Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1551 |
| ensemblid | ENSG00000160870.15 |
| hgncid | 2640 |
| symbol | CYP3A7 |
| name | cytochrome P450 family 3 subfamily A member 7 |
| refseq_nuc | NM_000765.5 |
| refseq_prot | NP_000756.3 |
| ensembl_nuc | ENST00000336374.4 |
| ensembl_prot | ENSP00000337450.2 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 99705036 |
| end | 99735196 |
| strand | - |
| ver | v1.2 |
| region | chr7:99705036-99735196 |
| region5000 | chr7:99700036-99740196 |
| regionname0 | CYP3A7_chr7_99705036_99735196 |
| regionname5000 | CYP3A7_chr7_99700036_99740196 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 503 | 146 | 62 | 10 | 52 | 4 | 17 | 45 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | MDLIP others(498): Show |
chr7 | 99700036 | 99740196 |
| a0002 | 1/0 | 503 | 134 | 26 | 26 | 57 | 7 | 17 | 45 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | MDLIP others(498): Show |
chr7 | 99700036 | 99740196 |
| a0003 | 0/0 | 503 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | MDLIP others(498): Show |
chr7 | 99700036 | 99740196 |
| a0004 | 0/0 | 503 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | MDLIP others(498): Show |
chr7 | 99700036 | 99740196 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/1 | 1509 | 133 | 50 | 9 | 52 | 4 | 17 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | ATGGA others(1504): Show |
chr7 | 99700036 | 99740196 | ||
| a0001c0003 | 0/0 | 1509 | 13 | 12 | 1 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | ATGGA others(1504): Show |
chr7 | 99700036 | 99740196 | ||
| a0002c0001 | 1/0 | 1509 | 133 | 26 | 26 | 56 | 7 | 17 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | ATGGA others(1504): Show |
chr7 | 99700036 | 99740196 | ||
| a0002c0005 | 0/0 | 1509 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | ATGGA others(1504): Show |
chr7 | 99700036 | 99740196 | ||
| a0003c0004 | 0/0 | 1509 | 1 | 0 | 0 | 0 | 1 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | ATGGA others(1504): Show |
chr7 | 99700036 | 99740196 | ||
| a0004c0006 | 0/0 | 1509 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | ATGGA others(1504): Show |
chr7 | 99700036 | 99740196 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/1 | 2079 | 115 | 36 | 7 | 51 | 4 | 16 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | ACTGC others(2074): Show |
chr7 | 99700036 | 99740196 |
| a0001c0002t0003 | 0/0 | 2079 | 10 | 8 | 2 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | ACTGC others(2074): Show |
chr7 | 99700036 | 99740196 |
| a0001c0002t0004 | 0/0 | 2079 | 5 | 5 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | ACTGC others(2074): Show |
chr7 | 99700036 | 99740196 |
| a0001c0002t0005 | 0/0 | 2079 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | ACTGC others(2074): Show |
chr7 | 99700036 | 99740196 |
| a0001c0002t0006 | 0/0 | 2079 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | ACTGC others(2074): Show |
chr7 | 99700036 | 99740196 |
| a0001c0002t0007 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | ACTGC others(2074): Show |
chr7 | 99700036 | 99740196 |
| a0001c0003t0001 | 0/0 | 2079 | 13 | 12 | 1 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | ACTGC others(2074): Show |
chr7 | 99700036 | 99740196 |
| a0002c0001t0001 | 0/0 | 2079 | 2 | 2 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | ACTGC others(2074): Show |
chr7 | 99700036 | 99740196 |
| a0002c0001t0002 | 1/0 | 2079 | 129 | 23 | 25 | 56 | 7 | 17 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | ACTGC others(2074): Show |
chr7 | 99700036 | 99740196 |
| a0002c0001t0003 | 0/0 | 2079 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | ACTGC others(2074): Show |
chr7 | 99700036 | 99740196 |
| a0002c0001t0008 | 0/0 | 2079 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | ACTGC others(2074): Show |
chr7 | 99700036 | 99740196 |
| a0002c0005t0002 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | ACTGC others(2074): Show |
chr7 | 99700036 | 99740196 |
| a0003c0004t0002 | 0/0 | 2079 | 1 | 0 | 0 | 0 | 1 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | ACTGC others(2074): Show |
chr7 | 99700036 | 99740196 |
| a0004c0006t0001 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | ACTGC others(2074): Show |
chr7 | 99700036 | 99740196 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0002 | 0/0 | 18 | 0 | 0 | 18 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0003 | 0/0 | 13 | 0 | 0 | 9 | 0 | 4 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0004 | 0/1 | 8 | 0 | 2 | 1 | 2 | 2 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0007 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0021 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0003g0012 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0004g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0004g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0006g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0002t0007g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0003t0001g0011 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0003t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0003t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0001c0003t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0001 | 0/0 | 38 | 2 | 7 | 22 | 0 | 7 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0005 | 0/0 | 7 | 0 | 5 | 0 | 1 | 1 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0006 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0126 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0001t0008g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0002c0005t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0003c0004t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| a0004c0006t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0119 | EUR | GBR | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG00099 | hp2 | a0002 | c0001 | t0002 | g0030 | EUR | GBR | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG00140 | hp1 | a0002 | c0001 | t0002 | g0051 | EUR | GBR | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG00140 | hp2 | a0002 | c0001 | t0002 | g0077 | EUR | GBR | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG00280 | hp1 | a0003 | c0004 | t0002 | g0085 | EUR | FIN | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0056 | EUR | FIN | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG00408 | hp1 | a0002 | c0001 | t0002 | g0055 | EAS | CHS | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | CHS | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG00423 | hp1 | a0002 | c0001 | t0002 | g0092 | EAS | CHS | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG00423 | hp2 | a0002 | c0001 | t0002 | g0071 | EAS | CHS | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG00438 | hp1 | a0002 | c0001 | t0002 | g0066 | EAS | CHS | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG00438 | hp2 | a0002 | c0001 | t0002 | g0132 | EAS | CHS | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG00597 | hp2 | a0002 | c0001 | t0002 | g0006 | EAS | CHS | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG00621 | hp2 | a0002 | c0001 | t0002 | g0001 | EAS | CHS | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG00639 | hp1 | a0002 | c0001 | t0002 | g0067 | AMR | PUR | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG00639 | hp2 | a0002 | c0001 | t0002 | g0001 | AMR | PUR | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG00642 | hp1 | a0002 | c0001 | t0002 | g0001 | AMR | PUR | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG00735 | hp1 | a0002 | c0001 | t0002 | g0030 | AMR | PUR | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG00735 | hp2 | a0002 | c0001 | t0002 | g0001 | AMR | PUR | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01074 | hp1 | a0002 | c0001 | t0002 | g0005 | AMR | PUR | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01074 | hp2 | a0002 | c0001 | t0002 | g0049 | AMR | PUR | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0110 | AMR | PUR | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01099 | hp2 | a0002 | c0001 | t0002 | g0005 | AMR | PUR | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01167 | hp1 | a0002 | c0001 | t0002 | g0001 | AMR | PUR | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01167 | hp2 | a0001 | c0002 | t0003 | g0012 | AMR | PUR | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01169 | hp1 | a0002 | c0001 | t0002 | g0005 | AMR | PUR | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01169 | hp2 | a0001 | c0002 | t0003 | g0012 | AMR | PUR | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01175 | hp2 | a0002 | c0001 | t0002 | g0001 | AMR | PUR | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01192 | hp1 | a0002 | c0001 | t0002 | g0005 | AMR | PUR | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0106 | AMR | PUR | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0011 | AMR | PUR | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01243 | hp2 | a0002 | c0001 | t0002 | g0001 | AMR | PUR | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01255 | hp1 | a0002 | c0001 | t0002 | g0005 | AMR | CLM | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01255 | hp2 | a0002 | c0001 | t0002 | g0068 | AMR | CLM | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01257 | hp1 | a0002 | c0001 | t0002 | g0027 | AMR | CLM | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01257 | hp2 | a0002 | c0001 | t0002 | g0028 | AMR | CLM | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01258 | hp1 | a0002 | c0001 | t0002 | g0024 | AMR | CLM | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01258 | hp2 | a0002 | c0001 | t0002 | g0028 | AMR | CLM | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | CLM | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01433 | hp2 | a0002 | c0001 | t0002 | g0046 | AMR | CLM | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01496 | hp1 | a0002 | c0001 | t0002 | g0024 | AMR | CLM | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | CLM | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01515 | hp1 | a0002 | c0001 | t0002 | g0072 | EUR | IBS | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0004 | EUR | IBS | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01516 | hp1 | a0002 | c0001 | t0002 | g0005 | EUR | IBS | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01516 | hp2 | a0002 | c0001 | t0002 | g0020 | EUR | IBS | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01517 | hp1 | a0002 | c0001 | t0002 | g0020 | EUR | IBS | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0004 | EUR | IBS | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01884 | hp1 | a0001 | c0002 | t0004 | g0036 | AFR | ACB | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01884 | hp2 | a0002 | c0001 | t0002 | g0008 | AFR | ACB | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | ACB | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PEL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01975 | hp2 | a0002 | c0001 | t0002 | g0006 | AMR | PEL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01993 | hp1 | a0002 | c0001 | t0002 | g0057 | AMR | PEL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG01993 | hp2 | a0002 | c0001 | t0008 | g0076 | AMR | PEL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02040 | hp1 | a0002 | c0001 | t0002 | g0075 | EAS | KHV | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02040 | hp2 | a0004 | c0006 | t0001 | g0108 | EAS | KHV | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0115 | AFR | ACB | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02055 | hp2 | a0002 | c0001 | t0002 | g0053 | AFR | ACB | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02056 | hp2 | a0002 | c0001 | t0002 | g0001 | EAS | KHV | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | KHV | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02071 | hp2 | a0002 | c0001 | t0002 | g0019 | EAS | KHV | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02083 | hp1 | a0002 | c0001 | t0002 | g0061 | EAS | KHV | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02083 | hp2 | a0002 | c0001 | t0002 | g0083 | EAS | KHV | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | ACB | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0128 | AFR | ACB | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02258 | hp1 | a0002 | c0001 | t0002 | g0082 | AFR | ACB | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02258 | hp2 | a0001 | c0003 | t0001 | g0130 | AFR | ACB | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0016 | AFR | ACB | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02280 | hp2 | a0002 | c0001 | t0002 | g0001 | AFR | ACB | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02293 | hp1 | a0002 | c0001 | t0002 | g0064 | AMR | PEL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02293 | hp2 | a0002 | c0001 | t0002 | g0001 | AMR | PEL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02451 | hp1 | a0002 | c0001 | t0002 | g0013 | AFR | ACB | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | ACB | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02572 | hp1 | a0002 | c0001 | t0002 | g0018 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02572 | hp2 | a0001 | c0002 | t0003 | g0012 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0093 | SAS | PJL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02602 | hp2 | a0002 | c0001 | t0002 | g0029 | SAS | PJL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02615 | hp1 | a0002 | c0001 | t0002 | g0013 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0125 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0016 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02630 | hp1 | a0002 | c0001 | t0002 | g0018 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0117 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02647 | hp1 | a0002 | c0001 | t0003 | g0042 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0032 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02717 | hp2 | a0001 | c0002 | t0003 | g0043 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0112 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02723 | hp2 | a0002 | c0001 | t0002 | g0052 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0021 | SAS | PJL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0087 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0124 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02818 | hp1 | a0001 | c0002 | t0004 | g0036 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02818 | hp2 | a0001 | c0002 | t0003 | g0038 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02886 | hp1 | a0001 | c0002 | t0005 | g0039 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02886 | hp2 | a0002 | c0001 | t0002 | g0018 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02895 | hp2 | a0001 | c0002 | t0004 | g0037 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02897 | hp1 | a0001 | c0002 | t0004 | g0037 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0123 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02922 | hp1 | a0001 | c0002 | t0003 | g0022 | AFR | ESN | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02922 | hp2 | a0002 | c0001 | t0002 | g0008 | AFR | ESN | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | ESN | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | ESN | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02970 | hp1 | a0002 | c0001 | t0002 | g0008 | AFR | ESN | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | ESN | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03017 | hp1 | a0002 | c0001 | t0002 | g0029 | SAS | PJL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0034 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03041 | hp2 | a0001 | c0002 | t0003 | g0041 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03098 | hp1 | a0002 | c0001 | t0002 | g0058 | AFR | MSL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03098 | hp2 | a0001 | c0002 | t0003 | g0012 | AFR | MSL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0122 | AFR | ESN | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | ESN | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03195 | hp1 | a0001 | c0002 | t0003 | g0040 | AFR | ESN | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03195 | hp2 | a0002 | c0001 | t0002 | g0059 | AFR | ESN | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03209 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | MSL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0104 | AFR | MSL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | MSL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0023 | AFR | MSL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03239 | hp1 | a0002 | c0001 | t0002 | g0001 | SAS | PJL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0094 | SAS | PJL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03453 | hp1 | a0002 | c0001 | t0002 | g0013 | AFR | MSL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03453 | hp2 | a0002 | c0001 | t0002 | g0008 | AFR | MSL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | MSL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0116 | AFR | MSL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0021 | SAS | PJL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03490 | hp2 | a0002 | c0001 | t0002 | g0001 | SAS | PJL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03492 | hp1 | a0002 | c0001 | t0002 | g0089 | SAS | PJL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0021 | SAS | PJL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | ESN | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | ESN | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0032 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03540 | hp2 | a0002 | c0001 | t0002 | g0001 | AFR | GWD | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0034 | AFR | MSL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03579 | hp2 | a0002 | c0001 | t0002 | g0008 | AFR | MSL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03654 | hp2 | a0002 | c0001 | t0002 | g0020 | SAS | PJL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03669 | hp1 | a0002 | c0001 | t0002 | g0001 | SAS | PJL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03669 | hp2 | a0002 | c0001 | t0002 | g0086 | SAS | PJL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | STU | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03688 | hp2 | a0002 | c0001 | t0002 | g0001 | SAS | STU | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03704 | hp1 | a0002 | c0001 | t0002 | g0045 | SAS | PJL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0120 | SAS | PJL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | BEB | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03831 | hp2 | a0002 | c0001 | t0002 | g0001 | SAS | BEB | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03927 | hp1 | a0002 | c0001 | t0002 | g0005 | SAS | BEB | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0103 | SAS | BEB | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG04115 | hp1 | a0002 | c0001 | t0002 | g0080 | SAS | STU | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0105 | SAS | STU | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG04184 | hp1 | a0002 | c0001 | t0002 | g0001 | SAS | BEB | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0101 | SAS | BEB | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG04199 | hp1 | a0002 | c0001 | t0002 | g0001 | SAS | STU | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0096 | SAS | STU | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG04204 | hp1 | a0002 | c0001 | t0002 | g0091 | SAS | STU | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | STU | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | YRI | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0113 | AFR | YRI | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18906 | hp1 | a0002 | c0001 | t0002 | g0008 | AFR | YRI | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0023 | AFR | YRI | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18944 | hp1 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18945 | hp1 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18947 | hp2 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18948 | hp2 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18949 | hp1 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18950 | hp2 | a0002 | c0005 | t0002 | g0074 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18954 | hp1 | a0002 | c0001 | t0002 | g0019 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18956 | hp2 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18959 | hp1 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18961 | hp1 | a0002 | c0001 | t0002 | g0084 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18963 | hp1 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18964 | hp2 | a0002 | c0001 | t0002 | g0026 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18965 | hp2 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18966 | hp1 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18967 | hp2 | a0002 | c0001 | t0002 | g0047 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18968 | hp1 | a0002 | c0001 | t0002 | g0026 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18968 | hp2 | a0002 | c0001 | t0002 | g0069 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18970 | hp1 | a0002 | c0001 | t0002 | g0006 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18971 | hp1 | a0002 | c0001 | t0002 | g0081 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18971 | hp2 | a0001 | c0002 | t0007 | g0121 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18973 | hp2 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18978 | hp2 | a0002 | c0001 | t0002 | g0065 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18979 | hp1 | a0002 | c0001 | t0002 | g0070 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18980 | hp2 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18982 | hp1 | a0002 | c0001 | t0002 | g0079 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18989 | hp1 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18995 | hp2 | a0002 | c0001 | t0002 | g0063 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18999 | hp1 | a0002 | c0001 | t0002 | g0060 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19000 | hp2 | a0002 | c0001 | t0002 | g0073 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19002 | hp1 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19004 | hp1 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19006 | hp1 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19009 | hp2 | a0002 | c0001 | t0002 | g0090 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19012 | hp2 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19030 | hp1 | a0002 | c0001 | t0002 | g0050 | AFR | LWK | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19030 | hp2 | a0002 | c0001 | t0002 | g0048 | AFR | LWK | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19043 | hp1 | a0002 | c0001 | t0002 | g0013 | AFR | LWK | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | LWK | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19054 | hp2 | a0002 | c0001 | t0002 | g0019 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19055 | hp1 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19055 | hp2 | a0002 | c0001 | t0002 | g0088 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19058 | hp1 | a0002 | c0001 | t0002 | g0006 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19075 | hp1 | a0002 | c0001 | t0002 | g0062 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19075 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19078 | hp2 | a0002 | c0001 | t0002 | g0054 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19079 | hp1 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19081 | hp2 | a0002 | c0001 | t0002 | g0006 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19083 | hp2 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19085 | hp1 | a0002 | c0001 | t0002 | g0006 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19086 | hp1 | a0002 | c0001 | t0002 | g0006 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19088 | hp2 | a0002 | c0001 | t0002 | g0078 | EAS | JPT | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19240 | hp1 | a0002 | c0001 | t0001 | g0025 | AFR | YRI | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | YRI | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | ASW | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0131 | AFR | ASW | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA20905 | hp1 | a0002 | c0001 | t0002 | g0044 | SAS | GIH | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| NA20905 | hp2 | a0001 | c0002 | t0006 | g0102 | SAS | GIH | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | ACB | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02486 | hp1 | a0002 | c0001 | t0001 | g0025 | AFR | ACB | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | ACB | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02559 | hp1 | a0001 | c0002 | t0003 | g0022 | AFR | ACB | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG02559 | hp2 | a0001 | c0002 | t0004 | g0129 | AFR | ACB | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0127 | AFR | MSL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0118 | AFR | MSL | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG06807 | hp1 | a0002 | c0001 | t0002 | g0027 | AFR | USA | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | USA | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0004 | REF | REF | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| homoSapiens | grch38p0 | a0002 | c0001 | t0002 | g0126 | REF | REF | CYP3A7_chr7_99700036_99740196 | CYP3A7 | chr7 | 99700036 | 99740196 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:99709062 | G | C | 2 | a0001 a0004 |
146 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(143): Show |
missense_variant | MODERATE | c.1226C>G | p.Thr409Arg | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 11/13 | 1329/2079 | 1226/1512 | 409/503 | chr7 | 99709062 | |||
| chr7:99709180 | C | T | 1 | a0004 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.1108G>A | p.Ala370Thr | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 11/13 | 1211/2079 | 1108/1512 | 370/503 | chr7 | 99709180 | |||
| chr7:99722302 | A | G | 1 | a0003 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.212T>C | p.Val71Ala | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 3/13 | 315/2079 | 212/1512 | 71/503 | chr7 | 99722302 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:99709223 | A | G | 1 | a0002c0005 | 1 | NA18950.hp2 | synonymous_variant | LOW | c.1065T>C | p.Tyr355Tyr | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 11/13 | 1168/2079 | 1065/1512 | 355/503 | chr7 | 99709223 | |||
| chr7:99720370 | G | A | 1 | a0001c0003 | 13 | HG01243.hp1 HG02109.hp2 HG02258.hp2 others(10): Show |
synonymous_variant | LOW | c.261C>T | p.Pro87Pro | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/13 | 364/2079 | 261/1512 | 87/503 | chr7 | 99720370 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:99705147 | C | G | 1 | a0001c0002t0004 | 5 | HG01884.hp1 HG02559.hp2 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*353G>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 13/13 | 353 | chr7 | 99705147 | ||||||
| chr7:99705167 | G | C | 1 | a0001c0002t0005 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*333C>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 13/13 | 333 | chr7 | 99705167 | ||||||
| chr7:99705321 | A | G | 1 | a0002c0001t0008 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*179T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 13/13 | 179 | chr7 | 99705321 | ||||||
| chr7:99705327 | C | T | 1 | a0001c0002t0006 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*173G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 13/13 | 173 | chr7 | 99705327 | ||||||
| chr7:99705371 | T | C | 10 | a0001c0002t0001 a0001c0002t0003 a0001c0002t0004 others(7): Show |
149 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*129A>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 13/13 | 129 | chr7 | 99705371 | ||||||
| chr7:99705378 | T | G | 1 | a0001c0002t0007 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*122A>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 13/13 | 122 | chr7 | 99705378 | ||||||
| chr7:99705471 | A | G | 10 | a0001c0002t0001 a0001c0002t0003 a0001c0002t0004 others(7): Show |
149 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*29T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 13/13 | 29 | chr7 | 99705471 | ||||||
| chr7:99735142 | C | T | 3 | a0001c0002t0003 a0001c0002t0005 a0002c0001t0003 |
12 | HG01167.hp2 HG01169.hp2 HG02559.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-49G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/13 | 49 | chr7 | 99735142 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:99705652 | A | G | 1 | a0001c0002t0001g0116 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1417-57T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 12/12 | chr7 | 99705652 | |||||||
| chr7:99705796 | A | G | 2 | a0001c0002t0001g0015 a0001c0002t0001g0114 |
5 | NA18939.hp1 NA18989.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.1417-201T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 12/12 | chr7 | 99705796 | |||||||
| chr7:99705921 | C | T | 1 | a0001c0002t0001g0120 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1417-326G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 12/12 | chr7 | 99705921 | |||||||
| chr7:99706178 | C | T | 2 | a0002c0001t0002g0075 a0002c0001t0002g0081 |
2 | HG02040.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1417-583G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 12/12 | chr7 | 99706178 | |||||||
| chr7:99706336 | C | T | 1 | a0001c0002t0001g0109 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1417-741G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 12/12 | chr7 | 99706336 | |||||||
| chr7:99706348 | T | C | 4 | a0002c0001t0002g0028 a0002c0001t0002g0046 a0002c0001t0002g0067 others(1): Show |
5 | HG00140.hp2 HG00639.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1417-753A>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 12/12 | chr7 | 99706348 | |||||||
| chr7:99706647 | T | G | 1 | a0002c0001t0002g0026 | 2 | NA18964.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.1417-1052A>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 12/12 | chr7 | 99706647 | |||||||
| chr7:99706674 | TA | T | 4 | a0002c0001t0002g0006 a0002c0001t0002g0019 a0002c0001t0002g0065 others(1): Show |
12 | HG00597.hp2 HG01975.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1417-1080delT | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 12/12 | chr7 | 99706674 | |||||||
| chr7:99706701 | T | C | 1 | a0002c0001t0002g0078 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1417-1106A>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 12/12 | chr7 | 99706701 | |||||||
| chr7:99706795 | C | T | 1 | a0002c0001t0002g0030 | 2 | HG00099.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.1416+1017G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 12/12 | chr7 | 99706795 | |||||||
| chr7:99706817 | C | T | 1 | a0002c0001t0002g0081 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1416+995G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 12/12 | chr7 | 99706817 | |||||||
| chr7:99706901 | A | G | 62 | a0002c0001t0002g0001 a0002c0001t0002g0005 a0002c0001t0002g0006 others(59): Show |
131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1416+911T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 12/12 | chr7 | 99706901 | |||||||
| chr7:99706995 | T | A | 62 | a0002c0001t0002g0001 a0002c0001t0002g0005 a0002c0001t0002g0006 others(59): Show |
131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1416+817A>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 12/12 | chr7 | 99706995 | |||||||
| chr7:99707089 | C | T | 62 | a0002c0001t0002g0001 a0002c0001t0002g0005 a0002c0001t0002g0006 others(59): Show |
131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1416+723G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 12/12 | chr7 | 99707089 | |||||||
| chr7:99707110 | C | T | 1 | a0002c0001t0002g0008 | 6 | HG01884.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1416+702G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 12/12 | chr7 | 99707110 | |||||||
| chr7:99707218 | C | A | 1 | a0002c0001t0002g0055 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1416+594G>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 12/12 | chr7 | 99707218 | |||||||
| chr7:99707288 | C | A | 16 | a0001c0002t0001g0004 a0001c0002t0001g0010 a0001c0002t0001g0015 others(13): Show |
32 | HG00099.hp1 HG00642.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.1416+524G>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 12/12 | chr7 | 99707288 | |||||||
| chr7:99707583 | A | G | 1 | a0002c0001t0002g0065 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1416+229T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 12/12 | chr7 | 99707583 | |||||||
| chr7:99707670 | T | A | 1 | a0001c0002t0001g0117 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1416+142A>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 12/12 | chr7 | 99707670 | |||||||
| chr7:99707687 | T | A | 1 | a0002c0001t0002g0061 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1416+125A>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 12/12 | chr7 | 99707687 | |||||||
| chr7:99707694 | C | G | 2 | a0001c0002t0001g0127 a0001c0002t0001g0128 |
2 | HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1416+118G>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 12/12 | chr7 | 99707694 | |||||||
| chr7:99707727 | G | A | 2 | a0001c0002t0001g0014 a0001c0002t0001g0104 |
5 | HG01891.hp2 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1416+85C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 12/12 | chr7 | 99707727 | |||||||
| chr7:99708144 | G | C | 1 | a0002c0001t0002g0028 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1254-170C>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 11/12 | chr7 | 99708144 | |||||||
| chr7:99708169 | C | T | 1 | a0002c0001t0002g0092 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1254-195G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 11/12 | chr7 | 99708169 | |||||||
| chr7:99708212 | T | A | 1 | a0001c0002t0001g0118 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1254-238A>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 11/12 | chr7 | 99708212 | |||||||
| chr7:99708267 | T | C | 1 | a0002c0001t0002g0079 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1254-293A>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 11/12 | chr7 | 99708267 | |||||||
| chr7:99708284 | C | T | 1 | a0001c0002t0001g0009 | 5 | NA18948.hp1 NA18950.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.1254-310G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 11/12 | chr7 | 99708284 | |||||||
| chr7:99708633 | A | T | 1 | a0001c0002t0001g0120 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1253+402T>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 11/12 | chr7 | 99708633 | |||||||
| chr7:99708645 | C | A | 2 | a0001c0002t0004g0036 a0001c0002t0004g0129 |
3 | HG01884.hp1 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1253+390G>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 11/12 | chr7 | 99708645 | |||||||
| chr7:99708659 | C | T | 1 | a0001c0002t0001g0087 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1253+376G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 11/12 | chr7 | 99708659 | |||||||
| chr7:99708698 | G | T | 62 | a0002c0001t0002g0001 a0002c0001t0002g0005 a0002c0001t0002g0006 others(59): Show |
131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1253+337C>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 11/12 | chr7 | 99708698 | |||||||
| chr7:99708729 | A | G | 1 | a0001c0003t0001g0011 | 5 | HG01243.hp1 HG02965.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1253+306T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 11/12 | chr7 | 99708729 | |||||||
| chr7:99708848 | A | G | 1 | a0001c0002t0001g0112 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1253+187T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 11/12 | chr7 | 99708848 | |||||||
| chr7:99708943 | C | T | 64 | a0002c0001t0001g0025 a0002c0001t0002g0001 a0002c0001t0002g0005 others(61): Show |
134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.1253+92G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 11/12 | chr7 | 99708943 | |||||||
| chr7:99709372 | G | A | 1 | a0001c0002t0001g0103 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1027-111C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 10/12 | chr7 | 99709372 | |||||||
| chr7:99709479 | G | A | 1 | a0002c0001t0002g0080 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1027-218C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 10/12 | chr7 | 99709479 | |||||||
| chr7:99709598 | A | C | 2 | a0001c0002t0004g0036 a0001c0002t0004g0129 |
3 | HG01884.hp1 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1027-337T>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 10/12 | chr7 | 99709598 | |||||||
| chr7:99709645 | G | A | 64 | a0002c0001t0001g0025 a0002c0001t0002g0001 a0002c0001t0002g0005 others(61): Show |
134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.1027-384C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 10/12 | chr7 | 99709645 | |||||||
| chr7:99709769 | T | C | 1 | a0001c0002t0001g0128 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1027-508A>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 10/12 | chr7 | 99709769 | |||||||
| chr7:99709774 | A | ATGTG | 60 | a0002c0001t0001g0025 a0002c0001t0002g0001 a0002c0001t0002g0005 others(57): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1027-517_1027-514d others(6): Show |
CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 10/12 | chr7 | 99709774 | |||||||
| chr7:99709786 | G | A | 1 | a0001c0002t0004g0037 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1027-525C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 10/12 | chr7 | 99709786 | |||||||
| chr7:99709786 | G | T | 2 | a0001c0002t0001g0034 a0001c0002t0001g0124 |
3 | HG02809.hp2 HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1027-525C>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 10/12 | chr7 | 99709786 | |||||||
| chr7:99709830 | T | A | 8 | a0001c0002t0001g0004 a0001c0002t0001g0015 a0001c0002t0001g0031 others(5): Show |
18 | HG00099.hp1 HG00642.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.1027-569A>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 10/12 | chr7 | 99709830 | |||||||
| chr7:99709876 | C | T | 2 | a0002c0001t0002g0051 a0003c0004t0002g0085 |
2 | HG00140.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.1027-615G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 10/12 | chr7 | 99709876 | |||||||
| chr7:99710037 | C | G | 1 | a0001c0002t0001g0115 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1026+695G>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 10/12 | chr7 | 99710037 | |||||||
| chr7:99710340 | C | T | 2 | a0001c0002t0001g0017 a0001c0002t0001g0023 |
5 | HG02970.hp2 HG03225.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1026+392G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 10/12 | chr7 | 99710340 | |||||||
| chr7:99710349 | C | T | 1 | a0001c0002t0001g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1026+383G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 10/12 | chr7 | 99710349 | |||||||
| chr7:99711061 | A | G | 2 | a0001c0002t0001g0127 a0001c0002t0001g0128 |
2 | HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.866-169T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 9/12 | chr7 | 99711061 | |||||||
| chr7:99711112 | G | A | 1 | a0001c0002t0001g0105 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.866-220C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 9/12 | chr7 | 99711112 | |||||||
| chr7:99711385 | T | G | 2 | a0001c0002t0001g0127 a0001c0002t0001g0128 |
2 | HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.866-493A>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 9/12 | chr7 | 99711385 | |||||||
| chr7:99711402 | C | T | 1 | a0002c0001t0002g0061 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.866-510G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 9/12 | chr7 | 99711402 | |||||||
| chr7:99711437 | A | G | 3 | a0001c0002t0001g0007 a0001c0002t0001g0106 a0001c0002t0001g0110 |
9 | HG01099.hp1 HG01192.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.866-545T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 9/12 | chr7 | 99711437 | |||||||
| chr7:99711715 | C | G | 1 | a0002c0001t0002g0073 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.866-823G>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 9/12 | chr7 | 99711715 | |||||||
| chr7:99711755 | C | T | 1 | a0002c0001t0002g0048 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.866-863G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 9/12 | chr7 | 99711755 | |||||||
| chr7:99711781 | A | AAAC | 57 | a0002c0001t0002g0001 a0002c0001t0002g0005 a0002c0001t0002g0006 others(54): Show |
118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.866-892_866-890dup others(3): Show |
CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 9/12 | chr7 | 99711781 | |||||||
| chr7:99712062 | T | C | 25 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(22): Show |
66 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.866-1170A>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 9/12 | chr7 | 99712062 | |||||||
| chr7:99712167 | G | A | 1 | a0002c0001t0002g0059 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.866-1275C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 9/12 | chr7 | 99712167 | |||||||
| chr7:99712261 | T | C | 1 | a0001c0002t0001g0034 | 2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.865+1208A>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 9/12 | chr7 | 99712261 | |||||||
| chr7:99712558 | A | C | 65 | a0001c0002t0001g0087 a0002c0001t0001g0025 a0002c0001t0002g0001 others(62): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.865+911T>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 9/12 | chr7 | 99712558 | |||||||
| chr7:99712650 | TGATA | T | 4 | a0001c0002t0001g0127 a0001c0002t0001g0128 a0002c0001t0002g0066 others(1): Show |
4 | HG00438.hp1 HG00438.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.865+815_865+818del others(4): Show |
CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 9/12 | chr7 | 99712650 | |||||||
| chr7:99712696 | A | G | 18 | a0001c0002t0001g0004 a0001c0002t0001g0010 a0001c0002t0001g0015 others(15): Show |
37 | HG00099.hp1 HG00642.hp2 HG01175.hp1 others(34): Show |
intron_variant | MODIFIER | c.865+773T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 9/12 | chr7 | 99712696 | |||||||
| chr7:99712708 | G | C | 65 | a0001c0002t0001g0087 a0002c0001t0001g0025 a0002c0001t0002g0001 others(62): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.865+761C>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 9/12 | chr7 | 99712708 | |||||||
| chr7:99713003 | A | G | 1 | a0002c0001t0002g0072 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.865+466T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 9/12 | chr7 | 99713003 | |||||||
| chr7:99713120 | G | A | 2 | a0002c0001t0002g0020 a0002c0001t0002g0086 |
4 | HG01516.hp2 HG01517.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.865+349C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 9/12 | chr7 | 99713120 | |||||||
| chr7:99713342 | C | T | 16 | a0001c0002t0001g0004 a0001c0002t0001g0010 a0001c0002t0001g0015 others(13): Show |
32 | HG00099.hp1 HG00642.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.865+127G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 9/12 | chr7 | 99713342 | |||||||
| chr7:99713627 | A | C | 2 | a0001c0002t0004g0036 a0001c0002t0004g0129 |
3 | HG01884.hp1 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.799-92T>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 8/12 | chr7 | 99713627 | |||||||
| chr7:99713686 | A | G | 1 | a0004c0006t0001g0108 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.799-151T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 8/12 | chr7 | 99713686 | |||||||
| chr7:99713779 | A | G | 1 | a0002c0001t0002g0029 | 2 | HG02602.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.799-244T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 8/12 | chr7 | 99713779 | |||||||
| chr7:99713927 | G | A | 64 | a0002c0001t0001g0025 a0002c0001t0002g0001 a0002c0001t0002g0005 others(61): Show |
134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.799-392C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 8/12 | chr7 | 99713927 | |||||||
| chr7:99714045 | A | G | 4 | a0001c0002t0003g0022 a0001c0002t0003g0038 a0001c0002t0003g0040 others(1): Show |
5 | HG02559.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.798+510T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 8/12 | chr7 | 99714045 | |||||||
| chr7:99714346 | T | C | 1 | a0002c0001t0002g0071 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.798+209A>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 8/12 | chr7 | 99714346 | |||||||
| chr7:99714348 | A | T | 1 | a0002c0001t0002g0071 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.798+207T>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 8/12 | chr7 | 99714348 | |||||||
| chr7:99714354 | C | G | 1 | a0002c0001t0002g0071 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.798+201G>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 8/12 | chr7 | 99714354 | |||||||
| chr7:99714378 | C | T | 2 | a0002c0001t0002g0051 a0003c0004t0002g0085 |
2 | HG00140.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.798+177G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 8/12 | chr7 | 99714378 | |||||||
| chr7:99714486 | C | T | 1 | a0001c0002t0001g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.798+69G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 8/12 | chr7 | 99714486 | |||||||
| chr7:99714701 | A | G | 1 | a0002c0001t0002g0049 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.671-19T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 7/12 | chr7 | 99714701 | |||||||
| chr7:99714755 | T | C | 2 | a0001c0002t0001g0034 a0001c0002t0001g0124 |
3 | HG02809.hp2 HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.671-73A>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 7/12 | chr7 | 99714755 | |||||||
| chr7:99715030 | C | G | 65 | a0001c0002t0001g0087 a0002c0001t0001g0025 a0002c0001t0002g0001 others(62): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.671-348G>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 7/12 | chr7 | 99715030 | |||||||
| chr7:99715309 | A | G | 1 | a0002c0001t0002g0048 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.670+449T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 7/12 | chr7 | 99715309 | |||||||
| chr7:99715332 | C | A | 1 | a0001c0002t0001g0110 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.670+426G>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 7/12 | chr7 | 99715332 | |||||||
| chr7:99715348 | A | G | 1 | a0001c0002t0001g0101 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.670+410T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 7/12 | chr7 | 99715348 | |||||||
| chr7:99715530 | C | T | 1 | a0001c0002t0001g0100 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.670+228G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 7/12 | chr7 | 99715530 | |||||||
| chr7:99715541 | T | A | 1 | a0002c0001t0002g0083 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.670+217A>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 7/12 | chr7 | 99715541 | |||||||
| chr7:99715630 | A | G | 1 | a0002c0001t0002g0028 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.670+128T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 7/12 | chr7 | 99715630 | |||||||
| chr7:99715942 | A | C | 1 | a0002c0001t0002g0088 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.522-36T>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 6/12 | chr7 | 99715942 | |||||||
| chr7:99716396 | C | T | 1 | a0002c0001t0002g0055 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.522-490G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 6/12 | chr7 | 99716396 | |||||||
| chr7:99716742 | C | G | 6 | a0001c0003t0001g0011 a0001c0003t0001g0016 a0001c0003t0001g0122 others(3): Show |
13 | HG01243.hp1 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.521+435G>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 6/12 | chr7 | 99716742 | |||||||
| chr7:99716856 | T | C | 1 | a0002c0001t0002g0061 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.521+321A>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 6/12 | chr7 | 99716856 | |||||||
| chr7:99717018 | G | A | 1 | a0001c0002t0004g0129 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.521+159C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 6/12 | chr7 | 99717018 | |||||||
| chr7:99717104 | A | G | 25 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(22): Show |
66 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.521+73T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 6/12 | chr7 | 99717104 | |||||||
| chr7:99717363 | A | G | 65 | a0001c0002t0001g0087 a0002c0001t0001g0025 a0002c0001t0002g0001 others(62): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.433-98T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 5/12 | chr7 | 99717363 | |||||||
| chr7:99717439 | C | T | 1 | a0002c0001t0002g0070 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.432+87G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 5/12 | chr7 | 99717439 | |||||||
| chr7:99717653 | C | T | 8 | a0001c0002t0001g0004 a0001c0002t0001g0015 a0001c0002t0001g0031 others(5): Show |
18 | HG00099.hp1 HG00642.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.319-14G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99717653 | |||||||
| chr7:99717691 | A | T | 5 | a0002c0001t0001g0025 a0002c0001t0002g0008 a0002c0001t0002g0013 others(2): Show |
14 | HG01884.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.319-52T>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99717691 | |||||||
| chr7:99717852 | A | T | 1 | a0002c0001t0002g0069 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.319-213T>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99717852 | |||||||
| chr7:99717920 | C | T | 5 | a0001c0002t0001g0127 a0001c0002t0001g0128 a0001c0002t0004g0036 others(2): Show |
7 | HG01884.hp1 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.319-281G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99717920 | |||||||
| chr7:99717988 | C | T | 1 | a0001c0003t0001g0122 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.319-349G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99717988 | |||||||
| chr7:99718135 | G | A | 1 | a0002c0001t0002g0008 | 6 | HG01884.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.319-496C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99718135 | |||||||
| chr7:99718233 | T | C | 43 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0004 others(40): Show |
103 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.319-594A>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99718233 | |||||||
| chr7:99718280 | G | T | 1 | a0002c0001t0002g0068 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.319-641C>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99718280 | |||||||
| chr7:99718281 | G | A | 65 | a0001c0002t0001g0087 a0002c0001t0001g0025 a0002c0001t0002g0001 others(62): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.319-642C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99718281 | |||||||
| chr7:99718303 | C | T | 1 | a0001c0002t0001g0107 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.319-664G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99718303 | |||||||
| chr7:99718324 | G | A | 1 | a0002c0001t0002g0084 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.319-685C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99718324 | |||||||
| chr7:99718507 | A | C | 6 | a0001c0003t0001g0011 a0001c0003t0001g0016 a0001c0003t0001g0122 others(3): Show |
13 | HG01243.hp1 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.319-868T>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99718507 | |||||||
| chr7:99718512 | A | C | 1 | a0001c0002t0001g0106 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.319-873T>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99718512 | |||||||
| chr7:99718687 | A | C | 1 | a0001c0002t0001g0099 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.319-1048T>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99718687 | |||||||
| chr7:99718800 | G | T | 117 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0004 others(114): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.319-1161C>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99718800 | |||||||
| chr7:99718830 | C | T | 1 | a0001c0002t0001g0032 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.319-1191G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99718830 | |||||||
| chr7:99718877 | A | G | 5 | a0001c0002t0001g0127 a0001c0002t0001g0128 a0001c0002t0004g0036 others(2): Show |
7 | HG01884.hp1 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.319-1238T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99718877 | |||||||
| chr7:99719202 | A | G | 131 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0004 others(128): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.318+1111T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99719202 | |||||||
| chr7:99719291 | A | G | 130 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0004 others(127): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.318+1022T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99719291 | |||||||
| chr7:99719303 | A | G | 65 | a0001c0002t0001g0087 a0002c0001t0001g0025 a0002c0001t0002g0001 others(62): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.318+1010T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99719303 | |||||||
| chr7:99719418 | C | T | 1 | a0002c0001t0002g0067 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.318+895G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99719418 | |||||||
| chr7:99719474 | C | G | 1 | a0001c0002t0003g0040 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.318+839G>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99719474 | |||||||
| chr7:99719495 | A | G | 1 | a0001c0002t0001g0023 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.318+818T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99719495 | |||||||
| chr7:99719597 | T | TA | 65 | a0001c0002t0001g0087 a0002c0001t0001g0025 a0002c0001t0002g0001 others(62): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.318+715dupT | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99719597 | |||||||
| chr7:99719836 | A | G | 1 | a0001c0002t0001g0098 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.318+477T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99719836 | |||||||
| chr7:99719974 | G | T | 1 | a0001c0002t0001g0097 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.318+339C>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99719974 | |||||||
| chr7:99719996 | G | GAAAAACA | 27 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(24): Show |
71 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.318+310_318+316dup others(7): Show |
CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99719996 | |||||||
| chr7:99720026 | C | G | 1 | a0001c0002t0003g0040 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.318+287G>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99720026 | |||||||
| chr7:99720119 | C | T | 1 | a0002c0001t0002g0089 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.318+194G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99720119 | |||||||
| chr7:99720141 | T | A | 2 | a0001c0002t0001g0017 a0001c0002t0001g0023 |
5 | HG02970.hp2 HG03225.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.318+172A>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99720141 | |||||||
| chr7:99720215 | G | T | 1 | a0002c0001t0002g0019 | 3 | HG02071.hp2 NA18954.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.318+98C>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99720215 | |||||||
| chr7:99720216 | C | T | 1 | a0002c0001t0002g0019 | 3 | HG02071.hp2 NA18954.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.318+97G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 4/12 | chr7 | 99720216 | |||||||
| chr7:99720602 | C | T | 1 | a0002c0001t0002g0066 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.219-190G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 3/12 | chr7 | 99720602 | |||||||
| chr7:99720627 | A | G | 1 | a0001c0002t0001g0009 | 5 | NA18948.hp1 NA18950.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-215T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 3/12 | chr7 | 99720627 | |||||||
| chr7:99720929 | A | G | 4 | a0002c0001t0002g0018 a0002c0001t0002g0052 a0002c0001t0002g0058 others(1): Show |
6 | HG02572.hp1 HG02630.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-517T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 3/12 | chr7 | 99720929 | |||||||
| chr7:99721021 | A | G | 65 | a0001c0002t0001g0087 a0002c0001t0001g0025 a0002c0001t0002g0001 others(62): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.219-609T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 3/12 | chr7 | 99721021 | |||||||
| chr7:99721061 | C | T | 2 | a0001c0002t0001g0021 a0001c0002t0001g0096 |
4 | HG02738.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-649G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 3/12 | chr7 | 99721061 | |||||||
| chr7:99721185 | C | T | 65 | a0001c0002t0001g0087 a0002c0001t0001g0025 a0002c0001t0002g0001 others(62): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.219-773G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 3/12 | chr7 | 99721185 | |||||||
| chr7:99721534 | G | A | 65 | a0001c0002t0001g0087 a0002c0001t0001g0025 a0002c0001t0002g0001 others(62): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.218+762C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 3/12 | chr7 | 99721534 | |||||||
| chr7:99721537 | G | A | 1 | a0002c0001t0002g0091 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.218+759C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 3/12 | chr7 | 99721537 | |||||||
| chr7:99721742 | C | CGT | 57 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0004 others(54): Show |
130 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.218+552_218+553dup others(2): Show |
CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 3/12 | chr7 | 99721742 | |||||||
| chr7:99721788 | T | TA | 3 | a0001c0002t0004g0036 a0001c0002t0004g0037 a0001c0002t0004g0129 |
5 | HG01884.hp1 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+507dupT | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 3/12 | chr7 | 99721788 | |||||||
| chr7:99721872 | T | C | 45 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0004 others(42): Show |
108 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.218+424A>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 3/12 | chr7 | 99721872 | |||||||
| chr7:99721908 | C | G | 1 | a0001c0002t0005g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.218+388G>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 3/12 | chr7 | 99721908 | |||||||
| chr7:99722147 | A | G | 1 | a0001c0002t0001g0093 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.218+149T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 3/12 | chr7 | 99722147 | |||||||
| chr7:99722169 | C | A | 1 | a0001c0002t0001g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.218+127G>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 3/12 | chr7 | 99722169 | |||||||
| chr7:99722228 | C | A | 1 | a0001c0003t0001g0011 | 5 | HG01243.hp1 HG02965.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+68G>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 3/12 | chr7 | 99722228 | |||||||
| chr7:99722494 | G | A | 1 | a0002c0001t0002g0089 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.166-146C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99722494 | |||||||
| chr7:99722507 | A | G | 8 | a0001c0002t0001g0010 a0001c0002t0001g0032 a0001c0002t0001g0033 others(5): Show |
14 | HG02055.hp1 HG02257.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.166-159T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99722507 | |||||||
| chr7:99722622 | G | A | 1 | a0002c0001t0002g0088 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.166-274C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99722622 | |||||||
| chr7:99722676 | C | T | 1 | a0002c0001t0002g0044 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.166-328G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99722676 | |||||||
| chr7:99722725 | C | T | 2 | a0001c0002t0001g0017 a0001c0002t0001g0023 |
5 | HG02970.hp2 HG03225.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-377G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99722725 | |||||||
| chr7:99722846 | C | T | 65 | a0001c0002t0001g0087 a0002c0001t0001g0025 a0002c0001t0002g0001 others(62): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.166-498G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99722846 | |||||||
| chr7:99722947 | A | G | 65 | a0001c0002t0001g0087 a0002c0001t0001g0025 a0002c0001t0002g0001 others(62): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.166-599T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99722947 | |||||||
| chr7:99723027 | T | TA | 70 | a0001c0002t0001g0087 a0001c0003t0001g0011 a0001c0003t0001g0016 others(67): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.166-680dupT | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99723027 | |||||||
| chr7:99723037 | C | T | 5 | a0002c0001t0001g0025 a0002c0001t0002g0008 a0002c0001t0002g0013 others(2): Show |
14 | HG01884.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.166-689G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99723037 | |||||||
| chr7:99723102 | A | C | 5 | a0002c0001t0001g0025 a0002c0001t0002g0008 a0002c0001t0002g0013 others(2): Show |
14 | HG01884.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.166-754T>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99723102 | |||||||
| chr7:99723295 | C | G | 1 | a0002c0001t0002g0065 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.166-947G>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99723295 | |||||||
| chr7:99723376 | C | A | 1 | a0003c0004t0002g0085 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.166-1028G>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99723376 | |||||||
| chr7:99723633 | C | T | 1 | a0001c0002t0004g0037 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.166-1285G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99723633 | |||||||
| chr7:99723718 | C | T | 1 | a0002c0001t0002g0064 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.166-1370G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99723718 | |||||||
| chr7:99723818 | G | A | 65 | a0001c0002t0001g0087 a0002c0001t0001g0025 a0002c0001t0002g0001 others(62): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.166-1470C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99723818 | |||||||
| chr7:99723856 | T | C | 65 | a0001c0002t0001g0087 a0002c0001t0001g0025 a0002c0001t0002g0001 others(62): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.166-1508A>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99723856 | |||||||
| chr7:99723989 | A | G | 65 | a0001c0002t0001g0087 a0002c0001t0001g0025 a0002c0001t0002g0001 others(62): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.166-1641T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99723989 | |||||||
| chr7:99724093 | T | C | 65 | a0001c0002t0001g0087 a0002c0001t0001g0025 a0002c0001t0002g0001 others(62): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.166-1745A>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99724093 | |||||||
| chr7:99724315 | A | G | 1 | a0001c0002t0001g0095 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.166-1967T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99724315 | |||||||
| chr7:99724337 | A | G | 1 | a0001c0002t0004g0037 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.166-1989T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99724337 | |||||||
| chr7:99724376 | A | T | 1 | a0001c0002t0001g0094 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.166-2028T>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99724376 | |||||||
| chr7:99724697 | T | A | 65 | a0001c0002t0001g0087 a0002c0001t0001g0025 a0002c0001t0002g0001 others(62): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.166-2349A>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99724697 | |||||||
| chr7:99724719 | T | C | 65 | a0001c0002t0001g0087 a0002c0001t0001g0025 a0002c0001t0002g0001 others(62): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.166-2371A>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99724719 | |||||||
| chr7:99724781 | G | A | 2 | a0001c0002t0001g0017 a0001c0002t0001g0023 |
5 | HG02970.hp2 HG03225.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-2433C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99724781 | |||||||
| chr7:99724907 | T | C | 1 | a0002c0001t0002g0086 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.166-2559A>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99724907 | |||||||
| chr7:99724912 | C | G | 1 | a0001c0002t0001g0031 | 2 | HG01891.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.166-2564G>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99724912 | |||||||
| chr7:99724993 | T | C | 1 | a0002c0001t0002g0091 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.166-2645A>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99724993 | |||||||
| chr7:99725160 | G | A | 1 | a0001c0002t0004g0037 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.166-2812C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99725160 | |||||||
| chr7:99725225 | C | T | 5 | a0002c0001t0001g0025 a0002c0001t0002g0008 a0002c0001t0002g0013 others(2): Show |
14 | HG01884.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.166-2877G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99725225 | |||||||
| chr7:99725451 | A | C | 65 | a0001c0002t0001g0087 a0002c0001t0001g0025 a0002c0001t0002g0001 others(62): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.166-3103T>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99725451 | |||||||
| chr7:99725494 | A | G | 1 | a0001c0002t0001g0093 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.166-3146T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99725494 | |||||||
| chr7:99725564 | G | A | 1 | a0001c0002t0001g0087 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.166-3216C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99725564 | |||||||
| chr7:99725602 | G | A | 1 | a0002c0001t0002g0088 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.166-3254C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99725602 | |||||||
| chr7:99725771 | C | T | 1 | a0002c0001t0002g0005 | 7 | HG01074.hp1 HG01099.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.166-3423G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99725771 | |||||||
| chr7:99725889 | C | G | 1 | a0002c0001t0002g0063 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.166-3541G>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99725889 | |||||||
| chr7:99726461 | C | T | 1 | a0001c0003t0001g0122 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.166-4113G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99726461 | |||||||
| chr7:99726483 | C | T | 1 | a0002c0001t0002g0048 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.166-4135G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99726483 | |||||||
| chr7:99726594 | C | T | 1 | a0002c0001t0002g0027 | 2 | HG01257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.166-4246G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99726594 | |||||||
| chr7:99726747 | C | A | 1 | a0002c0001t0002g0089 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.165+4312G>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99726747 | |||||||
| chr7:99726857 | G | A | 2 | a0001c0002t0001g0127 a0001c0002t0001g0128 |
2 | HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.165+4202C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99726857 | |||||||
| chr7:99726892 | G | C | 65 | a0001c0002t0001g0087 a0002c0001t0001g0025 a0002c0001t0002g0001 others(62): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.165+4167C>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99726892 | |||||||
| chr7:99726894 | C | G | 1 | a0002c0001t0002g0062 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.165+4165G>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99726894 | |||||||
| chr7:99726936 | C | G | 1 | a0001c0002t0001g0114 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.165+4123G>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99726936 | |||||||
| chr7:99727120 | T | C | 65 | a0001c0002t0001g0087 a0002c0001t0001g0025 a0002c0001t0002g0001 others(62): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.165+3939A>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99727120 | |||||||
| chr7:99727151 | A | G | 1 | a0002c0001t0002g0061 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.165+3908T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99727151 | |||||||
| chr7:99727173 | A | G | 65 | a0001c0002t0001g0087 a0002c0001t0001g0025 a0002c0001t0002g0001 others(62): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.165+3886T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99727173 | |||||||
| chr7:99727198 | T | C | 1 | a0001c0002t0001g0105 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.165+3861A>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99727198 | |||||||
| chr7:99727242 | A | G | 1 | a0001c0002t0001g0021 | 3 | HG02738.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.165+3817T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99727242 | |||||||
| chr7:99727270 | G | T | 1 | a0001c0002t0001g0113 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.165+3789C>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99727270 | |||||||
| chr7:99727492 | G | A | 65 | a0001c0002t0001g0087 a0002c0001t0001g0025 a0002c0001t0002g0001 others(62): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.165+3567C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99727492 | |||||||
| chr7:99727519 | C | G | 1 | a0002c0001t0002g0060 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.165+3540G>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99727519 | |||||||
| chr7:99727639 | C | T | 4 | a0002c0001t0002g0018 a0002c0001t0002g0052 a0002c0001t0002g0058 others(1): Show |
6 | HG02572.hp1 HG02630.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+3420G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99727639 | |||||||
| chr7:99727729 | C | T | 1 | a0002c0001t0003g0042 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.165+3330G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99727729 | |||||||
| chr7:99728101 | T | C | 5 | a0002c0001t0001g0025 a0002c0001t0002g0008 a0002c0001t0002g0013 others(2): Show |
14 | HG01884.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+2958A>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99728101 | |||||||
| chr7:99728259 | C | T | 65 | a0001c0002t0001g0087 a0002c0001t0001g0025 a0002c0001t0002g0001 others(62): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.165+2800G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99728259 | |||||||
| chr7:99728299 | T | G | 1 | a0001c0002t0003g0012 | 4 | HG01167.hp2 HG01169.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+2760A>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99728299 | |||||||
| chr7:99728408 | A | G | 2 | a0001c0002t0001g0034 a0001c0002t0001g0124 |
3 | HG02809.hp2 HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.165+2651T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99728408 | |||||||
| chr7:99728686 | T | G | 60 | a0001c0002t0001g0087 a0002c0001t0002g0001 a0002c0001t0002g0005 others(57): Show |
121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.165+2373A>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99728686 | |||||||
| chr7:99728756 | G | C | 1 | a0001c0002t0001g0111 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.165+2303C>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99728756 | |||||||
| chr7:99728875 | A | G | 16 | a0001c0002t0001g0004 a0001c0002t0001g0010 a0001c0002t0001g0015 others(13): Show |
32 | HG00099.hp1 HG00642.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.165+2184T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99728875 | |||||||
| chr7:99728940 | G | A | 1 | a0002c0001t0002g0090 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.165+2119C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99728940 | |||||||
| chr7:99729036 | G | A | 16 | a0001c0002t0001g0004 a0001c0002t0001g0010 a0001c0002t0001g0015 others(13): Show |
32 | HG00099.hp1 HG00642.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.165+2023C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99729036 | |||||||
| chr7:99729040 | A | G | 45 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0004 others(42): Show |
108 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.165+2019T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99729040 | |||||||
| chr7:99729107 | C | G | 27 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(24): Show |
71 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.165+1952G>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99729107 | |||||||
| chr7:99729185 | C | T | 1 | a0002c0001t0002g0026 | 2 | NA18964.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.165+1874G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99729185 | |||||||
| chr7:99729202 | A | G | 6 | a0002c0001t0001g0025 a0002c0001t0002g0008 a0002c0001t0002g0013 others(3): Show |
15 | HG01884.hp2 HG01993.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.165+1857T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99729202 | |||||||
| chr7:99729356 | C | A | 1 | a0002c0001t0002g0091 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.165+1703G>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99729356 | |||||||
| chr7:99729535 | G | A | 65 | a0001c0002t0001g0087 a0002c0001t0001g0025 a0002c0001t0002g0001 others(62): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.165+1524C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99729535 | |||||||
| chr7:99729769 | A | G | 2 | a0001c0002t0001g0034 a0001c0002t0001g0124 |
3 | HG02809.hp2 HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.165+1290T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99729769 | |||||||
| chr7:99729979 | C | T | 2 | a0002c0001t0002g0054 a0002c0001t0002g0055 |
2 | HG00408.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.165+1080G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99729979 | |||||||
| chr7:99730059 | T | C | 8 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0106 others(5): Show |
31 | HG00408.hp2 HG00597.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.165+1000A>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99730059 | |||||||
| chr7:99730499 | C | T | 1 | a0002c0001t0002g0053 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.165+560G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99730499 | |||||||
| chr7:99730858 | A | C | 2 | a0001c0002t0001g0127 a0001c0002t0001g0128 |
2 | HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.165+201T>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99730858 | |||||||
| chr7:99730885 | A | G | 1 | a0002c0001t0002g0052 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.165+174T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99730885 | |||||||
| chr7:99730923 | C | A | 6 | a0001c0003t0001g0011 a0001c0003t0001g0016 a0001c0003t0001g0122 others(3): Show |
13 | HG01243.hp1 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.165+136G>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 2/12 | chr7 | 99730923 | |||||||
| chr7:99731185 | A | T | 1 | a0001c0002t0001g0023 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.72-33T>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99731185 | |||||||
| chr7:99731233 | T | C | 1 | a0001c0002t0001g0133 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.72-81A>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99731233 | |||||||
| chr7:99731572 | G | A | 1 | a0002c0001t0002g0092 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.72-420C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99731572 | |||||||
| chr7:99731846 | C | T | 1 | a0002c0001t0002g0051 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.72-694G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99731846 | |||||||
| chr7:99731933 | A | G | 1 | a0002c0001t0002g0050 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.72-781T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99731933 | |||||||
| chr7:99731943 | A | G | 1 | a0001c0002t0001g0112 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.72-791T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99731943 | |||||||
| chr7:99732258 | C | A | 1 | a0001c0002t0001g0010 | 5 | HG02257.hp1 HG02965.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.72-1106G>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99732258 | |||||||
| chr7:99732275 | A | G | 1 | a0002c0001t0002g0049 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.72-1123T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99732275 | |||||||
| chr7:99732332 | A | G | 4 | a0002c0001t0001g0025 a0002c0001t0002g0008 a0002c0001t0002g0013 others(1): Show |
13 | HG01884.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.72-1180T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99732332 | |||||||
| chr7:99732360 | C | A | 26 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(23): Show |
70 | HG00408.hp2 HG00597.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.72-1208G>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99732360 | |||||||
| chr7:99732390 | A | AT | 3 | a0001c0003t0001g0011 a0001c0003t0001g0122 a0001c0003t0001g0123 |
7 | HG01243.hp1 HG02897.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.72-1239dupA | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99732390 | |||||||
| chr7:99732666 | T | C | 2 | a0001c0002t0001g0017 a0001c0002t0001g0023 |
5 | HG02970.hp2 HG03225.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.72-1514A>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99732666 | |||||||
| chr7:99732872 | C | T | 1 | a0002c0001t0002g0047 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.72-1720G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99732872 | |||||||
| chr7:99732873 | C | T | 1 | a0002c0001t0002g0047 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.72-1721G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99732873 | |||||||
| chr7:99732884 | C | T | 1 | a0002c0001t0002g0046 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.72-1732G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99732884 | |||||||
| chr7:99733006 | A | G | 6 | a0001c0003t0001g0011 a0001c0003t0001g0016 a0001c0003t0001g0122 others(3): Show |
13 | HG01243.hp1 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.72-1854T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99733006 | |||||||
| chr7:99733115 | A | G | 3 | a0001c0002t0004g0036 a0001c0002t0004g0037 a0001c0002t0004g0129 |
5 | HG01884.hp1 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+1908T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99733115 | |||||||
| chr7:99733123 | C | T | 1 | a0001c0002t0003g0038 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.71+1900G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99733123 | |||||||
| chr7:99733194 | G | A | 1 | a0001c0002t0003g0043 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.71+1829C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99733194 | |||||||
| chr7:99733419 | T | G | 65 | a0001c0002t0001g0056 a0001c0002t0001g0087 a0002c0001t0001g0025 others(62): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.71+1604A>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99733419 | |||||||
| chr7:99733426 | A | G | 26 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(23): Show |
70 | HG00408.hp2 HG00597.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.71+1597T>C | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99733426 | |||||||
| chr7:99733669 | G | A | 2 | a0001c0002t0001g0127 a0001c0002t0001g0128 |
2 | HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.71+1354C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99733669 | |||||||
| chr7:99733729 | C | A | 3 | a0001c0002t0004g0036 a0001c0002t0004g0037 a0001c0002t0004g0129 |
5 | HG01884.hp1 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+1294G>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99733729 | |||||||
| chr7:99733850 | C | T | 42 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0004 others(39): Show |
102 | HG00099.hp1 HG00408.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.71+1173G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99733850 | |||||||
| chr7:99734230 | G | T | 2 | a0002c0001t0002g0044 a0002c0001t0002g0045 |
2 | HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.71+793C>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99734230 | |||||||
| chr7:99734297 | T | C | 2 | a0001c0003t0001g0130 a0001c0003t0001g0131 |
2 | HG02258.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.71+726A>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99734297 | |||||||
| chr7:99734460 | C | T | 65 | a0001c0002t0001g0056 a0001c0002t0001g0087 a0002c0001t0001g0025 others(62): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.71+563G>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99734460 | |||||||
| chr7:99734510 | G | A | 1 | a0002c0001t0002g0132 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.71+513C>T | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99734510 | |||||||
| chr7:99734539 | A | C | 1 | a0002c0001t0002g0024 | 2 | HG01258.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.71+484T>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99734539 | |||||||
| chr7:99734628 | T | C | 1 | a0001c0002t0001g0133 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.71+395A>G | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99734628 | |||||||
| chr7:99734833 | G | T | 2 | a0001c0002t0001g0017 a0001c0002t0001g0023 |
5 | HG02970.hp2 HG03225.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+190C>A | CYP3A7 | ENSG00000160870.15 | transcript | ENST00000336374.4 | protein_coding | 1/12 | chr7 | 99734833 |