Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MDTSS others(707): Show |
chr12 | 20690332 | 20758386 |
| a0002 | 0/0 | 712 | 7 | 0 | 6 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | MDTSS others(707): Show |
chr12 | 20690332 | 20758386 |
| a0003 | 0/0 | 712 | 3 | 0 | 2 | 1 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | MDTSS others(707): Show |
chr12 | 20690332 | 20758386 |
| a0004 | 0/0 | 712 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | MDTSS others(707): Show |
chr12 | 20690332 | 20758386 |
| a0005 | 0/0 | 712 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | MDTSS others(707): Show |
chr12 | 20690332 | 20758386 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2136 | 97 | 50 | 15 | 22 | 1 | 8 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | ATGGA others(2131): Show |
chr12 | 20690332 | 20758386 | ||
| a0001c0002 | 0/1 | 2136 | 95 | 13 | 24 | 43 | 2 | 12 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | ATGGA others(2131): Show |
chr12 | 20690332 | 20758386 | ||
| a0001c0003 | 0/0 | 2136 | 31 | 16 | 6 | 2 | 1 | 6 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | ATGGA others(2131): Show |
chr12 | 20690332 | 20758386 | ||
| a0001c0004 | 0/0 | 2136 | 18 | 3 | 2 | 13 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | ATGGA others(2131): Show |
chr12 | 20690332 | 20758386 | ||
| a0001c0005 | 0/0 | 2136 | 16 | 4 | 2 | 1 | 3 | 6 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | ATGGA others(2131): Show |
chr12 | 20690332 | 20758386 | ||
| a0001c0006 | 0/0 | 2136 | 9 | 0 | 0 | 7 | 0 | 2 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | ATGGA others(2131): Show |
chr12 | 20690332 | 20758386 | ||
| a0001c0008 | 0/0 | 2136 | 4 | 0 | 2 | 0 | 2 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | ATGGA others(2131): Show |
chr12 | 20690332 | 20758386 | ||
| a0001c0009 | 0/0 | 2136 | 3 | 0 | 0 | 3 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | ATGGA others(2131): Show |
chr12 | 20690332 | 20758386 | ||
| a0001c0013 | 0/0 | 2136 | 2 | 0 | 2 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | ATGGA others(2131): Show |
chr12 | 20690332 | 20758386 | ||
| a0001c0014 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | ATGGA others(2131): Show |
chr12 | 20690332 | 20758386 | ||
| a0001c0015 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | ATGGA others(2131): Show |
chr12 | 20690332 | 20758386 | ||
| a0001c0016 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | ATGGA others(2131): Show |
chr12 | 20690332 | 20758386 | ||
| a0001c0017 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | ATGGA others(2131): Show |
chr12 | 20690332 | 20758386 | ||
| a0001c0018 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | ATGGA others(2131): Show |
chr12 | 20690332 | 20758386 | ||
| a0001c0020 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | ATGGA others(2131): Show |
chr12 | 20690332 | 20758386 | ||
| a0001c0021 | 0/0 | 2136 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | ATGGA others(2131): Show |
chr12 | 20690332 | 20758386 | ||
| a0001c0022 | 0/0 | 2136 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | ATGGA others(2131): Show |
chr12 | 20690332 | 20758386 | ||
| a0002c0007 | 0/0 | 2136 | 5 | 0 | 4 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | ATGGA others(2131): Show |
chr12 | 20690332 | 20758386 | ||
| a0002c0010 | 0/0 | 2136 | 2 | 0 | 2 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | ATGGA others(2131): Show |
chr12 | 20690332 | 20758386 | ||
| a0003c0012 | 0/0 | 2136 | 2 | 0 | 1 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | ATGGA others(2131): Show |
chr12 | 20690332 | 20758386 | ||
| a0003c0023 | 0/0 | 2136 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | ATGGA others(2131): Show |
chr12 | 20690332 | 20758386 | ||
| a0004c0011 | 0/0 | 2136 | 2 | 2 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | ATGGA others(2131): Show |
chr12 | 20690332 | 20758386 | ||
| a0005c0019 | 0/0 | 2136 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | ATGGA others(2131): Show |
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 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0001t0003 | 0/0 | 3498 | 13 | 8 | 0 | 5 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0001t0004 | 0/0 | 3498 | 6 | 1 | 2 | 0 | 1 | 2 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0001t0005 | 0/0 | 3498 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0001t0010 | 0/0 | 3498 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0001t0013 | 0/0 | 3498 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0002t0002 | 0/1 | 3498 | 92 | 13 | 24 | 42 | 2 | 10 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0002t0006 | 0/0 | 3498 | 2 | 0 | 0 | 0 | 0 | 2 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0002t0011 | 0/0 | 3498 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0003t0001 | 0/0 | 3498 | 19 | 8 | 3 | 2 | 1 | 5 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0003t0003 | 0/0 | 3498 | 3 | 1 | 2 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0003t0004 | 0/0 | 3498 | 2 | 0 | 1 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0003t0005 | 0/0 | 3498 | 4 | 4 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0003t0007 | 0/0 | 3498 | 2 | 2 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0003t0012 | 0/0 | 3498 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0004t0001 | 0/0 | 3498 | 11 | 2 | 2 | 7 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0004t0003 | 0/0 | 3498 | 7 | 1 | 0 | 6 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0005t0002 | 0/0 | 3498 | 15 | 4 | 2 | 1 | 3 | 5 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0005t0006 | 0/0 | 3498 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0006t0001 | 0/0 | 3498 | 7 | 0 | 0 | 5 | 0 | 2 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0006t0008 | 0/0 | 3498 | 2 | 0 | 0 | 2 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0008t0002 | 0/0 | 3498 | 4 | 0 | 2 | 0 | 2 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0009t0002 | 0/0 | 3498 | 3 | 0 | 0 | 3 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0013t0001 | 0/0 | 3498 | 2 | 0 | 2 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0014t0003 | 0/0 | 3498 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0015t0001 | 0/0 | 3498 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0016t0001 | 0/0 | 3498 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0017t0001 | 0/0 | 3498 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0018t0002 | 0/0 | 3498 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0020t0009 | 0/0 | 3498 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0021t0001 | 0/0 | 3498 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0001c0022t0002 | 0/0 | 3498 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0002c0007t0001 | 0/0 | 3498 | 3 | 0 | 2 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0002c0007t0004 | 0/0 | 3498 | 2 | 0 | 2 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0002c0010t0002 | 0/0 | 3498 | 2 | 0 | 2 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0003c0012t0001 | 0/0 | 3498 | 2 | 0 | 1 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0003c0023t0001 | 0/0 | 3498 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0004c0011t0002 | 0/0 | 3498 | 2 | 2 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| a0005c0019t0002 | 0/0 | 3498 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | CCTTA others(3493): Show |
chr12 | 20690332 | 20758386 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 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 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0057 | 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 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0105 | 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 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0113 | 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 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0134 | 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 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0171 | 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 |
| 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 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0211 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0229 | 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 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0257 | 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 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0001g0286 | 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 |
| a0001c0001t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0004g0283 | 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 |
| a0001c0001t0010g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0001t0013g0147 | 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 |
| a0001c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 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 |
| a0001c0002t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0032 | 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 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0065 | 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 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0079 | 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 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0112 | 0/1 | 1 | 0 | 0 | 0 | 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 |
| a0001c0002t0002g0119 | 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 |
| a0001c0002t0002g0125 | 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 |
| a0001c0002t0002g0130 | 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 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0228 | 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 |
| a0001c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0006g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0006g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0002t0011g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0234 | 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 |
| a0001c0003t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0004g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0004g0236 | 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 |
| a0001c0003t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0003t0012g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0001g0043 | 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 |
| a0001c0004t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0004t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0005t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0005t0006g0173 | 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 |
| a0001c0006t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0006t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0006t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0006t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0006t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0006t0008g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0006t0008g0203 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0008t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0008t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0008t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0009t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0009t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0009t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0013t0001g0220 | 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 |
| a0001c0014t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0015t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0016t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0017t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0018t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0020t0009g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0021t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0001c0022t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0002c0007t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0002c0007t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0002c0007t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0002c0007t0004g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0002c0010t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0002c0010t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0003c0012t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0003c0012t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0003c0023t0001g0227 | 0/0 | 1 | 0 | 1 | 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 |
| a0004c0011t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| a0005c0019t0002g0074 | 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 | g0166 | EUR | GBR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0284 | EUR | GBR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00280 | hp1 | a0002 | c0007 | t0001 | g0256 | EUR | FIN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00280 | hp2 | a0001 | c0008 | t0002 | g0218 | EUR | FIN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0055 | EAS | CHS | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00544 | hp2 | a0001 | c0004 | t0003 | g0270 | EAS | CHS | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00558 | hp1 | a0001 | c0009 | t0002 | g0099 | EAS | CHS | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0148 | EAS | CHS | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00597 | hp1 | a0001 | c0004 | t0001 | g0151 | EAS | CHS | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0255 | 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 | g0078 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0101 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0283 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0037 | 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 | g0169 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00735 | hp2 | a0001 | c0005 | t0002 | g0246 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00738 | hp2 | a0003 | c0023 | t0001 | g0227 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00741 | hp1 | a0001 | c0022 | t0002 | g0116 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01069 | hp1 | a0002 | c0007 | t0004 | g0008 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0093 | 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 | g0008 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01081 | hp2 | a0001 | c0004 | t0001 | g0096 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0135 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01167 | hp1 | a0001 | c0008 | t0002 | g0222 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01168 | hp1 | a0001 | c0003 | t0004 | g0236 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01168 | hp2 | a0001 | c0003 | t0003 | g0198 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01169 | hp1 | a0001 | c0003 | t0003 | g0197 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0240 | 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 | g0121 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0046 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01256 | hp2 | a0002 | c0010 | t0002 | g0225 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0070 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0228 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01258 | hp2 | a0002 | c0010 | t0002 | g0226 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0154 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0069 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0065 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0175 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0265 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0204 | 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 | g0253 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0059 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0264 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0239 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01496 | hp2 | a0002 | c0007 | t0001 | g0219 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01515 | hp1 | a0001 | c0008 | t0002 | g0223 | EUR | IBS | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01515 | hp2 | a0001 | c0005 | t0002 | g0233 | EUR | IBS | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0286 | 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 | g0196 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01928 | hp1 | a0001 | c0008 | t0002 | g0221 | AMR | PEL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0267 | AMR | PEL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0249 | AMR | PEL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0185 | AMR | PEL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0274 | AMR | PEL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01975 | hp2 | a0001 | c0013 | t0001 | g0220 | AMR | PEL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01978 | hp1 | a0003 | c0012 | t0001 | g0129 | AMR | PEL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0266 | 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 | g0064 | AMR | PEL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0100 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02015 | hp2 | a0001 | c0001 | t0013 | g0147 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02027 | hp1 | a0001 | c0004 | t0003 | g0152 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0091 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0214 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02055 | hp1 | a0001 | c0020 | t0009 | g0018 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02056 | hp1 | a0001 | c0003 | t0001 | g0136 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0191 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0111 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02071 | hp2 | a0001 | c0004 | t0001 | g0090 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0237 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02080 | hp2 | a0001 | c0006 | t0001 | g0149 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0275 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0282 | AMR | PEL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0073 | 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 | g0079 | EAS | CDX | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0205 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0258 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0260 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0161 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0263 | AMR | PEL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0176 | 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 | g0124 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02523 | hp2 | a0001 | c0004 | t0003 | g0157 | EAS | KHV | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0208 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02602 | hp2 | a0001 | c0003 | t0001 | g0199 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0177 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0017 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0201 | 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 | g0025 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02683 | hp1 | a0001 | c0003 | t0001 | g0234 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02683 | hp2 | a0005 | c0019 | t0002 | g0074 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02717 | hp1 | a0001 | c0003 | t0012 | g0029 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0102 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0261 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0200 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02895 | hp1 | a0004 | c0011 | t0002 | g0209 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0153 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02897 | hp1 | a0004 | c0011 | t0002 | g0210 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02922 | hp2 | a0001 | c0001 | t0010 | g0024 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0273 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03041 | hp2 | a0001 | c0005 | t0002 | g0044 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0285 | 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 | g0011 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0165 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0021 | 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 | g0195 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0077 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03453 | hp2 | a0001 | c0014 | t0003 | g0262 | AFR | MSL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0164 | AFR | MSL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0115 | 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 | g0097 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03516 | hp1 | a0001 | c0005 | t0002 | g0202 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0170 | AFR | ESN | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03540 | hp1 | a0001 | c0005 | t0002 | g0184 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0281 | AFR | GWD | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03579 | hp2 | a0001 | c0003 | t0007 | g0020 | AFR | MSL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03654 | hp1 | a0001 | c0005 | t0006 | g0173 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0278 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03688 | hp1 | a0001 | c0003 | t0001 | g0034 | SAS | STU | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0048 | SAS | STU | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0268 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0094 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0095 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03710 | hp2 | a0001 | c0005 | t0002 | g0066 | SAS | PJL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03831 | hp1 | a0001 | c0003 | t0001 | g0174 | SAS | BEB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03831 | hp2 | a0001 | c0005 | t0002 | g0141 | SAS | BEB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03834 | hp1 | a0001 | c0006 | t0001 | g0084 | SAS | BEB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03834 | hp2 | a0001 | c0003 | t0004 | g0168 | SAS | BEB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03927 | hp1 | a0001 | c0021 | t0001 | g0159 | SAS | BEB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0172 | SAS | BEB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03942 | hp1 | a0001 | c0002 | t0006 | g0235 | SAS | BEB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03942 | hp2 | a0001 | c0005 | t0002 | g0279 | SAS | BEB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG04115 | hp1 | a0001 | c0006 | t0001 | g0217 | SAS | STU | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG04115 | hp2 | a0001 | c0002 | t0006 | g0123 | SAS | STU | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0160 | SAS | BEB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0238 | SAS | STU | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | STU | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0156 | 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 | g0189 | AFR | YRI | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18522 | hp2 | a0001 | c0003 | t0001 | g0287 | AFR | YRI | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0224 | EAS | CHB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18612 | hp2 | a0001 | c0004 | t0003 | g0042 | EAS | CHB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18747 | hp1 | a0001 | c0009 | t0002 | g0128 | EAS | CHB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | CHB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0259 | AFR | YRI | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18941 | hp1 | a0001 | c0018 | t0002 | g0216 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0144 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18951 | hp1 | a0001 | c0004 | t0001 | g0043 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18951 | hp2 | a0001 | c0003 | t0001 | g0137 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0092 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0247 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18953 | hp2 | a0001 | c0004 | t0003 | g0082 | 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 | g0145 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18959 | hp1 | a0001 | c0015 | t0001 | g0192 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18959 | hp2 | a0001 | c0016 | t0001 | g0051 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18962 | hp1 | a0001 | c0002 | t0011 | g0085 | 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 | g0053 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18964 | hp2 | a0001 | c0004 | t0001 | g0120 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0089 | 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 | g0035 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18979 | hp1 | a0001 | c0006 | t0008 | g0041 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18983 | hp2 | a0003 | c0012 | t0001 | g0131 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0127 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0119 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18989 | hp1 | a0001 | c0006 | t0008 | g0203 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18989 | hp2 | a0001 | c0002 | t0002 | g0125 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18999 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19004 | hp1 | a0001 | c0004 | t0001 | g0088 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19005 | hp1 | a0001 | c0006 | t0001 | g0194 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0269 | 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 | g0252 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19030 | hp1 | a0001 | c0004 | t0003 | g0182 | AFR | LWK | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | LWK | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | LWK | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19043 | hp2 | a0001 | c0003 | t0005 | g0028 | AFR | LWK | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19058 | hp1 | a0001 | c0005 | t0002 | g0049 | 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 | g0158 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19072 | hp2 | a0001 | c0006 | t0001 | g0193 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19074 | hp1 | a0001 | c0009 | t0002 | g0087 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19074 | hp2 | a0001 | c0017 | t0001 | g0040 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19078 | hp1 | a0001 | c0002 | t0002 | g0122 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19078 | hp2 | a0001 | c0002 | t0002 | g0143 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0277 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0134 | 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 | g0015 | AFR | YRI | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA20129 | hp1 | a0001 | c0003 | t0003 | g0056 | AFR | ASW | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA20129 | hp2 | a0001 | c0005 | t0002 | g0186 | AFR | ASW | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA20752 | hp1 | a0001 | c0005 | t0002 | g0045 | EUR | TSI | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA20752 | hp2 | a0001 | c0005 | t0002 | g0109 | EUR | TSI | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0280 | EUR | TSI | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0103 | EUR | TSI | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0167 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG01123 | hp2 | a0001 | c0004 | t0001 | g0155 | AMR | CLM | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02109 | hp1 | a0001 | c0003 | t0007 | g0019 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0063 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0232 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG02486 | hp2 | a0001 | c0004 | t0001 | g0016 | 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 | g0181 | AFR | ACB | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | MSL | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | USA | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| HG06807 | hp2 | a0001 | c0004 | t0001 | g0107 | AFR | USA | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0130 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | USA | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | USA | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | LWK | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0112 | REF | REF | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0211 | REF | REF | SLCO1C1_chr12_20690332_20758386 | SLCO1C1 | chr12 | 20690332 | 20758386 |
| view | 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 |
| view | 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 | a0001c0008 a0001c0013 a0003c0023 |
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 | a0001c0003 a0001c0005 a0001c0020 others(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 | a0001c0017 a0001c0018 |
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 | a0001c0004 a0001c0009 a0001c0016 others(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 | a0001c0014 a0001c0020 |
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 | a0001c0002 a0001c0005 a0001c0008 others(6): Show |
124 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(121): 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 | a0001c0006 a0001c0015 a0001c0021 others(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 |
| view | 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 | a0001c0003t0007 a0001c0020t0009 |
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 | a0001c0001t0005 a0001c0003t0005 a0001c0003t0012 |
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 | a0001c0002t0002 a0001c0002t0006 a0001c0002t0011 others(9): Show |
124 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(121): 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 | a0001c0002t0002 a0001c0002t0006 a0001c0002t0011 others(9): Show |
124 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(121): 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 | a0001c0001t0004 a0001c0003t0004 a0002c0007t0004 |
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 | a0001c0002t0006 a0001c0005t0006 |
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 | a0001c0002t0002 a0001c0002t0006 a0001c0002t0011 others(9): Show |
124 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(121): 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 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(20): Show |
165 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(162): 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 |
| view | 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 | a0001c0001t0001g0288 a0001c0003t0001g0287 |
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 | a0001c0001t0001g0288 a0001c0003t0001g0287 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0288 a0001c0003t0001g0287 |
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 | a0001c0001t0001g0285 a0001c0001t0001g0286 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(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 | 157 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0037 others(154): Show |
159 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(156): 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 | a0001c0005t0002g0184 | 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 | a0001c0002t0002g0183 | 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 | a0001c0001t0001g0030 | 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 | a0001c0002t0002g0185 | 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 | a0001c0001t0004g0283 a0001c0003t0001g0284 |
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 | a0001c0001t0004g0031 | 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 | a0001c0002t0002g0032 | 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 | a0001c0001t0005g0027 a0001c0003t0005g0002 a0001c0003t0005g0026 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0288 a0001c0001t0004g0283 others(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 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0288 a0001c0001t0004g0283 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0288 a0001c0003t0001g0287 |
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 | a0001c0005t0002g0186 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0013 others(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 | a0001c0002t0002g0282 | 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 | a0001c0003t0001g0034 | 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 | a0001c0001t0001g0037 a0001c0002t0002g0036 a0001c0002t0002g0038 others(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 | a0001c0003t0001g0199 | 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 | a0001c0001t0001g0190 a0001c0002t0002g0191 a0001c0002t0002g0196 others(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 | a0001c0001t0001g0288 a0001c0003t0001g0287 |
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 | a0001c0001t0001g0190 a0001c0002t0002g0191 a0001c0002t0002g0196 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0187 a0001c0001t0001g0188 others(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 | a0001c0002t0002g0196 a0001c0003t0003g0197 a0001c0003t0003g0198 |
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 | a0001c0004t0003g0182 | 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 | a0001c0004t0001g0043 a0001c0004t0003g0042 a0001c0006t0008g0041 |
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 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(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 | a0001c0001t0004g0283 a0001c0003t0001g0284 |
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 | 137 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0037 others(134): Show |
139 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(136): 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 | a0001c0002t0002g0161 | 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 | a0001c0003t0001g0205 | 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 | 137 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0037 others(134): Show |
139 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(136): 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 | a0001c0001t0001g0023 a0001c0001t0001g0187 a0001c0001t0001g0188 others(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 | a0001c0001t0004g0283 a0001c0003t0001g0284 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0288 a0001c0003t0001g0287 |
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 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0288 a0001c0001t0004g0283 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0171 others(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 | a0001c0002t0002g0160 | 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 | a0001c0004t0003g0182 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0190 a0001c0001t0001g0288 others(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 | 171 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0037 others(168): Show |
174 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(171): 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 | 160 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0037 others(157): Show |
162 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(159): 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 | a0001c0002t0002g0281 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0288 a0001c0001t0004g0283 others(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 | a0001c0002t0002g0046 a0001c0005t0002g0044 a0001c0005t0002g0045 |
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 | a0001c0001t0004g0283 a0001c0003t0001g0284 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0190 a0001c0002t0002g0191 a0001c0002t0002g0196 others(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 | a0001c0001t0005g0027 a0001c0003t0005g0002 a0001c0003t0005g0026 others(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 | 204 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0013 others(201): Show |
209 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(206): 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 | a0001c0001t0001g0023 a0001c0001t0003g0021 a0001c0001t0003g0022 others(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 | a0001c0001t0004g0283 a0001c0003t0001g0284 |
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 | a0002c0007t0004g0008 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(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 | 168 | a0001c0001t0001g0023 a0001c0001t0001g0030 a0001c0001t0001g0033 others(165): Show |
170 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(167): 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0037 a0001c0002t0002g0036 a0001c0002t0002g0038 others(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 | a0001c0001t0001g0023 a0001c0001t0003g0021 a0001c0001t0003g0022 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(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 | a0001c0002t0002g0052 a0001c0002t0002g0053 a0001c0002t0002g0054 others(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 | a0001c0002t0002g0208 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0003t0003g0056 |
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 | 283 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(280): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): 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 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 |
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 | a0001c0001t0001g0023 a0001c0001t0003g0021 a0001c0001t0003g0022 others(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 | a0001c0003t0007g0019 a0001c0003t0007g0020 a0001c0020t0009g0018 |
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 | a0001c0001t0001g0190 a0001c0002t0002g0191 a0001c0002t0002g0196 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(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 | a0001c0001t0004g0283 a0001c0003t0001g0284 a0001c0005t0002g0184 |
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 | 135 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0037 others(132): Show |
137 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(134): 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 | a0001c0002t0002g0280 | 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 | a0001c0001t0005g0027 a0001c0003t0005g0002 a0001c0003t0005g0026 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0003g0164 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(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 | a0001c0006t0008g0203 | 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 | 199 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0013 others(196): Show |
204 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(201): 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 | a0001c0001t0004g0283 a0001c0003t0001g0284 a0001c0005t0002g0184 |
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 | a0001c0003t0001g0278 a0001c0005t0002g0279 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0190 a0001c0002t0002g0191 a0001c0002t0002g0196 others(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 | a0001c0001t0001g0276 a0001c0002t0002g0275 a0001c0002t0002g0277 |
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 | 200 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0013 others(197): Show |
205 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(202): 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 | a0001c0001t0001g0033 a0001c0001t0001g0060 a0001c0001t0001g0061 others(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 | 61 | a0001c0001t0001g0009 a0001c0001t0001g0037 a0001c0001t0001g0113 others(58): Show |
61 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(58): 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 | a0001c0001t0001g0162 a0001c0001t0001g0171 a0001c0001t0003g0170 others(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 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0001c0001t0001g0190 others(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 | a0001c0001t0001g0163 a0001c0001t0001g0179 a0001c0001t0001g0180 others(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 | a0001c0001t0001g0023 a0001c0001t0010g0024 a0001c0003t0001g0025 others(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 | a0001c0002t0002g0177 a0001c0003t0007g0020 |
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 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(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 | a0001c0002t0002g0165 | 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 | a0001c0001t0001g0171 a0001c0001t0003g0170 |
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 | a0001c0001t0001g0171 a0001c0001t0003g0170 |
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 | 34 | a0001c0001t0001g0006 a0001c0001t0001g0229 a0001c0001t0001g0242 others(31): 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 | a0001c0001t0001g0171 a0001c0001t0003g0170 a0001c0002t0002g0255 others(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 | a0001c0001t0001g0171 a0001c0001t0003g0170 a0001c0002t0002g0255 others(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 | a0001c0001t0001g0171 a0001c0001t0003g0170 a0001c0002t0002g0255 others(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 | a0001c0001t0001g0190 a0001c0002t0002g0191 a0001c0002t0002g0196 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0288 a0001c0003t0001g0287 |
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 | a0001c0001t0001g0011 a0001c0001t0004g0172 a0001c0002t0002g0244 others(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 | 187 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0030 others(184): Show |
190 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(187): 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 | 187 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0030 others(184): Show |
190 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(187): Show |
intron_variant | MODIFIER | c.272-1609G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20704340 | |||||||
| chr12:20704533 | A | C | 202 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0013 others(199): Show |
207 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(204): Show |
intron_variant | MODIFIER | c.272-1416A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 3/14 | chr12 | 20704533 | |||||||
| chr12:20704542 | G | A | 187 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0030 others(184): Show |
190 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(187): 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 | a0001c0004t0003g0157 | 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 | 187 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0030 others(184): Show |
190 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(187): 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 | a0001c0001t0001g0190 a0001c0002t0002g0191 a0001c0002t0002g0196 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(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 | 187 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0030 others(184): Show |
190 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(187): 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 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0190 a0001c0002t0002g0191 a0001c0002t0002g0196 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(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 | a0001c0005t0002g0044 | 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 | a0001c0002t0002g0111 | 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 | a0001c0001t0001g0023 a0001c0001t0003g0021 a0001c0001t0003g0022 others(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 | a0001c0001t0004g0103 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(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 | a0001c0005t0002g0184 | 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 | a0001c0001t0003g0273 | 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 | 175 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0030 others(172): Show |
177 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(174): 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 | a0001c0005t0002g0184 | 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 | a0001c0004t0003g0158 | 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 | 201 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0013 others(198): Show |
206 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(203): 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 | 164 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0033 others(161): Show |
166 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(163): 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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0003g0164 others(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 | a0001c0002t0002g0167 | 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 | a0001c0004t0003g0182 | 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 | a0001c0001t0001g0181 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(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 | a0001c0001t0004g0283 a0001c0003t0001g0284 |
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 | a0001c0001t0001g0190 a0001c0002t0002g0191 a0001c0002t0002g0196 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0285 a0001c0001t0001g0286 |
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 | a0001c0001t0001g0156 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.404+2016C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20708097 | |||||||
| chr12:20708164 | C | T | 2 | a0001c0001t0001g0288 a0001c0003t0001g0287 |
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 | a0001c0001t0001g0181 | 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 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(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 | a0001c0002t0002g0191 a0001c0006t0001g0005 a0001c0006t0001g0193 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0171 others(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 | 165 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0033 others(162): Show |
167 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(164): 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 | a0001c0004t0001g0155 | 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 | 279 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(276): Show |
287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): 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 | a0001c0002t0002g0214 | 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 | a0001c0001t0001g0288 a0001c0003t0001g0287 |
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 | a0001c0003t0003g0197 a0001c0003t0003g0198 |
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 | a0001c0001t0001g0285 a0001c0001t0001g0286 |
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 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
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 | a0001c0002t0002g0154 | 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 | a0001c0005t0002g0066 | 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 | 183 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0030 others(180): Show |
187 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(184): 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 | a0001c0002t0002g0263 | 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 | 32 | a0001c0001t0001g0006 a0001c0001t0001g0033 a0001c0001t0001g0113 others(29): 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 | a0001c0001t0001g0011 a0001c0001t0001g0114 a0001c0001t0001g0254 others(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 | a0001c0002t0002g0012 | 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 | a0001c0004t0001g0016 | 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 | a0001c0001t0001g0156 | 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 | a0001c0003t0012g0029 | 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 | a0001c0001t0001g0068 a0001c0001t0001g0104 a0001c0001t0001g0105 others(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 | a0001c0001t0001g0067 | 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 | 3 | a0001c0001t0001g0006 a0001c0002t0002g0239 a0001c0002t0002g0240 |
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 | a0001c0001t0001g0288 a0001c0003t0001g0287 |
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 | 145 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0037 others(142): Show |
148 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(145): 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 | a0001c0001t0004g0283 a0001c0003t0001g0284 |
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 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0005t0002g0184 |
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 | a0001c0001t0004g0238 a0001c0003t0001g0284 a0001c0005t0002g0279 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(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 | a0001c0001t0010g0024 | 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 | a0001c0001t0003g0021 a0001c0003t0001g0025 |
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 | a0001c0001t0003g0022 | 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 | a0001c0001t0001g0110 a0001c0001t0001g0171 a0001c0001t0001g0288 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0104 others(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 | 19 | a0001c0001t0001g0006 a0001c0001t0001g0050 a0001c0001t0001g0206 others(16): Show |
19 | HG00597.hp2 HG00735.hp1 HG00735.hp2 others(16): 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 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0106 a0001c0001t0001g0139 a0001c0001t0003g0118 others(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 | a0001c0003t0003g0056 | 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 | 86 | a0001c0001t0001g0030 a0001c0001t0001g0037 a0001c0001t0001g0071 others(83): 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 | a0001c0001t0001g0271 a0001c0002t0002g0092 |
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 | a0001c0001t0001g0009 | 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 | a0001c0004t0003g0270 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0104 others(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 | 105 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0013 others(102): Show |
109 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(106): 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 | a0001c0002t0002g0280 a0001c0008t0002g0218 |
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 | 61 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(58): Show |
62 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.405-771C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 4/14 | chr12 | 20710615 | |||||||
| chr12:20710621 | G | T | 40 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(37): 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 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0162 others(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 | 104 | a0001c0001t0001g0030 a0001c0001t0001g0037 a0001c0001t0001g0071 others(101): Show |
106 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(103): 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 | a0001c0001t0001g0047 a0001c0001t0001g0050 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0285 a0001c0002t0002g0239 a0005c0019t0002g0074 |
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 | a0001c0003t0001g0034 a0001c0003t0001g0284 a0005c0019t0002g0074 |
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 | a0001c0001t0001g0254 a0001c0001t0003g0022 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0047 a0001c0001t0001g0062 others(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 | a0001c0002t0002g0153 a0001c0002t0002g0255 a0001c0003t0001g0136 others(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 | |||||||
| chr12:20711200 | T | C | 3 | a0001c0001t0001g0207 a0001c0003t0001g0287 a0001c0003t0012g0029 |
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 | a0001c0001t0001g0009 | 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 | a0001c0001t0001g0285 | 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 | a0001c0001t0001g0013 a0001c0002t0002g0079 a0001c0021t0001g0159 others(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 | a0001c0003t0001g0025 a0001c0003t0001g0205 a0001c0003t0001g0245 others(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 | a0001c0001t0001g0050 a0001c0001t0001g0104 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0254 a0001c0001t0003g0022 a0001c0003t0004g0236 others(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 | a0001c0001t0001g0009 | 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 | a0001c0001t0001g0078 a0001c0001t0001g0133 a0001c0001t0001g0134 others(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 | 19 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0162 others(16): 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 | 12 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0229 others(9): 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 | a0001c0002t0002g0036 | 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 | 23 | a0001c0001t0001g0006 a0001c0001t0001g0078 a0001c0001t0001g0142 others(20): 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 | a0001c0001t0001g0189 | 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 | a0001c0005t0006g0173 | 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 | 149 | a0001c0001t0001g0006 a0001c0001t0001g0050 a0001c0001t0001g0076 others(146): 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 | a0001c0001t0001g0108 a0001c0003t0001g0287 a0001c0003t0012g0029 |
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 | a0001c0001t0001g0050 a0001c0001t0001g0073 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0050 a0001c0001t0001g0104 a0001c0001t0001g0110 others(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 | a0001c0003t0001g0261 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0108 a0001c0003t0001g0287 others(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 | 59 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0050 others(56): 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 | 7 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0229 others(4): 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 | a0001c0001t0001g0288 | 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 | 240 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(237): Show |
246 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(243): 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 | a0001c0001t0001g0037 a0001c0002t0002g0038 a0001c0002t0002g0039 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 others(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 | a0001c0001t0004g0031 a0001c0003t0004g0236 a0001c0003t0005g0002 others(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 | a0001c0001t0003g0083 | 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 | a0001c0006t0008g0041 a0003c0012t0001g0129 |
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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 others(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 | a0001c0001t0001g0015 | 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0189 a0001c0001t0005g0027 a0001c0005t0002g0044 |
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 | a0001c0002t0002g0079 a0001c0003t0001g0101 a0001c0003t0001g0121 others(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 | 216 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0023 others(213): Show |
220 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(217): 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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 others(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 | a0001c0002t0002g0091 a0001c0004t0001g0043 a0001c0004t0001g0090 |
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 | a0001c0001t0001g0254 | 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 | 220 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0023 others(217): Show |
224 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(221): Show |
intron_variant | MODIFIER | c.530-1337A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 5/14 | chr12 | 20713802 | |||||||
| chr12:20713879 | A | G | 2 | a0001c0001t0001g0006 a0001c0002t0002g0231 |
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 | a0001c0002t0002g0079 a0001c0003t0001g0101 a0001c0003t0001g0169 others(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 | a0001c0001t0004g0238 a0001c0003t0001g0034 a0001c0003t0001g0284 others(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 | a0001c0001t0004g0238 a0001c0003t0001g0034 a0001c0003t0001g0284 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 others(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 | 253 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(250): Show |
258 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(255): 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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 others(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 | a0001c0003t0003g0056 a0001c0003t0003g0197 a0001c0003t0003g0198 others(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 | a0001c0002t0002g0079 a0001c0003t0001g0101 a0001c0003t0001g0169 others(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 | a0001c0003t0003g0056 a0001c0003t0003g0197 a0001c0003t0003g0198 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0060 a0001c0001t0001g0061 others(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 | 7 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0229 others(4): 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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 others(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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0108 |
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 | a0001c0001t0001g0257 | 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 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0132 | 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 | 215 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0023 others(212): Show |
219 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(216): 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 | a0001c0005t0002g0066 | 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 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0257 | 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 | a0001c0001t0001g0257 | 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 | a0001c0001t0001g0257 | 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 | 7 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0229 others(4): 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 | a0001c0002t0002g0079 a0001c0003t0001g0101 a0001c0003t0001g0169 others(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 | 44 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0050 others(41): 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 | a0001c0002t0002g0079 | 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 | a0001c0004t0001g0252 | 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 | a0001c0004t0001g0252 | 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 | a0001c0001t0001g0023 a0001c0001t0001g0037 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0058 a0001c0001t0001g0105 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0179 a0001c0001t0001g0213 others(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 | a0001c0002t0002g0046 | 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 | a0001c0001t0001g0206 | 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 | 72 | a0001c0001t0001g0030 a0001c0001t0001g0071 a0001c0001t0001g0072 others(69): Show |
74 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(71): 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 | a0001c0001t0001g0133 a0001c0001t0001g0139 a0001c0001t0004g0238 others(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 | a0001c0001t0001g0113 a0001c0001t0004g0031 |
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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 others(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 | a0001c0001t0003g0164 | 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 | a0001c0001t0001g0009 | 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 | a0001c0001t0001g0189 a0001c0001t0001g0242 |
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 | a0001c0001t0001g0286 | 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 | a0001c0001t0001g0015 a0001c0001t0005g0027 a0001c0003t0001g0017 others(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 | a0001c0001t0001g0050 a0001c0002t0002g0001 a0001c0002t0002g0079 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0104 a0001c0001t0001g0108 others(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 | a0001c0002t0002g0165 | 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 | 7 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0229 others(4): 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 | a0001c0001t0003g0215 a0001c0002t0002g0004 a0001c0002t0002g0239 others(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 | a0001c0005t0002g0202 | 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 | a0001c0001t0001g0033 a0001c0003t0003g0056 a0001c0003t0003g0197 others(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 | a0001c0003t0003g0198 | 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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 others(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 | a0001c0001t0001g0276 | 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 | 274 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(271): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): 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 | a0001c0001t0001g0033 a0001c0003t0003g0056 a0001c0003t0003g0197 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 others(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 | a0001c0001t0004g0238 a0001c0003t0001g0034 a0001c0003t0001g0284 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0108 |
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 | a0001c0001t0001g0013 a0001c0001t0001g0108 |
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 | a0001c0001t0001g0033 a0001c0003t0003g0056 a0001c0003t0003g0197 others(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 | 66 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(63): 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 | a0002c0010t0002g0225 a0002c0010t0002g0226 |
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 | 40 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0050 others(37): 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 | a0001c0001t0001g0013 a0001c0001t0001g0108 |
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 | a0001c0001t0005g0027 a0001c0005t0002g0044 |
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 | a0001c0005t0006g0173 | 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 | a0001c0003t0003g0056 | 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 | a0001c0001t0001g0023 a0001c0001t0001g0106 a0001c0001t0001g0108 others(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 | a0001c0001t0004g0238 a0001c0002t0002g0079 a0001c0002t0002g0183 others(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 | a0001c0001t0001g0050 a0001c0002t0002g0281 a0001c0003t0001g0121 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0033 others(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 |
3 | a0001c0001t0001g0006 a0001c0002t0002g0231 a0001c0003t0012g0029 |
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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0050 a0001c0001t0001g0104 others(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 | a0001c0002t0002g0055 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0060 a0001c0001t0001g0061 others(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 | a0001c0001t0005g0027 a0001c0005t0002g0044 |
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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 others(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 | 215 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0023 others(212): Show |
219 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(216): Show |
intron_variant | MODIFIER | c.776-1602A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 7/14 | chr12 | 20720202 | |||||||
| chr12:20720204 | T | A | 7 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0229 others(4): 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 | a0001c0005t0002g0044 | 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 | 242 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0015 others(239): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(243): 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 | a0001c0001t0001g0011 a0001c0001t0001g0060 a0001c0001t0001g0061 others(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 | a0001c0002t0002g0111 | 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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 others(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 | 7 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0229 others(4): 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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0050 a0001c0001t0001g0108 others(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 | 23 | a0001c0001t0001g0006 a0001c0001t0001g0104 a0001c0001t0001g0142 others(20): 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 | a0001c0002t0002g0239 a0001c0002t0002g0240 |
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 | a0001c0002t0002g0059 | 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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 others(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 | a0001c0002t0002g0079 a0001c0002t0002g0095 a0001c0003t0001g0101 others(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 | a0001c0004t0003g0182 | 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 | a0001c0004t0003g0270 | 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 | 23 | a0001c0001t0001g0081 a0001c0001t0001g0138 a0001c0001t0001g0140 others(20): 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 | a0001c0006t0001g0149 a0001c0021t0001g0159 |
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 | 42 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0050 others(39): 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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 others(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 | a0001c0022t0002g0116 | 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 | a0001c0001t0004g0238 a0001c0003t0001g0034 a0001c0003t0001g0284 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 others(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 | 7 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0229 others(4): 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 | a0001c0005t0002g0186 | 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 | a0001c0003t0001g0034 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0050 others(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 | a0001c0006t0008g0041 a0003c0012t0001g0129 |
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 | a0001c0002t0002g0277 | 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 | a0001c0002t0002g0275 | 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 | a0001c0001t0001g0288 | 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 | a0001c0005t0002g0044 | 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 | a0001c0001t0001g0009 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0050 a0001c0001t0001g0104 others(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 | 2 | a0001c0001t0001g0006 a0001c0002t0002g0231 |
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 | a0001c0005t0002g0246 a0001c0008t0002g0222 |
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 | 65 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(62): 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 | a0001c0001t0001g0011 | 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 | 7 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0229 others(4): 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 | 72 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(69): 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 | a0001c0001t0001g0288 | 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 | a0001c0001t0001g0009 | 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 | a0001c0002t0002g0079 a0001c0002t0002g0095 a0001c0003t0001g0101 others(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 | 72 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(69): 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 | a0001c0002t0002g0094 a0001c0002t0002g0263 a0001c0002t0002g0282 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 others(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 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0139 others(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 | a0001c0002t0002g0281 | 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 | a0001c0001t0001g0050 a0001c0001t0001g0207 a0001c0001t0003g0022 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0104 a0001c0001t0001g0110 others(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 | a0001c0002t0002g0001 a0001c0002t0002g0177 |
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 | a0001c0002t0002g0091 a0001c0004t0001g0090 |
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 | a0001c0001t0001g0108 | 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 | a0001c0001t0004g0238 a0001c0001t0005g0027 a0001c0005t0006g0173 |
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 | a0001c0003t0001g0034 a0001c0003t0001g0284 a0001c0005t0002g0044 others(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 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 others(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 | a0001c0003t0005g0002 a0001c0003t0005g0026 a0001c0003t0005g0028 |
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 | 7 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0229 others(4): 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 | a0001c0002t0002g0232 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0076 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0071 a0001c0001t0001g0073 others(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 | 64 | a0001c0001t0001g0037 a0001c0001t0001g0047 a0001c0001t0001g0057 others(61): Show |
66 | HG00544.hp1 HG00558.hp1 HG00673.hp1 others(63): 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 | a0001c0001t0001g0058 a0001c0001t0001g0126 a0001c0001t0001g0133 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0093 a0001c0001t0004g0103 others(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 | a0001c0001t0001g0276 a0001c0002t0002g0154 |
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 | a0001c0001t0004g0283 a0001c0005t0002g0202 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0060 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0078 others(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 | a0001c0002t0002g0032 a0001c0002t0002g0148 a0001c0004t0001g0096 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0002t0002g0038 others(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 | a0001c0001t0001g0086 a0001c0001t0001g0106 a0001c0001t0001g0285 others(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 | a0001c0009t0002g0128 | 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 | a0001c0003t0003g0197 a0001c0003t0003g0198 a0001c0003t0007g0019 |
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 | a0001c0001t0001g0288 | 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 | a0001c0003t0001g0101 | 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 | a0001c0001t0001g0180 | 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 | a0002c0007t0001g0256 a0002c0007t0004g0008 |
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 | a0001c0001t0001g0013 a0001c0002t0002g0036 a0001c0002t0002g0095 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0037 a0001c0001t0001g0050 others(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 | a0002c0007t0001g0064 | 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 | a0001c0001t0001g0105 a0001c0001t0001g0190 a0001c0002t0002g0004 others(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 | a0001c0001t0001g0023 a0001c0001t0003g0170 a0001c0001t0004g0172 others(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 | 231 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0015 others(228): Show |
236 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.1186+1197A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20724451 | |||||||
| chr12:20724453 | G | A | 25 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0033 others(22): 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 | 7 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0229 others(4): 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 | a0001c0005t0002g0253 | 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 | a0001c0020t0009g0018 | 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 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0003t0001g0205 others(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 | a0001c0002t0002g0249 a0001c0005t0002g0246 a0001c0008t0002g0222 |
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 | a0001c0001t0004g0172 a0001c0002t0002g0048 a0001c0006t0001g0217 |
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 | a0001c0001t0001g0086 a0001c0002t0002g0092 a0001c0002t0011g0085 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0050 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 others(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 | 212 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0023 others(209): Show |
216 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(213): 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 | 7 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0229 others(4): 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 | a0001c0001t0001g0047 a0001c0001t0001g0057 a0001c0001t0001g0058 others(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 | a0001c0001t0001g0081 a0001c0002t0002g0130 a0001c0004t0001g0120 others(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 | a0001c0003t0005g0002 a0001c0003t0005g0026 a0001c0003t0005g0028 |
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 | a0001c0002t0002g0038 a0001c0002t0002g0039 |
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 | a0001c0001t0001g0288 | 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 | a0001c0001t0001g0108 a0001c0001t0004g0172 a0001c0006t0001g0217 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0060 a0001c0001t0001g0061 others(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 | 39 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0050 others(36): 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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 others(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 | a0001c0001t0004g0238 a0001c0003t0001g0034 a0001c0003t0001g0284 others(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 | a0001c0001t0001g0093 a0001c0001t0004g0103 a0001c0001t0004g0283 |
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 | a0001c0002t0002g0239 a0001c0002t0002g0240 |
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 | a0001c0004t0003g0182 | 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0115 a0001c0001t0001g0242 a0001c0005t0002g0279 |
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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 others(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 | a0001c0005t0002g0186 | 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 | a0001c0005t0006g0173 | 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 | a0001c0001t0001g0013 | 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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 others(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 | a0001c0002t0002g0089 | 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 | a0001c0001t0001g0075 a0001c0002t0002g0280 |
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 | a0001c0002t0002g0281 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(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 | 7 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0229 others(4): 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 | a0001c0001t0003g0170 | 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 | a0001c0001t0001g0050 a0001c0001t0001g0104 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0062 | 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 | a0001c0002t0002g0079 a0001c0002t0002g0095 a0001c0003t0001g0101 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0171 |
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 | a0001c0002t0002g0255 | 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 | a0001c0001t0001g0013 | 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 | 56 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0050 others(53): 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 | a0001c0001t0001g0204 a0001c0002t0002g0077 a0001c0002t0002g0166 |
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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0050 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0288 | 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 | a0001c0001t0005g0027 a0001c0005t0002g0044 |
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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0178 others(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 | a0001c0006t0001g0149 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0060 a0001c0001t0001g0061 others(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 | a0001c0005t0006g0173 | 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 | 263 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0015 others(260): Show |
270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): 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 | a0001c0001t0001g0288 | 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 | a0001c0002t0002g0048 | 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 | a0001c0003t0003g0056 | 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 | a0001c0001t0001g0181 a0001c0014t0003g0262 |
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 | a0001c0002t0002g0191 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0050 others(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 | a0002c0007t0001g0256 | 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 | 58 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(55): 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 | a0001c0002t0002g0255 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0050 a0001c0001t0001g0104 others(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 | a0001c0002t0002g0280 | 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 | 53 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(50): 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 | 53 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(50): 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 | 53 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(50): 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 | 53 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(50): 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 | a0002c0007t0001g0219 | 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 | a0001c0005t0002g0066 a0001c0005t0002g0109 a0001c0005t0002g0233 |
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 | a0001c0002t0002g0077 a0001c0002t0002g0166 |
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 | 51 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(48): 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 | 178 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0030 others(175): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): 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 | a0001c0001t0001g0047 a0001c0001t0001g0057 a0001c0001t0001g0058 others(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 | a0001c0002t0002g0240 | 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 | 249 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(246): Show |
256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): 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 | a0001c0001t0001g0015 a0001c0001t0001g0050 a0001c0001t0001g0178 others(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 | a0001c0001t0004g0031 a0001c0001t0004g0238 a0001c0002t0002g0065 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(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 | a0001c0001t0003g0022 | 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 | a0001c0001t0003g0022 | 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 | 285 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(282): Show |
293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.1187-206C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 9/14 | chr12 | 20732703 | |||||||
| chr12:20732707 | T | C | 120 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(117): Show |
124 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(121): 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 | a0001c0001t0003g0022 | 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 | a0001c0002t0002g0153 a0001c0003t0001g0017 |
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 | a0001c0001t0003g0083 a0001c0001t0003g0118 a0001c0001t0003g0215 others(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 | 108 | a0001c0001t0001g0110 a0001c0001t0004g0172 a0001c0002t0002g0003 others(105): Show |
112 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(109): 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 | a0001c0001t0001g0104 a0001c0001t0001g0106 a0001c0002t0002g0001 others(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 | a0001c0001t0001g0104 a0001c0001t0001g0106 a0001c0002t0002g0001 others(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 | 111 | a0001c0001t0001g0110 a0001c0001t0004g0172 a0001c0002t0002g0003 others(108): Show |
115 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(112): 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 | a0001c0002t0002g0274 | 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 | a0001c0003t0005g0028 | 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 | a0001c0005t0002g0186 a0001c0020t0009g0018 |
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 | a0001c0001t0004g0031 a0001c0001t0004g0103 a0001c0001t0004g0135 others(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 | 111 | a0001c0001t0001g0110 a0001c0001t0004g0172 a0001c0002t0002g0003 others(108): Show |
115 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(112): 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 | a0001c0002t0002g0089 a0001c0009t0002g0087 |
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 | 104 | a0001c0001t0004g0172 a0001c0002t0002g0003 a0001c0002t0002g0004 others(101): Show |
107 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(104): 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 | a0001c0002t0002g0077 | 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 | a0002c0007t0001g0064 a0002c0007t0001g0219 a0002c0007t0004g0008 |
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 | a0001c0001t0001g0013 a0001c0001t0003g0014 a0001c0001t0003g0021 others(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 | a0001c0001t0003g0083 a0001c0001t0003g0118 a0001c0001t0003g0215 others(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 | a0001c0003t0001g0234 | 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 | a0001c0003t0012g0029 | 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 | a0001c0001t0001g0114 a0001c0003t0001g0199 |
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 | a0001c0001t0001g0013 a0001c0001t0003g0014 a0001c0001t0003g0021 others(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 | a0001c0016t0001g0051 | 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 | a0001c0002t0006g0235 a0001c0005t0006g0173 |
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 | a0001c0001t0003g0083 a0001c0001t0003g0118 a0001c0001t0003g0215 others(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 | a0001c0001t0001g0163 | 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 | 234 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(231): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): 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 | a0001c0001t0004g0031 a0001c0001t0004g0103 a0001c0001t0004g0135 others(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 | a0001c0002t0002g0161 a0001c0002t0002g0230 a0001c0002t0002g0244 others(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 | 112 | a0001c0001t0001g0110 a0001c0001t0004g0172 a0001c0002t0002g0003 others(109): Show |
116 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(113): 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 | 123 | a0001c0001t0001g0030 a0001c0001t0001g0093 a0001c0001t0001g0098 others(120): Show |
128 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(125): 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 | a0001c0003t0012g0029 | 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 | 104 | a0001c0001t0004g0172 a0001c0002t0002g0003 a0001c0002t0002g0004 others(101): Show |
107 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.1383-590G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 10/14 | chr12 | 20736517 | |||||||
| chr12:20736726 | A | T | 111 | a0001c0001t0001g0110 a0001c0001t0004g0172 a0001c0002t0002g0003 others(108): Show |
115 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(112): 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 | a0001c0001t0001g0030 a0001c0001t0001g0072 a0001c0001t0001g0093 others(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 | a0001c0001t0001g0013 a0001c0001t0003g0014 a0001c0001t0003g0021 others(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 | 235 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(232): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): 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 | a0001c0002t0002g0089 a0001c0009t0002g0087 |
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 | a0001c0003t0001g0234 | 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 | a0001c0001t0004g0172 a0001c0002t0002g0268 a0001c0006t0001g0217 |
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 | a0001c0003t0001g0261 | 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 | a0001c0002t0006g0235 | 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 | a0001c0001t0001g0013 a0001c0001t0003g0014 a0001c0001t0003g0021 others(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 | a0001c0002t0002g0038 | 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 | a0002c0007t0004g0008 | 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 | a0001c0002t0002g0263 | 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 | 109 | a0001c0001t0004g0172 a0001c0002t0002g0003 a0001c0002t0002g0004 others(106): Show |
113 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(110): 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 | a0001c0003t0005g0028 | 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 | a0001c0004t0003g0082 | 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 | a0001c0002t0002g0122 | 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 | a0001c0001t0001g0288 | 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 | a0001c0004t0001g0035 | 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 | a0001c0001t0001g0104 a0001c0001t0003g0273 a0001c0002t0002g0001 others(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 | a0001c0001t0003g0083 a0001c0001t0003g0118 a0001c0001t0003g0215 others(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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1549-259T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 11/14 | chr12 | 20739925 | |||||||
| chr12:20739963 | C | T | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): 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 | a0001c0001t0001g0132 a0001c0001t0001g0145 a0001c0001t0001g0146 |
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 | a0001c0018t0002g0216 | 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 | 157 | a0001c0001t0001g0013 a0001c0001t0003g0014 a0001c0001t0003g0021 others(154): Show |
163 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.1549-66C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 11/14 | chr12 | 20740118 | |||||||
| chr12:20740174 | C | T | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): 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 | a0001c0001t0003g0021 a0001c0001t0003g0201 a0001c0001t0005g0027 others(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 | a0001c0001t0001g0067 | 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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): 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 | a0001c0001t0001g0011 a0001c0001t0001g0176 a0001c0001t0001g0212 others(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 | a0003c0012t0001g0129 | 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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): 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 | a0001c0001t0001g0207 a0001c0001t0003g0273 |
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 | a0001c0005t0002g0141 | 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 | a0001c0005t0002g0233 | 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 | a0001c0005t0002g0233 | 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 | a0001c0002t0002g0175 | 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 | a0001c0002t0002g0036 a0001c0002t0002g0119 a0001c0002t0002g0154 others(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 | a0001c0002t0002g0069 a0001c0002t0002g0125 a0001c0002t0002g0230 others(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 | a0001c0002t0002g0007 a0001c0002t0002g0055 a0001c0002t0002g0094 others(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 | a0001c0002t0002g0004 a0001c0002t0002g0038 a0001c0002t0002g0039 others(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 | a0001c0002t0002g0048 a0001c0002t0002g0089 a0001c0002t0002g0122 others(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 | a0001c0002t0002g0003 a0001c0002t0002g0077 a0001c0002t0002g0079 others(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 | a0001c0002t0002g0059 a0001c0002t0002g0185 a0001c0002t0002g0208 |
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 |
4 | a0001c0002t0002g0231 a0001c0002t0002g0249 a0001c0002t0002g0265 others(1): Show |
4 | HG01255.hp1 HG01358.hp1 HG01952.hp1 others(1): 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 | a0001c0002t0002g0007 a0001c0002t0002g0032 a0001c0002t0002g0053 others(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 | a0001c0009t0002g0128 | 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 | a0001c0003t0005g0002 a0001c0003t0005g0026 a0001c0003t0005g0028 |
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 | 101 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(98): Show |
104 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(101): 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 | a0001c0006t0001g0005 a0001c0006t0001g0193 a0001c0006t0001g0194 others(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 | a0001c0001t0004g0103 a0001c0001t0004g0135 a0001c0001t0004g0238 others(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 | a0002c0007t0001g0064 | 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 | a0001c0001t0003g0083 a0001c0001t0003g0118 a0001c0001t0004g0172 others(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 | a0001c0001t0004g0031 a0001c0003t0004g0236 |
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 | a0001c0001t0001g0072 a0001c0001t0003g0215 a0001c0006t0008g0041 others(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 | a0001c0001t0004g0283 a0001c0006t0008g0203 a0003c0012t0001g0131 |
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 | a0001c0003t0004g0168 a0001c0021t0001g0159 |
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 | 132 | a0001c0001t0001g0072 a0001c0001t0003g0083 a0001c0001t0003g0118 others(129): Show |
137 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(134): 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 | a0001c0002t0002g0281 | 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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0047 a0001c0001t0001g0057 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0050 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0060 a0001c0001t0001g0093 others(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 | a0001c0003t0001g0174 a0001c0016t0001g0051 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0086 a0001c0001t0001g0139 others(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 | a0001c0001t0001g0189 a0001c0001t0003g0124 a0001c0001t0003g0164 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0106 others(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 | a0001c0001t0001g0142 | 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 |
5 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0178 others(2): 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 | a0001c0001t0001g0078 a0001c0001t0001g0105 a0001c0001t0001g0110 |
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 | a0001c0001t0003g0080 a0001c0013t0001g0241 |
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 | a0001c0001t0003g0014 a0001c0001t0013g0147 a0001c0004t0003g0158 |
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 | a0001c0001t0001g0076 a0001c0001t0001g0180 a0001c0004t0003g0042 others(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 | a0001c0020t0009g0018 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0162 others(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 | 106 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(103): Show |
110 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(107): 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 | a0001c0002t0006g0235 a0001c0005t0006g0173 |
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 | a0001c0001t0001g0013 a0001c0001t0003g0014 a0001c0001t0003g0021 others(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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): 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 | a0001c0002t0002g0077 | 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 | a0001c0001t0001g0110 | 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 | 233 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(230): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): 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 | a0001c0014t0003g0262 | 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 | 102 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(99): Show |
105 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(102): 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 | a0001c0001t0001g0181 | 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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1733+1280G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20741648 | |||||||
| chr12:20741737 | TATA | T | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): 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 | a0001c0001t0001g0013 a0001c0001t0003g0014 a0001c0001t0003g0022 others(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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1734-1124T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20742181 | |||||||
| chr12:20742265 | T | C | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1734-1040T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20742265 | |||||||
| chr12:20742329 | T | C | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1734-976T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20742329 | |||||||
| chr12:20742333 | G | GT | 95 | a0001c0001t0001g0139 a0001c0001t0004g0031 a0001c0002t0002g0003 others(92): Show |
99 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(96): 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 | a0001c0002t0002g0095 a0001c0002t0002g0100 a0001c0002t0002g0231 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0037 a0001c0001t0001g0132 others(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 | a0001c0002t0006g0235 | 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 | 233 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(230): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): 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 | a0001c0006t0001g0149 | 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 | a0001c0005t0002g0186 a0001c0020t0009g0018 |
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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): 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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): 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 | a0001c0004t0003g0157 | 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 | a0001c0006t0001g0005 a0001c0006t0001g0193 a0001c0006t0001g0194 others(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 | a0001c0002t0002g0046 a0001c0002t0002g0069 a0001c0002t0002g0070 others(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 | 77 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0037 others(74): 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 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0093 others(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 | 104 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(101): Show |
108 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(105): 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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1734-589T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 12/14 | chr12 | 20742716 | |||||||
| chr12:20742781 | C | T | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): 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 | a0001c0001t0001g0030 a0001c0001t0001g0072 a0001c0001t0001g0093 others(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 | a0001c0001t0001g0013 a0001c0001t0003g0014 a0001c0001t0003g0021 others(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 | a0001c0003t0005g0002 a0001c0003t0005g0026 a0001c0003t0005g0028 |
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 | a0001c0004t0001g0043 | 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 | a0001c0001t0001g0110 | 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 | a0001c0002t0002g0079 | 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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): 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 | a0001c0005t0002g0186 a0001c0020t0009g0018 |
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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1798+461T>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20743830 | |||||||
| chr12:20743875 | G | GT | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): 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 | a0001c0002t0002g0070 a0001c0002t0002g0228 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0176 a0001c0001t0001g0212 others(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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1798+698C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20744067 | |||||||
| chr12:20744190 | A | G | 54 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0071 others(51): 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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1798+971C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20744340 | |||||||
| chr12:20744452 | G | T | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): 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 | a0001c0002t0002g0036 a0001c0002t0002g0119 |
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 | a0001c0003t0003g0197 a0001c0003t0003g0198 |
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 | a0001c0001t0001g0013 a0001c0001t0003g0014 a0001c0001t0003g0021 others(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 | a0001c0001t0003g0273 a0001c0002t0002g0001 a0001c0002t0002g0010 others(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 | a0001c0002t0006g0235 a0001c0005t0006g0173 |
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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1798+1457C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20744826 | |||||||
| chr12:20744883 | C | T | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): 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 | a0001c0001t0003g0083 a0001c0001t0003g0118 a0001c0001t0003g0215 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0072 a0001c0001t0001g0093 others(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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): 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 | a0001c0003t0012g0029 | 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 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(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 | a0001c0001t0004g0031 a0001c0001t0004g0103 a0001c0001t0004g0135 others(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 | |||||||
| chr12:20745148 | G | A | 1 | a0001c0020t0009g0018 | 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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): 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 | a0001c0002t0006g0123 a0001c0002t0006g0235 a0001c0005t0006g0173 |
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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1798+1848A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20745217 | |||||||
| chr12:20745223 | A | T | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): 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 | a0001c0001t0003g0083 a0001c0001t0003g0118 a0001c0001t0003g0215 |
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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1798+1992A>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20745361 | |||||||
| chr12:20745546 | T | C | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): 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 | a0001c0003t0005g0002 a0001c0003t0005g0026 a0001c0003t0005g0028 |
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 | a0001c0001t0001g0108 | 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 | a0001c0002t0002g0077 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1798+2402G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20745771 | |||||||
| chr12:20745832 | A | G | 13 | a0001c0001t0001g0013 a0001c0001t0003g0014 a0001c0001t0003g0022 others(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 | a0001c0002t0002g0089 | 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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1798+2488C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20745857 | |||||||
| chr12:20746011 | T | A | 101 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(98): Show |
104 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(101): 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 | a0001c0001t0003g0258 | 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 | a0001c0002t0002g0046 a0001c0002t0002g0069 a0001c0002t0002g0070 others(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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1798+2850A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20746219 | |||||||
| chr12:20746221 | C | A | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): 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 | a0001c0001t0004g0031 a0001c0001t0004g0103 a0001c0001t0004g0135 others(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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): 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 | a0001c0001t0001g0104 | 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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): 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 | a0001c0005t0002g0186 a0001c0020t0009g0018 |
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 | 109 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(106): Show |
113 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(110): 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 | a0001c0002t0006g0123 a0001c0002t0006g0235 a0001c0005t0006g0173 |
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 | a0001c0001t0003g0021 a0001c0001t0003g0201 a0001c0001t0010g0024 |
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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1798+3391A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20746760 | |||||||
| chr12:20746782 | A | C | 194 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(191): Show |
201 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(198): 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 | a0001c0002t0002g0248 a0001c0002t0006g0123 a0001c0002t0006g0235 others(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 | 100 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(97): Show |
103 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(100): 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 | a0001c0003t0001g0017 a0001c0003t0001g0025 a0001c0003t0007g0019 |
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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1798+3625T>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20746994 | |||||||
| chr12:20747014 | TAGG | T | 104 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(101): Show |
108 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(105): 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 | a0001c0002t0002g0237 | 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 | a0001c0003t0005g0002 a0001c0003t0005g0026 a0001c0003t0005g0028 |
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 | a0001c0003t0001g0017 a0001c0003t0001g0025 a0001c0003t0007g0019 |
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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): 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 | a0001c0001t0001g0288 | 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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): 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 | a0001c0002t0002g0032 a0001c0002t0002g0053 a0001c0002t0002g0117 others(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 | 2 | a0001c0002t0002g0007 a0001c0002t0002g0250 |
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 | 101 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(98): Show |
104 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(101): 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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): 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 | a0001c0002t0002g0143 | 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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): 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 | a0001c0001t0001g0110 | 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 | a0001c0003t0001g0234 | 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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): 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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): 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 | a0001c0002t0002g0160 | 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 | a0001c0002t0002g0160 | 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 | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1799-2929C>T | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20747746 | |||||||
| chr12:20747767 | A | T | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(108): 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 | a0001c0001t0001g0037 a0001c0001t0001g0110 a0001c0001t0001g0132 others(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 | 35 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0071 others(32): 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 | a0001c0003t0012g0029 | 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 | a0001c0003t0003g0197 a0001c0003t0003g0198 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0176 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0288 | 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 | 117 | a0001c0001t0001g0207 a0001c0001t0003g0273 a0001c0002t0002g0001 others(114): Show |
121 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.1799-2465A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20748210 | |||||||
| chr12:20748215 | C | T | 117 | a0001c0001t0001g0207 a0001c0001t0003g0273 a0001c0002t0002g0001 others(114): Show |
121 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(118): 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 | a0001c0001t0001g0013 a0001c0001t0003g0014 a0001c0001t0003g0022 others(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 | a0001c0001t0001g0115 | 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 | 117 | a0001c0001t0001g0207 a0001c0001t0003g0273 a0001c0002t0002g0001 others(114): Show |
121 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(118): 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 | a0001c0001t0001g0288 | 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 | 117 | a0001c0001t0001g0207 a0001c0001t0003g0273 a0001c0002t0002g0001 others(114): Show |
121 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(118): 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 | a0001c0001t0004g0031 a0001c0001t0004g0103 a0001c0001t0004g0135 others(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 | a0001c0001t0001g0189 | 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 | a0001c0001t0004g0172 a0001c0006t0001g0217 |
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 | 36 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0071 others(33): 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 | a0001c0001t0004g0238 | 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 | 117 | a0001c0001t0001g0207 a0001c0001t0003g0273 a0001c0002t0002g0001 others(114): Show |
121 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.1799-1321T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20749354 | |||||||
| chr12:20749380 | T | C | 117 | a0001c0001t0001g0207 a0001c0001t0003g0273 a0001c0002t0002g0001 others(114): Show |
121 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.1799-1295T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20749380 | |||||||
| chr12:20749494 | G | C | 117 | a0001c0001t0001g0207 a0001c0001t0003g0273 a0001c0002t0002g0001 others(114): Show |
121 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.1799-1181G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20749494 | |||||||
| chr12:20749581 | A | G | 117 | a0001c0001t0001g0207 a0001c0001t0003g0273 a0001c0002t0002g0001 others(114): Show |
121 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(118): 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 | a0001c0001t0001g0037 a0001c0001t0001g0132 a0001c0001t0001g0140 others(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 | 117 | a0001c0001t0001g0207 a0001c0001t0003g0273 a0001c0002t0002g0001 others(114): Show |
121 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.1799-1021A>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20749654 | |||||||
| chr12:20749714 | G | A | 117 | a0001c0001t0001g0207 a0001c0001t0003g0273 a0001c0002t0002g0001 others(114): Show |
121 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.1799-961G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20749714 | |||||||
| chr12:20749809 | G | T | 116 | a0001c0001t0003g0273 a0001c0002t0002g0001 a0001c0002t0002g0003 others(113): Show |
120 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(117): 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 | a0001c0001t0001g0030 a0001c0001t0001g0072 a0001c0001t0001g0093 others(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 | a0001c0002t0006g0235 | 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 | 117 | a0001c0001t0001g0207 a0001c0001t0003g0273 a0001c0002t0002g0001 others(114): Show |
121 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.1799-652A>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20750023 | |||||||
| chr12:20750027 | A | G | 117 | a0001c0001t0001g0207 a0001c0001t0003g0273 a0001c0002t0002g0001 others(114): Show |
121 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(118): 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 | a0001c0001t0001g0047 a0001c0001t0001g0057 a0001c0001t0001g0058 others(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 | a0001c0002t0002g0089 | 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 | 116 | a0001c0001t0001g0207 a0001c0001t0003g0273 a0001c0002t0002g0001 others(113): Show |
120 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(117): 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 | a0001c0001t0003g0083 a0001c0001t0003g0118 a0001c0001t0003g0215 others(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 | a0001c0009t0002g0099 | 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 | 117 | a0001c0001t0001g0207 a0001c0001t0003g0273 a0001c0002t0002g0001 others(114): Show |
121 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.1799-374C>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20750301 | |||||||
| chr12:20750536 | T | G | 116 | a0001c0001t0001g0207 a0001c0001t0003g0273 a0001c0002t0002g0001 others(113): Show |
120 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.1799-139T>G | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20750536 | |||||||
| chr12:20750586 | T | C | 118 | a0001c0001t0001g0207 a0001c0001t0003g0273 a0001c0002t0002g0001 others(115): Show |
122 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.1799-89T>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 13/14 | chr12 | 20750586 | |||||||
| chr12:20750823 | T | C | 117 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0004 others(114): Show |
121 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(118): 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 | a0001c0002t0002g0250 | 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 | 117 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0004 others(114): Show |
121 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(118): 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 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(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 | a0001c0001t0001g0207 a0001c0001t0003g0273 a0001c0020t0009g0018 |
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 | a0001c0006t0001g0005 a0001c0006t0001g0084 a0001c0006t0001g0149 others(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 | a0001c0003t0003g0197 a0001c0003t0003g0198 |
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 | 119 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0004 others(116): Show |
123 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(120): 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 | a0001c0002t0002g0196 | 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 | a0001c0001t0001g0207 a0001c0001t0003g0273 a0001c0020t0009g0018 |
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 |
119 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0004 others(116): Show |
123 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(120): 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 | a0001c0003t0001g0261 | 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 | 137 | a0001c0001t0001g0207 a0001c0001t0003g0258 a0001c0001t0003g0273 others(134): Show |
143 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(140): 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 | a0001c0002t0002g0038 | 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 | 119 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0004 others(116): Show |
123 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(120): 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 | a0002c0007t0001g0256 | 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 | a0001c0006t0001g0005 a0001c0006t0001g0193 a0001c0006t0001g0194 others(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 | 120 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0004 others(117): Show |
124 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.1917-336G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 14/14 | chr12 | 20751970 | |||||||
| chr12:20751997 | G | A | 120 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0004 others(117): Show |
124 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.1917-309G>A | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 14/14 | chr12 | 20751997 | |||||||
| chr12:20752072 | G | A | 120 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0004 others(117): Show |
124 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(121): 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 | a0001c0002t0002g0079 | 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 | a0001c0003t0003g0197 a0001c0003t0003g0198 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1917-42G>C | SLCO1C1 | ENSG00000139155.9 | transcript | ENST00000266509.7 | protein_coding | 14/14 | chr12 | 20752264 |