Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1577 |
| ensemblid | ENSG00000106258.16 |
| hgncid | 2638 |
| symbol | CYP3A5 |
| name | cytochrome P450 family 3 subfamily A member 5 |
| refseq_nuc | NM_000777.5 |
| refseq_prot | NP_000768.1 |
| ensembl_nuc | ENST00000222982.8 |
| ensembl_prot | ENSP00000222982.4 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 99648194 |
| end | 99679996 |
| strand | - |
| ver | v1.2 |
| region | chr7:99648194-99679996 |
| region5000 | chr7:99643194-99684996 |
| regionname0 | CYP3A5_chr7_99648194_99679996 |
| regionname5000 | CYP3A5_chr7_99643194_99684996 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 502 | 270 | 77 | 31 | 117 | 7 | 37 | 93 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | MDLIP others(497): Show |
chr7 | 99643194 | 99684996 |
| a0002 | 0/0 | 347 | 14 | 14 | 0 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | MDLIP others(342): Show |
chr7 | 99643194 | 99684996 |
| a0003 | 0/1 | 502 | 3 | 0 | 0 | 0 | 1 | 1 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | MDLIP others(497): Show |
chr7 | 99643194 | 99684996 |
| a0004 | 0/0 | 502 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | MDLIP others(497): Show |
chr7 | 99643194 | 99684996 |
| a0005 | 0/0 | 373 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | MDLIP others(368): Show |
chr7 | 99643194 | 99684996 |
| a0006 | 0/0 | 502 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | MDLIP others(497): Show |
chr7 | 99643194 | 99684996 |
| a0007 | 0/0 | 502 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | MDLIP others(497): Show |
chr7 | 99643194 | 99684996 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1506 | 252 | 62 | 29 | 117 | 6 | 37 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | ATGGA others(1501): Show |
chr7 | 99643194 | 99684996 | ||
| a0001c0002 | 0/0 | 1506 | 14 | 12 | 2 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | ATGGA others(1501): Show |
chr7 | 99643194 | 99684996 | ||
| a0001c0004 | 0/0 | 1506 | 3 | 3 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | ATGGA others(1501): Show |
chr7 | 99643194 | 99684996 | ||
| a0001c0007 | 0/0 | 1506 | 1 | 0 | 0 | 0 | 1 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | ATGGA others(1501): Show |
chr7 | 99643194 | 99684996 | ||
| a0002c0003 | 0/0 | 1507 | 14 | 14 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | ATGGA others(1502): Show |
chr7 | 99643194 | 99684996 | ||
| a0003c0006 | 0/1 | 1506 | 2 | 0 | 0 | 0 | 1 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | ATGGA others(1501): Show |
chr7 | 99643194 | 99684996 | ||
| a0003c0011 | 0/0 | 1506 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | ATGGA others(1501): Show |
chr7 | 99643194 | 99684996 | ||
| a0004c0005 | 0/0 | 1506 | 2 | 0 | 1 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | ATGGA others(1501): Show |
chr7 | 99643194 | 99684996 | ||
| a0005c0008 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | ATGGA others(1114): Show |
chr7 | 99643194 | 99684996 | ||
| a0006c0010 | 0/0 | 1506 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | ATGGA others(1501): Show |
chr7 | 99643194 | 99684996 | ||
| a0007c0009 | 0/0 | 1506 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | ATGGA others(1501): Show |
chr7 | 99643194 | 99684996 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1720 | 119 | 38 | 6 | 56 | 2 | 17 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | GCTGT others(1715): Show |
chr7 | 99643194 | 99684996 |
| a0001c0001t0002 | 1/0 | 1720 | 131 | 24 | 23 | 61 | 4 | 18 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | GCTGT others(1715): Show |
chr7 | 99643194 | 99684996 |
| a0001c0001t0003 | 0/0 | 1720 | 2 | 0 | 0 | 0 | 0 | 2 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | GCTGT others(1715): Show |
chr7 | 99643194 | 99684996 |
| a0001c0002t0001 | 0/0 | 1720 | 14 | 12 | 2 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | GCTGT others(1715): Show |
chr7 | 99643194 | 99684996 |
| a0001c0004t0001 | 0/0 | 1720 | 3 | 3 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | GCTGT others(1715): Show |
chr7 | 99643194 | 99684996 |
| a0001c0007t0002 | 0/0 | 1720 | 1 | 0 | 0 | 0 | 1 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | GCTGT others(1715): Show |
chr7 | 99643194 | 99684996 |
| a0002c0003t0001 | 0/0 | 1721 | 14 | 14 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | GCTGT others(1716): Show |
chr7 | 99643194 | 99684996 |
| a0003c0006t0002 | 0/1 | 1720 | 2 | 0 | 0 | 0 | 1 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | GCTGT others(1715): Show |
chr7 | 99643194 | 99684996 |
| a0003c0011t0002 | 0/0 | 1720 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | GCTGT others(1715): Show |
chr7 | 99643194 | 99684996 |
| a0004c0005t0002 | 0/0 | 1720 | 2 | 0 | 1 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | GCTGT others(1715): Show |
chr7 | 99643194 | 99684996 |
| a0005c0008t0001 | 0/0 | 1333 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | GCTGT others(1328): Show |
chr7 | 99643194 | 99684996 |
| a0006c0010t0002 | 0/0 | 1720 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | GCTGT others(1715): Show |
chr7 | 99643194 | 99684996 |
| a0007c0009t0002 | 0/0 | 1720 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | GCTGT others(1715): Show |
chr7 | 99643194 | 99684996 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0001 | 0/0 | 18 | 0 | 4 | 12 | 0 | 2 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0011 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0105 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0001t0003g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0002t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0004t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0001c0007t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0002c0003t0001g0002 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0002c0003t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0002c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0002c0003t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0002c0003t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0002c0003t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0003c0006t0002g0207 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0003c0006t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0003c0011t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0004c0005t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0004c0005t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0005c0008t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0006c0010t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| a0007c0009t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0199 | EUR | GBR | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0145 | EUR | GBR | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0056 | EUR | FIN | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | FIN | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | CHS | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | CHS | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | CHS | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG00642 | hp2 | a0004 | c0005 | t0002 | g0205 | AMR | PUR | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | CHS | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0182 | AMR | PUR | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0181 | AMR | PUR | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | CLM | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | CLM | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | CLM | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01515 | hp1 | a0001 | c0007 | t0002 | g0114 | EUR | IBS | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01515 | hp2 | a0003 | c0006 | t0002 | g0208 | EUR | IBS | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0196 | AFR | ACB | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PEL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PEL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | PEL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | PEL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | ACB | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02055 | hp2 | a0002 | c0003 | t0001 | g0046 | AFR | ACB | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | KHV | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | KHV | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02257 | hp1 | a0002 | c0003 | t0001 | g0014 | AFR | ACB | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | ACB | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0102 | AFR | ACB | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0170 | AFR | ACB | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | ACB | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0184 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0148 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0176 | SAS | PJL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0175 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02630 | hp1 | a0002 | c0003 | t0001 | g0002 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02717 | hp1 | a0002 | c0003 | t0001 | g0002 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0179 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02723 | hp2 | a0002 | c0003 | t0001 | g0002 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02738 | hp2 | a0003 | c0011 | t0002 | g0209 | SAS | PJL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02886 | hp2 | a0005 | c0008 | t0001 | g0180 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02895 | hp1 | a0002 | c0003 | t0001 | g0014 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | ESN | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02965 | hp1 | a0002 | c0003 | t0001 | g0002 | AFR | ESN | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02970 | hp1 | a0001 | c0004 | t0001 | g0007 | AFR | ESN | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | ESN | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0101 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0183 | AFR | MSL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | MSL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03139 | hp1 | a0002 | c0003 | t0001 | g0002 | AFR | ESN | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | ESN | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | ESN | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | PJL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | MSL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03486 | hp1 | a0002 | c0003 | t0001 | g0058 | AFR | MSL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0169 | AFR | ESN | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03540 | hp2 | a0002 | c0003 | t0001 | g0002 | AFR | GWD | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | MSL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03654 | hp1 | a0004 | c0005 | t0002 | g0206 | SAS | PJL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0043 | SAS | PJL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0043 | SAS | PJL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | STU | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | STU | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0151 | SAS | BEB | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | BEB | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | STU | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0012 | SAS | STU | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | BEB | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0161 | SAS | STU | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | STU | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG04204 | hp2 | a0006 | c0010 | t0002 | g0147 | SAS | STU | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | STU | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | STU | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | YRI | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18522 | hp2 | a0002 | c0003 | t0001 | g0002 | AFR | YRI | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | YRI | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | LWK | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | LWK | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | LWK | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | LWK | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19054 | hp1 | a0007 | c0009 | t0002 | g0129 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA19240 | hp2 | a0001 | c0004 | t0001 | g0007 | AFR | YRI | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA20129 | hp1 | a0002 | c0003 | t0001 | g0002 | AFR | ASW | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ASW | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0116 | EUR | TSI | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0039 | EUR | TSI | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | GIH | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | GIH | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | CLM | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | CLM | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02486 | hp1 | a0002 | c0003 | t0001 | g0193 | AFR | ACB | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0107 | AFR | ACB | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03471 | hp1 | a0002 | c0003 | t0001 | g0195 | AFR | MSL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | USA | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| HG06807 | hp2 | a0001 | c0004 | t0001 | g0007 | AFR | USA | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0006 | t0002 | g0207 | REF | REF | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0105 | REF | REF | CYP3A5_chr7_99643194_99684996 | CYP3A5 | chr7 | 99643194 | 99684996 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:99648651 | CTTGTGGA others(8479): Show |
C | 1 | a0005 | 1 | HG02886.hp2 | exon_loss_variant | HIGH | c.1026+3362_1414-252 others(3): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 12/13 | chr7 | 99648651 | |||||||
| chr7:99650179 | G | C | 1 | a0004 | 2 | HG00642.hp2 HG03654.hp1 |
missense_variant | MODERATE | c.1307C>G | p.Thr436Ser | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 12/13 | 1407/1720 | 1307/1509 | 436/502 | chr7 | 99650179 | |||
| chr7:99652770 | T | TA | 1 | a0002 | 14 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(11): Show |
frameshift_variant | HIGH | c.1035dupT | p.Thr346fs | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 11/13 | 1135/1720 | 1035/1509 | 345/502 | chr7 | 99652770 | |||
| chr7:99660585 | G | T | 1 | a0007 | 1 | NA19054.hp1 | missense_variant | MODERATE | c.940C>A | p.Leu314Ile | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/13 | 1040/1720 | 940/1509 | 314/502 | chr7 | 99660585 | |||
| chr7:99666601 | T | C | 1 | a0006 | 1 | HG04204.hp2 | missense_variant&splice_region_variant | MODERATE | c.521A>G | p.Asp174Gly | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 6/13 | 621/1720 | 521/1509 | 174/502 | chr7 | 99666601 | |||
| chr7:99676192 | G | A | 1 | a0003 | 3 | HG01515.hp2 HG02738.hp2 homoSapiens_chm13v2.hp1 |
missense_variant | MODERATE | c.88C>T | p.His30Tyr | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/13 | 188/1720 | 88/1509 | 30/502 | chr7 | 99676192 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:99665182 | T | C | 1 | a0001c0004 | 3 | HG02970.hp1 HG06807.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.654A>G | p.Pro218Pro | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 7/13 | 754/1720 | 654/1509 | 218/502 | chr7 | 99665182 | |||
| chr7:99665212 | C | T | 2 | a0001c0002 a0005c0008 |
15 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(12): Show |
synonymous_variant | LOW | c.624G>A | p.Lys208Lys | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 7/13 | 724/1720 | 624/1509 | 208/502 | chr7 | 99665212 | |||
| chr7:99666990 | A | G | 1 | a0001c0007 | 1 | HG01515.hp1 | synonymous_variant | LOW | c.394T>C | p.Leu132Leu | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 5/13 | 494/1720 | 394/1509 | 132/502 | chr7 | 99666990 | |||
| chr7:99672613 | C | A | 1 | a0003c0011 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.285G>T | p.Val95Val | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/13 | 385/1720 | 285/1509 | 95/502 | chr7 | 99672613 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:99648291 | A | G | 5 | a0001c0001t0001 a0001c0002t0001 a0001c0004t0001 others(2): Show |
151 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*14T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 13/13 | 14 | chr7 | 99648291 | ||||||
| chr7:99679970 | G | A | 1 | a0001c0001t0003 | 2 | HG03654.hp2 HG03669.hp1 |
5_prime_UTR_variant | MODIFIER | c.-74C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/13 | 74 | chr7 | 99679970 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:99648403 | A | G | 1 | a0001c0001t0002g0131 | 1 | HG03540.hp1 | splice_region_variant&intron_variant | LOW | c.1414-3T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 12/12 | chr7 | 99648403 | |||||||
| chr7:99648664 | G | GT | 13 | a0001c0001t0001g0063 a0001c0002t0001g0013 a0001c0002t0001g0101 others(10): Show |
15 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1414-265dupA | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 12/12 | chr7 | 99648664 | |||||||
| chr7:99648664 | GT | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0004t0001g0007 |
7 | HG02647.hp1 HG02970.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1414-265delA | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 12/12 | chr7 | 99648664 | |||||||
| chr7:99648865 | C | T | 2 | a0001c0001t0001g0020 a0001c0004t0001g0007 |
5 | HG02970.hp1 HG03225.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1414-465G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 12/12 | chr7 | 99648865 | |||||||
| chr7:99649017 | A | G | 1 | a0001c0001t0002g0126 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1414-617T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 12/12 | chr7 | 99649017 | |||||||
| chr7:99649084 | A | T | 2 | a0001c0001t0002g0116 a0001c0001t0002g0117 |
2 | HG04228.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1414-684T>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 12/12 | chr7 | 99649084 | |||||||
| chr7:99649106 | A | G | 1 | a0001c0001t0002g0131 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1414-706T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 12/12 | chr7 | 99649106 | |||||||
| chr7:99649202 | C | T | 1 | a0001c0001t0002g0144 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1414-802G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 12/12 | chr7 | 99649202 | |||||||
| chr7:99649205 | A | T | 1 | a0001c0001t0002g0144 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1414-805T>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 12/12 | chr7 | 99649205 | |||||||
| chr7:99649369 | A | G | 12 | a0001c0002t0001g0013 a0001c0002t0001g0101 a0001c0002t0001g0107 others(9): Show |
14 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1413+704T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 12/12 | chr7 | 99649369 | |||||||
| chr7:99649506 | C | T | 1 | a0001c0001t0002g0143 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1413+567G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 12/12 | chr7 | 99649506 | |||||||
| chr7:99649879 | CT | C | 7 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0060 others(4): Show |
11 | HG01884.hp1 HG02451.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.1413+193delA | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 12/12 | chr7 | 99649879 | |||||||
| chr7:99650013 | A | T | 1 | a0001c0001t0001g0197 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1413+60T>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 12/12 | chr7 | 99650013 | |||||||
| chr7:99650332 | AACCAGTA others(11): Show |
A | 1 | a0001c0001t0001g0031 | 2 | HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1254-118_1254-101d others(20): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 11/12 | chr7 | 99650332 | |||||||
| chr7:99650380 | C | G | 1 | a0001c0001t0001g0190 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1254-148G>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 11/12 | chr7 | 99650380 | |||||||
| chr7:99650681 | C | T | 20 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(17): Show |
25 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.1254-449G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 11/12 | chr7 | 99650681 | |||||||
| chr7:99650975 | T | G | 63 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(60): Show |
87 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1254-743A>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 11/12 | chr7 | 99650975 | |||||||
| chr7:99651119 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0106 |
3 | HG01884.hp2 HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1254-887C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 11/12 | chr7 | 99651119 | |||||||
| chr7:99651260 | A | G | 3 | a0001c0001t0001g0020 a0001c0001t0002g0061 a0001c0004t0001g0007 |
6 | HG02615.hp1 HG02970.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1254-1028T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 11/12 | chr7 | 99651260 | |||||||
| chr7:99651316 | A | G | 1 | a0001c0001t0002g0125 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1254-1084T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 11/12 | chr7 | 99651316 | |||||||
| chr7:99651318 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1254-1086C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 11/12 | chr7 | 99651318 | |||||||
| chr7:99651597 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1253+956G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 11/12 | chr7 | 99651597 | |||||||
| chr7:99651607 | A | G | 1 | a0001c0001t0002g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1253+946T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 11/12 | chr7 | 99651607 | |||||||
| chr7:99651614 | C | T | 4 | a0001c0001t0001g0040 a0001c0001t0001g0188 a0001c0001t0001g0189 others(1): Show |
5 | HG02647.hp1 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1253+939G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 11/12 | chr7 | 99651614 | |||||||
| chr7:99651649 | A | G | 1 | a0001c0001t0002g0135 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1253+904T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 11/12 | chr7 | 99651649 | |||||||
| chr7:99651944 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1253+609C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 11/12 | chr7 | 99651944 | |||||||
| chr7:99652376 | G | A | 15 | a0001c0001t0001g0041 a0001c0001t0001g0192 a0001c0001t0001g0194 others(12): Show |
24 | HG00099.hp1 HG02055.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.1253+177C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 11/12 | chr7 | 99652376 | |||||||
| chr7:99652381 | G | GT | 2 | a0001c0001t0001g0031 a0001c0001t0001g0106 |
3 | HG01884.hp2 HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1253+171dupA | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 11/12 | chr7 | 99652381 | |||||||
| chr7:99652412 | A | T | 1 | a0001c0001t0002g0036 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1253+141T>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 11/12 | chr7 | 99652412 | |||||||
| chr7:99652485 | T | G | 1 | a0001c0001t0001g0199 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1253+68A>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 11/12 | chr7 | 99652485 | |||||||
| chr7:99652852 | T | C | 6 | a0001c0001t0002g0011 a0001c0001t0002g0113 a0001c0001t0002g0138 others(3): Show |
8 | HG00099.hp2 HG01070.hp2 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.1027-73A>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99652852 | |||||||
| chr7:99653343 | C | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0047 |
3 | HG02896.hp2 HG02897.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1027-564G>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99653343 | |||||||
| chr7:99653450 | C | CAAAT | 88 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0020 others(85): Show |
126 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1027-675_1027-672d others(6): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99653450 | |||||||
| chr7:99653450 | C | CAAATAAA others(1): Show |
112 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(109): Show |
153 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.1027-679_1027-672d others(10): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99653450 | |||||||
| chr7:99653450 | C | CAAATAAA others(5): Show |
3 | a0001c0001t0001g0041 a0001c0001t0002g0039 a0001c0001t0002g0116 |
5 | HG04228.hp1 NA19054.hp2 NA19075.hp2 others(2): Show |
intron_variant | MODIFIER | c.1027-683_1027-672d others(14): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99653450 | |||||||
| chr7:99653450 | C | CAAATAAA others(9): Show |
1 | a0001c0001t0001g0075 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1027-687_1027-672d others(18): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99653450 | |||||||
| chr7:99653450 | CAAATAAA others(1): Show |
C | 3 | a0001c0001t0002g0119 a0001c0001t0002g0137 a0001c0001t0002g0210 |
3 | NA18944.hp1 NA18979.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1027-679_1027-672d others(10): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99653450 | |||||||
| chr7:99653450 | CAAATAAA others(9): Show |
C | 1 | a0001c0001t0002g0139 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1027-687_1027-672d others(18): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99653450 | |||||||
| chr7:99653522 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1027-743C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99653522 | |||||||
| chr7:99653924 | A | G | 4 | a0001c0001t0001g0040 a0001c0001t0001g0188 a0001c0001t0001g0189 others(1): Show |
5 | HG02647.hp1 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1027-1145T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99653924 | |||||||
| chr7:99653968 | G | C | 1 | a0001c0001t0001g0019 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1027-1189C>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99653968 | |||||||
| chr7:99654050 | A | C | 9 | a0001c0001t0001g0108 a0001c0001t0002g0006 a0001c0001t0002g0021 others(6): Show |
13 | HG01884.hp1 HG02451.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1027-1271T>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99654050 | |||||||
| chr7:99654082 | T | TG | 4 | a0001c0001t0001g0040 a0001c0001t0001g0188 a0001c0001t0001g0189 others(1): Show |
5 | HG02647.hp1 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1027-1304dupC | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99654082 | |||||||
| chr7:99654084 | A | G | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(109): Show |
157 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1027-1305T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99654084 | |||||||
| chr7:99654085 | A | T | 4 | a0001c0001t0001g0040 a0001c0001t0001g0188 a0001c0001t0001g0189 others(1): Show |
5 | HG02647.hp1 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1027-1306T>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99654085 | |||||||
| chr7:99654105 | A | C | 1 | a0001c0001t0001g0052 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1027-1326T>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99654105 | |||||||
| chr7:99654128 | C | G | 3 | a0001c0001t0001g0020 a0001c0001t0002g0061 a0001c0004t0001g0007 |
6 | HG02615.hp1 HG02970.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1027-1349G>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99654128 | |||||||
| chr7:99654128 | C | T | 1 | a0001c0001t0002g0142 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1027-1349G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99654128 | |||||||
| chr7:99654245 | A | C | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(116): Show |
165 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.1027-1466T>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99654245 | |||||||
| chr7:99654286 | G | GA | 10 | a0001c0001t0001g0041 a0001c0001t0001g0192 a0001c0001t0001g0194 others(7): Show |
11 | HG00099.hp1 HG02523.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1027-1508_1027-150 others(5): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99654286 | |||||||
| chr7:99654313 | C | T | 6 | a0001c0001t0001g0009 a0001c0001t0001g0069 a0001c0001t0001g0071 others(3): Show |
8 | HG01099.hp2 HG01192.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.1027-1534G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99654313 | |||||||
| chr7:99654358 | T | C | 7 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0060 others(4): Show |
11 | HG01884.hp1 HG02451.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.1027-1579A>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99654358 | |||||||
| chr7:99654402 | G | T | 1 | a0001c0001t0002g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1027-1623C>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99654402 | |||||||
| chr7:99654523 | A | G | 1 | a0001c0001t0002g0036 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1027-1744T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99654523 | |||||||
| chr7:99654552 | G | C | 1 | a0001c0001t0002g0123 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1027-1773C>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99654552 | |||||||
| chr7:99654556 | G | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(114): Show |
163 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.1027-1777C>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99654556 | |||||||
| chr7:99654768 | C | T | 3 | a0001c0001t0002g0006 a0001c0001t0002g0186 a0001c0001t0002g0187 |
6 | HG01884.hp1 HG02922.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1027-1989G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99654768 | |||||||
| chr7:99655013 | T | C | 4 | a0001c0001t0002g0125 a0001c0001t0002g0127 a0001c0001t0002g0146 others(1): Show |
4 | HG02040.hp1 HG02080.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.1027-2234A>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99655013 | |||||||
| chr7:99655194 | G | A | 2 | a0001c0001t0002g0037 a0001c0001t0002g0139 |
3 | NA18948.hp1 NA18999.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1027-2415C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99655194 | |||||||
| chr7:99655428 | A | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0098 |
2 | HG02523.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1027-2649T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99655428 | |||||||
| chr7:99655507 | T | C | 1 | a0001c0001t0002g0211 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1027-2728A>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99655507 | |||||||
| chr7:99655559 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1027-2780G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99655559 | |||||||
| chr7:99655605 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1027-2826C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99655605 | |||||||
| chr7:99655627 | T | C | 1 | a0001c0001t0002g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1027-2848A>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99655627 | |||||||
| chr7:99655841 | A | C | 1 | a0001c0001t0002g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1027-3062T>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99655841 | |||||||
| chr7:99655934 | C | G | 54 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(51): Show |
75 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1027-3155G>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99655934 | |||||||
| chr7:99655987 | G | A | 2 | a0001c0002t0001g0101 a0001c0002t0001g0196 |
2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1027-3208C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99655987 | |||||||
| chr7:99656012 | A | G | 16 | a0001c0001t0001g0041 a0001c0001t0001g0192 a0001c0001t0001g0194 others(13): Show |
25 | HG00099.hp1 HG02055.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1027-3233T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99656012 | |||||||
| chr7:99656229 | G | T | 1 | a0001c0001t0002g0141 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1027-3450C>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99656229 | |||||||
| chr7:99656354 | G | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(103): Show |
148 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.1027-3575C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99656354 | |||||||
| chr7:99656556 | T | A | 1 | a0001c0001t0002g0160 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1027-3777A>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99656556 | |||||||
| chr7:99656692 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1026+3807G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99656692 | |||||||
| chr7:99656825 | G | A | 1 | a0003c0011t0002g0209 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1026+3674C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99656825 | |||||||
| chr7:99656879 | A | G | 1 | a0001c0001t0001g0192 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1026+3620T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99656879 | |||||||
| chr7:99656908 | C | G | 1 | a0001c0001t0001g0015 | 2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1026+3591G>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99656908 | |||||||
| chr7:99657055 | G | A | 1 | a0001c0001t0002g0140 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1026+3444C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99657055 | |||||||
| chr7:99657834 | G | A | 1 | a0001c0001t0002g0155 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1026+2665C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99657834 | |||||||
| chr7:99657897 | G | T | 10 | a0001c0002t0001g0013 a0001c0002t0001g0101 a0001c0002t0001g0107 others(7): Show |
12 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1026+2602C>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99657897 | |||||||
| chr7:99657905 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1026+2594G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99657905 | |||||||
| chr7:99657962 | T | G | 1 | a0001c0001t0002g0113 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1026+2537A>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99657962 | |||||||
| chr7:99658014 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1026+2485G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99658014 | |||||||
| chr7:99658137 | A | G | 109 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(106): Show |
151 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1026+2362T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99658137 | |||||||
| chr7:99658149 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0031 a0001c0001t0001g0106 |
5 | HG01884.hp2 HG02559.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1026+2350C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99658149 | |||||||
| chr7:99658262 | T | G | 10 | a0001c0002t0001g0013 a0001c0002t0001g0101 a0001c0002t0001g0107 others(7): Show |
12 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1026+2237A>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99658262 | |||||||
| chr7:99658316 | T | G | 1 | a0001c0001t0001g0063 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1026+2183A>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99658316 | |||||||
| chr7:99658347 | G | A | 1 | a0002c0003t0001g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1026+2152C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99658347 | |||||||
| chr7:99658468 | T | C | 1 | a0001c0004t0001g0007 | 3 | HG02970.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1026+2031A>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99658468 | |||||||
| chr7:99658471 | G | C | 1 | a0001c0004t0001g0007 | 3 | HG02970.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1026+2028C>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99658471 | |||||||
| chr7:99658472 | T | C | 1 | a0001c0004t0001g0007 | 3 | HG02970.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1026+2027A>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99658472 | |||||||
| chr7:99658473 | G | C | 1 | a0001c0004t0001g0007 | 3 | HG02970.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1026+2026C>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99658473 | |||||||
| chr7:99658595 | G | T | 16 | a0001c0001t0001g0041 a0001c0001t0001g0192 a0001c0001t0001g0194 others(13): Show |
25 | HG00099.hp1 HG02055.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1026+1904C>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99658595 | |||||||
| chr7:99658620 | T | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0106 |
3 | HG01884.hp2 HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1026+1879A>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99658620 | |||||||
| chr7:99658727 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1026+1772G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99658727 | |||||||
| chr7:99658787 | A | G | 1 | a0001c0004t0001g0007 | 3 | HG02970.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1026+1712T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99658787 | |||||||
| chr7:99658815 | T | G | 89 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(86): Show |
119 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.1026+1684A>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99658815 | |||||||
| chr7:99658933 | C | T | 2 | a0001c0001t0002g0060 a0001c0001t0002g0062 |
2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1026+1566G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99658933 | |||||||
| chr7:99659143 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1026+1356T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99659143 | |||||||
| chr7:99659221 | A | G | 109 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(106): Show |
151 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1026+1278T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99659221 | |||||||
| chr7:99659298 | A | G | 1 | a0001c0001t0002g0140 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1026+1201T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99659298 | |||||||
| chr7:99659374 | G | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1026+1125C>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99659374 | |||||||
| chr7:99659485 | A | G | 3 | a0001c0002t0001g0169 a0001c0002t0001g0170 a0001c0002t0001g0175 |
3 | HG02451.hp1 HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1026+1014T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99659485 | |||||||
| chr7:99659495 | G | T | 1 | a0001c0001t0001g0190 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1026+1004C>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99659495 | |||||||
| chr7:99659499 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1026+1000G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99659499 | |||||||
| chr7:99659510 | T | A | 4 | a0001c0002t0001g0181 a0001c0002t0001g0182 a0001c0002t0001g0183 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026+989A>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99659510 | |||||||
| chr7:99659533 | TGAG | T | 7 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0060 others(4): Show |
11 | HG01884.hp1 HG02451.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.1026+963_1026+965d others(5): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99659533 | |||||||
| chr7:99659605 | C | G | 2 | a0001c0001t0002g0165 a0001c0001t0002g0167 |
2 | NA18959.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1026+894G>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99659605 | |||||||
| chr7:99659796 | T | C | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(107): Show |
152 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.1026+703A>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99659796 | |||||||
| chr7:99659849 | T | TCCATGGG others(16): Show |
3 | a0001c0001t0002g0021 a0001c0001t0002g0060 a0001c0001t0002g0062 |
4 | HG02451.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026+627_1026+649d others(25): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99659849 | |||||||
| chr7:99659858 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1026+641C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99659858 | |||||||
| chr7:99659880 | C | T | 1 | a0001c0001t0002g0034 | 2 | NA19004.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1026+619G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99659880 | |||||||
| chr7:99659971 | G | A | 1 | a0001c0001t0002g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1026+528C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99659971 | |||||||
| chr7:99660008 | C | T | 1 | a0001c0001t0002g0034 | 2 | NA19004.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1026+491G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99660008 | |||||||
| chr7:99660092 | T | G | 1 | a0001c0001t0002g0159 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1026+407A>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99660092 | |||||||
| chr7:99660133 | A | T | 7 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0060 others(4): Show |
11 | HG01884.hp1 HG02451.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.1026+366T>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99660133 | |||||||
| chr7:99660163 | G | C | 3 | a0001c0001t0001g0020 a0001c0001t0002g0061 a0001c0004t0001g0007 |
6 | HG02615.hp1 HG02970.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026+336C>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99660163 | |||||||
| chr7:99660214 | C | CT | 32 | a0001c0001t0001g0018 a0001c0001t0001g0040 a0001c0001t0001g0050 others(29): Show |
43 | HG00280.hp1 HG00621.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.1026+284dupA | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99660214 | |||||||
| chr7:99660214 | C | CTTTT | 22 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0026 others(19): Show |
30 | HG00408.hp1 HG02040.hp2 HG02071.hp1 others(27): Show |
intron_variant | MODIFIER | c.1026+281_1026+284d others(6): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99660214 | |||||||
| chr7:99660214 | C | CTTTTT | 16 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(13): Show |
25 | HG00597.hp2 HG01099.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1026+280_1026+284d others(7): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99660214 | |||||||
| chr7:99660214 | C | CTTTTTT | 10 | a0001c0001t0001g0022 a0001c0001t0001g0063 a0001c0001t0001g0067 others(7): Show |
11 | HG00621.hp2 HG01192.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.1026+279_1026+284d others(8): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99660214 | |||||||
| chr7:99660214 | CT | C | 18 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0002g0021 others(15): Show |
24 | HG01169.hp1 HG01891.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.1026+284delA | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99660214 | |||||||
| chr7:99660214 | CTT | C | 4 | a0001c0001t0002g0006 a0001c0001t0002g0186 a0001c0001t0002g0187 others(1): Show |
7 | HG01167.hp2 HG01884.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1026+283_1026+284d others(4): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99660214 | |||||||
| chr7:99660214 | CTTTTTTT others(10): Show |
C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0106 |
3 | HG01884.hp2 HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1026+268_1026+284d others(19): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99660214 | |||||||
| chr7:99660214 | CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0001g0019 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1026+267_1026+284d others(20): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99660214 | |||||||
| chr7:99660323 | G | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0076 |
3 | HG02132.hp1 NA18939.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1026+176C>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99660323 | |||||||
| chr7:99660377 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1026+122G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 10/12 | chr7 | 99660377 | |||||||
| chr7:99660901 | G | A | 8 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(5): Show |
11 | HG01243.hp2 HG02486.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.866-242C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 9/12 | chr7 | 99660901 | |||||||
| chr7:99661020 | G | A | 7 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0060 others(4): Show |
11 | HG01884.hp1 HG02451.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.866-361C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 9/12 | chr7 | 99661020 | |||||||
| chr7:99661025 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.866-366C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 9/12 | chr7 | 99661025 | |||||||
| chr7:99661278 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.866-619C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 9/12 | chr7 | 99661278 | |||||||
| chr7:99661551 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.866-892C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 9/12 | chr7 | 99661551 | |||||||
| chr7:99661704 | T | C | 1 | a0001c0001t0001g0191 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.866-1045A>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 9/12 | chr7 | 99661704 | |||||||
| chr7:99662054 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.865+762C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 9/12 | chr7 | 99662054 | |||||||
| chr7:99662188 | A | T | 1 | a0001c0001t0001g0100 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.865+628T>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 9/12 | chr7 | 99662188 | |||||||
| chr7:99662194 | G | A | 13 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(10): Show |
17 | HG01243.hp2 HG02109.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.865+622C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 9/12 | chr7 | 99662194 | |||||||
| chr7:99662291 | G | A | 1 | a0001c0002t0001g0101 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.865+525C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 9/12 | chr7 | 99662291 | |||||||
| chr7:99662469 | T | C | 89 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(86): Show |
119 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.865+347A>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 9/12 | chr7 | 99662469 | |||||||
| chr7:99662739 | C | A | 54 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(51): Show |
75 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.865+77G>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 9/12 | chr7 | 99662739 | |||||||
| chr7:99662909 | G | C | 2 | a0001c0001t0001g0083 a0001c0001t0001g0089 |
2 | NA19004.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.799-27C>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 8/12 | chr7 | 99662909 | |||||||
| chr7:99663111 | C | T | 5 | a0001c0001t0002g0038 a0001c0001t0002g0122 a0001c0001t0002g0148 others(2): Show |
6 | HG02572.hp2 HG02630.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.799-229G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 8/12 | chr7 | 99663111 | |||||||
| chr7:99663124 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.799-242G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 8/12 | chr7 | 99663124 | |||||||
| chr7:99663296 | C | G | 10 | a0001c0002t0001g0013 a0001c0002t0001g0101 a0001c0002t0001g0107 others(7): Show |
12 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.799-414G>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 8/12 | chr7 | 99663296 | |||||||
| chr7:99663392 | G | C | 1 | a0002c0003t0001g0058 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.799-510C>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 8/12 | chr7 | 99663392 | |||||||
| chr7:99663482 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.798+486G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 8/12 | chr7 | 99663482 | |||||||
| chr7:99663569 | C | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.798+399G>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 8/12 | chr7 | 99663569 | |||||||
| chr7:99663697 | G | A | 1 | a0001c0001t0002g0130 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.798+271C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 8/12 | chr7 | 99663697 | |||||||
| chr7:99663757 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.798+211C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 8/12 | chr7 | 99663757 | |||||||
| chr7:99663941 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.798+27G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 8/12 | chr7 | 99663941 | |||||||
| chr7:99664114 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0031 a0001c0001t0001g0106 |
5 | HG01884.hp2 HG02559.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-19T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 7/12 | chr7 | 99664114 | |||||||
| chr7:99664403 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.671-308C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 7/12 | chr7 | 99664403 | |||||||
| chr7:99664573 | A | T | 1 | a0001c0001t0001g0091 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.671-478T>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 7/12 | chr7 | 99664573 | |||||||
| chr7:99664664 | A | T | 3 | a0001c0001t0002g0119 a0001c0001t0002g0137 a0001c0001t0002g0210 |
3 | NA18944.hp1 NA18979.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.670+502T>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 7/12 | chr7 | 99664664 | |||||||
| chr7:99664949 | G | A | 210 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(207): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.670+217C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 7/12 | chr7 | 99664949 | |||||||
| chr7:99664996 | A | G | 1 | a0001c0001t0002g0123 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.670+170T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 7/12 | chr7 | 99664996 | |||||||
| chr7:99664999 | T | C | 7 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0060 others(4): Show |
11 | HG01884.hp1 HG02451.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.670+167A>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 7/12 | chr7 | 99664999 | |||||||
| chr7:99665489 | G | C | 1 | a0001c0001t0001g0054 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.522-175C>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 6/12 | chr7 | 99665489 | |||||||
| chr7:99665516 | T | G | 4 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0097 others(1): Show |
8 | HG00621.hp2 HG02056.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.522-202A>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 6/12 | chr7 | 99665516 | |||||||
| chr7:99665874 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0106 |
3 | HG01884.hp2 HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.522-560G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 6/12 | chr7 | 99665874 | |||||||
| chr7:99665875 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0185 |
2 | HG02735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.522-561C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 6/12 | chr7 | 99665875 | |||||||
| chr7:99665950 | T | C | 13 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(10): Show |
17 | HG01243.hp2 HG02109.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.522-636A>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 6/12 | chr7 | 99665950 | |||||||
| chr7:99666116 | T | C | 1 | a0001c0001t0001g0015 | 2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.521+485A>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 6/12 | chr7 | 99666116 | |||||||
| chr7:99666260 | G | T | 1 | a0002c0003t0001g0058 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.521+341C>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 6/12 | chr7 | 99666260 | |||||||
| chr7:99666526 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.521+75G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 6/12 | chr7 | 99666526 | |||||||
| chr7:99667236 | C | G | 1 | a0001c0001t0001g0192 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.319-171G>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99667236 | |||||||
| chr7:99667537 | G | A | 7 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0060 others(4): Show |
11 | HG01884.hp1 HG02451.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.319-472C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99667537 | |||||||
| chr7:99667538 | T | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.319-473A>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99667538 | |||||||
| chr7:99667684 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.319-619T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99667684 | |||||||
| chr7:99668050 | A | G | 1 | a0001c0001t0002g0160 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.319-985T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99668050 | |||||||
| chr7:99668312 | C | T | 10 | a0001c0002t0001g0013 a0001c0002t0001g0101 a0001c0002t0001g0107 others(7): Show |
12 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.319-1247G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99668312 | |||||||
| chr7:99668313 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0106 |
3 | HG01884.hp2 HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.319-1248C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99668313 | |||||||
| chr7:99668493 | T | C | 1 | a0001c0001t0002g0166 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.319-1428A>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99668493 | |||||||
| chr7:99668685 | C | T | 2 | a0001c0002t0001g0181 a0001c0002t0001g0182 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.319-1620G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99668685 | |||||||
| chr7:99668695 | G | A | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(126): Show |
177 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.319-1630C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99668695 | |||||||
| chr7:99668820 | C | T | 53 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(50): Show |
74 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.319-1755G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99668820 | |||||||
| chr7:99669165 | A | G | 10 | a0001c0001t0001g0133 a0001c0001t0001g0136 a0001c0001t0002g0005 others(7): Show |
14 | HG00408.hp2 HG00673.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.319-2100T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99669165 | |||||||
| chr7:99669196 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0092 |
5 | NA18949.hp2 NA18970.hp1 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-2131C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99669196 | |||||||
| chr7:99669257 | A | G | 1 | a0003c0011t0002g0209 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.319-2192T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99669257 | |||||||
| chr7:99669267 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.319-2202C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99669267 | |||||||
| chr7:99669399 | G | A | 1 | a0001c0001t0002g0151 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.319-2334C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99669399 | |||||||
| chr7:99669460 | T | C | 4 | a0001c0001t0001g0040 a0001c0001t0001g0188 a0001c0001t0001g0189 others(1): Show |
5 | HG02647.hp1 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.319-2395A>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99669460 | |||||||
| chr7:99669863 | G | A | 2 | a0001c0001t0002g0034 a0001c0001t0002g0132 |
3 | NA19004.hp2 NA19063.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.318+2717C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99669863 | |||||||
| chr7:99669923 | C | G | 1 | a0001c0001t0002g0152 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.318+2657G>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99669923 | |||||||
| chr7:99669975 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.318+2605G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99669975 | |||||||
| chr7:99669976 | A | G | 7 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0047 others(4): Show |
9 | HG01243.hp2 HG02896.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.318+2604T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99669976 | |||||||
| chr7:99669996 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.318+2584C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99669996 | |||||||
| chr7:99670053 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.318+2527G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99670053 | |||||||
| chr7:99670075 | A | G | 2 | a0001c0001t0001g0020 a0001c0004t0001g0007 |
5 | HG02970.hp1 HG03225.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.318+2505T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99670075 | |||||||
| chr7:99670085 | T | G | 3 | a0001c0001t0002g0039 a0001c0001t0002g0159 a0001c0001t0002g0164 |
4 | HG01106.hp1 HG03239.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.318+2495A>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99670085 | |||||||
| chr7:99670543 | A | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.318+2037T>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99670543 | |||||||
| chr7:99670591 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0106 |
3 | HG01884.hp2 HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.318+1989C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99670591 | |||||||
| chr7:99670767 | C | T | 53 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(50): Show |
74 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.318+1813G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99670767 | |||||||
| chr7:99671052 | T | C | 1 | a0001c0001t0002g0211 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.318+1528A>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99671052 | |||||||
| chr7:99671116 | TTTGTGTG others(12): Show |
T | 1 | a0005c0008t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.318+1445_318+1463d others(21): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99671116 | |||||||
| chr7:99671117 | T | TTG | 4 | a0001c0001t0002g0160 a0001c0001t0002g0161 a0001c0001t0002g0162 others(1): Show |
4 | HG00544.hp2 HG04199.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.318+1461_318+1462d others(4): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99671117 | |||||||
| chr7:99671117 | T | TTGTG | 5 | a0001c0001t0001g0066 a0001c0001t0001g0084 a0001c0001t0002g0163 others(2): Show |
5 | HG00280.hp2 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.318+1459_318+1462d others(6): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99671117 | |||||||
| chr7:99671117 | TTG | T | 51 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0053 others(48): Show |
76 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.318+1461_318+1462d others(4): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99671117 | |||||||
| chr7:99671117 | TTGTG | T | 21 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0048 others(18): Show |
28 | HG01243.hp1 HG01243.hp2 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.318+1459_318+1462d others(6): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99671117 | |||||||
| chr7:99671117 | TTGTGTG | T | 23 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0069 others(20): Show |
29 | HG00621.hp1 HG01070.hp2 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.318+1457_318+1462d others(8): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99671117 | |||||||
| chr7:99671117 | TTGTGTGT others(1): Show |
T | 5 | a0001c0001t0001g0078 a0001c0001t0002g0119 a0001c0001t0002g0120 others(2): Show |
5 | HG00673.hp1 HG01975.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.318+1455_318+1462d others(10): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99671117 | |||||||
| chr7:99671117 | TTGTGTGT others(3): Show |
T | 5 | a0001c0001t0001g0020 a0001c0001t0001g0031 a0001c0002t0001g0101 others(2): Show |
9 | HG01891.hp1 HG02559.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.318+1453_318+1462d others(12): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99671117 | |||||||
| chr7:99671117 | TTGTGTGT others(5): Show |
T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.318+1451_318+1462d others(14): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99671117 | |||||||
| chr7:99671117 | TTGTGTGT others(7): Show |
T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0090 a0001c0001t0001g0095 others(1): Show |
5 | HG02738.hp1 HG03471.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.318+1449_318+1462d others(16): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99671117 | |||||||
| chr7:99671117 | TTGTGTGT others(9): Show |
T | 35 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(32): Show |
50 | HG00408.hp1 HG00621.hp2 HG01891.hp2 others(47): Show |
intron_variant | MODIFIER | c.318+1447_318+1462d others(18): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99671117 | |||||||
| chr7:99671117 | TTGTGTGT others(13): Show |
T | 1 | a0001c0001t0001g0108 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.318+1443_318+1462d others(22): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99671117 | |||||||
| chr7:99671117 | TTGTGTGT others(15): Show |
T | 8 | a0001c0001t0001g0040 a0001c0001t0002g0006 a0001c0001t0002g0116 others(5): Show |
12 | HG01884.hp1 HG02559.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.318+1441_318+1462d others(24): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99671117 | |||||||
| chr7:99671117 | TTGTGTGT others(17): Show |
T | 12 | a0001c0001t0001g0041 a0001c0001t0001g0192 a0001c0001t0001g0194 others(9): Show |
13 | HG00099.hp1 HG01192.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.318+1439_318+1462d others(26): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99671117 | |||||||
| chr7:99671117 | TTGTGTGT others(19): Show |
T | 8 | a0001c0001t0001g0190 a0001c0001t0002g0021 a0001c0001t0002g0060 others(5): Show |
17 | HG02257.hp1 HG02451.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.318+1437_318+1462d others(28): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99671117 | |||||||
| chr7:99671170 | A | T | 11 | a0001c0001t0001g0106 a0001c0002t0001g0013 a0001c0002t0001g0101 others(8): Show |
13 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.318+1410T>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99671170 | |||||||
| chr7:99671774 | T | C | 17 | a0001c0001t0001g0041 a0001c0001t0001g0192 a0001c0001t0001g0194 others(14): Show |
26 | HG00099.hp1 HG01891.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.318+806A>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99671774 | |||||||
| chr7:99671778 | A | C | 3 | a0002c0003t0001g0058 a0002c0003t0001g0193 a0002c0003t0001g0195 |
3 | HG02486.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.318+802T>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99671778 | |||||||
| chr7:99672002 | A | T | 3 | a0001c0001t0002g0011 a0001c0001t0002g0113 a0001c0007t0002g0114 |
5 | HG01070.hp2 HG01167.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.318+578T>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99672002 | |||||||
| chr7:99672042 | T | TTTG | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | NA18959.hp2 NA19010.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.318+535_318+537dup others(3): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99672042 | |||||||
| chr7:99672042 | T | TTTGTTGT others(11): Show |
2 | a0001c0001t0001g0031 a0001c0001t0001g0106 |
3 | HG01884.hp2 HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.318+520_318+537dup others(18): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99672042 | |||||||
| chr7:99672042 | T | TTTGTTGT others(17): Show |
1 | a0001c0001t0001g0019 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.318+514_318+537dup others(24): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99672042 | |||||||
| chr7:99672084 | T | C | 1 | a0004c0005t0002g0206 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.318+496A>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99672084 | |||||||
| chr7:99672353 | AG | A | 4 | a0001c0001t0001g0041 a0001c0001t0001g0194 a0001c0001t0001g0202 others(1): Show |
5 | NA18939.hp1 NA18989.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.318+226delC | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 4/12 | chr7 | 99672353 | |||||||
| chr7:99672695 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0085 a0001c0001t0001g0096 |
5 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-16C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 3/12 | chr7 | 99672695 | |||||||
| chr7:99672720 | G | T | 1 | a0001c0001t0001g0066 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.219-41C>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 3/12 | chr7 | 99672720 | |||||||
| chr7:99672785 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.219-106G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 3/12 | chr7 | 99672785 | |||||||
| chr7:99672864 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.219-185T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 3/12 | chr7 | 99672864 | |||||||
| chr7:99672916 | T | C | 95 | a0001c0001t0001g0133 a0001c0001t0001g0136 a0001c0001t0002g0001 others(92): Show |
130 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.219-237A>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 3/12 | chr7 | 99672916 | |||||||
| chr7:99673232 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.219-553G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 3/12 | chr7 | 99673232 | |||||||
| chr7:99673325 | T | A | 1 | a0001c0002t0001g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.219-646A>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 3/12 | chr7 | 99673325 | |||||||
| chr7:99673328 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.219-649T>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 3/12 | chr7 | 99673328 | |||||||
| chr7:99673636 | T | C | 9 | a0001c0002t0001g0013 a0001c0002t0001g0101 a0001c0002t0001g0107 others(6): Show |
11 | HG01167.hp2 HG01169.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.218+897A>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 3/12 | chr7 | 99673636 | |||||||
| chr7:99673730 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.218+803C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 3/12 | chr7 | 99673730 | |||||||
| chr7:99673923 | C | T | 1 | a0001c0001t0001g0040 | 2 | HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.218+610G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 3/12 | chr7 | 99673923 | |||||||
| chr7:99673983 | G | T | 1 | a0001c0001t0002g0112 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.218+550C>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 3/12 | chr7 | 99673983 | |||||||
| chr7:99674155 | T | C | 1 | a0001c0001t0001g0019 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.218+378A>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 3/12 | chr7 | 99674155 | |||||||
| chr7:99674185 | T | C | 17 | a0001c0001t0001g0041 a0001c0001t0001g0192 a0001c0001t0001g0194 others(14): Show |
18 | HG00099.hp1 HG00642.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.218+348A>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 3/12 | chr7 | 99674185 | |||||||
| chr7:99674230 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0085 a0001c0001t0001g0096 |
5 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+303A>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 3/12 | chr7 | 99674230 | |||||||
| chr7:99674305 | G | A | 2 | a0001c0001t0001g0020 a0001c0004t0001g0007 |
5 | HG02970.hp1 HG03225.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+228C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 3/12 | chr7 | 99674305 | |||||||
| chr7:99674386 | A | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0031 a0001c0001t0001g0106 |
5 | HG01884.hp2 HG02559.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+147T>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 3/12 | chr7 | 99674386 | |||||||
| chr7:99674477 | G | A | 1 | a0001c0001t0002g0103 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.218+56C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 3/12 | chr7 | 99674477 | |||||||
| chr7:99674687 | G | A | 17 | a0001c0001t0001g0041 a0001c0001t0001g0192 a0001c0001t0001g0194 others(14): Show |
18 | HG00099.hp1 HG00642.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.166-102C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99674687 | |||||||
| chr7:99674888 | A | G | 1 | a0001c0001t0002g0060 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.166-303T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99674888 | |||||||
| chr7:99675438 | A | T | 1 | a0001c0001t0001g0071 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.165+677T>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675438 | |||||||
| chr7:99675633 | T | TCCCCACT others(199): Show |
1 | a0002c0003t0001g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.165+481_165+482ins others(206): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675633 | |||||||
| chr7:99675633 | T | TCCCCACT others(163): Show |
1 | a0002c0003t0001g0193 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.165+481_165+482ins others(170): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675633 | |||||||
| chr7:99675633 | T | TCCCCACT others(183): Show |
18 | a0001c0001t0001g0041 a0001c0001t0001g0192 a0001c0001t0001g0197 others(15): Show |
19 | HG00099.hp1 HG00642.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.165+481_165+482ins others(190): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675633 | |||||||
| chr7:99675633 | T | TCCCCACT others(198): Show |
2 | a0002c0003t0001g0002 a0002c0003t0001g0014 |
10 | HG02257.hp1 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.165+481_165+482ins others(205): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675633 | |||||||
| chr7:99675633 | T | TCCCCACT others(145): Show |
1 | a0001c0001t0001g0194 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.165+481_165+482ins others(152): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675633 | |||||||
| chr7:99675638 | T | C | 23 | a0001c0001t0001g0041 a0001c0001t0001g0192 a0001c0001t0001g0194 others(20): Show |
32 | HG00099.hp1 HG00642.hp2 HG01515.hp2 others(29): Show |
intron_variant | MODIFIER | c.165+477A>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCCCCACT others(269): Show |
1 | a0001c0001t0001g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.165+476_165+477ins others(276): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCC others(193): Show |
1 | a0001c0001t0002g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.165+476_165+477ins others(200): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(180): Show |
1 | a0001c0001t0002g0111 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.165+476_165+477ins others(187): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(305): Show |
1 | a0001c0001t0001g0091 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.165+476_165+477ins others(312): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(190): Show |
1 | a0001c0001t0001g0047 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.165+476_165+477ins others(197): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(168): Show |
1 | a0001c0001t0001g0048 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.165+476_165+477ins others(175): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(188): Show |
2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
4 | HG02486.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+476_165+477ins others(195): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(208): Show |
8 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0049 others(5): Show |
10 | HG01243.hp2 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.165+476_165+477ins others(215): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(228): Show |
1 | a0001c0001t0001g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.165+476_165+477ins others(235): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(325): Show |
1 | a0001c0001t0001g0086 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.165+476_165+477ins others(332): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(228): Show |
2 | a0001c0001t0001g0020 a0001c0004t0001g0007 |
5 | HG02970.hp1 HG03225.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+476_165+477ins others(235): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(221): Show |
1 | a0001c0002t0001g0175 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.165+476_165+477ins others(228): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(220): Show |
2 | a0001c0002t0001g0169 a0001c0002t0001g0170 |
2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.165+476_165+477ins others(227): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(239): Show |
1 | a0001c0002t0001g0107 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.165+476_165+477ins others(246): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(263): Show |
1 | a0001c0001t0001g0070 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.165+476_165+477ins others(270): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(179): Show |
1 | a0001c0001t0002g0173 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.165+476_165+477ins others(186): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(283): Show |
1 | a0001c0001t0001g0092 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.165+476_165+477ins others(290): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(303): Show |
1 | a0001c0001t0001g0093 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.165+476_165+477ins others(310): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(243): Show |
1 | a0001c0001t0001g0097 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.165+476_165+477ins others(250): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(283): Show |
1 | a0001c0001t0001g0094 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.165+476_165+477ins others(290): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(303): Show |
1 | a0001c0001t0001g0095 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.165+476_165+477ins others(310): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(263): Show |
2 | a0001c0001t0001g0098 a0001c0001t0001g0185 |
2 | HG04204.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.165+476_165+477ins others(270): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(322): Show |
1 | a0001c0001t0001g0090 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.165+476_165+477ins others(329): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(302): Show |
4 | a0001c0001t0001g0029 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
5 | HG03017.hp1 HG03239.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+476_165+477ins others(309): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(282): Show |
26 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
42 | HG00408.hp1 HG00597.hp2 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.165+476_165+477ins others(289): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(262): Show |
5 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(2): Show |
5 | HG00280.hp2 HG03831.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+476_165+477ins others(269): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(242): Show |
3 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0064 |
7 | HG00621.hp2 NA18948.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.165+476_165+477ins others(249): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(301): Show |
1 | a0001c0001t0001g0065 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.165+476_165+477ins others(308): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(159): Show |
1 | a0001c0001t0002g0057 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.165+476_165+477ins others(166): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(179): Show |
1 | a0001c0001t0002g0174 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.165+476_165+477ins others(186): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(158): Show |
2 | a0001c0001t0002g0109 a0001c0001t0002g0110 |
2 | HG00642.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.165+476_165+477ins others(165): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(178): Show |
77 | a0001c0001t0001g0133 a0001c0001t0001g0136 a0001c0001t0002g0001 others(74): Show |
112 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.165+476_165+477ins others(185): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(179): Show |
1 | a0001c0001t0002g0176 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.165+476_165+477ins others(186): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(198): Show |
7 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0060 others(4): Show |
11 | HG01884.hp1 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.165+476_165+477ins others(205): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(237): Show |
1 | a0001c0001t0001g0040 | 2 | HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.165+476_165+477ins others(244): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(217): Show |
2 | a0001c0001t0001g0019 a0001c0001t0001g0188 |
3 | HG02895.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.165+476_165+477ins others(224): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(197): Show |
4 | a0001c0001t0001g0031 a0001c0001t0001g0044 a0001c0001t0001g0045 others(1): Show |
5 | HG01884.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+476_165+477ins others(204): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(195): Show |
1 | a0001c0001t0002g0059 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.165+476_165+477ins others(202): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(215): Show |
1 | a0001c0001t0001g0190 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.165+476_165+477ins others(222): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(254): Show |
1 | a0001c0001t0001g0108 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.165+476_165+477ins others(261): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(162): Show |
1 | a0001c0001t0001g0189 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.165+476_165+477ins others(169): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675638 | T | TCTCCTCT others(178): Show |
1 | a0001c0001t0002g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.165+476_165+477ins others(185): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675638 | |||||||
| chr7:99675643 | T | TCTCCCTC others(184): Show |
1 | a0001c0001t0002g0178 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.165+471_165+472ins others(191): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675643 | |||||||
| chr7:99675643 | T | TCTCCTCC others(304): Show |
1 | a0001c0001t0001g0100 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.165+471_165+472ins others(311): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675643 | |||||||
| chr7:99675643 | T | TCTCCTCC others(252): Show |
4 | a0001c0002t0001g0181 a0001c0002t0001g0182 a0001c0002t0001g0183 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+471_165+472ins others(259): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675643 | |||||||
| chr7:99675643 | T | TCTCCTCC others(252): Show |
2 | a0001c0002t0001g0101 a0005c0008t0001g0180 |
2 | HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.165+471_165+472ins others(259): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675643 | |||||||
| chr7:99675643 | T | TCTCCTCC others(232): Show |
2 | a0001c0002t0001g0013 a0001c0002t0001g0179 |
4 | HG02717.hp2 HG02818.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+471_165+472ins others(239): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675643 | |||||||
| chr7:99675643 | T | TCTCCTCC others(243): Show |
1 | a0001c0001t0001g0099 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.165+471_165+472ins others(250): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675643 | |||||||
| chr7:99675643 | T | TCTCCTCC others(178): Show |
1 | a0001c0001t0002g0104 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.165+471_165+472ins others(185): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675643 | |||||||
| chr7:99675643 | T | TCTCCTCC others(179): Show |
1 | a0001c0001t0002g0177 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.165+471_165+472ins others(186): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675643 | |||||||
| chr7:99675645 | C | T | 1 | a0001c0001t0002g0104 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.165+470G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675645 | |||||||
| chr7:99675647 | C | T | 8 | a0001c0002t0001g0013 a0001c0002t0001g0101 a0001c0002t0001g0179 others(5): Show |
10 | HG01167.hp2 HG01169.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.165+468G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675647 | |||||||
| chr7:99675650 | T | TCC | 8 | a0001c0002t0001g0013 a0001c0002t0001g0101 a0001c0002t0001g0179 others(5): Show |
10 | HG01167.hp2 HG01169.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.165+463_165+464dup others(2): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675650 | |||||||
| chr7:99675662 | C | T | 1 | a0001c0001t0002g0103 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.165+453G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99675662 | |||||||
| chr7:99676079 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.165+36G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 2/12 | chr7 | 99676079 | |||||||
| chr7:99676319 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.72-111C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99676319 | |||||||
| chr7:99676614 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.72-406G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99676614 | |||||||
| chr7:99676693 | A | G | 1 | a0001c0001t0002g0102 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.72-485T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99676693 | |||||||
| chr7:99676835 | A | G | 1 | a0001c0001t0002g0030 | 2 | HG01256.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.72-627T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99676835 | |||||||
| chr7:99677369 | A | G | 1 | a0001c0002t0001g0101 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.72-1161T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99677369 | |||||||
| chr7:99677460 | C | T | 53 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(50): Show |
74 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.72-1252G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99677460 | |||||||
| chr7:99677495 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.72-1287G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99677495 | |||||||
| chr7:99677496 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.72-1288G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99677496 | |||||||
| chr7:99677745 | C | G | 1 | a0001c0001t0002g0186 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.72-1537G>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99677745 | |||||||
| chr7:99677763 | C | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0053 others(2): Show |
6 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.72-1555G>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99677763 | |||||||
| chr7:99677887 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.72-1679A>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99677887 | |||||||
| chr7:99677897 | AGG | A | 3 | a0001c0001t0002g0006 a0001c0001t0002g0186 a0001c0001t0002g0187 |
6 | HG01884.hp1 HG02922.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.72-1691_72-1690del others(2): Show |
CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99677897 | |||||||
| chr7:99678103 | T | A | 4 | a0001c0001t0001g0040 a0001c0001t0001g0188 a0001c0001t0001g0189 others(1): Show |
5 | HG02647.hp1 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+1723A>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99678103 | |||||||
| chr7:99678282 | C | T | 4 | a0001c0001t0002g0021 a0001c0001t0002g0060 a0001c0001t0002g0061 others(1): Show |
5 | HG02451.hp2 HG02615.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+1544G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99678282 | |||||||
| chr7:99678283 | G | T | 1 | a0001c0001t0001g0192 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.71+1543C>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99678283 | |||||||
| chr7:99678482 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.71+1344C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99678482 | |||||||
| chr7:99678681 | A | C | 1 | a0001c0001t0002g0059 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.71+1145T>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99678681 | |||||||
| chr7:99678713 | A | T | 2 | a0001c0001t0001g0020 a0001c0004t0001g0007 |
5 | HG02970.hp1 HG03225.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+1113T>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99678713 | |||||||
| chr7:99678787 | G | T | 1 | a0001c0001t0001g0019 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.71+1039C>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99678787 | |||||||
| chr7:99678885 | C | A | 23 | a0001c0001t0001g0041 a0001c0001t0001g0192 a0001c0001t0001g0194 others(20): Show |
32 | HG00099.hp1 HG00642.hp2 HG01515.hp2 others(29): Show |
intron_variant | MODIFIER | c.71+941G>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99678885 | |||||||
| chr7:99678928 | C | A | 1 | a0001c0001t0002g0042 | 2 | NA18980.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.71+898G>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99678928 | |||||||
| chr7:99679096 | G | A | 1 | a0001c0001t0002g0210 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.71+730C>T | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99679096 | |||||||
| chr7:99679125 | C | G | 1 | a0002c0003t0001g0058 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.71+701G>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99679125 | |||||||
| chr7:99679263 | G | C | 1 | a0001c0001t0002g0211 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.71+563C>G | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99679263 | |||||||
| chr7:99679433 | A | G | 2 | a0001c0001t0002g0056 a0001c0001t0002g0057 |
2 | HG00280.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.71+393T>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99679433 | |||||||
| chr7:99679445 | C | T | 13 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(10): Show |
17 | HG01243.hp2 HG02109.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.71+381G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99679445 | |||||||
| chr7:99679578 | C | T | 3 | a0002c0003t0001g0002 a0002c0003t0001g0014 a0002c0003t0001g0046 |
11 | HG02055.hp2 HG02257.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.71+248G>A | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99679578 | |||||||
| chr7:99679607 | C | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.71+219G>C | CYP3A5 | ENSG00000106258.16 | transcript | ENST00000222982.8 | protein_coding | 1/12 | chr7 | 99679607 |