Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 133688 |
| ensemblid | ENSG00000145626.12 |
| hgncid | 26625 |
| symbol | UGT3A1 |
| name | UDP glycosyltransferase family 3 member A1 |
| refseq_nuc | NM_152404.4 |
| refseq_prot | NP_689617.3 |
| ensembl_nuc | ENST00000274278.8 |
| ensembl_prot | ENSP00000274278.3 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 35951006 |
| end | 35991390 |
| strand | - |
| ver | v1.2 |
| region | chr5:35951006-35991390 |
| region5000 | chr5:35946006-35996390 |
| regionname0 | UGT3A1_chr5_35951006_35991390 |
| regionname5000 | UGT3A1_chr5_35946006_35996390 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 523 | 306 | 87 | 54 | 123 | 12 | 28 | 93 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | MVGQR others(518): Show |
chr5 | 35946006 | 35996390 |
| a0002 | 0/0 | 523 | 75 | 3 | 8 | 47 | 2 | 15 | 33 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | MVGQR others(518): Show |
chr5 | 35946006 | 35996390 |
| a0003 | 0/0 | 523 | 8 | 0 | 0 | 8 | 0 | 0 | 7 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | MVGQR others(518): Show |
chr5 | 35946006 | 35996390 |
| a0004 | 0/0 | 523 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | MVGQR others(518): Show |
chr5 | 35946006 | 35996390 |
| a0005 | 0/0 | 523 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | MVGQR others(518): Show |
chr5 | 35946006 | 35996390 |
| a0006 | 0/0 | 523 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | MVGQR others(518): Show |
chr5 | 35946006 | 35996390 |
| a0007 | 0/0 | 523 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | MVGQR others(518): Show |
chr5 | 35946006 | 35996390 |
| a0008 | 0/0 | 399 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | MVGQR others(394): Show |
chr5 | 35946006 | 35996390 |
| a0009 | 0/0 | 523 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | MVGQR others(518): Show |
chr5 | 35946006 | 35996390 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1569 | 297 | 80 | 52 | 123 | 12 | 28 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | ATGGT others(1564): Show |
chr5 | 35946006 | 35996390 | ||
| a0001c0004 | 0/0 | 1569 | 5 | 3 | 2 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | ATGGT others(1564): Show |
chr5 | 35946006 | 35996390 | ||
| a0001c0006 | 0/0 | 1569 | 4 | 4 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | ATGGT others(1564): Show |
chr5 | 35946006 | 35996390 | ||
| a0002c0002 | 0/0 | 1569 | 75 | 3 | 8 | 47 | 2 | 15 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | ATGGT others(1564): Show |
chr5 | 35946006 | 35996390 | ||
| a0003c0003 | 0/0 | 1569 | 8 | 0 | 0 | 8 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | ATGGT others(1564): Show |
chr5 | 35946006 | 35996390 | ||
| a0004c0005 | 0/0 | 1569 | 4 | 0 | 0 | 4 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | ATGGT others(1564): Show |
chr5 | 35946006 | 35996390 | ||
| a0005c0007 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | ATGGT others(1564): Show |
chr5 | 35946006 | 35996390 | ||
| a0006c0011 | 0/0 | 1569 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | ATGGT others(1564): Show |
chr5 | 35946006 | 35996390 | ||
| a0007c0008 | 0/0 | 1569 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | ATGGT others(1564): Show |
chr5 | 35946006 | 35996390 | ||
| a0008c0009 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | ATGGT others(1564): Show |
chr5 | 35946006 | 35996390 | ||
| a0009c0010 | 0/0 | 1569 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | ATGGT others(1564): Show |
chr5 | 35946006 | 35996390 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4918 | 61 | 1 | 7 | 51 | 0 | 2 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0002 | 0/0 | 4918 | 44 | 5 | 12 | 12 | 5 | 10 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0003 | 0/1 | 4918 | 28 | 7 | 2 | 12 | 0 | 6 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0004 | 0/0 | 4918 | 18 | 13 | 0 | 2 | 0 | 3 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0005 | 0/0 | 4918 | 19 | 2 | 9 | 3 | 3 | 2 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0006 | 0/0 | 4918 | 20 | 1 | 1 | 18 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0007 | 0/0 | 4918 | 14 | 12 | 2 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0008 | 0/0 | 4918 | 11 | 0 | 7 | 0 | 2 | 2 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0009 | 0/0 | 4918 | 11 | 0 | 7 | 0 | 2 | 2 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0010 | 0/0 | 4918 | 9 | 0 | 0 | 9 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0011 | 0/0 | 4918 | 7 | 0 | 0 | 7 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0012 | 0/0 | 4918 | 7 | 7 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0013 | 0/0 | 4918 | 6 | 6 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0014 | 0/0 | 4918 | 5 | 4 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0015 | 0/0 | 4918 | 5 | 5 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0016 | 0/0 | 4918 | 5 | 5 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0017 | 0/0 | 4918 | 3 | 3 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0018 | 0/0 | 4918 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0019 | 0/0 | 4918 | 4 | 4 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0020 | 0/0 | 4918 | 3 | 0 | 3 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0021 | 0/0 | 4918 | 3 | 0 | 0 | 3 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0023 | 1/0 | 4918 | 2 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0024 | 0/0 | 4918 | 2 | 0 | 0 | 2 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0025 | 0/0 | 4918 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0027 | 0/0 | 4918 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0033 | 0/0 | 4918 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0035 | 0/0 | 4918 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0036 | 0/0 | 4918 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0037 | 0/0 | 4918 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0038 | 0/0 | 4918 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0039 | 0/0 | 4918 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0001t0040 | 0/0 | 4918 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0004t0005 | 0/0 | 4918 | 5 | 3 | 2 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0006t0018 | 0/0 | 4918 | 3 | 3 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0001c0006t0032 | 0/0 | 4918 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0002c0002t0001 | 0/0 | 4918 | 67 | 1 | 8 | 43 | 2 | 13 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0002c0002t0007 | 0/0 | 4918 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0002c0002t0022 | 0/0 | 4918 | 2 | 0 | 0 | 2 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0002c0002t0026 | 0/0 | 4918 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0002c0002t0028 | 0/0 | 4918 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0002c0002t0029 | 0/0 | 4918 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0002c0002t0030 | 0/0 | 4918 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0002c0002t0031 | 0/0 | 4918 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0003c0003t0004 | 0/0 | 4918 | 8 | 0 | 0 | 8 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0004c0005t0002 | 0/0 | 4918 | 4 | 0 | 0 | 4 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0005c0007t0001 | 0/0 | 4918 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0006c0011t0017 | 0/0 | 4918 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0007c0008t0034 | 0/0 | 4918 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0008c0009t0006 | 0/0 | 4918 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| a0009c0010t0001 | 0/0 | 4918 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | AGAAG others(4913): Show |
chr5 | 35946006 | 35996390 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 14 | 0 | 0 | 14 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0018 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0002 | 0/0 | 8 | 0 | 2 | 3 | 0 | 3 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0004 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0027 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0003g0003 | 0/0 | 5 | 0 | 0 | 2 | 0 | 3 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0003g0238 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0004g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0004g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0005g0017 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0005g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0005g0045 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0005g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0005g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0005g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0005g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0005g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0005g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0005g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0006g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0006g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0006g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0006g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0006g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0006g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0006g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0006g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0006g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0006g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0007g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0007g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0007g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0007g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0007g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0007g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0007g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0007g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0007g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0008g0022 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0008g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0008g0054 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0008g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0008g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0008g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0008g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0009g0023 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0009g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0009g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0009g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0009g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0009g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0009g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0009g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0009g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0010g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0010g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0010g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0010g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0010g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0010g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0011g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0011g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0011g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0011g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0011g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0012g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0012g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0012g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0012g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0012g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0012g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0013g0059 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0013g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0013g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0013g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0013g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0014g0007 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0014g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0015g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0015g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0015g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0016g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0016g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0016g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0017g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0017g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0017g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0018g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0019g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0019g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0019g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0019g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0020g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0021g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0023g0152 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0023g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0024g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0025g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0027g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0033g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0035g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0036g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0037g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0038g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0039g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0001t0040g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0004t0005g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0004t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0004t0005g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0004t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0004t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0006t0018g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0006t0018g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0001c0006t0032g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0005 | 0/0 | 4 | 0 | 1 | 1 | 2 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0010 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0007g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0022g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0026g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0028g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0029g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0030g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0002c0002t0031g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0003c0003t0004g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0003c0003t0004g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0003c0003t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0003c0003t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0004c0005t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0005c0007t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0006c0011t0017g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0007c0008t0034g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0008c0009t0006g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| a0009c0010t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0214 | EUR | GBR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG00099 | hp2 | a0001 | c0001 | t0009 | g0244 | EUR | GBR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0275 | EUR | GBR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0017 | EUR | GBR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG00323 | hp1 | a0001 | c0001 | t0005 | g0045 | EUR | FIN | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0260 | EUR | FIN | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG00408 | hp2 | a0001 | c0001 | t0006 | g0151 | EAS | CHS | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG00438 | hp1 | a0005 | c0007 | t0001 | g0095 | EAS | CHS | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | CHS | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG00544 | hp2 | a0001 | c0001 | t0027 | g0131 | EAS | CHS | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | CHS | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG00597 | hp2 | a0002 | c0002 | t0022 | g0033 | EAS | CHS | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | CHS | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG00621 | hp2 | a0001 | c0001 | t0033 | g0132 | EAS | CHS | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0237 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0169 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG00642 | hp1 | a0001 | c0001 | t0009 | g0023 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG00642 | hp2 | a0001 | c0001 | t0008 | g0053 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0167 | EAS | CHS | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG00735 | hp1 | a0001 | c0001 | t0009 | g0245 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0094 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0045 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01070 | hp1 | a0001 | c0001 | t0008 | g0022 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0165 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01071 | hp2 | a0001 | c0001 | t0008 | g0022 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0251 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0098 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0272 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0030 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01099 | hp1 | a0001 | c0001 | t0014 | g0007 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0265 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0201 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01109 | hp2 | a0001 | c0001 | t0009 | g0246 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01168 | hp1 | a0001 | c0001 | t0008 | g0217 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01169 | hp1 | a0001 | c0001 | t0008 | g0231 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01169 | hp2 | a0001 | c0001 | t0020 | g0024 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01175 | hp1 | a0001 | c0001 | t0006 | g0171 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01175 | hp2 | a0001 | c0001 | t0009 | g0250 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0117 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0164 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01243 | hp1 | a0001 | c0001 | t0007 | g0039 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01243 | hp2 | a0001 | c0004 | t0005 | g0178 | AMR | PUR | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01256 | hp1 | a0001 | c0001 | t0009 | g0248 | AMR | CLM | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0043 | AMR | CLM | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01257 | hp2 | a0001 | c0001 | t0020 | g0024 | AMR | CLM | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0043 | AMR | CLM | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01346 | hp1 | a0001 | c0001 | t0009 | g0023 | AMR | CLM | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01346 | hp2 | a0001 | c0004 | t0005 | g0176 | AMR | CLM | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | CLM | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01358 | hp2 | a0001 | c0001 | t0008 | g0053 | AMR | CLM | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0074 | AMR | CLM | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0070 | AMR | CLM | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0103 | AMR | CLM | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0017 | AMR | CLM | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0274 | EUR | IBS | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0005 | EUR | IBS | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01516 | hp1 | a0001 | c0001 | t0008 | g0054 | EUR | IBS | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0273 | EUR | IBS | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01517 | hp1 | a0001 | c0001 | t0008 | g0054 | EUR | IBS | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0005 | EUR | IBS | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01884 | hp1 | a0001 | c0001 | t0014 | g0007 | AFR | ACB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01884 | hp2 | a0001 | c0001 | t0019 | g0281 | AFR | ACB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01891 | hp1 | a0001 | c0001 | t0023 | g0282 | AFR | ACB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PEL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01952 | hp2 | a0001 | c0001 | t0020 | g0024 | AMR | PEL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0283 | AMR | PEL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | PEL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01981 | hp1 | a0001 | c0001 | t0008 | g0223 | AMR | PEL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02015 | hp1 | a0001 | c0001 | t0006 | g0153 | EAS | KHV | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | KHV | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02027 | hp1 | a0001 | c0001 | t0011 | g0130 | EAS | KHV | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | KHV | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | KHV | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02055 | hp2 | a0001 | c0001 | t0012 | g0139 | AFR | ACB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | KHV | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | KHV | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02074 | hp2 | a0002 | c0002 | t0026 | g0078 | EAS | KHV | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | KHV | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | KHV | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | KHV | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02129 | hp1 | a0002 | c0002 | t0022 | g0033 | EAS | KHV | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02129 | hp2 | a0001 | c0001 | t0006 | g0148 | EAS | KHV | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02132 | hp1 | a0003 | c0003 | t0004 | g0006 | EAS | KHV | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02132 | hp2 | a0001 | c0001 | t0005 | g0226 | EAS | KHV | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | KHV | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02145 | hp1 | a0001 | c0001 | t0038 | g0118 | AFR | ACB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0061 | AFR | ACB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02148 | hp1 | a0001 | c0001 | t0025 | g0187 | AMR | PEL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PEL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0084 | EAS | CDX | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02155 | hp2 | a0001 | c0001 | t0005 | g0227 | EAS | CDX | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0166 | EAS | CDX | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | CDX | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02257 | hp1 | a0001 | c0001 | t0015 | g0025 | AFR | ACB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0066 | AFR | ACB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02258 | hp1 | a0001 | c0001 | t0016 | g0016 | AFR | ACB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02258 | hp2 | a0001 | c0001 | t0007 | g0127 | AFR | ACB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PEL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02280 | hp1 | a0001 | c0001 | t0013 | g0204 | AFR | ACB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | ACB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0116 | AFR | ACB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02451 | hp2 | a0001 | c0006 | t0018 | g0052 | AFR | ACB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0285 | AFR | GWD | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02572 | hp2 | a0001 | c0001 | t0040 | g0287 | AFR | GWD | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02630 | hp1 | a0001 | c0001 | t0012 | g0158 | AFR | GWD | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0160 | AFR | GWD | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0051 | AFR | GWD | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02647 | hp2 | a0001 | c0001 | t0014 | g0007 | AFR | GWD | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02683 | hp1 | a0001 | c0001 | t0008 | g0240 | SAS | PJL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0017 | SAS | PJL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0010 | SAS | PJL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0270 | SAS | PJL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | GWD | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02717 | hp2 | a0002 | c0002 | t0007 | g0082 | AFR | GWD | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | GWD | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0196 | AFR | GWD | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0104 | SAS | PJL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02809 | hp1 | a0001 | c0001 | t0013 | g0277 | AFR | GWD | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0065 | AFR | GWD | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0060 | AFR | GWD | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02818 | hp2 | a0001 | c0001 | t0012 | g0203 | AFR | GWD | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0067 | AFR | GWD | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0202 | AFR | GWD | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02895 | hp1 | a0001 | c0001 | t0012 | g0047 | AFR | GWD | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02895 | hp2 | a0001 | c0001 | t0017 | g0124 | AFR | GWD | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02896 | hp1 | a0001 | c0001 | t0013 | g0059 | AFR | GWD | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0051 | AFR | GWD | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02897 | hp1 | a0001 | c0001 | t0013 | g0059 | AFR | GWD | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02897 | hp2 | a0001 | c0001 | t0017 | g0109 | AFR | GWD | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0126 | AFR | ESN | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0206 | AFR | ESN | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02965 | hp1 | a0001 | c0001 | t0016 | g0162 | AFR | ESN | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02965 | hp2 | a0001 | c0001 | t0019 | g0205 | AFR | ESN | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0128 | AFR | ESN | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02970 | hp2 | a0001 | c0006 | t0018 | g0211 | AFR | ESN | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02976 | hp1 | a0001 | c0006 | t0018 | g0052 | AFR | ESN | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0170 | AFR | ESN | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0069 | SAS | PJL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03017 | hp2 | a0001 | c0001 | t0009 | g0249 | SAS | PJL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | GWD | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0194 | AFR | GWD | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0123 | AFR | MSL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03098 | hp2 | a0001 | c0001 | t0014 | g0199 | AFR | MSL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03130 | hp1 | a0001 | c0001 | t0015 | g0252 | AFR | ESN | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0063 | AFR | ESN | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0039 | AFR | ESN | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03195 | hp2 | a0001 | c0001 | t0016 | g0016 | AFR | ESN | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0193 | AFR | MSL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03209 | hp2 | a0001 | c0001 | t0017 | g0125 | AFR | MSL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0119 | AFR | MSL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03225 | hp2 | a0001 | c0004 | t0005 | g0180 | AFR | MSL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03453 | hp1 | a0001 | c0001 | t0018 | g0209 | AFR | MSL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0062 | AFR | MSL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03486 | hp1 | a0001 | c0001 | t0012 | g0173 | AFR | MSL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03486 | hp2 | a0001 | c0004 | t0005 | g0177 | AFR | MSL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0010 | SAS | PJL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0035 | SAS | PJL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0010 | SAS | PJL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03516 | hp2 | a0001 | c0001 | t0019 | g0207 | AFR | ESN | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | GWD | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03540 | hp2 | a0001 | c0001 | t0015 | g0025 | AFR | GWD | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03579 | hp1 | a0001 | c0001 | t0019 | g0208 | AFR | MSL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03579 | hp2 | a0001 | c0001 | t0015 | g0025 | AFR | MSL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0266 | SAS | PJL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03654 | hp2 | a0002 | c0002 | t0028 | g0089 | SAS | PJL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0035 | SAS | PJL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0276 | SAS | PJL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0106 | SAS | STU | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0086 | SAS | STU | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0235 | SAS | PJL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03704 | hp2 | a0007 | c0008 | t0034 | g0110 | SAS | PJL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0236 | SAS | PJL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0083 | SAS | BEB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0072 | SAS | BEB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0271 | SAS | BEB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0163 | SAS | BEB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03927 | hp1 | a0001 | c0001 | t0008 | g0022 | SAS | BEB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0175 | SAS | BEB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0044 | SAS | BEB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0255 | SAS | BEB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG04115 | hp1 | a0001 | c0001 | t0009 | g0023 | SAS | STU | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | STU | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0213 | SAS | BEB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG04184 | hp2 | a0001 | c0001 | t0039 | g0247 | SAS | BEB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0263 | SAS | STU | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0044 | SAS | STU | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0090 | SAS | STU | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | STU | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | YRI | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0120 | AFR | YRI | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18612 | hp1 | a0001 | c0001 | t0010 | g0114 | EAS | CHB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18747 | hp1 | a0001 | c0001 | t0011 | g0015 | EAS | CHB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18747 | hp2 | a0001 | c0001 | t0005 | g0225 | EAS | CHB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18940 | hp2 | a0001 | c0001 | t0021 | g0026 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18942 | hp1 | a0001 | c0001 | t0011 | g0115 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18942 | hp2 | a0001 | c0001 | t0010 | g0014 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18943 | hp2 | a0001 | c0001 | t0006 | g0138 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18945 | hp2 | a0001 | c0001 | t0006 | g0137 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18946 | hp2 | a0001 | c0001 | t0006 | g0041 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18947 | hp1 | a0004 | c0005 | t0002 | g0009 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18948 | hp1 | a0001 | c0001 | t0006 | g0154 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18951 | hp2 | a0001 | c0001 | t0010 | g0111 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18952 | hp2 | a0001 | c0001 | t0010 | g0038 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18960 | hp1 | a0001 | c0001 | t0024 | g0058 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18961 | hp1 | a0001 | c0001 | t0006 | g0156 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18963 | hp1 | a0008 | c0009 | t0006 | g0195 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18965 | hp2 | a0001 | c0001 | t0010 | g0014 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18966 | hp1 | a0001 | c0001 | t0006 | g0149 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18971 | hp2 | a0003 | c0003 | t0004 | g0046 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18973 | hp2 | a0001 | c0001 | t0010 | g0112 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18977 | hp1 | a0004 | c0005 | t0002 | g0009 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18977 | hp2 | a0003 | c0003 | t0004 | g0161 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18982 | hp1 | a0001 | c0001 | t0006 | g0147 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18983 | hp2 | a0003 | c0003 | t0004 | g0006 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18992 | hp1 | a0003 | c0003 | t0004 | g0157 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18998 | hp1 | a0001 | c0001 | t0006 | g0155 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA18999 | hp2 | a0001 | c0001 | t0006 | g0041 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19002 | hp1 | a0002 | c0002 | t0030 | g0079 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19003 | hp1 | a0001 | c0001 | t0006 | g0042 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19003 | hp2 | a0001 | c0001 | t0010 | g0038 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19004 | hp1 | a0001 | c0001 | t0021 | g0026 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19006 | hp1 | a0001 | c0001 | t0036 | g0232 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19007 | hp2 | a0003 | c0003 | t0004 | g0006 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19010 | hp1 | a0001 | c0001 | t0006 | g0135 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19011 | hp1 | a0003 | c0003 | t0004 | g0006 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19030 | hp1 | a0001 | c0001 | t0016 | g0016 | AFR | LWK | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19030 | hp2 | a0001 | c0001 | t0035 | g0253 | AFR | LWK | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19043 | hp1 | a0001 | c0001 | t0012 | g0172 | AFR | LWK | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19043 | hp2 | a0001 | c0001 | t0013 | g0279 | AFR | LWK | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19056 | hp2 | a0004 | c0005 | t0002 | g0009 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19057 | hp2 | a0001 | c0001 | t0006 | g0146 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19060 | hp1 | a0001 | c0001 | t0006 | g0150 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19060 | hp2 | a0001 | c0001 | t0011 | g0133 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19062 | hp2 | a0001 | c0001 | t0010 | g0113 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19064 | hp2 | a0001 | c0001 | t0011 | g0015 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19066 | hp2 | a0001 | c0001 | t0010 | g0014 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19070 | hp1 | a0001 | c0001 | t0024 | g0058 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19070 | hp2 | a0001 | c0001 | t0011 | g0015 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19074 | hp2 | a0001 | c0001 | t0021 | g0026 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19078 | hp1 | a0001 | c0001 | t0006 | g0042 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19079 | hp1 | a0003 | c0003 | t0004 | g0046 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19081 | hp1 | a0001 | c0001 | t0006 | g0136 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19085 | hp1 | a0001 | c0001 | t0037 | g0228 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19087 | hp1 | a0001 | c0001 | t0011 | g0197 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19090 | hp1 | a0004 | c0005 | t0002 | g0009 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0200 | AFR | YRI | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA19240 | hp2 | a0002 | c0002 | t0029 | g0077 | AFR | YRI | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA20129 | hp1 | a0001 | c0001 | t0012 | g0047 | AFR | ASW | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ASW | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA20752 | hp1 | a0001 | c0001 | t0009 | g0242 | EUR | TSI | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0256 | EUR | TSI | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0068 | SAS | GIH | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA20905 | hp2 | a0002 | c0002 | t0031 | g0224 | SAS | GIH | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01123 | hp1 | a0001 | c0001 | t0009 | g0243 | AMR | CLM | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0174 | AMR | CLM | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | ACB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02109 | hp2 | a0001 | c0001 | t0016 | g0159 | AFR | ACB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02486 | hp1 | a0001 | c0004 | t0005 | g0179 | AFR | ACB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0210 | AFR | ACB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02559 | hp1 | a0006 | c0011 | t0017 | g0286 | AFR | ACB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0064 | AFR | ACB | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03471 | hp1 | a0001 | c0001 | t0013 | g0278 | AFR | MSL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG03471 | hp2 | a0001 | c0001 | t0014 | g0007 | AFR | MSL | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0258 | AFR | USA | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| HG06807 | hp2 | a0001 | c0006 | t0032 | g0212 | AFR | USA | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA20300 | hp1 | a0009 | c0010 | t0001 | g0182 | AFR | USA | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0008 | AFR | USA | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0088 | AFR | LWK | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| NA21309 | hp2 | a0001 | c0001 | t0015 | g0280 | AFR | LWK | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0238 | REF | REF | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0023 | g0152 | REF | REF | UGT3A1_chr5_35946006_35996390 | UGT3A1 | chr5 | 35946006 | 35996390 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:35954207 | T | A | 1 | a0003 | 8 | HG02132.hp1 NA18971.hp2 NA18977.hp2 others(5): Show |
missense_variant | MODERATE | c.1567A>T | p.Thr523Ser | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 1717/4918 | 1567/1572 | 523/523 | chr5 | 35954207 | |||
| chr5:35954275 | A | G | 1 | a0004 | 4 | NA18947.hp1 NA18977.hp1 NA19056.hp2 others(1): Show |
missense_variant | MODERATE | c.1499T>C | p.Met500Thr | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 1649/4918 | 1499/1572 | 500/523 | chr5 | 35954275 | |||
| chr5:35955709 | G | A | 1 | a0007 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.1231C>T | p.Arg411Trp | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 6/7 | 1381/4918 | 1231/1572 | 411/523 | chr5 | 35955709 | |||
| chr5:35955742 | G | A | 1 | a0008 | 1 | NA18963.hp1 | stop_gained | HIGH | c.1198C>T | p.Arg400* | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 6/7 | 1348/4918 | 1198/1572 | 400/523 | chr5 | 35955742 | |||
| chr5:35957385 | G | A | 1 | a0009 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.878C>T | p.Ala293Val | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 5/7 | 1028/4918 | 878/1572 | 293/523 | chr5 | 35957385 | |||
| chr5:35965454 | G | A | 1 | a0006 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.775C>T | p.Arg259Trp | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/7 | 925/4918 | 775/1572 | 259/523 | chr5 | 35965454 | |||
| chr5:35965719 | G | T | 1 | a0005 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.510C>A | p.Phe170Leu | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/7 | 660/4918 | 510/1572 | 170/523 | chr5 | 35965719 | |||
| chr5:35965868 | A | C | 2 | a0002 a0005 |
76 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(73): Show |
missense_variant | MODERATE | c.361T>G | p.Cys121Gly | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/7 | 511/4918 | 361/1572 | 121/523 | chr5 | 35965868 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:35955773 | T | G | 1 | a0001c0006 | 4 | HG02451.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
synonymous_variant | LOW | c.1167A>C | p.Pro389Pro | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 6/7 | 1317/4918 | 1167/1572 | 389/523 | chr5 | 35955773 | |||
| chr5:35957360 | G | A | 1 | a0001c0004 | 5 | HG01243.hp2 HG01346.hp2 HG02486.hp1 others(2): Show |
synonymous_variant | LOW | c.903C>T | p.Gly301Gly | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 5/7 | 1053/4918 | 903/1572 | 301/523 | chr5 | 35957360 | |||
| chr5:35965509 | A | G | 1 | a0001c0001 | 4 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
synonymous_variant | LOW | c.720T>C | p.Leu240Leu | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/7 | 870/4918 | 720/1572 | 240/523 | chr5 | 35965509 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:35951009 | G | A | 1 | a0002c0002t0029 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3193C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 3193 | chr5 | 35951009 | ||||||
| chr5:35951025 | T | A | 2 | a0001c0001t0010 a0001c0001t0033 |
10 | HG00621.hp2 NA18612.hp1 NA18942.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3177A>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 3177 | chr5 | 35951025 | ||||||
| chr5:35951032 | G | T | 31 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(28): Show |
248 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*3170C>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 3170 | chr5 | 35951032 | ||||||
| chr5:35951078 | G | A | 1 | a0001c0006t0032 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3124C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 3124 | chr5 | 35951078 | ||||||
| chr5:35951225 | T | C | 1 | a0001c0001t0024 | 2 | NA18960.hp1 NA19070.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2977A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 2977 | chr5 | 35951225 | ||||||
| chr5:35951408 | A | T | 1 | a0002c0002t0028 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2794T>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 2794 | chr5 | 35951408 | ||||||
| chr5:35951525 | A | G | 1 | a0001c0001t0037 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2677T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 2677 | chr5 | 35951525 | ||||||
| chr5:35951541 | T | C | 3 | a0001c0001t0004 a0001c0001t0016 a0003c0003t0004 |
31 | HG00673.hp2 HG02109.hp2 HG02132.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2661A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 2661 | chr5 | 35951541 | ||||||
| chr5:35951561 | T | C | 3 | a0001c0001t0007 a0001c0001t0040 a0002c0002t0007 |
16 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2641A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 2641 | chr5 | 35951561 | ||||||
| chr5:35951802 | G | A | 1 | a0001c0001t0019 | 4 | HG01884.hp2 HG02965.hp2 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2400C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 2400 | chr5 | 35951802 | ||||||
| chr5:35951846 | A | T | 49 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(46): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
3_prime_UTR_variant | MODIFIER | c.*2356T>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 2356 | chr5 | 35951846 | ||||||
| chr5:35951923 | C | A | 1 | a0001c0001t0019 | 4 | HG01884.hp2 HG02965.hp2 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2279G>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 2279 | chr5 | 35951923 | ||||||
| chr5:35951985 | C | T | 3 | a0001c0001t0007 a0001c0001t0040 a0002c0002t0007 |
16 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2217G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 2217 | chr5 | 35951985 | ||||||
| chr5:35952038 | C | T | 4 | a0001c0001t0002 a0001c0001t0021 a0001c0001t0024 others(1): Show |
53 | HG00140.hp1 HG00323.hp2 HG01074.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*2164G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 2164 | chr5 | 35952038 | ||||||
| chr5:35952039 | G | A | 1 | a0001c0001t0033 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2163C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 2163 | chr5 | 35952039 | ||||||
| chr5:35952201 | G | T | 1 | a0001c0001t0027 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2001C>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 2001 | chr5 | 35952201 | ||||||
| chr5:35952277 | A | C | 1 | a0001c0001t0016 | 5 | HG02109.hp2 HG02258.hp1 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1925T>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 1925 | chr5 | 35952277 | ||||||
| chr5:35952351 | C | A | 3 | a0001c0001t0007 a0001c0001t0040 a0002c0002t0007 |
16 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1851G>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 1851 | chr5 | 35952351 | ||||||
| chr5:35952555 | G | A | 1 | a0002c0002t0022 | 2 | HG00597.hp2 HG02129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1647C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 1647 | chr5 | 35952555 | ||||||
| chr5:35952584 | G | C | 1 | a0001c0001t0020 | 3 | HG01169.hp2 HG01257.hp2 HG01952.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1618C>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 1618 | chr5 | 35952584 | ||||||
| chr5:35952584 | G | T | 1 | a0001c0001t0039 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1618C>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 1618 | chr5 | 35952584 | ||||||
| chr5:35952706 | T | C | 1 | a0001c0001t0014 | 5 | HG01099.hp1 HG01884.hp1 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1496A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 1496 | chr5 | 35952706 | ||||||
| chr5:35952800 | C | T | 1 | a0007c0008t0034 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1402G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 1402 | chr5 | 35952800 | ||||||
| chr5:35952801 | G | A | 1 | a0002c0002t0030 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1401C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 1401 | chr5 | 35952801 | ||||||
| chr5:35952995 | C | T | 20 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(17): Show |
205 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*1207G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 1207 | chr5 | 35952995 | ||||||
| chr5:35953067 | G | A | 8 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0012 others(5): Show |
66 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*1135C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 1135 | chr5 | 35953067 | ||||||
| chr5:35953218 | C | T | 21 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(18): Show |
206 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*984G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 984 | chr5 | 35953218 | ||||||
| chr5:35953249 | G | A | 1 | a0007c0008t0034 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*953C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 953 | chr5 | 35953249 | ||||||
| chr5:35953358 | G | A | 2 | a0001c0001t0006 a0008c0009t0006 |
21 | HG00408.hp2 HG01175.hp1 HG02015.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*844C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 844 | chr5 | 35953358 | ||||||
| chr5:35953442 | C | A | 49 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(46): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
3_prime_UTR_variant | MODIFIER | c.*760G>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 760 | chr5 | 35953442 | ||||||
| chr5:35953595 | A | G | 22 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(19): Show |
213 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*607T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 607 | chr5 | 35953595 | ||||||
| chr5:35953720 | T | G | 1 | a0001c0001t0035 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*482A>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 482 | chr5 | 35953720 | ||||||
| chr5:35953798 | G | T | 1 | a0001c0001t0021 | 3 | NA18940.hp2 NA19004.hp1 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*404C>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 404 | chr5 | 35953798 | ||||||
| chr5:35953847 | G | A | 4 | a0001c0001t0002 a0001c0001t0021 a0001c0001t0024 others(1): Show |
53 | HG00140.hp1 HG00323.hp2 HG01074.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*355C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 355 | chr5 | 35953847 | ||||||
| chr5:35953949 | G | A | 1 | a0001c0001t0038 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*253C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 253 | chr5 | 35953949 | ||||||
| chr5:35954041 | C | T | 8 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0012 others(5): Show |
61 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*161G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 161 | chr5 | 35954041 | ||||||
| chr5:35954047 | G | T | 1 | a0001c0001t0008 | 11 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*155C>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 155 | chr5 | 35954047 | ||||||
| chr5:35954080 | C | T | 1 | a0001c0001t0025 | 1 | HG02148.hp1 | 3_prime_UTR_variant | MODIFIER | c.*122G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 122 | chr5 | 35954080 | ||||||
| chr5:35954089 | G | A | 12 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(9): Show |
88 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*113C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 113 | chr5 | 35954089 | ||||||
| chr5:35954106 | A | G | 2 | a0001c0001t0017 a0006c0011t0017 |
4 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*96T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 96 | chr5 | 35954106 | ||||||
| chr5:35954117 | G | C | 1 | a0001c0001t0012 | 7 | HG02055.hp2 HG02630.hp1 HG02818.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*85C>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 85 | chr5 | 35954117 | ||||||
| chr5:35954126 | G | C | 2 | a0001c0001t0009 a0001c0001t0039 |
12 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*76C>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 7/7 | 76 | chr5 | 35954126 | ||||||
| chr5:35991290 | G | A | 1 | a0001c0001t0040 | 1 | HG02572.hp2 | 5_prime_UTR_variant | MODIFIER | c.-50C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/7 | 50 | chr5 | 35991290 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:35954486 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(88): Show |
137 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(134): Show |
splice_region_variant&intron_variant | LOW | c.1296-8G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 6/6 | chr5 | 35954486 | |||||||
| chr5:35954487 | G | A | 1 | a0001c0001t0010g0038 | 2 | NA18952.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1296-9C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 6/6 | chr5 | 35954487 | |||||||
| chr5:35954512 | C | T | 7 | a0001c0001t0010g0014 a0001c0001t0010g0038 a0001c0001t0010g0111 others(4): Show |
10 | HG00621.hp2 NA18612.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.1296-34G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 6/6 | chr5 | 35954512 | |||||||
| chr5:35954513 | G | A | 7 | a0001c0001t0008g0022 a0001c0001t0008g0053 a0001c0001t0008g0054 others(4): Show |
11 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.1296-35C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 6/6 | chr5 | 35954513 | |||||||
| chr5:35954585 | A | G | 7 | a0001c0001t0001g0040 a0001c0001t0001g0140 a0001c0001t0001g0141 others(4): Show |
8 | NA18940.hp1 NA18941.hp1 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.1296-107T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 6/6 | chr5 | 35954585 | |||||||
| chr5:35954829 | G | T | 1 | a0001c0001t0002g0283 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1296-351C>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 6/6 | chr5 | 35954829 | |||||||
| chr5:35954843 | A | T | 4 | a0001c0001t0019g0205 a0001c0001t0019g0207 a0001c0001t0019g0208 others(1): Show |
4 | HG01884.hp2 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296-365T>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 6/6 | chr5 | 35954843 | |||||||
| chr5:35954851 | T | C | 1 | a0007c0008t0034g0110 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1296-373A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 6/6 | chr5 | 35954851 | |||||||
| chr5:35955031 | A | G | 7 | a0001c0001t0010g0014 a0001c0001t0010g0038 a0001c0001t0010g0111 others(4): Show |
10 | HG00621.hp2 NA18612.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.1296-553T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 6/6 | chr5 | 35955031 | |||||||
| chr5:35955072 | A | T | 5 | a0001c0001t0004g0060 a0001c0001t0004g0061 a0001c0001t0004g0062 others(2): Show |
5 | HG02145.hp2 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1295+573T>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 6/6 | chr5 | 35955072 | |||||||
| chr5:35955228 | A | T | 1 | a0001c0001t0002g0256 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1295+417T>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 6/6 | chr5 | 35955228 | |||||||
| chr5:35955301 | G | A | 1 | a0001c0004t0005g0179 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1295+344C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 6/6 | chr5 | 35955301 | |||||||
| chr5:35955423 | C | T | 78 | a0001c0001t0001g0267 a0001c0001t0002g0002 a0001c0001t0002g0004 others(75): Show |
114 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(111): Show |
intron_variant | MODIFIER | c.1295+222G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 6/6 | chr5 | 35955423 | |||||||
| chr5:35955434 | C | G | 36 | a0001c0001t0003g0003 a0001c0001t0003g0213 a0001c0001t0003g0215 others(33): Show |
42 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1295+211G>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 6/6 | chr5 | 35955434 | |||||||
| chr5:35955580 | C | G | 78 | a0001c0001t0001g0267 a0001c0001t0002g0002 a0001c0001t0002g0004 others(75): Show |
116 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(113): Show |
intron_variant | MODIFIER | c.1295+65G>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 6/6 | chr5 | 35955580 | |||||||
| chr5:35955923 | G | A | 1 | a0007c0008t0034g0110 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1076-59C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 5/6 | chr5 | 35955923 | |||||||
| chr5:35955924 | T | C | 76 | a0001c0001t0001g0267 a0001c0001t0002g0002 a0001c0001t0002g0004 others(73): Show |
111 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(108): Show |
intron_variant | MODIFIER | c.1076-60A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 5/6 | chr5 | 35955924 | |||||||
| chr5:35956005 | C | G | 1 | a0001c0001t0002g0273 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1076-141G>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 5/6 | chr5 | 35956005 | |||||||
| chr5:35956311 | C | T | 32 | a0001c0001t0003g0116 a0001c0001t0003g0117 a0001c0001t0003g0119 others(29): Show |
40 | HG00673.hp2 HG01192.hp1 HG02109.hp2 others(37): Show |
intron_variant | MODIFIER | c.1076-447G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 5/6 | chr5 | 35956311 | |||||||
| chr5:35956684 | T | C | 1 | a0001c0001t0005g0164 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1075+504A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 5/6 | chr5 | 35956684 | |||||||
| chr5:35956713 | T | C | 138 | a0001c0001t0001g0267 a0001c0001t0002g0002 a0001c0001t0002g0004 others(135): Show |
193 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1075+475A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 5/6 | chr5 | 35956713 | |||||||
| chr5:35956958 | G | A | 6 | a0001c0001t0010g0014 a0001c0001t0010g0038 a0001c0001t0010g0111 others(3): Show |
9 | NA18612.hp1 NA18942.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.1075+230C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 5/6 | chr5 | 35956958 | |||||||
| chr5:35957100 | A | G | 133 | a0001c0001t0001g0267 a0001c0001t0002g0002 a0001c0001t0002g0004 others(130): Show |
186 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1075+88T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 5/6 | chr5 | 35957100 | |||||||
| chr5:35957134 | G | A | 4 | a0001c0001t0001g0143 a0001c0001t0007g0039 a0001c0001t0007g0126 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1075+54C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 5/6 | chr5 | 35957134 | |||||||
| chr5:35957181 | T | G | 32 | a0001c0001t0003g0116 a0001c0001t0003g0117 a0001c0001t0003g0119 others(29): Show |
40 | HG00673.hp2 HG01192.hp1 HG02109.hp2 others(37): Show |
splice_region_variant&intron_variant | LOW | c.1075+7A>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 5/6 | chr5 | 35957181 | |||||||
| chr5:35957693 | G | A | 2 | a0001c0001t0019g0205 a0001c0001t0019g0207 |
2 | HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.844-274C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35957693 | |||||||
| chr5:35957879 | G | C | 1 | a0001c0001t0003g0221 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.844-460C>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35957879 | |||||||
| chr5:35957951 | T | G | 1 | a0008c0009t0006g0195 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.844-532A>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35957951 | |||||||
| chr5:35957969 | C | T | 54 | a0001c0001t0003g0003 a0001c0001t0003g0213 a0001c0001t0003g0215 others(51): Show |
69 | HG00099.hp2 HG00621.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.844-550G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35957969 | |||||||
| chr5:35957999 | C | T | 7 | a0001c0001t0007g0008 a0001c0001t0007g0051 a0001c0001t0007g0196 others(4): Show |
11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.844-580G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35957999 | |||||||
| chr5:35958009 | C | A | 54 | a0001c0001t0003g0003 a0001c0001t0003g0213 a0001c0001t0003g0215 others(51): Show |
69 | HG00099.hp2 HG00621.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.844-590G>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35958009 | |||||||
| chr5:35958073 | T | G | 2 | a0001c0006t0018g0052 a0001c0006t0018g0211 |
3 | HG02451.hp2 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.844-654A>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35958073 | |||||||
| chr5:35958096 | T | G | 1 | a0008c0009t0006g0195 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.844-677A>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35958096 | |||||||
| chr5:35958480 | C | G | 4 | a0001c0001t0013g0059 a0001c0001t0013g0277 a0001c0001t0013g0278 others(1): Show |
5 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.844-1061G>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35958480 | |||||||
| chr5:35958497 | G | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(94): Show |
145 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.844-1078C>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35958497 | |||||||
| chr5:35958545 | AT | A | 54 | a0001c0001t0003g0003 a0001c0001t0003g0213 a0001c0001t0003g0215 others(51): Show |
69 | HG00099.hp2 HG00621.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.844-1127delA | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35958545 | |||||||
| chr5:35958672 | T | A | 1 | a0008c0009t0006g0195 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.844-1253A>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35958672 | |||||||
| chr5:35958673 | G | T | 1 | a0008c0009t0006g0195 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.844-1254C>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35958673 | |||||||
| chr5:35958674 | C | G | 1 | a0008c0009t0006g0195 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.844-1255G>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35958674 | |||||||
| chr5:35958705 | A | G | 1 | a0001c0001t0002g0269 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.844-1286T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35958705 | |||||||
| chr5:35958708 | A | T | 1 | a0001c0001t0002g0269 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.844-1289T>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35958708 | |||||||
| chr5:35958709 | A | T | 1 | a0001c0001t0002g0269 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.844-1290T>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35958709 | |||||||
| chr5:35958761 | C | T | 1 | a0002c0002t0007g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.844-1342G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35958761 | |||||||
| chr5:35958795 | G | T | 2 | a0001c0001t0004g0065 a0001c0001t0004g0193 |
2 | HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.844-1376C>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35958795 | |||||||
| chr5:35958837 | T | C | 40 | a0001c0001t0003g0116 a0001c0001t0003g0117 a0001c0001t0003g0119 others(37): Show |
55 | HG00642.hp2 HG00673.hp2 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.844-1418A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35958837 | |||||||
| chr5:35959082 | G | A | 76 | a0001c0001t0001g0267 a0001c0001t0002g0002 a0001c0001t0002g0004 others(73): Show |
111 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(108): Show |
intron_variant | MODIFIER | c.844-1663C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35959082 | |||||||
| chr5:35959382 | C | T | 1 | a0001c0001t0005g0226 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.844-1963G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35959382 | |||||||
| chr5:35959824 | A | G | 32 | a0001c0001t0003g0116 a0001c0001t0003g0117 a0001c0001t0003g0119 others(29): Show |
40 | HG00673.hp2 HG01192.hp1 HG02109.hp2 others(37): Show |
intron_variant | MODIFIER | c.844-2405T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35959824 | |||||||
| chr5:35959859 | G | A | 1 | a0003c0003t0004g0157 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.844-2440C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35959859 | |||||||
| chr5:35959902 | C | T | 4 | a0001c0001t0010g0014 a0001c0001t0010g0111 a0001c0001t0010g0112 others(1): Show |
6 | NA18612.hp1 NA18942.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.844-2483G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35959902 | |||||||
| chr5:35959922 | A | G | 7 | a0001c0001t0010g0014 a0001c0001t0010g0038 a0001c0001t0010g0111 others(4): Show |
10 | HG00621.hp2 NA18612.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.844-2503T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35959922 | |||||||
| chr5:35959935 | G | A | 1 | a0001c0001t0001g0189 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.844-2516C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35959935 | |||||||
| chr5:35959944 | T | TTCA | 233 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(230): Show |
334 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(331): Show |
intron_variant | MODIFIER | c.844-2528_844-2526d others(5): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35959944 | |||||||
| chr5:35960009 | A | T | 1 | a0007c0008t0034g0110 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.844-2590T>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35960009 | |||||||
| chr5:35960015 | A | T | 4 | a0001c0001t0013g0059 a0001c0001t0013g0277 a0001c0001t0013g0278 others(1): Show |
5 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.844-2596T>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35960015 | |||||||
| chr5:35960143 | C | T | 1 | a0001c0001t0006g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.844-2724G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35960143 | |||||||
| chr5:35960157 | A | G | 3 | a0001c0001t0003g0117 a0001c0001t0003g0119 a0001c0001t0038g0118 |
3 | HG01192.hp1 HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.844-2738T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35960157 | |||||||
| chr5:35960259 | C | A | 1 | a0001c0001t0001g0040 | 2 | NA18940.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.844-2840G>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35960259 | |||||||
| chr5:35960336 | T | C | 10 | a0001c0001t0001g0181 a0002c0002t0001g0012 a0002c0002t0001g0013 others(7): Show |
14 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.844-2917A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35960336 | |||||||
| chr5:35960341 | C | G | 2 | a0001c0001t0003g0218 a0001c0001t0003g0221 |
2 | NA18939.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.844-2922G>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35960341 | |||||||
| chr5:35960356 | C | G | 133 | a0001c0001t0001g0267 a0001c0001t0002g0002 a0001c0001t0002g0004 others(130): Show |
186 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.844-2937G>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35960356 | |||||||
| chr5:35960430 | C | G | 2 | a0001c0001t0014g0007 a0001c0001t0014g0199 |
5 | HG01099.hp1 HG01884.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.844-3011G>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35960430 | |||||||
| chr5:35960581 | T | C | 6 | a0001c0001t0008g0022 a0001c0001t0008g0053 a0001c0001t0008g0054 others(3): Show |
10 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.844-3162A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35960581 | |||||||
| chr5:35960593 | T | C | 1 | a0002c0002t0001g0097 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.844-3174A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35960593 | |||||||
| chr5:35960615 | C | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(235): Show |
340 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(337): Show |
intron_variant | MODIFIER | c.844-3196G>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35960615 | |||||||
| chr5:35960739 | T | C | 3 | a0001c0001t0001g0050 a0001c0001t0001g0183 a0001c0001t0001g0233 |
4 | HG02027.hp2 NA18954.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.844-3320A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35960739 | |||||||
| chr5:35960746 | T | C | 1 | a0007c0008t0034g0110 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.844-3327A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35960746 | |||||||
| chr5:35960771 | G | T | 3 | a0001c0006t0018g0052 a0001c0006t0018g0211 a0001c0006t0032g0212 |
4 | HG02451.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.844-3352C>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35960771 | |||||||
| chr5:35960963 | G | T | 1 | a0002c0002t0001g0088 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.844-3544C>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35960963 | |||||||
| chr5:35961029 | C | T | 1 | a0001c0001t0009g0244 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.844-3610G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35961029 | |||||||
| chr5:35961171 | C | T | 1 | a0007c0008t0034g0110 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.844-3752G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35961171 | |||||||
| chr5:35961189 | T | G | 1 | a0001c0001t0033g0132 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.844-3770A>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35961189 | |||||||
| chr5:35961307 | C | T | 7 | a0001c0001t0007g0008 a0001c0001t0007g0051 a0001c0001t0007g0196 others(4): Show |
11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.844-3888G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35961307 | |||||||
| chr5:35961338 | C | T | 2 | a0001c0001t0014g0007 a0001c0001t0014g0199 |
5 | HG01099.hp1 HG01884.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.844-3919G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35961338 | |||||||
| chr5:35961374 | G | A | 54 | a0001c0001t0003g0003 a0001c0001t0003g0213 a0001c0001t0003g0215 others(51): Show |
69 | HG00099.hp2 HG00621.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.844-3955C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35961374 | |||||||
| chr5:35961437 | A | G | 7 | a0001c0001t0010g0014 a0001c0001t0010g0038 a0001c0001t0010g0111 others(4): Show |
10 | HG00621.hp2 NA18612.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.843+3949T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35961437 | |||||||
| chr5:35961651 | A | G | 136 | a0001c0001t0001g0267 a0001c0001t0002g0002 a0001c0001t0002g0004 others(133): Show |
190 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.843+3735T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35961651 | |||||||
| chr5:35961927 | G | T | 1 | a0001c0001t0003g0237 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.843+3459C>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35961927 | |||||||
| chr5:35962030 | GATCC | G | 136 | a0001c0001t0001g0267 a0001c0001t0002g0002 a0001c0001t0002g0004 others(133): Show |
190 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.843+3352_843+3355d others(6): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35962030 | |||||||
| chr5:35962266 | G | T | 3 | a0001c0006t0018g0052 a0001c0006t0018g0211 a0001c0006t0032g0212 |
4 | HG02451.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.843+3120C>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35962266 | |||||||
| chr5:35962345 | G | T | 1 | a0006c0011t0017g0286 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.843+3041C>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35962345 | |||||||
| chr5:35962372 | G | A | 1 | a0001c0001t0006g0153 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.843+3014C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35962372 | |||||||
| chr5:35962415 | G | C | 1 | a0001c0001t0001g0168 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.843+2971C>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35962415 | |||||||
| chr5:35962516 | G | A | 6 | a0001c0001t0003g0116 a0001c0001t0003g0120 a0001c0001t0003g0121 others(3): Show |
6 | HG02280.hp2 HG02451.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.843+2870C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35962516 | |||||||
| chr5:35962546 | C | T | 7 | a0001c0001t0010g0014 a0001c0001t0010g0038 a0001c0001t0010g0111 others(4): Show |
10 | HG00621.hp2 NA18612.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.843+2840G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35962546 | |||||||
| chr5:35962551 | C | A | 42 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0181 others(39): Show |
57 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.843+2835G>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35962551 | |||||||
| chr5:35962555 | C | T | 4 | a0001c0001t0013g0059 a0001c0001t0013g0277 a0001c0001t0013g0278 others(1): Show |
5 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.843+2831G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35962555 | |||||||
| chr5:35962639 | C | T | 2 | a0001c0001t0006g0170 a0001c0001t0006g0171 |
2 | HG01175.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.843+2747G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35962639 | |||||||
| chr5:35962675 | G | A | 54 | a0001c0001t0003g0003 a0001c0001t0003g0213 a0001c0001t0003g0215 others(51): Show |
69 | HG00099.hp2 HG00621.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.843+2711C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35962675 | |||||||
| chr5:35962771 | C | T | 33 | a0001c0001t0003g0003 a0001c0001t0003g0213 a0001c0001t0003g0215 others(30): Show |
39 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.843+2615G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35962771 | |||||||
| chr5:35962780 | G | A | 10 | a0001c0001t0007g0008 a0001c0001t0007g0039 a0001c0001t0007g0051 others(7): Show |
15 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.843+2606C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35962780 | |||||||
| chr5:35962827 | T | C | 1 | a0001c0001t0011g0130 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.843+2559A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35962827 | |||||||
| chr5:35962879 | G | A | 1 | a0001c0001t0006g0153 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.843+2507C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35962879 | |||||||
| chr5:35962882 | A | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(230): Show |
335 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(332): Show |
intron_variant | MODIFIER | c.843+2504T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35962882 | |||||||
| chr5:35963246 | G | T | 1 | a0007c0008t0034g0110 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.843+2140C>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35963246 | |||||||
| chr5:35963405 | T | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(129): Show |
188 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.843+1981A>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35963405 | |||||||
| chr5:35963644 | C | T | 1 | a0001c0001t0016g0159 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.843+1742G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35963644 | |||||||
| chr5:35963866 | C | T | 1 | a0001c0001t0002g0264 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.843+1520G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35963866 | |||||||
| chr5:35963965 | C | T | 5 | a0001c0001t0003g0216 a0001c0001t0003g0218 a0001c0001t0003g0219 others(2): Show |
5 | NA18939.hp1 NA18939.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.843+1421G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35963965 | |||||||
| chr5:35964004 | T | C | 2 | a0002c0002t0001g0010 a0002c0002t0001g0104 |
4 | HG02698.hp1 HG02735.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.843+1382A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35964004 | |||||||
| chr5:35964093 | ATGGT | A | 159 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0181 others(156): Show |
209 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.843+1289_843+1292d others(6): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35964093 | |||||||
| chr5:35964098 | TA | T | 34 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(31): Show |
61 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.843+1287delT | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35964098 | |||||||
| chr5:35964154 | A | G | 2 | a0001c0001t0014g0007 a0001c0001t0014g0199 |
5 | HG01099.hp1 HG01884.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.843+1232T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35964154 | |||||||
| chr5:35964184 | A | G | 133 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0239 others(130): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.843+1202T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35964184 | |||||||
| chr5:35964357 | A | G | 2 | a0001c0001t0014g0007 a0001c0001t0014g0199 |
5 | HG01099.hp1 HG01884.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.843+1029T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35964357 | |||||||
| chr5:35964378 | G | A | 1 | a0001c0001t0003g0234 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.843+1008C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35964378 | |||||||
| chr5:35964543 | T | C | 1 | a0001c0001t0024g0058 | 2 | NA18960.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.843+843A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35964543 | |||||||
| chr5:35964656 | T | C | 2 | a0001c0001t0015g0252 a0006c0011t0017g0286 |
2 | HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.843+730A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35964656 | |||||||
| chr5:35964717 | G | A | 7 | a0001c0001t0010g0014 a0001c0001t0010g0038 a0001c0001t0010g0111 others(4): Show |
10 | HG00621.hp2 NA18612.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.843+669C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35964717 | |||||||
| chr5:35964756 | T | G | 4 | a0001c0001t0017g0109 a0001c0001t0017g0124 a0001c0001t0017g0125 others(1): Show |
4 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.843+630A>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35964756 | |||||||
| chr5:35964987 | A | T | 197 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(194): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.843+399T>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35964987 | |||||||
| chr5:35965136 | A | T | 9 | a0001c0001t0007g0008 a0001c0001t0007g0039 a0001c0001t0007g0051 others(6): Show |
14 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.843+250T>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35965136 | |||||||
| chr5:35965247 | T | A | 2 | a0001c0001t0014g0007 a0001c0001t0014g0199 |
5 | HG01099.hp1 HG01884.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.843+139A>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 4/6 | chr5 | 35965247 | |||||||
| chr5:35965925 | A | T | 1 | a0001c0001t0006g0151 | 1 | HG00408.hp2 | splice_region_variant&intron_variant | LOW | c.312-8T>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 3/6 | chr5 | 35965925 | |||||||
| chr5:35966076 | T | C | 14 | a0001c0001t0007g0008 a0001c0001t0007g0039 a0001c0001t0007g0051 others(11): Show |
23 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.312-159A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 3/6 | chr5 | 35966076 | |||||||
| chr5:35966112 | C | T | 1 | a0006c0011t0017g0286 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.312-195G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 3/6 | chr5 | 35966112 | |||||||
| chr5:35966128 | C | T | 1 | a0001c0001t0002g0266 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.312-211G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 3/6 | chr5 | 35966128 | |||||||
| chr5:35966237 | T | C | 5 | a0002c0002t0001g0032 a0002c0002t0001g0081 a0002c0002t0001g0084 others(2): Show |
7 | HG00597.hp2 HG02129.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.312-320A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 3/6 | chr5 | 35966237 | |||||||
| chr5:35966306 | G | T | 1 | a0001c0001t0033g0132 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.312-389C>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 3/6 | chr5 | 35966306 | |||||||
| chr5:35966434 | A | G | 5 | a0002c0002t0001g0010 a0002c0002t0001g0068 a0002c0002t0001g0069 others(2): Show |
7 | HG02698.hp1 HG02735.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.312-517T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 3/6 | chr5 | 35966434 | |||||||
| chr5:35966450 | C | T | 1 | a0001c0001t0033g0132 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.312-533G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 3/6 | chr5 | 35966450 | |||||||
| chr5:35966471 | A | G | 2 | a0001c0001t0014g0007 a0001c0001t0014g0199 |
5 | HG01099.hp1 HG01884.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.312-554T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 3/6 | chr5 | 35966471 | |||||||
| chr5:35966473 | G | A | 1 | a0001c0001t0004g0065 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.312-556C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 3/6 | chr5 | 35966473 | |||||||
| chr5:35966579 | A | G | 44 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0002g0002 others(41): Show |
68 | HG00140.hp1 HG00323.hp2 HG01074.hp1 others(65): Show |
intron_variant | MODIFIER | c.312-662T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 3/6 | chr5 | 35966579 | |||||||
| chr5:35966647 | G | A | 1 | a0001c0001t0002g0269 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.312-730C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 3/6 | chr5 | 35966647 | |||||||
| chr5:35966714 | A | T | 1 | a0001c0001t0010g0111 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.312-797T>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 3/6 | chr5 | 35966714 | |||||||
| chr5:35967281 | T | C | 11 | a0002c0002t0001g0032 a0002c0002t0001g0034 a0002c0002t0001g0037 others(8): Show |
15 | HG00597.hp2 HG02040.hp1 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.311+738A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 3/6 | chr5 | 35967281 | |||||||
| chr5:35967797 | T | C | 1 | a0001c0001t0002g0271 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.311+222A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 3/6 | chr5 | 35967797 | |||||||
| chr5:35967815 | G | C | 196 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(193): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.311+204C>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 3/6 | chr5 | 35967815 | |||||||
| chr5:35967898 | C | A | 83 | a0001c0001t0003g0116 a0001c0001t0003g0117 a0001c0001t0003g0119 others(80): Show |
107 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.311+121G>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 3/6 | chr5 | 35967898 | |||||||
| chr5:35968304 | G | A | 1 | a0001c0001t0003g0222 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.197-171C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35968304 | |||||||
| chr5:35968392 | C | T | 1 | a0002c0002t0001g0092 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.197-259G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35968392 | |||||||
| chr5:35968397 | A | G | 7 | a0001c0001t0010g0014 a0001c0001t0010g0038 a0001c0001t0010g0111 others(4): Show |
10 | HG00621.hp2 NA18612.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.197-264T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35968397 | |||||||
| chr5:35968531 | C | T | 1 | a0002c0002t0001g0090 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.197-398G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35968531 | |||||||
| chr5:35968664 | C | G | 1 | a0002c0002t0001g0085 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.197-531G>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35968664 | |||||||
| chr5:35968741 | T | A | 53 | a0002c0002t0001g0005 a0002c0002t0001g0010 a0002c0002t0001g0011 others(50): Show |
73 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.197-608A>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35968741 | |||||||
| chr5:35968763 | C | G | 1 | a0001c0001t0002g0259 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.197-630G>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35968763 | |||||||
| chr5:35968958 | A | C | 1 | a0001c0001t0006g0150 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.197-825T>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35968958 | |||||||
| chr5:35968998 | C | A | 7 | a0001c0001t0010g0014 a0001c0001t0010g0038 a0001c0001t0010g0111 others(4): Show |
10 | HG00621.hp2 NA18612.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.197-865G>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35968998 | |||||||
| chr5:35969118 | C | T | 6 | a0001c0001t0004g0206 a0001c0001t0004g0210 a0001c0001t0018g0209 others(3): Show |
6 | HG02486.hp2 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-985G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35969118 | |||||||
| chr5:35969157 | T | A | 91 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(88): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.197-1024A>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35969157 | |||||||
| chr5:35969317 | G | A | 1 | a0001c0001t0005g0163 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.197-1184C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35969317 | |||||||
| chr5:35969697 | G | C | 6 | a0001c0001t0004g0206 a0001c0001t0004g0210 a0001c0001t0018g0209 others(3): Show |
6 | HG02486.hp2 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-1564C>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35969697 | |||||||
| chr5:35969843 | C | T | 1 | a0001c0001t0003g0236 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.197-1710G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35969843 | |||||||
| chr5:35969844 | G | A | 1 | a0001c0001t0012g0173 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.197-1711C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35969844 | |||||||
| chr5:35969950 | A | G | 20 | a0001c0001t0004g0206 a0001c0001t0004g0210 a0001c0001t0007g0008 others(17): Show |
29 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.197-1817T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35969950 | |||||||
| chr5:35970113 | G | A | 54 | a0002c0002t0001g0005 a0002c0002t0001g0010 a0002c0002t0001g0011 others(51): Show |
74 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.197-1980C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35970113 | |||||||
| chr5:35970252 | C | A | 1 | a0001c0001t0001g0188 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.197-2119G>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35970252 | |||||||
| chr5:35970253 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.197-2120C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35970253 | |||||||
| chr5:35970272 | G | A | 1 | a0001c0001t0002g0262 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.197-2139C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35970272 | |||||||
| chr5:35970305 | T | A | 3 | a0001c0001t0002g0027 a0001c0001t0002g0269 a0001c0001t0002g0283 |
5 | HG01358.hp1 HG01952.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-2172A>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35970305 | |||||||
| chr5:35970390 | C | CA | 12 | a0001c0001t0001g0040 a0001c0001t0001g0142 a0001c0001t0001g0143 others(9): Show |
15 | HG02071.hp1 HG02257.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.197-2258dupT | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35970390 | |||||||
| chr5:35970390 | CA | C | 86 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(83): Show |
109 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.197-2258delT | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35970390 | |||||||
| chr5:35970445 | G | A | 91 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(88): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.197-2312C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35970445 | |||||||
| chr5:35970506 | G | A | 1 | a0002c0002t0001g0101 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.197-2373C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35970506 | |||||||
| chr5:35970539 | C | G | 2 | a0001c0001t0014g0007 a0001c0001t0014g0199 |
5 | HG01099.hp1 HG01884.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-2406G>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35970539 | |||||||
| chr5:35970843 | T | G | 1 | a0001c0001t0005g0163 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.197-2710A>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35970843 | |||||||
| chr5:35970929 | C | T | 1 | a0001c0004t0005g0177 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.197-2796G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35970929 | |||||||
| chr5:35971005 | TC | T | 18 | a0001c0001t0003g0116 a0001c0001t0003g0117 a0001c0001t0003g0119 others(15): Show |
19 | HG01192.hp1 HG02145.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.197-2873delG | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35971005 | |||||||
| chr5:35971085 | G | A | 91 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(88): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.197-2952C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35971085 | |||||||
| chr5:35971096 | A | G | 1 | a0001c0001t0003g0123 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.197-2963T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35971096 | |||||||
| chr5:35971128 | C | T | 1 | a0001c0001t0004g0066 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.197-2995G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35971128 | |||||||
| chr5:35971274 | C | T | 5 | a0002c0002t0001g0010 a0002c0002t0001g0068 a0002c0002t0001g0069 others(2): Show |
7 | HG02698.hp1 HG02735.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.197-3141G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35971274 | |||||||
| chr5:35971329 | G | T | 1 | a0001c0001t0002g0272 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.197-3196C>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35971329 | |||||||
| chr5:35971463 | T | TAC | 53 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(50): Show |
87 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.197-3332_197-3331d others(4): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35971463 | |||||||
| chr5:35971463 | T | TACAC | 7 | a0001c0001t0001g0021 a0001c0001t0001g0144 a0001c0001t0001g0181 others(4): Show |
9 | HG00597.hp1 HG02004.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.197-3334_197-3331d others(6): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35971463 | |||||||
| chr5:35971463 | T | TACACAC | 6 | a0001c0001t0010g0014 a0001c0001t0010g0038 a0001c0001t0010g0111 others(3): Show |
9 | NA18612.hp1 NA18942.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.197-3336_197-3331d others(8): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35971463 | |||||||
| chr5:35971463 | TAC | T | 36 | a0001c0001t0004g0206 a0001c0001t0004g0210 a0001c0001t0006g0170 others(33): Show |
48 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.197-3332_197-3331d others(4): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35971463 | |||||||
| chr5:35971463 | TACAC | T | 25 | a0001c0001t0002g0271 a0001c0001t0006g0156 a0001c0001t0015g0025 others(22): Show |
33 | HG00438.hp2 HG01071.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.197-3334_197-3331d others(6): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35971463 | |||||||
| chr5:35971463 | TACACAC | T | 39 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0002g0002 others(36): Show |
61 | HG00140.hp1 HG00323.hp2 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.197-3336_197-3331d others(8): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35971463 | |||||||
| chr5:35971503 | T | C | 202 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0134 others(199): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.197-3370A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35971503 | |||||||
| chr5:35971529 | A | T | 1 | a0007c0008t0034g0110 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.197-3396T>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35971529 | |||||||
| chr5:35971561 | C | A | 2 | a0001c0001t0014g0007 a0001c0001t0014g0199 |
5 | HG01099.hp1 HG01884.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-3428G>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35971561 | |||||||
| chr5:35971853 | C | T | 18 | a0001c0001t0003g0116 a0001c0001t0003g0117 a0001c0001t0003g0119 others(15): Show |
19 | HG01192.hp1 HG02145.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.197-3720G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35971853 | |||||||
| chr5:35971938 | A | T | 91 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(88): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.197-3805T>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35971938 | |||||||
| chr5:35972059 | C | G | 1 | a0001c0001t0006g0146 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.197-3926G>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35972059 | |||||||
| chr5:35972085 | A | AT | 76 | a0001c0001t0003g0116 a0001c0001t0003g0117 a0001c0001t0003g0119 others(73): Show |
97 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.197-3953dupA | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35972085 | |||||||
| chr5:35972152 | G | C | 1 | a0007c0008t0034g0110 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.197-4019C>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35972152 | |||||||
| chr5:35972355 | G | A | 1 | a0001c0001t0006g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.197-4222C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35972355 | |||||||
| chr5:35972494 | C | CGT | 25 | a0001c0001t0001g0021 a0001c0001t0001g0048 a0001c0001t0001g0181 others(22): Show |
34 | HG00597.hp1 HG00621.hp1 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.197-4363_197-4362d others(4): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35972494 | |||||||
| chr5:35972494 | C | CGTGT | 56 | a0001c0001t0001g0020 a0001c0001t0001g0055 a0001c0001t0001g0129 others(53): Show |
85 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.197-4365_197-4362d others(6): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35972494 | |||||||
| chr5:35972494 | C | CGTGTGT | 20 | a0001c0001t0001g0220 a0001c0001t0001g0239 a0001c0001t0002g0255 others(17): Show |
21 | HG00140.hp1 HG01099.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.197-4367_197-4362d others(8): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35972494 | |||||||
| chr5:35972494 | C | CGTGTGTG others(1): Show |
6 | a0001c0001t0002g0258 a0001c0001t0003g0229 a0001c0001t0009g0245 others(3): Show |
6 | HG00735.hp1 HG01256.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-4369_197-4362d others(10): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35972494 | |||||||
| chr5:35972494 | C | CGTGTGTG others(3): Show |
2 | a0001c0001t0009g0023 a0001c0001t0009g0244 |
4 | HG00099.hp2 HG00642.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-4371_197-4362d others(12): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35972494 | |||||||
| chr5:35972494 | C | CGTGTGTG others(5): Show |
1 | a0001c0001t0033g0132 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.197-4373_197-4362d others(14): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35972494 | |||||||
| chr5:35972494 | CGT | C | 50 | a0001c0001t0001g0049 a0001c0001t0001g0134 a0001c0001t0001g0188 others(47): Show |
67 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.197-4363_197-4362d others(4): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35972494 | |||||||
| chr5:35972494 | CGTGT | C | 24 | a0001c0001t0004g0067 a0001c0001t0004g0193 a0001c0001t0005g0017 others(21): Show |
29 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.197-4365_197-4362d others(6): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35972494 | |||||||
| chr5:35972494 | CGTGTGT | C | 18 | a0001c0001t0015g0025 a0001c0001t0015g0252 a0001c0001t0015g0280 others(15): Show |
25 | HG01071.hp1 HG01361.hp2 HG02071.hp1 others(22): Show |
intron_variant | MODIFIER | c.197-4367_197-4362d others(8): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35972494 | |||||||
| chr5:35972494 | CGTGTGTG others(3): Show |
C | 10 | a0001c0001t0001g0140 a0001c0001t0007g0008 a0001c0001t0007g0039 others(7): Show |
15 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.197-4371_197-4362d others(12): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35972494 | |||||||
| chr5:35972494 | CGTGTGTG others(5): Show |
C | 6 | a0001c0001t0001g0040 a0001c0001t0001g0141 a0001c0001t0001g0142 others(3): Show |
7 | NA18940.hp1 NA18961.hp2 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.197-4373_197-4362d others(14): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35972494 | |||||||
| chr5:35972665 | A | G | 1 | a0001c0001t0006g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.197-4532T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35972665 | |||||||
| chr5:35972694 | T | G | 1 | a0007c0008t0034g0110 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.197-4561A>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35972694 | |||||||
| chr5:35972887 | G | GA | 141 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0189 others(138): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.197-4755dupT | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35972887 | |||||||
| chr5:35972887 | GA | G | 5 | a0001c0001t0007g0127 a0001c0001t0014g0007 a0001c0001t0014g0199 others(2): Show |
8 | HG01099.hp1 HG01884.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.197-4755delT | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35972887 | |||||||
| chr5:35972925 | G | A | 1 | a0006c0011t0017g0286 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.197-4792C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35972925 | |||||||
| chr5:35973062 | T | C | 6 | a0002c0002t0001g0034 a0002c0002t0001g0037 a0002c0002t0001g0092 others(3): Show |
8 | HG02040.hp1 NA18945.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.197-4929A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35973062 | |||||||
| chr5:35973088 | A | T | 1 | a0001c0001t0013g0204 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.197-4955T>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35973088 | |||||||
| chr5:35973123 | A | C | 3 | a0001c0006t0018g0052 a0001c0006t0018g0211 a0001c0006t0032g0212 |
4 | HG02451.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-4990T>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35973123 | |||||||
| chr5:35973278 | C | A | 6 | a0001c0001t0004g0206 a0001c0001t0004g0210 a0001c0001t0018g0209 others(3): Show |
6 | HG02486.hp2 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-5145G>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35973278 | |||||||
| chr5:35973351 | G | A | 1 | a0001c0001t0007g0201 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.197-5218C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35973351 | |||||||
| chr5:35973382 | T | C | 5 | a0001c0001t0004g0060 a0001c0001t0004g0061 a0001c0001t0004g0062 others(2): Show |
5 | HG02145.hp2 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-5249A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35973382 | |||||||
| chr5:35973403 | G | A | 1 | a0002c0002t0001g0102 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.197-5270C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35973403 | |||||||
| chr5:35973403 | G | C | 9 | a0001c0001t0007g0008 a0001c0001t0007g0039 a0001c0001t0007g0051 others(6): Show |
14 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.197-5270C>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35973403 | |||||||
| chr5:35973572 | C | T | 1 | a0007c0008t0034g0110 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.197-5439G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35973572 | |||||||
| chr5:35973629 | A | C | 91 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(88): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.197-5496T>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35973629 | |||||||
| chr5:35973630 | A | G | 47 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(44): Show |
60 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.197-5497T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35973630 | |||||||
| chr5:35973773 | T | G | 202 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0134 others(199): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.197-5640A>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35973773 | |||||||
| chr5:35974086 | A | T | 54 | a0002c0002t0001g0005 a0002c0002t0001g0010 a0002c0002t0001g0011 others(51): Show |
74 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.197-5953T>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35974086 | |||||||
| chr5:35974148 | G | C | 2 | a0002c0002t0001g0074 a0002c0002t0001g0094 |
2 | HG00741.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.197-6015C>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35974148 | |||||||
| chr5:35974164 | C | T | 44 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0002g0002 others(41): Show |
68 | HG00140.hp1 HG00323.hp2 HG01074.hp1 others(65): Show |
intron_variant | MODIFIER | c.197-6031G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35974164 | |||||||
| chr5:35974226 | G | A | 1 | a0001c0001t0006g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.197-6093C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35974226 | |||||||
| chr5:35974703 | G | A | 3 | a0001c0001t0007g0008 a0001c0001t0007g0200 a0001c0001t0007g0202 |
6 | HG02109.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-6570C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35974703 | |||||||
| chr5:35974901 | G | A | 3 | a0001c0001t0007g0008 a0001c0001t0007g0200 a0001c0001t0007g0202 |
6 | HG02109.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-6768C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35974901 | |||||||
| chr5:35974906 | G | A | 2 | a0001c0001t0005g0165 a0001c0001t0014g0199 |
2 | HG01070.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.197-6773C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35974906 | |||||||
| chr5:35974957 | T | C | 1 | a0001c0001t0003g0213 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.197-6824A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35974957 | |||||||
| chr5:35975002 | A | G | 1 | a0007c0008t0034g0110 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.197-6869T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35975002 | |||||||
| chr5:35975154 | C | G | 3 | a0001c0001t0002g0057 a0001c0001t0002g0254 a0001c0001t0002g0261 |
4 | NA18946.hp1 NA18959.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-7021G>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35975154 | |||||||
| chr5:35975341 | C | A | 91 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(88): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.197-7208G>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35975341 | |||||||
| chr5:35975361 | G | A | 1 | a0001c0001t0005g0227 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.197-7228C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35975361 | |||||||
| chr5:35975366 | T | C | 91 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(88): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.197-7233A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35975366 | |||||||
| chr5:35975399 | G | C | 1 | a0006c0011t0017g0286 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.197-7266C>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35975399 | |||||||
| chr5:35975464 | A | G | 105 | a0001c0001t0003g0116 a0001c0001t0003g0117 a0001c0001t0003g0119 others(102): Show |
138 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.197-7331T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35975464 | |||||||
| chr5:35975521 | G | A | 3 | a0001c0006t0018g0052 a0001c0006t0018g0211 a0001c0006t0032g0212 |
4 | HG02451.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-7388C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35975521 | |||||||
| chr5:35975580 | C | T | 1 | a0001c0001t0003g0236 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.197-7447G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35975580 | |||||||
| chr5:35975662 | A | AT | 42 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0002g0002 others(39): Show |
64 | HG00140.hp1 HG00323.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.197-7530dupA | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35975662 | |||||||
| chr5:35975662 | AT | A | 5 | a0001c0001t0001g0055 a0001c0001t0004g0062 a0001c0001t0006g0154 others(2): Show |
6 | HG01975.hp2 HG02004.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-7530delA | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35975662 | |||||||
| chr5:35975718 | T | C | 1 | a0001c0001t0003g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.197-7585A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35975718 | |||||||
| chr5:35975731 | C | T | 3 | a0001c0001t0007g0039 a0001c0001t0007g0126 a0001c0001t0007g0127 |
4 | HG01243.hp1 HG02258.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-7598G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35975731 | |||||||
| chr5:35975743 | G | C | 2 | a0001c0001t0005g0226 a0001c0001t0005g0227 |
2 | HG02132.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.197-7610C>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35975743 | |||||||
| chr5:35975757 | C | T | 91 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(88): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.197-7624G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35975757 | |||||||
| chr5:35975762 | G | C | 91 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(88): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.197-7629C>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35975762 | |||||||
| chr5:35975809 | A | T | 7 | a0001c0001t0010g0014 a0001c0001t0010g0038 a0001c0001t0010g0111 others(4): Show |
10 | HG00621.hp2 NA18612.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.197-7676T>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35975809 | |||||||
| chr5:35975829 | T | A | 91 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(88): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.197-7696A>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35975829 | |||||||
| chr5:35975982 | T | C | 1 | a0001c0001t0006g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.197-7849A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35975982 | |||||||
| chr5:35976668 | C | T | 1 | a0001c0001t0002g0260 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.197-8535G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35976668 | |||||||
| chr5:35976833 | C | CAA | 268 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(265): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.197-8702_197-8701d others(4): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35976833 | |||||||
| chr5:35976839 | T | A | 268 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(265): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.197-8706A>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35976839 | |||||||
| chr5:35976871 | C | T | 2 | a0001c0001t0014g0007 a0001c0001t0014g0199 |
5 | HG01099.hp1 HG01884.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-8738G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35976871 | |||||||
| chr5:35976887 | G | GGGAA | 164 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0220 others(161): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.197-8758_197-8755d others(6): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35976887 | |||||||
| chr5:35976887 | G | GGGAAGGA others(5): Show |
5 | a0001c0001t0010g0014 a0001c0001t0010g0038 a0001c0001t0010g0111 others(2): Show |
8 | NA18612.hp1 NA18942.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.197-8766_197-8755d others(14): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35976887 | |||||||
| chr5:35976887 | G | GGGAAGGA others(9): Show |
1 | a0001c0001t0010g0113 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.197-8770_197-8755d others(18): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35976887 | |||||||
| chr5:35976911 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.197-8778C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35976911 | |||||||
| chr5:35976912 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.197-8779T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35976912 | |||||||
| chr5:35976918 | AAAGAAAA others(6): Show |
A | 1 | a0001c0001t0001g0198 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.197-8798_197-8786d others(15): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35976918 | |||||||
| chr5:35976932 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.197-8799T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35976932 | |||||||
| chr5:35976970 | G | A | 1 | a0001c0001t0004g0060 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.197-8837C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35976970 | |||||||
| chr5:35977022 | GAGAA | G | 19 | a0001c0001t0004g0206 a0001c0001t0004g0210 a0001c0001t0007g0008 others(16): Show |
25 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.197-8893_197-8890d others(6): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35977022 | |||||||
| chr5:35977030 | A | AAGAG | 2 | a0001c0001t0014g0007 a0001c0001t0014g0199 |
5 | HG01099.hp1 HG01884.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-8898_197-8897i others(6): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35977030 | |||||||
| chr5:35977037 | A | G | 2 | a0001c0001t0014g0007 a0001c0001t0014g0199 |
5 | HG01099.hp1 HG01884.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-8904T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35977037 | |||||||
| chr5:35977044 | G | GAGA | 2 | a0001c0001t0014g0007 a0001c0001t0014g0199 |
5 | HG01099.hp1 HG01884.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-8912_197-8911i others(5): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35977044 | |||||||
| chr5:35977045 | G | A | 2 | a0001c0001t0014g0007 a0001c0001t0014g0199 |
5 | HG01099.hp1 HG01884.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-8912C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35977045 | |||||||
| chr5:35977073 | G | A | 7 | a0001c0001t0010g0014 a0001c0001t0010g0038 a0001c0001t0010g0111 others(4): Show |
10 | HG00621.hp2 NA18612.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.197-8940C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35977073 | |||||||
| chr5:35977074 | A | G | 7 | a0001c0001t0010g0014 a0001c0001t0010g0038 a0001c0001t0010g0111 others(4): Show |
10 | HG00621.hp2 NA18612.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.197-8941T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35977074 | |||||||
| chr5:35977088 | A | G | 7 | a0001c0001t0010g0014 a0001c0001t0010g0038 a0001c0001t0010g0111 others(4): Show |
10 | HG00621.hp2 NA18612.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.197-8955T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35977088 | |||||||
| chr5:35977090 | G | A | 7 | a0001c0001t0010g0014 a0001c0001t0010g0038 a0001c0001t0010g0111 others(4): Show |
10 | HG00621.hp2 NA18612.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.197-8957C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35977090 | |||||||
| chr5:35977094 | AAGAAAGA others(3): Show |
A | 18 | a0001c0001t0003g0116 a0001c0001t0003g0117 a0001c0001t0003g0119 others(15): Show |
19 | HG01192.hp1 HG02145.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.197-8971_197-8962d others(12): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35977094 | |||||||
| chr5:35977102 | A | G | 7 | a0001c0001t0010g0014 a0001c0001t0010g0038 a0001c0001t0010g0111 others(4): Show |
10 | HG00621.hp2 NA18612.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.197-8969T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35977102 | |||||||
| chr5:35977104 | G | A | 7 | a0001c0001t0010g0014 a0001c0001t0010g0038 a0001c0001t0010g0111 others(4): Show |
10 | HG00621.hp2 NA18612.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.197-8971C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35977104 | |||||||
| chr5:35977104 | G | GAGAA | 171 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(168): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.197-8975_197-8972d others(6): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35977104 | |||||||
| chr5:35977176 | G | T | 90 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(87): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.197-9043C>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35977176 | |||||||
| chr5:35977286 | T | C | 2 | a0001c0001t0003g0236 a0001c0001t0003g0237 |
2 | HG00639.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.197-9153A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35977286 | |||||||
| chr5:35977477 | G | A | 6 | a0001c0001t0004g0206 a0001c0001t0004g0210 a0001c0001t0018g0209 others(3): Show |
6 | HG02486.hp2 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-9344C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35977477 | |||||||
| chr5:35977514 | G | T | 1 | a0002c0002t0001g0076 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.197-9381C>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35977514 | |||||||
| chr5:35977536 | T | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(265): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.197-9403A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35977536 | |||||||
| chr5:35977705 | T | C | 2 | a0001c0001t0014g0007 a0001c0001t0014g0199 |
5 | HG01099.hp1 HG01884.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-9572A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35977705 | |||||||
| chr5:35977740 | A | G | 1 | a0004c0005t0002g0009 | 4 | NA18947.hp1 NA18977.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-9607T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35977740 | |||||||
| chr5:35977803 | A | G | 4 | a0001c0001t0017g0109 a0001c0001t0017g0124 a0001c0001t0017g0125 others(1): Show |
4 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-9670T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35977803 | |||||||
| chr5:35977824 | G | A | 196 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(193): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.197-9691C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35977824 | |||||||
| chr5:35977835 | A | C | 1 | a0001c0001t0002g0259 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.197-9702T>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35977835 | |||||||
| chr5:35977878 | C | T | 76 | a0001c0001t0003g0116 a0001c0001t0003g0117 a0001c0001t0003g0119 others(73): Show |
97 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.197-9745G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35977878 | |||||||
| chr5:35977975 | T | C | 89 | a0001c0001t0001g0134 a0001c0001t0003g0116 a0001c0001t0003g0117 others(86): Show |
115 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.197-9842A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35977975 | |||||||
| chr5:35978359 | T | A | 6 | a0001c0001t0010g0014 a0001c0001t0010g0038 a0001c0001t0010g0111 others(3): Show |
9 | NA18612.hp1 NA18942.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.196+10091A>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35978359 | |||||||
| chr5:35978413 | T | C | 1 | a0001c0001t0006g0138 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.196+10037A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35978413 | |||||||
| chr5:35978430 | T | C | 1 | a0007c0008t0034g0110 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.196+10020A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35978430 | |||||||
| chr5:35978516 | A | C | 1 | a0001c0001t0004g0166 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.196+9934T>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35978516 | |||||||
| chr5:35978588 | T | C | 1 | a0001c0001t0007g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.196+9862A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35978588 | |||||||
| chr5:35978616 | G | C | 44 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0002g0002 others(41): Show |
68 | HG00140.hp1 HG00323.hp2 HG01074.hp1 others(65): Show |
intron_variant | MODIFIER | c.196+9834C>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35978616 | |||||||
| chr5:35978680 | C | T | 6 | a0001c0001t0004g0206 a0001c0001t0004g0210 a0001c0001t0018g0209 others(3): Show |
6 | HG02486.hp2 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+9770G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35978680 | |||||||
| chr5:35978700 | C | T | 1 | a0007c0008t0034g0110 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.196+9750G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35978700 | |||||||
| chr5:35978909 | C | T | 7 | a0001c0001t0010g0014 a0001c0001t0010g0038 a0001c0001t0010g0111 others(4): Show |
10 | HG00621.hp2 NA18612.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.196+9541G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35978909 | |||||||
| chr5:35979025 | C | T | 7 | a0001c0001t0007g0196 a0001c0001t0012g0047 a0001c0001t0012g0139 others(4): Show |
8 | HG02055.hp2 HG02630.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.196+9425G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35979025 | |||||||
| chr5:35979111 | C | T | 1 | a0001c0001t0005g0043 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.196+9339G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35979111 | |||||||
| chr5:35979237 | C | T | 7 | a0001c0001t0010g0014 a0001c0001t0010g0038 a0001c0001t0010g0111 others(4): Show |
10 | HG00621.hp2 NA18612.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.196+9213G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35979237 | |||||||
| chr5:35979268 | A | G | 2 | a0001c0001t0002g0251 a0001c0001t0002g0258 |
2 | HG01074.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.196+9182T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35979268 | |||||||
| chr5:35979326 | C | T | 1 | a0001c0001t0006g0135 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.196+9124G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35979326 | |||||||
| chr5:35979362 | C | T | 21 | a0001c0001t0004g0206 a0001c0001t0004g0210 a0001c0001t0007g0008 others(18): Show |
30 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.196+9088G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35979362 | |||||||
| chr5:35979364 | C | T | 1 | a0001c0001t0004g0067 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.196+9086G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35979364 | |||||||
| chr5:35979428 | T | C | 39 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0002g0002 others(36): Show |
61 | HG00140.hp1 HG00323.hp2 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.196+9022A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35979428 | |||||||
| chr5:35979443 | G | T | 54 | a0002c0002t0001g0005 a0002c0002t0001g0010 a0002c0002t0001g0011 others(51): Show |
74 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.196+9007C>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35979443 | |||||||
| chr5:35979447 | C | A | 4 | a0001c0001t0017g0109 a0001c0001t0017g0124 a0001c0001t0017g0125 others(1): Show |
4 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+9003G>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35979447 | |||||||
| chr5:35979451 | A | G | 47 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(44): Show |
60 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.196+8999T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35979451 | |||||||
| chr5:35979559 | T | C | 5 | a0002c0002t0001g0011 a0002c0002t0001g0071 a0002c0002t0001g0076 others(2): Show |
7 | HG01071.hp1 NA18960.hp2 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.196+8891A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35979559 | |||||||
| chr5:35979569 | TA | T | 14 | a0001c0001t0007g0008 a0001c0001t0007g0039 a0001c0001t0007g0051 others(11): Show |
23 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.196+8880delT | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35979569 | |||||||
| chr5:35979715 | C | T | 7 | a0001c0001t0004g0166 a0001c0001t0004g0167 a0001c0001t0004g0175 others(4): Show |
11 | HG00673.hp2 HG02132.hp1 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.196+8735G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35979715 | |||||||
| chr5:35979764 | G | A | 6 | a0001c0001t0004g0206 a0001c0001t0004g0210 a0001c0001t0018g0209 others(3): Show |
6 | HG02486.hp2 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+8686C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35979764 | |||||||
| chr5:35979779 | G | A | 3 | a0001c0001t0003g0117 a0001c0001t0003g0119 a0001c0001t0038g0118 |
3 | HG01192.hp1 HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.196+8671C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35979779 | |||||||
| chr5:35979809 | T | C | 1 | a0002c0002t0001g0072 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.196+8641A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35979809 | |||||||
| chr5:35979814 | T | C | 47 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(44): Show |
60 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.196+8636A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35979814 | |||||||
| chr5:35979918 | A | G | 39 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0002g0002 others(36): Show |
61 | HG00140.hp1 HG00323.hp2 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.196+8532T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35979918 | |||||||
| chr5:35980002 | T | A | 1 | a0001c0001t0004g0060 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.196+8448A>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35980002 | |||||||
| chr5:35980037 | A | G | 91 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(88): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.196+8413T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35980037 | |||||||
| chr5:35980087 | G | C | 197 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(194): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.196+8363C>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35980087 | |||||||
| chr5:35980152 | AC | A | 3 | a0001c0001t0004g0061 a0001c0001t0004g0063 a0001c0001t0004g0064 |
3 | HG02145.hp2 HG02559.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.196+8297delG | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35980152 | |||||||
| chr5:35980156 | CT | C | 47 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(44): Show |
60 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.196+8293delA | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35980156 | |||||||
| chr5:35980168 | T | A | 9 | a0001c0001t0007g0008 a0001c0001t0007g0039 a0001c0001t0007g0051 others(6): Show |
14 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.196+8282A>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35980168 | |||||||
| chr5:35980204 | T | C | 1 | a0001c0001t0008g0240 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.196+8246A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35980204 | |||||||
| chr5:35980319 | T | C | 2 | a0001c0001t0014g0007 a0001c0001t0014g0199 |
5 | HG01099.hp1 HG01884.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+8131A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35980319 | |||||||
| chr5:35980373 | C | T | 111 | a0001c0001t0001g0134 a0001c0001t0003g0116 a0001c0001t0003g0117 others(108): Show |
146 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.196+8077G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35980373 | |||||||
| chr5:35980522 | A | G | 1 | a0001c0001t0006g0148 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.196+7928T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35980522 | |||||||
| chr5:35980569 | T | A | 1 | a0001c0004t0005g0180 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.196+7881A>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35980569 | |||||||
| chr5:35980575 | A | G | 4 | a0003c0003t0004g0006 a0003c0003t0004g0046 a0003c0003t0004g0157 others(1): Show |
8 | HG02132.hp1 NA18971.hp2 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.196+7875T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35980575 | |||||||
| chr5:35980586 | C | G | 1 | a0006c0011t0017g0286 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.196+7864G>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35980586 | |||||||
| chr5:35980617 | C | T | 13 | a0001c0001t0001g0134 a0001c0001t0010g0014 a0001c0001t0010g0038 others(10): Show |
18 | HG00544.hp2 HG00621.hp2 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.196+7833G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35980617 | |||||||
| chr5:35980752 | C | A | 1 | a0007c0008t0034g0110 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.196+7698G>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35980752 | |||||||
| chr5:35981019 | C | A | 4 | a0003c0003t0004g0006 a0003c0003t0004g0046 a0003c0003t0004g0157 others(1): Show |
8 | HG02132.hp1 NA18971.hp2 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.196+7431G>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35981019 | |||||||
| chr5:35981082 | C | T | 91 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(88): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.196+7368G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35981082 | |||||||
| chr5:35981089 | T | C | 2 | a0001c0001t0004g0028 a0001c0001t0004g0067 |
3 | HG02723.hp1 HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.196+7361A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35981089 | |||||||
| chr5:35981176 | G | T | 1 | a0001c0001t0013g0204 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.196+7274C>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35981176 | |||||||
| chr5:35981233 | C | T | 4 | a0001c0001t0017g0109 a0001c0001t0017g0124 a0001c0001t0017g0125 others(1): Show |
4 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+7217G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35981233 | |||||||
| chr5:35981336 | G | C | 2 | a0001c0001t0009g0248 a0001c0001t0009g0249 |
2 | HG01256.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.196+7114C>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35981336 | |||||||
| chr5:35981509 | G | A | 2 | a0001c0001t0018g0209 a0001c0001t0019g0208 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.196+6941C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35981509 | |||||||
| chr5:35981511 | T | C | 1 | a0001c0001t0008g0022 | 3 | HG01070.hp1 HG01071.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.196+6939A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35981511 | |||||||
| chr5:35981649 | C | G | 3 | a0001c0001t0003g0117 a0001c0001t0003g0119 a0001c0001t0038g0118 |
3 | HG01192.hp1 HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.196+6801G>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35981649 | |||||||
| chr5:35981684 | G | T | 1 | a0001c0001t0023g0282 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.196+6766C>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35981684 | |||||||
| chr5:35981876 | A | G | 1 | a0001c0001t0004g0175 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.196+6574T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35981876 | |||||||
| chr5:35981897 | C | T | 6 | a0001c0001t0004g0206 a0001c0001t0004g0210 a0001c0001t0018g0209 others(3): Show |
6 | HG02486.hp2 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+6553G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35981897 | |||||||
| chr5:35981958 | C | T | 5 | a0002c0002t0001g0029 a0002c0002t0001g0031 a0002c0002t0001g0073 others(2): Show |
7 | HG02074.hp2 NA18947.hp2 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.196+6492G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35981958 | |||||||
| chr5:35982177 | T | A | 1 | a0001c0001t0004g0210 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.196+6273A>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35982177 | |||||||
| chr5:35982237 | A | G | 1 | a0002c0002t0029g0077 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.196+6213T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35982237 | |||||||
| chr5:35982272 | T | C | 6 | a0001c0001t0010g0014 a0001c0001t0010g0038 a0001c0001t0010g0111 others(3): Show |
9 | NA18612.hp1 NA18942.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.196+6178A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35982272 | |||||||
| chr5:35982358 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0239 |
3 | HG01975.hp2 HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.196+6092C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35982358 | |||||||
| chr5:35982391 | C | A | 46 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(43): Show |
59 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.196+6059G>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35982391 | |||||||
| chr5:35982539 | G | T | 9 | a0001c0001t0007g0008 a0001c0001t0007g0039 a0001c0001t0007g0051 others(6): Show |
14 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.196+5911C>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35982539 | |||||||
| chr5:35982564 | C | A | 1 | a0002c0002t0001g0093 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.196+5886G>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35982564 | |||||||
| chr5:35982573 | T | C | 2 | a0001c0001t0014g0007 a0001c0001t0014g0199 |
5 | HG01099.hp1 HG01884.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+5877A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35982573 | |||||||
| chr5:35982611 | C | T | 1 | a0001c0001t0003g0122 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.196+5839G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35982611 | |||||||
| chr5:35982713 | C | T | 1 | a0005c0007t0001g0095 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.196+5737G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35982713 | |||||||
| chr5:35982766 | G | A | 18 | a0001c0001t0003g0116 a0001c0001t0003g0117 a0001c0001t0003g0119 others(15): Show |
19 | HG01192.hp1 HG02145.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.196+5684C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35982766 | |||||||
| chr5:35982947 | T | A | 1 | a0002c0002t0001g0094 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.196+5503A>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35982947 | |||||||
| chr5:35982971 | T | A | 18 | a0001c0001t0003g0116 a0001c0001t0003g0117 a0001c0001t0003g0119 others(15): Show |
19 | HG01192.hp1 HG02145.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.196+5479A>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35982971 | |||||||
| chr5:35983135 | T | G | 1 | a0002c0002t0001g0073 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.196+5315A>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35983135 | |||||||
| chr5:35983181 | CA | C | 111 | a0001c0001t0001g0134 a0001c0001t0003g0116 a0001c0001t0003g0117 others(108): Show |
146 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.196+5268delT | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35983181 | |||||||
| chr5:35983327 | G | A | 6 | a0001c0001t0004g0206 a0001c0001t0004g0210 a0001c0001t0018g0209 others(3): Show |
6 | HG02486.hp2 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+5123C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35983327 | |||||||
| chr5:35983479 | C | T | 90 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(87): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.196+4971G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35983479 | |||||||
| chr5:35983550 | G | A | 20 | a0001c0001t0004g0206 a0001c0001t0004g0210 a0001c0001t0007g0008 others(17): Show |
29 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.196+4900C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35983550 | |||||||
| chr5:35983596 | A | G | 46 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(43): Show |
59 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.196+4854T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35983596 | |||||||
| chr5:35983656 | A | G | 1 | a0001c0001t0027g0131 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.196+4794T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35983656 | |||||||
| chr5:35983711 | G | A | 1 | a0001c0001t0023g0282 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.196+4739C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35983711 | |||||||
| chr5:35983781 | G | A | 3 | a0001c0006t0018g0052 a0001c0006t0018g0211 a0001c0006t0032g0212 |
4 | HG02451.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+4669C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35983781 | |||||||
| chr5:35983819 | G | A | 4 | a0001c0001t0013g0059 a0001c0001t0013g0277 a0001c0001t0013g0278 others(1): Show |
5 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+4631C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35983819 | |||||||
| chr5:35983861 | A | T | 1 | a0001c0001t0015g0280 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.196+4589T>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35983861 | |||||||
| chr5:35983903 | T | A | 1 | a0002c0002t0001g0074 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.196+4547A>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35983903 | |||||||
| chr5:35983951 | A | G | 202 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0134 others(199): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.196+4499T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35983951 | |||||||
| chr5:35984110 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.196+4340A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35984110 | |||||||
| chr5:35984141 | A | T | 1 | a0001c0001t0003g0121 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.196+4309T>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35984141 | |||||||
| chr5:35984301 | T | C | 1 | a0001c0001t0008g0240 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.196+4149A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35984301 | |||||||
| chr5:35984337 | T | C | 44 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0002g0002 others(41): Show |
68 | HG00140.hp1 HG00323.hp2 HG01074.hp1 others(65): Show |
intron_variant | MODIFIER | c.196+4113A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35984337 | |||||||
| chr5:35984449 | G | A | 1 | a0002c0002t0001g0035 | 2 | HG03491.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.196+4001C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35984449 | |||||||
| chr5:35984472 | A | AT | 103 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(100): Show |
165 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.196+3977dupA | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35984472 | |||||||
| chr5:35984472 | A | ATT | 93 | a0001c0001t0001g0019 a0001c0001t0003g0116 a0001c0001t0003g0117 others(90): Show |
123 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.196+3976_196+3977d others(4): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35984472 | |||||||
| chr5:35984472 | A | ATTT | 13 | a0001c0001t0001g0134 a0001c0001t0007g0051 a0001c0001t0007g0201 others(10): Show |
16 | HG00544.hp2 HG00621.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.196+3975_196+3977d others(5): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35984472 | |||||||
| chr5:35984472 | AT | A | 41 | a0001c0001t0001g0055 a0001c0001t0001g0198 a0001c0001t0001g0220 others(38): Show |
54 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.196+3977delA | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35984472 | |||||||
| chr5:35984476 | T | G | 4 | a0001c0001t0001g0129 a0001c0001t0005g0225 a0001c0001t0005g0226 others(1): Show |
4 | HG02132.hp2 HG02155.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+3974A>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35984476 | |||||||
| chr5:35984477 | T | G | 41 | a0001c0001t0001g0055 a0001c0001t0001g0198 a0001c0001t0001g0220 others(38): Show |
54 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.196+3973A>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35984477 | |||||||
| chr5:35984526 | G | T | 1 | a0001c0001t0023g0282 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.196+3924C>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35984526 | |||||||
| chr5:35984555 | C | T | 1 | a0006c0011t0017g0286 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.196+3895G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35984555 | |||||||
| chr5:35984571 | C | G | 90 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(87): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.196+3879G>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35984571 | |||||||
| chr5:35984640 | T | G | 45 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(42): Show |
58 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.196+3810A>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35984640 | |||||||
| chr5:35984691 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.196+3759A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35984691 | |||||||
| chr5:35984843 | G | A | 89 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(86): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.196+3607C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35984843 | |||||||
| chr5:35985060 | G | A | 1 | a0001c0001t0004g0175 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.196+3390C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35985060 | |||||||
| chr5:35985079 | T | TA | 35 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(32): Show |
58 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.196+3370dupT | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35985079 | |||||||
| chr5:35985079 | T | TAA | 28 | a0001c0001t0002g0108 a0001c0001t0002g0254 a0001c0001t0002g0255 others(25): Show |
34 | HG01081.hp2 HG01168.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.196+3369_196+3370d others(4): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35985079 | |||||||
| chr5:35985079 | T | TAAA | 101 | a0001c0001t0001g0134 a0001c0001t0001g0220 a0001c0001t0001g0267 others(98): Show |
147 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.196+3368_196+3370d others(5): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35985079 | |||||||
| chr5:35985079 | T | TAAAA | 51 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(48): Show |
66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.196+3367_196+3370d others(6): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35985079 | |||||||
| chr5:35985079 | T | TAAAAA | 6 | a0001c0001t0004g0206 a0001c0001t0004g0210 a0001c0001t0009g0250 others(3): Show |
6 | HG01175.hp2 HG02486.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+3366_196+3370d others(7): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35985079 | |||||||
| chr5:35985079 | T | TTAAA | 7 | a0001c0001t0007g0008 a0001c0001t0007g0039 a0001c0001t0007g0051 others(4): Show |
12 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.196+3370_196+3371i others(6): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35985079 | |||||||
| chr5:35985079 | TA | T | 8 | a0001c0001t0005g0160 a0001c0001t0006g0146 a0001c0001t0006g0147 others(5): Show |
10 | HG02109.hp2 HG02258.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.196+3370delT | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35985079 | |||||||
| chr5:35985092 | A | AG | 4 | a0001c0001t0017g0109 a0001c0001t0017g0124 a0001c0001t0017g0125 others(1): Show |
4 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+3357_196+3358i others(3): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35985092 | |||||||
| chr5:35985273 | C | T | 1 | a0001c0001t0014g0199 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.196+3177G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35985273 | |||||||
| chr5:35985276 | A | G | 1 | a0001c0001t0003g0216 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.196+3174T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35985276 | |||||||
| chr5:35985284 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(268): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.196+3166A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35985284 | |||||||
| chr5:35985293 | C | T | 39 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0002g0002 others(36): Show |
61 | HG00140.hp1 HG00323.hp2 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.196+3157G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35985293 | |||||||
| chr5:35985306 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.196+3144A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35985306 | |||||||
| chr5:35985489 | G | A | 1 | a0001c0001t0004g0193 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.196+2961C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35985489 | |||||||
| chr5:35986025 | A | C | 1 | a0003c0003t0004g0157 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.196+2425T>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35986025 | |||||||
| chr5:35986032 | A | G | 20 | a0001c0001t0004g0206 a0001c0001t0004g0210 a0001c0001t0007g0008 others(17): Show |
29 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.196+2418T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35986032 | |||||||
| chr5:35986148 | C | T | 14 | a0001c0001t0007g0008 a0001c0001t0007g0039 a0001c0001t0007g0051 others(11): Show |
23 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.196+2302G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35986148 | |||||||
| chr5:35986221 | T | C | 1 | a0001c0001t0013g0204 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.196+2229A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35986221 | |||||||
| chr5:35986354 | G | A | 3 | a0001c0001t0015g0025 a0001c0001t0015g0252 a0001c0001t0035g0253 |
5 | HG02257.hp1 HG03130.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+2096C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35986354 | |||||||
| chr5:35986525 | T | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(265): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.196+1925A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35986525 | |||||||
| chr5:35986551 | T | C | 1 | a0006c0011t0017g0286 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.196+1899A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35986551 | |||||||
| chr5:35986555 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.196+1895C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35986555 | |||||||
| chr5:35986633 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.196+1817C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35986633 | |||||||
| chr5:35986867 | T | C | 4 | a0001c0001t0017g0109 a0001c0001t0017g0124 a0001c0001t0017g0125 others(1): Show |
4 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+1583A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35986867 | |||||||
| chr5:35986894 | G | C | 2 | a0001c0001t0014g0007 a0001c0001t0014g0199 |
5 | HG01099.hp1 HG01884.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+1556C>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35986894 | |||||||
| chr5:35987330 | G | T | 2 | a0001c0001t0014g0007 a0001c0001t0014g0199 |
5 | HG01099.hp1 HG01884.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+1120C>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35987330 | |||||||
| chr5:35987435 | C | T | 1 | a0001c0001t0003g0215 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.196+1015G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35987435 | |||||||
| chr5:35987449 | G | A | 12 | a0001c0001t0005g0214 a0001c0001t0009g0023 a0001c0001t0009g0242 others(9): Show |
16 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.196+1001C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35987449 | |||||||
| chr5:35987479 | CA | C | 3 | a0001c0001t0015g0025 a0001c0001t0015g0252 a0001c0001t0035g0253 |
5 | HG02257.hp1 HG03130.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+970delT | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35987479 | |||||||
| chr5:35987517 | A | G | 13 | a0001c0001t0001g0134 a0001c0001t0010g0014 a0001c0001t0010g0038 others(10): Show |
18 | HG00544.hp2 HG00621.hp2 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.196+933T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35987517 | |||||||
| chr5:35987979 | G | A | 3 | a0001c0001t0004g0028 a0001c0001t0004g0067 a0001c0001t0023g0282 |
4 | HG01891.hp1 HG02723.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+471C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 2/6 | chr5 | 35987979 | |||||||
| chr5:35988684 | G | A | 3 | a0001c0006t0018g0052 a0001c0006t0018g0211 a0001c0006t0032g0212 |
4 | HG02451.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-133C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35988684 | |||||||
| chr5:35988753 | T | C | 1 | a0001c0001t0005g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.95-202A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35988753 | |||||||
| chr5:35988798 | G | T | 1 | a0001c0001t0005g0214 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.95-247C>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35988798 | |||||||
| chr5:35988848 | C | T | 68 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0198 others(65): Show |
90 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.95-297G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35988848 | |||||||
| chr5:35989103 | C | T | 1 | a0007c0008t0034g0110 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.95-552G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35989103 | |||||||
| chr5:35989110 | C | T | 1 | a0001c0001t0002g0251 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.95-559G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35989110 | |||||||
| chr5:35989176 | T | C | 1 | a0002c0002t0001g0013 | 3 | NA18956.hp1 NA18966.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.95-625A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35989176 | |||||||
| chr5:35989358 | A | G | 1 | a0001c0001t0003g0116 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.95-807T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35989358 | |||||||
| chr5:35989508 | T | C | 1 | a0002c0002t0001g0104 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.95-957A>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35989508 | |||||||
| chr5:35989637 | C | T | 201 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0134 others(198): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.95-1086G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35989637 | |||||||
| chr5:35989704 | C | T | 55 | a0001c0001t0002g0056 a0002c0002t0001g0005 a0002c0002t0001g0010 others(52): Show |
76 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.95-1153G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35989704 | |||||||
| chr5:35989887 | A | G | 77 | a0001c0001t0002g0056 a0001c0001t0003g0116 a0001c0001t0003g0117 others(74): Show |
99 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.94+1260T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35989887 | |||||||
| chr5:35990043 | G | T | 5 | a0001c0001t0004g0060 a0001c0001t0004g0061 a0001c0001t0004g0062 others(2): Show |
5 | HG02145.hp2 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+1104C>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35990043 | |||||||
| chr5:35990091 | C | CA | 20 | a0001c0001t0001g0050 a0001c0001t0003g0116 a0001c0001t0003g0117 others(17): Show |
23 | HG01192.hp1 HG01243.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.94+1055dupT | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35990091 | |||||||
| chr5:35990091 | C | CAA | 8 | a0001c0001t0001g0129 a0001c0001t0001g0134 a0001c0001t0003g0128 others(5): Show |
10 | HG00544.hp2 HG00621.hp2 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+1054_94+1055dup others(2): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35990091 | |||||||
| chr5:35990097 | A | G | 50 | a0001c0001t0001g0055 a0001c0001t0001g0198 a0001c0001t0001g0220 others(47): Show |
63 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.94+1050T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35990097 | |||||||
| chr5:35990105 | A | AG | 58 | a0001c0001t0004g0060 a0001c0001t0004g0061 a0001c0001t0004g0062 others(55): Show |
78 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.94+1041_94+1042ins others(1): Show |
UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35990105 | |||||||
| chr5:35990105 | A | G | 123 | a0001c0001t0001g0040 a0001c0001t0001g0055 a0001c0001t0001g0140 others(120): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.94+1042T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35990105 | |||||||
| chr5:35990211 | C | T | 54 | a0002c0002t0001g0005 a0002c0002t0001g0010 a0002c0002t0001g0011 others(51): Show |
74 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.94+936G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35990211 | |||||||
| chr5:35990269 | A | G | 10 | a0001c0001t0007g0008 a0001c0001t0007g0051 a0001c0001t0007g0200 others(7): Show |
17 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.94+878T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35990269 | |||||||
| chr5:35990306 | C | T | 19 | a0001c0001t0004g0206 a0001c0001t0004g0210 a0001c0001t0007g0008 others(16): Show |
27 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.94+841G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35990306 | |||||||
| chr5:35990338 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.94+809T>C | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35990338 | |||||||
| chr5:35990443 | C | A | 1 | a0001c0001t0002g0283 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.94+704G>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35990443 | |||||||
| chr5:35990581 | A | C | 203 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0134 others(200): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.94+566T>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35990581 | |||||||
| chr5:35990656 | C | T | 1 | a0002c0002t0001g0068 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.94+491G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35990656 | |||||||
| chr5:35990935 | G | A | 1 | a0001c0001t0002g0285 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.94+212C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35990935 | |||||||
| chr5:35990937 | G | A | 1 | a0006c0011t0017g0286 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.94+210C>T | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35990937 | |||||||
| chr5:35990937 | G | C | 109 | a0001c0001t0001g0055 a0001c0001t0001g0198 a0001c0001t0001g0220 others(106): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.94+210C>G | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35990937 | |||||||
| chr5:35991106 | C | T | 9 | a0001c0001t0004g0028 a0001c0001t0004g0060 a0001c0001t0004g0061 others(6): Show |
10 | HG02145.hp2 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.94+41G>A | UGT3A1 | ENSG00000145626.12 | transcript | ENST00000274278.8 | protein_coding | 1/6 | chr5 | 35991106 |