Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 85320 |
|---|---|
| ensemblid | ENSG00000121270.16 |
| hgncid | 14639 |
| symbol | ABCC11 |
| name | ATP binding cassette subfamily C member 11 |
| refseq_nuc | NM_001370497.1 |
| refseq_prot | NP_001357426.1 |
| ensembl_nuc | ENST00000356608.7 |
| ensembl_prot | ENSP00000349017.2 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 48165773 |
| end | 48247539 |
| strand | - |
| ver | v1.2 |
| region | chr16:48165773-48247539 |
| region5000 | chr16:48160773-48252539 |
| regionname0 | ABCC11_chr16_48165773_48247539 |
| regionname5000 | ABCC11_chr16_48160773_48252539 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1382 | 60 | 27 | 16 | 9 | 1 | 6 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0002 | 0/1 | 1382 | 19 | 0 | 6 | 6 | 0 | 6 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0003 | 0/0 | 1382 | 10 | 4 | 2 | 3 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0004 | 0/0 | 1382 | 9 | 7 | 1 | 0 | 0 | 1 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0005 | 0/0 | 1382 | 8 | 1 | 2 | 5 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0006 | 0/0 | 1382 | 7 | 1 | 5 | 0 | 0 | 1 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0007 | 0/0 | 1382 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0008 | 0/0 | 1382 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0009 | 0/0 | 1382 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0010 | 0/0 | 1382 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0011 | 0/0 | 1382 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0012 | 0/0 | 1382 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0013 | 0/0 | 1382 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0014 | 0/0 | 1382 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0015 | 0/0 | 1382 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0016 | 0/0 | 1382 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0017 | 0/0 | 1382 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0018 | 0/0 | 1382 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0019 | 0/0 | 1382 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0020 | 0/0 | 1373 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0021 | 0/0 | 1382 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0022 | 0/0 | 1382 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0023 | 0/0 | 1382 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 4149 | 40 | 19 | 7 | 6 | 1 | 6 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0002 | 0/1 | 4149 | 13 | 0 | 1 | 6 | 0 | 5 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0003 | 0/0 | 4149 | 13 | 4 | 7 | 2 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0004 | 0/0 | 4149 | 8 | 1 | 2 | 5 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0005 | 0/0 | 4149 | 7 | 1 | 5 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0006 | 0/0 | 4149 | 6 | 0 | 2 | 3 | 1 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0007 | 0/0 | 4149 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0008 | 0/0 | 4149 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0009 | 0/0 | 4149 | 5 | 5 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0010 | 0/0 | 4149 | 4 | 3 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0011 | 0/0 | 4149 | 4 | 4 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0012 | 0/0 | 4149 | 4 | 4 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0013 | 0/0 | 4149 | 3 | 0 | 3 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0014 | 0/0 | 4149 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0015 | 0/0 | 4149 | 3 | 2 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0016 | 0/0 | 4149 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0017 | 0/0 | 4149 | 2 | 0 | 1 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0018 | 0/0 | 4149 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0019 | 0/0 | 4149 | 2 | 0 | 1 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0020 | 0/0 | 4149 | 2 | 0 | 2 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0021 | 0/0 | 4149 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0022 | 0/0 | 4149 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0023 | 0/0 | 4149 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0024 | 0/0 | 4149 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0025 | 0/0 | 4149 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0026 | 0/0 | 4149 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0027 | 0/0 | 4149 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0028 | 0/0 | 4149 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0029 | 0/0 | 4149 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0030 | 0/0 | 4149 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0031 | 0/0 | 4149 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0032 | 0/0 | 4149 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0033 | 0/0 | 4122 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0034 | 0/0 | 4149 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0035 | 0/0 | 4149 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0036 | 0/0 | 4149 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0037 | 0/0 | 4149 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0038 | 0/0 | 4149 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0039 | 0/0 | 4149 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| c0040 | 0/0 | 4149 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2203 | 94 | 31 | 27 | 21 | 1 | 13 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| t0002 | 0/0 | 2203 | 13 | 12 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| t0003 | 0/0 | 2204 | 8 | 8 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| t0004 | 0/0 | 2203 | 7 | 1 | 2 | 3 | 1 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| t0005 | 0/0 | 2203 | 7 | 1 | 5 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| t0006 | 0/0 | 2203 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| t0007 | 0/0 | 2203 | 4 | 4 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| t0008 | 0/0 | 2203 | 4 | 3 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| t0009 | 0/0 | 2203 | 2 | 0 | 0 | 0 | 0 | 2 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| t0010 | 0/0 | 2203 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| t0011 | 0/0 | 2203 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| t0012 | 0/0 | 2203 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| t0013 | 1/0 | 1746 | 2 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| t0014 | 0/0 | 2203 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| t0015 | 0/0 | 2203 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| t0016 | 0/0 | 2203 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| t0017 | 0/0 | 2203 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| t0018 | 0/0 | 2203 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0095 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0140 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 4149 | 40 | 19 | 7 | 6 | 1 | 6 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0001c0003 | 0/0 | 4149 | 13 | 4 | 7 | 2 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0001c0020 | 0/0 | 4149 | 2 | 0 | 2 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0001c0021 | 0/0 | 4149 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0001c0037 | 0/0 | 4149 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0001c0039 | 0/0 | 4149 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0001c0040 | 0/0 | 4149 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0002c0002 | 0/1 | 4149 | 13 | 0 | 1 | 6 | 0 | 5 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0002c0013 | 0/0 | 4149 | 3 | 0 | 3 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0002c0019 | 0/0 | 4149 | 2 | 0 | 1 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0002c0031 | 0/0 | 4149 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0003c0006 | 0/0 | 4149 | 6 | 0 | 2 | 3 | 1 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0003c0018 | 0/0 | 4149 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0003c0023 | 0/0 | 4149 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0003c0029 | 0/0 | 4149 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0004c0009 | 0/0 | 4149 | 5 | 5 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0004c0017 | 0/0 | 4149 | 2 | 0 | 1 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0004c0027 | 0/0 | 4149 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0004c0028 | 0/0 | 4149 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0005c0004 | 0/0 | 4149 | 8 | 1 | 2 | 5 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0006c0005 | 0/0 | 4149 | 7 | 1 | 5 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0007c0008 | 0/0 | 4149 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0008c0007 | 0/0 | 4149 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0009c0010 | 0/0 | 4149 | 4 | 3 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0010c0012 | 0/0 | 4149 | 4 | 4 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0011c0011 | 0/0 | 4149 | 4 | 4 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0012c0015 | 0/0 | 4149 | 3 | 2 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0013c0014 | 0/0 | 4149 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0014c0016 | 0/0 | 4149 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0015c0024 | 0/0 | 4149 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0015c0026 | 0/0 | 4149 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0016c0035 | 0/0 | 4149 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0016c0038 | 0/0 | 4149 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0017c0022 | 0/0 | 4149 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0018c0025 | 0/0 | 4149 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0019c0036 | 0/0 | 4149 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0020c0033 | 0/0 | 4122 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0021c0034 | 0/0 | 4149 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0022c0032 | 0/0 | 4149 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0023c0030 | 0/0 | 4149 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6351 | 38 | 18 | 7 | 6 | 1 | 6 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0001c0001t0013 | 1/0 | 5894 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0001c0001t0014 | 0/0 | 6351 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0001c0003t0001 | 0/0 | 6351 | 12 | 4 | 6 | 2 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0001c0003t0013 | 0/0 | 5894 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0001c0020t0001 | 0/0 | 6351 | 2 | 0 | 2 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0001c0021t0001 | 0/0 | 6351 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0001c0037t0001 | 0/0 | 6351 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0001c0039t0001 | 0/0 | 6351 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0001c0040t0001 | 0/0 | 6351 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0002c0002t0001 | 0/1 | 6351 | 12 | 0 | 1 | 6 | 0 | 4 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0002c0002t0009 | 0/0 | 6351 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0002c0013t0001 | 0/0 | 6351 | 3 | 0 | 3 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0002c0019t0001 | 0/0 | 6351 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0002c0019t0009 | 0/0 | 6351 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0002c0031t0001 | 0/0 | 6351 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0003c0006t0004 | 0/0 | 6351 | 6 | 0 | 2 | 3 | 1 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0003c0018t0002 | 0/0 | 6351 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0003c0018t0018 | 0/0 | 6351 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0003c0023t0004 | 0/0 | 6351 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0003c0029t0015 | 0/0 | 6351 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0004c0009t0001 | 0/0 | 6351 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0004c0009t0010 | 0/0 | 6351 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0004c0017t0001 | 0/0 | 6351 | 2 | 0 | 1 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0004c0027t0001 | 0/0 | 6351 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0004c0028t0012 | 0/0 | 6351 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0005c0004t0001 | 0/0 | 6351 | 8 | 1 | 2 | 5 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0006c0005t0005 | 0/0 | 6351 | 7 | 1 | 5 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0007c0008t0003 | 0/0 | 6352 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0008c0007t0006 | 0/0 | 6351 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0009c0010t0008 | 0/0 | 6351 | 4 | 3 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0010c0012t0007 | 0/0 | 6351 | 4 | 4 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0011c0011t0002 | 0/0 | 6351 | 4 | 4 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0012c0015t0002 | 0/0 | 6351 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0012c0015t0003 | 0/0 | 6352 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0013c0014t0002 | 0/0 | 6351 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0014c0016t0002 | 0/0 | 6351 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0015c0024t0012 | 0/0 | 6351 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0015c0026t0017 | 0/0 | 6351 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0016c0035t0002 | 0/0 | 6351 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0016c0038t0016 | 0/0 | 6351 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0017c0022t0011 | 0/0 | 6351 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0018c0025t0001 | 0/0 | 6351 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0019c0036t0001 | 0/0 | 6351 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0020c0033t0001 | 0/0 | 6324 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0021c0034t0001 | 0/0 | 6351 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0022c0032t0001 | 0/0 | 6351 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| a0023c0030t0001 | 0/0 | 6351 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | copy fasta | chr16 | 48160773 | 48252539 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0013g0140 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0001t0014g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0003t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0003t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0003t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0003t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0003t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0003t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0003t0013g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0020t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0020t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0021t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0021t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0037t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0039t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0001c0040t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0002c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0002c0002t0001g0095 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0002c0002t0009g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0002c0013t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0002c0013t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0002c0013t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0002c0019t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0002c0019t0009g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0002c0031t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0003c0006t0004g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0003c0006t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0003c0006t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0003c0006t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0003c0006t0004g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0003c0006t0004g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0003c0018t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0003c0018t0018g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0003c0023t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0003c0029t0015g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0004c0009t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0004c0009t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0004c0009t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0004c0009t0010g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0004c0009t0010g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0004c0017t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0004c0017t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0004c0027t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0004c0028t0012g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0005c0004t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0005c0004t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0005c0004t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0005c0004t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0005c0004t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0005c0004t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0005c0004t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0006c0005t0005g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0006c0005t0005g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0006c0005t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0006c0005t0005g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0006c0005t0005g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0007c0008t0003g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0007c0008t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0007c0008t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0007c0008t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0007c0008t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0008c0007t0006g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0008c0007t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0008c0007t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0008c0007t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0008c0007t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0008c0007t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0009c0010t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0009c0010t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0009c0010t0008g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0009c0010t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0010c0012t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0010c0012t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0010c0012t0007g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0010c0012t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0011c0011t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0011c0011t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0011c0011t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0012c0015t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0012c0015t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0012c0015t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0013c0014t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0013c0014t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0014c0016t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0014c0016t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0014c0016t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0015c0024t0012g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0015c0026t0017g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0016c0035t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0016c0038t0016g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0017c0022t0011g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0017c0022t0011g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0018c0025t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0019c0036t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0020c0033t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0021c0034t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0022c0032t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| a0023c0030t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | CHS | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG00558 | hp1 | a0005 | c0004 | t0001 | g0004 | EAS | CHS | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG00738 | hp1 | a0006 | c0005 | t0005 | g0150 | AMR | PUR | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG00741 | hp1 | a0006 | c0005 | t0005 | g0151 | AMR | PUR | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01070 | hp1 | a0006 | c0005 | t0005 | g0001 | AMR | PUR | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0064 | AMR | PUR | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01071 | hp1 | a0002 | c0019 | t0001 | g0096 | AMR | PUR | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01071 | hp2 | a0006 | c0005 | t0005 | g0001 | AMR | PUR | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0045 | AMR | PUR | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01099 | hp2 | a0003 | c0006 | t0004 | g0026 | AMR | PUR | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01106 | hp1 | a0004 | c0017 | t0001 | g0031 | AMR | PUR | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01106 | hp2 | a0023 | c0030 | t0001 | g0112 | AMR | PUR | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01109 | hp1 | a0016 | c0038 | t0016 | g0058 | AMR | PUR | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01109 | hp2 | a0009 | c0010 | t0008 | g0035 | AMR | PUR | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0087 | AMR | PUR | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01175 | hp2 | a0003 | c0006 | t0004 | g0028 | AMR | PUR | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01243 | hp2 | a0018 | c0025 | t0001 | g0030 | AMR | PUR | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01256 | hp2 | a0001 | c0020 | t0001 | g0061 | AMR | CLM | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01258 | hp1 | a0005 | c0004 | t0001 | g0099 | AMR | CLM | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01258 | hp2 | a0001 | c0020 | t0001 | g0075 | AMR | CLM | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01433 | hp2 | a0001 | c0003 | t0013 | g0141 | AMR | CLM | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01496 | hp1 | a0002 | c0013 | t0001 | g0092 | AMR | CLM | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01496 | hp2 | a0012 | c0015 | t0002 | g0080 | AMR | CLM | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01884 | hp1 | a0004 | c0009 | t0001 | g0126 | AFR | ACB | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01884 | hp2 | a0007 | c0008 | t0003 | g0006 | AFR | ACB | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01891 | hp1 | a0010 | c0012 | t0007 | g0021 | AFR | ACB | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01891 | hp2 | a0008 | c0007 | t0006 | g0145 | AFR | ACB | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0017 | AMR | PEL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01975 | hp1 | a0002 | c0013 | t0001 | g0043 | AMR | PEL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01975 | hp2 | a0001 | c0003 | t0001 | g0081 | AMR | PEL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01978 | hp1 | a0005 | c0004 | t0001 | g0107 | AMR | PEL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01978 | hp2 | a0002 | c0013 | t0001 | g0108 | AMR | PEL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02027 | hp1 | a0005 | c0004 | t0001 | g0101 | EAS | KHV | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02040 | hp1 | a0021 | c0034 | t0001 | g0039 | EAS | KHV | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02040 | hp2 | a0001 | c0003 | t0001 | g0050 | EAS | KHV | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02055 | hp1 | a0003 | c0023 | t0004 | g0032 | AFR | ACB | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02056 | hp1 | a0001 | c0040 | t0001 | g0057 | EAS | KHV | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02056 | hp2 | a0005 | c0004 | t0001 | g0119 | EAS | KHV | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02074 | hp1 | a0003 | c0006 | t0004 | g0013 | EAS | KHV | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | KHV | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | KHV | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02080 | hp2 | a0005 | c0004 | t0001 | g0098 | EAS | KHV | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | KHV | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02083 | hp2 | a0003 | c0006 | t0004 | g0011 | EAS | KHV | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02129 | hp2 | a0001 | c0003 | t0001 | g0056 | EAS | KHV | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | KHV | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02135 | hp2 | a0003 | c0006 | t0004 | g0012 | EAS | KHV | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02145 | hp1 | a0009 | c0010 | t0008 | g0024 | AFR | ACB | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02145 | hp2 | a0004 | c0009 | t0010 | g0130 | AFR | ACB | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CDX | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | CDX | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02258 | hp1 | a0008 | c0007 | t0006 | g0144 | AFR | ACB | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02273 | hp1 | a0001 | c0003 | t0001 | g0082 | AMR | PEL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02273 | hp2 | a0002 | c0031 | t0001 | g0091 | AMR | PEL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02280 | hp1 | a0003 | c0018 | t0002 | g0010 | AFR | ACB | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02293 | hp1 | a0020 | c0033 | t0001 | g0117 | AMR | PEL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02572 | hp1 | a0001 | c0021 | t0001 | g0042 | AFR | GWD | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02572 | hp2 | a0008 | c0007 | t0006 | g0146 | AFR | GWD | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02622 | hp1 | a0012 | c0015 | t0003 | g0134 | AFR | GWD | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02647 | hp2 | a0007 | c0008 | t0003 | g0138 | AFR | GWD | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02698 | hp1 | a0002 | c0019 | t0009 | g0008 | SAS | PJL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02723 | hp1 | a0012 | c0015 | t0003 | g0135 | AFR | GWD | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02723 | hp2 | a0007 | c0008 | t0003 | g0137 | AFR | GWD | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0103 | SAS | PJL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02809 | hp1 | a0014 | c0016 | t0002 | g0067 | AFR | GWD | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02886 | hp2 | a0004 | c0009 | t0001 | g0128 | AFR | GWD | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02895 | hp1 | a0001 | c0021 | t0001 | g0041 | AFR | GWD | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02895 | hp2 | a0011 | c0011 | t0002 | g0005 | AFR | GWD | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02896 | hp1 | a0003 | c0018 | t0018 | g0132 | AFR | GWD | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02897 | hp1 | a0011 | c0011 | t0002 | g0005 | AFR | GWD | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0054 | AFR | ESN | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02965 | hp2 | a0010 | c0012 | t0007 | g0023 | AFR | ESN | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02970 | hp2 | a0010 | c0012 | t0007 | g0022 | AFR | ESN | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02976 | hp1 | a0013 | c0014 | t0002 | g0002 | AFR | ESN | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02976 | hp2 | a0007 | c0008 | t0003 | g0136 | AFR | ESN | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03098 | hp1 | a0008 | c0007 | t0006 | g0147 | AFR | MSL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03098 | hp2 | a0004 | c0009 | t0001 | g0129 | AFR | MSL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03130 | hp1 | a0014 | c0016 | t0002 | g0077 | AFR | ESN | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03130 | hp2 | a0008 | c0007 | t0006 | g0143 | AFR | ESN | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03139 | hp1 | a0007 | c0008 | t0003 | g0139 | AFR | ESN | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0114 | AFR | ESN | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03195 | hp2 | a0009 | c0010 | t0008 | g0025 | AFR | ESN | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03209 | hp2 | a0011 | c0011 | t0002 | g0124 | AFR | MSL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03225 | hp1 | a0009 | c0010 | t0008 | g0036 | AFR | MSL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03239 | hp2 | a0004 | c0017 | t0001 | g0029 | SAS | PJL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03453 | hp1 | a0004 | c0028 | t0012 | g0131 | AFR | MSL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03453 | hp2 | a0016 | c0035 | t0002 | g0123 | AFR | MSL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03486 | hp1 | a0010 | c0012 | t0007 | g0020 | AFR | MSL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03486 | hp2 | a0001 | c0037 | t0001 | g0070 | AFR | MSL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03492 | hp2 | a0006 | c0005 | t0005 | g0148 | SAS | PJL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0060 | AFR | MSL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | STU | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | STU | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0109 | SAS | PJL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | STU | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG04115 | hp2 | a0019 | c0036 | t0001 | g0040 | SAS | STU | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| NA18906 | hp1 | a0015 | c0026 | t0017 | g0033 | AFR | YRI | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| NA18906 | hp2 | a0003 | c0029 | t0015 | g0019 | AFR | YRI | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| NA18983 | hp2 | a0005 | c0004 | t0001 | g0004 | EAS | JPT | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| NA19043 | hp1 | a0004 | c0009 | t0010 | g0127 | AFR | LWK | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| NA19043 | hp2 | a0001 | c0039 | t0001 | g0066 | AFR | LWK | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| NA19240 | hp1 | a0001 | c0001 | t0014 | g0007 | AFR | YRI | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| NA19240 | hp2 | a0004 | c0027 | t0001 | g0034 | AFR | YRI | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| NA20129 | hp1 | a0007 | c0008 | t0003 | g0006 | AFR | ASW | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| NA20129 | hp2 | a0005 | c0004 | t0001 | g0102 | AFR | ASW | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| NA20752 | hp1 | a0003 | c0006 | t0004 | g0027 | EUR | TSI | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0051 | EUR | TSI | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| NA20905 | hp1 | a0022 | c0032 | t0001 | g0100 | SAS | GIH | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| NA20905 | hp2 | a0002 | c0002 | t0009 | g0009 | SAS | GIH | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01123 | hp1 | a0006 | c0005 | t0005 | g0001 | AMR | CLM | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0097 | AMR | CLM | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02109 | hp1 | a0014 | c0016 | t0002 | g0078 | AFR | ACB | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02109 | hp2 | a0017 | c0022 | t0011 | g0015 | AFR | ACB | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02486 | hp1 | a0011 | c0011 | t0002 | g0125 | AFR | ACB | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02486 | hp2 | a0008 | c0007 | t0006 | g0142 | AFR | ACB | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02559 | hp1 | a0017 | c0022 | t0011 | g0014 | AFR | ACB | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG02559 | hp2 | a0013 | c0014 | t0002 | g0002 | AFR | ACB | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03471 | hp1 | a0015 | c0024 | t0012 | g0133 | AFR | MSL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG03471 | hp2 | a0013 | c0014 | t0002 | g0110 | AFR | MSL | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG06807 | hp1 | a0001 | c0003 | t0001 | g0065 | AFR | USA | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| HG06807 | hp2 | a0006 | c0005 | t0005 | g0149 | AFR | USA | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0095 | REF | REF | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0013 | g0140 | REF | REF | ABCC11_chr16_48160773_48252539 | ABCC11 | chr16 | 48160773 | 48252539 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:48167521
|
T | C | 12 | a0003a0006a0007others(9): Show | 54 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(51): Show |
missense_variant | MODERATE | c.4031A>G | p.His1344Arg | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 29/30 | 4275/5894 | 4031/4149 | 1344/1382 | chr16 | 48167521 | ||
| chr16:48167586
|
TTCACGGA others(20): Show |
T | 1 | a0020 | 1 | HG02293.hp1 | disruptive_inframe_deletion | MODERATE | c.3939_3965delCACCCT others(21): Show |
p.Asp1313_Arg1321del | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 29/30 | 4209/5894 | 3939/4149 | 1313/1382 | chr16 | 48167586 | ||
| chr16:48170166
|
T | A | 1 | a0010 | 4 | HG01891.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
missense_variant | MODERATE | c.3830A>T | p.Asn1277Ile | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 28/30 | 4074/5894 | 3830/4149 | 1277/1382 | chr16 | 48170166 | ||
| chr16:48170167
|
T | A | 4 | a0006a0011a0014others(1): Show | 16 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(13): Show |
missense_variant | MODERATE | c.3829A>T | p.Asn1277Tyr | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 28/30 | 4073/5894 | 3829/4149 | 1277/1382 | chr16 | 48170167 | ||
| chr16:48170932
|
T | A | 1 | a0019 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.3734A>T | p.Gln1245Leu | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 27/30 | 3978/5894 | 3734/4149 | 1245/1382 | chr16 | 48170932 | ||
| chr16:48175267
|
C | T | 1 | a0009 | 4 | HG01109.hp2 HG02145.hp1 HG03195.hp2 others(1): Show |
missense_variant | MODERATE | c.3689G>A | p.Gly1230Glu | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 26/30 | 3933/5894 | 3689/4149 | 1230/1382 | chr16 | 48175267 | ||
| chr16:48187040
|
C | T | 1 | a0008 | 6 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
missense_variant | MODERATE | c.2984G>A | p.Arg995Gln | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 22/30 | 3228/5894 | 2984/4149 | 995/1382 | chr16 | 48187040 | ||
| chr16:48187408
|
C | T | 1 | a0021 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.2726G>A | p.Ser909Asn | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 21/30 | 2970/5894 | 2726/4149 | 909/1382 | chr16 | 48187408 | ||
| chr16:48198043
|
T | C | 2 | a0008a0017 | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
missense_variant | MODERATE | c.2242A>G | p.Ile748Val | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 17/30 | 2486/5894 | 2242/4149 | 748/1382 | chr16 | 48198043 | ||
| chr16:48198154
|
T | C | 1 | a0012 | 3 | HG01496.hp2 HG02622.hp1 HG02723.hp1 |
missense_variant | MODERATE | c.2204A>G | p.Lys735Arg | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 16/30 | 2448/5894 | 2204/4149 | 735/1382 | chr16 | 48198154 | ||
| chr16:48200299
|
C | T | 1 | a0012 | 3 | HG01496.hp2 HG02622.hp1 HG02723.hp1 |
missense_variant | MODERATE | c.2059G>A | p.Val687Ile | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 15/30 | 2303/5894 | 2059/4149 | 687/1382 | chr16 | 48200299 | ||
| chr16:48200416
|
C | T | 3 | a0005a0020a0022 | 10 | HG00558.hp1 HG01258.hp1 HG01978.hp1 others(7): Show |
missense_variant | MODERATE | c.1942G>A | p.Val648Ile | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 15/30 | 2186/5894 | 1942/4149 | 648/1382 | chr16 | 48200416 | ||
| chr16:48200470
|
G | A | 1 | a0018 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.1888C>T | p.Arg630Trp | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 15/30 | 2132/5894 | 1888/4149 | 630/1382 | chr16 | 48200470 | ||
| chr16:48208468
|
G | A | 1 | a0006 | 7 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(4): Show |
missense_variant | MODERATE | c.1637C>T | p.Thr546Met | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 12/30 | 1881/5894 | 1637/4149 | 546/1382 | chr16 | 48208468 | ||
| chr16:48211085
|
C | T | 2 | a0007a0012 | 9 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
missense_variant | MODERATE | c.1471G>A | p.Val491Ile | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 11/30 | 1715/5894 | 1471/4149 | 491/1382 | chr16 | 48211085 | ||
| chr16:48211091
|
C | T | 1 | a0022 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.1465G>A | p.Gly489Arg | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 11/30 | 1709/5894 | 1465/4149 | 489/1382 | chr16 | 48211091 | ||
| chr16:48216115
|
G | T | 7 | a0003a0004a0009others(4): Show | 35 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(32): Show |
missense_variant&splice_region_variant | MODERATE | c.950C>A | p.Ala317Glu | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 7/30 | 1194/5894 | 950/4149 | 317/1382 | chr16 | 48216115 | ||
| chr16:48224287
|
C | T | 5 | a0002a0005a0020others(2): Show | 30 | HG00438.hp2 HG00558.hp1 HG01071.hp1 others(27): Show |
missense_variant | MODERATE | c.538G>A | p.Gly180Arg | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 5/30 | 782/5894 | 538/4149 | 180/1382 | chr16 | 48224287 | ||
| chr16:48230441
|
G | A | 1 | a0007 | 6 | HG01884.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
missense_variant | MODERATE | c.232C>T | p.Pro78Ser | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/30 | 476/5894 | 232/4149 | 78/1382 | chr16 | 48230441 | ||
| chr16:48231858
|
C | T | 1 | a0023 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.64G>A | p.Asp22Asn | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 2/30 | 308/5894 | 64/4149 | 22/1382 | chr16 | 48231858 | ||
| chr16:48231866
|
C | T | 7 | a0003a0004a0009others(4): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
missense_variant | MODERATE | c.56G>A | p.Arg19His | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 2/30 | 300/5894 | 56/4149 | 19/1382 | chr16 | 48231866 | ||
| chr16:48231898
|
C | A | 1 | a0007 | 6 | HG01884.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
missense_variant | MODERATE | c.24G>T | p.Trp8Cys | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 2/30 | 268/5894 | 24/4149 | 8/1382 | chr16 | 48231898 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:48178681
|
C | T | 2 | a0002c0013a0002c0031 | 4 | HG01496.hp1 HG01975.hp1 HG01978.hp2 others(1): Show |
synonymous_variant | LOW | c.3264G>A | p.Ala1088Ala | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 24/30 | 3508/5894 | 3264/4149 | 1088/1382 | chr16 | 48178681 | ||
| chr16:48187350
|
T | C | 1 | a0001c0021 | 2 | HG02572.hp1 HG02895.hp1 |
synonymous_variant | LOW | c.2784A>G | p.Glu928Glu | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 21/30 | 3028/5894 | 2784/4149 | 928/1382 | chr16 | 48187350 | ||
| chr16:48192568
|
C | T | 6 | a0001c0003a0001c0020a0001c0040others(3): Show | 20 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(17): Show |
synonymous_variant | LOW | c.2658G>A | p.Lys886Lys | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/30 | 2902/5894 | 2658/4149 | 886/1382 | chr16 | 48192568 | ||
| chr16:48193951
|
G | A | 14 | a0001c0037a0003c0006a0003c0018others(11): Show | 46 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(43): Show |
synonymous_variant | LOW | c.2436C>T | p.Phe812Phe | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 19/30 | 2680/5894 | 2436/4149 | 812/1382 | chr16 | 48193951 | ||
| chr16:48193978
|
G | A | 1 | a0001c0039 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.2409C>T | p.Tyr803Tyr | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 19/30 | 2653/5894 | 2409/4149 | 803/1382 | chr16 | 48193978 | ||
| chr16:48198237
|
A | G | 1 | a0001c0020 | 2 | HG01256.hp2 HG01258.hp2 |
synonymous_variant | LOW | c.2121T>C | p.Asn707Asn | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 16/30 | 2365/5894 | 2121/4149 | 707/1382 | chr16 | 48198237 | ||
| chr16:48200303
|
C | T | 3 | a0011c0011a0014c0016a0016c0035 | 8 | HG02109.hp1 HG02486.hp1 HG02809.hp1 others(5): Show |
synonymous_variant | LOW | c.2055G>A | p.Thr685Thr | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 15/30 | 2299/5894 | 2055/4149 | 685/1382 | chr16 | 48200303 | ||
| chr16:48205430
|
G | A | 1 | a0001c0040 | 1 | HG02056.hp1 | synonymous_variant | LOW | c.1788C>T | p.Gly596Gly | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 13/30 | 2032/5894 | 1788/4149 | 596/1382 | chr16 | 48205430 | ||
| chr16:48208448
|
G | A | 2 | a0007c0008a0012c0015 | 9 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
synonymous_variant | LOW | c.1657C>T | p.Leu553Leu | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 12/30 | 1901/5894 | 1657/4149 | 553/1382 | chr16 | 48208448 | ||
| chr16:48213473
|
C | T | 1 | a0002c0031 | 1 | HG02273.hp2 | synonymous_variant | LOW | c.1326G>A | p.Thr442Thr | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 10/30 | 1570/5894 | 1326/4149 | 442/1382 | chr16 | 48213473 | ||
| chr16:48214887
|
C | T | 1 | a0004c0009 | 5 | HG01884.hp1 HG02145.hp2 HG02886.hp2 others(2): Show |
synonymous_variant | LOW | c.1242G>A | p.Ala414Ala | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 9/30 | 1486/5894 | 1242/4149 | 414/1382 | chr16 | 48214887 | ||
| chr16:48214932
|
C | T | 1 | a0004c0027 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.1197G>A | p.Ala399Ala | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 9/30 | 1441/5894 | 1197/4149 | 399/1382 | chr16 | 48214932 | ||
| chr16:48215007
|
T | C | 16 | a0003c0006a0003c0018a0003c0023others(13): Show | 51 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(48): Show |
synonymous_variant | LOW | c.1122A>G | p.Lys374Lys | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 9/30 | 1366/5894 | 1122/4149 | 374/1382 | chr16 | 48215007 | ||
| chr16:48216120
|
T | C | 8 | a0003c0018a0003c0029a0004c0009others(5): Show | 21 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(18): Show |
synonymous_variant | LOW | c.945A>G | p.Pro315Pro | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 7/30 | 1189/5894 | 945/4149 | 315/1382 | chr16 | 48216120 | ||
| chr16:48222691
|
T | C | 14 | a0003c0006a0003c0018a0003c0023others(11): Show | 36 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(33): Show |
synonymous_variant | LOW | c.684A>G | p.Gln228Gln | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/30 | 928/5894 | 684/4149 | 228/1382 | chr16 | 48222691 | ||
| chr16:48227916
|
G | A | 1 | a0003c0029 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.285C>T | p.Leu95Leu | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/30 | 529/5894 | 285/4149 | 95/1382 | chr16 | 48227916 | ||
| chr16:48230484
|
C | T | 1 | a0003c0023 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.189G>A | p.Lys63Lys | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/30 | 433/5894 | 189/4149 | 63/1382 | chr16 | 48230484 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:48165893
|
T | C | 1 | a0009c0010t0008 | 4 | HG01109.hp2 HG02145.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1381A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 30/30 | 1381 | chr16 | 48165893 | |||||
| chr16:48165895
|
G | A | 1 | a0015c0026t0017 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1379C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 30/30 | 1379 | chr16 | 48165895 | |||||
| chr16:48166090
|
A | C | 2 | a0008c0007t0006a0017c0022t0011 | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1184T>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 30/30 | 1184 | chr16 | 48166090 | |||||
| chr16:48166302
|
T | C | 16 | a0003c0006t0004a0003c0018t0002a0003c0018t0018others(13): Show | 46 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*972A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 30/30 | 972 | chr16 | 48166302 | |||||
| chr16:48166463
|
C | T | 1 | a0010c0012t0007 | 4 | HG01891.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*811G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 30/30 | 811 | chr16 | 48166463 | |||||
| chr16:48166526
|
G | C | 1 | a0003c0029t0015 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*748C>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 30/30 | 748 | chr16 | 48166526 | |||||
| chr16:48166821
|
C | A | 5 | a0003c0006t0004a0003c0023t0004a0003c0029t0015others(2): Show | 16 | HG01099.hp2 HG01109.hp2 HG01175.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*453G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 30/30 | 453 | chr16 | 48166821 | |||||
| chr16:48166930
|
A | G | 2 | a0006c0005t0005a0016c0038t0016 | 8 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*344T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 30/30 | 344 | chr16 | 48166930 | |||||
| chr16:48167086
|
C | T | 1 | a0004c0009t0010 | 2 | HG02145.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*188G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 30/30 | 188 | chr16 | 48167086 | |||||
| chr16:48167220
|
C | G | 5 | a0003c0006t0004a0003c0023t0004a0003c0029t0015others(2): Show | 16 | HG01099.hp2 HG01109.hp2 HG01175.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*54G>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 30/30 | 54 | chr16 | 48167220 | |||||
| chr16:48247353
|
C | G | 2 | a0007c0008t0003a0012c0015t0003 | 8 | HG01884.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-58G>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/30 | 15432 | chr16 | 48247353 | |||||
| chr16:48247382
|
C | T | 2 | a0002c0002t0009a0002c0019t0009 | 2 | HG02698.hp1 NA20905.hp2 |
5_prime_UTR_variant | MODIFIER | c.-87G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/30 | 15461 | chr16 | 48247382 | |||||
| chr16:48247412
|
A | AGAGCAGC others(451): Show |
2 | a0007c0008t0003a0012c0015t0003 | 8 | HG01884.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-118_-117insCTTGAA others(452): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/30 | 15492 | chr16 | 48247412 | |||||
| chr16:48247412
|
A | AGAGCAGC others(450): Show |
3 | a0003c0018t0018a0004c0028t0012a0015c0024t0012 | 3 | HG02896.hp1 HG03453.hp1 HG03471.hp1 |
5_prime_UTR_variant | MODIFIER | c.-118_-117insCTTGAA others(451): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/30 | 15492 | chr16 | 48247412 | |||||
| chr16:48247412
|
A | AGAGCAGC others(450): Show |
41 | a0001c0001t0001a0001c0001t0014a0001c0003t0001others(38): Show | 145 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(142): Show |
5_prime_UTR_variant | MODIFIER | c.-118_-117insCTTGAA others(451): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/30 | 15492 | chr16 | 48247412 | |||||
| chr16:48247455
|
G | C | 1 | a0008c0007t0006 | 6 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-160C>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/30 | chr16 | 48247455 | ||||||
| chr16:48247491
|
T | C | 1 | a0006c0005t0005 | 7 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-196A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/30 | 15570 | chr16 | 48247491 | |||||
| chr16:48247527
|
C | G | 1 | a0001c0001t0014 | 1 | NA19240.hp1 | 5_prime_UTR_variant | MODIFIER | c.-232G>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/30 | 15606 | chr16 | 48247527 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:48167485
|
G | T | 1 | a0017c0022t0011g0015 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4056+11C>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 29/29 | chr16 | 48167485 | ||||||
| chr16:48167767
|
C | A | 25 | a0003c0018t0002g0010a0003c0018t0018g0132a0006c0005t0005g0001others(22): Show | 30 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.3892-107G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 28/29 | chr16 | 48167767 | ||||||
| chr16:48167791
|
G | A | 13 | a0006c0005t0005g0001a0006c0005t0005g0148a0006c0005t0005g0149others(10): Show | 16 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.3892-131C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 28/29 | chr16 | 48167791 | ||||||
| chr16:48167792
|
A | T | 13 | a0006c0005t0005g0001a0006c0005t0005g0148a0006c0005t0005g0149others(10): Show | 16 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.3892-132T>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 28/29 | chr16 | 48167792 | ||||||
| chr16:48167796
|
A | G | 49 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(46): Show | 54 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.3892-136T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 28/29 | chr16 | 48167796 | ||||||
| chr16:48168222
|
ACAAAAAT others(28): Show |
A | 2 | a0001c0001t0001g0083a0002c0002t0001g0097 | 2 | HG00738.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.3892-597_3892-563d others(37): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 28/29 | chr16 | 48168222 | ||||||
| chr16:48168237
|
T | C | 5 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.3892-577A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 28/29 | chr16 | 48168237 | ||||||
| chr16:48168364
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3892-704T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 28/29 | chr16 | 48168364 | ||||||
| chr16:48168449
|
G | A | 2 | a0017c0022t0011g0014a0017c0022t0011g0015 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.3892-789C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 28/29 | chr16 | 48168449 | ||||||
| chr16:48168505
|
G | T | 1 | a0003c0018t0002g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3892-845C>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 28/29 | chr16 | 48168505 | ||||||
| chr16:48168564
|
A | G | 1 | a0003c0018t0002g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3892-904T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 28/29 | chr16 | 48168564 | ||||||
| chr16:48168592
|
G | T | 25 | a0003c0018t0002g0010a0003c0018t0018g0132a0006c0005t0005g0001others(22): Show | 30 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.3892-932C>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 28/29 | chr16 | 48168592 | ||||||
| chr16:48168677
|
G | A | 16 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(13): Show | 16 | HG01099.hp2 HG01109.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.3892-1017C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 28/29 | chr16 | 48168677 | ||||||
| chr16:48168936
|
T | C | 10 | a0006c0005t0005g0001a0006c0005t0005g0148a0006c0005t0005g0149others(7): Show | 12 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.3891+1169A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 28/29 | chr16 | 48168936 | ||||||
| chr16:48169136
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3891+969C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 28/29 | chr16 | 48169136 | ||||||
| chr16:48169138
|
T | C | 5 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.3891+967A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 28/29 | chr16 | 48169138 | ||||||
| chr16:48169564
|
C | T | 1 | a0002c0002t0009g0009 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3891+541G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 28/29 | chr16 | 48169564 | ||||||
| chr16:48169622
|
T | C | 1 | a0004c0027t0001g0034 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3891+483A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 28/29 | chr16 | 48169622 | ||||||
| chr16:48169639
|
C | T | 16 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(13): Show | 16 | HG01099.hp2 HG01109.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.3891+466G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 28/29 | chr16 | 48169639 | ||||||
| chr16:48169860
|
A | G | 8 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.3891+245T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 28/29 | chr16 | 48169860 | ||||||
| chr16:48169918
|
TA | T | 4 | a0002c0013t0001g0043a0002c0013t0001g0092a0002c0013t0001g0108others(1): Show | 4 | HG01496.hp1 HG01975.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.3891+186delT | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 28/29 | chr16 | 48169918 | ||||||
| chr16:48169966
|
T | TTGTTGC | 41 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(38): Show | 46 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.3891+138_3891+139i others(8): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 28/29 | chr16 | 48169966 | ||||||
| chr16:48170033
|
G | A | 3 | a0014c0016t0002g0067a0014c0016t0002g0077a0014c0016t0002g0078 | 3 | HG02109.hp1 HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3891+72C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 28/29 | chr16 | 48170033 | ||||||
| chr16:48170058
|
T | A | 8 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.3891+47A>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 28/29 | chr16 | 48170058 | ||||||
| chr16:48170058
|
T | G | 1 | a0003c0029t0015g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3891+47A>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 28/29 | chr16 | 48170058 | ||||||
| chr16:48170219
|
C | T | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG01433.hp1 NA20752.hp2 |
splice_acceptor_variant&intron_variant | HIGH | c.3778-1G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 27/29 | chr16 | 48170219 | ||||||
| chr16:48170351
|
C | A | 1 | a0015c0024t0012g0133 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3778-133G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 27/29 | chr16 | 48170351 | ||||||
| chr16:48170725
|
T | A | 1 | a0002c0019t0009g0008 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3777+164A>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 27/29 | chr16 | 48170725 | ||||||
| chr16:48170785
|
C | T | 8 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.3777+104G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 27/29 | chr16 | 48170785 | ||||||
| chr16:48170840
|
C | T | 1 | a0009c0010t0008g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3777+49G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 27/29 | chr16 | 48170840 | ||||||
| chr16:48170888
|
C | T | 1 | a0002c0002t0001g0095 | 1 | homoSapiens_chm13v2.hp1 | splice_donor_variant&intron_variant | HIGH | c.3777+1G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 27/29 | chr16 | 48170888 | ||||||
| chr16:48171197
|
A | G | 1 | a0018c0025t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3699-230T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 26/29 | chr16 | 48171197 | ||||||
| chr16:48171198
|
T | A | 1 | a0018c0025t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3699-231A>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 26/29 | chr16 | 48171198 | ||||||
| chr16:48171214
|
C | G | 5 | a0004c0009t0001g0126a0004c0009t0001g0128a0004c0009t0001g0129others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3699-247G>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 26/29 | chr16 | 48171214 | ||||||
| chr16:48171273
|
A | G | 49 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(46): Show | 54 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.3699-306T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 26/29 | chr16 | 48171273 | ||||||
| chr16:48171682
|
T | C | 41 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(38): Show | 46 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.3699-715A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 26/29 | chr16 | 48171682 | ||||||
| chr16:48171737
|
G | A | 4 | a0001c0001t0001g0088a0005c0004t0001g0099a0005c0004t0001g0102others(1): Show | 4 | HG01258.hp1 HG01978.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.3699-770C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 26/29 | chr16 | 48171737 | ||||||
| chr16:48171956
|
C | T | 6 | a0006c0005t0005g0001a0006c0005t0005g0148a0006c0005t0005g0149others(3): Show | 8 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.3699-989G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 26/29 | chr16 | 48171956 | ||||||
| chr16:48172427
|
C | CT | 13 | a0001c0001t0001g0079a0002c0019t0009g0008a0003c0006t0004g0028others(10): Show | 13 | HG01175.hp2 HG01243.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.3699-1461dupA | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 26/29 | chr16 | 48172427 | ||||||
| chr16:48172427
|
CT | C | 20 | a0001c0003t0001g0054a0002c0019t0001g0096a0003c0006t0004g0011others(17): Show | 21 | HG01071.hp1 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.3699-1461delA | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 26/29 | chr16 | 48172427 | ||||||
| chr16:48172467
|
T | G | 41 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(38): Show | 46 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.3699-1500A>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 26/29 | chr16 | 48172467 | ||||||
| chr16:48172469
|
C | A | 1 | a0001c0001t0001g0016 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3699-1502G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 26/29 | chr16 | 48172469 | ||||||
| chr16:48172586
|
C | A | 3 | a0001c0001t0001g0037a0001c0001t0001g0044a0020c0033t0001g0117 | 3 | HG01256.hp1 HG02293.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.3699-1619G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 26/29 | chr16 | 48172586 | ||||||
| chr16:48172629
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3699-1662A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 26/29 | chr16 | 48172629 | ||||||
| chr16:48173666
|
C | T | 41 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(38): Show | 46 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.3698+1592G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 26/29 | chr16 | 48173666 | ||||||
| chr16:48173813
|
CAG | C | 18 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(15): Show | 19 | HG01099.hp2 HG01109.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.3698+1443_3698+144 others(6): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 26/29 | chr16 | 48173813 | ||||||
| chr16:48173920
|
C | G | 23 | a0003c0018t0002g0010a0003c0018t0018g0132a0006c0005t0005g0001others(20): Show | 27 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.3698+1338G>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 26/29 | chr16 | 48173920 | ||||||
| chr16:48174047
|
G | A | 8 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(5): Show | 9 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.3698+1211C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 26/29 | chr16 | 48174047 | ||||||
| chr16:48174103
|
G | A | 23 | a0003c0018t0002g0010a0003c0018t0018g0132a0006c0005t0005g0001others(20): Show | 27 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.3698+1155C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 26/29 | chr16 | 48174103 | ||||||
| chr16:48174495
|
A | G | 1 | a0004c0017t0001g0029 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3698+763T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 26/29 | chr16 | 48174495 | ||||||
| chr16:48174496
|
G | A | 8 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.3698+762C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 26/29 | chr16 | 48174496 | ||||||
| chr16:48174895
|
G | A | 1 | a0018c0025t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3698+363C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 26/29 | chr16 | 48174895 | ||||||
| chr16:48174970
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3698+288G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 26/29 | chr16 | 48174970 | ||||||
| chr16:48175135
|
C | T | 6 | a0006c0005t0005g0001a0006c0005t0005g0148a0006c0005t0005g0149others(3): Show | 8 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.3698+123G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 26/29 | chr16 | 48175135 | ||||||
| chr16:48175451
|
C | T | 1 | a0014c0016t0002g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3539-34G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 25/29 | chr16 | 48175451 | ||||||
| chr16:48175566
|
G | A | 8 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.3539-149C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 25/29 | chr16 | 48175566 | ||||||
| chr16:48175591
|
G | A | 1 | a0018c0025t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3539-174C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 25/29 | chr16 | 48175591 | ||||||
| chr16:48175630
|
C | T | 3 | a0011c0011t0002g0005a0011c0011t0002g0124a0011c0011t0002g0125 | 4 | HG02486.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.3539-213G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 25/29 | chr16 | 48175630 | ||||||
| chr16:48175959
|
T | A | 41 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(38): Show | 46 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.3539-542A>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 25/29 | chr16 | 48175959 | ||||||
| chr16:48176258
|
C | T | 6 | a0006c0005t0005g0001a0006c0005t0005g0148a0006c0005t0005g0149others(3): Show | 8 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.3538+666G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 25/29 | chr16 | 48176258 | ||||||
| chr16:48176271
|
C | T | 49 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(46): Show | 54 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.3538+653G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 25/29 | chr16 | 48176271 | ||||||
| chr16:48176604
|
A | T | 1 | a0002c0002t0001g0003 | 2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.3538+320T>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 25/29 | chr16 | 48176604 | ||||||
| chr16:48176621
|
G | A | 41 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(38): Show | 46 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.3538+303C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 25/29 | chr16 | 48176621 | ||||||
| chr16:48176696
|
C | T | 1 | a0003c0029t0015g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3538+228G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 25/29 | chr16 | 48176696 | ||||||
| chr16:48176808
|
A | G | 41 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(38): Show | 46 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.3538+116T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 25/29 | chr16 | 48176808 | ||||||
| chr16:48176903
|
C | T | 1 | a0002c0002t0001g0090 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3538+21G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 25/29 | chr16 | 48176903 | ||||||
| chr16:48177240
|
C | G | 1 | a0003c0029t0015g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3349-127G>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 24/29 | chr16 | 48177240 | ||||||
| chr16:48177438
|
C | T | 5 | a0004c0009t0001g0126a0004c0009t0001g0128a0004c0009t0001g0129others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3349-325G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 24/29 | chr16 | 48177438 | ||||||
| chr16:48177694
|
C | T | 2 | a0001c0001t0001g0044a0003c0006t0004g0026 | 2 | HG01099.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.3349-581G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 24/29 | chr16 | 48177694 | ||||||
| chr16:48177707
|
G | A | 1 | a0018c0025t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3349-594C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 24/29 | chr16 | 48177707 | ||||||
| chr16:48178712
|
G | C | 3 | a0011c0011t0002g0005a0011c0011t0002g0124a0011c0011t0002g0125 | 4 | HG02486.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.3259-26C>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48178712 | ||||||
| chr16:48178924
|
G | A | 1 | a0015c0024t0012g0133 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3259-238C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48178924 | ||||||
| chr16:48179256
|
T | C | 49 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(46): Show | 54 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.3259-570A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48179256 | ||||||
| chr16:48179438
|
G | T | 1 | a0005c0004t0001g0099 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.3259-752C>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48179438 | ||||||
| chr16:48179681
|
C | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0055 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3259-995G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48179681 | ||||||
| chr16:48179772
|
G | C | 1 | a0001c0001t0001g0049 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3259-1086C>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48179772 | ||||||
| chr16:48179962
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3259-1276T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48179962 | ||||||
| chr16:48179965
|
A | C | 3 | a0012c0015t0002g0080a0012c0015t0003g0134a0012c0015t0003g0135 | 3 | HG01496.hp2 HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.3259-1279T>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48179965 | ||||||
| chr16:48180042
|
T | C | 10 | a0003c0018t0002g0010a0003c0018t0018g0132a0007c0008t0003g0006others(7): Show | 11 | HG01496.hp2 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.3259-1356A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48180042 | ||||||
| chr16:48180206
|
G | A | 6 | a0006c0005t0005g0001a0006c0005t0005g0148a0006c0005t0005g0149others(3): Show | 8 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.3259-1520C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48180206 | ||||||
| chr16:48180429
|
G | C | 8 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(5): Show | 9 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.3259-1743C>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48180429 | ||||||
| chr16:48180512
|
T | C | 6 | a0006c0005t0005g0001a0006c0005t0005g0148a0006c0005t0005g0149others(3): Show | 8 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.3259-1826A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48180512 | ||||||
| chr16:48180859
|
A | G | 1 | a0019c0036t0001g0040 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3259-2173T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48180859 | ||||||
| chr16:48180978
|
G | C | 1 | a0001c0001t0001g0016 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3259-2292C>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48180978 | ||||||
| chr16:48181236
|
G | A | 1 | a0023c0030t0001g0112 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3259-2550C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48181236 | ||||||
| chr16:48181611
|
C | CT | 10 | a0003c0018t0002g0010a0003c0018t0018g0132a0007c0008t0003g0006others(7): Show | 11 | HG01496.hp2 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.3258+2828dupA | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48181611 | ||||||
| chr16:48181650
|
A | G | 41 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(38): Show | 46 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.3258+2790T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48181650 | ||||||
| chr16:48181893
|
G | A | 1 | a0004c0027t0001g0034 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3258+2547C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48181893 | ||||||
| chr16:48181983
|
G | C | 10 | a0003c0018t0002g0010a0003c0018t0018g0132a0007c0008t0003g0006others(7): Show | 11 | HG01496.hp2 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.3258+2457C>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48181983 | ||||||
| chr16:48182087
|
C | T | 1 | a0003c0018t0002g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3258+2353G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48182087 | ||||||
| chr16:48182212
|
C | T | 1 | a0007c0008t0003g0006 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3258+2228G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48182212 | ||||||
| chr16:48182243
|
C | T | 1 | a0002c0002t0001g0003 | 2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.3258+2197G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48182243 | ||||||
| chr16:48182256
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3258+2184T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48182256 | ||||||
| chr16:48182440
|
ATT | A | 5 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.3258+1998_3258+199 others(6): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48182440 | ||||||
| chr16:48182553
|
G | A | 8 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.3258+1887C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48182553 | ||||||
| chr16:48182596
|
A | G | 1 | a0003c0029t0015g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3258+1844T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48182596 | ||||||
| chr16:48182782
|
C | CA | 9 | a0002c0002t0001g0118a0008c0007t0006g0142a0008c0007t0006g0143others(6): Show | 9 | HG01891.hp2 HG02083.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.3258+1657dupT | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48182782 | ||||||
| chr16:48182812
|
T | C | 1 | a0005c0004t0001g0098 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3258+1628A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48182812 | ||||||
| chr16:48183032
|
C | T | 1 | a0005c0004t0001g0098 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3258+1408G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48183032 | ||||||
| chr16:48183088
|
C | T | 3 | a0007c0008t0003g0136a0007c0008t0003g0137a0007c0008t0003g0139 | 3 | HG02723.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3258+1352G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48183088 | ||||||
| chr16:48183133
|
G | T | 17 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(14): Show | 18 | HG01099.hp2 HG01109.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.3258+1307C>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48183133 | ||||||
| chr16:48183280
|
C | T | 1 | a0001c0001t0014g0007 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3258+1160G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48183280 | ||||||
| chr16:48183527
|
C | T | 1 | a0003c0029t0015g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3258+913G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48183527 | ||||||
| chr16:48183565
|
C | T | 1 | a0003c0029t0015g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3258+875G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48183565 | ||||||
| chr16:48183854
|
G | A | 9 | a0001c0003t0001g0050a0001c0003t0001g0054a0001c0003t0001g0056others(6): Show | 9 | HG01106.hp2 HG02040.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.3258+586C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48183854 | ||||||
| chr16:48183890
|
C | A | 52 | a0001c0001t0001g0079a0003c0006t0004g0011a0003c0006t0004g0012others(49): Show | 57 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.3258+550G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 23/29 | chr16 | 48183890 | ||||||
| chr16:48184644
|
G | C | 6 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(3): Show | 6 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.3072-18C>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 22/29 | chr16 | 48184644 | ||||||
| chr16:48184874
|
C | T | 1 | a0003c0018t0018g0132 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3072-248G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 22/29 | chr16 | 48184874 | ||||||
| chr16:48184923
|
G | T | 1 | a0001c0001t0001g0085 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3072-297C>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 22/29 | chr16 | 48184923 | ||||||
| chr16:48185057
|
A | G | 1 | a0004c0027t0001g0034 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3072-431T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 22/29 | chr16 | 48185057 | ||||||
| chr16:48185437
|
G | A | 10 | a0003c0018t0002g0010a0003c0018t0018g0132a0007c0008t0003g0006others(7): Show | 11 | HG01496.hp2 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.3072-811C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 22/29 | chr16 | 48185437 | ||||||
| chr16:48185475
|
T | C | 1 | a0003c0029t0015g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3072-849A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 22/29 | chr16 | 48185475 | ||||||
| chr16:48185766
|
T | C | 1 | a0015c0024t0012g0133 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3072-1140A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 22/29 | chr16 | 48185766 | ||||||
| chr16:48186332
|
C | T | 1 | a0001c0003t0001g0054 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3071+621G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 22/29 | chr16 | 48186332 | ||||||
| chr16:48186438
|
C | T | 1 | a0006c0005t0005g0148 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.3071+515G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 22/29 | chr16 | 48186438 | ||||||
| chr16:48186591
|
C | A | 1 | a0001c0003t0013g0141 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3071+362G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 22/29 | chr16 | 48186591 | ||||||
| chr16:48186783
|
A | G | 1 | a0004c0027t0001g0034 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3071+170T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 22/29 | chr16 | 48186783 | ||||||
| chr16:48187446
|
C | A | 1 | a0001c0003t0001g0017 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2707-19G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48187446 | ||||||
| chr16:48187626
|
G | A | 1 | a0014c0016t0002g0077 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2707-199C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48187626 | ||||||
| chr16:48187668
|
C | A | 6 | a0006c0005t0005g0001a0006c0005t0005g0148a0006c0005t0005g0149others(3): Show | 8 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.2707-241G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48187668 | ||||||
| chr16:48187761
|
C | T | 1 | a0001c0039t0001g0066 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2707-334G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48187761 | ||||||
| chr16:48187844
|
C | A | 6 | a0006c0005t0005g0001a0006c0005t0005g0148a0006c0005t0005g0149others(3): Show | 8 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.2707-417G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48187844 | ||||||
| chr16:48187860
|
T | A | 3 | a0001c0001t0001g0116a0002c0002t0001g0103a0002c0002t0009g0009 | 3 | HG02698.hp2 HG02738.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2707-433A>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48187860 | ||||||
| chr16:48188166
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2707-739A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48188166 | ||||||
| chr16:48188201
|
A | G | 1 | a0008c0007t0006g0142 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2707-774T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48188201 | ||||||
| chr16:48188310
|
C | T | 8 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2707-883G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48188310 | ||||||
| chr16:48188358
|
G | C | 13 | a0006c0005t0005g0001a0006c0005t0005g0148a0006c0005t0005g0149others(10): Show | 16 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.2707-931C>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48188358 | ||||||
| chr16:48188694
|
T | A | 1 | a0001c0001t0001g0046 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2707-1267A>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48188694 | ||||||
| chr16:48188881
|
T | A | 17 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(14): Show | 18 | HG01099.hp2 HG01109.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.2707-1454A>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48188881 | ||||||
| chr16:48188907
|
G | A | 1 | a0003c0029t0015g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2707-1480C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48188907 | ||||||
| chr16:48189232
|
C | T | 1 | a0015c0024t0012g0133 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2707-1805G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48189232 | ||||||
| chr16:48189261
|
C | G | 2 | a0001c0001t0001g0079a0004c0028t0012g0131 | 2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2707-1834G>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48189261 | ||||||
| chr16:48189323
|
T | G | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG01433.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2707-1896A>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48189323 | ||||||
| chr16:48189433
|
AT | A | 8 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2707-2007delA | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48189433 | ||||||
| chr16:48189462
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2707-2035C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48189462 | ||||||
| chr16:48189524
|
T | G | 3 | a0001c0001t0001g0084a0001c0037t0001g0070a0001c0039t0001g0066 | 3 | HG03486.hp2 HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2707-2097A>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48189524 | ||||||
| chr16:48189664
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2707-2237A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48189664 | ||||||
| chr16:48189881
|
C | T | 3 | a0012c0015t0002g0080a0012c0015t0003g0134a0012c0015t0003g0135 | 3 | HG01496.hp2 HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2707-2454G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48189881 | ||||||
| chr16:48189924
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2707-2497G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48189924 | ||||||
| chr16:48190031
|
C | A | 2 | a0001c0020t0001g0061a0001c0020t0001g0075 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2706+2489G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48190031 | ||||||
| chr16:48190171
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2706+2349G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48190171 | ||||||
| chr16:48190172
|
G | A | 1 | a0002c0002t0001g0090 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2706+2348C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48190172 | ||||||
| chr16:48190178
|
G | C | 8 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2706+2342C>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48190178 | ||||||
| chr16:48190354
|
A | C | 6 | a0003c0029t0015g0019a0004c0009t0001g0126a0004c0009t0001g0128others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2706+2166T>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48190354 | ||||||
| chr16:48190354
|
A | G | 14 | a0001c0037t0001g0070a0006c0005t0005g0001a0006c0005t0005g0148others(11): Show | 17 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.2706+2166T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48190354 | ||||||
| chr16:48190371
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2706+2149A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48190371 | ||||||
| chr16:48190470
|
C | T | 8 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2706+2050G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48190470 | ||||||
| chr16:48190824
|
G | A | 1 | a0003c0029t0015g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2706+1696C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48190824 | ||||||
| chr16:48190967
|
A | G | 1 | a0003c0029t0015g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2706+1553T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48190967 | ||||||
| chr16:48191058
|
G | A | 1 | a0006c0005t0005g0150 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2706+1462C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48191058 | ||||||
| chr16:48191517
|
G | A | 8 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2706+1003C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48191517 | ||||||
| chr16:48191566
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2706+954G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48191566 | ||||||
| chr16:48191841
|
A | T | 1 | a0003c0029t0015g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2706+679T>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48191841 | ||||||
| chr16:48192421
|
G | T | 2 | a0001c0021t0001g0041a0001c0021t0001g0042 | 2 | HG02572.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2706+99C>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 20/29 | chr16 | 48192421 | ||||||
| chr16:48192774
|
G | A | 5 | a0004c0009t0001g0126a0004c0009t0001g0128a0004c0009t0001g0129others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2509-57C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 19/29 | chr16 | 48192774 | ||||||
| chr16:48193286
|
C | G | 1 | a0018c0025t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2509-569G>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 19/29 | chr16 | 48193286 | ||||||
| chr16:48193528
|
C | G | 2 | a0001c0001t0001g0079a0004c0028t0012g0131 | 2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2508+351G>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 19/29 | chr16 | 48193528 | ||||||
| chr16:48193837
|
C | CG | 13 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(10): Show | 14 | HG01099.hp2 HG01109.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.2508+41_2508+42ins others(1): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 19/29 | chr16 | 48193837 | ||||||
| chr16:48194494
|
A | G | 3 | a0004c0017t0001g0029a0004c0017t0001g0031a0018c0025t0001g0030 | 3 | HG01106.hp1 HG01243.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.2405-512T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 18/29 | chr16 | 48194494 | ||||||
| chr16:48194678
|
T | C | 5 | a0004c0009t0001g0126a0004c0009t0001g0128a0004c0009t0001g0129others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2405-696A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 18/29 | chr16 | 48194678 | ||||||
| chr16:48194695
|
T | C | 1 | a0003c0029t0015g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2405-713A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 18/29 | chr16 | 48194695 | ||||||
| chr16:48194727
|
T | C | 2 | a0008c0007t0006g0144a0008c0007t0006g0145 | 2 | HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.2405-745A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 18/29 | chr16 | 48194727 | ||||||
| chr16:48194731
|
G | A | 2 | a0001c0020t0001g0061a0001c0020t0001g0075 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2405-749C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 18/29 | chr16 | 48194731 | ||||||
| chr16:48195605
|
T | G | 5 | a0004c0009t0001g0126a0004c0009t0001g0128a0004c0009t0001g0129others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2404+627A>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 18/29 | chr16 | 48195605 | ||||||
| chr16:48195679
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2404+553G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 18/29 | chr16 | 48195679 | ||||||
| chr16:48195818
|
C | G | 1 | a0002c0002t0001g0095 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2404+414G>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 18/29 | chr16 | 48195818 | ||||||
| chr16:48195878
|
G | C | 31 | a0001c0037t0001g0070a0003c0006t0004g0011a0003c0006t0004g0012others(28): Show | 35 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.2404+354C>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 18/29 | chr16 | 48195878 | ||||||
| chr16:48196820
|
A | T | 17 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(14): Show | 18 | HG01099.hp2 HG01109.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.2315-499T>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 17/29 | chr16 | 48196820 | ||||||
| chr16:48196823
|
G | A | 150 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0037others(147): Show | 157 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.2315-502C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 17/29 | chr16 | 48196823 | ||||||
| chr16:48196888
|
T | C | 2 | a0003c0018t0002g0010a0003c0018t0018g0132 | 2 | HG02280.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.2315-567A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 17/29 | chr16 | 48196888 | ||||||
| chr16:48196997
|
G | A | 2 | a0013c0014t0002g0002a0013c0014t0002g0110 | 3 | HG02559.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2315-676C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 17/29 | chr16 | 48196997 | ||||||
| chr16:48197182
|
G | A | 1 | a0003c0029t0015g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2314+789C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 17/29 | chr16 | 48197182 | ||||||
| chr16:48197309
|
C | G | 150 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0037others(147): Show | 157 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.2314+662G>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 17/29 | chr16 | 48197309 | ||||||
| chr16:48197312
|
A | AG | 150 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0037others(147): Show | 157 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.2314+658_2314+659i others(3): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 17/29 | chr16 | 48197312 | ||||||
| chr16:48197616
|
C | G | 1 | a0001c0001t0014g0007 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2314+355G>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 17/29 | chr16 | 48197616 | ||||||
| chr16:48197709
|
G | T | 10 | a0003c0018t0002g0010a0003c0018t0018g0132a0007c0008t0003g0006others(7): Show | 11 | HG01496.hp2 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2314+262C>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 17/29 | chr16 | 48197709 | ||||||
| chr16:48197754
|
C | A | 1 | a0004c0027t0001g0034 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2314+217G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 17/29 | chr16 | 48197754 | ||||||
| chr16:48198124
|
A | T | 1 | a0001c0001t0001g0071 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2217+17T>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 16/29 | chr16 | 48198124 | ||||||
| chr16:48198537
|
T | C | 2 | a0001c0001t0001g0113a0001c0001t0001g0115 | 2 | HG02622.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2083-262A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 15/29 | chr16 | 48198537 | ||||||
| chr16:48198625
|
A | G | 57 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(54): Show | 62 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.2083-350T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 15/29 | chr16 | 48198625 | ||||||
| chr16:48198637
|
AT | A | 24 | a0001c0001t0001g0089a0001c0003t0001g0064a0002c0002t0001g0093others(21): Show | 26 | HG01070.hp2 HG01496.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.2083-363delA | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 15/29 | chr16 | 48198637 | ||||||
| chr16:48198685
|
T | C | 6 | a0003c0029t0015g0019a0004c0009t0001g0126a0004c0009t0001g0128others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2083-410A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 15/29 | chr16 | 48198685 | ||||||
| chr16:48199041
|
T | A | 32 | a0001c0001t0001g0044a0003c0006t0004g0011a0003c0006t0004g0012others(29): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.2083-766A>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 15/29 | chr16 | 48199041 | ||||||
| chr16:48199043
|
T | A | 1 | a0014c0016t0002g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2083-768A>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 15/29 | chr16 | 48199043 | ||||||
| chr16:48199146
|
G | T | 7 | a0011c0011t0002g0005a0011c0011t0002g0124a0011c0011t0002g0125others(4): Show | 8 | HG02109.hp1 HG02486.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2083-871C>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 15/29 | chr16 | 48199146 | ||||||
| chr16:48199345
|
T | C | 2 | a0001c0001t0001g0079a0004c0028t0012g0131 | 2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2082+931A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 15/29 | chr16 | 48199345 | ||||||
| chr16:48199672
|
AT | A | 33 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0059others(30): Show | 35 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.2082+603delA | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 15/29 | chr16 | 48199672 | ||||||
| chr16:48199672
|
ATT | A | 51 | a0001c0001t0001g0016a0001c0001t0001g0037a0001c0001t0001g0044others(48): Show | 51 | HG00558.hp2 HG00741.hp2 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.2082+602_2082+603d others(4): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 15/29 | chr16 | 48199672 | ||||||
| chr16:48199672
|
ATTT | A | 26 | a0001c0001t0001g0018a0001c0001t0001g0048a0001c0001t0001g0084others(23): Show | 27 | HG00738.hp1 HG01109.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.2082+601_2082+603d others(5): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 15/29 | chr16 | 48199672 | ||||||
| chr16:48199672
|
ATTTT | A | 3 | a0003c0023t0004g0032a0006c0005t0005g0001a0010c0012t0007g0020 | 5 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.2082+600_2082+603d others(6): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 15/29 | chr16 | 48199672 | ||||||
| chr16:48199672
|
ATTTTT | A | 6 | a0009c0010t0008g0024a0010c0012t0007g0021a0010c0012t0007g0022others(3): Show | 7 | HG01891.hp1 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2082+599_2082+603d others(7): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 15/29 | chr16 | 48199672 | ||||||
| chr16:48199672
|
ATTTTTT | A | 12 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(9): Show | 12 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2082+598_2082+603d others(8): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 15/29 | chr16 | 48199672 | ||||||
| chr16:48199846
|
T | A | 3 | a0012c0015t0002g0080a0012c0015t0003g0134a0012c0015t0003g0135 | 3 | HG01496.hp2 HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2082+430A>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 15/29 | chr16 | 48199846 | ||||||
| chr16:48199848
|
A | G | 1 | a0002c0002t0001g0093 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2082+428T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 15/29 | chr16 | 48199848 | ||||||
| chr16:48199878
|
G | A | 1 | a0003c0018t0002g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2082+398C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 15/29 | chr16 | 48199878 | ||||||
| chr16:48199938
|
A | G | 1 | a0003c0023t0004g0032 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2082+338T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 15/29 | chr16 | 48199938 | ||||||
| chr16:48199988
|
T | C | 5 | a0004c0009t0001g0126a0004c0009t0001g0128a0004c0009t0001g0129others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2082+288A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 15/29 | chr16 | 48199988 | ||||||
| chr16:48200046
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2082+230T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 15/29 | chr16 | 48200046 | ||||||
| chr16:48200245
|
A | G | 2 | a0001c0001t0001g0089a0002c0002t0001g0093 | 2 | HG02129.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.2082+31T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 15/29 | chr16 | 48200245 | ||||||
| chr16:48200641
|
A | G | 1 | a0001c0003t0001g0064 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1879-162T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 14/29 | chr16 | 48200641 | ||||||
| chr16:48200653
|
C | G | 1 | a0001c0001t0001g0088 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1879-174G>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 14/29 | chr16 | 48200653 | ||||||
| chr16:48200927
|
C | G | 8 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(5): Show | 9 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1879-448G>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 14/29 | chr16 | 48200927 | ||||||
| chr16:48201369
|
C | G | 6 | a0001c0001t0001g0079a0004c0009t0001g0126a0004c0009t0001g0128others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1879-890G>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 14/29 | chr16 | 48201369 | ||||||
| chr16:48201374
|
A | T | 10 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(7): Show | 11 | HG01496.hp2 HG01884.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1879-895T>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 14/29 | chr16 | 48201374 | ||||||
| chr16:48201458
|
C | T | 6 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(3): Show | 6 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1879-979G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 14/29 | chr16 | 48201458 | ||||||
| chr16:48201465
|
T | A | 5 | a0004c0009t0001g0126a0004c0009t0001g0128a0004c0009t0001g0129others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1879-986A>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 14/29 | chr16 | 48201465 | ||||||
| chr16:48201474
|
C | CT | 31 | a0001c0001t0001g0120a0003c0006t0004g0011a0003c0006t0004g0012others(28): Show | 33 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1879-996dupA | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 14/29 | chr16 | 48201474 | ||||||
| chr16:48201474
|
C | CTT | 5 | a0004c0009t0001g0126a0004c0009t0001g0128a0004c0009t0001g0129others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1879-997_1879-996d others(4): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 14/29 | chr16 | 48201474 | ||||||
| chr16:48201474
|
CT | C | 32 | a0001c0001t0001g0018a0001c0001t0001g0048a0001c0003t0001g0017others(29): Show | 34 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.1879-996delA | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 14/29 | chr16 | 48201474 | ||||||
| chr16:48201478
|
T | C | 1 | a0001c0003t0001g0050 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1879-999A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 14/29 | chr16 | 48201478 | ||||||
| chr16:48201607
|
C | T | 1 | a0015c0024t0012g0133 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1879-1128G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 14/29 | chr16 | 48201607 | ||||||
| chr16:48201666
|
C | G | 54 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(51): Show | 58 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.1879-1187G>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 14/29 | chr16 | 48201666 | ||||||
| chr16:48202383
|
G | A | 5 | a0004c0009t0001g0126a0004c0009t0001g0128a0004c0009t0001g0129others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1878+845C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 14/29 | chr16 | 48202383 | ||||||
| chr16:48202553
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1878+675C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 14/29 | chr16 | 48202553 | ||||||
| chr16:48202594
|
G | A | 11 | a0004c0027t0001g0034a0010c0012t0007g0020a0010c0012t0007g0021others(8): Show | 12 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1878+634C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 14/29 | chr16 | 48202594 | ||||||
| chr16:48202676
|
A | G | 1 | a0004c0009t0001g0129 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1878+552T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 14/29 | chr16 | 48202676 | ||||||
| chr16:48202748
|
G | T | 1 | a0003c0029t0015g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1878+480C>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 14/29 | chr16 | 48202748 | ||||||
| chr16:48202755
|
A | C | 54 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(51): Show | 58 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.1878+473T>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 14/29 | chr16 | 48202755 | ||||||
| chr16:48203901
|
C | T | 1 | a0002c0002t0001g0003 | 2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1806-601G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 13/29 | chr16 | 48203901 | ||||||
| chr16:48204118
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1806-818A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 13/29 | chr16 | 48204118 | ||||||
| chr16:48204140
|
C | T | 14 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(11): Show | 14 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1806-840G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 13/29 | chr16 | 48204140 | ||||||
| chr16:48204206
|
G | T | 54 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(51): Show | 58 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.1806-906C>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 13/29 | chr16 | 48204206 | ||||||
| chr16:48204491
|
T | C | 3 | a0014c0016t0002g0067a0014c0016t0002g0077a0014c0016t0002g0078 | 3 | HG02109.hp1 HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1805+922A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 13/29 | chr16 | 48204491 | ||||||
| chr16:48204749
|
T | C | 3 | a0012c0015t0002g0080a0012c0015t0003g0134a0012c0015t0003g0135 | 3 | HG01496.hp2 HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1805+664A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 13/29 | chr16 | 48204749 | ||||||
| chr16:48204859
|
G | A | 11 | a0004c0027t0001g0034a0010c0012t0007g0020a0010c0012t0007g0021others(8): Show | 12 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1805+554C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 13/29 | chr16 | 48204859 | ||||||
| chr16:48204923
|
C | T | 8 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1805+490G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 13/29 | chr16 | 48204923 | ||||||
| chr16:48205282
|
G | C | 3 | a0012c0015t0002g0080a0012c0015t0003g0134a0012c0015t0003g0135 | 3 | HG01496.hp2 HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1805+131C>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 13/29 | chr16 | 48205282 | ||||||
| chr16:48205678
|
C | T | 8 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1681-141G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 12/29 | chr16 | 48205678 | ||||||
| chr16:48205802
|
G | GT | 8 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1681-266dupA | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 12/29 | chr16 | 48205802 | ||||||
| chr16:48205812
|
C | CT | 32 | a0003c0018t0018g0132a0003c0023t0004g0032a0004c0009t0001g0126others(29): Show | 36 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1681-276dupA | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 12/29 | chr16 | 48205812 | ||||||
| chr16:48205812
|
C | CTT | 15 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(12): Show | 15 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1681-277_1681-276d others(4): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 12/29 | chr16 | 48205812 | ||||||
| chr16:48205834
|
G | A | 15 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(12): Show | 15 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1681-297C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 12/29 | chr16 | 48205834 | ||||||
| chr16:48205903
|
C | A | 1 | a0003c0018t0018g0132 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1681-366G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 12/29 | chr16 | 48205903 | ||||||
| chr16:48205972
|
G | A | 15 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(12): Show | 15 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1681-435C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 12/29 | chr16 | 48205972 | ||||||
| chr16:48206012
|
G | A | 8 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(5): Show | 9 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1681-475C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 12/29 | chr16 | 48206012 | ||||||
| chr16:48206061
|
C | T | 1 | a0010c0012t0007g0022 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1681-524G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 12/29 | chr16 | 48206061 | ||||||
| chr16:48206070
|
A | G | 8 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1681-533T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 12/29 | chr16 | 48206070 | ||||||
| chr16:48206306
|
A | T | 11 | a0004c0027t0001g0034a0010c0012t0007g0020a0010c0012t0007g0021others(8): Show | 12 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1681-769T>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 12/29 | chr16 | 48206306 | ||||||
| chr16:48206392
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1681-855T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 12/29 | chr16 | 48206392 | ||||||
| chr16:48206991
|
C | T | 8 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1680+1434G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 12/29 | chr16 | 48206991 | ||||||
| chr16:48207116
|
G | A | 1 | a0003c0018t0002g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1680+1309C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 12/29 | chr16 | 48207116 | ||||||
| chr16:48207151
|
G | T | 1 | a0003c0018t0018g0132 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1680+1274C>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 12/29 | chr16 | 48207151 | ||||||
| chr16:48207176
|
A | G | 39 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(36): Show | 42 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1680+1249T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 12/29 | chr16 | 48207176 | ||||||
| chr16:48207637
|
T | C | 35 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(32): Show | 37 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.1680+788A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 12/29 | chr16 | 48207637 | ||||||
| chr16:48207695
|
A | AAAGGG | 4 | a0007c0008t0003g0136a0007c0008t0003g0137a0007c0008t0003g0138others(1): Show | 4 | HG02647.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1680+725_1680+729d others(7): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 12/29 | chr16 | 48207695 | ||||||
| chr16:48207856
|
TACCCC | T | 2 | a0001c0001t0001g0016a0002c0002t0001g0109 | 2 | HG03704.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1680+564_1680+568d others(7): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 12/29 | chr16 | 48207856 | ||||||
| chr16:48207858
|
CCCCACTG | C | 9 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0072others(6): Show | 9 | HG00741.hp2 HG01109.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1680+560_1680+566d others(9): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 12/29 | chr16 | 48207858 | ||||||
| chr16:48208041
|
C | CT | 7 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(4): Show | 8 | HG01496.hp2 HG01884.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1680+383dupA | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 12/29 | chr16 | 48208041 | ||||||
| chr16:48208283
|
A | G | 8 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1680+142T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 12/29 | chr16 | 48208283 | ||||||
| chr16:48208291
|
T | C | 1 | a0003c0018t0018g0132 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1680+134A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 12/29 | chr16 | 48208291 | ||||||
| chr16:48208324
|
T | C | 5 | a0003c0018t0002g0010a0009c0010t0008g0024a0009c0010t0008g0025others(2): Show | 5 | HG01109.hp2 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1680+101A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 12/29 | chr16 | 48208324 | ||||||
| chr16:48208545
|
A | G | 11 | a0004c0027t0001g0034a0010c0012t0007g0020a0010c0012t0007g0021others(8): Show | 12 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1609-49T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 11/29 | chr16 | 48208545 | ||||||
| chr16:48208768
|
G | T | 1 | a0003c0018t0018g0132 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1609-272C>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 11/29 | chr16 | 48208768 | ||||||
| chr16:48208863
|
C | T | 1 | a0002c0013t0001g0043 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1609-367G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 11/29 | chr16 | 48208863 | ||||||
| chr16:48208987
|
T | G | 12 | a0003c0018t0018g0132a0004c0009t0001g0126a0004c0009t0001g0128others(9): Show | 14 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.1609-491A>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 11/29 | chr16 | 48208987 | ||||||
| chr16:48209077
|
T | C | 3 | a0011c0011t0002g0005a0011c0011t0002g0124a0011c0011t0002g0125 | 4 | HG02486.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1609-581A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 11/29 | chr16 | 48209077 | ||||||
| chr16:48209319
|
T | G | 1 | a0014c0016t0002g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1609-823A>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 11/29 | chr16 | 48209319 | ||||||
| chr16:48209522
|
A | G | 11 | a0004c0027t0001g0034a0010c0012t0007g0020a0010c0012t0007g0021others(8): Show | 12 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1609-1026T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 11/29 | chr16 | 48209522 | ||||||
| chr16:48209558
|
C | T | 1 | a0003c0018t0002g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1609-1062G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 11/29 | chr16 | 48209558 | ||||||
| chr16:48209596
|
G | A | 5 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1609-1100C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 11/29 | chr16 | 48209596 | ||||||
| chr16:48209913
|
G | A | 1 | a0004c0028t0012g0131 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1608+1035C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 11/29 | chr16 | 48209913 | ||||||
| chr16:48209933
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1608+1015C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 11/29 | chr16 | 48209933 | ||||||
| chr16:48210065
|
G | A | 4 | a0010c0012t0007g0020a0010c0012t0007g0021a0010c0012t0007g0022others(1): Show | 4 | HG01891.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1608+883C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 11/29 | chr16 | 48210065 | ||||||
| chr16:48210159
|
C | T | 23 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(20): Show | 23 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1608+789G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 11/29 | chr16 | 48210159 | ||||||
| chr16:48210364
|
A | T | 1 | a0003c0018t0018g0132 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1608+584T>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 11/29 | chr16 | 48210364 | ||||||
| chr16:48210401
|
T | C | 1 | a0004c0009t0010g0127 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1608+547A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 11/29 | chr16 | 48210401 | ||||||
| chr16:48210465
|
G | A | 55 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(52): Show | 59 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.1608+483C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 11/29 | chr16 | 48210465 | ||||||
| chr16:48210574
|
G | C | 35 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(32): Show | 37 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.1608+374C>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 11/29 | chr16 | 48210574 | ||||||
| chr16:48210638
|
A | G | 3 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013 | 3 | HG02074.hp1 HG02083.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.1608+310T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 11/29 | chr16 | 48210638 | ||||||
| chr16:48210806
|
T | C | 12 | a0003c0018t0018g0132a0004c0009t0001g0126a0004c0009t0001g0128others(9): Show | 14 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.1608+142A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 11/29 | chr16 | 48210806 | ||||||
| chr16:48210927
|
G | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0059 | 2 | HG00438.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1608+21C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 11/29 | chr16 | 48210927 | ||||||
| chr16:48210928
|
C | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0059 | 2 | HG00438.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1608+20G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 11/29 | chr16 | 48210928 | ||||||
| chr16:48211421
|
T | C | 1 | a0004c0027t0001g0034 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1357-222A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 10/29 | chr16 | 48211421 | ||||||
| chr16:48211681
|
TA | T | 10 | a0001c0001t0001g0111a0008c0007t0006g0142a0008c0007t0006g0143others(7): Show | 10 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1357-483delT | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 10/29 | chr16 | 48211681 | ||||||
| chr16:48211801
|
C | G | 1 | a0006c0005t0005g0149 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1357-602G>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 10/29 | chr16 | 48211801 | ||||||
| chr16:48211843
|
A | G | 4 | a0006c0005t0005g0148a0006c0005t0005g0149a0006c0005t0005g0150others(1): Show | 4 | HG00738.hp1 HG00741.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1357-644T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 10/29 | chr16 | 48211843 | ||||||
| chr16:48211877
|
G | C | 1 | a0001c0001t0001g0104 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1357-678C>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 10/29 | chr16 | 48211877 | ||||||
| chr16:48212065
|
T | C | 35 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(32): Show | 37 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.1357-866A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 10/29 | chr16 | 48212065 | ||||||
| chr16:48212216
|
C | T | 11 | a0004c0027t0001g0034a0010c0012t0007g0020a0010c0012t0007g0021others(8): Show | 12 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1357-1017G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 10/29 | chr16 | 48212216 | ||||||
| chr16:48212260
|
C | T | 1 | a0001c0039t0001g0066 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1357-1061G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 10/29 | chr16 | 48212260 | ||||||
| chr16:48212331
|
C | T | 1 | a0007c0008t0003g0136 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1356+1112G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 10/29 | chr16 | 48212331 | ||||||
| chr16:48212406
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1356+1037T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 10/29 | chr16 | 48212406 | ||||||
| chr16:48212580
|
T | C | 1 | a0003c0018t0002g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1356+863A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 10/29 | chr16 | 48212580 | ||||||
| chr16:48212609
|
C | T | 2 | a0001c0001t0001g0053a0001c0003t0001g0054 | 2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1356+834G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 10/29 | chr16 | 48212609 | ||||||
| chr16:48212669
|
C | G | 1 | a0008c0007t0006g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1356+774G>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 10/29 | chr16 | 48212669 | ||||||
| chr16:48212673
|
A | G | 6 | a0004c0009t0001g0126a0004c0009t0001g0128a0004c0009t0001g0129others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1356+770T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 10/29 | chr16 | 48212673 | ||||||
| chr16:48212783
|
T | C | 1 | a0001c0003t0001g0082 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1356+660A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 10/29 | chr16 | 48212783 | ||||||
| chr16:48212901
|
G | A | 2 | a0001c0020t0001g0061a0001c0020t0001g0075 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1356+542C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 10/29 | chr16 | 48212901 | ||||||
| chr16:48213612
|
T | G | 55 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(52): Show | 59 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.1249-62A>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 9/29 | chr16 | 48213612 | ||||||
| chr16:48213618
|
G | A | 2 | a0004c0028t0012g0131a0008c0007t0006g0146 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1249-68C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 9/29 | chr16 | 48213618 | ||||||
| chr16:48213887
|
T | A | 1 | a0003c0018t0002g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1249-337A>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 9/29 | chr16 | 48213887 | ||||||
| chr16:48214007
|
C | T | 8 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1249-457G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 9/29 | chr16 | 48214007 | ||||||
| chr16:48214087
|
A | G | 1 | a0002c0002t0001g0118 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1249-537T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 9/29 | chr16 | 48214087 | ||||||
| chr16:48214165
|
T | A | 1 | a0006c0005t0005g0148 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1249-615A>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 9/29 | chr16 | 48214165 | ||||||
| chr16:48214457
|
A | T | 55 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(52): Show | 59 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.1248+424T>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 9/29 | chr16 | 48214457 | ||||||
| chr16:48214506
|
C | T | 1 | a0015c0024t0012g0133 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1248+375G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 9/29 | chr16 | 48214506 | ||||||
| chr16:48214532
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0051a0001c0001t0001g0052others(1): Show | 4 | HG01433.hp1 HG01943.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1248+349C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 9/29 | chr16 | 48214532 | ||||||
| chr16:48214650
|
C | A | 8 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1248+231G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 9/29 | chr16 | 48214650 | ||||||
| chr16:48214821
|
G | C | 5 | a0006c0005t0005g0001a0006c0005t0005g0148a0006c0005t0005g0149others(2): Show | 7 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.1248+60C>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 9/29 | chr16 | 48214821 | ||||||
| chr16:48214827
|
G | A | 5 | a0006c0005t0005g0001a0006c0005t0005g0148a0006c0005t0005g0149others(2): Show | 7 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.1248+54C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 9/29 | chr16 | 48214827 | ||||||
| chr16:48215038
|
T | TA | 5 | a0006c0005t0005g0001a0006c0005t0005g0148a0006c0005t0005g0149others(2): Show | 7 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.1100-10dupT | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 8/29 | chr16 | 48215038 | ||||||
| chr16:48215499
|
T | A | 6 | a0004c0009t0001g0126a0004c0009t0001g0128a0004c0009t0001g0129others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.952-155A>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 7/29 | chr16 | 48215499 | ||||||
| chr16:48215814
|
G | T | 34 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(31): Show | 35 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.951+300C>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 7/29 | chr16 | 48215814 | ||||||
| chr16:48215823
|
C | T | 5 | a0006c0005t0005g0001a0006c0005t0005g0148a0006c0005t0005g0149others(2): Show | 7 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.951+291G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 7/29 | chr16 | 48215823 | ||||||
| chr16:48215840
|
A | G | 1 | a0003c0029t0015g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.951+274T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 7/29 | chr16 | 48215840 | ||||||
| chr16:48215936
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.951+178A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 7/29 | chr16 | 48215936 | ||||||
| chr16:48215938
|
C | A | 34 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(31): Show | 35 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.951+176G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 7/29 | chr16 | 48215938 | ||||||
| chr16:48216100
|
G | A | 34 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(31): Show | 35 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.951+14C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 7/29 | chr16 | 48216100 | ||||||
| chr16:48216307
|
T | C | 34 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(31): Show | 35 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.778-20A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48216307 | ||||||
| chr16:48216310
|
G | A | 34 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(31): Show | 35 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.778-23C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48216310 | ||||||
| chr16:48216336
|
C | A | 34 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(31): Show | 35 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.778-49G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48216336 | ||||||
| chr16:48216521
|
C | T | 1 | a0003c0018t0002g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.778-234G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48216521 | ||||||
| chr16:48216525
|
C | G | 14 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(11): Show | 14 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.778-238G>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48216525 | ||||||
| chr16:48216573
|
A | T | 1 | a0004c0009t0001g0129 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.778-286T>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48216573 | ||||||
| chr16:48216574
|
C | T | 1 | a0002c0002t0001g0093 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.778-287G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48216574 | ||||||
| chr16:48216650
|
A | C | 34 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(31): Show | 35 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.778-363T>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48216650 | ||||||
| chr16:48216822
|
C | T | 6 | a0004c0009t0001g0126a0004c0009t0001g0128a0004c0009t0001g0129others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-535G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48216822 | ||||||
| chr16:48216918
|
C | T | 34 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(31): Show | 35 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.778-631G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48216918 | ||||||
| chr16:48216931
|
C | A | 34 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(31): Show | 35 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.778-644G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48216931 | ||||||
| chr16:48217224
|
C | A | 34 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(31): Show | 35 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.778-937G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48217224 | ||||||
| chr16:48217321
|
C | T | 3 | a0011c0011t0002g0005a0011c0011t0002g0124a0011c0011t0002g0125 | 4 | HG02486.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.778-1034G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48217321 | ||||||
| chr16:48217325
|
A | G | 1 | a0001c0003t0001g0114 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.778-1038T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48217325 | ||||||
| chr16:48217461
|
G | T | 34 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(31): Show | 35 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.778-1174C>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48217461 | ||||||
| chr16:48217564
|
T | C | 34 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(31): Show | 35 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.778-1277A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48217564 | ||||||
| chr16:48217755
|
T | A | 1 | a0001c0001t0001g0085 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.778-1468A>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48217755 | ||||||
| chr16:48217905
|
CAT | C | 3 | a0004c0017t0001g0029a0004c0017t0001g0031a0018c0025t0001g0030 | 3 | HG01106.hp1 HG01243.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.778-1620_778-1619d others(4): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48217905 | ||||||
| chr16:48217967
|
G | A | 34 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(31): Show | 35 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.778-1680C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48217967 | ||||||
| chr16:48217990
|
A | G | 34 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(31): Show | 35 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.778-1703T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48217990 | ||||||
| chr16:48218040
|
C | T | 1 | a0003c0018t0018g0132 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.778-1753G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48218040 | ||||||
| chr16:48218151
|
C | T | 1 | a0003c0018t0002g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.778-1864G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48218151 | ||||||
| chr16:48218170
|
C | T | 39 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(36): Show | 42 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.778-1883G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48218170 | ||||||
| chr16:48218441
|
C | T | 36 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(33): Show | 38 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.778-2154G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48218441 | ||||||
| chr16:48218609
|
T | G | 39 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(36): Show | 42 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.778-2322A>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48218609 | ||||||
| chr16:48218710
|
G | A | 7 | a0004c0027t0001g0034a0011c0011t0002g0005a0011c0011t0002g0124others(4): Show | 8 | HG02109.hp1 HG02486.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.778-2423C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48218710 | ||||||
| chr16:48218778
|
C | T | 2 | a0001c0001t0001g0068a0002c0002t0001g0094 | 2 | HG00438.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.778-2491G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48218778 | ||||||
| chr16:48218806
|
C | T | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG01433.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.778-2519G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48218806 | ||||||
| chr16:48218919
|
G | A | 3 | a0004c0017t0001g0029a0004c0017t0001g0031a0018c0025t0001g0030 | 3 | HG01106.hp1 HG01243.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.778-2632C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48218919 | ||||||
| chr16:48219062
|
C | T | 35 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(32): Show | 36 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.778-2775G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48219062 | ||||||
| chr16:48219169
|
G | GT | 20 | a0001c0001t0001g0037a0001c0001t0001g0120a0001c0003t0001g0045others(17): Show | 22 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.778-2883dupA | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48219169 | ||||||
| chr16:48219169
|
GT | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0076a0001c0003t0001g0017others(2): Show | 5 | HG01943.hp1 HG01943.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-2883delA | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48219169 | ||||||
| chr16:48219169
|
GTTTT | G | 35 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(32): Show | 36 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.778-2886_778-2883d others(6): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48219169 | ||||||
| chr16:48219180
|
T | C | 5 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-2893A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48219180 | ||||||
| chr16:48219187
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.778-2900A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48219187 | ||||||
| chr16:48219223
|
T | G | 48 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(45): Show | 52 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.778-2936A>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48219223 | ||||||
| chr16:48219239
|
A | G | 35 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(32): Show | 36 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.778-2952T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48219239 | ||||||
| chr16:48219253
|
TA | T | 12 | a0004c0027t0001g0034a0010c0012t0007g0020a0010c0012t0007g0021others(9): Show | 13 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.778-2967delT | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48219253 | ||||||
| chr16:48219255
|
T | G | 12 | a0004c0027t0001g0034a0010c0012t0007g0020a0010c0012t0007g0021others(9): Show | 13 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.778-2968A>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48219255 | ||||||
| chr16:48219294
|
T | C | 60 | a0001c0001t0001g0079a0001c0001t0001g0113a0001c0001t0001g0115others(57): Show | 64 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.778-3007A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48219294 | ||||||
| chr16:48219363
|
A | G | 48 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(45): Show | 52 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.778-3076T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48219363 | ||||||
| chr16:48219367
|
C | T | 2 | a0002c0002t0001g0038a0002c0002t0001g0105 | 2 | HG02074.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.778-3080G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48219367 | ||||||
| chr16:48219537
|
G | A | 4 | a0009c0010t0008g0024a0009c0010t0008g0025a0009c0010t0008g0035others(1): Show | 4 | HG01109.hp2 HG02145.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.777+3061C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48219537 | ||||||
| chr16:48219607
|
A | T | 48 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(45): Show | 52 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.777+2991T>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48219607 | ||||||
| chr16:48219670
|
T | A | 35 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(32): Show | 36 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.777+2928A>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48219670 | ||||||
| chr16:48219772
|
G | A | 35 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(32): Show | 36 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.777+2826C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48219772 | ||||||
| chr16:48219810
|
G | A | 35 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(32): Show | 36 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.777+2788C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48219810 | ||||||
| chr16:48219932
|
G | C | 35 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(32): Show | 36 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.777+2666C>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48219932 | ||||||
| chr16:48220075
|
A | G | 35 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(32): Show | 36 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.777+2523T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48220075 | ||||||
| chr16:48220201
|
G | A | 35 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(32): Show | 36 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.777+2397C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48220201 | ||||||
| chr16:48220225
|
C | T | 35 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(32): Show | 36 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.777+2373G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48220225 | ||||||
| chr16:48220808
|
G | A | 6 | a0003c0029t0015g0019a0004c0009t0001g0126a0004c0009t0001g0128others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.777+1790C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48220808 | ||||||
| chr16:48221224
|
G | T | 35 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(32): Show | 36 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.777+1374C>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48221224 | ||||||
| chr16:48221511
|
T | C | 3 | a0012c0015t0002g0080a0012c0015t0003g0134a0012c0015t0003g0135 | 3 | HG01496.hp2 HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.777+1087A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48221511 | ||||||
| chr16:48221534
|
A | T | 12 | a0004c0027t0001g0034a0010c0012t0007g0020a0010c0012t0007g0021others(9): Show | 13 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.777+1064T>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48221534 | ||||||
| chr16:48221623
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0116 | 2 | HG02129.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.777+975C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48221623 | ||||||
| chr16:48221628
|
C | T | 35 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(32): Show | 36 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.777+970G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48221628 | ||||||
| chr16:48221737
|
GGT | G | 34 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(31): Show | 35 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.777+859_777+860del others(2): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48221737 | ||||||
| chr16:48221778
|
A | G | 35 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(32): Show | 36 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.777+820T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48221778 | ||||||
| chr16:48221888
|
T | A | 1 | a0007c0008t0003g0138 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.777+710A>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48221888 | ||||||
| chr16:48221916
|
C | CT | 4 | a0003c0006t0004g0028a0003c0018t0002g0010a0011c0011t0002g0005others(1): Show | 5 | HG01175.hp2 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.777+681dupA | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48221916 | ||||||
| chr16:48221929
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.777+669A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48221929 | ||||||
| chr16:48222049
|
G | A | 1 | a0010c0012t0007g0020 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.777+549C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48222049 | ||||||
| chr16:48222081
|
A | AT | 50 | a0001c0001t0001g0046a0001c0001t0001g0062a0001c0001t0001g0063others(47): Show | 54 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.777+516dupA | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48222081 | ||||||
| chr16:48222121
|
G | A | 14 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(11): Show | 14 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.777+477C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48222121 | ||||||
| chr16:48222171
|
C | T | 35 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(32): Show | 36 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.777+427G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48222171 | ||||||
| chr16:48222369
|
C | T | 2 | a0001c0021t0001g0041a0001c0021t0001g0042 | 2 | HG02572.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.777+229G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48222369 | ||||||
| chr16:48222469
|
G | A | 5 | a0004c0009t0001g0126a0004c0009t0001g0128a0004c0009t0001g0129others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.777+129C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48222469 | ||||||
| chr16:48222478
|
T | C | 1 | a0001c0003t0001g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.777+120A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48222478 | ||||||
| chr16:48222573
|
A | G | 40 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(37): Show | 42 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.777+25T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 6/29 | chr16 | 48222573 | ||||||
| chr16:48222991
|
C | T | 1 | a0001c0003t0001g0050 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.544-160G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 5/29 | chr16 | 48222991 | ||||||
| chr16:48222994
|
G | T | 5 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0120others(2): Show | 5 | HG02055.hp2 HG02809.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.544-163C>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 5/29 | chr16 | 48222994 | ||||||
| chr16:48223089
|
G | A | 32 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(29): Show | 33 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.544-258C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 5/29 | chr16 | 48223089 | ||||||
| chr16:48223096
|
G | A | 1 | a0015c0024t0012g0133 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.544-265C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 5/29 | chr16 | 48223096 | ||||||
| chr16:48223175
|
G | A | 8 | a0003c0018t0002g0010a0003c0018t0018g0132a0004c0009t0001g0126others(5): Show | 8 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.544-344C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 5/29 | chr16 | 48223175 | ||||||
| chr16:48223549
|
C | T | 1 | a0003c0029t0015g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.544-718G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 5/29 | chr16 | 48223549 | ||||||
| chr16:48223591
|
G | A | 2 | a0008c0007t0006g0143a0008c0007t0006g0147 | 2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.543+691C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 5/29 | chr16 | 48223591 | ||||||
| chr16:48223885
|
T | C | 32 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(29): Show | 33 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.543+397A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 5/29 | chr16 | 48223885 | ||||||
| chr16:48223985
|
G | A | 1 | a0003c0029t0015g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.543+297C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 5/29 | chr16 | 48223985 | ||||||
| chr16:48224470
|
T | A | 32 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(29): Show | 33 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.396-41A>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48224470 | ||||||
| chr16:48224508
|
C | A | 32 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(29): Show | 33 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.396-79G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48224508 | ||||||
| chr16:48224513
|
T | C | 32 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(29): Show | 33 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.396-84A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48224513 | ||||||
| chr16:48224812
|
C | T | 5 | a0006c0005t0005g0001a0006c0005t0005g0148a0006c0005t0005g0149others(2): Show | 7 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.396-383G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48224812 | ||||||
| chr16:48224814
|
G | A | 1 | a0013c0014t0002g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.396-385C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48224814 | ||||||
| chr16:48224821
|
G | A | 32 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(29): Show | 33 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.396-392C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48224821 | ||||||
| chr16:48224895
|
C | T | 14 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(11): Show | 14 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.396-466G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48224895 | ||||||
| chr16:48224903
|
A | C | 1 | a0001c0001t0014g0007 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.396-474T>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48224903 | ||||||
| chr16:48225043
|
C | CA | 13 | a0006c0005t0005g0001a0006c0005t0005g0148a0006c0005t0005g0149others(10): Show | 16 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.396-615dupT | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48225043 | ||||||
| chr16:48225043
|
C | CAAAA | 23 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(20): Show | 23 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.396-618_396-615dup others(4): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48225043 | ||||||
| chr16:48225043
|
C | CAAAAA | 9 | a0003c0018t0002g0010a0004c0009t0001g0126a0004c0009t0001g0128others(6): Show | 10 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.396-619_396-615dup others(5): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48225043 | ||||||
| chr16:48225071
|
C | G | 3 | a0001c0003t0001g0045a0001c0020t0001g0061a0001c0020t0001g0075 | 3 | HG01099.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.396-642G>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48225071 | ||||||
| chr16:48225169
|
C | T | 32 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(29): Show | 33 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.396-740G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48225169 | ||||||
| chr16:48225192
|
G | A | 40 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(37): Show | 41 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.396-763C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48225192 | ||||||
| chr16:48225200
|
G | A | 14 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(11): Show | 14 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.396-771C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48225200 | ||||||
| chr16:48225534
|
A | ATCCCCTG others(4): Show |
2 | a0003c0018t0018g0132a0004c0028t0012g0131 | 2 | HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.396-1106_396-1105i others(13): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48225534 | ||||||
| chr16:48225539
|
T | C | 48 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(45): Show | 52 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.396-1110A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48225539 | ||||||
| chr16:48225657
|
G | A | 32 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(29): Show | 33 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.396-1228C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48225657 | ||||||
| chr16:48225847
|
C | T | 32 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(29): Show | 33 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.396-1418G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48225847 | ||||||
| chr16:48225931
|
G | A | 1 | a0012c0015t0003g0134 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.396-1502C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48225931 | ||||||
| chr16:48226069
|
G | A | 7 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(4): Show | 8 | HG01884.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.396-1640C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48226069 | ||||||
| chr16:48226072
|
C | CATTATTA others(8): Show |
11 | a0004c0009t0001g0126a0004c0009t0001g0128a0004c0009t0001g0129others(8): Show | 12 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.396-1658_396-1644d others(17): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48226072 | ||||||
| chr16:48226072
|
C | CATTATTA others(11): Show |
9 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(6): Show | 9 | HG01099.hp2 HG01175.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.396-1661_396-1644d others(20): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48226072 | ||||||
| chr16:48226072
|
C | CATTATTA others(14): Show |
6 | a0004c0017t0001g0029a0004c0017t0001g0031a0009c0010t0008g0024others(3): Show | 6 | HG01106.hp1 HG01243.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.396-1664_396-1644d others(23): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48226072 | ||||||
| chr16:48226072
|
C | CATTATTA others(17): Show |
5 | a0003c0018t0002g0010a0003c0023t0004g0032a0003c0029t0015g0019others(2): Show | 5 | HG02055.hp1 HG02280.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.396-1644_396-1643i others(26): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48226072 | ||||||
| chr16:48226072
|
C | CATTATTA others(20): Show |
1 | a0010c0012t0007g0020 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.396-1644_396-1643i others(29): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48226072 | ||||||
| chr16:48226072
|
C | CATTATTA others(23): Show |
1 | a0003c0018t0018g0132 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.396-1644_396-1643i others(32): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48226072 | ||||||
| chr16:48226169
|
C | T | 1 | a0004c0028t0012g0131 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.395+1637G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48226169 | ||||||
| chr16:48226335
|
C | G | 2 | a0012c0015t0003g0134a0012c0015t0003g0135 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.395+1471G>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48226335 | ||||||
| chr16:48226352
|
A | G | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.395+1454T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48226352 | ||||||
| chr16:48226442
|
A | G | 8 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.395+1364T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48226442 | ||||||
| chr16:48226528
|
T | C | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.395+1278A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48226528 | ||||||
| chr16:48226546
|
G | A | 19 | a0001c0001t0001g0037a0001c0001t0001g0044a0001c0001t0001g0046others(16): Show | 19 | HG00558.hp2 HG01070.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.395+1260C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48226546 | ||||||
| chr16:48226566
|
T | C | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.395+1240A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48226566 | ||||||
| chr16:48226572
|
C | T | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.395+1234G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48226572 | ||||||
| chr16:48226719
|
G | A | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.395+1087C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48226719 | ||||||
| chr16:48226787
|
G | A | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.395+1019C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48226787 | ||||||
| chr16:48226893
|
AT | A | 5 | a0006c0005t0005g0001a0006c0005t0005g0148a0006c0005t0005g0149others(2): Show | 7 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+912delA | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48226893 | ||||||
| chr16:48226937
|
T | G | 1 | a0003c0018t0002g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.395+869A>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48226937 | ||||||
| chr16:48227033
|
G | A | 1 | a0002c0002t0001g0038 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.395+773C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48227033 | ||||||
| chr16:48227040
|
A | C | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.395+766T>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48227040 | ||||||
| chr16:48227046
|
A | T | 8 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.395+760T>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48227046 | ||||||
| chr16:48227330
|
C | T | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.395+476G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48227330 | ||||||
| chr16:48227418
|
C | G | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.395+388G>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48227418 | ||||||
| chr16:48227475
|
C | CA | 14 | a0001c0001t0001g0120a0006c0005t0005g0001a0006c0005t0005g0148others(11): Show | 16 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.395+330dupT | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48227475 | ||||||
| chr16:48227475
|
CA | C | 34 | a0001c0001t0001g0016a0001c0001t0001g0115a0001c0001t0001g0121others(31): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.395+330delT | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48227475 | ||||||
| chr16:48227475
|
CAA | C | 7 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(4): Show | 9 | HG01884.hp2 HG02486.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.395+329_395+330del others(2): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48227475 | ||||||
| chr16:48227753
|
C | A | 1 | a0001c0001t0001g0068 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.395+53G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 4/29 | chr16 | 48227753 | ||||||
| chr16:48228106
|
T | C | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.237-142A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48228106 | ||||||
| chr16:48228412
|
T | C | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.237-448A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48228412 | ||||||
| chr16:48228521
|
G | C | 5 | a0004c0009t0001g0126a0004c0009t0001g0128a0004c0009t0001g0129others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-557C>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48228521 | ||||||
| chr16:48228551
|
A | G | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.237-587T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48228551 | ||||||
| chr16:48228586
|
G | A | 1 | a0002c0002t0009g0009 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.237-622C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48228586 | ||||||
| chr16:48228601
|
G | GA | 31 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(28): Show | 32 | HG01099.hp2 HG01109.hp2 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.237-638dupT | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48228601 | ||||||
| chr16:48228772
|
T | C | 5 | a0001c0001t0001g0018a0001c0003t0001g0081a0001c0003t0001g0082others(2): Show | 5 | HG01175.hp1 HG01496.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.237-808A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48228772 | ||||||
| chr16:48229031
|
G | A | 1 | a0003c0029t0015g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.237-1067C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48229031 | ||||||
| chr16:48229052
|
G | A | 3 | a0003c0018t0018g0132a0004c0028t0012g0131a0015c0024t0012g0133 | 3 | HG02896.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.237-1088C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48229052 | ||||||
| chr16:48229128
|
G | A | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.237-1164C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48229128 | ||||||
| chr16:48229260
|
C | T | 5 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(2): Show | 5 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.236+1177G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48229260 | ||||||
| chr16:48229302
|
A | G | 1 | a0004c0027t0001g0034 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.236+1135T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48229302 | ||||||
| chr16:48229453
|
C | CT | 21 | a0001c0001t0001g0072a0003c0006t0004g0011a0003c0006t0004g0012others(18): Show | 23 | HG00741.hp2 HG01099.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.236+983dupA | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48229453 | ||||||
| chr16:48229453
|
C | CTT | 15 | a0003c0018t0002g0010a0003c0018t0018g0132a0003c0023t0004g0032others(12): Show | 16 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.236+982_236+983dup others(2): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48229453 | ||||||
| chr16:48229453
|
C | CTTT | 5 | a0003c0029t0015g0019a0004c0009t0001g0129a0004c0009t0010g0130others(2): Show | 5 | HG02145.hp2 HG03098.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.236+981_236+983dup others(3): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48229453 | ||||||
| chr16:48229482
|
G | A | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.236+955C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48229482 | ||||||
| chr16:48229485
|
G | T | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.236+952C>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48229485 | ||||||
| chr16:48229489
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.236+948C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48229489 | ||||||
| chr16:48229497
|
A | G | 53 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(50): Show | 57 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.236+940T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48229497 | ||||||
| chr16:48229512
|
C | T | 3 | a0001c0001t0014g0007a0002c0002t0009g0009a0002c0019t0009g0008 | 3 | HG02698.hp1 NA19240.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.236+925G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48229512 | ||||||
| chr16:48229534
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.236+903C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48229534 | ||||||
| chr16:48229566
|
A | G | 28 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(25): Show | 29 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.236+871T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48229566 | ||||||
| chr16:48229589
|
T | C | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.236+848A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48229589 | ||||||
| chr16:48229622
|
A | G | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.236+815T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48229622 | ||||||
| chr16:48229682
|
T | A | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.236+755A>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48229682 | ||||||
| chr16:48229808
|
T | C | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.236+629A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48229808 | ||||||
| chr16:48229917
|
C | T | 2 | a0008c0007t0006g0142a0008c0007t0006g0146 | 2 | HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.236+520G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48229917 | ||||||
| chr16:48229935
|
C | T | 2 | a0012c0015t0003g0134a0012c0015t0003g0135 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.236+502G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48229935 | ||||||
| chr16:48230133
|
T | C | 5 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.236+304A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48230133 | ||||||
| chr16:48230337
|
G | T | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.236+100C>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48230337 | ||||||
| chr16:48230417
|
C | T | 1 | a0002c0002t0001g0109 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.236+20G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 3/29 | chr16 | 48230417 | ||||||
| chr16:48230706
|
A | G | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.100-133T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 2/29 | chr16 | 48230706 | ||||||
| chr16:48230864
|
T | C | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.100-291A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 2/29 | chr16 | 48230864 | ||||||
| chr16:48231149
|
C | T | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.100-576G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 2/29 | chr16 | 48231149 | ||||||
| chr16:48231190
|
C | CTTA | 2 | a0006c0005t0005g0149a0006c0005t0005g0151 | 2 | HG00741.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.100-620_100-618dup others(3): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 2/29 | chr16 | 48231190 | ||||||
| chr16:48231311
|
G | T | 1 | a0001c0001t0001g0049 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.99+512C>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 2/29 | chr16 | 48231311 | ||||||
| chr16:48231430
|
C | T | 4 | a0002c0013t0001g0043a0002c0013t0001g0092a0002c0013t0001g0108others(1): Show | 4 | HG01496.hp1 HG01975.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+393G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 2/29 | chr16 | 48231430 | ||||||
| chr16:48231474
|
C | A | 4 | a0009c0010t0008g0024a0009c0010t0008g0025a0009c0010t0008g0035others(1): Show | 4 | HG01109.hp2 HG02145.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+349G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 2/29 | chr16 | 48231474 | ||||||
| chr16:48231660
|
C | CA | 9 | a0001c0001t0001g0069a0001c0001t0001g0113a0002c0002t0001g0103others(6): Show | 11 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.99+162dupT | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 2/29 | chr16 | 48231660 | ||||||
| chr16:48231660
|
C | CAA | 5 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+161_99+162dupTT | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 2/29 | chr16 | 48231660 | ||||||
| chr16:48231673
|
AAAAG | A | 6 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(3): Show | 6 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+146_99+149delCT others(2): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 2/29 | chr16 | 48231673 | ||||||
| chr16:48231674
|
AAAG | A | 24 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(21): Show | 24 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.99+146_99+148delCT others(1): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 2/29 | chr16 | 48231674 | ||||||
| chr16:48231675
|
AAG | A | 10 | a0004c0009t0001g0126a0004c0009t0001g0128a0004c0009t0001g0129others(7): Show | 11 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+146_99+147delCT | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 2/29 | chr16 | 48231675 | ||||||
| chr16:48231998
|
T | A | 5 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18-59A>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48231998 | ||||||
| chr16:48232278
|
C | T | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-339G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48232278 | ||||||
| chr16:48232493
|
A | G | 5 | a0001c0001t0001g0018a0001c0003t0001g0081a0001c0003t0001g0082others(2): Show | 5 | HG01175.hp1 HG01496.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-554T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48232493 | ||||||
| chr16:48232554
|
TA | T | 5 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18-616delT | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48232554 | ||||||
| chr16:48232555
|
A | T | 27 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(24): Show | 28 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-616T>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48232555 | ||||||
| chr16:48232556
|
A | T | 13 | a0003c0018t0002g0010a0003c0018t0018g0132a0003c0029t0015g0019others(10): Show | 15 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18-617T>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48232556 | ||||||
| chr16:48232569
|
A | C | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-630T>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48232569 | ||||||
| chr16:48232628
|
T | C | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-689A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48232628 | ||||||
| chr16:48232920
|
C | T | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-981G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48232920 | ||||||
| chr16:48233100
|
C | G | 2 | a0004c0027t0001g0034a0015c0026t0017g0033 | 2 | NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-18-1161G>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48233100 | ||||||
| chr16:48233165
|
T | C | 3 | a0004c0017t0001g0029a0004c0017t0001g0031a0018c0025t0001g0030 | 3 | HG01106.hp1 HG01243.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-18-1226A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48233165 | ||||||
| chr16:48233419
|
G | T | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-1480C>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48233419 | ||||||
| chr16:48233436
|
C | A | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-1497G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48233436 | ||||||
| chr16:48233591
|
T | G | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-1652A>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48233591 | ||||||
| chr16:48233664
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-18-1725G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48233664 | ||||||
| chr16:48233667
|
A | G | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-1728T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48233667 | ||||||
| chr16:48233732
|
C | T | 1 | a0003c0029t0015g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-18-1793G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48233732 | ||||||
| chr16:48233767
|
C | T | 2 | a0004c0027t0001g0034a0015c0026t0017g0033 | 2 | NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-18-1828G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48233767 | ||||||
| chr16:48233972
|
T | C | 1 | a0005c0004t0001g0098 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-18-2033A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48233972 | ||||||
| chr16:48234152
|
T | C | 1 | a0014c0016t0002g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-18-2213A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48234152 | ||||||
| chr16:48234156
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-18-2217C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48234156 | ||||||
| chr16:48234174
|
A | G | 2 | a0012c0015t0003g0134a0012c0015t0003g0135 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-18-2235T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48234174 | ||||||
| chr16:48234376
|
T | G | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-2437A>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48234376 | ||||||
| chr16:48234377
|
T | A | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-2438A>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48234377 | ||||||
| chr16:48234384
|
T | A | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-2445A>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48234384 | ||||||
| chr16:48234407
|
T | C | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-2468A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48234407 | ||||||
| chr16:48234714
|
G | A | 2 | a0001c0037t0001g0070a0016c0035t0002g0123 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-18-2775C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48234714 | ||||||
| chr16:48234808
|
G | C | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-2869C>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48234808 | ||||||
| chr16:48234826
|
G | A | 2 | a0011c0011t0002g0005a0011c0011t0002g0125 | 3 | HG02486.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-18-2887C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48234826 | ||||||
| chr16:48234947
|
T | TGA | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-3010_-18-3009d others(4): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48234947 | ||||||
| chr16:48234972
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0115 | 2 | HG02622.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-18-3033C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48234972 | ||||||
| chr16:48235018
|
G | A | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-3079C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48235018 | ||||||
| chr16:48235209
|
TAGAGATG others(3): Show |
T | 34 | a0001c0001t0001g0047a0003c0006t0004g0011a0003c0006t0004g0012others(31): Show | 35 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.-18-3280_-18-3271d others(12): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48235209 | ||||||
| chr16:48235352
|
C | T | 5 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18-3413G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48235352 | ||||||
| chr16:48235650
|
A | G | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-3711T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48235650 | ||||||
| chr16:48236007
|
T | C | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-4068A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48236007 | ||||||
| chr16:48236048
|
G | A | 1 | a0015c0026t0017g0033 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-18-4109C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48236048 | ||||||
| chr16:48236057
|
T | C | 1 | a0003c0029t0015g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-18-4118A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48236057 | ||||||
| chr16:48236518
|
C | T | 27 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(24): Show | 28 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-4579G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48236518 | ||||||
| chr16:48236597
|
T | C | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-4658A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48236597 | ||||||
| chr16:48236651
|
C | T | 1 | a0001c0003t0001g0017 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-18-4712G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48236651 | ||||||
| chr16:48236663
|
A | G | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-4724T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48236663 | ||||||
| chr16:48236712
|
T | G | 3 | a0003c0018t0018g0132a0004c0028t0012g0131a0015c0024t0012g0133 | 3 | HG02896.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-18-4773A>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48236712 | ||||||
| chr16:48236820
|
T | G | 2 | a0012c0015t0003g0134a0012c0015t0003g0135 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-18-4881A>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48236820 | ||||||
| chr16:48236952
|
C | T | 3 | a0003c0018t0018g0132a0004c0028t0012g0131a0015c0024t0012g0133 | 3 | HG02896.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-18-5013G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48236952 | ||||||
| chr16:48237196
|
C | T | 1 | a0002c0002t0001g0090 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-18-5257G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48237196 | ||||||
| chr16:48237551
|
G | A | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-5612C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48237551 | ||||||
| chr16:48237604
|
A | G | 2 | a0017c0022t0011g0014a0017c0022t0011g0015 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-18-5665T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48237604 | ||||||
| chr16:48237613
|
C | A | 5 | a0006c0005t0005g0001a0006c0005t0005g0148a0006c0005t0005g0149others(2): Show | 7 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18-5674G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48237613 | ||||||
| chr16:48237633
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-18-5694A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48237633 | ||||||
| chr16:48237641
|
G | A | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-5702C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48237641 | ||||||
| chr16:48237687
|
C | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0115 | 2 | HG02622.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-18-5748G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48237687 | ||||||
| chr16:48237770
|
A | G | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-5831T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48237770 | ||||||
| chr16:48237777
|
C | T | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-5838G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48237777 | ||||||
| chr16:48237907
|
C | T | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-5968G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48237907 | ||||||
| chr16:48237990
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-18-6051C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48237990 | ||||||
| chr16:48238295
|
T | C | 6 | a0004c0027t0001g0034a0010c0012t0007g0020a0010c0012t0007g0021others(3): Show | 6 | HG01891.hp1 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18-6356A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48238295 | ||||||
| chr16:48238441
|
G | C | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-6502C>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48238441 | ||||||
| chr16:48238475
|
C | T | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-6536G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48238475 | ||||||
| chr16:48238603
|
CA | C | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-6665delT | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48238603 | ||||||
| chr16:48238660
|
G | A | 2 | a0012c0015t0003g0134a0012c0015t0003g0135 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-18-6721C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48238660 | ||||||
| chr16:48238805
|
T | C | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-6866A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48238805 | ||||||
| chr16:48238885
|
C | T | 3 | a0011c0011t0002g0005a0011c0011t0002g0124a0011c0011t0002g0125 | 4 | HG02486.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-6946G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48238885 | ||||||
| chr16:48238906
|
C | T | 7 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(4): Show | 8 | HG01884.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18-6967G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48238906 | ||||||
| chr16:48238915
|
C | T | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-6976G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48238915 | ||||||
| chr16:48238934
|
T | TA | 37 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(34): Show | 38 | HG00741.hp2 HG01099.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.-18-6996dupT | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48238934 | ||||||
| chr16:48238934
|
T | TAAA | 8 | a0003c0006t0004g0026a0003c0006t0004g0027a0004c0009t0001g0126others(5): Show | 8 | HG01099.hp2 HG01884.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18-6998_-18-6996d others(5): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48238934 | ||||||
| chr16:48238934
|
T | TAAAA | 13 | a0003c0006t0004g0011a0003c0006t0004g0028a0003c0023t0004g0032others(10): Show | 14 | HG01106.hp1 HG01175.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-18-6999_-18-6996d others(6): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48238934 | ||||||
| chr16:48238934
|
T | TAAAAA | 10 | a0003c0006t0004g0012a0003c0006t0004g0013a0003c0018t0002g0010others(7): Show | 10 | HG01109.hp2 HG01243.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18-7000_-18-6996d others(7): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48238934 | ||||||
| chr16:48238934
|
TA | T | 9 | a0001c0001t0001g0018a0001c0003t0001g0081a0001c0003t0001g0087others(6): Show | 11 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18-6996delT | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48238934 | ||||||
| chr16:48239138
|
G | T | 5 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(2): Show | 5 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18-7199C>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48239138 | ||||||
| chr16:48239183
|
T | C | 2 | a0001c0001t0001g0113a0001c0001t0001g0115 | 2 | HG02622.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-18-7244A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48239183 | ||||||
| chr16:48239284
|
T | C | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-7345A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48239284 | ||||||
| chr16:48239288
|
C | T | 34 | a0001c0001t0001g0046a0003c0006t0004g0011a0003c0006t0004g0012others(31): Show | 35 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.-18-7349G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48239288 | ||||||
| chr16:48239313
|
A | G | 5 | a0006c0005t0005g0001a0006c0005t0005g0148a0006c0005t0005g0149others(2): Show | 7 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18-7374T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48239313 | ||||||
| chr16:48239333
|
C | T | 5 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18-7394G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48239333 | ||||||
| chr16:48239385
|
AC | A | 5 | a0001c0001t0001g0018a0001c0003t0001g0081a0001c0003t0001g0082others(2): Show | 5 | HG01175.hp1 HG01496.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-7447delG | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48239385 | ||||||
| chr16:48239387
|
C | T | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-7448G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48239387 | ||||||
| chr16:48239433
|
A | G | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-7494T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48239433 | ||||||
| chr16:48239454
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-18-7515G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48239454 | ||||||
| chr16:48239561
|
C | CA | 15 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(12): Show | 15 | HG00738.hp2 HG01175.hp1 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18-7623dupT | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48239561 | ||||||
| chr16:48239561
|
CA | C | 18 | a0001c0001t0001g0088a0001c0003t0001g0045a0003c0006t0004g0011others(15): Show | 19 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.-18-7623delT | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48239561 | ||||||
| chr16:48239561
|
CAA | C | 6 | a0004c0027t0001g0034a0010c0012t0007g0020a0010c0012t0007g0021others(3): Show | 6 | HG01891.hp1 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18-7624_-18-7623d others(4): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48239561 | ||||||
| chr16:48239561
|
CAAA | C | 8 | a0003c0018t0002g0010a0003c0018t0018g0132a0003c0029t0015g0019others(5): Show | 9 | HG02280.hp1 HG02486.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18-7625_-18-7623d others(5): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48239561 | ||||||
| chr16:48239561
|
CAAAAAAA others(4): Show |
C | 5 | a0004c0009t0001g0126a0004c0009t0001g0128a0004c0009t0001g0129others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18-7633_-18-7623d others(13): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48239561 | ||||||
| chr16:48239870
|
T | C | 7 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(4): Show | 8 | HG01884.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+7444A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48239870 | ||||||
| chr16:48239932
|
A | G | 6 | a0004c0027t0001g0034a0010c0012t0007g0020a0010c0012t0007g0021others(3): Show | 6 | HG01891.hp1 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+7382T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48239932 | ||||||
| chr16:48240101
|
C | T | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+7213G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48240101 | ||||||
| chr16:48240213
|
G | A | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+7101C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48240213 | ||||||
| chr16:48240493
|
G | A | 3 | a0004c0017t0001g0029a0004c0017t0001g0031a0018c0025t0001g0030 | 3 | HG01106.hp1 HG01243.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-19+6821C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48240493 | ||||||
| chr16:48240496
|
G | A | 1 | a0003c0018t0018g0132 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-19+6818C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48240496 | ||||||
| chr16:48240511
|
T | C | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+6803A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48240511 | ||||||
| chr16:48240622
|
G | A | 1 | a0006c0005t0005g0150 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-19+6692C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48240622 | ||||||
| chr16:48240707
|
C | T | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+6607G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48240707 | ||||||
| chr16:48240728
|
G | T | 1 | a0007c0008t0003g0136 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-19+6586C>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48240728 | ||||||
| chr16:48240729
|
C | T | 1 | a0007c0008t0003g0136 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-19+6585G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48240729 | ||||||
| chr16:48240870
|
G | A | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+6444C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48240870 | ||||||
| chr16:48240875
|
G | T | 3 | a0003c0018t0018g0132a0004c0028t0012g0131a0015c0024t0012g0133 | 3 | HG02896.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-19+6439C>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48240875 | ||||||
| chr16:48241016
|
C | T | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+6298G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48241016 | ||||||
| chr16:48241203
|
C | T | 7 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(4): Show | 8 | HG01884.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+6111G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48241203 | ||||||
| chr16:48241221
|
C | T | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+6093G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48241221 | ||||||
| chr16:48241258
|
T | G | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+6056A>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48241258 | ||||||
| chr16:48241290
|
G | T | 3 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013 | 3 | HG02074.hp1 HG02083.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.-19+6024C>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48241290 | ||||||
| chr16:48241383
|
C | T | 8 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19+5931G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48241383 | ||||||
| chr16:48241658
|
T | C | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+5656A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48241658 | ||||||
| chr16:48241664
|
C | A | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+5650G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48241664 | ||||||
| chr16:48241718
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-19+5596G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48241718 | ||||||
| chr16:48241807
|
T | C | 1 | a0015c0026t0017g0033 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-19+5507A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48241807 | ||||||
| chr16:48242092
|
A | G | 6 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(3): Show | 6 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+5222T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48242092 | ||||||
| chr16:48242119
|
T | A | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+5195A>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48242119 | ||||||
| chr16:48242206
|
TCAAA | T | 3 | a0003c0006t0004g0026a0003c0006t0004g0027a0003c0006t0004g0028 | 3 | HG01099.hp2 HG01175.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-19+5104_-19+5107d others(6): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48242206 | ||||||
| chr16:48242226
|
G | C | 1 | a0011c0011t0002g0124 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-19+5088C>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48242226 | ||||||
| chr16:48242342
|
T | C | 3 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0116 | 3 | HG02129.hp1 HG02293.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.-19+4972A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48242342 | ||||||
| chr16:48242368
|
A | C | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+4946T>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48242368 | ||||||
| chr16:48242373
|
A | G | 45 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(42): Show | 49 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.-19+4941T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48242373 | ||||||
| chr16:48242491
|
T | A | 2 | a0001c0021t0001g0041a0001c0021t0001g0042 | 2 | HG02572.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-19+4823A>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48242491 | ||||||
| chr16:48242610
|
G | A | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+4704C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48242610 | ||||||
| chr16:48242643
|
A | C | 5 | a0006c0005t0005g0001a0006c0005t0005g0148a0006c0005t0005g0149others(2): Show | 7 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19+4671T>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48242643 | ||||||
| chr16:48242671
|
A | G | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+4643T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48242671 | ||||||
| chr16:48242778
|
G | A | 1 | a0002c0002t0001g0109 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-19+4536C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48242778 | ||||||
| chr16:48242912
|
G | A | 33 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0120others(30): Show | 35 | HG00438.hp2 HG00558.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-19+4402C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48242912 | ||||||
| chr16:48243063
|
T | A | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+4251A>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48243063 | ||||||
| chr16:48243076
|
G | GAA | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+4236_-19+4237d others(4): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48243076 | ||||||
| chr16:48243102
|
T | TAA | 5 | a0006c0005t0005g0001a0006c0005t0005g0148a0006c0005t0005g0149others(2): Show | 7 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19+4210_-19+4211d others(4): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48243102 | ||||||
| chr16:48243107
|
A | G | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+4207T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48243107 | ||||||
| chr16:48243269
|
C | T | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+4045G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48243269 | ||||||
| chr16:48243273
|
T | A | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+4041A>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48243273 | ||||||
| chr16:48243401
|
C | CA | 12 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0115others(9): Show | 12 | HG01106.hp2 HG02055.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.-19+3912dupT | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48243401 | ||||||
| chr16:48243401
|
CA | C | 5 | a0001c0021t0001g0041a0001c0021t0001g0042a0002c0013t0001g0043others(2): Show | 5 | HG01975.hp1 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+3912delT | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48243401 | ||||||
| chr16:48243401
|
CAAA | C | 18 | a0003c0023t0004g0032a0004c0009t0001g0129a0004c0009t0010g0130others(15): Show | 22 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19+3910_-19+3912d others(5): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48243401 | ||||||
| chr16:48243401
|
CAAAA | C | 20 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(17): Show | 20 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-19+3909_-19+3912d others(6): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48243401 | ||||||
| chr16:48243595
|
G | GT | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+3718dupA | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48243595 | ||||||
| chr16:48243939
|
T | C | 45 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(42): Show | 49 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.-19+3375A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48243939 | ||||||
| chr16:48243968
|
C | T | 1 | a0021c0034t0001g0039 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-19+3346G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48243968 | ||||||
| chr16:48243993
|
G | GAATAAAT others(1): Show |
4 | a0003c0018t0018g0132a0003c0029t0015g0019a0004c0028t0012g0131others(1): Show | 4 | HG02896.hp1 HG03453.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+3313_-19+3320d others(10): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48243993 | ||||||
| chr16:48243993
|
G | GAATAAAT others(5): Show |
11 | a0003c0018t0002g0010a0004c0009t0001g0126a0004c0009t0001g0128others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-19+3309_-19+3320d others(14): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48243993 | ||||||
| chr16:48243993
|
G | GAATAAAT others(9): Show |
12 | a0003c0006t0004g0026a0003c0006t0004g0027a0003c0006t0004g0028others(9): Show | 13 | HG01099.hp2 HG01106.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19+3305_-19+3320d others(18): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48243993 | ||||||
| chr16:48243993
|
G | GAATAAAT others(13): Show |
6 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(3): Show | 6 | HG02055.hp1 HG02074.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+3301_-19+3320d others(22): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48243993 | ||||||
| chr16:48244070
|
C | T | 33 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(30): Show | 34 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+3244G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48244070 | ||||||
| chr16:48244196
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-19+3118C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48244196 | ||||||
| chr16:48244279
|
C | A | 5 | a0004c0009t0001g0126a0004c0009t0001g0128a0004c0009t0001g0129others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19+3035G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48244279 | ||||||
| chr16:48244556
|
C | T | 1 | a0002c0002t0001g0038 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-19+2758G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48244556 | ||||||
| chr16:48244580
|
T | C | 3 | a0011c0011t0002g0005a0011c0011t0002g0124a0011c0011t0002g0125 | 4 | HG02486.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+2734A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48244580 | ||||||
| chr16:48244714
|
A | G | 32 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(29): Show | 33 | HG01099.hp2 HG01106.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.-19+2600T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48244714 | ||||||
| chr16:48244751
|
T | C | 32 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(29): Show | 33 | HG01099.hp2 HG01106.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.-19+2563A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48244751 | ||||||
| chr16:48244790
|
C | T | 2 | a0004c0027t0001g0034a0015c0026t0017g0033 | 2 | NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-19+2524G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48244790 | ||||||
| chr16:48244798
|
C | G | 1 | a0001c0001t0001g0037 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-19+2516G>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48244798 | ||||||
| chr16:48244812
|
G | T | 3 | a0003c0018t0018g0132a0004c0028t0012g0131a0015c0024t0012g0133 | 3 | HG02896.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-19+2502C>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48244812 | ||||||
| chr16:48244889
|
T | C | 1 | a0003c0018t0002g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-19+2425A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48244889 | ||||||
| chr16:48244897
|
T | C | 1 | a0012c0015t0003g0134 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-19+2417A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48244897 | ||||||
| chr16:48245107
|
C | A | 5 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+2207G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48245107 | ||||||
| chr16:48245181
|
C | G | 14 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(11): Show | 14 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-19+2133G>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48245181 | ||||||
| chr16:48245241
|
C | T | 3 | a0003c0018t0018g0132a0004c0028t0012g0131a0015c0024t0012g0133 | 3 | HG02896.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-19+2073G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48245241 | ||||||
| chr16:48245333
|
G | C | 1 | a0001c0001t0001g0122 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-19+1981C>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48245333 | ||||||
| chr16:48245339
|
T | C | 7 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(4): Show | 8 | HG01884.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+1975A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48245339 | ||||||
| chr16:48245422
|
A | T | 44 | a0003c0006t0004g0011a0003c0006t0004g0012a0003c0006t0004g0013others(41): Show | 47 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.-19+1892T>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48245422 | ||||||
| chr16:48245512
|
T | C | 1 | a0016c0035t0002g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-19+1802A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48245512 | ||||||
| chr16:48245600
|
C | T | 4 | a0010c0012t0007g0020a0010c0012t0007g0021a0010c0012t0007g0022others(1): Show | 4 | HG01891.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+1714G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48245600 | ||||||
| chr16:48245604
|
C | T | 5 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+1710G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48245604 | ||||||
| chr16:48245621
|
GGA | G | 3 | a0011c0011t0002g0005a0011c0011t0002g0124a0011c0011t0002g0125 | 4 | HG02486.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+1691_-19+1692d others(4): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48245621 | ||||||
| chr16:48245635
|
C | T | 1 | a0012c0015t0003g0134 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-19+1679G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48245635 | ||||||
| chr16:48245895
|
C | T | 5 | a0006c0005t0005g0001a0006c0005t0005g0148a0006c0005t0005g0149others(2): Show | 7 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19+1419G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48245895 | ||||||
| chr16:48245926
|
T | G | 7 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(4): Show | 8 | HG01884.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+1388A>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48245926 | ||||||
| chr16:48245944
|
C | T | 5 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+1370G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48245944 | ||||||
| chr16:48246004
|
C | T | 1 | a0003c0029t0015g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-19+1310G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48246004 | ||||||
| chr16:48246044
|
G | C | 3 | a0003c0018t0018g0132a0004c0028t0012g0131a0015c0024t0012g0133 | 3 | HG02896.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-19+1270C>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48246044 | ||||||
| chr16:48246211
|
C | A | 5 | a0006c0005t0005g0001a0006c0005t0005g0148a0006c0005t0005g0149others(2): Show | 7 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19+1103G>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48246211 | ||||||
| chr16:48246334
|
C | T | 7 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(4): Show | 8 | HG01884.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+980G>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48246334 | ||||||
| chr16:48246368
|
A | T | 7 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(4): Show | 8 | HG01884.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+946T>A | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48246368 | ||||||
| chr16:48246493
|
A | C | 5 | a0006c0005t0005g0001a0006c0005t0005g0148a0006c0005t0005g0149others(2): Show | 7 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19+821T>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48246493 | ||||||
| chr16:48246715
|
T | C | 7 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(4): Show | 8 | HG01884.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+599A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48246715 | ||||||
| chr16:48246799
|
T | C | 6 | a0008c0007t0006g0142a0008c0007t0006g0143a0008c0007t0006g0144others(3): Show | 6 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+515A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48246799 | ||||||
| chr16:48246883
|
T | C | 5 | a0003c0018t0002g0010a0003c0029t0015g0019a0011c0011t0002g0005others(2): Show | 6 | HG02280.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+431A>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48246883 | ||||||
| chr16:48247053
|
G | A | 1 | a0003c0018t0002g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-19+261C>T | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48247053 | ||||||
| chr16:48247155
|
A | G | 1 | a0003c0018t0002g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-19+159T>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48247155 | ||||||
| chr16:48247217
|
T | TAA | 6 | a0004c0009t0001g0126a0004c0009t0001g0128a0004c0009t0001g0129others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+95_-19+96dupTT | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48247217 | ||||||
| chr16:48247217
|
T | TAAAGA | 5 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+96_-19+97insTC others(3): Show |
ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48247217 | ||||||
| chr16:48247217
|
TA | T | 16 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0003t0001g0017others(13): Show | 16 | HG01891.hp2 HG01943.hp1 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19+96delT | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48247217 | ||||||
| chr16:48247238
|
G | C | 7 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(4): Show | 8 | HG01884.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+76C>G | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48247238 | ||||||
| chr16:48247283
|
T | G | 7 | a0007c0008t0003g0006a0007c0008t0003g0136a0007c0008t0003g0137others(4): Show | 8 | HG01884.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+31A>C | ABCC11 | ENSG00000121270.16 | transcript | ENST00000356608.7 | protein_coding | 1/29 | chr16 | 48247283 |