Item | Value |
---|---|
geneid | 8529 |
ensemblid | ENSG00000186115.13 |
hgncid | 2645 |
symbol | CYP4F2 |
name | cytochrome P450 family 4 subfamily F member 2 |
refseq_nuc | NM_001082.5 |
refseq_prot | NP_001073.3 |
ensembl_nuc | ENST00000221700.11 |
ensembl_prot | ENSP00000221700.3 |
mane_status | MANE Select |
chr | chr19 |
start | 15878023 |
end | 15898074 |
strand | - |
ver | v1.2 |
region | chr19:15878023-15898074 |
region5000 | chr19:15873023-15903074 |
regionname0 | CYP4F2_chr19_15878023_15898074 |
regionname5000 | CYP4F2_chr19_15873023_15903074 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 520 | 378 | 90 | 80 | 149 | 18 | 40 | 111 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | MSQLS others(515): Show |
chr19 | 15873023 | 15903074 |
a0002 | 0/0 | 0 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 | |
a0003 | 0/1 | 520 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | MSQLS others(515): Show |
chr19 | 15873023 | 15903074 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1560 | 378 | 90 | 80 | 149 | 18 | 40 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | ATGTC others(1555): Show |
chr19 | 15873023 | 15903074 | ||
a0002c0000 | 0/0 | 0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 | |||
a0003c0003 | 0/1 | 1560 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | ATGTC others(1555): Show |
chr19 | 15873023 | 15903074 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2360 | 378 | 90 | 80 | 149 | 18 | 40 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | AGCAG others(2355): Show |
chr19 | 15873023 | 15903074 |
a0002c0000t0000 | 0/0 | 0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 | |
a0003c0003t0001 | 0/1 | 2360 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | AGCAG others(2355): Show |
chr19 | 15873023 | 15903074 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 1/0 | 378 | 90 | 80 | 149 | 18 | 40 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0002c0000t0000g0000 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0003c0003t0001g0003 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19054 | hp2 | a0002 | c0000 | t0000 | g0000 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
homoSapiens | chm13v2 | a0003 | c0003 | t0001 | g0003 | REF | REF | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:15878779 | G | T | 1 | a0001 | 14 | HG01346.hp2 HG02055.hp1 HG02109.hp2 others(11): Show |
missense_variant | MODERATE | c.1555C>A | p.Leu519Met | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 13/13 | 1605/2361 | 1555/1563 | 519/520 | chr19 | 15878779 | |||
chr19:15879621 | C | T | 1 | a0001 | 86 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(83): Show |
missense_variant | MODERATE | c.1297G>A | p.Val433Met | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 11/13 | 1347/2361 | 1297/1563 | 433/520 | chr19 | 15879621 | |||
chr19:15879844 | C | T | 1 | a0001 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.1169G>A | p.Arg390Gln | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 10/13 | 1219/2361 | 1169/1563 | 390/520 | chr19 | 15879844 | |||
chr19:15886018 | G | C | 1 | a0001 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.1021C>G | p.Leu341Val | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/13 | 1071/2361 | 1021/1563 | 341/520 | chr19 | 15886018 | |||
chr19:15890405 | C | A | 1 | a0001 | 7 | HG01069.hp2 HG02895.hp1 HG02896.hp1 others(4): Show |
missense_variant | MODERATE | c.554G>T | p.Gly185Val | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 6/13 | 604/2361 | 554/1563 | 185/520 | chr19 | 15890405 | |||
chr19:15897475 | C | T | 1 | a0001 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.137G>A | p.Arg46His | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/13 | 187/2361 | 137/1563 | 46/520 | chr19 | 15897475 | |||
chr19:15897476 | G | A | 1 | a0001 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.136C>T | p.Arg46Cys | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/13 | 186/2361 | 136/1563 | 46/520 | chr19 | 15897476 | |||
chr19:15897566 | C | G | 1 | a0001 | 2 | HG03453.hp1 HG03486.hp2 |
missense_variant | MODERATE | c.46G>C | p.Ala16Pro | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/13 | 96/2361 | 46/1563 | 16/520 | chr19 | 15897566 | |||
chr19:15897578 | A | C | 1 | a0001 | 49 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(46): Show |
missense_variant | MODERATE | c.34T>G | p.Trp12Gly | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/13 | 84/2361 | 34/1563 | 12/520 | chr19 | 15897578 | |||
chr19:15897592 | G | T | 1 | a0001 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.20C>A | p.Ser7Tyr | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/13 | 70/2361 | 20/1563 | 7/520 | chr19 | 15897592 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:15878813 | G | A | 1 | a0001c0001 | 1 | NA18989.hp1 | synonymous_variant | LOW | c.1521C>T | p.Arg507Arg | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 13/13 | 1571/2361 | 1521/1563 | 507/520 | chr19 | 15878813 | |||
chr19:15885947 | G | A | 1 | a0001c0001 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.1092C>T | p.Asp364Asp | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/13 | 1142/2361 | 1092/1563 | 364/520 | chr19 | 15885947 | |||
chr19:15886010 | G | A | 1 | a0001c0001 | 80 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(77): Show |
synonymous_variant | LOW | c.1029C>T | p.His343His | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/13 | 1079/2361 | 1029/1563 | 343/520 | chr19 | 15886010 | |||
chr19:15889510 | A | G | 1 | a0001c0001 | 2 | HG02257.hp2 HG02922.hp2 |
synonymous_variant | LOW | c.831T>C | p.Thr277Thr | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/13 | 881/2361 | 831/1563 | 277/520 | chr19 | 15889510 | |||
chr19:15889516 | G | A | 1 | a0001c0001 | 3 | HG01070.hp2 HG01071.hp2 HG02071.hp2 |
synonymous_variant | LOW | c.825C>T | p.Arg275Arg | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/13 | 875/2361 | 825/1563 | 275/520 | chr19 | 15889516 | |||
chr19:15889549 | G | A | 1 | a0001c0001 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.792C>T | p.His264His | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/13 | 842/2361 | 792/1563 | 264/520 | chr19 | 15889549 | |||
chr19:15892578 | G | C | 1 | a0001c0001 | 2 | HG02257.hp2 HG02922.hp2 |
synonymous_variant | LOW | c.348C>G | p.Ala116Ala | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 4/13 | 398/2361 | 348/1563 | 116/520 | chr19 | 15892578 | |||
chr19:15895513 | G | A | 1 | a0001c0001 | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
synonymous_variant | LOW | c.336C>T | p.Asn112Asn | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/13 | 386/2361 | 336/1563 | 112/520 | chr19 | 15895513 | |||
chr19:15895570 | T | G | 1 | a0001c0001 | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
synonymous_variant | LOW | c.279A>C | p.Gly93Gly | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/13 | 329/2361 | 279/1563 | 93/520 | chr19 | 15895570 | |||
chr19:15895603 | G | A | 1 | a0001c0001 | 37 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(34): Show |
synonymous_variant | LOW | c.246C>T | p.Ala82Ala | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/13 | 296/2361 | 246/1563 | 82/520 | chr19 | 15895603 | |||
chr19:15897447 | T | C | 1 | a0001c0001 | 64 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(61): Show |
synonymous_variant | LOW | c.165A>G | p.Pro55Pro | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/13 | 215/2361 | 165/1563 | 55/520 | chr19 | 15897447 | |||
chr19:15897513 | A | G | 1 | a0001c0001 | 1 | HG01123.hp2 | synonymous_variant | LOW | c.99T>C | p.His33His | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/13 | 149/2361 | 99/1563 | 33/520 | chr19 | 15897513 | |||
chr19:15897537 | G | A | 1 | a0001c0001 | 1 | NA18990.hp1 | synonymous_variant | LOW | c.75C>T | p.Val25Val | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/13 | 125/2361 | 75/1563 | 25/520 | chr19 | 15897537 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:15878230 | C | G | 1 | a0001c0001t0001 | 53 | HG00280.hp2 HG00733.hp2 HG01099.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*541G>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 13/13 | 541 | chr19 | 15878230 | ||||||
chr19:15878310 | C | T | 1 | a0001c0001t0001 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*461G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 13/13 | 461 | chr19 | 15878310 | ||||||
chr19:15878357 | C | T | 1 | a0001c0001t0001 | 15 | HG01346.hp2 HG02055.hp1 HG02109.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*414G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 13/13 | 414 | chr19 | 15878357 | ||||||
chr19:15878374 | G | A | 1 | a0001c0001t0001 | 81 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*397C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 13/13 | 397 | chr19 | 15878374 | ||||||
chr19:15878595 | C | T | 1 | a0001c0001t0001 | 179 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*176G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 13/13 | 176 | chr19 | 15878595 | ||||||
chr19:15878644 | A | G | 1 | a0001c0001t0001 | 4 | HG02451.hp2 HG02572.hp1 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*127T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 13/13 | 127 | chr19 | 15878644 | ||||||
chr19:15878699 | G | T | 1 | a0001c0001t0001 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*72C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 13/13 | 72 | chr19 | 15878699 | ||||||
chr19:15878713 | T | C | 1 | a0001c0001t0001 | 4 | HG01891.hp2 HG02698.hp2 HG02896.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*58A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 13/13 | 58 | chr19 | 15878713 | ||||||
chr19:15878744 | T | C | 1 | a0001c0001t0001 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*27A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 13/13 | 27 | chr19 | 15878744 | ||||||
chr19:15898051 | G | A | 1 | a0001c0001t0001 | 3 | HG02486.hp2 HG02717.hp1 HG03486.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-27C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/13 | chr19 | 15898051 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:15879061 | T | A | 1 | a0001c0001t0001g0001 | 99 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1398-125A>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 12/12 | chr19 | 15879061 | |||||||
chr19:15879238 | A | G | 1 | a0001c0001t0001g0001 | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.1397+108T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 12/12 | chr19 | 15879238 | |||||||
chr19:15879454 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1315-26A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 11/12 | chr19 | 15879454 | |||||||
chr19:15879455 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1315-27A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 11/12 | chr19 | 15879455 | |||||||
chr19:15879700 | G | T | 1 | a0001c0001t0001g0001 | 5 | HG02145.hp1 HG02559.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1250-32C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 10/12 | chr19 | 15879700 | |||||||
chr19:15879747 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1249+17G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 10/12 | chr19 | 15879747 | |||||||
chr19:15880200 | G | GA | 1 | a0001c0001t0001g0001 | 8 | HG00438.hp1 HG00544.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.1116-304dupT | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15880200 | |||||||
chr19:15880327 | G | GA | 1 | a0001c0001t0001g0001 | 10 | HG00741.hp2 HG01515.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.1116-431dupT | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15880327 | |||||||
chr19:15880623 | C | T | 1 | a0001c0001t0001g0001 | 79 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1116-726G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15880623 | |||||||
chr19:15880623 | CA | C | 1 | a0001c0001t0001g0001 | 44 | HG01069.hp1 HG01071.hp1 HG01346.hp2 others(41): Show |
intron_variant | MODIFIER | c.1116-727delT | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15880623 | |||||||
chr19:15880866 | C | T | 1 | a0001c0001t0001g0001 | 78 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.1116-969G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15880866 | |||||||
chr19:15880968 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1116-1071C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15880968 | |||||||
chr19:15881002 | T | TG | 1 | a0001c0001t0001g0001 | 3 | NA18986.hp2 NA18992.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1116-1106_1116-110 others(5): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881002 | |||||||
chr19:15881007 | GTGCACAC others(1): Show |
G | 1 | a0001c0001t0001g0001 | 3 | NA18986.hp2 NA18992.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1116-1118_1116-111 others(12): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881007 | |||||||
chr19:15881104 | C | G | 1 | a0001c0001t0001g0001 | 95 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.1116-1207G>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881104 | |||||||
chr19:15881382 | A | T | 1 | a0001c0001t0001g0001 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1116-1485T>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881382 | |||||||
chr19:15881509 | G | A | 1 | a0001c0001t0001g0001 | 12 | HG01891.hp1 HG02145.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1116-1612C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881509 | |||||||
chr19:15881543 | T | C | 1 | a0001c0001t0001g0001 | 7 | HG01192.hp1 HG01255.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1116-1646A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881543 | |||||||
chr19:15881565 | G | GGATA | 1 | a0001c0001t0001g0001 | 118 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.1116-1672_1116-166 others(8): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881565 | |||||||
chr19:15881565 | G | GGATAGAT others(1): Show |
1 | a0001c0001t0001g0001 | 20 | HG00408.hp1 HG00673.hp2 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.1116-1676_1116-166 others(12): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881565 | |||||||
chr19:15881565 | G | GGATAGAT others(5): Show |
1 | a0001c0001t0001g0001 | 2 | NA19081.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1116-1680_1116-166 others(16): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881565 | |||||||
chr19:15881565 | GGATA | G | 1 | a0001c0001t0001g0001 | 3 | HG02257.hp2 HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1116-1672_1116-166 others(8): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881565 | |||||||
chr19:15881565 | GGATAGAT others(13): Show |
G | 1 | a0001c0001t0001g0001 | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.1116-1688_1116-166 others(24): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881565 | |||||||
chr19:15881569 | A | G | 1 | a0001c0001t0001g0001 | 2 | HG01361.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1116-1672T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881569 | |||||||
chr19:15881712 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1116-1815C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881712 | |||||||
chr19:15881743 | A | G | 1 | a0001c0001t0001g0001 | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.1116-1846T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881743 | |||||||
chr19:15881801 | TA | T | 1 | a0001c0001t0001g0001 | 6 | HG01074.hp1 HG01168.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1116-1905delT | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881801 | |||||||
chr19:15881808 | A | T | 1 | a0001c0001t0001g0001 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1116-1911T>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881808 | |||||||
chr19:15881970 | C | T | 1 | a0001c0001t0001g0001 | 22 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1116-2073G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881970 | |||||||
chr19:15881972 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1116-2075G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881972 | |||||||
chr19:15882008 | G | T | 1 | a0001c0001t0001g0001 | 2 | HG00597.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1116-2111C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15882008 | |||||||
chr19:15882184 | G | A | 1 | a0001c0001t0001g0001 | 3 | HG02896.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1116-2287C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15882184 | |||||||
chr19:15882214 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1116-2317G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15882214 | |||||||
chr19:15882231 | C | T | 1 | a0001c0001t0001g0001 | 98 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1116-2334G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15882231 | |||||||
chr19:15882251 | G | GAA | 1 | a0001c0001t0001g0001 | 81 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.1116-2356_1116-235 others(6): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15882251 | |||||||
chr19:15882273 | A | G | 1 | a0001c0001t0001g0001 | 2 | HG00408.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1116-2376T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15882273 | |||||||
chr19:15882312 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1116-2415G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15882312 | |||||||
chr19:15882375 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1116-2478G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15882375 | |||||||
chr19:15882463 | AATGTTCT others(111): Show |
A | 1 | a0001c0001t0001g0001 | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.1116-2684_1116-256 others(4): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15882463 | |||||||
chr19:15882725 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1116-2828T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15882725 | |||||||
chr19:15882756 | G | T | 1 | a0001c0001t0001g0001 | 2 | NA18991.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.1116-2859C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15882756 | |||||||
chr19:15882795 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1116-2898T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15882795 | |||||||
chr19:15883016 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1115+2908G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883016 | |||||||
chr19:15883179 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1115+2745T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883179 | |||||||
chr19:15883301 | T | TAAAAATG others(312): Show |
1 | a0001c0001t0001g0001 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1115+2622_1115+262 others(323): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883301 | |||||||
chr19:15883301 | T | TAAAAATG others(313): Show |
1 | a0001c0001t0001g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1115+2622_1115+262 others(324): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883301 | |||||||
chr19:15883301 | T | TAAAAATG others(325): Show |
1 | a0001c0001t0001g0001 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1115+2622_1115+262 others(336): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883301 | |||||||
chr19:15883301 | T | TAAAAATG others(325): Show |
1 | a0001c0001t0001g0001 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1115+2622_1115+262 others(336): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883301 | |||||||
chr19:15883622 | C | T | 1 | a0001c0001t0001g0001 | 10 | HG01891.hp1 HG02145.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1115+2302G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883622 | |||||||
chr19:15883668 | A | T | 1 | a0001c0001t0001g0001 | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.1115+2256T>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883668 | |||||||
chr19:15883683 | T | C | 1 | a0001c0001t0001g0001 | 10 | HG01891.hp1 HG02145.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1115+2241A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883683 | |||||||
chr19:15883733 | AATCAACC others(9): Show |
A | 1 | a0001c0001t0001g0001 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1115+2175_1115+219 others(20): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883733 | |||||||
chr19:15883861 | C | T | 1 | a0001c0001t0001g0001 | 5 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1115+2063G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883861 | |||||||
chr19:15883920 | A | G | 1 | a0001c0001t0001g0001 | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1115+2004T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883920 | |||||||
chr19:15883931 | C | G | 1 | a0001c0001t0001g0001 | 2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1115+1993G>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883931 | |||||||
chr19:15883936 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1115+1988T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883936 | |||||||
chr19:15883988 | G | A | 1 | a0001c0001t0001g0001 | 2 | NA18994.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1115+1936C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883988 | |||||||
chr19:15884114 | G | A | 1 | a0001c0001t0001g0001 | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.1115+1810C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884114 | |||||||
chr19:15884223 | G | A | 1 | a0001c0001t0001g0001 | 10 | HG01891.hp1 HG02145.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1115+1701C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884223 | |||||||
chr19:15884338 | G | A | 1 | a0001c0001t0001g0001 | 35 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1115+1586C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884338 | |||||||
chr19:15884426 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1115+1498C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884426 | |||||||
chr19:15884429 | T | A | 1 | a0001c0001t0001g0001 | 2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1115+1495A>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884429 | |||||||
chr19:15884485 | A | T | 1 | a0001c0001t0001g0001 | 10 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1115+1439T>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884485 | |||||||
chr19:15884599 | C | A | 1 | a0001c0001t0001g0001 | 10 | HG01891.hp1 HG02145.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1115+1325G>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884599 | |||||||
chr19:15884678 | A | C | 1 | a0001c0001t0001g0001 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1115+1246T>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884678 | |||||||
chr19:15884711 | G | C | 1 | a0001c0001t0001g0001 | 2 | NA18979.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1115+1213C>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884711 | |||||||
chr19:15884741 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1115+1183G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884741 | |||||||
chr19:15884751 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1115+1173C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884751 | |||||||
chr19:15884755 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1115+1169T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884755 | |||||||
chr19:15884852 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1115+1072G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884852 | |||||||
chr19:15884944 | C | T | 1 | a0001c0001t0001g0001 | 6 | HG02145.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1115+980G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884944 | |||||||
chr19:15884978 | C | T | 1 | a0001c0001t0001g0001 | 35 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1115+946G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884978 | |||||||
chr19:15884992 | G | GCCTTGCT others(1): Show |
1 | a0001c0001t0001g0001 | 29 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.1115+931_1115+932i others(10): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884992 | |||||||
chr19:15884996 | G | T | 1 | a0001c0001t0001g0001 | 29 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.1115+928C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884996 | |||||||
chr19:15884997 | C | CT | 1 | a0001c0001t0001g0001 | 29 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.1115+926_1115+927i others(3): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884997 | |||||||
chr19:15885039 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1115+885C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885039 | |||||||
chr19:15885053 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1115+871G>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885053 | |||||||
chr19:15885092 | T | C | 1 | a0001c0001t0001g0001 | 7 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1115+832A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885092 | |||||||
chr19:15885118 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1115+806C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885118 | |||||||
chr19:15885164 | C | A | 1 | a0001c0001t0001g0001 | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1115+760G>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885164 | |||||||
chr19:15885168 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1115+756C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885168 | |||||||
chr19:15885198 | C | G | 1 | a0001c0001t0001g0001 | 5 | HG02818.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1115+726G>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885198 | |||||||
chr19:15885198 | C | T | 1 | a0001c0001t0001g0001 | 29 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.1115+726G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885198 | |||||||
chr19:15885211 | T | A | 1 | a0001c0001t0001g0001 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1115+713A>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885211 | |||||||
chr19:15885435 | A | G | 1 | a0001c0001t0001g0001 | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1115+489T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885435 | |||||||
chr19:15885482 | A | G | 1 | a0001c0001t0001g0001 | 35 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1115+442T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885482 | |||||||
chr19:15885539 | A | T | 1 | a0001c0001t0001g0001 | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1115+385T>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885539 | |||||||
chr19:15885672 | T | TA | 1 | a0001c0001t0001g0001 | 12 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1115+251_1115+252i others(3): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885672 | |||||||
chr19:15885672 | T | TG | 1 | a0001c0001t0001g0001 | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.1115+251_1115+252i others(3): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885672 | |||||||
chr19:15885687 | C | T | 1 | a0001c0001t0001g0001 | 14 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1115+237G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885687 | |||||||
chr19:15885775 | G | T | 1 | a0001c0001t0001g0001 | 4 | HG00280.hp1 HG00738.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1115+149C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885775 | |||||||
chr19:15885870 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG02559.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1115+54C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885870 | |||||||
chr19:15885914 | C | T | 1 | a0001c0001t0001g0001 | 7 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1115+10G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885914 | |||||||
chr19:15886097 | C | T | 1 | a0001c0001t0001g0001 | 29 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.986-44G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 8/12 | chr19 | 15886097 | |||||||
chr19:15886207 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.985+35G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 8/12 | chr19 | 15886207 | |||||||
chr19:15886326 | A | AC | 1 | a0001c0001t0001g0001 | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.919-19dupG | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15886326 | |||||||
chr19:15886332 | C | A | 1 | a0001c0001t0001g0001 | 4 | HG03130.hp2 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.919-24G>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15886332 | |||||||
chr19:15886506 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.919-198G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15886506 | |||||||
chr19:15886587 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.919-279A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15886587 | |||||||
chr19:15886612 | A | C | 1 | a0001c0001t0001g0001 | 35 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.919-304T>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15886612 | |||||||
chr19:15886711 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.919-403G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15886711 | |||||||
chr19:15886726 | G | C | 1 | a0001c0001t0001g0001 | 35 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.919-418C>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15886726 | |||||||
chr19:15886754 | G | A | 1 | a0001c0001t0001g0001 | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.919-446C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15886754 | |||||||
chr19:15886891 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.919-583A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15886891 | |||||||
chr19:15887101 | A | T | 1 | a0001c0001t0001g0001 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.919-793T>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887101 | |||||||
chr19:15887112 | C | T | 1 | a0001c0001t0001g0001 | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.919-804G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887112 | |||||||
chr19:15887131 | T | A | 1 | a0001c0001t0001g0001 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.919-823A>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887131 | |||||||
chr19:15887193 | G | GAC | 1 | a0001c0001t0001g0001 | 35 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.919-887_919-886dup others(2): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887193 | |||||||
chr19:15887209 | G | T | 1 | a0001c0001t0001g0001 | 10 | HG01891.hp1 HG02145.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.919-901C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887209 | |||||||
chr19:15887327 | T | A | 1 | a0001c0001t0001g0001 | 8 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.919-1019A>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887327 | |||||||
chr19:15887333 | T | G | 1 | a0001c0001t0001g0001 | 10 | HG01891.hp1 HG02145.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.919-1025A>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887333 | |||||||
chr19:15887372 | G | A | 1 | a0001c0001t0001g0001 | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.919-1064C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887372 | |||||||
chr19:15887385 | AAAACACA others(7): Show |
A | 1 | a0001c0001t0001g0001 | 5 | NA18965.hp2 NA18979.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.919-1091_919-1078d others(16): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887385 | |||||||
chr19:15887388 | A | T | 1 | a0001c0001t0001g0001 | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.919-1080T>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887388 | |||||||
chr19:15887492 | ATAGACAT others(81): Show |
A | 1 | a0001c0001t0001g0001 | 4 | HG03130.hp2 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.919-1272_919-1185d others(90): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887492 | |||||||
chr19:15887519 | GAC | G | 1 | a0001c0001t0001g0001 | 35 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.919-1213_919-1212d others(4): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887519 | |||||||
chr19:15887573 | C | T | 1 | a0001c0001t0001g0001 | 5 | NA18965.hp2 NA18979.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.919-1265G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887573 | |||||||
chr19:15887574 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG03491.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.919-1266C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887574 | |||||||
chr19:15887601 | G | C | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.919-1293C>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887601 | |||||||
chr19:15887822 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.919-1514T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887822 | |||||||
chr19:15887867 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.918+1556G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887867 | |||||||
chr19:15887898 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.918+1525C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887898 | |||||||
chr19:15887931 | C | T | 1 | a0001c0001t0001g0001 | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.918+1492G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887931 | |||||||
chr19:15888001 | C | T | 1 | a0001c0001t0001g0001 | 5 | HG02818.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+1422G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15888001 | |||||||
chr19:15888021 | CAGATAT | C | 1 | a0001c0001t0001g0001 | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.918+1396_918+1401d others(8): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15888021 | |||||||
chr19:15888194 | A | T | 1 | a0001c0001t0001g0001 | 4 | HG03130.hp2 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+1229T>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15888194 | |||||||
chr19:15888285 | C | T | 1 | a0001c0001t0001g0001 | 7 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.918+1138G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15888285 | |||||||
chr19:15888369 | T | C | 1 | a0001c0001t0001g0001 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.918+1054A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15888369 | |||||||
chr19:15888447 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.918+976G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15888447 | |||||||
chr19:15888614 | G | T | 1 | a0001c0001t0001g0001 | 6 | HG01069.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.918+809C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15888614 | |||||||
chr19:15888647 | AAC | A | 1 | a0001c0001t0001g0001 | 8 | HG02055.hp2 HG02257.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.918+774_918+775del others(2): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15888647 | |||||||
chr19:15888668 | A | G | 1 | a0001c0001t0001g0001 | 10 | HG01891.hp1 HG02145.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.918+755T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15888668 | |||||||
chr19:15888778 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.918+645A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15888778 | |||||||
chr19:15888788 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG01069.hp2 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.918+635T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15888788 | |||||||
chr19:15888817 | C | T | 1 | a0001c0001t0001g0001 | 35 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.918+606G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15888817 | |||||||
chr19:15889075 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.918+348A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15889075 | |||||||
chr19:15889091 | A | G | 1 | a0001c0001t0001g0001 | 10 | HG01891.hp1 HG02145.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.918+332T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15889091 | |||||||
chr19:15889134 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.918+289T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15889134 | |||||||
chr19:15889356 | C | T | 1 | a0001c0001t0001g0001 | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.918+67G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15889356 | |||||||
chr19:15889700 | G | T | 1 | a0001c0001t0001g0001 | 1 | HG01346.hp1 | splice_region_variant&intron_variant | LOW | c.648-7C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 6/12 | chr19 | 15889700 | |||||||
chr19:15889758 | C | A | 1 | a0001c0001t0001g0001 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.648-65G>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 6/12 | chr19 | 15889758 | |||||||
chr19:15889799 | T | A | 1 | a0001c0001t0001g0001 | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.648-106A>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 6/12 | chr19 | 15889799 | |||||||
chr19:15889906 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.648-213C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 6/12 | chr19 | 15889906 | |||||||
chr19:15889929 | G | A | 1 | a0001c0001t0001g0001 | 5 | NA18965.hp2 NA18979.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.648-236C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 6/12 | chr19 | 15889929 | |||||||
chr19:15890118 | C | A | 1 | a0001c0001t0001g0001 | 4 | HG00408.hp2 HG02056.hp1 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.647+194G>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 6/12 | chr19 | 15890118 | |||||||
chr19:15890230 | GT | G | 1 | a0001c0001t0001g0001 | 3 | HG02486.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.647+81delA | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 6/12 | chr19 | 15890230 | |||||||
chr19:15890465 | G | T | 1 | a0001c0001t0001g0001 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.526-32C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15890465 | |||||||
chr19:15890574 | A | C | 1 | a0001c0001t0001g0001 | 2 | HG00280.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.526-141T>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15890574 | |||||||
chr19:15890782 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.526-349G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15890782 | |||||||
chr19:15890789 | G | A | 1 | a0001c0001t0001g0001 | 5 | HG02818.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-356C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15890789 | |||||||
chr19:15890819 | G | A | 1 | a0001c0001t0001g0001 | 7 | HG01069.hp2 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.526-386C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15890819 | |||||||
chr19:15890924 | A | G | 1 | a0001c0001t0001g0001 | 2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.526-491T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15890924 | |||||||
chr19:15890930 | G | A | 1 | a0001c0001t0001g0001 | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.526-497C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15890930 | |||||||
chr19:15890934 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.526-501G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15890934 | |||||||
chr19:15890980 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.526-547T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15890980 | |||||||
chr19:15891000 | G | A | 1 | a0001c0001t0001g0001 | 5 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-567C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891000 | |||||||
chr19:15891010 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.526-577A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891010 | |||||||
chr19:15891038 | T | A | 1 | a0001c0001t0001g0001 | 4 | HG03130.hp2 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.526-605A>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891038 | |||||||
chr19:15891042 | G | T | 1 | a0001c0001t0001g0001 | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.526-609C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891042 | |||||||
chr19:15891378 | C | T | 1 | a0001c0001t0001g0001 | 5 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.525+931G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891378 | |||||||
chr19:15891487 | C | T | 1 | a0001c0001t0001g0001 | 72 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.525+822G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891487 | |||||||
chr19:15891552 | A | G | 1 | a0001c0001t0001g0001 | 5 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+757T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891552 | |||||||
chr19:15891583 | T | C | 1 | a0001c0001t0001g0001 | 9 | HG02818.hp2 HG02965.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.525+726A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891583 | |||||||
chr19:15891694 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.525+615C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891694 | |||||||
chr19:15891711 | G | A | 1 | a0001c0001t0001g0001 | 22 | HG01891.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.525+598C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891711 | |||||||
chr19:15891727 | C | A | 1 | a0001c0001t0001g0001 | 5 | HG02818.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.525+582G>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891727 | |||||||
chr19:15891792 | C | T | 1 | a0001c0001t0001g0001 | 5 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+517G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891792 | |||||||
chr19:15891846 | G | C | 1 | a0001c0001t0001g0001 | 6 | HG01109.hp1 HG02109.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.525+463C>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891846 | |||||||
chr19:15891951 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.525+358G>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891951 | |||||||
chr19:15892163 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.525+146G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15892163 | |||||||
chr19:15892600 | A | T | 1 | a0001c0001t0001g0001 | 2 | HG01361.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.344-18T>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15892600 | |||||||
chr19:15892833 | C | T | 1 | a0001c0001t0001g0001 | 10 | HG01891.hp1 HG02145.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.344-251G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15892833 | |||||||
chr19:15892841 | T | C | 1 | a0001c0001t0001g0001 | 60 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.344-259A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15892841 | |||||||
chr19:15892885 | C | T | 1 | a0001c0001t0001g0001 | 72 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.344-303G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15892885 | |||||||
chr19:15892908 | A | C | 1 | a0001c0001t0001g0001 | 2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.344-326T>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15892908 | |||||||
chr19:15892942 | T | C | 1 | a0001c0001t0001g0001 | 9 | HG01069.hp2 HG02895.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.344-360A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15892942 | |||||||
chr19:15893046 | A | G | 1 | a0001c0001t0001g0001 | 2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.344-464T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893046 | |||||||
chr19:15893053 | A | G | 1 | a0001c0001t0001g0001 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.344-471T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893053 | |||||||
chr19:15893061 | T | C | 1 | a0001c0001t0001g0001 | 10 | HG01891.hp1 HG02145.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.344-479A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893061 | |||||||
chr19:15893110 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.344-528C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893110 | |||||||
chr19:15893129 | T | C | 1 | a0001c0001t0001g0001 | 22 | HG01891.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.344-547A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893129 | |||||||
chr19:15893270 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.344-688C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893270 | |||||||
chr19:15893280 | T | TCCCAGAC others(11): Show |
1 | a0001c0001t0001g0001 | 3 | HG01070.hp2 HG01071.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.344-716_344-699dup others(18): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893280 | |||||||
chr19:15893323 | T | C | 1 | a0001c0001t0001g0001 | 3 | HG02074.hp1 HG02083.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.344-741A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893323 | |||||||
chr19:15893561 | A | T | 1 | a0001c0001t0001g0001 | 37 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.344-979T>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893561 | |||||||
chr19:15893586 | C | G | 1 | a0001c0001t0001g0001 | 49 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.344-1004G>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893586 | |||||||
chr19:15893672 | G | A | 1 | a0001c0001t0001g0001 | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.344-1090C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893672 | |||||||
chr19:15893728 | G | A | 1 | a0001c0001t0001g0001 | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.344-1146C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893728 | |||||||
chr19:15893771 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.344-1189C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893771 | |||||||
chr19:15893955 | C | G | 1 | a0001c0001t0001g0001 | 15 | HG01070.hp2 HG01071.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.344-1373G>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893955 | |||||||
chr19:15893990 | C | A | 1 | a0001c0001t0001g0001 | 37 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.344-1408G>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893990 | |||||||
chr19:15894042 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.344-1460C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894042 | |||||||
chr19:15894170 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.343+1336G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894170 | |||||||
chr19:15894179 | A | C | 1 | a0001c0001t0001g0001 | 4 | HG03130.hp2 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.343+1327T>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894179 | |||||||
chr19:15894180 | C | T | 1 | a0001c0001t0001g0001 | 5 | HG02818.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.343+1326G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894180 | |||||||
chr19:15894193 | C | T | 1 | a0001c0001t0001g0001 | 49 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.343+1313G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894193 | |||||||
chr19:15894206 | G | A | 1 | a0001c0001t0001g0001 | 37 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.343+1300C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894206 | |||||||
chr19:15894209 | T | C | 1 | a0001c0001t0001g0001 | 37 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.343+1297A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894209 | |||||||
chr19:15894271 | C | T | 1 | a0001c0001t0001g0001 | 6 | HG02818.hp2 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.343+1235G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894271 | |||||||
chr19:15894294 | C | T | 1 | a0001c0001t0001g0001 | 37 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.343+1212G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894294 | |||||||
chr19:15894344 | TGGTCCTG others(7): Show |
T | 1 | a0001c0001t0001g0001 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.343+1148_343+1161d others(16): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894344 | |||||||
chr19:15894350 | T | C | 1 | a0001c0001t0001g0001 | 15 | HG01070.hp2 HG01071.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.343+1156A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894350 | |||||||
chr19:15894375 | C | T | 1 | a0001c0001t0001g0001 | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.343+1131G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894375 | |||||||
chr19:15894386 | T | A | 1 | a0001c0001t0001g0001 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.343+1120A>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894386 | |||||||
chr19:15894422 | A | G | 1 | a0001c0001t0001g0001 | 37 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.343+1084T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894422 | |||||||
chr19:15894427 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.343+1079G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894427 | |||||||
chr19:15894432 | C | G | 1 | a0001c0001t0001g0001 | 3 | HG02486.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.343+1074G>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894432 | |||||||
chr19:15894466 | G | C | 1 | a0001c0001t0001g0001 | 37 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.343+1040C>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894466 | |||||||
chr19:15894467 | G | T | 1 | a0001c0001t0001g0001 | 37 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.343+1039C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894467 | |||||||
chr19:15894486 | C | T | 1 | a0001c0001t0001g0001 | 37 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.343+1020G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894486 | |||||||
chr19:15894490 | A | G | 1 | a0001c0001t0001g0001 | 27 | HG01070.hp2 HG01071.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.343+1016T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894490 | |||||||
chr19:15894593 | C | A | 1 | a0001c0001t0001g0001 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.343+913G>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894593 | |||||||
chr19:15894711 | G | T | 1 | a0001c0001t0001g0001 | 9 | HG01069.hp2 HG02895.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.343+795C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894711 | |||||||
chr19:15894764 | C | T | 1 | a0001c0001t0001g0001 | 37 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.343+742G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894764 | |||||||
chr19:15894775 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.343+731G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894775 | |||||||
chr19:15894805 | A | T | 1 | a0001c0001t0001g0001 | 37 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.343+701T>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894805 | |||||||
chr19:15894835 | G | A | 1 | a0001c0001t0001g0001 | 4 | HG03130.hp2 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.343+671C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894835 | |||||||
chr19:15894865 | G | T | 1 | a0001c0001t0001g0001 | 3 | HG01070.hp2 HG01071.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.343+641C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894865 | |||||||
chr19:15894931 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.343+575C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894931 | |||||||
chr19:15894972 | C | T | 1 | a0001c0001t0001g0001 | 8 | HG00639.hp1 HG00741.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.343+534G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894972 | |||||||
chr19:15894984 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.343+522G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894984 | |||||||
chr19:15895010 | G | T | 1 | a0001c0001t0001g0001 | 4 | HG03130.hp2 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.343+496C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895010 | |||||||
chr19:15895049 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.343+457G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895049 | |||||||
chr19:15895166 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.343+340C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895166 | |||||||
chr19:15895211 | G | C | 1 | a0001c0001t0001g0001 | 15 | HG01070.hp2 HG01071.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.343+295C>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895211 | |||||||
chr19:15895264 | T | A | 1 | a0001c0001t0001g0001 | 73 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.343+242A>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895264 | |||||||
chr19:15895288 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.343+218C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895288 | |||||||
chr19:15895291 | T | C | 1 | a0001c0001t0001g0001 | 49 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.343+215A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895291 | |||||||
chr19:15895335 | A | G | 1 | a0001c0001t0001g0001 | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.343+171T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895335 | |||||||
chr19:15895358 | A | G | 1 | a0001c0001t0001g0001 | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.343+148T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895358 | |||||||
chr19:15895368 | A | G | 1 | a0001c0001t0001g0001 | 49 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.343+138T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895368 | |||||||
chr19:15895425 | T | C | 1 | a0001c0001t0001g0001 | 2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.343+81A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895425 | |||||||
chr19:15895430 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.343+76C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895430 | |||||||
chr19:15895438 | C | A | 1 | a0001c0001t0001g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.343+68G>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895438 | |||||||
chr19:15895455 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.343+51G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895455 | |||||||
chr19:15895459 | A | G | 1 | a0001c0001t0001g0001 | 4 | HG03130.hp2 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.343+47T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895459 | |||||||
chr19:15895484 | C | CA | 1 | a0001c0001t0001g0001 | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.343+21dupT | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895484 | |||||||
chr19:15895735 | T | C | 1 | a0001c0001t0001g0001 | 15 | HG01070.hp2 HG01071.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.199-85A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15895735 | |||||||
chr19:15895801 | T | C | 1 | a0001c0001t0001g0001 | 37 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.199-151A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15895801 | |||||||
chr19:15895838 | T | A | 1 | a0001c0001t0001g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.199-188A>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15895838 | |||||||
chr19:15895867 | ATCTG | A | 1 | a0001c0001t0001g0001 | 37 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.199-221_199-218del others(4): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15895867 | |||||||
chr19:15895907 | C | CATCT | 1 | a0001c0001t0001g0001 | 46 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.199-258_199-257ins others(4): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15895907 | |||||||
chr19:15895908 | G | A | 1 | a0001c0001t0001g0001 | 4 | HG03017.hp2 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-258C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15895908 | |||||||
chr19:15896011 | C | A | 1 | a0001c0001t0001g0001 | 6 | HG02818.hp2 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-361G>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896011 | |||||||
chr19:15896044 | A | C | 1 | a0001c0001t0001g0001 | 49 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.199-394T>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896044 | |||||||
chr19:15896058 | GTCTA | G | 1 | a0001c0001t0001g0001 | 3 | HG02040.hp2 HG02451.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.199-412_199-409del others(4): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896058 | |||||||
chr19:15896065 | T | TATCC | 1 | a0001c0001t0001g0001 | 9 | HG01069.hp2 HG01981.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.199-416_199-415ins others(4): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896065 | |||||||
chr19:15896065 | T | TATCCATC others(1): Show |
1 | a0001c0001t0001g0001 | 11 | HG01891.hp1 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.199-416_199-415ins others(8): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896065 | |||||||
chr19:15896065 | T | TATCCATC others(5): Show |
1 | a0001c0001t0001g0001 | 4 | HG01070.hp2 HG01071.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-416_199-415ins others(12): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896065 | |||||||
chr19:15896065 | TATCTATC others(1): Show |
T | 1 | a0001c0001t0001g0001 | 7 | HG02257.hp2 HG02922.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-423_199-416del others(8): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896065 | |||||||
chr19:15896065 | TATCTATC others(5): Show |
T | 1 | a0001c0001t0001g0001 | 7 | HG02074.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.199-427_199-416del others(12): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896065 | |||||||
chr19:15896069 | T | C | 1 | a0001c0001t0001g0001 | 105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.199-419A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896069 | |||||||
chr19:15896069 | T | TATCC | 1 | a0001c0001t0001g0001 | 78 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.199-423_199-420dup others(4): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896069 | |||||||
chr19:15896069 | T | TATCCATC others(1): Show |
1 | a0001c0001t0001g0001 | 3 | HG02486.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.199-427_199-420dup others(8): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896069 | |||||||
chr19:15896069 | TATCC | T | 1 | a0001c0001t0001g0001 | 10 | HG01109.hp1 HG01123.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.199-423_199-420del others(4): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896069 | |||||||
chr19:15896182 | C | T | 1 | a0001c0001t0001g0001 | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.199-532G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896182 | |||||||
chr19:15896233 | G | GCTAT | 1 | a0001c0001t0001g0001 | 194 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.199-587_199-584dup others(4): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896233 | |||||||
chr19:15896233 | G | GCTATCTA others(1): Show |
1 | a0001c0001t0001g0001 | 11 | HG01081.hp2 HG01993.hp2 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.199-591_199-584dup others(8): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896233 | |||||||
chr19:15896233 | G | GCTATCTA others(5): Show |
1 | a0001c0001t0001g0001 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.199-595_199-584dup others(12): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896233 | |||||||
chr19:15896233 | GCTAT | G | 1 | a0001c0001t0001g0001 | 27 | HG00140.hp1 HG00438.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.199-587_199-584del others(4): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896233 | |||||||
chr19:15896233 | GCTATCTA others(1): Show |
G | 1 | a0001c0001t0001g0001 | 67 | HG00099.hp2 HG00544.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.199-591_199-584del others(8): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896233 | |||||||
chr19:15896233 | GCTATCTA others(5): Show |
G | 1 | a0001c0001t0001g0001 | 2 | HG00621.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.199-595_199-584del others(12): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896233 | |||||||
chr19:15896335 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.199-685C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896335 | |||||||
chr19:15896380 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.199-730C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896380 | |||||||
chr19:15896407 | G | T | 1 | a0001c0001t0001g0001 | 10 | HG01891.hp1 HG02145.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.199-757C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896407 | |||||||
chr19:15896508 | C | T | 1 | a0001c0001t0001g0001 | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.199-858G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896508 | |||||||
chr19:15896543 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.198+871A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896543 | |||||||
chr19:15896647 | G | A | 1 | a0001c0001t0001g0001 | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.198+767C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896647 | |||||||
chr19:15896652 | T | G | 1 | a0001c0001t0001g0001 | 2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.198+762A>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896652 | |||||||
chr19:15896723 | C | T | 1 | a0001c0001t0001g0001 | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.198+691G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896723 | |||||||
chr19:15896743 | T | C | 1 | a0001c0001t0001g0001 | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.198+671A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896743 | |||||||
chr19:15896830 | G | A | 1 | a0001c0001t0001g0001 | 3 | HG01109.hp1 HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.198+584C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896830 | |||||||
chr19:15896840 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.198+574G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896840 | |||||||
chr19:15896877 | G | A | 1 | a0001c0001t0001g0001 | 6 | HG01109.hp1 HG02109.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+537C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896877 | |||||||
chr19:15896960 | G | A | 1 | a0001c0001t0001g0001 | 15 | HG01070.hp2 HG01071.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.198+454C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896960 | |||||||
chr19:15896974 | A | G | 1 | a0001c0001t0001g0001 | 49 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.198+440T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896974 | |||||||
chr19:15896990 | G | A | 1 | a0001c0001t0001g0001 | 2 | NA18943.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.198+424C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896990 | |||||||
chr19:15897012 | C | T | 1 | a0001c0001t0001g0001 | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.198+402G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15897012 | |||||||
chr19:15897072 | T | G | 1 | a0001c0001t0001g0001 | 2 | HG02040.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.198+342A>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15897072 | |||||||
chr19:15897094 | T | C | 1 | a0001c0001t0001g0001 | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.198+320A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15897094 | |||||||
chr19:15897225 | A | T | 1 | a0001c0001t0001g0001 | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.198+189T>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15897225 | |||||||
chr19:15897289 | T | C | 1 | a0001c0001t0001g0001 | 37 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.198+125A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15897289 | |||||||
chr19:15897359 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.198+55G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15897359 | |||||||
chr19:15897624 | A | G | 1 | a0001c0001t0001g0001 | 37 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.-1-12T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/12 | chr19 | 15897624 | |||||||
chr19:15897634 | C | T | 1 | a0001c0001t0001g0001 | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.-1-22G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/12 | chr19 | 15897634 | |||||||
chr19:15897654 | G | A | 1 | a0001c0001t0001g0001 | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.-1-42C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/12 | chr19 | 15897654 | |||||||
chr19:15897659 | C | G | 1 | a0001c0001t0001g0001 | 49 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.-1-47G>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/12 | chr19 | 15897659 | |||||||
chr19:15897668 | G | C | 1 | a0001c0001t0001g0001 | 3 | HG03130.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-1-56C>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/12 | chr19 | 15897668 | |||||||
chr19:15897688 | A | G | 1 | a0001c0001t0001g0001 | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.-1-76T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/12 | chr19 | 15897688 | |||||||
chr19:15897702 | A | G | 1 | a0001c0001t0001g0001 | 64 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.-1-90T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/12 | chr19 | 15897702 | |||||||
chr19:15897829 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-2+197C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/12 | chr19 | 15897829 | |||||||
chr19:15897831 | A | AAGAG | 1 | a0001c0001t0001g0001 | 64 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.-2+191_-2+194dupCT others(2): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/12 | chr19 | 15897831 | |||||||
chr19:15897833 | G | A | 1 | a0001c0001t0001g0001 | 71 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.-2+193C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/12 | chr19 | 15897833 | |||||||
chr19:15897879 | CTG | C | 1 | a0001c0001t0001g0001 | 81 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.-2+145_-2+146delCA | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/12 | chr19 | 15897879 | |||||||
chr19:15897992 | A | AC | 1 | a0001c0001t0001g0001 | 15 | HG02257.hp2 HG02486.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.-2+33dupG | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/12 | chr19 | 15897992 | |||||||
chr19:15898012 | C | A | 1 | a0001c0001t0001g0001 | 15 | HG02257.hp2 HG02486.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.-2+14G>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/12 | chr19 | 15898012 |