Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 10599 |
|---|---|
| ensemblid | ENSG00000134538.3 |
| hgncid | 10959 |
| symbol | SLCO1B1 |
| name | solute carrier organic anion transporter family member 1B1 |
| refseq_nuc | NM_006446.5 |
| refseq_prot | NP_006437.3 |
| ensembl_nuc | ENST00000256958.3 |
| ensembl_prot | ENSP00000256958.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 21131194 |
| end | 21239796 |
| strand | + |
| ver | v1.2 |
| region | chr12:21131194-21239796 |
| region5000 | chr12:21126194-21244796 |
| regionname0 | SLCO1B1_chr12_21131194_21239796 |
| regionname5000 | SLCO1B1_chr12_21126194_21244796 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 691 | 159 | 49 | 11 | 87 | 0 | 12 | 66 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0002 | 1/1 | 691 | 84 | 13 | 20 | 35 | 4 | 10 | 30 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0003 | 0/0 | 691 | 27 | 1 | 7 | 19 | 0 | 0 | 14 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0004 | 0/0 | 691 | 13 | 7 | 4 | 1 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0005 | 0/0 | 691 | 11 | 4 | 2 | 0 | 3 | 2 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0006 | 0/0 | 691 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0007 | 0/0 | 691 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0008 | 0/0 | 691 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0009 | 0/0 | 691 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0010 | 0/0 | 691 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0011 | 0/0 | 691 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0012 | 0/0 | 691 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0013 | 0/0 | 691 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0014 | 0/0 | 691 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0015 | 0/0 | 691 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0016 | 0/0 | 691 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0017 | 0/0 | 579 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0018 | 0/0 | 691 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0019 | 0/0 | 691 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2076 | 89 | 34 | 4 | 42 | 0 | 9 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| c0002 | 0/1 | 2076 | 68 | 3 | 15 | 35 | 4 | 10 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| c0003 | 0/0 | 2076 | 68 | 13 | 7 | 45 | 0 | 3 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| c0004 | 0/0 | 2076 | 27 | 1 | 7 | 19 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| c0005 | 1/0 | 2076 | 16 | 10 | 5 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| c0006 | 0/0 | 2076 | 13 | 7 | 4 | 1 | 1 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| c0007 | 0/0 | 2076 | 8 | 1 | 2 | 0 | 3 | 2 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| c0008 | 0/0 | 2076 | 3 | 3 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| c0009 | 0/0 | 2076 | 3 | 3 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| c0010 | 0/0 | 2076 | 3 | 3 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| c0011 | 0/0 | 2076 | 2 | 0 | 0 | 2 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| c0012 | 0/0 | 2076 | 2 | 0 | 0 | 2 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| c0013 | 0/0 | 2076 | 2 | 0 | 0 | 2 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| c0014 | 0/0 | 2076 | 2 | 2 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| c0015 | 0/0 | 2076 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| c0016 | 0/0 | 2076 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| c0017 | 0/0 | 2076 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| c0018 | 0/0 | 2076 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| c0019 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| c0020 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| c0021 | 0/0 | 2076 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| c0022 | 0/0 | 2076 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| c0023 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| c0024 | 0/0 | 2076 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| c0025 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| c0026 | 0/0 | 2076 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 712 | 129 | 52 | 25 | 31 | 6 | 14 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| t0002 | 0/1 | 712 | 114 | 27 | 17 | 66 | 0 | 3 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| t0003 | 0/0 | 712 | 51 | 0 | 2 | 46 | 0 | 3 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| t0004 | 0/0 | 712 | 10 | 0 | 2 | 0 | 2 | 6 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| t0005 | 0/0 | 712 | 5 | 0 | 0 | 5 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| t0006 | 0/0 | 712 | 3 | 3 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| t0007 | 0/0 | 712 | 3 | 0 | 0 | 3 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| t0008 | 0/0 | 712 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| t0009 | 0/0 | 712 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| t0010 | 0/0 | 712 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0191 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0300 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2076 | 89 | 34 | 4 | 42 | 0 | 9 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0001c0003 | 0/0 | 2076 | 68 | 13 | 7 | 45 | 0 | 3 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0001c0020 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0001c0023 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0002c0002 | 0/1 | 2076 | 68 | 3 | 15 | 35 | 4 | 10 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0002c0005 | 1/0 | 2076 | 16 | 10 | 5 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0003c0004 | 0/0 | 2076 | 27 | 1 | 7 | 19 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0004c0006 | 0/0 | 2076 | 13 | 7 | 4 | 1 | 1 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0005c0007 | 0/0 | 2076 | 8 | 1 | 2 | 0 | 3 | 2 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0005c0009 | 0/0 | 2076 | 3 | 3 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0006c0010 | 0/0 | 2076 | 3 | 3 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0006c0014 | 0/0 | 2076 | 2 | 2 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0007c0008 | 0/0 | 2076 | 3 | 3 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0007c0019 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0008c0013 | 0/0 | 2076 | 2 | 0 | 0 | 2 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0009c0011 | 0/0 | 2076 | 2 | 0 | 0 | 2 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0010c0012 | 0/0 | 2076 | 2 | 0 | 0 | 2 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0011c0025 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0012c0026 | 0/0 | 2076 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0013c0021 | 0/0 | 2076 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0014c0022 | 0/0 | 2076 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0015c0024 | 0/0 | 2076 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0016c0018 | 0/0 | 2076 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0017c0017 | 0/0 | 2076 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0018c0016 | 0/0 | 2076 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0019c0015 | 0/0 | 2076 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2787 | 28 | 20 | 1 | 5 | 0 | 2 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0001c0001t0002 | 0/0 | 2787 | 15 | 13 | 1 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0001c0001t0003 | 0/0 | 2787 | 42 | 0 | 2 | 37 | 0 | 3 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0001c0001t0004 | 0/0 | 2787 | 3 | 0 | 0 | 0 | 0 | 3 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0001c0001t0009 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0001c0003t0001 | 0/0 | 2787 | 9 | 6 | 0 | 2 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0001c0003t0002 | 0/0 | 2787 | 53 | 7 | 7 | 37 | 0 | 2 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0001c0003t0003 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0001c0003t0005 | 0/0 | 2787 | 5 | 0 | 0 | 5 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0001c0020t0001 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0001c0023t0001 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0002c0002t0001 | 0/0 | 2787 | 48 | 3 | 14 | 18 | 4 | 9 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0002c0002t0002 | 0/1 | 2787 | 11 | 0 | 1 | 9 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0002c0002t0003 | 0/0 | 2787 | 4 | 0 | 0 | 4 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0002c0002t0004 | 0/0 | 2787 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0002c0002t0007 | 0/0 | 2787 | 3 | 0 | 0 | 3 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0002c0002t0010 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0002c0005t0001 | 1/0 | 2787 | 14 | 8 | 5 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0002c0005t0002 | 0/0 | 2787 | 2 | 2 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0003c0004t0001 | 0/0 | 2787 | 2 | 0 | 0 | 2 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0003c0004t0002 | 0/0 | 2787 | 22 | 1 | 7 | 14 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0003c0004t0003 | 0/0 | 2787 | 3 | 0 | 0 | 3 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0004c0006t0001 | 0/0 | 2787 | 13 | 7 | 4 | 1 | 1 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0005c0007t0001 | 0/0 | 2787 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0005c0007t0004 | 0/0 | 2787 | 6 | 0 | 2 | 0 | 2 | 2 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0005c0007t0008 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0005c0009t0002 | 0/0 | 2787 | 3 | 3 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0006c0010t0001 | 0/0 | 2787 | 3 | 3 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0006c0014t0001 | 0/0 | 2787 | 2 | 2 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0007c0008t0006 | 0/0 | 2787 | 3 | 3 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0007c0019t0002 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0008c0013t0002 | 0/0 | 2787 | 2 | 0 | 0 | 2 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0009c0011t0002 | 0/0 | 2787 | 2 | 0 | 0 | 2 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0010c0012t0001 | 0/0 | 2787 | 2 | 0 | 0 | 2 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0011c0025t0001 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0012c0026t0003 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0013c0021t0002 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0014c0022t0002 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0015c0024t0001 | 0/0 | 2787 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0016c0018t0001 | 0/0 | 2787 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0017c0017t0001 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0018c0016t0001 | 0/0 | 2787 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| a0019c0015t0002 | 0/0 | 2787 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | copy fasta | chr12 | 21126194 | 21244796 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0001t0009g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0005g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0005g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0005g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0003t0005g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0020t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0001c0023t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0002g0191 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0004g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0007g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0007g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0007g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0002t0010g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0005t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0005t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0005t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0005t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0005t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0005t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0005t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0005t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0005t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0005t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0005t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0005t0001g0300 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0005t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0005t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0005t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0002c0005t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0003c0004t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0003c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0003c0004t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0003c0004t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0003c0004t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0003c0004t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0003c0004t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0003c0004t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0003c0004t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0003c0004t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0003c0004t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0003c0004t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0003c0004t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0003c0004t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0003c0004t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0003c0004t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0003c0004t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0003c0004t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0003c0004t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0003c0004t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0003c0004t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0003c0004t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0003c0004t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0003c0004t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0003c0004t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0004c0006t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0004c0006t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0004c0006t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0004c0006t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0004c0006t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0004c0006t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0004c0006t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0004c0006t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0004c0006t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0004c0006t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0004c0006t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0004c0006t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0004c0006t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0005c0007t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0005c0007t0004g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0005c0007t0004g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0005c0007t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0005c0007t0004g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0005c0007t0004g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0005c0007t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0005c0007t0008g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0005c0009t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0005c0009t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0005c0009t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0006c0010t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0006c0010t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0006c0010t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0006c0014t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0006c0014t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0007c0008t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0007c0008t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0007c0008t0006g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0007c0019t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0008c0013t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0008c0013t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0009c0011t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0009c0011t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0010c0012t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0010c0012t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0011c0025t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0012c0026t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0013c0021t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0014c0022t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0015c0024t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0016c0018t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0017c0017t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0018c0016t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| a0019c0015t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0181 | EUR | GBR | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG00099 | hp2 | a0005 | c0007 | t0004 | g0099 | EUR | GBR | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG00280 | hp1 | a0004 | c0006 | t0001 | g0028 | EUR | FIN | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0208 | EUR | FIN | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG00423 | hp1 | a0001 | c0003 | t0001 | g0297 | EAS | CHS | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | CHS | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG00438 | hp2 | a0001 | c0003 | t0002 | g0196 | EAS | CHS | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | CHS | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG00544 | hp2 | a0001 | c0003 | t0002 | g0224 | EAS | CHS | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG00609 | hp1 | a0003 | c0004 | t0002 | g0036 | EAS | CHS | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG00609 | hp2 | a0002 | c0002 | t0007 | g0149 | EAS | CHS | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG00642 | hp1 | a0004 | c0006 | t0001 | g0235 | AMR | PUR | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG00642 | hp2 | a0002 | c0005 | t0001 | g0258 | AMR | PUR | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG00673 | hp1 | a0001 | c0003 | t0002 | g0213 | EAS | CHS | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | CHS | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG00735 | hp1 | a0016 | c0018 | t0001 | g0140 | AMR | PUR | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG00735 | hp2 | a0001 | c0003 | t0002 | g0005 | AMR | PUR | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0200 | AMR | PUR | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0197 | AMR | PUR | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01069 | hp1 | a0001 | c0003 | t0002 | g0302 | AMR | PUR | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01069 | hp2 | a0004 | c0006 | t0001 | g0233 | AMR | PUR | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01071 | hp2 | a0004 | c0006 | t0001 | g0234 | AMR | PUR | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01081 | hp1 | a0002 | c0005 | t0001 | g0143 | AMR | PUR | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01081 | hp2 | a0003 | c0004 | t0002 | g0098 | AMR | PUR | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01167 | hp2 | a0001 | c0003 | t0002 | g0005 | AMR | PUR | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01168 | hp1 | a0004 | c0006 | t0001 | g0029 | AMR | PUR | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0100 | AMR | PUR | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01175 | hp2 | a0001 | c0003 | t0002 | g0228 | AMR | PUR | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01258 | hp2 | a0003 | c0004 | t0002 | g0003 | AMR | CLM | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0153 | AMR | CLM | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01261 | hp2 | a0003 | c0004 | t0002 | g0003 | AMR | CLM | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01346 | hp1 | a0005 | c0007 | t0004 | g0095 | AMR | CLM | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0139 | AMR | CLM | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01358 | hp1 | a0003 | c0004 | t0002 | g0027 | AMR | CLM | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0190 | AMR | CLM | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01433 | hp1 | a0005 | c0007 | t0004 | g0180 | AMR | CLM | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0240 | AMR | CLM | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0174 | AMR | CLM | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01496 | hp2 | a0003 | c0004 | t0002 | g0097 | AMR | CLM | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01515 | hp1 | a0005 | c0007 | t0001 | g0101 | EUR | IBS | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0205 | EUR | IBS | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01884 | hp1 | a0007 | c0008 | t0006 | g0245 | AFR | ACB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0285 | AFR | ACB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01891 | hp1 | a0006 | c0014 | t0001 | g0309 | AFR | ACB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01891 | hp2 | a0004 | c0006 | t0001 | g0127 | AFR | ACB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01928 | hp1 | a0003 | c0004 | t0002 | g0260 | AMR | PEL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0210 | AMR | PEL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01943 | hp1 | a0003 | c0004 | t0002 | g0254 | AMR | PEL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | PEL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01975 | hp1 | a0002 | c0005 | t0001 | g0253 | AMR | PEL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01975 | hp2 | a0001 | c0003 | t0002 | g0218 | AMR | PEL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0209 | AMR | PEL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01978 | hp2 | a0002 | c0005 | t0001 | g0265 | AMR | PEL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0144 | AMR | PEL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG01993 | hp2 | a0001 | c0003 | t0002 | g0215 | AMR | PEL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0054 | AMR | PEL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0203 | AMR | PEL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | KHV | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02015 | hp2 | a0003 | c0004 | t0002 | g0287 | EAS | KHV | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | KHV | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0092 | EAS | KHV | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | KHV | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02040 | hp2 | a0001 | c0003 | t0002 | g0176 | EAS | KHV | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02055 | hp1 | a0001 | c0003 | t0002 | g0116 | AFR | ACB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0085 | AFR | ACB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02071 | hp1 | a0001 | c0003 | t0002 | g0223 | EAS | KHV | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | KHV | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02074 | hp2 | a0003 | c0004 | t0001 | g0091 | EAS | KHV | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02080 | hp1 | a0001 | c0003 | t0002 | g0178 | EAS | KHV | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | KHV | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02083 | hp1 | a0001 | c0003 | t0002 | g0273 | EAS | KHV | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | KHV | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | KHV | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02129 | hp2 | a0001 | c0003 | t0003 | g0291 | EAS | KHV | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | KHV | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | KHV | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02145 | hp1 | a0004 | c0006 | t0001 | g0272 | AFR | ACB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0310 | AFR | ACB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02155 | hp1 | a0004 | c0006 | t0001 | g0078 | EAS | CDX | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02155 | hp2 | a0003 | c0004 | t0002 | g0021 | EAS | CDX | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02257 | hp2 | a0002 | c0005 | t0001 | g0270 | AFR | ACB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02258 | hp1 | a0006 | c0014 | t0001 | g0298 | AFR | ACB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02258 | hp2 | a0002 | c0005 | t0001 | g0117 | AFR | ACB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0206 | AFR | ACB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02280 | hp2 | a0004 | c0006 | t0001 | g0138 | AFR | ACB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0152 | AMR | PEL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02293 | hp2 | a0001 | c0003 | t0002 | g0201 | AMR | PEL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02300 | hp1 | a0002 | c0005 | t0001 | g0164 | AMR | PEL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02300 | hp2 | a0019 | c0015 | t0002 | g0217 | AMR | PEL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02451 | hp2 | a0004 | c0006 | t0001 | g0246 | AFR | ACB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02572 | hp1 | a0005 | c0007 | t0008 | g0102 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02572 | hp2 | a0001 | c0001 | t0009 | g0243 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0103 | SAS | PJL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0154 | SAS | PJL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02615 | hp1 | a0001 | c0003 | t0002 | g0252 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0284 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0268 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02622 | hp2 | a0002 | c0005 | t0001 | g0301 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0249 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02630 | hp2 | a0006 | c0010 | t0001 | g0264 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0269 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02683 | hp1 | a0018 | c0016 | t0001 | g0185 | SAS | PJL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02683 | hp2 | a0005 | c0007 | t0004 | g0096 | SAS | PJL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0202 | SAS | PJL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0022 | SAS | PJL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02723 | hp1 | a0011 | c0025 | t0001 | g0019 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0278 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0274 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02895 | hp2 | a0001 | c0003 | t0002 | g0266 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02896 | hp1 | a0004 | c0006 | t0001 | g0256 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02896 | hp2 | a0002 | c0005 | t0001 | g0016 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02897 | hp1 | a0004 | c0006 | t0001 | g0255 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02922 | hp1 | a0005 | c0009 | t0002 | g0084 | AFR | ESN | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0207 | SAS | PJL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03017 | hp2 | a0001 | c0003 | t0002 | g0241 | SAS | PJL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03098 | hp1 | a0004 | c0006 | t0001 | g0081 | AFR | MSL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03098 | hp2 | a0001 | c0003 | t0002 | g0305 | AFR | MSL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03130 | hp1 | a0007 | c0008 | t0006 | g0244 | AFR | ESN | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03130 | hp2 | a0001 | c0003 | t0002 | g0110 | AFR | ESN | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | ESN | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | MSL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03225 | hp1 | a0006 | c0010 | t0001 | g0263 | AFR | MSL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03225 | hp2 | a0002 | c0005 | t0001 | g0257 | AFR | MSL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0173 | SAS | PJL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03239 | hp2 | a0001 | c0003 | t0002 | g0175 | SAS | PJL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03453 | hp1 | a0005 | c0009 | t0002 | g0109 | AFR | MSL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0168 | SAS | PJL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0204 | SAS | PJL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | ESN | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03516 | hp2 | a0007 | c0008 | t0006 | g0247 | AFR | ESN | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0251 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03540 | hp2 | a0001 | c0003 | t0002 | g0271 | AFR | GWD | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | MSL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03579 | hp2 | a0001 | c0020 | t0001 | g0282 | AFR | MSL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0030 | SAS | PJL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03654 | hp2 | a0015 | c0024 | t0001 | g0017 | SAS | PJL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0166 | SAS | PJL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0172 | SAS | PJL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03710 | hp2 | a0002 | c0002 | t0004 | g0199 | SAS | PJL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0198 | SAS | BEB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0089 | SAS | BEB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03834 | hp1 | a0005 | c0007 | t0004 | g0094 | SAS | BEB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0167 | SAS | BEB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0141 | SAS | STU | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG04115 | hp2 | a0001 | c0003 | t0001 | g0193 | SAS | STU | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0023 | SAS | BEB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18522 | hp1 | a0001 | c0023 | t0001 | g0088 | AFR | YRI | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18522 | hp2 | a0002 | c0005 | t0002 | g0011 | AFR | YRI | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18747 | hp1 | a0003 | c0004 | t0002 | g0037 | EAS | CHB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18747 | hp2 | a0001 | c0003 | t0002 | g0229 | EAS | CHB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18940 | hp1 | a0001 | c0003 | t0002 | g0106 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18941 | hp1 | a0001 | c0003 | t0002 | g0280 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18942 | hp2 | a0001 | c0003 | t0002 | g0160 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18943 | hp1 | a0002 | c0002 | t0007 | g0150 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18943 | hp2 | a0001 | c0003 | t0002 | g0303 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18946 | hp2 | a0003 | c0004 | t0001 | g0090 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0165 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0157 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18948 | hp2 | a0001 | c0003 | t0002 | g0293 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18951 | hp2 | a0001 | c0003 | t0002 | g0018 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18954 | hp2 | a0003 | c0004 | t0002 | g0039 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18957 | hp2 | a0001 | c0003 | t0005 | g0290 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18959 | hp2 | a0001 | c0003 | t0002 | g0275 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18960 | hp2 | a0003 | c0004 | t0002 | g0040 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18962 | hp2 | a0001 | c0003 | t0002 | g0231 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18965 | hp1 | a0001 | c0003 | t0002 | g0194 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18965 | hp2 | a0003 | c0004 | t0002 | g0041 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18967 | hp1 | a0001 | c0003 | t0002 | g0188 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18971 | hp1 | a0002 | c0002 | t0003 | g0220 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18972 | hp2 | a0002 | c0002 | t0002 | g0281 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18973 | hp2 | a0001 | c0003 | t0002 | g0230 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18975 | hp1 | a0001 | c0003 | t0002 | g0145 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0239 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18979 | hp2 | a0017 | c0017 | t0001 | g0219 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18981 | hp2 | a0001 | c0003 | t0002 | g0295 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18982 | hp1 | a0002 | c0002 | t0003 | g0212 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18982 | hp2 | a0012 | c0026 | t0003 | g0045 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18983 | hp1 | a0001 | c0003 | t0002 | g0211 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18983 | hp2 | a0001 | c0003 | t0002 | g0158 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18986 | hp2 | a0001 | c0003 | t0002 | g0242 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18988 | hp1 | a0003 | c0004 | t0002 | g0043 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18988 | hp2 | a0001 | c0003 | t0002 | g0156 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18989 | hp1 | a0013 | c0021 | t0002 | g0232 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18990 | hp1 | a0010 | c0012 | t0001 | g0189 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18990 | hp2 | a0014 | c0022 | t0002 | g0146 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18991 | hp1 | a0001 | c0003 | t0005 | g0286 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18991 | hp2 | a0001 | c0003 | t0002 | g0107 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18992 | hp2 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18993 | hp2 | a0001 | c0003 | t0005 | g0307 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18994 | hp1 | a0001 | c0003 | t0002 | g0226 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18999 | hp1 | a0002 | c0002 | t0003 | g0237 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19003 | hp2 | a0001 | c0003 | t0002 | g0195 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19004 | hp2 | a0001 | c0003 | t0002 | g0294 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19005 | hp1 | a0001 | c0003 | t0002 | g0289 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19006 | hp1 | a0001 | c0003 | t0001 | g0296 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19006 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19009 | hp1 | a0009 | c0011 | t0002 | g0192 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19012 | hp1 | a0003 | c0004 | t0003 | g0047 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19012 | hp2 | a0001 | c0003 | t0002 | g0214 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19030 | hp1 | a0001 | c0003 | t0002 | g0250 | AFR | LWK | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | LWK | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19054 | hp1 | a0003 | c0004 | t0002 | g0038 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19057 | hp2 | a0003 | c0004 | t0002 | g0033 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19065 | hp1 | a0001 | c0003 | t0002 | g0276 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19065 | hp2 | a0010 | c0012 | t0001 | g0155 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19066 | hp1 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19066 | hp2 | a0003 | c0004 | t0003 | g0024 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19074 | hp1 | a0001 | c0003 | t0002 | g0187 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19074 | hp2 | a0008 | c0013 | t0002 | g0035 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19077 | hp1 | a0009 | c0011 | t0002 | g0105 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19077 | hp2 | a0003 | c0004 | t0002 | g0034 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19079 | hp2 | a0001 | c0003 | t0005 | g0292 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19081 | hp1 | a0003 | c0004 | t0003 | g0046 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19082 | hp2 | a0001 | c0003 | t0002 | g0308 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19083 | hp1 | a0001 | c0003 | t0002 | g0216 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19083 | hp2 | a0008 | c0013 | t0002 | g0044 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19084 | hp2 | a0002 | c0002 | t0007 | g0148 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19088 | hp1 | a0003 | c0004 | t0002 | g0042 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19088 | hp2 | a0001 | c0003 | t0002 | g0313 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19090 | hp1 | a0001 | c0003 | t0002 | g0306 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19090 | hp2 | a0001 | c0003 | t0005 | g0159 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19091 | hp1 | a0002 | c0002 | t0010 | g0238 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19091 | hp2 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | YRI | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA20129 | hp1 | a0006 | c0010 | t0001 | g0262 | AFR | ASW | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA20129 | hp2 | a0002 | c0005 | t0001 | g0312 | AFR | ASW | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0163 | EUR | TSI | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA20752 | hp2 | a0005 | c0007 | t0004 | g0093 | EUR | TSI | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02486 | hp1 | a0002 | c0005 | t0001 | g0261 | AFR | ACB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02486 | hp2 | a0001 | c0003 | t0001 | g0299 | AFR | ACB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG02559 | hp2 | a0007 | c0019 | t0002 | g0124 | AFR | ACB | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03471 | hp1 | a0002 | c0005 | t0002 | g0122 | AFR | MSL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0259 | AFR | MSL | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG06807 | hp1 | a0003 | c0004 | t0002 | g0288 | AFR | USA | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| HG06807 | hp2 | a0005 | c0009 | t0002 | g0083 | AFR | USA | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA21309 | hp1 | a0002 | c0005 | t0001 | g0086 | AFR | LWK | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | LWK | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0191 | REF | REF | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| homoSapiens_grch38 | hp1 | a0002 | c0005 | t0001 | g0300 | REF | REF | SLCO1B1_chr12_21126194_21244796 | SLCO1B1 | chr12 | 21126194 | 21244796 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:21174684
|
G | A | 1 | a0019 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.334G>A | p.Ala112Thr | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 4/15 | 438/2787 | 334/2076 | 112/691 | chr12 | 21174684 | ||
| chr12:21176804
|
A | G | 14 | a0001a0003a0004others(11): Show | 228 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(225): Show |
missense_variant | MODERATE | c.388A>G | p.Asn130Asp | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 5/15 | 492/2787 | 388/2076 | 130/691 | chr12 | 21176804 | ||
| chr12:21176868
|
A | G | 1 | a0010 | 2 | NA18990.hp1 NA19065.hp2 |
missense_variant | MODERATE | c.452A>G | p.Asn151Ser | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 5/15 | 556/2787 | 452/2076 | 151/691 | chr12 | 21176868 | ||
| chr12:21176879
|
C | A | 3 | a0005a0007a0016 | 16 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(13): Show |
missense_variant | MODERATE | c.463C>A | p.Pro155Thr | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 5/15 | 567/2787 | 463/2076 | 155/691 | chr12 | 21176879 | ||
| chr12:21178615
|
T | C | 2 | a0003a0008 | 29 | HG00609.hp1 HG01081.hp2 HG01258.hp2 others(26): Show |
missense_variant | MODERATE | c.521T>C | p.Val174Ala | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 6/15 | 625/2787 | 521/2076 | 174/691 | chr12 | 21178615 | ||
| chr12:21178926
|
A | G | 1 | a0015 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.633A>G | p.Ile211Met | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/15 | 737/2787 | 633/2076 | 211/691 | chr12 | 21178926 | ||
| chr12:21196951
|
A | G | 2 | a0007a0015 | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
missense_variant | MODERATE | c.733A>G | p.Ile245Val | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/15 | 837/2787 | 733/2076 | 245/691 | chr12 | 21196951 | ||
| chr12:21200544
|
C | G | 1 | a0008 | 2 | NA19074.hp2 NA19083.hp2 |
missense_variant | MODERATE | c.1007C>G | p.Pro336Arg | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/15 | 1111/2787 | 1007/2076 | 336/691 | chr12 | 21200544 | ||
| chr12:21202541
|
A | C | 1 | a0014 | 1 | NA18990.hp2 | missense_variant | MODERATE | c.1186A>C | p.Ile396Leu | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/15 | 1290/2787 | 1186/2076 | 396/691 | chr12 | 21202541 | ||
| chr12:21202555
|
C | G | 1 | a0006 | 5 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(2): Show |
missense_variant | MODERATE | c.1200C>G | p.Phe400Leu | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/15 | 1304/2787 | 1200/2076 | 400/691 | chr12 | 21202555 | ||
| chr12:21205999
|
G | C | 1 | a0011 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.1463G>C | p.Gly488Ala | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/15 | 1567/2787 | 1463/2076 | 488/691 | chr12 | 21205999 | ||
| chr12:21206001
|
T | A | 1 | a0013 | 1 | NA18989.hp1 | missense_variant | MODERATE | c.1465T>A | p.Cys489Ser | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/15 | 1569/2787 | 1465/2076 | 489/691 | chr12 | 21206001 | ||
| chr12:21206010
|
T | A | 1 | a0018 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.1474T>A | p.Ser492Thr | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/15 | 1578/2787 | 1474/2076 | 492/691 | chr12 | 21206010 | ||
| chr12:21206031
|
A | G | 1 | a0007 | 4 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.1495A>G | p.Ile499Val | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/15 | 1599/2787 | 1495/2076 | 499/691 | chr12 | 21206031 | ||
| chr12:21217249
|
T | G | 1 | a0009 | 2 | NA19009.hp1 NA19077.hp1 |
missense_variant | MODERATE | c.1628T>G | p.Leu543Trp | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/15 | 1732/2787 | 1628/2076 | 543/691 | chr12 | 21217249 | ||
| chr12:21222332
|
T | C | 1 | a0012 | 1 | NA18982.hp2 | missense_variant | MODERATE | c.1715T>C | p.Leu572Pro | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/15 | 1819/2787 | 1715/2076 | 572/691 | chr12 | 21222332 | ||
| chr12:21222355
|
C | T | 1 | a0017 | 1 | NA18979.hp2 | stop_gained | HIGH | c.1738C>T | p.Arg580* | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/15 | 1842/2787 | 1738/2076 | 580/691 | chr12 | 21222355 | ||
| chr12:21239042
|
A | C | 3 | a0004a0015a0016 | 15 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(12): Show |
missense_variant | MODERATE | c.1929A>C | p.Leu643Phe | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 15/15 | 2033/2787 | 1929/2076 | 643/691 | chr12 | 21239042 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:21176827
|
G | A | 3 | a0005c0007a0007c0019a0016c0018 | 10 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(7): Show |
synonymous_variant | LOW | c.411G>A | p.Ser137Ser | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 5/15 | 515/2787 | 411/2076 | 137/691 | chr12 | 21176827 | ||
| chr12:21178665
|
T | C | 11 | a0001c0020a0002c0002a0005c0007others(8): Show | 91 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(88): Show |
synonymous_variant | LOW | c.571T>C | p.Leu191Leu | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 6/15 | 675/2787 | 571/2076 | 191/691 | chr12 | 21178665 | ||
| chr12:21178691
|
C | T | 13 | a0001c0001a0001c0020a0003c0004others(10): Show | 152 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(149): Show |
synonymous_variant | LOW | c.597C>T | p.Phe199Phe | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 6/15 | 701/2787 | 597/2076 | 199/691 | chr12 | 21178691 | ||
| chr12:21197100
|
G | A | 3 | a0007c0008a0007c0019a0015c0024 | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
synonymous_variant | LOW | c.882G>A | p.Leu294Leu | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/15 | 986/2787 | 882/2076 | 294/691 | chr12 | 21197100 | ||
| chr12:21200623
|
C | T | 3 | a0001c0023a0006c0010a0006c0014 | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
synonymous_variant | LOW | c.1086C>T | p.Tyr362Tyr | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/15 | 1190/2787 | 1086/2076 | 362/691 | chr12 | 21200623 | ||
| chr12:21202603
|
G | A | 6 | a0001c0023a0006c0010a0006c0014others(3): Show | 11 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(8): Show |
synonymous_variant | LOW | c.1248G>A | p.Val416Val | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/15 | 1352/2787 | 1248/2076 | 416/691 | chr12 | 21202603 | ||
| chr12:21205988
|
C | T | 3 | a0007c0008a0007c0019a0015c0024 | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
synonymous_variant | LOW | c.1452C>T | p.Pro484Pro | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/15 | 1556/2787 | 1452/2076 | 484/691 | chr12 | 21205988 | ||
| chr12:21224768
|
G | A | 1 | a0015c0024 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.1794G>A | p.Thr598Thr | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/15 | 1898/2787 | 1794/2076 | 598/691 | chr12 | 21224768 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:21141572
|
A | C | 1 | a0002c0002t0010 | 1 | NA19091.hp1 | 5_prime_UTR_variant | MODIFIER | c.-3A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/15 | 3 | chr12 | 21141572 | |||||
| chr12:21239229
|
C | G | 1 | a0002c0002t0007 | 3 | HG00609.hp2 NA18943.hp1 NA19084.hp2 |
3_prime_UTR_variant | MODIFIER | c.*40C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 15/15 | 40 | chr12 | 21239229 | |||||
| chr12:21239271
|
C | T | 1 | a0001c0001t0009 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*82C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 15/15 | 82 | chr12 | 21239271 | |||||
| chr12:21239310
|
G | C | 1 | a0007c0008t0006 | 3 | HG01884.hp1 HG03130.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*121G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 15/15 | 121 | chr12 | 21239310 | |||||
| chr12:21239356
|
T | C | 5 | a0001c0001t0003a0001c0003t0003a0002c0002t0003others(2): Show | 51 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*167T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 15/15 | 167 | chr12 | 21239356 | |||||
| chr12:21239517
|
A | G | 1 | a0001c0003t0005 | 5 | NA18957.hp2 NA18991.hp1 NA18993.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*328A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 15/15 | 328 | chr12 | 21239517 | |||||
| chr12:21239628
|
T | G | 23 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(20): Show | 184 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*439T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 15/15 | 439 | chr12 | 21239628 | |||||
| chr12:21239638
|
A | C | 3 | a0001c0001t0004a0002c0002t0004a0005c0007t0004 | 10 | HG00099.hp2 HG01346.hp1 HG01433.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*449A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 15/15 | 449 | chr12 | 21239638 | |||||
| chr12:21239638
|
A | G | 1 | a0005c0007t0008 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*449A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 15/15 | 449 | chr12 | 21239638 | |||||
| chr12:21239652
|
A | G | 23 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(20): Show | 184 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*463A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 15/15 | 463 | chr12 | 21239652 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:21131301
|
G | C | 4 | a0002c0002t0001g0006a0002c0002t0002g0007a0002c0002t0002g0009others(1): Show | 4 | NA18957.hp1 NA18999.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.-62+65G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21131301 | ||||||
| chr12:21131390
|
T | C | 1 | a0001c0001t0002g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-62+154T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21131390 | ||||||
| chr12:21131412
|
T | G | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(3): Show | 6 | HG02559.hp1 HG02896.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-62+176T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21131412 | ||||||
| chr12:21131542
|
T | G | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-62+306T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21131542 | ||||||
| chr12:21131654
|
G | A | 1 | a0001c0003t0002g0018 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-62+418G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21131654 | ||||||
| chr12:21131687
|
T | TA | 87 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0087others(84): Show | 88 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-62+457dupA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 21131687 | |||||
| chr12:21131822
|
A | G | 1 | a0001c0001t0003g0103 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-62+586A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21131822 | ||||||
| chr12:21131965
|
C | T | 10 | a0002c0002t0001g0100a0003c0004t0002g0097a0003c0004t0002g0098others(7): Show | 10 | HG00099.hp2 HG01081.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.-62+729C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21131965 | ||||||
| chr12:21132033
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-62+797G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21132033 | ||||||
| chr12:21132034
|
T | G | 148 | a0001c0001t0001g0002a0001c0001t0001g0113a0001c0001t0001g0114others(145): Show | 152 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.-62+798T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21132034 | ||||||
| chr12:21132047
|
T | C | 1 | a0011c0025t0001g0019 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-62+811T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21132047 | ||||||
| chr12:21132078
|
C | T | 1 | a0001c0003t0002g0313 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-62+842C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21132078 | ||||||
| chr12:21132310
|
C | A | 1 | a0002c0002t0002g0020 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-62+1074C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21132310 | ||||||
| chr12:21132376
|
G | T | 1 | a0002c0002t0002g0092 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-62+1140G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21132376 | ||||||
| chr12:21132415
|
T | A | 1 | a0009c0011t0002g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-62+1179T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21132415 | ||||||
| chr12:21132481
|
A | G | 3 | a0002c0002t0002g0092a0003c0004t0001g0090a0003c0004t0001g0091 | 3 | HG02027.hp2 HG02074.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.-62+1245A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21132481 | ||||||
| chr12:21132613
|
T | C | 10 | a0002c0002t0001g0100a0003c0004t0002g0097a0003c0004t0002g0098others(7): Show | 10 | HG00099.hp2 HG01081.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.-62+1377T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21132613 | ||||||
| chr12:21132679
|
G | A | 31 | a0001c0001t0003g0026a0001c0001t0003g0031a0001c0001t0003g0032others(28): Show | 32 | HG00280.hp1 HG00609.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.-62+1443G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21132679 | ||||||
| chr12:21132900
|
C | T | 1 | a0001c0001t0003g0089 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-62+1664C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21132900 | ||||||
| chr12:21132920
|
T | G | 1 | a0003c0004t0002g0021 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-62+1684T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21132920 | ||||||
| chr12:21132950
|
G | A | 35 | a0001c0001t0001g0079a0001c0001t0003g0048a0001c0001t0003g0049others(32): Show | 35 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.-62+1714G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21132950 | ||||||
| chr12:21132975
|
T | G | 4 | a0001c0001t0001g0082a0001c0001t0002g0080a0004c0006t0001g0081others(1): Show | 4 | HG03041.hp2 HG03098.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-62+1739T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21132975 | ||||||
| chr12:21133009
|
G | A | 264 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(261): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.-62+1773G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21133009 | ||||||
| chr12:21133016
|
G | A | 1 | a0001c0001t0009g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-62+1780G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21133016 | ||||||
| chr12:21133069
|
G | A | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(3): Show | 6 | HG02559.hp1 HG02896.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-62+1833G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21133069 | ||||||
| chr12:21133183
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-62+1947T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21133183 | ||||||
| chr12:21133186
|
G | A | 3 | a0001c0003t0001g0085a0005c0009t0002g0084a0011c0025t0001g0019 | 3 | HG02055.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-62+1950G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21133186 | ||||||
| chr12:21133264
|
G | T | 264 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(261): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.-62+2028G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21133264 | ||||||
| chr12:21133290
|
C | G | 2 | a0001c0001t0001g0079a0001c0003t0002g0242 | 2 | HG02071.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.-62+2054C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21133290 | ||||||
| chr12:21133308
|
T | G | 1 | a0001c0001t0001g0079 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-62+2072T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21133308 | ||||||
| chr12:21133383
|
C | T | 1 | a0002c0005t0001g0265 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-62+2147C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21133383 | ||||||
| chr12:21133669
|
T | C | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-62+2433T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21133669 | ||||||
| chr12:21133739
|
T | C | 1 | a0001c0003t0002g0106 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-62+2503T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21133739 | ||||||
| chr12:21133740
|
G | A | 1 | a0001c0003t0002g0106 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-62+2504G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21133740 | ||||||
| chr12:21133911
|
C | A | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-62+2675C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21133911 | ||||||
| chr12:21133911
|
C | T | 2 | a0001c0003t0002g0241a0004c0006t0001g0078 | 2 | HG02155.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.-62+2675C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21133911 | ||||||
| chr12:21133913
|
T | G | 5 | a0001c0001t0009g0243a0004c0006t0001g0246a0007c0008t0006g0244others(2): Show | 5 | HG01884.hp1 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-62+2677T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21133913 | ||||||
| chr12:21133949
|
G | A | 1 | a0001c0003t0002g0107 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-62+2713G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21133949 | ||||||
| chr12:21133954
|
A | G | 16 | a0001c0001t0002g0251a0001c0003t0001g0259a0001c0003t0002g0250others(13): Show | 16 | HG00642.hp2 HG01928.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.-62+2718A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21133954 | ||||||
| chr12:21134001
|
C | T | 5 | a0001c0001t0002g0249a0004c0006t0001g0246a0007c0008t0006g0244others(2): Show | 5 | HG01884.hp1 HG02451.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-62+2765C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21134001 | ||||||
| chr12:21134002
|
A | G | 5 | a0001c0001t0002g0249a0004c0006t0001g0246a0007c0008t0006g0244others(2): Show | 5 | HG01884.hp1 HG02451.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-62+2766A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21134002 | ||||||
| chr12:21134146
|
C | T | 5 | a0001c0001t0001g0082a0001c0001t0002g0080a0002c0002t0001g0240others(2): Show | 5 | HG01433.hp2 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-62+2910C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21134146 | ||||||
| chr12:21134147
|
G | A | 1 | a0001c0001t0004g0022 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-62+2911G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21134147 | ||||||
| chr12:21134213
|
T | G | 1 | a0001c0001t0004g0023 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-62+2977T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21134213 | ||||||
| chr12:21134214
|
G | T | 15 | a0003c0004t0002g0001a0003c0004t0002g0034a0003c0004t0002g0036others(12): Show | 16 | HG00609.hp1 NA18747.hp1 NA18954.hp2 others(13): Show |
intron_variant | MODIFIER | c.-62+2978G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21134214 | ||||||
| chr12:21134237
|
G | T | 1 | a0001c0001t0002g0249 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-62+3001G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21134237 | ||||||
| chr12:21134247
|
G | T | 115 | a0001c0001t0001g0177a0001c0001t0001g0186a0001c0001t0002g0141others(112): Show | 118 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.-62+3011G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21134247 | ||||||
| chr12:21134275
|
G | C | 1 | a0002c0002t0001g0139 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-62+3039G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21134275 | ||||||
| chr12:21134331
|
G | A | 2 | a0001c0001t0001g0087a0002c0005t0001g0086 | 2 | HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-62+3095G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21134331 | ||||||
| chr12:21134379
|
T | C | 1 | a0005c0007t0004g0093 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-62+3143T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21134379 | ||||||
| chr12:21134380
|
A | G | 4 | a0001c0001t0001g0082a0001c0001t0002g0080a0004c0006t0001g0081others(1): Show | 4 | HG03041.hp2 HG03098.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-62+3144A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21134380 | ||||||
| chr12:21134426
|
A | G | 3 | a0002c0002t0002g0239a0002c0002t0003g0237a0002c0002t0010g0238 | 3 | NA18975.hp2 NA18999.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-62+3190A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21134426 | ||||||
| chr12:21134445
|
T | C | 1 | a0001c0001t0003g0108 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-62+3209T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21134445 | ||||||
| chr12:21134446
|
G | C | 7 | a0001c0001t0001g0267a0001c0003t0002g0266a0001c0003t0002g0271others(4): Show | 7 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-62+3210G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21134446 | ||||||
| chr12:21134456
|
C | G | 30 | a0001c0001t0003g0026a0001c0001t0003g0031a0001c0001t0003g0032others(27): Show | 31 | HG00280.hp1 HG00609.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.-62+3220C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21134456 | ||||||
| chr12:21134510
|
A | C | 1 | a0001c0001t0002g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-62+3274A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21134510 | ||||||
| chr12:21134511
|
G | T | 1 | a0001c0001t0002g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-62+3275G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21134511 | ||||||
| chr12:21134619
|
C | G | 10 | a0002c0002t0001g0100a0003c0004t0002g0097a0003c0004t0002g0098others(7): Show | 10 | HG00099.hp2 HG01081.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.-62+3383C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21134619 | ||||||
| chr12:21134669
|
C | G | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-62+3433C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21134669 | ||||||
| chr12:21134670
|
G | A | 1 | a0016c0018t0001g0140 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-62+3434G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21134670 | ||||||
| chr12:21134769
|
G | A | 7 | a0001c0001t0001g0267a0001c0003t0002g0266a0001c0003t0002g0271others(4): Show | 7 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-62+3533G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21134769 | ||||||
| chr12:21134784
|
G | T | 1 | a0001c0001t0003g0077 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-62+3548G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21134784 | ||||||
| chr12:21134819
|
G | A | 1 | a0005c0009t0002g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-62+3583G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21134819 | ||||||
| chr12:21135002
|
T | A | 10 | a0002c0002t0001g0100a0003c0004t0002g0097a0003c0004t0002g0098others(7): Show | 10 | HG00099.hp2 HG01081.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.-62+3766T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21135002 | ||||||
| chr12:21135214
|
TC | T | 30 | a0001c0001t0003g0026a0001c0001t0003g0031a0001c0001t0003g0032others(27): Show | 31 | HG00280.hp1 HG00609.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.-62+3979delC | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21135214 | ||||||
| chr12:21135217
|
G | T | 5 | a0001c0001t0002g0249a0004c0006t0001g0246a0007c0008t0006g0244others(2): Show | 5 | HG01884.hp1 HG02451.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-62+3981G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21135217 | ||||||
| chr12:21135303
|
A | G | 3 | a0002c0002t0002g0092a0003c0004t0001g0090a0003c0004t0001g0091 | 3 | HG02027.hp2 HG02074.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.-62+4067A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21135303 | ||||||
| chr12:21135390
|
G | A | 4 | a0004c0006t0001g0246a0007c0008t0006g0244a0007c0008t0006g0245others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-62+4154G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21135390 | ||||||
| chr12:21135390
|
G | T | 3 | a0006c0010t0001g0262a0006c0010t0001g0263a0006c0010t0001g0264 | 3 | HG02630.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-62+4154G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21135390 | ||||||
| chr12:21135425
|
A | T | 1 | a0001c0001t0002g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-62+4189A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21135425 | ||||||
| chr12:21135432
|
G | A | 1 | a0005c0007t0004g0094 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-62+4196G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21135432 | ||||||
| chr12:21135535
|
A | G | 8 | a0001c0001t0001g0267a0001c0003t0002g0266a0001c0003t0002g0271others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-62+4299A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21135535 | ||||||
| chr12:21135545
|
T | G | 6 | a0001c0001t0002g0248a0001c0001t0002g0249a0004c0006t0001g0246others(3): Show | 6 | HG01884.hp1 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-62+4309T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21135545 | ||||||
| chr12:21135553
|
G | A | 9 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(6): Show | 9 | HG02559.hp1 HG02630.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.-62+4317G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21135553 | ||||||
| chr12:21135553
|
G | T | 1 | a0002c0002t0001g0236 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-62+4317G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21135553 | ||||||
| chr12:21135588
|
A | G | 32 | a0001c0001t0001g0002a0001c0001t0001g0113a0001c0001t0001g0114others(29): Show | 33 | HG00438.hp1 HG01167.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.-62+4352A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21135588 | ||||||
| chr12:21135612
|
C | T | 1 | a0001c0001t0002g0248 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-62+4376C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21135612 | ||||||
| chr12:21135624
|
A | G | 1 | a0001c0001t0002g0248 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-62+4388A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21135624 | ||||||
| chr12:21135675
|
T | C | 1 | a0011c0025t0001g0019 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-62+4439T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21135675 | ||||||
| chr12:21135738
|
G | T | 1 | a0001c0001t0001g0137 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-62+4502G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21135738 | ||||||
| chr12:21135743
|
G | C | 1 | a0001c0001t0002g0141 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-62+4507G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21135743 | ||||||
| chr12:21135789
|
A | G | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-62+4553A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21135789 | ||||||
| chr12:21135793
|
G | A | 4 | a0001c0001t0001g0082a0001c0001t0002g0080a0004c0006t0001g0081others(1): Show | 4 | HG03041.hp2 HG03098.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-62+4557G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21135793 | ||||||
| chr12:21135874
|
A | T | 2 | a0001c0001t0002g0248a0001c0001t0002g0249 | 2 | HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-62+4638A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21135874 | ||||||
| chr12:21135877
|
G | A | 2 | a0001c0001t0002g0248a0001c0001t0002g0249 | 2 | HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-62+4641G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21135877 | ||||||
| chr12:21135890
|
G | A | 10 | a0002c0002t0001g0100a0003c0004t0002g0097a0003c0004t0002g0098others(7): Show | 10 | HG00099.hp2 HG01081.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.-62+4654G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21135890 | ||||||
| chr12:21136102
|
C | G | 38 | a0001c0001t0001g0079a0001c0001t0003g0048a0001c0001t0003g0049others(35): Show | 38 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.-62+4866C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21136102 | ||||||
| chr12:21136190
|
C | T | 1 | a0003c0004t0002g0033 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-62+4954C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21136190 | ||||||
| chr12:21136262
|
T | C | 39 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0002g0080others(36): Show | 40 | HG00280.hp1 HG00609.hp1 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.-62+5026T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21136262 | ||||||
| chr12:21136304
|
G | A | 1 | a0001c0023t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-62+5068G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21136304 | ||||||
| chr12:21136323
|
C | T | 38 | a0001c0001t0001g0079a0001c0001t0003g0048a0001c0001t0003g0049others(35): Show | 38 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.-62+5087C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21136323 | ||||||
| chr12:21136344
|
G | A | 8 | a0001c0001t0001g0267a0001c0003t0002g0266a0001c0003t0002g0271others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-62+5108G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21136344 | ||||||
| chr12:21136441
|
C | T | 147 | a0001c0001t0001g0002a0001c0001t0001g0113a0001c0001t0001g0114others(144): Show | 151 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-61-5073C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21136441 | ||||||
| chr12:21136494
|
A | T | 3 | a0004c0006t0001g0233a0004c0006t0001g0234a0004c0006t0001g0235 | 3 | HG00642.hp1 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-61-5020A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21136494 | ||||||
| chr12:21136583
|
G | A | 7 | a0001c0001t0001g0267a0001c0003t0002g0266a0001c0003t0002g0271others(4): Show | 7 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-61-4931G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21136583 | ||||||
| chr12:21136601
|
C | A | 1 | a0001c0001t0002g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-61-4913C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21136601 | ||||||
| chr12:21136684
|
A | G | 271 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(268): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.-61-4830A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21136684 | ||||||
| chr12:21136829
|
C | G | 1 | a0005c0007t0008g0102 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-61-4685C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21136829 | ||||||
| chr12:21136862
|
C | T | 1 | a0001c0001t0002g0249 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-61-4652C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21136862 | ||||||
| chr12:21136863
|
G | A | 34 | a0001c0001t0001g0087a0001c0001t0003g0026a0001c0001t0003g0031others(31): Show | 35 | HG00280.hp1 HG00609.hp1 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.-61-4651G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21136863 | ||||||
| chr12:21136904
|
G | A | 1 | a0001c0003t0002g0273 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-61-4610G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21136904 | ||||||
| chr12:21136970
|
C | G | 3 | a0006c0010t0001g0262a0006c0010t0001g0263a0006c0010t0001g0264 | 3 | HG02630.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-61-4544C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21136970 | ||||||
| chr12:21136993
|
G | A | 1 | a0001c0003t0002g0250 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-61-4521G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21136993 | ||||||
| chr12:21137013
|
C | T | 236 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(233): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.-61-4501C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21137013 | ||||||
| chr12:21137144
|
C | T | 1 | a0001c0001t0003g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-61-4370C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21137144 | ||||||
| chr12:21137242
|
C | T | 3 | a0001c0003t0002g0271a0002c0005t0001g0270a0004c0006t0001g0272 | 3 | HG02145.hp1 HG02257.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-61-4272C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21137242 | ||||||
| chr12:21137264
|
G | C | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-61-4250G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21137264 | ||||||
| chr12:21137309
|
T | A | 1 | a0001c0001t0003g0142 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-61-4205T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21137309 | ||||||
| chr12:21137314
|
G | C | 1 | a0002c0005t0001g0143 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-61-4200G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21137314 | ||||||
| chr12:21137326
|
C | T | 1 | a0003c0004t0003g0047 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-61-4188C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21137326 | ||||||
| chr12:21137327
|
G | A | 7 | a0001c0001t0001g0267a0001c0003t0002g0266a0001c0003t0002g0271others(4): Show | 7 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-61-4187G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21137327 | ||||||
| chr12:21137455
|
G | A | 10 | a0002c0002t0001g0100a0003c0004t0002g0097a0003c0004t0002g0098others(7): Show | 10 | HG00099.hp2 HG01081.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.-61-4059G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21137455 | ||||||
| chr12:21137487
|
G | A | 1 | a0002c0002t0001g0144 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-61-4027G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21137487 | ||||||
| chr12:21137498
|
C | T | 1 | a0002c0005t0001g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-61-4016C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21137498 | ||||||
| chr12:21137499
|
C | T | 3 | a0001c0003t0001g0085a0005c0009t0002g0084a0011c0025t0001g0019 | 3 | HG02055.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-61-4015C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21137499 | ||||||
| chr12:21137534
|
A | G | 1 | a0001c0003t0002g0241 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-61-3980A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21137534 | ||||||
| chr12:21137538
|
T | C | 3 | a0001c0001t0001g0082a0001c0001t0002g0080a0004c0006t0001g0081 | 3 | HG03041.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-61-3976T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21137538 | ||||||
| chr12:21137680
|
G | T | 4 | a0001c0003t0002g0229a0001c0003t0002g0230a0001c0003t0002g0231others(1): Show | 4 | NA18747.hp2 NA18962.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.-61-3834G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21137680 | ||||||
| chr12:21137693
|
A | C | 3 | a0001c0001t0001g0082a0001c0001t0002g0080a0004c0006t0001g0081 | 3 | HG03041.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-61-3821A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21137693 | ||||||
| chr12:21137856
|
G | A | 1 | a0001c0001t0002g0248 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-61-3658G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21137856 | ||||||
| chr12:21137966
|
G | A | 1 | a0001c0001t0009g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-61-3548G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21137966 | ||||||
| chr12:21138180
|
T | C | 2 | a0001c0001t0001g0087a0002c0005t0001g0086 | 2 | HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-61-3334T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21138180 | ||||||
| chr12:21138269
|
T | A | 39 | a0001c0001t0001g0079a0001c0001t0003g0048a0001c0001t0003g0049others(36): Show | 39 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.-61-3245T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21138269 | ||||||
| chr12:21138364
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-61-3150A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21138364 | ||||||
| chr12:21138450
|
T | C | 1 | a0003c0004t0002g0034 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-61-3064T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21138450 | ||||||
| chr12:21138543
|
T | C | 3 | a0001c0003t0002g0018a0001c0003t0002g0145a0014c0022t0002g0146 | 3 | NA18951.hp2 NA18975.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.-61-2971T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21138543 | ||||||
| chr12:21138556
|
G | A | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(3): Show | 6 | HG02559.hp1 HG02896.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-61-2958G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21138556 | ||||||
| chr12:21138567
|
T | C | 122 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(119): Show | 125 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.-61-2947T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21138567 | ||||||
| chr12:21138601
|
T | C | 1 | a0001c0001t0003g0142 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-61-2913T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21138601 | ||||||
| chr12:21138627
|
T | G | 43 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0002g0080others(40): Show | 43 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.-61-2887T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21138627 | ||||||
| chr12:21138644
|
G | A | 32 | a0001c0001t0001g0002a0001c0001t0001g0113a0001c0001t0001g0114others(29): Show | 33 | HG00438.hp1 HG01167.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.-61-2870G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21138644 | ||||||
| chr12:21138726
|
T | C | 1 | a0002c0002t0001g0147 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-61-2788T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21138726 | ||||||
| chr12:21138773
|
A | AG | 270 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(267): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.-61-2741_-61-2740i others(3): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21138773 | ||||||
| chr12:21138859
|
G | T | 10 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0135others(7): Show | 10 | HG00438.hp1 HG03669.hp2 NA18942.hp1 others(7): Show |
intron_variant | MODIFIER | c.-61-2655G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21138859 | ||||||
| chr12:21139044
|
A | G | 32 | a0001c0001t0001g0002a0001c0001t0001g0113a0001c0001t0001g0114others(29): Show | 33 | HG00438.hp1 HG01167.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.-61-2470A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21139044 | ||||||
| chr12:21139077
|
A | G | 11 | a0001c0003t0001g0259a0001c0003t0002g0250a0002c0005t0001g0253others(8): Show | 11 | HG00642.hp2 HG01928.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.-61-2437A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21139077 | ||||||
| chr12:21139091
|
A | G | 1 | a0001c0001t0002g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-61-2423A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21139091 | ||||||
| chr12:21139121
|
C | T | 24 | a0001c0001t0002g0141a0001c0003t0002g0005a0001c0003t0002g0018others(21): Show | 25 | HG00544.hp2 HG00673.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.-61-2393C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21139121 | ||||||
| chr12:21139122
|
G | A | 232 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(229): Show | 236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.-61-2392G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21139122 | ||||||
| chr12:21139193
|
T | A | 2 | a0001c0001t0002g0248a0001c0001t0002g0249 | 2 | HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-61-2321T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21139193 | ||||||
| chr12:21139194
|
T | A | 123 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(120): Show | 125 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.-61-2320T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21139194 | ||||||
| chr12:21139195
|
A | T | 77 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0087others(74): Show | 78 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.-61-2319A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21139195 | ||||||
| chr12:21139272
|
A | T | 87 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0087others(84): Show | 88 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-61-2242A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21139272 | ||||||
| chr12:21139346
|
C | T | 30 | a0001c0001t0003g0026a0001c0001t0003g0031a0001c0001t0003g0032others(27): Show | 31 | HG00280.hp1 HG00609.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.-61-2168C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21139346 | ||||||
| chr12:21139471
|
T | C | 2 | a0001c0001t0001g0087a0002c0005t0001g0086 | 2 | HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-61-2043T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21139471 | ||||||
| chr12:21139626
|
A | G | 1 | a0011c0025t0001g0019 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-61-1888A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21139626 | ||||||
| chr12:21139898
|
T | C | 1 | a0001c0001t0003g0049 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-61-1616T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21139898 | ||||||
| chr12:21139925
|
AGAGTATC others(1): Show |
A | 11 | a0001c0003t0001g0259a0001c0003t0002g0250a0002c0005t0001g0253others(8): Show | 11 | HG00642.hp2 HG01928.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.-61-1585_-61-1578d others(10): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 21139925 | |||||
| chr12:21140128
|
A | G | 1 | a0006c0010t0001g0264 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-61-1386A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21140128 | ||||||
| chr12:21140202
|
C | G | 1 | a0001c0001t0003g0075 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-61-1312C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21140202 | ||||||
| chr12:21140218
|
C | T | 2 | a0002c0002t0001g0197a0002c0002t0001g0198 | 2 | HG00741.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-61-1296C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21140218 | ||||||
| chr12:21140400
|
G | T | 7 | a0001c0003t0002g0194a0001c0003t0002g0195a0001c0003t0002g0196others(4): Show | 7 | HG00438.hp2 NA18957.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-61-1114G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21140400 | ||||||
| chr12:21140503
|
T | C | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-61-1011T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21140503 | ||||||
| chr12:21140652
|
C | G | 1 | a0001c0001t0002g0249 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-61-862C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21140652 | ||||||
| chr12:21140710
|
A | T | 1 | a0001c0003t0001g0193 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-61-804A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21140710 | ||||||
| chr12:21140929
|
A | G | 1 | a0001c0001t0001g0311 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-61-585A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21140929 | ||||||
| chr12:21140953
|
T | C | 1 | a0001c0001t0002g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-61-561T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21140953 | ||||||
| chr12:21141035
|
C | T | 11 | a0001c0003t0001g0259a0001c0003t0002g0250a0002c0005t0001g0253others(8): Show | 11 | HG00642.hp2 HG01928.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.-61-479C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21141035 | ||||||
| chr12:21141067
|
A | G | 4 | a0001c0001t0001g0082a0001c0001t0002g0080a0004c0006t0001g0081others(1): Show | 4 | HG03041.hp2 HG03098.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-61-447A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21141067 | ||||||
| chr12:21141123
|
T | C | 6 | a0001c0001t0002g0248a0001c0001t0002g0249a0004c0006t0001g0246others(3): Show | 6 | HG01884.hp1 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-61-391T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21141123 | ||||||
| chr12:21141261
|
ATTAC | A | 43 | a0001c0001t0001g0087a0001c0001t0003g0026a0001c0001t0003g0031others(40): Show | 44 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.-61-246_-61-243del others(4): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 21141261 | |||||
| chr12:21141292
|
AATTT | A | 30 | a0001c0001t0003g0026a0001c0001t0003g0031a0001c0001t0003g0032others(27): Show | 31 | HG00280.hp1 HG00609.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.-61-217_-61-214del others(4): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 21141292 | |||||
| chr12:21141359
|
T | G | 271 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(268): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.-61-155T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21141359 | ||||||
| chr12:21141395
|
T | C | 2 | a0001c0001t0002g0251a0001c0003t0002g0252 | 2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-61-119T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 1/14 | chr12 | 21141395 | ||||||
| chr12:21141740
|
C | T | 2 | a0001c0001t0003g0031a0001c0001t0003g0032 | 2 | NA18979.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.84+82C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21141740 | ||||||
| chr12:21141776
|
A | G | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(3): Show | 6 | HG02559.hp1 HG02896.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+118A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21141776 | ||||||
| chr12:21141826
|
T | C | 3 | a0002c0002t0007g0148a0002c0002t0007g0149a0002c0002t0007g0150 | 3 | HG00609.hp2 NA18943.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.84+168T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21141826 | ||||||
| chr12:21141850
|
C | T | 2 | a0009c0011t0002g0105a0009c0011t0002g0192 | 2 | NA19009.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.84+192C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21141850 | ||||||
| chr12:21141851
|
G | A | 24 | a0001c0001t0003g0026a0001c0001t0003g0031a0001c0001t0003g0032others(21): Show | 25 | HG00609.hp1 HG02027.hp2 HG02074.hp2 others(22): Show |
intron_variant | MODIFIER | c.84+193G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21141851 | ||||||
| chr12:21141861
|
A | T | 11 | a0001c0003t0001g0259a0001c0003t0002g0250a0002c0005t0001g0253others(8): Show | 11 | HG00642.hp2 HG01928.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.84+203A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21141861 | ||||||
| chr12:21141865
|
T | C | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(3): Show | 6 | HG02559.hp1 HG02896.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+207T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21141865 | ||||||
| chr12:21141866
|
T | A | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(3): Show | 6 | HG02559.hp1 HG02896.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+208T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21141866 | ||||||
| chr12:21141906
|
A | G | 16 | a0001c0001t0002g0251a0001c0003t0001g0259a0001c0003t0002g0250others(13): Show | 16 | HG00642.hp2 HG01928.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.84+248A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21141906 | ||||||
| chr12:21141969
|
A | T | 1 | a0001c0001t0003g0074 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.84+311A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21141969 | ||||||
| chr12:21142066
|
C | A | 7 | a0001c0001t0001g0267a0001c0003t0002g0266a0001c0003t0002g0271others(4): Show | 7 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.84+408C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21142066 | ||||||
| chr12:21142069
|
T | TA | 32 | a0001c0001t0001g0002a0001c0001t0001g0113a0001c0001t0001g0114others(29): Show | 33 | HG00438.hp1 HG01167.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.84+411_84+412insA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21142069 | ||||||
| chr12:21142069
|
T | TAA | 4 | a0001c0001t0001g0082a0001c0001t0001g0129a0001c0001t0002g0080others(1): Show | 4 | HG03041.hp2 HG03098.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.84+411_84+412insAA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21142069 | ||||||
| chr12:21142070
|
T | A | 37 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0113others(34): Show | 38 | HG00438.hp1 HG01167.hp1 HG01168.hp2 others(35): Show |
intron_variant | MODIFIER | c.84+412T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21142070 | ||||||
| chr12:21142070
|
T | TA | 218 | a0001c0001t0001g0079a0001c0001t0001g0087a0001c0001t0001g0177others(215): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.84+423dupA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21142070 | |||||
| chr12:21142146
|
A | G | 1 | a0002c0002t0002g0191 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.84+488A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21142146 | ||||||
| chr12:21142345
|
G | A | 2 | a0002c0002t0001g0152a0002c0002t0001g0153 | 2 | HG01261.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.84+687G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21142345 | ||||||
| chr12:21142419
|
C | G | 1 | a0001c0001t0001g0129 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.84+761C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21142419 | ||||||
| chr12:21142514
|
G | A | 1 | a0001c0001t0002g0249 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.84+856G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21142514 | ||||||
| chr12:21142678
|
G | A | 86 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0087others(83): Show | 87 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.84+1020G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21142678 | ||||||
| chr12:21142887
|
G | C | 4 | a0004c0006t0001g0246a0007c0008t0006g0244a0007c0008t0006g0245others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.84+1229G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21142887 | ||||||
| chr12:21143065
|
A | G | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.84+1407A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21143065 | ||||||
| chr12:21143175
|
C | T | 1 | a0001c0001t0003g0026 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.84+1517C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21143175 | ||||||
| chr12:21143293
|
T | A | 10 | a0002c0002t0001g0100a0003c0004t0002g0097a0003c0004t0002g0098others(7): Show | 10 | HG00099.hp2 HG01081.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.84+1635T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21143293 | ||||||
| chr12:21143337
|
C | T | 10 | a0002c0002t0001g0100a0003c0004t0002g0097a0003c0004t0002g0098others(7): Show | 10 | HG00099.hp2 HG01081.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.84+1679C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21143337 | ||||||
| chr12:21143410
|
A | G | 149 | a0001c0001t0001g0002a0001c0001t0001g0113a0001c0001t0001g0114others(146): Show | 153 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.84+1752A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21143410 | ||||||
| chr12:21143541
|
T | A | 117 | a0001c0001t0001g0177a0001c0001t0001g0186a0001c0001t0002g0010others(114): Show | 120 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.84+1883T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21143541 | ||||||
| chr12:21143650
|
C | A | 3 | a0001c0001t0001g0082a0001c0001t0002g0080a0004c0006t0001g0081 | 3 | HG03041.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.84+1992C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21143650 | ||||||
| chr12:21143773
|
C | G | 236 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(233): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.84+2115C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21143773 | ||||||
| chr12:21143872
|
C | G | 42 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0002g0080others(39): Show | 42 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.84+2214C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21143872 | ||||||
| chr12:21144024
|
TC | T | 115 | a0001c0001t0001g0177a0001c0001t0001g0186a0001c0001t0002g0141others(112): Show | 118 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.84+2367delC | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21144024 | ||||||
| chr12:21144616
|
A | G | 145 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(142): Show | 148 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.84+2958A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21144616 | ||||||
| chr12:21144836
|
A | C | 1 | a0001c0001t0003g0072 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.84+3178A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21144836 | ||||||
| chr12:21144864
|
A | G | 32 | a0001c0001t0001g0002a0001c0001t0001g0113a0001c0001t0001g0114others(29): Show | 33 | HG00438.hp1 HG01167.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.84+3206A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21144864 | ||||||
| chr12:21144940
|
A | G | 7 | a0001c0001t0001g0267a0001c0003t0002g0266a0001c0003t0002g0271others(4): Show | 7 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.84+3282A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21144940 | ||||||
| chr12:21145473
|
A | AT | 45 | a0001c0001t0001g0002a0001c0001t0001g0113a0001c0001t0001g0114others(42): Show | 46 | HG01167.hp1 HG01168.hp2 HG01891.hp1 others(43): Show |
intron_variant | MODIFIER | c.84+3841dupT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21145473 | |||||
| chr12:21145473
|
A | ATTT | 19 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(16): Show | 19 | HG00642.hp2 HG01069.hp2 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.84+3839_84+3841dup others(3): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21145473 | |||||
| chr12:21145473
|
A | ATTTT | 116 | a0001c0001t0001g0177a0001c0001t0001g0186a0001c0001t0002g0010others(113): Show | 119 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.84+3838_84+3841dup others(4): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21145473 | |||||
| chr12:21145473
|
A | ATTTTT | 9 | a0001c0003t0002g0106a0001c0003t0002g0228a0002c0002t0001g0190others(6): Show | 9 | HG01175.hp2 HG01358.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.84+3837_84+3841dup others(5): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21145473 | |||||
| chr12:21145473
|
A | T | 1 | a0011c0025t0001g0019 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.84+3815A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21145473 | ||||||
| chr12:21145473
|
AT | A | 43 | a0001c0001t0001g0079a0001c0001t0003g0048a0001c0001t0003g0049others(40): Show | 43 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.84+3841delT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21145473 | |||||
| chr12:21145566
|
G | A | 4 | a0002c0002t0001g0198a0006c0010t0001g0262a0006c0010t0001g0263others(1): Show | 4 | HG02630.hp2 HG03225.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.84+3908G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21145566 | ||||||
| chr12:21145635
|
G | A | 2 | a0010c0012t0001g0155a0010c0012t0001g0189 | 2 | NA18990.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.84+3977G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21145635 | ||||||
| chr12:21145768
|
A | G | 271 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(268): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.84+4110A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21145768 | ||||||
| chr12:21145820
|
A | G | 32 | a0001c0001t0001g0002a0001c0001t0001g0113a0001c0001t0001g0114others(29): Show | 33 | HG00438.hp1 HG01167.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.84+4162A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21145820 | ||||||
| chr12:21146138
|
C | T | 1 | a0005c0007t0001g0101 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.84+4480C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21146138 | ||||||
| chr12:21146180
|
T | G | 1 | a0001c0001t0002g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.84+4522T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21146180 | ||||||
| chr12:21146182
|
G | T | 3 | a0001c0003t0002g0107a0001c0003t0002g0187a0001c0003t0002g0188 | 3 | NA18967.hp1 NA18991.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.84+4524G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21146182 | ||||||
| chr12:21146201
|
T | A | 1 | a0001c0001t0002g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.84+4543T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21146201 | ||||||
| chr12:21146539
|
A | G | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(3): Show | 6 | HG02559.hp1 HG02896.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+4881A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21146539 | ||||||
| chr12:21146654
|
A | C | 10 | a0002c0002t0001g0100a0003c0004t0002g0097a0003c0004t0002g0098others(7): Show | 10 | HG00099.hp2 HG01081.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.84+4996A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21146654 | ||||||
| chr12:21147068
|
T | G | 10 | a0002c0002t0001g0100a0003c0004t0002g0097a0003c0004t0002g0098others(7): Show | 10 | HG00099.hp2 HG01081.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.84+5410T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21147068 | ||||||
| chr12:21147130
|
T | C | 1 | a0001c0001t0002g0249 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.84+5472T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21147130 | ||||||
| chr12:21147141
|
GA | G | 10 | a0002c0002t0001g0100a0003c0004t0002g0097a0003c0004t0002g0098others(7): Show | 10 | HG00099.hp2 HG01081.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.84+5485delA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21147141 | |||||
| chr12:21147230
|
G | T | 11 | a0001c0003t0001g0259a0001c0003t0002g0250a0002c0005t0001g0253others(8): Show | 11 | HG00642.hp2 HG01928.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.84+5572G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21147230 | ||||||
| chr12:21147265
|
G | T | 1 | a0001c0003t0002g0228 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.84+5607G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21147265 | ||||||
| chr12:21147276
|
T | G | 1 | a0005c0007t0004g0095 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.84+5618T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21147276 | ||||||
| chr12:21147394
|
G | A | 3 | a0001c0003t0002g0211a0001c0003t0002g0213a0001c0003t0002g0214 | 3 | HG00673.hp1 NA18983.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.84+5736G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21147394 | ||||||
| chr12:21147803
|
G | T | 1 | a0001c0001t0002g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.84+6145G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21147803 | ||||||
| chr12:21147863
|
T | A | 1 | a0001c0001t0001g0130 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.84+6205T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21147863 | ||||||
| chr12:21147898
|
G | A | 6 | a0001c0001t0002g0248a0001c0001t0002g0249a0004c0006t0001g0246others(3): Show | 6 | HG01884.hp1 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+6240G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21147898 | ||||||
| chr12:21147903
|
C | T | 2 | a0001c0001t0002g0251a0001c0003t0002g0252 | 2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.84+6245C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21147903 | ||||||
| chr12:21147911
|
G | A | 7 | a0001c0001t0001g0267a0001c0003t0002g0266a0001c0003t0002g0271others(4): Show | 7 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.84+6253G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21147911 | ||||||
| chr12:21148166
|
C | T | 1 | a0001c0001t0003g0070 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.84+6508C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21148166 | ||||||
| chr12:21148183
|
C | A | 3 | a0001c0003t0002g0275a0001c0003t0002g0276a0001c0003t0002g0303 | 3 | NA18943.hp2 NA18959.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.84+6525C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21148183 | ||||||
| chr12:21148318
|
G | C | 270 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(267): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.84+6660G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21148318 | ||||||
| chr12:21148392
|
G | A | 38 | a0001c0001t0001g0079a0001c0001t0003g0048a0001c0001t0003g0049others(35): Show | 38 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.84+6734G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21148392 | ||||||
| chr12:21148587
|
A | C | 2 | a0002c0002t0001g0268a0002c0002t0001g0269 | 2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.84+6929A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21148587 | ||||||
| chr12:21148643
|
A | G | 2 | a0001c0001t0002g0251a0001c0003t0002g0252 | 2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.84+6985A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21148643 | ||||||
| chr12:21148650
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.84+6992C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21148650 | ||||||
| chr12:21148695
|
C | CT | 7 | a0001c0003t0002g0271a0002c0002t0001g0025a0002c0002t0002g0092others(4): Show | 7 | HG02027.hp2 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.84+7057dupT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21148695 | |||||
| chr12:21148695
|
CT | C | 23 | a0001c0001t0001g0082a0001c0001t0001g0186a0001c0001t0002g0080others(20): Show | 23 | HG01261.hp1 HG01928.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.84+7057delT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21148695 | |||||
| chr12:21148695
|
CTT | C | 115 | a0001c0001t0001g0177a0001c0001t0001g0304a0001c0001t0002g0010others(112): Show | 118 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.84+7056_84+7057del others(2): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21148695 | |||||
| chr12:21148695
|
CTTT | C | 12 | a0001c0003t0002g0106a0001c0003t0002g0156a0001c0003t0002g0158others(9): Show | 12 | HG01993.hp1 HG01993.hp2 NA18747.hp2 others(9): Show |
intron_variant | MODIFIER | c.84+7055_84+7057del others(3): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21148695 | |||||
| chr12:21148695
|
CTTTT | C | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(3): Show | 6 | HG02559.hp1 HG02896.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+7054_84+7057del others(4): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21148695 | |||||
| chr12:21148708
|
T | C | 1 | a0001c0001t0003g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.84+7050T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21148708 | ||||||
| chr12:21148744
|
T | G | 3 | a0001c0001t0001g0082a0001c0001t0002g0080a0004c0006t0001g0081 | 3 | HG03041.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.84+7086T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21148744 | ||||||
| chr12:21148920
|
C | T | 1 | a0001c0003t0002g0302 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.84+7262C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21148920 | ||||||
| chr12:21148921
|
G | A | 10 | a0001c0001t0003g0161a0001c0003t0002g0160a0002c0002t0001g0147others(7): Show | 11 | HG00609.hp2 HG01258.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.84+7263G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21148921 | ||||||
| chr12:21149003
|
C | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(3): Show | 6 | HG02559.hp1 HG02896.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+7345C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21149003 | ||||||
| chr12:21149174
|
G | A | 4 | a0001c0001t0001g0082a0001c0001t0002g0080a0004c0006t0001g0081others(1): Show | 4 | HG03041.hp2 HG03098.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.84+7516G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21149174 | ||||||
| chr12:21149302
|
G | A | 1 | a0003c0004t0002g0003 | 2 | HG01258.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.84+7644G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21149302 | ||||||
| chr12:21149342
|
A | G | 4 | a0001c0001t0001g0082a0001c0001t0002g0080a0004c0006t0001g0081others(1): Show | 4 | HG03041.hp2 HG03098.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.84+7684A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21149342 | ||||||
| chr12:21149364
|
T | C | 87 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0087others(84): Show | 88 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.84+7706T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21149364 | ||||||
| chr12:21149516
|
T | A | 1 | a0002c0002t0007g0148 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.84+7858T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21149516 | ||||||
| chr12:21149703
|
T | C | 309 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(306): Show | 314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.84+8045T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21149703 | ||||||
| chr12:21149704
|
G | A | 2 | a0010c0012t0001g0155a0010c0012t0001g0189 | 2 | NA18990.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.84+8046G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21149704 | ||||||
| chr12:21149914
|
C | G | 1 | a0001c0001t0003g0071 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.84+8256C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21149914 | ||||||
| chr12:21149994
|
G | A | 3 | a0001c0003t0002g0196a0002c0002t0001g0163a0002c0002t0002g0191 | 3 | HG00438.hp2 NA20752.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.84+8336G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21149994 | ||||||
| chr12:21150027
|
T | A | 1 | a0001c0001t0003g0103 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.84+8369T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21150027 | ||||||
| chr12:21150197
|
C | A | 11 | a0001c0003t0001g0259a0001c0003t0002g0250a0002c0005t0001g0253others(8): Show | 11 | HG00642.hp2 HG01928.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.84+8539C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21150197 | ||||||
| chr12:21150237
|
C | CCTGGGAG others(9): Show |
7 | a0001c0001t0001g0267a0001c0003t0002g0266a0001c0003t0002g0271others(4): Show | 7 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.84+8583_84+8598dup others(16): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21150237 | |||||
| chr12:21150382
|
C | G | 2 | a0001c0001t0001g0087a0002c0005t0001g0086 | 2 | HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.84+8724C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21150382 | ||||||
| chr12:21150406
|
C | T | 3 | a0006c0010t0001g0262a0006c0010t0001g0263a0006c0010t0001g0264 | 3 | HG02630.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.84+8748C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21150406 | ||||||
| chr12:21150461
|
T | C | 86 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0087others(83): Show | 87 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.84+8803T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21150461 | ||||||
| chr12:21150505
|
G | A | 10 | a0002c0002t0001g0100a0003c0004t0002g0097a0003c0004t0002g0098others(7): Show | 10 | HG00099.hp2 HG01081.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.84+8847G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21150505 | ||||||
| chr12:21150594
|
G | A | 116 | a0001c0001t0001g0177a0001c0001t0001g0186a0001c0001t0002g0010others(113): Show | 119 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.84+8936G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21150594 | ||||||
| chr12:21150618
|
A | G | 261 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.84+8960A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21150618 | ||||||
| chr12:21150682
|
C | G | 3 | a0001c0001t0001g0082a0001c0001t0002g0080a0004c0006t0001g0081 | 3 | HG03041.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.84+9024C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21150682 | ||||||
| chr12:21150962
|
G | A | 1 | a0001c0001t0002g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.84+9304G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21150962 | ||||||
| chr12:21151036
|
C | A | 11 | a0001c0003t0001g0259a0001c0003t0002g0250a0002c0005t0001g0253others(8): Show | 11 | HG00642.hp2 HG01928.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.84+9378C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21151036 | ||||||
| chr12:21151047
|
A | G | 1 | a0005c0007t0004g0093 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.84+9389A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21151047 | ||||||
| chr12:21151139
|
A | G | 3 | a0002c0002t0002g0007a0002c0002t0002g0009a0002c0002t0003g0008 | 3 | NA18999.hp2 NA19066.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.84+9481A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21151139 | ||||||
| chr12:21151319
|
G | A | 1 | a0001c0001t0002g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.84+9661G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21151319 | ||||||
| chr12:21151359
|
A | G | 1 | a0001c0003t0001g0193 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.84+9701A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21151359 | ||||||
| chr12:21151359
|
A | T | 1 | a0001c0001t0002g0248 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.84+9701A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21151359 | ||||||
| chr12:21151417
|
T | C | 1 | a0001c0001t0003g0108 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.84+9759T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21151417 | ||||||
| chr12:21151435
|
A | G | 77 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0087others(74): Show | 78 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.84+9777A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21151435 | ||||||
| chr12:21151638
|
T | G | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.84+9980T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21151638 | ||||||
| chr12:21151773
|
G | T | 10 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0135others(7): Show | 10 | HG00438.hp1 HG03669.hp2 NA18942.hp1 others(7): Show |
intron_variant | MODIFIER | c.84+10115G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21151773 | ||||||
| chr12:21151779
|
G | GGGAAGGT others(10): Show |
1 | a0002c0002t0001g0227 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.84+10122_84+10138d others(19): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21151779 | |||||
| chr12:21152116
|
A | C | 1 | a0002c0002t0004g0199 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.84+10458A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21152116 | ||||||
| chr12:21152219
|
T | G | 39 | a0001c0001t0001g0079a0001c0001t0003g0048a0001c0001t0003g0049others(36): Show | 39 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.84+10561T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21152219 | ||||||
| chr12:21152319
|
T | C | 1 | a0001c0003t0002g0110 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.84+10661T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21152319 | ||||||
| chr12:21152364
|
C | A | 1 | a0002c0005t0001g0164 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.84+10706C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21152364 | ||||||
| chr12:21152412
|
T | A | 1 | a0005c0007t0004g0096 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.84+10754T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21152412 | ||||||
| chr12:21152413
|
T | A | 2 | a0001c0001t0001g0279a0001c0001t0001g0304 | 2 | HG02886.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.84+10755T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21152413 | ||||||
| chr12:21152442
|
T | G | 1 | a0002c0002t0004g0199 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.84+10784T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21152442 | ||||||
| chr12:21152533
|
C | CTTTTTTT others(3): Show |
9 | a0002c0002t0001g0100a0003c0004t0002g0097a0003c0004t0002g0098others(6): Show | 9 | HG00099.hp2 HG01081.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.84+10884_84+10893d others(12): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21152533 | |||||
| chr12:21152533
|
C | CTTTTTTT others(5): Show |
11 | a0001c0001t0001g0087a0001c0001t0001g0267a0001c0003t0001g0274others(8): Show | 11 | HG02486.hp2 HG02622.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.84+10882_84+10893d others(14): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21152533 | |||||
| chr12:21152533
|
C | CTTTTTTT others(6): Show |
30 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0131others(27): Show | 31 | HG00280.hp1 HG00609.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.84+10881_84+10893d others(15): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21152533 | |||||
| chr12:21152533
|
C | CTTTTTTT others(7): Show |
34 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0003g0026others(31): Show | 34 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.84+10880_84+10893d others(16): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21152533 | |||||
| chr12:21152533
|
C | CTTTTTTT others(8): Show |
106 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0121others(103): Show | 109 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.84+10879_84+10893d others(17): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21152533 | |||||
| chr12:21152533
|
C | CTTTTTTT others(9): Show |
47 | a0001c0001t0001g0137a0001c0001t0002g0126a0001c0001t0003g0069others(44): Show | 47 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.84+10878_84+10893d others(18): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21152533 | |||||
| chr12:21152533
|
C | CTTTTTTT others(10): Show |
3 | a0001c0003t0002g0242a0001c0003t0005g0159a0009c0011t0002g0192 | 3 | NA18986.hp2 NA19009.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.84+10877_84+10893d others(19): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21152533 | |||||
| chr12:21152533
|
C | CTTTTTTT others(11): Show |
5 | a0002c0005t0001g0016a0002c0005t0002g0011a0004c0006t0001g0246others(2): Show | 5 | HG01884.hp1 HG02451.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+10876_84+10893d others(20): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21152533 | |||||
| chr12:21152533
|
C | CTTTTTTT others(12): Show |
5 | a0001c0001t0002g0249a0001c0003t0002g0230a0001c0003t0002g0231others(2): Show | 5 | HG02630.hp1 HG03516.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+10893_84+10894i others(21): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21152533 | |||||
| chr12:21152533
|
C | CTTTTTTT others(13): Show |
3 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0002g0080 | 3 | HG03041.hp2 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.84+10893_84+10894i others(22): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21152533 | |||||
| chr12:21152533
|
C | CTTTTTTT others(14): Show |
5 | a0001c0001t0001g0015a0001c0001t0001g0082a0001c0001t0002g0014others(2): Show | 5 | HG02559.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.84+10893_84+10894i others(23): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21152533 | |||||
| chr12:21152533
|
C | CTTTTTTT others(16): Show |
1 | a0001c0001t0002g0248 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.84+10893_84+10894i others(25): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21152533 | |||||
| chr12:21152580
|
T | G | 3 | a0002c0002t0002g0239a0002c0002t0003g0237a0002c0002t0010g0238 | 3 | NA18975.hp2 NA18999.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.84+10922T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21152580 | ||||||
| chr12:21152776
|
A | G | 1 | a0001c0003t0002g0213 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.84+11118A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21152776 | ||||||
| chr12:21152777
|
A | G | 10 | a0002c0002t0001g0100a0003c0004t0002g0097a0003c0004t0002g0098others(7): Show | 10 | HG00099.hp2 HG01081.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.84+11119A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21152777 | ||||||
| chr12:21153059
|
C | G | 1 | a0001c0003t0002g0231 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.84+11401C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21153059 | ||||||
| chr12:21153114
|
AG | A | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(3): Show | 6 | HG02559.hp1 HG02896.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+11458delG | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21153114 | |||||
| chr12:21153121
|
C | T | 1 | a0001c0001t0004g0030 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.84+11463C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21153121 | ||||||
| chr12:21153187
|
G | C | 1 | a0005c0007t0004g0096 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.84+11529G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21153187 | ||||||
| chr12:21153418
|
C | T | 3 | a0006c0010t0001g0262a0006c0010t0001g0263a0006c0010t0001g0264 | 3 | HG02630.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.84+11760C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21153418 | ||||||
| chr12:21153458
|
A | T | 145 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(142): Show | 148 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.84+11800A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21153458 | ||||||
| chr12:21153909
|
C | T | 1 | a0002c0002t0002g0020 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.84+12251C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21153909 | ||||||
| chr12:21153943
|
ATAAAAAG others(3): Show |
A | 1 | a0002c0002t0001g0227 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.84+12286_84+12295d others(12): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21153943 | ||||||
| chr12:21154051
|
G | A | 8 | a0001c0003t0002g0250a0002c0005t0001g0253a0002c0005t0001g0257others(5): Show | 8 | HG00642.hp2 HG01928.hp1 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.84+12393G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21154051 | ||||||
| chr12:21154082
|
T | TGATTTTC others(337): Show |
1 | a0002c0005t0001g0270 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.84+12440_84+12441i others(346): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21154082 | |||||
| chr12:21154140
|
A | G | 1 | a0001c0001t0002g0125 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.84+12482A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21154140 | ||||||
| chr12:21154313
|
G | A | 5 | a0001c0001t0002g0249a0004c0006t0001g0246a0007c0008t0006g0244others(2): Show | 5 | HG01884.hp1 HG02451.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.84+12655G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21154313 | ||||||
| chr12:21154516
|
A | G | 10 | a0002c0002t0001g0100a0003c0004t0002g0097a0003c0004t0002g0098others(7): Show | 10 | HG00099.hp2 HG01081.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.84+12858A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21154516 | ||||||
| chr12:21154595
|
T | C | 1 | a0002c0002t0001g0139 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.84+12937T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21154595 | ||||||
| chr12:21154649
|
C | A | 3 | a0001c0003t0002g0280a0001c0003t0002g0313a0002c0002t0002g0281 | 3 | NA18941.hp1 NA18972.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.84+12991C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21154649 | ||||||
| chr12:21154712
|
G | A | 2 | a0003c0004t0002g0036a0003c0004t0002g0037 | 2 | HG00609.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.84+13054G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21154712 | ||||||
| chr12:21154792
|
G | A | 6 | a0001c0001t0001g0283a0001c0001t0001g0311a0001c0001t0002g0285others(3): Show | 6 | HG01884.hp2 HG02451.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.84+13134G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21154792 | ||||||
| chr12:21154923
|
C | A | 1 | a0005c0007t0004g0093 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.84+13265C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21154923 | ||||||
| chr12:21154993
|
T | A | 1 | a0002c0002t0001g0227 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.84+13335T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21154993 | ||||||
| chr12:21155021
|
T | G | 1 | a0001c0001t0003g0103 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.84+13363T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21155021 | ||||||
| chr12:21155060
|
T | C | 3 | a0006c0010t0001g0262a0006c0010t0001g0263a0006c0010t0001g0264 | 3 | HG02630.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.84+13402T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21155060 | ||||||
| chr12:21155072
|
A | C | 1 | a0001c0003t0002g0187 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.84+13414A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21155072 | ||||||
| chr12:21155099
|
A | AT | 268 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(265): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.84+13447dupT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21155099 | |||||
| chr12:21155106
|
G | T | 1 | a0002c0002t0001g0227 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.84+13448G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21155106 | ||||||
| chr12:21155110
|
T | G | 3 | a0006c0010t0001g0262a0006c0010t0001g0263a0006c0010t0001g0264 | 3 | HG02630.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.84+13452T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21155110 | ||||||
| chr12:21155243
|
T | C | 1 | a0001c0001t0002g0248 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.84+13585T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21155243 | ||||||
| chr12:21155282
|
A | C | 10 | a0002c0002t0001g0100a0003c0004t0002g0097a0003c0004t0002g0098others(7): Show | 10 | HG00099.hp2 HG01081.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.84+13624A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21155282 | ||||||
| chr12:21155365
|
A | G | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.84+13707A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21155365 | ||||||
| chr12:21155372
|
C | T | 1 | a0001c0001t0003g0048 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.84+13714C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21155372 | ||||||
| chr12:21155407
|
A | G | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(9): Show | 12 | HG01884.hp1 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.84+13749A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21155407 | ||||||
| chr12:21155689
|
A | G | 10 | a0002c0002t0001g0100a0003c0004t0002g0097a0003c0004t0002g0098others(7): Show | 10 | HG00099.hp2 HG01081.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.84+14031A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21155689 | ||||||
| chr12:21155737
|
C | T | 1 | a0001c0001t0002g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.84+14079C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21155737 | ||||||
| chr12:21155750
|
A | C | 1 | a0001c0001t0002g0285 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.84+14092A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21155750 | ||||||
| chr12:21155800
|
G | A | 1 | a0001c0003t0002g0280 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.84+14142G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21155800 | ||||||
| chr12:21155971
|
C | T | 1 | a0001c0001t0009g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.84+14313C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21155971 | ||||||
| chr12:21156305
|
A | G | 1 | a0007c0019t0002g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.84+14647A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21156305 | ||||||
| chr12:21156352
|
C | T | 1 | a0018c0016t0001g0185 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.84+14694C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21156352 | ||||||
| chr12:21156496
|
A | C | 1 | a0001c0001t0003g0068 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.84+14838A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21156496 | ||||||
| chr12:21156523
|
G | T | 36 | a0001c0001t0001g0087a0001c0001t0002g0141a0001c0001t0003g0026others(33): Show | 37 | HG00280.hp1 HG00609.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.84+14865G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21156523 | ||||||
| chr12:21156589
|
A | T | 36 | a0001c0001t0001g0087a0001c0001t0002g0141a0001c0001t0003g0026others(33): Show | 37 | HG00280.hp1 HG00609.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.84+14931A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21156589 | ||||||
| chr12:21156673
|
A | C | 1 | a0004c0006t0001g0272 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.84+15015A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21156673 | ||||||
| chr12:21156780
|
T | C | 10 | a0002c0002t0001g0100a0003c0004t0002g0097a0003c0004t0002g0098others(7): Show | 10 | HG00099.hp2 HG01081.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.84+15122T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21156780 | ||||||
| chr12:21157075
|
A | T | 36 | a0001c0001t0001g0079a0001c0001t0003g0048a0001c0001t0003g0049others(33): Show | 36 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.84+15417A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21157075 | ||||||
| chr12:21157145
|
T | G | 1 | a0001c0001t0003g0051 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.84+15487T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21157145 | ||||||
| chr12:21157311
|
G | A | 1 | a0001c0003t0002g0273 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.85-15339G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21157311 | ||||||
| chr12:21157373
|
A | G | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(9): Show | 12 | HG01884.hp1 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.85-15277A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21157373 | ||||||
| chr12:21157505
|
C | A | 1 | a0001c0001t0003g0068 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-15145C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21157505 | ||||||
| chr12:21157600
|
A | AT | 54 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0113others(51): Show | 55 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.85-15031dupT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21157600 | |||||
| chr12:21157600
|
A | T | 1 | a0001c0001t0003g0068 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-15050A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21157600 | ||||||
| chr12:21157600
|
AT | A | 49 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(46): Show | 50 | HG00280.hp1 HG00609.hp1 HG01168.hp1 others(47): Show |
intron_variant | MODIFIER | c.85-15031delT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21157600 | |||||
| chr12:21157636
|
C | CT | 3 | a0002c0002t0001g0221a0002c0002t0001g0222a0002c0002t0001g0225 | 3 | NA18970.hp1 NA18993.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.85-15013dupT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21157636 | |||||
| chr12:21157665
|
G | A | 3 | a0001c0001t0001g0087a0001c0023t0001g0088a0002c0005t0001g0086 | 3 | HG02818.hp2 NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.85-14985G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21157665 | ||||||
| chr12:21157700
|
C | G | 10 | a0002c0002t0001g0100a0003c0004t0002g0097a0003c0004t0002g0098others(7): Show | 10 | HG00099.hp2 HG01081.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.85-14950C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21157700 | ||||||
| chr12:21157722
|
C | T | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(9): Show | 12 | HG01884.hp1 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.85-14928C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21157722 | ||||||
| chr12:21157790
|
C | A | 3 | a0001c0001t0001g0082a0001c0001t0002g0080a0004c0006t0001g0081 | 3 | HG03041.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.85-14860C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21157790 | ||||||
| chr12:21157847
|
A | G | 2 | a0001c0001t0001g0123a0001c0001t0001g0128 | 2 | HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.85-14803A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21157847 | ||||||
| chr12:21157848
|
C | T | 2 | a0001c0003t0002g0250a0002c0005t0001g0257 | 2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.85-14802C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21157848 | ||||||
| chr12:21157962
|
T | G | 3 | a0001c0001t0001g0082a0001c0001t0002g0080a0004c0006t0001g0081 | 3 | HG03041.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.85-14688T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21157962 | ||||||
| chr12:21158031
|
A | G | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(9): Show | 12 | HG01884.hp1 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.85-14619A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21158031 | ||||||
| chr12:21158091
|
T | C | 10 | a0002c0002t0001g0100a0003c0004t0002g0097a0003c0004t0002g0098others(7): Show | 10 | HG00099.hp2 HG01081.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.85-14559T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21158091 | ||||||
| chr12:21158144
|
A | G | 3 | a0002c0002t0003g0212a0002c0002t0003g0220a0017c0017t0001g0219 | 3 | NA18971.hp1 NA18979.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.85-14506A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21158144 | ||||||
| chr12:21158303
|
G | C | 1 | a0001c0023t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.85-14347G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21158303 | ||||||
| chr12:21158314
|
T | C | 40 | a0001c0001t0001g0087a0001c0001t0002g0141a0001c0001t0003g0026others(37): Show | 41 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.85-14336T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21158314 | ||||||
| chr12:21158368
|
A | G | 10 | a0002c0002t0001g0100a0003c0004t0002g0097a0003c0004t0002g0098others(7): Show | 10 | HG00099.hp2 HG01081.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.85-14282A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21158368 | ||||||
| chr12:21158369
|
T | C | 6 | a0001c0001t0001g0087a0001c0003t0001g0274a0001c0003t0001g0299others(3): Show | 6 | HG02486.hp2 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.85-14281T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21158369 | ||||||
| chr12:21158510
|
A | C | 1 | a0002c0002t0001g0184 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.85-14140A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21158510 | ||||||
| chr12:21158650
|
C | T | 1 | a0001c0003t0002g0178 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.85-14000C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21158650 | ||||||
| chr12:21158784
|
A | G | 141 | a0001c0001t0001g0002a0001c0001t0001g0079a0001c0001t0001g0082others(138): Show | 143 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.85-13866A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21158784 | ||||||
| chr12:21158793
|
C | A | 1 | a0003c0004t0003g0047 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.85-13857C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21158793 | ||||||
| chr12:21158833
|
A | C | 112 | a0001c0001t0001g0177a0001c0001t0001g0186a0001c0001t0003g0161others(109): Show | 115 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.85-13817A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21158833 | ||||||
| chr12:21158838
|
A | G | 3 | a0006c0010t0001g0262a0006c0010t0001g0263a0006c0010t0001g0264 | 3 | HG02630.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.85-13812A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21158838 | ||||||
| chr12:21158936
|
G | T | 1 | a0018c0016t0001g0185 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.85-13714G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21158936 | ||||||
| chr12:21159112
|
T | C | 298 | a0001c0001t0001g0002a0001c0001t0001g0079a0001c0001t0001g0082others(295): Show | 303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.85-13538T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21159112 | ||||||
| chr12:21159229
|
T | C | 6 | a0001c0001t0002g0251a0001c0001t0009g0243a0001c0003t0001g0259others(3): Show | 6 | HG02572.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-13421T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21159229 | ||||||
| chr12:21159280
|
G | A | 26 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0121others(23): Show | 26 | HG00438.hp1 HG01167.hp1 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.85-13370G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21159280 | ||||||
| chr12:21159386
|
T | G | 33 | a0001c0001t0002g0141a0001c0001t0003g0026a0001c0001t0003g0031others(30): Show | 34 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.85-13264T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21159386 | ||||||
| chr12:21159474
|
T | C | 36 | a0001c0001t0001g0079a0001c0001t0003g0048a0001c0001t0003g0049others(33): Show | 36 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.85-13176T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21159474 | ||||||
| chr12:21159529
|
G | A | 36 | a0001c0001t0001g0079a0001c0001t0003g0048a0001c0001t0003g0049others(33): Show | 36 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.85-13121G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21159529 | ||||||
| chr12:21159576
|
G | A | 146 | a0001c0001t0001g0002a0001c0001t0001g0079a0001c0001t0001g0082others(143): Show | 148 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.85-13074G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21159576 | ||||||
| chr12:21159632
|
T | A | 1 | a0001c0003t0002g0187 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.85-13018T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21159632 | ||||||
| chr12:21159723
|
A | G | 1 | a0011c0025t0001g0019 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.85-12927A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21159723 | ||||||
| chr12:21159844
|
G | A | 12 | a0001c0001t0001g0267a0001c0003t0001g0085a0001c0003t0002g0266others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.85-12806G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21159844 | ||||||
| chr12:21159874
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.85-12776T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21159874 | ||||||
| chr12:21159990
|
A | G | 58 | a0001c0001t0001g0002a0001c0001t0001g0087a0001c0001t0001g0104others(55): Show | 59 | HG00423.hp1 HG00642.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.85-12660A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21159990 | ||||||
| chr12:21160024
|
A | T | 1 | a0001c0001t0003g0068 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-12626A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21160024 | ||||||
| chr12:21160026
|
T | A | 1 | a0001c0001t0003g0068 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-12624T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21160026 | ||||||
| chr12:21160106
|
T | TA | 79 | a0001c0001t0001g0002a0001c0001t0001g0087a0001c0001t0001g0104others(76): Show | 81 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.85-12524dupA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21160106 | |||||
| chr12:21160106
|
T | TAA | 30 | a0001c0001t0001g0082a0001c0001t0001g0267a0001c0001t0002g0010others(27): Show | 30 | HG00099.hp2 HG00673.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.85-12525_85-12524d others(4): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21160106 | |||||
| chr12:21160106
|
T | TAAA | 30 | a0001c0001t0001g0079a0001c0001t0003g0048a0001c0001t0003g0049others(27): Show | 30 | HG00423.hp2 HG00544.hp1 HG01943.hp2 others(27): Show |
intron_variant | MODIFIER | c.85-12526_85-12524d others(5): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21160106 | |||||
| chr12:21160106
|
TA | T | 6 | a0001c0001t0002g0141a0001c0001t0003g0131a0001c0001t0004g0023others(3): Show | 6 | HG02622.hp2 HG04115.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-12524delA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21160106 | |||||
| chr12:21160106
|
TAA | T | 31 | a0001c0001t0003g0026a0001c0001t0003g0031a0001c0001t0003g0032others(28): Show | 32 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.85-12525_85-12524d others(4): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21160106 | |||||
| chr12:21160154
|
A | C | 36 | a0001c0001t0001g0079a0001c0001t0003g0048a0001c0001t0003g0049others(33): Show | 36 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.85-12496A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21160154 | ||||||
| chr12:21160167
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.85-12483G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21160167 | ||||||
| chr12:21160211
|
G | A | 5 | a0001c0001t0001g0082a0001c0001t0002g0080a0001c0001t0002g0111others(2): Show | 5 | HG02895.hp1 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.85-12439G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21160211 | ||||||
| chr12:21160226
|
A | G | 35 | a0001c0001t0002g0141a0001c0001t0003g0026a0001c0001t0003g0031others(32): Show | 36 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.85-12424A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21160226 | ||||||
| chr12:21160322
|
G | A | 5 | a0001c0001t0003g0131a0001c0001t0003g0132a0001c0001t0003g0133others(2): Show | 5 | HG02293.hp2 NA18942.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.85-12328G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21160322 | ||||||
| chr12:21160442
|
G | C | 139 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0121others(136): Show | 142 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.85-12208G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21160442 | ||||||
| chr12:21160451
|
C | T | 10 | a0002c0002t0001g0100a0003c0004t0002g0097a0003c0004t0002g0098others(7): Show | 10 | HG00099.hp2 HG01081.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.85-12199C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21160451 | ||||||
| chr12:21160497
|
G | GA | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(4): Show | 7 | HG02559.hp1 HG02896.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.85-12143dupA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21160497 | |||||
| chr12:21160635
|
A | C | 1 | a0001c0003t0002g0213 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.85-12015A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21160635 | ||||||
| chr12:21160691
|
G | T | 1 | a0001c0001t0001g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.85-11959G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21160691 | ||||||
| chr12:21160839
|
T | A | 298 | a0001c0001t0001g0002a0001c0001t0001g0079a0001c0001t0001g0082others(295): Show | 303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.85-11811T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21160839 | ||||||
| chr12:21160887
|
T | C | 1 | a0001c0003t0002g0196 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.85-11763T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21160887 | ||||||
| chr12:21160913
|
C | G | 1 | a0001c0001t0003g0161 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.85-11737C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21160913 | ||||||
| chr12:21160995
|
A | C | 59 | a0001c0001t0001g0002a0001c0001t0001g0087a0001c0001t0001g0104others(56): Show | 60 | HG00423.hp1 HG00642.hp2 HG01069.hp1 others(57): Show |
intron_variant | MODIFIER | c.85-11655A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21160995 | ||||||
| chr12:21161049
|
T | C | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.85-11601T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21161049 | ||||||
| chr12:21161059
|
G | C | 9 | a0001c0001t0001g0267a0001c0003t0002g0266a0001c0003t0002g0271others(6): Show | 9 | HG02145.hp1 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.85-11591G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21161059 | ||||||
| chr12:21161262
|
A | G | 10 | a0002c0002t0001g0100a0003c0004t0002g0097a0003c0004t0002g0098others(7): Show | 10 | HG00099.hp2 HG01081.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.85-11388A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21161262 | ||||||
| chr12:21161344
|
A | G | 8 | a0001c0001t0001g0186a0002c0002t0001g0163a0002c0002t0001g0166others(5): Show | 8 | HG00099.hp1 HG00735.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.85-11306A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21161344 | ||||||
| chr12:21161443
|
A | G | 15 | a0001c0001t0002g0141a0001c0001t0004g0022a0001c0001t0004g0023others(12): Show | 15 | HG00280.hp1 HG00642.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.85-11207A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21161443 | ||||||
| chr12:21161499
|
G | A | 1 | a0005c0009t0002g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.85-11151G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21161499 | ||||||
| chr12:21161551
|
G | A | 309 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(306): Show | 314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.85-11099G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21161551 | ||||||
| chr12:21161638
|
T | C | 245 | a0001c0001t0001g0002a0001c0001t0001g0079a0001c0001t0001g0082others(242): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.85-11012T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21161638 | ||||||
| chr12:21161663
|
A | C | 305 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(302): Show | 310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.85-10987A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21161663 | ||||||
| chr12:21161773
|
C | T | 1 | a0006c0010t0001g0262 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.85-10877C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21161773 | ||||||
| chr12:21161798
|
G | A | 5 | a0001c0001t0001g0082a0001c0001t0002g0080a0001c0001t0002g0111others(2): Show | 5 | HG02895.hp1 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.85-10852G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21161798 | ||||||
| chr12:21161802
|
G | A | 9 | a0003c0004t0002g0097a0003c0004t0002g0098a0005c0007t0001g0101others(6): Show | 9 | HG00099.hp2 HG01081.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.85-10848G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21161802 | ||||||
| chr12:21161845
|
T | C | 1 | a0001c0003t0002g0241 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.85-10805T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21161845 | ||||||
| chr12:21161865
|
A | G | 1 | a0004c0006t0001g0138 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.85-10785A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21161865 | ||||||
| chr12:21161924
|
C | G | 1 | a0008c0013t0002g0044 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.85-10726C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21161924 | ||||||
| chr12:21162039
|
A | T | 210 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0015others(207): Show | 214 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(211): Show |
intron_variant | MODIFIER | c.85-10611A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21162039 | ||||||
| chr12:21162126
|
A | T | 33 | a0001c0001t0001g0079a0001c0001t0003g0048a0001c0001t0003g0049others(30): Show | 33 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.85-10524A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21162126 | ||||||
| chr12:21162158
|
C | T | 1 | a0002c0002t0002g0200 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.85-10492C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21162158 | ||||||
| chr12:21162457
|
T | C | 10 | a0001c0001t0002g0141a0001c0001t0004g0022a0001c0001t0004g0023others(7): Show | 10 | HG00280.hp1 HG00642.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.85-10193T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21162457 | ||||||
| chr12:21162481
|
A | C | 85 | a0001c0001t0001g0079a0001c0001t0002g0141a0001c0001t0002g0251others(82): Show | 87 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.85-10169A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21162481 | ||||||
| chr12:21162510
|
G | C | 17 | a0001c0003t0002g0195a0003c0004t0002g0001a0003c0004t0002g0034others(14): Show | 18 | HG00609.hp1 HG01928.hp1 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.85-10140G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21162510 | ||||||
| chr12:21162563
|
T | A | 1 | a0003c0004t0002g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.85-10087T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21162563 | ||||||
| chr12:21162580
|
A | C | 1 | a0002c0005t0001g0117 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.85-10070A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21162580 | ||||||
| chr12:21162588
|
A | G | 61 | a0001c0001t0001g0079a0001c0001t0001g0177a0001c0001t0002g0141others(58): Show | 61 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.85-10062A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21162588 | ||||||
| chr12:21162770
|
G | C | 1 | a0005c0007t0008g0102 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.85-9880G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21162770 | ||||||
| chr12:21163018
|
T | C | 52 | a0001c0001t0001g0079a0001c0001t0001g0119a0001c0001t0002g0141others(49): Show | 52 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.85-9632T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21163018 | ||||||
| chr12:21163125
|
A | G | 159 | a0001c0001t0001g0012a0001c0001t0001g0119a0001c0001t0001g0177others(156): Show | 161 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.85-9525A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21163125 | ||||||
| chr12:21163279
|
A | G | 145 | a0001c0001t0001g0177a0001c0001t0003g0077a0001c0001t0003g0108others(142): Show | 147 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.85-9371A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21163279 | ||||||
| chr12:21163693
|
A | G | 1 | a0001c0001t0003g0048 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.85-8957A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21163693 | ||||||
| chr12:21163817
|
G | A | 82 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(79): Show | 82 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.85-8833G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21163817 | ||||||
| chr12:21163942
|
G | A | 2 | a0001c0001t0002g0285a0001c0001t0009g0243 | 2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.85-8708G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21163942 | ||||||
| chr12:21163942
|
GA | G | 146 | a0001c0001t0001g0177a0001c0001t0003g0077a0001c0001t0003g0108others(143): Show | 148 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.85-8696delA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21163942 | |||||
| chr12:21163986
|
A | G | 71 | a0001c0003t0001g0193a0001c0003t0001g0259a0001c0003t0001g0274others(68): Show | 72 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.85-8664A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21163986 | ||||||
| chr12:21164039
|
T | C | 1 | a0001c0003t0002g0213 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.85-8611T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21164039 | ||||||
| chr12:21164104
|
A | G | 8 | a0005c0007t0001g0101a0005c0007t0004g0093a0005c0007t0004g0094others(5): Show | 8 | HG00099.hp2 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.85-8546A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21164104 | ||||||
| chr12:21164227
|
G | A | 1 | a0005c0007t0004g0096 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.85-8423G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21164227 | ||||||
| chr12:21164279
|
A | G | 2 | a0002c0002t0001g0268a0002c0002t0001g0269 | 2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.85-8371A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21164279 | ||||||
| chr12:21164394
|
T | C | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.85-8256T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21164394 | ||||||
| chr12:21164395
|
A | G | 3 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247 | 3 | HG01884.hp1 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.85-8255A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21164395 | ||||||
| chr12:21164418
|
C | G | 77 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(74): Show | 77 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.85-8232C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21164418 | ||||||
| chr12:21164665
|
T | C | 21 | a0001c0001t0001g0119a0001c0001t0001g0283a0001c0001t0001g0311others(18): Show | 21 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.85-7985T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21164665 | ||||||
| chr12:21164734
|
T | C | 8 | a0005c0007t0001g0101a0005c0007t0004g0093a0005c0007t0004g0094others(5): Show | 8 | HG00099.hp2 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.85-7916T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21164734 | ||||||
| chr12:21164857
|
C | T | 186 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(183): Show | 187 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.85-7793C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21164857 | ||||||
| chr12:21164867
|
G | C | 11 | a0001c0003t0001g0085a0001c0003t0002g0250a0001c0003t0002g0252others(8): Show | 11 | HG01884.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.85-7783G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21164867 | ||||||
| chr12:21164875
|
A | T | 3 | a0005c0009t0002g0083a0005c0009t0002g0084a0005c0009t0002g0109 | 3 | HG02922.hp1 HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.85-7775A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21164875 | ||||||
| chr12:21164876
|
A | G | 260 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(257): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.85-7774A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21164876 | ||||||
| chr12:21164944
|
G | A | 1 | a0001c0001t0003g0134 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.85-7706G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21164944 | ||||||
| chr12:21164988
|
G | A | 178 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(175): Show | 179 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.85-7662G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21164988 | ||||||
| chr12:21165150
|
G | A | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.85-7500G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21165150 | ||||||
| chr12:21165165
|
T | G | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.85-7485T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21165165 | ||||||
| chr12:21165216
|
A | G | 1 | a0001c0020t0001g0282 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.85-7434A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21165216 | ||||||
| chr12:21165305
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.85-7345A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21165305 | ||||||
| chr12:21165331
|
T | C | 234 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(231): Show | 236 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.85-7319T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21165331 | ||||||
| chr12:21165362
|
T | C | 2 | a0001c0001t0003g0052a0001c0001t0003g0142 | 2 | HG02040.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.85-7288T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21165362 | ||||||
| chr12:21165488
|
T | C | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.85-7162T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21165488 | ||||||
| chr12:21165699
|
G | C | 1 | a0001c0003t0002g0306 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.85-6951G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21165699 | ||||||
| chr12:21165755
|
G | C | 71 | a0001c0003t0001g0193a0001c0003t0001g0259a0001c0003t0001g0274others(68): Show | 72 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.85-6895G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21165755 | ||||||
| chr12:21165795
|
T | C | 3 | a0001c0001t0003g0131a0001c0001t0003g0132a0001c0001t0003g0133 | 3 | NA18942.hp1 NA18959.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.85-6855T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21165795 | ||||||
| chr12:21165866
|
A | C | 1 | a0002c0002t0001g0167 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.85-6784A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21165866 | ||||||
| chr12:21165958
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.85-6692C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21165958 | ||||||
| chr12:21166019
|
C | T | 1 | a0003c0004t0001g0090 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.85-6631C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21166019 | ||||||
| chr12:21166379
|
G | A | 66 | a0001c0003t0001g0259a0001c0003t0001g0278a0001c0003t0001g0296others(63): Show | 67 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.85-6271G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21166379 | ||||||
| chr12:21166592
|
G | A | 173 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(170): Show | 174 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.85-6058G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21166592 | ||||||
| chr12:21166661
|
A | ACAAGAAC others(339): Show |
1 | a0001c0001t0003g0134 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.85-5978_85-5977ins others(346): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21166661 | |||||
| chr12:21166661
|
A | ACAAGAAC others(352): Show |
2 | a0001c0001t0003g0131a0001c0001t0003g0132 | 2 | NA18942.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.85-5978_85-5977ins others(359): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21166661 | |||||
| chr12:21166661
|
A | ACAAGAAC others(353): Show |
1 | a0001c0001t0003g0133 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.85-5978_85-5977ins others(360): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21166661 | |||||
| chr12:21166705
|
G | A | 10 | a0001c0003t0002g0018a0001c0003t0002g0145a0001c0003t0002g0211others(7): Show | 10 | HG00544.hp2 HG00673.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.85-5945G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21166705 | ||||||
| chr12:21166829
|
C | T | 2 | a0002c0002t0003g0212a0002c0002t0003g0220 | 2 | NA18971.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.85-5821C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21166829 | ||||||
| chr12:21166831
|
G | C | 2 | a0001c0001t0001g0177a0002c0002t0001g0154 | 2 | HG02602.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.85-5819G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21166831 | ||||||
| chr12:21166856
|
C | G | 2 | a0001c0003t0001g0296a0001c0003t0001g0297 | 2 | HG00423.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.85-5794C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21166856 | ||||||
| chr12:21166925
|
C | A | 1 | a0001c0003t0002g0195 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.85-5725C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21166925 | ||||||
| chr12:21166925
|
C | G | 2 | a0005c0007t0004g0094a0005c0007t0004g0095 | 2 | HG01346.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.85-5725C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21166925 | ||||||
| chr12:21167158
|
G | T | 3 | a0001c0003t0001g0274a0001c0003t0001g0284a0001c0003t0001g0299 | 3 | HG02486.hp2 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.85-5492G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21167158 | ||||||
| chr12:21167219
|
A | C | 1 | a0002c0002t0001g0147 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.85-5431A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21167219 | ||||||
| chr12:21167331
|
A | G | 312 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(309): Show | 317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.85-5319A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21167331 | ||||||
| chr12:21167391
|
A | T | 3 | a0001c0003t0002g0211a0001c0003t0002g0213a0001c0003t0002g0214 | 3 | HG00673.hp1 NA18983.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.85-5259A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21167391 | ||||||
| chr12:21167439
|
A | T | 1 | a0001c0001t0001g0082 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.85-5211A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21167439 | ||||||
| chr12:21167472
|
C | T | 3 | a0001c0003t0001g0274a0001c0003t0001g0284a0001c0003t0001g0299 | 3 | HG02486.hp2 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.85-5178C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21167472 | ||||||
| chr12:21167506
|
G | C | 1 | a0001c0001t0003g0071 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.85-5144G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21167506 | ||||||
| chr12:21167567
|
C | T | 3 | a0003c0004t0002g0027a0003c0004t0002g0097a0003c0004t0002g0098 | 3 | HG01081.hp2 HG01358.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.85-5083C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21167567 | ||||||
| chr12:21167661
|
T | C | 2 | a0001c0001t0001g0177a0002c0002t0001g0154 | 2 | HG02602.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.85-4989T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21167661 | ||||||
| chr12:21167752
|
A | G | 71 | a0001c0003t0001g0193a0001c0003t0001g0259a0001c0003t0001g0274others(68): Show | 72 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.85-4898A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21167752 | ||||||
| chr12:21167795
|
T | C | 1 | a0001c0023t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.85-4855T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21167795 | ||||||
| chr12:21167818
|
C | CT | 9 | a0001c0001t0001g0079a0001c0001t0003g0056a0001c0001t0003g0057others(6): Show | 9 | HG00544.hp1 HG00673.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.85-4816dupT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21167818 | |||||
| chr12:21167818
|
CT | C | 16 | a0001c0001t0001g0118a0001c0001t0003g0071a0001c0003t0002g0187others(13): Show | 16 | HG01167.hp1 HG01884.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.85-4816delT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21167818 | |||||
| chr12:21167873
|
G | T | 1 | a0001c0001t0001g0082 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.85-4777G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21167873 | ||||||
| chr12:21167952
|
G | T | 1 | a0002c0002t0001g0208 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.85-4698G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21167952 | ||||||
| chr12:21167963
|
A | C | 296 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(293): Show | 301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.85-4687A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21167963 | ||||||
| chr12:21167983
|
A | AT | 142 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(139): Show | 145 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.85-4656dupT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21167983 | |||||
| chr12:21168181
|
T | G | 3 | a0001c0003t0001g0274a0001c0003t0001g0284a0001c0003t0001g0299 | 3 | HG02486.hp2 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.85-4469T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21168181 | ||||||
| chr12:21168199
|
C | G | 1 | a0001c0001t0002g0251 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.85-4451C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21168199 | ||||||
| chr12:21168212
|
CATATT | C | 72 | a0001c0001t0001g0177a0001c0001t0003g0108a0002c0002t0001g0004others(69): Show | 73 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.85-4437_85-4433del others(5): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21168212 | ||||||
| chr12:21168229
|
T | C | 1 | a0005c0009t0002g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.85-4421T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21168229 | ||||||
| chr12:21168336
|
C | T | 208 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(205): Show | 212 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.85-4314C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21168336 | ||||||
| chr12:21168348
|
T | C | 1 | a0001c0001t0003g0168 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.85-4302T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21168348 | ||||||
| chr12:21168384
|
G | C | 9 | a0005c0007t0001g0101a0005c0007t0004g0093a0005c0007t0004g0094others(6): Show | 9 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.85-4266G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21168384 | ||||||
| chr12:21168436
|
T | C | 74 | a0001c0003t0001g0193a0001c0003t0001g0259a0001c0003t0001g0278others(71): Show | 75 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.85-4214T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21168436 | ||||||
| chr12:21168495
|
T | C | 296 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(293): Show | 301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.85-4155T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21168495 | ||||||
| chr12:21168496
|
G | A | 3 | a0001c0001t0002g0251a0001c0003t0002g0107a0001c0003t0002g0187 | 3 | HG03540.hp1 NA18991.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.85-4154G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21168496 | ||||||
| chr12:21168523
|
C | T | 9 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0135others(6): Show | 9 | HG00438.hp1 HG03669.hp2 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.85-4127C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21168523 | ||||||
| chr12:21168548
|
C | T | 74 | a0001c0001t0001g0177a0002c0002t0001g0004a0002c0002t0001g0006others(71): Show | 75 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.85-4102C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21168548 | ||||||
| chr12:21168573
|
G | T | 63 | a0001c0003t0001g0193a0001c0003t0001g0259a0001c0003t0001g0278others(60): Show | 64 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.85-4077G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21168573 | ||||||
| chr12:21168599
|
A | T | 1 | a0001c0023t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.85-4051A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21168599 | ||||||
| chr12:21168710
|
C | T | 1 | a0002c0002t0002g0157 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.85-3940C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21168710 | ||||||
| chr12:21168750
|
T | G | 144 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(141): Show | 147 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.85-3900T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21168750 | ||||||
| chr12:21168790
|
T | G | 1 | a0004c0006t0001g0028 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.85-3860T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21168790 | ||||||
| chr12:21168797
|
T | C | 2 | a0002c0002t0001g0152a0002c0002t0001g0153 | 2 | HG01261.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.85-3853T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21168797 | ||||||
| chr12:21168896
|
G | A | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.85-3754G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21168896 | ||||||
| chr12:21168971
|
C | CTTTTAT | 70 | a0001c0003t0001g0193a0001c0003t0001g0259a0001c0003t0001g0274others(67): Show | 71 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.85-3674_85-3669dup others(6): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21168971 | |||||
| chr12:21169042
|
A | T | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.85-3608A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21169042 | ||||||
| chr12:21169078
|
A | T | 39 | a0001c0001t0001g0079a0001c0001t0003g0026a0001c0001t0003g0048others(36): Show | 39 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.85-3572A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21169078 | ||||||
| chr12:21169122
|
G | A | 11 | a0005c0007t0001g0101a0005c0007t0004g0093a0005c0007t0004g0094others(8): Show | 11 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.85-3528G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21169122 | ||||||
| chr12:21169278
|
T | A | 70 | a0001c0003t0001g0193a0001c0003t0001g0259a0001c0003t0001g0274others(67): Show | 71 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.85-3372T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21169278 | ||||||
| chr12:21169301
|
A | T | 221 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(218): Show | 225 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.85-3349A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21169301 | ||||||
| chr12:21169341
|
T | C | 2 | a0002c0005t0001g0258a0002c0005t0001g0261 | 2 | HG00642.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.85-3309T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21169341 | ||||||
| chr12:21169633
|
A | G | 1 | a0016c0018t0001g0140 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.85-3017A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21169633 | ||||||
| chr12:21169745
|
A | AT | 82 | a0001c0001t0001g0177a0002c0002t0001g0004a0002c0002t0001g0006others(79): Show | 83 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.85-2896dupT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21169745 | |||||
| chr12:21169745
|
A | ATT | 132 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(129): Show | 135 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.85-2897_85-2896dup others(2): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 21169745 | |||||
| chr12:21169932
|
C | G | 75 | a0001c0001t0001g0177a0002c0002t0001g0004a0002c0002t0001g0006others(72): Show | 76 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.85-2718C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21169932 | ||||||
| chr12:21169944
|
C | T | 3 | a0001c0003t0002g0250a0001c0003t0002g0252a0001c0003t0002g0271 | 3 | HG02615.hp1 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.85-2706C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21169944 | ||||||
| chr12:21170038
|
G | C | 70 | a0001c0003t0001g0193a0001c0003t0001g0259a0001c0003t0001g0274others(67): Show | 71 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.85-2612G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21170038 | ||||||
| chr12:21170234
|
T | C | 12 | a0001c0001t0001g0002a0001c0001t0001g0104a0001c0001t0001g0114others(9): Show | 13 | HG01167.hp1 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.85-2416T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21170234 | ||||||
| chr12:21170338
|
A | G | 10 | a0005c0007t0001g0101a0005c0007t0004g0093a0005c0007t0004g0094others(7): Show | 10 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.85-2312A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21170338 | ||||||
| chr12:21170404
|
TG | T | 50 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(47): Show | 52 | HG00438.hp1 HG00609.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.85-2245delG | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21170404 | ||||||
| chr12:21170540
|
A | G | 6 | a0005c0009t0002g0083a0005c0009t0002g0084a0005c0009t0002g0109others(3): Show | 6 | HG01884.hp1 HG02922.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-2110A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21170540 | ||||||
| chr12:21170593
|
T | C | 75 | a0001c0001t0001g0177a0002c0002t0001g0004a0002c0002t0001g0006others(72): Show | 76 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.85-2057T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21170593 | ||||||
| chr12:21170622
|
C | T | 74 | a0001c0001t0001g0177a0002c0002t0001g0004a0002c0002t0001g0006others(71): Show | 75 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.85-2028C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21170622 | ||||||
| chr12:21170632
|
T | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(132): Show | 138 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.85-2018T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21170632 | ||||||
| chr12:21170677
|
C | T | 70 | a0001c0003t0001g0193a0001c0003t0001g0259a0001c0003t0001g0274others(67): Show | 71 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.85-1973C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21170677 | ||||||
| chr12:21170852
|
G | A | 2 | a0003c0004t0002g0254a0003c0004t0002g0260 | 2 | HG01928.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.85-1798G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21170852 | ||||||
| chr12:21170869
|
G | T | 1 | a0001c0001t0003g0072 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.85-1781G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21170869 | ||||||
| chr12:21170909
|
C | T | 1 | a0001c0003t0002g0302 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.85-1741C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21170909 | ||||||
| chr12:21170946
|
C | T | 1 | a0002c0002t0001g0162 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.85-1704C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21170946 | ||||||
| chr12:21170999
|
G | A | 1 | a0007c0019t0002g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.85-1651G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21170999 | ||||||
| chr12:21171244
|
G | A | 1 | a0003c0004t0003g0024 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.85-1406G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21171244 | ||||||
| chr12:21171433
|
G | A | 1 | a0001c0003t0002g0289 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.85-1217G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21171433 | ||||||
| chr12:21171708
|
A | G | 39 | a0001c0001t0001g0079a0001c0001t0003g0026a0001c0001t0003g0048others(36): Show | 39 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.85-942A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21171708 | ||||||
| chr12:21171814
|
A | G | 148 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(145): Show | 151 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.85-836A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21171814 | ||||||
| chr12:21172013
|
A | T | 10 | a0001c0001t0001g0002a0001c0001t0001g0104a0001c0001t0001g0114others(7): Show | 11 | HG01167.hp1 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.85-637A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21172013 | ||||||
| chr12:21172092
|
G | A | 33 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0087others(30): Show | 34 | HG01167.hp1 HG01884.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.85-558G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21172092 | ||||||
| chr12:21172249
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(1): Show | 4 | HG02559.hp1 HG03209.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.85-401G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21172249 | ||||||
| chr12:21172287
|
C | A | 1 | a0001c0001t0002g0248 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.85-363C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21172287 | ||||||
| chr12:21172413
|
G | A | 296 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(293): Show | 301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.85-237G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 2/14 | chr12 | 21172413 | ||||||
| chr12:21172826
|
G | C | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.226+35G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 3/14 | chr12 | 21172826 | ||||||
| chr12:21172874
|
G | A | 10 | a0001c0001t0001g0119a0001c0001t0001g0283a0004c0006t0001g0081others(7): Show | 10 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.226+83G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 3/14 | chr12 | 21172874 | ||||||
| chr12:21172880
|
T | G | 117 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(114): Show | 118 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.226+89T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 3/14 | chr12 | 21172880 | ||||||
| chr12:21172947
|
G | A | 1 | a0004c0006t0001g0235 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.226+156G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 3/14 | chr12 | 21172947 | ||||||
| chr12:21173015
|
A | G | 69 | a0001c0003t0001g0259a0001c0003t0001g0274a0001c0003t0001g0278others(66): Show | 70 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.226+224A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 3/14 | chr12 | 21173015 | ||||||
| chr12:21173160
|
T | C | 6 | a0001c0003t0001g0274a0001c0003t0001g0284a0001c0003t0001g0299others(3): Show | 6 | HG02486.hp2 HG02615.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.226+369T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 3/14 | chr12 | 21173160 | ||||||
| chr12:21173414
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.226+623T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 3/14 | chr12 | 21173414 | ||||||
| chr12:21173574
|
C | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(136): Show | 142 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.226+783C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 3/14 | chr12 | 21173574 | ||||||
| chr12:21173626
|
T | TA | 139 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(136): Show | 142 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.226+845dupA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 21173626 | |||||
| chr12:21173626
|
TA | T | 7 | a0002c0005t0001g0086a0002c0005t0001g0143a0002c0005t0001g0164others(4): Show | 7 | HG00642.hp2 HG01081.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.226+845delA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 21173626 | |||||
| chr12:21173711
|
T | G | 2 | a0001c0001t0002g0010a0001c0001t0002g0310 | 2 | HG02145.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.227-866T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 3/14 | chr12 | 21173711 | ||||||
| chr12:21173738
|
C | A | 215 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(212): Show | 219 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(216): Show |
intron_variant | MODIFIER | c.227-839C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 3/14 | chr12 | 21173738 | ||||||
| chr12:21173771
|
C | CT | 12 | a0001c0001t0001g0118a0001c0001t0002g0111a0001c0001t0003g0063others(9): Show | 12 | HG01167.hp1 HG02055.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.227-787dupT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 21173771 | |||||
| chr12:21173771
|
C | CTT | 129 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(126): Show | 132 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.227-788_227-787dup others(2): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 21173771 | |||||
| chr12:21173794
|
A | G | 54 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(51): Show | 56 | HG00438.hp1 HG00609.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.227-783A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 3/14 | chr12 | 21173794 | ||||||
| chr12:21173812
|
G | T | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.227-765G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 3/14 | chr12 | 21173812 | ||||||
| chr12:21173822
|
T | G | 223 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(220): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.227-755T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 3/14 | chr12 | 21173822 | ||||||
| chr12:21173876
|
T | G | 297 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(294): Show | 302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.227-701T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 3/14 | chr12 | 21173876 | ||||||
| chr12:21173912
|
T | C | 2 | a0004c0006t0001g0246a0004c0006t0001g0272 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.227-665T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 3/14 | chr12 | 21173912 | ||||||
| chr12:21173914
|
T | C | 2 | a0004c0006t0001g0246a0004c0006t0001g0272 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.227-663T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 3/14 | chr12 | 21173914 | ||||||
| chr12:21174170
|
T | G | 3 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247 | 3 | HG01884.hp1 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.227-407T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 3/14 | chr12 | 21174170 | ||||||
| chr12:21174244
|
T | C | 1 | a0001c0001t0003g0068 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.227-333T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 3/14 | chr12 | 21174244 | ||||||
| chr12:21174385
|
C | CT | 65 | a0001c0003t0001g0259a0001c0003t0001g0274a0001c0003t0001g0278others(62): Show | 66 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.227-183dupT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 21174385 | |||||
| chr12:21174505
|
C | G | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.227-72C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 3/14 | chr12 | 21174505 | ||||||
| chr12:21174718
|
T | TA | 121 | a0001c0001t0003g0026a0001c0003t0001g0193a0001c0003t0001g0259others(118): Show | 122 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.359+23dupA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 21174718 | |||||
| chr12:21174718
|
T | TAA | 23 | a0001c0003t0003g0291a0001c0003t0005g0286a0001c0003t0005g0290others(20): Show | 24 | HG00741.hp1 HG00741.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.359+22_359+23dupAA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 21174718 | |||||
| chr12:21174767
|
A | G | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.359+58A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 4/14 | chr12 | 21174767 | ||||||
| chr12:21174806
|
C | A | 139 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(136): Show | 142 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.359+97C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 4/14 | chr12 | 21174806 | ||||||
| chr12:21174864
|
A | G | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.359+155A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 4/14 | chr12 | 21174864 | ||||||
| chr12:21174972
|
G | A | 1 | a0002c0005t0001g0261 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.359+263G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 4/14 | chr12 | 21174972 | ||||||
| chr12:21175065
|
A | C | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.359+356A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 4/14 | chr12 | 21175065 | ||||||
| chr12:21175277
|
A | G | 66 | a0001c0003t0001g0259a0001c0003t0001g0274a0001c0003t0001g0278others(63): Show | 67 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.359+568A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 4/14 | chr12 | 21175277 | ||||||
| chr12:21175308
|
A | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(136): Show | 142 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.359+599A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 4/14 | chr12 | 21175308 | ||||||
| chr12:21175451
|
AT | A | 66 | a0001c0003t0001g0259a0001c0003t0001g0274a0001c0003t0001g0278others(63): Show | 67 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.359+744delT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 21175451 | |||||
| chr12:21175462
|
T | A | 139 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(136): Show | 142 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.359+753T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 4/14 | chr12 | 21175462 | ||||||
| chr12:21175490
|
G | C | 216 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(213): Show | 220 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(217): Show |
intron_variant | MODIFIER | c.359+781G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 4/14 | chr12 | 21175490 | ||||||
| chr12:21175528
|
G | T | 2 | a0002c0005t0001g0143a0002c0005t0001g0164 | 2 | HG01081.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.359+819G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 4/14 | chr12 | 21175528 | ||||||
| chr12:21175631
|
T | C | 10 | a0005c0007t0001g0101a0005c0007t0004g0093a0005c0007t0004g0094others(7): Show | 10 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.359+922T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 4/14 | chr12 | 21175631 | ||||||
| chr12:21175905
|
G | T | 63 | a0001c0003t0001g0259a0001c0003t0001g0278a0001c0003t0001g0296others(60): Show | 64 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.360-871G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 4/14 | chr12 | 21175905 | ||||||
| chr12:21175938
|
T | C | 142 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(139): Show | 145 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.360-838T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 4/14 | chr12 | 21175938 | ||||||
| chr12:21175995
|
A | G | 1 | a0005c0009t0002g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.360-781A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 4/14 | chr12 | 21175995 | ||||||
| chr12:21176257
|
G | A | 1 | a0001c0001t0003g0026 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.360-519G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 4/14 | chr12 | 21176257 | ||||||
| chr12:21176343
|
T | G | 1 | a0001c0001t0002g0141 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.360-433T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 4/14 | chr12 | 21176343 | ||||||
| chr12:21176456
|
C | T | 297 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(294): Show | 302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.360-320C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 4/14 | chr12 | 21176456 | ||||||
| chr12:21176490
|
T | C | 296 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(293): Show | 301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.360-286T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 4/14 | chr12 | 21176490 | ||||||
| chr12:21176615
|
T | C | 1 | a0001c0003t0002g0216 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.360-161T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 4/14 | chr12 | 21176615 | ||||||
| chr12:21176710
|
A | G | 1 | a0007c0019t0002g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.360-66A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 4/14 | chr12 | 21176710 | ||||||
| chr12:21176898
|
G | T | 2 | a0002c0005t0001g0016a0002c0005t0002g0011 | 2 | HG02896.hp2 NA18522.hp2 |
splice_donor_variant&intron_variant | HIGH | c.481+1G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 5/14 | chr12 | 21176898 | ||||||
| chr12:21177057
|
C | T | 10 | a0005c0007t0001g0101a0005c0007t0004g0093a0005c0007t0004g0094others(7): Show | 10 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.481+160C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 5/14 | chr12 | 21177057 | ||||||
| chr12:21177062
|
A | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(136): Show | 142 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.481+165A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 5/14 | chr12 | 21177062 | ||||||
| chr12:21177086
|
G | A | 139 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(136): Show | 142 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.481+189G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 5/14 | chr12 | 21177086 | ||||||
| chr12:21177088
|
G | A | 73 | a0002c0002t0001g0004a0002c0002t0001g0006a0002c0002t0001g0025others(70): Show | 74 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.481+191G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 5/14 | chr12 | 21177088 | ||||||
| chr12:21177139
|
C | T | 1 | a0007c0019t0002g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.481+242C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 5/14 | chr12 | 21177139 | ||||||
| chr12:21177223
|
A | G | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.481+326A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 5/14 | chr12 | 21177223 | ||||||
| chr12:21177277
|
A | G | 3 | a0004c0006t0001g0233a0004c0006t0001g0234a0004c0006t0001g0235 | 3 | HG00642.hp1 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.481+380A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 5/14 | chr12 | 21177277 | ||||||
| chr12:21177404
|
C | T | 5 | a0001c0001t0003g0050a0001c0001t0003g0063a0001c0001t0003g0065others(2): Show | 5 | HG02074.hp1 HG02129.hp1 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.481+507C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 5/14 | chr12 | 21177404 | ||||||
| chr12:21177417
|
A | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(136): Show | 142 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.481+520A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 5/14 | chr12 | 21177417 | ||||||
| chr12:21177479
|
G | A | 1 | a0007c0019t0002g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.481+582G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 5/14 | chr12 | 21177479 | ||||||
| chr12:21177676
|
A | T | 1 | a0001c0003t0002g0229 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.481+779A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 5/14 | chr12 | 21177676 | ||||||
| chr12:21177753
|
A | G | 66 | a0001c0003t0001g0193a0001c0003t0001g0259a0001c0003t0001g0274others(63): Show | 67 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.482-823A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 5/14 | chr12 | 21177753 | ||||||
| chr12:21178054
|
T | C | 142 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(139): Show | 145 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.482-522T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 5/14 | chr12 | 21178054 | ||||||
| chr12:21178069
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.482-507G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 5/14 | chr12 | 21178069 | ||||||
| chr12:21178123
|
A | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(140): Show | 146 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.482-453A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 5/14 | chr12 | 21178123 | ||||||
| chr12:21178125
|
A | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(140): Show | 146 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.482-451A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 5/14 | chr12 | 21178125 | ||||||
| chr12:21178201
|
G | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(132): Show | 138 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.482-375G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 5/14 | chr12 | 21178201 | ||||||
| chr12:21178211
|
A | G | 1 | a0002c0002t0001g0171 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.482-365A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 5/14 | chr12 | 21178211 | ||||||
| chr12:21178245
|
G | A | 134 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(131): Show | 137 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.482-331G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 5/14 | chr12 | 21178245 | ||||||
| chr12:21178304
|
G | A | 40 | a0001c0001t0001g0079a0001c0001t0002g0251a0001c0001t0002g0285others(37): Show | 40 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.482-272G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 5/14 | chr12 | 21178304 | ||||||
| chr12:21178455
|
TTACTTG | T | 153 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(150): Show | 156 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.482-112_482-107del others(6): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 21178455 | |||||
| chr12:21178565
|
T | C | 2 | a0001c0001t0002g0285a0001c0001t0009g0243 | 2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.482-11T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 5/14 | chr12 | 21178565 | ||||||
| chr12:21178824
|
T | C | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.629-98T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 6/14 | chr12 | 21178824 | ||||||
| chr12:21179053
|
C | T | 73 | a0002c0002t0001g0004a0002c0002t0001g0006a0002c0002t0001g0025others(70): Show | 74 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.727+33C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21179053 | ||||||
| chr12:21179287
|
T | A | 216 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(213): Show | 220 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(217): Show |
intron_variant | MODIFIER | c.727+267T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21179287 | ||||||
| chr12:21179293
|
C | T | 2 | a0001c0003t0002g0295a0001c0003t0002g0308 | 2 | NA18981.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.727+273C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21179293 | ||||||
| chr12:21179489
|
G | A | 10 | a0005c0007t0001g0101a0005c0007t0004g0093a0005c0007t0004g0094others(7): Show | 10 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.727+469G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21179489 | ||||||
| chr12:21179530
|
A | C | 1 | a0005c0007t0008g0102 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.727+510A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21179530 | ||||||
| chr12:21179625
|
T | C | 1 | a0002c0002t0001g0151 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.727+605T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21179625 | ||||||
| chr12:21179819
|
C | T | 1 | a0001c0001t0003g0068 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.727+799C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21179819 | ||||||
| chr12:21179909
|
A | G | 284 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(281): Show | 288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.727+889A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21179909 | ||||||
| chr12:21180106
|
A | G | 11 | a0005c0007t0001g0101a0005c0007t0004g0093a0005c0007t0004g0094others(8): Show | 11 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.727+1086A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21180106 | ||||||
| chr12:21180280
|
A | G | 130 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(127): Show | 132 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.727+1260A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21180280 | ||||||
| chr12:21180332
|
C | T | 212 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(209): Show | 215 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.727+1312C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21180332 | ||||||
| chr12:21180349
|
A | G | 1 | a0002c0002t0001g0139 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.727+1329A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21180349 | ||||||
| chr12:21180385
|
T | C | 1 | a0001c0001t0002g0251 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.727+1365T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21180385 | ||||||
| chr12:21180406
|
G | A | 130 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(127): Show | 132 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.727+1386G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21180406 | ||||||
| chr12:21180492
|
G | A | 67 | a0001c0003t0001g0193a0001c0003t0001g0259a0001c0003t0001g0274others(64): Show | 68 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.727+1472G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21180492 | ||||||
| chr12:21180619
|
C | G | 1 | a0001c0001t0003g0073 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.727+1599C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21180619 | ||||||
| chr12:21180623
|
G | A | 1 | a0008c0013t0002g0035 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.727+1603G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21180623 | ||||||
| chr12:21180717
|
C | A | 76 | a0002c0002t0001g0004a0002c0002t0001g0006a0002c0002t0001g0025others(73): Show | 77 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.727+1697C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21180717 | ||||||
| chr12:21180761
|
C | T | 1 | a0001c0001t0003g0061 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.727+1741C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21180761 | ||||||
| chr12:21180811
|
G | A | 10 | a0005c0007t0001g0101a0005c0007t0004g0093a0005c0007t0004g0094others(7): Show | 10 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.727+1791G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21180811 | ||||||
| chr12:21180875
|
G | C | 22 | a0001c0001t0001g0087a0001c0001t0001g0119a0001c0001t0001g0123others(19): Show | 22 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.727+1855G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21180875 | ||||||
| chr12:21180924
|
A | G | 3 | a0001c0003t0002g0250a0001c0003t0002g0252a0001c0003t0002g0271 | 3 | HG02615.hp1 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.727+1904A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21180924 | ||||||
| chr12:21180951
|
T | C | 1 | a0001c0003t0002g0242 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.727+1931T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21180951 | ||||||
| chr12:21180978
|
G | T | 9 | a0005c0007t0001g0101a0005c0007t0004g0093a0005c0007t0004g0094others(6): Show | 9 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.727+1958G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21180978 | ||||||
| chr12:21181076
|
T | C | 14 | a0001c0020t0001g0282a0005c0007t0001g0101a0005c0007t0004g0093others(11): Show | 14 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.727+2056T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21181076 | ||||||
| chr12:21181102
|
A | G | 1 | a0002c0002t0001g0197 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.727+2082A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21181102 | ||||||
| chr12:21181125
|
C | T | 1 | a0001c0023t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.727+2105C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21181125 | ||||||
| chr12:21181223
|
G | T | 3 | a0002c0002t0003g0212a0002c0002t0003g0220a0017c0017t0001g0219 | 3 | NA18971.hp1 NA18979.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.727+2203G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21181223 | ||||||
| chr12:21181237
|
A | C | 1 | a0002c0002t0002g0092 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.727+2217A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21181237 | ||||||
| chr12:21181280
|
G | A | 2 | a0002c0002t0001g0163a0002c0002t0002g0191 | 2 | NA20752.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.727+2260G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21181280 | ||||||
| chr12:21181292
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.727+2272G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21181292 | ||||||
| chr12:21181293
|
C | T | 127 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(124): Show | 129 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.727+2273C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21181293 | ||||||
| chr12:21181315
|
T | C | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.727+2295T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21181315 | ||||||
| chr12:21181435
|
G | C | 14 | a0001c0020t0001g0282a0005c0007t0001g0101a0005c0007t0004g0093others(11): Show | 14 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.727+2415G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21181435 | ||||||
| chr12:21181453
|
T | C | 14 | a0001c0020t0001g0282a0005c0007t0001g0101a0005c0007t0004g0093others(11): Show | 14 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.727+2433T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21181453 | ||||||
| chr12:21181527
|
T | A | 14 | a0001c0020t0001g0282a0005c0007t0001g0101a0005c0007t0004g0093others(11): Show | 14 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.727+2507T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21181527 | ||||||
| chr12:21181544
|
C | A | 10 | a0001c0003t0002g0018a0001c0003t0002g0145a0001c0003t0002g0211others(7): Show | 10 | HG00544.hp2 HG00673.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.727+2524C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21181544 | ||||||
| chr12:21181636
|
T | C | 108 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(105): Show | 110 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.727+2616T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21181636 | ||||||
| chr12:21181665
|
T | C | 14 | a0001c0020t0001g0282a0005c0007t0001g0101a0005c0007t0004g0093others(11): Show | 14 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.727+2645T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21181665 | ||||||
| chr12:21181666
|
A | G | 288 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(285): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.727+2646A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21181666 | ||||||
| chr12:21181797
|
A | C | 1 | a0002c0002t0001g0147 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.727+2777A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21181797 | ||||||
| chr12:21181810
|
T | A | 1 | a0001c0003t0002g0223 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.727+2790T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21181810 | ||||||
| chr12:21182036
|
C | T | 10 | a0005c0007t0001g0101a0005c0007t0004g0093a0005c0007t0004g0094others(7): Show | 10 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.727+3016C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21182036 | ||||||
| chr12:21182127
|
T | G | 8 | a0001c0001t0001g0079a0001c0001t0003g0056a0001c0001t0003g0057others(5): Show | 8 | HG00544.hp1 HG02071.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.727+3107T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21182127 | ||||||
| chr12:21182212
|
G | T | 1 | a0001c0001t0001g0136 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.727+3192G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21182212 | ||||||
| chr12:21182224
|
G | T | 1 | a0007c0019t0002g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.727+3204G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21182224 | ||||||
| chr12:21182256
|
C | G | 78 | a0001c0003t0001g0193a0002c0002t0001g0004a0002c0002t0001g0006others(75): Show | 79 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.727+3236C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21182256 | ||||||
| chr12:21182338
|
A | G | 2 | a0001c0001t0003g0054a0001c0001t0003g0055 | 2 | HG01943.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.727+3318A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21182338 | ||||||
| chr12:21182356
|
T | G | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(10): Show | 13 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.727+3336T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21182356 | ||||||
| chr12:21182411
|
G | A | 2 | a0001c0001t0002g0249a0007c0019t0002g0124 | 2 | HG02559.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.727+3391G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21182411 | ||||||
| chr12:21182447
|
G | C | 78 | a0001c0003t0001g0193a0002c0002t0001g0004a0002c0002t0001g0006others(75): Show | 79 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.727+3427G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21182447 | ||||||
| chr12:21182458
|
A | C | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(10): Show | 13 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.727+3438A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21182458 | ||||||
| chr12:21182508
|
G | A | 1 | a0005c0007t0004g0094 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.727+3488G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21182508 | ||||||
| chr12:21182520
|
T | C | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(10): Show | 13 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.727+3500T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21182520 | ||||||
| chr12:21182544
|
C | T | 1 | a0001c0001t0002g0115 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.727+3524C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21182544 | ||||||
| chr12:21182586
|
G | A | 1 | a0002c0002t0001g0151 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.727+3566G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21182586 | ||||||
| chr12:21182636
|
A | C | 4 | a0001c0001t0001g0119a0001c0001t0001g0283a0004c0006t0001g0081others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.727+3616A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21182636 | ||||||
| chr12:21182705
|
G | C | 1 | a0007c0019t0002g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.727+3685G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21182705 | ||||||
| chr12:21182791
|
G | GCACT | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(10): Show | 13 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.727+3774_727+3777d others(6): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 21182791 | |||||
| chr12:21182815
|
G | C | 182 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0104others(179): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.727+3795G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21182815 | ||||||
| chr12:21182847
|
C | T | 93 | a0001c0003t0001g0085a0002c0002t0001g0004a0002c0002t0001g0006others(90): Show | 94 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.727+3827C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21182847 | ||||||
| chr12:21182949
|
T | C | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(10): Show | 13 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.727+3929T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21182949 | ||||||
| chr12:21183015
|
A | G | 182 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0104others(179): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.727+3995A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21183015 | ||||||
| chr12:21183019
|
G | C | 20 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0104others(17): Show | 21 | HG01081.hp1 HG01167.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.727+3999G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21183019 | ||||||
| chr12:21183034
|
T | A | 307 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(304): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.727+4014T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21183034 | ||||||
| chr12:21183076
|
C | T | 1 | a0002c0002t0004g0199 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.727+4056C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21183076 | ||||||
| chr12:21183129
|
C | T | 181 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0104others(178): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.727+4109C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21183129 | ||||||
| chr12:21183151
|
C | G | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(10): Show | 13 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.727+4131C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21183151 | ||||||
| chr12:21183178
|
A | T | 102 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0104others(99): Show | 104 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.727+4158A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21183178 | ||||||
| chr12:21183202
|
G | A | 307 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(304): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.727+4182G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21183202 | ||||||
| chr12:21183210
|
A | G | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(10): Show | 13 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.727+4190A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21183210 | ||||||
| chr12:21183223
|
C | T | 181 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0104others(178): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.727+4203C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21183223 | ||||||
| chr12:21183230
|
CTG | C | 20 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0104others(17): Show | 21 | HG01081.hp1 HG01167.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.727+4212_727+4213d others(4): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 21183230 | |||||
| chr12:21183247
|
G | A | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(10): Show | 13 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.727+4227G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21183247 | ||||||
| chr12:21183248
|
C | T | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.727+4228C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21183248 | ||||||
| chr12:21183513
|
G | A | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(10): Show | 13 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.727+4493G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21183513 | ||||||
| chr12:21183639
|
T | C | 3 | a0002c0002t0001g0166a0002c0002t0001g0167a0002c0002t0001g0181 | 3 | HG00099.hp1 HG03669.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.727+4619T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21183639 | ||||||
| chr12:21183783
|
G | A | 65 | a0001c0001t0002g0141a0001c0003t0001g0259a0001c0003t0001g0274others(62): Show | 66 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.727+4763G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21183783 | ||||||
| chr12:21183826
|
C | T | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.727+4806C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21183826 | ||||||
| chr12:21183929
|
A | G | 1 | a0006c0010t0001g0262 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.727+4909A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21183929 | ||||||
| chr12:21183994
|
C | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0104a0001c0001t0001g0114others(20): Show | 24 | HG01081.hp1 HG01167.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.727+4974C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21183994 | ||||||
| chr12:21183994
|
C | T | 1 | a0016c0018t0001g0140 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.727+4974C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21183994 | ||||||
| chr12:21183998
|
G | C | 2 | a0001c0003t0002g0289a0001c0003t0002g0293 | 2 | NA18948.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.727+4978G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21183998 | ||||||
| chr12:21184007
|
A | T | 1 | a0001c0001t0001g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.727+4987A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21184007 | ||||||
| chr12:21184024
|
C | A | 277 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(274): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.727+5004C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21184024 | ||||||
| chr12:21184050
|
G | GA | 14 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(11): Show | 14 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.727+5039dupA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 21184050 | |||||
| chr12:21184176
|
T | C | 1 | a0002c0002t0001g0173 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.727+5156T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21184176 | ||||||
| chr12:21184237
|
C | A | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(10): Show | 13 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.727+5217C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21184237 | ||||||
| chr12:21184677
|
C | A | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(10): Show | 13 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.727+5657C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21184677 | ||||||
| chr12:21184692
|
C | T | 66 | a0001c0001t0002g0141a0001c0003t0001g0259a0001c0003t0001g0274others(63): Show | 67 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.727+5672C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21184692 | ||||||
| chr12:21185001
|
C | T | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.727+5981C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21185001 | ||||||
| chr12:21185047
|
A | T | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(10): Show | 13 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.727+6027A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21185047 | ||||||
| chr12:21185051
|
G | C | 46 | a0001c0001t0001g0079a0001c0001t0003g0026a0001c0001t0003g0031others(43): Show | 46 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.727+6031G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21185051 | ||||||
| chr12:21185198
|
A | ACAGG | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(10): Show | 13 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.727+6178_727+6179i others(6): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21185198 | ||||||
| chr12:21185263
|
A | G | 81 | a0001c0003t0001g0193a0001c0003t0002g0250a0001c0003t0002g0252others(78): Show | 82 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.727+6243A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21185263 | ||||||
| chr12:21185297
|
T | A | 102 | a0001c0001t0001g0002a0001c0001t0001g0104a0001c0001t0001g0114others(99): Show | 104 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.727+6277T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21185297 | ||||||
| chr12:21185350
|
T | C | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(10): Show | 13 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.727+6330T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21185350 | ||||||
| chr12:21185420
|
G | A | 66 | a0001c0001t0002g0141a0001c0003t0001g0259a0001c0003t0001g0274others(63): Show | 67 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.727+6400G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21185420 | ||||||
| chr12:21185472
|
T | C | 207 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(204): Show | 211 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.727+6452T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21185472 | ||||||
| chr12:21185628
|
A | G | 19 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0104others(16): Show | 20 | HG01081.hp1 HG01167.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.727+6608A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21185628 | ||||||
| chr12:21185632
|
A | G | 4 | a0001c0003t0002g0280a0001c0003t0002g0289a0001c0003t0002g0293others(1): Show | 4 | NA18941.hp1 NA18948.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.727+6612A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21185632 | ||||||
| chr12:21185830
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.727+6810A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21185830 | ||||||
| chr12:21185863
|
G | A | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.727+6843G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21185863 | ||||||
| chr12:21185916
|
A | C | 1 | a0002c0002t0001g0151 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.727+6896A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21185916 | ||||||
| chr12:21185927
|
T | C | 20 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0104others(17): Show | 21 | HG01081.hp1 HG01167.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.727+6907T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21185927 | ||||||
| chr12:21185955
|
G | A | 102 | a0001c0001t0001g0002a0001c0001t0001g0104a0001c0001t0001g0114others(99): Show | 104 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.727+6935G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21185955 | ||||||
| chr12:21186324
|
G | A | 12 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(9): Show | 12 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.727+7304G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21186324 | ||||||
| chr12:21186414
|
G | A | 4 | a0001c0020t0001g0282a0007c0008t0006g0244a0007c0008t0006g0245others(1): Show | 4 | HG01884.hp1 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+7394G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21186414 | ||||||
| chr12:21186434
|
A | ATTGT | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(10): Show | 13 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.727+7415_727+7418d others(6): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 21186434 | |||||
| chr12:21186446
|
G | C | 5 | a0005c0007t0001g0101a0005c0007t0004g0093a0005c0007t0004g0096others(2): Show | 5 | HG00099.hp2 HG00735.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.727+7426G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21186446 | ||||||
| chr12:21186456
|
A | T | 1 | a0007c0019t0002g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.727+7436A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21186456 | ||||||
| chr12:21186464
|
T | C | 41 | a0001c0001t0001g0079a0001c0001t0003g0026a0001c0001t0003g0031others(38): Show | 41 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.727+7444T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21186464 | ||||||
| chr12:21186495
|
G | A | 11 | a0001c0003t0002g0106a0001c0003t0002g0156a0001c0003t0002g0158others(8): Show | 11 | NA18747.hp2 NA18940.hp1 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.727+7475G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21186495 | ||||||
| chr12:21186504
|
A | G | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.727+7484A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21186504 | ||||||
| chr12:21186546
|
C | T | 1 | a0001c0001t0004g0023 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.727+7526C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21186546 | ||||||
| chr12:21186556
|
T | A | 47 | a0001c0001t0001g0079a0001c0001t0003g0026a0001c0001t0003g0031others(44): Show | 47 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.727+7536T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21186556 | ||||||
| chr12:21186557
|
C | A | 47 | a0001c0001t0001g0079a0001c0001t0003g0026a0001c0001t0003g0031others(44): Show | 47 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.727+7537C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21186557 | ||||||
| chr12:21186678
|
G | GA | 8 | a0001c0001t0001g0113a0001c0001t0002g0080a0001c0001t0002g0111others(5): Show | 8 | HG01168.hp2 HG02647.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.727+7667dupA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 21186678 | |||||
| chr12:21186679
|
A | G | 2 | a0001c0001t0001g0129a0001c0001t0001g0177 | 2 | HG03669.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.727+7659A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21186679 | ||||||
| chr12:21186680
|
A | G | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(10): Show | 13 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.727+7660A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21186680 | ||||||
| chr12:21186719
|
C | G | 1 | a0002c0002t0001g0207 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.727+7699C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21186719 | ||||||
| chr12:21186756
|
C | T | 65 | a0001c0001t0002g0141a0001c0003t0001g0259a0001c0003t0001g0274others(62): Show | 66 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.727+7736C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21186756 | ||||||
| chr12:21186757
|
G | A | 3 | a0001c0003t0002g0250a0001c0003t0002g0252a0001c0003t0002g0271 | 3 | HG02615.hp1 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.727+7737G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21186757 | ||||||
| chr12:21186784
|
G | T | 4 | a0006c0010t0001g0262a0006c0010t0001g0263a0006c0010t0001g0264others(1): Show | 4 | HG02630.hp2 HG03225.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+7764G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21186784 | ||||||
| chr12:21186803
|
T | C | 1 | a0001c0001t0003g0052 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.727+7783T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21186803 | ||||||
| chr12:21186889
|
G | A | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(10): Show | 13 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.727+7869G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21186889 | ||||||
| chr12:21187076
|
T | A | 1 | a0001c0001t0003g0026 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.727+8056T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21187076 | ||||||
| chr12:21187083
|
G | C | 1 | a0001c0023t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.727+8063G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21187083 | ||||||
| chr12:21187115
|
C | T | 1 | a0003c0004t0002g0021 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.727+8095C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21187115 | ||||||
| chr12:21187153
|
A | G | 1 | a0001c0003t0002g0176 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.727+8133A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21187153 | ||||||
| chr12:21187196
|
A | G | 307 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(304): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.727+8176A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21187196 | ||||||
| chr12:21187273
|
T | C | 3 | a0003c0004t0002g0027a0003c0004t0002g0097a0003c0004t0002g0098 | 3 | HG01081.hp2 HG01358.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.727+8253T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21187273 | ||||||
| chr12:21187464
|
T | C | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(10): Show | 13 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.727+8444T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21187464 | ||||||
| chr12:21187566
|
C | A | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(10): Show | 13 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.727+8546C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21187566 | ||||||
| chr12:21187573
|
G | A | 79 | a0001c0001t0002g0141a0001c0001t0004g0022a0001c0001t0004g0023others(76): Show | 80 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.727+8553G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21187573 | ||||||
| chr12:21187668
|
G | GA | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(10): Show | 13 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.727+8658dupA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 21187668 | |||||
| chr12:21187668
|
GA | G | 105 | a0001c0001t0001g0079a0001c0001t0002g0141a0001c0001t0003g0026others(102): Show | 106 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.727+8658delA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 21187668 | |||||
| chr12:21187668
|
GAA | G | 11 | a0002c0005t0001g0016a0002c0005t0001g0086a0002c0005t0001g0117others(8): Show | 11 | HG01081.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.727+8657_727+8658d others(4): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 21187668 | |||||
| chr12:21187735
|
T | A | 1 | a0001c0023t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.727+8715T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21187735 | ||||||
| chr12:21187815
|
T | G | 1 | a0005c0009t0002g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.727+8795T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21187815 | ||||||
| chr12:21187922
|
G | A | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(10): Show | 13 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.727+8902G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21187922 | ||||||
| chr12:21187929
|
T | C | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(10): Show | 13 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.727+8909T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21187929 | ||||||
| chr12:21187997
|
C | G | 1 | a0007c0019t0002g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.728-8949C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21187997 | ||||||
| chr12:21188072
|
A | G | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(10): Show | 13 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.728-8874A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21188072 | ||||||
| chr12:21188085
|
G | A | 1 | a0002c0002t0001g0169 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.728-8861G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21188085 | ||||||
| chr12:21188162
|
C | T | 97 | a0001c0001t0002g0141a0001c0001t0004g0022a0001c0001t0004g0023others(94): Show | 98 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.728-8784C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21188162 | ||||||
| chr12:21188206
|
T | C | 11 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(8): Show | 11 | HG01346.hp1 HG01433.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.728-8740T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21188206 | ||||||
| chr12:21188216
|
T | G | 11 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(8): Show | 11 | HG01346.hp1 HG01433.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.728-8730T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21188216 | ||||||
| chr12:21188422
|
A | G | 4 | a0001c0020t0001g0282a0007c0008t0006g0244a0007c0008t0006g0245others(1): Show | 4 | HG01884.hp1 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.728-8524A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21188422 | ||||||
| chr12:21188577
|
G | A | 3 | a0002c0002t0001g0197a0002c0002t0001g0198a0018c0016t0001g0185 | 3 | HG00741.hp2 HG02683.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.728-8369G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21188577 | ||||||
| chr12:21188621
|
A | G | 2 | a0004c0006t0001g0233a0004c0006t0001g0234 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.728-8325A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21188621 | ||||||
| chr12:21188634
|
C | T | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(10): Show | 13 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.728-8312C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21188634 | ||||||
| chr12:21189094
|
A | G | 4 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(1): Show | 4 | HG02630.hp2 HG03225.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.728-7852A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21189094 | ||||||
| chr12:21189237
|
C | T | 4 | a0001c0003t0001g0259a0001c0003t0001g0274a0001c0003t0001g0284others(1): Show | 4 | HG02486.hp2 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.728-7709C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21189237 | ||||||
| chr12:21189315
|
A | G | 1 | a0007c0019t0002g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.728-7631A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21189315 | ||||||
| chr12:21189358
|
A | G | 1 | a0007c0019t0002g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.728-7588A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21189358 | ||||||
| chr12:21189455
|
AT | A | 185 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(182): Show | 188 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.728-7479delT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 21189455 | |||||
| chr12:21189474
|
C | G | 1 | a0007c0019t0002g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.728-7472C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21189474 | ||||||
| chr12:21189474
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.728-7472C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21189474 | ||||||
| chr12:21189528
|
A | G | 4 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(1): Show | 4 | HG02630.hp2 HG03225.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.728-7418A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21189528 | ||||||
| chr12:21189538
|
G | C | 1 | a0007c0019t0002g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.728-7408G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21189538 | ||||||
| chr12:21189631
|
G | C | 1 | a0007c0019t0002g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.728-7315G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21189631 | ||||||
| chr12:21189647
|
A | G | 1 | a0007c0019t0002g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.728-7299A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21189647 | ||||||
| chr12:21189738
|
T | C | 5 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(2): Show | 5 | HG02559.hp2 HG02630.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-7208T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21189738 | ||||||
| chr12:21189771
|
GTACACTC | G | 4 | a0002c0005t0001g0257a0002c0005t0001g0270a0002c0005t0001g0301others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.728-7172_728-7166d others(9): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 21189771 | |||||
| chr12:21189825
|
A | T | 1 | a0005c0007t0004g0095 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.728-7121A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21189825 | ||||||
| chr12:21190114
|
C | G | 4 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(1): Show | 4 | HG02630.hp2 HG03225.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.728-6832C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21190114 | ||||||
| chr12:21190295
|
C | G | 167 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(164): Show | 170 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.728-6651C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21190295 | ||||||
| chr12:21190334
|
C | T | 4 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(1): Show | 4 | HG02630.hp2 HG03225.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.728-6612C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21190334 | ||||||
| chr12:21190470
|
A | G | 231 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(228): Show | 236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.728-6476A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21190470 | ||||||
| chr12:21190554
|
G | A | 5 | a0001c0003t0003g0291a0001c0003t0005g0286a0001c0003t0005g0290others(2): Show | 5 | HG02129.hp2 NA18957.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-6392G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21190554 | ||||||
| chr12:21190625
|
T | G | 1 | a0003c0004t0002g0021 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.728-6321T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21190625 | ||||||
| chr12:21190670
|
T | C | 1 | a0002c0002t0001g0144 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.728-6276T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21190670 | ||||||
| chr12:21190679
|
C | T | 3 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247 | 3 | HG01884.hp1 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.728-6267C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21190679 | ||||||
| chr12:21190716
|
T | C | 4 | a0001c0001t0002g0310a0001c0003t0002g0250a0001c0003t0002g0252others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.728-6230T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21190716 | ||||||
| chr12:21190875
|
G | A | 1 | a0001c0003t0002g0216 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.728-6071G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21190875 | ||||||
| chr12:21190887
|
C | T | 1 | a0002c0002t0001g0100 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.728-6059C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21190887 | ||||||
| chr12:21190889
|
T | A | 2 | a0001c0001t0002g0285a0001c0001t0009g0243 | 2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.728-6057T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21190889 | ||||||
| chr12:21190899
|
A | C | 41 | a0001c0001t0002g0080a0001c0001t0002g0111a0001c0001t0002g0112others(38): Show | 43 | HG00609.hp1 HG01081.hp2 HG01258.hp2 others(40): Show |
intron_variant | MODIFIER | c.728-6047A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21190899 | ||||||
| chr12:21190952
|
A | G | 55 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(52): Show | 56 | HG00438.hp1 HG00609.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.728-5994A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21190952 | ||||||
| chr12:21191056
|
A | G | 4 | a0001c0001t0001g0113a0001c0001t0002g0120a0001c0001t0002g0125others(1): Show | 4 | HG01168.hp2 HG02647.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.728-5890A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21191056 | ||||||
| chr12:21191179
|
A | G | 3 | a0001c0001t0002g0080a0001c0001t0002g0111a0001c0001t0002g0112 | 3 | HG02895.hp1 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.728-5767A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21191179 | ||||||
| chr12:21191213
|
A | G | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-5733A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21191213 | ||||||
| chr12:21191261
|
T | TA | 228 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(225): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.728-5684dupA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 21191261 | |||||
| chr12:21191373
|
C | A | 4 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(1): Show | 4 | HG02630.hp2 HG03225.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.728-5573C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21191373 | ||||||
| chr12:21191379
|
GA | G | 18 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(15): Show | 18 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.728-5566delA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21191379 | ||||||
| chr12:21191390
|
A | C | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-5556A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21191390 | ||||||
| chr12:21191609
|
T | A | 75 | a0001c0001t0001g0283a0001c0003t0001g0284a0001c0003t0001g0296others(72): Show | 76 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.728-5337T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21191609 | ||||||
| chr12:21191612
|
G | A | 1 | a0002c0005t0001g0258 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.728-5334G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21191612 | ||||||
| chr12:21191636
|
G | C | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-5310G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21191636 | ||||||
| chr12:21191746
|
G | C | 1 | a0005c0009t0002g0084 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.728-5200G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21191746 | ||||||
| chr12:21191785
|
G | A | 1 | a0011c0025t0001g0019 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.728-5161G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21191785 | ||||||
| chr12:21192218
|
C | T | 3 | a0002c0002t0001g0166a0002c0002t0001g0167a0002c0002t0001g0181 | 3 | HG00099.hp1 HG03669.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.728-4728C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21192218 | ||||||
| chr12:21192223
|
CAGTA | C | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-4721_728-4718d others(6): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 21192223 | |||||
| chr12:21192335
|
CT | C | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-4610delT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21192335 | ||||||
| chr12:21192441
|
T | A | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-4505T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21192441 | ||||||
| chr12:21192544
|
G | A | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-4402G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21192544 | ||||||
| chr12:21192709
|
A | G | 1 | a0002c0005t0001g0016 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.728-4237A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21192709 | ||||||
| chr12:21192722
|
G | A | 2 | a0004c0006t0001g0246a0004c0006t0001g0272 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.728-4224G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21192722 | ||||||
| chr12:21192748
|
A | G | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-4198A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21192748 | ||||||
| chr12:21192839
|
T | C | 1 | a0003c0004t0002g0287 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.728-4107T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21192839 | ||||||
| chr12:21192841
|
T | A | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.728-4105T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21192841 | ||||||
| chr12:21192918
|
C | T | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.728-4028C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21192918 | ||||||
| chr12:21193001
|
A | T | 2 | a0002c0005t0001g0143a0002c0005t0001g0164 | 2 | HG01081.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.728-3945A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21193001 | ||||||
| chr12:21193153
|
A | T | 1 | a0001c0001t0009g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.728-3793A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21193153 | ||||||
| chr12:21193206
|
C | A | 12 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(9): Show | 12 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.728-3740C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21193206 | ||||||
| chr12:21193206
|
C | T | 5 | a0001c0001t0003g0060a0001c0023t0001g0088a0006c0010t0001g0262others(2): Show | 5 | HG02630.hp2 HG03225.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-3740C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21193206 | ||||||
| chr12:21193207
|
G | T | 12 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(9): Show | 12 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.728-3739G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21193207 | ||||||
| chr12:21193365
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.728-3581G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21193365 | ||||||
| chr12:21193523
|
T | C | 3 | a0006c0010t0001g0262a0006c0010t0001g0263a0006c0010t0001g0264 | 3 | HG02630.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.728-3423T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21193523 | ||||||
| chr12:21193572
|
G | T | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-3374G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21193572 | ||||||
| chr12:21193789
|
T | G | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-3157T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21193789 | ||||||
| chr12:21193802
|
T | A | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-3144T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21193802 | ||||||
| chr12:21193802
|
T | C | 103 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(100): Show | 104 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.728-3144T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21193802 | ||||||
| chr12:21193853
|
C | T | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-3093C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21193853 | ||||||
| chr12:21193859
|
C | T | 5 | a0001c0001t0001g0113a0001c0001t0002g0115a0001c0001t0002g0120others(2): Show | 5 | HG01168.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-3087C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21193859 | ||||||
| chr12:21193894
|
T | C | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-3052T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21193894 | ||||||
| chr12:21193905
|
T | C | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-3041T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21193905 | ||||||
| chr12:21193923
|
T | G | 1 | a0001c0001t0003g0056 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.728-3023T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21193923 | ||||||
| chr12:21193944
|
C | T | 1 | a0001c0001t0003g0071 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.728-3002C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21193944 | ||||||
| chr12:21194013
|
G | C | 2 | a0002c0002t0001g0152a0002c0002t0001g0153 | 2 | HG01261.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.728-2933G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21194013 | ||||||
| chr12:21194058
|
T | C | 4 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(1): Show | 4 | HG02630.hp2 HG03225.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.728-2888T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21194058 | ||||||
| chr12:21194071
|
G | A | 1 | a0002c0005t0002g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.728-2875G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21194071 | ||||||
| chr12:21194087
|
G | A | 17 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.728-2859G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21194087 | ||||||
| chr12:21194087
|
G | T | 85 | a0001c0001t0001g0079a0001c0001t0001g0113a0001c0001t0002g0010others(82): Show | 87 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.728-2859G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21194087 | ||||||
| chr12:21194088
|
G | A | 45 | a0001c0001t0001g0079a0001c0001t0003g0026a0001c0001t0003g0031others(42): Show | 45 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.728-2858G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21194088 | ||||||
| chr12:21194132
|
G | A | 4 | a0001c0001t0003g0131a0001c0001t0003g0132a0001c0001t0003g0133others(1): Show | 4 | NA18942.hp1 NA18959.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.728-2814G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21194132 | ||||||
| chr12:21194142
|
A | C | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-2804A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21194142 | ||||||
| chr12:21194205
|
C | T | 7 | a0002c0002t0001g0210a0004c0006t0001g0028a0004c0006t0001g0029others(4): Show | 7 | HG00280.hp1 HG00642.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.728-2741C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21194205 | ||||||
| chr12:21194244
|
C | T | 1 | a0008c0013t0002g0035 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.728-2702C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21194244 | ||||||
| chr12:21194264
|
G | A | 72 | a0001c0001t0001g0283a0001c0003t0001g0296a0001c0003t0001g0297others(69): Show | 73 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.728-2682G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21194264 | ||||||
| chr12:21194290
|
G | T | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-2656G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21194290 | ||||||
| chr12:21194309
|
G | A | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-2637G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21194309 | ||||||
| chr12:21194408
|
A | T | 3 | a0001c0001t0003g0131a0001c0001t0003g0132a0001c0001t0003g0133 | 3 | NA18942.hp1 NA18959.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.728-2538A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21194408 | ||||||
| chr12:21194417
|
A | C | 12 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(9): Show | 12 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.728-2529A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21194417 | ||||||
| chr12:21194500
|
T | G | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-2446T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21194500 | ||||||
| chr12:21194586
|
C | T | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-2360C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21194586 | ||||||
| chr12:21194706
|
A | G | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-2240A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21194706 | ||||||
| chr12:21194782
|
A | G | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-2164A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21194782 | ||||||
| chr12:21194812
|
T | C | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-2134T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21194812 | ||||||
| chr12:21195102
|
G | A | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-1844G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21195102 | ||||||
| chr12:21195203
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.728-1743G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21195203 | ||||||
| chr12:21195292
|
A | T | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-1654A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21195292 | ||||||
| chr12:21195346
|
T | G | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.728-1600T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21195346 | ||||||
| chr12:21195420
|
T | TTTTGATT others(1): Show |
4 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(1): Show | 4 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.728-1522_728-1521i others(10): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 21195420 | |||||
| chr12:21195465
|
C | T | 1 | a0016c0018t0001g0140 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.728-1481C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21195465 | ||||||
| chr12:21195779
|
A | G | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-1167A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21195779 | ||||||
| chr12:21195875
|
A | G | 1 | a0001c0003t0001g0274 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.728-1071A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21195875 | ||||||
| chr12:21195937
|
T | A | 1 | a0001c0001t0001g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.728-1009T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21195937 | ||||||
| chr12:21196062
|
T | G | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-884T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21196062 | ||||||
| chr12:21196108
|
C | T | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-838C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21196108 | ||||||
| chr12:21196162
|
G | C | 1 | a0001c0001t0002g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.728-784G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21196162 | ||||||
| chr12:21196191
|
T | C | 1 | a0001c0003t0002g0005 | 2 | HG00735.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.728-755T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21196191 | ||||||
| chr12:21196253
|
CT | C | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-686delT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 21196253 | |||||
| chr12:21196273
|
G | A | 1 | a0001c0003t0002g0107 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.728-673G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21196273 | ||||||
| chr12:21196297
|
G | C | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-649G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21196297 | ||||||
| chr12:21196393
|
T | A | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-553T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21196393 | ||||||
| chr12:21196440
|
T | C | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-506T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21196440 | ||||||
| chr12:21196563
|
T | C | 5 | a0001c0003t0002g0005a0001c0003t0002g0201a0001c0003t0002g0215others(2): Show | 6 | HG00735.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.728-383T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21196563 | ||||||
| chr12:21196677
|
C | T | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-269C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21196677 | ||||||
| chr12:21196723
|
A | C | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-223A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21196723 | ||||||
| chr12:21196724
|
G | A | 4 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(1): Show | 4 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.728-222G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21196724 | ||||||
| chr12:21196865
|
A | G | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.728-81A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21196865 | ||||||
| chr12:21196928
|
TATAA | T | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-17_728-14delAT others(2): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 7/14 | chr12 | 21196928 | ||||||
| chr12:21197252
|
A | C | 1 | a0001c0001t0003g0051 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.970+64A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21197252 | ||||||
| chr12:21197462
|
T | C | 12 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(9): Show | 12 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.970+274T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21197462 | ||||||
| chr12:21197467
|
A | T | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.970+279A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21197467 | ||||||
| chr12:21197613
|
G | A | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.970+425G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21197613 | ||||||
| chr12:21197632
|
A | T | 1 | a0001c0003t0002g0218 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.970+444A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21197632 | ||||||
| chr12:21197681
|
A | C | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.970+493A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21197681 | ||||||
| chr12:21197715
|
C | T | 1 | a0002c0002t0001g0100 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.970+527C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21197715 | ||||||
| chr12:21197734
|
T | C | 210 | a0001c0001t0001g0002a0001c0001t0001g0079a0001c0001t0001g0082others(207): Show | 214 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(211): Show |
intron_variant | MODIFIER | c.970+546T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21197734 | ||||||
| chr12:21197753
|
A | C | 211 | a0001c0001t0001g0002a0001c0001t0001g0079a0001c0001t0001g0082others(208): Show | 215 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.970+565A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21197753 | ||||||
| chr12:21197755
|
T | G | 18 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(15): Show | 18 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.970+567T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21197755 | ||||||
| chr12:21197802
|
G | A | 1 | a0001c0003t0002g0295 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.970+614G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21197802 | ||||||
| chr12:21197856
|
G | T | 84 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0104others(81): Show | 86 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(83): Show |
intron_variant | MODIFIER | c.970+668G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21197856 | ||||||
| chr12:21197927
|
A | G | 84 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0104others(81): Show | 86 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(83): Show |
intron_variant | MODIFIER | c.970+739A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21197927 | ||||||
| chr12:21198184
|
A | C | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.970+996A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21198184 | ||||||
| chr12:21198199
|
C | T | 1 | a0002c0002t0001g0206 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.970+1011C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21198199 | ||||||
| chr12:21198333
|
C | T | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.970+1145C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21198333 | ||||||
| chr12:21198396
|
A | G | 2 | a0001c0001t0003g0072a0012c0026t0003g0045 | 2 | NA18951.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.970+1208A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21198396 | ||||||
| chr12:21198467
|
C | A | 1 | a0001c0003t0001g0297 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.970+1279C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21198467 | ||||||
| chr12:21198483
|
C | T | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.970+1295C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21198483 | ||||||
| chr12:21198637
|
GAATA | G | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.970+1450_970+1453d others(6): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21198637 | ||||||
| chr12:21198712
|
G | T | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.970+1524G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21198712 | ||||||
| chr12:21198772
|
G | C | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.970+1584G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21198772 | ||||||
| chr12:21198785
|
A | G | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.970+1597A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21198785 | ||||||
| chr12:21198824
|
C | T | 2 | a0004c0006t0001g0028a0004c0006t0001g0029 | 2 | HG00280.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.970+1636C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21198824 | ||||||
| chr12:21198905
|
G | T | 1 | a0002c0002t0001g0147 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.971-1603G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21198905 | ||||||
| chr12:21199013
|
G | A | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.971-1495G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21199013 | ||||||
| chr12:21199043
|
T | C | 5 | a0001c0003t0002g0005a0001c0003t0002g0201a0001c0003t0002g0215others(2): Show | 6 | HG00735.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.971-1465T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21199043 | ||||||
| chr12:21199066
|
A | C | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.971-1442A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21199066 | ||||||
| chr12:21199074
|
T | C | 1 | a0001c0001t0009g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.971-1434T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21199074 | ||||||
| chr12:21199102
|
T | G | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.971-1406T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21199102 | ||||||
| chr12:21199116
|
T | C | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.971-1392T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21199116 | ||||||
| chr12:21199126
|
CCTT | C | 4 | a0001c0003t0003g0291a0001c0003t0005g0290a0001c0003t0005g0292others(1): Show | 4 | HG02129.hp2 NA18957.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.971-1381_971-1379d others(5): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21199126 | ||||||
| chr12:21199239
|
T | G | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.971-1269T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21199239 | ||||||
| chr12:21199252
|
A | C | 3 | a0006c0010t0001g0262a0006c0010t0001g0263a0006c0010t0001g0264 | 3 | HG02630.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.971-1256A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21199252 | ||||||
| chr12:21199252
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.971-1256A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21199252 | ||||||
| chr12:21199342
|
T | C | 1 | a0001c0001t0004g0030 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.971-1166T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21199342 | ||||||
| chr12:21199367
|
C | T | 1 | a0002c0005t0002g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.971-1141C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21199367 | ||||||
| chr12:21199381
|
A | G | 91 | a0001c0001t0001g0079a0001c0001t0001g0113a0001c0001t0002g0010others(88): Show | 93 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.971-1127A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21199381 | ||||||
| chr12:21199489
|
C | G | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.971-1019C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21199489 | ||||||
| chr12:21199559
|
A | G | 2 | a0001c0003t0002g0295a0001c0003t0002g0308 | 2 | NA18981.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.971-949A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21199559 | ||||||
| chr12:21199607
|
A | G | 90 | a0001c0001t0001g0079a0001c0001t0001g0113a0001c0001t0002g0010others(87): Show | 92 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.971-901A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21199607 | ||||||
| chr12:21199621
|
T | C | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.971-887T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21199621 | ||||||
| chr12:21199662
|
G | A | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.971-846G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21199662 | ||||||
| chr12:21199737
|
A | G | 12 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(9): Show | 12 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.971-771A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21199737 | ||||||
| chr12:21199789
|
T | TTTTG | 6 | a0001c0003t0002g0294a0001c0003t0003g0291a0001c0003t0005g0292others(3): Show | 6 | HG00099.hp1 HG02129.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.971-694_971-691dup others(4): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 21199789 | |||||
| chr12:21199789
|
TTTTG | T | 11 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.971-694_971-691del others(4): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 21199789 | |||||
| chr12:21199876
|
A | ACTGCAAC others(6): Show |
1 | a0001c0023t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.971-629_971-617dup others(13): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 21199876 | |||||
| chr12:21199927
|
A | G | 15 | a0001c0001t0002g0310a0001c0003t0002g0250a0001c0003t0002g0252others(12): Show | 15 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.971-581A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21199927 | ||||||
| chr12:21199957
|
G | A | 1 | a0001c0001t0002g0285 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.971-551G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21199957 | ||||||
| chr12:21200097
|
G | A | 3 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0009g0243 | 3 | HG02572.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.971-411G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21200097 | ||||||
| chr12:21200104
|
A | G | 10 | a0001c0001t0002g0310a0001c0003t0002g0250a0001c0003t0002g0252others(7): Show | 10 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.971-404A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21200104 | ||||||
| chr12:21200253
|
C | A | 1 | a0001c0001t0001g0129 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.971-255C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21200253 | ||||||
| chr12:21200383
|
T | G | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.971-125T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 8/14 | chr12 | 21200383 | ||||||
| chr12:21200686
|
T | G | 1 | a0001c0003t0003g0291 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1135+14T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21200686 | ||||||
| chr12:21200695
|
G | A | 2 | a0002c0005t0001g0253a0002c0005t0001g0265 | 2 | HG01975.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1135+23G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21200695 | ||||||
| chr12:21200714
|
A | C | 11 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1135+42A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21200714 | ||||||
| chr12:21200738
|
G | A | 11 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1135+66G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21200738 | ||||||
| chr12:21200848
|
G | T | 2 | a0001c0003t0002g0250a0001c0003t0002g0271 | 2 | HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1135+176G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21200848 | ||||||
| chr12:21200854
|
C | T | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1135+182C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21200854 | ||||||
| chr12:21200892
|
A | G | 11 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1135+220A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21200892 | ||||||
| chr12:21200938
|
A | G | 84 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0104others(81): Show | 86 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(83): Show |
intron_variant | MODIFIER | c.1135+266A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21200938 | ||||||
| chr12:21200976
|
C | T | 3 | a0001c0001t0002g0141a0001c0001t0003g0067a0001c0001t0003g0069 | 3 | HG04115.hp1 NA18971.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1135+304C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21200976 | ||||||
| chr12:21200977
|
C | G | 176 | a0001c0001t0001g0002a0001c0001t0001g0079a0001c0001t0001g0082others(173): Show | 180 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(177): Show |
intron_variant | MODIFIER | c.1135+305C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21200977 | ||||||
| chr12:21201044
|
C | G | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1135+372C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21201044 | ||||||
| chr12:21201097
|
A | G | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1135+425A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21201097 | ||||||
| chr12:21201128
|
A | G | 1 | a0002c0002t0001g0147 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1135+456A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21201128 | ||||||
| chr12:21201176
|
G | T | 1 | a0007c0019t0002g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1135+504G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21201176 | ||||||
| chr12:21201238
|
T | C | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1135+566T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21201238 | ||||||
| chr12:21201406
|
C | T | 1 | a0001c0001t0009g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1135+734C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21201406 | ||||||
| chr12:21201434
|
C | T | 1 | a0011c0025t0001g0019 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1135+762C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21201434 | ||||||
| chr12:21201465
|
T | C | 1 | a0001c0023t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1135+793T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21201465 | ||||||
| chr12:21201485
|
G | A | 1 | a0001c0001t0009g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1135+813G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21201485 | ||||||
| chr12:21201536
|
G | A | 304 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(301): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1135+864G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21201536 | ||||||
| chr12:21201560
|
T | C | 75 | a0001c0001t0001g0283a0001c0003t0001g0284a0001c0003t0001g0296others(72): Show | 76 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1135+888T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21201560 | ||||||
| chr12:21201759
|
C | T | 3 | a0005c0009t0002g0083a0005c0009t0002g0084a0005c0009t0002g0109 | 3 | HG02922.hp1 HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1136-732C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21201759 | ||||||
| chr12:21201772
|
C | T | 1 | a0002c0002t0002g0092 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1136-719C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21201772 | ||||||
| chr12:21201788
|
A | T | 1 | a0003c0004t0002g0037 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1136-703A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21201788 | ||||||
| chr12:21201863
|
T | A | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1136-628T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21201863 | ||||||
| chr12:21202002
|
A | G | 1 | a0004c0006t0001g0127 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1136-489A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21202002 | ||||||
| chr12:21202004
|
G | A | 11 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1136-487G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21202004 | ||||||
| chr12:21202151
|
T | C | 79 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0104others(76): Show | 81 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.1136-340T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21202151 | ||||||
| chr12:21202181
|
G | A | 5 | a0001c0001t0002g0310a0001c0001t0009g0243a0001c0003t0002g0250others(2): Show | 5 | HG02145.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1136-310G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21202181 | ||||||
| chr12:21202233
|
G | T | 4 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(1): Show | 4 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1136-258G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21202233 | ||||||
| chr12:21202356
|
T | C | 3 | a0001c0003t0001g0299a0002c0005t0001g0016a0010c0012t0001g0189 | 3 | HG02486.hp2 HG02896.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1136-135T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 9/14 | chr12 | 21202356 | ||||||
| chr12:21202789
|
TTTAAG | T | 4 | a0001c0001t0002g0080a0001c0001t0002g0111a0001c0001t0002g0112others(1): Show | 4 | HG02630.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1331+109_1331+113d others(7): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 21202789 | |||||
| chr12:21202818
|
A | G | 1 | a0001c0003t0002g0266 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1331+132A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21202818 | ||||||
| chr12:21202857
|
C | A | 1 | a0002c0002t0001g0181 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1331+171C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21202857 | ||||||
| chr12:21203004
|
C | G | 10 | a0001c0001t0002g0080a0001c0001t0002g0111a0001c0001t0002g0112others(7): Show | 10 | HG02145.hp2 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1331+318C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21203004 | ||||||
| chr12:21203084
|
A | T | 1 | a0002c0002t0004g0199 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1331+398A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21203084 | ||||||
| chr12:21203086
|
G | T | 1 | a0002c0002t0004g0199 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1331+400G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21203086 | ||||||
| chr12:21203087
|
G | T | 1 | a0002c0002t0004g0199 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1331+401G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21203087 | ||||||
| chr12:21203146
|
G | A | 1 | a0001c0003t0002g0175 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1331+460G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21203146 | ||||||
| chr12:21203324
|
A | T | 4 | a0001c0001t0002g0080a0001c0001t0002g0111a0001c0001t0002g0112others(1): Show | 4 | HG02630.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1331+638A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21203324 | ||||||
| chr12:21203443
|
G | A | 1 | a0005c0007t0008g0102 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1331+757G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21203443 | ||||||
| chr12:21203692
|
T | C | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1331+1006T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21203692 | ||||||
| chr12:21203788
|
ACTTTC | A | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1331+1107_1331+111 others(9): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 21203788 | |||||
| chr12:21203802
|
T | C | 2 | a0005c0007t0004g0094a0005c0007t0004g0095 | 2 | HG01346.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1331+1116T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21203802 | ||||||
| chr12:21203868
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1331+1182A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21203868 | ||||||
| chr12:21204127
|
G | T | 2 | a0006c0014t0001g0298a0006c0014t0001g0309 | 2 | HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1331+1441G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21204127 | ||||||
| chr12:21204138
|
G | T | 1 | a0001c0001t0003g0032 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1331+1452G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21204138 | ||||||
| chr12:21204156
|
A | G | 1 | a0001c0003t0002g0275 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1331+1470A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21204156 | ||||||
| chr12:21204304
|
A | G | 1 | a0002c0005t0002g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1332-1564A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21204304 | ||||||
| chr12:21204425
|
A | G | 2 | a0002c0005t0001g0143a0002c0005t0001g0164 | 2 | HG01081.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1332-1443A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21204425 | ||||||
| chr12:21204444
|
A | T | 2 | a0001c0003t0001g0259a0001c0003t0001g0274 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1332-1424A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21204444 | ||||||
| chr12:21204518
|
C | CA | 20 | a0001c0001t0001g0304a0001c0001t0002g0125a0001c0001t0003g0031others(17): Show | 20 | HG00673.hp2 HG01175.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1332-1336dupA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 21204518 | |||||
| chr12:21204676
|
G | A | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1332-1192G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21204676 | ||||||
| chr12:21204682
|
G | A | 1 | a0001c0001t0003g0063 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1332-1186G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21204682 | ||||||
| chr12:21204697
|
C | T | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1332-1171C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21204697 | ||||||
| chr12:21204777
|
C | T | 85 | a0001c0001t0001g0079a0001c0001t0001g0113a0001c0001t0002g0010others(82): Show | 87 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.1332-1091C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21204777 | ||||||
| chr12:21204797
|
C | T | 174 | a0001c0001t0001g0002a0001c0001t0001g0079a0001c0001t0001g0104others(171): Show | 178 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(175): Show |
intron_variant | MODIFIER | c.1332-1071C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21204797 | ||||||
| chr12:21204819
|
G | C | 85 | a0001c0001t0001g0079a0001c0001t0001g0113a0001c0001t0002g0010others(82): Show | 87 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.1332-1049G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21204819 | ||||||
| chr12:21204835
|
C | T | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1332-1033C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21204835 | ||||||
| chr12:21205014
|
T | C | 71 | a0001c0001t0002g0141a0001c0001t0002g0310a0001c0003t0001g0193others(68): Show | 72 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.1332-854T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21205014 | ||||||
| chr12:21205166
|
AT | A | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1332-696delT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 21205166 | |||||
| chr12:21205495
|
G | GTC | 3 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247 | 3 | HG01884.hp1 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1332-372_1332-371d others(4): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 21205495 | |||||
| chr12:21205520
|
C | T | 2 | a0002c0002t0002g0157a0002c0002t0002g0281 | 2 | NA18948.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1332-348C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21205520 | ||||||
| chr12:21205573
|
A | G | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1332-295A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21205573 | ||||||
| chr12:21205608
|
T | TTGGTTTA others(342): Show |
1 | a0007c0019t0002g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1332-249_1332-248i others(351): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 21205608 | |||||
| chr12:21205608
|
T | TTGGTTTA others(341): Show |
3 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247 | 3 | HG01884.hp1 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1332-249_1332-248i others(350): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 21205608 | |||||
| chr12:21205608
|
T | TTGGTTTA others(324): Show |
1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1332-249_1332-248i others(333): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 21205608 | |||||
| chr12:21205654
|
T | C | 1 | a0002c0002t0001g0227 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1332-214T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21205654 | ||||||
| chr12:21205710
|
GTCA | G | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1332-151_1332-149d others(5): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 21205710 | |||||
| chr12:21205737
|
TA | T | 6 | a0004c0006t0001g0028a0004c0006t0001g0029a0004c0006t0001g0078others(3): Show | 6 | HG00280.hp1 HG00642.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.1332-128delA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 21205737 | |||||
| chr12:21205761
|
T | TTTC | 208 | a0001c0001t0001g0002a0001c0001t0001g0079a0001c0001t0001g0082others(205): Show | 212 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(209): Show |
intron_variant | MODIFIER | c.1332-105_1332-104i others(5): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 21205761 | |||||
| chr12:21205808
|
CTTCT | C | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1332-57_1332-54del others(4): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 21205808 | |||||
| chr12:21205849
|
G | C | 3 | a0006c0010t0001g0262a0006c0010t0001g0263a0006c0010t0001g0264 | 3 | HG02630.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1332-19G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 10/14 | chr12 | 21205849 | ||||||
| chr12:21206167
|
T | C | 3 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247 | 3 | HG01884.hp1 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1497+134T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21206167 | ||||||
| chr12:21206217
|
G | C | 1 | a0001c0003t0002g0223 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1497+184G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21206217 | ||||||
| chr12:21206352
|
G | C | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1497+319G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21206352 | ||||||
| chr12:21206516
|
T | C | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1497+483T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21206516 | ||||||
| chr12:21206552
|
G | A | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1497+519G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21206552 | ||||||
| chr12:21206678
|
C | G | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1497+645C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21206678 | ||||||
| chr12:21206745
|
T | C | 1 | a0002c0002t0001g0062 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1497+712T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21206745 | ||||||
| chr12:21206775
|
C | A | 1 | a0001c0001t0003g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1497+742C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21206775 | ||||||
| chr12:21206900
|
C | T | 1 | a0001c0003t0002g0275 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1497+867C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21206900 | ||||||
| chr12:21206934
|
A | G | 5 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1497+901A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21206934 | ||||||
| chr12:21207023
|
A | G | 1 | a0001c0001t0002g0080 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1497+990A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21207023 | ||||||
| chr12:21207150
|
T | C | 4 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(1): Show | 4 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1497+1117T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21207150 | ||||||
| chr12:21207165
|
G | A | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1497+1132G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21207165 | ||||||
| chr12:21207230
|
C | T | 1 | a0002c0002t0001g0172 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1497+1197C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21207230 | ||||||
| chr12:21207246
|
T | G | 1 | a0001c0001t0002g0141 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1497+1213T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21207246 | ||||||
| chr12:21207756
|
A | G | 1 | a0002c0005t0002g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1497+1723A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21207756 | ||||||
| chr12:21207801
|
G | A | 72 | a0001c0001t0001g0311a0001c0001t0002g0141a0001c0003t0002g0005others(69): Show | 73 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1497+1768G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21207801 | ||||||
| chr12:21207827
|
G | A | 68 | a0001c0001t0001g0079a0001c0001t0001g0113a0001c0001t0002g0010others(65): Show | 69 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.1497+1794G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21207827 | ||||||
| chr12:21207848
|
G | A | 1 | a0001c0003t0002g0289 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1497+1815G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21207848 | ||||||
| chr12:21207992
|
T | C | 17 | a0001c0001t0001g0002a0001c0001t0001g0104a0001c0001t0001g0113others(14): Show | 18 | HG01167.hp1 HG01891.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1497+1959T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21207992 | ||||||
| chr12:21208015
|
C | G | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1497+1982C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21208015 | ||||||
| chr12:21208114
|
T | TTTC | 97 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(94): Show | 99 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.1497+2083_1497+208 others(7): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 21208114 | |||||
| chr12:21208124
|
GCAGAAGC others(1): Show |
G | 90 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(87): Show | 92 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1497+2094_1497+210 others(12): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 21208124 | |||||
| chr12:21208207
|
T | G | 75 | a0001c0001t0001g0283a0001c0003t0001g0193a0001c0003t0001g0284others(72): Show | 76 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1497+2174T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21208207 | ||||||
| chr12:21208279
|
A | C | 91 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(88): Show | 93 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.1497+2246A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21208279 | ||||||
| chr12:21208284
|
G | T | 1 | a0001c0001t0001g0013 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1497+2251G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21208284 | ||||||
| chr12:21208529
|
G | T | 6 | a0004c0006t0001g0028a0004c0006t0001g0029a0004c0006t0001g0078others(3): Show | 6 | HG00280.hp1 HG00642.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.1497+2496G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21208529 | ||||||
| chr12:21208572
|
A | G | 7 | a0001c0001t0002g0285a0001c0023t0001g0088a0006c0010t0001g0262others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1497+2539A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21208572 | ||||||
| chr12:21208626
|
G | T | 306 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(303): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1497+2593G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21208626 | ||||||
| chr12:21208641
|
T | C | 5 | a0001c0001t0002g0248a0001c0001t0002g0310a0001c0003t0002g0250others(2): Show | 5 | HG02145.hp2 HG02615.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1497+2608T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21208641 | ||||||
| chr12:21208650
|
A | G | 12 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(9): Show | 12 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1497+2617A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21208650 | ||||||
| chr12:21208653
|
T | G | 96 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(93): Show | 98 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1497+2620T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21208653 | ||||||
| chr12:21208667
|
T | C | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1497+2634T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21208667 | ||||||
| chr12:21208668
|
G | C | 7 | a0001c0001t0002g0285a0001c0023t0001g0088a0006c0010t0001g0262others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1497+2635G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21208668 | ||||||
| chr12:21208702
|
A | G | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1497+2669A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21208702 | ||||||
| chr12:21208727
|
T | A | 1 | a0001c0001t0002g0285 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1497+2694T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21208727 | ||||||
| chr12:21208805
|
C | T | 1 | a0001c0001t0002g0285 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1497+2772C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21208805 | ||||||
| chr12:21208825
|
G | A | 1 | a0002c0002t0001g0147 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1497+2792G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21208825 | ||||||
| chr12:21208882
|
G | A | 1 | a0016c0018t0001g0140 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1497+2849G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21208882 | ||||||
| chr12:21208934
|
C | T | 17 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(14): Show | 17 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.1497+2901C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21208934 | ||||||
| chr12:21209038
|
T | G | 2 | a0001c0001t0009g0243a0015c0024t0001g0017 | 2 | HG02572.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1497+3005T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21209038 | ||||||
| chr12:21209055
|
A | T | 43 | a0001c0001t0003g0026a0001c0001t0003g0031a0001c0001t0003g0032others(40): Show | 43 | HG00423.hp2 HG00673.hp2 HG01943.hp2 others(40): Show |
intron_variant | MODIFIER | c.1497+3022A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21209055 | ||||||
| chr12:21209059
|
T | A | 7 | a0001c0001t0002g0285a0001c0023t0001g0088a0006c0010t0001g0262others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1497+3026T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21209059 | ||||||
| chr12:21209178
|
A | C | 7 | a0001c0001t0002g0285a0001c0023t0001g0088a0006c0010t0001g0262others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1497+3145A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21209178 | ||||||
| chr12:21209202
|
T | TC | 7 | a0001c0001t0002g0285a0001c0023t0001g0088a0006c0010t0001g0262others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1497+3175dupC | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 21209202 | |||||
| chr12:21209207
|
C | T | 3 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247 | 3 | HG01884.hp1 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1497+3174C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21209207 | ||||||
| chr12:21209248
|
C | A | 1 | a0001c0001t0002g0285 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1497+3215C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21209248 | ||||||
| chr12:21209284
|
C | T | 1 | a0002c0005t0002g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1497+3251C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21209284 | ||||||
| chr12:21209305
|
G | A | 7 | a0004c0006t0001g0028a0004c0006t0001g0029a0004c0006t0001g0078others(4): Show | 7 | HG00280.hp1 HG00642.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1497+3272G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21209305 | ||||||
| chr12:21209330
|
C | T | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1497+3297C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21209330 | ||||||
| chr12:21209425
|
A | G | 17 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(14): Show | 17 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.1497+3392A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21209425 | ||||||
| chr12:21209458
|
C | A | 96 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(93): Show | 98 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1497+3425C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21209458 | ||||||
| chr12:21209621
|
G | A | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1497+3588G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21209621 | ||||||
| chr12:21209628
|
C | T | 96 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(93): Show | 98 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1497+3595C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21209628 | ||||||
| chr12:21209629
|
G | A | 1 | a0001c0023t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1497+3596G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21209629 | ||||||
| chr12:21209653
|
A | G | 96 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(93): Show | 98 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1497+3620A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21209653 | ||||||
| chr12:21209673
|
CAACAGTG others(2): Show |
C | 3 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247 | 3 | HG01884.hp1 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1497+3643_1497+365 others(13): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 21209673 | |||||
| chr12:21209735
|
T | A | 70 | a0001c0001t0001g0283a0001c0003t0001g0193a0001c0003t0001g0284others(67): Show | 71 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1497+3702T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21209735 | ||||||
| chr12:21209861
|
T | A | 3 | a0004c0006t0001g0233a0004c0006t0001g0234a0004c0006t0001g0235 | 3 | HG00642.hp1 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1497+3828T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21209861 | ||||||
| chr12:21209885
|
C | T | 97 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(94): Show | 99 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.1497+3852C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21209885 | ||||||
| chr12:21210026
|
G | A | 2 | a0006c0014t0001g0298a0006c0014t0001g0309 | 2 | HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1497+3993G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210026 | ||||||
| chr12:21210034
|
T | C | 85 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0080others(82): Show | 87 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.1497+4001T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210034 | ||||||
| chr12:21210043
|
T | C | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1497+4010T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210043 | ||||||
| chr12:21210087
|
T | G | 96 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(93): Show | 98 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1497+4054T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210087 | ||||||
| chr12:21210107
|
T | C | 96 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(93): Show | 98 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1497+4074T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210107 | ||||||
| chr12:21210125
|
T | G | 7 | a0001c0001t0002g0285a0001c0023t0001g0088a0006c0010t0001g0262others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1497+4092T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210125 | ||||||
| chr12:21210134
|
C | A | 1 | a0001c0023t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1497+4101C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210134 | ||||||
| chr12:21210175
|
G | C | 95 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(92): Show | 97 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.1497+4142G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210175 | ||||||
| chr12:21210199
|
C | T | 1 | a0007c0019t0002g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1497+4166C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210199 | ||||||
| chr12:21210218
|
T | A | 4 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(1): Show | 4 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1497+4185T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210218 | ||||||
| chr12:21210221
|
T | C | 1 | a0001c0003t0002g0187 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1497+4188T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210221 | ||||||
| chr12:21210245
|
A | C | 1 | a0001c0001t0001g0283 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1497+4212A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210245 | ||||||
| chr12:21210292
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1497+4259C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210292 | ||||||
| chr12:21210299
|
C | G | 120 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1497+4266C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210299 | ||||||
| chr12:21210341
|
C | T | 1 | a0002c0005t0002g0011 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1497+4308C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210341 | ||||||
| chr12:21210377
|
C | T | 2 | a0005c0009t0002g0083a0005c0009t0002g0084 | 2 | HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1497+4344C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210377 | ||||||
| chr12:21210381
|
A | G | 7 | a0001c0001t0002g0285a0001c0023t0001g0088a0006c0010t0001g0262others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1497+4348A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210381 | ||||||
| chr12:21210421
|
C | T | 1 | a0002c0002t0001g0173 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1497+4388C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210421 | ||||||
| chr12:21210424
|
T | C | 2 | a0001c0003t0001g0259a0001c0003t0001g0274 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1497+4391T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210424 | ||||||
| chr12:21210442
|
A | G | 81 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0104others(78): Show | 83 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.1497+4409A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210442 | ||||||
| chr12:21210492
|
GTGA | G | 204 | a0001c0001t0001g0002a0001c0001t0001g0079a0001c0001t0001g0104others(201): Show | 208 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(205): Show |
intron_variant | MODIFIER | c.1497+4465_1497+446 others(7): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 21210492 | |||||
| chr12:21210539
|
G | A | 17 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(14): Show | 17 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.1497+4506G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210539 | ||||||
| chr12:21210543
|
T | C | 211 | a0001c0001t0001g0002a0001c0001t0001g0079a0001c0001t0001g0104others(208): Show | 215 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.1497+4510T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210543 | ||||||
| chr12:21210672
|
T | C | 1 | a0001c0001t0002g0080 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1497+4639T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210672 | ||||||
| chr12:21210683
|
T | C | 1 | a0002c0002t0001g0210 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1497+4650T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210683 | ||||||
| chr12:21210685
|
C | T | 1 | a0004c0006t0001g0028 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1497+4652C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210685 | ||||||
| chr12:21210701
|
G | A | 4 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(1): Show | 4 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1497+4668G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210701 | ||||||
| chr12:21210718
|
T | C | 1 | a0001c0001t0002g0310 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1497+4685T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210718 | ||||||
| chr12:21210778
|
C | T | 4 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG00438.hp1 NA18950.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.1497+4745C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210778 | ||||||
| chr12:21210779
|
G | C | 108 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(105): Show | 110 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.1497+4746G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210779 | ||||||
| chr12:21210816
|
A | G | 1 | a0012c0026t0003g0045 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1497+4783A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210816 | ||||||
| chr12:21210932
|
G | T | 50 | a0001c0001t0001g0079a0001c0001t0003g0026a0001c0001t0003g0031others(47): Show | 50 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1497+4899G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210932 | ||||||
| chr12:21210966
|
A | C | 17 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(14): Show | 17 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.1497+4933A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210966 | ||||||
| chr12:21210967
|
C | T | 17 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(14): Show | 17 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.1497+4934C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210967 | ||||||
| chr12:21210968
|
A | G | 17 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(14): Show | 17 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.1497+4935A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21210968 | ||||||
| chr12:21211046
|
A | C | 1 | a0002c0005t0001g0253 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1497+5013A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21211046 | ||||||
| chr12:21211140
|
G | A | 1 | a0001c0001t0002g0285 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1497+5107G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21211140 | ||||||
| chr12:21211149
|
C | T | 62 | a0001c0001t0002g0141a0001c0003t0002g0005a0001c0003t0002g0018others(59): Show | 63 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.1497+5116C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21211149 | ||||||
| chr12:21211168
|
G | T | 6 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0135others(3): Show | 6 | HG00438.hp1 HG03669.hp2 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.1497+5135G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21211168 | ||||||
| chr12:21211230
|
G | A | 1 | a0002c0002t0001g0203 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1497+5197G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21211230 | ||||||
| chr12:21211355
|
G | T | 95 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(92): Show | 97 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.1497+5322G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21211355 | ||||||
| chr12:21211374
|
T | C | 2 | a0004c0006t0001g0028a0004c0006t0001g0029 | 2 | HG00280.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.1497+5341T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21211374 | ||||||
| chr12:21211531
|
T | C | 79 | a0001c0001t0001g0002a0001c0001t0001g0104a0001c0001t0001g0113others(76): Show | 81 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.1497+5498T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21211531 | ||||||
| chr12:21211546
|
G | A | 3 | a0002c0002t0002g0007a0002c0002t0002g0239a0002c0002t0010g0238 | 3 | NA18975.hp2 NA18999.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1497+5513G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21211546 | ||||||
| chr12:21211613
|
C | T | 8 | a0001c0003t0001g0284a0002c0002t0001g0268a0002c0002t0001g0269others(5): Show | 8 | HG01891.hp1 HG02258.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1498-5506C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21211613 | ||||||
| chr12:21211655
|
C | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(3): Show | 6 | HG02723.hp2 HG03195.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1498-5464C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21211655 | ||||||
| chr12:21211694
|
AC | A | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1498-5424delC | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21211694 | ||||||
| chr12:21211738
|
A | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0104a0001c0001t0001g0113others(76): Show | 81 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.1498-5381A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21211738 | ||||||
| chr12:21211788
|
C | G | 7 | a0001c0001t0002g0285a0001c0023t0001g0088a0006c0010t0001g0262others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1498-5331C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21211788 | ||||||
| chr12:21211814
|
A | C | 1 | a0001c0001t0002g0285 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1498-5305A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21211814 | ||||||
| chr12:21211825
|
C | G | 7 | a0001c0001t0002g0285a0001c0023t0001g0088a0006c0010t0001g0262others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1498-5294C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21211825 | ||||||
| chr12:21211898
|
G | A | 31 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(28): Show | 31 | HG00099.hp2 HG00438.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.1498-5221G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21211898 | ||||||
| chr12:21211919
|
G | A | 120 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1498-5200G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21211919 | ||||||
| chr12:21211938
|
A | T | 1 | a0001c0001t0002g0249 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1498-5181A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21211938 | ||||||
| chr12:21211976
|
C | T | 102 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(99): Show | 104 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.1498-5143C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21211976 | ||||||
| chr12:21211977
|
G | A | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1498-5142G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21211977 | ||||||
| chr12:21211978
|
G | A | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1498-5141G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21211978 | ||||||
| chr12:21212039
|
GT | G | 7 | a0001c0001t0002g0285a0001c0023t0001g0088a0006c0010t0001g0262others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1498-5071delT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 21212039 | |||||
| chr12:21212040
|
T | G | 112 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(109): Show | 114 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.1498-5079T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212040 | ||||||
| chr12:21212041
|
T | G | 7 | a0001c0001t0002g0285a0001c0023t0001g0088a0006c0010t0001g0262others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1498-5078T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212041 | ||||||
| chr12:21212128
|
C | A | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1498-4991C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212128 | ||||||
| chr12:21212147
|
T | G | 5 | a0001c0001t0003g0067a0001c0003t0001g0085a0002c0002t0002g0009others(2): Show | 5 | HG02055.hp2 NA18971.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498-4972T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212147 | ||||||
| chr12:21212158
|
G | C | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1498-4961G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212158 | ||||||
| chr12:21212188
|
C | T | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1498-4931C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212188 | ||||||
| chr12:21212194
|
G | A | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1498-4925G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212194 | ||||||
| chr12:21212203
|
T | A | 96 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(93): Show | 98 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1498-4916T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212203 | ||||||
| chr12:21212260
|
C | T | 205 | a0001c0001t0001g0002a0001c0001t0001g0079a0001c0001t0001g0104others(202): Show | 209 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.1498-4859C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212260 | ||||||
| chr12:21212328
|
A | T | 1 | a0002c0002t0001g0173 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1498-4791A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212328 | ||||||
| chr12:21212338
|
G | C | 96 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(93): Show | 98 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1498-4781G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212338 | ||||||
| chr12:21212370
|
G | A | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1498-4749G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212370 | ||||||
| chr12:21212386
|
C | A | 91 | a0001c0001t0001g0002a0001c0001t0001g0104a0001c0001t0001g0113others(88): Show | 93 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.1498-4733C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212386 | ||||||
| chr12:21212400
|
C | G | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1498-4719C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212400 | ||||||
| chr12:21212455
|
C | A | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1498-4664C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212455 | ||||||
| chr12:21212462
|
C | T | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1498-4657C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212462 | ||||||
| chr12:21212494
|
A | T | 2 | a0004c0006t0001g0028a0004c0006t0001g0029 | 2 | HG00280.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.1498-4625A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212494 | ||||||
| chr12:21212495
|
G | A | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1498-4624G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212495 | ||||||
| chr12:21212516
|
G | A | 29 | a0001c0001t0001g0283a0001c0003t0001g0193a0002c0002t0001g0004others(26): Show | 30 | HG00099.hp1 HG00280.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.1498-4603G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212516 | ||||||
| chr12:21212536
|
T | G | 12 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(9): Show | 12 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1498-4583T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212536 | ||||||
| chr12:21212557
|
A | G | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1498-4562A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212557 | ||||||
| chr12:21212581
|
C | T | 1 | a0001c0003t0002g0005 | 2 | HG00735.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1498-4538C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212581 | ||||||
| chr12:21212635
|
C | T | 79 | a0001c0001t0001g0002a0001c0001t0001g0104a0001c0001t0001g0113others(76): Show | 81 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.1498-4484C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212635 | ||||||
| chr12:21212636
|
A | G | 304 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(301): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1498-4483A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212636 | ||||||
| chr12:21212720
|
A | C | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1498-4399A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212720 | ||||||
| chr12:21212728
|
C | T | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1498-4391C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212728 | ||||||
| chr12:21212740
|
T | G | 8 | a0001c0001t0002g0285a0001c0003t0001g0085a0001c0023t0001g0088others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1498-4379T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212740 | ||||||
| chr12:21212750
|
G | C | 7 | a0001c0001t0002g0285a0001c0023t0001g0088a0006c0010t0001g0262others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1498-4369G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212750 | ||||||
| chr12:21212760
|
C | T | 95 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(92): Show | 97 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.1498-4359C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212760 | ||||||
| chr12:21212850
|
T | G | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1498-4269T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212850 | ||||||
| chr12:21212891
|
A | G | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1498-4228A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212891 | ||||||
| chr12:21212892
|
A | C | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1498-4227A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212892 | ||||||
| chr12:21212929
|
C | T | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1498-4190C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212929 | ||||||
| chr12:21212950
|
A | T | 80 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0104others(77): Show | 82 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.1498-4169A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212950 | ||||||
| chr12:21212966
|
G | A | 2 | a0006c0014t0001g0298a0006c0014t0001g0309 | 2 | HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1498-4153G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212966 | ||||||
| chr12:21212977
|
C | A | 1 | a0002c0005t0002g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1498-4142C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212977 | ||||||
| chr12:21212977
|
C | T | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1498-4142C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21212977 | ||||||
| chr12:21213102
|
T | C | 2 | a0006c0014t0001g0298a0006c0014t0001g0309 | 2 | HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1498-4017T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213102 | ||||||
| chr12:21213104
|
T | A | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1498-4015T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213104 | ||||||
| chr12:21213132
|
T | G | 2 | a0001c0001t0002g0285a0001c0003t0001g0085 | 2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1498-3987T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213132 | ||||||
| chr12:21213141
|
C | T | 121 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(118): Show | 123 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.1498-3978C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213141 | ||||||
| chr12:21213160
|
T | C | 207 | a0001c0001t0001g0002a0001c0001t0001g0079a0001c0001t0001g0082others(204): Show | 211 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.1498-3959T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213160 | ||||||
| chr12:21213161
|
G | A | 12 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(9): Show | 12 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1498-3958G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213161 | ||||||
| chr12:21213193
|
T | C | 9 | a0001c0003t0001g0085a0001c0023t0001g0088a0004c0006t0001g0028others(6): Show | 9 | HG00280.hp1 HG01168.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1498-3926T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213193 | ||||||
| chr12:21213204
|
A | G | 3 | a0001c0003t0001g0085a0006c0014t0001g0298a0006c0014t0001g0309 | 3 | HG01891.hp1 HG02055.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1498-3915A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213204 | ||||||
| chr12:21213226
|
C | T | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1498-3893C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213226 | ||||||
| chr12:21213249
|
G | A | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1498-3870G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213249 | ||||||
| chr12:21213269
|
G | A | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1498-3850G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213269 | ||||||
| chr12:21213293
|
G | T | 1 | a0001c0003t0002g0176 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1498-3826G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213293 | ||||||
| chr12:21213299
|
T | G | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1498-3820T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213299 | ||||||
| chr12:21213316
|
G | A | 81 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0104others(78): Show | 83 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.1498-3803G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213316 | ||||||
| chr12:21213367
|
G | T | 2 | a0001c0001t0002g0310a0001c0003t0001g0085 | 2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1498-3752G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213367 | ||||||
| chr12:21213408
|
C | T | 1 | a0004c0006t0001g0078 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1498-3711C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213408 | ||||||
| chr12:21213411
|
A | G | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1498-3708A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213411 | ||||||
| chr12:21213424
|
C | T | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1498-3695C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213424 | ||||||
| chr12:21213425
|
G | A | 1 | a0001c0001t0002g0285 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1498-3694G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213425 | ||||||
| chr12:21213433
|
C | A | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1498-3686C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213433 | ||||||
| chr12:21213470
|
C | T | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1498-3649C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213470 | ||||||
| chr12:21213495
|
A | G | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1498-3624A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213495 | ||||||
| chr12:21213527
|
C | G | 1 | a0013c0021t0002g0232 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1498-3592C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213527 | ||||||
| chr12:21213560
|
A | G | 121 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(118): Show | 123 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.1498-3559A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213560 | ||||||
| chr12:21213578
|
A | G | 1 | a0001c0003t0002g0302 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1498-3541A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213578 | ||||||
| chr12:21213604
|
G | A | 6 | a0004c0006t0001g0028a0004c0006t0001g0029a0004c0006t0001g0078others(3): Show | 6 | HG00280.hp1 HG00642.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.1498-3515G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213604 | ||||||
| chr12:21213624
|
T | C | 1 | a0001c0001t0002g0285 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1498-3495T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213624 | ||||||
| chr12:21213634
|
C | G | 2 | a0006c0014t0001g0298a0006c0014t0001g0309 | 2 | HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1498-3485C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213634 | ||||||
| chr12:21213710
|
C | T | 4 | a0001c0003t0001g0284a0001c0003t0002g0273a0002c0002t0001g0268others(1): Show | 4 | HG02083.hp1 HG02615.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1498-3409C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213710 | ||||||
| chr12:21213760
|
G | A | 1 | a0002c0002t0001g0197 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1498-3359G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213760 | ||||||
| chr12:21213826
|
T | C | 97 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(94): Show | 99 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.1498-3293T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213826 | ||||||
| chr12:21213853
|
G | A | 2 | a0001c0003t0002g0145a0007c0019t0002g0124 | 2 | HG02559.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1498-3266G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213853 | ||||||
| chr12:21213853
|
G | C | 1 | a0002c0002t0002g0092 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1498-3266G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213853 | ||||||
| chr12:21213894
|
G | A | 7 | a0001c0001t0002g0285a0001c0023t0001g0088a0006c0010t0001g0262others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1498-3225G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213894 | ||||||
| chr12:21213902
|
G | T | 16 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(13): Show | 16 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.1498-3217G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213902 | ||||||
| chr12:21213914
|
A | G | 5 | a0001c0001t0002g0248a0001c0001t0002g0310a0001c0003t0002g0250others(2): Show | 5 | HG02145.hp2 HG02615.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498-3205A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213914 | ||||||
| chr12:21213929
|
C | T | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1498-3190C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21213929 | ||||||
| chr12:21214012
|
G | A | 1 | a0001c0001t0003g0048 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1498-3107G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214012 | ||||||
| chr12:21214036
|
T | C | 10 | a0001c0001t0002g0014a0001c0001t0002g0251a0001c0003t0002g0110others(7): Show | 10 | HG02055.hp1 HG02559.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1498-3083T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214036 | ||||||
| chr12:21214062
|
C | T | 2 | a0010c0012t0001g0155a0010c0012t0001g0189 | 2 | NA18990.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1498-3057C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214062 | ||||||
| chr12:21214063
|
G | A | 9 | a0004c0006t0001g0028a0004c0006t0001g0029a0004c0006t0001g0078others(6): Show | 9 | HG00280.hp1 HG00642.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.1498-3056G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214063 | ||||||
| chr12:21214113
|
A | G | 207 | a0001c0001t0001g0002a0001c0001t0001g0079a0001c0001t0001g0082others(204): Show | 211 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.1498-3006A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214113 | ||||||
| chr12:21214197
|
G | C | 1 | a0002c0002t0001g0172 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1498-2922G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214197 | ||||||
| chr12:21214239
|
C | T | 13 | a0001c0001t0002g0285a0001c0023t0001g0088a0004c0006t0001g0028others(10): Show | 13 | HG00280.hp1 HG00642.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.1498-2880C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214239 | ||||||
| chr12:21214252
|
G | C | 1 | a0002c0002t0007g0150 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1498-2867G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214252 | ||||||
| chr12:21214267
|
T | C | 1 | a0002c0002t0001g0100 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1498-2852T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214267 | ||||||
| chr12:21214274
|
T | C | 1 | a0001c0023t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1498-2845T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214274 | ||||||
| chr12:21214311
|
A | G | 1 | a0002c0005t0001g0301 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1498-2808A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214311 | ||||||
| chr12:21214318
|
G | A | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1498-2801G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214318 | ||||||
| chr12:21214321
|
G | C | 1 | a0002c0002t0001g0154 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1498-2798G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214321 | ||||||
| chr12:21214351
|
C | G | 18 | a0001c0001t0002g0010a0001c0001t0002g0080a0001c0001t0002g0111others(15): Show | 18 | HG00673.hp1 HG01168.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1498-2768C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214351 | ||||||
| chr12:21214352
|
G | GC | 7 | a0001c0001t0002g0285a0001c0023t0001g0088a0006c0010t0001g0262others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1498-2767_1498-276 others(5): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214352 | ||||||
| chr12:21214358
|
C | A | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1498-2761C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214358 | ||||||
| chr12:21214378
|
G | A | 1 | a0003c0004t0002g0260 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1498-2741G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214378 | ||||||
| chr12:21214397
|
C | T | 4 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(1): Show | 4 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1498-2722C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214397 | ||||||
| chr12:21214411
|
G | C | 194 | a0001c0001t0001g0002a0001c0001t0001g0079a0001c0001t0001g0082others(191): Show | 198 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.1498-2708G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214411 | ||||||
| chr12:21214441
|
C | T | 120 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1498-2678C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214441 | ||||||
| chr12:21214448
|
A | C | 93 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(90): Show | 95 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.1498-2671A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214448 | ||||||
| chr12:21214547
|
C | T | 12 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(9): Show | 12 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1498-2572C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214547 | ||||||
| chr12:21214561
|
A | C | 1 | a0003c0004t0002g0027 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1498-2558A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214561 | ||||||
| chr12:21214570
|
T | G | 6 | a0004c0006t0001g0028a0004c0006t0001g0029a0004c0006t0001g0078others(3): Show | 6 | HG00280.hp1 HG00642.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.1498-2549T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214570 | ||||||
| chr12:21214577
|
T | C | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1498-2542T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214577 | ||||||
| chr12:21214582
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1498-2537G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214582 | ||||||
| chr12:21214587
|
C | T | 3 | a0005c0009t0002g0083a0005c0009t0002g0084a0005c0009t0002g0109 | 3 | HG02922.hp1 HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1498-2532C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214587 | ||||||
| chr12:21214604
|
C | A | 1 | a0001c0001t0003g0075 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1498-2515C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214604 | ||||||
| chr12:21214605
|
A | C | 1 | a0001c0001t0003g0075 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1498-2514A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214605 | ||||||
| chr12:21214606
|
G | A | 1 | a0001c0001t0003g0075 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1498-2513G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214606 | ||||||
| chr12:21214609
|
C | T | 120 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1498-2510C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214609 | ||||||
| chr12:21214615
|
GT | G | 120 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1498-2499delT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 21214615 | |||||
| chr12:21214620
|
T | A | 120 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1498-2499T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214620 | ||||||
| chr12:21214665
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1498-2454G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214665 | ||||||
| chr12:21214666
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1498-2453C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214666 | ||||||
| chr12:21214699
|
G | A | 95 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(92): Show | 97 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.1498-2420G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214699 | ||||||
| chr12:21214858
|
G | C | 7 | a0001c0001t0002g0285a0001c0023t0001g0088a0006c0010t0001g0262others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1498-2261G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214858 | ||||||
| chr12:21214859
|
G | A | 7 | a0001c0001t0002g0285a0001c0023t0001g0088a0006c0010t0001g0262others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1498-2260G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214859 | ||||||
| chr12:21214895
|
C | T | 120 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1498-2224C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214895 | ||||||
| chr12:21214896
|
C | G | 203 | a0001c0001t0001g0079a0001c0001t0001g0311a0001c0001t0002g0010others(200): Show | 206 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.1498-2223C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214896 | ||||||
| chr12:21214934
|
C | T | 3 | a0001c0003t0002g0211a0001c0003t0002g0213a0001c0003t0002g0214 | 3 | HG00673.hp1 NA18983.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1498-2185C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214934 | ||||||
| chr12:21214935
|
G | A | 7 | a0001c0001t0002g0285a0001c0023t0001g0088a0006c0010t0001g0262others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1498-2184G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214935 | ||||||
| chr12:21214987
|
C | G | 7 | a0001c0001t0002g0285a0001c0023t0001g0088a0006c0010t0001g0262others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1498-2132C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21214987 | ||||||
| chr12:21215019
|
G | A | 1 | a0002c0002t0001g0100 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1498-2100G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21215019 | ||||||
| chr12:21215070
|
G | A | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1498-2049G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21215070 | ||||||
| chr12:21215080
|
G | C | 1 | a0013c0021t0002g0232 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1498-2039G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21215080 | ||||||
| chr12:21215081
|
C | T | 96 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(93): Show | 98 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1498-2038C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21215081 | ||||||
| chr12:21215106
|
A | G | 1 | a0005c0007t0004g0180 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1498-2013A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21215106 | ||||||
| chr12:21215137
|
G | T | 1 | a0001c0001t0003g0070 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1498-1982G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21215137 | ||||||
| chr12:21215272
|
G | A | 1 | a0001c0023t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1498-1847G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21215272 | ||||||
| chr12:21215354
|
C | T | 2 | a0002c0002t0001g0152a0002c0002t0001g0153 | 2 | HG01261.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1498-1765C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21215354 | ||||||
| chr12:21215356
|
A | G | 2 | a0001c0003t0002g0302a0002c0002t0002g0200 | 2 | HG00741.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.1498-1763A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21215356 | ||||||
| chr12:21215356
|
A | T | 2 | a0001c0003t0002g0289a0001c0003t0002g0293 | 2 | NA18948.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1498-1763A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21215356 | ||||||
| chr12:21215426
|
G | T | 120 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1498-1693G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21215426 | ||||||
| chr12:21215466
|
G | C | 51 | a0001c0001t0001g0079a0001c0001t0003g0026a0001c0001t0003g0031others(48): Show | 51 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.1498-1653G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21215466 | ||||||
| chr12:21215489
|
G | A | 5 | a0001c0001t0002g0248a0001c0001t0002g0310a0001c0003t0002g0250others(2): Show | 5 | HG02145.hp2 HG02615.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498-1630G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21215489 | ||||||
| chr12:21215604
|
C | CCTATATG others(3): Show |
1 | a0002c0005t0001g0253 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1498-1508_1498-149 others(14): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 21215604 | |||||
| chr12:21215779
|
A | G | 1 | a0017c0017t0001g0219 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1498-1340A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21215779 | ||||||
| chr12:21215788
|
T | C | 95 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(92): Show | 97 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.1498-1331T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21215788 | ||||||
| chr12:21215863
|
T | A | 25 | a0001c0003t0002g0273a0002c0002t0002g0191a0003c0004t0002g0001others(22): Show | 27 | HG00609.hp1 HG01081.hp2 HG01258.hp2 others(24): Show |
intron_variant | MODIFIER | c.1498-1256T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21215863 | ||||||
| chr12:21215928
|
G | A | 5 | a0006c0010t0001g0262a0006c0010t0001g0263a0006c0010t0001g0264others(2): Show | 5 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1498-1191G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21215928 | ||||||
| chr12:21216031
|
G | C | 1 | a0001c0001t0009g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1498-1088G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21216031 | ||||||
| chr12:21216056
|
G | A | 7 | a0001c0001t0002g0285a0001c0023t0001g0088a0006c0010t0001g0262others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1498-1063G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21216056 | ||||||
| chr12:21216056
|
G | C | 298 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(295): Show | 303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.1498-1063G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21216056 | ||||||
| chr12:21216115
|
A | G | 1 | a0001c0001t0002g0120 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1498-1004A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21216115 | ||||||
| chr12:21216257
|
T | C | 65 | a0001c0001t0002g0141a0001c0003t0002g0005a0001c0003t0002g0018others(62): Show | 66 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.1498-862T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21216257 | ||||||
| chr12:21216318
|
G | C | 2 | a0001c0003t0002g0295a0001c0003t0002g0308 | 2 | NA18981.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1498-801G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21216318 | ||||||
| chr12:21216392
|
G | C | 214 | a0001c0001t0001g0002a0001c0001t0001g0079a0001c0001t0001g0104others(211): Show | 218 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(215): Show |
intron_variant | MODIFIER | c.1498-727G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21216392 | ||||||
| chr12:21216405
|
T | G | 1 | a0001c0001t0002g0285 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1498-714T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21216405 | ||||||
| chr12:21216492
|
A | G | 1 | a0001c0001t0001g0311 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1498-627A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21216492 | ||||||
| chr12:21216578
|
C | A | 2 | a0001c0001t0003g0026a0001c0001t0003g0056 | 2 | HG02083.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1498-541C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21216578 | ||||||
| chr12:21216626
|
C | T | 12 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(9): Show | 12 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1498-493C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21216626 | ||||||
| chr12:21216851
|
G | A | 1 | a0001c0023t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1498-268G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21216851 | ||||||
| chr12:21216949
|
C | G | 101 | a0001c0001t0001g0002a0001c0001t0001g0104a0001c0001t0001g0113others(98): Show | 103 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1498-170C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21216949 | ||||||
| chr12:21217030
|
T | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0104a0001c0001t0001g0113others(91): Show | 96 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.1498-89T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21217030 | ||||||
| chr12:21217041
|
TA | T | 96 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(93): Show | 98 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1498-75delA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 21217041 | |||||
| chr12:21217051
|
G | A | 74 | a0001c0001t0001g0002a0001c0001t0001g0104a0001c0001t0001g0113others(71): Show | 76 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.1498-68G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 11/14 | chr12 | 21217051 | ||||||
| chr12:21217581
|
C | T | 1 | a0002c0005t0001g0086 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1682+278C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21217581 | ||||||
| chr12:21217607
|
T | G | 1 | a0001c0001t0002g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1682+304T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21217607 | ||||||
| chr12:21217745
|
C | T | 64 | a0001c0001t0001g0283a0001c0003t0001g0193a0001c0003t0001g0296others(61): Show | 65 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.1682+442C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21217745 | ||||||
| chr12:21217748
|
C | T | 113 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(110): Show | 115 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.1682+445C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21217748 | ||||||
| chr12:21217750
|
C | A | 113 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(110): Show | 115 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.1682+447C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21217750 | ||||||
| chr12:21217966
|
G | A | 14 | a0001c0020t0001g0282a0004c0006t0001g0028a0004c0006t0001g0029others(11): Show | 14 | HG00280.hp1 HG00642.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.1682+663G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21217966 | ||||||
| chr12:21217970
|
T | C | 1 | a0005c0007t0004g0095 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1682+667T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21217970 | ||||||
| chr12:21218089
|
A | T | 7 | a0001c0001t0002g0285a0001c0023t0001g0088a0006c0010t0001g0262others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1682+786A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21218089 | ||||||
| chr12:21218141
|
G | A | 17 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(14): Show | 17 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.1682+838G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21218141 | ||||||
| chr12:21218155
|
C | A | 1 | a0002c0005t0002g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1682+852C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21218155 | ||||||
| chr12:21218210
|
T | C | 113 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(110): Show | 115 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.1682+907T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21218210 | ||||||
| chr12:21218254
|
A | G | 2 | a0001c0001t0003g0053a0001c0001t0003g0070 | 2 | HG00423.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1682+951A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21218254 | ||||||
| chr12:21218462
|
G | GA | 119 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(116): Show | 121 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.1682+1169dupA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 21218462 | |||||
| chr12:21218604
|
A | G | 2 | a0001c0003t0002g0302a0002c0002t0002g0200 | 2 | HG00741.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.1682+1301A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21218604 | ||||||
| chr12:21218609
|
ATGT | A | 96 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(93): Show | 98 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1682+1310_1682+131 others(7): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 21218609 | |||||
| chr12:21218658
|
C | T | 1 | a0001c0001t0009g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1682+1355C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21218658 | ||||||
| chr12:21218739
|
A | T | 14 | a0001c0020t0001g0282a0004c0006t0001g0028a0004c0006t0001g0029others(11): Show | 14 | HG00280.hp1 HG00642.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.1682+1436A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21218739 | ||||||
| chr12:21218923
|
T | C | 1 | a0001c0001t0003g0061 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1682+1620T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21218923 | ||||||
| chr12:21219195
|
C | G | 199 | a0001c0001t0001g0079a0001c0001t0001g0311a0001c0001t0002g0010others(196): Show | 202 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.1682+1892C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21219195 | ||||||
| chr12:21219251
|
G | A | 3 | a0001c0003t0005g0286a0001c0003t0005g0292a0001c0003t0005g0307 | 3 | NA18991.hp1 NA18993.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1682+1948G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21219251 | ||||||
| chr12:21219290
|
A | G | 17 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(14): Show | 17 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.1682+1987A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21219290 | ||||||
| chr12:21219316
|
GC | G | 3 | a0002c0002t0002g0009a0002c0002t0003g0008a0002c0002t0003g0237 | 3 | NA18999.hp1 NA19066.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1682+2014delC | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21219316 | ||||||
| chr12:21219410
|
A | G | 17 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(14): Show | 17 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.1682+2107A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21219410 | ||||||
| chr12:21219701
|
TAAATG | T | 51 | a0001c0001t0001g0079a0001c0001t0003g0026a0001c0001t0003g0031others(48): Show | 51 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.1682+2405_1682+240 others(9): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 21219701 | |||||
| chr12:21219720
|
A | G | 1 | a0001c0001t0003g0134 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1682+2417A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21219720 | ||||||
| chr12:21219732
|
G | C | 7 | a0001c0001t0002g0285a0001c0023t0001g0088a0006c0010t0001g0262others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1682+2429G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21219732 | ||||||
| chr12:21219795
|
C | G | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1682+2492C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21219795 | ||||||
| chr12:21219795
|
C | T | 1 | a0018c0016t0001g0185 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1682+2492C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21219795 | ||||||
| chr12:21219818
|
T | C | 1 | a0001c0001t0001g0311 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1683-2482T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21219818 | ||||||
| chr12:21219841
|
AC | A | 206 | a0001c0001t0001g0079a0001c0001t0001g0311a0001c0001t0002g0010others(203): Show | 209 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.1683-2456delC | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 21219841 | |||||
| chr12:21219847
|
C | T | 7 | a0001c0001t0002g0285a0001c0023t0001g0088a0006c0010t0001g0262others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1683-2453C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21219847 | ||||||
| chr12:21219848
|
G | A | 72 | a0001c0001t0001g0311a0001c0001t0002g0141a0001c0001t0002g0248others(69): Show | 73 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1683-2452G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21219848 | ||||||
| chr12:21219856
|
G | A | 1 | a0001c0001t0003g0103 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1683-2444G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21219856 | ||||||
| chr12:21219864
|
C | T | 1 | a0001c0003t0002g0158 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1683-2436C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21219864 | ||||||
| chr12:21219925
|
C | T | 1 | a0001c0023t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1683-2375C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21219925 | ||||||
| chr12:21219936
|
A | T | 1 | a0001c0003t0002g0223 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1683-2364A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21219936 | ||||||
| chr12:21219950
|
C | G | 113 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(110): Show | 115 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.1683-2350C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21219950 | ||||||
| chr12:21220024
|
G | A | 3 | a0002c0002t0007g0148a0002c0002t0007g0149a0002c0002t0007g0150 | 3 | HG00609.hp2 NA18943.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1683-2276G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21220024 | ||||||
| chr12:21220124
|
A | G | 1 | a0001c0001t0002g0285 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1683-2176A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21220124 | ||||||
| chr12:21220167
|
G | A | 1 | a0002c0005t0001g0257 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1683-2133G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21220167 | ||||||
| chr12:21220360
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1683-1940A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21220360 | ||||||
| chr12:21220679
|
A | G | 3 | a0001c0001t0003g0131a0001c0001t0003g0132a0001c0001t0003g0133 | 3 | NA18942.hp1 NA18959.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1683-1621A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21220679 | ||||||
| chr12:21220772
|
C | T | 1 | a0001c0003t0005g0292 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1683-1528C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21220772 | ||||||
| chr12:21220815
|
T | TA | 25 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(22): Show | 25 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.1683-1470dupA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 21220815 | |||||
| chr12:21220815
|
T | TAA | 72 | a0001c0001t0001g0113a0001c0001t0001g0311a0001c0001t0002g0141others(69): Show | 73 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1683-1471_1683-147 others(6): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 21220815 | |||||
| chr12:21220815
|
TAAAAAAA others(4): Show |
T | 1 | a0001c0001t0002g0285 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1683-1480_1683-147 others(15): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 21220815 | |||||
| chr12:21220826
|
A | AG | 96 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(93): Show | 98 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1683-1474_1683-147 others(5): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21220826 | ||||||
| chr12:21220881
|
C | T | 113 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(110): Show | 115 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.1683-1419C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21220881 | ||||||
| chr12:21220938
|
T | C | 5 | a0006c0010t0001g0262a0006c0010t0001g0263a0006c0010t0001g0264others(2): Show | 5 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1683-1362T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21220938 | ||||||
| chr12:21220981
|
T | C | 113 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(110): Show | 115 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.1683-1319T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21220981 | ||||||
| chr12:21221009
|
T | A | 120 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1683-1291T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21221009 | ||||||
| chr12:21221087
|
GA | G | 120 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1683-1208delA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 21221087 | |||||
| chr12:21221252
|
A | G | 5 | a0001c0001t0002g0248a0001c0001t0002g0310a0001c0003t0002g0250others(2): Show | 5 | HG02145.hp2 HG02615.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1683-1048A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21221252 | ||||||
| chr12:21221275
|
T | C | 120 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1683-1025T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21221275 | ||||||
| chr12:21221285
|
G | C | 17 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(14): Show | 17 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.1683-1015G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21221285 | ||||||
| chr12:21221300
|
A | T | 113 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(110): Show | 115 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.1683-1000A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21221300 | ||||||
| chr12:21221316
|
A | G | 1 | a0001c0001t0003g0048 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1683-984A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21221316 | ||||||
| chr12:21221351
|
T | C | 8 | a0001c0020t0001g0282a0004c0006t0001g0081a0004c0006t0001g0127others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1683-949T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21221351 | ||||||
| chr12:21221379
|
T | C | 2 | a0001c0003t0002g0266a0002c0005t0002g0011 | 2 | HG02895.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1683-921T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21221379 | ||||||
| chr12:21221530
|
C | T | 12 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(9): Show | 12 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1683-770C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21221530 | ||||||
| chr12:21221604
|
C | T | 199 | a0001c0001t0001g0079a0001c0001t0001g0311a0001c0001t0002g0010others(196): Show | 202 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.1683-696C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21221604 | ||||||
| chr12:21221669
|
C | G | 17 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(14): Show | 17 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.1683-631C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21221669 | ||||||
| chr12:21221732
|
C | T | 120 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1683-568C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21221732 | ||||||
| chr12:21221904
|
A | G | 205 | a0001c0001t0001g0079a0001c0001t0001g0311a0001c0001t0002g0010others(202): Show | 208 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(205): Show |
intron_variant | MODIFIER | c.1683-396A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21221904 | ||||||
| chr12:21222013
|
A | G | 1 | a0002c0005t0002g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1683-287A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21222013 | ||||||
| chr12:21222127
|
T | A | 17 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(14): Show | 17 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.1683-173T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21222127 | ||||||
| chr12:21222129
|
G | C | 22 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(19): Show | 22 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.1683-171G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21222129 | ||||||
| chr12:21222189
|
C | T | 4 | a0003c0004t0002g0001a0003c0004t0002g0041a0003c0004t0002g0042others(1): Show | 5 | NA18965.hp2 NA18988.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.1683-111C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21222189 | ||||||
| chr12:21222225
|
A | G | 5 | a0001c0001t0002g0248a0001c0001t0002g0310a0001c0003t0002g0250others(2): Show | 5 | HG02145.hp2 HG02615.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1683-75A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 12/14 | chr12 | 21222225 | ||||||
| chr12:21222372
|
G | GA | 24 | a0001c0001t0001g0121a0001c0001t0001g0130a0001c0001t0001g0135others(21): Show | 24 | HG00438.hp1 HG01175.hp1 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.1747+34dupA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222372 | |||||
| chr12:21222372
|
G | GAA | 11 | a0001c0001t0001g0012a0001c0001t0001g0104a0001c0001t0001g0113others(8): Show | 11 | HG02109.hp1 HG02258.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1747+33_1747+34dup others(2): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222372 | |||||
| chr12:21222372
|
G | GAAA | 10 | a0001c0001t0001g0082a0001c0001t0001g0118a0001c0001t0001g0267others(7): Show | 10 | HG01167.hp1 HG01168.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1747+32_1747+34dup others(3): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222372 | |||||
| chr12:21222373
|
A | G | 4 | a0004c0006t0001g0028a0004c0006t0001g0233a0004c0006t0001g0234others(1): Show | 4 | HG00280.hp1 HG00642.hp1 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.1747+9A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222373 | ||||||
| chr12:21222391
|
A | C | 1 | a0002c0002t0001g0227 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1747+27A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222391 | ||||||
| chr12:21222391
|
AAAAAAAA others(11): Show |
A | 1 | a0001c0003t0002g0242 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1747+29_1747+46del others(18): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222391 | |||||
| chr12:21222393
|
A | AATATATA others(3): Show |
1 | a0001c0001t0003g0064 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1747+30_1747+31ins others(10): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222393 | |||||
| chr12:21222393
|
A | ATATAT | 4 | a0001c0001t0001g0079a0001c0001t0003g0060a0001c0001t0003g0072others(1): Show | 4 | HG02071.hp2 NA18951.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1747+29_1747+30ins others(5): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222393 | ||||||
| chr12:21222393
|
A | T | 2 | a0001c0001t0003g0051a0001c0001t0003g0069 | 2 | NA18947.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1747+29A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222393 | ||||||
| chr12:21222393
|
AAAAAATA others(7): Show |
A | 1 | a0001c0001t0003g0055 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1747+31_1747+44del others(14): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222393 | |||||
| chr12:21222394
|
AAAAATAT others(4): Show |
A | 1 | a0001c0003t0002g0156 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1747+32_1747+42del others(11): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222394 | |||||
| chr12:21222394
|
AAAAATAT others(6): Show |
A | 2 | a0001c0001t0003g0054a0001c0001t0003g0076 | 2 | HG02004.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1747+32_1747+44del others(13): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222394 | |||||
| chr12:21222395
|
A | AATATATA others(3): Show |
1 | a0001c0001t0003g0061 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1747+32_1747+33ins others(10): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222395 | |||||
| chr12:21222395
|
A | AATATATA others(29): Show |
1 | a0002c0005t0001g0164 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1747+32_1747+33ins others(36): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222395 | |||||
| chr12:21222395
|
A | ATATAT | 5 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0067others(2): Show | 5 | HG00544.hp1 NA18954.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.1747+31_1747+32ins others(5): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222395 | ||||||
| chr12:21222395
|
A | ATATATAT | 5 | a0001c0001t0003g0049a0001c0001t0003g0068a0001c0001t0003g0074others(2): Show | 5 | NA18944.hp2 NA18946.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1747+31_1747+32ins others(7): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222395 | ||||||
| chr12:21222395
|
A | ATATATAT others(2): Show |
5 | a0001c0001t0003g0026a0001c0001t0003g0031a0001c0001t0003g0032others(2): Show | 5 | HG02083.hp2 NA18979.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.1747+31_1747+32ins others(9): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222395 | ||||||
| chr12:21222395
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0003g0168 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1747+31_1747+32ins others(11): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222395 | ||||||
| chr12:21222395
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0003g0071 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1747+31_1747+32ins others(13): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222395 | ||||||
| chr12:21222395
|
A | T | 20 | a0001c0001t0001g0079a0001c0001t0001g0087a0001c0001t0002g0249others(17): Show | 20 | HG00423.hp2 HG01515.hp2 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1747+31A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222395 | ||||||
| chr12:21222395
|
AAAATATA others(5): Show |
A | 3 | a0001c0003t0002g0178a0001c0003t0002g0188a0001c0003t0002g0313 | 3 | HG02080.hp1 NA18967.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1747+33_1747+44del others(12): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222395 | |||||
| chr12:21222396
|
AAATATAT others(4): Show |
A | 11 | a0001c0001t0002g0141a0001c0003t0002g0211a0001c0003t0002g0294others(8): Show | 11 | HG02015.hp1 HG02027.hp2 HG04115.hp1 others(8): Show |
intron_variant | MODIFIER | c.1747+34_1747+44del others(11): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222396 | |||||
| chr12:21222397
|
A | AAAAAAAA others(8): Show |
1 | a0003c0004t0002g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1747+34_1747+35ins others(15): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222397 | |||||
| chr12:21222397
|
A | AAAAAAAT others(6): Show |
1 | a0003c0004t0002g0034 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1747+34_1747+35ins others(13): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222397 | |||||
| chr12:21222397
|
A | AAAAAATA others(3): Show |
1 | a0008c0013t0002g0035 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1747+34_1747+35ins others(10): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222397 | |||||
| chr12:21222397
|
A | AAAAAATA others(5): Show |
1 | a0002c0002t0002g0191 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1747+34_1747+35ins others(12): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222397 | |||||
| chr12:21222397
|
A | AAAAATAT others(4): Show |
3 | a0003c0004t0002g0003a0003c0004t0002g0038a0008c0013t0002g0044 | 4 | HG01258.hp2 HG01261.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.1747+34_1747+35ins others(11): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222397 | |||||
| chr12:21222397
|
A | AAAAATAT others(6): Show |
2 | a0003c0004t0002g0027a0003c0004t0002g0036 | 2 | HG00609.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1747+34_1747+35ins others(13): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222397 | |||||
| chr12:21222397
|
A | AAAAATAT others(8): Show |
1 | a0003c0004t0002g0039 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1747+34_1747+35ins others(15): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222397 | |||||
| chr12:21222397
|
A | AAAATATA others(3): Show |
1 | a0005c0009t0002g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1747+34_1747+35ins others(10): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222397 | |||||
| chr12:21222397
|
A | AAAATATA others(5): Show |
2 | a0003c0004t0002g0037a0003c0004t0002g0043 | 2 | NA18747.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.1747+34_1747+35ins others(12): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222397 | |||||
| chr12:21222397
|
A | AAAATATA others(7): Show |
3 | a0003c0004t0002g0021a0003c0004t0002g0040a0003c0004t0002g0288 | 3 | HG02155.hp2 HG06807.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1747+34_1747+35ins others(14): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222397 | |||||
| chr12:21222397
|
A | AAAATATA others(9): Show |
2 | a0001c0001t0003g0052a0003c0004t0002g0033 | 2 | NA19057.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1747+34_1747+35ins others(16): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222397 | |||||
| chr12:21222397
|
A | AAATATAT others(4): Show |
2 | a0003c0004t0002g0001a0003c0004t0002g0260 | 3 | HG01928.hp1 NA18992.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1747+34_1747+35ins others(11): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222397 | |||||
| chr12:21222397
|
A | AAATATAT others(6): Show |
1 | a0003c0004t0002g0041 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1747+34_1747+35ins others(13): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222397 | |||||
| chr12:21222397
|
A | AAATATAT others(8): Show |
1 | a0003c0004t0002g0287 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1747+34_1747+35ins others(15): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222397 | |||||
| chr12:21222397
|
A | AATATATA others(3): Show |
1 | a0003c0004t0003g0024 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1747+55_1747+64dup others(10): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222397 | |||||
| chr12:21222397
|
A | AATATATA others(5): Show |
1 | a0003c0004t0002g0254 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1747+53_1747+64dup others(12): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222397 | |||||
| chr12:21222397
|
A | AT | 4 | a0001c0001t0001g0015a0002c0002t0001g0182a0006c0014t0001g0309others(1): Show | 4 | HG01891.hp1 HG03209.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.1747+33_1747+34ins others(1): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222397 | ||||||
| chr12:21222397
|
A | ATATAT | 4 | a0001c0001t0003g0131a0001c0001t0003g0132a0001c0003t0002g0116others(1): Show | 4 | HG02055.hp1 NA18942.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.1747+33_1747+34ins others(5): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222397 | ||||||
| chr12:21222397
|
A | ATATATAT | 3 | a0001c0001t0002g0080a0001c0001t0003g0048a0001c0001t0003g0077 | 3 | HG03041.hp2 NA18967.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.1747+33_1747+34ins others(7): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222397 | ||||||
| chr12:21222397
|
A | ATATATAT others(4): Show |
2 | a0001c0001t0003g0075a0002c0002t0003g0237 | 2 | NA18945.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1747+33_1747+34ins others(11): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222397 | ||||||
| chr12:21222397
|
A | ATATATAT others(52): Show |
1 | a0002c0005t0001g0143 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1747+33_1747+34ins others(59): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222397 | ||||||
| chr12:21222397
|
A | T | 48 | a0001c0001t0001g0079a0001c0001t0001g0087a0001c0001t0001g0119others(45): Show | 48 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.1747+33A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222397 | ||||||
| chr12:21222397
|
AAT | A | 7 | a0002c0002t0001g0144a0002c0002t0001g0147a0002c0002t0001g0166others(4): Show | 7 | HG00099.hp1 HG01993.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1747+63_1747+64del others(2): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222397 | |||||
| chr12:21222398
|
AT | A | 5 | a0002c0002t0001g0240a0002c0005t0001g0253a0003c0004t0001g0090others(2): Show | 5 | HG01433.hp2 HG01891.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1747+35delT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222398 | ||||||
| chr12:21222398
|
ATAT | A | 8 | a0002c0002t0004g0199a0004c0006t0001g0138a0005c0007t0004g0094others(5): Show | 8 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.1747+35_1747+37del others(3): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222398 | ||||||
| chr12:21222398
|
ATATATAT others(4): Show |
A | 29 | a0001c0003t0002g0005a0001c0003t0002g0145a0001c0003t0002g0158others(26): Show | 30 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.1747+35_1747+45del others(11): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222398 | ||||||
| chr12:21222399
|
T | A | 82 | a0001c0001t0001g0082a0001c0001t0001g0104a0001c0001t0001g0113others(79): Show | 83 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1747+35T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222399 | ||||||
| chr12:21222401
|
T | A | 42 | a0001c0001t0001g0283a0001c0001t0002g0285a0001c0001t0009g0243others(39): Show | 42 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1747+37T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222401 | ||||||
| chr12:21222403
|
T | A | 20 | a0001c0020t0001g0282a0002c0002t0001g0152a0002c0002t0001g0153others(17): Show | 20 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.1747+39T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222403 | ||||||
| chr12:21222405
|
T | A | 9 | a0004c0006t0001g0127a0004c0006t0001g0138a0004c0006t0001g0255others(6): Show | 9 | HG01346.hp1 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1747+41T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222405 | ||||||
| chr12:21222407
|
T | A | 4 | a0004c0006t0001g0138a0007c0008t0006g0244a0007c0008t0006g0245others(1): Show | 4 | HG01884.hp1 HG02280.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1747+43T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222407 | ||||||
| chr12:21222409
|
T | A | 3 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247 | 3 | HG01884.hp1 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1747+45T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222409 | ||||||
| chr12:21222411
|
T | A | 3 | a0001c0003t0002g0145a0001c0003t0002g0226a0001c0003t0002g0293 | 3 | NA18948.hp2 NA18975.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1747+47T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222411 | ||||||
| chr12:21222417
|
TATATATA others(5): Show |
T | 8 | a0001c0003t0002g0018a0001c0003t0002g0106a0001c0003t0002g0176others(5): Show | 8 | HG01975.hp2 HG02040.hp2 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.1747+55_1747+66del others(12): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222417 | |||||
| chr12:21222419
|
TATATATA others(3): Show |
T | 12 | a0001c0001t0001g0311a0001c0003t0002g0107a0001c0003t0002g0201others(9): Show | 12 | HG02129.hp2 HG02293.hp2 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.1747+57_1747+66del others(10): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222419 | |||||
| chr12:21222427
|
T | C | 11 | a0001c0001t0001g0087a0001c0001t0002g0010a0001c0003t0001g0299others(8): Show | 11 | HG02027.hp1 HG02486.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1747+63T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222427 | ||||||
| chr12:21222427
|
TAC | T | 4 | a0004c0006t0001g0233a0004c0006t0001g0234a0004c0006t0001g0235others(1): Show | 4 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1747+73_1747+74del others(2): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222427 | |||||
| chr12:21222427
|
TACAC | T | 9 | a0001c0001t0009g0243a0004c0006t0001g0028a0004c0006t0001g0029others(6): Show | 9 | HG00280.hp1 HG01168.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1747+71_1747+74del others(4): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21222427 | |||||
| chr12:21222429
|
C | T | 64 | a0001c0001t0002g0141a0001c0001t0002g0248a0001c0001t0002g0310others(61): Show | 65 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.1747+65C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222429 | ||||||
| chr12:21222431
|
C | T | 3 | a0004c0006t0001g0233a0004c0006t0001g0234a0004c0006t0001g0235 | 3 | HG00642.hp1 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1747+67C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222431 | ||||||
| chr12:21222592
|
A | T | 3 | a0006c0010t0001g0262a0006c0010t0001g0263a0006c0010t0001g0264 | 3 | HG02630.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1747+228A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222592 | ||||||
| chr12:21222836
|
G | A | 4 | a0001c0001t0002g0080a0001c0001t0002g0111a0001c0001t0002g0112others(1): Show | 4 | HG02630.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1747+472G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21222836 | ||||||
| chr12:21223234
|
G | A | 120 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1747+870G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21223234 | ||||||
| chr12:21223279
|
A | G | 1 | a0001c0001t0002g0285 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1747+915A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21223279 | ||||||
| chr12:21223369
|
A | C | 3 | a0006c0010t0001g0262a0006c0010t0001g0263a0006c0010t0001g0264 | 3 | HG02630.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1747+1005A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21223369 | ||||||
| chr12:21223575
|
C | T | 187 | a0001c0001t0001g0079a0001c0001t0001g0311a0001c0001t0002g0010others(184): Show | 190 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.1748-1147C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21223575 | ||||||
| chr12:21223742
|
C | CA | 113 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(110): Show | 115 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.1748-971dupA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21223742 | |||||
| chr12:21223852
|
G | A | 1 | a0006c0010t0001g0262 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1748-870G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21223852 | ||||||
| chr12:21223904
|
T | C | 1 | a0001c0001t0003g0058 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1748-818T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21223904 | ||||||
| chr12:21224242
|
A | G | 2 | a0005c0009t0002g0083a0005c0009t0002g0084 | 2 | HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1748-480A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21224242 | ||||||
| chr12:21224279
|
TA | T | 13 | a0001c0001t0002g0285a0001c0023t0001g0088a0002c0002t0001g0182others(10): Show | 13 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1748-430delA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 21224279 | |||||
| chr12:21224299
|
T | C | 120 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1748-423T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21224299 | ||||||
| chr12:21224314
|
G | A | 1 | a0001c0001t0003g0049 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1748-408G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21224314 | ||||||
| chr12:21224358
|
A | T | 5 | a0001c0001t0002g0248a0001c0001t0002g0310a0001c0003t0002g0250others(2): Show | 5 | HG02145.hp2 HG02615.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1748-364A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21224358 | ||||||
| chr12:21224512
|
T | A | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1748-210T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21224512 | ||||||
| chr12:21224519
|
A | T | 1 | a0002c0005t0002g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1748-203A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21224519 | ||||||
| chr12:21224524
|
G | A | 2 | a0001c0001t0001g0311a0011c0025t0001g0019 | 2 | HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1748-198G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21224524 | ||||||
| chr12:21224563
|
C | A | 17 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(14): Show | 17 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.1748-159C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21224563 | ||||||
| chr12:21224625
|
G | C | 96 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(93): Show | 98 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1748-97G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 13/14 | chr12 | 21224625 | ||||||
| chr12:21224889
|
T | G | 1 | a0017c0017t0001g0219 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1865+50T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21224889 | ||||||
| chr12:21224988
|
G | A | 8 | a0001c0020t0001g0282a0004c0006t0001g0081a0004c0006t0001g0127others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1865+149G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21224988 | ||||||
| chr12:21225087
|
G | A | 96 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(93): Show | 98 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1865+248G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21225087 | ||||||
| chr12:21225488
|
CA | C | 3 | a0006c0010t0001g0262a0006c0010t0001g0263a0006c0010t0001g0264 | 3 | HG02630.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1865+650delA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21225488 | ||||||
| chr12:21225491
|
G | T | 3 | a0006c0010t0001g0262a0006c0010t0001g0263a0006c0010t0001g0264 | 3 | HG02630.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1865+652G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21225491 | ||||||
| chr12:21225529
|
C | T | 2 | a0005c0007t0004g0099a0016c0018t0001g0140 | 2 | HG00099.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.1865+690C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21225529 | ||||||
| chr12:21225704
|
C | T | 2 | a0004c0006t0001g0246a0004c0006t0001g0272 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1865+865C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21225704 | ||||||
| chr12:21225705
|
G | A | 1 | a0002c0002t0001g0190 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1865+866G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21225705 | ||||||
| chr12:21225731
|
C | A | 120 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1865+892C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21225731 | ||||||
| chr12:21226004
|
C | T | 9 | a0002c0002t0001g0147a0002c0002t0001g0151a0002c0002t0001g0162others(6): Show | 9 | HG00609.hp2 NA18943.hp1 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.1865+1165C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21226004 | ||||||
| chr12:21226035
|
C | T | 2 | a0003c0004t0002g0287a0003c0004t0002g0288 | 2 | HG02015.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1865+1196C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21226035 | ||||||
| chr12:21226085
|
T | C | 120 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1865+1246T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21226085 | ||||||
| chr12:21226181
|
A | G | 120 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1865+1342A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21226181 | ||||||
| chr12:21226203
|
C | T | 4 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(1): Show | 4 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1865+1364C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21226203 | ||||||
| chr12:21226233
|
A | G | 120 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1865+1394A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21226233 | ||||||
| chr12:21226241
|
C | T | 120 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1865+1402C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21226241 | ||||||
| chr12:21226318
|
G | T | 21 | a0001c0003t0002g0194a0001c0003t0002g0195a0001c0003t0002g0196others(18): Show | 21 | HG00438.hp2 HG02129.hp2 NA18941.hp1 others(18): Show |
intron_variant | MODIFIER | c.1865+1479G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21226318 | ||||||
| chr12:21226346
|
G | A | 120 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1865+1507G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21226346 | ||||||
| chr12:21226355
|
A | G | 12 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(9): Show | 12 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1865+1516A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21226355 | ||||||
| chr12:21226383
|
C | T | 120 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1865+1544C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21226383 | ||||||
| chr12:21226421
|
G | GA | 96 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(93): Show | 98 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1865+1591dupA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21226421 | |||||
| chr12:21226427
|
A | C | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1865+1588A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21226427 | ||||||
| chr12:21226464
|
G | A | 120 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1865+1625G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21226464 | ||||||
| chr12:21226631
|
C | A | 65 | a0001c0001t0001g0311a0001c0001t0002g0141a0001c0003t0002g0005others(62): Show | 66 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.1865+1792C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21226631 | ||||||
| chr12:21226636
|
T | C | 1 | a0002c0005t0002g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1865+1797T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21226636 | ||||||
| chr12:21226698
|
A | G | 120 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1865+1859A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21226698 | ||||||
| chr12:21226766
|
A | AC | 120 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1865+1928dupC | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21226766 | |||||
| chr12:21226899
|
A | C | 1 | a0001c0001t0003g0089 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1865+2060A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21226899 | ||||||
| chr12:21226926
|
C | T | 1 | a0001c0001t0009g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1865+2087C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21226926 | ||||||
| chr12:21226945
|
T | C | 114 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(111): Show | 116 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.1865+2106T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21226945 | ||||||
| chr12:21226976
|
A | G | 12 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(9): Show | 12 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1865+2137A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21226976 | ||||||
| chr12:21226996
|
C | A | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(10): Show | 13 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.1865+2157C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21226996 | ||||||
| chr12:21227037
|
T | G | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1865+2198T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21227037 | ||||||
| chr12:21227046
|
G | A | 95 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(92): Show | 97 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.1865+2207G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21227046 | ||||||
| chr12:21227227
|
G | T | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1865+2388G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21227227 | ||||||
| chr12:21227230
|
C | CCTGCAGA others(9): Show |
6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1865+2391_1865+239 others(20): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21227230 | ||||||
| chr12:21227232
|
A | T | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1865+2393A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21227232 | ||||||
| chr12:21227237
|
C | A | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1865+2398C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21227237 | ||||||
| chr12:21227302
|
C | G | 114 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(111): Show | 116 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.1865+2463C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21227302 | ||||||
| chr12:21227423
|
C | G | 1 | a0001c0001t0001g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1865+2584C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21227423 | ||||||
| chr12:21227573
|
G | T | 1 | a0001c0001t0003g0048 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1865+2734G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21227573 | ||||||
| chr12:21227629
|
T | G | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1865+2790T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21227629 | ||||||
| chr12:21227696
|
A | T | 25 | a0001c0003t0002g0273a0002c0002t0002g0009a0002c0002t0002g0191others(22): Show | 27 | HG00609.hp1 HG01081.hp2 HG01258.hp2 others(24): Show |
intron_variant | MODIFIER | c.1865+2857A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21227696 | ||||||
| chr12:21227697
|
C | T | 5 | a0001c0001t0003g0067a0001c0001t0003g0069a0002c0002t0003g0008others(2): Show | 5 | NA18971.hp2 NA18999.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.1865+2858C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21227697 | ||||||
| chr12:21227808
|
CTA | C | 14 | a0001c0001t0002g0285a0001c0001t0004g0022a0001c0001t0004g0023others(11): Show | 14 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.1865+2971_1865+297 others(6): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21227808 | |||||
| chr12:21227855
|
T | A | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1865+3016T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21227855 | ||||||
| chr12:21228036
|
C | T | 1 | a0001c0001t0002g0285 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1865+3197C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21228036 | ||||||
| chr12:21228093
|
T | A | 215 | a0001c0001t0001g0002a0001c0001t0001g0079a0001c0001t0001g0082others(212): Show | 219 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(216): Show |
intron_variant | MODIFIER | c.1865+3254T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21228093 | ||||||
| chr12:21228179
|
T | G | 114 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(111): Show | 116 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.1865+3340T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21228179 | ||||||
| chr12:21228257
|
T | G | 102 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(99): Show | 104 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.1865+3418T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21228257 | ||||||
| chr12:21228298
|
TAAAAG | T | 4 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(1): Show | 4 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1865+3463_1865+346 others(9): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21228298 | |||||
| chr12:21228306
|
A | G | 3 | a0006c0010t0001g0262a0006c0010t0001g0263a0006c0010t0001g0264 | 3 | HG02630.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1865+3467A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21228306 | ||||||
| chr12:21228336
|
A | G | 12 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(9): Show | 12 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1865+3497A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21228336 | ||||||
| chr12:21228668
|
T | C | 125 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(122): Show | 127 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.1865+3829T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21228668 | ||||||
| chr12:21228725
|
C | T | 4 | a0001c0003t0002g0195a0001c0003t0002g0196a0002c0002t0002g0007others(1): Show | 4 | HG00438.hp2 NA18975.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1865+3886C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21228725 | ||||||
| chr12:21228726
|
G | T | 11 | a0001c0001t0002g0248a0001c0001t0002g0310a0001c0003t0002g0250others(8): Show | 11 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1865+3887G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21228726 | ||||||
| chr12:21228804
|
A | C | 11 | a0001c0001t0002g0248a0001c0001t0002g0310a0001c0003t0002g0250others(8): Show | 11 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1865+3965A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21228804 | ||||||
| chr12:21228920
|
C | G | 1 | a0001c0003t0002g0295 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1865+4081C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21228920 | ||||||
| chr12:21229001
|
TA | T | 9 | a0001c0001t0003g0063a0001c0003t0002g0156a0001c0003t0002g0160others(6): Show | 9 | HG01069.hp1 HG02004.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.1865+4175delA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21229001 | |||||
| chr12:21229071
|
T | C | 1 | a0002c0005t0001g0117 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1865+4232T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21229071 | ||||||
| chr12:21229254
|
G | GAGTCCAC | 125 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(122): Show | 127 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.1865+4419_1865+442 others(11): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21229254 | |||||
| chr12:21229282
|
C | A | 14 | a0001c0020t0001g0282a0004c0006t0001g0028a0004c0006t0001g0029others(11): Show | 14 | HG00280.hp1 HG00642.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.1865+4443C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21229282 | ||||||
| chr12:21229288
|
A | G | 114 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(111): Show | 116 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.1865+4449A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21229288 | ||||||
| chr12:21229297
|
T | TC | 125 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(122): Show | 127 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.1865+4458_1865+445 others(5): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21229297 | ||||||
| chr12:21229317
|
A | G | 3 | a0006c0010t0001g0262a0006c0010t0001g0263a0006c0010t0001g0264 | 3 | HG02630.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1865+4478A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21229317 | ||||||
| chr12:21229333
|
A | G | 1 | a0005c0007t0004g0094 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1865+4494A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21229333 | ||||||
| chr12:21229394
|
A | T | 2 | a0006c0014t0001g0298a0006c0014t0001g0309 | 2 | HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1865+4555A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21229394 | ||||||
| chr12:21229408
|
T | C | 114 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(111): Show | 116 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.1865+4569T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21229408 | ||||||
| chr12:21229574
|
G | A | 65 | a0001c0001t0001g0311a0001c0001t0002g0141a0001c0003t0002g0005others(62): Show | 66 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.1865+4735G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21229574 | ||||||
| chr12:21229577
|
T | C | 1 | a0001c0001t0002g0141 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1865+4738T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21229577 | ||||||
| chr12:21229685
|
T | C | 96 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(93): Show | 98 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1865+4846T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21229685 | ||||||
| chr12:21229706
|
C | G | 1 | a0002c0002t0001g0062 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1865+4867C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21229706 | ||||||
| chr12:21229796
|
T | G | 65 | a0001c0001t0002g0141a0001c0003t0002g0005a0001c0003t0002g0018others(62): Show | 66 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.1865+4957T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21229796 | ||||||
| chr12:21229868
|
A | C | 1 | a0001c0001t0001g0114 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1865+5029A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21229868 | ||||||
| chr12:21229896
|
C | T | 14 | a0001c0001t0002g0285a0001c0001t0004g0022a0001c0001t0004g0023others(11): Show | 14 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.1865+5057C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21229896 | ||||||
| chr12:21229944
|
C | T | 1 | a0001c0001t0003g0056 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1865+5105C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21229944 | ||||||
| chr12:21229966
|
T | C | 114 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(111): Show | 116 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.1865+5127T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21229966 | ||||||
| chr12:21230140
|
T | C | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1865+5301T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21230140 | ||||||
| chr12:21230166
|
G | A | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1865+5327G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21230166 | ||||||
| chr12:21230175
|
C | T | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1865+5336C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21230175 | ||||||
| chr12:21230185
|
G | A | 3 | a0006c0010t0001g0262a0006c0010t0001g0263a0006c0010t0001g0264 | 3 | HG02630.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1865+5346G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21230185 | ||||||
| chr12:21230288
|
G | A | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1865+5449G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21230288 | ||||||
| chr12:21230323
|
C | CT | 57 | a0001c0001t0003g0064a0001c0001t0004g0023a0001c0001t0004g0030others(54): Show | 58 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.1865+5507dupT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21230323 | |||||
| chr12:21230323
|
CT | C | 75 | a0001c0001t0001g0130a0001c0001t0001g0311a0001c0001t0002g0141others(72): Show | 76 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.1865+5507delT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21230323 | |||||
| chr12:21230346
|
TG | T | 14 | a0001c0001t0002g0014a0001c0001t0002g0251a0001c0001t0003g0050others(11): Show | 14 | HG00544.hp1 HG02040.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1865+5509delG | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21230346 | |||||
| chr12:21230347
|
G | T | 100 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0080others(97): Show | 102 | HG00099.hp2 HG00423.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.1865+5508G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21230347 | ||||||
| chr12:21230416
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0186 | 2 | HG02109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1865+5577C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21230416 | ||||||
| chr12:21230419
|
T | C | 120 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1865+5580T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21230419 | ||||||
| chr12:21230451
|
C | T | 1 | a0002c0002t0007g0148 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1865+5612C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21230451 | ||||||
| chr12:21230522
|
G | C | 1 | a0001c0001t0009g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1865+5683G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21230522 | ||||||
| chr12:21230572
|
C | T | 134 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1865+5733C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21230572 | ||||||
| chr12:21230582
|
G | A | 101 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(98): Show | 103 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.1865+5743G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21230582 | ||||||
| chr12:21230930
|
C | G | 120 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1865+6091C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21230930 | ||||||
| chr12:21230950
|
C | T | 114 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(111): Show | 116 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.1865+6111C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21230950 | ||||||
| chr12:21230974
|
C | T | 1 | a0002c0002t0001g0205 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1865+6135C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21230974 | ||||||
| chr12:21231078
|
T | C | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1865+6239T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21231078 | ||||||
| chr12:21231088
|
C | T | 1 | a0002c0005t0002g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1865+6249C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21231088 | ||||||
| chr12:21231134
|
C | T | 1 | a0002c0002t0001g0167 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1865+6295C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21231134 | ||||||
| chr12:21231416
|
C | CA | 114 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(111): Show | 116 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.1865+6578dupA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21231416 | |||||
| chr12:21231448
|
G | C | 18 | a0001c0001t0002g0285a0001c0001t0004g0022a0001c0001t0004g0023others(15): Show | 18 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.1865+6609G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21231448 | ||||||
| chr12:21231521
|
G | A | 8 | a0001c0020t0001g0282a0004c0006t0001g0081a0004c0006t0001g0127others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1865+6682G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21231521 | ||||||
| chr12:21231559
|
T | A | 1 | a0015c0024t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1865+6720T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21231559 | ||||||
| chr12:21231562
|
GAAAAAT | G | 14 | a0001c0020t0001g0282a0004c0006t0001g0028a0004c0006t0001g0029others(11): Show | 14 | HG00280.hp1 HG00642.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.1865+6727_1865+673 others(10): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21231562 | |||||
| chr12:21231565
|
A | C | 1 | a0007c0019t0002g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1865+6726A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21231565 | ||||||
| chr12:21231629
|
G | A | 1 | a0001c0003t0002g0308 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1865+6790G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21231629 | ||||||
| chr12:21231662
|
C | T | 3 | a0002c0002t0001g0166a0002c0002t0001g0167a0002c0002t0001g0181 | 3 | HG00099.hp1 HG03669.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1865+6823C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21231662 | ||||||
| chr12:21231703
|
A | G | 1 | a0001c0003t0002g0156 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1865+6864A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21231703 | ||||||
| chr12:21231764
|
G | T | 3 | a0006c0010t0001g0262a0006c0010t0001g0263a0006c0010t0001g0264 | 3 | HG02630.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1865+6925G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21231764 | ||||||
| chr12:21232018
|
T | C | 4 | a0002c0002t0001g0170a0002c0002t0001g0182a0002c0002t0001g0183others(1): Show | 4 | NA18950.hp2 NA18962.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.1866-6961T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21232018 | ||||||
| chr12:21232313
|
C | T | 3 | a0001c0003t0001g0299a0002c0005t0001g0016a0002c0005t0001g0117 | 3 | HG02258.hp2 HG02486.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1866-6666C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21232313 | ||||||
| chr12:21232314
|
G | A | 18 | a0001c0001t0002g0285a0001c0001t0004g0022a0001c0001t0004g0023others(15): Show | 18 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.1866-6665G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21232314 | ||||||
| chr12:21232400
|
A | G | 125 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(122): Show | 127 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.1866-6579A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21232400 | ||||||
| chr12:21232421
|
C | A | 125 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(122): Show | 127 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.1866-6558C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21232421 | ||||||
| chr12:21232493
|
C | T | 14 | a0001c0020t0001g0282a0004c0006t0001g0028a0004c0006t0001g0029others(11): Show | 14 | HG00280.hp1 HG00642.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.1866-6486C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21232493 | ||||||
| chr12:21232494
|
G | A | 1 | a0005c0007t0004g0095 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1866-6485G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21232494 | ||||||
| chr12:21232555
|
ATT | A | 64 | a0001c0001t0001g0311a0001c0001t0002g0141a0001c0003t0002g0005others(61): Show | 65 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.1866-6423_1866-642 others(6): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21232555 | ||||||
| chr12:21232670
|
A | G | 108 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(105): Show | 110 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.1866-6309A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21232670 | ||||||
| chr12:21232691
|
C | CAG | 10 | a0001c0020t0001g0282a0004c0006t0001g0028a0004c0006t0001g0029others(7): Show | 10 | HG00280.hp1 HG01168.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1866-6270_1866-626 others(6): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21232691 | |||||
| chr12:21232711
|
CAGAAAGA others(5): Show |
C | 1 | a0001c0001t0002g0120 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1866-6264_1866-625 others(16): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21232711 | |||||
| chr12:21232715
|
AAGACAGA others(1): Show |
A | 123 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(120): Show | 125 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.1866-6246_1866-623 others(12): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21232715 | |||||
| chr12:21232735
|
C | A | 1 | a0003c0004t0003g0024 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1866-6244C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21232735 | ||||||
| chr12:21232739
|
G | C | 1 | a0003c0004t0003g0024 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1866-6240G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21232739 | ||||||
| chr12:21232741
|
A | AAGACAG | 191 | a0001c0001t0001g0079a0001c0001t0001g0311a0001c0001t0002g0010others(188): Show | 194 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(191): Show |
intron_variant | MODIFIER | c.1866-6222_1866-621 others(10): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21232741 | |||||
| chr12:21232741
|
A | AAGACAGA others(5): Show |
12 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(9): Show | 12 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1866-6228_1866-621 others(16): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21232741 | |||||
| chr12:21232741
|
A | G | 1 | a0003c0004t0003g0024 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1866-6238A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21232741 | ||||||
| chr12:21233059
|
A | G | 1 | a0001c0003t0002g0158 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1866-5920A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21233059 | ||||||
| chr12:21233084
|
A | G | 108 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(105): Show | 110 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.1866-5895A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21233084 | ||||||
| chr12:21233097
|
C | T | 6 | a0004c0006t0001g0028a0004c0006t0001g0029a0004c0006t0001g0078others(3): Show | 6 | HG00280.hp1 HG00642.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.1866-5882C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21233097 | ||||||
| chr12:21233127
|
A | G | 17 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(14): Show | 17 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.1866-5852A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21233127 | ||||||
| chr12:21233162
|
A | C | 17 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(14): Show | 17 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.1866-5817A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21233162 | ||||||
| chr12:21233226
|
CT | C | 125 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(122): Show | 127 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.1866-5748delT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21233226 | |||||
| chr12:21233277
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1866-5702G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21233277 | ||||||
| chr12:21233511
|
T | TAGAG | 125 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(122): Show | 127 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.1866-5467_1866-546 others(8): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21233511 | |||||
| chr12:21233535
|
G | A | 50 | a0001c0001t0001g0079a0001c0001t0003g0026a0001c0001t0003g0031others(47): Show | 50 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1866-5444G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21233535 | ||||||
| chr12:21233552
|
CA | C | 10 | a0001c0003t0002g0018a0001c0003t0002g0145a0001c0003t0002g0211others(7): Show | 10 | HG00544.hp2 HG00673.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.1866-5417delA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21233552 | |||||
| chr12:21233559
|
A | C | 96 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(93): Show | 98 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1866-5420A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21233559 | ||||||
| chr12:21233560
|
AAAC | A | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(10): Show | 13 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.1866-5416_1866-541 others(7): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21233560 | |||||
| chr12:21233571
|
C | CA | 18 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0082others(15): Show | 19 | HG01167.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1866-5395dupA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21233571 | |||||
| chr12:21233571
|
C | CAAAAA | 6 | a0004c0006t0001g0028a0004c0006t0001g0029a0004c0006t0001g0078others(3): Show | 6 | HG00280.hp1 HG00642.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.1866-5399_1866-539 others(9): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21233571 | |||||
| chr12:21233571
|
CA | C | 99 | a0001c0001t0001g0079a0001c0001t0001g0130a0001c0001t0002g0010others(96): Show | 101 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1866-5395delA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21233571 | |||||
| chr12:21233574
|
A | C | 1 | a0001c0003t0002g0214 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1866-5405A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21233574 | ||||||
| chr12:21233575
|
A | C | 46 | a0001c0001t0002g0248a0001c0001t0002g0310a0001c0001t0004g0022others(43): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1866-5404A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21233575 | ||||||
| chr12:21233576
|
A | C | 3 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247 | 3 | HG01884.hp1 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1866-5403A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21233576 | ||||||
| chr12:21233582
|
AAAC | A | 60 | a0001c0001t0001g0311a0001c0001t0002g0141a0001c0003t0002g0005others(57): Show | 61 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.1866-5394_1866-539 others(7): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21233582 | |||||
| chr12:21233585
|
C | A | 4 | a0001c0003t0002g0018a0001c0003t0002g0145a0001c0003t0002g0226others(1): Show | 4 | NA18951.hp2 NA18975.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.1866-5394C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21233585 | ||||||
| chr12:21233593
|
C | T | 1 | a0002c0002t0001g0227 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1866-5386C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21233593 | ||||||
| chr12:21233909
|
T | C | 114 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(111): Show | 116 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.1866-5070T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21233909 | ||||||
| chr12:21234086
|
C | G | 15 | a0001c0020t0001g0282a0004c0006t0001g0028a0004c0006t0001g0029others(12): Show | 15 | HG00280.hp1 HG00642.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.1866-4893C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21234086 | ||||||
| chr12:21234138
|
G | A | 1 | a0003c0004t0001g0090 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1866-4841G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21234138 | ||||||
| chr12:21234139
|
G | A | 1 | a0003c0004t0001g0090 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1866-4840G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21234139 | ||||||
| chr12:21234181
|
A | C | 10 | a0001c0001t0002g0014a0001c0001t0002g0251a0001c0003t0002g0110others(7): Show | 10 | HG02055.hp1 HG02559.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1866-4798A>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21234181 | ||||||
| chr12:21234544
|
C | G | 12 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(9): Show | 12 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1866-4435C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21234544 | ||||||
| chr12:21234797
|
A | G | 1 | a0001c0003t0002g0176 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1866-4182A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21234797 | ||||||
| chr12:21234994
|
T | TA | 14 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(11): Show | 14 | HG01346.hp1 HG01433.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1866-3979dupA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21234994 | |||||
| chr12:21235081
|
A | AT | 106 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(103): Show | 108 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.1866-3880dupT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21235081 | |||||
| chr12:21235081
|
AT | A | 9 | a0001c0003t0002g0295a0001c0003t0002g0302a0002c0002t0001g0144others(6): Show | 9 | HG01069.hp1 HG01081.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1866-3880delT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21235081 | |||||
| chr12:21235133
|
C | CCT | 12 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(9): Show | 12 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1866-3846_1866-384 others(6): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21235133 | ||||||
| chr12:21235134
|
T | A | 12 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(9): Show | 12 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1866-3845T>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21235134 | ||||||
| chr12:21235283
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1866-3696A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21235283 | ||||||
| chr12:21235294
|
A | G | 1 | a0002c0005t0002g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1866-3685A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21235294 | ||||||
| chr12:21235687
|
G | A | 15 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(12): Show | 15 | HG00099.hp2 HG01346.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.1866-3292G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21235687 | ||||||
| chr12:21235836
|
C | CATT | 304 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(301): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1866-3136_1866-313 others(7): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21235836 | |||||
| chr12:21235853
|
T | G | 4 | a0007c0008t0006g0244a0007c0008t0006g0245a0007c0008t0006g0247others(1): Show | 4 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1866-3126T>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21235853 | ||||||
| chr12:21235895
|
T | C | 96 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(93): Show | 98 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1866-3084T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21235895 | ||||||
| chr12:21235922
|
T | C | 1 | a0002c0005t0002g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1866-3057T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21235922 | ||||||
| chr12:21235971
|
G | T | 112 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(109): Show | 114 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.1866-3008G>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21235971 | ||||||
| chr12:21236103
|
A | T | 112 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(109): Show | 114 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.1866-2876A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21236103 | ||||||
| chr12:21236175
|
C | T | 9 | a0001c0001t0002g0010a0001c0001t0002g0080a0001c0001t0002g0111others(6): Show | 9 | HG01168.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1866-2804C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21236175 | ||||||
| chr12:21236206
|
C | G | 1 | a0002c0005t0002g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1866-2773C>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21236206 | ||||||
| chr12:21236246
|
T | C | 1 | a0001c0001t0003g0103 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1866-2733T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21236246 | ||||||
| chr12:21236297
|
C | T | 112 | a0001c0001t0001g0079a0001c0001t0002g0010a0001c0001t0002g0014others(109): Show | 114 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.1866-2682C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21236297 | ||||||
| chr12:21236434
|
A | T | 2 | a0001c0001t0001g0311a0011c0025t0001g0019 | 2 | HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1866-2545A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21236434 | ||||||
| chr12:21236581
|
A | G | 14 | a0004c0006t0001g0028a0004c0006t0001g0029a0004c0006t0001g0078others(11): Show | 14 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1866-2398A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21236581 | ||||||
| chr12:21236621
|
G | C | 1 | a0001c0003t0002g0252 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1866-2358G>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21236621 | ||||||
| chr12:21236700
|
C | T | 6 | a0001c0023t0001g0088a0006c0010t0001g0262a0006c0010t0001g0263others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1866-2279C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21236700 | ||||||
| chr12:21236718
|
T | C | 1 | a0002c0005t0001g0117 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1866-2261T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21236718 | ||||||
| chr12:21236774
|
A | G | 212 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(209): Show | 216 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.1866-2205A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21236774 | ||||||
| chr12:21236883
|
T | C | 16 | a0001c0001t0002g0285a0001c0001t0004g0022a0001c0001t0004g0023others(13): Show | 16 | HG00099.hp2 HG01346.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.1866-2096T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21236883 | ||||||
| chr12:21236921
|
A | T | 181 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0002g0080others(178): Show | 184 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.1866-2058A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21236921 | ||||||
| chr12:21236922
|
T | TA | 181 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0002g0080others(178): Show | 184 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.1866-2055dupA | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21236922 | |||||
| chr12:21237036
|
T | C | 181 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0002g0080others(178): Show | 184 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.1866-1943T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21237036 | ||||||
| chr12:21237211
|
G | A | 181 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0002g0080others(178): Show | 184 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.1866-1768G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21237211 | ||||||
| chr12:21237276
|
A | G | 1 | a0001c0001t0001g0283 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1866-1703A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21237276 | ||||||
| chr12:21237430
|
T | C | 16 | a0001c0001t0002g0285a0001c0001t0004g0022a0001c0001t0004g0023others(13): Show | 16 | HG00099.hp2 HG01346.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.1866-1549T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21237430 | ||||||
| chr12:21237468
|
T | C | 1 | a0002c0002t0001g0147 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1866-1511T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21237468 | ||||||
| chr12:21237502
|
A | T | 5 | a0006c0010t0001g0262a0006c0010t0001g0263a0006c0010t0001g0264others(2): Show | 5 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1866-1477A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21237502 | ||||||
| chr12:21237548
|
C | T | 1 | a0002c0005t0001g0257 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1866-1431C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21237548 | ||||||
| chr12:21237719
|
A | AT | 168 | a0001c0001t0002g0010a0001c0001t0002g0080a0001c0001t0002g0111others(165): Show | 169 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.1866-1247dupT | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21237719 | |||||
| chr12:21237719
|
A | ATT | 25 | a0002c0002t0002g0009a0002c0002t0002g0191a0003c0004t0002g0001others(22): Show | 27 | HG00609.hp1 HG01081.hp2 HG01258.hp2 others(24): Show |
intron_variant | MODIFIER | c.1866-1248_1866-124 others(6): Show |
SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 21237719 | |||||
| chr12:21237903
|
C | T | 16 | a0004c0006t0001g0028a0004c0006t0001g0029a0004c0006t0001g0078others(13): Show | 16 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.1866-1076C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21237903 | ||||||
| chr12:21238017
|
A | T | 1 | a0001c0003t0001g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1866-962A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21238017 | ||||||
| chr12:21238399
|
C | T | 1 | a0002c0002t0001g0208 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1866-580C>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21238399 | ||||||
| chr12:21238402
|
T | C | 165 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0002g0080others(162): Show | 168 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(165): Show |
intron_variant | MODIFIER | c.1866-577T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21238402 | ||||||
| chr12:21238418
|
G | A | 95 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0002g0080others(92): Show | 97 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.1866-561G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21238418 | ||||||
| chr12:21238427
|
A | T | 1 | a0003c0004t0002g0034 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1866-552A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21238427 | ||||||
| chr12:21238500
|
C | A | 2 | a0001c0003t0002g0230a0001c0003t0002g0231 | 2 | NA18962.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1866-479C>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21238500 | ||||||
| chr12:21238674
|
A | G | 95 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0002g0080others(92): Show | 97 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.1866-305A>G | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21238674 | ||||||
| chr12:21238747
|
G | A | 2 | a0001c0001t0003g0053a0001c0001t0003g0070 | 2 | HG00423.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1866-232G>A | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21238747 | ||||||
| chr12:21238748
|
T | C | 51 | a0001c0001t0003g0026a0001c0001t0003g0031a0001c0001t0003g0032others(48): Show | 51 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.1866-231T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21238748 | ||||||
| chr12:21238764
|
A | T | 1 | a0002c0002t0001g0205 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1866-215A>T | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21238764 | ||||||
| chr12:21238884
|
T | C | 16 | a0001c0001t0002g0285a0001c0001t0004g0022a0001c0001t0004g0023others(13): Show | 16 | HG00099.hp2 HG01346.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.1866-95T>C | SLCO1B1 | ENSG00000134538.3 | transcript | ENST00000256958.3 | protein_coding | 14/14 | chr12 | 21238884 |