Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4051 |
| ensemblid | ENSG00000186529.16 |
| hgncid | 2646 |
| symbol | CYP4F3 |
| name | cytochrome P450 family 4 subfamily F member 3 |
| refseq_nuc | NM_000896.3 |
| refseq_prot | NP_000887.2 |
| ensembl_nuc | ENST00000221307.13 |
| ensembl_prot | ENSP00000221307.6 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 15640897 |
| end | 15662825 |
| strand | + |
| ver | v1.2 |
| region | chr19:15640897-15662825 |
| region5000 | chr19:15635897-15667825 |
| regionname0 | CYP4F3_chr19_15640897_15662825 |
| regionname5000 | CYP4F3_chr19_15635897_15667825 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 520 | 336 | 82 | 64 | 135 | 12 | 41 | 105 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | MPQLS others(515): Show |
chr19 | 15635897 | 15667825 |
| a0002 | 0/0 | 520 | 64 | 8 | 8 | 39 | 3 | 6 | 32 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | MPQLS others(515): Show |
chr19 | 15635897 | 15667825 |
| a0003 | 0/0 | 520 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | MPQLS others(515): Show |
chr19 | 15635897 | 15667825 |
| a0004 | 0/0 | 520 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | MPQLS others(515): Show |
chr19 | 15635897 | 15667825 |
| a0005 | 0/0 | 520 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | MPQLS others(515): Show |
chr19 | 15635897 | 15667825 |
| a0006 | 0/0 | 520 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | MPQLS others(515): Show |
chr19 | 15635897 | 15667825 |
| a0007 | 0/0 | 520 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | MPQLS others(515): Show |
chr19 | 15635897 | 15667825 |
| a0008 | 0/0 | 520 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | MPQLS others(515): Show |
chr19 | 15635897 | 15667825 |
| a0009 | 0/0 | 520 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | MPQLS others(515): Show |
chr19 | 15635897 | 15667825 |
| a0010 | 0/0 | 520 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | MPQLS others(515): Show |
chr19 | 15635897 | 15667825 |
| a0011 | 0/0 | 520 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | MPQLS others(515): Show |
chr19 | 15635897 | 15667825 |
| a0012 | 0/0 | 520 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | MPQLS others(515): Show |
chr19 | 15635897 | 15667825 |
| a0013 | 0/0 | 520 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | MPQLS others(515): Show |
chr19 | 15635897 | 15667825 |
| a0014 | 0/0 | 520 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | MPQLS others(515): Show |
chr19 | 15635897 | 15667825 |
| a0015 | 0/0 | 520 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | MPQLS others(515): Show |
chr19 | 15635897 | 15667825 |
| a0016 | 0/0 | 520 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | MPQLS others(515): Show |
chr19 | 15635897 | 15667825 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1560 | 174 | 52 | 27 | 84 | 1 | 10 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | ATGCC others(1555): Show |
chr19 | 15635897 | 15667825 | ||
| a0001c0002 | 1/1 | 1560 | 86 | 17 | 21 | 19 | 9 | 18 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | ATGCC others(1555): Show |
chr19 | 15635897 | 15667825 | ||
| a0001c0004 | 0/0 | 1560 | 41 | 8 | 6 | 19 | 0 | 8 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | ATGCC others(1555): Show |
chr19 | 15635897 | 15667825 | ||
| a0001c0005 | 0/0 | 1560 | 31 | 3 | 9 | 12 | 2 | 5 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | ATGCC others(1555): Show |
chr19 | 15635897 | 15667825 | ||
| a0001c0010 | 0/0 | 1560 | 2 | 1 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | ATGCC others(1555): Show |
chr19 | 15635897 | 15667825 | ||
| a0001c0018 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | ATGCC others(1555): Show |
chr19 | 15635897 | 15667825 | ||
| a0001c0021 | 0/0 | 1560 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | ATGCC others(1555): Show |
chr19 | 15635897 | 15667825 | ||
| a0002c0003 | 0/0 | 1560 | 60 | 8 | 8 | 35 | 3 | 6 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | ATGCC others(1555): Show |
chr19 | 15635897 | 15667825 | ||
| a0002c0007 | 0/0 | 1560 | 4 | 0 | 0 | 4 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | ATGCC others(1555): Show |
chr19 | 15635897 | 15667825 | ||
| a0003c0006 | 0/0 | 1560 | 5 | 0 | 0 | 5 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | ATGCC others(1555): Show |
chr19 | 15635897 | 15667825 | ||
| a0004c0008 | 0/0 | 1560 | 4 | 0 | 0 | 4 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | ATGCC others(1555): Show |
chr19 | 15635897 | 15667825 | ||
| a0005c0012 | 0/0 | 1560 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | ATGCC others(1555): Show |
chr19 | 15635897 | 15667825 | ||
| a0006c0009 | 0/0 | 1560 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | ATGCC others(1555): Show |
chr19 | 15635897 | 15667825 | ||
| a0007c0011 | 0/0 | 1560 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | ATGCC others(1555): Show |
chr19 | 15635897 | 15667825 | ||
| a0008c0013 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | ATGCC others(1555): Show |
chr19 | 15635897 | 15667825 | ||
| a0009c0022 | 0/0 | 1560 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | ATGCC others(1555): Show |
chr19 | 15635897 | 15667825 | ||
| a0010c0020 | 0/0 | 1560 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | ATGCC others(1555): Show |
chr19 | 15635897 | 15667825 | ||
| a0011c0016 | 0/0 | 1560 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | ATGCC others(1555): Show |
chr19 | 15635897 | 15667825 | ||
| a0012c0015 | 0/0 | 1560 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | ATGCC others(1555): Show |
chr19 | 15635897 | 15667825 | ||
| a0013c0023 | 0/0 | 1560 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | ATGCC others(1555): Show |
chr19 | 15635897 | 15667825 | ||
| a0014c0014 | 0/0 | 1560 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | ATGCC others(1555): Show |
chr19 | 15635897 | 15667825 | ||
| a0015c0019 | 0/0 | 1560 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | ATGCC others(1555): Show |
chr19 | 15635897 | 15667825 | ||
| a0016c0017 | 0/0 | 1560 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | ATGCC others(1555): Show |
chr19 | 15635897 | 15667825 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 5058 | 71 | 0 | 15 | 49 | 1 | 6 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5053): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0003 | 0/0 | 5048 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5043): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0006 | 0/0 | 5059 | 13 | 0 | 3 | 10 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5054): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0008 | 0/0 | 5068 | 7 | 3 | 4 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5063): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0009 | 0/0 | 5066 | 8 | 8 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5061): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0010 | 0/0 | 5069 | 6 | 3 | 2 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5064): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0012 | 0/0 | 5067 | 5 | 4 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5062): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0013 | 0/0 | 5071 | 4 | 4 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5066): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0014 | 0/0 | 5057 | 4 | 0 | 1 | 3 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5052): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0015 | 0/0 | 5071 | 4 | 2 | 1 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5066): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0016 | 0/0 | 5066 | 4 | 4 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5061): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0018 | 0/0 | 5070 | 4 | 3 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5065): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0019 | 0/0 | 5070 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5065): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0020 | 0/0 | 5069 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5064): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0022 | 0/0 | 5068 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5063): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0024 | 0/0 | 5057 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5052): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0025 | 0/0 | 5052 | 2 | 0 | 0 | 1 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5047): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0026 | 0/0 | 5058 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5053): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0027 | 0/0 | 5058 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5053): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0029 | 0/0 | 5059 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5054): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0034 | 0/0 | 5068 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5063): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0039 | 0/0 | 5063 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5058): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0043 | 0/0 | 5061 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5056): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0045 | 0/0 | 5068 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5063): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0046 | 0/0 | 5057 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5052): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0047 | 0/0 | 5055 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5050): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0048 | 0/0 | 5067 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5062): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0049 | 0/0 | 5058 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5053): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0053 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5068): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0054 | 0/0 | 5069 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5064): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0055 | 0/0 | 5062 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5057): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0056 | 0/0 | 5060 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5055): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0057 | 0/0 | 5058 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5053): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0058 | 0/0 | 5059 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5054): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0059 | 0/0 | 5057 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5052): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0061 | 0/0 | 5057 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5052): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0076 | 0/0 | 5052 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5047): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0077 | 0/0 | 5057 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5052): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0078 | 0/0 | 5058 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5053): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0079 | 0/0 | 5058 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5053): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0081 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5059): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0082 | 0/0 | 5063 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5058): Show |
chr19 | 15635897 | 15667825 |
| a0001c0001t0083 | 0/0 | 5068 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5063): Show |
chr19 | 15635897 | 15667825 |
| a0001c0002t0001 | 1/1 | 5052 | 69 | 7 | 18 | 18 | 9 | 15 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5047): Show |
chr19 | 15635897 | 15667825 |
| a0001c0002t0017 | 0/0 | 5075 | 4 | 2 | 2 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5070): Show |
chr19 | 15635897 | 15667825 |
| a0001c0002t0023 | 0/0 | 5062 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5057): Show |
chr19 | 15635897 | 15667825 |
| a0001c0002t0031 | 0/0 | 5076 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5071): Show |
chr19 | 15635897 | 15667825 |
| a0001c0002t0032 | 0/0 | 5053 | 2 | 0 | 1 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5048): Show |
chr19 | 15635897 | 15667825 |
| a0001c0002t0044 | 0/0 | 5052 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5047): Show |
chr19 | 15635897 | 15667825 |
| a0001c0002t0065 | 0/0 | 5047 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5042): Show |
chr19 | 15635897 | 15667825 |
| a0001c0002t0066 | 0/0 | 5052 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5047): Show |
chr19 | 15635897 | 15667825 |
| a0001c0002t0067 | 0/0 | 5078 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5073): Show |
chr19 | 15635897 | 15667825 |
| a0001c0002t0068 | 0/0 | 5074 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5069): Show |
chr19 | 15635897 | 15667825 |
| a0001c0002t0069 | 0/0 | 5057 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5052): Show |
chr19 | 15635897 | 15667825 |
| a0001c0002t0070 | 0/0 | 5075 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5070): Show |
chr19 | 15635897 | 15667825 |
| a0001c0004t0005 | 0/0 | 5060 | 16 | 2 | 3 | 8 | 0 | 3 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5055): Show |
chr19 | 15635897 | 15667825 |
| a0001c0004t0007 | 0/0 | 5061 | 11 | 2 | 1 | 7 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5056): Show |
chr19 | 15635897 | 15667825 |
| a0001c0004t0011 | 0/0 | 5062 | 5 | 0 | 0 | 2 | 0 | 3 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5057): Show |
chr19 | 15635897 | 15667825 |
| a0001c0004t0036 | 0/0 | 5062 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5057): Show |
chr19 | 15635897 | 15667825 |
| a0001c0004t0037 | 0/0 | 5055 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5050): Show |
chr19 | 15635897 | 15667825 |
| a0001c0004t0038 | 0/0 | 5060 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5055): Show |
chr19 | 15635897 | 15667825 |
| a0001c0004t0040 | 0/0 | 5066 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5061): Show |
chr19 | 15635897 | 15667825 |
| a0001c0004t0041 | 0/0 | 5059 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5054): Show |
chr19 | 15635897 | 15667825 |
| a0001c0004t0071 | 0/0 | 5050 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5045): Show |
chr19 | 15635897 | 15667825 |
| a0001c0004t0073 | 0/0 | 5050 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5045): Show |
chr19 | 15635897 | 15667825 |
| a0001c0004t0074 | 0/0 | 5051 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5046): Show |
chr19 | 15635897 | 15667825 |
| a0001c0004t0080 | 0/0 | 5061 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5056): Show |
chr19 | 15635897 | 15667825 |
| a0001c0005t0004 | 0/0 | 5051 | 27 | 2 | 9 | 10 | 2 | 4 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5046): Show |
chr19 | 15635897 | 15667825 |
| a0001c0005t0033 | 0/0 | 5052 | 2 | 1 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5047): Show |
chr19 | 15635897 | 15667825 |
| a0001c0005t0072 | 0/0 | 5050 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5045): Show |
chr19 | 15635897 | 15667825 |
| a0001c0005t0075 | 0/0 | 5052 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5047): Show |
chr19 | 15635897 | 15667825 |
| a0001c0010t0021 | 0/0 | 5057 | 2 | 1 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5052): Show |
chr19 | 15635897 | 15667825 |
| a0001c0018t0001 | 0/0 | 5052 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5047): Show |
chr19 | 15635897 | 15667825 |
| a0001c0021t0001 | 0/0 | 5052 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5047): Show |
chr19 | 15635897 | 15667825 |
| a0002c0003t0001 | 0/0 | 5052 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5047): Show |
chr19 | 15635897 | 15667825 |
| a0002c0003t0002 | 0/0 | 5058 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5053): Show |
chr19 | 15635897 | 15667825 |
| a0002c0003t0003 | 0/0 | 5048 | 50 | 6 | 8 | 30 | 1 | 5 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5043): Show |
chr19 | 15635897 | 15667825 |
| a0002c0003t0010 | 0/0 | 5069 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5064): Show |
chr19 | 15635897 | 15667825 |
| a0002c0003t0028 | 0/0 | 5047 | 2 | 1 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5042): Show |
chr19 | 15635897 | 15667825 |
| a0002c0003t0030 | 0/0 | 5050 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5045): Show |
chr19 | 15635897 | 15667825 |
| a0002c0003t0060 | 0/0 | 5049 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5044): Show |
chr19 | 15635897 | 15667825 |
| a0002c0003t0062 | 0/0 | 5048 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5043): Show |
chr19 | 15635897 | 15667825 |
| a0002c0003t0063 | 0/0 | 5049 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5044): Show |
chr19 | 15635897 | 15667825 |
| a0002c0003t0064 | 0/0 | 5049 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5044): Show |
chr19 | 15635897 | 15667825 |
| a0002c0007t0001 | 0/0 | 5052 | 3 | 0 | 0 | 3 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5047): Show |
chr19 | 15635897 | 15667825 |
| a0002c0007t0006 | 0/0 | 5059 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5054): Show |
chr19 | 15635897 | 15667825 |
| a0003c0006t0001 | 0/0 | 5052 | 5 | 0 | 0 | 5 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5047): Show |
chr19 | 15635897 | 15667825 |
| a0004c0008t0003 | 0/0 | 5048 | 3 | 0 | 0 | 3 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5043): Show |
chr19 | 15635897 | 15667825 |
| a0004c0008t0030 | 0/0 | 5050 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5045): Show |
chr19 | 15635897 | 15667825 |
| a0005c0012t0002 | 0/0 | 5058 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5053): Show |
chr19 | 15635897 | 15667825 |
| a0006c0009t0051 | 0/0 | 5075 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5070): Show |
chr19 | 15635897 | 15667825 |
| a0006c0009t0052 | 0/0 | 5074 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5069): Show |
chr19 | 15635897 | 15667825 |
| a0007c0011t0008 | 0/0 | 5068 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5063): Show |
chr19 | 15635897 | 15667825 |
| a0008c0013t0001 | 0/0 | 5052 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5047): Show |
chr19 | 15635897 | 15667825 |
| a0009c0022t0001 | 0/0 | 5052 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5047): Show |
chr19 | 15635897 | 15667825 |
| a0010c0020t0001 | 0/0 | 5052 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5047): Show |
chr19 | 15635897 | 15667825 |
| a0011c0016t0042 | 0/0 | 5048 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5043): Show |
chr19 | 15635897 | 15667825 |
| a0012c0015t0004 | 0/0 | 5051 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5046): Show |
chr19 | 15635897 | 15667825 |
| a0013c0023t0006 | 0/0 | 5059 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5054): Show |
chr19 | 15635897 | 15667825 |
| a0014c0014t0050 | 0/0 | 5069 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5064): Show |
chr19 | 15635897 | 15667825 |
| a0015c0019t0001 | 0/0 | 5052 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5047): Show |
chr19 | 15635897 | 15667825 |
| a0016c0017t0035 | 0/0 | 5054 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | AGAAG others(5049): Show |
chr19 | 15635897 | 15667825 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0006g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0006g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0006g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0006g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0006g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0006g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0006g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0006g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0006g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0006g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0006g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0006g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0006g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0008g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0008g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0008g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0008g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0008g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0008g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0008g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0009g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0009g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0009g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0009g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0009g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0009g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0009g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0009g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0010g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0010g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0010g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0010g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0010g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0010g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0012g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0012g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0012g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0012g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0012g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0013g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0013g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0013g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0013g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0014g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0014g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0014g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0014g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0015g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0015g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0015g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0015g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0016g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0016g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0016g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0016g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0018g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0018g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0018g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0018g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0019g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0019g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0019g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0020g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0020g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0020g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0022g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0022g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0024g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0024g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0025g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0025g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0026g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0026g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0027g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0027g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0029g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0029g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0034g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0039g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0043g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0045g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0046g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0047g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0048g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0049g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0053g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0054g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0055g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0056g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0057g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0058g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0059g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0061g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0076g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0077g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0078g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0079g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0081g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0082g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0001t0083g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0371 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0382 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0383 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0384 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0387 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0001g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0017g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0017g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0017g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0017g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0023g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0023g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0031g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0031g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0032g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0032g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0044g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0065g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0066g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0067g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0068g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0069g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0002t0070g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0005g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0005g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0005g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0005g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0005g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0005g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0005g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0007g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0007g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0007g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0007g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0007g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0007g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0007g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0007g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0007g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0011g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0011g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0011g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0011g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0011g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0036g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0037g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0038g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0040g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0041g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0071g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0073g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0074g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0004t0080g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0005t0004g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0005t0004g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0005t0004g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0005t0004g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0005t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0005t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0005t0004g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0005t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0005t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0005t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0005t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0005t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0005t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0005t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0005t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0005t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0005t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0005t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0005t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0005t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0005t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0005t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0005t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0005t0033g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0005t0033g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0005t0072g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0005t0075g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0010t0021g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0010t0021g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0018t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0001c0021t0001g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0010g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0028g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0028g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0030g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0060g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0062g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0063g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0003t0064g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0007t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0007t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0007t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0002c0007t0006g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0003c0006t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0003c0006t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0003c0006t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0003c0006t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0003c0006t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0004c0008t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0004c0008t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0004c0008t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0004c0008t0030g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0005c0012t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0005c0012t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0006c0009t0051g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0006c0009t0052g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0007c0011t0008g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0007c0011t0008g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0008c0013t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0009c0022t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0010c0020t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0011c0016t0042g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0012c0015t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0013c0023t0006g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0014c0014t0050g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0015c0019t0001g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| a0016c0017t0035g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0241 | EUR | GBR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0026 | EUR | GBR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0343 | EUR | GBR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0357 | EUR | GBR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00280 | hp1 | a0002 | c0003 | t0003 | g0097 | EUR | FIN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0340 | EUR | FIN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0330 | EUR | FIN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00323 | hp2 | a0002 | c0003 | t0010 | g0118 | EUR | FIN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00408 | hp2 | a0002 | c0003 | t0003 | g0103 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00438 | hp2 | a0002 | c0003 | t0003 | g0133 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00558 | hp1 | a0008 | c0013 | t0001 | g0310 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00558 | hp2 | a0001 | c0004 | t0038 | g0068 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00597 | hp1 | a0001 | c0004 | t0005 | g0080 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00597 | hp2 | a0005 | c0012 | t0002 | g0272 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00609 | hp1 | a0002 | c0007 | t0001 | g0129 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0319 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00621 | hp1 | a0002 | c0007 | t0001 | g0128 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00621 | hp2 | a0001 | c0001 | t0039 | g0227 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00639 | hp1 | a0001 | c0005 | t0004 | g0055 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0352 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0026 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00642 | hp2 | a0001 | c0005 | t0004 | g0008 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00673 | hp1 | a0001 | c0001 | t0006 | g0302 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00673 | hp2 | a0002 | c0007 | t0006 | g0131 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00733 | hp1 | a0002 | c0003 | t0003 | g0126 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0332 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00735 | hp2 | a0001 | c0004 | t0005 | g0089 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0338 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG00741 | hp2 | a0001 | c0005 | t0004 | g0007 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01069 | hp2 | a0009 | c0022 | t0001 | g0027 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01070 | hp1 | a0001 | c0005 | t0004 | g0044 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01070 | hp2 | a0001 | c0005 | t0004 | g0006 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01071 | hp2 | a0001 | c0005 | t0004 | g0006 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0362 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01074 | hp2 | a0002 | c0003 | t0003 | g0139 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01081 | hp1 | a0001 | c0001 | t0015 | g0179 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0375 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01099 | hp2 | a0001 | c0005 | t0004 | g0048 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0342 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01109 | hp2 | a0001 | c0001 | t0018 | g0195 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01167 | hp1 | a0010 | c0020 | t0001 | g0096 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01168 | hp1 | a0002 | c0003 | t0003 | g0017 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01168 | hp2 | a0001 | c0001 | t0008 | g0202 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01169 | hp1 | a0002 | c0003 | t0003 | g0017 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01169 | hp2 | a0001 | c0001 | t0014 | g0004 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0359 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01175 | hp2 | a0001 | c0004 | t0007 | g0069 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0374 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01192 | hp2 | a0001 | c0005 | t0004 | g0045 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01243 | hp1 | a0001 | c0004 | t0005 | g0012 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01243 | hp2 | a0001 | c0002 | t0032 | g0385 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01255 | hp2 | a0001 | c0001 | t0008 | g0207 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0291 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01256 | hp2 | a0001 | c0004 | t0041 | g0011 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0168 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01257 | hp2 | a0001 | c0001 | t0008 | g0019 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01258 | hp1 | a0001 | c0001 | t0010 | g0019 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01258 | hp2 | a0001 | c0004 | t0005 | g0011 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0250 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0377 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0367 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01346 | hp2 | a0002 | c0003 | t0003 | g0142 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01358 | hp1 | a0001 | c0001 | t0010 | g0180 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0245 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01361 | hp1 | a0002 | c0003 | t0003 | g0099 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01361 | hp2 | a0001 | c0010 | t0021 | g0146 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0388 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01496 | hp2 | a0002 | c0003 | t0003 | g0101 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01515 | hp1 | a0001 | c0005 | t0004 | g0007 | EUR | IBS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0335 | EUR | IBS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01516 | hp1 | a0011 | c0016 | t0042 | g0071 | EUR | IBS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0024 | EUR | IBS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0024 | EUR | IBS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01517 | hp2 | a0001 | c0005 | t0004 | g0008 | EUR | IBS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01891 | hp1 | a0006 | c0009 | t0051 | g0304 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01891 | hp2 | a0002 | c0003 | t0060 | g0003 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01928 | hp1 | a0001 | c0005 | t0004 | g0047 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01928 | hp2 | a0001 | c0001 | t0006 | g0022 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0271 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01943 | hp2 | a0001 | c0001 | t0006 | g0004 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0285 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01952 | hp2 | a0001 | c0001 | t0006 | g0247 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0295 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01975 | hp2 | a0002 | c0003 | t0003 | g0125 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01978 | hp1 | a0012 | c0015 | t0004 | g0040 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0373 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0341 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01981 | hp2 | a0013 | c0023 | t0006 | g0022 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0246 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02004 | hp2 | a0001 | c0001 | t0008 | g0186 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02015 | hp2 | a0001 | c0001 | t0079 | g0169 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02040 | hp1 | a0001 | c0004 | t0005 | g0070 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02040 | hp2 | a0002 | c0003 | t0003 | g0107 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02055 | hp1 | a0001 | c0001 | t0082 | g0092 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02055 | hp2 | a0001 | c0001 | t0045 | g0211 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02074 | hp2 | a0001 | c0001 | t0006 | g0236 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02080 | hp2 | a0001 | c0004 | t0005 | g0081 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02083 | hp2 | a0001 | c0001 | t0024 | g0263 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02132 | hp2 | a0002 | c0003 | t0003 | g0003 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02135 | hp1 | a0004 | c0008 | t0003 | g0002 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02145 | hp1 | a0001 | c0001 | t0012 | g0159 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02145 | hp2 | a0002 | c0003 | t0003 | g0143 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02155 | hp1 | a0001 | c0001 | t0057 | g0237 | EAS | CDX | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | CDX | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | CDX | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | CDX | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02257 | hp1 | a0001 | c0001 | t0061 | g0095 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02257 | hp2 | a0001 | c0001 | t0053 | g0201 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0386 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02258 | hp2 | a0007 | c0011 | t0008 | g0185 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0376 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02273 | hp2 | a0001 | c0004 | t0037 | g0083 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02280 | hp1 | a0006 | c0009 | t0052 | g0305 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02280 | hp2 | a0001 | c0001 | t0010 | g0204 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0276 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0356 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0379 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02451 | hp1 | a0001 | c0001 | t0081 | g0093 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02451 | hp2 | a0001 | c0002 | t0017 | g0324 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02572 | hp1 | a0001 | c0002 | t0023 | g0318 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0199 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02602 | hp1 | a0001 | c0005 | t0075 | g0039 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0274 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02615 | hp1 | a0001 | c0004 | t0005 | g0059 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02615 | hp2 | a0001 | c0002 | t0017 | g0325 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0381 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02622 | hp2 | a0001 | c0002 | t0031 | g0321 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02630 | hp1 | a0001 | c0004 | t0074 | g0052 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02630 | hp2 | a0001 | c0001 | t0029 | g0155 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02647 | hp1 | a0001 | c0001 | t0012 | g0184 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02647 | hp2 | a0001 | c0001 | t0083 | g0196 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02683 | hp1 | a0001 | c0004 | t0005 | g0075 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02683 | hp2 | a0001 | c0001 | t0025 | g0197 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02698 | hp1 | a0002 | c0003 | t0002 | g0127 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02698 | hp2 | a0001 | c0001 | t0048 | g0206 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02717 | hp1 | a0001 | c0001 | t0077 | g0161 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02717 | hp2 | a0002 | c0003 | t0003 | g0132 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02723 | hp1 | a0001 | c0001 | t0009 | g0176 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02723 | hp2 | a0001 | c0001 | t0029 | g0094 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02735 | hp1 | a0015 | c0019 | t0001 | g0380 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0365 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0382 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0358 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02809 | hp1 | a0001 | c0001 | t0034 | g0018 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02809 | hp2 | a0001 | c0001 | t0054 | g0187 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02818 | hp1 | a0001 | c0005 | t0004 | g0031 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02818 | hp2 | a0001 | c0001 | t0009 | g0148 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02886 | hp1 | a0001 | c0001 | t0019 | g0177 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02886 | hp2 | a0001 | c0005 | t0004 | g0046 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02895 | hp1 | a0002 | c0003 | t0003 | g0119 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02895 | hp2 | a0001 | c0002 | t0068 | g0326 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02896 | hp1 | a0001 | c0001 | t0034 | g0018 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0023 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02897 | hp1 | a0002 | c0003 | t0003 | g0116 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0023 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02922 | hp1 | a0001 | c0001 | t0020 | g0200 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02922 | hp2 | a0001 | c0002 | t0067 | g0322 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02965 | hp1 | a0001 | c0004 | t0071 | g0053 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02965 | hp2 | a0001 | c0021 | t0001 | g0378 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02970 | hp1 | a0001 | c0010 | t0021 | g0145 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0178 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0173 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02976 | hp2 | a0001 | c0001 | t0019 | g0210 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0351 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03017 | hp2 | a0002 | c0003 | t0003 | g0136 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03041 | hp1 | a0001 | c0001 | t0055 | g0270 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03041 | hp2 | a0001 | c0001 | t0016 | g0166 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03098 | hp1 | a0001 | c0001 | t0009 | g0175 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03098 | hp2 | a0001 | c0002 | t0070 | g0372 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03130 | hp1 | a0001 | c0002 | t0044 | g0028 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03130 | hp2 | a0001 | c0004 | t0073 | g0054 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03139 | hp1 | a0007 | c0011 | t0008 | g0192 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03139 | hp2 | a0001 | c0001 | t0010 | g0165 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03195 | hp1 | a0001 | c0001 | t0013 | g0153 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03195 | hp2 | a0001 | c0001 | t0013 | g0154 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03209 | hp1 | a0002 | c0003 | t0003 | g0141 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03209 | hp2 | a0001 | c0002 | t0031 | g0323 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03225 | hp1 | a0001 | c0001 | t0020 | g0160 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03225 | hp2 | a0001 | c0002 | t0023 | g0028 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0364 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03453 | hp1 | a0001 | c0001 | t0016 | g0183 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03453 | hp2 | a0001 | c0001 | t0076 | g0389 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03486 | hp1 | a0001 | c0004 | t0007 | g0061 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0182 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03490 | hp1 | a0001 | c0005 | t0004 | g0009 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03490 | hp2 | a0001 | c0004 | t0040 | g0065 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03492 | hp1 | a0001 | c0005 | t0004 | g0009 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03492 | hp2 | a0001 | c0002 | t0066 | g0353 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03516 | hp1 | a0002 | c0003 | t0003 | g0140 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03516 | hp2 | a0001 | c0001 | t0043 | g0091 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03540 | hp1 | a0001 | c0001 | t0013 | g0152 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0327 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03579 | hp1 | a0001 | c0001 | t0012 | g0157 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03579 | hp2 | a0001 | c0001 | t0020 | g0189 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0346 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03654 | hp2 | a0001 | c0005 | t0004 | g0056 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03669 | hp1 | a0001 | c0004 | t0007 | g0088 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03669 | hp2 | a0001 | c0002 | t0032 | g0029 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0280 | SAS | STU | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0348 | SAS | STU | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03704 | hp1 | a0001 | c0004 | t0005 | g0090 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0360 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03710 | hp1 | a0001 | c0004 | t0005 | g0087 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0334 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03831 | hp1 | a0002 | c0003 | t0003 | g0106 | SAS | BEB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03831 | hp2 | a0001 | c0004 | t0011 | g0074 | SAS | BEB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03834 | hp1 | a0001 | c0004 | t0011 | g0084 | SAS | BEB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03834 | hp2 | a0001 | c0004 | t0011 | g0012 | SAS | BEB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0361 | SAS | BEB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03927 | hp2 | a0001 | c0005 | t0004 | g0032 | SAS | BEB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03942 | hp1 | a0001 | c0001 | t0010 | g0181 | SAS | BEB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03942 | hp2 | a0001 | c0002 | t0065 | g0066 | SAS | BEB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0230 | SAS | STU | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG04115 | hp2 | a0002 | c0003 | t0003 | g0115 | SAS | STU | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0239 | SAS | BEB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0337 | SAS | BEB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0281 | SAS | STU | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG04199 | hp2 | a0002 | c0003 | t0003 | g0015 | SAS | STU | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0387 | SAS | STU | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0368 | SAS | STU | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG04228 | hp1 | a0001 | c0001 | t0015 | g0198 | SAS | STU | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0339 | SAS | STU | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0174 | AFR | YRI | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18522 | hp2 | a0001 | c0001 | t0009 | g0150 | AFR | YRI | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | CHB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0366 | EAS | CHB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | CHB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | CHB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18906 | hp1 | a0001 | c0001 | t0018 | g0306 | AFR | YRI | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18906 | hp2 | a0001 | c0001 | t0016 | g0188 | AFR | YRI | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18939 | hp1 | a0001 | c0001 | t0056 | g0294 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18939 | hp2 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0333 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18940 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18941 | hp1 | a0001 | c0001 | t0024 | g0225 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0363 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0350 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18945 | hp1 | a0001 | c0005 | t0004 | g0030 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18946 | hp1 | a0001 | c0001 | t0006 | g0218 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18946 | hp2 | a0001 | c0001 | t0006 | g0283 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18947 | hp1 | a0003 | c0006 | t0001 | g0314 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18947 | hp2 | a0001 | c0001 | t0047 | g0298 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18948 | hp2 | a0002 | c0003 | t0003 | g0100 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18951 | hp1 | a0002 | c0003 | t0028 | g0003 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18953 | hp1 | a0001 | c0005 | t0072 | g0043 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18954 | hp2 | a0002 | c0003 | t0030 | g0102 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18957 | hp1 | a0002 | c0003 | t0003 | g0013 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18957 | hp2 | a0001 | c0001 | t0027 | g0292 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18959 | hp2 | a0001 | c0004 | t0007 | g0076 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18960 | hp1 | a0001 | c0005 | t0004 | g0038 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18960 | hp2 | a0001 | c0004 | t0011 | g0082 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18961 | hp1 | a0002 | c0003 | t0003 | g0112 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18962 | hp2 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18963 | hp1 | a0002 | c0003 | t0003 | g0013 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0370 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18965 | hp1 | a0001 | c0005 | t0004 | g0041 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18965 | hp2 | a0003 | c0006 | t0001 | g0316 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18966 | hp2 | a0001 | c0005 | t0033 | g0049 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18968 | hp1 | a0002 | c0003 | t0063 | g0014 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18968 | hp2 | a0001 | c0005 | t0004 | g0033 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18969 | hp1 | a0002 | c0003 | t0003 | g0111 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18969 | hp2 | a0001 | c0001 | t0014 | g0217 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18971 | hp2 | a0001 | c0004 | t0007 | g0073 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18972 | hp1 | a0001 | c0005 | t0004 | g0051 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18972 | hp2 | a0002 | c0007 | t0001 | g0130 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18973 | hp1 | a0002 | c0003 | t0062 | g0014 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18973 | hp2 | a0001 | c0001 | t0026 | g0277 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18978 | hp1 | a0002 | c0003 | t0003 | g0120 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18978 | hp2 | a0001 | c0005 | t0004 | g0036 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18979 | hp1 | a0001 | c0001 | t0006 | g0021 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18979 | hp2 | a0002 | c0003 | t0003 | g0108 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18981 | hp2 | a0004 | c0008 | t0030 | g0144 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0369 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18983 | hp2 | a0002 | c0003 | t0003 | g0110 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18985 | hp1 | a0001 | c0004 | t0036 | g0063 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18986 | hp1 | a0002 | c0003 | t0003 | g0104 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18986 | hp2 | a0001 | c0004 | t0005 | g0064 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18987 | hp1 | a0002 | c0003 | t0064 | g0122 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18987 | hp2 | a0001 | c0004 | t0005 | g0078 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18989 | hp1 | a0001 | c0004 | t0007 | g0077 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18990 | hp1 | a0002 | c0003 | t0003 | g0124 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18990 | hp2 | a0005 | c0012 | t0002 | g0266 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18992 | hp1 | a0001 | c0018 | t0001 | g0355 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18992 | hp2 | a0001 | c0004 | t0007 | g0072 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18994 | hp1 | a0001 | c0005 | t0004 | g0050 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18994 | hp2 | a0001 | c0001 | t0078 | g0282 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18998 | hp1 | a0002 | c0003 | t0003 | g0117 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0345 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18999 | hp1 | a0001 | c0001 | t0014 | g0216 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18999 | hp2 | a0001 | c0001 | t0014 | g0354 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19000 | hp1 | a0001 | c0004 | t0011 | g0086 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19000 | hp2 | a0002 | c0003 | t0003 | g0109 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19001 | hp1 | a0001 | c0001 | t0006 | g0267 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19001 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19002 | hp1 | a0001 | c0005 | t0004 | g0035 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19002 | hp2 | a0001 | c0004 | t0007 | g0010 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19004 | hp1 | a0003 | c0006 | t0001 | g0315 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19005 | hp1 | a0001 | c0004 | t0005 | g0067 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19005 | hp2 | a0003 | c0006 | t0001 | g0312 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19007 | hp1 | a0002 | c0003 | t0003 | g0135 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19009 | hp1 | a0001 | c0001 | t0022 | g0209 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19010 | hp1 | a0001 | c0004 | t0005 | g0085 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19010 | hp2 | a0001 | c0001 | t0025 | g0269 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19011 | hp1 | a0001 | c0001 | t0006 | g0214 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19011 | hp2 | a0001 | c0001 | t0058 | g0289 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19012 | hp1 | a0002 | c0003 | t0003 | g0121 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19012 | hp2 | a0001 | c0001 | t0006 | g0219 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19030 | hp1 | a0001 | c0001 | t0013 | g0151 | AFR | LWK | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19030 | hp2 | a0001 | c0004 | t0007 | g0058 | AFR | LWK | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19043 | hp1 | a0001 | c0001 | t0015 | g0212 | AFR | LWK | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19043 | hp2 | a0001 | c0001 | t0019 | g0307 | AFR | LWK | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19055 | hp1 | a0001 | c0001 | t0059 | g0255 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19056 | hp1 | a0002 | c0003 | t0003 | g0134 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19056 | hp2 | a0002 | c0003 | t0003 | g0123 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0317 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19057 | hp2 | a0001 | c0004 | t0005 | g0079 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19058 | hp1 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19060 | hp1 | a0001 | c0002 | t0069 | g0328 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19063 | hp1 | a0001 | c0001 | t0049 | g0297 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19063 | hp2 | a0001 | c0001 | t0027 | g0238 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19065 | hp1 | a0002 | c0003 | t0003 | g0015 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19066 | hp1 | a0001 | c0004 | t0007 | g0171 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19068 | hp1 | a0001 | c0001 | t0022 | g0194 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0329 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19070 | hp1 | a0001 | c0005 | t0004 | g0042 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19070 | hp2 | a0001 | c0001 | t0006 | g0235 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0344 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19080 | hp1 | a0001 | c0001 | t0012 | g0205 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19081 | hp1 | a0001 | c0001 | t0006 | g0278 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0347 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19083 | hp1 | a0004 | c0008 | t0003 | g0137 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19084 | hp1 | a0001 | c0005 | t0004 | g0034 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19084 | hp2 | a0002 | c0003 | t0003 | g0016 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19085 | hp1 | a0002 | c0003 | t0003 | g0016 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19087 | hp2 | a0001 | c0001 | t0026 | g0287 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19088 | hp1 | a0003 | c0006 | t0001 | g0313 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19090 | hp1 | a0001 | c0004 | t0007 | g0010 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19090 | hp2 | a0001 | c0001 | t0046 | g0021 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19091 | hp1 | a0002 | c0003 | t0003 | g0114 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA19091 | hp2 | a0004 | c0008 | t0003 | g0138 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA20129 | hp1 | a0001 | c0001 | t0008 | g0193 | AFR | ASW | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA20129 | hp2 | a0016 | c0017 | t0035 | g0057 | AFR | ASW | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA20752 | hp1 | a0002 | c0003 | t0001 | g0105 | EUR | TSI | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0383 | EUR | TSI | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0336 | SAS | GIH | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA20905 | hp2 | a0002 | c0003 | t0003 | g0098 | SAS | GIH | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01123 | hp1 | a0001 | c0002 | t0017 | g0331 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG01123 | hp2 | a0001 | c0002 | t0017 | g0320 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02109 | hp1 | a0001 | c0001 | t0018 | g0190 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02109 | hp2 | a0001 | c0001 | t0008 | g0208 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02486 | hp1 | a0001 | c0004 | t0005 | g0060 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02486 | hp2 | a0001 | c0001 | t0018 | g0203 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02559 | hp1 | a0001 | c0001 | t0016 | g0158 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG02559 | hp2 | a0014 | c0014 | t0050 | g0191 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03471 | hp1 | a0001 | c0001 | t0012 | g0156 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG03471 | hp2 | a0001 | c0001 | t0009 | g0149 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0147 | AFR | USA | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| HG06807 | hp2 | a0002 | c0003 | t0028 | g0113 | AFR | USA | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0349 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA18955 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA20300 | hp1 | a0001 | c0001 | t0009 | g0172 | AFR | USA | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA20300 | hp2 | a0001 | c0001 | t0015 | g0213 | AFR | USA | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA21309 | hp1 | a0001 | c0005 | t0033 | g0037 | AFR | LWK | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| NA21309 | hp2 | a0001 | c0004 | t0080 | g0062 | AFR | LWK | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0371 | REF | REF | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0384 | REF | REF | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:15641444 | G | A | 1 | a0008 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.29G>A | p.Gly10Asp | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/13 | 79/5053 | 29/1563 | 10/520 | chr19 | 15641444 | |||
| chr19:15641555 | G | A | 1 | a0014 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.140G>A | p.Arg47His | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/13 | 190/5053 | 140/1563 | 47/520 | chr19 | 15641555 | |||
| chr19:15645729 | C | T | 1 | a0004 | 4 | HG02135.hp1 NA18981.hp2 NA19083.hp1 others(1): Show |
missense_variant | MODERATE | c.209C>T | p.Ser70Leu | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/13 | 259/5053 | 209/1563 | 70/520 | chr19 | 15645729 | |||
| chr19:15645786 | G | A | 1 | a0006 | 2 | HG01891.hp1 HG02280.hp1 |
missense_variant | MODERATE | c.266G>A | p.Cys89Tyr | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/13 | 316/5053 | 266/1563 | 89/520 | chr19 | 15645786 | |||
| chr19:15645818 | C | T | 1 | a0013 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.298C>T | p.Arg100Cys | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/13 | 348/5053 | 298/1563 | 100/520 | chr19 | 15645818 | |||
| chr19:15649236 | A | G | 1 | a0005 | 2 | HG00597.hp2 NA18990.hp2 |
missense_variant | MODERATE | c.602A>G | p.Asp201Gly | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 6/13 | 652/5053 | 602/1563 | 201/520 | chr19 | 15649236 | |||
| chr19:15650071 | C | A | 2 | a0002 a0004 |
68 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
missense_variant | MODERATE | c.806C>A | p.Ala269Asp | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/13 | 856/5053 | 806/1563 | 269/520 | chr19 | 15650071 | |||
| chr19:15650073 | G | A | 1 | a0011 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.808G>A | p.Val270Ile | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/13 | 858/5053 | 808/1563 | 270/520 | chr19 | 15650073 | |||
| chr19:15650092 | G | A | 1 | a0016 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.827G>A | p.Arg276His | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/13 | 877/5053 | 827/1563 | 276/520 | chr19 | 15650092 | |||
| chr19:15650164 | A | T | 1 | a0009 | 1 | HG01069.hp2 | missense_variant | MODERATE | c.899A>T | p.Asp300Val | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/13 | 949/5053 | 899/1563 | 300/520 | chr19 | 15650164 | |||
| chr19:15658340 | G | A | 1 | a0007 | 2 | HG02258.hp2 HG03139.hp1 |
missense_variant | MODERATE | c.1192G>A | p.Val398Ile | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 10/13 | 1242/5053 | 1192/1563 | 398/520 | chr19 | 15658340 | |||
| chr19:15658376 | G | A | 1 | a0015 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.1228G>A | p.Asp410Asn | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 10/13 | 1278/5053 | 1228/1563 | 410/520 | chr19 | 15658376 | |||
| chr19:15659242 | G | A | 1 | a0003 | 5 | NA18947.hp1 NA18965.hp2 NA19004.hp1 others(2): Show |
missense_variant | MODERATE | c.1420G>A | p.Ala474Thr | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1470/5053 | 1420/1563 | 474/520 | chr19 | 15659242 | |||
| chr19:15659249 | C | A | 1 | a0010 | 1 | HG01167.hp1 | missense_variant | MODERATE | c.1427C>A | p.Ala476Glu | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1477/5053 | 1427/1563 | 476/520 | chr19 | 15659249 | |||
| chr19:15659270 | G | C | 1 | a0014 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.1448G>C | p.Gly483Ala | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1498/5053 | 1448/1563 | 483/520 | chr19 | 15659270 | |||
| chr19:15659341 | C | G | 1 | a0012 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.1519C>G | p.Arg507Gly | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1569/5053 | 1519/1563 | 507/520 | chr19 | 15659341 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:15649243 | G | A | 2 | a0001c0005 a0012c0015 |
32 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(29): Show |
synonymous_variant | LOW | c.609G>A | p.Leu203Leu | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 6/13 | 659/5053 | 609/1563 | 203/520 | chr19 | 15649243 | |||
| chr19:15652881 | G | A | 6 | a0001c0004 a0001c0005 a0001c0010 others(3): Show |
77 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(74): Show |
synonymous_variant | LOW | c.1044G>A | p.Pro348Pro | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/13 | 1094/5053 | 1044/1563 | 348/520 | chr19 | 15652881 | |||
| chr19:15652911 | G | A | 8 | a0001c0001 a0002c0003 a0004c0008 others(5): Show |
246 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(243): Show |
synonymous_variant | LOW | c.1074G>A | p.Val358Val | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/13 | 1124/5053 | 1074/1563 | 358/520 | chr19 | 15652911 | |||
| chr19:15652917 | G | A | 1 | a0001c0018 | 1 | NA18992.hp1 | synonymous_variant | LOW | c.1080G>A | p.Glu360Glu | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/13 | 1130/5053 | 1080/1563 | 360/520 | chr19 | 15652917 | |||
| chr19:15658549 | C | T | 1 | a0001c0010 | 2 | HG01361.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.1308C>T | p.Asp436Asp | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 11/13 | 1358/5053 | 1308/1563 | 436/520 | chr19 | 15658549 | |||
| chr19:15659241 | C | T | 1 | a0001c0010 | 2 | HG01361.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.1419C>T | p.Phe473Phe | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1469/5053 | 1419/1563 | 473/520 | chr19 | 15659241 | |||
| chr19:15659250 | G | T | 1 | a0001c0021 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.1428G>T | p.Ala476Ala | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1478/5053 | 1428/1563 | 476/520 | chr19 | 15659250 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:15659443 | G | A | 1 | a0001c0010t0021 | 2 | HG01361.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*58G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 58 | chr19 | 15659443 | ||||||
| chr19:15659546 | G | A | 1 | a0001c0010t0021 | 2 | HG01361.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*161G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 161 | chr19 | 15659546 | ||||||
| chr19:15659561 | A | G | 4 | a0001c0001t0018 a0001c0001t0020 a0001c0001t0034 others(1): Show |
10 | HG01109.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*176A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 176 | chr19 | 15659561 | ||||||
| chr19:15659580 | A | G | 2 | a0001c0001t0081 a0001c0001t0082 |
2 | HG02055.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*195A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 195 | chr19 | 15659580 | ||||||
| chr19:15659625 | T | G | 1 | a0016c0017t0035 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*240T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 240 | chr19 | 15659625 | ||||||
| chr19:15659626 | A | G | 1 | a0001c0004t0080 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*241A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 241 | chr19 | 15659626 | ||||||
| chr19:15659635 | A | G | 1 | a0001c0010t0021 | 2 | HG01361.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*250A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 250 | chr19 | 15659635 | ||||||
| chr19:15659636 | T | C | 1 | a0001c0001t0022 | 2 | NA19009.hp1 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*251T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 251 | chr19 | 15659636 | ||||||
| chr19:15659653 | G | A | 2 | a0001c0001t0029 a0001c0001t0061 |
2 | HG02257.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*268G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 268 | chr19 | 15659653 | ||||||
| chr19:15659665 | A | T | 1 | a0001c0001t0079 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*280A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 280 | chr19 | 15659665 | ||||||
| chr19:15659695 | C | T | 1 | a0001c0010t0021 | 2 | HG01361.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*310C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 310 | chr19 | 15659695 | ||||||
| chr19:15659742 | A | G | 1 | a0001c0001t0078 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*357A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 357 | chr19 | 15659742 | ||||||
| chr19:15659817 | A | G | 1 | a0001c0001t0077 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*432A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 432 | chr19 | 15659817 | ||||||
| chr19:15659880 | G | T | 1 | a0001c0010t0021 | 2 | HG01361.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*495G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 495 | chr19 | 15659880 | ||||||
| chr19:15659890 | C | T | 9 | a0001c0001t0076 a0001c0004t0071 a0001c0004t0073 others(6): Show |
36 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*505C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 505 | chr19 | 15659890 | ||||||
| chr19:15659942 | G | A | 12 | a0001c0001t0039 a0001c0004t0005 a0001c0004t0007 others(9): Show |
41 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*557G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 557 | chr19 | 15659942 | ||||||
| chr19:15659974 | G | A | 70 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(67): Show |
283 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*589G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 589 | chr19 | 15659974 | ||||||
| chr19:15660045 | A | G | 1 | a0001c0010t0021 | 2 | HG01361.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*660A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 660 | chr19 | 15660045 | ||||||
| chr19:15660214 | GT | G | 46 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(43): Show |
178 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*833delT | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 833 | INFO_REALIGN_3_PRIME | chr19 | 15660214 | |||||
| chr19:15660279 | A | G | 1 | a0001c0001t0076 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*894A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 894 | chr19 | 15660279 | ||||||
| chr19:15660323 | T | A | 3 | a0001c0001t0009 a0001c0001t0013 a0001c0001t0043 |
13 | HG02723.hp1 HG02818.hp2 HG02976.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*938T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 938 | chr19 | 15660323 | ||||||
| chr19:15660377 | A | G | 1 | a0001c0010t0021 | 2 | HG01361.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*992A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 992 | chr19 | 15660377 | ||||||
| chr19:15660440 | T | G | 70 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(67): Show |
283 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*1055T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1055 | chr19 | 15660440 | ||||||
| chr19:15660443 | G | C | 70 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(67): Show |
283 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*1058G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1058 | chr19 | 15660443 | ||||||
| chr19:15660447 | T | C | 70 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(67): Show |
283 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*1062T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1062 | chr19 | 15660447 | ||||||
| chr19:15660558 | C | CTG | 82 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(79): Show |
324 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(321): Show |
3_prime_UTR_variant | MODIFIER | c.*1174_*1175dupTG | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1176 | INFO_REALIGN_3_PRIME | chr19 | 15660558 | |||||
| chr19:15660589 | G | A | 2 | a0001c0004t0036 a0001c0004t0071 |
2 | HG02965.hp1 NA18985.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1204G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1204 | chr19 | 15660589 | ||||||
| chr19:15660708 | A | T | 2 | a0001c0001t0027 a0001c0001t0059 |
3 | NA18957.hp2 NA19055.hp1 NA19063.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1323A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1323 | chr19 | 15660708 | ||||||
| chr19:15660719 | A | ACTT | 2 | a0001c0002t0023 a0001c0002t0044 |
3 | HG02572.hp1 HG03130.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1334_*1335insCTT | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1335 | chr19 | 15660719 | ||||||
| chr19:15660719 | A | AT | 11 | a0001c0001t0003 a0001c0001t0029 a0001c0001t0061 others(8): Show |
65 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1349dupT | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1350 | INFO_REALIGN_3_PRIME | chr19 | 15660719 | |||||
| chr19:15660719 | A | ATT | 14 | a0001c0001t0014 a0001c0001t0034 a0001c0001t0048 others(11): Show |
45 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1348_*1349dupTT | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1350 | INFO_REALIGN_3_PRIME | chr19 | 15660719 | |||||
| chr19:15660719 | A | ATTT | 40 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(37): Show |
167 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*1347_*1349dupTTT | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1350 | INFO_REALIGN_3_PRIME | chr19 | 15660719 | |||||
| chr19:15660757 | C | T | 1 | a0002c0003t0062 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1372C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1372 | chr19 | 15660757 | ||||||
| chr19:15660792 | C | T | 83 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(80): Show |
326 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(323): Show |
3_prime_UTR_variant | MODIFIER | c.*1407C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1407 | chr19 | 15660792 | ||||||
| chr19:15660803 | G | A | 1 | a0001c0010t0021 | 2 | HG01361.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1418G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1418 | chr19 | 15660803 | ||||||
| chr19:15660809 | T | G | 1 | a0001c0010t0021 | 2 | HG01361.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1424T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1424 | chr19 | 15660809 | ||||||
| chr19:15660825 | T | A | 70 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(67): Show |
283 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*1440T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1440 | chr19 | 15660825 | ||||||
| chr19:15660839 | C | T | 2 | a0001c0004t0071 a0001c0004t0074 |
2 | HG02630.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1454C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1454 | chr19 | 15660839 | ||||||
| chr19:15660913 | C | T | 2 | a0001c0001t0081 a0001c0001t0082 |
2 | HG02055.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1528C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1528 | chr19 | 15660913 | ||||||
| chr19:15660922 | G | A | 70 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(67): Show |
283 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*1537G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1537 | chr19 | 15660922 | ||||||
| chr19:15660963 | C | T | 70 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(67): Show |
283 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*1578C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1578 | chr19 | 15660963 | ||||||
| chr19:15660975 | C | G | 1 | a0001c0001t0076 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1590C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1590 | chr19 | 15660975 | ||||||
| chr19:15660998 | C | T | 70 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(67): Show |
283 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*1613C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1613 | chr19 | 15660998 | ||||||
| chr19:15660999 | G | T | 12 | a0001c0001t0039 a0001c0004t0005 a0001c0004t0007 others(9): Show |
41 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1614G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1614 | chr19 | 15660999 | ||||||
| chr19:15661001 | T | C | 70 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(67): Show |
283 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*1616T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1616 | chr19 | 15661001 | ||||||
| chr19:15661161 | C | T | 67 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(64): Show |
270 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*1776C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1776 | chr19 | 15661161 | ||||||
| chr19:15661168 | G | A | 79 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(76): Show |
311 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(308): Show |
3_prime_UTR_variant | MODIFIER | c.*1783G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1783 | chr19 | 15661168 | ||||||
| chr19:15661268 | A | AAAAAC | 3 | a0001c0001t0009 a0001c0001t0043 a0001c0002t0069 |
10 | HG02723.hp1 HG02818.hp2 HG02976.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1913_*1917dupCAAA others(1): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1918 | INFO_REALIGN_3_PRIME | chr19 | 15661268 | |||||
| chr19:15661268 | A | AAAAACAA others(3): Show |
1 | a0001c0001t0013 | 4 | HG03195.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1908_*1917dupCAAA others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1918 | INFO_REALIGN_3_PRIME | chr19 | 15661268 | |||||
| chr19:15661268 | AAAAAC | A | 69 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(66): Show |
272 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*1913_*1917delCAAA others(1): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1913 | INFO_REALIGN_3_PRIME | chr19 | 15661268 | |||||
| chr19:15661303 | A | C | 5 | a0001c0001t0009 a0001c0001t0013 a0001c0001t0043 others(2): Show |
16 | HG01361.hp2 HG02723.hp1 HG02818.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1918A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1918 | chr19 | 15661303 | ||||||
| chr19:15661355 | C | A | 4 | a0001c0001t0009 a0001c0001t0013 a0001c0001t0043 others(1): Show |
15 | HG01361.hp2 HG02723.hp1 HG02818.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1970C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1970 | chr19 | 15661355 | ||||||
| chr19:15661356 | G | A | 5 | a0001c0001t0018 a0001c0001t0020 a0001c0001t0034 others(2): Show |
11 | HG01109.hp2 HG02109.hp1 HG02486.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1971G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1971 | chr19 | 15661356 | ||||||
| chr19:15661423 | T | G | 67 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(64): Show |
270 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*2038T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2038 | chr19 | 15661423 | ||||||
| chr19:15661567 | T | A | 57 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(54): Show |
207 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*2182T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2182 | chr19 | 15661567 | ||||||
| chr19:15661604 | G | A | 57 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(54): Show |
207 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*2219G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2219 | chr19 | 15661604 | ||||||
| chr19:15661652 | C | T | 3 | a0001c0004t0071 a0001c0004t0073 a0001c0004t0074 |
3 | HG02630.hp1 HG02965.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2267C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2267 | chr19 | 15661652 | ||||||
| chr19:15661689 | T | A | 56 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(53): Show |
206 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*2304T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2304 | chr19 | 15661689 | ||||||
| chr19:15661711 | T | C | 11 | a0001c0001t0039 a0001c0004t0005 a0001c0004t0007 others(8): Show |
40 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2326T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2326 | chr19 | 15661711 | ||||||
| chr19:15661720 | C | T | 57 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(54): Show |
207 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*2335C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2335 | chr19 | 15661720 | ||||||
| chr19:15661738 | A | G | 57 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(54): Show |
207 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*2353A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2353 | chr19 | 15661738 | ||||||
| chr19:15661754 | T | A | 57 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(54): Show |
207 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*2369T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2369 | chr19 | 15661754 | ||||||
| chr19:15661804 | T | C | 1 | a0014c0014t0050 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2419T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2419 | chr19 | 15661804 | ||||||
| chr19:15661906 | T | C | 11 | a0001c0001t0039 a0001c0004t0005 a0001c0004t0007 others(8): Show |
40 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2521T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2521 | chr19 | 15661906 | ||||||
| chr19:15661907 | A | G | 57 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(54): Show |
207 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*2522A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2522 | chr19 | 15661907 | ||||||
| chr19:15661925 | T | C | 5 | a0001c0001t0009 a0001c0001t0013 a0001c0001t0043 others(2): Show |
16 | HG01361.hp2 HG02723.hp1 HG02818.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2540T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2540 | chr19 | 15661925 | ||||||
| chr19:15661928 | G | A | 55 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(52): Show |
204 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*2543G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2543 | chr19 | 15661928 | ||||||
| chr19:15661971 | T | G | 1 | a0001c0002t0066 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2586T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2586 | chr19 | 15661971 | ||||||
| chr19:15662000 | C | T | 1 | a0002c0003t0064 | 1 | NA18987.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2615C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2615 | chr19 | 15662000 | ||||||
| chr19:15662043 | T | C | 1 | a0001c0004t0038 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2658T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2658 | chr19 | 15662043 | ||||||
| chr19:15662262 | TTC | T | 3 | a0001c0004t0071 a0001c0004t0073 a0001c0005t0072 |
3 | HG02965.hp1 HG03130.hp2 NA18953.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2886_*2887delTC | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | INFO_REALIGN_3_PRIME | chr19 | 15662262 | |||||
| chr19:15662266 | C | G | 54 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(51): Show |
204 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*2881C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2881 | chr19 | 15662266 | ||||||
| chr19:15662268 | C | G | 3 | a0001c0004t0071 a0001c0004t0073 a0001c0005t0072 |
3 | HG02965.hp1 HG03130.hp2 NA18953.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2883C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2883 | chr19 | 15662268 | ||||||
| chr19:15662270 | C | CAAAAA | 2 | a0001c0001t0024 a0001c0001t0059 |
3 | HG02083.hp2 NA18941.hp1 NA19055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(1): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | ||||||
| chr19:15662270 | C | CAAAAAA | 12 | a0001c0001t0002 a0001c0001t0014 a0001c0001t0026 others(9): Show |
88 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(2): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | ||||||
| chr19:15662270 | C | CAAAAAAA | 5 | a0001c0001t0006 a0001c0001t0049 a0001c0001t0058 others(2): Show |
17 | HG00673.hp1 HG00673.hp2 HG01928.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(3): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | ||||||
| chr19:15662270 | C | CAAAAAAA others(1): Show |
3 | a0001c0001t0029 a0001c0001t0046 a0001c0001t0056 |
4 | HG02630.hp2 HG02723.hp2 NA18939.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(4): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | ||||||
| chr19:15662270 | C | CAAAAAAA others(3): Show |
3 | a0001c0001t0055 a0001c0001t0082 a0001c0002t0023 |
4 | HG02055.hp1 HG02572.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | ||||||
| chr19:15662270 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0081 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(7): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | ||||||
| chr19:15662270 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0016 | 4 | HG02559.hp1 HG03041.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | ||||||
| chr19:15662270 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0012 | 5 | HG02145.hp1 HG02647.hp1 HG03471.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(11): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | ||||||
| chr19:15662270 | C | CAAAAAAA others(9): Show |
5 | a0001c0001t0008 a0001c0001t0022 a0001c0001t0048 others(2): Show |
13 | HG01168.hp2 HG01255.hp2 HG01257.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | ||||||
| chr19:15662270 | C | CAAAAAAA others(10): Show |
6 | a0001c0001t0010 a0001c0001t0020 a0001c0001t0034 others(3): Show |
14 | HG00323.hp2 HG01258.hp1 HG01358.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(13): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | ||||||
| chr19:15662270 | C | CAAAAAAA others(11): Show |
2 | a0001c0001t0018 a0001c0001t0019 |
7 | HG01109.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(14): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | ||||||
| chr19:15662270 | C | CAAAAAAA others(12): Show |
2 | a0001c0001t0015 a0001c0001t0045 |
5 | HG01081.hp1 HG02055.hp2 HG04228.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(15): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | ||||||
| chr19:15662270 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0053 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(17): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | ||||||
| chr19:15662270 | C | CAAAAAAA others(15): Show |
1 | a0006c0009t0052 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(18): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | ||||||
| chr19:15662270 | C | CAAAAAAA others(16): Show |
1 | a0006c0009t0051 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(19): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | ||||||
| chr19:15662270 | CT | C | 4 | a0001c0004t0074 a0001c0005t0004 a0001c0005t0075 others(1): Show |
30 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2886delT | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | ||||||
| chr19:15662271 | T | A | 49 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(46): Show |
173 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*2886T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662271 | ||||||
| chr19:15662272 | C | A | 53 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(50): Show |
203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
3_prime_UTR_variant | MODIFIER | c.*2887C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2887 | chr19 | 15662272 | ||||||
| chr19:15662272 | C | CAAAAA | 3 | a0001c0001t0009 a0001c0001t0013 a0001c0010t0021 |
14 | HG01361.hp2 HG02723.hp1 HG02818.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2903_*2907dupAAAA others(1): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2908 | INFO_REALIGN_3_PRIME | chr19 | 15662272 | |||||
| chr19:15662272 | C | CAAAAAAA others(4): Show |
1 | a0001c0004t0041 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2897_*2907dupAAAA others(7): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2908 | INFO_REALIGN_3_PRIME | chr19 | 15662272 | |||||
| chr19:15662272 | C | CAAAAAAA others(5): Show |
4 | a0001c0004t0005 a0001c0004t0037 a0001c0004t0038 others(1): Show |
19 | HG00558.hp2 HG00597.hp1 HG00735.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2896_*2907dupAAAA others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2908 | INFO_REALIGN_3_PRIME | chr19 | 15662272 | |||||
| chr19:15662272 | C | CAAAAAAA others(6): Show |
2 | a0001c0004t0007 a0001c0004t0080 |
12 | HG01175.hp2 HG03486.hp1 HG03669.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2895_*2907dupAAAA others(9): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2908 | INFO_REALIGN_3_PRIME | chr19 | 15662272 | |||||
| chr19:15662272 | C | CAAAAAAA others(7): Show |
2 | a0001c0004t0011 a0001c0004t0036 |
6 | HG03831.hp2 HG03834.hp1 HG03834.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2894_*2907dupAAAA others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2908 | INFO_REALIGN_3_PRIME | chr19 | 15662272 | |||||
| chr19:15662272 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0039 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2893_*2907dupAAAA others(11): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2908 | INFO_REALIGN_3_PRIME | chr19 | 15662272 | |||||
| chr19:15662272 | C | CAAAAAAA others(15): Show |
2 | a0001c0002t0068 a0001c0002t0070 |
2 | HG02895.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2907_*2908insAAAA others(18): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2908 | INFO_REALIGN_3_PRIME | chr19 | 15662272 | |||||
| chr19:15662272 | C | CAAAAAAA others(16): Show |
1 | a0001c0002t0017 | 4 | HG01123.hp1 HG01123.hp2 HG02451.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2907_*2908insAAAA others(19): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2908 | INFO_REALIGN_3_PRIME | chr19 | 15662272 | |||||
| chr19:15662272 | C | CAAAAAAA others(17): Show |
1 | a0001c0002t0031 | 2 | HG02622.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2907_*2908insAAAA others(20): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2908 | INFO_REALIGN_3_PRIME | chr19 | 15662272 | |||||
| chr19:15662272 | C | CAAAAAAA others(19): Show |
1 | a0001c0002t0067 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2907_*2908insAAAA others(22): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2908 | INFO_REALIGN_3_PRIME | chr19 | 15662272 | |||||
| chr19:15662272 | CAA | C | 7 | a0001c0001t0003 a0002c0003t0003 a0002c0003t0028 others(4): Show |
60 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*2906_*2907delAA | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2906 | INFO_REALIGN_3_PRIME | chr19 | 15662272 | |||||
| chr19:15662354 | A | G | 1 | a0001c0001t0057 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2969A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2969 | chr19 | 15662354 | ||||||
| chr19:15662451 | TTATAGTA | T | 10 | a0001c0001t0039 a0001c0004t0005 a0001c0004t0007 others(7): Show |
39 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*3070_*3076delAGTA others(3): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 3070 | INFO_REALIGN_3_PRIME | chr19 | 15662451 | |||||
| chr19:15662494 | A | AT | 67 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(64): Show |
246 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(243): Show |
3_prime_UTR_variant | MODIFIER | c.*3115dupT | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 3116 | INFO_REALIGN_3_PRIME | chr19 | 15662494 | |||||
| chr19:15662529 | C | T | 58 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(55): Show |
208 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(205): Show |
3_prime_UTR_variant | MODIFIER | c.*3144C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 3144 | chr19 | 15662529 | ||||||
| chr19:15662559 | G | T | 9 | a0001c0001t0003 a0002c0003t0003 a0002c0003t0028 others(6): Show |
62 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*3174G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 3174 | chr19 | 15662559 | ||||||
| chr19:15662560 | T | C | 1 | a0016c0017t0035 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3175T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 3175 | chr19 | 15662560 | ||||||
| chr19:15662617 | A | G | 5 | a0001c0001t0009 a0001c0001t0013 a0001c0001t0043 others(2): Show |
16 | HG01361.hp2 HG02723.hp1 HG02818.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3232A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 3232 | chr19 | 15662617 | ||||||
| chr19:15662627 | C | A | 1 | a0001c0001t0054 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3242C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 3242 | chr19 | 15662627 | ||||||
| chr19:15662661 | A | G | 2 | a0001c0001t0081 a0001c0001t0082 |
2 | HG02055.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3276A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 3276 | chr19 | 15662661 | ||||||
| chr19:15662722 | T | C | 10 | a0001c0001t0039 a0001c0004t0005 a0001c0004t0007 others(7): Show |
39 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*3337T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 3337 | chr19 | 15662722 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:15640956 | G | T | 1 | a0001c0001t0076g0389 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-2+11G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 1/12 | chr19 | 15640956 | |||||||
| chr19:15641087 | T | G | 137 | a0001c0001t0029g0094 a0001c0001t0043g0091 a0001c0001t0061g0095 others(134): Show |
150 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.-2+142T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 1/12 | chr19 | 15641087 | |||||||
| chr19:15641213 | G | A | 72 | a0001c0002t0065g0066 a0001c0004t0005g0011 a0001c0004t0005g0012 others(69): Show |
77 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.-1-202G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 1/12 | chr19 | 15641213 | |||||||
| chr19:15641327 | C | T | 70 | a0001c0002t0065g0066 a0001c0004t0005g0011 a0001c0004t0005g0012 others(67): Show |
75 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.-1-88C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 1/12 | chr19 | 15641327 | |||||||
| chr19:15641687 | G | A | 1 | a0001c0002t0001g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.198+74G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15641687 | |||||||
| chr19:15641840 | C | G | 38 | a0001c0002t0065g0066 a0001c0004t0005g0011 a0001c0004t0005g0012 others(35): Show |
39 | HG00558.hp2 HG00597.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.198+227C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15641840 | |||||||
| chr19:15641871 | G | T | 60 | a0002c0003t0001g0105 a0002c0003t0002g0127 a0002c0003t0003g0001 others(57): Show |
68 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.198+258G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15641871 | |||||||
| chr19:15641964 | T | C | 311 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(308): Show |
328 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(325): Show |
intron_variant | MODIFIER | c.198+351T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15641964 | |||||||
| chr19:15641983 | T | G | 7 | a0001c0001t0009g0148 a0001c0001t0009g0149 a0001c0001t0009g0150 others(4): Show |
7 | HG02818.hp2 HG03195.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+370T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15641983 | |||||||
| chr19:15642005 | G | T | 1 | a0001c0001t0002g0308 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.198+392G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642005 | |||||||
| chr19:15642129 | T | C | 5 | a0001c0001t0012g0156 a0001c0001t0012g0157 a0001c0001t0012g0159 others(2): Show |
5 | HG02145.hp1 HG02559.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+516T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642129 | |||||||
| chr19:15642231 | G | A | 1 | a0001c0002t0001g0309 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.198+618G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642231 | |||||||
| chr19:15642460 | T | C | 1 | a0001c0005t0004g0030 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.198+847T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642460 | |||||||
| chr19:15642529 | C | T | 33 | a0001c0002t0065g0066 a0001c0004t0005g0011 a0001c0004t0005g0012 others(30): Show |
34 | HG00558.hp2 HG00597.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.198+916C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642529 | |||||||
| chr19:15642531 | C | T | 311 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(308): Show |
328 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(325): Show |
intron_variant | MODIFIER | c.198+918C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642531 | |||||||
| chr19:15642535 | G | C | 1 | a0001c0001t0029g0155 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.198+922G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642535 | |||||||
| chr19:15642602 | A | T | 1 | a0001c0001t0019g0307 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.198+989A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642602 | |||||||
| chr19:15642613 | T | C | 389 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(386): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.198+1000T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642613 | |||||||
| chr19:15642686 | G | A | 1 | a0002c0003t0003g0013 | 2 | NA18957.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.198+1073G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642686 | |||||||
| chr19:15642779 | G | A | 1 | a0001c0001t0020g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.198+1166G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642779 | |||||||
| chr19:15642873 | A | G | 241 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(238): Show |
253 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.198+1260A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642873 | |||||||
| chr19:15642884 | A | AGATG | 5 | a0001c0002t0001g0373 a0001c0002t0001g0374 a0001c0002t0001g0375 others(2): Show |
5 | HG01081.hp2 HG01192.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+1307_198+1310d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15642884 | ||||||
| chr19:15642884 | AGATG | A | 12 | a0001c0001t0029g0094 a0001c0001t0061g0095 a0002c0003t0003g0136 others(9): Show |
12 | HG01074.hp2 HG01346.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.198+1307_198+1310d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15642884 | ||||||
| chr19:15642884 | AGATGGAT others(1): Show |
A | 299 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(296): Show |
316 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(313): Show |
intron_variant | MODIFIER | c.198+1303_198+1310d others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15642884 | ||||||
| chr19:15642915 | T | C | 1 | a0001c0001t0077g0161 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.198+1302T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642915 | |||||||
| chr19:15642949 | G | A | 241 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(238): Show |
253 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.198+1336G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642949 | |||||||
| chr19:15642979 | A | C | 1 | a0001c0002t0001g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.198+1366A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642979 | |||||||
| chr19:15642992 | G | A | 3 | a0001c0001t0002g0162 a0001c0001t0002g0163 a0001c0001t0002g0164 |
3 | HG00544.hp1 HG02074.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.198+1379G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642992 | |||||||
| chr19:15642994 | T | C | 3 | a0001c0001t0043g0091 a0001c0001t0081g0093 a0001c0001t0082g0092 |
3 | HG02055.hp1 HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.198+1381T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642994 | |||||||
| chr19:15643076 | AGATG | A | 3 | a0001c0005t0004g0055 a0001c0005t0004g0056 a0016c0017t0035g0057 |
3 | HG00639.hp1 HG03654.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.198+1485_198+1488d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643076 | ||||||
| chr19:15643127 | TTAGA | T | 60 | a0002c0003t0001g0105 a0002c0003t0002g0127 a0002c0003t0003g0001 others(57): Show |
68 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.198+1518_198+1521d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643127 | ||||||
| chr19:15643160 | AATAG | A | 3 | a0001c0001t0018g0306 a0001c0002t0070g0372 a0002c0003t0003g0017 |
4 | HG01168.hp1 HG01169.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+1556_198+1559d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643160 | ||||||
| chr19:15643192 | G | T | 1 | a0001c0001t0076g0389 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.198+1579G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643192 | |||||||
| chr19:15643232 | GGATA | G | 10 | a0001c0001t0012g0156 a0001c0001t0012g0157 a0001c0001t0012g0159 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.198+1626_198+1629d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643232 | ||||||
| chr19:15643239 | TAGAC | T | 63 | a0001c0004t0071g0053 a0001c0004t0073g0054 a0001c0004t0074g0052 others(60): Show |
71 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.198+1630_198+1633d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643239 | ||||||
| chr19:15643296 | C | T | 1 | a0002c0003t0003g0135 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.198+1683C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643296 | |||||||
| chr19:15643314 | TTAGA | T | 79 | a0001c0002t0001g0311 a0001c0002t0001g0317 a0001c0002t0065g0066 others(76): Show |
84 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.198+1718_198+1721d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643314 | ||||||
| chr19:15643331 | T | C | 71 | a0001c0001t0010g0165 a0001c0001t0012g0156 a0001c0001t0012g0157 others(68): Show |
79 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.198+1718T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643331 | |||||||
| chr19:15643335 | C | T | 71 | a0001c0001t0010g0165 a0001c0001t0012g0156 a0001c0001t0012g0157 others(68): Show |
79 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.198+1722C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643335 | |||||||
| chr19:15643341 | G | C | 72 | a0001c0001t0010g0165 a0001c0001t0012g0156 a0001c0001t0012g0157 others(69): Show |
80 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.198+1728G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643341 | |||||||
| chr19:15643341 | G | GATAC | 165 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
169 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.198+1744_198+1747d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643341 | ||||||
| chr19:15643397 | TATAGGTA others(5): Show |
T | 1 | a0001c0010t0021g0145 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.198+1789_198+1800d others(14): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643397 | ||||||
| chr19:15643402 | G | GTAGA | 6 | a0001c0001t0002g0163 a0001c0001t0002g0167 a0001c0001t0002g0168 others(3): Show |
6 | HG01257.hp1 HG02074.hp1 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+1791_198+1792i others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643402 | ||||||
| chr19:15643402 | GTAAA | G | 81 | a0001c0001t0002g0005 a0001c0001t0002g0256 a0001c0001t0002g0257 others(78): Show |
86 | HG00597.hp2 HG00673.hp2 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.198+1792_198+1795d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643402 | ||||||
| chr19:15643402 | GTAAATAG others(1): Show |
G | 95 | a0001c0001t0002g0004 a0001c0001t0002g0020 a0001c0001t0002g0162 others(92): Show |
101 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.198+1792_198+1799d others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643402 | ||||||
| chr19:15643402 | GTAAATAG others(5): Show |
G | 22 | a0001c0001t0013g0151 a0001c0001t0029g0094 a0002c0003t0003g0099 others(19): Show |
22 | HG00323.hp2 HG00438.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.198+1792_198+1803d others(14): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643402 | ||||||
| chr19:15643405 | A | AATAG | 16 | a0001c0002t0001g0023 a0001c0002t0001g0026 a0001c0002t0001g0334 others(13): Show |
17 | HG00642.hp1 HG01074.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.198+1842_198+1845d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643405 | ||||||
| chr19:15643405 | A | AATAGATA others(1): Show |
3 | a0001c0001t0014g0354 a0001c0002t0001g0027 a0001c0002t0001g0382 |
3 | HG02738.hp1 NA18999.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.198+1838_198+1845d others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643405 | ||||||
| chr19:15643405 | A | G | 38 | a0001c0001t0002g0164 a0001c0001t0002g0293 a0001c0001t0002g0295 others(35): Show |
38 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.198+1792A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643405 | |||||||
| chr19:15643405 | A | T | 4 | a0001c0001t0002g0163 a0001c0001t0002g0167 a0001c0001t0002g0168 others(1): Show |
4 | HG01257.hp1 HG02074.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+1792A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643405 | |||||||
| chr19:15643405 | AATAG | A | 76 | a0001c0002t0001g0024 a0001c0002t0001g0025 a0001c0002t0001g0026 others(73): Show |
82 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.198+1842_198+1845d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643405 | ||||||
| chr19:15643405 | AATAGATA others(1): Show |
A | 9 | a0001c0002t0001g0329 a0001c0002t0001g0369 a0001c0002t0001g0370 others(6): Show |
9 | HG00639.hp1 HG01978.hp1 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.198+1838_198+1845d others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643405 | ||||||
| chr19:15643405 | AATAGATA others(5): Show |
A | 1 | a0001c0004t0080g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.198+1834_198+1845d others(14): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643405 | ||||||
| chr19:15643405 | AATAGATA others(9): Show |
A | 1 | a0016c0017t0035g0057 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.198+1830_198+1845d others(18): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643405 | ||||||
| chr19:15643409 | G | T | 17 | a0001c0001t0002g0164 a0001c0001t0002g0293 a0001c0001t0002g0295 others(14): Show |
17 | HG00438.hp1 HG00673.hp1 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.198+1796G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643409 | |||||||
| chr19:15643413 | G | T | 38 | a0001c0001t0002g0005 a0001c0001t0002g0256 a0001c0001t0002g0257 others(35): Show |
40 | HG00597.hp2 HG01256.hp1 HG01943.hp1 others(37): Show |
intron_variant | MODIFIER | c.198+1800G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643413 | |||||||
| chr19:15643417 | G | T | 46 | a0001c0001t0002g0004 a0001c0001t0002g0020 a0001c0001t0002g0215 others(43): Show |
47 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.198+1804G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643417 | |||||||
| chr19:15643433 | G | C | 1 | a0001c0002t0070g0372 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.198+1820G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643433 | |||||||
| chr19:15643461 | G | C | 2 | a0001c0004t0071g0053 a0001c0004t0074g0052 |
2 | HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.198+1848G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643461 | |||||||
| chr19:15643465 | G | A | 10 | a0001c0001t0012g0156 a0001c0001t0012g0157 a0001c0001t0012g0159 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.198+1852G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643465 | |||||||
| chr19:15643507 | G | A | 1 | a0001c0001t0006g0214 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.198+1894G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643507 | |||||||
| chr19:15643644 | G | A | 1 | a0001c0004t0036g0063 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.198+2031G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643644 | |||||||
| chr19:15643870 | C | T | 2 | a0001c0001t0029g0094 a0001c0001t0061g0095 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.199-1849C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643870 | |||||||
| chr19:15643928 | A | G | 2 | a0001c0002t0001g0369 a0001c0002t0001g0370 |
2 | NA18963.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.199-1791A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643928 | |||||||
| chr19:15644083 | A | G | 241 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(238): Show |
253 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.199-1636A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15644083 | |||||||
| chr19:15644098 | C | T | 4 | a0001c0001t0015g0212 a0001c0001t0015g0213 a0001c0001t0019g0210 others(1): Show |
4 | HG02055.hp2 HG02976.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-1621C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15644098 | |||||||
| chr19:15644163 | C | T | 2 | a0001c0002t0001g0367 a0001c0002t0001g0368 |
2 | HG01346.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.199-1556C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15644163 | |||||||
| chr19:15644165 | C | T | 239 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(236): Show |
251 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.199-1554C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15644165 | |||||||
| chr19:15644299 | C | A | 1 | a0001c0005t0004g0031 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.199-1420C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15644299 | |||||||
| chr19:15644302 | G | A | 239 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(236): Show |
251 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.199-1417G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15644302 | |||||||
| chr19:15644432 | C | A | 2 | a0001c0002t0001g0023 a0001c0002t0023g0318 |
3 | HG02572.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.199-1287C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15644432 | |||||||
| chr19:15644582 | G | C | 241 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(238): Show |
253 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.199-1137G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15644582 | |||||||
| chr19:15644592 | T | TGAG | 241 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(238): Show |
253 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.199-1124_199-1122d others(5): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15644592 | ||||||
| chr19:15644632 | T | C | 311 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(308): Show |
328 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(325): Show |
intron_variant | MODIFIER | c.199-1087T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15644632 | |||||||
| chr19:15644816 | C | A | 1 | a0001c0004t0005g0064 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.199-903C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15644816 | |||||||
| chr19:15644819 | G | A | 2 | a0001c0010t0021g0145 a0001c0010t0021g0146 |
2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.199-900G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15644819 | |||||||
| chr19:15644875 | G | A | 1 | a0001c0021t0001g0378 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.199-844G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15644875 | |||||||
| chr19:15645030 | T | C | 241 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(238): Show |
253 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.199-689T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15645030 | |||||||
| chr19:15645105 | C | T | 2 | a0001c0010t0021g0145 a0001c0010t0021g0146 |
2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.199-614C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15645105 | |||||||
| chr19:15645143 | G | A | 1 | a0001c0001t0016g0166 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.199-576G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15645143 | |||||||
| chr19:15645234 | G | T | 3 | a0001c0001t0043g0091 a0001c0001t0081g0093 a0001c0001t0082g0092 |
3 | HG02055.hp1 HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.199-485G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15645234 | |||||||
| chr19:15645354 | A | C | 311 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(308): Show |
328 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(325): Show |
intron_variant | MODIFIER | c.199-365A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15645354 | |||||||
| chr19:15645673 | C | T | 2 | a0001c0002t0023g0028 a0001c0002t0044g0028 |
2 | HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.199-46C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15645673 | |||||||
| chr19:15645703 | G | A | 25 | a0001c0001t0002g0005 a0001c0001t0002g0215 a0001c0001t0002g0220 others(22): Show |
27 | HG00621.hp2 HG02080.hp1 HG02155.hp2 others(24): Show |
intron_variant | MODIFIER | c.199-16G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15645703 | |||||||
| chr19:15645947 | G | A | 2 | a0001c0001t0029g0094 a0001c0001t0061g0095 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.343+84G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15645947 | |||||||
| chr19:15645952 | G | A | 108 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(105): Show |
111 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.343+89G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15645952 | |||||||
| chr19:15646161 | T | C | 69 | a0001c0002t0065g0066 a0001c0004t0005g0011 a0001c0004t0005g0012 others(66): Show |
74 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.343+298T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646161 | |||||||
| chr19:15646181 | A | C | 1 | a0001c0002t0001g0366 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.343+318A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646181 | |||||||
| chr19:15646346 | G | A | 38 | a0001c0002t0065g0066 a0001c0004t0005g0011 a0001c0004t0005g0012 others(35): Show |
39 | HG00558.hp2 HG00597.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.343+483G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646346 | |||||||
| chr19:15646365 | C | G | 168 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(165): Show |
172 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.343+502C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646365 | |||||||
| chr19:15646405 | G | A | 1 | a0001c0002t0001g0319 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.343+542G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646405 | |||||||
| chr19:15646564 | G | C | 4 | a0001c0005t0004g0032 a0001c0005t0004g0033 a0001c0005t0004g0034 others(1): Show |
4 | HG03927.hp2 NA18968.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.344-488G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646564 | |||||||
| chr19:15646601 | T | C | 2 | a0001c0010t0021g0145 a0001c0010t0021g0146 |
2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.344-451T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646601 | |||||||
| chr19:15646618 | T | A | 240 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(237): Show |
252 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.344-434T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646618 | |||||||
| chr19:15646712 | G | A | 1 | a0001c0001t0043g0091 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.344-340G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646712 | |||||||
| chr19:15646718 | A | G | 240 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(237): Show |
252 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.344-334A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646718 | |||||||
| chr19:15646833 | C | T | 238 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(235): Show |
250 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.344-219C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646833 | |||||||
| chr19:15646951 | G | C | 2 | a0001c0001t0029g0094 a0001c0001t0061g0095 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.344-101G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646951 | |||||||
| chr19:15646988 | C | A | 1 | a0001c0001t0076g0389 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.344-64C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646988 | |||||||
| chr19:15646991 | C | CA | 10 | a0001c0001t0012g0156 a0001c0001t0012g0157 a0001c0001t0012g0159 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.344-60dupA | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr19 | 15646991 | ||||||
| chr19:15646993 | C | A | 2 | a0001c0001t0027g0292 a0001c0001t0059g0255 |
2 | NA18957.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.344-59C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646993 | |||||||
| chr19:15647117 | T | C | 321 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(318): Show |
338 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(335): Show |
intron_variant | MODIFIER | c.397+12T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 4/12 | chr19 | 15647117 | |||||||
| chr19:15647563 | C | T | 1 | a0001c0001t0076g0389 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.525+239C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15647563 | |||||||
| chr19:15647587 | A | C | 311 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(308): Show |
328 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(325): Show |
intron_variant | MODIFIER | c.525+263A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15647587 | |||||||
| chr19:15647591 | A | C | 3 | a0001c0001t0002g0162 a0001c0001t0002g0163 a0001c0001t0002g0164 |
3 | HG00544.hp1 HG02074.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.525+267A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15647591 | |||||||
| chr19:15647693 | C | T | 2 | a0001c0002t0001g0369 a0001c0002t0001g0370 |
2 | NA18963.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.525+369C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15647693 | |||||||
| chr19:15647778 | G | A | 1 | a0001c0004t0040g0065 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.525+454G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15647778 | |||||||
| chr19:15647908 | T | C | 1 | a0001c0005t0004g0006 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.525+584T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15647908 | |||||||
| chr19:15647936 | A | C | 7 | a0001c0004t0005g0011 a0001c0004t0005g0012 a0001c0004t0005g0087 others(4): Show |
7 | HG00735.hp2 HG01243.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.525+612A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15647936 | |||||||
| chr19:15647997 | A | G | 2 | a0001c0001t0002g0253 a0001c0001t0002g0254 |
2 | NA18985.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.525+673A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15647997 | |||||||
| chr19:15648005 | A | G | 1 | a0002c0003t0003g0133 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.525+681A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15648005 | |||||||
| chr19:15648007 | G | A | 1 | a0001c0002t0001g0327 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.525+683G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15648007 | |||||||
| chr19:15648075 | A | G | 1 | a0001c0002t0070g0372 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.525+751A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15648075 | |||||||
| chr19:15648121 | T | C | 240 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(237): Show |
252 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.525+797T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15648121 | |||||||
| chr19:15648221 | G | A | 1 | a0016c0017t0035g0057 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.525+897G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15648221 | |||||||
| chr19:15648393 | T | C | 1 | a0016c0017t0035g0057 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.526-767T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15648393 | |||||||
| chr19:15648404 | G | A | 2 | a0002c0003t0003g0097 a0002c0003t0003g0098 |
2 | HG00280.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.526-756G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15648404 | |||||||
| chr19:15648664 | G | A | 71 | a0001c0001t0012g0156 a0001c0001t0012g0157 a0001c0001t0012g0159 others(68): Show |
79 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.526-496G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15648664 | |||||||
| chr19:15648671 | T | C | 2 | a0001c0010t0021g0145 a0001c0010t0021g0146 |
2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.526-489T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15648671 | |||||||
| chr19:15648747 | C | A | 12 | a0001c0001t0009g0148 a0001c0001t0009g0149 a0001c0001t0009g0150 others(9): Show |
12 | HG02723.hp1 HG02818.hp2 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.526-413C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15648747 | |||||||
| chr19:15648866 | C | G | 2 | a0001c0002t0001g0364 a0001c0002t0001g0365 |
2 | HG02735.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.526-294C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15648866 | |||||||
| chr19:15648954 | C | T | 240 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(237): Show |
252 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.526-206C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15648954 | |||||||
| chr19:15648999 | A | G | 60 | a0002c0003t0001g0105 a0002c0003t0002g0127 a0002c0003t0003g0001 others(57): Show |
68 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.526-161A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15648999 | |||||||
| chr19:15649018 | A | G | 240 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(237): Show |
252 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.526-142A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15649018 | |||||||
| chr19:15649033 | C | T | 1 | a0001c0004t0080g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.526-127C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15649033 | |||||||
| chr19:15649337 | G | A | 6 | a0001c0001t0010g0165 a0001c0001t0015g0212 a0001c0001t0015g0213 others(3): Show |
6 | HG02055.hp2 HG02886.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.647+56G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 6/12 | chr19 | 15649337 | |||||||
| chr19:15649403 | C | T | 71 | a0001c0001t0012g0156 a0001c0001t0012g0157 a0001c0001t0012g0159 others(68): Show |
79 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.647+122C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 6/12 | chr19 | 15649403 | |||||||
| chr19:15649767 | C | T | 240 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(237): Show |
252 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.648-146C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 6/12 | chr19 | 15649767 | |||||||
| chr19:15649912 | G | A | 1 | a0001c0001t0010g0178 | 1 | HG02970.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.648-1G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 6/12 | chr19 | 15649912 | |||||||
| chr19:15650264 | C | T | 2 | a0001c0001t0081g0093 a0001c0001t0082g0092 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.918+81C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650264 | |||||||
| chr19:15650274 | C | A | 1 | a0001c0002t0065g0066 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.918+91C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650274 | |||||||
| chr19:15650399 | C | T | 2 | a0001c0001t0002g0308 a0001c0001t0039g0227 |
2 | HG00621.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.918+216C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650399 | |||||||
| chr19:15650494 | GTCTTTCT others(4): Show |
G | 1 | a0001c0001t0024g0263 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.918+312_918+322del others(11): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650494 | |||||||
| chr19:15650570 | T | C | 2 | a0001c0002t0001g0319 a0001c0002t0069g0328 |
2 | HG00609.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.918+387T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650570 | |||||||
| chr19:15650623 | T | C | 1 | a0001c0001t0002g0228 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.918+440T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650623 | |||||||
| chr19:15650655 | C | CTTCTTT | 10 | a0001c0001t0002g0252 a0001c0001t0002g0291 a0001c0001t0008g0207 others(7): Show |
11 | HG00735.hp1 HG01255.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.918+479_918+484dup others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650655 | ||||||
| chr19:15650658 | C | CTTTTTCT others(32): Show |
2 | a0001c0004t0005g0011 a0001c0004t0041g0011 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.918+478_918+516dup others(39): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650658 | ||||||
| chr19:15650660 | T | C | 3 | a0001c0004t0071g0053 a0001c0004t0073g0054 a0001c0004t0074g0052 |
3 | HG02630.hp1 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.918+477T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650660 | |||||||
| chr19:15650660 | T | TTTTC | 11 | a0001c0002t0001g0147 a0001c0002t0001g0338 a0001c0002t0001g0339 others(8): Show |
11 | HG00280.hp2 HG00741.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.918+553_918+556dup others(4): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650660 | ||||||
| chr19:15650660 | T | TTTTCTTT others(1): Show |
4 | a0001c0002t0001g0334 a0001c0005t0004g0032 a0001c0005t0004g0038 others(1): Show |
4 | HG02602.hp1 HG03710.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+549_918+556dup others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650660 | ||||||
| chr19:15650660 | T | TTTTCTTT others(5): Show |
3 | a0001c0002t0001g0381 a0001c0005t0033g0037 a0015c0019t0001g0380 |
3 | HG02622.hp1 HG02735.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.918+545_918+556dup others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650660 | ||||||
| chr19:15650660 | T | TTTTCTTT others(9): Show |
1 | a0001c0005t0004g0036 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.918+541_918+556dup others(16): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650660 | ||||||
| chr19:15650660 | T | TTTTCTTT others(17): Show |
1 | a0001c0002t0001g0379 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.918+533_918+556dup others(24): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650660 | ||||||
| chr19:15650660 | T | TTTTCTTT others(3): Show |
2 | a0001c0001t0019g0307 a0001c0001t0081g0093 |
2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.918+484_918+485ins others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650660 | ||||||
| chr19:15650660 | TTTTC | T | 15 | a0001c0002t0001g0026 a0001c0002t0001g0311 a0001c0002t0001g0345 others(12): Show |
17 | HG00099.hp2 HG00642.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.918+553_918+556del others(4): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650660 | ||||||
| chr19:15650660 | TTTTCTTT others(9): Show |
T | 2 | a0001c0002t0001g0387 a0001c0002t0001g0388 |
2 | HG01496.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.918+541_918+556del others(16): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650660 | ||||||
| chr19:15650664 | C | CTT | 199 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(196): Show |
210 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.918+483_918+484dup others(2): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650664 | ||||||
| chr19:15650664 | C | CTTTCTTT others(28): Show |
2 | a0001c0004t0005g0064 a0001c0004t0005g0070 |
2 | HG02040.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.918+482_918+516dup others(35): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650664 | ||||||
| chr19:15650666 | TTC | T | 23 | a0001c0001t0002g0170 a0001c0001t0002g0226 a0001c0001t0002g0228 others(20): Show |
23 | HG00438.hp1 HG01952.hp1 HG02129.hp2 others(20): Show |
intron_variant | MODIFIER | c.918+485_918+486del others(2): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650666 | ||||||
| chr19:15650668 | C | CTTTCTTT others(20): Show |
2 | a0001c0004t0007g0058 a0001c0004t0007g0069 |
2 | HG01175.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.918+486_918+512dup others(27): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650668 | ||||||
| chr19:15650668 | C | CTTTCTTT others(24): Show |
1 | a0001c0004t0005g0067 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.918+486_918+516dup others(31): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650668 | ||||||
| chr19:15650668 | C | CTTTCTTT others(40): Show |
1 | a0011c0016t0042g0071 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.918+486_918+532dup others(47): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650668 | ||||||
| chr19:15650672 | C | CTTTCTTT others(16): Show |
1 | a0001c0004t0005g0059 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.918+490_918+512dup others(23): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650672 | ||||||
| chr19:15650672 | C | CTTTCTTT others(20): Show |
7 | a0001c0004t0005g0078 a0001c0004t0005g0079 a0001c0004t0005g0080 others(4): Show |
7 | HG00597.hp1 HG02080.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.918+490_918+516dup others(27): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650672 | ||||||
| chr19:15650676 | C | CTTTCTTT others(12): Show |
1 | a0001c0004t0005g0060 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.918+494_918+512dup others(19): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650676 | ||||||
| chr19:15650676 | C | CTTTCTTT others(14): Show |
1 | a0001c0004t0007g0076 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.918+496_918+516dup others(21): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650676 | ||||||
| chr19:15650676 | C | CTTTCTTT others(16): Show |
5 | a0001c0004t0005g0085 a0001c0004t0005g0087 a0001c0004t0007g0010 others(2): Show |
6 | HG03490.hp2 HG03710.hp1 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.918+494_918+516dup others(23): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650676 | ||||||
| chr19:15650676 | C | CTTTCTTT others(20): Show |
4 | a0001c0002t0065g0066 a0001c0004t0005g0075 a0001c0004t0005g0090 others(1): Show |
4 | HG02683.hp1 HG03704.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+494_918+520dup others(27): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650676 | ||||||
| chr19:15650680 | C | CTTTCTTT others(8): Show |
1 | a0001c0004t0007g0061 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.918+498_918+512dup others(15): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650680 | ||||||
| chr19:15650680 | C | CTTTCTTT others(12): Show |
5 | a0001c0004t0005g0012 a0001c0004t0005g0089 a0001c0004t0007g0088 others(2): Show |
5 | HG00735.hp2 HG01243.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+498_918+516dup others(19): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650680 | ||||||
| chr19:15650682 | T | C | 1 | a0001c0005t0004g0006 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.918+499T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650682 | |||||||
| chr19:15650684 | C | CTTTCTTT others(8): Show |
1 | a0001c0004t0007g0171 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.918+502_918+516dup others(15): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650684 | ||||||
| chr19:15650688 | C | CTTTCTTT others(4): Show |
1 | a0001c0004t0011g0086 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.918+506_918+516dup others(11): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650688 | ||||||
| chr19:15650688 | C | CTTTCTTT others(12): Show |
1 | a0001c0004t0007g0073 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.918+506_918+524dup others(19): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650688 | ||||||
| chr19:15650698 | T | TTTTTCTT others(141): Show |
1 | a0001c0004t0011g0084 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.918+516_918+517ins others(148): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650698 | ||||||
| chr19:15650700 | C | CTT | 4 | a0001c0001t0008g0019 a0001c0001t0008g0202 a0001c0001t0010g0019 others(1): Show |
4 | HG01168.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+519_918+520dup others(2): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650700 | ||||||
| chr19:15650702 | T | C | 2 | a0001c0001t0010g0180 a0001c0001t0015g0179 |
2 | HG01081.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.918+519T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650702 | |||||||
| chr19:15650706 | T | C | 4 | a0001c0001t0008g0019 a0001c0001t0008g0202 a0001c0001t0010g0019 others(1): Show |
4 | HG01168.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+523T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650706 | |||||||
| chr19:15650706 | T | TTTTTCTT others(141): Show |
1 | a0016c0017t0035g0057 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.918+524_918+525ins others(148): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650706 | ||||||
| chr19:15650709 | T | TTTCTTTC others(109): Show |
1 | a0001c0002t0066g0353 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.918+544_918+545ins others(116): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650709 | ||||||
| chr19:15650710 | T | A | 1 | a0001c0001t0077g0161 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.918+527T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650710 | |||||||
| chr19:15650710 | T | C | 2 | a0001c0001t0010g0181 a0001c0001t0081g0093 |
2 | HG02451.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.918+527T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650710 | |||||||
| chr19:15650710 | T | TTCTTTCT others(86): Show |
1 | a0001c0004t0073g0054 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.918+536_918+537ins others(93): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650710 | ||||||
| chr19:15650710 | T | TTTTCTC | 8 | a0001c0001t0002g0252 a0001c0001t0002g0291 a0001c0001t0008g0207 others(5): Show |
8 | HG00735.hp1 HG01255.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.918+528_918+529ins others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650710 | ||||||
| chr19:15650713 | T | TTTCTTTC others(123): Show |
1 | a0001c0002t0001g0369 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.918+546_918+547ins others(130): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | ||||||
| chr19:15650713 | T | TTTCTTTC others(127): Show |
1 | a0001c0002t0001g0370 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.918+550_918+551ins others(134): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | ||||||
| chr19:15650713 | T | TTTCTTTC others(123): Show |
1 | a0010c0020t0001g0096 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(130): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | ||||||
| chr19:15650713 | T | TTTCTTTC others(133): Show |
2 | a0001c0002t0001g0329 a0001c0002t0001g0330 |
2 | HG00323.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.918+556_918+557ins others(140): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | ||||||
| chr19:15650713 | T | TTTCTTTC others(129): Show |
3 | a0001c0002t0001g0364 a0001c0002t0017g0320 a0001c0002t0017g0331 |
3 | HG01123.hp1 HG01123.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.918+556_918+557ins others(136): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | ||||||
| chr19:15650713 | T | TTTCTTTC others(125): Show |
2 | a0001c0002t0001g0332 a0001c0002t0001g0333 |
2 | HG00733.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.918+556_918+557ins others(132): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | ||||||
| chr19:15650713 | T | TTTCTTTC others(121): Show |
7 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 others(4): Show |
7 | HG00558.hp1 HG01515.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.918+556_918+557ins others(128): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | ||||||
| chr19:15650713 | T | TTTCTTTC others(117): Show |
1 | a0001c0002t0001g0342 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.918+614_918+615ins others(124): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | ||||||
| chr19:15650713 | T | TTTCTTTC others(113): Show |
5 | a0001c0002t0001g0346 a0001c0002t0001g0347 a0001c0002t0001g0348 others(2): Show |
5 | HG00621.hp1 HG01346.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+552_918+553ins others(120): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | ||||||
| chr19:15650713 | T | TTTCTTTC others(109): Show |
11 | a0001c0002t0001g0023 a0001c0002t0001g0027 a0001c0002t0001g0309 others(8): Show |
12 | HG00609.hp1 HG00639.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.918+548_918+549ins others(116): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | ||||||
| chr19:15650713 | T | TTTCTTTC others(105): Show |
10 | a0001c0001t0014g0354 a0001c0002t0001g0319 a0001c0002t0001g0356 others(7): Show |
10 | HG00140.hp2 HG00609.hp2 HG00673.hp2 others(7): Show |
intron_variant | MODIFIER | c.918+544_918+545ins others(112): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | ||||||
| chr19:15650713 | T | TTTCTTTC others(101): Show |
7 | a0001c0002t0001g0317 a0001c0002t0001g0327 a0001c0002t0001g0359 others(4): Show |
7 | HG01175.hp1 HG03540.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.918+540_918+541ins others(108): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | ||||||
| chr19:15650713 | T | TTTCTTTT others(97): Show |
1 | a0001c0002t0001g0361 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.918+536_918+537ins others(104): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | ||||||
| chr19:15650713 | T | TTTTCCTT others(93): Show |
1 | a0001c0002t0001g0362 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.918+532_918+533ins others(100): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | ||||||
| chr19:15650714 | T | C | 3 | a0002c0003t0003g0016 a0002c0003t0003g0099 a0002c0003t0003g0132 |
4 | HG01361.hp1 HG02717.hp2 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+531T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650714 | |||||||
| chr19:15650717 | T | TTTCTTTC others(145): Show |
1 | a0001c0004t0007g0072 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.918+556_918+557ins others(152): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650717 | ||||||
| chr19:15650717 | T | TTTCTTTC others(117): Show |
1 | a0001c0005t0004g0008 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.918+552_918+553ins others(124): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650717 | ||||||
| chr19:15650717 | T | TTTCTTTC others(105): Show |
1 | a0001c0002t0070g0372 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.918+548_918+549ins others(112): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650717 | ||||||
| chr19:15650717 | T | TTTCTTTC others(113): Show |
4 | a0001c0004t0074g0052 a0001c0005t0004g0008 a0001c0005t0004g0046 others(1): Show |
4 | HG00642.hp2 HG01928.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+548_918+549ins others(120): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650717 | ||||||
| chr19:15650717 | T | TTTCTTTC others(105): Show |
1 | a0001c0005t0004g0031 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.918+544_918+545ins others(112): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650717 | ||||||
| chr19:15650717 | T | TTTCTTTC others(109): Show |
3 | a0001c0004t0071g0053 a0001c0005t0004g0030 a0001c0005t0004g0045 |
3 | HG01192.hp2 HG02965.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.918+544_918+545ins others(116): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650717 | ||||||
| chr19:15650718 | T | TTC | 4 | a0001c0001t0008g0019 a0001c0001t0008g0202 a0001c0001t0010g0019 others(1): Show |
4 | HG01168.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+537_918+538dup others(2): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | ||||||
| chr19:15650718 | T | TTCTCTCT others(124): Show |
1 | a0002c0003t0003g0126 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.918+538_918+539ins others(131): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | ||||||
| chr19:15650718 | T | TTCTCTCT others(128): Show |
1 | a0002c0003t0003g0015 | 2 | HG04199.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.918+538_918+539ins others(135): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | ||||||
| chr19:15650718 | T | TTCTTTCT others(150): Show |
2 | a0001c0001t0010g0165 a0001c0001t0020g0189 |
2 | HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.918+548_918+549ins others(157): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | ||||||
| chr19:15650718 | T | TTCTTTCT others(154): Show |
1 | a0001c0001t0012g0184 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.918+548_918+549ins others(161): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | ||||||
| chr19:15650718 | T | TTCTTTCT others(150): Show |
13 | a0001c0001t0002g0005 a0001c0001t0002g0167 a0001c0001t0002g0239 others(10): Show |
14 | HG00099.hp1 HG02004.hp1 HG03239.hp2 others(11): Show |
intron_variant | MODIFIER | c.918+548_918+549ins others(157): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | ||||||
| chr19:15650718 | T | TTCTTTCT others(147): Show |
2 | a0001c0001t0009g0172 a0001c0001t0013g0151 |
2 | NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.918+548_918+549ins others(154): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | ||||||
| chr19:15650718 | T | TTCTTTCT others(153): Show |
1 | a0001c0001t0002g0220 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.918+544_918+545ins others(160): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | ||||||
| chr19:15650718 | T | TTCTTTCT others(146): Show |
4 | a0001c0001t0018g0306 a0001c0001t0019g0177 a0001c0001t0025g0197 others(1): Show |
4 | HG02559.hp2 HG02683.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+544_918+545ins others(153): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | ||||||
| chr19:15650718 | T | TTCTTTCT others(142): Show |
1 | a0001c0001t0002g0273 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.918+544_918+545ins others(149): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | ||||||
| chr19:15650718 | T | TTCTTTCT others(150): Show |
1 | a0001c0001t0016g0183 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.918+544_918+545ins others(157): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | ||||||
| chr19:15650718 | T | TTCTTTCT others(146): Show |
8 | a0001c0001t0002g0005 a0001c0001t0002g0242 a0001c0001t0002g0243 others(5): Show |
8 | HG02602.hp2 HG02698.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.918+544_918+545ins others(153): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | ||||||
| chr19:15650718 | T | TTCTTTCT others(143): Show |
2 | a0001c0001t0009g0148 a0001c0001t0009g0150 |
2 | HG02818.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.918+544_918+545ins others(150): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | ||||||
| chr19:15650718 | T | TTCTTTTT others(142): Show |
12 | a0001c0001t0008g0186 a0001c0001t0010g0178 a0001c0001t0015g0198 others(9): Show |
12 | HG01109.hp2 HG01891.hp1 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.918+540_918+541ins others(149): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | ||||||
| chr19:15650718 | T | TTCTTTTT others(142): Show |
5 | a0001c0001t0002g0245 a0001c0001t0002g0248 a0001c0001t0002g0276 others(2): Show |
5 | HG01358.hp2 HG01952.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+540_918+541ins others(149): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | ||||||
| chr19:15650718 | T | TTCTTTTT others(139): Show |
2 | a0001c0001t0009g0149 a0001c0001t0013g0152 |
2 | HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.918+540_918+541ins others(146): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | ||||||
| chr19:15650718 | T | TTCTTTTT others(139): Show |
1 | a0002c0003t0003g0125 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.918+540_918+541ins others(146): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | ||||||
| chr19:15650718 | T | TTTTCTCT others(138): Show |
5 | a0001c0001t0008g0193 a0001c0001t0015g0212 a0001c0001t0015g0213 others(2): Show |
5 | HG02809.hp2 HG02976.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+536_918+537ins others(145): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | ||||||
| chr19:15650718 | T | TTTTCTCT others(138): Show |
1 | a0001c0001t0002g0244 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.918+536_918+537ins others(145): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | ||||||
| chr19:15650718 | T | TTTTCTCT others(135): Show |
1 | a0001c0001t0009g0173 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.918+536_918+537ins others(142): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | ||||||
| chr19:15650718 | T | TTTTCTCT others(138): Show |
2 | a0007c0011t0008g0185 a0007c0011t0008g0192 |
2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.918+536_918+537ins others(145): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | ||||||
| chr19:15650721 | T | TTCCTTCC others(91): Show |
1 | a0001c0002t0023g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.918+539_918+540ins others(98): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650721 | ||||||
| chr19:15650721 | T | TTTCTTTT others(101): Show |
1 | a0001c0002t0044g0028 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.918+544_918+545ins others(108): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650721 | ||||||
| chr19:15650722 | T | C | 1 | a0001c0001t0082g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.918+539T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650722 | |||||||
| chr19:15650722 | T | TTC | 13 | a0001c0001t0002g0252 a0001c0001t0002g0291 a0001c0001t0008g0207 others(10): Show |
14 | HG00735.hp1 HG01255.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.918+541_918+542dup others(2): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650722 | ||||||
| chr19:15650722 | T | TTCTCTCT others(15): Show |
1 | a0001c0010t0021g0146 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.918+542_918+543ins others(22): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650722 | ||||||
| chr19:15650722 | T | TTCTCTCT others(7): Show |
1 | a0001c0005t0004g0048 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.918+542_918+543ins others(14): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650722 | ||||||
| chr19:15650722 | T | TTCTTTCT others(21): Show |
2 | a0001c0001t0027g0238 a0001c0001t0049g0297 |
2 | NA19063.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.918+548_918+549ins others(28): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650722 | ||||||
| chr19:15650722 | T | TTCTTTTT others(17): Show |
2 | a0001c0001t0008g0182 a0001c0001t0043g0091 |
2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.918+544_918+545ins others(24): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650722 | ||||||
| chr19:15650726 | T | C | 4 | a0002c0003t0003g0002 a0002c0003t0062g0014 a0002c0003t0063g0014 others(1): Show |
5 | HG02135.hp1 NA18939.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.918+543T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650726 | |||||||
| chr19:15650730 | T | C | 10 | a0001c0001t0012g0156 a0002c0003t0003g0003 a0002c0003t0003g0013 others(7): Show |
11 | HG00408.hp2 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.918+547T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650730 | |||||||
| chr19:15650734 | T | C | 8 | a0001c0001t0029g0094 a0001c0001t0029g0155 a0002c0003t0001g0105 others(5): Show |
8 | HG00438.hp2 HG02040.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.918+551T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650734 | |||||||
| chr19:15650736 | C | T | 6 | a0001c0001t0008g0019 a0001c0001t0008g0202 a0001c0001t0010g0019 others(3): Show |
6 | HG01081.hp1 HG01168.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.918+553C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650736 | |||||||
| chr19:15650737 | T | C | 6 | a0001c0001t0008g0019 a0001c0001t0008g0202 a0001c0001t0010g0019 others(3): Show |
6 | HG01081.hp1 HG01168.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.918+554T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650737 | |||||||
| chr19:15650737 | T | TCTCTTTC others(144): Show |
3 | a0001c0001t0077g0161 a0002c0003t0003g0017 a0002c0003t0003g0109 |
4 | HG01168.hp1 HG01169.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+554_918+555ins others(151): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650737 | |||||||
| chr19:15650737 | T | TCTCTTTC others(148): Show |
10 | a0002c0003t0003g0001 a0002c0003t0003g0110 a0002c0003t0003g0111 others(7): Show |
13 | HG03017.hp2 HG04115.hp2 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.918+554_918+555ins others(155): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650737 | |||||||
| chr19:15650737 | T | TCTCTTTC others(160): Show |
1 | a0001c0001t0012g0157 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.918+554_918+555ins others(167): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650737 | |||||||
| chr19:15650737 | T | TCTCTTTC others(164): Show |
1 | a0001c0001t0016g0158 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.918+554_918+555ins others(171): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650737 | |||||||
| chr19:15650737 | T | TCTTTCTT others(11): Show |
1 | a0001c0001t0082g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.918+554_918+555ins others(18): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650737 | |||||||
| chr19:15650737 | T | TCTTTCTT others(132): Show |
2 | a0002c0003t0062g0014 a0002c0003t0063g0014 |
2 | NA18968.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.918+554_918+555ins others(139): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650737 | |||||||
| chr19:15650737 | T | TCTTTCTT others(136): Show |
2 | a0002c0003t0003g0002 a0004c0008t0003g0002 |
3 | HG02135.hp1 NA18939.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.918+554_918+555ins others(143): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650737 | |||||||
| chr19:15650738 | T | C | 26 | a0001c0001t0008g0019 a0001c0001t0008g0202 a0001c0001t0010g0019 others(23): Show |
31 | HG01081.hp1 HG01168.hp1 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.918+555T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650738 | |||||||
| chr19:15650738 | T | TCTCTCTT others(156): Show |
1 | a0001c0001t0013g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.918+555_918+556ins others(163): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650738 | |||||||
| chr19:15650738 | T | TCTTTCTC others(163): Show |
1 | a0001c0001t0002g0293 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.918+555_918+556ins others(170): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650738 | |||||||
| chr19:15650738 | T | TTCTCTCT others(35): Show |
1 | a0001c0010t0021g0145 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(42): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTCTCT others(148): Show |
1 | a0002c0003t0003g0116 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(155): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTCTCT others(152): Show |
3 | a0002c0003t0003g0117 a0002c0003t0003g0139 a0002c0003t0003g0140 |
3 | HG01074.hp2 HG03516.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.918+556_918+557ins others(159): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTCTCT others(148): Show |
1 | a0002c0003t0010g0118 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.918+556_918+557ins others(155): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTCTCT others(156): Show |
1 | a0002c0003t0003g0141 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(163): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTCTCT others(160): Show |
1 | a0001c0001t0002g0264 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.918+556_918+557ins others(167): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTCTTT others(136): Show |
1 | a0002c0003t0003g0100 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.918+556_918+557ins others(143): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTCTTT others(136): Show |
1 | a0002c0003t0003g0101 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.918+556_918+557ins others(143): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTCTTT others(140): Show |
7 | a0002c0003t0003g0003 a0002c0003t0003g0013 a0002c0003t0003g0103 others(4): Show |
8 | HG00408.hp2 HG01891.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.918+556_918+557ins others(147): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTCTC others(151): Show |
1 | a0002c0003t0003g0119 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(158): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTTCT others(152): Show |
1 | a0002c0003t0003g0120 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(159): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTTCT others(156): Show |
3 | a0002c0003t0003g0121 a0002c0003t0003g0134 a0002c0003t0003g0142 |
3 | HG01346.hp2 NA19012.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.918+556_918+557ins others(163): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTTCT others(160): Show |
1 | a0002c0003t0003g0143 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.918+556_918+557ins others(167): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTTCT others(156): Show |
1 | a0001c0001t0012g0159 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(163): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTTCT others(160): Show |
1 | a0001c0001t0012g0156 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(167): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTTCT others(140): Show |
2 | a0002c0003t0003g0104 a0002c0003t0003g0133 |
2 | HG00438.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.918+556_918+557ins others(147): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTTCT others(140): Show |
1 | a0002c0003t0001g0105 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(147): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTTCT others(144): Show |
2 | a0002c0003t0003g0106 a0002c0003t0003g0107 |
2 | HG02040.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.918+556_918+557ins others(151): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTTCT others(148): Show |
1 | a0002c0003t0003g0108 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.918+556_918+557ins others(155): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTTCT others(148): Show |
1 | a0001c0001t0076g0389 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.918+556_918+557ins others(155): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTTCT others(156): Show |
1 | a0002c0003t0064g0122 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(163): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTTCT others(160): Show |
2 | a0002c0003t0003g0123 a0004c0008t0030g0144 |
2 | NA18981.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.918+556_918+557ins others(167): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTTCT others(168): Show |
1 | a0001c0001t0061g0095 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(175): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTTCT others(164): Show |
1 | a0001c0001t0029g0155 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.918+556_918+557ins others(171): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTTCT others(148): Show |
1 | a0001c0001t0029g0094 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.918+556_918+557ins others(155): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTTCT others(164): Show |
1 | a0002c0003t0003g0124 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(171): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTTCT others(178): Show |
1 | a0001c0001t0002g0215 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(185): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTTCT others(182): Show |
1 | a0001c0001t0002g0229 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(189): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTTCT others(174): Show |
5 | a0001c0001t0002g0162 a0001c0001t0002g0230 a0001c0001t0002g0265 others(2): Show |
5 | HG00544.hp1 HG02083.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.918+556_918+557ins others(181): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTTCT others(41): Show |
1 | a0002c0003t0003g0097 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(48): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTTCT others(166): Show |
1 | a0001c0001t0003g0231 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(173): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTTCT others(166): Show |
1 | a0001c0001t0002g0232 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(173): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTTCT others(170): Show |
9 | a0001c0001t0002g0020 a0001c0001t0002g0163 a0001c0001t0002g0253 others(6): Show |
10 | HG01069.hp1 HG01071.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.918+556_918+557ins others(177): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTTTT others(162): Show |
2 | a0001c0001t0003g0233 a0001c0001t0014g0216 |
2 | HG00544.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.918+556_918+557ins others(169): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTTTT others(166): Show |
18 | a0001c0001t0002g0004 a0001c0001t0002g0164 a0001c0001t0002g0234 others(15): Show |
18 | HG00597.hp2 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.918+556_918+557ins others(173): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTTTT others(170): Show |
1 | a0001c0001t0006g0219 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.918+556_918+557ins others(177): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTCTTTTT others(166): Show |
1 | a0001c0001t0057g0237 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(173): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTTCC | 79 | a0001c0001t0002g0005 a0001c0001t0002g0167 a0001c0001t0002g0220 others(76): Show |
82 | HG00099.hp1 HG00733.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.918+564_918+567dup others(4): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTTTCTCT others(33): Show |
1 | a0002c0003t0003g0098 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.918+557_918+558ins others(40): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTTTCTCT others(162): Show |
5 | a0001c0001t0018g0203 a0001c0001t0020g0160 a0001c0001t0020g0200 others(2): Show |
6 | HG02486.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.918+557_918+558ins others(169): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTTTCTCT others(158): Show |
2 | a0001c0001t0002g0228 a0001c0001t0002g0249 |
2 | HG00408.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.918+557_918+558ins others(165): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTTTCTCT others(158): Show |
1 | a0001c0001t0002g0251 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.918+557_918+558ins others(165): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTTTCTCT others(162): Show |
31 | a0001c0001t0002g0168 a0001c0001t0002g0170 a0001c0001t0002g0221 others(28): Show |
31 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.918+557_918+558ins others(169): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650738 | T | TTTTCTCT others(159): Show |
4 | a0001c0001t0009g0174 a0001c0001t0009g0175 a0001c0001t0009g0176 others(1): Show |
4 | HG02723.hp1 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+557_918+558ins others(166): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | ||||||
| chr19:15650751 | A | T | 4 | a0001c0005t0004g0048 a0002c0003t0003g0016 a0002c0003t0003g0099 others(1): Show |
5 | HG01099.hp2 HG01361.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.918+568A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650751 | |||||||
| chr19:15650754 | T | C | 4 | a0001c0005t0004g0048 a0002c0003t0003g0016 a0002c0003t0003g0099 others(1): Show |
5 | HG01099.hp2 HG01361.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.918+571T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650754 | |||||||
| chr19:15650755 | T | A | 4 | a0001c0005t0004g0048 a0002c0003t0003g0016 a0002c0003t0003g0099 others(1): Show |
5 | HG01099.hp2 HG01361.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.918+572T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650755 | |||||||
| chr19:15650776 | G | A | 2 | a0001c0001t0081g0093 a0001c0001t0082g0092 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.918+593G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650776 | |||||||
| chr19:15650776 | G | GTTCTTTC others(12): Show |
4 | a0001c0005t0004g0030 a0001c0005t0004g0031 a0001c0005t0004g0045 others(1): Show |
4 | HG01192.hp2 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+596_918+614dup others(19): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650776 | ||||||
| chr19:15650776 | G | GTTCTTTC others(16): Show |
2 | a0001c0004t0011g0084 a0016c0017t0035g0057 |
2 | HG03834.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.918+614_918+615ins others(23): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650776 | ||||||
| chr19:15650776 | G | GTTCTTTC others(132): Show |
1 | a0001c0004t0007g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.918+614_918+615ins others(139): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650776 | ||||||
| chr19:15650776 | G | GTTCTTTC others(136): Show |
1 | a0012c0015t0004g0040 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.918+614_918+615ins others(143): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650776 | ||||||
| chr19:15650776 | G | GTTCTTTC others(140): Show |
17 | a0001c0005t0004g0006 a0001c0005t0004g0009 a0001c0005t0004g0032 others(14): Show |
19 | HG00639.hp1 HG01070.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.918+614_918+615ins others(147): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650776 | ||||||
| chr19:15650776 | G | GTTCTTTC others(144): Show |
9 | a0001c0004t0005g0059 a0001c0004t0005g0060 a0001c0004t0005g0078 others(6): Show |
10 | HG02486.hp1 HG02615.hp1 HG03486.hp1 others(7): Show |
intron_variant | MODIFIER | c.918+614_918+615ins others(151): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650776 | ||||||
| chr19:15650776 | G | GTTCTTTC others(203): Show |
1 | a0001c0005t0033g0049 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.918+614_918+615ins others(210): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650776 | ||||||
| chr19:15650776 | G | GTTCTTTC others(144): Show |
1 | a0001c0005t0004g0036 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.918+614_918+615ins others(151): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650776 | ||||||
| chr19:15650776 | G | GTTCTTTC others(32): Show |
1 | a0001c0001t0002g0224 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.918+617_918+618ins others(39): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650776 | ||||||
| chr19:15650776 | GTTCT | G | 3 | a0001c0002t0001g0023 a0001c0002t0001g0350 a0001c0002t0023g0318 |
4 | HG02572.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+614_918+617del others(4): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650776 | ||||||
| chr19:15650779 | C | CGTTCTTT others(12): Show |
2 | a0001c0010t0021g0145 a0001c0010t0021g0146 |
2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.918+596_918+597ins others(19): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | |||||||
| chr19:15650779 | C | CGTTCTTT others(138): Show |
1 | a0001c0001t0053g0201 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.918+596_918+597ins others(145): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | |||||||
| chr19:15650779 | C | CGTTCTTT others(149): Show |
1 | a0001c0001t0010g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.918+596_918+597ins others(156): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | |||||||
| chr19:15650779 | C | CGTTCTTT others(149): Show |
2 | a0001c0001t0012g0205 a0001c0001t0019g0307 |
2 | NA19043.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.918+596_918+597ins others(156): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | |||||||
| chr19:15650779 | C | CGTTCTTT others(153): Show |
4 | a0001c0001t0008g0202 a0001c0001t0008g0207 a0001c0001t0010g0181 others(1): Show |
4 | HG01168.hp2 HG01255.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+596_918+597ins others(160): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | |||||||
| chr19:15650779 | C | CGTTCTTT others(157): Show |
4 | a0001c0001t0008g0019 a0001c0001t0008g0208 a0001c0001t0010g0019 others(1): Show |
4 | HG01081.hp1 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+596_918+597ins others(164): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | |||||||
| chr19:15650779 | C | CGTTCTTT others(161): Show |
1 | a0001c0001t0022g0209 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.918+596_918+597ins others(168): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | |||||||
| chr19:15650779 | C | CGTTCTTT others(161): Show |
1 | a0001c0001t0010g0180 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.918+596_918+597ins others(168): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | |||||||
| chr19:15650779 | C | CGTTCTTT others(153): Show |
1 | a0001c0001t0008g0182 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.918+596_918+597ins others(160): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | |||||||
| chr19:15650779 | C | CGTTCTTT others(152): Show |
2 | a0001c0001t0027g0238 a0001c0001t0049g0297 |
2 | NA19063.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.918+596_918+597ins others(159): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | |||||||
| chr19:15650779 | C | CGTTCTTT others(157): Show |
2 | a0001c0001t0002g0252 a0001c0001t0002g0291 |
2 | HG00735.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.918+596_918+597ins others(164): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | |||||||
| chr19:15650779 | C | CGTTCTTT others(145): Show |
1 | a0002c0003t0003g0097 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.918+596_918+597ins others(152): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | |||||||
| chr19:15650779 | C | CGTTCTTT others(157): Show |
1 | a0002c0003t0003g0098 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.918+596_918+597ins others(164): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | |||||||
| chr19:15650779 | C | CGTTCTTT others(28): Show |
2 | a0001c0001t0002g0168 a0001c0001t0002g0285 |
2 | HG01257.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.918+596_918+597ins others(35): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | |||||||
| chr19:15650780 | T | C | 25 | a0001c0001t0002g0168 a0001c0001t0002g0252 a0001c0001t0002g0285 others(22): Show |
25 | HG00280.hp1 HG00735.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.918+597T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650780 | |||||||
| chr19:15650780 | T | G | 1 | a0001c0001t0043g0091 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.918+597T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650780 | |||||||
| chr19:15650780 | T | TTTCTTTC others(4): Show |
1 | a0001c0001t0076g0389 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.918+600_918+610dup others(11): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650780 | ||||||
| chr19:15650780 | T | TTTCTTTC others(8): Show |
31 | a0001c0002t0065g0066 a0001c0004t0005g0011 a0001c0004t0005g0012 others(28): Show |
33 | HG00558.hp2 HG00597.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.918+600_918+614dup others(15): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650780 | ||||||
| chr19:15650780 | T | TTTCTTTC others(113): Show |
4 | a0001c0002t0001g0345 a0001c0002t0001g0374 a0001c0002t0001g0375 others(1): Show |
4 | HG01081.hp2 HG01192.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+614_918+615ins others(120): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650780 | ||||||
| chr19:15650780 | T | TTTCTTTC others(12): Show |
2 | a0001c0001t0009g0148 a0001c0001t0077g0161 |
2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.918+599_918+617dup others(19): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650780 | ||||||
| chr19:15650780 | T | TTTCTTTC others(16): Show |
16 | a0001c0001t0002g0170 a0001c0001t0002g0295 a0001c0001t0006g0022 others(13): Show |
16 | HG01928.hp2 HG01975.hp1 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.918+617_918+618ins others(23): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650780 | ||||||
| chr19:15650780 | T | TTTCTTTC others(20): Show |
8 | a0001c0001t0002g0167 a0001c0001t0002g0229 a0001c0001t0002g0254 others(5): Show |
8 | HG00438.hp1 HG01255.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.918+617_918+618ins others(27): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650780 | ||||||
| chr19:15650780 | T | TTTCTTTC others(24): Show |
47 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(44): Show |
50 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.918+617_918+618ins others(31): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650780 | ||||||
| chr19:15650780 | T | TTTCTTTC others(28): Show |
37 | a0001c0001t0002g0223 a0001c0001t0002g0232 a0001c0001t0002g0240 others(34): Show |
37 | HG00099.hp1 HG01261.hp1 HG02015.hp1 others(34): Show |
intron_variant | MODIFIER | c.918+617_918+618ins others(35): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650780 | ||||||
| chr19:15650780 | T | TTTCTTTC others(32): Show |
23 | a0001c0001t0002g0162 a0001c0001t0002g0163 a0001c0001t0002g0164 others(20): Show |
24 | HG00544.hp1 HG00544.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.918+617_918+618ins others(39): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650780 | ||||||
| chr19:15650780 | T | TTTCTTTC others(36): Show |
5 | a0001c0001t0002g0271 a0001c0001t0006g0247 a0001c0001t0015g0213 others(2): Show |
5 | HG01943.hp1 HG01952.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+617_918+618ins others(43): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650780 | ||||||
| chr19:15650780 | T | TTTCTTTC others(40): Show |
2 | a0001c0001t0002g0226 a0001c0001t0015g0198 |
2 | HG04228.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.918+617_918+618ins others(47): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650780 | ||||||
| chr19:15650780 | T | TTTCTTTC others(44): Show |
1 | a0005c0012t0002g0272 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.918+617_918+618ins others(51): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650780 | ||||||
| chr19:15650783 | C | CTTTCTTT others(6): Show |
1 | a0011c0016t0042g0071 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.918+603_918+615dup others(13): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650783 | ||||||
| chr19:15650784 | T | TTTCTTTC others(4): Show |
22 | a0001c0001t0029g0155 a0001c0002t0001g0024 a0001c0002t0001g0025 others(19): Show |
25 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(22): Show |
intron_variant | MODIFIER | c.918+604_918+614dup others(11): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650784 | ||||||
| chr19:15650784 | T | TTTCTTTC others(8): Show |
39 | a0001c0001t0016g0158 a0002c0003t0001g0105 a0002c0003t0003g0001 others(36): Show |
45 | HG00408.hp2 HG00438.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.918+603_918+617dup others(15): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650784 | ||||||
| chr19:15650784 | T | TTTCTTTC others(12): Show |
1 | a0002c0003t0003g0115 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.918+617_918+618ins others(19): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650784 | ||||||
| chr19:15650784 | T | TTTCTTTC others(137): Show |
2 | a0002c0003t0003g0016 a0002c0003t0003g0132 |
3 | HG02717.hp2 NA19084.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.918+617_918+618ins others(144): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650784 | ||||||
| chr19:15650785 | T | TTCTTTCT others(25): Show |
1 | a0001c0001t0010g0178 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.918+617_918+618ins others(32): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650785 | ||||||
| chr19:15650788 | T | TTTCTTTC others(4): Show |
1 | a0002c0003t0010g0118 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.918+607_918+617dup others(11): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650788 | ||||||
| chr19:15650793 | T | TCCTTTCT others(23): Show |
1 | a0001c0001t0012g0159 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.918+610_918+611ins others(30): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650793 | |||||||
| chr19:15650793 | T | TTCTTTCT others(23): Show |
2 | a0001c0001t0012g0156 a0001c0001t0012g0157 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.918+617_918+618ins others(30): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650793 | ||||||
| chr19:15650797 | T | C | 2 | a0001c0002t0001g0309 a0001c0002t0001g0377 |
2 | HG01261.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.918+614T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650797 | |||||||
| chr19:15650797 | T | TTTCTTCT others(157): Show |
1 | a0001c0001t0043g0091 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.918+615_918+616ins others(164): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650797 | ||||||
| chr19:15650799 | C | CT | 3 | a0002c0003t0003g0017 a0002c0003t0003g0136 a0002c0003t0003g0139 |
4 | HG01074.hp2 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+617dupT | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650799 | ||||||
| chr19:15650799 | C | CTTCTT | 5 | a0002c0003t0003g0101 a0002c0003t0003g0109 a0002c0003t0003g0120 others(2): Show |
5 | HG01496.hp2 HG01975.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+617_918+618ins others(5): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650799 | ||||||
| chr19:15650799 | C | CTTTCTTT others(35): Show |
1 | a0001c0001t0026g0287 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.918+617_918+618ins others(42): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650799 | ||||||
| chr19:15650799 | C | CTTTCTTT others(39): Show |
1 | a0001c0001t0002g0253 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.918+617_918+618ins others(46): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650799 | ||||||
| chr19:15650799 | C | CTTTCTTT others(43): Show |
1 | a0001c0001t0002g0244 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.918+617_918+618ins others(50): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650799 | ||||||
| chr19:15650799 | C | CTTTCTTT others(47): Show |
1 | a0001c0001t0002g0248 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.918+617_918+618ins others(54): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650799 | ||||||
| chr19:15650799 | C | T | 1 | a0001c0004t0007g0072 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.918+616C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650799 | |||||||
| chr19:15650801 | C | T | 6 | a0001c0001t0081g0093 a0001c0001t0082g0092 a0001c0005t0004g0008 others(3): Show |
7 | HG00642.hp2 HG01099.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.918+618C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650801 | |||||||
| chr19:15650803 | C | T | 9 | a0001c0004t0007g0072 a0002c0003t0003g0017 a0002c0003t0003g0101 others(6): Show |
10 | HG01074.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.918+620C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650803 | |||||||
| chr19:15650805 | C | CT | 5 | a0002c0003t0003g0101 a0002c0003t0003g0109 a0002c0003t0003g0120 others(2): Show |
5 | HG01496.hp2 HG01975.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+624dupT | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650805 | ||||||
| chr19:15650805 | C | CTTCT | 11 | a0001c0001t0002g0020 a0001c0001t0002g0256 a0001c0001t0006g0219 others(8): Show |
13 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.918+623_918+626dup others(4): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650805 | ||||||
| chr19:15650805 | C | T | 5 | a0001c0001t0081g0093 a0001c0001t0082g0092 a0001c0005t0004g0047 others(2): Show |
5 | HG01099.hp2 HG01361.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+622C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650805 | |||||||
| chr19:15650806 | T | C | 2 | a0001c0005t0004g0048 a0002c0003t0003g0099 |
2 | HG01099.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.918+623T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650806 | |||||||
| chr19:15650806 | T | TC | 4 | a0001c0001t0002g0244 a0001c0001t0002g0248 a0001c0001t0002g0253 others(1): Show |
4 | NA18952.hp2 NA18985.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+623_918+624ins others(1): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650806 | |||||||
| chr19:15650806 | T | TTCTCTCT others(7): Show |
1 | a0001c0001t0002g0243 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.918+628_918+629ins others(14): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650806 | ||||||
| chr19:15650806 | T | TTCTCTTT others(3): Show |
5 | a0001c0001t0016g0158 a0001c0001t0029g0094 a0002c0003t0003g0114 others(2): Show |
5 | HG02559.hp1 HG02723.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+632_918+633ins others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650806 | ||||||
| chr19:15650806 | T | TTCTTTC | 3 | a0001c0001t0009g0172 a0001c0001t0013g0153 a0001c0002t0001g0199 |
3 | HG02572.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.918+626_918+627ins others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650806 | ||||||
| chr19:15650806 | T | TTCTTTCT others(1): Show |
7 | a0001c0001t0002g0220 a0001c0001t0002g0279 a0001c0001t0008g0019 others(4): Show |
7 | HG01081.hp1 HG01255.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.918+626_918+627ins others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650806 | ||||||
| chr19:15650806 | T | TTCTTTCT others(3): Show |
16 | a0001c0001t0002g0251 a0001c0001t0002g0258 a0001c0001t0002g0259 others(13): Show |
16 | HG01891.hp1 HG02129.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.918+626_918+627ins others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650806 | ||||||
| chr19:15650806 | T | TTCTTTCT others(5): Show |
41 | a0001c0001t0002g0163 a0001c0001t0002g0167 a0001c0001t0002g0221 others(38): Show |
41 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.918+626_918+627ins others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650806 | ||||||
| chr19:15650806 | T | TTTC | 3 | a0001c0001t0012g0157 a0001c0001t0012g0159 a0001c0002t0001g0309 |
3 | HG02145.hp1 HG03579.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.918+624_918+625ins others(3): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650806 | ||||||
| chr19:15650807 | T | C | 2 | a0001c0001t0081g0093 a0001c0001t0082g0092 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.918+624T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650807 | |||||||
| chr19:15650807 | TC | T | 9 | a0001c0001t0012g0156 a0001c0001t0043g0091 a0001c0002t0001g0377 others(6): Show |
10 | HG01074.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.918+625delC | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650807 | |||||||
| chr19:15650808 | C | CTCTT | 9 | a0001c0002t0001g0029 a0001c0002t0001g0329 a0001c0002t0001g0330 others(6): Show |
9 | HG00323.hp1 HG00621.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.918+683_918+686dup others(4): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650808 | ||||||
| chr19:15650808 | C | CTCTTTCT others(15): Show |
1 | a0002c0003t0003g0142 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.918+632_918+633ins others(22): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650808 | ||||||
| chr19:15650808 | C | CTCTTTCT others(1): Show |
5 | a0001c0002t0001g0317 a0001c0002t0001g0332 a0001c0002t0001g0346 others(2): Show |
5 | HG00733.hp2 HG02273.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+679_918+686dup others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650808 | ||||||
| chr19:15650808 | C | CTCTTTCT others(5): Show |
1 | a0001c0018t0001g0355 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.918+675_918+686dup others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650808 | ||||||
| chr19:15650808 | C | CTTTCTCT others(9): Show |
20 | a0001c0001t0002g0168 a0001c0001t0002g0170 a0001c0001t0002g0228 others(17): Show |
20 | HG01257.hp1 HG01358.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.918+626_918+627ins others(16): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650808 | ||||||
| chr19:15650808 | C | CTTTCTCT others(7): Show |
2 | a0001c0001t0009g0149 a0001c0001t0009g0174 |
2 | HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.918+626_918+627ins others(14): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650808 | ||||||
| chr19:15650808 | C | T | 7 | a0001c0001t0012g0157 a0001c0001t0012g0159 a0001c0001t0081g0093 others(4): Show |
7 | HG01099.hp2 HG01361.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.918+625C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650808 | |||||||
| chr19:15650808 | CTCTT | C | 22 | a0001c0001t0014g0354 a0001c0002t0001g0023 a0001c0002t0001g0319 others(19): Show |
23 | HG00609.hp2 HG00673.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.918+683_918+686del others(4): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650808 | ||||||
| chr19:15650808 | CTCTTTCT others(1): Show |
C | 7 | a0001c0002t0001g0327 a0001c0002t0001g0357 a0001c0002t0001g0358 others(4): Show |
7 | HG00140.hp2 HG01243.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.918+679_918+686del others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650808 | ||||||
| chr19:15650808 | CTCTTTCT others(5): Show |
C | 4 | a0001c0002t0001g0360 a0001c0002t0001g0382 a0001c0002t0001g0386 others(1): Show |
4 | HG02258.hp1 HG02735.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+675_918+686del others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650808 | ||||||
| chr19:15650810 | C | T | 64 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0162 others(61): Show |
66 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.918+627C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650810 | |||||||
| chr19:15650812 | T | C | 93 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(90): Show |
97 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.918+629T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650812 | |||||||
| chr19:15650812 | T | TTC | 9 | a0002c0003t0001g0105 a0002c0003t0003g0013 a0002c0003t0003g0106 others(6): Show |
10 | HG02040.hp2 HG02895.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.918+631_918+632dup others(2): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650812 | ||||||
| chr19:15650812 | T | TTCTCTC | 5 | a0001c0001t0029g0155 a0001c0001t0076g0389 a0002c0003t0003g0115 others(2): Show |
5 | HG02630.hp2 HG03453.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.918+632_918+633ins others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650812 | ||||||
| chr19:15650812 | T | TTCTCTCT others(3): Show |
1 | a0001c0001t0061g0095 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.918+632_918+633ins others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650812 | ||||||
| chr19:15650812 | T | TTCTTTCT others(98): Show |
1 | a0001c0002t0001g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.918+645_918+646ins others(105): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650812 | ||||||
| chr19:15650812 | T | TTCTTTCT others(102): Show |
4 | a0001c0002t0001g0343 a0001c0002t0001g0344 a0001c0002t0001g0365 others(1): Show |
4 | HG00140.hp1 HG02735.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+645_918+646ins others(109): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650812 | ||||||
| chr19:15650812 | T | TTCTTTCT others(94): Show |
1 | a0001c0002t0001g0349 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.918+645_918+646ins others(101): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650812 | ||||||
| chr19:15650812 | T | TTCTTTCT others(106): Show |
1 | a0001c0002t0001g0339 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.918+649_918+650ins others(113): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650812 | ||||||
| chr19:15650812 | T | TTCTTTCT others(121): Show |
1 | a0001c0005t0004g0007 | 2 | HG00741.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.918+649_918+650ins others(128): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650812 | ||||||
| chr19:15650812 | T | TTCTTTCT others(125): Show |
6 | a0001c0004t0005g0079 a0001c0004t0005g0085 a0001c0004t0005g0090 others(3): Show |
6 | HG03704.hp1 HG03831.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.918+649_918+650ins others(132): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650812 | ||||||
| chr19:15650814 | CTT | C | 22 | a0001c0001t0077g0161 a0002c0003t0003g0001 a0002c0003t0003g0002 others(19): Show |
26 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.918+633_918+634del others(2): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650814 | ||||||
| chr19:15650814 | CTTTCTT | C | 5 | a0002c0003t0003g0015 a0002c0003t0003g0016 a0002c0003t0003g0111 others(2): Show |
7 | HG04199.hp2 NA18954.hp2 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.918+633_918+638del others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650814 | ||||||
| chr19:15650816 | T | C | 86 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(83): Show |
92 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.918+633T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650816 | |||||||
| chr19:15650816 | T | TC | 6 | a0001c0005t0004g0047 a0002c0003t0003g0101 a0002c0003t0003g0109 others(3): Show |
6 | HG01496.hp2 HG01928.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.918+633_918+634ins others(1): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650816 | |||||||
| chr19:15650816 | T | TTCTTTCT others(102): Show |
1 | a0001c0002t0001g0334 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.918+645_918+646ins others(109): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650816 | ||||||
| chr19:15650816 | T | TTCTTTCT others(94): Show |
1 | a0001c0002t0001g0366 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.918+645_918+646ins others(101): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650816 | ||||||
| chr19:15650816 | T | TTCTTTCT others(98): Show |
5 | a0001c0002t0001g0025 a0001c0002t0001g0026 a0001c0002t0001g0340 others(2): Show |
7 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(4): Show |
intron_variant | MODIFIER | c.918+645_918+646ins others(105): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650816 | ||||||
| chr19:15650816 | T | TTCTTTCT others(117): Show |
1 | a0001c0004t0005g0089 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.918+645_918+646ins others(124): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650816 | ||||||
| chr19:15650816 | T | TTCTTTCT others(121): Show |
5 | a0001c0004t0005g0070 a0001c0004t0005g0075 a0001c0004t0005g0087 others(2): Show |
5 | HG01175.hp2 HG02040.hp1 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.918+649_918+650ins others(128): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650816 | ||||||
| chr19:15650816 | T | TTCTTTCT others(126): Show |
1 | a0001c0004t0011g0082 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.918+649_918+650ins others(133): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650816 | ||||||
| chr19:15650819 | T | A | 1 | a0001c0001t0009g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.918+636T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650819 | |||||||
| chr19:15650819 | T | TC | 2 | a0002c0003t0003g0017 a0002c0003t0003g0139 |
3 | HG01074.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.918+636_918+637ins others(1): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650819 | |||||||
| chr19:15650820 | T | C | 89 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0162 others(86): Show |
95 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.918+637T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650820 | |||||||
| chr19:15650820 | T | TTC | 5 | a0002c0003t0003g0101 a0002c0003t0003g0109 a0002c0003t0003g0120 others(2): Show |
5 | HG01496.hp2 HG01975.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+639_918+640dup others(2): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650820 | ||||||
| chr19:15650820 | T | TTCTTTCT others(94): Show |
2 | a0001c0002t0001g0024 a0001c0002t0001g0338 |
3 | HG00741.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.918+645_918+646ins others(101): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650820 | ||||||
| chr19:15650820 | T | TTCTTTCT others(117): Show |
5 | a0001c0004t0005g0011 a0001c0004t0005g0012 a0001c0004t0007g0088 others(2): Show |
5 | HG01243.hp1 HG01256.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.918+649_918+650ins others(124): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650820 | ||||||
| chr19:15650820 | T | TTCTTTCT others(121): Show |
1 | a0011c0016t0042g0071 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.918+649_918+650ins others(128): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650820 | ||||||
| chr19:15650822 | C | T | 1 | a0002c0003t0003g0136 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.918+639C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650822 | |||||||
| chr19:15650824 | T | C | 13 | a0002c0003t0003g0015 a0002c0003t0003g0016 a0002c0003t0003g0017 others(10): Show |
16 | HG01074.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.918+641T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650824 | |||||||
| chr19:15650824 | T | TCTTTCTT others(131): Show |
2 | a0001c0005t0004g0048 a0002c0003t0003g0099 |
2 | HG01099.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.918+641_918+642ins others(138): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650824 | |||||||
| chr19:15650824 | T | TTCTTCTT others(90): Show |
2 | a0001c0002t0001g0311 a0001c0002t0017g0324 |
2 | HG02451.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.918+645_918+646ins others(97): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650824 | ||||||
| chr19:15650824 | T | TTCTTCTT others(371): Show |
1 | a0001c0002t0001g0341 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.918+645_918+646ins others(378): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650824 | ||||||
| chr19:15650824 | T | TTCTTTCT others(121): Show |
1 | a0001c0004t0005g0067 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.918+649_918+650ins others(128): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650824 | ||||||
| chr19:15650824 | T | TTCTTTCT others(113): Show |
2 | a0001c0002t0065g0066 a0001c0004t0007g0171 |
2 | HG03942.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.918+649_918+650ins others(120): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650824 | ||||||
| chr19:15650824 | T | TTCTTTCT others(117): Show |
3 | a0001c0004t0005g0064 a0001c0004t0005g0080 a0001c0004t0036g0063 |
3 | HG00597.hp1 NA18985.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.918+649_918+650ins others(124): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650824 | ||||||
| chr19:15650826 | C | T | 2 | a0002c0003t0003g0017 a0002c0003t0003g0139 |
3 | HG01074.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.918+643C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650826 | |||||||
| chr19:15650828 | T | C | 6 | a0001c0004t0007g0072 a0002c0003t0003g0017 a0002c0003t0003g0110 others(3): Show |
7 | HG01074.hp2 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.918+645T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650828 | |||||||
| chr19:15650828 | T | TTCTTCTT others(113): Show |
2 | a0001c0004t0005g0081 a0001c0004t0038g0068 |
2 | HG00558.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.918+649_918+650ins others(120): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650828 | ||||||
| chr19:15650830 | C | T | 2 | a0002c0003t0003g0110 a0002c0003t0003g0121 |
2 | NA18983.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.918+647C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650830 | |||||||
| chr19:15650832 | T | C | 4 | a0002c0003t0003g0017 a0002c0003t0003g0110 a0002c0003t0003g0121 others(1): Show |
5 | HG01074.hp2 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+649T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650832 | |||||||
| chr19:15650836 | T | C | 2 | a0002c0003t0003g0110 a0002c0003t0003g0121 |
2 | NA18983.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.918+653T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650836 | |||||||
| chr19:15650836 | T | TTCTCTCT others(120): Show |
2 | a0001c0001t0081g0093 a0001c0001t0082g0092 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.918+656_918+657ins others(127): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650836 | ||||||
| chr19:15650836 | T | TTCTTTCT others(75): Show |
2 | a0001c0002t0017g0325 a0001c0002t0068g0326 |
2 | HG02615.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.918+666_918+667ins others(82): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650836 | ||||||
| chr19:15650844 | T | TTCTCTCT others(8): Show |
1 | a0001c0001t0076g0389 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.918+664_918+665ins others(15): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650844 | ||||||
| chr19:15650848 | T | C | 1 | a0005c0012t0002g0266 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.918+665T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650848 | |||||||
| chr19:15650852 | T | C | 12 | a0001c0001t0002g0168 a0001c0001t0002g0228 a0001c0001t0002g0285 others(9): Show |
12 | HG00597.hp2 HG01257.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.918+669T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650852 | |||||||
| chr19:15650856 | T | C | 44 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0170 others(41): Show |
45 | HG00438.hp1 HG00597.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.918+673T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650856 | |||||||
| chr19:15650856 | T | TTC | 3 | a0001c0001t0009g0148 a0001c0001t0010g0181 a0001c0001t0013g0153 |
3 | HG02818.hp2 HG03195.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.918+675_918+676dup others(2): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650856 | ||||||
| chr19:15650856 | T | TTCTCTCT others(3): Show |
3 | a0001c0001t0002g0232 a0001c0001t0002g0258 a0001c0001t0002g0262 |
3 | HG02015.hp1 NA18945.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.918+676_918+677ins others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650856 | ||||||
| chr19:15650860 | T | C | 53 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0170 others(50): Show |
54 | HG00438.hp1 HG00597.hp2 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.918+677T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650860 | |||||||
| chr19:15650860 | T | TTCTCTC | 3 | a0001c0001t0009g0150 a0001c0001t0013g0151 a0001c0001t0055g0270 |
3 | HG03041.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.918+680_918+681ins others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650860 | ||||||
| chr19:15650860 | T | TTCTCTCT others(1): Show |
8 | a0001c0001t0008g0186 a0001c0001t0008g0208 a0001c0001t0012g0184 others(5): Show |
8 | HG02004.hp2 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.918+680_918+681ins others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650860 | ||||||
| chr19:15650860 | T | TTCTCTCT others(3): Show |
2 | a0001c0001t0019g0307 a0006c0009t0052g0305 |
2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.918+680_918+681ins others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650860 | ||||||
| chr19:15650860 | T | TTCTCTCT others(5): Show |
10 | a0001c0001t0002g0252 a0001c0001t0002g0275 a0001c0001t0002g0286 others(7): Show |
10 | HG00735.hp1 NA18953.hp2 NA18957.hp2 others(7): Show |
intron_variant | MODIFIER | c.918+680_918+681ins others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650860 | ||||||
| chr19:15650860 | T | TTCTCTCT others(7): Show |
2 | a0001c0001t0002g0223 a0001c0001t0002g0239 |
2 | HG04184.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.918+680_918+681ins others(14): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650860 | ||||||
| chr19:15650864 | T | C | 82 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0170 others(79): Show |
83 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.918+681T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650864 | |||||||
| chr19:15650864 | T | TTCTCTCT others(1): Show |
4 | a0001c0001t0009g0173 a0001c0001t0009g0175 a0001c0001t0009g0176 others(1): Show |
4 | HG02723.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+684_918+685ins others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650864 | ||||||
| chr19:15650864 | T | TTCTCTCT others(3): Show |
2 | a0001c0001t0013g0152 a0001c0001t0013g0154 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.918+684_918+685ins others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650864 | ||||||
| chr19:15650864 | T | TTCTCTCT others(5): Show |
4 | a0001c0001t0008g0193 a0001c0001t0010g0204 a0001c0001t0015g0212 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+684_918+685ins others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650864 | ||||||
| chr19:15650864 | T | TTCTCTCT others(7): Show |
2 | a0001c0001t0010g0178 a0001c0001t0054g0187 |
2 | HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.918+684_918+685ins others(14): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650864 | ||||||
| chr19:15650864 | T | TTCTCTCT others(9): Show |
8 | a0001c0001t0002g0163 a0001c0001t0002g0243 a0001c0001t0002g0251 others(5): Show |
8 | HG02074.hp1 HG02129.hp2 HG04199.hp1 others(5): Show |
intron_variant | MODIFIER | c.918+684_918+685ins others(16): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650864 | ||||||
| chr19:15650864 | T | TTCTCTCT others(11): Show |
4 | a0001c0001t0002g0229 a0001c0001t0002g0245 a0001c0001t0006g0021 others(1): Show |
4 | HG01255.hp1 HG01358.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+684_918+685ins others(18): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650864 | ||||||
| chr19:15650864 | T | TTCTCTCT others(13): Show |
2 | a0001c0001t0002g0271 a0001c0001t0006g0218 |
2 | HG01943.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.918+684_918+685ins others(20): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650864 | ||||||
| chr19:15650864 | T | TTCTCTCT others(15): Show |
1 | a0001c0001t0002g0250 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.918+684_918+685ins others(22): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650864 | ||||||
| chr19:15650866 | C | CTTTCTTT others(5): Show |
4 | a0001c0004t0005g0060 a0001c0004t0011g0084 a0001c0005t0004g0041 others(1): Show |
4 | HG02486.hp1 HG03834.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+686_918+687ins others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650866 | ||||||
| chr19:15650866 | C | CTTTCTTT others(1): Show |
7 | a0001c0004t0007g0077 a0001c0004t0073g0054 a0001c0005t0004g0042 others(4): Show |
7 | HG00639.hp1 HG01192.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.918+686_918+687ins others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650866 | ||||||
| chr19:15650866 | C | CTTTG | 7 | a0001c0004t0005g0059 a0001c0004t0007g0058 a0001c0004t0007g0061 others(4): Show |
8 | HG01070.hp2 HG01071.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.918+686_918+687ins others(4): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650866 | ||||||
| chr19:15650866 | C | G | 52 | a0001c0002t0065g0066 a0001c0004t0005g0011 a0001c0004t0005g0012 others(49): Show |
56 | HG00558.hp2 HG00597.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.918+683C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650866 | |||||||
| chr19:15650866 | CTT | C | 5 | a0002c0003t0003g0103 a0002c0003t0003g0107 a0002c0003t0003g0108 others(2): Show |
5 | HG00408.hp2 HG02040.hp2 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+687_918+688del others(2): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650866 | ||||||
| chr19:15650868 | T | C | 160 | a0001c0001t0002g0163 a0001c0001t0002g0167 a0001c0001t0002g0168 others(157): Show |
169 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.918+685T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650868 | |||||||
| chr19:15650868 | T | TCTCTCTC others(15): Show |
1 | a0001c0001t0002g0220 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.918+685_918+686ins others(22): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650868 | |||||||
| chr19:15650868 | T | TCTCTCTC others(10): Show |
1 | a0001c0001t0049g0297 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.918+685_918+686ins others(17): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650868 | |||||||
| chr19:15650868 | T | TCTCTCTC others(12): Show |
1 | a0001c0001t0057g0237 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.918+685_918+686ins others(19): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650868 | |||||||
| chr19:15650868 | T | TTC | 9 | a0001c0001t0012g0156 a0001c0001t0012g0157 a0001c0001t0012g0159 others(6): Show |
9 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.918+686_918+687ins others(2): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650868 | ||||||
| chr19:15650868 | T | TTCTCTCT others(5): Show |
1 | a0001c0001t0076g0389 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.918+686_918+687ins others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650868 | ||||||
| chr19:15650868 | T | TTCTCTCT others(7): Show |
4 | a0001c0001t0002g0261 a0001c0001t0009g0149 a0001c0001t0025g0197 others(1): Show |
4 | HG02165.hp2 HG02683.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+686_918+687ins others(14): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650868 | ||||||
| chr19:15650868 | T | TTCTCTCT others(9): Show |
2 | a0001c0001t0008g0182 a0001c0001t0008g0202 |
2 | HG01168.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.918+686_918+687ins others(16): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650868 | ||||||
| chr19:15650868 | T | TTCTCTCT others(11): Show |
1 | a0001c0001t0027g0238 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.918+686_918+687ins others(18): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650868 | ||||||
| chr19:15650868 | T | TTCTCTCT others(13): Show |
28 | a0001c0001t0002g0162 a0001c0001t0002g0164 a0001c0001t0002g0222 others(25): Show |
28 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.918+686_918+687ins others(20): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650868 | ||||||
| chr19:15650868 | T | TTCTCTCT others(15): Show |
18 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(15): Show |
21 | HG00099.hp1 HG00280.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.918+686_918+687ins others(22): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650868 | ||||||
| chr19:15650868 | T | TTCTCTCT others(17): Show |
3 | a0001c0001t0002g0253 a0001c0001t0002g0257 a0001c0001t0002g0260 |
3 | NA18985.hp2 NA19065.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.918+686_918+687ins others(24): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650868 | ||||||
| chr19:15650868 | T | TTCTCTCT others(19): Show |
1 | a0001c0001t0002g0256 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.918+686_918+687ins others(26): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650868 | ||||||
| chr19:15650868 | T | TTCTTTCT others(3): Show |
1 | a0001c0010t0021g0145 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.918+686_918+687ins others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650868 | ||||||
| chr19:15650870 | T | C | 236 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(233): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.918+687T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650870 | |||||||
| chr19:15650883 | T | TCTCTCTC others(10): Show |
1 | a0001c0001t0002g0273 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.918+700_918+701ins others(17): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650883 | |||||||
| chr19:15650883 | T | TCTCTCTC others(14): Show |
1 | a0001c0001t0002g0264 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.918+700_918+701ins others(21): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650883 | |||||||
| chr19:15650883 | T | TCTCTCTC others(16): Show |
1 | a0001c0001t0006g0219 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.918+700_918+701ins others(23): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650883 | |||||||
| chr19:15650897 | C | T | 7 | a0001c0001t0009g0148 a0001c0001t0009g0149 a0001c0001t0009g0150 others(4): Show |
7 | HG02818.hp2 HG03195.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.918+714C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650897 | |||||||
| chr19:15651099 | C | T | 8 | a0001c0004t0005g0064 a0001c0004t0005g0067 a0001c0004t0005g0080 others(5): Show |
8 | HG00558.hp2 HG00597.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.918+916C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651099 | |||||||
| chr19:15651126 | GGCCTCCC others(466): Show |
G | 70 | a0001c0004t0005g0011 a0001c0004t0005g0012 a0001c0004t0005g0059 others(67): Show |
75 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.918+956_919-958del | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15651126 | ||||||
| chr19:15651169 | C | T | 1 | a0001c0001t0083g0196 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.918+986C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651169 | |||||||
| chr19:15651268 | C | T | 1 | a0001c0001t0002g0220 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.918+1085C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651268 | |||||||
| chr19:15651372 | CT | C | 240 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(237): Show |
252 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.919-1184delT | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15651372 | ||||||
| chr19:15651392 | G | A | 1 | a0001c0002t0001g0351 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.919-1177G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651392 | |||||||
| chr19:15651398 | C | T | 1 | a0002c0003t0003g0111 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.919-1171C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651398 | |||||||
| chr19:15651403 | T | C | 1 | a0001c0001t0043g0091 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.919-1166T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651403 | |||||||
| chr19:15651437 | G | A | 2 | a0001c0010t0021g0145 a0001c0010t0021g0146 |
2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.919-1132G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651437 | |||||||
| chr19:15651460 | T | C | 1 | a0001c0001t0002g0220 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.919-1109T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651460 | |||||||
| chr19:15651461 | G | T | 1 | a0001c0001t0002g0220 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.919-1108G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651461 | |||||||
| chr19:15651495 | C | G | 2 | a0001c0010t0021g0145 a0001c0010t0021g0146 |
2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.919-1074C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651495 | |||||||
| chr19:15651529 | G | A | 1 | a0001c0002t0065g0066 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.919-1040G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651529 | |||||||
| chr19:15651563 | A | G | 2 | a0001c0010t0021g0145 a0001c0010t0021g0146 |
2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.919-1006A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651563 | |||||||
| chr19:15651691 | CTGT | C | 234 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(231): Show |
246 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.919-877_919-875del others(3): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651691 | |||||||
| chr19:15651793 | T | C | 72 | a0001c0004t0005g0011 a0001c0004t0005g0012 a0001c0004t0005g0059 others(69): Show |
77 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.919-776T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651793 | |||||||
| chr19:15651868 | A | T | 72 | a0001c0004t0005g0011 a0001c0004t0005g0012 a0001c0004t0005g0059 others(69): Show |
77 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.919-701A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651868 | |||||||
| chr19:15651903 | C | T | 72 | a0001c0004t0005g0011 a0001c0004t0005g0012 a0001c0004t0005g0059 others(69): Show |
77 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.919-666C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651903 | |||||||
| chr19:15651979 | G | A | 2 | a0001c0010t0021g0145 a0001c0010t0021g0146 |
2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.919-590G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651979 | |||||||
| chr19:15652058 | T | TAGAGAG | 69 | a0001c0004t0005g0011 a0001c0004t0005g0012 a0001c0004t0005g0059 others(66): Show |
74 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.919-500_919-495dup others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15652058 | ||||||
| chr19:15652058 | T | TAGAGAGA others(3): Show |
1 | a0016c0017t0035g0057 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.919-504_919-495dup others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15652058 | ||||||
| chr19:15652128 | T | A | 72 | a0001c0004t0005g0011 a0001c0004t0005g0012 a0001c0004t0005g0059 others(69): Show |
77 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.919-441T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15652128 | |||||||
| chr19:15652283 | AT | A | 306 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(303): Show |
323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.919-279delT | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15652283 | ||||||
| chr19:15652438 | A | T | 306 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(303): Show |
323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.919-131A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15652438 | |||||||
| chr19:15652460 | C | G | 306 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(303): Show |
323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.919-109C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15652460 | |||||||
| chr19:15652710 | G | A | 5 | a0001c0001t0029g0094 a0001c0001t0029g0155 a0001c0001t0061g0095 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.985+75G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 8/12 | chr19 | 15652710 | |||||||
| chr19:15652767 | A | C | 72 | a0001c0004t0005g0011 a0001c0004t0005g0012 a0001c0004t0005g0059 others(69): Show |
77 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.986-56A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 8/12 | chr19 | 15652767 | |||||||
| chr19:15652957 | G | A | 1 | a0001c0002t0001g0346 | 1 | HG03654.hp1 | splice_region_variant&intron_variant | LOW | c.1115+5G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15652957 | |||||||
| chr19:15652962 | G | C | 5 | a0003c0006t0001g0312 a0003c0006t0001g0313 a0003c0006t0001g0314 others(2): Show |
5 | NA18947.hp1 NA18965.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1115+10G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15652962 | |||||||
| chr19:15652965 | G | A | 31 | a0001c0004t0071g0053 a0001c0004t0073g0054 a0001c0004t0074g0052 others(28): Show |
35 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1115+13G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15652965 | |||||||
| chr19:15652987 | T | A | 2 | a0001c0001t0009g0148 a0001c0001t0009g0150 |
2 | HG02818.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1115+35T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15652987 | |||||||
| chr19:15652988 | G | C | 72 | a0001c0004t0005g0011 a0001c0004t0005g0012 a0001c0004t0005g0059 others(69): Show |
77 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.1115+36G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15652988 | |||||||
| chr19:15653021 | G | A | 1 | a0001c0001t0077g0161 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1115+69G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653021 | |||||||
| chr19:15653119 | C | G | 72 | a0001c0004t0005g0011 a0001c0004t0005g0012 a0001c0004t0005g0059 others(69): Show |
77 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.1115+167C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653119 | |||||||
| chr19:15653179 | T | C | 2 | a0001c0010t0021g0145 a0001c0010t0021g0146 |
2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1115+227T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653179 | |||||||
| chr19:15653183 | A | T | 1 | a0002c0003t0003g0142 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1115+231A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653183 | |||||||
| chr19:15653188 | A | T | 70 | a0001c0004t0005g0011 a0001c0004t0005g0012 a0001c0004t0005g0059 others(67): Show |
75 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1115+236A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653188 | |||||||
| chr19:15653261 | T | G | 38 | a0001c0004t0005g0011 a0001c0004t0005g0012 a0001c0004t0005g0059 others(35): Show |
39 | HG00558.hp2 HG00597.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1115+309T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653261 | |||||||
| chr19:15653295 | T | G | 1 | a0001c0001t0002g0268 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1115+343T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653295 | |||||||
| chr19:15653320 | C | T | 306 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(303): Show |
323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.1115+368C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653320 | |||||||
| chr19:15653321 | A | G | 306 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(303): Show |
323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.1115+369A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653321 | |||||||
| chr19:15653410 | C | T | 234 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(231): Show |
246 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.1115+458C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653410 | |||||||
| chr19:15653506 | C | A | 33 | a0001c0004t0005g0011 a0001c0004t0005g0012 a0001c0004t0005g0064 others(30): Show |
34 | HG00558.hp2 HG00597.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.1115+554C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653506 | |||||||
| chr19:15653557 | A | C | 2 | a0006c0009t0051g0304 a0006c0009t0052g0305 |
2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1115+605A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653557 | |||||||
| chr19:15653560 | C | T | 1 | a0001c0002t0001g0199 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1115+608C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653560 | |||||||
| chr19:15653585 | G | A | 2 | a0007c0011t0008g0185 a0007c0011t0008g0192 |
2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1115+633G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653585 | |||||||
| chr19:15653593 | T | C | 1 | a0001c0002t0001g0343 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1115+641T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653593 | |||||||
| chr19:15653598 | G | A | 71 | a0001c0001t0039g0227 a0001c0004t0005g0011 a0001c0004t0005g0012 others(68): Show |
76 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.1115+646G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653598 | |||||||
| chr19:15653663 | T | C | 2 | a0001c0010t0021g0145 a0001c0010t0021g0146 |
2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1115+711T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653663 | |||||||
| chr19:15653704 | A | G | 309 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(306): Show |
326 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(323): Show |
intron_variant | MODIFIER | c.1115+752A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653704 | |||||||
| chr19:15653725 | AAGAGAGA others(4): Show |
A | 1 | a0001c0018t0001g0355 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1115+784_1115+794d others(13): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653725 | ||||||
| chr19:15653735 | G | GGA | 16 | a0001c0002t0001g0024 a0001c0002t0001g0026 a0001c0002t0001g0029 others(13): Show |
16 | HG00099.hp2 HG00140.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1115+833_1115+834d others(4): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | ||||||
| chr19:15653735 | G | GGAGA | 11 | a0001c0002t0001g0024 a0001c0002t0001g0147 a0001c0002t0001g0330 others(8): Show |
11 | HG00323.hp1 HG00639.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.1115+831_1115+834d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | ||||||
| chr19:15653735 | G | GGAGAGA | 9 | a0001c0002t0001g0199 a0001c0002t0001g0317 a0001c0002t0001g0334 others(6): Show |
9 | HG00140.hp1 HG00621.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1115+829_1115+834d others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | ||||||
| chr19:15653735 | G | GGAGAGAG others(1): Show |
3 | a0001c0002t0032g0029 a0003c0006t0001g0312 a0003c0006t0001g0313 |
3 | HG03669.hp2 NA19005.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1115+827_1115+834d others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | ||||||
| chr19:15653735 | G | GGAGAGAG others(3): Show |
1 | a0002c0007t0001g0130 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1115+825_1115+834d others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | ||||||
| chr19:15653735 | G | GGAGAGAG others(7): Show |
2 | a0001c0002t0023g0028 a0001c0002t0044g0028 |
2 | HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1115+821_1115+834d others(16): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | ||||||
| chr19:15653735 | G | GGAGAGAG others(9): Show |
1 | a0002c0007t0006g0131 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1115+819_1115+834d others(18): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | ||||||
| chr19:15653735 | G | GGAGAGAG others(19): Show |
1 | a0001c0002t0023g0318 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1115+809_1115+834d others(28): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | ||||||
| chr19:15653735 | GGA | G | 8 | a0001c0002t0001g0319 a0001c0002t0001g0336 a0001c0002t0001g0347 others(5): Show |
8 | HG00609.hp2 HG00639.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.1115+833_1115+834d others(4): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | ||||||
| chr19:15653735 | GGAGA | G | 25 | a0001c0002t0001g0026 a0001c0002t0001g0339 a0001c0002t0001g0340 others(22): Show |
29 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1115+831_1115+834d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | ||||||
| chr19:15653735 | GGAGAGA | G | 20 | a0001c0002t0001g0023 a0001c0002t0001g0025 a0001c0002t0001g0338 others(17): Show |
21 | HG00741.hp1 HG01070.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.1115+829_1115+834d others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | ||||||
| chr19:15653735 | GGAGAGAG others(1): Show |
G | 6 | a0001c0001t0006g0021 a0001c0001t0046g0021 a0001c0002t0001g0344 others(3): Show |
6 | HG00558.hp1 HG02622.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1115+827_1115+834d others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | ||||||
| chr19:15653735 | GGAGAGAG others(3): Show |
G | 189 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(186): Show |
194 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.1115+825_1115+834d others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | ||||||
| chr19:15653735 | GGAGAGAG others(5): Show |
G | 2 | a0001c0001t0043g0091 a0001c0002t0001g0335 |
2 | HG01515.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1115+823_1115+834d others(14): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | ||||||
| chr19:15653735 | GGAGAGAG others(7): Show |
G | 64 | a0001c0001t0002g0232 a0001c0001t0003g0231 a0001c0001t0003g0233 others(61): Show |
72 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.1115+821_1115+834d others(16): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | ||||||
| chr19:15653735 | GGAGAGAG others(9): Show |
G | 7 | a0001c0001t0029g0094 a0001c0001t0029g0155 a0001c0001t0061g0095 others(4): Show |
7 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1115+819_1115+834d others(18): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | ||||||
| chr19:15653757 | A | AGAGT | 12 | a0001c0001t0009g0148 a0001c0001t0009g0149 a0001c0001t0009g0150 others(9): Show |
12 | HG02723.hp1 HG02818.hp2 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.1115+808_1115+809i others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653757 | ||||||
| chr19:15653768 | G | T | 1 | a0001c0005t0004g0048 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1115+816G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653768 | |||||||
| chr19:15653773 | A | AGAGAGAG others(7): Show |
1 | a0001c0004t0074g0052 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1115+834_1115+835i others(16): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653773 | ||||||
| chr19:15653773 | A | AGAGAGAG others(5): Show |
1 | a0001c0004t0071g0053 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1115+832_1115+833i others(14): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653773 | ||||||
| chr19:15653773 | A | T | 303 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(300): Show |
320 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.1115+821A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653773 | |||||||
| chr19:15653857 | T | A | 2 | a0001c0001t0081g0093 a0001c0001t0082g0092 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1115+905T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653857 | |||||||
| chr19:15653875 | C | A | 2 | a0001c0001t0029g0094 a0001c0001t0061g0095 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1115+923C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653875 | |||||||
| chr19:15653958 | A | AG | 305 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(302): Show |
322 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(319): Show |
intron_variant | MODIFIER | c.1115+1009dupG | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653958 | ||||||
| chr19:15654060 | C | T | 218 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(215): Show |
230 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.1115+1108C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654060 | |||||||
| chr19:15654082 | CA | C | 72 | a0001c0001t0039g0227 a0001c0004t0005g0011 a0001c0004t0005g0012 others(69): Show |
77 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.1115+1131delA | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654082 | |||||||
| chr19:15654083 | A | C | 1 | a0016c0017t0035g0057 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1115+1131A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654083 | |||||||
| chr19:15654117 | G | C | 1 | a0002c0003t0003g0133 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1115+1165G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654117 | |||||||
| chr19:15654127 | T | C | 31 | a0001c0004t0071g0053 a0001c0004t0073g0054 a0001c0004t0074g0052 others(28): Show |
35 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1115+1175T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654127 | |||||||
| chr19:15654132 | C | T | 306 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(303): Show |
323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.1115+1180C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654132 | |||||||
| chr19:15654145 | C | T | 40 | a0001c0001t0039g0227 a0001c0001t0076g0389 a0001c0004t0005g0011 others(37): Show |
41 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1115+1193C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654145 | |||||||
| chr19:15654151 | T | C | 306 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(303): Show |
323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.1115+1199T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654151 | |||||||
| chr19:15654203 | C | T | 73 | a0001c0001t0039g0227 a0001c0004t0005g0011 a0001c0004t0005g0012 others(70): Show |
78 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1115+1251C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654203 | |||||||
| chr19:15654218 | T | G | 3 | a0001c0001t0008g0186 a0001c0001t0008g0207 a0001c0001t0048g0206 |
3 | HG01255.hp2 HG02004.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1115+1266T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654218 | |||||||
| chr19:15654347 | C | A | 1 | a0001c0001t0012g0205 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1115+1395C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654347 | |||||||
| chr19:15654351 | T | C | 306 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(303): Show |
323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.1115+1399T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654351 | |||||||
| chr19:15654476 | T | G | 3 | a0001c0002t0023g0028 a0001c0002t0023g0318 a0001c0002t0044g0028 |
3 | HG02572.hp1 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1115+1524T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654476 | |||||||
| chr19:15654615 | T | G | 16 | a0001c0001t0002g0162 a0001c0001t0002g0163 a0001c0001t0002g0164 others(13): Show |
16 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.1115+1663T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654615 | |||||||
| chr19:15654746 | A | C | 306 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(303): Show |
323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.1115+1794A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654746 | |||||||
| chr19:15654789 | G | A | 73 | a0001c0001t0039g0227 a0001c0004t0005g0011 a0001c0004t0005g0012 others(70): Show |
78 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1115+1837G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654789 | |||||||
| chr19:15654792 | G | A | 28 | a0001c0005t0004g0006 a0001c0005t0004g0007 a0001c0005t0004g0008 others(25): Show |
32 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.1115+1840G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654792 | |||||||
| chr19:15654792 | G | C | 61 | a0001c0001t0003g0231 a0001c0001t0003g0233 a0001c0001t0029g0094 others(58): Show |
69 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1115+1840G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654792 | |||||||
| chr19:15654959 | C | T | 4 | a0001c0001t0009g0172 a0001c0001t0009g0174 a0001c0001t0009g0176 others(1): Show |
4 | HG02723.hp1 HG03516.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1115+2007C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654959 | |||||||
| chr19:15654998 | G | A | 73 | a0001c0001t0039g0227 a0001c0004t0005g0011 a0001c0004t0005g0012 others(70): Show |
78 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1115+2046G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654998 | |||||||
| chr19:15655012 | C | A | 71 | a0001c0001t0039g0227 a0001c0004t0005g0011 a0001c0004t0005g0012 others(68): Show |
76 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.1115+2060C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655012 | |||||||
| chr19:15655259 | G | A | 73 | a0001c0001t0039g0227 a0001c0004t0005g0011 a0001c0004t0005g0012 others(70): Show |
78 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1115+2307G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655259 | |||||||
| chr19:15655265 | T | C | 2 | a0001c0010t0021g0145 a0001c0010t0021g0146 |
2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1115+2313T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655265 | |||||||
| chr19:15655277 | G | A | 1 | a0002c0003t0001g0105 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1115+2325G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655277 | |||||||
| chr19:15655344 | T | A | 1 | a0001c0001t0015g0179 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1115+2392T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655344 | |||||||
| chr19:15655403 | C | T | 13 | a0001c0001t0009g0148 a0001c0001t0009g0149 a0001c0001t0009g0150 others(10): Show |
13 | HG02723.hp1 HG02818.hp2 HG02976.hp1 others(10): Show |
intron_variant | MODIFIER | c.1115+2451C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655403 | |||||||
| chr19:15655404 | T | G | 2 | a0001c0001t0029g0094 a0001c0001t0061g0095 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1115+2452T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655404 | |||||||
| chr19:15655451 | G | A | 1 | a0001c0001t0015g0179 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1115+2499G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655451 | |||||||
| chr19:15655609 | G | A | 236 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(233): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.1116-2655G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655609 | |||||||
| chr19:15655634 | A | G | 2 | a0001c0010t0021g0145 a0001c0010t0021g0146 |
2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1116-2630A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655634 | |||||||
| chr19:15655660 | T | A | 306 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(303): Show |
323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.1116-2604T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655660 | |||||||
| chr19:15655705 | G | A | 28 | a0001c0005t0004g0006 a0001c0005t0004g0007 a0001c0005t0004g0008 others(25): Show |
32 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.1116-2559G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655705 | |||||||
| chr19:15655723 | G | A | 1 | a0001c0005t0004g0056 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1116-2541G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655723 | |||||||
| chr19:15655728 | C | T | 1 | a0001c0002t0001g0366 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1116-2536C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655728 | |||||||
| chr19:15655765 | G | A | 2 | a0001c0010t0021g0145 a0001c0010t0021g0146 |
2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1116-2499G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655765 | |||||||
| chr19:15655799 | A | G | 46 | a0001c0001t0008g0019 a0001c0001t0008g0182 a0001c0001t0008g0186 others(43): Show |
47 | HG00323.hp2 HG01081.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.1116-2465A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655799 | |||||||
| chr19:15655811 | T | A | 1 | a0001c0002t0001g0199 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1116-2453T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655811 | |||||||
| chr19:15655841 | G | A | 306 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(303): Show |
323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.1116-2423G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655841 | |||||||
| chr19:15655855 | C | T | 2 | a0001c0001t0029g0094 a0001c0001t0061g0095 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1116-2409C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655855 | |||||||
| chr19:15655890 | T | C | 1 | a0001c0018t0001g0355 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1116-2374T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655890 | |||||||
| chr19:15656056 | C | T | 171 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(168): Show |
175 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1116-2208C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656056 | |||||||
| chr19:15656084 | C | G | 306 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(303): Show |
323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.1116-2180C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656084 | |||||||
| chr19:15656085 | C | A | 2 | a0001c0010t0021g0145 a0001c0010t0021g0146 |
2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1116-2179C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656085 | |||||||
| chr19:15656117 | A | G | 1 | a0001c0002t0001g0023 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1116-2147A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656117 | |||||||
| chr19:15656205 | T | G | 3 | a0001c0002t0023g0028 a0001c0002t0023g0318 a0001c0002t0044g0028 |
3 | HG02572.hp1 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1116-2059T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656205 | |||||||
| chr19:15656241 | A | G | 158 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(155): Show |
162 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1116-2023A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656241 | |||||||
| chr19:15656247 | T | A | 2 | a0001c0001t0002g0271 a0001c0001t0002g0295 |
2 | HG01943.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.1116-2017T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656247 | |||||||
| chr19:15656284 | GTA | G | 31 | a0001c0004t0071g0053 a0001c0004t0073g0054 a0001c0004t0074g0052 others(28): Show |
35 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1116-1963_1116-196 others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656284 | ||||||
| chr19:15656284 | GTATA | G | 275 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(272): Show |
288 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.1116-1965_1116-196 others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656284 | ||||||
| chr19:15656469 | T | C | 233 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(230): Show |
245 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.1116-1795T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656469 | |||||||
| chr19:15656469 | T | TTATC | 4 | a0001c0002t0001g0363 a0001c0002t0001g0367 a0001c0002t0001g0382 others(1): Show |
4 | HG01346.hp1 HG02735.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1116-1743_1116-174 others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656469 | ||||||
| chr19:15656469 | TTATC | T | 35 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(32): Show |
38 | HG00280.hp2 HG00323.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1116-1743_1116-174 others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656469 | ||||||
| chr19:15656469 | TTATCTAT others(1): Show |
T | 24 | a0001c0002t0001g0026 a0001c0002t0001g0319 a0001c0002t0001g0327 others(21): Show |
25 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(22): Show |
intron_variant | MODIFIER | c.1116-1747_1116-174 others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656469 | ||||||
| chr19:15656469 | TTATCTAT others(5): Show |
T | 3 | a0001c0002t0001g0358 a0001c0002t0001g0366 a0001c0021t0001g0378 |
3 | HG02738.hp2 HG02965.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1116-1751_1116-174 others(16): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656469 | ||||||
| chr19:15656497 | CTATCTAT others(20): Show |
C | 3 | a0001c0002t0023g0028 a0001c0002t0023g0318 a0001c0002t0044g0028 |
3 | HG02572.hp1 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1116-1765_1116-173 others(31): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656497 | ||||||
| chr19:15656501 | C | G | 1 | a0001c0004t0007g0072 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1116-1763C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656501 | |||||||
| chr19:15656505 | CTATCTAT others(12): Show |
C | 4 | a0001c0001t0009g0173 a0002c0003t0003g0107 a0002c0003t0003g0116 others(1): Show |
4 | HG02040.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1116-1757_1116-173 others(23): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656505 | ||||||
| chr19:15656509 | C | G | 4 | a0001c0004t0005g0064 a0001c0004t0005g0067 a0001c0004t0005g0080 others(1): Show |
4 | HG00597.hp1 NA18985.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1116-1755C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656509 | |||||||
| chr19:15656509 | CTATCTAT others(8): Show |
C | 43 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0170 others(40): Show |
44 | HG00597.hp2 HG00673.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.1116-1753_1116-173 others(19): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656509 | ||||||
| chr19:15656513 | C | G | 3 | a0001c0004t0005g0081 a0001c0004t0007g0171 a0001c0004t0038g0068 |
3 | HG00558.hp2 HG02080.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1116-1751C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656513 | |||||||
| chr19:15656513 | CTATCTAT others(4): Show |
C | 165 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
169 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.1116-1749_1116-173 others(15): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656513 | ||||||
| chr19:15656517 | CTATCTAT | C | 26 | a0001c0001t0002g0162 a0001c0001t0002g0221 a0001c0001t0002g0222 others(23): Show |
26 | HG00544.hp1 HG01074.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1116-1745_1116-173 others(11): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656517 | ||||||
| chr19:15656521 | C | G | 13 | a0001c0001t0039g0227 a0001c0004t0005g0059 a0001c0004t0005g0060 others(10): Show |
14 | HG00621.hp2 HG00735.hp2 HG02273.hp2 others(11): Show |
intron_variant | MODIFIER | c.1116-1743C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656521 | |||||||
| chr19:15656521 | CTAT | C | 9 | a0001c0001t0002g0005 a0001c0001t0002g0254 a0001c0001t0002g0257 others(6): Show |
9 | HG02451.hp2 NA18945.hp2 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.1116-1741_1116-173 others(7): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656521 | ||||||
| chr19:15656524 | T | TC | 7 | a0001c0001t0002g0005 a0001c0001t0002g0284 a0001c0001t0025g0197 others(4): Show |
7 | HG00597.hp1 HG02165.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.1116-1740_1116-173 others(5): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656524 | |||||||
| chr19:15656524 | T | TCTATC | 3 | a0001c0004t0005g0081 a0001c0004t0007g0171 a0001c0004t0038g0068 |
3 | HG00558.hp2 HG02080.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1116-1740_1116-173 others(9): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656524 | |||||||
| chr19:15656524 | T | TCTATCTA others(6): Show |
12 | a0001c0001t0039g0227 a0001c0004t0005g0059 a0001c0004t0005g0060 others(9): Show |
13 | HG00621.hp2 HG00735.hp2 HG02273.hp2 others(10): Show |
intron_variant | MODIFIER | c.1116-1740_1116-173 others(17): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656524 | |||||||
| chr19:15656524 | T | TCTATCTA others(10): Show |
1 | a0001c0004t0071g0053 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1116-1740_1116-173 others(21): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656524 | |||||||
| chr19:15656524 | T | TCTATCTA others(30): Show |
1 | a0001c0005t0004g0030 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1116-1740_1116-173 others(41): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656524 | |||||||
| chr19:15656524 | T | TCTATCTA others(26): Show |
6 | a0001c0005t0004g0007 a0001c0005t0004g0033 a0001c0005t0004g0034 others(3): Show |
6 | HG00741.hp2 HG03654.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1116-1740_1116-173 others(37): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656524 | |||||||
| chr19:15656524 | T | TCTATCTA others(18): Show |
4 | a0001c0004t0005g0012 a0001c0004t0005g0070 a0001c0010t0021g0145 others(1): Show |
4 | HG01243.hp1 HG01361.hp2 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1116-1740_1116-173 others(29): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656524 | |||||||
| chr19:15656524 | T | TCTATCTA others(22): Show |
13 | a0001c0005t0004g0008 a0001c0005t0004g0031 a0001c0005t0004g0036 others(10): Show |
13 | HG00639.hp1 HG00642.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1116-1740_1116-173 others(33): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656524 | |||||||
| chr19:15656524 | T | TCTATGTA others(14): Show |
6 | a0001c0004t0005g0011 a0001c0004t0005g0075 a0001c0004t0005g0090 others(3): Show |
6 | HG01256.hp2 HG01258.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1116-1740_1116-173 others(25): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656524 | |||||||
| chr19:15656524 | T | TCTATGTA others(18): Show |
12 | a0001c0004t0073g0054 a0001c0004t0074g0052 a0001c0005t0004g0006 others(9): Show |
14 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1116-1740_1116-173 others(29): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656524 | |||||||
| chr19:15656524 | T | TGTATCTA others(10): Show |
11 | a0001c0004t0005g0078 a0001c0004t0005g0085 a0001c0004t0005g0087 others(8): Show |
11 | HG01175.hp2 HG01516.hp1 HG03710.hp1 others(8): Show |
intron_variant | MODIFIER | c.1116-1740_1116-173 others(21): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656524 | |||||||
| chr19:15656524 | T | TGTATCTA others(14): Show |
1 | a0001c0005t0004g0050 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1116-1740_1116-173 others(25): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656524 | |||||||
| chr19:15656550 | C | G | 1 | a0001c0002t0001g0364 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1116-1714C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656550 | |||||||
| chr19:15656570 | A | T | 1 | a0001c0001t0053g0201 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1116-1694A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656570 | |||||||
| chr19:15656582 | A | G | 233 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(230): Show |
245 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.1116-1682A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656582 | |||||||
| chr19:15656598 | ATCTG | A | 17 | a0001c0001t0009g0148 a0001c0001t0009g0149 a0001c0001t0009g0150 others(14): Show |
18 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1116-1662_1116-165 others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656598 | ||||||
| chr19:15656602 | GTCTA | G | 71 | a0001c0001t0039g0227 a0001c0004t0005g0011 a0001c0004t0005g0012 others(68): Show |
76 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.1116-1651_1116-164 others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656602 | ||||||
| chr19:15656626 | T | A | 4 | a0001c0001t0029g0094 a0001c0001t0061g0095 a0001c0001t0081g0093 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1116-1638T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656626 | |||||||
| chr19:15656728 | T | C | 74 | a0001c0001t0002g0234 a0001c0001t0039g0227 a0001c0004t0005g0011 others(71): Show |
79 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.1116-1536T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656728 | |||||||
| chr19:15656728 | T | TTATC | 26 | a0001c0001t0002g0271 a0001c0002t0001g0319 a0001c0002t0001g0330 others(23): Show |
26 | HG00323.hp1 HG00609.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.1116-1499_1116-149 others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656728 | ||||||
| chr19:15656728 | T | TTATCTAT others(1): Show |
45 | a0001c0002t0001g0025 a0001c0002t0001g0026 a0001c0002t0001g0027 others(42): Show |
47 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(44): Show |
intron_variant | MODIFIER | c.1116-1503_1116-149 others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656728 | ||||||
| chr19:15656728 | T | TTATCTAT others(5): Show |
11 | a0001c0001t0002g0295 a0001c0002t0001g0024 a0001c0002t0001g0311 others(8): Show |
12 | HG00558.hp1 HG01261.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.1116-1507_1116-149 others(16): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656728 | ||||||
| chr19:15656728 | TTATC | T | 4 | a0001c0001t0016g0166 a0001c0001t0016g0183 a0001c0002t0001g0327 others(1): Show |
4 | HG02735.hp2 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1116-1499_1116-149 others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656728 | ||||||
| chr19:15656760 | CT | C | 6 | a0001c0001t0015g0179 a0001c0001t0020g0160 a0001c0001t0020g0200 others(3): Show |
6 | HG01081.hp1 HG01175.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1116-1503delT | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656760 | |||||||
| chr19:15656764 | CTAT | C | 8 | a0001c0001t0015g0179 a0001c0001t0020g0160 a0001c0001t0020g0200 others(5): Show |
8 | HG01081.hp1 HG01175.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.1116-1499_1116-149 others(7): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656764 | |||||||
| chr19:15656765 | T | A | 39 | a0001c0001t0002g0268 a0001c0001t0008g0019 a0001c0001t0008g0186 others(36): Show |
42 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1116-1499T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656765 | |||||||
| chr19:15656766 | A | T | 39 | a0001c0001t0002g0268 a0001c0001t0008g0019 a0001c0001t0008g0186 others(36): Show |
42 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1116-1498A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656766 | |||||||
| chr19:15656767 | T | C | 39 | a0001c0001t0002g0268 a0001c0001t0008g0019 a0001c0001t0008g0186 others(36): Show |
42 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1116-1497T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656767 | |||||||
| chr19:15656767 | T | TCTATCAT others(1): Show |
78 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0162 others(75): Show |
81 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1116-1496_1116-149 others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656767 | ||||||
| chr19:15656767 | T | TCTATCTA others(5): Show |
109 | a0001c0001t0002g0004 a0001c0001t0002g0163 a0001c0001t0002g0168 others(106): Show |
112 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1116-1496_1116-149 others(16): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656767 | ||||||
| chr19:15656767 | T | TCTATCTA others(9): Show |
14 | a0001c0001t0002g0005 a0001c0001t0002g0215 a0001c0001t0002g0242 others(11): Show |
14 | HG01891.hp1 HG01981.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.1116-1496_1116-149 others(20): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656767 | ||||||
| chr19:15656780 | C | A | 248 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(245): Show |
262 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.1116-1484C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656780 | |||||||
| chr19:15656780 | C | CATCA | 58 | a0001c0001t0002g0234 a0001c0001t0002g0240 a0001c0001t0002g0264 others(55): Show |
61 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1116-1482_1116-148 others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656780 | ||||||
| chr19:15656797 | C | T | 306 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(303): Show |
323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.1116-1467C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656797 | |||||||
| chr19:15656826 | A | G | 158 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(155): Show |
162 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1116-1438A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656826 | |||||||
| chr19:15656841 | T | A | 3 | a0001c0001t0018g0190 a0001c0001t0018g0195 a0001c0001t0020g0189 |
3 | HG01109.hp2 HG02109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1116-1423T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656841 | |||||||
| chr19:15657000 | C | A | 306 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(303): Show |
323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.1116-1264C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657000 | |||||||
| chr19:15657001 | A | G | 309 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(306): Show |
326 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(323): Show |
intron_variant | MODIFIER | c.1116-1263A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657001 | |||||||
| chr19:15657059 | T | C | 2 | a0001c0010t0021g0145 a0001c0010t0021g0146 |
2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1116-1205T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657059 | |||||||
| chr19:15657096 | G | T | 2 | a0001c0001t0081g0093 a0001c0001t0082g0092 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1116-1168G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657096 | |||||||
| chr19:15657099 | A | G | 73 | a0001c0001t0039g0227 a0001c0004t0005g0011 a0001c0004t0005g0012 others(70): Show |
78 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1116-1165A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657099 | |||||||
| chr19:15657149 | A | G | 31 | a0001c0004t0071g0053 a0001c0004t0073g0054 a0001c0004t0074g0052 others(28): Show |
35 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1116-1115A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657149 | |||||||
| chr19:15657150 | T | A | 4 | a0001c0001t0029g0094 a0001c0001t0061g0095 a0001c0001t0081g0093 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1116-1114T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657150 | |||||||
| chr19:15657160 | G | T | 4 | a0001c0001t0012g0156 a0001c0001t0012g0157 a0001c0001t0012g0159 others(1): Show |
4 | HG02145.hp1 HG02559.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1116-1104G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657160 | |||||||
| chr19:15657188 | A | T | 1 | a0011c0016t0042g0071 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1116-1076A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657188 | |||||||
| chr19:15657189 | C | G | 71 | a0001c0001t0039g0227 a0001c0004t0005g0011 a0001c0004t0005g0012 others(68): Show |
76 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.1116-1075C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657189 | |||||||
| chr19:15657197 | T | A | 73 | a0001c0001t0039g0227 a0001c0004t0005g0011 a0001c0004t0005g0012 others(70): Show |
78 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1116-1067T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657197 | |||||||
| chr19:15657363 | C | A | 73 | a0001c0001t0039g0227 a0001c0004t0005g0011 a0001c0004t0005g0012 others(70): Show |
78 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1116-901C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657363 | |||||||
| chr19:15657377 | G | A | 73 | a0001c0001t0039g0227 a0001c0004t0005g0011 a0001c0004t0005g0012 others(70): Show |
78 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1116-887G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657377 | |||||||
| chr19:15657399 | C | A | 2 | a0001c0001t0029g0094 a0001c0001t0061g0095 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1116-865C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657399 | |||||||
| chr19:15657445 | C | G | 2 | a0001c0010t0021g0145 a0001c0010t0021g0146 |
2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1116-819C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657445 | |||||||
| chr19:15657504 | G | C | 73 | a0001c0001t0039g0227 a0001c0004t0005g0011 a0001c0004t0005g0012 others(70): Show |
78 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1116-760G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657504 | |||||||
| chr19:15657573 | G | A | 73 | a0001c0001t0039g0227 a0001c0004t0005g0011 a0001c0004t0005g0012 others(70): Show |
78 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1116-691G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657573 | |||||||
| chr19:15657593 | C | T | 73 | a0001c0001t0039g0227 a0001c0004t0005g0011 a0001c0004t0005g0012 others(70): Show |
78 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1116-671C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657593 | |||||||
| chr19:15657624 | C | T | 2 | a0001c0010t0021g0145 a0001c0010t0021g0146 |
2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1116-640C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657624 | |||||||
| chr19:15657660 | GTAT | G | 233 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(230): Show |
245 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.1116-599_1116-597d others(5): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15657660 | ||||||
| chr19:15657689 | T | C | 73 | a0001c0001t0039g0227 a0001c0004t0005g0011 a0001c0004t0005g0012 others(70): Show |
78 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1116-575T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657689 | |||||||
| chr19:15657754 | G | T | 2 | a0001c0010t0021g0145 a0001c0010t0021g0146 |
2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1116-510G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657754 | |||||||
| chr19:15657862 | T | G | 5 | a0001c0002t0001g0026 a0001c0002t0001g0330 a0001c0002t0001g0341 others(2): Show |
6 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(3): Show |
intron_variant | MODIFIER | c.1116-402T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657862 | |||||||
| chr19:15657981 | A | C | 306 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(303): Show |
323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.1116-283A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657981 | |||||||
| chr19:15657983 | C | T | 306 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(303): Show |
323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.1116-281C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657983 | |||||||
| chr19:15658214 | G | A | 1 | a0001c0001t0002g0279 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1116-50G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15658214 | |||||||
| chr19:15658429 | G | T | 1 | a0001c0005t0004g0009 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1249+32G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 10/12 | chr19 | 15658429 | |||||||
| chr19:15658443 | C | A | 233 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(230): Show |
245 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.1249+46C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 10/12 | chr19 | 15658443 | |||||||
| chr19:15658460 | A | C | 235 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(232): Show |
247 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.1250-31A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 10/12 | chr19 | 15658460 | |||||||
| chr19:15658569 | G | C | 236 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(233): Show |
247 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.1314+14G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 11/12 | chr19 | 15658569 | |||||||
| chr19:15658639 | A | G | 237 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(234): Show |
249 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.1314+84A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 11/12 | chr19 | 15658639 | |||||||
| chr19:15658668 | C | T | 158 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(155): Show |
162 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1315-59C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 11/12 | chr19 | 15658668 | |||||||
| chr19:15658719 | G | T | 236 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(233): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(245): Show |
splice_region_variant&intron_variant | LOW | c.1315-8G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 11/12 | chr19 | 15658719 | |||||||
| chr19:15658720 | C | T | 236 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(233): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(245): Show |
splice_region_variant&intron_variant | LOW | c.1315-7C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 11/12 | chr19 | 15658720 | |||||||
| chr19:15658815 | A | G | 309 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(306): Show |
326 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(323): Show |
splice_region_variant&intron_variant | LOW | c.1397+6A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15658815 | |||||||
| chr19:15658854 | A | G | 50 | a0001c0001t0008g0019 a0001c0001t0008g0182 a0001c0001t0008g0186 others(47): Show |
51 | HG00323.hp2 HG01081.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.1397+45A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15658854 | |||||||
| chr19:15658881 | A | G | 1 | a0001c0001t0006g0267 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1397+72A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15658881 | |||||||
| chr19:15658897 | C | G | 3 | a0001c0004t0071g0053 a0001c0004t0073g0054 a0001c0004t0074g0052 |
3 | HG02630.hp1 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1397+88C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15658897 | |||||||
| chr19:15658903 | G | A | 4 | a0001c0001t0008g0182 a0001c0001t0012g0184 a0001c0001t0016g0166 others(1): Show |
4 | HG02647.hp1 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1397+94G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15658903 | |||||||
| chr19:15658955 | A | G | 1 | a0001c0005t0075g0039 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1397+146A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15658955 | |||||||
| chr19:15658956 | C | T | 2 | a0001c0010t0021g0145 a0001c0010t0021g0146 |
2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1397+147C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15658956 | |||||||
| chr19:15658965 | A | G | 237 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(234): Show |
249 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.1397+156A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15658965 | |||||||
| chr19:15658968 | G | A | 1 | a0001c0004t0080g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1397+159G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15658968 | |||||||
| chr19:15658976 | C | T | 3 | a0001c0004t0007g0069 a0001c0004t0037g0083 a0011c0016t0042g0071 |
3 | HG01175.hp2 HG01516.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1397+167C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15658976 | |||||||
| chr19:15658995 | A | T | 237 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(234): Show |
249 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.1397+186A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15658995 | |||||||
| chr19:15659017 | C | G | 32 | a0001c0001t0053g0201 a0001c0004t0071g0053 a0001c0004t0073g0054 others(29): Show |
36 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.1398-203C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659017 | |||||||
| chr19:15659025 | T | TCTAGGCT others(12): Show |
5 | a0001c0002t0017g0324 a0001c0002t0017g0325 a0001c0002t0031g0321 others(2): Show |
5 | HG02451.hp2 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1398-192_1398-174d others(21): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 15659025 | ||||||
| chr19:15659032 | TG | T | 238 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(235): Show |
250 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.1398-182delG | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 15659032 | ||||||
| chr19:15659039 | T | C | 237 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(234): Show |
249 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.1398-181T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659039 | |||||||
| chr19:15659044 | G | T | 237 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(234): Show |
249 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.1398-176G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659044 | |||||||
| chr19:15659047 | C | G | 237 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(234): Show |
249 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.1398-173C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659047 | |||||||
| chr19:15659062 | G | T | 236 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(233): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.1398-158G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659062 | |||||||
| chr19:15659092 | C | T | 2 | a0001c0010t0021g0145 a0001c0010t0021g0146 |
2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1398-128C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659092 | |||||||
| chr19:15659100 | C | G | 2 | a0001c0001t0013g0151 a0001c0001t0013g0153 |
2 | HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1398-120C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659100 | |||||||
| chr19:15659101 | C | G | 1 | a0001c0005t0004g0048 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1398-119C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659101 | |||||||
| chr19:15659107 | C | T | 1 | a0001c0001t0002g0291 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1398-113C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659107 | |||||||
| chr19:15659155 | A | C | 135 | a0001c0001t0003g0231 a0001c0001t0003g0233 a0001c0001t0029g0094 others(132): Show |
148 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.1398-65A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659155 | |||||||
| chr19:15659157 | C | T | 2 | a0001c0010t0021g0145 a0001c0010t0021g0146 |
2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1398-63C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659157 | |||||||
| chr19:15659182 | A | T | 395 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(392): Show |
416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.1398-38A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659182 | |||||||
| chr19:15659183 | C | T | 2 | a0001c0010t0021g0145 a0001c0010t0021g0146 |
2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1398-37C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659183 | |||||||
| chr19:15659202 | T | C | 267 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(264): Show |
283 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.1398-18T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659202 | |||||||
| chr19:15659204 | C | T | 2 | a0001c0010t0021g0145 a0001c0010t0021g0146 |
2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1398-16C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659204 | |||||||
| chr19:15659208 | T | C | 126 | a0001c0001t0039g0227 a0001c0002t0001g0023 a0001c0002t0001g0024 others(123): Show |
131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1398-12T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659208 | |||||||
| chr19:15659209 | C | A | 1 | a0001c0002t0023g0318 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1398-11C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659209 | |||||||
| chr19:15659210 | C | T | 126 | a0001c0001t0039g0227 a0001c0002t0001g0023 a0001c0002t0001g0024 others(123): Show |
131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1398-10C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659210 | |||||||
| chr19:15659216 | C | G | 16 | a0001c0001t0009g0148 a0001c0001t0009g0149 a0001c0001t0009g0150 others(13): Show |
16 | HG02572.hp1 HG02723.hp1 HG02818.hp2 others(13): Show |
splice_region_variant&intron_variant | LOW | c.1398-4C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659216 | |||||||
| chr19:15659217 | A | T | 267 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(264): Show |
283 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(280): Show |
splice_region_variant&intron_variant | LOW | c.1398-3A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659217 |