Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1562 |
| ensemblid | ENSG00000108242.13 |
| hgncid | 2620 |
| symbol | CYP2C18 |
| name | cytochrome P450 family 2 subfamily C member 18 |
| refseq_nuc | NM_000772.3 |
| refseq_prot | NP_000763.1 |
| ensembl_nuc | ENST00000285979.11 |
| ensembl_prot | ENSP00000285979.6 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 94683729 |
| end | 94736190 |
| strand | + |
| ver | v1.2 |
| region | chr10:94683729-94736190 |
| region5000 | chr10:94678729-94741190 |
| regionname0 | CYP2C18_chr10_94683729_94736190 |
| regionname5000 | CYP2C18_chr10_94678729_94741190 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 490 | 253 | 70 | 49 | 92 | 15 | 25 | 71 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | MDPAV others(485): Show |
chr10 | 94678729 | 94741190 |
| a0002 | 0/0 | 490 | 86 | 9 | 6 | 57 | 1 | 13 | 42 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | MDPAV others(485): Show |
chr10 | 94678729 | 94741190 |
| a0003 | 0/0 | 67 | 24 | 7 | 0 | 13 | 0 | 4 | 13 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | MDPAV others(62): Show |
chr10 | 94678729 | 94741190 |
| a0004 | 0/0 | 490 | 7 | 0 | 3 | 0 | 2 | 2 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | MDPAV others(485): Show |
chr10 | 94678729 | 94741190 |
| a0005 | 0/0 | 490 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | MDPAV others(485): Show |
chr10 | 94678729 | 94741190 |
| a0006 | 0/0 | 490 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | MDPAV others(485): Show |
chr10 | 94678729 | 94741190 |
| a0007 | 0/0 | 490 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | MDPAV others(485): Show |
chr10 | 94678729 | 94741190 |
| a0008 | 0/0 | 490 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | MDPAV others(485): Show |
chr10 | 94678729 | 94741190 |
| a0009 | 0/0 | 419 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | MDPAV others(414): Show |
chr10 | 94678729 | 94741190 |
| a0010 | 0/0 | 490 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | MDPAV others(485): Show |
chr10 | 94678729 | 94741190 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1470 | 236 | 62 | 47 | 85 | 15 | 25 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | ATGGA others(1465): Show |
chr10 | 94678729 | 94741190 | ||
| a0001c0004 | 0/0 | 1470 | 9 | 0 | 2 | 7 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | ATGGA others(1465): Show |
chr10 | 94678729 | 94741190 | ||
| a0001c0005 | 0/0 | 1470 | 8 | 8 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | ATGGA others(1465): Show |
chr10 | 94678729 | 94741190 | ||
| a0002c0002 | 0/0 | 1470 | 85 | 9 | 6 | 56 | 1 | 13 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | ATGGA others(1465): Show |
chr10 | 94678729 | 94741190 | ||
| a0002c0011 | 0/0 | 1470 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | ATGGA others(1465): Show |
chr10 | 94678729 | 94741190 | ||
| a0003c0003 | 0/0 | 1470 | 20 | 3 | 0 | 13 | 0 | 4 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | ATGGA others(1465): Show |
chr10 | 94678729 | 94741190 | ||
| a0003c0007 | 0/0 | 1470 | 3 | 3 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | ATGGA others(1465): Show |
chr10 | 94678729 | 94741190 | ||
| a0003c0010 | 0/0 | 1470 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | ATGGA others(1465): Show |
chr10 | 94678729 | 94741190 | ||
| a0004c0006 | 0/0 | 1470 | 7 | 0 | 3 | 0 | 2 | 2 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | ATGGA others(1465): Show |
chr10 | 94678729 | 94741190 | ||
| a0005c0008 | 0/0 | 1470 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | ATGGA others(1465): Show |
chr10 | 94678729 | 94741190 | ||
| a0006c0009 | 0/0 | 1470 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | ATGGA others(1465): Show |
chr10 | 94678729 | 94741190 | ||
| a0007c0015 | 0/0 | 1470 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | ATGGA others(1465): Show |
chr10 | 94678729 | 94741190 | ||
| a0008c0014 | 0/0 | 1470 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | ATGGA others(1465): Show |
chr10 | 94678729 | 94741190 | ||
| a0009c0012 | 0/0 | 1470 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | ATGGA others(1465): Show |
chr10 | 94678729 | 94741190 | ||
| a0010c0013 | 0/0 | 1470 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | ATGGA others(1465): Show |
chr10 | 94678729 | 94741190 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2310 | 158 | 57 | 27 | 50 | 9 | 14 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | AGAGT others(2305): Show |
chr10 | 94678729 | 94741190 |
| a0001c0001t0002 | 0/1 | 2310 | 55 | 2 | 17 | 22 | 5 | 8 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | AGAGT others(2305): Show |
chr10 | 94678729 | 94741190 |
| a0001c0001t0004 | 0/0 | 2310 | 3 | 2 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | AGAGT others(2305): Show |
chr10 | 94678729 | 94741190 |
| a0001c0001t0005 | 0/0 | 2311 | 18 | 0 | 2 | 12 | 1 | 3 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | AGAGT others(2306): Show |
chr10 | 94678729 | 94741190 |
| a0001c0001t0009 | 0/0 | 2310 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | AGAGT others(2305): Show |
chr10 | 94678729 | 94741190 |
| a0001c0001t0011 | 0/0 | 2310 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | AGAGT others(2305): Show |
chr10 | 94678729 | 94741190 |
| a0001c0004t0002 | 0/0 | 2310 | 9 | 0 | 2 | 7 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | AGAGT others(2305): Show |
chr10 | 94678729 | 94741190 |
| a0001c0005t0001 | 0/0 | 2310 | 8 | 8 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | AGAGT others(2305): Show |
chr10 | 94678729 | 94741190 |
| a0002c0002t0003 | 0/0 | 2310 | 48 | 0 | 1 | 41 | 0 | 6 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | AGAGT others(2305): Show |
chr10 | 94678729 | 94741190 |
| a0002c0002t0004 | 0/0 | 2310 | 34 | 9 | 3 | 15 | 0 | 7 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | AGAGT others(2305): Show |
chr10 | 94678729 | 94741190 |
| a0002c0002t0007 | 0/0 | 2310 | 2 | 0 | 1 | 0 | 1 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | AGAGT others(2305): Show |
chr10 | 94678729 | 94741190 |
| a0002c0002t0008 | 0/0 | 2310 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | AGAGT others(2305): Show |
chr10 | 94678729 | 94741190 |
| a0002c0011t0003 | 0/0 | 2310 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | AGAGT others(2305): Show |
chr10 | 94678729 | 94741190 |
| a0003c0003t0001 | 0/0 | 2310 | 3 | 3 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | AGAGT others(2305): Show |
chr10 | 94678729 | 94741190 |
| a0003c0003t0006 | 0/0 | 2310 | 17 | 0 | 0 | 13 | 0 | 4 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | AGAGT others(2305): Show |
chr10 | 94678729 | 94741190 |
| a0003c0007t0001 | 0/0 | 2310 | 3 | 3 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | AGAGT others(2305): Show |
chr10 | 94678729 | 94741190 |
| a0003c0010t0010 | 0/0 | 2310 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | AGAGT others(2305): Show |
chr10 | 94678729 | 94741190 |
| a0004c0006t0001 | 0/0 | 2310 | 7 | 0 | 3 | 0 | 2 | 2 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | AGAGT others(2305): Show |
chr10 | 94678729 | 94741190 |
| a0005c0008t0004 | 0/0 | 2310 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | AGAGT others(2305): Show |
chr10 | 94678729 | 94741190 |
| a0006c0009t0003 | 0/0 | 2310 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | AGAGT others(2305): Show |
chr10 | 94678729 | 94741190 |
| a0007c0015t0012 | 0/0 | 2310 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | AGAGT others(2305): Show |
chr10 | 94678729 | 94741190 |
| a0008c0014t0001 | 0/0 | 2310 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | AGAGT others(2305): Show |
chr10 | 94678729 | 94741190 |
| a0009c0012t0002 | 0/0 | 2310 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | AGAGT others(2305): Show |
chr10 | 94678729 | 94741190 |
| a0010c0013t0001 | 0/0 | 2310 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | AGAGT others(2305): Show |
chr10 | 94678729 | 94741190 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0002 | 0/0 | 11 | 4 | 3 | 0 | 0 | 4 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0003 | 0/0 | 10 | 10 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0006 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0234 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0005 | 0/0 | 8 | 0 | 6 | 0 | 2 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0012 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0045 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0002g0219 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0004g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0005g0004 | 0/0 | 8 | 0 | 0 | 6 | 0 | 2 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0005g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0009g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0001t0011g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0004t0002g0007 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0004t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0004t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0004t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0005t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0005t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0005t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0005t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0005t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0001c0005t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0007g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0002t0008g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0002c0011t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0003c0003t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0003c0003t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0003c0003t0006g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0003c0003t0006g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0003c0003t0006g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0003c0003t0006g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0003c0003t0006g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0003c0003t0006g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0003c0003t0006g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0003c0003t0006g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0003c0003t0006g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0003c0003t0006g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0003c0003t0006g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0003c0007t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0003c0007t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0003c0010t0010g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0004c0006t0001g0001 | 0/0 | 6 | 0 | 2 | 0 | 2 | 2 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0004c0006t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0005c0008t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0005c0008t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0006c0009t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0006c0009t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0007c0015t0012g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0008c0014t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0009c0012t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| a0010c0013t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0206 | EUR | GBR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | GBR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | GBR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | GBR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG00280 | hp1 | a0002 | c0002 | t0007 | g0032 | EUR | FIN | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0196 | EUR | FIN | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | FIN | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0201 | EUR | FIN | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0059 | EAS | CHS | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG00423 | hp2 | a0002 | c0002 | t0003 | g0073 | EAS | CHS | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG00438 | hp1 | a0002 | c0002 | t0003 | g0011 | EAS | CHS | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | CHS | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG00609 | hp2 | a0002 | c0002 | t0003 | g0125 | EAS | CHS | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG00621 | hp1 | a0002 | c0002 | t0004 | g0009 | EAS | CHS | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG00621 | hp2 | a0002 | c0002 | t0003 | g0072 | EAS | CHS | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0028 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG00639 | hp2 | a0004 | c0006 | t0001 | g0001 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG00673 | hp2 | a0002 | c0002 | t0004 | g0091 | EAS | CHS | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG00741 | hp2 | a0002 | c0002 | t0004 | g0097 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01071 | hp1 | a0002 | c0002 | t0004 | g0100 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01074 | hp1 | a0002 | c0002 | t0008 | g0030 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01192 | hp2 | a0002 | c0002 | t0004 | g0123 | AMR | PUR | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0065 | AMR | CLM | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01358 | hp2 | a0004 | c0006 | t0001 | g0001 | AMR | CLM | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01496 | hp1 | a0002 | c0002 | t0007 | g0032 | AMR | CLM | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0177 | EUR | IBS | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01515 | hp2 | a0004 | c0006 | t0001 | g0001 | EUR | IBS | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | IBS | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01517 | hp2 | a0004 | c0006 | t0001 | g0001 | EUR | IBS | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01884 | hp1 | a0003 | c0003 | t0001 | g0236 | AFR | ACB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PEL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0064 | AMR | PEL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01981 | hp1 | a0001 | c0004 | t0002 | g0180 | AMR | PEL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02027 | hp2 | a0002 | c0002 | t0004 | g0051 | EAS | KHV | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02040 | hp1 | a0002 | c0002 | t0003 | g0016 | EAS | KHV | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02040 | hp2 | a0001 | c0001 | t0005 | g0058 | EAS | KHV | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | ACB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | KHV | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02074 | hp2 | a0002 | c0002 | t0003 | g0076 | EAS | KHV | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02080 | hp2 | a0002 | c0002 | t0003 | g0090 | EAS | KHV | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | KHV | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02083 | hp2 | a0001 | c0001 | t0011 | g0188 | EAS | KHV | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02129 | hp2 | a0002 | c0002 | t0004 | g0009 | EAS | KHV | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02132 | hp1 | a0002 | c0002 | t0004 | g0031 | EAS | KHV | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02135 | hp2 | a0002 | c0002 | t0004 | g0098 | EAS | KHV | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02145 | hp1 | a0001 | c0005 | t0001 | g0055 | AFR | ACB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02145 | hp2 | a0002 | c0002 | t0004 | g0102 | AFR | ACB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02155 | hp1 | a0002 | c0002 | t0003 | g0103 | EAS | CDX | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02155 | hp2 | a0001 | c0004 | t0002 | g0161 | EAS | CDX | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02257 | hp2 | a0007 | c0015 | t0012 | g0251 | AFR | ACB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02258 | hp1 | a0005 | c0008 | t0004 | g0249 | AFR | ACB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02258 | hp2 | a0003 | c0007 | t0001 | g0252 | AFR | ACB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02280 | hp1 | a0002 | c0002 | t0004 | g0246 | AFR | ACB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02293 | hp1 | a0001 | c0004 | t0002 | g0007 | AMR | PEL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02293 | hp2 | a0002 | c0002 | t0003 | g0085 | AMR | PEL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0124 | AFR | ACB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02602 | hp2 | a0002 | c0002 | t0003 | g0119 | SAS | PJL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02630 | hp2 | a0003 | c0010 | t0010 | g0245 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02698 | hp1 | a0002 | c0002 | t0004 | g0086 | SAS | PJL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0175 | SAS | PJL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02723 | hp2 | a0002 | c0002 | t0004 | g0112 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02735 | hp2 | a0002 | c0002 | t0004 | g0082 | SAS | PJL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02886 | hp1 | a0003 | c0003 | t0001 | g0048 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02886 | hp2 | a0001 | c0005 | t0001 | g0066 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02895 | hp1 | a0002 | c0002 | t0004 | g0110 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02896 | hp2 | a0001 | c0005 | t0001 | g0027 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02897 | hp2 | a0001 | c0005 | t0001 | g0027 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02922 | hp1 | a0003 | c0007 | t0001 | g0050 | AFR | ESN | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02922 | hp2 | a0005 | c0008 | t0004 | g0248 | AFR | ESN | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02970 | hp1 | a0002 | c0002 | t0004 | g0074 | AFR | ESN | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02976 | hp1 | a0002 | c0002 | t0004 | g0101 | AFR | ESN | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03017 | hp1 | a0002 | c0002 | t0004 | g0113 | SAS | PJL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03041 | hp2 | a0002 | c0002 | t0004 | g0104 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03139 | hp1 | a0001 | c0005 | t0001 | g0026 | AFR | ESN | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03195 | hp1 | a0001 | c0005 | t0001 | g0054 | AFR | ESN | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03453 | hp1 | a0003 | c0003 | t0001 | g0048 | AFR | MSL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03486 | hp2 | a0002 | c0002 | t0004 | g0099 | AFR | MSL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03490 | hp1 | a0003 | c0003 | t0006 | g0049 | SAS | PJL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03490 | hp2 | a0001 | c0001 | t0005 | g0004 | SAS | PJL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03491 | hp2 | a0002 | c0002 | t0004 | g0087 | SAS | PJL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03492 | hp1 | a0003 | c0003 | t0006 | g0049 | SAS | PJL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03579 | hp2 | a0003 | c0007 | t0001 | g0050 | AFR | MSL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03654 | hp1 | a0002 | c0002 | t0003 | g0118 | SAS | PJL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0164 | SAS | PJL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03669 | hp2 | a0002 | c0002 | t0004 | g0078 | SAS | PJL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03688 | hp1 | a0002 | c0002 | t0003 | g0121 | SAS | STU | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03704 | hp1 | a0004 | c0006 | t0001 | g0001 | SAS | PJL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0062 | SAS | PJL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03831 | hp2 | a0003 | c0003 | t0006 | g0239 | SAS | BEB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03834 | hp1 | a0002 | c0002 | t0004 | g0088 | SAS | BEB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | BEB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0171 | SAS | BEB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03927 | hp2 | a0004 | c0006 | t0001 | g0001 | SAS | BEB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | BEB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03942 | hp2 | a0002 | c0002 | t0003 | g0122 | SAS | BEB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG04115 | hp1 | a0002 | c0002 | t0003 | g0075 | SAS | STU | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0165 | SAS | STU | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG04204 | hp1 | a0002 | c0002 | t0004 | g0089 | SAS | STU | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG04204 | hp2 | a0003 | c0003 | t0006 | g0238 | SAS | STU | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG04228 | hp1 | a0002 | c0002 | t0003 | g0081 | SAS | STU | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | STU | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18612 | hp2 | a0002 | c0002 | t0003 | g0029 | EAS | CHB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18939 | hp2 | a0002 | c0002 | t0003 | g0092 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18940 | hp1 | a0002 | c0002 | t0003 | g0015 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18943 | hp1 | a0002 | c0002 | t0003 | g0010 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18943 | hp2 | a0003 | c0003 | t0006 | g0237 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18944 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18944 | hp2 | a0002 | c0002 | t0003 | g0070 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18945 | hp1 | a0002 | c0002 | t0004 | g0009 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18947 | hp1 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18948 | hp1 | a0003 | c0003 | t0006 | g0014 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18948 | hp2 | a0001 | c0004 | t0002 | g0007 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18949 | hp1 | a0002 | c0002 | t0003 | g0071 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18950 | hp2 | a0003 | c0003 | t0006 | g0242 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18951 | hp2 | a0002 | c0002 | t0004 | g0010 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18952 | hp1 | a0001 | c0001 | t0005 | g0057 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18953 | hp1 | a0002 | c0002 | t0003 | g0111 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18959 | hp2 | a0001 | c0001 | t0005 | g0061 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18960 | hp1 | a0001 | c0001 | t0005 | g0060 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18960 | hp2 | a0002 | c0002 | t0004 | g0009 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18964 | hp1 | a0008 | c0014 | t0001 | g0200 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18964 | hp2 | a0002 | c0002 | t0003 | g0015 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18965 | hp1 | a0006 | c0009 | t0003 | g0084 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18967 | hp2 | a0002 | c0002 | t0004 | g0010 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18969 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18977 | hp2 | a0002 | c0002 | t0003 | g0107 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18978 | hp2 | a0002 | c0002 | t0003 | g0108 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18979 | hp1 | a0003 | c0003 | t0006 | g0240 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18982 | hp2 | a0002 | c0002 | t0003 | g0106 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18983 | hp2 | a0002 | c0002 | t0003 | g0016 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18984 | hp1 | a0002 | c0002 | t0003 | g0117 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18985 | hp2 | a0002 | c0002 | t0003 | g0080 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18986 | hp1 | a0002 | c0002 | t0003 | g0105 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18990 | hp2 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18991 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18993 | hp1 | a0002 | c0002 | t0003 | g0011 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18993 | hp2 | a0003 | c0003 | t0006 | g0243 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18995 | hp2 | a0001 | c0004 | t0002 | g0159 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18998 | hp1 | a0002 | c0002 | t0003 | g0115 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18999 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19000 | hp1 | a0002 | c0011 | t0003 | g0077 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19001 | hp1 | a0003 | c0003 | t0006 | g0014 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19003 | hp1 | a0001 | c0004 | t0002 | g0007 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19003 | hp2 | a0002 | c0002 | t0003 | g0079 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19005 | hp2 | a0002 | c0002 | t0003 | g0109 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19006 | hp2 | a0002 | c0002 | t0004 | g0011 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19007 | hp2 | a0001 | c0004 | t0002 | g0007 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19011 | hp1 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19011 | hp2 | a0003 | c0003 | t0006 | g0023 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | LWK | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19054 | hp1 | a0003 | c0003 | t0006 | g0023 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19055 | hp1 | a0002 | c0002 | t0003 | g0093 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19056 | hp1 | a0002 | c0002 | t0003 | g0029 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19058 | hp1 | a0002 | c0002 | t0004 | g0011 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19060 | hp1 | a0003 | c0003 | t0006 | g0014 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19060 | hp2 | a0001 | c0001 | t0005 | g0056 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19062 | hp1 | a0009 | c0012 | t0002 | g0253 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19062 | hp2 | a0006 | c0009 | t0003 | g0083 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19065 | hp1 | a0003 | c0003 | t0006 | g0023 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19065 | hp2 | a0002 | c0002 | t0003 | g0030 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19066 | hp1 | a0002 | c0002 | t0003 | g0015 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19067 | hp1 | a0002 | c0002 | t0004 | g0069 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19068 | hp1 | a0003 | c0003 | t0006 | g0244 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19072 | hp1 | a0002 | c0002 | t0003 | g0016 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19072 | hp2 | a0001 | c0004 | t0002 | g0007 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19074 | hp2 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19075 | hp1 | a0001 | c0004 | t0002 | g0007 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19075 | hp2 | a0002 | c0002 | t0003 | g0096 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19076 | hp1 | a0003 | c0003 | t0006 | g0014 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19076 | hp2 | a0002 | c0002 | t0003 | g0114 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19080 | hp2 | a0002 | c0002 | t0003 | g0010 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19084 | hp2 | a0002 | c0002 | t0003 | g0120 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19085 | hp1 | a0002 | c0002 | t0003 | g0116 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19089 | hp1 | a0002 | c0002 | t0004 | g0031 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19089 | hp2 | a0003 | c0003 | t0006 | g0241 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ASW | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA20129 | hp2 | a0010 | c0013 | t0001 | g0235 | AFR | ASW | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | TSI | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0247 | EUR | TSI | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0179 | EUR | TSI | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0063 | EUR | TSI | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | GIH | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0004 | SAS | GIH | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG01123 | hp2 | a0004 | c0006 | t0001 | g0207 | AMR | CLM | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02109 | hp1 | a0001 | c0005 | t0001 | g0026 | AFR | ACB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG02486 | hp2 | a0001 | c0005 | t0001 | g0067 | AFR | ACB | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG06807 | hp1 | a0002 | c0002 | t0004 | g0095 | AFR | USA | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | USA | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18955 | hp1 | a0002 | c0002 | t0004 | g0094 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | USA | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | USA | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | LWK | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| NA21309 | hp2 | a0001 | c0001 | t0009 | g0185 | AFR | LWK | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0219 | REF | REF | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0234 | REF | REF | CYP2C18_chr10_94678729_94741190 | CYP2C18 | chr10 | 94678729 | 94741190 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:94687805 | T | A | 1 | a0003 | 24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
stop_gained | HIGH | c.204T>A | p.Tyr68* | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 2/9 | 295/2310 | 204/1473 | 68/490 | chr10 | 94687805 | |||
| chr10:94688224 | G | A | 1 | a0005 | 2 | HG02258.hp1 HG02922.hp2 |
missense_variant | MODERATE | c.431G>A | p.Arg144His | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/9 | 522/2310 | 431/1473 | 144/490 | chr10 | 94688224 | |||
| chr10:94720400 | A | G | 1 | a0008 | 1 | NA18964.hp1 | missense_variant | MODERATE | c.824A>G | p.Lys275Arg | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/9 | 915/2310 | 824/1473 | 275/490 | chr10 | 94720400 | |||
| chr10:94720472 | C | T | 1 | a0010 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.896C>T | p.Thr299Ile | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/9 | 987/2310 | 896/1473 | 299/490 | chr10 | 94720472 | |||
| chr10:94724372 | G | T | 1 | a0007 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.988G>T | p.Val330Leu | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/9 | 1079/2310 | 988/1473 | 330/490 | chr10 | 94724372 | |||
| chr10:94724388 | G | A | 1 | a0004 | 7 | HG00639.hp2 HG01123.hp2 HG01358.hp2 others(4): Show |
missense_variant | MODERATE | c.1004G>A | p.Arg335Gln | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/9 | 1095/2310 | 1004/1473 | 335/490 | chr10 | 94724388 | |||
| chr10:94733301 | C | T | 2 | a0002 a0006 |
88 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(85): Show |
missense_variant | MODERATE | c.1154C>T | p.Thr385Met | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/9 | 1245/2310 | 1154/1473 | 385/490 | chr10 | 94733301 | |||
| chr10:94733401 | C | A | 1 | a0009 | 1 | NA19062.hp1 | missense_variant | MODERATE | c.1254C>A | p.Asn418Lys | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/9 | 1345/2310 | 1254/1473 | 418/490 | chr10 | 94733401 | |||
| chr10:94733402 | T | C | 1 | a0009 | 1 | NA19062.hp1 | missense_variant | MODERATE | c.1255T>C | p.Phe419Leu | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/9 | 1346/2310 | 1255/1473 | 419/490 | chr10 | 94733402 | |||
| chr10:94733405 | A | T | 1 | a0009 | 1 | NA19062.hp1 | stop_gained | HIGH | c.1258A>T | p.Lys420* | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/9 | 1349/2310 | 1258/1473 | 420/490 | chr10 | 94733405 | |||
| chr10:94735295 | C | T | 1 | a0006 | 2 | NA18965.hp1 NA19062.hp2 |
missense_variant | MODERATE | c.1324C>T | p.Arg442Cys | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 9/9 | 1415/2310 | 1324/1473 | 442/490 | chr10 | 94735295 | |||
| chr10:94735296 | G | T | 1 | a0010 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.1325G>T | p.Arg442Leu | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 9/9 | 1416/2310 | 1325/1473 | 442/490 | chr10 | 94735296 | |||
| chr10:94735401 | G | C | 1 | a0009 | 1 | NA19062.hp1 | missense_variant | MODERATE | c.1430G>C | p.Gly477Ala | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 9/9 | 1521/2310 | 1430/1473 | 477/490 | chr10 | 94735401 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:94683966 | C | T | 2 | a0001c0005 a0003c0007 |
11 | HG02109.hp1 HG02145.hp1 HG02258.hp2 others(8): Show |
synonymous_variant | LOW | c.147C>T | p.Asp49Asp | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/9 | 238/2310 | 147/1473 | 49/490 | chr10 | 94683966 | |||
| chr10:94706810 | C | T | 1 | a0007c0015 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.669C>T | p.Ile223Ile | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/9 | 760/2310 | 669/1473 | 223/490 | chr10 | 94706810 | |||
| chr10:94724476 | C | T | 2 | a0001c0004 a0009c0012 |
10 | HG01981.hp1 HG02155.hp2 HG02293.hp1 others(7): Show |
synonymous_variant | LOW | c.1092C>T | p.Thr364Thr | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/9 | 1183/2310 | 1092/1473 | 364/490 | chr10 | 94724476 | |||
| chr10:94733302 | G | A | 1 | a0003c0010 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.1155G>A | p.Thr385Thr | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/9 | 1246/2310 | 1155/1473 | 385/490 | chr10 | 94733302 | |||
| chr10:94733326 | T | C | 1 | a0007c0015 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.1179T>C | p.Ser393Ser | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/9 | 1270/2310 | 1179/1473 | 393/490 | chr10 | 94733326 | |||
| chr10:94733437 | A | G | 1 | a0002c0011 | 1 | NA19000.hp1 | splice_region_variant&synonymous_variant | LOW | c.1290A>G | p.Ala430Ala | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/9 | 1381/2310 | 1290/1473 | 430/490 | chr10 | 94733437 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:94683807 | A | G | 1 | a0007c0015t0012 | 1 | HG02257.hp2 | 5_prime_UTR_variant | MODIFIER | c.-13A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/9 | 13 | chr10 | 94683807 | ||||||
| chr10:94735475 | C | T | 3 | a0001c0001t0002 a0001c0004t0002 a0009c0012t0002 |
64 | HG00323.hp1 HG00735.hp2 HG00741.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*31C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 9/9 | 31 | chr10 | 94735475 | ||||||
| chr10:94735509 | G | A | 2 | a0001c0001t0005 a0007c0015t0012 |
19 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*65G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 9/9 | 65 | chr10 | 94735509 | ||||||
| chr10:94735527 | G | A | 8 | a0001c0001t0004 a0002c0002t0003 a0002c0002t0004 others(5): Show |
93 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*83G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 9/9 | 83 | chr10 | 94735527 | ||||||
| chr10:94735527 | G | C | 1 | a0003c0003t0006 | 17 | HG03490.hp1 HG03492.hp1 HG03831.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*83G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 9/9 | 83 | chr10 | 94735527 | ||||||
| chr10:94735584 | A | G | 1 | a0001c0001t0011 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*140A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 9/9 | 140 | chr10 | 94735584 | ||||||
| chr10:94735653 | C | T | 1 | a0002c0002t0008 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*209C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 9/9 | 209 | chr10 | 94735653 | ||||||
| chr10:94735727 | G | T | 8 | a0001c0001t0004 a0002c0002t0003 a0002c0002t0004 others(5): Show |
93 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*283G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 9/9 | 283 | chr10 | 94735727 | ||||||
| chr10:94735798 | G | T | 1 | a0002c0002t0007 | 2 | HG00280.hp1 HG01496.hp1 |
3_prime_UTR_variant | MODIFIER | c.*354G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 9/9 | 354 | chr10 | 94735798 | ||||||
| chr10:94735830 | C | A | 1 | a0001c0001t0009 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*386C>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 9/9 | 386 | chr10 | 94735830 | ||||||
| chr10:94735870 | T | C | 1 | a0003c0010t0010 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*426T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 9/9 | 426 | chr10 | 94735870 | ||||||
| chr10:94735990 | G | GA | 1 | a0001c0001t0005 | 18 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*555dupA | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 9/9 | 556 | INFO_REALIGN_3_PRIME | chr10 | 94735990 | |||||
| chr10:94736036 | C | A | 3 | a0002c0002t0003 a0002c0011t0003 a0006c0009t0003 |
51 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*592C>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 9/9 | 592 | chr10 | 94736036 | ||||||
| chr10:94736128 | T | G | 1 | a0003c0010t0010 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*684T>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 9/9 | 684 | chr10 | 94736128 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:94684025 | T | G | 1 | a0001c0001t0002g0024 | 2 | NA18949.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.168+38T>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94684025 | |||||||
| chr10:94684117 | A | G | 1 | a0009c0012t0002g0253 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.168+130A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94684117 | |||||||
| chr10:94684151 | G | A | 1 | a0002c0002t0004g0051 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.168+164G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94684151 | |||||||
| chr10:94684151 | G | T | 2 | a0003c0007t0001g0050 a0003c0007t0001g0252 |
3 | HG02258.hp2 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.168+164G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94684151 | |||||||
| chr10:94684169 | A | G | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.168+182A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94684169 | |||||||
| chr10:94684185 | A | C | 1 | a0001c0001t0001g0250 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.168+198A>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94684185 | |||||||
| chr10:94684240 | C | G | 2 | a0005c0008t0004g0248 a0005c0008t0004g0249 |
2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.168+253C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94684240 | |||||||
| chr10:94684312 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.168+325G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94684312 | |||||||
| chr10:94684427 | A | G | 1 | a0001c0001t0001g0247 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.168+440A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94684427 | |||||||
| chr10:94684513 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.168+526G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94684513 | |||||||
| chr10:94684622 | C | T | 1 | a0002c0002t0004g0246 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.168+635C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94684622 | |||||||
| chr10:94684755 | T | G | 20 | a0001c0001t0001g0025 a0001c0001t0005g0004 a0001c0001t0005g0056 others(17): Show |
31 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.168+768T>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94684755 | |||||||
| chr10:94684823 | T | G | 2 | a0001c0005t0001g0054 a0001c0005t0001g0055 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.168+836T>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94684823 | |||||||
| chr10:94684915 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.168+928G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94684915 | |||||||
| chr10:94684983 | A | G | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.168+996A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94684983 | |||||||
| chr10:94685024 | TTTAA | T | 110 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0033 others(107): Show |
145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.168+1063_168+1066d others(6): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 94685024 | ||||||
| chr10:94685037 | TTAA | T | 8 | a0001c0005t0001g0026 a0001c0005t0001g0027 a0001c0005t0001g0054 others(5): Show |
11 | HG02109.hp1 HG02145.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.168+1052_168+1054d others(5): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 94685037 | ||||||
| chr10:94685222 | T | C | 2 | a0003c0007t0001g0050 a0003c0007t0001g0252 |
3 | HG02258.hp2 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.168+1235T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94685222 | |||||||
| chr10:94685285 | T | A | 8 | a0001c0005t0001g0026 a0001c0005t0001g0027 a0001c0005t0001g0054 others(5): Show |
11 | HG02109.hp1 HG02145.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.168+1298T>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94685285 | |||||||
| chr10:94685330 | GA | G | 8 | a0001c0005t0001g0026 a0001c0005t0001g0027 a0001c0005t0001g0054 others(5): Show |
11 | HG02109.hp1 HG02145.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.168+1344delA | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94685330 | |||||||
| chr10:94685501 | T | TA | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.168+1515dupA | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 94685501 | ||||||
| chr10:94685716 | T | G | 1 | a0001c0001t0002g0149 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.168+1729T>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94685716 | |||||||
| chr10:94685751 | T | A | 76 | a0001c0001t0001g0025 a0001c0001t0004g0028 a0001c0001t0004g0124 others(73): Show |
95 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.168+1764T>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94685751 | |||||||
| chr10:94685852 | A | G | 144 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0033 others(141): Show |
196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.168+1865A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94685852 | |||||||
| chr10:94686000 | C | A | 1 | a0001c0001t0002g0150 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.169-1770C>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94686000 | |||||||
| chr10:94686106 | C | A | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.169-1664C>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94686106 | |||||||
| chr10:94686409 | G | A | 8 | a0001c0005t0001g0026 a0001c0005t0001g0027 a0001c0005t0001g0054 others(5): Show |
11 | HG02109.hp1 HG02145.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.169-1361G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94686409 | |||||||
| chr10:94686418 | C | G | 1 | a0003c0010t0010g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.169-1352C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94686418 | |||||||
| chr10:94686497 | T | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0220 |
5 | HG02451.hp2 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.169-1273T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94686497 | |||||||
| chr10:94686579 | G | A | 3 | a0001c0001t0001g0039 a0001c0001t0001g0151 a0001c0001t0001g0152 |
4 | HG01361.hp2 HG01952.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-1191G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94686579 | |||||||
| chr10:94686799 | T | C | 1 | a0002c0002t0004g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.169-971T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94686799 | |||||||
| chr10:94686838 | T | G | 2 | a0005c0008t0004g0248 a0005c0008t0004g0249 |
2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.169-932T>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94686838 | |||||||
| chr10:94686871 | G | T | 5 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(2): Show |
5 | HG00140.hp1 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-899G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94686871 | |||||||
| chr10:94686875 | G | A | 117 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0025 others(114): Show |
157 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.169-895G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94686875 | |||||||
| chr10:94686931 | A | G | 1 | a0002c0002t0003g0125 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.169-839A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94686931 | |||||||
| chr10:94686981 | T | C | 1 | a0005c0008t0004g0248 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.169-789T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94686981 | |||||||
| chr10:94686984 | C | T | 1 | a0010c0013t0001g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.169-786C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94686984 | |||||||
| chr10:94686992 | A | C | 1 | a0010c0013t0001g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.169-778A>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94686992 | |||||||
| chr10:94687252 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.169-518T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94687252 | |||||||
| chr10:94687528 | G | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0151 a0001c0001t0001g0152 |
4 | HG01361.hp2 HG01952.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-242G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 1/8 | chr10 | 94687528 | |||||||
| chr10:94688042 | A | G | 1 | a0001c0001t0004g0124 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.332-83A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 2/8 | chr10 | 94688042 | |||||||
| chr10:94688098 | C | T | 1 | a0003c0010t0010g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.332-27C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 2/8 | chr10 | 94688098 | |||||||
| chr10:94688313 | A | T | 1 | a0003c0010t0010g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.481+39A>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94688313 | |||||||
| chr10:94688372 | A | G | 145 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0033 others(142): Show |
197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.481+98A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94688372 | |||||||
| chr10:94688488 | A | G | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.481+214A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94688488 | |||||||
| chr10:94688499 | C | T | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.481+225C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94688499 | |||||||
| chr10:94688527 | A | G | 11 | a0003c0003t0006g0014 a0003c0003t0006g0023 a0003c0003t0006g0049 others(8): Show |
17 | HG03490.hp1 HG03492.hp1 HG03831.hp2 others(14): Show |
intron_variant | MODIFIER | c.481+253A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94688527 | |||||||
| chr10:94688529 | G | C | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.481+255G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94688529 | |||||||
| chr10:94688623 | C | G | 33 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(30): Show |
49 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.481+349C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94688623 | |||||||
| chr10:94688704 | G | C | 3 | a0002c0002t0003g0015 a0002c0002t0003g0070 a0002c0002t0003g0071 |
5 | NA18940.hp1 NA18944.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.481+430G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94688704 | |||||||
| chr10:94688818 | A | T | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.481+544A>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94688818 | |||||||
| chr10:94688828 | G | A | 2 | a0002c0002t0003g0072 a0002c0002t0003g0073 |
2 | HG00423.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.481+554G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94688828 | |||||||
| chr10:94689062 | T | A | 1 | a0001c0001t0001g0154 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.481+788T>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94689062 | |||||||
| chr10:94689296 | T | C | 1 | a0001c0001t0001g0155 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.481+1022T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94689296 | |||||||
| chr10:94689307 | CTTTA | C | 5 | a0001c0001t0001g0013 a0001c0001t0001g0220 a0001c0001t0001g0226 others(2): Show |
8 | HG01081.hp2 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.481+1035_481+1038d others(6): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 94689307 | ||||||
| chr10:94689324 | T | A | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.481+1050T>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94689324 | |||||||
| chr10:94689370 | GA | G | 103 | a0001c0001t0004g0028 a0001c0001t0004g0124 a0001c0001t0005g0004 others(100): Show |
136 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.481+1099delA | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 94689370 | ||||||
| chr10:94689373 | A | T | 103 | a0001c0001t0004g0028 a0001c0001t0004g0124 a0001c0001t0005g0004 others(100): Show |
136 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.481+1099A>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94689373 | |||||||
| chr10:94689374 | T | G | 103 | a0001c0001t0004g0028 a0001c0001t0004g0124 a0001c0001t0005g0004 others(100): Show |
136 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.481+1100T>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94689374 | |||||||
| chr10:94689467 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.481+1193A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94689467 | |||||||
| chr10:94689686 | A | G | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.481+1412A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94689686 | |||||||
| chr10:94689693 | A | C | 11 | a0001c0001t0005g0004 a0001c0001t0005g0056 a0001c0001t0005g0057 others(8): Show |
18 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.481+1419A>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94689693 | |||||||
| chr10:94689978 | T | C | 1 | a0001c0001t0002g0156 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.481+1704T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94689978 | |||||||
| chr10:94689982 | G | A | 72 | a0001c0001t0004g0028 a0002c0002t0003g0008 a0002c0002t0003g0010 others(69): Show |
90 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.481+1708G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94689982 | |||||||
| chr10:94690182 | G | A | 1 | a0001c0001t0002g0149 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.481+1908G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94690182 | |||||||
| chr10:94690199 | C | T | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.481+1925C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94690199 | |||||||
| chr10:94690208 | G | T | 1 | a0001c0001t0001g0217 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.481+1934G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94690208 | |||||||
| chr10:94690233 | C | G | 2 | a0002c0002t0004g0123 a0002c0002t0007g0032 |
3 | HG00280.hp1 HG01192.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.481+1959C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94690233 | |||||||
| chr10:94690278 | C | T | 1 | a0002c0002t0003g0122 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.481+2004C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94690278 | |||||||
| chr10:94690405 | C | G | 1 | a0002c0002t0003g0121 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.481+2131C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94690405 | |||||||
| chr10:94690412 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.481+2138G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94690412 | |||||||
| chr10:94690412 | G | T | 11 | a0001c0001t0005g0004 a0001c0001t0005g0056 a0001c0001t0005g0057 others(8): Show |
18 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.481+2138G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94690412 | |||||||
| chr10:94690453 | C | T | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.481+2179C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94690453 | |||||||
| chr10:94690464 | C | G | 1 | a0002c0002t0003g0120 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.481+2190C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94690464 | |||||||
| chr10:94690490 | G | A | 2 | a0003c0007t0001g0050 a0003c0007t0001g0252 |
3 | HG02258.hp2 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.481+2216G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94690490 | |||||||
| chr10:94690783 | A | C | 1 | a0001c0001t0005g0065 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.481+2509A>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94690783 | |||||||
| chr10:94690859 | G | C | 3 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0010t0010g0245 |
4 | HG01884.hp1 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+2585G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94690859 | |||||||
| chr10:94690909 | A | T | 2 | a0001c0001t0002g0215 a0001c0001t0002g0216 |
2 | NA19002.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.481+2635A>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94690909 | |||||||
| chr10:94690974 | AC | A | 73 | a0001c0001t0004g0028 a0001c0001t0004g0124 a0002c0002t0003g0008 others(70): Show |
91 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.481+2703delC | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 94690974 | ||||||
| chr10:94691004 | G | C | 1 | a0001c0001t0001g0226 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.481+2730G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94691004 | |||||||
| chr10:94691036 | G | A | 1 | a0001c0005t0001g0054 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.481+2762G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94691036 | |||||||
| chr10:94691050 | G | T | 1 | a0002c0002t0003g0119 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.481+2776G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94691050 | |||||||
| chr10:94691107 | T | G | 1 | a0001c0001t0001g0033 | 2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.481+2833T>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94691107 | |||||||
| chr10:94691142 | C | T | 33 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(30): Show |
49 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.481+2868C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94691142 | |||||||
| chr10:94691143 | G | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(30): Show |
49 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.481+2869G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94691143 | |||||||
| chr10:94691157 | C | T | 103 | a0001c0001t0004g0028 a0001c0001t0004g0124 a0001c0001t0005g0004 others(100): Show |
136 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.481+2883C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94691157 | |||||||
| chr10:94691235 | C | T | 1 | a0010c0013t0001g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.481+2961C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94691235 | |||||||
| chr10:94691252 | A | G | 15 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(12): Show |
23 | HG01884.hp1 HG02258.hp2 HG02886.hp1 others(20): Show |
intron_variant | MODIFIER | c.481+2978A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94691252 | |||||||
| chr10:94691303 | C | A | 11 | a0001c0001t0005g0004 a0001c0001t0005g0056 a0001c0001t0005g0057 others(8): Show |
18 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.481+3029C>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94691303 | |||||||
| chr10:94691390 | G | C | 2 | a0005c0008t0004g0248 a0005c0008t0004g0249 |
2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.481+3116G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94691390 | |||||||
| chr10:94691416 | A | G | 51 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(48): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.481+3142A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94691416 | |||||||
| chr10:94691572 | G | C | 103 | a0001c0001t0004g0028 a0001c0001t0004g0124 a0001c0001t0005g0004 others(100): Show |
136 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.481+3298G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94691572 | |||||||
| chr10:94691659 | A | T | 2 | a0005c0008t0004g0248 a0005c0008t0004g0249 |
2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.482-3258A>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94691659 | |||||||
| chr10:94691706 | G | A | 15 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(12): Show |
23 | HG01884.hp1 HG02258.hp2 HG02886.hp1 others(20): Show |
intron_variant | MODIFIER | c.482-3211G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94691706 | |||||||
| chr10:94691720 | A | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(31): Show |
50 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(47): Show |
intron_variant | MODIFIER | c.482-3197A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94691720 | |||||||
| chr10:94691848 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.482-3069A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94691848 | |||||||
| chr10:94691932 | C | A | 1 | a0002c0002t0004g0074 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.482-2985C>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94691932 | |||||||
| chr10:94691954 | G | T | 4 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0007t0001g0050 others(1): Show |
6 | HG01884.hp1 HG02258.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.482-2963G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94691954 | |||||||
| chr10:94692003 | C | A | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.482-2914C>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94692003 | |||||||
| chr10:94692006 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(242): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.482-2911T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94692006 | |||||||
| chr10:94692053 | C | T | 1 | a0002c0002t0003g0121 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.482-2864C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94692053 | |||||||
| chr10:94692054 | G | C | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.482-2863G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94692054 | |||||||
| chr10:94692065 | A | G | 1 | a0001c0004t0002g0180 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.482-2852A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94692065 | |||||||
| chr10:94692070 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.482-2847C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94692070 | |||||||
| chr10:94692131 | A | G | 1 | a0002c0002t0003g0118 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.482-2786A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94692131 | |||||||
| chr10:94692185 | A | G | 1 | a0001c0001t0002g0213 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.482-2732A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94692185 | |||||||
| chr10:94692267 | C | A | 11 | a0001c0001t0005g0004 a0001c0001t0005g0056 a0001c0001t0005g0057 others(8): Show |
18 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.482-2650C>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94692267 | |||||||
| chr10:94692377 | A | C | 15 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(12): Show |
23 | HG01884.hp1 HG02258.hp2 HG02886.hp1 others(20): Show |
intron_variant | MODIFIER | c.482-2540A>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94692377 | |||||||
| chr10:94692404 | C | CA | 142 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0033 others(139): Show |
194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.482-2508dupA | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 94692404 | ||||||
| chr10:94692405 | A | C | 1 | a0001c0001t0001g0212 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.482-2512A>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94692405 | |||||||
| chr10:94692415 | G | GA | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.482-2497dupA | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 94692415 | ||||||
| chr10:94692468 | G | T | 1 | a0010c0013t0001g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.482-2449G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94692468 | |||||||
| chr10:94692668 | TG | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(42): Show |
80 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.482-2246delG | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 94692668 | ||||||
| chr10:94692678 | C | T | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.482-2239C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94692678 | |||||||
| chr10:94692701 | G | A | 1 | a0003c0003t0006g0237 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.482-2216G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94692701 | |||||||
| chr10:94692734 | C | T | 1 | a0002c0002t0003g0121 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.482-2183C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94692734 | |||||||
| chr10:94692773 | A | G | 6 | a0001c0005t0001g0026 a0001c0005t0001g0027 a0001c0005t0001g0054 others(3): Show |
8 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.482-2144A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94692773 | |||||||
| chr10:94692854 | A | C | 3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 |
3 | HG01081.hp2 HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.482-2063A>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94692854 | |||||||
| chr10:94692875 | C | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0210 a0001c0001t0001g0211 |
12 | HG01891.hp1 HG02280.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.482-2042C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94692875 | |||||||
| chr10:94692921 | C | T | 11 | a0003c0003t0006g0014 a0003c0003t0006g0023 a0003c0003t0006g0049 others(8): Show |
17 | HG03490.hp1 HG03492.hp1 HG03831.hp2 others(14): Show |
intron_variant | MODIFIER | c.482-1996C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94692921 | |||||||
| chr10:94692952 | G | A | 1 | a0002c0002t0003g0075 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.482-1965G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94692952 | |||||||
| chr10:94693023 | G | C | 1 | a0002c0002t0003g0076 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.482-1894G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94693023 | |||||||
| chr10:94693061 | C | T | 11 | a0001c0001t0005g0004 a0001c0001t0005g0056 a0001c0001t0005g0057 others(8): Show |
18 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.482-1856C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94693061 | |||||||
| chr10:94693103 | C | T | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.482-1814C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94693103 | |||||||
| chr10:94693129 | G | A | 1 | a0002c0002t0003g0118 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.482-1788G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94693129 | |||||||
| chr10:94693282 | C | G | 76 | a0001c0001t0001g0025 a0001c0001t0004g0028 a0001c0001t0004g0124 others(73): Show |
95 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.482-1635C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94693282 | |||||||
| chr10:94693342 | A | G | 105 | a0001c0001t0001g0025 a0001c0001t0001g0126 a0001c0001t0004g0028 others(102): Show |
139 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.482-1575A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94693342 | |||||||
| chr10:94693367 | C | T | 1 | a0003c0010t0010g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.482-1550C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94693367 | |||||||
| chr10:94693384 | G | A | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.482-1533G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94693384 | |||||||
| chr10:94693385 | T | A | 1 | a0001c0001t0001g0025 | 2 | HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.482-1532T>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94693385 | |||||||
| chr10:94693396 | C | T | 2 | a0001c0001t0002g0178 a0001c0001t0002g0179 |
2 | HG03669.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.482-1521C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94693396 | |||||||
| chr10:94693397 | G | A | 1 | a0010c0013t0001g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.482-1520G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94693397 | |||||||
| chr10:94693703 | A | C | 1 | a0001c0001t0001g0209 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.482-1214A>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94693703 | |||||||
| chr10:94694147 | G | T | 75 | a0001c0001t0004g0028 a0001c0001t0004g0124 a0002c0002t0003g0008 others(72): Show |
93 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.482-770G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94694147 | |||||||
| chr10:94694175 | T | A | 1 | a0001c0001t0002g0040 | 2 | NA18991.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.482-742T>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94694175 | |||||||
| chr10:94694399 | G | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(30): Show |
49 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.482-518G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94694399 | |||||||
| chr10:94694423 | T | C | 2 | a0003c0003t0001g0048 a0003c0003t0001g0236 |
3 | HG01884.hp1 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.482-494T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94694423 | |||||||
| chr10:94694458 | A | G | 3 | a0001c0001t0005g0062 a0001c0001t0005g0063 a0001c0001t0005g0064 |
3 | HG01978.hp2 HG03710.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.482-459A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94694458 | |||||||
| chr10:94694480 | A | G | 1 | a0001c0001t0002g0177 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.482-437A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94694480 | |||||||
| chr10:94694569 | T | A | 1 | a0002c0011t0003g0077 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.482-348T>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94694569 | |||||||
| chr10:94694681 | G | A | 7 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0221 others(4): Show |
11 | HG00642.hp2 HG01099.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.482-236G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94694681 | |||||||
| chr10:94694684 | C | T | 2 | a0001c0005t0001g0027 a0002c0002t0003g0117 |
3 | HG02896.hp2 HG02897.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.482-233C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 3/8 | chr10 | 94694684 | |||||||
| chr10:94695144 | T | A | 1 | a0003c0003t0006g0049 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.642+67T>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94695144 | |||||||
| chr10:94695168 | G | T | 2 | a0003c0007t0001g0050 a0003c0007t0001g0252 |
3 | HG02258.hp2 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.642+91G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94695168 | |||||||
| chr10:94695212 | A | G | 1 | a0003c0010t0010g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.642+135A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94695212 | |||||||
| chr10:94695225 | G | A | 72 | a0001c0001t0004g0028 a0002c0002t0003g0008 a0002c0002t0003g0010 others(69): Show |
90 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.642+148G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94695225 | |||||||
| chr10:94695250 | G | A | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.642+173G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94695250 | |||||||
| chr10:94695317 | G | T | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.642+240G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94695317 | |||||||
| chr10:94695401 | T | C | 1 | a0001c0001t0002g0177 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.642+324T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94695401 | |||||||
| chr10:94695455 | C | T | 6 | a0001c0005t0001g0026 a0001c0005t0001g0027 a0001c0005t0001g0054 others(3): Show |
8 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.642+378C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94695455 | |||||||
| chr10:94695681 | A | G | 1 | a0002c0002t0003g0116 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.642+604A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94695681 | |||||||
| chr10:94695696 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0220 |
5 | HG02451.hp2 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.642+619C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94695696 | |||||||
| chr10:94695768 | C | T | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.642+691C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94695768 | |||||||
| chr10:94695769 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.642+692G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94695769 | |||||||
| chr10:94695773 | C | G | 1 | a0001c0001t0001g0208 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.642+696C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94695773 | |||||||
| chr10:94695778 | C | T | 1 | a0002c0002t0004g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.642+701C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94695778 | |||||||
| chr10:94695809 | T | C | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.642+732T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94695809 | |||||||
| chr10:94695943 | C | G | 1 | a0001c0001t0002g0149 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.642+866C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94695943 | |||||||
| chr10:94695981 | C | T | 2 | a0002c0002t0003g0070 a0002c0002t0003g0071 |
2 | NA18944.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.642+904C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94695981 | |||||||
| chr10:94696043 | T | C | 11 | a0001c0001t0005g0004 a0001c0001t0005g0056 a0001c0001t0005g0057 others(8): Show |
18 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.642+966T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94696043 | |||||||
| chr10:94696052 | G | T | 11 | a0001c0001t0005g0004 a0001c0001t0005g0056 a0001c0001t0005g0057 others(8): Show |
18 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.642+975G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94696052 | |||||||
| chr10:94696070 | A | C | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.642+993A>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94696070 | |||||||
| chr10:94696125 | AAG | A | 6 | a0001c0005t0001g0026 a0001c0005t0001g0027 a0001c0005t0001g0054 others(3): Show |
8 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.642+1053_642+1054d others(4): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 94696125 | ||||||
| chr10:94696169 | C | T | 1 | a0001c0001t0002g0176 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.642+1092C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94696169 | |||||||
| chr10:94696181 | G | A | 1 | a0001c0001t0002g0041 | 2 | HG01123.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.642+1104G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94696181 | |||||||
| chr10:94696296 | G | A | 1 | a0001c0001t0005g0056 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.642+1219G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94696296 | |||||||
| chr10:94696364 | C | A | 11 | a0001c0001t0005g0004 a0001c0001t0005g0056 a0001c0001t0005g0057 others(8): Show |
18 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.642+1287C>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94696364 | |||||||
| chr10:94696404 | C | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(31): Show |
50 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(47): Show |
intron_variant | MODIFIER | c.642+1327C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94696404 | |||||||
| chr10:94696408 | C | G | 1 | a0001c0001t0002g0179 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.642+1331C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94696408 | |||||||
| chr10:94696482 | G | A | 73 | a0001c0001t0004g0028 a0001c0001t0004g0124 a0002c0002t0003g0008 others(70): Show |
91 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.642+1405G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94696482 | |||||||
| chr10:94696740 | T | G | 2 | a0005c0008t0004g0248 a0005c0008t0004g0249 |
2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.642+1663T>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94696740 | |||||||
| chr10:94696742 | G | C | 1 | a0001c0001t0001g0126 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.642+1665G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94696742 | |||||||
| chr10:94696809 | C | T | 2 | a0002c0002t0004g0123 a0002c0002t0007g0032 |
3 | HG00280.hp1 HG01192.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.642+1732C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94696809 | |||||||
| chr10:94696928 | A | G | 28 | a0001c0001t0005g0004 a0001c0001t0005g0056 a0001c0001t0005g0057 others(25): Show |
43 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(40): Show |
intron_variant | MODIFIER | c.642+1851A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94696928 | |||||||
| chr10:94696933 | A | C | 2 | a0003c0007t0001g0050 a0003c0007t0001g0252 |
3 | HG02258.hp2 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.642+1856A>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94696933 | |||||||
| chr10:94696941 | G | A | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.642+1864G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94696941 | |||||||
| chr10:94697023 | C | T | 2 | a0003c0007t0001g0050 a0003c0007t0001g0252 |
3 | HG02258.hp2 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.642+1946C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94697023 | |||||||
| chr10:94697024 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.642+1947G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94697024 | |||||||
| chr10:94697099 | G | A | 2 | a0003c0007t0001g0050 a0003c0007t0001g0252 |
3 | HG02258.hp2 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.642+2022G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94697099 | |||||||
| chr10:94697189 | G | A | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.642+2112G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94697189 | |||||||
| chr10:94697199 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.642+2122T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94697199 | |||||||
| chr10:94697262 | T | G | 11 | a0001c0001t0005g0004 a0001c0001t0005g0056 a0001c0001t0005g0057 others(8): Show |
18 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.642+2185T>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94697262 | |||||||
| chr10:94697274 | C | G | 7 | a0001c0001t0001g0025 a0001c0005t0001g0026 a0001c0005t0001g0027 others(4): Show |
10 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.642+2197C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94697274 | |||||||
| chr10:94697419 | C | A | 1 | a0001c0001t0005g0057 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.642+2342C>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94697419 | |||||||
| chr10:94697451 | C | G | 1 | a0001c0001t0001g0033 | 2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.642+2374C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94697451 | |||||||
| chr10:94697451 | C | T | 12 | a0001c0001t0005g0004 a0001c0001t0005g0056 a0001c0001t0005g0057 others(9): Show |
19 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.642+2374C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94697451 | |||||||
| chr10:94697545 | A | G | 1 | a0001c0001t0001g0033 | 2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.642+2468A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94697545 | |||||||
| chr10:94697547 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.642+2470C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94697547 | |||||||
| chr10:94697591 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.642+2514A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94697591 | |||||||
| chr10:94697629 | A | C | 1 | a0002c0002t0003g0115 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.642+2552A>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94697629 | |||||||
| chr10:94697996 | C | G | 1 | a0002c0002t0003g0114 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.642+2919C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94697996 | |||||||
| chr10:94697999 | C | T | 73 | a0001c0001t0004g0028 a0002c0002t0003g0008 a0002c0002t0003g0010 others(70): Show |
91 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.642+2922C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94697999 | |||||||
| chr10:94698005 | G | C | 72 | a0001c0001t0004g0028 a0002c0002t0003g0008 a0002c0002t0003g0010 others(69): Show |
90 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.642+2928G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94698005 | |||||||
| chr10:94698038 | T | C | 1 | a0001c0001t0001g0155 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.642+2961T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94698038 | |||||||
| chr10:94698188 | G | T | 1 | a0001c0001t0001g0220 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.642+3111G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94698188 | |||||||
| chr10:94698231 | G | T | 1 | a0001c0005t0001g0026 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.642+3154G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94698231 | |||||||
| chr10:94698241 | C | T | 13 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(10): Show |
20 | HG01884.hp1 HG02886.hp1 HG03453.hp1 others(17): Show |
intron_variant | MODIFIER | c.642+3164C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94698241 | |||||||
| chr10:94698292 | T | C | 1 | a0002c0002t0004g0078 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.642+3215T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94698292 | |||||||
| chr10:94698293 | G | A | 1 | a0002c0002t0004g0078 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.642+3216G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94698293 | |||||||
| chr10:94698410 | T | G | 1 | a0001c0001t0002g0040 | 2 | NA18991.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.642+3333T>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94698410 | |||||||
| chr10:94698414 | A | G | 1 | a0001c0001t0002g0040 | 2 | NA18991.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.642+3337A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94698414 | |||||||
| chr10:94698418 | T | G | 1 | a0001c0001t0002g0040 | 2 | NA18991.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.642+3341T>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94698418 | |||||||
| chr10:94698438 | C | G | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.642+3361C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94698438 | |||||||
| chr10:94698482 | T | C | 2 | a0003c0003t0001g0048 a0003c0003t0001g0236 |
3 | HG01884.hp1 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.642+3405T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94698482 | |||||||
| chr10:94698564 | T | A | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.642+3487T>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94698564 | |||||||
| chr10:94698681 | TG | T | 75 | a0001c0001t0004g0028 a0001c0001t0004g0124 a0002c0002t0003g0008 others(72): Show |
93 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.642+3605delG | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94698681 | |||||||
| chr10:94698696 | G | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0144 |
2 | HG01884.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.642+3619G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94698696 | |||||||
| chr10:94698703 | T | G | 1 | a0001c0001t0001g0212 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.642+3626T>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94698703 | |||||||
| chr10:94698800 | A | T | 1 | a0002c0002t0004g0113 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.642+3723A>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94698800 | |||||||
| chr10:94698886 | G | T | 1 | a0001c0001t0002g0177 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.642+3809G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94698886 | |||||||
| chr10:94698940 | A | G | 3 | a0001c0005t0001g0054 a0001c0005t0001g0055 a0001c0005t0001g0067 |
3 | HG02145.hp1 HG02486.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.642+3863A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94698940 | |||||||
| chr10:94698942 | C | T | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.642+3865C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94698942 | |||||||
| chr10:94698943 | C | T | 71 | a0002c0002t0003g0008 a0002c0002t0003g0010 a0002c0002t0003g0011 others(68): Show |
88 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.642+3866C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94698943 | |||||||
| chr10:94698995 | C | G | 1 | a0004c0006t0001g0207 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.642+3918C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94698995 | |||||||
| chr10:94699214 | G | A | 13 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(10): Show |
20 | HG01884.hp1 HG02886.hp1 HG03453.hp1 others(17): Show |
intron_variant | MODIFIER | c.642+4137G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94699214 | |||||||
| chr10:94699562 | A | T | 8 | a0001c0001t0005g0004 a0001c0001t0005g0056 a0001c0001t0005g0057 others(5): Show |
15 | HG00609.hp1 HG01978.hp2 HG03490.hp2 others(12): Show |
intron_variant | MODIFIER | c.642+4485A>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94699562 | |||||||
| chr10:94699567 | C | G | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.642+4490C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94699567 | |||||||
| chr10:94699581 | C | T | 1 | a0002c0002t0004g0112 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.642+4504C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94699581 | |||||||
| chr10:94699590 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.642+4513T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94699590 | |||||||
| chr10:94699672 | G | C | 5 | a0001c0001t0001g0013 a0001c0001t0001g0220 a0001c0001t0001g0226 others(2): Show |
8 | HG01081.hp2 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.642+4595G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94699672 | |||||||
| chr10:94699958 | C | G | 1 | a0001c0001t0002g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.642+4881C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94699958 | |||||||
| chr10:94700015 | G | T | 42 | a0001c0001t0001g0042 a0001c0001t0001g0160 a0001c0001t0001g0169 others(39): Show |
67 | HG00323.hp1 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.642+4938G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94700015 | |||||||
| chr10:94700022 | G | T | 1 | a0002c0002t0003g0111 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.642+4945G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94700022 | |||||||
| chr10:94700052 | C | T | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.642+4975C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94700052 | |||||||
| chr10:94700087 | A | G | 15 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(12): Show |
23 | HG01884.hp1 HG02258.hp2 HG02886.hp1 others(20): Show |
intron_variant | MODIFIER | c.642+5010A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94700087 | |||||||
| chr10:94700146 | C | G | 1 | a0001c0001t0001g0206 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.642+5069C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94700146 | |||||||
| chr10:94700160 | G | A | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.642+5083G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94700160 | |||||||
| chr10:94700184 | G | A | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.642+5107G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94700184 | |||||||
| chr10:94700209 | A | G | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.642+5132A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94700209 | |||||||
| chr10:94700233 | C | G | 1 | a0001c0001t0002g0046 | 2 | NA18942.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.642+5156C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94700233 | |||||||
| chr10:94700279 | G | C | 2 | a0003c0007t0001g0050 a0003c0007t0001g0252 |
3 | HG02258.hp2 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.642+5202G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94700279 | |||||||
| chr10:94700375 | G | A | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.642+5298G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94700375 | |||||||
| chr10:94700381 | G | A | 2 | a0003c0007t0001g0050 a0003c0007t0001g0252 |
3 | HG02258.hp2 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.642+5304G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94700381 | |||||||
| chr10:94700395 | T | G | 2 | a0005c0008t0004g0248 a0005c0008t0004g0249 |
2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.642+5318T>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94700395 | |||||||
| chr10:94700408 | T | G | 1 | a0001c0001t0001g0186 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.642+5331T>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94700408 | |||||||
| chr10:94700466 | G | T | 73 | a0001c0001t0004g0028 a0001c0001t0004g0124 a0002c0002t0003g0008 others(70): Show |
91 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.642+5389G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94700466 | |||||||
| chr10:94700520 | C | T | 3 | a0003c0003t0006g0023 a0003c0003t0006g0243 a0003c0003t0006g0244 |
5 | NA18993.hp2 NA19011.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.642+5443C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94700520 | |||||||
| chr10:94700521 | G | A | 12 | a0001c0001t0001g0129 a0001c0001t0005g0004 a0001c0001t0005g0056 others(9): Show |
19 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.642+5444G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94700521 | |||||||
| chr10:94700537 | G | A | 11 | a0001c0001t0005g0004 a0001c0001t0005g0056 a0001c0001t0005g0057 others(8): Show |
18 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.642+5460G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94700537 | |||||||
| chr10:94700605 | A | G | 7 | a0001c0001t0001g0025 a0001c0005t0001g0026 a0001c0005t0001g0027 others(4): Show |
10 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.642+5528A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94700605 | |||||||
| chr10:94700760 | CTCAAACT others(17): Show |
C | 1 | a0001c0001t0001g0187 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.642+5684_642+5707d others(26): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94700760 | |||||||
| chr10:94700811 | T | C | 1 | a0001c0001t0001g0021 | 3 | HG02071.hp1 NA19063.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.642+5734T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94700811 | |||||||
| chr10:94700824 | C | A | 2 | a0001c0001t0002g0178 a0001c0001t0002g0179 |
2 | HG03669.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.642+5747C>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94700824 | |||||||
| chr10:94700935 | A | G | 144 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0034 others(141): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.643-5849A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94700935 | |||||||
| chr10:94700939 | G | A | 8 | a0001c0001t0001g0006 a0001c0001t0001g0189 a0001c0001t0001g0190 others(5): Show |
15 | HG00438.hp2 HG00673.hp1 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.643-5845G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94700939 | |||||||
| chr10:94701017 | G | C | 1 | a0003c0010t0010g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.643-5767G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94701017 | |||||||
| chr10:94701062 | G | T | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.643-5722G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94701062 | |||||||
| chr10:94701195 | A | C | 1 | a0001c0001t0009g0185 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.643-5589A>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94701195 | |||||||
| chr10:94701296 | A | G | 7 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0221 others(4): Show |
11 | HG00642.hp2 HG01099.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.643-5488A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94701296 | |||||||
| chr10:94701296 | A | T | 1 | a0001c0004t0002g0180 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.643-5488A>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94701296 | |||||||
| chr10:94701314 | T | G | 7 | a0002c0002t0003g0008 a0002c0002t0003g0029 a0002c0002t0003g0079 others(4): Show |
11 | NA18612.hp2 NA18947.hp1 NA18953.hp1 others(8): Show |
intron_variant | MODIFIER | c.643-5470T>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94701314 | |||||||
| chr10:94701474 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.643-5310C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94701474 | |||||||
| chr10:94701515 | G | A | 1 | a0001c0001t0011g0188 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.643-5269G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94701515 | |||||||
| chr10:94701527 | G | A | 72 | a0001c0001t0004g0028 a0002c0002t0003g0008 a0002c0002t0003g0010 others(69): Show |
90 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.643-5257G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94701527 | |||||||
| chr10:94701559 | G | C | 1 | a0001c0001t0001g0193 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.643-5225G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94701559 | |||||||
| chr10:94701561 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.643-5223A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94701561 | |||||||
| chr10:94701834 | A | G | 3 | a0001c0001t0001g0039 a0001c0001t0001g0151 a0001c0001t0001g0152 |
4 | HG01361.hp2 HG01952.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.643-4950A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94701834 | |||||||
| chr10:94701995 | TA | T | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0187 others(8): Show |
15 | HG00642.hp2 HG01081.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.643-4779delA | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 94701995 | ||||||
| chr10:94702229 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.643-4555G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94702229 | |||||||
| chr10:94702335 | C | T | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.643-4449C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94702335 | |||||||
| chr10:94702352 | C | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0033 others(47): Show |
76 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.643-4432C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94702352 | |||||||
| chr10:94702494 | G | C | 11 | a0001c0001t0005g0004 a0001c0001t0005g0056 a0001c0001t0005g0057 others(8): Show |
18 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.643-4290G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94702494 | |||||||
| chr10:94702731 | G | A | 2 | a0003c0007t0001g0050 a0003c0007t0001g0252 |
3 | HG02258.hp2 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.643-4053G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94702731 | |||||||
| chr10:94702734 | A | G | 1 | a0002c0002t0003g0073 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.643-4050A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94702734 | |||||||
| chr10:94702864 | T | C | 1 | a0003c0010t0010g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.643-3920T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94702864 | |||||||
| chr10:94702944 | A | G | 11 | a0001c0001t0005g0004 a0001c0001t0005g0056 a0001c0001t0005g0057 others(8): Show |
18 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.643-3840A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94702944 | |||||||
| chr10:94703025 | C | A | 1 | a0001c0001t0001g0226 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.643-3759C>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94703025 | |||||||
| chr10:94703063 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.643-3721G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94703063 | |||||||
| chr10:94703073 | C | G | 1 | a0002c0002t0004g0110 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.643-3711C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94703073 | |||||||
| chr10:94703087 | G | C | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.643-3697G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94703087 | |||||||
| chr10:94703112 | A | C | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.643-3672A>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94703112 | |||||||
| chr10:94703175 | G | A | 1 | a0002c0002t0003g0081 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.643-3609G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94703175 | |||||||
| chr10:94703187 | G | A | 6 | a0001c0005t0001g0026 a0001c0005t0001g0027 a0001c0005t0001g0054 others(3): Show |
8 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.643-3597G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94703187 | |||||||
| chr10:94703370 | G | A | 1 | a0001c0001t0005g0060 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.643-3414G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94703370 | |||||||
| chr10:94703466 | C | T | 7 | a0003c0003t0006g0014 a0003c0003t0006g0023 a0003c0003t0006g0240 others(4): Show |
12 | NA18948.hp1 NA18950.hp2 NA18979.hp1 others(9): Show |
intron_variant | MODIFIER | c.643-3318C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94703466 | |||||||
| chr10:94703474 | T | C | 2 | a0003c0007t0001g0050 a0003c0007t0001g0252 |
3 | HG02258.hp2 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.643-3310T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94703474 | |||||||
| chr10:94703604 | G | C | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.643-3180G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94703604 | |||||||
| chr10:94703618 | A | G | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.643-3166A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94703618 | |||||||
| chr10:94703943 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.643-2841G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94703943 | |||||||
| chr10:94704004 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.643-2780C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94704004 | |||||||
| chr10:94704121 | C | T | 2 | a0001c0001t0004g0124 a0003c0007t0001g0050 |
3 | HG02451.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.643-2663C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94704121 | |||||||
| chr10:94704133 | A | G | 1 | a0003c0010t0010g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.643-2651A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94704133 | |||||||
| chr10:94704211 | T | C | 1 | a0002c0002t0004g0082 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.643-2573T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94704211 | |||||||
| chr10:94704309 | T | C | 1 | a0001c0001t0002g0157 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.643-2475T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94704309 | |||||||
| chr10:94704324 | G | GT | 8 | a0001c0001t0001g0142 a0001c0001t0002g0173 a0001c0001t0002g0174 others(5): Show |
8 | HG02738.hp2 HG03471.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.643-2455dupT | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 94704324 | ||||||
| chr10:94704330 | A | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.643-2454A>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94704330 | |||||||
| chr10:94704375 | A | G | 7 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0221 others(4): Show |
11 | HG00642.hp2 HG01099.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.643-2409A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94704375 | |||||||
| chr10:94704394 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.643-2390T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94704394 | |||||||
| chr10:94704432 | G | T | 1 | a0001c0001t0001g0205 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.643-2352G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94704432 | |||||||
| chr10:94704536 | G | A | 71 | a0002c0002t0003g0008 a0002c0002t0003g0010 a0002c0002t0003g0011 others(68): Show |
88 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.643-2248G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94704536 | |||||||
| chr10:94704540 | G | A | 2 | a0006c0009t0003g0083 a0006c0009t0003g0084 |
2 | NA18965.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.643-2244G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94704540 | |||||||
| chr10:94704602 | G | A | 11 | a0003c0003t0006g0014 a0003c0003t0006g0023 a0003c0003t0006g0049 others(8): Show |
17 | HG03490.hp1 HG03492.hp1 HG03831.hp2 others(14): Show |
intron_variant | MODIFIER | c.643-2182G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94704602 | |||||||
| chr10:94704625 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.643-2159C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94704625 | |||||||
| chr10:94704934 | G | A | 1 | a0006c0009t0003g0083 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.643-1850G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94704934 | |||||||
| chr10:94704973 | G | A | 28 | a0001c0001t0005g0004 a0001c0001t0005g0056 a0001c0001t0005g0057 others(25): Show |
43 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(40): Show |
intron_variant | MODIFIER | c.643-1811G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94704973 | |||||||
| chr10:94705009 | A | AT | 7 | a0001c0001t0001g0025 a0001c0005t0001g0026 a0001c0005t0001g0027 others(4): Show |
10 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.643-1769dupT | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 94705009 | ||||||
| chr10:94705062 | T | C | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.643-1722T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94705062 | |||||||
| chr10:94705173 | A | G | 1 | a0003c0010t0010g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.643-1611A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94705173 | |||||||
| chr10:94705288 | A | C | 1 | a0001c0001t0001g0141 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.643-1496A>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94705288 | |||||||
| chr10:94705370 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.643-1414G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94705370 | |||||||
| chr10:94705377 | G | T | 1 | a0001c0001t0002g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.643-1407G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94705377 | |||||||
| chr10:94705454 | A | G | 13 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(10): Show |
20 | HG01884.hp1 HG02886.hp1 HG03453.hp1 others(17): Show |
intron_variant | MODIFIER | c.643-1330A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94705454 | |||||||
| chr10:94705485 | C | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(48): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.643-1299C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94705485 | |||||||
| chr10:94705496 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0204 |
3 | NA18951.hp1 NA18979.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.643-1288C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94705496 | |||||||
| chr10:94705549 | T | A | 13 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0153 others(10): Show |
22 | HG00438.hp2 HG00673.hp1 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.643-1235T>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94705549 | |||||||
| chr10:94705731 | G | A | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0141 |
3 | HG02109.hp2 HG02572.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.643-1053G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94705731 | |||||||
| chr10:94705859 | A | G | 76 | a0001c0001t0001g0025 a0001c0001t0004g0028 a0001c0001t0004g0124 others(73): Show |
95 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.643-925A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94705859 | |||||||
| chr10:94706045 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.643-739G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94706045 | |||||||
| chr10:94706181 | G | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.643-603G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94706181 | |||||||
| chr10:94706316 | T | A | 75 | a0001c0001t0004g0028 a0001c0001t0004g0124 a0002c0002t0003g0008 others(72): Show |
93 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.643-468T>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94706316 | |||||||
| chr10:94706321 | G | T | 42 | a0001c0001t0001g0042 a0001c0001t0001g0160 a0001c0001t0001g0169 others(39): Show |
67 | HG00323.hp1 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.643-463G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94706321 | |||||||
| chr10:94706390 | A | T | 72 | a0001c0001t0004g0028 a0002c0002t0003g0008 a0002c0002t0003g0010 others(69): Show |
90 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.643-394A>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94706390 | |||||||
| chr10:94706404 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.643-380C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94706404 | |||||||
| chr10:94706457 | A | G | 1 | a0001c0001t0005g0056 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.643-327A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94706457 | |||||||
| chr10:94706513 | C | A | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.643-271C>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94706513 | |||||||
| chr10:94706585 | C | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(30): Show |
48 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(45): Show |
intron_variant | MODIFIER | c.643-199C>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94706585 | |||||||
| chr10:94706626 | A | G | 5 | a0001c0001t0001g0038 a0001c0001t0001g0127 a0001c0001t0001g0140 others(2): Show |
6 | HG01884.hp2 HG02976.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.643-158A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94706626 | |||||||
| chr10:94706634 | A | G | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.643-150A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94706634 | |||||||
| chr10:94706650 | C | T | 1 | a0001c0001t0004g0028 | 2 | HG00639.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.643-134C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94706650 | |||||||
| chr10:94706668 | T | C | 1 | a0002c0002t0003g0117 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.643-116T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94706668 | |||||||
| chr10:94706733 | T | G | 1 | a0002c0002t0003g0085 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.643-51T>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 4/8 | chr10 | 94706733 | |||||||
| chr10:94706982 | T | C | 2 | a0001c0001t0001g0038 a0001c0001t0001g0142 |
3 | HG03130.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.819+22T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94706982 | |||||||
| chr10:94707014 | C | T | 2 | a0001c0001t0002g0171 a0001c0001t0002g0172 |
2 | HG01361.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.819+54C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94707014 | |||||||
| chr10:94707067 | C | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.819+107C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94707067 | |||||||
| chr10:94707098 | G | A | 6 | a0001c0005t0001g0026 a0001c0005t0001g0027 a0001c0005t0001g0054 others(3): Show |
8 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.819+138G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94707098 | |||||||
| chr10:94707127 | T | TATA | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(242): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.819+168_819+170dup others(3): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94707127 | ||||||
| chr10:94707181 | G | A | 74 | a0001c0001t0001g0025 a0001c0001t0004g0028 a0001c0001t0004g0124 others(71): Show |
93 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.819+221G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94707181 | |||||||
| chr10:94707228 | A | G | 1 | a0001c0001t0005g0065 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.819+268A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94707228 | |||||||
| chr10:94707320 | A | G | 1 | a0003c0010t0010g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.819+360A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94707320 | |||||||
| chr10:94707358 | A | G | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.819+398A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94707358 | |||||||
| chr10:94707586 | G | A | 4 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0005c0008t0004g0248 others(1): Show |
6 | HG01257.hp1 HG01258.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.819+626G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94707586 | |||||||
| chr10:94707629 | A | G | 7 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0221 others(4): Show |
11 | HG00642.hp2 HG01099.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.819+669A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94707629 | |||||||
| chr10:94707703 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.819+743G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94707703 | |||||||
| chr10:94707952 | G | GC | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.819+993dupC | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94707952 | ||||||
| chr10:94707954 | T | C | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.819+994T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94707954 | |||||||
| chr10:94708021 | G | T | 3 | a0001c0005t0001g0054 a0001c0005t0001g0055 a0001c0005t0001g0067 |
3 | HG02145.hp1 HG02486.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.819+1061G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94708021 | |||||||
| chr10:94708078 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.819+1118G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94708078 | |||||||
| chr10:94708093 | G | A | 2 | a0002c0002t0004g0123 a0002c0002t0007g0032 |
3 | HG00280.hp1 HG01192.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.819+1133G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94708093 | |||||||
| chr10:94708193 | G | C | 4 | a0002c0002t0004g0086 a0002c0002t0004g0087 a0002c0002t0004g0088 others(1): Show |
4 | HG02698.hp1 HG03491.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.819+1233G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94708193 | |||||||
| chr10:94708214 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.819+1254T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94708214 | |||||||
| chr10:94708245 | A | G | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.819+1285A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94708245 | |||||||
| chr10:94708362 | G | C | 76 | a0001c0001t0001g0025 a0001c0001t0004g0028 a0001c0001t0004g0124 others(73): Show |
95 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.819+1402G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94708362 | |||||||
| chr10:94708508 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.819+1548A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94708508 | |||||||
| chr10:94708767 | A | C | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.819+1807A>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94708767 | |||||||
| chr10:94708877 | A | G | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.819+1917A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94708877 | |||||||
| chr10:94708914 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0220 |
5 | HG02451.hp2 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.819+1954C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94708914 | |||||||
| chr10:94708981 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.819+2021G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94708981 | |||||||
| chr10:94708998 | T | C | 11 | a0001c0001t0005g0004 a0001c0001t0005g0056 a0001c0001t0005g0057 others(8): Show |
18 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.819+2038T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94708998 | |||||||
| chr10:94709051 | T | C | 33 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(30): Show |
49 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.819+2091T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94709051 | |||||||
| chr10:94709087 | G | C | 1 | a0001c0001t0001g0129 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.819+2127G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94709087 | |||||||
| chr10:94709113 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.819+2153C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94709113 | |||||||
| chr10:94709142 | G | A | 5 | a0001c0001t0002g0005 a0001c0001t0002g0041 a0001c0001t0002g0158 others(2): Show |
13 | HG00735.hp2 HG01123.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.819+2182G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94709142 | |||||||
| chr10:94709152 | C | G | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.819+2192C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94709152 | |||||||
| chr10:94709333 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.819+2373T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94709333 | |||||||
| chr10:94709445 | TAGGTTAT others(10): Show |
T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0220 |
5 | HG02451.hp2 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.819+2487_819+2503d others(19): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94709445 | ||||||
| chr10:94709465 | A | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0220 |
5 | HG02451.hp2 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.819+2505A>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94709465 | |||||||
| chr10:94709522 | AT | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0220 |
5 | HG02451.hp2 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.819+2564delT | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94709522 | ||||||
| chr10:94709545 | T | C | 1 | a0002c0002t0003g0071 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.819+2585T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94709545 | |||||||
| chr10:94709629 | G | C | 2 | a0005c0008t0004g0248 a0005c0008t0004g0249 |
2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.819+2669G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94709629 | |||||||
| chr10:94709656 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.819+2696C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94709656 | |||||||
| chr10:94709698 | C | T | 1 | a0001c0001t0009g0185 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.819+2738C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94709698 | |||||||
| chr10:94709818 | C | CAT | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.819+2859_819+2860d others(4): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94709818 | ||||||
| chr10:94709874 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.819+2914T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94709874 | |||||||
| chr10:94709875 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(46): Show |
73 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.819+2915C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94709875 | |||||||
| chr10:94709912 | C | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(31): Show |
50 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(47): Show |
intron_variant | MODIFIER | c.819+2952C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94709912 | |||||||
| chr10:94710010 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.819+3050G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94710010 | |||||||
| chr10:94710167 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.819+3207C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94710167 | |||||||
| chr10:94710236 | G | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0221 others(4): Show |
11 | HG00642.hp2 HG01099.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.819+3276G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94710236 | |||||||
| chr10:94710485 | C | T | 13 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(10): Show |
20 | HG01884.hp1 HG02886.hp1 HG03453.hp1 others(17): Show |
intron_variant | MODIFIER | c.819+3525C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94710485 | |||||||
| chr10:94710567 | G | T | 1 | a0002c0002t0003g0106 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.819+3607G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94710567 | |||||||
| chr10:94710744 | G | C | 1 | a0010c0013t0001g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.819+3784G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94710744 | |||||||
| chr10:94710767 | G | T | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.819+3807G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94710767 | |||||||
| chr10:94711197 | A | C | 33 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(30): Show |
49 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.819+4237A>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94711197 | |||||||
| chr10:94711333 | C | T | 1 | a0001c0001t0002g0176 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.819+4373C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94711333 | |||||||
| chr10:94711596 | G | A | 1 | a0001c0004t0002g0159 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.819+4636G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94711596 | |||||||
| chr10:94711750 | T | C | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.819+4790T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94711750 | |||||||
| chr10:94711753 | G | A | 104 | a0001c0001t0001g0025 a0001c0001t0004g0028 a0001c0001t0004g0124 others(101): Show |
138 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.819+4793G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94711753 | |||||||
| chr10:94711755 | G | C | 1 | a0002c0002t0004g0246 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.819+4795G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94711755 | |||||||
| chr10:94711804 | G | A | 1 | a0002c0002t0004g0009 | 4 | HG00621.hp1 HG02129.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.819+4844G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94711804 | |||||||
| chr10:94711824 | CT | C | 4 | a0001c0001t0001g0042 a0001c0001t0001g0160 a0001c0001t0002g0017 others(1): Show |
8 | HG01109.hp2 HG03453.hp2 NA18991.hp2 others(5): Show |
intron_variant | MODIFIER | c.819+4874delT | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94711824 | ||||||
| chr10:94711848 | T | A | 7 | a0001c0001t0001g0020 a0001c0001t0001g0039 a0001c0001t0001g0047 others(4): Show |
11 | HG01361.hp2 HG01952.hp1 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.819+4888T>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94711848 | |||||||
| chr10:94712008 | A | AT | 23 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0132 others(20): Show |
35 | HG01891.hp1 HG02027.hp1 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.819+5068dupT | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712008 | ||||||
| chr10:94712008 | A | ATTT | 13 | a0001c0001t0009g0185 a0002c0002t0003g0073 a0003c0003t0006g0014 others(10): Show |
19 | HG00423.hp2 HG02922.hp2 HG03490.hp1 others(16): Show |
intron_variant | MODIFIER | c.819+5066_819+5068d others(5): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712008 | ||||||
| chr10:94712008 | A | ATTTTTTT others(3): Show |
1 | a0002c0002t0007g0032 | 2 | HG00280.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.819+5059_819+5068d others(12): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712008 | ||||||
| chr10:94712008 | A | ATTTTTTT others(5): Show |
2 | a0002c0002t0003g0070 a0003c0007t0001g0252 |
2 | HG02258.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.819+5057_819+5068d others(14): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712008 | ||||||
| chr10:94712008 | A | ATTTTTTT others(6): Show |
4 | a0002c0002t0003g0015 a0002c0002t0003g0071 a0002c0002t0003g0111 others(1): Show |
7 | HG02922.hp1 HG03579.hp2 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.819+5056_819+5068d others(15): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712008 | ||||||
| chr10:94712008 | A | ATTTTTTT others(7): Show |
1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.819+5055_819+5068d others(16): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712008 | ||||||
| chr10:94712008 | A | ATTTTTTT others(8): Show |
1 | a0002c0002t0003g0106 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.819+5054_819+5068d others(17): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712008 | ||||||
| chr10:94712008 | A | ATTTTTTT others(11): Show |
1 | a0003c0003t0001g0236 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.819+5051_819+5068d others(20): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712008 | ||||||
| chr10:94712008 | A | ATTTTTTT others(12): Show |
3 | a0002c0002t0003g0008 a0002c0002t0003g0079 a0003c0003t0001g0048 |
7 | HG02886.hp1 HG03453.hp1 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.819+5050_819+5068d others(21): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712008 | ||||||
| chr10:94712008 | A | ATTTTTTT others(13): Show |
3 | a0002c0002t0003g0029 a0002c0002t0003g0114 a0002c0002t0003g0120 |
4 | NA18612.hp2 NA19056.hp1 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.819+5049_819+5068d others(22): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712008 | ||||||
| chr10:94712008 | A | ATTTTTTT others(14): Show |
4 | a0001c0001t0004g0028 a0001c0001t0004g0124 a0002c0002t0003g0080 others(1): Show |
5 | HG00639.hp1 HG02293.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.819+5068_819+5069i others(23): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712008 | ||||||
| chr10:94712008 | A | ATTTTTTT others(16): Show |
1 | a0002c0002t0003g0081 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.819+5068_819+5069i others(25): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712008 | ||||||
| chr10:94712008 | A | ATTTTTTT others(17): Show |
1 | a0002c0002t0003g0092 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.819+5068_819+5069i others(26): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712008 | ||||||
| chr10:94712008 | A | ATTTTTTT others(18): Show |
12 | a0002c0002t0003g0030 a0002c0002t0003g0075 a0002c0002t0003g0093 others(9): Show |
12 | HG01074.hp1 HG03017.hp1 HG04115.hp1 others(9): Show |
intron_variant | MODIFIER | c.819+5068_819+5069i others(27): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712008 | ||||||
| chr10:94712008 | A | ATTTTTTT others(19): Show |
19 | a0001c0001t0001g0025 a0002c0002t0003g0010 a0002c0002t0003g0072 others(16): Show |
22 | HG00609.hp2 HG00621.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.819+5068_819+5069i others(28): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712008 | ||||||
| chr10:94712008 | A | ATTTTTTT others(20): Show |
8 | a0002c0002t0003g0076 a0002c0002t0004g0031 a0002c0002t0004g0082 others(5): Show |
9 | HG01192.hp2 HG02074.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.819+5068_819+5069i others(29): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712008 | ||||||
| chr10:94712008 | A | ATTTTTTT others(21): Show |
5 | a0002c0002t0003g0011 a0002c0002t0003g0103 a0002c0002t0004g0011 others(2): Show |
7 | HG00438.hp1 HG02027.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.819+5068_819+5069i others(30): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712008 | ||||||
| chr10:94712008 | A | ATTTTTTT others(22): Show |
2 | a0002c0002t0003g0016 a0002c0002t0004g0104 |
4 | HG02040.hp1 HG03041.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.819+5068_819+5069i others(31): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712008 | ||||||
| chr10:94712008 | A | ATTTTTTT others(23): Show |
2 | a0002c0002t0003g0108 a0002c0002t0003g0121 |
2 | HG03688.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.819+5068_819+5069i others(32): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712008 | ||||||
| chr10:94712008 | A | ATTTTTTT others(24): Show |
1 | a0002c0002t0004g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.819+5068_819+5069i others(33): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712008 | ||||||
| chr10:94712008 | A | ATTTTTTT others(25): Show |
1 | a0002c0002t0003g0109 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.819+5068_819+5069i others(34): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712008 | ||||||
| chr10:94712008 | A | ATTTTTTT others(30): Show |
1 | a0002c0002t0003g0105 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.819+5068_819+5069i others(39): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712008 | ||||||
| chr10:94712008 | AT | A | 39 | a0001c0001t0001g0042 a0001c0001t0001g0146 a0001c0001t0001g0160 others(36): Show |
61 | HG00735.hp2 HG00741.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.819+5068delT | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712008 | ||||||
| chr10:94712008 | ATTTT | A | 10 | a0001c0001t0005g0004 a0001c0001t0005g0056 a0001c0001t0005g0057 others(7): Show |
17 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.819+5065_819+5068d others(6): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712008 | ||||||
| chr10:94712015 | T | A | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.819+5055T>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94712015 | |||||||
| chr10:94712030 | T | G | 76 | a0001c0001t0001g0025 a0001c0001t0004g0028 a0001c0001t0004g0124 others(73): Show |
95 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.819+5070T>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94712030 | |||||||
| chr10:94712071 | C | T | 1 | a0001c0001t0009g0185 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.819+5111C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94712071 | |||||||
| chr10:94712158 | A | AT | 10 | a0001c0001t0001g0169 a0001c0001t0001g0212 a0001c0001t0001g0229 others(7): Show |
14 | HG02056.hp1 HG02451.hp1 NA18944.hp2 others(11): Show |
intron_variant | MODIFIER | c.819+5213dupT | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712158 | ||||||
| chr10:94712158 | A | ATT | 70 | a0001c0001t0001g0025 a0001c0001t0004g0028 a0002c0002t0003g0008 others(67): Show |
89 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.819+5212_819+5213d others(4): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712158 | ||||||
| chr10:94712158 | AT | A | 14 | a0001c0001t0001g0210 a0001c0001t0001g0222 a0001c0001t0005g0004 others(11): Show |
21 | HG00423.hp1 HG00609.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.819+5213delT | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712158 | ||||||
| chr10:94712158 | ATT | A | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.819+5212_819+5213d others(4): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94712158 | ||||||
| chr10:94712323 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.819+5363C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94712323 | |||||||
| chr10:94712400 | C | T | 6 | a0001c0001t0001g0036 a0001c0001t0001g0128 a0001c0001t0001g0131 others(3): Show |
7 | HG02109.hp2 HG02572.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.819+5440C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94712400 | |||||||
| chr10:94712481 | G | A | 1 | a0002c0002t0004g0094 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.819+5521G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94712481 | |||||||
| chr10:94712888 | G | T | 1 | a0003c0010t0010g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.819+5928G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94712888 | |||||||
| chr10:94713018 | A | G | 1 | a0001c0001t0002g0150 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.819+6058A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94713018 | |||||||
| chr10:94713100 | A | C | 1 | a0003c0010t0010g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.819+6140A>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94713100 | |||||||
| chr10:94713149 | G | A | 1 | a0003c0010t0010g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.819+6189G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94713149 | |||||||
| chr10:94713168 | T | G | 76 | a0001c0001t0001g0025 a0001c0001t0004g0028 a0001c0001t0004g0124 others(73): Show |
95 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.819+6208T>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94713168 | |||||||
| chr10:94713255 | A | T | 1 | a0001c0001t0001g0204 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.819+6295A>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94713255 | |||||||
| chr10:94713333 | C | T | 1 | a0001c0001t0002g0044 | 2 | HG00741.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.819+6373C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94713333 | |||||||
| chr10:94713427 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0139 |
3 | HG02965.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.819+6467C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94713427 | |||||||
| chr10:94713521 | T | A | 1 | a0001c0001t0001g0151 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.819+6561T>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94713521 | |||||||
| chr10:94713541 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.819+6581T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94713541 | |||||||
| chr10:94713651 | G | A | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.819+6691G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94713651 | |||||||
| chr10:94713694 | C | G | 1 | a0001c0001t0005g0059 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.820-6702C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94713694 | |||||||
| chr10:94713718 | A | G | 1 | a0003c0003t0006g0244 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.820-6678A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94713718 | |||||||
| chr10:94713751 | G | T | 75 | a0001c0001t0004g0028 a0001c0001t0004g0124 a0002c0002t0003g0008 others(72): Show |
93 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.820-6645G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94713751 | |||||||
| chr10:94713802 | G | A | 1 | a0001c0001t0002g0177 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.820-6594G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94713802 | |||||||
| chr10:94713803 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.820-6593T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94713803 | |||||||
| chr10:94713854 | T | C | 1 | a0003c0010t0010g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.820-6542T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94713854 | |||||||
| chr10:94713935 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.820-6461G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94713935 | |||||||
| chr10:94713940 | A | G | 6 | a0001c0001t0001g0022 a0001c0001t0001g0221 a0001c0001t0001g0222 others(3): Show |
8 | HG00642.hp2 HG01099.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.820-6456A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94713940 | |||||||
| chr10:94714121 | T | G | 1 | a0001c0001t0001g0126 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.820-6275T>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94714121 | |||||||
| chr10:94714169 | C | G | 7 | a0001c0001t0002g0046 a0001c0001t0002g0166 a0001c0001t0002g0167 others(4): Show |
8 | HG02129.hp1 NA18942.hp1 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.820-6227C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94714169 | |||||||
| chr10:94714205 | T | G | 1 | a0001c0001t0001g0152 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.820-6191T>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94714205 | |||||||
| chr10:94714334 | C | A | 75 | a0001c0001t0004g0028 a0001c0001t0004g0124 a0002c0002t0003g0008 others(72): Show |
93 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.820-6062C>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94714334 | |||||||
| chr10:94714340 | G | A | 1 | a0002c0002t0004g0097 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.820-6056G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94714340 | |||||||
| chr10:94714390 | A | C | 1 | a0001c0001t0001g0129 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.820-6006A>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94714390 | |||||||
| chr10:94714495 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0202 |
2 | HG03225.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.820-5901C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94714495 | |||||||
| chr10:94714894 | A | G | 92 | a0001c0001t0001g0025 a0001c0001t0004g0028 a0001c0001t0004g0124 others(89): Show |
119 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.820-5502A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94714894 | |||||||
| chr10:94715032 | T | G | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.820-5364T>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94715032 | |||||||
| chr10:94715163 | C | A | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.820-5233C>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94715163 | |||||||
| chr10:94715235 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.820-5161A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94715235 | |||||||
| chr10:94715374 | G | C | 1 | a0001c0001t0001g0230 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.820-5022G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94715374 | |||||||
| chr10:94715397 | G | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(31): Show |
50 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(47): Show |
intron_variant | MODIFIER | c.820-4999G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94715397 | |||||||
| chr10:94715606 | G | A | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.820-4790G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94715606 | |||||||
| chr10:94715617 | C | T | 1 | a0001c0001t0005g0061 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.820-4779C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94715617 | |||||||
| chr10:94715721 | C | G | 1 | a0001c0001t0001g0153 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.820-4675C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94715721 | |||||||
| chr10:94715746 | C | A | 1 | a0001c0001t0005g0062 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.820-4650C>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94715746 | |||||||
| chr10:94715804 | T | C | 6 | a0003c0003t0006g0014 a0003c0003t0006g0023 a0003c0003t0006g0240 others(3): Show |
11 | NA18948.hp1 NA18979.hp1 NA18993.hp2 others(8): Show |
intron_variant | MODIFIER | c.820-4592T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94715804 | |||||||
| chr10:94715816 | C | CT | 75 | a0001c0001t0001g0025 a0001c0001t0004g0028 a0001c0001t0004g0124 others(72): Show |
94 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.820-4571dupT | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94715816 | ||||||
| chr10:94715867 | G | T | 11 | a0001c0001t0005g0004 a0001c0001t0005g0056 a0001c0001t0005g0057 others(8): Show |
18 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.820-4529G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94715867 | |||||||
| chr10:94715969 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.820-4427G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94715969 | |||||||
| chr10:94716018 | T | A | 1 | a0001c0001t0002g0215 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.820-4378T>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94716018 | |||||||
| chr10:94716039 | A | C | 1 | a0002c0011t0003g0077 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.820-4357A>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94716039 | |||||||
| chr10:94716235 | G | T | 72 | a0001c0001t0004g0028 a0002c0002t0003g0008 a0002c0002t0003g0010 others(69): Show |
90 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.820-4161G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94716235 | |||||||
| chr10:94716265 | T | C | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.820-4131T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94716265 | |||||||
| chr10:94716345 | C | G | 11 | a0001c0001t0005g0004 a0001c0001t0005g0056 a0001c0001t0005g0057 others(8): Show |
18 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.820-4051C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94716345 | |||||||
| chr10:94716352 | A | G | 2 | a0001c0001t0002g0164 a0001c0001t0002g0165 |
2 | HG03654.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.820-4044A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94716352 | |||||||
| chr10:94716356 | G | A | 2 | a0001c0001t0002g0164 a0001c0001t0002g0165 |
2 | HG03654.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.820-4040G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94716356 | |||||||
| chr10:94716421 | G | A | 1 | a0001c0001t0004g0124 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.820-3975G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94716421 | |||||||
| chr10:94716462 | G | T | 76 | a0001c0001t0001g0025 a0001c0001t0004g0028 a0001c0001t0004g0124 others(73): Show |
95 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.820-3934G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94716462 | |||||||
| chr10:94716532 | T | C | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.820-3864T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94716532 | |||||||
| chr10:94716644 | G | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(31): Show |
50 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(47): Show |
intron_variant | MODIFIER | c.820-3752G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94716644 | |||||||
| chr10:94716674 | A | G | 2 | a0003c0003t0001g0048 a0003c0003t0001g0236 |
3 | HG01884.hp1 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.820-3722A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94716674 | |||||||
| chr10:94716706 | G | A | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.820-3690G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94716706 | |||||||
| chr10:94716735 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.820-3661T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94716735 | |||||||
| chr10:94716792 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.820-3604C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94716792 | |||||||
| chr10:94716859 | G | A | 1 | a0001c0001t0002g0164 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.820-3537G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94716859 | |||||||
| chr10:94716867 | G | C | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.820-3529G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94716867 | |||||||
| chr10:94716938 | G | A | 2 | a0003c0007t0001g0050 a0003c0007t0001g0252 |
3 | HG02258.hp2 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.820-3458G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94716938 | |||||||
| chr10:94717006 | C | T | 1 | a0003c0003t0006g0239 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.820-3390C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94717006 | |||||||
| chr10:94717029 | G | A | 11 | a0001c0001t0005g0004 a0001c0001t0005g0056 a0001c0001t0005g0057 others(8): Show |
18 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.820-3367G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94717029 | |||||||
| chr10:94717166 | A | C | 2 | a0003c0007t0001g0050 a0003c0007t0001g0252 |
3 | HG02258.hp2 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.820-3230A>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94717166 | |||||||
| chr10:94717209 | T | C | 6 | a0001c0005t0001g0026 a0001c0005t0001g0027 a0001c0005t0001g0054 others(3): Show |
8 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.820-3187T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94717209 | |||||||
| chr10:94717221 | A | G | 2 | a0001c0001t0002g0178 a0001c0001t0002g0179 |
2 | HG03669.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.820-3175A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94717221 | |||||||
| chr10:94717234 | C | T | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.820-3162C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94717234 | |||||||
| chr10:94717321 | G | A | 76 | a0001c0001t0001g0025 a0001c0001t0004g0028 a0001c0001t0004g0124 others(73): Show |
95 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.820-3075G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94717321 | |||||||
| chr10:94717355 | G | A | 6 | a0001c0005t0001g0026 a0001c0005t0001g0027 a0001c0005t0001g0054 others(3): Show |
8 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.820-3041G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94717355 | |||||||
| chr10:94717377 | G | T | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.820-3019G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94717377 | |||||||
| chr10:94717386 | A | G | 76 | a0001c0001t0001g0025 a0001c0001t0004g0028 a0001c0001t0004g0124 others(73): Show |
95 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.820-3010A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94717386 | |||||||
| chr10:94717456 | G | T | 76 | a0001c0001t0001g0025 a0001c0001t0004g0028 a0001c0001t0004g0124 others(73): Show |
95 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.820-2940G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94717456 | |||||||
| chr10:94717490 | A | G | 1 | a0001c0001t0004g0124 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.820-2906A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94717490 | |||||||
| chr10:94717505 | C | T | 17 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(14): Show |
25 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.820-2891C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94717505 | |||||||
| chr10:94717801 | G | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(30): Show |
49 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.820-2595G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94717801 | |||||||
| chr10:94717805 | G | T | 1 | a0001c0001t0002g0163 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.820-2591G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94717805 | |||||||
| chr10:94717867 | G | A | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.820-2529G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94717867 | |||||||
| chr10:94717910 | G | A | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.820-2486G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94717910 | |||||||
| chr10:94717929 | A | G | 1 | a0002c0002t0004g0113 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.820-2467A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94717929 | |||||||
| chr10:94717943 | G | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0139 |
3 | HG02965.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.820-2453G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94717943 | |||||||
| chr10:94717980 | A | G | 1 | a0002c0002t0004g0091 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.820-2416A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94717980 | |||||||
| chr10:94718022 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.820-2374A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94718022 | |||||||
| chr10:94718097 | T | C | 74 | a0001c0001t0001g0025 a0001c0001t0004g0028 a0001c0001t0004g0124 others(71): Show |
93 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.820-2299T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94718097 | |||||||
| chr10:94718235 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.820-2161T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94718235 | |||||||
| chr10:94718295 | G | A | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.820-2101G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94718295 | |||||||
| chr10:94718365 | G | C | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.820-2031G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94718365 | |||||||
| chr10:94718416 | CT | C | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.820-1977delT | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94718416 | ||||||
| chr10:94718575 | C | G | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.820-1821C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94718575 | |||||||
| chr10:94718606 | A | T | 1 | a0001c0005t0001g0026 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.820-1790A>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94718606 | |||||||
| chr10:94718680 | CTT | C | 6 | a0001c0005t0001g0026 a0001c0005t0001g0027 a0001c0005t0001g0054 others(3): Show |
8 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.820-1713_820-1712d others(4): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94718680 | ||||||
| chr10:94718751 | A | G | 13 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(10): Show |
20 | HG01884.hp1 HG02886.hp1 HG03453.hp1 others(17): Show |
intron_variant | MODIFIER | c.820-1645A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94718751 | |||||||
| chr10:94718851 | C | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(31): Show |
50 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(47): Show |
intron_variant | MODIFIER | c.820-1545C>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94718851 | |||||||
| chr10:94719245 | G | GA | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.820-1143dupA | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94719245 | ||||||
| chr10:94719281 | T | C | 13 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(10): Show |
20 | HG01884.hp1 HG02886.hp1 HG03453.hp1 others(17): Show |
intron_variant | MODIFIER | c.820-1115T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94719281 | |||||||
| chr10:94719410 | AT | A | 15 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(12): Show |
23 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(20): Show |
intron_variant | MODIFIER | c.820-975delT | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 94719410 | ||||||
| chr10:94719477 | C | T | 13 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(10): Show |
20 | HG01884.hp1 HG02886.hp1 HG03453.hp1 others(17): Show |
intron_variant | MODIFIER | c.820-919C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94719477 | |||||||
| chr10:94719563 | G | C | 1 | a0001c0001t0001g0132 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.820-833G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94719563 | |||||||
| chr10:94719582 | A | T | 2 | a0003c0007t0001g0050 a0003c0007t0001g0252 |
3 | HG02258.hp2 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.820-814A>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94719582 | |||||||
| chr10:94719718 | G | A | 5 | a0001c0004t0002g0007 a0001c0004t0002g0159 a0001c0004t0002g0161 others(2): Show |
10 | HG01981.hp1 HG02155.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.820-678G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94719718 | |||||||
| chr10:94719775 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.820-621A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94719775 | |||||||
| chr10:94720008 | G | A | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0141 |
3 | HG02109.hp2 HG02572.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.820-388G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94720008 | |||||||
| chr10:94720108 | A | C | 11 | a0003c0003t0006g0014 a0003c0003t0006g0023 a0003c0003t0006g0049 others(8): Show |
17 | HG03490.hp1 HG03492.hp1 HG03831.hp2 others(14): Show |
intron_variant | MODIFIER | c.820-288A>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 5/8 | chr10 | 94720108 | |||||||
| chr10:94720867 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.961+330G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/8 | chr10 | 94720867 | |||||||
| chr10:94721026 | T | C | 1 | a0001c0001t0001g0033 | 2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.961+489T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/8 | chr10 | 94721026 | |||||||
| chr10:94721106 | C | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0221 others(4): Show |
11 | HG00642.hp2 HG01099.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.961+569C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/8 | chr10 | 94721106 | |||||||
| chr10:94721133 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.961+596C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/8 | chr10 | 94721133 | |||||||
| chr10:94721246 | C | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0220 |
5 | HG02451.hp2 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.961+709C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/8 | chr10 | 94721246 | |||||||
| chr10:94721452 | T | A | 1 | a0001c0001t0002g0149 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.961+915T>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/8 | chr10 | 94721452 | |||||||
| chr10:94721501 | G | A | 1 | a0003c0003t0006g0238 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.961+964G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/8 | chr10 | 94721501 | |||||||
| chr10:94721757 | A | G | 1 | a0002c0002t0004g0113 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.961+1220A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/8 | chr10 | 94721757 | |||||||
| chr10:94721791 | C | T | 3 | a0001c0001t0001g0037 a0001c0001t0001g0130 a0001c0001t0001g0138 |
4 | HG01192.hp1 HG02735.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.961+1254C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/8 | chr10 | 94721791 | |||||||
| chr10:94721904 | CTGT | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(46): Show |
86 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.961+1370_961+1372d others(5): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr10 | 94721904 | ||||||
| chr10:94722349 | C | A | 1 | a0001c0001t0004g0028 | 2 | HG00639.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.961+1812C>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/8 | chr10 | 94722349 | |||||||
| chr10:94722362 | A | G | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.961+1825A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/8 | chr10 | 94722362 | |||||||
| chr10:94722754 | G | C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0047 a0001c0001t0001g0197 others(1): Show |
7 | HG02071.hp2 NA18942.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.962-1592G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/8 | chr10 | 94722754 | |||||||
| chr10:94722882 | C | T | 13 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(10): Show |
20 | HG01884.hp1 HG02886.hp1 HG03453.hp1 others(17): Show |
intron_variant | MODIFIER | c.962-1464C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/8 | chr10 | 94722882 | |||||||
| chr10:94723012 | A | G | 1 | a0002c0002t0004g0087 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.962-1334A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/8 | chr10 | 94723012 | |||||||
| chr10:94723023 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.962-1323G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/8 | chr10 | 94723023 | |||||||
| chr10:94723095 | A | G | 11 | a0001c0001t0005g0004 a0001c0001t0005g0056 a0001c0001t0005g0057 others(8): Show |
18 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.962-1251A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/8 | chr10 | 94723095 | |||||||
| chr10:94723215 | A | G | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.962-1131A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/8 | chr10 | 94723215 | |||||||
| chr10:94723251 | G | C | 11 | a0001c0001t0005g0004 a0001c0001t0005g0056 a0001c0001t0005g0057 others(8): Show |
18 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.962-1095G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/8 | chr10 | 94723251 | |||||||
| chr10:94723360 | G | A | 2 | a0003c0007t0001g0050 a0003c0007t0001g0252 |
3 | HG02258.hp2 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.962-986G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/8 | chr10 | 94723360 | |||||||
| chr10:94723530 | A | G | 1 | a0001c0001t0002g0170 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.962-816A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/8 | chr10 | 94723530 | |||||||
| chr10:94723618 | A | G | 2 | a0003c0003t0001g0048 a0003c0003t0001g0236 |
3 | HG01884.hp1 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.962-728A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/8 | chr10 | 94723618 | |||||||
| chr10:94723734 | A | G | 1 | a0002c0002t0003g0103 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.962-612A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/8 | chr10 | 94723734 | |||||||
| chr10:94723775 | C | CT | 103 | a0001c0001t0004g0028 a0001c0001t0004g0124 a0001c0001t0005g0004 others(100): Show |
136 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.962-571_962-570ins others(1): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/8 | chr10 | 94723775 | |||||||
| chr10:94723807 | G | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0183 a0001c0001t0001g0184 |
5 | HG01074.hp2 HG01257.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.962-539G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/8 | chr10 | 94723807 | |||||||
| chr10:94723867 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.962-479C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/8 | chr10 | 94723867 | |||||||
| chr10:94724215 | A | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0221 others(4): Show |
11 | HG00642.hp2 HG01099.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.962-131A>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 6/8 | chr10 | 94724215 | |||||||
| chr10:94724737 | A | G | 1 | a0001c0001t0001g0154 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1149+204A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94724737 | |||||||
| chr10:94724758 | A | AT | 89 | a0001c0001t0004g0028 a0001c0001t0004g0124 a0002c0002t0003g0008 others(86): Show |
115 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1149+235dupT | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr10 | 94724758 | ||||||
| chr10:94724783 | GT | G | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.1149+252delT | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr10 | 94724783 | ||||||
| chr10:94724814 | T | C | 7 | a0001c0001t0001g0025 a0001c0005t0001g0026 a0001c0005t0001g0027 others(4): Show |
10 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1149+281T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94724814 | |||||||
| chr10:94724824 | T | C | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1149+291T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94724824 | |||||||
| chr10:94724842 | G | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(31): Show |
50 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(47): Show |
intron_variant | MODIFIER | c.1149+309G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94724842 | |||||||
| chr10:94724888 | A | G | 1 | a0002c0002t0004g0097 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1149+355A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94724888 | |||||||
| chr10:94724945 | C | G | 1 | a0001c0001t0001g0128 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1149+412C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94724945 | |||||||
| chr10:94724947 | T | C | 1 | a0003c0010t0010g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1149+414T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94724947 | |||||||
| chr10:94725020 | G | A | 91 | a0001c0001t0004g0028 a0001c0001t0004g0124 a0002c0002t0003g0008 others(88): Show |
117 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.1149+487G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94725020 | |||||||
| chr10:94725189 | C | T | 13 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(10): Show |
20 | HG01884.hp1 HG02886.hp1 HG03453.hp1 others(17): Show |
intron_variant | MODIFIER | c.1149+656C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94725189 | |||||||
| chr10:94725449 | A | G | 1 | a0002c0002t0003g0117 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1149+916A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94725449 | |||||||
| chr10:94725802 | G | A | 1 | a0001c0001t0001g0025 | 2 | HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1149+1269G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94725802 | |||||||
| chr10:94725827 | A | G | 76 | a0001c0001t0001g0025 a0001c0001t0004g0028 a0001c0001t0004g0124 others(73): Show |
95 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1149+1294A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94725827 | |||||||
| chr10:94725922 | C | T | 1 | a0002c0002t0004g0089 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1149+1389C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94725922 | |||||||
| chr10:94725923 | A | G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(365): Show |
intron_variant | MODIFIER | c.1149+1390A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94725923 | |||||||
| chr10:94726182 | CA | C | 13 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(10): Show |
20 | HG01884.hp1 HG02886.hp1 HG03453.hp1 others(17): Show |
intron_variant | MODIFIER | c.1149+1657delA | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr10 | 94726182 | ||||||
| chr10:94726190 | AT | A | 3 | a0003c0007t0001g0050 a0003c0007t0001g0252 a0003c0010t0010g0245 |
4 | HG02258.hp2 HG02630.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1149+1665delT | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr10 | 94726190 | ||||||
| chr10:94726201 | AT | A | 105 | a0001c0001t0001g0025 a0001c0001t0004g0028 a0001c0001t0005g0004 others(102): Show |
141 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.1149+1678delT | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr10 | 94726201 | ||||||
| chr10:94726202 | T | G | 1 | a0001c0001t0004g0124 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1149+1669T>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94726202 | |||||||
| chr10:94726274 | G | A | 1 | a0002c0002t0003g0093 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1149+1741G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94726274 | |||||||
| chr10:94726289 | G | A | 1 | a0003c0010t0010g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1149+1756G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94726289 | |||||||
| chr10:94726344 | C | T | 1 | a0002c0002t0003g0079 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1149+1811C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94726344 | |||||||
| chr10:94726433 | A | T | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.1149+1900A>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94726433 | |||||||
| chr10:94726436 | C | T | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1149+1903C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94726436 | |||||||
| chr10:94726496 | A | C | 103 | a0001c0001t0001g0025 a0001c0001t0004g0028 a0001c0001t0004g0124 others(100): Show |
137 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.1149+1963A>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94726496 | |||||||
| chr10:94726541 | T | C | 76 | a0001c0001t0001g0025 a0001c0001t0004g0028 a0001c0001t0004g0124 others(73): Show |
95 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1149+2008T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94726541 | |||||||
| chr10:94726599 | A | T | 76 | a0001c0001t0001g0025 a0001c0001t0004g0028 a0001c0001t0004g0124 others(73): Show |
95 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1149+2066A>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94726599 | |||||||
| chr10:94726707 | A | AG | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.1149+2175dupG | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr10 | 94726707 | ||||||
| chr10:94726747 | A | G | 144 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0033 others(141): Show |
196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.1149+2214A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94726747 | |||||||
| chr10:94727014 | C | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0221 others(4): Show |
11 | HG00642.hp2 HG01099.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.1149+2481C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94727014 | |||||||
| chr10:94727025 | T | A | 3 | a0001c0001t0005g0062 a0001c0001t0005g0063 a0001c0001t0005g0064 |
3 | HG01978.hp2 HG03710.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1149+2492T>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94727025 | |||||||
| chr10:94727153 | G | A | 1 | a0002c0002t0004g0097 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1149+2620G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94727153 | |||||||
| chr10:94727242 | T | A | 1 | a0001c0001t0001g0230 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1149+2709T>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94727242 | |||||||
| chr10:94727367 | C | A | 1 | a0001c0001t0002g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1149+2834C>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94727367 | |||||||
| chr10:94727492 | G | A | 1 | a0003c0010t0010g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1149+2959G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94727492 | |||||||
| chr10:94727550 | C | G | 91 | a0001c0001t0004g0028 a0001c0001t0004g0124 a0002c0002t0003g0008 others(88): Show |
117 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.1149+3017C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94727550 | |||||||
| chr10:94727570 | G | A | 1 | a0002c0002t0003g0096 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1149+3037G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94727570 | |||||||
| chr10:94727605 | G | A | 1 | a0001c0001t0001g0033 | 2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1149+3072G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94727605 | |||||||
| chr10:94727614 | C | CA | 15 | a0001c0001t0001g0192 a0003c0003t0001g0048 a0003c0003t0001g0236 others(12): Show |
23 | HG01884.hp1 HG02258.hp2 HG02886.hp1 others(20): Show |
intron_variant | MODIFIER | c.1149+3089dupA | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr10 | 94727614 | ||||||
| chr10:94727623 | C | A | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.1149+3090C>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94727623 | |||||||
| chr10:94727694 | C | T | 145 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0033 others(142): Show |
197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.1149+3161C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94727694 | |||||||
| chr10:94727774 | T | C | 75 | a0001c0001t0004g0028 a0001c0001t0004g0124 a0002c0002t0003g0008 others(72): Show |
93 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.1149+3241T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94727774 | |||||||
| chr10:94727821 | C | T | 1 | a0002c0002t0004g0082 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1149+3288C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94727821 | |||||||
| chr10:94727831 | A | G | 1 | a0003c0010t0010g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1149+3298A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94727831 | |||||||
| chr10:94727892 | G | A | 1 | a0001c0001t0009g0185 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1149+3359G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94727892 | |||||||
| chr10:94728006 | C | T | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1149+3473C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94728006 | |||||||
| chr10:94728055 | C | A | 13 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(10): Show |
20 | HG01884.hp1 HG02886.hp1 HG03453.hp1 others(17): Show |
intron_variant | MODIFIER | c.1149+3522C>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94728055 | |||||||
| chr10:94728172 | A | G | 1 | a0001c0004t0002g0161 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1149+3639A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94728172 | |||||||
| chr10:94728179 | C | T | 1 | a0001c0001t0002g0162 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1149+3646C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94728179 | |||||||
| chr10:94728357 | TG | T | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.1149+3825delG | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94728357 | |||||||
| chr10:94728532 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1149+3999T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94728532 | |||||||
| chr10:94728712 | C | T | 73 | a0001c0001t0004g0028 a0001c0001t0004g0124 a0002c0002t0003g0008 others(70): Show |
91 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1149+4179C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94728712 | |||||||
| chr10:94728812 | A | G | 1 | a0010c0013t0001g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1149+4279A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94728812 | |||||||
| chr10:94729131 | G | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(31): Show |
50 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(47): Show |
intron_variant | MODIFIER | c.1150-4166G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94729131 | |||||||
| chr10:94729183 | A | G | 1 | a0002c0002t0004g0087 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1150-4114A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94729183 | |||||||
| chr10:94729231 | A | G | 1 | a0003c0010t0010g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1150-4066A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94729231 | |||||||
| chr10:94729240 | T | A | 91 | a0001c0001t0004g0028 a0001c0001t0004g0124 a0002c0002t0003g0008 others(88): Show |
117 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.1150-4057T>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94729240 | |||||||
| chr10:94729248 | C | T | 2 | a0002c0002t0004g0102 a0002c0002t0004g0112 |
2 | HG02145.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1150-4049C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94729248 | |||||||
| chr10:94729305 | G | A | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.1150-3992G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94729305 | |||||||
| chr10:94729501 | T | G | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.1150-3796T>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94729501 | |||||||
| chr10:94729562 | A | G | 75 | a0001c0001t0004g0028 a0001c0001t0004g0124 a0002c0002t0003g0008 others(72): Show |
93 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.1150-3735A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94729562 | |||||||
| chr10:94729657 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1150-3640G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94729657 | |||||||
| chr10:94729724 | C | T | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.1150-3573C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94729724 | |||||||
| chr10:94729823 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1150-3474A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94729823 | |||||||
| chr10:94730085 | A | G | 1 | a0003c0003t0006g0239 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1150-3212A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94730085 | |||||||
| chr10:94730139 | A | T | 2 | a0005c0008t0004g0248 a0005c0008t0004g0249 |
2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1150-3158A>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94730139 | |||||||
| chr10:94730233 | A | C | 1 | a0001c0001t0002g0157 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1150-3064A>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94730233 | |||||||
| chr10:94730334 | G | T | 1 | a0002c0002t0003g0115 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1150-2963G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94730334 | |||||||
| chr10:94730402 | C | A | 1 | a0001c0001t0002g0171 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1150-2895C>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94730402 | |||||||
| chr10:94730449 | A | G | 2 | a0003c0007t0001g0050 a0003c0007t0001g0252 |
3 | HG02258.hp2 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1150-2848A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94730449 | |||||||
| chr10:94730677 | G | C | 1 | a0001c0001t0002g0166 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1150-2620G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94730677 | |||||||
| chr10:94730717 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1150-2580A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94730717 | |||||||
| chr10:94730872 | G | A | 145 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0033 others(142): Show |
197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.1150-2425G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94730872 | |||||||
| chr10:94730874 | A | G | 11 | a0003c0003t0006g0014 a0003c0003t0006g0023 a0003c0003t0006g0049 others(8): Show |
17 | HG03490.hp1 HG03492.hp1 HG03831.hp2 others(14): Show |
intron_variant | MODIFIER | c.1150-2423A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94730874 | |||||||
| chr10:94730972 | A | G | 16 | a0003c0003t0001g0048 a0003c0003t0001g0236 a0003c0003t0006g0014 others(13): Show |
24 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.1150-2325A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94730972 | |||||||
| chr10:94731057 | T | A | 1 | a0009c0012t0002g0253 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1150-2240T>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94731057 | |||||||
| chr10:94731108 | C | T | 1 | a0003c0010t0010g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1150-2189C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94731108 | |||||||
| chr10:94731116 | C | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0019 others(38): Show |
67 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.1150-2181C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94731116 | |||||||
| chr10:94731126 | A | T | 1 | a0009c0012t0002g0253 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1150-2171A>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94731126 | |||||||
| chr10:94731247 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1150-2050G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94731247 | |||||||
| chr10:94731296 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1150-2001C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94731296 | |||||||
| chr10:94731316 | C | T | 75 | a0001c0001t0004g0028 a0001c0001t0004g0124 a0002c0002t0003g0008 others(72): Show |
93 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.1150-1981C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94731316 | |||||||
| chr10:94731319 | G | A | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1150-1978G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94731319 | |||||||
| chr10:94731352 | G | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0033 others(142): Show |
197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.1150-1945G>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94731352 | |||||||
| chr10:94731379 | C | CA | 53 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(50): Show |
90 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1150-1908dupA | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr10 | 94731379 | ||||||
| chr10:94731453 | C | G | 10 | a0003c0003t0006g0014 a0003c0003t0006g0023 a0003c0003t0006g0237 others(7): Show |
15 | HG03831.hp2 HG04204.hp2 NA18943.hp2 others(12): Show |
intron_variant | MODIFIER | c.1150-1844C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94731453 | |||||||
| chr10:94731571 | T | G | 1 | a0009c0012t0002g0253 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1150-1726T>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94731571 | |||||||
| chr10:94731587 | C | A | 1 | a0009c0012t0002g0253 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1150-1710C>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94731587 | |||||||
| chr10:94731726 | C | G | 1 | a0002c0002t0003g0075 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1150-1571C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94731726 | |||||||
| chr10:94732015 | A | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(31): Show |
50 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(47): Show |
intron_variant | MODIFIER | c.1150-1282A>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94732015 | |||||||
| chr10:94732174 | G | A | 2 | a0003c0007t0001g0050 a0003c0007t0001g0252 |
3 | HG02258.hp2 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1150-1123G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94732174 | |||||||
| chr10:94732382 | A | T | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1150-915A>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94732382 | |||||||
| chr10:94732579 | C | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0138 |
2 | HG01192.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1150-718C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94732579 | |||||||
| chr10:94732786 | G | A | 28 | a0001c0001t0005g0004 a0001c0001t0005g0056 a0001c0001t0005g0057 others(25): Show |
43 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(40): Show |
intron_variant | MODIFIER | c.1150-511G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94732786 | |||||||
| chr10:94732791 | G | A | 1 | a0007c0015t0012g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1150-506G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94732791 | |||||||
| chr10:94732916 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0134 |
3 | HG00099.hp2 HG00140.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.1150-381G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94732916 | |||||||
| chr10:94732925 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1150-372C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94732925 | |||||||
| chr10:94733009 | CACCAGGG others(17): Show |
C | 7 | a0001c0001t0001g0025 a0001c0005t0001g0026 a0001c0005t0001g0027 others(4): Show |
10 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1150-284_1150-261d others(26): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr10 | 94733009 | ||||||
| chr10:94733058 | G | A | 3 | a0001c0005t0001g0054 a0001c0005t0001g0055 a0001c0005t0001g0067 |
3 | HG02145.hp1 HG02486.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1150-239G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94733058 | |||||||
| chr10:94733069 | T | C | 2 | a0001c0001t0002g0215 a0001c0001t0002g0216 |
2 | NA19002.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1150-228T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94733069 | |||||||
| chr10:94733116 | C | T | 75 | a0001c0001t0004g0028 a0001c0001t0004g0124 a0002c0002t0003g0008 others(72): Show |
93 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.1150-181C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 7/8 | chr10 | 94733116 | |||||||
| chr10:94733571 | C | T | 75 | a0001c0001t0004g0028 a0001c0001t0004g0124 a0002c0002t0003g0008 others(72): Show |
93 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.1291+133C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/8 | chr10 | 94733571 | |||||||
| chr10:94733575 | C | T | 11 | a0001c0001t0005g0004 a0001c0001t0005g0056 a0001c0001t0005g0057 others(8): Show |
18 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.1291+137C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/8 | chr10 | 94733575 | |||||||
| chr10:94733601 | A | G | 145 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0033 others(142): Show |
197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.1291+163A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/8 | chr10 | 94733601 | |||||||
| chr10:94733613 | G | A | 1 | a0002c0002t0004g0098 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1291+175G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/8 | chr10 | 94733613 | |||||||
| chr10:94733867 | C | G | 7 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0221 others(4): Show |
11 | HG00642.hp2 HG01099.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.1291+429C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/8 | chr10 | 94733867 | |||||||
| chr10:94733952 | A | G | 33 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(30): Show |
49 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.1291+514A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/8 | chr10 | 94733952 | |||||||
| chr10:94733993 | G | A | 11 | a0001c0001t0005g0004 a0001c0001t0005g0056 a0001c0001t0005g0057 others(8): Show |
18 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.1291+555G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/8 | chr10 | 94733993 | |||||||
| chr10:94734034 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1291+596G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/8 | chr10 | 94734034 | |||||||
| chr10:94734452 | G | A | 2 | a0003c0003t0001g0048 a0003c0003t0001g0236 |
3 | HG01884.hp1 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1292-811G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/8 | chr10 | 94734452 | |||||||
| chr10:94734631 | T | C | 8 | a0002c0002t0004g0074 a0002c0002t0004g0099 a0002c0002t0004g0101 others(5): Show |
8 | HG02145.hp2 HG02280.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1292-632T>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/8 | chr10 | 94734631 | |||||||
| chr10:94734820 | T | G | 5 | a0002c0002t0004g0009 a0002c0002t0004g0095 a0002c0002t0004g0100 others(2): Show |
9 | HG00280.hp1 HG00621.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1292-443T>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/8 | chr10 | 94734820 | |||||||
| chr10:94734974 | G | T | 1 | a0001c0001t0001g0140 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1292-289G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/8 | chr10 | 94734974 | |||||||
| chr10:94735003 | G | T | 1 | a0001c0001t0001g0226 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1292-260G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/8 | chr10 | 94735003 | |||||||
| chr10:94735005 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1292-258A>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/8 | chr10 | 94735005 | |||||||
| chr10:94735008 | C | G | 1 | a0001c0001t0001g0226 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1292-255C>G | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/8 | chr10 | 94735008 | |||||||
| chr10:94735014 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1292-249G>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/8 | chr10 | 94735014 | |||||||
| chr10:94735015 | A | C | 1 | a0001c0001t0001g0226 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1292-248A>C | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/8 | chr10 | 94735015 | |||||||
| chr10:94735101 | G | T | 1 | a0001c0001t0001g0226 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1292-162G>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/8 | chr10 | 94735101 | |||||||
| chr10:94735102 | T | A | 1 | a0001c0001t0001g0226 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1292-161T>A | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/8 | chr10 | 94735102 | |||||||
| chr10:94735111 | T | TTC | 91 | a0001c0001t0004g0028 a0001c0001t0004g0124 a0002c0002t0003g0008 others(88): Show |
117 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.1292-151_1292-150i others(4): Show |
CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 94735111 | ||||||
| chr10:94735155 | C | T | 11 | a0001c0001t0005g0004 a0001c0001t0005g0056 a0001c0001t0005g0057 others(8): Show |
18 | HG00423.hp1 HG00609.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.1292-108C>T | CYP2C18 | ENSG00000108242.13 | transcript | ENST00000285979.11 | protein_coding | 8/8 | chr10 | 94735155 |