Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 53919 |
|---|---|
| ensemblid | ENSG00000139155.9 |
| hgncid | 13819 |
| symbol | SLCO1C1 |
| name | solute carrier organic anion transporter family member 1C1 |
| refseq_nuc | NM_017435.5 |
| refseq_prot | NP_059131.1 |
| ensembl_nuc | ENST00000266509.7 |
| ensembl_prot | ENSP00000266509.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 20695332 |
| end | 20753386 |
| strand | + |
| ver | v1.2 |
| region | chr12:20695332-20753386 |
| region5000 | chr12:20690332-20758386 |
| regionname0 | SLCO1C1_chr12_20695332_20753386 |
| regionname5000 | SLCO1C1_chr12_20690332_20758386 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 712 | 283 | 88 | 54 | 95 | 9 | 35 | 65 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0002 | 0/0 | 712 | 7 | 0 | 6 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0003 | 0/0 | 712 | 3 | 0 | 2 | 1 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0004 | 0/0 | 712 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0005 | 0/0 | 712 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| 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 | 1/0 | 2139 | 97 | 50 | 15 | 22 | 1 | 8 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| c0002 | 0/1 | 2139 | 95 | 13 | 24 | 43 | 2 | 12 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| c0003 | 0/0 | 2139 | 31 | 16 | 6 | 2 | 1 | 6 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| c0004 | 0/0 | 2139 | 18 | 3 | 2 | 13 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| c0005 | 0/0 | 2139 | 16 | 4 | 2 | 1 | 3 | 6 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| c0006 | 0/0 | 2139 | 9 | 0 | 0 | 7 | 0 | 2 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| c0007 | 0/0 | 2139 | 5 | 0 | 4 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| c0008 | 0/0 | 2139 | 4 | 0 | 2 | 0 | 2 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| c0009 | 0/0 | 2139 | 3 | 0 | 0 | 3 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| c0010 | 0/0 | 2139 | 2 | 0 | 2 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| c0011 | 0/0 | 2139 | 2 | 2 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| c0012 | 0/0 | 2139 | 2 | 0 | 1 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| c0013 | 0/0 | 2139 | 2 | 0 | 2 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| c0014 | 0/0 | 2139 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| c0015 | 0/0 | 2139 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| c0016 | 0/0 | 2139 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| c0017 | 0/0 | 2139 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| c0018 | 0/0 | 2139 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| c0019 | 0/0 | 2139 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| c0020 | 0/0 | 2139 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| c0021 | 0/0 | 2139 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| c0022 | 0/0 | 2139 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| c0023 | 0/0 | 2139 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| 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 | 1360 | 124 | 49 | 24 | 34 | 2 | 14 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| t0002 | 0/1 | 1360 | 121 | 19 | 31 | 47 | 7 | 16 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| t0003 | 0/0 | 1360 | 24 | 11 | 2 | 11 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| t0004 | 0/0 | 1360 | 10 | 1 | 5 | 0 | 1 | 3 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| t0005 | 0/0 | 1360 | 5 | 5 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| t0006 | 0/0 | 1360 | 3 | 0 | 0 | 0 | 0 | 3 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| t0007 | 0/0 | 1360 | 2 | 2 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| t0008 | 0/0 | 1360 | 2 | 0 | 0 | 2 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| t0009 | 0/0 | 1360 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| t0010 | 0/0 | 1360 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| t0011 | 0/0 | 1360 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| t0012 | 0/0 | 1360 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| t0013 | 0/0 | 1360 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| 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 | 2 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0208 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| 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 | 1/0 | 2139 | 97 | 50 | 15 | 22 | 1 | 8 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0002 | 0/1 | 2139 | 95 | 13 | 24 | 43 | 2 | 12 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0003 | 0/0 | 2139 | 31 | 16 | 6 | 2 | 1 | 6 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0004 | 0/0 | 2139 | 18 | 3 | 2 | 13 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0005 | 0/0 | 2139 | 16 | 4 | 2 | 1 | 3 | 6 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0006 | 0/0 | 2139 | 9 | 0 | 0 | 7 | 0 | 2 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0008 | 0/0 | 2139 | 4 | 0 | 2 | 0 | 2 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0009 | 0/0 | 2139 | 3 | 0 | 0 | 3 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0013 | 0/0 | 2139 | 2 | 0 | 2 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0014 | 0/0 | 2139 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0015 | 0/0 | 2139 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0016 | 0/0 | 2139 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0017 | 0/0 | 2139 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0018 | 0/0 | 2139 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0020 | 0/0 | 2139 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0021 | 0/0 | 2139 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0022 | 0/0 | 2139 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0002c0007 | 0/0 | 2139 | 5 | 0 | 4 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0002c0010 | 0/0 | 2139 | 2 | 0 | 2 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0003c0012 | 0/0 | 2139 | 2 | 0 | 1 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0003c0023 | 0/0 | 2139 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0004c0011 | 0/0 | 2139 | 2 | 2 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0005c0019 | 0/0 | 2139 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3498 | 75 | 39 | 13 | 16 | 0 | 6 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0001t0003 | 0/0 | 3498 | 13 | 8 | 0 | 5 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0001t0004 | 0/0 | 3498 | 6 | 1 | 2 | 0 | 1 | 2 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0001t0005 | 0/0 | 3498 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0001t0010 | 0/0 | 3498 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0001t0013 | 0/0 | 3498 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0002t0002 | 0/1 | 3498 | 92 | 13 | 24 | 42 | 2 | 10 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0002t0006 | 0/0 | 3498 | 2 | 0 | 0 | 0 | 0 | 2 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0002t0011 | 0/0 | 3498 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0003t0001 | 0/0 | 3498 | 19 | 8 | 3 | 2 | 1 | 5 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0003t0003 | 0/0 | 3498 | 3 | 1 | 2 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0003t0004 | 0/0 | 3498 | 2 | 0 | 1 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0003t0005 | 0/0 | 3498 | 4 | 4 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0003t0007 | 0/0 | 3498 | 2 | 2 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0003t0012 | 0/0 | 3498 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0004t0001 | 0/0 | 3498 | 11 | 2 | 2 | 7 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0004t0003 | 0/0 | 3498 | 7 | 1 | 0 | 6 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0005t0002 | 0/0 | 3498 | 15 | 4 | 2 | 1 | 3 | 5 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0005t0006 | 0/0 | 3498 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0006t0001 | 0/0 | 3498 | 7 | 0 | 0 | 5 | 0 | 2 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0006t0008 | 0/0 | 3498 | 2 | 0 | 0 | 2 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0008t0002 | 0/0 | 3498 | 4 | 0 | 2 | 0 | 2 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0009t0002 | 0/0 | 3498 | 3 | 0 | 0 | 3 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0013t0001 | 0/0 | 3498 | 2 | 0 | 2 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0014t0003 | 0/0 | 3498 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0015t0001 | 0/0 | 3498 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0016t0001 | 0/0 | 3498 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0017t0001 | 0/0 | 3498 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0018t0002 | 0/0 | 3498 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0020t0009 | 0/0 | 3498 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0021t0001 | 0/0 | 3498 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0001c0022t0002 | 0/0 | 3498 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0002c0007t0001 | 0/0 | 3498 | 3 | 0 | 2 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0002c0007t0004 | 0/0 | 3498 | 2 | 0 | 2 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0002c0010t0002 | 0/0 | 3498 | 2 | 0 | 2 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0003c0012t0001 | 0/0 | 3498 | 2 | 0 | 1 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0003c0023t0001 | 0/0 | 3498 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0004c0011t0002 | 0/0 | 3498 | 2 | 2 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| a0005c0019t0002 | 0/0 | 3498 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | copy fasta | chr12 | 20690332 | 20758386 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0208 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0010g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0013g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0006g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0006g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0011g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0004g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0005g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0012g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0006g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0006t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0006t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0006t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0006t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0006t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0006t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0006t0008g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0006t0008g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0008t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0008t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0008t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0008t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0009t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0009t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0009t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0013t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0013t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0014t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0015t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0016t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0017t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0018t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0020t0009g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0021t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0022t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0002c0007t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0002c0007t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0002c0007t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0002c0007t0004g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0002c0010t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0002c0010t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0003c0012t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0003c0012t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0003c0023t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0004c0011t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0004c0011t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0005c0019t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0164 | EUR | GBR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0286 | EUR | GBR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00280 | hp1 | a0002 | c0007 | t0001 | g0260 | EUR | FIN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00280 | hp2 | a0001 | c0008 | t0002 | g0236 | EUR | FIN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | CHS | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00544 | hp2 | a0001 | c0004 | t0003 | g0247 | EAS | CHS | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00558 | hp1 | a0001 | c0009 | t0002 | g0097 | EAS | CHS | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0143 | EAS | CHS | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00597 | hp1 | a0001 | c0004 | t0001 | g0146 | EAS | CHS | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0273 | EAS | CHS | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0230 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0099 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0285 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0243 | EAS | CHS | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00735 | hp1 | a0001 | c0003 | t0001 | g0167 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00735 | hp2 | a0001 | c0005 | t0002 | g0254 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00738 | hp2 | a0003 | c0023 | t0001 | g0221 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00741 | hp1 | a0001 | c0022 | t0002 | g0115 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01069 | hp1 | a0002 | c0007 | t0004 | g0006 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0244 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01071 | hp2 | a0002 | c0007 | t0004 | g0006 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01081 | hp2 | a0001 | c0004 | t0001 | g0094 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0132 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01167 | hp1 | a0001 | c0008 | t0002 | g0217 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01168 | hp1 | a0001 | c0003 | t0004 | g0238 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01168 | hp2 | a0001 | c0003 | t0003 | g0196 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01169 | hp1 | a0001 | c0003 | t0003 | g0195 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0234 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0231 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01255 | hp2 | a0001 | c0003 | t0001 | g0119 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0044 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01256 | hp2 | a0002 | c0010 | t0002 | g0219 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0069 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0229 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01258 | hp2 | a0002 | c0010 | t0002 | g0220 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0152 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0068 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0063 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0171 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0266 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01361 | hp1 | a0001 | c0013 | t0001 | g0241 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01361 | hp2 | a0001 | c0005 | t0002 | g0269 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0057 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0265 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0233 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01496 | hp2 | a0002 | c0007 | t0001 | g0226 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01515 | hp1 | a0001 | c0008 | t0002 | g0218 | EUR | IBS | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01515 | hp2 | a0001 | c0005 | t0002 | g0224 | EUR | IBS | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0194 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01928 | hp1 | a0001 | c0008 | t0002 | g0227 | AMR | PEL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0270 | AMR | PEL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0250 | AMR | PEL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0183 | AMR | PEL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0276 | AMR | PEL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01975 | hp2 | a0001 | c0013 | t0001 | g0216 | AMR | PEL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01978 | hp1 | a0003 | c0012 | t0001 | g0126 | AMR | PEL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0267 | AMR | PEL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0272 | AMR | PEL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01981 | hp2 | a0002 | c0007 | t0001 | g0062 | AMR | PEL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0098 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02015 | hp2 | a0001 | c0001 | t0013 | g0142 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02027 | hp1 | a0001 | c0004 | t0003 | g0150 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0089 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0212 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02055 | hp1 | a0001 | c0020 | t0009 | g0016 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02056 | hp1 | a0001 | c0003 | t0001 | g0133 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0189 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0109 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02071 | hp2 | a0001 | c0004 | t0001 | g0088 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0240 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02080 | hp2 | a0001 | c0006 | t0001 | g0144 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0277 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0284 | AMR | PEL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CDX | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | CDX | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0203 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0261 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0253 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0159 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0246 | AMR | PEL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0245 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02523 | hp2 | a0001 | c0004 | t0003 | g0155 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0206 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02602 | hp2 | a0001 | c0003 | t0001 | g0197 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0175 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0199 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0023 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02683 | hp1 | a0001 | c0003 | t0001 | g0239 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02683 | hp2 | a0005 | c0019 | t0002 | g0073 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02717 | hp1 | a0001 | c0003 | t0012 | g0024 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0100 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0263 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0198 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02895 | hp1 | a0004 | c0011 | t0002 | g0207 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0151 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02897 | hp1 | a0004 | c0011 | t0002 | g0209 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02922 | hp2 | a0001 | c0001 | t0010 | g0022 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0275 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03041 | hp2 | a0001 | c0005 | t0002 | g0042 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | MSL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0163 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | MSL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03209 | hp2 | a0001 | c0003 | t0005 | g0002 | AFR | MSL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03239 | hp1 | a0001 | c0005 | t0002 | g0193 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0067 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03453 | hp2 | a0001 | c0014 | t0003 | g0264 | AFR | MSL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0162 | AFR | MSL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03492 | hp2 | a0001 | c0005 | t0002 | g0095 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03516 | hp1 | a0001 | c0005 | t0002 | g0200 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0174 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03540 | hp1 | a0001 | c0005 | t0002 | g0182 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0283 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03579 | hp2 | a0001 | c0003 | t0007 | g0018 | AFR | MSL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03654 | hp1 | a0001 | c0005 | t0006 | g0169 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0280 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03688 | hp1 | a0001 | c0003 | t0001 | g0032 | SAS | STU | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0046 | SAS | STU | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0274 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0092 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0093 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03710 | hp2 | a0001 | c0005 | t0002 | g0064 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03831 | hp1 | a0001 | c0003 | t0001 | g0170 | SAS | BEB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03831 | hp2 | a0001 | c0005 | t0002 | g0137 | SAS | BEB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03834 | hp1 | a0001 | c0006 | t0001 | g0082 | SAS | BEB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03834 | hp2 | a0001 | c0003 | t0004 | g0166 | SAS | BEB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03927 | hp1 | a0001 | c0021 | t0001 | g0157 | SAS | BEB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0168 | SAS | BEB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03942 | hp1 | a0001 | c0002 | t0006 | g0223 | SAS | BEB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03942 | hp2 | a0001 | c0005 | t0002 | g0281 | SAS | BEB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG04115 | hp1 | a0001 | c0006 | t0001 | g0215 | SAS | STU | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG04115 | hp2 | a0001 | c0002 | t0006 | g0147 | SAS | STU | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0158 | SAS | BEB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0225 | SAS | STU | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | STU | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | STU | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | STU | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | YRI | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18522 | hp2 | a0001 | c0003 | t0001 | g0289 | AFR | YRI | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0228 | EAS | CHB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18612 | hp2 | a0001 | c0004 | t0003 | g0040 | EAS | CHB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18747 | hp1 | a0001 | c0009 | t0002 | g0125 | EAS | CHB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | CHB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0262 | AFR | YRI | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18941 | hp1 | a0001 | c0018 | t0002 | g0214 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0140 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18951 | hp1 | a0001 | c0004 | t0001 | g0041 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18951 | hp2 | a0001 | c0003 | t0001 | g0134 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0255 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18953 | hp2 | a0001 | c0004 | t0003 | g0080 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18959 | hp1 | a0001 | c0015 | t0001 | g0191 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18959 | hp2 | a0001 | c0016 | t0001 | g0050 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0116 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18962 | hp1 | a0001 | c0002 | t0011 | g0083 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18964 | hp2 | a0001 | c0004 | t0001 | g0118 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18977 | hp1 | a0001 | c0004 | t0001 | g0033 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18979 | hp1 | a0001 | c0006 | t0008 | g0039 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18983 | hp2 | a0003 | c0012 | t0001 | g0128 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0124 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18989 | hp1 | a0001 | c0006 | t0008 | g0201 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18989 | hp2 | a0001 | c0002 | t0002 | g0122 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18999 | hp2 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19004 | hp1 | a0001 | c0004 | t0001 | g0086 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19005 | hp1 | a0001 | c0006 | t0001 | g0192 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0268 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19010 | hp1 | a0001 | c0006 | t0001 | g0005 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19010 | hp2 | a0001 | c0004 | t0001 | g0259 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19030 | hp1 | a0001 | c0004 | t0003 | g0180 | AFR | LWK | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | LWK | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | LWK | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19043 | hp2 | a0001 | c0003 | t0005 | g0025 | AFR | LWK | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19058 | hp1 | a0001 | c0005 | t0002 | g0047 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19058 | hp2 | a0001 | c0006 | t0001 | g0005 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19066 | hp1 | a0001 | c0004 | t0003 | g0156 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0258 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0145 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19072 | hp2 | a0001 | c0006 | t0001 | g0190 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19074 | hp1 | a0001 | c0009 | t0002 | g0085 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19074 | hp2 | a0001 | c0017 | t0001 | g0038 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19078 | hp1 | a0001 | c0002 | t0002 | g0120 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19078 | hp2 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0279 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19240 | hp1 | a0001 | c0003 | t0005 | g0002 | AFR | YRI | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA20129 | hp1 | a0001 | c0003 | t0003 | g0054 | AFR | ASW | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA20129 | hp2 | a0001 | c0005 | t0002 | g0184 | AFR | ASW | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA20752 | hp1 | a0001 | c0005 | t0002 | g0043 | EUR | TSI | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA20752 | hp2 | a0001 | c0005 | t0002 | g0108 | EUR | TSI | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0282 | EUR | TSI | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0101 | EUR | TSI | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0165 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01123 | hp2 | a0001 | c0004 | t0001 | g0153 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02109 | hp1 | a0001 | c0003 | t0007 | g0017 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0061 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0222 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02486 | hp2 | a0001 | c0004 | t0001 | g0015 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02559 | hp1 | a0001 | c0003 | t0005 | g0026 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | MSL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | USA | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG06807 | hp2 | a0001 | c0004 | t0001 | g0105 | AFR | USA | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0127 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | USA | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | USA | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | LWK | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0110 | REF | REF | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0208 | REF | REF | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:20711408
|
C | A | 1 | a0002 | 7 | HG00280.hp1 HG01069.hp1 HG01071.hp2 others(4): Show |
missense_variant | MODERATE | c.427C>A | p.Pro143Thr | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/15 | 928/3498 | 427/2139 | 143/712 | chr12 | 20711408 | ||
| chr12:20711502
|
T | A | 1 | a0005 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.521T>A | p.Ile174Lys | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/15 | 1022/3498 | 521/2139 | 174/712 | chr12 | 20711502 | ||
| chr12:20721955
|
T | G | 1 | a0004 | 2 | HG02895.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.927T>G | p.Asn309Lys | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 8/15 | 1428/3498 | 927/2139 | 309/712 | chr12 | 20721955 | ||
| chr12:20740325
|
A | G | 1 | a0003 | 3 | HG00738.hp2 HG01978.hp1 NA18983.hp2 |
missense_variant | MODERATE | c.1690A>G | p.Thr564Ala | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/15 | 2191/3498 | 1690/2139 | 564/712 | chr12 | 20740325 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:20699612
|
C | T | 3 | a0001c0008a0001c0013a0003c0023 | 7 | HG00280.hp2 HG00738.hp2 HG01167.hp1 others(4): Show |
synonymous_variant | LOW | c.36C>T | p.Phe12Phe | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 2/15 | 537/3498 | 36/2139 | 12/712 | chr12 | 20699612 | ||
| chr12:20711422
|
C | T | 9 | a0001c0003a0001c0005a0001c0020others(6): Show | 59 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(56): Show |
synonymous_variant | LOW | c.441C>T | p.Ser147Ser | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/15 | 942/3498 | 441/2139 | 147/712 | chr12 | 20711422 | ||
| chr12:20717160
|
A | T | 2 | a0001c0017a0001c0018 | 2 | NA18941.hp1 NA19074.hp2 |
synonymous_variant | LOW | c.705A>T | p.Gly235Gly | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/15 | 1206/3498 | 705/2139 | 235/712 | chr12 | 20717160 | ||
| chr12:20732997
|
A | G | 4 | a0001c0004a0001c0009a0001c0016others(1): Show | 23 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(20): Show |
synonymous_variant | LOW | c.1275A>G | p.Ala425Ala | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/15 | 1776/3498 | 1275/2139 | 425/712 | chr12 | 20732997 | ||
| chr12:20733007
|
T | C | 2 | a0001c0014a0001c0020 | 2 | HG02055.hp1 HG03453.hp2 |
synonymous_variant | LOW | c.1285T>C | p.Leu429Leu | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/15 | 1786/3498 | 1285/2139 | 429/712 | chr12 | 20733007 | ||
| chr12:20737251
|
C | A | 1 | a0001c0016 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.1527C>A | p.Ser509Ser | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 11/15 | 2028/3498 | 1527/2139 | 509/712 | chr12 | 20737251 | ||
| chr12:20750676
|
A | G | 1 | a0001c0015 | 1 | NA18959.hp1 | splice_region_variant&synonymous_variant | LOW | c.1800A>G | p.Ala600Ala | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 14/15 | 2301/3498 | 1800/2139 | 600/712 | chr12 | 20750676 | ||
| chr12:20752316
|
C | T | 9 | a0001c0002a0001c0005a0001c0008others(6): Show | 125 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(122): Show |
synonymous_variant | LOW | c.1927C>T | p.Leu643Leu | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 15/15 | 2428/3498 | 1927/2139 | 643/712 | chr12 | 20752316 | ||
| chr12:20752345
|
G | T | 5 | a0001c0006a0001c0015a0001c0021others(2): Show | 14 | HG00738.hp2 HG01978.hp1 HG02080.hp2 others(11): Show |
synonymous_variant | LOW | c.1956G>T | p.Val652Val | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 15/15 | 2457/3498 | 1956/2139 | 652/712 | chr12 | 20752345 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:20695521
|
C | T | 1 | a0001c0001t0013 | 1 | HG02015.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-312C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/15 | chr12 | 20695521 | ||||||
| chr12:20695580
|
G | A | 2 | a0001c0003t0007a0001c0020t0009 | 3 | HG02055.hp1 HG02109.hp1 HG03579.hp2 |
5_prime_UTR_variant | MODIFIER | c.-253G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/15 | 3997 | chr12 | 20695580 | |||||
| chr12:20695742
|
G | T | 3 | a0001c0001t0005a0001c0003t0005a0001c0003t0012 | 6 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-91G>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/15 | chr12 | 20695742 | ||||||
| chr12:20752693
|
C | T | 12 | a0001c0002t0002a0001c0002t0006a0001c0002t0011others(9): Show | 125 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*165C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 15/15 | 165 | chr12 | 20752693 | |||||
| chr12:20752748
|
A | T | 1 | a0001c0006t0008 | 2 | NA18979.hp1 NA18989.hp1 |
3_prime_UTR_variant | MODIFIER | c.*220A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 15/15 | 220 | chr12 | 20752748 | |||||
| chr12:20752763
|
C | T | 12 | a0001c0002t0002a0001c0002t0006a0001c0002t0011others(9): Show | 125 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*235C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 15/15 | 235 | chr12 | 20752763 | |||||
| chr12:20752895
|
T | A | 1 | a0001c0002t0011 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*367T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 15/15 | 367 | chr12 | 20752895 | |||||
| chr12:20753030
|
G | A | 3 | a0001c0001t0004a0001c0003t0004a0002c0007t0004 | 10 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*502G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 15/15 | 502 | chr12 | 20753030 | |||||
| chr12:20753032
|
T | C | 2 | a0001c0002t0006a0001c0005t0006 | 3 | HG03654.hp1 HG03942.hp1 HG04115.hp2 |
3_prime_UTR_variant | MODIFIER | c.*504T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 15/15 | 504 | chr12 | 20753032 | |||||
| chr12:20753056
|
T | C | 12 | a0001c0002t0002a0001c0002t0006a0001c0002t0011others(9): Show | 125 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*528T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 15/15 | 528 | chr12 | 20753056 | |||||
| chr12:20753238
|
C | T | 23 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(20): Show | 166 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*710C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 15/15 | 710 | chr12 | 20753238 | |||||
| chr12:20753349
|
C | A | 1 | a0001c0001t0010 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*821C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 15/15 | 821 | chr12 | 20753349 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:20695872
|
C | T | 2 | a0001c0001t0001g0290a0001c0003t0001g0289 | 2 | HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-26+65C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20695872 | ||||||
| chr12:20695988
|
T | A | 2 | a0001c0001t0001g0290a0001c0003t0001g0289 | 2 | HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-26+181T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20695988 | ||||||
| chr12:20696042
|
C | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0290a0001c0003t0001g0289 | 3 | HG03453.hp1 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-26+235C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20696042 | ||||||
| chr12:20696043
|
A | C | 2 | a0001c0001t0001g0287a0001c0001t0001g0288 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-26+236A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20696043 | ||||||
| chr12:20696110
|
G | C | 22 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(19): Show | 24 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-26+303G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20696110 | ||||||
| chr12:20696133
|
G | A | 158 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0035others(155): Show | 160 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.-26+326G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20696133 | ||||||
| chr12:20696177
|
G | C | 1 | a0001c0005t0002g0182 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-26+370G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20696177 | ||||||
| chr12:20696245
|
C | T | 1 | a0001c0002t0002g0181 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-26+438C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20696245 | ||||||
| chr12:20696317
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-26+510T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20696317 | ||||||
| chr12:20696419
|
T | C | 1 | a0001c0002t0002g0183 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-26+612T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20696419 | ||||||
| chr12:20696465
|
C | T | 2 | a0001c0001t0004g0285a0001c0003t0001g0286 | 2 | HG00099.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.-26+658C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20696465 | ||||||
| chr12:20696533
|
T | C | 1 | a0001c0001t0004g0029 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-26+726T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20696533 | ||||||
| chr12:20696642
|
G | A | 1 | a0001c0002t0002g0030 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-26+835G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20696642 | ||||||
| chr12:20696653
|
C | T | 5 | a0001c0001t0005g0027a0001c0003t0005g0002a0001c0003t0005g0025others(2): Show | 6 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-26+846C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20696653 | ||||||
| chr12:20696681
|
G | A | 14 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(11): Show | 16 | HG01884.hp2 HG02486.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.-26+874G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20696681 | ||||||
| chr12:20696793
|
G | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0290a0001c0001t0004g0285others(3): Show | 6 | HG00099.hp2 HG00642.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-26+986G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20696793 | ||||||
| chr12:20697023
|
T | G | 1 | a0001c0001t0001g0031 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-26+1216T>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20697023 | ||||||
| chr12:20697064
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0290a0001c0001t0004g0285others(3): Show | 6 | HG00099.hp2 HG00642.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-26+1257A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20697064 | ||||||
| chr12:20697251
|
TATG | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0290a0001c0003t0001g0289 | 3 | HG03453.hp1 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-26+1447_-26+1449d others(5): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 20697251 | |||||
| chr12:20697280
|
G | A | 1 | a0001c0005t0002g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-26+1473G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20697280 | ||||||
| chr12:20697351
|
G | A | 38 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(35): Show | 41 | HG01167.hp2 HG01168.hp2 HG01169.hp1 others(38): Show |
intron_variant | MODIFIER | c.-26+1544G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20697351 | ||||||
| chr12:20697428
|
T | A | 1 | a0001c0002t0002g0003 | 2 | NA18962.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.-26+1621T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20697428 | ||||||
| chr12:20697704
|
A | C | 1 | a0001c0002t0002g0284 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-25-1848A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20697704 | ||||||
| chr12:20697708
|
T | C | 1 | a0001c0003t0001g0032 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-25-1844T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20697708 | ||||||
| chr12:20697754
|
T | C | 6 | a0001c0001t0001g0035a0001c0002t0002g0034a0001c0002t0002g0036others(3): Show | 6 | HG00673.hp1 NA18955.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25-1798T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20697754 | ||||||
| chr12:20697879
|
T | C | 1 | a0001c0003t0001g0197 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-25-1673T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20697879 | ||||||
| chr12:20698277
|
CTTCT | C | 10 | a0001c0001t0001g0188a0001c0002t0002g0189a0001c0002t0002g0194others(7): Show | 11 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-25-1272_-25-1269d others(6): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 20698277 | |||||
| chr12:20698394
|
C | T | 2 | a0001c0001t0001g0290a0001c0003t0001g0289 | 2 | HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-25-1158C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20698394 | ||||||
| chr12:20698411
|
C | T | 10 | a0001c0001t0001g0188a0001c0002t0002g0189a0001c0002t0002g0194others(7): Show | 11 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-25-1141C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20698411 | ||||||
| chr12:20698679
|
T | C | 14 | a0001c0001t0001g0021a0001c0001t0001g0185a0001c0001t0001g0186others(11): Show | 14 | HG01167.hp2 HG01169.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-25-873T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20698679 | ||||||
| chr12:20698827
|
A | G | 3 | a0001c0002t0002g0194a0001c0003t0003g0195a0001c0003t0003g0196 | 3 | HG01168.hp2 HG01169.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.-25-725A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20698827 | ||||||
| chr12:20698874
|
C | G | 1 | a0001c0004t0003g0180 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-25-678C>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20698874 | ||||||
| chr12:20698926
|
T | C | 3 | a0001c0004t0001g0041a0001c0004t0003g0040a0001c0006t0008g0039 | 3 | NA18612.hp2 NA18951.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.-25-626T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20698926 | ||||||
| chr12:20699051
|
T | A | 6 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-25-501T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20699051 | ||||||
| chr12:20699149
|
A | C | 2 | a0001c0001t0004g0285a0001c0003t0001g0286 | 2 | HG00099.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.-25-403A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20699149 | ||||||
| chr12:20699152
|
G | A | 138 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0035others(135): Show | 140 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.-25-400G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20699152 | ||||||
| chr12:20699314
|
A | C | 1 | a0001c0002t0002g0159 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-25-238A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20699314 | ||||||
| chr12:20699371
|
G | A | 1 | a0001c0003t0001g0203 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-25-181G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20699371 | ||||||
| chr12:20699387
|
T | G | 138 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0035others(135): Show | 140 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.-25-165T>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20699387 | ||||||
| chr12:20699389
|
T | G | 14 | a0001c0001t0001g0021a0001c0001t0001g0185a0001c0001t0001g0186others(11): Show | 14 | HG01167.hp2 HG01169.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-25-163T>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20699389 | ||||||
| chr12:20699510
|
G | A | 2 | a0001c0001t0004g0285a0001c0003t0001g0286 | 2 | HG00099.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.-25-42G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | chr12 | 20699510 | ||||||
| chr12:20699515
|
A | ATTTG | 44 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(41): Show | 47 | HG00099.hp2 HG00642.hp2 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.-25-34_-25-33insGT others(2): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 20699515 | |||||
| chr12:20699778
|
T | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0290a0001c0003t0001g0289 | 3 | HG03453.hp1 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129+73T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 2/14 | chr12 | 20699778 | ||||||
| chr12:20699796
|
C | A | 2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.129+91C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 2/14 | chr12 | 20699796 | ||||||
| chr12:20699797
|
T | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0290a0001c0001t0004g0285others(3): Show | 6 | HG00099.hp2 HG00642.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.129+92T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 2/14 | chr12 | 20699797 | ||||||
| chr12:20699802
|
T | TA | 23 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0172others(20): Show | 23 | HG00099.hp1 HG00735.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.129+110dupA | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 20699802 | |||||
| chr12:20699827
|
C | G | 1 | a0001c0002t0002g0158 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.129+122C>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 2/14 | chr12 | 20699827 | ||||||
| chr12:20699854
|
G | A | 1 | a0001c0004t0003g0180 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.129+149G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 2/14 | chr12 | 20699854 | ||||||
| chr12:20699916
|
G | GC | 30 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(27): Show | 32 | HG00099.hp2 HG00642.hp2 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.129+218dupC | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 20699916 | |||||
| chr12:20699916
|
G | GCC | 13 | a0001c0001t0001g0007a0001c0001t0001g0188a0001c0001t0001g0290others(10): Show | 14 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.129+217_129+218dup others(2): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 20699916 | |||||
| chr12:20700088
|
CT | C | 172 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0035others(169): Show | 175 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(172): Show |
intron_variant | MODIFIER | c.129+397delT | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 20700088 | |||||
| chr12:20700091
|
T | A | 161 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0035others(158): Show | 163 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(160): Show |
intron_variant | MODIFIER | c.129+386T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 2/14 | chr12 | 20700091 | ||||||
| chr12:20700112
|
G | T | 1 | a0001c0002t0002g0283 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.129+407G>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 2/14 | chr12 | 20700112 | ||||||
| chr12:20700126
|
T | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0290a0001c0001t0004g0285others(3): Show | 6 | HG00099.hp2 HG00642.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.129+421T>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 2/14 | chr12 | 20700126 | ||||||
| chr12:20700187
|
T | C | 3 | a0001c0002t0002g0044a0001c0005t0002g0042a0001c0005t0002g0043 | 3 | HG01256.hp1 HG03041.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.129+482T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 2/14 | chr12 | 20700187 | ||||||
| chr12:20700205
|
A | C | 2 | a0001c0001t0004g0285a0001c0003t0001g0286 | 2 | HG00099.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.129+500A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 2/14 | chr12 | 20700205 | ||||||
| chr12:20700575
|
T | G | 32 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(29): Show | 35 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.130-743T>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 2/14 | chr12 | 20700575 | ||||||
| chr12:20700597
|
G | A | 10 | a0001c0001t0001g0188a0001c0002t0002g0189a0001c0002t0002g0194others(7): Show | 11 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.130-721G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 2/14 | chr12 | 20700597 | ||||||
| chr12:20700598
|
C | T | 5 | a0001c0001t0005g0027a0001c0003t0005g0002a0001c0003t0005g0025others(2): Show | 6 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.130-720C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 2/14 | chr12 | 20700598 | ||||||
| chr12:20700607
|
T | C | 205 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(202): Show | 210 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(207): Show |
intron_variant | MODIFIER | c.130-711T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 2/14 | chr12 | 20700607 | ||||||
| chr12:20700676
|
C | T | 8 | a0001c0001t0001g0021a0001c0001t0003g0019a0001c0001t0003g0020others(5): Show | 8 | HG02055.hp1 HG02109.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.130-642C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 2/14 | chr12 | 20700676 | ||||||
| chr12:20701082
|
G | A | 2 | a0001c0001t0004g0285a0001c0003t0001g0286 | 2 | HG00099.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.130-236G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 2/14 | chr12 | 20701082 | ||||||
| chr12:20701165
|
C | T | 1 | a0002c0007t0004g0006 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.130-153C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 2/14 | chr12 | 20701165 | ||||||
| chr12:20701572
|
C | CT | 26 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(23): Show | 29 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.271+128dupT | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 20701572 | |||||
| chr12:20701572
|
C | CTT | 169 | a0001c0001t0001g0021a0001c0001t0001g0028a0001c0001t0001g0031others(166): Show | 171 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.271+127_271+128dup others(2): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 20701572 | |||||
| chr12:20701726
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.271+267T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20701726 | ||||||
| chr12:20701852
|
G | T | 31 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(28): Show | 34 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.271+393G>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20701852 | ||||||
| chr12:20701934
|
T | A | 6 | a0001c0001t0001g0035a0001c0002t0002g0034a0001c0002t0002g0036others(3): Show | 6 | HG00673.hp1 NA18955.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.271+475T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20701934 | ||||||
| chr12:20702050
|
A | G | 8 | a0001c0001t0001g0021a0001c0001t0003g0019a0001c0001t0003g0020others(5): Show | 8 | HG02055.hp1 HG02109.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.271+591A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20702050 | ||||||
| chr12:20702062
|
G | T | 37 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(34): Show | 40 | HG01167.hp2 HG01168.hp2 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.271+603G>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20702062 | ||||||
| chr12:20702104
|
T | C | 5 | a0001c0002t0002g0049a0001c0002t0002g0051a0001c0002t0002g0052others(2): Show | 5 | HG00544.hp1 NA18959.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.271+645T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20702104 | ||||||
| chr12:20702127
|
G | A | 1 | a0001c0002t0002g0206 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.271+668G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20702127 | ||||||
| chr12:20702203
|
C | T | 34 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(31): Show | 37 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.271+744C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20702203 | ||||||
| chr12:20702246
|
G | A | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0003t0003g0054 | 3 | HG02896.hp1 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.271+787G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20702246 | ||||||
| chr12:20702303
|
A | G | 286 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(283): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.271+844A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20702303 | ||||||
| chr12:20702335
|
A | G | 13 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(10): Show | 15 | HG01884.hp2 HG02486.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.271+876A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20702335 | ||||||
| chr12:20702365
|
A | G | 3 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178 | 3 | HG02818.hp2 HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.271+906A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20702365 | ||||||
| chr12:20702414
|
TC | T | 8 | a0001c0001t0001g0021a0001c0001t0003g0019a0001c0001t0003g0020others(5): Show | 8 | HG02055.hp1 HG02109.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.271+957delC | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 20702414 | |||||
| chr12:20702579
|
T | C | 3 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0020t0009g0016 | 3 | HG02055.hp1 HG02109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.271+1120T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20702579 | ||||||
| chr12:20702685
|
C | T | 10 | a0001c0001t0001g0188a0001c0002t0002g0189a0001c0002t0002g0194others(7): Show | 11 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.271+1226C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20702685 | ||||||
| chr12:20702721
|
A | G | 37 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(34): Show | 40 | HG01167.hp2 HG01168.hp2 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.271+1262A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20702721 | ||||||
| chr12:20702762
|
A | G | 3 | a0001c0001t0004g0285a0001c0003t0001g0286a0001c0005t0002g0182 | 3 | HG00099.hp2 HG00642.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.271+1303A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20702762 | ||||||
| chr12:20702827
|
T | C | 136 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0035others(133): Show | 138 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.271+1368T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20702827 | ||||||
| chr12:20703014
|
C | T | 1 | a0001c0002t0002g0282 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.271+1555C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20703014 | ||||||
| chr12:20703153
|
G | C | 5 | a0001c0001t0005g0027a0001c0003t0005g0002a0001c0003t0005g0025others(2): Show | 6 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.271+1694G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20703153 | ||||||
| chr12:20703274
|
T | C | 4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0003g0162others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.271+1815T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20703274 | ||||||
| chr12:20703391
|
G | A | 4 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(1): Show | 4 | HG02109.hp2 HG02970.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.271+1932G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20703391 | ||||||
| chr12:20703396
|
T | A | 1 | a0001c0006t0008g0201 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.271+1937T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20703396 | ||||||
| chr12:20703418
|
TTGA | T | 200 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(197): Show | 205 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(202): Show |
intron_variant | MODIFIER | c.271+1961_271+1963d others(5): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 20703418 | |||||
| chr12:20703421
|
A | T | 3 | a0001c0001t0004g0285a0001c0003t0001g0286a0001c0005t0002g0182 | 3 | HG00099.hp2 HG00642.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.271+1962A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20703421 | ||||||
| chr12:20703435
|
C | T | 2 | a0001c0003t0001g0280a0001c0005t0002g0281 | 2 | HG03654.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.271+1976C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20703435 | ||||||
| chr12:20703466
|
A | C | 13 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(10): Show | 15 | HG01884.hp2 HG02486.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.271+2007A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20703466 | ||||||
| chr12:20703473
|
A | G | 10 | a0001c0001t0001g0188a0001c0002t0002g0189a0001c0002t0002g0194others(7): Show | 11 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.271+2014A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20703473 | ||||||
| chr12:20703565
|
C | T | 3 | a0001c0001t0001g0278a0001c0002t0002g0277a0001c0002t0002g0279 | 3 | HG02135.hp1 NA19070.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.271+2106C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20703565 | ||||||
| chr12:20703645
|
T | C | 201 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(198): Show | 206 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(203): Show |
intron_variant | MODIFIER | c.271+2186T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20703645 | ||||||
| chr12:20703955
|
C | CTG | 18 | a0001c0001t0001g0031a0001c0001t0001g0058a0001c0001t0001g0059others(15): Show | 19 | HG01256.hp1 HG01975.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.272-1963_272-1962d others(4): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 20703955 | |||||
| chr12:20703955
|
C | CTGTG | 62 | a0001c0001t0001g0007a0001c0001t0001g0035a0001c0001t0001g0111others(59): Show | 62 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.272-1965_272-1962d others(6): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 20703955 | |||||
| chr12:20703955
|
C | CTGTGTG | 7 | a0001c0001t0001g0160a0001c0001t0001g0173a0001c0001t0003g0174others(4): Show | 7 | HG00735.hp1 HG03041.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.272-1967_272-1962d others(8): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 20703955 | |||||
| chr12:20703955
|
C | CTGTGTGT others(1): Show |
19 | a0001c0001t0001g0172a0001c0001t0001g0176a0001c0001t0001g0188others(16): Show | 20 | HG01168.hp2 HG01169.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.272-1969_272-1962d others(10): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 20703955 | |||||
| chr12:20703955
|
C | CTGTGTGT others(3): Show |
9 | a0001c0001t0001g0161a0001c0001t0001g0177a0001c0001t0001g0178others(6): Show | 9 | HG02055.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.272-1971_272-1962d others(12): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 20703955 | |||||
| chr12:20703955
|
C | CTGTGTGT others(5): Show |
5 | a0001c0001t0001g0021a0001c0001t0010g0022a0001c0003t0001g0023others(2): Show | 5 | HG02109.hp1 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.272-1973_272-1962d others(14): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 20703955 | |||||
| chr12:20703955
|
C | CTGTGTGT others(7): Show |
2 | a0001c0002t0002g0175a0001c0003t0007g0018 | 2 | HG02615.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.272-1975_272-1962d others(16): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 20703955 | |||||
| chr12:20703955
|
CTG | C | 10 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0210others(7): Show | 10 | HG01167.hp2 HG01169.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.272-1963_272-1962d others(4): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 20703955 | |||||
| chr12:20703955
|
CTGTG | C | 10 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(7): Show | 11 | HG00099.hp2 HG00642.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.272-1965_272-1962d others(6): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 20703955 | |||||
| chr12:20703955
|
CTGTGTGT others(5): Show |
C | 1 | a0001c0002t0002g0163 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.272-1973_272-1962d others(14): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 20703955 | |||||
| chr12:20703988
|
C | T | 2 | a0001c0001t0001g0173a0001c0001t0003g0174 | 2 | HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.272-1961C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20703988 | ||||||
| chr12:20703989
|
A | G | 2 | a0001c0001t0001g0173a0001c0001t0003g0174 | 2 | HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.272-1960A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20703989 | ||||||
| chr12:20703990
|
TAGAC | T | 35 | a0001c0001t0001g0232a0001c0001t0001g0235a0001c0001t0001g0237others(32): Show | 35 | HG00280.hp2 HG00639.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.272-1951_272-1948d others(6): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 20703990 | |||||
| chr12:20703991
|
A | G | 4 | a0001c0001t0001g0173a0001c0001t0003g0174a0001c0002t0002g0273others(1): Show | 4 | HG00597.hp2 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.272-1958A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20703991 | ||||||
| chr12:20703992
|
G | C | 4 | a0001c0001t0001g0173a0001c0001t0003g0174a0001c0002t0002g0273others(1): Show | 4 | HG00597.hp2 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.272-1957G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20703992 | ||||||
| chr12:20703994
|
C | T | 4 | a0001c0001t0001g0173a0001c0001t0003g0174a0001c0002t0002g0273others(1): Show | 4 | HG00597.hp2 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.272-1955C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20703994 | ||||||
| chr12:20704073
|
T | C | 11 | a0001c0001t0001g0188a0001c0002t0002g0189a0001c0002t0002g0194others(8): Show | 12 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.272-1876T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20704073 | ||||||
| chr12:20704183
|
T | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0290a0001c0003t0001g0289 | 3 | HG03453.hp1 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.272-1766T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20704183 | ||||||
| chr12:20704242
|
G | GAT | 8 | a0001c0001t0001g0009a0001c0001t0004g0168a0001c0002t0002g0244others(5): Show | 8 | HG00735.hp1 HG01071.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.272-1694_272-1693d others(4): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 20704242 | |||||
| chr12:20704339
|
T | TC | 188 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0028others(185): Show | 191 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(188): Show |
intron_variant | MODIFIER | c.272-1610_272-1609i others(3): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20704339 | ||||||
| chr12:20704340
|
G | C | 188 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0028others(185): Show | 191 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(188): Show |
intron_variant | MODIFIER | c.272-1609G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20704340 | ||||||
| chr12:20704533
|
A | C | 203 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(200): Show | 208 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(205): Show |
intron_variant | MODIFIER | c.272-1416A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20704533 | ||||||
| chr12:20704542
|
G | A | 188 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0028others(185): Show | 191 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(188): Show |
intron_variant | MODIFIER | c.272-1407G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20704542 | ||||||
| chr12:20704686
|
C | G | 1 | a0001c0004t0003g0155 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.272-1263C>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20704686 | ||||||
| chr12:20704728
|
C | CAGAT | 188 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0028others(185): Show | 191 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(188): Show |
intron_variant | MODIFIER | c.272-1220_272-1217d others(6): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 20704728 | |||||
| chr12:20705126
|
T | C | 10 | a0001c0001t0001g0188a0001c0002t0002g0189a0001c0002t0002g0194others(7): Show | 11 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.272-823T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20705126 | ||||||
| chr12:20705169
|
A | G | 13 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(10): Show | 15 | HG01884.hp2 HG02486.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.272-780A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20705169 | ||||||
| chr12:20705351
|
C | T | 188 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0028others(185): Show | 191 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(188): Show |
intron_variant | MODIFIER | c.272-598C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20705351 | ||||||
| chr12:20705601
|
TAAG | T | 13 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(10): Show | 15 | HG01884.hp2 HG02486.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.272-344_272-342del others(3): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 20705601 | |||||
| chr12:20705746
|
T | C | 10 | a0001c0001t0001g0188a0001c0002t0002g0189a0001c0002t0002g0194others(7): Show | 11 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.272-203T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20705746 | ||||||
| chr12:20705748
|
C | T | 13 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(10): Show | 15 | HG01884.hp2 HG02486.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.272-201C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20705748 | ||||||
| chr12:20705840
|
C | A | 1 | a0001c0005t0002g0042 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.272-109C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20705840 | ||||||
| chr12:20705851
|
G | C | 1 | a0001c0002t0002g0109 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.272-98G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20705851 | ||||||
| chr12:20705865
|
G | T | 8 | a0001c0001t0001g0021a0001c0001t0003g0019a0001c0001t0003g0020others(5): Show | 8 | HG02055.hp1 HG02109.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.272-84G>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20705865 | ||||||
| chr12:20705941
|
C | T | 1 | a0001c0001t0004g0101 | 1 | NA20805.hp2 | splice_region_variant&intron_variant | LOW | c.272-8C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20705941 | ||||||
| chr12:20706265
|
A | C | 13 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(10): Show | 15 | HG01884.hp2 HG02486.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.404+184A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20706265 | ||||||
| chr12:20706437
|
C | T | 1 | a0001c0002t0002g0272 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.404+356C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20706437 | ||||||
| chr12:20706611
|
T | G | 1 | a0001c0005t0002g0182 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.404+530T>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20706611 | ||||||
| chr12:20706655
|
T | C | 1 | a0001c0001t0003g0275 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.404+574T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20706655 | ||||||
| chr12:20706716
|
C | T | 176 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0028others(173): Show | 178 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(175): Show |
intron_variant | MODIFIER | c.404+635C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20706716 | ||||||
| chr12:20706813
|
A | G | 1 | a0001c0005t0002g0182 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.404+732A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20706813 | ||||||
| chr12:20706935
|
T | C | 1 | a0001c0004t0003g0156 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.404+854T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20706935 | ||||||
| chr12:20707018
|
A | T | 1 | a0001c0002t0002g0243 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.404+937A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20707018 | ||||||
| chr12:20707050
|
AT | A | 202 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(199): Show | 207 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(204): Show |
intron_variant | MODIFIER | c.404+974delT | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 20707050 | |||||
| chr12:20707159
|
G | A | 165 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0031others(162): Show | 167 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(164): Show |
intron_variant | MODIFIER | c.404+1078G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20707159 | ||||||
| chr12:20707360
|
T | G | 4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0003g0162others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.404+1279T>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20707360 | ||||||
| chr12:20707443
|
C | T | 1 | a0001c0002t0002g0165 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.404+1362C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20707443 | ||||||
| chr12:20707446
|
A | G | 1 | a0001c0004t0003g0180 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.404+1365A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20707446 | ||||||
| chr12:20707470
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.404+1389C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20707470 | ||||||
| chr12:20707567
|
A | G | 13 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(10): Show | 15 | HG01884.hp2 HG02486.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.404+1486A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20707567 | ||||||
| chr12:20707601
|
T | G | 2 | a0001c0001t0004g0285a0001c0003t0001g0286 | 2 | HG00099.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.404+1520T>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20707601 | ||||||
| chr12:20707706
|
T | C | 10 | a0001c0001t0001g0188a0001c0002t0002g0189a0001c0002t0002g0194others(7): Show | 11 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.404+1625T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20707706 | ||||||
| chr12:20707823
|
GA | G | 34 | a0001c0001t0001g0021a0001c0001t0001g0160a0001c0001t0001g0161others(31): Show | 35 | HG00099.hp1 HG00735.hp1 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.404+1751delA | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 20707823 | |||||
| chr12:20707824
|
A | G | 2 | a0001c0001t0001g0287a0001c0001t0001g0288 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.404+1743A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20707824 | ||||||
| chr12:20708097
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.404+2016C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20708097 | ||||||
| chr12:20708143
|
G | A | 1 | a0001c0002t0002g0110 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.404+2062G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20708143 | ||||||
| chr12:20708164
|
C | T | 2 | a0001c0001t0001g0290a0001c0003t0001g0289 | 2 | HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.404+2083C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20708164 | ||||||
| chr12:20708198
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.404+2117G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20708198 | ||||||
| chr12:20708299
|
G | GTA | 4 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.404+2226_404+2227d others(4): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 20708299 | |||||
| chr12:20708401
|
A | G | 1 | a0001c0002t0002g0004 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.404+2320A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20708401 | ||||||
| chr12:20708485
|
A | T | 5 | a0001c0002t0002g0189a0001c0006t0001g0005a0001c0006t0001g0190others(2): Show | 6 | HG02056.hp2 NA18959.hp1 NA19005.hp1 others(3): Show |
intron_variant | MODIFIER | c.404+2404A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20708485 | ||||||
| chr12:20708510
|
T | C | 21 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0172others(18): Show | 21 | HG00099.hp1 HG00735.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.404+2429T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20708510 | ||||||
| chr12:20708517
|
A | T | 166 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0031others(163): Show | 168 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(165): Show |
intron_variant | MODIFIER | c.404+2436A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20708517 | ||||||
| chr12:20708591
|
C | T | 1 | a0001c0004t0001g0153 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.404+2510C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20708591 | ||||||
| chr12:20708834
|
A | G | 282 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(279): Show | 288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.405-2552A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20708834 | ||||||
| chr12:20708892
|
C | A | 1 | a0001c0002t0002g0212 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.405-2494C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20708892 | ||||||
| chr12:20708947
|
C | T | 2 | a0001c0001t0001g0290a0001c0003t0001g0289 | 2 | HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.405-2439C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20708947 | ||||||
| chr12:20708962
|
C | T | 2 | a0001c0003t0003g0195a0001c0003t0003g0196 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.405-2424C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20708962 | ||||||
| chr12:20709146
|
G | A | 2 | a0001c0001t0001g0287a0001c0001t0001g0288 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.405-2240G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20709146 | ||||||
| chr12:20709147
|
G | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.405-2239G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20709147 | ||||||
| chr12:20709233
|
A | T | 1 | a0001c0002t0002g0152 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.405-2153A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20709233 | ||||||
| chr12:20709338
|
A | G | 1 | a0001c0003t0001g0245 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.405-2048A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20709338 | ||||||
| chr12:20709452
|
T | C | 1 | a0001c0005t0002g0064 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.405-1934T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20709452 | ||||||
| chr12:20709585
|
TAAGAATT others(331): Show |
T | 184 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0028others(181): Show | 188 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(185): Show |
intron_variant | MODIFIER | c.405-1785_405-1448d others(2): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 20709585 | |||||
| chr12:20709700
|
T | C | 1 | a0001c0002t0002g0246 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.405-1686T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20709700 | ||||||
| chr12:20709887
|
C | CA | 33 | a0001c0001t0001g0031a0001c0001t0001g0112a0001c0001t0001g0210others(30): Show | 34 | HG00597.hp2 HG00639.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.405-1461dupA | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 20709887 | |||||
| chr12:20709887
|
C | CAA | 16 | a0001c0001t0001g0009a0001c0001t0001g0111a0001c0001t0001g0248others(13): Show | 16 | HG00544.hp2 HG00738.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.405-1462_405-1461d others(4): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 20709887 | |||||
| chr12:20709887
|
C | CAAAAAAA others(4): Show |
1 | a0001c0002t0002g0010 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.405-1471_405-1461d others(13): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 20709887 | |||||
| chr12:20709887
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0004t0001g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.405-1471_405-1461d others(13): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 20709887 | |||||
| chr12:20709887
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0154 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.405-1472_405-1461d others(14): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 20709887 | |||||
| chr12:20709887
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0003t0012g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.405-1477_405-1461d others(19): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 20709887 | |||||
| chr12:20709887
|
CAAAAAAA others(11): Show |
C | 7 | a0001c0001t0001g0065a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 8 | HG02559.hp1 HG02630.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.405-1478_405-1461d others(20): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 20709887 | |||||
| chr12:20709887
|
CAAAAAAA others(12): Show |
C | 1 | a0001c0001t0001g0066 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.405-1479_405-1461d others(21): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 20709887 | |||||
| chr12:20709935
|
A | G | 4 | a0001c0001t0001g0232a0001c0001t0001g0235a0001c0002t0002g0233others(1): Show | 4 | HG01081.hp1 HG01106.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.405-1451A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20709935 | ||||||
| chr12:20709996
|
A | G | 2 | a0001c0001t0001g0290a0001c0003t0001g0289 | 2 | HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.405-1390A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20709996 | ||||||
| chr12:20710005
|
G | A | 146 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0035others(143): Show | 149 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(146): Show |
intron_variant | MODIFIER | c.405-1381G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20710005 | ||||||
| chr12:20710078
|
T | C | 2 | a0001c0001t0004g0285a0001c0003t0001g0286 | 2 | HG00099.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.405-1308T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20710078 | ||||||
| chr12:20710174
|
T | G | 3 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0005t0002g0182 | 3 | HG01884.hp1 HG03130.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.405-1212T>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20710174 | ||||||
| chr12:20710195
|
C | CT | 3 | a0001c0001t0004g0225a0001c0003t0001g0286a0001c0005t0002g0281 | 3 | HG00099.hp2 HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.405-1187dupT | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 20710195 | |||||
| chr12:20710195
|
C | CTTTTTTT others(3): Show |
6 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(3): Show | 6 | HG02486.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.405-1187_405-1186i others(12): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 20710195 | |||||
| chr12:20710195
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0010g0022 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.405-1187_405-1186i others(13): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 20710195 | |||||
| chr12:20710195
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0003g0019a0001c0003t0001g0023 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.405-1187_405-1186i others(14): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 20710195 | |||||
| chr12:20710195
|
C | CTTTTTTT others(8): Show |
1 | a0001c0002t0002g0001 | 2 | HG01884.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.405-1187_405-1186i others(17): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 20710195 | |||||
| chr12:20710195
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0003g0020 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.405-1187_405-1186i others(20): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 20710195 | |||||
| chr12:20710198
|
TTC | T | 8 | a0001c0001t0001g0107a0001c0001t0001g0173a0001c0001t0001g0290others(5): Show | 8 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.405-1186_405-1185d others(4): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 20710198 | |||||
| chr12:20710199
|
TC | T | 14 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0102others(11): Show | 14 | HG01884.hp1 HG02109.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.405-1186delC | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20710199 | ||||||
| chr12:20710200
|
C | CT | 20 | a0001c0001t0001g0048a0001c0001t0001g0205a0001c0001t0001g0235others(17): Show | 20 | HG00597.hp2 HG00735.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.405-1161dupT | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 20710200 | |||||
| chr12:20710200
|
C | T | 38 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(35): Show | 40 | HG00099.hp2 HG00642.hp2 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.405-1186C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20710200 | ||||||
| chr12:20710200
|
CT | C | 9 | a0001c0001t0001g0104a0001c0001t0001g0121a0001c0001t0003g0113others(6): Show | 9 | HG02280.hp2 HG02523.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.405-1161delT | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 20710200 | |||||
| chr12:20710206
|
T | C | 1 | a0001c0003t0003g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.405-1180T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20710206 | ||||||
| chr12:20710223
|
T | C | 87 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0070others(84): Show | 90 | HG00280.hp2 HG00544.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.405-1163T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20710223 | ||||||
| chr12:20710268
|
C | T | 2 | a0001c0001t0001g0271a0001c0002t0002g0090 | 2 | HG02155.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.405-1118C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20710268 | ||||||
| chr12:20710282
|
A | G | 1 | a0001c0001t0001g0007 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.405-1104A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20710282 | ||||||
| chr12:20710293
|
C | T | 1 | a0001c0004t0003g0247 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.405-1093C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20710293 | ||||||
| chr12:20710322
|
C | G | 1 | a0001c0002t0002g0001 | 2 | HG01884.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.405-1064C>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20710322 | ||||||
| chr12:20710360
|
TATGC | T | 12 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(9): Show | 13 | HG00099.hp2 HG01884.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.405-1021_405-1018d others(6): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 20710360 | |||||
| chr12:20710372
|
T | C | 10 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(7): Show | 11 | HG01884.hp2 HG02486.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.405-1014T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20710372 | ||||||
| chr12:20710386
|
A | G | 43 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0102others(40): Show | 44 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.405-1000A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20710386 | ||||||
| chr12:20710535
|
C | T | 107 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(104): Show | 110 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(107): Show |
intron_variant | MODIFIER | c.405-851C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20710535 | ||||||
| chr12:20710550
|
T | C | 2 | a0001c0002t0002g0282a0001c0008t0002g0236 | 2 | HG00280.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.405-836T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20710550 | ||||||
| chr12:20710615
|
C | A | 63 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(60): Show | 63 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.405-771C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20710615 | ||||||
| chr12:20710621
|
G | T | 41 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(38): Show | 41 | HG01081.hp1 HG01106.hp1 HG01168.hp2 others(38): Show |
intron_variant | MODIFIER | c.405-765G>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20710621 | ||||||
| chr12:20710635
|
T | C | 14 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0160others(11): Show | 14 | HG01884.hp1 HG02055.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.405-751T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20710635 | ||||||
| chr12:20710639
|
A | G | 105 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0070others(102): Show | 107 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.405-747A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20710639 | ||||||
| chr12:20710673
|
A | C | 17 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0172others(14): Show | 17 | HG01346.hp2 HG01358.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.405-713A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20710673 | ||||||
| chr12:20710684
|
C | A | 3 | a0001c0001t0001g0287a0001c0002t0002g0233a0005c0019t0002g0073 | 3 | HG01496.hp1 HG02683.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.405-702C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20710684 | ||||||
| chr12:20710916
|
G | A | 3 | a0001c0003t0001g0032a0001c0003t0001g0286a0005c0019t0002g0073 | 3 | HG00099.hp2 HG02683.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.405-470G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20710916 | ||||||
| chr12:20710980
|
T | C | 2 | a0001c0001t0001g0248a0001c0001t0003g0020 | 2 | HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.405-406T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20710980 | ||||||
| chr12:20711009
|
GGAA | G | 17 | a0001c0001t0001g0031a0001c0001t0001g0045a0001c0001t0001g0060others(14): Show | 17 | HG00099.hp2 HG01346.hp2 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.405-367_405-365del others(3): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 20711009 | |||||
| chr12:20711062
|
T | C | 9 | a0001c0002t0002g0151a0001c0002t0002g0273a0001c0003t0001g0133others(6): Show | 9 | HG00544.hp2 HG00597.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.405-324T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20711062 | ||||||
| chr12:20711199
|
A | G | 1 | a0001c0002t0002g0110 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.405-187A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20711199 | ||||||
| chr12:20711200
|
T | C | 3 | a0001c0001t0001g0204a0001c0003t0001g0289a0001c0003t0012g0024 | 3 | HG02717.hp1 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.405-186T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20711200 | ||||||
| chr12:20711312
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.405-74C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20711312 | ||||||
| chr12:20711313
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.405-73G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20711313 | ||||||
| chr12:20711517
|
T | A | 9 | a0001c0001t0001g0011a0001c0002t0002g0077a0001c0021t0001g0157others(6): Show | 10 | HG00280.hp1 HG01069.hp1 HG01071.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.529+7T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20711517 | ||||||
| chr12:20711535
|
T | C | 8 | a0001c0003t0001g0023a0001c0003t0001g0203a0001c0003t0001g0245others(5): Show | 8 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.529+25T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20711535 | ||||||
| chr12:20711547
|
T | A | 5 | a0001c0001t0001g0048a0001c0001t0001g0102a0001c0001t0001g0107others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.529+37T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20711547 | ||||||
| chr12:20711562
|
A | G | 6 | a0001c0001t0001g0248a0001c0001t0003g0020a0001c0003t0004g0238others(3): Show | 7 | HG01168.hp1 HG02559.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.529+52A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20711562 | ||||||
| chr12:20711586
|
G | C | 1 | a0001c0001t0001g0007 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.529+76G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20711586 | ||||||
| chr12:20711688
|
GAA | G | 19 | a0001c0001t0001g0076a0001c0001t0001g0130a0001c0001t0001g0131others(16): Show | 19 | HG00639.hp2 HG00738.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.529+181_529+182del others(2): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 20711688 | |||||
| chr12:20711695
|
T | C | 20 | a0001c0001t0001g0138a0001c0001t0001g0160a0001c0001t0001g0161others(17): Show | 21 | HG01081.hp1 HG01106.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.529+185T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20711695 | ||||||
| chr12:20711717
|
GA | G | 13 | a0001c0001t0001g0138a0001c0001t0001g0232a0001c0001t0001g0235others(10): Show | 14 | HG01081.hp1 HG01106.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.529+214delA | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 20711717 | |||||
| chr12:20711850
|
T | G | 1 | a0001c0002t0002g0034 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.529+340T>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20711850 | ||||||
| chr12:20711927
|
C | G | 24 | a0001c0001t0001g0076a0001c0001t0001g0138a0001c0001t0001g0172others(21): Show | 25 | HG00639.hp2 HG01081.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.529+417C>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20711927 | ||||||
| chr12:20711994
|
C | A | 1 | a0001c0001t0001g0187 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.529+484C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20711994 | ||||||
| chr12:20712000
|
T | C | 1 | a0001c0005t0006g0169 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.529+490T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20712000 | ||||||
| chr12:20712055
|
C | T | 151 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0079others(148): Show | 156 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.529+545C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20712055 | ||||||
| chr12:20712056
|
G | A | 3 | a0001c0001t0001g0106a0001c0003t0001g0289a0001c0003t0012g0024 | 3 | HG02717.hp1 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.529+546G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20712056 | ||||||
| chr12:20712168
|
A | G | 38 | a0001c0001t0001g0048a0001c0001t0001g0072a0001c0001t0001g0102others(35): Show | 41 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.529+658A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20712168 | ||||||
| chr12:20712178
|
C | T | 33 | a0001c0001t0001g0048a0001c0001t0001g0102a0001c0001t0001g0107others(30): Show | 36 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.529+668C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20712178 | ||||||
| chr12:20712217
|
A | G | 1 | a0001c0003t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.529+707A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20712217 | ||||||
| chr12:20712225
|
T | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0106a0001c0003t0001g0289others(1): Show | 4 | HG02717.hp1 HG03195.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.529+715T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20712225 | ||||||
| chr12:20712367
|
G | A | 60 | a0001c0001t0001g0011a0001c0001t0001g0048a0001c0001t0001g0102others(57): Show | 63 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.529+857G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20712367 | ||||||
| chr12:20712763
|
T | C | 8 | a0001c0001t0001g0138a0001c0001t0001g0232a0001c0001t0001g0235others(5): Show | 8 | HG01081.hp1 HG01106.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.529+1253T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20712763 | ||||||
| chr12:20712874
|
C | A | 1 | a0001c0001t0001g0290 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.529+1364C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20712874 | ||||||
| chr12:20713083
|
C | CT | 243 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(240): Show | 247 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.529+1587dupT | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 20713083 | |||||
| chr12:20713083
|
C | CTT | 6 | a0001c0001t0001g0035a0001c0002t0002g0036a0001c0002t0002g0037others(3): Show | 6 | HG00673.hp1 HG02040.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.529+1586_529+1587d others(4): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 20713083 | |||||
| chr12:20713083
|
C | CTTTTTTT | 7 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.529+1581_529+1587d others(9): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 20713083 | |||||
| chr12:20713083
|
C | CTTTTTTT others(1): Show |
5 | a0001c0001t0004g0029a0001c0003t0004g0238a0001c0003t0005g0002others(2): Show | 6 | HG01168.hp1 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.529+1580_529+1587d others(10): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 20713083 | |||||
| chr12:20713102
|
C | T | 1 | a0001c0001t0003g0081 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.529+1592C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20713102 | ||||||
| chr12:20713140
|
C | G | 2 | a0001c0006t0008g0039a0003c0012t0001g0126 | 2 | HG01978.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.529+1630C>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20713140 | ||||||
| chr12:20713197
|
A | G | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(9): Show | 13 | HG01168.hp1 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.529+1687A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20713197 | ||||||
| chr12:20713225
|
G | A | 1 | a0001c0001t0001g0013 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.529+1715G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20713225 | ||||||
| chr12:20713230
|
C | A | 1 | a0001c0001t0001g0187 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.529+1720C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20713230 | ||||||
| chr12:20713231
|
T | C | 3 | a0001c0001t0001g0187a0001c0001t0005g0027a0001c0005t0002g0042 | 3 | HG02630.hp1 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.529+1721T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20713231 | ||||||
| chr12:20713281
|
T | G | 13 | a0001c0002t0002g0077a0001c0003t0001g0099a0001c0003t0001g0119others(10): Show | 14 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.529+1771T>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20713281 | ||||||
| chr12:20713356
|
G | C | 218 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0021others(215): Show | 221 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(218): Show |
intron_variant | MODIFIER | c.530-1783G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20713356 | ||||||
| chr12:20713441
|
G | C | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(9): Show | 13 | HG01168.hp1 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.530-1698G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20713441 | ||||||
| chr12:20713511
|
A | C | 3 | a0001c0002t0002g0089a0001c0004t0001g0041a0001c0004t0001g0088 | 3 | HG02027.hp2 HG02071.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.530-1628A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20713511 | ||||||
| chr12:20713777
|
T | A | 1 | a0001c0001t0001g0248 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.530-1362T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20713777 | ||||||
| chr12:20713802
|
A | G | 222 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0021others(219): Show | 225 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(222): Show |
intron_variant | MODIFIER | c.530-1337A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20713802 | ||||||
| chr12:20713879
|
A | G | 3 | a0001c0001t0001g0232a0001c0001t0001g0235a0001c0002t0002g0231 | 3 | HG01081.hp1 HG01106.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.530-1260A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20713879 | ||||||
| chr12:20714095
|
C | T | 9 | a0001c0002t0002g0077a0001c0003t0001g0099a0001c0003t0001g0167others(6): Show | 10 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.530-1044C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20714095 | ||||||
| chr12:20714262
|
A | G | 6 | a0001c0001t0004g0225a0001c0003t0001g0032a0001c0003t0001g0286others(3): Show | 6 | HG00099.hp2 HG02683.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.530-877A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20714262 | ||||||
| chr12:20714820
|
C | A | 5 | a0001c0001t0004g0225a0001c0003t0001g0032a0001c0003t0001g0286others(2): Show | 5 | HG00099.hp2 HG02683.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.530-319C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20714820 | ||||||
| chr12:20714830
|
T | C | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(9): Show | 13 | HG01168.hp1 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.530-309T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20714830 | ||||||
| chr12:20714891
|
A | G | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(9): Show | 13 | HG01168.hp1 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.530-248A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20714891 | ||||||
| chr12:20714959
|
C | T | 256 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(253): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.530-180C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20714959 | ||||||
| chr12:20714993
|
C | T | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(9): Show | 13 | HG01168.hp1 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.530-146C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20714993 | ||||||
| chr12:20715059
|
A | T | 5 | a0001c0003t0003g0054a0001c0003t0003g0195a0001c0003t0003g0196others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.530-80A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20715059 | ||||||
| chr12:20715313
|
C | T | 9 | a0001c0002t0002g0077a0001c0003t0001g0099a0001c0003t0001g0167others(6): Show | 10 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.676+28C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 6/14 | chr12 | 20715313 | ||||||
| chr12:20715517
|
C | T | 5 | a0001c0003t0003g0054a0001c0003t0003g0195a0001c0003t0003g0196others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.676+232C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 6/14 | chr12 | 20715517 | ||||||
| chr12:20715535
|
C | T | 5 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(2): Show | 5 | HG01175.hp1 HG02148.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.676+250C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 6/14 | chr12 | 20715535 | ||||||
| chr12:20715582
|
T | C | 11 | a0001c0001t0001g0009a0001c0001t0001g0058a0001c0001t0001g0059others(8): Show | 11 | HG01361.hp1 HG01891.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.676+297T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 6/14 | chr12 | 20715582 | ||||||
| chr12:20715664
|
C | CCA | 8 | a0001c0001t0001g0138a0001c0001t0001g0232a0001c0001t0001g0235others(5): Show | 8 | HG01081.hp1 HG01106.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.676+380_676+381dup others(2): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 20715664 | |||||
| chr12:20715675
|
G | GC | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(9): Show | 13 | HG01168.hp1 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.676+392dupC | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 20715675 | |||||
| chr12:20715914
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.676+629T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 6/14 | chr12 | 20715914 | ||||||
| chr12:20716148
|
T | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0106 | 2 | HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.676+863T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 6/14 | chr12 | 20716148 | ||||||
| chr12:20716335
|
G | C | 1 | a0001c0001t0001g0252 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.677-797G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 6/14 | chr12 | 20716335 | ||||||
| chr12:20716343
|
G | T | 1 | a0001c0001t0001g0106 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.677-789G>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 6/14 | chr12 | 20716343 | ||||||
| chr12:20716443
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.677-689A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 6/14 | chr12 | 20716443 | ||||||
| chr12:20716500
|
G | A | 217 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0021others(214): Show | 220 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(217): Show |
intron_variant | MODIFIER | c.677-632G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 6/14 | chr12 | 20716500 | ||||||
| chr12:20716631
|
C | T | 1 | a0001c0005t0002g0064 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.677-501C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 6/14 | chr12 | 20716631 | ||||||
| chr12:20716737
|
CATTTG | C | 9 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0172others(6): Show | 9 | HG00639.hp2 HG01891.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.677-393_677-389del others(5): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 20716737 | |||||
| chr12:20716774
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.677-358C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 6/14 | chr12 | 20716774 | ||||||
| chr12:20716936
|
G | T | 1 | a0001c0002t0002g0001 | 2 | HG01884.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.677-196G>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 6/14 | chr12 | 20716936 | ||||||
| chr12:20717009
|
G | T | 1 | a0001c0001t0001g0252 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.677-123G>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 6/14 | chr12 | 20717009 | ||||||
| chr12:20717010
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.677-122C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 6/14 | chr12 | 20717010 | ||||||
| chr12:20717099
|
C | CT | 8 | a0001c0001t0001g0138a0001c0001t0001g0232a0001c0001t0001g0235others(5): Show | 8 | HG01081.hp1 HG01106.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.677-22dupT | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 20717099 | |||||
| chr12:20717099
|
CTTTT | C | 9 | a0001c0002t0002g0077a0001c0003t0001g0099a0001c0003t0001g0167others(6): Show | 10 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.677-25_677-22delTT others(2): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 20717099 | |||||
| chr12:20717331
|
T | C | 45 | a0001c0001t0001g0011a0001c0001t0001g0048a0001c0001t0001g0102others(42): Show | 48 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.775+101T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20717331 | ||||||
| chr12:20717371
|
A | C | 1 | a0001c0002t0002g0077 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.775+141A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20717371 | ||||||
| chr12:20717531
|
G | T | 1 | a0001c0004t0001g0259 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.775+301G>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20717531 | ||||||
| chr12:20717645
|
CTTCTTTT others(22): Show |
C | 1 | a0001c0004t0001g0259 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.775+418_775+446del others(29): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20717645 | |||||
| chr12:20717648
|
C | CT | 35 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0096others(32): Show | 35 | HG00597.hp1 HG00639.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.775+462dupT | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20717648 | |||||
| chr12:20717648
|
C | CTTTT | 11 | a0001c0001t0001g0056a0001c0001t0001g0103a0001c0001t0001g0136others(8): Show | 11 | HG00099.hp2 HG02015.hp2 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.775+459_775+462dup others(4): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20717648 | |||||
| chr12:20717648
|
C | CTTTTTTT | 6 | a0001c0001t0001g0045a0001c0001t0001g0177a0001c0001t0001g0211others(3): Show | 6 | HG01891.hp2 HG02622.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.775+456_775+462dup others(7): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20717648 | |||||
| chr12:20717648
|
C | CTTTTTTT others(4): Show |
1 | a0001c0002t0002g0044 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.775+452_775+462dup others(11): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20717648 | |||||
| chr12:20717648
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.775+418C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20717648 | ||||||
| chr12:20717648
|
CT | C | 74 | a0001c0001t0001g0028a0001c0001t0001g0070a0001c0001t0001g0071others(71): Show | 75 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.775+462delT | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20717648 | |||||
| chr12:20717648
|
CTT | C | 6 | a0001c0001t0001g0121a0001c0001t0001g0130a0001c0001t0004g0225others(3): Show | 6 | HG00280.hp2 HG00558.hp2 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.775+461_775+462del others(2): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20717648 | |||||
| chr12:20717648
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0001g0112a0001c0001t0004g0029 | 2 | HG02572.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.775+450_775+462del others(13): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20717648 | |||||
| chr12:20717648
|
CTTTTTTT others(7): Show |
C | 10 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(7): Show | 11 | HG01168.hp1 HG02559.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.775+449_775+462del others(14): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20717648 | |||||
| chr12:20717648
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0003g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.775+448_775+462del others(15): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20717648 | |||||
| chr12:20717648
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0007 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.775+447_775+462del others(16): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20717648 | |||||
| chr12:20717648
|
CTTTTTTT others(11): Show |
C | 2 | a0001c0001t0001g0187a0001c0001t0001g0242 | 2 | HG04228.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.775+445_775+462del others(18): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20717648 | |||||
| chr12:20717648
|
CTTTTTTT others(12): Show |
C | 1 | a0001c0001t0001g0288 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.775+444_775+462del others(19): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20717648 | |||||
| chr12:20717648
|
CTTTTTTT others(13): Show |
C | 5 | a0001c0001t0001g0013a0001c0001t0005g0027a0001c0003t0001g0014others(2): Show | 5 | HG02622.hp1 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.775+443_775+462del others(20): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20717648 | |||||
| chr12:20717648
|
CTTTTTTT others(14): Show |
C | 11 | a0001c0001t0001g0048a0001c0002t0002g0001a0001c0002t0002g0077others(8): Show | 13 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.775+442_775+462del others(21): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20717648 | |||||
| chr12:20717648
|
CTTTTTTT others(15): Show |
C | 10 | a0001c0001t0001g0011a0001c0001t0001g0102a0001c0001t0001g0106others(7): Show | 10 | HG01496.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.775+441_775+462del others(22): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20717648 | |||||
| chr12:20717648
|
CTTTTTTT others(16): Show |
C | 1 | a0001c0002t0002g0163 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.775+440_775+462del others(23): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20717648 | |||||
| chr12:20717648
|
CTTTTTTT others(19): Show |
C | 8 | a0001c0001t0001g0138a0001c0001t0001g0232a0001c0001t0001g0235others(5): Show | 8 | HG01081.hp1 HG01106.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.775+437_775+462del others(26): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20717648 | |||||
| chr12:20717648
|
CTTTTTTT others(22): Show |
C | 4 | a0001c0001t0003g0213a0001c0002t0002g0004a0001c0002t0002g0233others(1): Show | 5 | HG01175.hp2 HG01496.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.775+434_775+462del others(29): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20717648 | |||||
| chr12:20717655
|
T | C | 1 | a0001c0005t0002g0200 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.775+425T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20717655 | ||||||
| chr12:20717657
|
T | C | 4 | a0001c0001t0001g0031a0001c0003t0003g0054a0001c0003t0003g0195others(1): Show | 4 | HG01169.hp1 HG02109.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.775+427T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20717657 | ||||||
| chr12:20717658
|
T | C | 1 | a0001c0003t0003g0196 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.775+428T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20717658 | ||||||
| chr12:20717682
|
T | C | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(9): Show | 13 | HG01168.hp1 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.775+452T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20717682 | ||||||
| chr12:20717730
|
C | A | 1 | a0001c0001t0001g0278 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.775+500C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20717730 | ||||||
| chr12:20717766
|
G | A | 277 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(274): Show | 282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.775+536G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20717766 | ||||||
| chr12:20717798
|
A | G | 6 | a0001c0001t0001g0031a0001c0003t0003g0054a0001c0003t0003g0195others(3): Show | 6 | HG01168.hp2 HG01169.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.775+568A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20717798 | ||||||
| chr12:20717813
|
T | C | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(9): Show | 13 | HG01168.hp1 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.775+583T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20717813 | ||||||
| chr12:20717922
|
G | A | 5 | a0001c0001t0004g0225a0001c0003t0001g0032a0001c0003t0001g0286others(2): Show | 5 | HG00099.hp2 HG02683.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.775+692G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20717922 | ||||||
| chr12:20718000
|
C | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0106 | 2 | HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.775+770C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20718000 | ||||||
| chr12:20718057
|
C | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0106 | 2 | HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.775+827C>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20718057 | ||||||
| chr12:20718084
|
A | T | 6 | a0001c0001t0001g0031a0001c0003t0003g0054a0001c0003t0003g0195others(3): Show | 6 | HG01168.hp2 HG01169.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.775+854A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20718084 | ||||||
| chr12:20718138
|
C | T | 67 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0031others(64): Show | 70 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.775+908C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20718138 | ||||||
| chr12:20718194
|
C | G | 2 | a0002c0010t0002g0219a0002c0010t0002g0220 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.775+964C>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20718194 | ||||||
| chr12:20718322
|
T | A | 41 | a0001c0001t0001g0011a0001c0001t0001g0048a0001c0001t0001g0102others(38): Show | 44 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.775+1092T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20718322 | ||||||
| chr12:20718427
|
C | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0106 | 2 | HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.775+1197C>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20718427 | ||||||
| chr12:20718512
|
A | G | 1 | a0001c0002t0002g0001 | 2 | HG01884.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.775+1282A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20718512 | ||||||
| chr12:20718825
|
G | A | 2 | a0001c0001t0005g0027a0001c0005t0002g0042 | 2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.775+1595G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20718825 | ||||||
| chr12:20718866
|
TATCTTGC others(14): Show |
T | 1 | a0001c0005t0006g0169 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.775+1637_775+1657d others(23): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20718866 | ||||||
| chr12:20719088
|
C | T | 1 | a0001c0003t0003g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.775+1858C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20719088 | ||||||
| chr12:20719100
|
C | CTAT | 18 | a0001c0001t0001g0021a0001c0001t0001g0104a0001c0001t0001g0106others(15): Show | 18 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.775+1900_775+1902d others(5): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20719100 | |||||
| chr12:20719100
|
C | CTATTAT | 18 | a0001c0001t0004g0225a0001c0002t0002g0077a0001c0002t0002g0181others(15): Show | 19 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.775+1897_775+1902d others(8): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20719100 | |||||
| chr12:20719100
|
C | CTATTATT others(2): Show |
7 | a0001c0001t0001g0048a0001c0002t0002g0283a0001c0003t0001g0119others(4): Show | 7 | HG01081.hp2 HG01123.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.775+1894_775+1902d others(11): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20719100 | |||||
| chr12:20719100
|
C | CTATTATT others(5): Show |
28 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0031others(25): Show | 29 | HG01257.hp2 HG01361.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.775+1891_775+1902d others(14): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20719100 | |||||
| chr12:20719100
|
C | CTATTATT others(8): Show |
4 | a0001c0001t0001g0232a0001c0001t0001g0235a0001c0002t0002g0231others(1): Show | 4 | HG01081.hp1 HG01106.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.775+1888_775+1902d others(17): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20719100 | |||||
| chr12:20719135
|
T | A | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(9): Show | 13 | HG01168.hp1 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.775+1905T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20719135 | ||||||
| chr12:20719196
|
G | A | 12 | a0001c0001t0001g0011a0001c0001t0001g0048a0001c0001t0001g0102others(9): Show | 13 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.775+1966G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20719196 | ||||||
| chr12:20719709
|
G | T | 1 | a0001c0002t0002g0053 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.776-2095G>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20719709 | ||||||
| chr12:20719886
|
C | A | 8 | a0001c0001t0001g0009a0001c0001t0001g0058a0001c0001t0001g0059others(5): Show | 8 | HG01891.hp1 HG02922.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.776-1918C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20719886 | ||||||
| chr12:20720017
|
A | T | 2 | a0001c0001t0005g0027a0001c0005t0002g0042 | 2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.776-1787A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20720017 | ||||||
| chr12:20720202
|
A | AT | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(9): Show | 13 | HG01168.hp1 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.776-1602_776-1601i others(3): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20720202 | ||||||
| chr12:20720202
|
A | T | 217 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0021others(214): Show | 220 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(217): Show |
intron_variant | MODIFIER | c.776-1602A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20720202 | ||||||
| chr12:20720204
|
T | A | 8 | a0001c0001t0001g0138a0001c0001t0001g0232a0001c0001t0001g0235others(5): Show | 8 | HG01081.hp1 HG01106.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.776-1600T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20720204 | ||||||
| chr12:20720236
|
C | T | 1 | a0001c0005t0002g0042 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.776-1568C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20720236 | ||||||
| chr12:20720300
|
A | T | 244 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(241): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.776-1504A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20720300 | ||||||
| chr12:20720317
|
G | A | 10 | a0001c0001t0001g0009a0001c0001t0001g0058a0001c0001t0001g0059others(7): Show | 10 | HG01361.hp1 HG01891.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.776-1487G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20720317 | ||||||
| chr12:20720387
|
C | T | 1 | a0001c0002t0002g0109 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.776-1417C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20720387 | ||||||
| chr12:20720678
|
C | T | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(9): Show | 13 | HG01168.hp1 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.776-1126C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20720678 | ||||||
| chr12:20720685
|
A | C | 8 | a0001c0001t0001g0138a0001c0001t0001g0232a0001c0001t0001g0235others(5): Show | 8 | HG01081.hp1 HG01106.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.776-1119A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20720685 | ||||||
| chr12:20720809
|
G | C | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(9): Show | 13 | HG01168.hp1 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.776-995G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20720809 | ||||||
| chr12:20720997
|
C | CA | 39 | a0001c0001t0001g0011a0001c0001t0001g0048a0001c0001t0001g0106others(36): Show | 41 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.776-785dupA | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20720997 | |||||
| chr12:20720997
|
C | CAA | 24 | a0001c0001t0001g0102a0001c0001t0001g0138a0001c0001t0001g0160others(21): Show | 25 | HG00735.hp1 HG01081.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.776-786_776-785dup others(2): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20720997 | |||||
| chr12:20721083
|
C | A | 2 | a0001c0002t0002g0233a0001c0002t0002g0234 | 2 | HG01175.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.776-721C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20721083 | ||||||
| chr12:20721100
|
T | A | 1 | a0001c0002t0002g0057 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.776-704T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20721100 | ||||||
| chr12:20721298
|
C | T | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(9): Show | 13 | HG01168.hp1 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.776-506C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20721298 | ||||||
| chr12:20721309
|
T | C | 14 | a0001c0002t0002g0077a0001c0002t0002g0093a0001c0003t0001g0099others(11): Show | 15 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.776-495T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20721309 | ||||||
| chr12:20721339
|
C | A | 1 | a0001c0004t0003g0180 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.776-465C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20721339 | ||||||
| chr12:20721381
|
T | C | 1 | a0001c0004t0003g0247 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.776-423T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20721381 | ||||||
| chr12:20721461
|
CT | C | 24 | a0001c0001t0001g0079a0001c0001t0001g0135a0001c0001t0001g0136others(21): Show | 25 | HG02056.hp2 HG02135.hp2 HG02523.hp1 others(22): Show |
intron_variant | MODIFIER | c.776-334delT | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20721461 | |||||
| chr12:20721524
|
A | G | 2 | a0001c0006t0001g0144a0001c0021t0001g0157 | 2 | HG02080.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.776-280A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20721524 | ||||||
| chr12:20721665
|
TA | T | 43 | a0001c0001t0001g0011a0001c0001t0001g0048a0001c0001t0001g0102others(40): Show | 45 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.776-128delA | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20721665 | |||||
| chr12:20721665
|
TAA | T | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(9): Show | 13 | HG01168.hp1 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.776-129_776-128del others(2): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 20721665 | |||||
| chr12:20721666
|
A | T | 1 | a0001c0022t0002g0115 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.776-138A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20721666 | ||||||
| chr12:20721667
|
A | T | 6 | a0001c0001t0004g0225a0001c0003t0001g0032a0001c0003t0001g0286others(3): Show | 6 | HG00099.hp2 HG02683.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.776-137A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20721667 | ||||||
| chr12:20722056
|
C | G | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(9): Show | 13 | HG01168.hp1 HG02559.hp1 HG02559.hp2 others(10): Show |
splice_region_variant&intron_variant | LOW | c.1021+7C>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 8/14 | chr12 | 20722056 | ||||||
| chr12:20722062
|
C | A | 8 | a0001c0001t0001g0138a0001c0001t0001g0232a0001c0001t0001g0235others(5): Show | 8 | HG01081.hp1 HG01106.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1021+13C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 8/14 | chr12 | 20722062 | ||||||
| chr12:20722098
|
T | C | 1 | a0001c0005t0002g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1021+49T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 8/14 | chr12 | 20722098 | ||||||
| chr12:20722348
|
A | G | 1 | a0001c0003t0001g0032 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1021+299A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 8/14 | chr12 | 20722348 | ||||||
| chr12:20722452
|
G | A | 47 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0048others(44): Show | 50 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1021+403G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 8/14 | chr12 | 20722452 | ||||||
| chr12:20722650
|
A | G | 2 | a0001c0006t0008g0039a0003c0012t0001g0126 | 2 | HG01978.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1022-440A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 8/14 | chr12 | 20722650 | ||||||
| chr12:20722727
|
G | T | 1 | a0001c0002t0002g0279 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1022-363G>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 8/14 | chr12 | 20722727 | ||||||
| chr12:20722767
|
G | C | 1 | a0001c0002t0002g0277 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1022-323G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 8/14 | chr12 | 20722767 | ||||||
| chr12:20722875
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1022-215A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 8/14 | chr12 | 20722875 | ||||||
| chr12:20723020
|
C | T | 1 | a0001c0005t0002g0042 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1022-70C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 8/14 | chr12 | 20723020 | ||||||
| chr12:20723047
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1022-43G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 8/14 | chr12 | 20723047 | ||||||
| chr12:20723049
|
G | T | 22 | a0001c0001t0001g0011a0001c0001t0001g0048a0001c0001t0001g0102others(19): Show | 24 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.1022-41G>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 8/14 | chr12 | 20723049 | ||||||
| chr12:20723051
|
C | T | 3 | a0001c0001t0001g0232a0001c0001t0001g0235a0001c0002t0002g0231 | 3 | HG01081.hp1 HG01106.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1022-39C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 8/14 | chr12 | 20723051 | ||||||
| chr12:20723262
|
C | T | 2 | a0001c0005t0002g0254a0001c0008t0002g0217 | 2 | HG00735.hp2 HG01167.hp1 |
splice_region_variant&intron_variant | LOW | c.1186+8C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20723262 | ||||||
| chr12:20723293
|
G | C | 66 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0048others(63): Show | 69 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.1186+39G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20723293 | ||||||
| chr12:20723548
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1186+294G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20723548 | ||||||
| chr12:20723640
|
G | A | 8 | a0001c0001t0001g0138a0001c0001t0001g0232a0001c0001t0001g0235others(5): Show | 8 | HG01081.hp1 HG01106.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1186+386G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20723640 | ||||||
| chr12:20723760
|
T | C | 73 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0031others(70): Show | 76 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.1186+506T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20723760 | ||||||
| chr12:20723933
|
C | G | 1 | a0001c0001t0001g0290 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1186+679C>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20723933 | ||||||
| chr12:20724013
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1186+759G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20724013 | ||||||
| chr12:20724144
|
A | G | 14 | a0001c0002t0002g0077a0001c0002t0002g0093a0001c0003t0001g0099others(11): Show | 15 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.1186+890A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20724144 | ||||||
| chr12:20724154
|
A | G | 73 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0031others(70): Show | 76 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.1186+900A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20724154 | ||||||
| chr12:20724244
|
T | C | 4 | a0001c0002t0002g0092a0001c0002t0002g0246a0001c0002t0002g0284others(1): Show | 4 | HG01928.hp1 HG02148.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1186+990T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20724244 | ||||||
| chr12:20724292
|
CTTTAT | C | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(9): Show | 13 | HG01168.hp1 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1186+1046_1186+105 others(9): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724292 | |||||
| chr12:20724393
|
ATG | A | 11 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0121others(8): Show | 11 | HG00735.hp1 HG01496.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.1186+1157_1186+115 others(6): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724393 | |||||
| chr12:20724405
|
GTGTGTGT others(3): Show |
G | 1 | a0001c0002t0002g0283 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1186+1153_1186+116 others(14): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724405 | |||||
| chr12:20724405
|
GTGTGTGT others(5): Show |
G | 4 | a0001c0001t0001g0048a0001c0001t0001g0204a0001c0001t0003g0020others(1): Show | 4 | HG02717.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1186+1153_1186+116 others(16): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724405 | |||||
| chr12:20724405
|
GTGTGTGT others(7): Show |
G | 6 | a0001c0001t0001g0011a0001c0001t0001g0102a0001c0001t0001g0107others(3): Show | 6 | HG02109.hp2 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1186+1153_1186+116 others(18): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724405 | |||||
| chr12:20724405
|
GTGTGTGT others(9): Show |
G | 2 | a0001c0002t0002g0001a0001c0002t0002g0175 | 3 | HG01884.hp2 HG02615.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1186+1153_1186+116 others(20): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724405 | |||||
| chr12:20724407
|
GTGTGTAT others(3): Show |
G | 2 | a0001c0002t0002g0089a0001c0004t0001g0088 | 2 | HG02027.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.1186+1155_1186+116 others(14): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724407 | |||||
| chr12:20724407
|
GTGTGTAT others(7): Show |
G | 1 | a0001c0001t0001g0106 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1186+1155_1186+116 others(18): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724407 | |||||
| chr12:20724407
|
GTGTGTAT others(9): Show |
G | 3 | a0001c0001t0004g0225a0001c0001t0005g0027a0001c0005t0006g0169 | 3 | HG02630.hp1 HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1186+1155_1186+117 others(20): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724407 | |||||
| chr12:20724407
|
GTGTGTAT others(11): Show |
G | 5 | a0001c0003t0001g0032a0001c0003t0001g0286a0001c0005t0002g0042others(2): Show | 5 | HG00099.hp2 HG02683.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1186+1155_1186+117 others(22): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724407 | |||||
| chr12:20724407
|
GTGTGTAT others(13): Show |
G | 1 | a0001c0001t0001g0031 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1186+1155_1186+117 others(24): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724407 | |||||
| chr12:20724407
|
GTGTGTAT others(15): Show |
G | 9 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(6): Show | 9 | HG01168.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1186+1155_1186+117 others(26): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724407 | |||||
| chr12:20724407
|
GTGTGTAT others(17): Show |
G | 3 | a0001c0003t0005g0002a0001c0003t0005g0025a0001c0003t0005g0026 | 4 | HG02559.hp1 HG03209.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1186+1155_1186+117 others(28): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724407 | |||||
| chr12:20724407
|
GTGTGTAT others(19): Show |
G | 8 | a0001c0001t0001g0138a0001c0001t0001g0232a0001c0001t0001g0235others(5): Show | 8 | HG01081.hp1 HG01106.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1186+1155_1186+118 others(30): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724407 | |||||
| chr12:20724407
|
GTGTGTAT others(23): Show |
G | 1 | a0001c0002t0002g0222 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1186+1155_1186+118 others(34): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724407 | |||||
| chr12:20724409
|
GTGTA | G | 23 | a0001c0001t0001g0013a0001c0001t0001g0074a0001c0001t0001g0075others(20): Show | 23 | HG00099.hp1 HG00639.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.1186+1157_1186+116 others(8): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724409 | |||||
| chr12:20724409
|
GTGTATA | G | 28 | a0001c0001t0001g0028a0001c0001t0001g0070a0001c0001t0001g0072others(25): Show | 29 | HG00738.hp1 HG00738.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1186+1157_1186+116 others(10): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724409 | |||||
| chr12:20724409
|
GTGTATAT others(1): Show |
G | 66 | a0001c0001t0001g0035a0001c0001t0001g0045a0001c0001t0001g0055others(63): Show | 67 | HG00544.hp1 HG00558.hp1 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.1186+1157_1186+116 others(12): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724409 | |||||
| chr12:20724409
|
GTGTATAT others(3): Show |
G | 29 | a0001c0001t0001g0056a0001c0001t0001g0123a0001c0001t0001g0130others(26): Show | 29 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.1186+1157_1186+116 others(14): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724409 | |||||
| chr12:20724409
|
GTGTATAT others(5): Show |
G | 7 | a0001c0001t0001g0079a0001c0001t0001g0091a0001c0001t0004g0101others(4): Show | 7 | HG01069.hp2 HG01106.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.1186+1157_1186+116 others(16): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724409 | |||||
| chr12:20724409
|
GTGTATAT others(7): Show |
G | 2 | a0001c0001t0001g0278a0001c0002t0002g0152 | 2 | HG01261.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1186+1157_1186+117 others(18): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724409 | |||||
| chr12:20724409
|
GTGTATAT others(9): Show |
G | 2 | a0001c0001t0004g0285a0001c0005t0002g0200 | 2 | HG00642.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1186+1157_1186+117 others(20): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724409 | |||||
| chr12:20724409
|
GTGTATAT others(11): Show |
G | 10 | a0001c0001t0001g0009a0001c0001t0001g0058a0001c0001t0001g0059others(7): Show | 10 | HG01515.hp1 HG01891.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.1186+1157_1186+117 others(22): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724409 | |||||
| chr12:20724409
|
GTGTATAT others(13): Show |
G | 1 | a0001c0013t0001g0241 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1186+1157_1186+117 others(24): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724409 | |||||
| chr12:20724411
|
G | A | 28 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0076others(25): Show | 30 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1186+1157G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20724411 | ||||||
| chr12:20724411
|
GTA | G | 4 | a0001c0002t0002g0030a0001c0002t0002g0143a0001c0004t0001g0094others(1): Show | 4 | HG00558.hp2 HG01081.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.1186+1197_1186+119 others(6): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724411 | |||||
| chr12:20724411
|
GTATA | G | 12 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0002t0002g0036others(9): Show | 12 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1186+1195_1186+119 others(8): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724411 | |||||
| chr12:20724411
|
GTATATA | G | 10 | a0001c0001t0001g0084a0001c0001t0001g0104a0001c0001t0001g0287others(7): Show | 10 | HG00597.hp2 HG02040.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1186+1193_1186+119 others(10): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724411 | |||||
| chr12:20724415
|
A | G | 1 | a0001c0009t0002g0125 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1186+1161A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20724415 | ||||||
| chr12:20724435
|
ATATATAT others(11): Show |
A | 3 | a0001c0003t0003g0195a0001c0003t0003g0196a0001c0003t0007g0017 | 3 | HG01168.hp2 HG01169.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1186+1183_1186+120 others(22): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724435 | |||||
| chr12:20724443
|
ATATATAT others(3): Show |
A | 1 | a0001c0001t0001g0290 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1186+1191_1186+120 others(14): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724443 | |||||
| chr12:20724445
|
A | G | 1 | a0001c0003t0001g0099 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1186+1191A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20724445 | ||||||
| chr12:20724445
|
ATATATAT others(3): Show |
A | 1 | a0001c0001t0001g0178 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1186+1193_1186+120 others(14): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724445 | |||||
| chr12:20724447
|
A | ATG | 2 | a0002c0007t0001g0260a0002c0007t0004g0006 | 3 | HG00280.hp1 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1186+1194_1186+119 others(6): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724447 | |||||
| chr12:20724447
|
A | G | 16 | a0001c0001t0001g0011a0001c0002t0002g0034a0001c0002t0002g0093others(13): Show | 17 | HG00642.hp1 HG00735.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1186+1193A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20724447 | ||||||
| chr12:20724449
|
A | G | 64 | a0001c0001t0001g0011a0001c0001t0001g0035a0001c0001t0001g0048others(61): Show | 66 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1186+1195A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20724449 | ||||||
| chr12:20724451
|
A | ATATATAT others(3): Show |
1 | a0002c0007t0001g0062 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1186+1198_1186+119 others(14): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724451 | |||||
| chr12:20724451
|
A | ATATG | 4 | a0001c0001t0001g0103a0001c0001t0001g0188a0001c0002t0002g0004others(1): Show | 5 | HG02055.hp2 HG02976.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.1186+1198_1186+119 others(8): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724451 | |||||
| chr12:20724451
|
A | ATG | 6 | a0001c0001t0001g0021a0001c0001t0003g0174a0001c0001t0004g0168others(3): Show | 6 | HG01175.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1186+1223_1186+122 others(6): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20724451 | |||||
| chr12:20724451
|
A | G | 232 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(229): Show | 237 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.1186+1197A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20724451 | ||||||
| chr12:20724453
|
G | A | 26 | a0001c0001t0001g0009a0001c0001t0001g0031a0001c0001t0001g0058others(23): Show | 26 | HG00099.hp2 HG00642.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.1186+1199G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20724453 | ||||||
| chr12:20724455
|
G | A | 8 | a0001c0001t0001g0138a0001c0001t0001g0232a0001c0001t0001g0235others(5): Show | 8 | HG01081.hp1 HG01106.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1186+1201G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20724455 | ||||||
| chr12:20724469
|
G | A | 1 | a0001c0005t0002g0269 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1186+1215G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20724469 | ||||||
| chr12:20724553
|
T | C | 1 | a0001c0020t0009g0016 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1186+1299T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20724553 | ||||||
| chr12:20724662
|
T | A | 8 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0003t0001g0203others(5): Show | 8 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1186+1408T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20724662 | ||||||
| chr12:20724683
|
T | C | 3 | a0001c0002t0002g0250a0001c0005t0002g0254a0001c0008t0002g0217 | 3 | HG00735.hp2 HG01167.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1186+1429T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20724683 | ||||||
| chr12:20724918
|
T | C | 3 | a0001c0001t0004g0168a0001c0002t0002g0046a0001c0006t0001g0215 | 3 | HG03688.hp2 HG03927.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1186+1664T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20724918 | ||||||
| chr12:20725025
|
A | G | 7 | a0001c0001t0001g0084a0001c0002t0002g0090a0001c0002t0011g0083others(4): Show | 7 | NA18952.hp1 NA18962.hp1 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.1186+1771A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20725025 | ||||||
| chr12:20725088
|
AAAT | A | 28 | a0001c0001t0001g0011a0001c0001t0001g0048a0001c0001t0001g0102others(25): Show | 30 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.1186+1839_1186+184 others(7): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20725088 | |||||
| chr12:20725162
|
AATT | A | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(9): Show | 13 | HG01168.hp1 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1186+1915_1186+191 others(7): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20725162 | |||||
| chr12:20725227
|
G | T | 214 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0021others(211): Show | 217 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(214): Show |
intron_variant | MODIFIER | c.1186+1973G>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20725227 | ||||||
| chr12:20725247
|
AAATATGT others(5): Show |
A | 8 | a0001c0001t0001g0138a0001c0001t0001g0232a0001c0001t0001g0235others(5): Show | 8 | HG01081.hp1 HG01106.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1186+2004_1186+201 others(16): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20725247 | |||||
| chr12:20725280
|
ATAT | A | 7 | a0001c0001t0001g0045a0001c0001t0001g0055a0001c0001t0001g0056others(4): Show | 7 | HG02723.hp1 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1186+2030_1186+203 others(7): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20725280 | |||||
| chr12:20725332
|
A | T | 11 | a0001c0001t0001g0079a0001c0002t0002g0127a0001c0004t0001g0118others(8): Show | 11 | HG00558.hp1 HG00597.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.1186+2078A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20725332 | ||||||
| chr12:20725382
|
GTATAA | G | 3 | a0001c0003t0005g0002a0001c0003t0005g0025a0001c0003t0005g0026 | 4 | HG02559.hp1 HG03209.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1186+2133_1186+213 others(9): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20725382 | |||||
| chr12:20725825
|
C | A | 2 | a0001c0002t0002g0036a0001c0002t0002g0037 | 2 | NA18983.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1186+2571C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20725825 | ||||||
| chr12:20725845
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1186+2591G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20725845 | ||||||
| chr12:20726056
|
G | A | 3 | a0001c0001t0001g0106a0001c0001t0004g0168a0001c0006t0001g0215 | 3 | HG03195.hp1 HG03927.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1186+2802G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20726056 | ||||||
| chr12:20726192
|
G | A | 10 | a0001c0001t0001g0009a0001c0001t0001g0058a0001c0001t0001g0059others(7): Show | 10 | HG01361.hp1 HG01891.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.1186+2938G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20726192 | ||||||
| chr12:20726251
|
AT | A | 40 | a0001c0001t0001g0011a0001c0001t0001g0048a0001c0001t0001g0102others(37): Show | 42 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1186+3009delT | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20726251 | |||||
| chr12:20726251
|
ATT | A | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(9): Show | 13 | HG01168.hp1 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1186+3008_1186+300 others(6): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20726251 | |||||
| chr12:20726296
|
A | G | 5 | a0001c0001t0004g0225a0001c0003t0001g0032a0001c0003t0001g0286others(2): Show | 5 | HG00099.hp2 HG02683.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1186+3042A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20726296 | ||||||
| chr12:20726330
|
C | T | 3 | a0001c0001t0001g0091a0001c0001t0004g0101a0001c0001t0004g0285 | 3 | HG00642.hp2 HG01069.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1186+3076C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20726330 | ||||||
| chr12:20726659
|
G | T | 2 | a0001c0002t0002g0233a0001c0002t0002g0234 | 2 | HG01175.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1186+3405G>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20726659 | ||||||
| chr12:20726673
|
C | A | 1 | a0001c0004t0003g0180 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1186+3419C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20726673 | ||||||
| chr12:20726785
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1186+3531A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20726785 | ||||||
| chr12:20726965
|
G | A | 3 | a0001c0001t0001g0114a0001c0001t0001g0242a0001c0005t0002g0281 | 3 | HG03490.hp1 HG03942.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1186+3711G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20726965 | ||||||
| chr12:20727146
|
G | C | 1 | a0001c0002t0002g0001 | 2 | HG01884.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1186+3892G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20727146 | ||||||
| chr12:20727260
|
C | A | 7 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1186+4006C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20727260 | ||||||
| chr12:20727322
|
C | A | 1 | a0001c0005t0002g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1186+4068C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20727322 | ||||||
| chr12:20727344
|
C | T | 1 | a0001c0005t0006g0169 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1186+4090C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20727344 | ||||||
| chr12:20727401
|
G | C | 1 | a0001c0001t0001g0011 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1186+4147G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20727401 | ||||||
| chr12:20727471
|
C | T | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(9): Show | 13 | HG01168.hp1 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1186+4217C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20727471 | ||||||
| chr12:20727472
|
A | G | 1 | a0001c0002t0002g0087 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1186+4218A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20727472 | ||||||
| chr12:20727596
|
G | C | 2 | a0001c0001t0001g0074a0001c0002t0002g0282 | 2 | HG01175.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1186+4342G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20727596 | ||||||
| chr12:20727661
|
C | T | 1 | a0001c0002t0002g0283 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1186+4407C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20727661 | ||||||
| chr12:20727981
|
T | C | 6 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(3): Show | 6 | HG01175.hp1 HG01433.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.1186+4727T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20727981 | ||||||
| chr12:20728004
|
C | T | 8 | a0001c0001t0001g0138a0001c0001t0001g0232a0001c0001t0001g0235others(5): Show | 8 | HG01081.hp1 HG01106.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1186+4750C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20728004 | ||||||
| chr12:20728083
|
T | G | 1 | a0001c0001t0003g0174 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1187-4826T>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20728083 | ||||||
| chr12:20728182
|
A | G | 9 | a0001c0001t0001g0048a0001c0001t0001g0102a0001c0001t0001g0107others(6): Show | 10 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1187-4727A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20728182 | ||||||
| chr12:20728235
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1187-4674T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20728235 | ||||||
| chr12:20728255
|
AT | A | 14 | a0001c0002t0002g0077a0001c0002t0002g0093a0001c0003t0001g0099others(11): Show | 15 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.1187-4651delT | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20728255 | |||||
| chr12:20728487
|
T | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0173 | 2 | HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1187-4422T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20728487 | ||||||
| chr12:20728814
|
G | A | 1 | a0001c0002t0002g0273 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1187-4095G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20728814 | ||||||
| chr12:20728827
|
A | C | 1 | a0001c0001t0001g0011 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1187-4082A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20728827 | ||||||
| chr12:20728828
|
A | G | 57 | a0001c0001t0001g0011a0001c0001t0001g0048a0001c0001t0001g0102others(54): Show | 60 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.1187-4081A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20728828 | ||||||
| chr12:20729064
|
A | G | 3 | a0001c0001t0001g0202a0001c0002t0002g0067a0001c0002t0002g0164 | 3 | HG00099.hp1 HG01358.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1187-3845A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20729064 | ||||||
| chr12:20729156
|
C | A | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(9): Show | 13 | HG01168.hp1 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1187-3753C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20729156 | ||||||
| chr12:20729271
|
G | A | 38 | a0001c0001t0001g0011a0001c0001t0001g0048a0001c0001t0001g0102others(35): Show | 41 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.1187-3638G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20729271 | ||||||
| chr12:20729332
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1187-3577A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20729332 | ||||||
| chr12:20729563
|
A | C | 2 | a0001c0001t0005g0027a0001c0005t0002g0042 | 2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1187-3346A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20729563 | ||||||
| chr12:20729631
|
C | T | 1 | a0001c0001t0005g0027 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1187-3278C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20729631 | ||||||
| chr12:20729776
|
G | T | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(9): Show | 13 | HG01168.hp1 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1187-3133G>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20729776 | ||||||
| chr12:20729856
|
A | G | 1 | a0001c0006t0001g0144 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1187-3053A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20729856 | ||||||
| chr12:20730146
|
G | C | 11 | a0001c0001t0001g0009a0001c0001t0001g0058a0001c0001t0001g0059others(8): Show | 11 | HG01361.hp1 HG01891.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.1187-2763G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20730146 | ||||||
| chr12:20730453
|
A | G | 1 | a0001c0005t0006g0169 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1187-2456A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20730453 | ||||||
| chr12:20730473
|
G | C | 266 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0021others(263): Show | 271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1187-2436G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20730473 | ||||||
| chr12:20730761
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1187-2148C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20730761 | ||||||
| chr12:20730872
|
C | T | 1 | a0001c0002t0002g0046 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1187-2037C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20730872 | ||||||
| chr12:20730877
|
A | G | 1 | a0001c0003t0003g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1187-2032A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20730877 | ||||||
| chr12:20730888
|
A | G | 2 | a0001c0001t0001g0179a0001c0014t0003g0264 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1187-2021A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20730888 | ||||||
| chr12:20730955
|
T | C | 1 | a0001c0002t0002g0189 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1187-1954T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20730955 | ||||||
| chr12:20731004
|
G | A | 39 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0048others(36): Show | 41 | HG01168.hp1 HG01361.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.1187-1905G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20731004 | ||||||
| chr12:20731186
|
C | T | 1 | a0002c0007t0001g0260 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1187-1723C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20731186 | ||||||
| chr12:20731391
|
GAACA | G | 59 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0048others(56): Show | 61 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.1187-1511_1187-150 others(8): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20731391 | |||||
| chr12:20731453
|
T | C | 1 | a0001c0002t0002g0273 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1187-1456T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20731453 | ||||||
| chr12:20731473
|
C | T | 9 | a0001c0001t0001g0011a0001c0001t0001g0048a0001c0001t0001g0102others(6): Show | 10 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1187-1436C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20731473 | ||||||
| chr12:20731474
|
A | G | 1 | a0001c0002t0002g0282 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1187-1435A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20731474 | ||||||
| chr12:20731780
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1187-1129C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20731780 | ||||||
| chr12:20731866
|
C | T | 54 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0048others(51): Show | 56 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1187-1043C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20731866 | ||||||
| chr12:20731867
|
AT | A | 54 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0048others(51): Show | 56 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1187-1033delT | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 20731867 | |||||
| chr12:20731877
|
A | G | 54 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0048others(51): Show | 56 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1187-1032A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20731877 | ||||||
| chr12:20731906
|
A | G | 1 | a0001c0013t0001g0241 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1187-1003A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20731906 | ||||||
| chr12:20731930
|
T | C | 54 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0048others(51): Show | 56 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1187-979T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20731930 | ||||||
| chr12:20731952
|
T | C | 1 | a0002c0007t0001g0226 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1187-957T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20731952 | ||||||
| chr12:20732159
|
A | G | 3 | a0001c0005t0002g0064a0001c0005t0002g0108a0001c0005t0002g0224 | 3 | HG01515.hp2 HG03710.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1187-750A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20732159 | ||||||
| chr12:20732212
|
A | G | 2 | a0001c0002t0002g0067a0001c0002t0002g0164 | 2 | HG00099.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1187-697A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20732212 | ||||||
| chr12:20732233
|
T | C | 52 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0058others(49): Show | 53 | HG00099.hp2 HG00642.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.1187-676T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20732233 | ||||||
| chr12:20732335
|
G | A | 180 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0028others(177): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1187-574G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20732335 | ||||||
| chr12:20732346
|
T | C | 7 | a0001c0001t0001g0045a0001c0001t0001g0055a0001c0001t0001g0056others(4): Show | 7 | HG02723.hp1 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1187-563T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20732346 | ||||||
| chr12:20732361
|
G | C | 1 | a0001c0002t0002g0234 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1187-548G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20732361 | ||||||
| chr12:20732380
|
T | C | 252 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(249): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.1187-529T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20732380 | ||||||
| chr12:20732411
|
T | C | 8 | a0001c0001t0001g0013a0001c0001t0001g0048a0001c0001t0001g0176others(5): Show | 8 | HG02055.hp2 HG02622.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1187-498T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20732411 | ||||||
| chr12:20732504
|
G | T | 5 | a0001c0001t0004g0029a0001c0001t0004g0225a0001c0002t0002g0063others(2): Show | 5 | HG01168.hp1 HG01346.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1187-405G>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20732504 | ||||||
| chr12:20732506
|
C | A | 8 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(5): Show | 8 | HG02922.hp1 HG02970.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1187-403C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20732506 | ||||||
| chr12:20732622
|
T | C | 1 | a0001c0001t0003g0020 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1187-287T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20732622 | ||||||
| chr12:20732649
|
A | C | 1 | a0001c0001t0003g0020 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1187-260A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20732649 | ||||||
| chr12:20732703
|
C | A | 288 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(285): Show | 294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.1187-206C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20732703 | ||||||
| chr12:20732707
|
T | C | 122 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(119): Show | 125 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.1187-202T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20732707 | ||||||
| chr12:20732716
|
C | T | 1 | a0001c0001t0003g0020 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1187-193C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20732716 | ||||||
| chr12:20732897
|
C | G | 2 | a0001c0002t0002g0151a0001c0003t0001g0014 | 2 | HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1187-12C>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20732897 | ||||||
| chr12:20733214
|
G | T | 15 | a0001c0001t0003g0081a0001c0001t0003g0113a0001c0001t0003g0213others(12): Show | 16 | HG00738.hp2 HG01978.hp1 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.1382+110G>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20733214 | ||||||
| chr12:20733251
|
C | T | 110 | a0001c0001t0001g0107a0001c0001t0004g0168a0001c0002t0002g0003others(107): Show | 113 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.1382+147C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20733251 | ||||||
| chr12:20733258
|
C | T | 13 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0002t0002g0001others(10): Show | 14 | HG01884.hp2 HG02109.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1382+154C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20733258 | ||||||
| chr12:20733306
|
T | C | 14 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0002t0002g0001others(11): Show | 15 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1382+202T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20733306 | ||||||
| chr12:20733500
|
T | C | 113 | a0001c0001t0001g0107a0001c0001t0004g0168a0001c0002t0002g0003others(110): Show | 116 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.1382+396T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20733500 | ||||||
| chr12:20733507
|
G | A | 1 | a0001c0002t0002g0276 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1382+403G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20733507 | ||||||
| chr12:20733644
|
G | C | 1 | a0001c0003t0005g0025 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1382+540G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20733644 | ||||||
| chr12:20733836
|
A | G | 2 | a0001c0005t0002g0184a0001c0020t0009g0016 | 2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1382+732A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20733836 | ||||||
| chr12:20733952
|
T | C | 10 | a0001c0001t0004g0029a0001c0001t0004g0101a0001c0001t0004g0132others(7): Show | 11 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.1382+848T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20733952 | ||||||
| chr12:20734057
|
A | G | 113 | a0001c0001t0001g0107a0001c0001t0004g0168a0001c0002t0002g0003others(110): Show | 116 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.1382+953A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20734057 | ||||||
| chr12:20734134
|
G | A | 2 | a0001c0002t0002g0087a0001c0009t0002g0085 | 2 | NA18971.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1382+1030G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20734134 | ||||||
| chr12:20734280
|
G | C | 106 | a0001c0001t0004g0168a0001c0002t0002g0003a0001c0002t0002g0004others(103): Show | 108 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.1382+1176G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20734280 | ||||||
| chr12:20734354
|
G | C | 1 | a0001c0002t0002g0067 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1382+1250G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20734354 | ||||||
| chr12:20734580
|
A | C | 3 | a0002c0007t0001g0062a0002c0007t0001g0226a0002c0007t0004g0006 | 4 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.1382+1476A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20734580 | ||||||
| chr12:20735028
|
A | T | 19 | a0001c0001t0001g0011a0001c0001t0003g0012a0001c0001t0003g0019others(16): Show | 19 | HG00544.hp2 HG02027.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.1382+1924A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20735028 | ||||||
| chr12:20735275
|
A | T | 15 | a0001c0001t0003g0081a0001c0001t0003g0113a0001c0001t0003g0213others(12): Show | 16 | HG00738.hp2 HG01978.hp1 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.1383-1832A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20735275 | ||||||
| chr12:20735278
|
A | G | 1 | a0001c0003t0001g0239 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1383-1829A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20735278 | ||||||
| chr12:20735323
|
A | G | 1 | a0001c0003t0012g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1383-1784A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20735323 | ||||||
| chr12:20735522
|
T | G | 2 | a0001c0001t0001g0111a0001c0003t0001g0197 | 2 | HG02602.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1383-1585T>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20735522 | ||||||
| chr12:20735581
|
T | C | 19 | a0001c0001t0001g0011a0001c0001t0003g0012a0001c0001t0003g0019others(16): Show | 19 | HG00544.hp2 HG02027.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.1383-1526T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20735581 | ||||||
| chr12:20735750
|
C | A | 1 | a0001c0016t0001g0050 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1383-1357C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20735750 | ||||||
| chr12:20736004
|
A | C | 2 | a0001c0002t0006g0223a0001c0005t0006g0169 | 2 | HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1383-1103A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20736004 | ||||||
| chr12:20736044
|
G | C | 15 | a0001c0001t0003g0081a0001c0001t0003g0113a0001c0001t0003g0213others(12): Show | 16 | HG00738.hp2 HG01978.hp1 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.1383-1063G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20736044 | ||||||
| chr12:20736152
|
C | A | 1 | a0001c0001t0001g0161 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1383-955C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20736152 | ||||||
| chr12:20736152
|
C | T | 237 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0028others(234): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1383-955C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20736152 | ||||||
| chr12:20736171
|
A | G | 10 | a0001c0001t0004g0029a0001c0001t0004g0101a0001c0001t0004g0132others(7): Show | 11 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.1383-936A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20736171 | ||||||
| chr12:20736252
|
C | A | 15 | a0001c0002t0002g0159a0001c0002t0002g0230a0001c0002t0002g0244others(12): Show | 15 | HG00639.hp1 HG00735.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1383-855C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20736252 | ||||||
| chr12:20736266
|
C | CA | 114 | a0001c0001t0001g0107a0001c0001t0004g0168a0001c0002t0002g0003others(111): Show | 117 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.1383-832dupA | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 20736266 | |||||
| chr12:20736336
|
T | TG | 125 | a0001c0001t0001g0028a0001c0001t0001g0091a0001c0001t0001g0096others(122): Show | 129 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1383-762dupG | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 20736336 | |||||
| chr12:20736399
|
G | A | 1 | a0001c0003t0012g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1383-708G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20736399 | ||||||
| chr12:20736517
|
G | C | 106 | a0001c0001t0004g0168a0001c0002t0002g0003a0001c0002t0002g0004others(103): Show | 108 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.1383-590G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20736517 | ||||||
| chr12:20736726
|
A | T | 113 | a0001c0001t0001g0107a0001c0001t0004g0168a0001c0002t0002g0003others(110): Show | 116 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.1383-381A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20736726 | ||||||
| chr12:20736735
|
A | G | 15 | a0001c0001t0001g0028a0001c0001t0001g0071a0001c0001t0001g0091others(12): Show | 15 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.1383-372A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20736735 | ||||||
| chr12:20736747
|
T | C | 29 | a0001c0001t0001g0011a0001c0001t0003g0012a0001c0001t0003g0019others(26): Show | 30 | HG00544.hp2 HG00642.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.1383-360T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20736747 | ||||||
| chr12:20737008
|
A | G | 238 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0028others(235): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1383-99A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20737008 | ||||||
| chr12:20737434
|
G | A | 2 | a0001c0002t0002g0087a0001c0009t0002g0085 | 2 | NA18971.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1548+162G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 11/14 | chr12 | 20737434 | ||||||
| chr12:20737461
|
G | T | 1 | a0001c0003t0001g0239 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1548+189G>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 11/14 | chr12 | 20737461 | ||||||
| chr12:20737567
|
C | T | 3 | a0001c0001t0004g0168a0001c0002t0002g0274a0001c0006t0001g0215 | 3 | HG03704.hp1 HG03927.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1548+295C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 11/14 | chr12 | 20737567 | ||||||
| chr12:20737762
|
C | T | 1 | a0001c0003t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1548+490C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 11/14 | chr12 | 20737762 | ||||||
| chr12:20737860
|
T | A | 1 | a0001c0002t0006g0223 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1548+588T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 11/14 | chr12 | 20737860 | ||||||
| chr12:20738041
|
T | C | 19 | a0001c0001t0001g0011a0001c0001t0003g0012a0001c0001t0003g0019others(16): Show | 19 | HG00544.hp2 HG02027.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.1548+769T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 11/14 | chr12 | 20738041 | ||||||
| chr12:20738085
|
A | C | 1 | a0001c0002t0002g0036 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1548+813A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 11/14 | chr12 | 20738085 | ||||||
| chr12:20738451
|
A | G | 1 | a0002c0007t0004g0006 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1548+1179A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 11/14 | chr12 | 20738451 | ||||||
| chr12:20738456
|
T | C | 1 | a0001c0002t0002g0246 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1548+1184T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 11/14 | chr12 | 20738456 | ||||||
| chr12:20738929
|
G | A | 111 | a0001c0001t0004g0168a0001c0002t0002g0003a0001c0002t0002g0004others(108): Show | 114 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.1549-1255G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 11/14 | chr12 | 20738929 | ||||||
| chr12:20738948
|
T | G | 1 | a0001c0003t0005g0025 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1549-1236T>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 11/14 | chr12 | 20738948 | ||||||
| chr12:20739124
|
T | C | 1 | a0001c0004t0003g0080 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1549-1060T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 11/14 | chr12 | 20739124 | ||||||
| chr12:20739209
|
G | A | 1 | a0001c0002t0002g0120 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1549-975G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 11/14 | chr12 | 20739209 | ||||||
| chr12:20739386
|
T | G | 1 | a0001c0001t0001g0290 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1549-798T>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 11/14 | chr12 | 20739386 | ||||||
| chr12:20739595
|
G | A | 1 | a0001c0004t0001g0033 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1549-589G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 11/14 | chr12 | 20739595 | ||||||
| chr12:20739603
|
G | A | 13 | a0001c0001t0001g0102a0001c0001t0003g0275a0001c0002t0002g0001others(10): Show | 14 | HG01884.hp2 HG02109.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1549-581G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 11/14 | chr12 | 20739603 | ||||||
| chr12:20739709
|
G | A | 17 | a0001c0001t0003g0081a0001c0001t0003g0113a0001c0001t0003g0213others(14): Show | 18 | HG00738.hp2 HG01978.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.1549-475G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 11/14 | chr12 | 20739709 | ||||||
| chr12:20739925
|
T | C | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1549-259T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 11/14 | chr12 | 20739925 | ||||||
| chr12:20739963
|
C | T | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1549-221C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 11/14 | chr12 | 20739963 | ||||||
| chr12:20740075
|
C | A | 3 | a0001c0001t0001g0129a0001c0001t0001g0139a0001c0001t0001g0141 | 3 | NA18952.hp2 NA18956.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1549-109C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 11/14 | chr12 | 20740075 | ||||||
| chr12:20740076
|
C | T | 1 | a0001c0018t0002g0214 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1549-108C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 11/14 | chr12 | 20740076 | ||||||
| chr12:20740118
|
C | A | 159 | a0001c0001t0001g0011a0001c0001t0003g0012a0001c0001t0003g0019others(156): Show | 164 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(161): Show |
intron_variant | MODIFIER | c.1549-66C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 11/14 | chr12 | 20740118 | ||||||
| chr12:20740174
|
C | T | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1549-10C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 11/14 | chr12 | 20740174 | ||||||
| chr12:20740175
|
G | T | 4 | a0001c0001t0003g0019a0001c0001t0003g0199a0001c0001t0005g0027others(1): Show | 4 | HG02622.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1549-9G>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 11/14 | chr12 | 20740175 | ||||||
| chr12:20740417
|
C | A | 1 | a0001c0001t0001g0066 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1733+49C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20740417 | ||||||
| chr12:20740420
|
G | C | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1733+52G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20740420 | ||||||
| chr12:20740547
|
GA | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0172a0001c0001t0001g0210others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1733+181delA | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740547 | |||||
| chr12:20740611
|
T | G | 1 | a0003c0012t0001g0126 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1733+243T>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20740611 | ||||||
| chr12:20740638
|
C | T | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1733+270C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20740638 | ||||||
| chr12:20740646
|
T | G | 2 | a0001c0001t0001g0204a0001c0001t0003g0275 | 2 | HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1733+278T>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20740646 | ||||||
| chr12:20740655
|
C | T | 1 | a0001c0005t0002g0137 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1733+287C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20740655 | ||||||
| chr12:20740775
|
A | ATTTATTA others(9): Show |
1 | a0001c0005t0002g0224 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1733+407_1733+408i others(18): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20740775 | ||||||
| chr12:20740778
|
T | A | 1 | a0001c0005t0002g0224 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1733+410T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20740778 | ||||||
| chr12:20740778
|
T | TATTATAT others(5): Show |
1 | a0001c0002t0002g0171 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1733+410_1733+411i others(14): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20740778 | ||||||
| chr12:20740781
|
T | TTA | 4 | a0001c0002t0002g0034a0001c0002t0002g0117a0001c0002t0002g0152others(1): Show | 4 | HG01261.hp1 HG01496.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.1733+414_1733+415i others(4): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740781 | |||||
| chr12:20740781
|
T | TTATA | 14 | a0001c0002t0002g0068a0001c0002t0002g0122a0001c0002t0002g0222others(11): Show | 14 | HG00639.hp1 HG00735.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1733+414_1733+415i others(6): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740781 | |||||
| chr12:20740781
|
T | TTATATA | 22 | a0001c0002t0002g0053a0001c0002t0002g0092a0001c0002t0002g0098others(19): Show | 22 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.1733+414_1733+415i others(8): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740781 | |||||
| chr12:20740781
|
T | TTATATAT others(1): Show |
28 | a0001c0002t0002g0004a0001c0002t0002g0036a0001c0002t0002g0037others(25): Show | 29 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.1733+414_1733+415i others(10): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740781 | |||||
| chr12:20740781
|
T | TTATATAT others(3): Show |
5 | a0001c0002t0002g0046a0001c0002t0002g0087a0001c0002t0002g0120others(2): Show | 5 | HG00099.hp1 HG03688.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.1733+414_1733+415i others(12): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740781 | |||||
| chr12:20740781
|
T | TTATATAT others(5): Show |
14 | a0001c0002t0002g0003a0001c0002t0002g0067a0001c0002t0002g0077others(11): Show | 15 | HG02155.hp2 HG03239.hp2 HG03710.hp2 others(12): Show |
intron_variant | MODIFIER | c.1733+414_1733+415i others(14): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740781 | |||||
| chr12:20740781
|
T | TTATATAT others(7): Show |
3 | a0001c0002t0002g0057a0001c0002t0002g0183a0001c0002t0002g0206 | 3 | HG01433.hp1 HG01952.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1733+414_1733+415i others(16): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740781 | |||||
| chr12:20740781
|
T | TTATATAT others(9): Show |
5 | a0001c0002t0002g0110a0001c0002t0002g0231a0001c0002t0002g0250others(2): Show | 5 | HG01255.hp1 HG01358.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1733+414_1733+415i others(18): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740781 | |||||
| chr12:20740781
|
T | TTATATAT others(11): Show |
4 | a0001c0002t0002g0030a0001c0002t0002g0052a0001c0002t0002g0249others(1): Show | 4 | HG01515.hp1 NA18747.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.1733+414_1733+415i others(20): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740781 | |||||
| chr12:20740781
|
T | TTATATAT others(13): Show |
1 | a0001c0009t0002g0125 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1733+414_1733+415i others(22): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740781 | |||||
| chr12:20740781
|
TTTTATTT others(17): Show |
T | 3 | a0001c0003t0005g0002a0001c0003t0005g0025a0001c0003t0005g0026 | 4 | HG02559.hp1 HG03209.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1733+415_1733+438d others(26): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740781 | |||||
| chr12:20740783
|
T | A | 103 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(100): Show | 105 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.1733+415T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20740783 | ||||||
| chr12:20740783
|
T | TTATATAT others(3): Show |
6 | a0001c0006t0001g0005a0001c0006t0001g0190a0001c0006t0001g0192others(3): Show | 8 | HG01069.hp1 HG01071.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.1733+418_1733+419i others(12): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740783 | |||||
| chr12:20740783
|
T | TTATATAT others(5): Show |
5 | a0001c0001t0004g0101a0001c0001t0004g0132a0001c0001t0004g0225others(2): Show | 5 | HG00738.hp2 HG01106.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.1733+418_1733+419i others(14): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740783 | |||||
| chr12:20740783
|
T | TTATATAT others(7): Show |
1 | a0002c0007t0001g0062 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1733+418_1733+419i others(16): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740783 | |||||
| chr12:20740783
|
T | TTATATAT others(9): Show |
6 | a0001c0001t0003g0081a0001c0001t0003g0113a0001c0001t0004g0168others(3): Show | 6 | HG02080.hp2 HG03834.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.1733+418_1733+419i others(18): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740783 | |||||
| chr12:20740783
|
T | TTATATAT others(11): Show |
2 | a0001c0001t0004g0029a0001c0003t0004g0238 | 2 | HG01168.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1733+418_1733+419i others(20): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740783 | |||||
| chr12:20740783
|
T | TTATATAT others(13): Show |
4 | a0001c0001t0001g0071a0001c0001t0003g0213a0001c0006t0008g0039others(1): Show | 4 | HG01496.hp2 HG04184.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1733+418_1733+419i others(22): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740783 | |||||
| chr12:20740783
|
T | TTATATAT others(15): Show |
3 | a0001c0001t0004g0285a0001c0006t0008g0201a0003c0012t0001g0128 | 3 | HG00642.hp2 NA18983.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1733+418_1733+419i others(24): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740783 | |||||
| chr12:20740783
|
T | TTATATAT others(17): Show |
2 | a0001c0003t0004g0166a0001c0021t0001g0157 | 2 | HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1733+418_1733+419i others(26): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740783 | |||||
| chr12:20740787
|
T | A | 134 | a0001c0001t0001g0071a0001c0001t0003g0081a0001c0001t0003g0113others(131): Show | 138 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.1733+419T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20740787 | ||||||
| chr12:20740787
|
T | TATATATA others(4): Show |
1 | a0001c0002t0002g0283 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1733+419_1733+420i others(13): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20740787 | ||||||
| chr12:20740787
|
T | TATATATA others(12): Show |
1 | a0001c0001t0001g0074 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1733+419_1733+420i others(21): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20740787 | ||||||
| chr12:20740787
|
T | TTA | 30 | a0001c0001t0001g0035a0001c0001t0001g0045a0001c0001t0001g0055others(27): Show | 30 | HG00673.hp1 HG01081.hp2 HG02135.hp2 others(27): Show |
intron_variant | MODIFIER | c.1733+449_1733+450d others(4): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740787 | |||||
| chr12:20740787
|
T | TTATA | 29 | a0001c0001t0001g0021a0001c0001t0001g0048a0001c0001t0001g0059others(26): Show | 30 | HG00099.hp2 HG00597.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.1733+447_1733+450d others(6): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740787 | |||||
| chr12:20740787
|
T | TTATATA | 9 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0114others(6): Show | 9 | HG00735.hp1 HG01169.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1733+445_1733+450d others(8): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740787 | |||||
| chr12:20740787
|
T | TTATATAT others(1): Show |
14 | a0001c0001t0001g0028a0001c0001t0001g0058a0001c0001t0001g0091others(11): Show | 14 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.1733+443_1733+450d others(10): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740787 | |||||
| chr12:20740787
|
T | TTATATAT others(3): Show |
2 | a0001c0003t0001g0170a0001c0016t0001g0050 | 2 | HG03831.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1733+441_1733+450d others(12): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740787 | |||||
| chr12:20740787
|
T | TTATATAT others(5): Show |
11 | a0001c0001t0001g0009a0001c0001t0001g0084a0001c0001t0001g0121others(8): Show | 11 | HG01257.hp2 HG01891.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.1733+439_1733+450d others(14): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740787 | |||||
| chr12:20740787
|
T | TTATATAT others(7): Show |
9 | a0001c0001t0001g0187a0001c0001t0003g0148a0001c0001t0003g0162others(6): Show | 9 | HG01168.hp2 HG01169.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.1733+437_1733+450d others(16): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740787 | |||||
| chr12:20740787
|
T | TTATATAT others(9): Show |
15 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0104others(12): Show | 15 | HG00544.hp2 HG02148.hp2 HG02300.hp2 others(12): Show |
intron_variant | MODIFIER | c.1733+435_1733+450d others(18): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740787 | |||||
| chr12:20740787
|
T | TTATATAT others(11): Show |
1 | a0001c0001t0001g0138 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1733+433_1733+450d others(20): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740787 | |||||
| chr12:20740787
|
T | TTATATAT others(13): Show |
6 | a0001c0001t0001g0011a0001c0001t0001g0176a0001c0001t0001g0232others(3): Show | 6 | HG01081.hp1 HG01106.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1733+431_1733+450d others(22): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740787 | |||||
| chr12:20740787
|
T | TTATATAT others(15): Show |
3 | a0001c0001t0001g0076a0001c0001t0001g0103a0001c0001t0001g0107 | 3 | HG00639.hp2 HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1733+429_1733+450d others(24): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740787 | |||||
| chr12:20740787
|
T | TTATATAT others(17): Show |
2 | a0001c0001t0003g0078a0001c0013t0001g0241 | 2 | HG01361.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1733+427_1733+450d others(26): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740787 | |||||
| chr12:20740787
|
T | TTATATAT others(19): Show |
3 | a0001c0001t0003g0012a0001c0001t0013g0142a0001c0004t0003g0156 | 3 | HG02015.hp2 HG02615.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1733+425_1733+450d others(28): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740787 | |||||
| chr12:20740787
|
T | TTATATAT others(21): Show |
4 | a0001c0001t0001g0075a0001c0001t0001g0178a0001c0004t0003g0040others(1): Show | 4 | HG02735.hp2 HG02818.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.1733+423_1733+450d others(30): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740787 | |||||
| chr12:20740787
|
T | TTTTATAT others(15): Show |
1 | a0001c0020t0009g0016 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1733+420_1733+421i others(24): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740787 | |||||
| chr12:20740787
|
TTA | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0160others(4): Show | 7 | HG02109.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1733+449_1733+450d others(4): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20740787 | |||||
| chr12:20740819
|
G | A | 108 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(105): Show | 111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1733+451G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20740819 | ||||||
| chr12:20741009
|
C | T | 2 | a0001c0002t0006g0223a0001c0005t0006g0169 | 2 | HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1733+641C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20741009 | ||||||
| chr12:20741046
|
G | A | 29 | a0001c0001t0001g0011a0001c0001t0003g0012a0001c0001t0003g0019others(26): Show | 30 | HG00544.hp2 HG00642.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.1733+678G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20741046 | ||||||
| chr12:20741118
|
A | C | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1733+750A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20741118 | ||||||
| chr12:20741241
|
C | T | 1 | a0001c0002t0002g0067 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1733+873C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20741241 | ||||||
| chr12:20741348
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1733+980A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20741348 | ||||||
| chr12:20741401
|
G | A | 236 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0028others(233): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1733+1033G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20741401 | ||||||
| chr12:20741492
|
A | C | 1 | a0001c0014t0003g0264 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1733+1124A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20741492 | ||||||
| chr12:20741500
|
G | C | 104 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(101): Show | 106 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.1733+1132G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20741500 | ||||||
| chr12:20741584
|
T | G | 1 | a0001c0001t0001g0179 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1733+1216T>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20741584 | ||||||
| chr12:20741648
|
G | A | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1733+1280G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20741648 | ||||||
| chr12:20741737
|
TATA | T | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1733+1373_1733+137 others(7): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20741737 | |||||
| chr12:20742057
|
A | G | 1 | a0001c0013t0001g0241 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1734-1248A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20742057 | ||||||
| chr12:20742059
|
T | C | 13 | a0001c0001t0001g0011a0001c0001t0003g0012a0001c0001t0003g0020others(10): Show | 13 | HG00544.hp2 HG02027.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.1734-1246T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20742059 | ||||||
| chr12:20742181
|
T | C | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1734-1124T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20742181 | ||||||
| chr12:20742265
|
T | C | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1734-1040T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20742265 | ||||||
| chr12:20742329
|
T | C | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1734-976T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20742329 | ||||||
| chr12:20742333
|
G | GT | 97 | a0001c0001t0001g0121a0001c0001t0004g0029a0001c0002t0002g0003others(94): Show | 100 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1734-959dupT | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20742333 | |||||
| chr12:20742333
|
G | GTT | 10 | a0001c0002t0002g0093a0001c0002t0002g0098a0001c0002t0002g0231others(7): Show | 10 | HG00735.hp2 HG01255.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1734-960_1734-959d others(4): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20742333 | |||||
| chr12:20742333
|
GT | G | 28 | a0001c0001t0001g0011a0001c0001t0001g0035a0001c0001t0001g0129others(25): Show | 28 | HG00099.hp2 HG00544.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.1734-959delT | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20742333 | |||||
| chr12:20742400
|
T | C | 1 | a0001c0002t0006g0223 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1734-905T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20742400 | ||||||
| chr12:20742426
|
C | T | 236 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0028others(233): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1734-879C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20742426 | ||||||
| chr12:20742469
|
A | C | 1 | a0001c0006t0001g0144 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1734-836A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20742469 | ||||||
| chr12:20742577
|
A | T | 2 | a0001c0005t0002g0184a0001c0020t0009g0016 | 2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1734-728A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20742577 | ||||||
| chr12:20742584
|
A | AG | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1734-718dupG | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20742584 | |||||
| chr12:20742595
|
A | G | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1734-710A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20742595 | ||||||
| chr12:20742598
|
A | G | 1 | a0001c0004t0003g0155 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1734-707A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20742598 | ||||||
| chr12:20742606
|
C | G | 4 | a0001c0006t0001g0005a0001c0006t0001g0190a0001c0006t0001g0192others(1): Show | 5 | NA18959.hp1 NA19005.hp1 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.1734-699C>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20742606 | ||||||
| chr12:20742617
|
T | C | 6 | a0001c0002t0002g0044a0001c0002t0002g0068a0001c0002t0002g0069others(3): Show | 6 | HG00741.hp1 HG01256.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1734-688T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20742617 | ||||||
| chr12:20742700
|
AT | A | 78 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0070others(75): Show | 80 | HG00099.hp2 HG00639.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.1734-584delT | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20742700 | |||||
| chr12:20742700
|
ATT | A | 42 | a0001c0001t0001g0011a0001c0001t0001g0028a0001c0001t0001g0091others(39): Show | 43 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1734-585_1734-584d others(4): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20742700 | |||||
| chr12:20742700
|
ATTTT | A | 106 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(103): Show | 109 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.1734-587_1734-584d others(6): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 20742700 | |||||
| chr12:20742716
|
T | A | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1734-589T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20742716 | ||||||
| chr12:20742781
|
C | T | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1734-524C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20742781 | ||||||
| chr12:20742846
|
T | A | 15 | a0001c0001t0001g0028a0001c0001t0001g0071a0001c0001t0001g0091others(12): Show | 15 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.1734-459T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20742846 | ||||||
| chr12:20742940
|
T | A | 29 | a0001c0001t0001g0011a0001c0001t0003g0012a0001c0001t0003g0019others(26): Show | 30 | HG00544.hp2 HG00642.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.1734-365T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20742940 | ||||||
| chr12:20742971
|
A | T | 3 | a0001c0003t0005g0002a0001c0003t0005g0025a0001c0003t0005g0026 | 4 | HG02559.hp1 HG03209.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1734-334A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20742971 | ||||||
| chr12:20743099
|
A | C | 1 | a0001c0004t0001g0041 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1734-206A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20743099 | ||||||
| chr12:20743626
|
A | T | 1 | a0001c0001t0001g0107 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1798+257A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20743626 | ||||||
| chr12:20743705
|
G | C | 1 | a0001c0002t0002g0077 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1798+336G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20743705 | ||||||
| chr12:20743725
|
AATATAT | A | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1798+357_1798+362d others(8): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20743725 | ||||||
| chr12:20743728
|
A | G | 2 | a0001c0005t0002g0184a0001c0020t0009g0016 | 2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1798+359A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20743728 | ||||||
| chr12:20743830
|
T | A | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1798+461T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20743830 | ||||||
| chr12:20743875
|
G | GT | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1798+512dupT | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 20743875 | |||||
| chr12:20744057
|
A | G | 2 | a0001c0002t0002g0069a0001c0002t0002g0229 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1798+688A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20744057 | ||||||
| chr12:20744058
|
A | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0172a0001c0001t0001g0210others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1798+689A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20744058 | ||||||
| chr12:20744067
|
C | T | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1798+698C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20744067 | ||||||
| chr12:20744190
|
A | G | 55 | a0001c0001t0001g0009a0001c0001t0001g0070a0001c0001t0001g0072others(52): Show | 56 | HG00639.hp2 HG00738.hp2 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.1798+821A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20744190 | ||||||
| chr12:20744340
|
C | T | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1798+971C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20744340 | ||||||
| chr12:20744452
|
G | T | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1798+1083G>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20744452 | ||||||
| chr12:20744529
|
A | G | 2 | a0001c0002t0002g0034a0001c0002t0002g0117 | 2 | NA18955.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1798+1160A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20744529 | ||||||
| chr12:20744714
|
A | G | 2 | a0001c0003t0003g0195a0001c0003t0003g0196 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1798+1345A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20744714 | ||||||
| chr12:20744732
|
T | C | 19 | a0001c0001t0001g0011a0001c0001t0003g0012a0001c0001t0003g0019others(16): Show | 19 | HG00544.hp2 HG02027.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.1798+1363T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20744732 | ||||||
| chr12:20744742
|
C | T | 12 | a0001c0001t0003g0275a0001c0002t0002g0001a0001c0002t0002g0008others(9): Show | 13 | HG01884.hp2 HG02109.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1798+1373C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20744742 | ||||||
| chr12:20744750
|
C | T | 2 | a0001c0002t0006g0223a0001c0005t0006g0169 | 2 | HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1798+1381C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20744750 | ||||||
| chr12:20744826
|
C | T | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1798+1457C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20744826 | ||||||
| chr12:20744883
|
C | T | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1798+1514C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20744883 | ||||||
| chr12:20744920
|
C | T | 19 | a0001c0001t0003g0081a0001c0001t0003g0113a0001c0001t0003g0213others(16): Show | 20 | HG00738.hp2 HG01168.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.1798+1551C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20744920 | ||||||
| chr12:20744968
|
G | A | 15 | a0001c0001t0001g0028a0001c0001t0001g0071a0001c0001t0001g0091others(12): Show | 15 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.1798+1599G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20744968 | ||||||
| chr12:20745023
|
G | A | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1798+1654G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20745023 | ||||||
| chr12:20745029
|
T | C | 1 | a0001c0003t0012g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1798+1660T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20745029 | ||||||
| chr12:20745132
|
T | A | 11 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0010others(8): Show | 12 | HG01884.hp2 HG02109.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1798+1763T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20745132 | ||||||
| chr12:20745140
|
G | A | 10 | a0001c0001t0004g0029a0001c0001t0004g0101a0001c0001t0004g0132others(7): Show | 11 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.1798+1771G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20745140 | ||||||
| chr12:20745147
|
T | C | 289 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.1798+1778T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20745147 | ||||||
| chr12:20745148
|
G | A | 1 | a0001c0020t0009g0016 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1798+1779G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20745148 | ||||||
| chr12:20745188
|
A | G | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1798+1819A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20745188 | ||||||
| chr12:20745191
|
A | T | 3 | a0001c0002t0006g0147a0001c0002t0006g0223a0001c0005t0006g0169 | 3 | HG03654.hp1 HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1798+1822A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20745191 | ||||||
| chr12:20745217
|
A | T | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1798+1848A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20745217 | ||||||
| chr12:20745223
|
A | T | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1798+1854A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20745223 | ||||||
| chr12:20745324
|
G | GCC | 3 | a0001c0001t0003g0081a0001c0001t0003g0113a0001c0001t0003g0213 | 3 | NA18941.hp2 NA18968.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1798+1956_1798+195 others(6): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 20745324 | |||||
| chr12:20745361
|
A | T | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1798+1992A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20745361 | ||||||
| chr12:20745546
|
T | C | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1798+2177T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20745546 | ||||||
| chr12:20745547
|
G | A | 1 | a0001c0002t0002g0004 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1798+2178G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20745547 | ||||||
| chr12:20745655
|
T | C | 3 | a0001c0003t0005g0002a0001c0003t0005g0025a0001c0003t0005g0026 | 4 | HG02559.hp1 HG03209.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1798+2286T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20745655 | ||||||
| chr12:20745681
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1798+2312C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20745681 | ||||||
| chr12:20745771
|
G | A | 1 | a0001c0002t0002g0067 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1798+2402G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20745771 | ||||||
| chr12:20745808
|
A | G | 289 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.1798+2439A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20745808 | ||||||
| chr12:20745832
|
A | G | 13 | a0001c0001t0001g0011a0001c0001t0003g0012a0001c0001t0003g0020others(10): Show | 13 | HG00544.hp2 HG02027.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.1798+2463A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20745832 | ||||||
| chr12:20745840
|
A | G | 1 | a0001c0002t0002g0087 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1798+2471A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20745840 | ||||||
| chr12:20745857
|
C | T | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1798+2488C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20745857 | ||||||
| chr12:20746011
|
T | A | 103 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(100): Show | 105 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.1798+2642T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20746011 | ||||||
| chr12:20746144
|
A | G | 1 | a0001c0001t0003g0261 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1798+2775A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20746144 | ||||||
| chr12:20746146
|
A | C | 6 | a0001c0002t0002g0044a0001c0002t0002g0068a0001c0002t0002g0069others(3): Show | 6 | HG00741.hp1 HG01256.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1798+2777A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20746146 | ||||||
| chr12:20746219
|
A | G | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1798+2850A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20746219 | ||||||
| chr12:20746221
|
C | A | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1798+2852C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20746221 | ||||||
| chr12:20746258
|
T | C | 10 | a0001c0001t0004g0029a0001c0001t0004g0101a0001c0001t0004g0132others(7): Show | 11 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.1798+2889T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20746258 | ||||||
| chr12:20746356
|
G | GA | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1798+2994dupA | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 20746356 | |||||
| chr12:20746358
|
A | C | 1 | a0001c0001t0001g0102 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1798+2989A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20746358 | ||||||
| chr12:20746386
|
A | G | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1798+3017A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20746386 | ||||||
| chr12:20746439
|
C | T | 2 | a0001c0005t0002g0184a0001c0020t0009g0016 | 2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1798+3070C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20746439 | ||||||
| chr12:20746477
|
T | TA | 111 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(108): Show | 114 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.1798+3119dupA | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 20746477 | |||||
| chr12:20746635
|
T | C | 3 | a0001c0002t0006g0147a0001c0002t0006g0223a0001c0005t0006g0169 | 3 | HG03654.hp1 HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1798+3266T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20746635 | ||||||
| chr12:20746745
|
C | A | 3 | a0001c0001t0003g0019a0001c0001t0003g0199a0001c0001t0010g0022 | 3 | HG02622.hp2 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1798+3376C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20746745 | ||||||
| chr12:20746760
|
A | G | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1798+3391A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20746760 | ||||||
| chr12:20746782
|
A | C | 197 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0070others(194): Show | 202 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.1798+3413A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20746782 | ||||||
| chr12:20746823
|
T | TTC | 7 | a0001c0002t0002g0256a0001c0002t0006g0147a0001c0002t0006g0223others(4): Show | 8 | HG02559.hp1 HG03209.hp2 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.1798+3454_1798+345 others(6): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20746823 | ||||||
| chr12:20746823
|
T | TTTC | 102 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(99): Show | 104 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.1798+3454_1798+345 others(7): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20746823 | ||||||
| chr12:20746840
|
GA | G | 3 | a0001c0003t0001g0014a0001c0003t0001g0023a0001c0003t0007g0017 | 3 | HG02109.hp1 HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1798+3478delA | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 20746840 | |||||
| chr12:20746994
|
T | G | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1798+3625T>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20746994 | ||||||
| chr12:20747014
|
TAGG | T | 106 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(103): Show | 109 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.1798+3648_1798+365 others(7): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 20747014 | |||||
| chr12:20747035
|
G | A | 1 | a0001c0002t0002g0240 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1799-3640G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20747035 | ||||||
| chr12:20747113
|
T | C | 3 | a0001c0003t0005g0002a0001c0003t0005g0025a0001c0003t0005g0026 | 4 | HG02559.hp1 HG03209.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1799-3562T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20747113 | ||||||
| chr12:20747160
|
C | G | 3 | a0001c0003t0001g0014a0001c0003t0001g0023a0001c0003t0007g0017 | 3 | HG02109.hp1 HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1799-3515C>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20747160 | ||||||
| chr12:20747204
|
A | C | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1799-3471A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20747204 | ||||||
| chr12:20747223
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1799-3452G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20747223 | ||||||
| chr12:20747300
|
T | C | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1799-3375T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20747300 | ||||||
| chr12:20747342
|
T | C | 7 | a0001c0002t0002g0030a0001c0002t0002g0052a0001c0002t0002g0116others(4): Show | 7 | HG00558.hp2 HG01952.hp2 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.1799-3333T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20747342 | ||||||
| chr12:20747397
|
C | A | 3 | a0001c0002t0002g0249a0001c0002t0002g0257a0001c0002t0002g0258 | 3 | NA18979.hp2 NA18999.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1799-3278C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20747397 | ||||||
| chr12:20747434
|
A | AC | 103 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(100): Show | 105 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.1799-3241_1799-324 others(5): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20747434 | ||||||
| chr12:20747449
|
A | G | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1799-3226A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20747449 | ||||||
| chr12:20747494
|
C | T | 1 | a0001c0002t0002g0149 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1799-3181C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20747494 | ||||||
| chr12:20747534
|
G | C | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1799-3141G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20747534 | ||||||
| chr12:20747585
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1799-3090C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20747585 | ||||||
| chr12:20747586
|
G | A | 1 | a0001c0003t0001g0239 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1799-3089G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20747586 | ||||||
| chr12:20747610
|
AT | A | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1799-3058delT | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 20747610 | |||||
| chr12:20747673
|
T | G | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1799-3002T>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20747673 | ||||||
| chr12:20747711
|
C | A | 1 | a0001c0002t0002g0158 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1799-2964C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20747711 | ||||||
| chr12:20747712
|
C | A | 1 | a0001c0002t0002g0158 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1799-2963C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20747712 | ||||||
| chr12:20747746
|
C | T | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1799-2929C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20747746 | ||||||
| chr12:20747767
|
A | T | 109 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0030others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1799-2908A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20747767 | ||||||
| chr12:20747779
|
G | A | 24 | a0001c0001t0001g0035a0001c0001t0001g0107a0001c0001t0001g0129others(21): Show | 25 | HG00099.hp2 HG00673.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.1799-2896G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20747779 | ||||||
| chr12:20747905
|
C | T | 36 | a0001c0001t0001g0009a0001c0001t0001g0070a0001c0001t0001g0072others(33): Show | 36 | HG00639.hp2 HG01081.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.1799-2770C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20747905 | ||||||
| chr12:20747941
|
C | G | 1 | a0001c0003t0012g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1799-2734C>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20747941 | ||||||
| chr12:20748011
|
A | G | 2 | a0001c0003t0003g0195a0001c0003t0003g0196 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1799-2664A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20748011 | ||||||
| chr12:20748047
|
T | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0172a0001c0001t0001g0210others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1799-2628T>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20748047 | ||||||
| chr12:20748163
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1799-2512G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20748163 | ||||||
| chr12:20748210
|
A | G | 119 | a0001c0001t0001g0204a0001c0001t0003g0275a0001c0002t0002g0001others(116): Show | 122 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1799-2465A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20748210 | ||||||
| chr12:20748215
|
C | T | 119 | a0001c0001t0001g0204a0001c0001t0003g0275a0001c0002t0002g0001others(116): Show | 122 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1799-2460C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20748215 | ||||||
| chr12:20748454
|
C | A | 13 | a0001c0001t0001g0011a0001c0001t0003g0012a0001c0001t0003g0020others(10): Show | 13 | HG00544.hp2 HG02027.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.1799-2221C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20748454 | ||||||
| chr12:20748648
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1799-2027T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20748648 | ||||||
| chr12:20748719
|
C | G | 119 | a0001c0001t0001g0204a0001c0001t0003g0275a0001c0002t0002g0001others(116): Show | 122 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1799-1956C>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20748719 | ||||||
| chr12:20748752
|
T | C | 1 | a0001c0001t0001g0290 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1799-1923T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20748752 | ||||||
| chr12:20748908
|
G | A | 119 | a0001c0001t0001g0204a0001c0001t0003g0275a0001c0002t0002g0001others(116): Show | 122 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1799-1767G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20748908 | ||||||
| chr12:20748987
|
T | C | 10 | a0001c0001t0004g0029a0001c0001t0004g0101a0001c0001t0004g0132others(7): Show | 11 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.1799-1688T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20748987 | ||||||
| chr12:20749067
|
C | T | 1 | a0001c0003t0005g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1799-1608C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20749067 | ||||||
| chr12:20749155
|
T | A | 1 | a0001c0001t0001g0187 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1799-1520T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20749155 | ||||||
| chr12:20749228
|
A | G | 2 | a0001c0001t0004g0168a0001c0006t0001g0215 | 2 | HG03927.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1799-1447A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20749228 | ||||||
| chr12:20749291
|
G | A | 37 | a0001c0001t0001g0009a0001c0001t0001g0070a0001c0001t0001g0072others(34): Show | 37 | HG00639.hp2 HG01081.hp1 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.1799-1384G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20749291 | ||||||
| chr12:20749291
|
G | T | 1 | a0001c0001t0004g0225 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1799-1384G>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20749291 | ||||||
| chr12:20749324
|
T | A | 1 | a0001c0003t0001g0245 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1799-1351T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20749324 | ||||||
| chr12:20749354
|
T | C | 119 | a0001c0001t0001g0204a0001c0001t0003g0275a0001c0002t0002g0001others(116): Show | 122 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1799-1321T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20749354 | ||||||
| chr12:20749380
|
T | C | 119 | a0001c0001t0001g0204a0001c0001t0003g0275a0001c0002t0002g0001others(116): Show | 122 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1799-1295T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20749380 | ||||||
| chr12:20749494
|
G | C | 119 | a0001c0001t0001g0204a0001c0001t0003g0275a0001c0002t0002g0001others(116): Show | 122 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1799-1181G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20749494 | ||||||
| chr12:20749581
|
A | G | 119 | a0001c0001t0001g0204a0001c0001t0003g0275a0001c0002t0002g0001others(116): Show | 122 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1799-1094A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20749581 | ||||||
| chr12:20749600
|
A | C | 10 | a0001c0001t0001g0035a0001c0001t0001g0129a0001c0001t0001g0136others(7): Show | 10 | HG00099.hp2 HG00673.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.1799-1075A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20749600 | ||||||
| chr12:20749654
|
A | C | 119 | a0001c0001t0001g0204a0001c0001t0003g0275a0001c0002t0002g0001others(116): Show | 122 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1799-1021A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20749654 | ||||||
| chr12:20749714
|
G | A | 119 | a0001c0001t0001g0204a0001c0001t0003g0275a0001c0002t0002g0001others(116): Show | 122 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1799-961G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20749714 | ||||||
| chr12:20749809
|
G | T | 118 | a0001c0001t0003g0275a0001c0002t0002g0001a0001c0002t0002g0003others(115): Show | 121 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.1799-866G>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20749809 | ||||||
| chr12:20749861
|
T | C | 16 | a0001c0001t0001g0028a0001c0001t0001g0071a0001c0001t0001g0091others(13): Show | 16 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.1799-814T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20749861 | ||||||
| chr12:20749987
|
G | A | 1 | a0001c0002t0006g0223 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1799-688G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20749987 | ||||||
| chr12:20750023
|
A | G | 119 | a0001c0001t0001g0204a0001c0001t0003g0275a0001c0002t0002g0001others(116): Show | 122 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1799-652A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20750023 | ||||||
| chr12:20750027
|
A | G | 119 | a0001c0001t0001g0204a0001c0001t0003g0275a0001c0002t0002g0001others(116): Show | 122 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1799-648A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20750027 | ||||||
| chr12:20750062
|
G | A | 6 | a0001c0001t0001g0045a0001c0001t0001g0055a0001c0001t0001g0056others(3): Show | 6 | HG02723.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1799-613G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20750062 | ||||||
| chr12:20750134
|
C | T | 1 | a0001c0002t0002g0087 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1799-541C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20750134 | ||||||
| chr12:20750160
|
C | T | 118 | a0001c0001t0001g0204a0001c0001t0003g0275a0001c0002t0002g0001others(115): Show | 121 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.1799-515C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20750160 | ||||||
| chr12:20750283
|
A | T | 16 | a0001c0001t0003g0081a0001c0001t0003g0113a0001c0001t0003g0213others(13): Show | 17 | HG00738.hp2 HG01978.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.1799-392A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20750283 | ||||||
| chr12:20750289
|
T | A | 1 | a0001c0009t0002g0097 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1799-386T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20750289 | ||||||
| chr12:20750301
|
C | A | 119 | a0001c0001t0001g0204a0001c0001t0003g0275a0001c0002t0002g0001others(116): Show | 122 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1799-374C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20750301 | ||||||
| chr12:20750536
|
T | G | 118 | a0001c0001t0001g0204a0001c0001t0003g0275a0001c0002t0002g0001others(115): Show | 121 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.1799-139T>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20750536 | ||||||
| chr12:20750586
|
T | C | 120 | a0001c0001t0001g0204a0001c0001t0003g0275a0001c0002t0002g0001others(117): Show | 123 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.1799-89T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20750586 | ||||||
| chr12:20750823
|
T | C | 119 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0004others(116): Show | 122 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.1916+31T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 14/14 | chr12 | 20750823 | ||||||
| chr12:20750893
|
A | G | 1 | a0001c0002t0002g0258 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1916+101A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 14/14 | chr12 | 20750893 | ||||||
| chr12:20750931
|
G | A | 119 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0004others(116): Show | 122 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.1916+139G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 14/14 | chr12 | 20750931 | ||||||
| chr12:20751120
|
A | G | 12 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0010others(9): Show | 13 | HG01884.hp2 HG02109.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1916+328A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 14/14 | chr12 | 20751120 | ||||||
| chr12:20751185
|
G | C | 3 | a0001c0001t0001g0204a0001c0001t0003g0275a0001c0020t0009g0016 | 3 | HG02055.hp1 HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1916+393G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 14/14 | chr12 | 20751185 | ||||||
| chr12:20751232
|
G | A | 13 | a0001c0006t0001g0005a0001c0006t0001g0082a0001c0006t0001g0144others(10): Show | 14 | HG00738.hp2 HG01978.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.1916+440G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 14/14 | chr12 | 20751232 | ||||||
| chr12:20751266
|
C | T | 2 | a0001c0003t0003g0195a0001c0003t0003g0196 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1916+474C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 14/14 | chr12 | 20751266 | ||||||
| chr12:20751334
|
G | A | 121 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0004others(118): Show | 124 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.1916+542G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 14/14 | chr12 | 20751334 | ||||||
| chr12:20751349
|
T | C | 1 | a0001c0002t0002g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1916+557T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 14/14 | chr12 | 20751349 | ||||||
| chr12:20751416
|
G | A | 3 | a0001c0001t0001g0204a0001c0001t0003g0275a0001c0020t0009g0016 | 3 | HG02055.hp1 HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1916+624G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 14/14 | chr12 | 20751416 | ||||||
| chr12:20751419
|
G | GCAATGCT others(1): Show |
121 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0004others(118): Show | 124 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.1916+632_1916+633i others(10): Show |
SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 20751419 | |||||
| chr12:20751478
|
A | G | 1 | a0001c0003t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1916+686A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 14/14 | chr12 | 20751478 | ||||||
| chr12:20751534
|
T | C | 139 | a0001c0001t0001g0204a0001c0001t0003g0261a0001c0001t0003g0275others(136): Show | 144 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.1916+742T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 14/14 | chr12 | 20751534 | ||||||
| chr12:20751535
|
G | A | 1 | a0001c0002t0002g0036 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1916+743G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 14/14 | chr12 | 20751535 | ||||||
| chr12:20751573
|
C | G | 121 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0004others(118): Show | 124 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.1917-733C>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 14/14 | chr12 | 20751573 | ||||||
| chr12:20751743
|
C | T | 1 | a0002c0007t0001g0260 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1917-563C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 14/14 | chr12 | 20751743 | ||||||
| chr12:20751878
|
A | G | 4 | a0001c0006t0001g0005a0001c0006t0001g0190a0001c0006t0001g0192others(1): Show | 5 | NA18959.hp1 NA19005.hp1 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.1917-428A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 14/14 | chr12 | 20751878 | ||||||
| chr12:20751970
|
G | A | 122 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0004others(119): Show | 125 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.1917-336G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 14/14 | chr12 | 20751970 | ||||||
| chr12:20751997
|
G | A | 122 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0004others(119): Show | 125 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.1917-309G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 14/14 | chr12 | 20751997 | ||||||
| chr12:20752072
|
G | A | 122 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0004others(119): Show | 125 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.1917-234G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 14/14 | chr12 | 20752072 | ||||||
| chr12:20752159
|
C | T | 1 | a0001c0002t0002g0077 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1917-147C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 14/14 | chr12 | 20752159 | ||||||
| chr12:20752264
|
G | C | 2 | a0001c0003t0003g0195a0001c0003t0003g0196 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1917-42G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 14/14 | chr12 | 20752264 |