2:69589974
|
A | T | 9 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(6): Show | 9 | HG01243.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-32996T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69589974 | ||||||
| chr2:69590056
|
G | A | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG01243.hp1 others(83): Show |
intron_variant | MODIFIER | c.164-33078C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69590056 | ||||||
| chr2:69590120
|
G | T | 4 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0063g0288others(1): Show | 4 | HG02257.hp1 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-33142C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69590120 | ||||||
| chr2:69590126
|
AC | A | 3 | a0001c0001t0004g0265a0001c0001t0004g0266a0001c0001t0004g0268 | 3 | NA18954.hp2 NA19005.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.164-33149delG | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69590126 | ||||||
| chr2:69590201
|
C | T | 9 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(6): Show | 9 | HG01243.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-33223G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69590201 | ||||||
| chr2:69590385
|
C | T | 3 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0063g0288 | 3 | HG02257.hp1 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.164-33407G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69590385 | ||||||
| chr2:69590414
|
A | T | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.164-33436T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69590414 | ||||||
| chr2:69590674
|
C | T | 1 | a0002c0002t0013g0112 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.164-33696G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69590674 | ||||||
| chr2:69590860
|
C | G | 8 | a0001c0001t0021g0278a0001c0007t0021g0276a0001c0007t0021g0279others(5): Show | 8 | HG02280.hp2 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-33882G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69590860 | ||||||
| chr2:69590877
|
C | A | 1 | a0002c0002t0005g0253 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.164-33899G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69590877 | ||||||
| chr2:69590878
|
A | C | 1 | a0002c0002t0005g0253 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.164-33900T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69590878 | ||||||
| chr2:69590901
|
T | C | 128 | a0001c0001t0007g0027a0001c0001t0007g0049a0001c0001t0007g0081others(125): Show | 128 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.164-33923A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69590901 | ||||||
| chr2:69590949
|
G | A | 1 | a0001c0001t0138g0209 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.164-33971C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69590949 | ||||||
| chr2:69591173
|
T | C | 1 | a0002c0002t0033g0200 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.164-34195A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69591173 | ||||||
| chr2:69591275
|
G | A | 2 | a0001c0001t0078g0055a0001c0003t0081g0080 | 2 | HG01167.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.164-34297C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69591275 | ||||||
| chr2:69591517
|
C | CT | 11 | a0001c0001t0004g0258a0001c0001t0004g0265a0001c0001t0045g0287others(8): Show | 11 | HG00735.hp2 HG02109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.164-34540dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69591517 | ||||||
| chr2:69591517
|
C | CTT | 58 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(55): Show | 58 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(55): Show |
intron_variant | MODIFIER | c.164-34541_164-3454 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69591517 | ||||||
| chr2:69591522
|
TC | T | 9 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(6): Show | 9 | HG01243.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-34545delG | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69591522 | ||||||
| chr2:69591523
|
C | CT | 86 | a0001c0001t0007g0027a0001c0001t0007g0049a0001c0001t0008g0022others(83): Show | 86 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.164-34546dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69591523 | ||||||
| chr2:69591523
|
C | T | 73 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(70): Show | 73 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.164-34545G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69591523 | ||||||
| chr2:69591552
|
GCTCTGTC others(43): Show |
G | 9 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(6): Show | 9 | HG01243.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-34624_164-3457 others(54): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69591552 | ||||||
| chr2:69591558
|
TCTCCCAG others(43): Show |
T | 3 | a0001c0001t0078g0055a0001c0003t0081g0080a0004c0012t0036g0283 | 3 | HG01167.hp1 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.164-34630_164-3458 others(54): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69591558 | ||||||
| chr2:69591753
|
C | T | 203 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(200): Show | 203 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.164-34775G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69591753 | ||||||
| chr2:69591867
|
C | T | 1 | a0001c0001t0090g0119 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.164-34889G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69591867 | ||||||
| chr2:69591894
|
C | A | 2 | a0001c0001t0014g0059a0001c0009t0141g0191 | 2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.164-34916G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69591894 | ||||||
| chr2:69592010
|
C | A | 1 | a0004c0012t0036g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.164-35032G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69592010 | ||||||
| chr2:69592034
|
A | G | 9 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066others(6): Show | 9 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-35056T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69592034 | ||||||
| chr2:69592154
|
T | C | 3 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0063g0288 | 3 | HG02257.hp1 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.164-35176A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69592154 | ||||||
| chr2:69592238
|
C | T | 83 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(80): Show | 83 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.164-35260G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69592238 | ||||||
| chr2:69592360
|
G | A | 8 | a0001c0001t0021g0278a0001c0007t0021g0276a0001c0007t0021g0279others(5): Show | 8 | HG02280.hp2 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-35382C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69592360 | ||||||
| chr2:69592426
|
C | T | 1 | a0001c0001t0140g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.164-35448G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69592426 | ||||||
| chr2:69592442
|
T | C | 226 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(223): Show | 226 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.164-35464A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69592442 | ||||||
| chr2:69592568
|
T | C | 1 | a0001c0001t0113g0178 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.164-35590A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69592568 | ||||||
| chr2:69592693
|
T | C | 83 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(80): Show | 83 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.164-35715A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69592693 | ||||||
| chr2:69592864
|
G | A | 2 | a0001c0001t0120g0187a0001c0001t0124g0188 | 2 | HG02280.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.164-35886C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69592864 | ||||||
| chr2:69593200
|
A | G | 109 | a0001c0001t0007g0027a0001c0001t0007g0049a0001c0001t0008g0022others(106): Show | 109 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.164-36222T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69593200 | ||||||
| chr2:69593272
|
T | C | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.164-36294A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69593272 | ||||||
| chr2:69593433
|
A | AT | 8 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0104g0292others(5): Show | 8 | HG00735.hp2 HG02109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-36456dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69593433 | ||||||
| chr2:69593546
|
T | C | 52 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(49): Show | 52 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(49): Show |
intron_variant | MODIFIER | c.164-36568A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69593546 | ||||||
| chr2:69593552
|
T | A | 10 | a0002c0002t0001g0029a0002c0002t0001g0034a0002c0002t0001g0042others(7): Show | 10 | HG00544.hp2 HG02080.hp2 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.164-36574A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69593552 | ||||||
| chr2:69593563
|
T | C | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.164-36585A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69593563 | ||||||
| chr2:69593603
|
A | T | 1 | a0002c0002t0023g0026 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.164-36625T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69593603 | ||||||
| chr2:69593876
|
A | C | 17 | a0001c0001t0007g0081a0001c0001t0037g0009a0001c0001t0077g0072others(14): Show | 17 | HG00099.hp2 HG01255.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.164-36898T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69593876 | ||||||
| chr2:69593934
|
G | A | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.164-36956C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69593934 | ||||||
| chr2:69594251
|
A | G | 2 | a0002c0005t0018g0064a0002c0005t0100g0116 | 2 | HG02559.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.164-37273T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69594251 | ||||||
| chr2:69594252
|
A | G | 1 | a0001c0001t0024g0087 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.164-37274T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69594252 | ||||||
| chr2:69594367
|
G | T | 1 | a0001c0004t0067g0077 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.164-37389C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69594367 | ||||||
| chr2:69594384
|
T | C | 62 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(59): Show | 62 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(59): Show |
intron_variant | MODIFIER | c.164-37406A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69594384 | ||||||
| chr2:69594436
|
G | A | 83 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(80): Show | 83 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.164-37458C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69594436 | ||||||
| chr2:69594609
|
C | T | 1 | a0004c0012t0036g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.164-37631G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69594609 | ||||||
| chr2:69594677
|
A | T | 62 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(59): Show | 62 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(59): Show |
intron_variant | MODIFIER | c.164-37699T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69594677 | ||||||
| chr2:69594896
|
A | G | 8 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0104g0292others(5): Show | 8 | HG00735.hp2 HG02109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-37918T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69594896 | ||||||
| chr2:69594909
|
T | C | 9 | a0002c0002t0001g0029a0002c0002t0001g0034a0002c0002t0001g0042others(6): Show | 9 | HG00544.hp2 HG02080.hp2 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-37931A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69594909 | ||||||
| chr2:69595706
|
A | AT | 8 | a0001c0001t0021g0278a0001c0007t0021g0276a0001c0007t0021g0279others(5): Show | 8 | HG02280.hp2 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-38729dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69595706 | ||||||
| chr2:69595712
|
A | G | 4 | a0001c0004t0017g0073a0001c0004t0017g0075a0001c0004t0067g0077others(1): Show | 4 | HG02572.hp1 HG03041.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-38734T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69595712 | ||||||
| chr2:69595799
|
G | A | 8 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0104g0292others(5): Show | 8 | HG00735.hp2 HG02109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-38821C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69595799 | ||||||
| chr2:69595915
|
T | C | 83 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(80): Show | 83 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.164-38937A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69595915 | ||||||
| chr2:69596221
|
C | CT | 79 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(76): Show | 79 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(76): Show |
intron_variant | MODIFIER | c.164-39244dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69596221 | ||||||
| chr2:69596221
|
C | CTTT | 14 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066others(11): Show | 14 | HG00735.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.164-39246_164-3924 others(7): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69596221 | ||||||
| chr2:69596221
|
CT | C | 8 | a0001c0001t0105g0108a0001c0004t0017g0073a0001c0004t0017g0075others(5): Show | 8 | HG02145.hp2 HG02572.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-39244delA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69596221 | ||||||
| chr2:69596253
|
C | T | 62 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(59): Show | 62 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(59): Show |
intron_variant | MODIFIER | c.164-39275G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69596253 | ||||||
| chr2:69596287
|
T | C | 92 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(89): Show | 92 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.164-39309A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69596287 | ||||||
| chr2:69596297
|
T | C | 2 | a0001c0001t0011g0195a0001c0001t0149g0280 | 2 | NA18747.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.164-39319A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69596297 | ||||||
| chr2:69596378
|
C | T | 1 | a0007c0018t0002g0165 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.164-39400G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69596378 | ||||||
| chr2:69596476
|
C | T | 10 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(7): Show | 10 | HG01243.hp2 HG01928.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.164-39498G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69596476 | ||||||
| chr2:69596643
|
A | G | 83 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(80): Show | 83 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.164-39665T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69596643 | ||||||
| chr2:69596770
|
C | A | 8 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0104g0292others(5): Show | 8 | HG00735.hp2 HG02109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-39792G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69596770 | ||||||
| chr2:69596785
|
G | C | 1 | a0001c0001t0008g0082 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.164-39807C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69596785 | ||||||
| chr2:69596821
|
G | A | 9 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066others(6): Show | 9 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-39843C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69596821 | ||||||
| chr2:69596895
|
A | G | 1 | a0001c0001t0002g0125 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.164-39917T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69596895 | ||||||
| chr2:69597005
|
G | A | 1 | a0001c0001t0138g0209 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.164-40027C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69597005 | ||||||
| chr2:69597019
|
G | T | 83 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(80): Show | 83 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.164-40041C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69597019 | ||||||
| chr2:69597073
|
T | C | 2 | a0001c0004t0014g0063a0002c0019t0065g0062 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.164-40095A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69597073 | ||||||
| chr2:69597196
|
CT | C | 83 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(80): Show | 83 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.164-40219delA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69597196 | ||||||
| chr2:69597580
|
C | A | 1 | a0001c0006t0016g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.164-40602G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69597580 | ||||||
| chr2:69597602
|
G | A | 8 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0104g0292others(5): Show | 8 | HG00735.hp2 HG02109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-40624C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69597602 | ||||||
| chr2:69597707
|
CA | C | 110 | a0001c0001t0007g0027a0001c0001t0007g0049a0001c0001t0008g0022others(107): Show | 110 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.164-40730delT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69597707 | ||||||
| chr2:69597707
|
CAA | C | 82 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(79): Show | 82 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.164-40731_164-4073 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69597707 | ||||||
| chr2:69597719
|
A | T | 9 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066others(6): Show | 9 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-40741T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69597719 | ||||||
| chr2:69597720
|
A | T | 9 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066others(6): Show | 9 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-40742T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69597720 | ||||||
| chr2:69597944
|
C | A | 1 | a0001c0009t0141g0191 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.164-40966G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69597944 | ||||||
| chr2:69598115
|
T | G | 1 | a0001c0001t0007g0065 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.164-41137A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69598115 | ||||||
| chr2:69598165
|
C | CA | 83 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(80): Show | 83 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.164-41188dupT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69598165 | ||||||
| chr2:69598496
|
G | T | 83 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(80): Show | 83 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.164-41518C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69598496 | ||||||
| chr2:69598505
|
G | A | 1 | a0002c0002t0111g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.164-41527C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69598505 | ||||||
| chr2:69598670
|
A | C | 1 | a0002c0002t0055g0021 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.164-41692T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69598670 | ||||||
| chr2:69598805
|
G | A | 1 | a0001c0001t0101g0118 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.164-41827C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69598805 | ||||||
| chr2:69598834
|
A | G | 9 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066others(6): Show | 9 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-41856T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69598834 | ||||||
| chr2:69598929
|
T | C | 1 | a0001c0001t0011g0196 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.164-41951A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69598929 | ||||||
| chr2:69599028
|
G | A | 9 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(6): Show | 9 | HG01243.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-42050C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69599028 | ||||||
| chr2:69599060
|
G | C | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.164-42082C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69599060 | ||||||
| chr2:69599063
|
G | A | 83 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(80): Show | 83 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.164-42085C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69599063 | ||||||
| chr2:69599263
|
T | C | 1 | a0001c0001t0057g0291 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.164-42285A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69599263 | ||||||
| chr2:69599305
|
C | T | 2 | a0002c0016t0103g0106a0004c0013t0107g0107 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.164-42327G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69599305 | ||||||
| chr2:69599313
|
T | C | 1 | a0001c0004t0146g0273 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.164-42335A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69599313 | ||||||
| chr2:69599379
|
T | TA | 78 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(75): Show | 78 | HG00544.hp1 HG00597.hp2 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.164-42402dupT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69599379 | ||||||
| chr2:69599379
|
T | TAA | 12 | a0001c0001t0007g0065a0001c0001t0045g0287a0001c0001t0057g0291others(9): Show | 12 | HG00735.hp2 HG02109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.164-42403_164-4240 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69599379 | ||||||
| chr2:69599398
|
AC | A | 85 | a0001c0001t0007g0027a0001c0001t0007g0049a0001c0001t0008g0022others(82): Show | 85 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.164-42421delG | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69599398 | ||||||
| chr2:69599399
|
C | A | 1 | a0002c0002t0015g0003 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.164-42421G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69599399 | ||||||
| chr2:69599400
|
T | A | 87 | a0001c0001t0007g0027a0001c0001t0007g0049a0001c0001t0008g0022others(84): Show | 87 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.164-42422A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69599400 | ||||||
| chr2:69599495
|
G | A | 1 | a0004c0012t0036g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.164-42517C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69599495 | ||||||
| chr2:69599545
|
C | T | 1 | a0001c0001t0014g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.164-42567G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69599545 | ||||||
| chr2:69599618
|
T | C | 83 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(80): Show | 83 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.164-42640A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69599618 | ||||||
| chr2:69599667
|
T | C | 83 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(80): Show | 83 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.164-42689A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69599667 | ||||||
| chr2:69599776
|
GTGTT | G | 5 | a0001c0001t0117g0189a0002c0005t0122g0182a0002c0005t0123g0183others(2): Show | 5 | HG02895.hp2 HG03098.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-42802_164-4279 others(8): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69599776 | ||||||
| chr2:69599944
|
A | AT | 14 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066others(11): Show | 14 | HG01243.hp1 HG02109.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.163+42933dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69599944 | ||||||
| chr2:69599944
|
AT | A | 10 | a0001c0001t0004g0265a0001c0001t0008g0012a0001c0001t0008g0013others(7): Show | 10 | HG01928.hp2 HG01943.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.163+42933delA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69599944 | ||||||
| chr2:69599944
|
ATT | A | 62 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(59): Show | 62 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(59): Show |
intron_variant | MODIFIER | c.163+42932_163+4293 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69599944 | ||||||
| chr2:69600271
|
G | A | 9 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066others(6): Show | 9 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.163+42607C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69600271 | ||||||
| chr2:69600290
|
G | GT | 12 | a0001c0001t0009g0129a0001c0001t0014g0059a0001c0001t0020g0193others(9): Show | 12 | HG02148.hp1 HG03831.hp1 NA18906.hp2 others(9): Show |
intron_variant | MODIFIER | c.163+42587dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69600290 | ||||||
| chr2:69600290
|
GT | G | 69 | a0001c0001t0002g0152a0001c0001t0004g0206a0001c0001t0004g0216others(66): Show | 69 | HG00099.hp2 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.163+42587delA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69600290 | ||||||
| chr2:69600311
|
TAACA | T | 62 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(59): Show | 62 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(59): Show |
intron_variant | MODIFIER | c.163+42563_163+4256 others(8): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69600311 | ||||||
| chr2:69600324
|
G | A | 108 | a0001c0001t0007g0027a0001c0001t0007g0049a0001c0001t0008g0022others(105): Show | 108 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.163+42554C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69600324 | ||||||
| chr2:69600363
|
G | A | 1 | a0001c0001t0004g0264 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.163+42515C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69600363 | ||||||
| chr2:69600608
|
G | C | 9 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066others(6): Show | 9 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.163+42270C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69600608 | ||||||
| chr2:69600883
|
A | G | 62 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(59): Show | 62 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(59): Show |
intron_variant | MODIFIER | c.163+41995T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69600883 | ||||||
| chr2:69600899
|
C | A | 92 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(89): Show | 92 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.163+41979G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69600899 | ||||||
| chr2:69601216
|
G | A | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.163+41662C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69601216 | ||||||
| chr2:69601245
|
C | T | 1 | a0004c0012t0061g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.163+41633G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69601245 | ||||||
| chr2:69601430
|
T | C | 2 | a0001c0006t0041g0008a0001c0006t0042g0007 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.163+41448A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69601430 | ||||||
| chr2:69601499
|
C | G | 52 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(49): Show | 52 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(49): Show |
intron_variant | MODIFIER | c.163+41379G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69601499 | ||||||
| chr2:69601671
|
T | TA | 67 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(64): Show | 67 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(64): Show |
intron_variant | MODIFIER | c.163+41206dupT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69601671 | ||||||
| chr2:69601835
|
A | G | 9 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066others(6): Show | 9 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.163+41043T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69601835 | ||||||
| chr2:69602119
|
A | C | 92 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(89): Show | 92 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.163+40759T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69602119 | ||||||
| chr2:69602324
|
A | G | 8 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0104g0292others(5): Show | 8 | HG00735.hp2 HG02109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.163+40554T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69602324 | ||||||
| chr2:69602433
|
T | A | 1 | a0001c0001t0076g0037 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.163+40445A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69602433 | ||||||
| chr2:69602472
|
A | G | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.163+40406T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69602472 | ||||||
| chr2:69602486
|
T | A | 1 | a0002c0002t0001g0043 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.163+40392A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69602486 | ||||||
| chr2:69602589
|
T | A | 2 | a0001c0001t0014g0059a0001c0009t0141g0191 | 2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.163+40289A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69602589 | ||||||
| chr2:69602659
|
C | A | 1 | a0004c0012t0036g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.163+40219G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69602659 | ||||||
| chr2:69602784
|
T | C | 202 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(199): Show | 202 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.163+40094A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69602784 | ||||||
| chr2:69602848
|
A | C | 62 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(59): Show | 62 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(59): Show |
intron_variant | MODIFIER | c.163+40030T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69602848 | ||||||
| chr2:69602856
|
C | T | 9 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(6): Show | 9 | HG00735.hp2 HG02109.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.163+40022G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69602856 | ||||||
| chr2:69603067
|
T | C | 1 | a0004c0012t0036g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.163+39811A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69603067 | ||||||
| chr2:69603131
|
C | G | 4 | a0001c0006t0016g0289a0001c0011t0029g0293a0001c0011t0029g0294others(1): Show | 4 | HG00735.hp2 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+39747G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69603131 | ||||||
| chr2:69603232
|
C | A | 2 | a0001c0001t0014g0059a0001c0009t0141g0191 | 2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.163+39646G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69603232 | ||||||
| chr2:69603393
|
C | T | 1 | a0001c0001t0137g0247 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.163+39485G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69603393 | ||||||
| chr2:69603740
|
A | AATC | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+39135_163+3913 others(7): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69603740 | ||||||
| chr2:69603795
|
G | A | 2 | a0001c0006t0041g0008a0001c0006t0042g0007 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.163+39083C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69603795 | ||||||
| chr2:69603851
|
G | A | 7 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+39027C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69603851 | ||||||
| chr2:69603930
|
T | A | 1 | a0004c0012t0036g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.163+38948A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69603930 | ||||||
| chr2:69603935
|
G | A | 2 | a0001c0001t0118g0184a0001c0001t0121g0186 | 2 | HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.163+38943C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69603935 | ||||||
| chr2:69604002
|
C | T | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.163+38876G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69604002 | ||||||
| chr2:69604095
|
G | C | 1 | a0002c0002t0039g0004 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.163+38783C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69604095 | ||||||
| chr2:69604170
|
A | G | 10 | a0002c0002t0003g0199a0002c0002t0003g0227a0002c0002t0003g0238others(7): Show | 10 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.163+38708T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69604170 | ||||||
| chr2:69604317
|
G | A | 203 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(200): Show | 203 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.163+38561C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69604317 | ||||||
| chr2:69604414
|
T | C | 2 | a0001c0001t0037g0009a0001c0001t0077g0072 | 2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.163+38464A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69604414 | ||||||
| chr2:69604442
|
C | G | 1 | a0004c0012t0036g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.163+38436G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69604442 | ||||||
| chr2:69604504
|
C | T | 205 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(202): Show | 205 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.163+38374G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69604504 | ||||||
| chr2:69604549
|
G | A | 1 | a0001c0001t0004g0259 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.163+38329C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69604549 | ||||||
| chr2:69604582
|
C | T | 1 | a0002c0002t0003g0215 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.163+38296G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69604582 | ||||||
| chr2:69604600
|
A | G | 225 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(222): Show | 225 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.163+38278T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69604600 | ||||||
| chr2:69604636
|
G | A | 1 | a0001c0003t0012g0097 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.163+38242C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69604636 | ||||||
| chr2:69604690
|
G | C | 11 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(8): Show | 11 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.163+38188C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69604690 | ||||||
| chr2:69604788
|
C | A | 1 | a0001c0003t0012g0096 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.163+38090G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69604788 | ||||||
| chr2:69605060
|
G | A | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+37818C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69605060 | ||||||
| chr2:69605124
|
C | T | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+37754G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69605124 | ||||||
| chr2:69605202
|
C | T | 66 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(63): Show | 66 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(63): Show |
intron_variant | MODIFIER | c.163+37676G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69605202 | ||||||
| chr2:69605210
|
C | T | 1 | a0004c0012t0061g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.163+37668G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69605210 | ||||||
| chr2:69605397
|
TC | T | 4 | a0001c0001t0117g0189a0002c0005t0122g0182a0002c0005t0123g0183others(1): Show | 4 | HG03098.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+37480delG | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69605397 | ||||||
| chr2:69605475
|
C | T | 1 | a0001c0009t0125g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.163+37403G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69605475 | ||||||
| chr2:69605614
|
G | A | 66 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(63): Show | 66 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(63): Show |
intron_variant | MODIFIER | c.163+37264C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69605614 | ||||||
| chr2:69605935
|
T | C | 1 | a0002c0002t0059g0032 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.163+36943A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69605935 | ||||||
| chr2:69606036
|
T | C | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+36842A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69606036 | ||||||
| chr2:69606189
|
C | A | 15 | a0001c0003t0012g0088a0001c0003t0012g0095a0001c0003t0012g0096others(12): Show | 15 | HG02451.hp1 HG02602.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.163+36689G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69606189 | ||||||
| chr2:69606250
|
G | T | 201 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(198): Show | 201 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.163+36628C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69606250 | ||||||
| chr2:69606344
|
C | T | 1 | a0002c0002t0059g0032 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.163+36534G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69606344 | ||||||
| chr2:69606363
|
C | T | 3 | a0001c0001t0007g0081a0001c0004t0071g0074a0007c0017t0066g0076 | 3 | HG01255.hp1 HG02132.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.163+36515G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69606363 | ||||||
| chr2:69606403
|
G | C | 1 | a0004c0012t0061g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.163+36475C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69606403 | ||||||
| chr2:69606408
|
A | G | 1 | a0001c0001t0140g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.163+36470T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69606408 | ||||||
| chr2:69606530
|
T | C | 7 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(4): Show | 7 | HG01243.hp2 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+36348A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69606530 | ||||||
| chr2:69606574
|
G | A | 1 | a0001c0001t0083g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.163+36304C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69606574 | ||||||
| chr2:69606654
|
C | A | 4 | a0001c0001t0014g0059a0001c0009t0035g0190a0001c0009t0125g0179others(1): Show | 4 | HG02280.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+36224G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69606654 | ||||||
| chr2:69607004
|
T | C | 201 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(198): Show | 201 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.163+35874A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69607004 | ||||||
| chr2:69607015
|
G | A | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+35863C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69607015 | ||||||
| chr2:69607046
|
C | CA | 27 | a0001c0001t0007g0081a0001c0001t0008g0082a0001c0001t0032g0172others(24): Show | 27 | HG00099.hp2 HG00438.hp1 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.163+35831dupT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69607046 | ||||||
| chr2:69607046
|
CA | C | 17 | a0001c0003t0012g0088a0001c0003t0012g0095a0001c0003t0012g0096others(14): Show | 17 | HG01074.hp1 HG01952.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.163+35831delT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69607046 | ||||||
| chr2:69607046
|
CAA | C | 9 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066others(6): Show | 9 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.163+35830_163+3583 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69607046 | ||||||
| chr2:69607046
|
CAAAAA | C | 65 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(62): Show | 65 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.163+35827_163+3583 others(9): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69607046 | ||||||
| chr2:69607046
|
CAAAAAA | C | 19 | a0001c0001t0014g0059a0001c0001t0021g0278a0001c0001t0045g0287others(16): Show | 19 | HG01243.hp2 HG01891.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.163+35826_163+3583 others(10): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69607046 | ||||||
| chr2:69607131
|
G | A | 3 | a0001c0011t0029g0293a0001c0011t0029g0294a0001c0011t0079g0290 | 3 | HG02486.hp1 HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.163+35747C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69607131 | ||||||
| chr2:69607151
|
G | A | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+35727C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69607151 | ||||||
| chr2:69607194
|
G | T | 4 | a0001c0001t0014g0059a0001c0009t0035g0190a0001c0009t0125g0179others(1): Show | 4 | HG02280.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+35684C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69607194 | ||||||
| chr2:69607238
|
T | C | 1 | a0001c0001t0078g0055 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.163+35640A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69607238 | ||||||
| chr2:69607257
|
A | T | 1 | a0001c0001t0004g0254 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.163+35621T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69607257 | ||||||
| chr2:69607373
|
G | A | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+35505C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69607373 | ||||||
| chr2:69607395
|
T | C | 3 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066 | 3 | HG01243.hp1 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.163+35483A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69607395 | ||||||
| chr2:69607435
|
G | A | 1 | a0002c0002t0133g0210 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.163+35443C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69607435 | ||||||
| chr2:69607497
|
C | A | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+35381G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69607497 | ||||||
| chr2:69607551
|
C | T | 1 | a0001c0001t0105g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.163+35327G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69607551 | ||||||
| chr2:69607598
|
C | T | 2 | a0001c0001t0078g0055a0002c0002t0001g0051 | 2 | HG01167.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.163+35280G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69607598 | ||||||
| chr2:69607623
|
A | G | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+35255T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69607623 | ||||||
| chr2:69607805
|
T | A | 1 | a0002c0002t0033g0200 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.163+35073A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69607805 | ||||||
| chr2:69607818
|
A | G | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+35060T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69607818 | ||||||
| chr2:69608315
|
T | A | 2 | a0006c0015t0001g0024a0006c0015t0013g0111 | 2 | HG00558.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.163+34563A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69608315 | ||||||
| chr2:69608384
|
A | G | 2 | a0001c0009t0035g0190a0001c0009t0125g0179 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.163+34494T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69608384 | ||||||
| chr2:69608552
|
G | C | 1 | a0001c0001t0136g0212 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.163+34326C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69608552 | ||||||
| chr2:69608634
|
A | G | 3 | a0001c0001t0002g0132a0001c0003t0106g0141a0001c0008t0098g0140 | 3 | HG00438.hp2 HG00558.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.163+34244T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69608634 | ||||||
| chr2:69608847
|
G | A | 1 | a0001c0001t0140g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.163+34031C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69608847 | ||||||
| chr2:69608930
|
T | C | 3 | a0002c0002t0005g0239a0002c0002t0005g0240a0002c0002t0127g0249 | 3 | HG01934.hp1 NA18950.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.163+33948A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69608930 | ||||||
| chr2:69609098
|
A | T | 1 | a0001c0001t0007g0099 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.163+33780T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69609098 | ||||||
| chr2:69609137
|
G | A | 7 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(4): Show | 7 | HG01243.hp2 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+33741C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69609137 | ||||||
| chr2:69609150
|
T | C | 1 | a0001c0003t0012g0097 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.163+33728A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69609150 | ||||||
| chr2:69609216
|
A | G | 1 | a0001c0001t0078g0055 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.163+33662T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69609216 | ||||||
| chr2:69609389
|
T | C | 7 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(4): Show | 7 | HG01243.hp2 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+33489A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69609389 | ||||||
| chr2:69609410
|
G | A | 1 | a0002c0002t0005g0228 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.163+33468C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69609410 | ||||||
| chr2:69609537
|
T | C | 221 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(218): Show | 221 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.163+33341A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69609537 | ||||||
| chr2:69609617
|
T | C | 1 | a0007c0018t0002g0165 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.163+33261A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69609617 | ||||||
| chr2:69609713
|
C | T | 1 | a0002c0002t0059g0032 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.163+33165G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69609713 | ||||||
| chr2:69609788
|
G | A | 1 | a0002c0002t0003g0215 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.163+33090C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69609788 | ||||||
| chr2:69609813
|
G | A | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.163+33065C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69609813 | ||||||
| chr2:69609846
|
G | A | 4 | a0001c0001t0014g0059a0001c0009t0035g0190a0001c0009t0125g0179others(1): Show | 4 | HG02280.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+33032C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69609846 | ||||||
| chr2:69609902
|
T | C | 1 | a0002c0024t0060g0031 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.163+32976A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69609902 | ||||||
| chr2:69609940
|
C | T | 1 | a0001c0009t0035g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.163+32938G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69609940 | ||||||
| chr2:69609942
|
C | T | 3 | a0001c0006t0041g0008a0001c0006t0042g0007a0002c0002t0015g0005 | 3 | HG01884.hp2 NA18993.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.163+32936G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69609942 | ||||||
| chr2:69609975
|
G | A | 1 | a0002c0002t0050g0035 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.163+32903C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69609975 | ||||||
| chr2:69609986
|
CT | C | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+32891delA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69609986 | ||||||
| chr2:69610014
|
G | A | 7 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(4): Show | 7 | HG01243.hp2 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+32864C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69610014 | ||||||
| chr2:69610030
|
G | A | 16 | a0001c0003t0012g0088a0001c0003t0012g0095a0001c0003t0012g0096others(13): Show | 16 | HG01433.hp1 HG02451.hp1 HG02602.hp1 others(13): Show |
intron_variant | MODIFIER | c.163+32848C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69610030 | ||||||
| chr2:69610045
|
T | C | 201 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(198): Show | 201 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.163+32833A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69610045 | ||||||
| chr2:69610050
|
C | CA | 7 | a0001c0001t0056g0058a0001c0001t0102g0113a0001c0001t0140g0269others(4): Show | 7 | HG01243.hp2 HG01928.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+32827dupT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69610050 | ||||||
| chr2:69610050
|
C | CAA | 6 | a0001c0001t0021g0278a0001c0007t0021g0276a0001c0007t0021g0279others(3): Show | 6 | HG02809.hp2 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+32826_163+3282 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69610050 | ||||||
| chr2:69610050
|
CA | C | 15 | a0001c0001t0002g0120a0001c0001t0009g0160a0001c0001t0014g0066others(12): Show | 15 | HG00323.hp1 HG01074.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.163+32827delT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69610050 | ||||||
| chr2:69610050
|
CAA | C | 60 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(57): Show | 60 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(57): Show |
intron_variant | MODIFIER | c.163+32826_163+3282 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69610050 | ||||||
| chr2:69610137
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.163+32741C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69610137 | ||||||
| chr2:69610208
|
T | C | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.163+32670A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69610208 | ||||||
| chr2:69610443
|
G | A | 12 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(9): Show | 12 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.163+32435C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69610443 | ||||||
| chr2:69610562
|
A | G | 32 | a0001c0001t0137g0247a0002c0002t0003g0199a0002c0002t0003g0203others(29): Show | 32 | HG00438.hp1 HG00735.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.163+32316T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69610562 | ||||||
| chr2:69610613
|
A | G | 1 | a0001c0001t0140g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.163+32265T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69610613 | ||||||
| chr2:69610945
|
T | C | 7 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066others(4): Show | 7 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+31933A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69610945 | ||||||
| chr2:69610975
|
A | G | 2 | a0001c0006t0041g0008a0001c0006t0042g0007 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.163+31903T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69610975 | ||||||
| chr2:69610976
|
G | A | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+31902C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69610976 | ||||||
| chr2:69611176
|
A | T | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+31702T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69611176 | ||||||
| chr2:69611207
|
A | G | 1 | a0001c0001t0136g0212 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.163+31671T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69611207 | ||||||
| chr2:69611360
|
G | T | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+31518C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69611360 | ||||||
| chr2:69611410
|
T | C | 1 | a0001c0001t0105g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.163+31468A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69611410 | ||||||
| chr2:69611413
|
A | G | 2 | a0001c0006t0041g0008a0001c0006t0042g0007 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.163+31465T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69611413 | ||||||
| chr2:69611487
|
G | A | 2 | a0002c0005t0123g0183a0002c0005t0150g0281 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.163+31391C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69611487 | ||||||
| chr2:69611653
|
C | G | 12 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(9): Show | 12 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.163+31225G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69611653 | ||||||
| chr2:69611682
|
G | A | 1 | a0001c0001t0078g0055 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.163+31196C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69611682 | ||||||
| chr2:69611762
|
T | C | 1 | a0002c0002t0001g0028 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.163+31116A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69611762 | ||||||
| chr2:69611975
|
G | A | 1 | a0001c0001t0083g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.163+30903C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69611975 | ||||||
| chr2:69612046
|
G | A | 7 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(4): Show | 7 | HG01243.hp2 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+30832C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69612046 | ||||||
| chr2:69612054
|
A | G | 1 | a0001c0001t0004g0206 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.163+30824T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69612054 | ||||||
| chr2:69612169
|
T | C | 11 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(8): Show | 11 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.163+30709A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69612169 | ||||||
| chr2:69612207
|
G | A | 2 | a0002c0002t0003g0242a0002c0002t0129g0241 | 2 | NA18948.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.163+30671C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69612207 | ||||||
| chr2:69612209
|
G | A | 1 | a0002c0002t0132g0236 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.163+30669C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69612209 | ||||||
| chr2:69612386
|
C | T | 11 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(8): Show | 11 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.163+30492G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69612386 | ||||||
| chr2:69612501
|
T | C | 201 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(198): Show | 201 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.163+30377A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69612501 | ||||||
| chr2:69612552
|
T | C | 33 | a0001c0001t0007g0065a0001c0001t0014g0059a0001c0001t0014g0060others(30): Show | 33 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.163+30326A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69612552 | ||||||
| chr2:69612553
|
G | A | 11 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(8): Show | 11 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.163+30325C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69612553 | ||||||
| chr2:69612693
|
T | A | 104 | a0001c0001t0007g0027a0001c0001t0007g0049a0001c0001t0008g0022others(101): Show | 104 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.163+30185A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69612693 | ||||||
| chr2:69613038
|
T | A | 1 | a0001c0001t0032g0175 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.163+29840A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69613038 | ||||||
| chr2:69613039
|
T | C | 29 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066others(26): Show | 29 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.163+29839A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69613039 | ||||||
| chr2:69613115
|
G | T | 4 | a0001c0001t0014g0059a0001c0009t0035g0190a0001c0009t0125g0179others(1): Show | 4 | HG02280.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+29763C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69613115 | ||||||
| chr2:69613243
|
T | C | 29 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066others(26): Show | 29 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.163+29635A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69613243 | ||||||
| chr2:69613568
|
T | A | 1 | a0004c0012t0036g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.163+29310A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69613568 | ||||||
| chr2:69613603
|
A | C | 62 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(59): Show | 62 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(59): Show |
intron_variant | MODIFIER | c.163+29275T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69613603 | ||||||
| chr2:69613731
|
A | G | 1 | a0001c0001t0011g0201 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.163+29147T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69613731 | ||||||
| chr2:69614012
|
G | C | 2 | a0001c0001t0120g0187a0001c0001t0124g0188 | 2 | HG02280.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.163+28866C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69614012 | ||||||
| chr2:69614059
|
G | GA | 11 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(8): Show | 11 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.163+28818dupT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69614059 | ||||||
| chr2:69614125
|
T | A | 1 | a0001c0004t0071g0074 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.163+28753A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69614125 | ||||||
| chr2:69614209
|
T | C | 7 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(4): Show | 7 | HG01243.hp2 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+28669A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69614209 | ||||||
| chr2:69614295
|
G | A | 29 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066others(26): Show | 29 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.163+28583C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69614295 | ||||||
| chr2:69614589
|
T | C | 32 | a0001c0001t0007g0065a0001c0001t0014g0059a0001c0001t0014g0060others(29): Show | 32 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.163+28289A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69614589 | ||||||
| chr2:69614590
|
G | A | 12 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(9): Show | 12 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.163+28288C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69614590 | ||||||
| chr2:69614649
|
C | T | 1 | a0001c0001t0083g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.163+28229G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69614649 | ||||||
| chr2:69614761
|
A | G | 1 | a0001c0004t0017g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.163+28117T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69614761 | ||||||
| chr2:69614781
|
T | C | 2 | a0001c0006t0041g0008a0001c0006t0042g0007 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.163+28097A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69614781 | ||||||
| chr2:69615035
|
G | T | 1 | a0001c0001t0057g0291 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.163+27843C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69615035 | ||||||
| chr2:69615081
|
G | A | 62 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(59): Show | 62 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(59): Show |
intron_variant | MODIFIER | c.163+27797C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69615081 | ||||||
| chr2:69615083
|
G | A | 1 | a0001c0001t0014g0060 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.163+27795C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69615083 | ||||||
| chr2:69615239
|
G | A | 2 | a0001c0006t0041g0008a0001c0006t0042g0007 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.163+27639C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69615239 | ||||||
| chr2:69615246
|
C | T | 2 | a0001c0001t0008g0012a0001c0001t0008g0013 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.163+27632G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69615246 | ||||||
| chr2:69615344
|
T | C | 1 | a0001c0001t0078g0055 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.163+27534A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69615344 | ||||||
| chr2:69615365
|
T | C | 1 | a0001c0001t0057g0291 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.163+27513A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69615365 | ||||||
| chr2:69615615
|
C | G | 4 | a0001c0001t0014g0059a0001c0009t0035g0190a0001c0009t0125g0179others(1): Show | 4 | HG02280.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+27263G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69615615 | ||||||
| chr2:69615688
|
G | A | 33 | a0001c0001t0007g0065a0001c0001t0014g0059a0001c0001t0014g0060others(30): Show | 33 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.163+27190C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69615688 | ||||||
| chr2:69615917
|
C | T | 3 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066 | 3 | HG01243.hp1 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.163+26961G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69615917 | ||||||
| chr2:69616106
|
C | T | 33 | a0001c0001t0007g0065a0001c0001t0014g0059a0001c0001t0014g0060others(30): Show | 33 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.163+26772G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69616106 | ||||||
| chr2:69616392
|
G | A | 1 | a0001c0008t0098g0140 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.163+26486C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69616392 | ||||||
| chr2:69616467
|
AT | A | 12 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(9): Show | 12 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.163+26410delA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69616467 | ||||||
| chr2:69616631
|
C | T | 62 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(59): Show | 62 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(59): Show |
intron_variant | MODIFIER | c.163+26247G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69616631 | ||||||
| chr2:69616639
|
G | A | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+26239C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69616639 | ||||||
| chr2:69616664
|
C | G | 12 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(9): Show | 12 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.163+26214G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69616664 | ||||||
| chr2:69616839
|
A | C | 2 | a0001c0001t0002g0132a0001c0008t0098g0140 | 2 | HG00438.hp2 HG00558.hp1 |
intron_variant | MODIFIER | c.163+26039T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69616839 | ||||||
| chr2:69616930
|
C | T | 9 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066others(6): Show | 9 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.163+25948G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69616930 | ||||||
| chr2:69616948
|
T | C | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.163+25930A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69616948 | ||||||
| chr2:69617067
|
T | C | 1 | a0001c0004t0070g0071 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.163+25811A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69617067 | ||||||
| chr2:69617184
|
C | G | 1 | a0001c0001t0004g0264 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.163+25694G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69617184 | ||||||
| chr2:69617389
|
T | C | 33 | a0001c0001t0007g0065a0001c0001t0014g0059a0001c0001t0014g0060others(30): Show | 33 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.163+25489A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69617389 | ||||||
| chr2:69617392
|
C | T | 168 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(165): Show | 168 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.163+25486G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69617392 | ||||||
| chr2:69617597
|
A | G | 7 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(4): Show | 7 | HG01243.hp2 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+25281T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69617597 | ||||||
| chr2:69617663
|
G | C | 1 | a0002c0002t0023g0036 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.163+25215C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69617663 | ||||||
| chr2:69617736
|
C | T | 2 | a0002c0005t0018g0064a0002c0005t0100g0116 | 2 | HG02559.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.163+25142G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69617736 | ||||||
| chr2:69617740
|
G | T | 16 | a0001c0003t0012g0088a0001c0003t0012g0095a0001c0003t0012g0096others(13): Show | 16 | HG01433.hp1 HG02451.hp1 HG02602.hp1 others(13): Show |
intron_variant | MODIFIER | c.163+25138C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69617740 | ||||||
| chr2:69617839
|
A | G | 1 | a0001c0001t0004g0261 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.163+25039T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69617839 | ||||||
| chr2:69617858
|
C | G | 12 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(9): Show | 12 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.163+25020G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69617858 | ||||||
| chr2:69617930
|
G | A | 19 | a0001c0003t0012g0088a0001c0003t0012g0095a0001c0003t0012g0096others(16): Show | 19 | HG01433.hp1 HG02257.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.163+24948C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69617930 | ||||||
| chr2:69617938
|
T | A | 221 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(218): Show | 221 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.163+24940A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69617938 | ||||||
| chr2:69618158
|
C | G | 4 | a0001c0001t0014g0059a0001c0009t0035g0190a0001c0009t0125g0179others(1): Show | 4 | HG02280.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+24720G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69618158 | ||||||
| chr2:69618192
|
G | A | 1 | a0001c0003t0026g0014 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.163+24686C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69618192 | ||||||
| chr2:69618232
|
G | T | 1 | a0001c0001t0032g0172 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.163+24646C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69618232 | ||||||
| chr2:69618465
|
C | T | 66 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(63): Show | 66 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(63): Show |
intron_variant | MODIFIER | c.163+24413G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69618465 | ||||||
| chr2:69618486
|
C | T | 1 | a0004c0012t0061g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.163+24392G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69618486 | ||||||
| chr2:69618660
|
TAACA | T | 4 | a0001c0001t0014g0059a0001c0009t0035g0190a0001c0009t0125g0179others(1): Show | 4 | HG02280.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+24214_163+2421 others(8): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69618660 | ||||||
| chr2:69618670
|
G | T | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+24208C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69618670 | ||||||
| chr2:69618697
|
C | G | 83 | a0001c0001t0007g0027a0001c0001t0007g0049a0001c0001t0008g0022others(80): Show | 83 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.163+24181G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69618697 | ||||||
| chr2:69618707
|
TCCTA | T | 62 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(59): Show | 62 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(59): Show |
intron_variant | MODIFIER | c.163+24167_163+2417 others(8): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69618707 | ||||||
| chr2:69618882
|
A | C | 7 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(4): Show | 7 | HG01243.hp2 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+23996T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69618882 | ||||||
| chr2:69618977
|
C | T | 1 | a0005c0010t0010g0123 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.163+23901G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69618977 | ||||||
| chr2:69619090
|
T | C | 1 | a0001c0001t0093g0121 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.163+23788A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69619090 | ||||||
| chr2:69619324
|
T | C | 66 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(63): Show | 66 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(63): Show |
intron_variant | MODIFIER | c.163+23554A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69619324 | ||||||
| chr2:69619343
|
C | T | 66 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(63): Show | 66 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(63): Show |
intron_variant | MODIFIER | c.163+23535G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69619343 | ||||||
| chr2:69619378
|
T | C | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+23500A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69619378 | ||||||
| chr2:69619431
|
C | T | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+23447G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69619431 | ||||||
| chr2:69619568
|
A | G | 62 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(59): Show | 62 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(59): Show |
intron_variant | MODIFIER | c.163+23310T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69619568 | ||||||
| chr2:69619600
|
T | C | 1 | a0001c0009t0141g0191 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.163+23278A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69619600 | ||||||
| chr2:69619763
|
C | T | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+23115G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69619763 | ||||||
| chr2:69619808
|
T | C | 1 | a0004c0012t0036g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.163+23070A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69619808 | ||||||
| chr2:69619832
|
G | A | 7 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(4): Show | 7 | HG01243.hp2 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+23046C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69619832 | ||||||
| chr2:69619872
|
G | A | 1 | a0002c0002t0008g0050 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.163+23006C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69619872 | ||||||
| chr2:69619976
|
A | T | 2 | a0001c0003t0022g0010a0001c0003t0064g0085 | 2 | NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.163+22902T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69619976 | ||||||
| chr2:69620123
|
G | C | 1 | a0002c0002t0049g0047 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.163+22755C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69620123 | ||||||
| chr2:69620178
|
A | C | 2 | a0001c0003t0026g0014a0001c0003t0026g0015 | 2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.163+22700T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69620178 | ||||||
| chr2:69620188
|
T | C | 3 | a0002c0002t0062g0054a0002c0002t0154g0297a0002c0002t0155g0298 | 3 | NA18945.hp1 NA18970.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.163+22690A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69620188 | ||||||
| chr2:69620225
|
G | C | 104 | a0001c0001t0007g0027a0001c0001t0007g0049a0001c0001t0008g0022others(101): Show | 104 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.163+22653C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69620225 | ||||||
| chr2:69620321
|
T | C | 1 | a0001c0004t0014g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.163+22557A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69620321 | ||||||
| chr2:69620409
|
A | G | 1 | a0001c0026t0152g0295 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+22469T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69620409 | ||||||
| chr2:69620416
|
C | T | 1 | a0004c0012t0036g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.163+22462G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69620416 | ||||||
| chr2:69620422
|
T | A | 1 | a0002c0002t0003g0203 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.163+22456A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69620422 | ||||||
| chr2:69620539
|
C | G | 1 | a0001c0008t0097g0131 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.163+22339G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69620539 | ||||||
| chr2:69620680
|
G | A | 1 | a0001c0001t0078g0055 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.163+22198C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69620680 | ||||||
| chr2:69620766
|
C | G | 2 | a0001c0009t0035g0190a0001c0009t0125g0179 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.163+22112G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69620766 | ||||||
| chr2:69620818
|
A | T | 1 | a0001c0001t0007g0081 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.163+22060T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69620818 | ||||||
| chr2:69620856
|
C | A | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.163+22022G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69620856 | ||||||
| chr2:69620861
|
T | C | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+22017A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69620861 | ||||||
| chr2:69620879
|
A | G | 7 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(4): Show | 7 | HG01243.hp2 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+21999T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69620879 | ||||||
| chr2:69620920
|
T | C | 1 | a0001c0008t0135g0262 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.163+21958A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69620920 | ||||||
| chr2:69620952
|
T | C | 1 | a0001c0001t0139g0231 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.163+21926A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69620952 | ||||||
| chr2:69621034
|
G | A | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+21844C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69621034 | ||||||
| chr2:69621114
|
G | A | 7 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(4): Show | 7 | HG01243.hp2 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+21764C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69621114 | ||||||
| chr2:69621208
|
G | A | 1 | a0001c0001t0008g0022 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.163+21670C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69621208 | ||||||
| chr2:69621266
|
G | A | 62 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(59): Show | 62 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(59): Show |
intron_variant | MODIFIER | c.163+21612C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69621266 | ||||||
| chr2:69621271
|
T | A | 2 | a0001c0001t0087g0135a0001c0001t0092g0164 | 2 | HG00140.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.163+21607A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69621271 | ||||||
| chr2:69621283
|
T | C | 221 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(218): Show | 221 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.163+21595A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69621283 | ||||||
| chr2:69621335
|
C | T | 1 | a0001c0001t0140g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.163+21543G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69621335 | ||||||
| chr2:69621336
|
G | A | 6 | a0001c0001t0021g0278a0001c0007t0021g0276a0001c0007t0021g0279others(3): Show | 6 | HG02809.hp2 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+21542C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69621336 | ||||||
| chr2:69621338
|
G | A | 9 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066others(6): Show | 9 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.163+21540C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69621338 | ||||||
| chr2:69621408
|
G | A | 1 | a0001c0001t0058g0092 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.163+21470C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69621408 | ||||||
| chr2:69621679
|
A | G | 2 | a0002c0005t0018g0064a0002c0005t0100g0116 | 2 | HG02559.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.163+21199T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69621679 | ||||||
| chr2:69621696
|
G | A | 1 | a0001c0026t0152g0295 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+21182C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69621696 | ||||||
| chr2:69621746
|
T | C | 12 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(9): Show | 12 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.163+21132A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69621746 | ||||||
| chr2:69621858
|
C | T | 1 | a0001c0001t0091g0117 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.163+21020G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69621858 | ||||||
| chr2:69621948
|
C | T | 1 | a0004c0012t0061g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.163+20930G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69621948 | ||||||
| chr2:69621949
|
G | A | 1 | a0002c0002t0001g0057 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.163+20929C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69621949 | ||||||
| chr2:69621953
|
C | T | 74 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(71): Show | 74 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+20925G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69621953 | ||||||
| chr2:69621987
|
T | C | 2 | a0003c0014t0025g0285a0003c0014t0025g0286 | 2 | HG01891.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.163+20891A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69621987 | ||||||
| chr2:69622008
|
G | A | 1 | a0001c0001t0144g0232 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.163+20870C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69622008 | ||||||
| chr2:69622009
|
C | G | 1 | a0001c0001t0144g0232 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.163+20869G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69622009 | ||||||
| chr2:69622081
|
A | G | 11 | a0001c0001t0007g0086a0001c0001t0007g0089a0001c0001t0007g0099others(8): Show | 11 | HG00408.hp2 HG02015.hp2 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.163+20797T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69622081 | ||||||
| chr2:69622092
|
C | T | 1 | a0003c0020t0084g0105 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.163+20786G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69622092 | ||||||
| chr2:69622093
|
G | A | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+20785C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69622093 | ||||||
| chr2:69622244
|
G | T | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+20634C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69622244 | ||||||
| chr2:69622254
|
T | C | 2 | a0001c0001t0076g0037a0001c0001t0102g0113 | 2 | NA18973.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.163+20624A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69622254 | ||||||
| chr2:69622267
|
G | A | 1 | a0002c0016t0134g0272 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.163+20611C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69622267 | ||||||
| chr2:69622268
|
C | T | 1 | a0002c0002t0005g0234 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.163+20610G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69622268 | ||||||
| chr2:69622314
|
C | G | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.163+20564G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69622314 | ||||||
| chr2:69622317
|
T | TC | 13 | a0001c0001t0002g0130a0001c0001t0002g0154a0001c0001t0020g0202others(10): Show | 13 | HG01192.hp1 HG01192.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.163+20560dupG | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69622317 | ||||||
| chr2:69622322
|
C | T | 1 | a0003c0020t0084g0105 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.163+20556G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69622322 | ||||||
| chr2:69622327
|
G | A | 2 | a0001c0006t0041g0008a0001c0006t0042g0007 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.163+20551C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69622327 | ||||||
| chr2:69622348
|
C | G | 7 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(4): Show | 7 | HG01243.hp2 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+20530G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69622348 | ||||||
| chr2:69622366
|
C | T | 1 | a0001c0001t0073g0052 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.163+20512G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69622366 | ||||||
| chr2:69622370
|
A | AC | 6 | a0001c0001t0117g0189a0001c0001t0118g0184a0001c0001t0120g0187others(3): Show | 6 | HG02145.hp2 HG02809.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+20507dupG | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69622370 | ||||||
| chr2:69622380
|
C | T | 11 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(8): Show | 11 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.163+20498G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69622380 | ||||||
| chr2:69622505
|
G | A | 4 | a0001c0001t0014g0059a0001c0009t0035g0190a0001c0009t0125g0179others(1): Show | 4 | HG02280.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+20373C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69622505 | ||||||
| chr2:69622506
|
A | G | 4 | a0001c0001t0014g0059a0001c0009t0035g0190a0001c0009t0125g0179others(1): Show | 4 | HG02280.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+20372T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69622506 | ||||||
| chr2:69622545
|
G | C | 12 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(9): Show | 12 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.163+20333C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69622545 | ||||||
| chr2:69622589
|
C | T | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+20289G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69622589 | ||||||
| chr2:69622611
|
C | A | 52 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(49): Show | 52 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(49): Show |
intron_variant | MODIFIER | c.163+20267G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69622611 | ||||||
| chr2:69622832
|
T | C | 1 | a0001c0004t0002g0137 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.163+20046A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69622832 | ||||||
| chr2:69622838
|
C | T | 2 | a0002c0005t0018g0103a0002c0005t0018g0104 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.163+20040G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69622838 | ||||||
| chr2:69622954
|
A | C | 2 | a0001c0004t0017g0073a0002c0005t0040g0006 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.163+19924T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69622954 | ||||||
| chr2:69622982
|
A | AAG | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+19894_163+1989 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69622982 | ||||||
| chr2:69623042
|
C | T | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+19836G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69623042 | ||||||
| chr2:69623131
|
A | G | 1 | a0001c0001t0031g0174 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.163+19747T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69623131 | ||||||
| chr2:69623133
|
C | T | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+19745G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69623133 | ||||||
| chr2:69623144
|
G | A | 1 | a0001c0001t0011g0201 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.163+19734C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69623144 | ||||||
| chr2:69623242
|
C | T | 4 | a0001c0001t0014g0059a0001c0009t0035g0190a0001c0009t0125g0179others(1): Show | 4 | HG02280.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+19636G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69623242 | ||||||
| chr2:69623276
|
G | A | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+19602C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69623276 | ||||||
| chr2:69623354
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.163+19524G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69623354 | ||||||
| chr2:69623435
|
G | A | 221 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(218): Show | 221 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.163+19443C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69623435 | ||||||
| chr2:69623437
|
T | C | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+19441A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69623437 | ||||||
| chr2:69623445
|
C | T | 6 | a0001c0001t0002g0130a0001c0001t0002g0155a0001c0001t0009g0124others(3): Show | 6 | HG02056.hp1 HG02165.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+19433G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69623445 | ||||||
| chr2:69623489
|
A | T | 1 | a0001c0001t0002g0125 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.163+19389T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69623489 | ||||||
| chr2:69623541
|
G | A | 7 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(4): Show | 7 | HG01243.hp2 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+19337C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69623541 | ||||||
| chr2:69623603
|
C | G | 1 | a0001c0001t0073g0052 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.163+19275G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69623603 | ||||||
| chr2:69623629
|
T | C | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+19249A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69623629 | ||||||
| chr2:69623707
|
A | G | 1 | a0002c0002t0015g0002 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.163+19171T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69623707 | ||||||
| chr2:69623772
|
CT | C | 9 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066others(6): Show | 9 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.163+19105delA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69623772 | ||||||
| chr2:69624032
|
A | C | 1 | a0001c0003t0012g0088 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.163+18846T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69624032 | ||||||
| chr2:69624131
|
G | T | 1 | a0001c0001t0149g0280 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.163+18747C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69624131 | ||||||
| chr2:69624445
|
C | T | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+18433G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69624445 | ||||||
| chr2:69624638
|
C | T | 1 | a0001c0001t0074g0048 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.163+18240G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69624638 | ||||||
| chr2:69624745
|
C | T | 6 | a0001c0001t0008g0084a0001c0001t0009g0160a0001c0001t0091g0117others(3): Show | 6 | HG02976.hp1 HG03098.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+18133G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69624745 | ||||||
| chr2:69624842
|
G | A | 19 | a0001c0003t0012g0088a0001c0003t0012g0095a0001c0003t0012g0096others(16): Show | 19 | HG01433.hp1 HG02257.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.163+18036C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69624842 | ||||||
| chr2:69624886
|
T | C | 17 | a0001c0001t0007g0081a0001c0001t0037g0009a0001c0001t0077g0072others(14): Show | 17 | HG00099.hp2 HG01255.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.163+17992A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69624886 | ||||||
| chr2:69624892
|
G | A | 11 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(8): Show | 11 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.163+17986C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69624892 | ||||||
| chr2:69625325
|
G | A | 4 | a0001c0001t0014g0059a0001c0009t0035g0190a0001c0009t0125g0179others(1): Show | 4 | HG02280.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+17553C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69625325 | ||||||
| chr2:69625361
|
A | C | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+17517T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69625361 | ||||||
| chr2:69625461
|
A | G | 9 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066others(6): Show | 9 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.163+17417T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69625461 | ||||||
| chr2:69625475
|
A | G | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+17403T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69625475 | ||||||
| chr2:69625486
|
C | A | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+17392G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69625486 | ||||||
| chr2:69625496
|
G | C | 1 | a0001c0001t0077g0072 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.163+17382C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69625496 | ||||||
| chr2:69625647
|
C | T | 1 | a0002c0002t0145g0275 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.163+17231G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69625647 | ||||||
| chr2:69626048
|
A | C | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+16830T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69626048 | ||||||
| chr2:69626076
|
T | C | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+16802A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69626076 | ||||||
| chr2:69626185
|
A | G | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+16693T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69626185 | ||||||
| chr2:69626245
|
T | C | 9 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066others(6): Show | 9 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.163+16633A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69626245 | ||||||
| chr2:69626272
|
G | C | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+16606C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69626272 | ||||||
| chr2:69626416
|
T | G | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+16462A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69626416 | ||||||
| chr2:69626431
|
C | T | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+16447G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69626431 | ||||||
| chr2:69626456
|
A | G | 4 | a0001c0001t0014g0059a0001c0009t0035g0190a0001c0009t0125g0179others(1): Show | 4 | HG02280.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+16422T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69626456 | ||||||
| chr2:69626505
|
A | AT | 62 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(59): Show | 62 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(59): Show |
intron_variant | MODIFIER | c.163+16372dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69626505 | ||||||
| chr2:69626505
|
A | T | 1 | a0004c0012t0036g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.163+16373T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69626505 | ||||||
| chr2:69626508
|
A | AT | 21 | a0001c0001t0014g0059a0001c0001t0021g0278a0001c0001t0045g0287others(18): Show | 21 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.163+16369dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69626508 | ||||||
| chr2:69626508
|
A | ATT | 8 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066others(5): Show | 8 | HG01243.hp1 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.163+16368_163+1636 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69626508 | ||||||
| chr2:69626508
|
A | T | 190 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(187): Show | 190 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.163+16370T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69626508 | ||||||
| chr2:69626572
|
T | TCACTGTA others(71): Show |
1 | a0002c0002t0019g0159 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.163+16228_163+1630 others(82): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69626572 | ||||||
| chr2:69626653
|
C | A | 12 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(9): Show | 12 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.163+16225G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69626653 | ||||||
| chr2:69626663
|
C | CT | 14 | a0001c0001t0007g0027a0001c0001t0007g0086a0001c0001t0009g0139others(11): Show | 14 | HG00738.hp2 HG01175.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.163+16214dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69626663 | ||||||
| chr2:69626663
|
C | CTT | 24 | a0001c0001t0004g0261a0001c0001t0014g0059a0001c0001t0021g0278others(21): Show | 24 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.163+16213_163+1621 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69626663 | ||||||
| chr2:69626663
|
C | CTTT | 63 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(60): Show | 63 | HG00544.hp1 HG00597.hp2 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.163+16212_163+1621 others(7): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69626663 | ||||||
| chr2:69626663
|
C | CTTTT | 8 | a0001c0001t0004g0258a0001c0001t0006g0204a0001c0001t0011g0201others(5): Show | 8 | HG01978.hp2 HG02559.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.163+16211_163+1621 others(8): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69626663 | ||||||
| chr2:69626711
|
A | T | 1 | a0001c0001t0027g0128 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.163+16167T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69626711 | ||||||
| chr2:69626736
|
G | A | 1 | a0002c0002t0001g0025 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.163+16142C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69626736 | ||||||
| chr2:69626765
|
G | A | 1 | a0001c0009t0141g0191 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.163+16113C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69626765 | ||||||
| chr2:69626798
|
C | T | 2 | a0002c0005t0018g0103a0002c0005t0018g0104 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.163+16080G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69626798 | ||||||
| chr2:69626855
|
T | G | 2 | a0002c0005t0018g0064a0002c0005t0100g0116 | 2 | HG02559.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.163+16023A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69626855 | ||||||
| chr2:69627117
|
C | T | 1 | a0001c0001t0014g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.163+15761G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69627117 | ||||||
| chr2:69627118
|
G | A | 1 | a0001c0001t0140g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.163+15760C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69627118 | ||||||
| chr2:69627187
|
G | C | 11 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(8): Show | 11 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.163+15691C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69627187 | ||||||
| chr2:69627276
|
G | A | 12 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(9): Show | 12 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.163+15602C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69627276 | ||||||
| chr2:69627296
|
G | GAA | 10 | a0001c0001t0045g0287a0001c0001t0063g0288a0001c0001t0104g0292others(7): Show | 10 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.163+15580_163+1558 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69627296 | ||||||
| chr2:69627296
|
GA | G | 64 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(61): Show | 64 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(61): Show |
intron_variant | MODIFIER | c.163+15581delT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69627296 | ||||||
| chr2:69627778
|
T | C | 1 | a0002c0005t0100g0116 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.163+15100A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69627778 | ||||||
| chr2:69627867
|
A | G | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+15011T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69627867 | ||||||
| chr2:69627962
|
G | C | 104 | a0001c0001t0007g0027a0001c0001t0007g0049a0001c0001t0008g0022others(101): Show | 104 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.163+14916C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69627962 | ||||||
| chr2:69628070
|
G | A | 4 | a0001c0001t0014g0059a0001c0009t0035g0190a0001c0009t0125g0179others(1): Show | 4 | HG02280.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+14808C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69628070 | ||||||
| chr2:69628164
|
G | A | 1 | a0001c0001t0104g0292 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.163+14714C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69628164 | ||||||
| chr2:69628284
|
C | CT | 82 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(79): Show | 82 | HG00544.hp1 HG00597.hp2 HG01243.hp1 others(79): Show |
intron_variant | MODIFIER | c.163+14593dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69628284 | ||||||
| chr2:69628284
|
C | CTT | 12 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(9): Show | 12 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.163+14592_163+1459 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69628284 | ||||||
| chr2:69628472
|
G | A | 2 | a0002c0016t0103g0106a0004c0013t0107g0107 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.163+14406C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69628472 | ||||||
| chr2:69628757
|
T | C | 3 | a0001c0003t0081g0080a0001c0004t0014g0063a0002c0019t0065g0062 | 3 | HG02257.hp2 HG02970.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.163+14121A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69628757 | ||||||
| chr2:69628766
|
A | G | 1 | a0001c0001t0021g0278 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.163+14112T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69628766 | ||||||
| chr2:69629129
|
T | A | 9 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066others(6): Show | 9 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.163+13749A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69629129 | ||||||
| chr2:69629147
|
G | A | 1 | a0001c0001t0078g0055 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.163+13731C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69629147 | ||||||
| chr2:69629165
|
G | C | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.163+13713C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69629165 | ||||||
| chr2:69629248
|
C | G | 3 | a0002c0002t0001g0038a0006c0015t0001g0024a0006c0015t0013g0111 | 3 | HG00558.hp2 NA18983.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.163+13630G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69629248 | ||||||
| chr2:69629302
|
G | A | 1 | a0002c0002t0003g0250 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.163+13576C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69629302 | ||||||
| chr2:69629391
|
G | C | 73 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(70): Show | 73 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(70): Show |
intron_variant | MODIFIER | c.163+13487C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69629391 | ||||||
| chr2:69629503
|
T | C | 7 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(4): Show | 7 | HG01243.hp2 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+13375A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69629503 | ||||||
| chr2:69629601
|
C | T | 95 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+13277G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69629601 | ||||||
| chr2:69629754
|
C | T | 1 | a0002c0002t0038g0001 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.163+13124G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69629754 | ||||||
| chr2:69629769
|
G | A | 1 | a0001c0001t0149g0280 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.163+13109C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69629769 | ||||||
| chr2:69629790
|
A | G | 2 | a0001c0003t0082g0098a0001c0003t0109g0166 | 2 | NA18939.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.163+13088T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69629790 | ||||||
| chr2:69629943
|
G | C | 7 | a0001c0001t0021g0278a0001c0001t0140g0269a0001c0007t0021g0276others(4): Show | 7 | HG01243.hp2 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+12935C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69629943 | ||||||
| chr2:69630016
|
A | C | 1 | a0001c0001t0002g0114 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.163+12862T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69630016 | ||||||
| chr2:69630077
|
G | A | 1 | a0002c0002t0062g0054 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.163+12801C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69630077 | ||||||
| chr2:69630104
|
C | T | 1 | a0003c0020t0084g0105 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.163+12774G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69630104 | ||||||
| chr2:69630243
|
A | C | 1 | a0001c0004t0146g0273 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.163+12635T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69630243 | ||||||
| chr2:69630314
|
G | A | 1 | a0001c0004t0071g0074 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.163+12564C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69630314 | ||||||
| chr2:69630328
|
T | C | 1 | a0004c0012t0061g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.163+12550A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69630328 | ||||||
| chr2:69630338
|
G | GGC | 6 | a0001c0001t0004g0206a0001c0001t0004g0258a0001c0001t0006g0205others(3): Show | 6 | HG01981.hp2 HG02293.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+12539_163+1254 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69630338 | ||||||
| chr2:69630339
|
G | C | 1 | a0001c0001t0004g0216 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.163+12539C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69630339 | ||||||
| chr2:69630339
|
G | GC | 40 | a0001c0001t0004g0254a0001c0001t0004g0259a0001c0001t0004g0264others(37): Show | 40 | HG00597.hp2 HG01243.hp2 HG01258.hp1 others(37): Show |
intron_variant | MODIFIER | c.163+12538_163+1253 others(5): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69630339 | ||||||
| chr2:69630340
|
T | C | 36 | a0001c0001t0004g0221a0001c0001t0004g0233a0001c0001t0004g0257others(33): Show | 36 | HG00544.hp1 HG00735.hp2 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.163+12538A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69630340 | ||||||
| chr2:69630340
|
T | G | 57 | a0001c0001t0002g0150a0001c0001t0004g0206a0001c0001t0004g0216others(54): Show | 57 | HG00597.hp1 HG00597.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.163+12538A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69630340 | ||||||
| chr2:69630340
|
T | TG | 80 | a0001c0001t0002g0125a0001c0001t0002g0155a0001c0001t0007g0027others(77): Show | 80 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.163+12537dupC | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69630340 | ||||||
| chr2:69630340
|
T | TGG | 67 | a0001c0001t0002g0149a0001c0001t0007g0049a0001c0001t0007g0065others(64): Show | 67 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.163+12536_163+1253 others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69630340 | ||||||
| chr2:69630349
|
A | G | 7 | a0001c0001t0004g0261a0001c0003t0012g0088a0002c0002t0033g0200others(4): Show | 7 | HG02602.hp1 HG02698.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+12529T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69630349 | ||||||
| chr2:69630380
|
G | A | 2 | a0003c0014t0025g0285a0003c0014t0025g0286 | 2 | HG01891.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.163+12498C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69630380 | ||||||
| chr2:69630461
|
C | A | 1 | a0001c0001t0004g0216 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.163+12417G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69630461 | ||||||
| chr2:69630462
|
A | C | 1 | a0001c0001t0004g0216 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.163+12416T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69630462 | ||||||
| chr2:69630491
|
A | T | 1 | a0004c0012t0036g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.163+12387T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69630491 | ||||||
| chr2:69630579
|
T | C | 83 | a0001c0001t0007g0027a0001c0001t0007g0049a0001c0001t0008g0022others(80): Show | 83 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.163+12299A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69630579 | ||||||
| chr2:69630617
|
T | A | 1 | a0001c0006t0016g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.163+12261A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69630617 | ||||||
| chr2:69630635
|
T | C | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.163+12243A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69630635 | ||||||
| chr2:69630708
|
A | G | 9 | a0001c0001t0007g0065a0001c0001t0014g0060a0001c0001t0014g0066others(6): Show | 9 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.163+12170T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69630708 | ||||||
| chr2:69630815
|
T | C | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+12063A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69630815 | ||||||
| chr2:69630853
|
A | C | 12 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(9): Show | 12 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.163+12025T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69630853 | ||||||
| chr2:69630953
|
A | G | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+11925T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69630953 | ||||||
| chr2:69631153
|
C | T | 1 | a0001c0001t0078g0055 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.163+11725G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69631153 | ||||||
| chr2:69631311
|
A | T | 2 | a0002c0005t0018g0103a0002c0005t0018g0104 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.163+11567T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69631311 | ||||||
| chr2:69631361
|
T | C | 1 | a0001c0001t0140g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.163+11517A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69631361 | ||||||
| chr2:69631373
|
C | A | 2 | a0002c0016t0103g0106a0004c0013t0107g0107 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.163+11505G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69631373 | ||||||
| chr2:69631911
|
C | T | 1 | a0001c0001t0091g0117 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.163+10967G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69631911 | ||||||
| chr2:69631912
|
G | A | 1 | a0001c0001t0013g0151 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.163+10966C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69631912 | ||||||
| chr2:69631934
|
C | T | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.163+10944G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69631934 | ||||||
| chr2:69632160
|
A | C | 1 | a0001c0001t0004g0216 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.163+10718T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69632160 | ||||||
| chr2:69632161
|
C | A | 64 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(61): Show | 64 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(61): Show |
intron_variant | MODIFIER | c.163+10717G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69632161 | ||||||
| chr2:69632590
|
TTTG | T | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+10285_163+1028 others(7): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69632590 | ||||||
| chr2:69632625
|
G | A | 1 | a0001c0001t0002g0152 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.163+10253C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69632625 | ||||||
| chr2:69632664
|
C | T | 6 | a0001c0001t0116g0185a0001c0001t0118g0184a0001c0001t0120g0187others(3): Show | 6 | HG02280.hp1 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+10214G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69632664 | ||||||
| chr2:69632972
|
G | A | 4 | a0001c0001t0014g0059a0001c0009t0035g0190a0001c0009t0125g0179others(1): Show | 4 | HG02280.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+9906C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69632972 | ||||||
| chr2:69633014
|
C | T | 1 | a0001c0004t0010g0127 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.163+9864G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633014 | ||||||
| chr2:69633042
|
A | T | 11 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(8): Show | 11 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.163+9836T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633042 | ||||||
| chr2:69633043
|
A | T | 63 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(60): Show | 63 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(60): Show |
intron_variant | MODIFIER | c.163+9835T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633043 | ||||||
| chr2:69633044
|
T | A | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+9834A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633044 | ||||||
| chr2:69633049
|
A | T | 1 | a0001c0001t0014g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.163+9829T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633049 | ||||||
| chr2:69633064
|
A | T | 4 | a0001c0001t0004g0216a0001c0003t0081g0080a0001c0004t0014g0063others(1): Show | 4 | HG02257.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+9814T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633064 | ||||||
| chr2:69633099
|
T | C | 10 | a0001c0001t0014g0059a0001c0001t0116g0185a0001c0001t0118g0184others(7): Show | 10 | HG02280.hp1 HG02280.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.163+9779A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633099 | ||||||
| chr2:69633175
|
C | T | 1 | a0002c0002t0052g0023 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.163+9703G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633175 | ||||||
| chr2:69633176
|
G | A | 1 | a0002c0002t0039g0004 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.163+9702C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633176 | ||||||
| chr2:69633177
|
C | T | 11 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(8): Show | 11 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.163+9701G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633177 | ||||||
| chr2:69633217
|
T | TAAAAAAA others(1): Show |
23 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(20): Show | 23 | HG00544.hp1 HG01257.hp1 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.163+9660_163+9661i others(10): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633217 | ||||||
| chr2:69633217
|
T | TAAAAAAA others(2): Show |
8 | a0001c0001t0004g0254a0001c0001t0004g0257a0001c0001t0004g0259others(5): Show | 8 | HG00597.hp2 HG01258.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.163+9660_163+9661i others(11): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633217 | ||||||
| chr2:69633217
|
T | TAAAAAAA others(3): Show |
1 | a0001c0001t0004g0258 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.163+9660_163+9661i others(12): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633217 | ||||||
| chr2:69633218
|
C | A | 33 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(30): Show | 33 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(30): Show |
intron_variant | MODIFIER | c.163+9660G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633218 | ||||||
| chr2:69633218
|
C | CA | 82 | a0001c0001t0007g0027a0001c0001t0007g0049a0001c0001t0008g0022others(79): Show | 82 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.163+9659dupT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633218 | ||||||
| chr2:69633218
|
C | CAAAAAAA | 16 | a0001c0001t0021g0278a0001c0001t0045g0287a0001c0001t0057g0291others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.163+9653_163+9659d others(9): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633218 | ||||||
| chr2:69633218
|
C | CAAAAAAA others(1): Show |
30 | a0001c0001t0004g0261a0001c0001t0011g0192a0001c0001t0011g0195others(27): Show | 30 | HG00735.hp2 HG01243.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.163+9652_163+9659d others(10): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633218 | ||||||
| chr2:69633465
|
G | A | 1 | a0001c0001t0074g0048 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.163+9413C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633465 | ||||||
| chr2:69633472
|
G | A | 1 | a0004c0012t0036g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.163+9406C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633472 | ||||||
| chr2:69633493
|
T | C | 221 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(218): Show | 221 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.163+9385A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633493 | ||||||
| chr2:69633545
|
G | T | 4 | a0001c0006t0016g0289a0001c0011t0029g0293a0001c0011t0029g0294others(1): Show | 4 | HG00735.hp2 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+9333C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633545 | ||||||
| chr2:69633547
|
G | T | 1 | a0001c0001t0136g0212 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.163+9331C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633547 | ||||||
| chr2:69633599
|
C | CA | 8 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0037g0009others(5): Show | 8 | HG01106.hp1 HG01361.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.163+9278dupT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633599 | ||||||
| chr2:69633599
|
CA | C | 108 | a0001c0001t0007g0027a0001c0001t0007g0065a0001c0001t0008g0022others(105): Show | 108 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.163+9278delT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633599 | ||||||
| chr2:69633599
|
CAA | C | 7 | a0001c0001t0004g0206a0001c0001t0004g0259a0001c0001t0004g0261others(4): Show | 7 | HG01258.hp1 HG01884.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+9277_163+9278d others(4): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633599 | ||||||
| chr2:69633599
|
CAAA | C | 81 | a0001c0001t0004g0216a0001c0001t0004g0221a0001c0001t0004g0233others(78): Show | 81 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.163+9276_163+9278d others(5): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633599 | ||||||
| chr2:69633768
|
A | G | 2 | a0002c0005t0018g0064a0002c0005t0100g0116 | 2 | HG02559.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.163+9110T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633768 | ||||||
| chr2:69633828
|
G | A | 2 | a0002c0005t0018g0103a0002c0005t0018g0104 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.163+9050C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633828 | ||||||
| chr2:69633917
|
C | T | 2 | a0001c0006t0041g0008a0001c0006t0042g0007 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.163+8961G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633917 | ||||||
| chr2:69633987
|
T | C | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+8891A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69633987 | ||||||
| chr2:69634149
|
G | A | 1 | a0001c0001t0007g0081 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.163+8729C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69634149 | ||||||
| chr2:69634175
|
T | C | 3 | a0002c0002t0005g0252a0002c0002t0005g0253a0002c0002t0145g0275 | 3 | HG01099.hp2 NA18939.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.163+8703A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69634175 | ||||||
| chr2:69634177
|
TA | T | 83 | a0001c0001t0007g0027a0001c0001t0007g0049a0001c0001t0008g0022others(80): Show | 83 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.163+8700delT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69634177 | ||||||
| chr2:69634223
|
C | T | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.163+8655G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69634223 | ||||||
| chr2:69634235
|
T | G | 11 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(8): Show | 11 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.163+8643A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69634235 | ||||||
| chr2:69634270
|
C | T | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+8608G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69634270 | ||||||
| chr2:69634285
|
T | C | 1 | a0002c0002t0033g0200 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.163+8593A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69634285 | ||||||
| chr2:69634544
|
G | C | 10 | a0001c0001t0014g0059a0001c0001t0116g0185a0001c0001t0118g0184others(7): Show | 10 | HG02280.hp1 HG02280.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.163+8334C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69634544 | ||||||
| chr2:69634611
|
A | C | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+8267T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69634611 | ||||||
| chr2:69634709
|
G | GAA | 104 | a0001c0001t0007g0027a0001c0001t0007g0049a0001c0001t0008g0022others(101): Show | 104 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.163+8167_163+8168d others(4): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69634709 | ||||||
| chr2:69634825
|
GTA | G | 11 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(8): Show | 11 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.163+8051_163+8052d others(4): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69634825 | ||||||
| chr2:69634829
|
A | C | 11 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(8): Show | 11 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.163+8049T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69634829 | ||||||
| chr2:69634886
|
A | G | 1 | a0001c0001t0008g0022 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.163+7992T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69634886 | ||||||
| chr2:69634904
|
T | C | 1 | a0002c0002t0008g0050 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.163+7974A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69634904 | ||||||
| chr2:69634959
|
G | A | 1 | a0001c0003t0082g0098 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.163+7919C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69634959 | ||||||
| chr2:69635057
|
A | G | 1 | a0002c0002t0001g0028 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.163+7821T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69635057 | ||||||
| chr2:69635069
|
A | T | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+7809T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69635069 | ||||||
| chr2:69635200
|
G | T | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+7678C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69635200 | ||||||
| chr2:69635337
|
T | TGTTGATG others(3): Show |
1 | a0001c0003t0030g0169 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.163+7531_163+7540d others(12): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69635337 | ||||||
| chr2:69635491
|
C | T | 1 | a0001c0001t0007g0027 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.163+7387G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69635491 | ||||||
| chr2:69635558
|
T | C | 1 | a0001c0001t0009g0124 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.163+7320A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69635558 | ||||||
| chr2:69635655
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.163+7223C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69635655 | ||||||
| chr2:69635762
|
C | T | 221 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(218): Show | 221 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.163+7116G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69635762 | ||||||
| chr2:69635812
|
T | C | 1 | a0001c0001t0078g0055 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.163+7066A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69635812 | ||||||
| chr2:69635902
|
C | T | 1 | a0001c0001t0139g0231 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.163+6976G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69635902 | ||||||
| chr2:69635945
|
G | A | 1 | a0001c0001t0002g0157 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.163+6933C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69635945 | ||||||
| chr2:69636201
|
T | TA | 13 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(10): Show | 13 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.163+6676dupT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69636201 | ||||||
| chr2:69636225
|
TA | T | 10 | a0001c0001t0014g0059a0001c0001t0116g0185a0001c0001t0118g0184others(7): Show | 10 | HG02280.hp1 HG02280.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.163+6652delT | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69636225 | ||||||
| chr2:69636266
|
T | C | 53 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(50): Show | 53 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.163+6612A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69636266 | ||||||
| chr2:69636291
|
A | G | 221 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(218): Show | 221 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.163+6587T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69636291 | ||||||
| chr2:69636679
|
T | G | 2 | a0001c0006t0041g0008a0001c0006t0042g0007 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.163+6199A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69636679 | ||||||
| chr2:69636697
|
T | G | 2 | a0001c0001t0014g0060a0001c0001t0014g0066 | 2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.163+6181A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69636697 | ||||||
| chr2:69636705
|
C | CT | 73 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(70): Show | 73 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(70): Show |
intron_variant | MODIFIER | c.163+6172dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69636705 | ||||||
| chr2:69636784
|
C | T | 1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.163+6094G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69636784 | ||||||
| chr2:69636802
|
C | A | 1 | a0001c0001t0007g0081 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.163+6076G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69636802 | ||||||
| chr2:69636803
|
G | A | 12 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(9): Show | 12 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.163+6075C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69636803 | ||||||
| chr2:69636845
|
A | G | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+6033T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69636845 | ||||||
| chr2:69636846
|
G | C | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+6032C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69636846 | ||||||
| chr2:69637104
|
C | A | 104 | a0001c0001t0007g0027a0001c0001t0007g0049a0001c0001t0008g0022others(101): Show | 104 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.163+5774G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69637104 | ||||||
| chr2:69637127
|
G | A | 6 | a0001c0001t0116g0185a0001c0001t0118g0184a0001c0001t0120g0187others(3): Show | 6 | HG02280.hp1 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+5751C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69637127 | ||||||
| chr2:69637186
|
T | C | 2 | a0002c0016t0103g0106a0004c0013t0107g0107 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.163+5692A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69637186 | ||||||
| chr2:69637243
|
TTCCCTGA others(59): Show |
T | 1 | a0001c0001t0149g0280 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.163+5569_163+5634d others(68): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69637243 | ||||||
| chr2:69637316
|
G | A | 1 | a0001c0001t0002g0158 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.163+5562C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69637316 | ||||||
| chr2:69637326
|
C | T | 63 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(60): Show | 63 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(60): Show |
intron_variant | MODIFIER | c.163+5552G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69637326 | ||||||
| chr2:69637537
|
C | T | 1 | a0001c0026t0152g0295 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+5341G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69637537 | ||||||
| chr2:69637555
|
A | G | 1 | a0001c0001t0096g0162 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.163+5323T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69637555 | ||||||
| chr2:69637704
|
T | G | 1 | a0001c0001t0056g0058 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.163+5174A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69637704 | ||||||
| chr2:69637777
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.163+5101C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69637777 | ||||||
| chr2:69637955
|
A | G | 6 | a0001c0001t0116g0185a0001c0001t0118g0184a0001c0001t0120g0187others(3): Show | 6 | HG02280.hp1 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+4923T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69637955 | ||||||
| chr2:69638048
|
C | G | 2 | a0002c0002t0154g0297a0002c0002t0155g0298 | 2 | NA18970.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.163+4830G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69638048 | ||||||
| chr2:69638159
|
T | C | 10 | a0001c0001t0021g0278a0001c0001t0117g0189a0001c0007t0021g0276others(7): Show | 10 | HG02809.hp2 HG02896.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.163+4719A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69638159 | ||||||
| chr2:69638224
|
A | G | 5 | a0001c0001t0075g0020a0002c0002t0001g0019a0002c0002t0007g0018others(2): Show | 5 | NA18954.hp1 NA18967.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+4654T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69638224 | ||||||
| chr2:69638406
|
C | T | 7 | a0001c0003t0012g0095a0001c0003t0012g0096a0001c0003t0012g0097others(4): Show | 7 | NA18961.hp2 NA18966.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+4472G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69638406 | ||||||
| chr2:69638433
|
C | T | 10 | a0001c0001t0014g0059a0001c0001t0116g0185a0001c0001t0118g0184others(7): Show | 10 | HG02280.hp1 HG02280.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.163+4445G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69638433 | ||||||
| chr2:69638626
|
G | C | 70 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(67): Show | 70 | HG00544.hp1 HG00597.hp2 HG01243.hp2 others(67): Show |
intron_variant | MODIFIER | c.163+4252C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69638626 | ||||||
| chr2:69638626
|
G | T | 4 | a0001c0001t0020g0193a0001c0001t0020g0202a0001c0001t0020g0208others(1): Show | 4 | NA18956.hp1 NA18963.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+4252C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69638626 | ||||||
| chr2:69638674
|
C | A | 1 | a0002c0002t0015g0003 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.163+4204G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69638674 | ||||||
| chr2:69638687
|
A | G | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+4191T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69638687 | ||||||
| chr2:69638733
|
ATCTGCTG others(7): Show |
A | 1 | a0003c0020t0084g0105 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.163+4131_163+4144d others(16): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69638733 | ||||||
| chr2:69638801
|
T | C | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+4077A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69638801 | ||||||
| chr2:69638885
|
G | A | 1 | a0001c0001t0056g0058 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.163+3993C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69638885 | ||||||
| chr2:69638896
|
GGCCTGTG others(41): Show |
G | 1 | a0001c0003t0030g0169 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.163+3934_163+3981d others(50): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69638896 | ||||||
| chr2:69638900
|
T | C | 1 | a0002c0002t0019g0159 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.163+3978A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69638900 | ||||||
| chr2:69638910
|
T | C | 86 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(83): Show | 86 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.163+3968A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69638910 | ||||||
| chr2:69638960
|
G | A | 4 | a0001c0001t0020g0193a0001c0001t0020g0202a0001c0001t0020g0208others(1): Show | 4 | NA18956.hp1 NA18963.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+3918C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69638960 | ||||||
| chr2:69638982
|
A | AGTTTGCT others(32): Show |
1 | a0001c0003t0030g0169 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.163+3895_163+3896i others(41): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69638982 | ||||||
| chr2:69638983
|
C | T | 1 | a0001c0003t0030g0169 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.163+3895G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69638983 | ||||||
| chr2:69638984
|
C | A | 1 | a0001c0003t0030g0169 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.163+3894G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69638984 | ||||||
| chr2:69638986
|
A | G | 1 | a0001c0003t0030g0169 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.163+3892T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69638986 | ||||||
| chr2:69638988
|
A | C | 1 | a0001c0003t0030g0169 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.163+3890T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69638988 | ||||||
| chr2:69638991
|
T | C | 1 | a0001c0003t0030g0169 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.163+3887A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69638991 | ||||||
| chr2:69638995
|
G | T | 1 | a0001c0003t0030g0169 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.163+3883C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69638995 | ||||||
| chr2:69639001
|
T | G | 1 | a0001c0003t0030g0169 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.163+3877A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69639001 | ||||||
| chr2:69639235
|
T | G | 1 | a0001c0001t0056g0058 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.163+3643A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69639235 | ||||||
| chr2:69639540
|
C | A | 1 | a0002c0002t0039g0004 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.163+3338G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69639540 | ||||||
| chr2:69639637
|
T | A | 101 | a0001c0001t0007g0027a0001c0001t0007g0049a0001c0001t0008g0022others(98): Show | 101 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.163+3241A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69639637 | ||||||
| chr2:69639637
|
T | C | 123 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(120): Show | 123 | HG00099.hp2 HG00544.hp1 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.163+3241A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69639637 | ||||||
| chr2:69639652
|
C | A | 11 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(8): Show | 11 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.163+3226G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69639652 | ||||||
| chr2:69639759
|
T | C | 1 | a0001c0006t0016g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.163+3119A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69639759 | ||||||
| chr2:69639807
|
A | G | 118 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(115): Show | 118 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.163+3071T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69639807 | ||||||
| chr2:69639842
|
G | A | 1 | a0001c0001t0096g0162 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.163+3036C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69639842 | ||||||
| chr2:69640014
|
A | AAC | 26 | a0001c0001t0002g0120a0001c0001t0002g0125a0001c0001t0004g0254others(23): Show | 26 | HG00597.hp2 HG00735.hp1 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.163+2862_163+2863d others(4): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640014 | ||||||
| chr2:69640014
|
A | AACAC | 26 | a0001c0001t0004g0233a0001c0001t0008g0012a0001c0001t0008g0013others(23): Show | 26 | HG00438.hp1 HG00738.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.163+2860_163+2863d others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640014 | ||||||
| chr2:69640014
|
A | AACACAC | 29 | a0001c0001t0004g0216a0001c0001t0004g0221a0001c0001t0006g0213others(26): Show | 29 | HG00544.hp1 HG01358.hp2 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.163+2858_163+2863d others(8): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640014 | ||||||
| chr2:69640014
|
A | AACACACA others(1): Show |
10 | a0001c0001t0004g0206a0001c0001t0006g0205a0001c0001t0006g0207others(7): Show | 10 | HG01257.hp1 HG01258.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.163+2856_163+2863d others(10): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640014 | ||||||
| chr2:69640014
|
A | AACACACA others(3): Show |
1 | a0001c0001t0006g0204 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.163+2854_163+2863d others(12): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640014 | ||||||
| chr2:69640014
|
A | AACACACA others(5): Show |
2 | a0001c0001t0020g0202a0002c0002t0003g0203 | 2 | HG02135.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.163+2852_163+2863d others(14): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640014 | ||||||
| chr2:69640014
|
AAC | A | 11 | a0001c0001t0007g0065a0001c0001t0014g0066a0001c0001t0073g0052others(8): Show | 11 | HG01192.hp2 HG01255.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.163+2862_163+2863d others(4): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640014 | ||||||
| chr2:69640014
|
AACAC | A | 4 | a0001c0001t0092g0164a0001c0003t0046g0100a0003c0020t0084g0105others(1): Show | 4 | HG01361.hp1 HG01433.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+2860_163+2863d others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640014 | ||||||
| chr2:69640043
|
ACACACAC others(5): Show |
A | 1 | a0001c0001t0007g0081 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.163+2823_163+2834d others(14): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640043 | ||||||
| chr2:69640047
|
A | T | 2 | a0001c0001t0007g0089a0001c0003t0109g0166 | 2 | HG02015.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.163+2831T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640047 | ||||||
| chr2:69640047
|
ACACACAC others(1): Show |
A | 11 | a0001c0001t0037g0009a0001c0003t0081g0080a0001c0004t0017g0073others(8): Show | 11 | HG02132.hp2 HG02145.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.163+2823_163+2830d others(10): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640047 | ||||||
| chr2:69640049
|
A | ACT | 5 | a0001c0001t0008g0084a0001c0003t0022g0010a0001c0003t0064g0085others(2): Show | 5 | HG03098.hp1 HG03540.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+2828_163+2829i others(4): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640049 | ||||||
| chr2:69640049
|
A | ACTCTCTC others(15): Show |
1 | a0003c0021t0151g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.163+2828_163+2829i others(24): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640049 | ||||||
| chr2:69640049
|
A | T | 23 | a0001c0001t0007g0086a0001c0001t0007g0089a0001c0001t0007g0101others(20): Show | 23 | HG00408.hp2 HG02015.hp2 HG02040.hp1 others(20): Show |
intron_variant | MODIFIER | c.163+2829T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640049 | ||||||
| chr2:69640049
|
ACACACT | A | 5 | a0001c0001t0077g0072a0001c0004t0070g0071a0001c0006t0041g0008others(2): Show | 5 | HG00099.hp2 HG01884.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.163+2823_163+2828d others(8): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640049 | ||||||
| chr2:69640051
|
A | ACT | 40 | a0001c0001t0007g0027a0001c0001t0007g0049a0001c0001t0056g0058others(37): Show | 40 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.163+2826_163+2827i others(4): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640051 | ||||||
| chr2:69640051
|
A | T | 34 | a0001c0001t0007g0086a0001c0001t0007g0089a0001c0001t0007g0099others(31): Show | 34 | HG00408.hp2 HG01243.hp1 HG01928.hp2 others(31): Show |
intron_variant | MODIFIER | c.163+2827T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640051 | ||||||
| chr2:69640053
|
A | ACACACAC others(5): Show |
1 | a0002c0016t0134g0272 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.163+2824_163+2825i others(14): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640053 | ||||||
| chr2:69640053
|
A | ACACACTC others(3): Show |
2 | a0001c0001t0116g0185a0001c0001t0121g0186 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.163+2824_163+2825i others(12): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640053 | ||||||
| chr2:69640053
|
A | ACACACTC others(5): Show |
2 | a0001c0001t0118g0184a0003c0014t0025g0286 | 2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.163+2824_163+2825i others(14): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640053 | ||||||
| chr2:69640053
|
A | ACACACTC others(7): Show |
1 | a0003c0014t0025g0285 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.163+2824_163+2825i others(16): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640053 | ||||||
| chr2:69640053
|
A | ACACTCT | 4 | a0001c0001t0002g0114a0001c0001t0104g0292a0001c0001t0120g0187others(1): Show | 4 | HG01884.hp1 HG02280.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+2824_163+2825i others(8): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640053 | ||||||
| chr2:69640053
|
A | ACTCT | 10 | a0001c0001t0008g0022a0001c0001t0014g0059a0001c0006t0016g0289others(7): Show | 10 | HG00558.hp2 HG00735.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.163+2821_163+2824d others(6): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640053 | ||||||
| chr2:69640053
|
A | ACTCTCT | 3 | a0001c0001t0045g0287a0001c0001t0063g0288a0004c0013t0043g0284 | 3 | HG02109.hp1 HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.163+2819_163+2824d others(8): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640053 | ||||||
| chr2:69640053
|
A | T | 85 | a0001c0001t0007g0027a0001c0001t0007g0049a0001c0001t0007g0065others(82): Show | 85 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.163+2825T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640053 | ||||||
| chr2:69640055
|
T | A | 82 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(79): Show | 82 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.163+2823A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640055 | ||||||
| chr2:69640057
|
T | A | 8 | a0001c0001t0004g0264a0001c0001t0004g0265a0001c0001t0004g0266others(5): Show | 8 | HG00735.hp1 HG02040.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.163+2821A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640057 | ||||||
| chr2:69640059
|
T | A | 5 | a0001c0001t0004g0264a0001c0001t0004g0265a0001c0001t0004g0266others(2): Show | 5 | HG02083.hp1 NA18954.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.163+2819A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640059 | ||||||
| chr2:69640079
|
T | C | 1 | a0001c0003t0046g0100 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.163+2799A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640079 | ||||||
| chr2:69640079
|
T | TC | 17 | a0001c0001t0007g0089a0001c0001t0007g0099a0001c0001t0024g0090others(14): Show | 17 | HG02015.hp2 HG02040.hp1 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.163+2798dupG | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640079 | ||||||
| chr2:69640081
|
C | T | 115 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(112): Show | 115 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.163+2797G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640081 | ||||||
| chr2:69640302
|
TCCA | T | 12 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(9): Show | 12 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.163+2573_163+2575d others(5): Show |
AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640302 | ||||||
| chr2:69640313
|
C | T | 3 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0105g0108 | 3 | HG02257.hp1 HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.163+2565G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640313 | ||||||
| chr2:69640396
|
C | T | 5 | a0001c0001t0075g0020a0002c0002t0001g0019a0002c0002t0007g0018others(2): Show | 5 | NA18954.hp1 NA18967.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+2482G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640396 | ||||||
| chr2:69640481
|
G | A | 1 | a0001c0001t0056g0058 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.163+2397C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640481 | ||||||
| chr2:69640481
|
G | GT | 117 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(114): Show | 117 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.163+2396dupA | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640481 | ||||||
| chr2:69640552
|
A | T | 117 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(114): Show | 117 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.163+2326T>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640552 | ||||||
| chr2:69640703
|
G | A | 12 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(9): Show | 12 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.163+2175C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640703 | ||||||
| chr2:69640739
|
C | T | 200 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(197): Show | 200 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.163+2139G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640739 | ||||||
| chr2:69640844
|
C | G | 1 | a0001c0001t0008g0082 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.163+2034G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640844 | ||||||
| chr2:69640905
|
A | C | 1 | a0001c0006t0016g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.163+1973T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640905 | ||||||
| chr2:69640933
|
T | G | 1 | a0001c0001t0007g0101 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.163+1945A>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69640933 | ||||||
| chr2:69641146
|
T | C | 117 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(114): Show | 117 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.163+1732A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69641146 | ||||||
| chr2:69641171
|
C | T | 2 | a0002c0016t0103g0106a0004c0013t0107g0107 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.163+1707G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69641171 | ||||||
| chr2:69641226
|
G | A | 28 | a0001c0001t0007g0086a0001c0001t0007g0089a0001c0001t0007g0099others(25): Show | 28 | HG00408.hp2 HG02015.hp2 HG02040.hp1 others(25): Show |
intron_variant | MODIFIER | c.163+1652C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69641226 | ||||||
| chr2:69641283
|
T | C | 1 | a0001c0001t0149g0280 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.163+1595A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69641283 | ||||||
| chr2:69641340
|
T | A | 6 | a0001c0001t0116g0185a0001c0001t0118g0184a0001c0001t0120g0187others(3): Show | 6 | HG02280.hp1 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+1538A>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69641340 | ||||||
| chr2:69641394
|
C | A | 117 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(114): Show | 117 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.163+1484G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69641394 | ||||||
| chr2:69641450
|
A | G | 1 | a0001c0001t0083g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.163+1428T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69641450 | ||||||
| chr2:69641477
|
C | G | 2 | a0001c0003t0026g0014a0001c0003t0026g0015 | 2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.163+1401G>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69641477 | ||||||
| chr2:69641583
|
A | G | 117 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(114): Show | 117 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.163+1295T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69641583 | ||||||
| chr2:69641700
|
T | C | 1 | a0001c0008t0069g0102 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.163+1178A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69641700 | ||||||
| chr2:69641799
|
G | C | 2 | a0002c0005t0018g0103a0002c0005t0018g0104 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.163+1079C>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69641799 | ||||||
| chr2:69641871
|
G | T | 1 | a0001c0001t0149g0280 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.163+1007C>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69641871 | ||||||
| chr2:69641872
|
T | C | 1 | a0001c0001t0149g0280 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.163+1006A>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69641872 | ||||||
| chr2:69641873
|
C | T | 1 | a0001c0001t0149g0280 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.163+1005G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69641873 | ||||||
| chr2:69641881
|
C | T | 85 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(82): Show | 85 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.163+997G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69641881 | ||||||
| chr2:69642187
|
C | A | 1 | a0001c0001t0117g0189 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.163+691G>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69642187 | ||||||
| chr2:69642515
|
A | C | 3 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0105g0108 | 3 | HG02257.hp1 HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.163+363T>G | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69642515 | ||||||
| chr2:69642603
|
G | A | 1 | a0004c0012t0036g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.163+275C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69642603 | ||||||
| chr2:69642658
|
C | T | 2 | a0002c0016t0103g0106a0004c0013t0107g0107 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.163+220G>A | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69642658 | ||||||
| chr2:69642769
|
A | G | 85 | a0001c0001t0004g0206a0001c0001t0004g0216a0001c0001t0004g0221others(82): Show | 85 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.163+109T>C | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 2/21 | chr2 | 69642769 | ||||||
| chr2:69643498
|
G | A | 12 | a0001c0001t0045g0287a0001c0001t0057g0291a0001c0001t0063g0288others(9): Show | 12 | HG00735.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-235+77C>T | AAK1 | ENSG00000115977.21 | transcript | ENST00000409085.9 | protein_coding | 1/21 | chr2 | 69643498 |