Item | Value |
---|---|
geneid | 1548 |
ensemblid | ENSG00000255974.8 |
hgncid | 2610 |
symbol | CYP2A6 |
name | cytochrome P450 family 2 subfamily A member 6 |
refseq_nuc | NM_000762.6 |
refseq_prot | NP_000753.3 |
ensembl_nuc | ENST00000301141.10 |
ensembl_prot | ENSP00000301141.4 |
mane_status | MANE Select |
chr | chr19 |
start | 40843541 |
end | 40850447 |
strand | - |
ver | v1.2 |
region | chr19:40843541-40850447 |
region5000 | chr19:40838541-40855447 |
regionname0 | CYP2A6_chr19_40843541_40850447 |
regionname5000 | CYP2A6_chr19_40838541_40855447 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1482 | 381 | 88 | 78 | 154 | 18 | 42 | CYP2A6_chr19_40838541_40855447 | CYP2A6 | ATGCT others(1477): Show |
chr19 | 40838541 | 40855447 | ||
a0001c0002 | 0/1 | 1482 | 1 | 0 | 0 | 0 | 0 | 0 | CYP2A6_chr19_40838541_40855447 | CYP2A6 | ATGCT others(1477): Show |
chr19 | 40838541 | 40855447 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1761 | 381 | 88 | 78 | 154 | 18 | 42 | CYP2A6_chr19_40838541_40855447 | CYP2A6 | ATCTA others(1756): Show |
chr19 | 40838541 | 40855447 |
a0001c0002t0002 | 0/1 | 1760 | 1 | 0 | 0 | 0 | 0 | 0 | CYP2A6_chr19_40838541_40855447 | CYP2A6 | ATCTA others(1755): Show |
chr19 | 40838541 | 40855447 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 1/0 | 381 | 88 | 78 | 154 | 18 | 42 | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
a0001c0002t0002g0002 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0002 | REF | REF | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | CYP2A6_chr19_40838541_40855447 | CYP2A6 | chr19 | 40838541 | 40855447 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:40843595 | TCCTTCCT others(11845): Show |
T | 1 | a0001 | 6 | HG00438.hp1 HG02165.hp1 HG02738.hp1 others(3): Show |
exon_loss_variant | HIGH | c.-5021_*200del | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/9 | 1706/1761 | chr19 | 40843595 | ||||||
chr19:40843812 | C | T | 1 | a0001 | 2 | HG02056.hp1 HG02083.hp1 |
missense_variant | MODERATE | c.1469G>A | p.Ser490Asn | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 1490/1761 | 1469/1485 | 490/494 | chr19 | 40843812 | |||
chr19:40843827 | C | A | 1 | a0001 | 6 | HG00597.hp1 HG02080.hp2 NA18951.hp2 others(3): Show |
missense_variant | MODERATE | c.1454G>T | p.Arg485Leu | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 1475/1761 | 1454/1485 | 485/494 | chr19 | 40843827 | |||
chr19:40843845 | C | A | 1 | a0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
missense_variant | MODERATE | c.1436G>T | p.Gly479Val | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 1457/1761 | 1436/1485 | 479/494 | chr19 | 40843845 | |||
chr19:40843854 | T | C | 1 | a0001 | 3 | HG01346.hp2 HG01978.hp2 HG02683.hp2 |
missense_variant | MODERATE | c.1427A>G | p.Lys476Arg | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 1448/1761 | 1427/1485 | 476/494 | chr19 | 40843854 | |||
chr19:40843869 | A | G | 1 | a0001 | 26 | HG00408.hp2 HG00597.hp1 HG00673.hp2 others(23): Show |
missense_variant | MODERATE | c.1412T>C | p.Ile471Thr | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 1433/1761 | 1412/1485 | 471/494 | chr19 | 40843869 | |||
chr19:40843969 | T | A | 1 | a0001 | 4 | HG02622.hp2 HG03195.hp2 NA18906.hp1 others(1): Show |
missense_variant | MODERATE | c.1312A>T | p.Asn438Tyr | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 1333/1761 | 1312/1485 | 438/494 | chr19 | 40843969 | |||
chr19:40844677 | C | G | 1 | a0001 | 8 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(5): Show |
missense_variant | MODERATE | c.1257G>C | p.Glu419Asp | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/9 | 1278/1761 | 1257/1485 | 419/494 | chr19 | 40844677 | |||
chr19:40844682 | T | C | 1 | a0001 | 9 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(6): Show |
missense_variant | MODERATE | c.1252A>G | p.Asn418Asp | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/9 | 1273/1761 | 1252/1485 | 418/494 | chr19 | 40844682 | |||
chr19:40844759 | T | A | 1 | a0001 | 12 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(9): Show |
missense_variant | MODERATE | c.1175A>T | p.Tyr392Phe | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/9 | 1196/1761 | 1175/1485 | 392/494 | chr19 | 40844759 | |||
chr19:40845352 | A | G | 1 | a0001 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.1103T>C | p.Met368Thr | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/9 | 1124/1761 | 1103/1485 | 368/494 | chr19 | 40845352 | |||
chr19:40845362 | C | T | 1 | a0001 | 9 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(6): Show |
missense_variant | MODERATE | c.1093G>A | p.Val365Met | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/9 | 1114/1761 | 1093/1485 | 365/494 | chr19 | 40845362 | |||
chr19:40845416 | C | T | 1 | a0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
missense_variant | MODERATE | c.1039G>A | p.Ala347Thr | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/9 | 1060/1761 | 1039/1485 | 347/494 | chr19 | 40845416 | |||
chr19:40845998 | G | A | 1 | a0001 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.931C>T | p.Arg311Cys | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/9 | 952/1761 | 931/1485 | 311/494 | chr19 | 40845998 | |||
chr19:40846027 | C | G | 1 | a0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
missense_variant | MODERATE | c.902G>C | p.Gly301Ala | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/9 | 923/1761 | 902/1485 | 301/494 | chr19 | 40846027 | |||
chr19:40846048 | G | C | 1 | a0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
missense_variant | MODERATE | c.881C>G | p.Thr294Ser | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/9 | 902/1761 | 881/1485 | 294/494 | chr19 | 40846048 | |||
chr19:40846055 | C | T | 1 | a0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
missense_variant | MODERATE | c.874G>A | p.Val292Met | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/9 | 895/1761 | 874/1485 | 292/494 | chr19 | 40846055 | |||
chr19:40846885 | C | T | 1 | a0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
missense_variant | MODERATE | c.821G>A | p.Arg274His | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/9 | 842/1761 | 821/1485 | 274/494 | chr19 | 40846885 | |||
chr19:40846912 | C | T | 1 | a0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
missense_variant | MODERATE | c.794G>A | p.Arg265Gln | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/9 | 815/1761 | 794/1485 | 265/494 | chr19 | 40846912 | |||
chr19:40846937 | G | A | 1 | a0001 | 1 | HG00733.hp2 | missense_variant | MODERATE | c.769C>T | p.Arg257Cys | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/9 | 790/1761 | 769/1485 | 257/494 | chr19 | 40846937 | |||
chr19:40846991 | G | T | 1 | a0001 | 8 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(5): Show |
missense_variant | MODERATE | c.715C>A | p.Gln239Lys | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/9 | 736/1761 | 715/1485 | 239/494 | chr19 | 40846991 | |||
chr19:40848265 | C | T | 1 | a0001 | 2 | HG03225.hp2 NA18522.hp1 |
missense_variant | MODERATE | c.608G>A | p.Arg203His | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/9 | 629/1761 | 608/1485 | 203/494 | chr19 | 40848265 | |||
chr19:40848266 | G | A | 1 | a0001 | 2 | HG02976.hp1 HG06807.hp2 |
missense_variant | MODERATE | c.607C>T | p.Arg203Cys | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/9 | 628/1761 | 607/1485 | 203/494 | chr19 | 40848266 | |||
chr19:40848266 | G | T | 1 | a0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
missense_variant | MODERATE | c.607C>A | p.Arg203Ser | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/9 | 628/1761 | 607/1485 | 203/494 | chr19 | 40848266 | |||
chr19:40848293 | T | C | 1 | a0001 | 10 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(7): Show |
missense_variant | MODERATE | c.580A>G | p.Lys194Glu | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/9 | 601/1761 | 580/1485 | 194/494 | chr19 | 40848293 | |||
chr19:40848366 | A | C | 1 | a0001 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.507T>G | p.Asp169Glu | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/9 | 528/1761 | 507/1485 | 169/494 | chr19 | 40848366 | |||
chr19:40848616 | C | T | 1 | a0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
missense_variant&splice_region_variant | MODERATE | c.491G>A | p.Gly164Asp | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 3/9 | 512/1761 | 491/1485 | 164/494 | chr19 | 40848616 | |||
chr19:40848617 | C | G | 1 | a0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
missense_variant | MODERATE | c.490G>C | p.Gly164Arg | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 3/9 | 511/1761 | 490/1485 | 164/494 | chr19 | 40848617 | |||
chr19:40848623 | C | T | 1 | a0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
missense_variant | MODERATE | c.484G>A | p.Gly162Ser | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 3/9 | 505/1761 | 484/1485 | 162/494 | chr19 | 40848623 | |||
chr19:40848629 | G | T | 1 | a0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
missense_variant | MODERATE | c.478C>A | p.Leu160Ile | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 3/9 | 499/1761 | 478/1485 | 160/494 | chr19 | 40848629 | |||
chr19:40848633 | G | C | 1 | a0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
missense_variant | MODERATE | c.474C>G | p.Asp158Glu | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 3/9 | 495/1761 | 474/1485 | 158/494 | chr19 | 40848633 | |||
chr19:40848650 | C | A | 1 | a0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
missense_variant | MODERATE | c.457G>T | p.Ala153Ser | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 3/9 | 478/1761 | 457/1485 | 153/494 | chr19 | 40848650 | |||
chr19:40848716 | A | C | 1 | a0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
missense_variant | MODERATE | c.391T>G | p.Ser131Ala | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 3/9 | 412/1761 | 391/1485 | 131/494 | chr19 | 40848716 | |||
chr19:40848724 | C | A | 1 | a0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
missense_variant | MODERATE | c.383G>T | p.Arg128Leu | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 3/9 | 404/1761 | 383/1485 | 128/494 | chr19 | 40848724 | |||
chr19:40848755 | A | G | 1 | a0001 | 3 | HG03225.hp2 NA18522.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.352T>C | p.Phe118Leu | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 3/9 | 373/1761 | 352/1485 | 118/494 | chr19 | 40848755 | |||
chr19:40848757 | A | G | 1 | a0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
missense_variant | MODERATE | c.350T>C | p.Val117Ala | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 3/9 | 371/1761 | 350/1485 | 117/494 | chr19 | 40848757 | |||
chr19:40849799 | CTCTTGGG others(5641): Show |
C | 1 | a0001 | 2 | HG01928.hp1 NA20805.hp2 |
exon_loss_variant | HIGH | c.-5021_343+18del | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/9 | chr19 | 40849799 | |||||||
chr19:40849833 | C | G | 1 | a0001 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.328G>C | p.Val110Leu | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/9 | 349/1761 | 328/1485 | 110/494 | chr19 | 40849833 | |||
chr19:40849872 | C | T | 1 | a0001 | 2 | HG03492.hp2 HG03927.hp2 |
missense_variant | MODERATE | c.289G>A | p.Glu97Lys | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/9 | 310/1761 | 289/1485 | 97/494 | chr19 | 40849872 | |||
chr19:40849971 | G | A | 1 | a0001 | 9 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(6): Show |
missense_variant | MODERATE | c.190C>T | p.Arg64Cys | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/9 | 211/1761 | 190/1485 | 64/494 | chr19 | 40849971 | |||
chr19:40849980 | T | A | 1 | a0001 | 9 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(6): Show |
missense_variant&splice_region_variant | MODERATE | c.181A>T | p.Ile61Phe | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/9 | 202/1761 | 181/1485 | 61/494 | chr19 | 40849980 | |||
chr19:40850255 | G | T | 1 | a0001 | 10 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(7): Show |
missense_variant | MODERATE | c.172C>A | p.Leu58Ile | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/9 | 193/1761 | 172/1485 | 58/494 | chr19 | 40850255 | |||
chr19:40850261 | T | C | 1 | a0001 | 10 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(7): Show |
missense_variant | MODERATE | c.166A>G | p.Asn56Asp | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/9 | 187/1761 | 166/1485 | 56/494 | chr19 | 40850261 | |||
chr19:40850263 | T | C | 1 | a0001 | 10 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(7): Show |
missense_variant | MODERATE | c.164A>G | p.Tyr55Cys | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/9 | 185/1761 | 164/1485 | 55/494 | chr19 | 40850263 | |||
chr19:40850265 | C | T | 1 | a0001 | 10 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(7): Show |
missense_variant | MODERATE | c.162G>A | p.Met54Ile | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/9 | 183/1761 | 162/1485 | 54/494 | chr19 | 40850265 | |||
chr19:40850268 | C | G | 1 | a0001 | 10 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(7): Show |
missense_variant | MODERATE | c.159G>C | p.Gln53His | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/9 | 180/1761 | 159/1485 | 53/494 | chr19 | 40850268 | |||
chr19:40850333 | T | C | 1 | a0001 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.94A>G | p.Lys32Glu | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/9 | 115/1761 | 94/1485 | 32/494 | chr19 | 40850333 | |||
chr19:40850338 | T | C | 1 | a0001 | 10 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(7): Show |
missense_variant | MODERATE | c.89A>G | p.Lys30Arg | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/9 | 110/1761 | 89/1485 | 30/494 | chr19 | 40850338 | |||
chr19:40850389 | A | G | 1 | a0001 | 10 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(7): Show |
missense_variant | MODERATE | c.38T>C | p.Val13Ala | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/9 | 59/1761 | 38/1485 | 13/494 | chr19 | 40850389 | |||
chr19:40850411 | T | G | 1 | a0001 | 11 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(8): Show |
missense_variant | MODERATE | c.16A>C | p.Met6Leu | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/9 | 37/1761 | 16/1485 | 6/494 | chr19 | 40850411 | |||
chr19:40850414 | C | T | 1 | a0001 | 2 | NA18956.hp2 NA18991.hp1 |
missense_variant | MODERATE | c.13G>A | p.Gly5Arg | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/9 | 34/1761 | 13/1485 | 5/494 | chr19 | 40850414 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:40843841 | A | G | 1 | a0001c0001 | 4 | HG02723.hp2 HG03225.hp2 NA18522.hp1 others(1): Show |
synonymous_variant | LOW | c.1440T>C | p.Phe480Phe | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 1461/1761 | 1440/1485 | 480/494 | chr19 | 40843841 | |||
chr19:40843961 | G | A | 1 | a0001c0001 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1320C>T | p.Phe440Phe | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 1341/1761 | 1320/1485 | 440/494 | chr19 | 40843961 | |||
chr19:40844689 | G | A | 1 | a0001c0001 | 21 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(18): Show |
synonymous_variant | LOW | c.1245C>T | p.His415His | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/9 | 1266/1761 | 1245/1485 | 415/494 | chr19 | 40844689 | |||
chr19:40844710 | G | A | 1 | a0001c0001 | 29 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(26): Show |
synonymous_variant | LOW | c.1224C>T | p.Pro408Pro | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/9 | 1245/1761 | 1224/1485 | 408/494 | chr19 | 40844710 | |||
chr19:40844725 | A | G | 1 | a0001c0001 | 8 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(5): Show |
synonymous_variant | LOW | c.1209T>C | p.Ser403Ser | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/9 | 1230/1761 | 1209/1485 | 403/494 | chr19 | 40844725 | |||
chr19:40844743 | A | G | 1 | a0001c0001 | 23 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(20): Show |
synonymous_variant | LOW | c.1191T>C | p.Ser397Ser | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/9 | 1212/1761 | 1191/1485 | 397/494 | chr19 | 40844743 | |||
chr19:40845306 | G | A | 1 | a0001c0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
synonymous_variant | LOW | c.1149C>T | p.Phe383Phe | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/9 | 1170/1761 | 1149/1485 | 383/494 | chr19 | 40845306 | |||
chr19:40845333 | G | A | 1 | a0001c0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
synonymous_variant | LOW | c.1122C>T | p.Val374Val | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/9 | 1143/1761 | 1122/1485 | 374/494 | chr19 | 40845333 | |||
chr19:40845336 | T | C | 1 | a0001c0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
synonymous_variant | LOW | c.1119A>G | p.Arg373Arg | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/9 | 1140/1761 | 1119/1485 | 373/494 | chr19 | 40845336 | |||
chr19:40845450 | G | A | 1 | a0001c0001 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.1005C>T | p.Ile335Ile | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/9 | 1026/1761 | 1005/1485 | 335/494 | chr19 | 40845450 | |||
chr19:40846014 | G | C | 1 | a0001c0001 | 8 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(5): Show |
synonymous_variant | LOW | c.915C>G | p.Thr305Thr | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/9 | 936/1761 | 915/1485 | 305/494 | chr19 | 40846014 | |||
chr19:40846026 | C | T | 1 | a0001c0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
synonymous_variant | LOW | c.903G>A | p.Gly301Gly | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/9 | 924/1761 | 903/1485 | 301/494 | chr19 | 40846026 | |||
chr19:40846062 | T | C | 1 | a0001c0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
synonymous_variant | LOW | c.867A>G | p.Lys289Lys | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/9 | 888/1761 | 867/1485 | 289/494 | chr19 | 40846062 | |||
chr19:40846077 | C | T | 1 | a0001c0001 | 3 | HG02896.hp2 HG02897.hp1 HG03453.hp2 |
synonymous_variant | LOW | c.852G>A | p.Thr284Thr | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/9 | 873/1761 | 852/1485 | 284/494 | chr19 | 40846077 | |||
chr19:40846902 | A | G | 1 | a0001c0001 | 9 | HG00609.hp2 HG00621.hp1 HG01433.hp2 others(6): Show |
synonymous_variant | LOW | c.804T>C | p.Ile268Ile | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/9 | 825/1761 | 804/1485 | 268/494 | chr19 | 40846902 | |||
chr19:40846935 | G | A | 1 | a0001c0001 | 13 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(10): Show |
synonymous_variant | LOW | c.771C>T | p.Arg257Arg | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/9 | 792/1761 | 771/1485 | 257/494 | chr19 | 40846935 | |||
chr19:40847031 | C | T | 1 | a0001c0001 | 5 | HG01074.hp1 HG01243.hp1 HG01515.hp1 others(2): Show |
synonymous_variant | LOW | c.675G>A | p.Ser225Ser | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/9 | 696/1761 | 675/1485 | 225/494 | chr19 | 40847031 | |||
chr19:40848269 | A | G | 1 | a0001c0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
synonymous_variant | LOW | c.604T>C | p.Leu202Leu | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/9 | 625/1761 | 604/1485 | 202/494 | chr19 | 40848269 | |||
chr19:40848618 | A | C | 1 | a0001c0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
synonymous_variant | LOW | c.489T>G | p.Thr163Thr | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 3/9 | 510/1761 | 489/1485 | 163/494 | chr19 | 40848618 | |||
chr19:40848648 | C | T | 1 | a0001c0001 | 17 | HG00639.hp2 HG01496.hp2 HG01884.hp1 others(14): Show |
synonymous_variant | LOW | c.459G>A | p.Ala153Ala | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 3/9 | 480/1761 | 459/1485 | 153/494 | chr19 | 40848648 | |||
chr19:40848701 | G | T | 1 | a0001c0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
synonymous_variant | LOW | c.406C>A | p.Arg136Arg | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 3/9 | 427/1761 | 406/1485 | 136/494 | chr19 | 40848701 | |||
chr19:40848717 | G | A | 1 | a0001c0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
synonymous_variant | LOW | c.390C>T | p.Phe130Phe | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 3/9 | 411/1761 | 390/1485 | 130/494 | chr19 | 40848717 | |||
chr19:40848756 | T | C | 1 | a0001c0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
synonymous_variant | LOW | c.351A>G | p.Val117Val | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 3/9 | 372/1761 | 351/1485 | 117/494 | chr19 | 40848756 | |||
chr19:40849849 | T | C | 1 | a0001c0001 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.312A>G | p.Gln104Gln | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/9 | 333/1761 | 312/1485 | 104/494 | chr19 | 40849849 | |||
chr19:40849870 | C | T | 1 | a0001c0001 | 4 | HG02280.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
synonymous_variant | LOW | c.291G>A | p.Glu97Glu | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/9 | 312/1761 | 291/1485 | 97/494 | chr19 | 40849870 | |||
chr19:40849944 | A | G | 1 | a0001c0001 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.217T>C | p.Leu73Leu | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/9 | 238/1761 | 217/1485 | 73/494 | chr19 | 40849944 | |||
chr19:40849960 | G | A | 1 | a0001c0001 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.201C>T | p.Pro67Pro | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/9 | 222/1761 | 201/1485 | 67/494 | chr19 | 40849960 | |||
chr19:40850262 | G | A | 1 | a0001c0001 | 10 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(7): Show |
synonymous_variant | LOW | c.165C>T | p.Tyr55Tyr | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/9 | 186/1761 | 165/1485 | 55/494 | chr19 | 40850262 | |||
chr19:40850283 | C | T | 1 | a0001c0001 | 13 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(10): Show |
synonymous_variant | LOW | c.144G>A | p.Gln48Gln | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/9 | 165/1761 | 144/1485 | 48/494 | chr19 | 40850283 | |||
chr19:40850286 | C | G | 1 | a0001c0001 | 10 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(7): Show |
synonymous_variant | LOW | c.141G>C | p.Leu47Leu | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/9 | 162/1761 | 141/1485 | 47/494 | chr19 | 40850286 | |||
chr19:40850309 | A | G | 1 | a0001c0001 | 10 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(7): Show |
synonymous_variant | LOW | c.118T>C | p.Leu40Leu | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/9 | 139/1761 | 118/1485 | 40/494 | chr19 | 40850309 | |||
chr19:40850358 | A | G | 1 | a0001c0001 | 10 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(7): Show |
synonymous_variant | LOW | c.69T>C | p.Val23Val | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/9 | 90/1761 | 69/1485 | 23/494 | chr19 | 40850358 | |||
chr19:40850376 | T | C | 1 | a0001c0001 | 302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
synonymous_variant | LOW | c.51A>G | p.Val17Val | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/9 | 72/1761 | 51/1485 | 17/494 | chr19 | 40850376 | |||
chr19:40850405 | G | A | 1 | a0001c0001 | 34 | HG00408.hp2 HG00597.hp1 HG00673.hp2 others(31): Show |
synonymous_variant | LOW | c.22C>T | p.Leu8Leu | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/9 | 43/1761 | 22/1485 | 8/494 | chr19 | 40850405 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:40843592 | G | T | 1 | a0001c0001t0001 | 34 | HG00408.hp2 HG00597.hp1 HG00673.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*204C>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 204 | chr19 | 40843592 | ||||||
chr19:40843595 | T | C | 1 | a0001c0001t0001 | 34 | HG00408.hp2 HG00597.hp1 HG00673.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*201A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 201 | chr19 | 40843595 | ||||||
chr19:40843645 | G | C | 1 | a0001c0001t0001 | 151 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*151C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 151 | chr19 | 40843645 | ||||||
chr19:40843692 | G | C | 1 | a0001c0001t0001 | 148 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*104C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 104 | chr19 | 40843692 | ||||||
chr19:40843693 | C | G | 1 | a0001c0001t0001 | 148 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*103G>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 103 | chr19 | 40843693 | ||||||
chr19:40843698 | C | T | 1 | a0001c0001t0001 | 149 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*98G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 98 | chr19 | 40843698 | ||||||
chr19:40843700 | G | C | 1 | a0001c0001t0001 | 148 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*96C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 96 | chr19 | 40843700 | ||||||
chr19:40843707 | G | T | 1 | a0001c0001t0001 | 148 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*89C>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 89 | chr19 | 40843707 | ||||||
chr19:40843713 | G | T | 1 | a0001c0001t0001 | 148 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*83C>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 83 | chr19 | 40843713 | ||||||
chr19:40843714 | C | A | 1 | a0001c0001t0001 | 148 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*82G>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 82 | chr19 | 40843714 | ||||||
chr19:40843715 | T | C | 1 | a0001c0001t0001 | 148 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*81A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 81 | chr19 | 40843715 | ||||||
chr19:40843716 | G | C | 1 | a0001c0001t0001 | 148 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*80C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 80 | chr19 | 40843716 | ||||||
chr19:40843721 | C | T | 1 | a0001c0001t0001 | 148 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*75G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 75 | chr19 | 40843721 | ||||||
chr19:40843724 | C | T | 1 | a0001c0001t0001 | 148 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*72G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 72 | chr19 | 40843724 | ||||||
chr19:40843725 | T | C | 1 | a0001c0001t0001 | 148 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*71A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 71 | chr19 | 40843725 | ||||||
chr19:40843727 | C | G | 1 | a0001c0001t0001 | 148 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*69G>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 69 | chr19 | 40843727 | ||||||
chr19:40843729 | A | G | 1 | a0001c0001t0001 | 148 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*67T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 67 | chr19 | 40843729 | ||||||
chr19:40843731 | G | A | 1 | a0001c0001t0001 | 148 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*65C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 65 | chr19 | 40843731 | ||||||
chr19:40843735 | G | C | 1 | a0001c0001t0001 | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
3_prime_UTR_variant | MODIFIER | c.*61C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 61 | chr19 | 40843735 | ||||||
chr19:40843737 | T | C | 1 | a0001c0001t0001 | 148 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*59A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 59 | chr19 | 40843737 | ||||||
chr19:40843739 | T | C | 1 | a0001c0001t0001 | 148 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*57A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 57 | chr19 | 40843739 | ||||||
chr19:40843742 | G | A | 1 | a0001c0001t0001 | 148 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*54C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 54 | chr19 | 40843742 | ||||||
chr19:40843746 | T | C | 1 | a0001c0001t0001 | 148 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*50A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 50 | chr19 | 40843746 | ||||||
chr19:40843747 | GC | G | 1 | a0001c0001t0001 | 148 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*48delG | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 48 | chr19 | 40843747 | ||||||
chr19:40843773 | A | C | 1 | a0001c0001t0001 | 3 | HG02896.hp2 HG02897.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*23T>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 9/9 | 23 | chr19 | 40843773 | ||||||
chr19:40850437 | G | A | 1 | a0001c0001t0001 | 10 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-11C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/9 | 11 | chr19 | 40850437 | ||||||
chr19:40850443 | T | C | 1 | a0001c0001t0001 | 10 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(7): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-17A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/9 | chr19 | 40850443 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:40844038 | G | C | 1 | a0001c0001t0001g0001 | 6 | HG01433.hp2 HG03017.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.1304-61C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/8 | chr19 | 40844038 | |||||||
chr19:40844065 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1304-88T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/8 | chr19 | 40844065 | |||||||
chr19:40844066 | G | T | 1 | a0001c0001t0001g0001 | 3 | HG03098.hp2 HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1304-89C>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/8 | chr19 | 40844066 | |||||||
chr19:40844073 | A | G | 1 | a0001c0001t0001g0001 | 87 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.1304-96T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/8 | chr19 | 40844073 | |||||||
chr19:40844134 | A | G | 1 | a0001c0001t0001g0001 | 16 | HG00609.hp2 HG00621.hp1 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.1304-157T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/8 | chr19 | 40844134 | |||||||
chr19:40844145 | T | C | 1 | a0001c0001t0001g0001 | 16 | HG00609.hp2 HG00621.hp1 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.1304-168A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/8 | chr19 | 40844145 | |||||||
chr19:40844151 | A | T | 1 | a0001c0001t0001g0001 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1304-174T>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/8 | chr19 | 40844151 | |||||||
chr19:40844188 | T | G | 1 | a0001c0001t0001g0001 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1304-211A>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/8 | chr19 | 40844188 | |||||||
chr19:40844209 | T | C | 1 | a0001c0001t0001g0001 | 14 | HG00609.hp2 HG00621.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.1304-232A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/8 | chr19 | 40844209 | |||||||
chr19:40844324 | CT | C | 1 | a0001c0001t0001g0001 | 8 | HG00609.hp2 HG00621.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.1303+306delA | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/8 | chr19 | 40844324 | |||||||
chr19:40844329 | C | T | 1 | a0001c0001t0001g0001 | 8 | HG00609.hp2 HG00621.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.1303+302G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/8 | chr19 | 40844329 | |||||||
chr19:40844336 | G | A | 1 | a0001c0001t0001g0001 | 8 | HG00609.hp2 HG00621.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.1303+295C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/8 | chr19 | 40844336 | |||||||
chr19:40844367 | A | G | 1 | a0001c0001t0001g0001 | 2 | HG01433.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1303+264T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/8 | chr19 | 40844367 | |||||||
chr19:40844444 | A | C | 1 | a0001c0001t0001g0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.1303+187T>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/8 | chr19 | 40844444 | |||||||
chr19:40844456 | C | T | 1 | a0001c0001t0001g0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.1303+175G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/8 | chr19 | 40844456 | |||||||
chr19:40844534 | T | G | 1 | a0001c0001t0001g0001 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1303+97A>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/8 | chr19 | 40844534 | |||||||
chr19:40844570 | A | T | 1 | a0001c0001t0001g0001 | 11 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.1303+61T>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/8 | chr19 | 40844570 | |||||||
chr19:40844584 | C | G | 1 | a0001c0001t0001g0001 | 20 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.1303+47G>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/8 | chr19 | 40844584 | |||||||
chr19:40844600 | C | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1303+31G>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/8 | chr19 | 40844600 | |||||||
chr19:40844602 | T | C | 1 | a0001c0001t0001g0001 | 17 | HG00639.hp2 HG01496.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1303+29A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/8 | chr19 | 40844602 | |||||||
chr19:40844604 | G | A | 1 | a0001c0001t0001g0001 | 9 | HG00323.hp2 HG00609.hp1 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.1303+27C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/8 | chr19 | 40844604 | |||||||
chr19:40844622 | G | C | 1 | a0001c0001t0001g0001 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1303+9C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 8/8 | chr19 | 40844622 | |||||||
chr19:40844791 | T | G | 1 | a0001c0001t0001g0001 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1162-19A>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40844791 | |||||||
chr19:40844799 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1162-27C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40844799 | |||||||
chr19:40844806 | A | C | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1162-34T>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40844806 | |||||||
chr19:40844807 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1162-35C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40844807 | |||||||
chr19:40844811 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1162-39G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40844811 | |||||||
chr19:40844812 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1162-40C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40844812 | |||||||
chr19:40844844 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1162-72C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40844844 | |||||||
chr19:40844852 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1162-80T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40844852 | |||||||
chr19:40844854 | T | G | 1 | a0001c0001t0001g0001 | 10 | HG02698.hp1 NA18941.hp1 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.1162-82A>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40844854 | |||||||
chr19:40844864 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1162-92C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40844864 | |||||||
chr19:40844882 | C | G | 1 | a0001c0001t0001g0001 | 5 | HG01074.hp1 HG01243.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.1162-110G>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40844882 | |||||||
chr19:40844902 | C | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1162-130G>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40844902 | |||||||
chr19:40844906 | T | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1162-134A>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40844906 | |||||||
chr19:40844922 | G | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1162-150C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40844922 | |||||||
chr19:40844977 | C | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1162-205G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40844977 | |||||||
chr19:40844979 | T | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1162-207A>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40844979 | |||||||
chr19:40844983 | G | C | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1162-211C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40844983 | |||||||
chr19:40844988 | G | GT | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1162-217_1162-216i others(3): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40844988 | |||||||
chr19:40844989 | A | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1162-217T>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40844989 | |||||||
chr19:40844990 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1162-218C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40844990 | |||||||
chr19:40845005 | G | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1162-233C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845005 | |||||||
chr19:40845010 | C | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1162-238G>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845010 | |||||||
chr19:40845019 | T | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1162-247A>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845019 | |||||||
chr19:40845031 | G | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1162-259C>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845031 | |||||||
chr19:40845071 | G | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161+223C>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845071 | |||||||
chr19:40845073 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG01433.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1161+221C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845073 | |||||||
chr19:40845077 | A | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161+217T>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845077 | |||||||
chr19:40845080 | T | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161+214A>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845080 | |||||||
chr19:40845091 | C | T | 1 | a0001c0001t0001g0001 | 13 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.1161+203G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845091 | |||||||
chr19:40845093 | T | C | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161+201A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845093 | |||||||
chr19:40845110 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161+184T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845110 | |||||||
chr19:40845151 | C | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161+143G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845151 | |||||||
chr19:40845174 | T | C | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161+120A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845174 | |||||||
chr19:40845186 | T | A | 1 | a0001c0001t0001g0001 | 2 | HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1161+108A>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845186 | |||||||
chr19:40845203 | G | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161+91C>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845203 | |||||||
chr19:40845205 | T | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161+89A>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845205 | |||||||
chr19:40845206 | C | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161+88G>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845206 | |||||||
chr19:40845223 | T | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161+71A>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845223 | |||||||
chr19:40845227 | T | C | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161+67A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845227 | |||||||
chr19:40845228 | G | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161+66C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845228 | |||||||
chr19:40845233 | G | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161+61C>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845233 | |||||||
chr19:40845249 | G | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161+45C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845249 | |||||||
chr19:40845264 | C | T | 1 | a0001c0001t0001g0001 | 22 | HG00639.hp2 HG01074.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.1161+30G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845264 | |||||||
chr19:40845265 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1161+29C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845265 | |||||||
chr19:40845272 | G | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161+22C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845272 | |||||||
chr19:40845278 | T | G | 1 | a0001c0001t0001g0001 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1161+16A>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845278 | |||||||
chr19:40845278 | TG | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161+15delC | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845278 | |||||||
chr19:40845284 | C | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161+10G>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 7/8 | chr19 | 40845284 | |||||||
chr19:40845495 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG00733.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.974-14C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845495 | |||||||
chr19:40845515 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.974-34T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845515 | |||||||
chr19:40845518 | G | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.974-37C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845518 | |||||||
chr19:40845542 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.974-61G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845542 | |||||||
chr19:40845543 | C | T | 1 | a0001c0001t0001g0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.974-62G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845543 | |||||||
chr19:40845551 | C | T | 1 | a0001c0001t0001g0001 | 8 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.974-70G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845551 | |||||||
chr19:40845556 | T | C | 1 | a0001c0001t0001g0001 | 8 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.974-75A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845556 | |||||||
chr19:40845570 | T | C | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.974-89A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845570 | |||||||
chr19:40845577 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.974-96C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845577 | |||||||
chr19:40845577 | G | C | 1 | a0001c0001t0001g0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.974-96C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845577 | |||||||
chr19:40845591 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.974-110T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845591 | |||||||
chr19:40845620 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.974-139T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845620 | |||||||
chr19:40845633 | G | T | 1 | a0001c0001t0001g0001 | 10 | HG00423.hp2 HG02027.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.974-152C>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845633 | |||||||
chr19:40845649 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.974-168C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845649 | |||||||
chr19:40845658 | G | A | 1 | a0001c0001t0001g0001 | 6 | HG01884.hp2 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.974-177C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845658 | |||||||
chr19:40845700 | G | A | 1 | a0001c0001t0001g0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.974-219C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845700 | |||||||
chr19:40845709 | G | A | 1 | a0001c0001t0001g0001 | 38 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.974-228C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845709 | |||||||
chr19:40845709 | G | C | 1 | a0001c0001t0001g0001 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.974-228C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845709 | |||||||
chr19:40845711 | T | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.974-230A>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845711 | |||||||
chr19:40845716 | C | G | 1 | a0001c0001t0001g0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.974-235G>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845716 | |||||||
chr19:40845723 | T | C | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.973+233A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845723 | |||||||
chr19:40845727 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.973+229G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845727 | |||||||
chr19:40845746 | A | C | 1 | a0001c0001t0001g0001 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.973+210T>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845746 | |||||||
chr19:40845791 | T | G | 1 | a0001c0001t0001g0001 | 11 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.973+165A>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845791 | |||||||
chr19:40845833 | T | A | 1 | a0001c0001t0001g0001 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.973+123A>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845833 | |||||||
chr19:40845850 | T | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.973+106A>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845850 | |||||||
chr19:40845866 | C | T | 1 | a0001c0001t0001g0001 | 8 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.973+90G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845866 | |||||||
chr19:40845883 | G | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.973+73C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845883 | |||||||
chr19:40845938 | G | A | 1 | a0001c0001t0001g0001 | 22 | HG00639.hp2 HG01074.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.973+18C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 6/8 | chr19 | 40845938 | |||||||
chr19:40846144 | A | G | 1 | a0001c0001t0001g0001 | 2 | HG01433.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.832-47T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846144 | |||||||
chr19:40846188 | T | C | 1 | a0001c0001t0001g0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.832-91A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846188 | |||||||
chr19:40846234 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG01433.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.832-137G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846234 | |||||||
chr19:40846283 | C | T | 1 | a0001c0001t0001g0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.832-186G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846283 | |||||||
chr19:40846301 | C | G | 1 | a0001c0001t0001g0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.832-204G>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846301 | |||||||
chr19:40846301 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.832-204G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846301 | |||||||
chr19:40846321 | C | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-224G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846321 | |||||||
chr19:40846342 | GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0001g0001 | 9 | HG00609.hp2 HG00621.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.832-256_832-246del others(11): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846342 | |||||||
chr19:40846352 | G | GT | 1 | a0001c0001t0001g0001 | 9 | HG00642.hp2 HG04115.hp2 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.832-256dupA | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846352 | |||||||
chr19:40846352 | G | T | 1 | a0001c0001t0001g0001 | 4 | HG02615.hp2 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-255C>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846352 | |||||||
chr19:40846352 | GT | G | 1 | a0001c0001t0001g0001 | 91 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.832-256delA | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846352 | |||||||
chr19:40846358 | T | G | 1 | a0001c0001t0001g0001 | 13 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.832-261A>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846358 | |||||||
chr19:40846368 | T | C | 1 | a0001c0001t0001g0001 | 9 | HG00609.hp2 HG00621.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.832-271A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846368 | |||||||
chr19:40846399 | C | T | 1 | a0001c0001t0001g0001 | 8 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.832-302G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846399 | |||||||
chr19:40846406 | C | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-309G>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846406 | |||||||
chr19:40846415 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-318T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846415 | |||||||
chr19:40846433 | G | C | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-336C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846433 | |||||||
chr19:40846437 | C | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-340G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846437 | |||||||
chr19:40846465 | T | C | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-368A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846465 | |||||||
chr19:40846521 | C | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+354G>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846521 | |||||||
chr19:40846528 | C | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+347G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846528 | |||||||
chr19:40846546 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+329T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846546 | |||||||
chr19:40846555 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.831+320G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846555 | |||||||
chr19:40846557 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+318T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846557 | |||||||
chr19:40846595 | T | G | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.831+280A>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846595 | |||||||
chr19:40846596 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.831+279G>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846596 | |||||||
chr19:40846606 | T | C | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+269A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846606 | |||||||
chr19:40846608 | C | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+267G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846608 | |||||||
chr19:40846609 | C | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+266G>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846609 | |||||||
chr19:40846612 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+263T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846612 | |||||||
chr19:40846639 | G | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+236C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846639 | |||||||
chr19:40846669 | C | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+206G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846669 | |||||||
chr19:40846743 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+132T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846743 | |||||||
chr19:40846768 | T | G | 1 | a0001c0001t0001g0001 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.831+107A>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846768 | |||||||
chr19:40846777 | T | C | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+98A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846777 | |||||||
chr19:40846787 | T | C | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+88A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846787 | |||||||
chr19:40846791 | C | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+84G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846791 | |||||||
chr19:40846799 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+76T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846799 | |||||||
chr19:40846806 | T | C | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+69A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846806 | |||||||
chr19:40846820 | A | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+55T>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846820 | |||||||
chr19:40846847 | T | C | 1 | a0001c0001t0001g0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+28A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846847 | |||||||
chr19:40846857 | G | C | 1 | a0001c0001t0001g0001 | 20 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.831+18C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 5/8 | chr19 | 40846857 | |||||||
chr19:40847095 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.655-44G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847095 | |||||||
chr19:40847112 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.655-61C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847112 | |||||||
chr19:40847145 | T | G | 1 | a0001c0001t0001g0001 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.655-94A>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847145 | |||||||
chr19:40847166 | G | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.655-115C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847166 | |||||||
chr19:40847189 | C | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.655-138G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847189 | |||||||
chr19:40847202 | T | C | 1 | a0001c0001t0001g0001 | 157 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.655-151A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847202 | |||||||
chr19:40847231 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.655-180G>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847231 | |||||||
chr19:40847271 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.655-220T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847271 | |||||||
chr19:40847294 | T | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.655-243A>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847294 | |||||||
chr19:40847295 | T | C | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.655-244A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847295 | |||||||
chr19:40847299 | C | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.655-248G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847299 | |||||||
chr19:40847342 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.655-291C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847342 | |||||||
chr19:40847433 | A | G | 1 | a0001c0001t0001g0001 | 109 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.655-382T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847433 | |||||||
chr19:40847506 | C | T | 1 | a0001c0001t0001g0001 | 22 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.655-455G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847506 | |||||||
chr19:40847545 | G | C | 1 | a0001c0001t0001g0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.655-494C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847545 | |||||||
chr19:40847582 | G | C | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.655-531C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847582 | |||||||
chr19:40847590 | T | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.655-539A>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847590 | |||||||
chr19:40847644 | T | G | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.654+575A>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847644 | |||||||
chr19:40847662 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.654+557C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847662 | |||||||
chr19:40847674 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.654+545T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847674 | |||||||
chr19:40847706 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.654+513G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847706 | |||||||
chr19:40847718 | T | C | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.654+501A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847718 | |||||||
chr19:40847740 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.654+479C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847740 | |||||||
chr19:40847743 | G | T | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.654+476C>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847743 | |||||||
chr19:40847752 | G | C | 1 | a0001c0001t0001g0001 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.654+467C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847752 | |||||||
chr19:40847822 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.654+397G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847822 | |||||||
chr19:40847837 | T | C | 1 | a0001c0001t0001g0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.654+382A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847837 | |||||||
chr19:40847849 | C | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.654+370G>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847849 | |||||||
chr19:40847864 | C | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.654+355G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847864 | |||||||
chr19:40847939 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.654+280C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847939 | |||||||
chr19:40847944 | C | T | 1 | a0001c0001t0001g0001 | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.654+275G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847944 | |||||||
chr19:40847978 | C | T | 1 | a0001c0001t0001g0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.654+241G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847978 | |||||||
chr19:40847984 | G | A | 1 | a0001c0001t0001g0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.654+235C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847984 | |||||||
chr19:40847992 | G | T | 1 | a0001c0001t0001g0001 | 5 | HG01074.hp1 HG01243.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.654+227C>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40847992 | |||||||
chr19:40848010 | T | G | 1 | a0001c0001t0001g0001 | 3 | HG01433.hp2 HG02698.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.654+209A>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40848010 | |||||||
chr19:40848014 | T | A | 1 | a0001c0001t0001g0001 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.654+205A>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40848014 | |||||||
chr19:40848041 | AGGGTATT others(13): Show |
A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.654+158_654+177del others(20): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40848041 | |||||||
chr19:40848064 | G | C | 1 | a0001c0001t0001g0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.654+155C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40848064 | |||||||
chr19:40848100 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.654+119T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40848100 | |||||||
chr19:40848128 | G | C | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.654+91C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40848128 | |||||||
chr19:40848130 | C | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.654+89G>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40848130 | |||||||
chr19:40848131 | G | A | 1 | a0001c0001t0001g0001 | 4 | HG02723.hp2 HG03225.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+88C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 4/8 | chr19 | 40848131 | |||||||
chr19:40848388 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.494-9T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 3/8 | chr19 | 40848388 | |||||||
chr19:40848392 | C | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.494-13G>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 3/8 | chr19 | 40848392 | |||||||
chr19:40848401 | G | A | 1 | a0001c0001t0001g0001 | 4 | HG01074.hp1 HG01243.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-22C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 3/8 | chr19 | 40848401 | |||||||
chr19:40848439 | G | A | 1 | a0001c0001t0001g0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.494-60C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 3/8 | chr19 | 40848439 | |||||||
chr19:40848512 | G | C | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.493+102C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 3/8 | chr19 | 40848512 | |||||||
chr19:40848537 | C | G | 1 | a0001c0001t0001g0001 | 21 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.493+77G>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 3/8 | chr19 | 40848537 | |||||||
chr19:40848553 | C | A | 1 | a0001c0001t0001g0001 | 5 | HG01074.hp1 HG01243.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.493+61G>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 3/8 | chr19 | 40848553 | |||||||
chr19:40848591 | C | A | 1 | a0001c0001t0001g0001 | 51 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.493+23G>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 3/8 | chr19 | 40848591 | |||||||
chr19:40848602 | T | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.493+12A>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 3/8 | chr19 | 40848602 | |||||||
chr19:40848603 | C | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.493+11G>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 3/8 | chr19 | 40848603 | |||||||
chr19:40848606 | C | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.493+8G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 3/8 | chr19 | 40848606 | |||||||
chr19:40848608 | G | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.493+6C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 3/8 | chr19 | 40848608 | |||||||
chr19:40848774 | G | C | 1 | a0001c0001t0001g0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.344-11C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848774 | |||||||
chr19:40848777 | C | G | 1 | a0001c0001t0001g0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.344-14G>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848777 | |||||||
chr19:40848783 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-20T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848783 | |||||||
chr19:40848784 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-21T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848784 | |||||||
chr19:40848791 | C | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-28G>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848791 | |||||||
chr19:40848794 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.344-31C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848794 | |||||||
chr19:40848795 | C | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-32G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848795 | |||||||
chr19:40848806 | C | CG | 1 | a0001c0001t0001g0001 | 4 | HG00642.hp2 HG01106.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.344-44_344-43insC | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848806 | |||||||
chr19:40848807 | A | G | 1 | a0001c0001t0001g0001 | 305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.344-44T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848807 | |||||||
chr19:40848809 | G | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-46C>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848809 | |||||||
chr19:40848814 | G | T | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.344-51C>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848814 | |||||||
chr19:40848822 | G | C | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-59C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848822 | |||||||
chr19:40848826 | C | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-63G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848826 | |||||||
chr19:40848852 | G | C | 1 | a0001c0001t0001g0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.344-89C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848852 | |||||||
chr19:40848852 | G | T | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.344-89C>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848852 | |||||||
chr19:40848857 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-94T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848857 | |||||||
chr19:40848860 | G | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-97C>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848860 | |||||||
chr19:40848864 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-101T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848864 | |||||||
chr19:40848888 | C | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-125G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848888 | |||||||
chr19:40848893 | T | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-130A>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848893 | |||||||
chr19:40848898 | CAGCAGAG others(134): Show |
C | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.344-276_344-136del | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848898 | |||||||
chr19:40848901 | C | G | 1 | a0001c0001t0001g0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.344-138G>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848901 | |||||||
chr19:40848903 | G | C | 1 | a0001c0001t0001g0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.344-140C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848903 | |||||||
chr19:40848906 | C | G | 1 | a0001c0001t0001g0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.344-143G>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848906 | |||||||
chr19:40848928 | ACGATGT | A | 1 | a0001c0001t0001g0001 | 4 | HG00609.hp2 HG02056.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.344-171_344-166del others(6): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848928 | |||||||
chr19:40848937 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.344-174T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848937 | |||||||
chr19:40848940 | T | G | 1 | a0001c0001t0001g0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.344-177A>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848940 | |||||||
chr19:40848940 | T | TAG | 1 | a0001c0001t0001g0001 | 19 | HG00408.hp2 HG00741.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.344-179_344-178dup others(2): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848940 | |||||||
chr19:40848940 | T | TAGAG | 1 | a0001c0001t0001g0001 | 6 | HG03453.hp2 NA18951.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.344-181_344-178dup others(4): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848940 | |||||||
chr19:40848940 | TAG | T | 1 | a0001c0001t0001g0001 | 51 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.344-179_344-178del others(2): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848940 | |||||||
chr19:40848940 | TAGAG | T | 1 | a0001c0001t0001g0001 | 54 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.344-181_344-178del others(4): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848940 | |||||||
chr19:40848940 | TAGAGAG | T | 1 | a0001c0001t0001g0001 | 53 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.344-183_344-178del others(6): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848940 | |||||||
chr19:40848940 | TAGAGAGA others(1): Show |
T | 1 | a0001c0001t0001g0001 | 8 | HG01496.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.344-185_344-178del others(8): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848940 | |||||||
chr19:40848940 | TAGAGAGA others(3): Show |
T | 1 | a0001c0001t0001g0001 | 24 | HG00558.hp1 HG01069.hp2 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.344-187_344-178del others(10): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848940 | |||||||
chr19:40848966 | G | GA | 1 | a0001c0001t0001g0001 | 34 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.344-204dupT | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848966 | |||||||
chr19:40848967 | AGAGAGAG others(71): Show |
A | 1 | a0001c0001t0001g0001 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.344-282_344-205del others(78): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848967 | |||||||
chr19:40848968 | G | GA | 1 | a0001c0001t0001g0001 | 5 | HG00621.hp2 HG02040.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.344-206dupT | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848968 | |||||||
chr19:40848971 | AGAG | A | 1 | a0001c0001t0001g0001 | 3 | HG02572.hp2 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.344-211_344-209del others(3): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848971 | |||||||
chr19:40848971 | AGAGAGAA others(67): Show |
A | 1 | a0001c0001t0001g0001 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.344-282_344-209del others(74): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848971 | |||||||
chr19:40848972 | GAGAGA | G | 1 | a0001c0001t0001g0001 | 3 | HG01106.hp2 HG01981.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.344-214_344-210del others(5): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848972 | |||||||
chr19:40848973 | AG | A | 1 | a0001c0001t0001g0001 | 4 | HG00438.hp2 HG01261.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.344-211delC | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848973 | |||||||
chr19:40848973 | AGAGAAGA others(65): Show |
A | 1 | a0001c0001t0001g0001 | 2 | HG02056.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.344-282_344-211del others(72): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848973 | |||||||
chr19:40848974 | GAGA | G | 1 | a0001c0001t0001g0001 | 5 | HG02109.hp2 HG02293.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.344-214_344-212del others(3): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848974 | |||||||
chr19:40848975 | AGAAGAGA others(63): Show |
A | 1 | a0001c0001t0001g0001 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.344-282_344-213del others(70): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848975 | |||||||
chr19:40848976 | G | A | 1 | a0001c0001t0001g0001 | 15 | HG00323.hp2 HG00609.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.344-213C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848976 | |||||||
chr19:40848976 | GA | G | 1 | a0001c0001t0001g0001 | 16 | HG00438.hp2 HG01261.hp1 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.344-214delT | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848976 | |||||||
chr19:40848976 | GAAGAGAG others(52): Show |
G | 1 | a0001c0001t0001g0001 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.344-272_344-214del others(59): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848976 | |||||||
chr19:40848977 | A | AG | 1 | a0001c0001t0001g0001 | 23 | HG00639.hp2 HG00642.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.344-215_344-214ins others(1): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848977 | |||||||
chr19:40848977 | A | AGAG | 1 | a0001c0001t0001g0001 | 4 | HG02258.hp1 HG02809.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.344-215_344-214ins others(3): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848977 | |||||||
chr19:40848977 | A | AGAGAGAG others(12): Show |
1 | a0001c0001t0001g0001 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.344-215_344-214ins others(19): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848977 | |||||||
chr19:40848977 | A | G | 1 | a0001c0001t0001g0001 | 50 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.344-214T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848977 | |||||||
chr19:40848978 | A | G | 1 | a0001c0001t0001g0001 | 11 | HG00621.hp2 HG00673.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.344-215T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848978 | |||||||
chr19:40848980 | A | AG | 1 | a0001c0001t0001g0001 | 4 | HG01496.hp2 HG02717.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.344-218dupC | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848980 | |||||||
chr19:40848980 | A | G | 1 | a0001c0001t0001g0001 | 9 | HG00639.hp2 HG01515.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.344-217T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848980 | |||||||
chr19:40848982 | A | G | 1 | a0001c0001t0001g0001 | 3 | HG02559.hp1 HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.344-219T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848982 | |||||||
chr19:40848986 | A | G | 1 | a0001c0001t0001g0001 | 20 | HG00323.hp2 HG00438.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.344-223T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848986 | |||||||
chr19:40848986 | AG | A | 1 | a0001c0001t0001g0001 | 5 | HG00733.hp1 HG00735.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.344-224delC | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848986 | |||||||
chr19:40848987 | G | A | 1 | a0001c0001t0001g0001 | 33 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.344-224C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848987 | |||||||
chr19:40848987 | G | GA | 1 | a0001c0001t0001g0001 | 56 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.344-225_344-224ins others(1): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848987 | |||||||
chr19:40848987 | G | GGA | 1 | a0001c0001t0001g0001 | 8 | HG00741.hp2 HG03130.hp1 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.344-226_344-225dup others(2): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848987 | |||||||
chr19:40848987 | GGAGA | G | 1 | a0001c0001t0001g0001 | 7 | HG01243.hp1 HG01433.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-228_344-225del others(4): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848987 | |||||||
chr19:40848988 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.344-225C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848988 | |||||||
chr19:40848990 | GA | G | 1 | a0001c0001t0001g0001 | 3 | HG01928.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.344-228delT | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848990 | |||||||
chr19:40848991 | A | AGAGAG | 1 | a0001c0001t0001g0001 | 6 | HG00639.hp2 HG01496.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.344-233_344-229dup others(5): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848991 | |||||||
chr19:40848992 | G | GAGAGAGA others(8): Show |
1 | a0001c0001t0001g0001 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.344-244_344-230dup others(15): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848992 | |||||||
chr19:40848996 | G | GA | 1 | a0001c0001t0001g0001 | 4 | HG01069.hp1 HG01071.hp1 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.344-234dupT | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848996 | |||||||
chr19:40848996 | GA | G | 1 | a0001c0001t0001g0001 | 7 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-234delT | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848996 | |||||||
chr19:40848999 | A | AAGAGAGA others(3): Show |
1 | a0001c0001t0001g0001 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.344-237_344-236ins others(10): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848999 | |||||||
chr19:40848999 | AG | A | 1 | a0001c0001t0001g0001 | 26 | HG00280.hp2 HG00423.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.344-237delC | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40848999 | |||||||
chr19:40849000 | G | GA | 1 | a0001c0001t0001g0001 | 11 | HG00597.hp2 HG00621.hp2 HG00673.hp2 others(8): Show |
intron_variant | MODIFIER | c.344-238dupT | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849000 | |||||||
chr19:40849005 | A | AG | 1 | a0001c0001t0001g0001 | 4 | HG01069.hp1 HG01071.hp1 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.344-243dupC | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849005 | |||||||
chr19:40849011 | A | AC | 1 | a0001c0001t0001g0001 | 3 | HG01069.hp1 HG01071.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.344-249_344-248ins others(1): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849011 | |||||||
chr19:40849011 | A | AG | 1 | a0001c0001t0001g0001 | 20 | HG01074.hp1 HG01109.hp2 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.344-249_344-248ins others(1): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849011 | |||||||
chr19:40849011 | A | AGAAGAGA others(8): Show |
1 | a0001c0001t0001g0001 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.344-249_344-248ins others(15): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849011 | |||||||
chr19:40849011 | A | AGAAGAGA others(14): Show |
1 | a0001c0001t0001g0001 | 2 | HG00733.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.344-249_344-248ins others(21): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849011 | |||||||
chr19:40849011 | A | AGAGAGAG others(6): Show |
1 | a0001c0001t0001g0001 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.344-249_344-248ins others(13): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849011 | |||||||
chr19:40849011 | A | AGAGAGAG others(49): Show |
1 | a0001c0001t0001g0001 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.344-249_344-248ins others(56): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849011 | |||||||
chr19:40849011 | A | AGAGAGAG others(13): Show |
1 | a0001c0001t0001g0001 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.344-249_344-248ins others(20): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849011 | |||||||
chr19:40849011 | A | G | 1 | a0001c0001t0001g0001 | 37 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.344-248T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849011 | |||||||
chr19:40849012 | A | G | 1 | a0001c0001t0001g0001 | 4 | HG02486.hp2 HG03492.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.344-249T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849012 | |||||||
chr19:40849017 | G | C | 1 | a0001c0001t0001g0001 | 33 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.344-254C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849017 | |||||||
chr19:40849019 | G | C | 1 | a0001c0001t0001g0001 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.344-256C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849019 | |||||||
chr19:40849020 | A | G | 1 | a0001c0001t0001g0001 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.344-257T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849020 | |||||||
chr19:40849020 | AG | A | 1 | a0001c0001t0001g0001 | 4 | HG02486.hp2 HG02559.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.344-258delC | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849020 | |||||||
chr19:40849021 | G | A | 1 | a0001c0001t0001g0001 | 6 | HG01069.hp1 HG01071.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.344-258C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849021 | |||||||
chr19:40849021 | G | GA | 1 | a0001c0001t0001g0001 | 48 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.344-259_344-258ins others(1): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849021 | |||||||
chr19:40849021 | G | GAGAGAGA others(22): Show |
1 | a0001c0001t0001g0001 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.344-259_344-258ins others(29): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849021 | |||||||
chr19:40849021 | G | GGA | 1 | a0001c0001t0001g0001 | 16 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.344-260_344-259dup others(2): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849021 | |||||||
chr19:40849021 | G | GGAGA | 1 | a0001c0001t0001g0001 | 15 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.344-262_344-259dup others(4): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849021 | |||||||
chr19:40849021 | G | GGAGAGA | 1 | a0001c0001t0001g0001 | 4 | HG02723.hp2 HG03225.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.344-264_344-259dup others(6): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849021 | |||||||
chr19:40849021 | G | GGAGAGAG others(7): Show |
1 | a0001c0001t0001g0001 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.344-272_344-259dup others(14): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849021 | |||||||
chr19:40849021 | G | GGAGAGAG others(13): Show |
1 | a0001c0001t0001g0001 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.344-259_344-258ins others(20): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849021 | |||||||
chr19:40849021 | G | GGAGAGAG others(15): Show |
1 | a0001c0001t0001g0001 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.344-259_344-258ins others(22): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849021 | |||||||
chr19:40849021 | G | GGAGAGAG others(4): Show |
1 | a0001c0001t0001g0001 | 4 | HG00738.hp1 HG01070.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.344-259_344-258ins others(11): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849021 | |||||||
chr19:40849022 | G | A | 1 | a0001c0001t0001g0001 | 3 | HG02109.hp1 NA18982.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.344-259C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849022 | |||||||
chr19:40849025 | AG | A | 1 | a0001c0001t0001g0001 | 34 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.344-263delC | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849025 | |||||||
chr19:40849026 | G | GAC | 1 | a0001c0001t0001g0001 | 18 | HG01069.hp2 HG02074.hp2 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.344-264_344-263ins others(2): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849026 | |||||||
chr19:40849026 | G | GACAGAGA others(4): Show |
1 | a0001c0001t0001g0001 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.344-264_344-263ins others(11): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849026 | |||||||
chr19:40849026 | G | GAGAGGAG others(13): Show |
1 | a0001c0001t0001g0001 | 2 | HG01168.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.344-264_344-263ins others(20): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849026 | |||||||
chr19:40849027 | A | AG | 1 | a0001c0001t0001g0001 | 3 | HG01069.hp1 HG03540.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.344-265dupC | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849027 | |||||||
chr19:40849027 | A | AGAGGAGA others(20): Show |
1 | a0001c0001t0001g0001 | 2 | HG01255.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.344-265_344-264ins others(27): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849027 | |||||||
chr19:40849027 | AGAGAGAG others(11): Show |
A | 1 | a0001c0001t0001g0001 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.344-282_344-265del others(18): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849027 | |||||||
chr19:40849028 | G | C | 1 | a0001c0001t0001g0001 | 9 | HG00558.hp1 HG01943.hp1 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.344-265C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849028 | |||||||
chr19:40849028 | G | GAGGAGAG others(11): Show |
1 | a0001c0001t0001g0001 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.344-266_344-265ins others(18): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849028 | |||||||
chr19:40849029 | A | AG | 1 | a0001c0001t0001g0001 | 8 | HG01099.hp1 HG01169.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.344-267dupC | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849029 | |||||||
chr19:40849035 | A | AAGAGAGA others(23): Show |
1 | a0001c0001t0001g0001 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.344-273_344-272ins others(30): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849035 | |||||||
chr19:40849035 | A | AG | 1 | a0001c0001t0001g0001 | 16 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.344-273_344-272ins others(1): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849035 | |||||||
chr19:40849035 | A | AGAAGAGA others(3): Show |
1 | a0001c0001t0001g0001 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.344-273_344-272ins others(10): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849035 | |||||||
chr19:40849035 | A | AGAAGAGA others(16): Show |
1 | a0001c0001t0001g0001 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.344-273_344-272ins others(23): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849035 | |||||||
chr19:40849035 | A | AGAAGAGA others(7): Show |
1 | a0001c0001t0001g0001 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.344-273_344-272ins others(14): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849035 | |||||||
chr19:40849035 | A | AGAAGAGA others(4): Show |
1 | a0001c0001t0001g0001 | 12 | HG01175.hp1 HG01358.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.344-273_344-272ins others(11): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849035 | |||||||
chr19:40849035 | A | AGAAGAGA others(6): Show |
1 | a0001c0001t0001g0001 | 18 | HG00140.hp1 HG00558.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.344-273_344-272ins others(13): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849035 | |||||||
chr19:40849035 | A | AGAAGAGA others(8): Show |
1 | a0001c0001t0001g0001 | 12 | HG00140.hp2 HG01255.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.344-273_344-272ins others(15): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849035 | |||||||
chr19:40849035 | A | AGAAGAGA others(10): Show |
1 | a0001c0001t0001g0001 | 4 | HG01081.hp1 HG01261.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.344-273_344-272ins others(17): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849035 | |||||||
chr19:40849035 | A | AGAAGAGA others(12): Show |
1 | a0001c0001t0001g0001 | 3 | HG00408.hp1 HG02015.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.344-273_344-272ins others(19): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849035 | |||||||
chr19:40849035 | A | AGAAGAGA others(14): Show |
1 | a0001c0001t0001g0001 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.344-273_344-272ins others(21): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849035 | |||||||
chr19:40849035 | A | AGAGAAGA others(8): Show |
1 | a0001c0001t0001g0001 | 4 | HG01884.hp1 HG01884.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.344-273_344-272ins others(15): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849035 | |||||||
chr19:40849035 | A | AGAGAAGA others(10): Show |
1 | a0001c0001t0001g0001 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.344-273_344-272ins others(17): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849035 | |||||||
chr19:40849035 | A | AGAGAAGA others(10): Show |
1 | a0001c0001t0001g0001 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.344-273_344-272ins others(17): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849035 | |||||||
chr19:40849035 | A | AGAGAGAG others(14): Show |
1 | a0001c0001t0001g0001 | 3 | HG01169.hp2 HG01981.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.344-273_344-272ins others(21): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849035 | |||||||
chr19:40849035 | A | AGAGAGAG others(16): Show |
1 | a0001c0001t0001g0001 | 3 | HG01099.hp1 HG01175.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.344-273_344-272ins others(23): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849035 | |||||||
chr19:40849035 | A | AGAGAGAG others(17): Show |
1 | a0001c0001t0001g0001 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.344-273_344-272ins others(24): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849035 | |||||||
chr19:40849035 | A | AGAGAGAG others(15): Show |
1 | a0001c0001t0001g0001 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.344-273_344-272ins others(22): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849035 | |||||||
chr19:40849035 | A | AGAGAGAG others(28): Show |
1 | a0001c0001t0001g0001 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.344-273_344-272ins others(35): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849035 | |||||||
chr19:40849035 | A | AGAGAGAG others(9): Show |
1 | a0001c0001t0001g0001 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.344-273_344-272ins others(16): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849035 | |||||||
chr19:40849035 | A | G | 1 | a0001c0001t0001g0001 | 43 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.344-272T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849035 | |||||||
chr19:40849036 | A | AGAGAGAG | 1 | a0001c0001t0001g0001 | 3 | HG01069.hp2 NA18950.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.344-280_344-274dup others(7): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849036 | |||||||
chr19:40849036 | A | G | 1 | a0001c0001t0001g0001 | 68 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.344-273T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849036 | |||||||
chr19:40849037 | G | A | 1 | a0001c0001t0001g0001 | 66 | HG00438.hp2 HG00558.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.344-274C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849037 | |||||||
chr19:40849038 | A | AGAGAG | 1 | a0001c0001t0001g0001 | 5 | HG01361.hp1 NA18522.hp2 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.344-280_344-276dup others(5): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849038 | |||||||
chr19:40849040 | A | AGAG | 1 | a0001c0001t0001g0001 | 8 | HG00738.hp1 HG01106.hp2 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.344-280_344-278dup others(3): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849040 | |||||||
chr19:40849040 | A | T | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.344-277T>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849040 | |||||||
chr19:40849042 | A | AG | 1 | a0001c0001t0001g0001 | 3 | NA18968.hp2 NA19089.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.344-280dupC | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849042 | |||||||
chr19:40849044 | A | AAGAGAGA others(8): Show |
1 | a0001c0001t0001g0001 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.344-282_344-281ins others(15): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849044 | |||||||
chr19:40849044 | A | AAGAGAGA others(10): Show |
1 | a0001c0001t0001g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.344-282_344-281ins others(17): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849044 | |||||||
chr19:40849044 | A | G | 1 | a0001c0001t0001g0001 | 16 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.344-281T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849044 | |||||||
chr19:40849044 | AG | A | 1 | a0001c0001t0001g0001 | 14 | HG00423.hp1 HG02559.hp2 HG02698.hp1 others(11): Show |
intron_variant | MODIFIER | c.344-282delC | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849044 | |||||||
chr19:40849045 | G | A | 1 | a0001c0001t0001g0001 | 18 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.344-282C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849045 | |||||||
chr19:40849045 | G | GA | 1 | a0001c0001t0001g0001 | 121 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.344-283_344-282ins others(1): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849045 | |||||||
chr19:40849045 | G | GAGA | 1 | a0001c0001t0001g0001 | 11 | HG00099.hp1 HG00673.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.344-283_344-282ins others(3): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849045 | |||||||
chr19:40849045 | G | GAGAGA | 1 | a0001c0001t0001g0001 | 12 | HG00280.hp2 HG00597.hp2 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.344-283_344-282ins others(5): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849045 | |||||||
chr19:40849045 | G | GAGAGAGA others(2): Show |
1 | a0001c0001t0001g0001 | 3 | NA18980.hp1 NA18991.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.344-283_344-282ins others(9): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849045 | |||||||
chr19:40849045 | G | GAGAGAGA others(6): Show |
1 | a0001c0001t0001g0001 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.344-283_344-282ins others(13): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849045 | |||||||
chr19:40849045 | G | GGA | 1 | a0001c0001t0001g0001 | 24 | HG00597.hp1 HG00639.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.344-284_344-283dup others(2): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849045 | |||||||
chr19:40849045 | G | GGAAGAGA others(6): Show |
1 | a0001c0001t0001g0001 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.344-283_344-282ins others(13): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849045 | |||||||
chr19:40849045 | G | GGAGA | 1 | a0001c0001t0001g0001 | 24 | HG00099.hp2 HG01081.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.344-286_344-283dup others(4): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849045 | |||||||
chr19:40849045 | G | GGAGAGA | 1 | a0001c0001t0001g0001 | 28 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.344-288_344-283dup others(6): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849045 | |||||||
chr19:40849045 | G | GGAGAGAG others(1): Show |
1 | a0001c0001t0001g0001 | 26 | HG01109.hp1 HG01257.hp1 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.344-290_344-283dup others(8): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849045 | |||||||
chr19:40849045 | G | GGAGAGAG others(3): Show |
1 | a0001c0001t0001g0001 | 21 | HG00741.hp1 HG01192.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.344-292_344-283dup others(10): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849045 | |||||||
chr19:40849045 | G | GGAGAGAG others(5): Show |
1 | a0001c0001t0001g0001 | 8 | HG00323.hp2 HG01928.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.344-294_344-283dup others(12): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849045 | |||||||
chr19:40849045 | G | GGAGAGAG others(7): Show |
1 | a0001c0001t0001g0001 | 8 | HG00408.hp2 HG01243.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.344-296_344-283dup others(14): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849045 | |||||||
chr19:40849045 | G | GGAGAGAG others(9): Show |
1 | a0001c0001t0001g0001 | 5 | HG01516.hp2 HG03579.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.344-298_344-283dup others(16): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849045 | |||||||
chr19:40849045 | G | GGAGAGAG others(11): Show |
1 | a0001c0001t0001g0001 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.344-300_344-283dup others(18): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849045 | |||||||
chr19:40849045 | G | GGAGGAGA others(6): Show |
1 | a0001c0001t0001g0001 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.344-283_344-282ins others(13): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849045 | |||||||
chr19:40849045 | GGA | G | 1 | a0001c0001t0001g0001 | 4 | HG00735.hp1 HG01099.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.344-284_344-283del others(2): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849045 | |||||||
chr19:40849045 | GGAGAGAG others(3): Show |
G | 1 | a0001c0001t0001g0001 | 3 | HG03704.hp1 HG03834.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.344-292_344-283del others(10): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849045 | |||||||
chr19:40849045 | GGAGAGAG others(5): Show |
G | 1 | a0001c0001t0001g0001 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.344-294_344-283del others(12): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849045 | |||||||
chr19:40849045 | GGAGAGAG others(19): Show |
G | 1 | a0001c0001t0001g0001 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.344-308_344-283del others(26): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849045 | |||||||
chr19:40849065 | A | AGAGAGAG others(4): Show |
1 | a0001c0001t0001g0001 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.344-313_344-303dup others(11): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849065 | |||||||
chr19:40849085 | A | AGAGAGAG others(6): Show |
1 | a0001c0001t0001g0001 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.344-323_344-322ins others(13): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849085 | |||||||
chr19:40849085 | A | AGAGAGAG others(12): Show |
1 | a0001c0001t0001g0001 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.344-323_344-322ins others(19): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849085 | |||||||
chr19:40849092 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-329T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849092 | |||||||
chr19:40849096 | T | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-333A>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849096 | |||||||
chr19:40849097 | T | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-334A>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849097 | |||||||
chr19:40849103 | A | C | 1 | a0001c0001t0001g0001 | 9 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.344-340T>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849103 | |||||||
chr19:40849109 | C | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-346G>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849109 | |||||||
chr19:40849118 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-355T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849118 | |||||||
chr19:40849135 | GAC | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-374_344-373del others(2): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849135 | |||||||
chr19:40849139 | G | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-376C>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849139 | |||||||
chr19:40849148 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-385T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849148 | |||||||
chr19:40849151 | T | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-388A>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849151 | |||||||
chr19:40849173 | C | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-410G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849173 | |||||||
chr19:40849191 | A | T | 1 | a0001c0001t0001g0001 | 8 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.344-428T>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849191 | |||||||
chr19:40849214 | GTGATGGA others(6): Show |
G | 1 | a0001c0001t0001g0001 | 2 | NA18970.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.344-464_344-452del others(13): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849214 | |||||||
chr19:40849215 | T | A | 1 | a0001c0001t0001g0001 | 8 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.344-452A>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849215 | |||||||
chr19:40849228 | G | A | 1 | a0001c0001t0001g0001 | 2 | NA18970.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.344-465C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849228 | |||||||
chr19:40849290 | G | C | 1 | a0001c0001t0001g0001 | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.344-527C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849290 | |||||||
chr19:40849325 | T | C | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+493A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849325 | |||||||
chr19:40849331 | T | C | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+487A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849331 | |||||||
chr19:40849354 | G | T | 1 | a0001c0001t0001g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.343+464C>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849354 | |||||||
chr19:40849386 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+432T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849386 | |||||||
chr19:40849400 | G | A | 1 | a0001c0001t0001g0001 | 8 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.343+418C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849400 | |||||||
chr19:40849406 | C | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+412G>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849406 | |||||||
chr19:40849408 | C | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+410G>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849408 | |||||||
chr19:40849421 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+397T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849421 | |||||||
chr19:40849422 | C | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+396G>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849422 | |||||||
chr19:40849430 | G | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+388C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849430 | |||||||
chr19:40849439 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+379T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849439 | |||||||
chr19:40849445 | T | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+373A>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849445 | |||||||
chr19:40849447 | C | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+371G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849447 | |||||||
chr19:40849455 | T | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+363A>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849455 | |||||||
chr19:40849464 | C | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+354G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849464 | |||||||
chr19:40849465 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+353T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849465 | |||||||
chr19:40849473 | C | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+345G>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849473 | |||||||
chr19:40849482 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+336T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849482 | |||||||
chr19:40849487 | G | C | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+331C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849487 | |||||||
chr19:40849488 | G | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+330C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849488 | |||||||
chr19:40849513 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+305T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849513 | |||||||
chr19:40849514 | A | G | 1 | a0001c0001t0001g0001 | 17 | HG00639.hp2 HG01496.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.343+304T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849514 | |||||||
chr19:40849521 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG01433.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.343+297G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849521 | |||||||
chr19:40849548 | T | C | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+270A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849548 | |||||||
chr19:40849565 | G | A | 1 | a0001c0001t0001g0001 | 5 | HG02698.hp1 HG03239.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.343+253C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849565 | |||||||
chr19:40849610 | A | C | 1 | a0001c0001t0001g0001 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.343+208T>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849610 | |||||||
chr19:40849624 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.343+194C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849624 | |||||||
chr19:40849630 | G | C | 1 | a0001c0001t0001g0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.343+188C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849630 | |||||||
chr19:40849659 | T | A | 1 | a0001c0001t0001g0001 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.343+159A>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849659 | |||||||
chr19:40849678 | A | G | 1 | a0001c0001t0001g0001 | 10 | HG00609.hp2 HG00621.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.343+140T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849678 | |||||||
chr19:40849696 | G | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+122C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849696 | |||||||
chr19:40849697 | G | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+121C>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849697 | |||||||
chr19:40849707 | C | T | 1 | a0001c0001t0001g0001 | 4 | HG02622.hp2 HG03195.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.343+111G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849707 | |||||||
chr19:40849708 | T | C | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+110A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849708 | |||||||
chr19:40849713 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+105T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849713 | |||||||
chr19:40849714 | C | T | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+104G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849714 | |||||||
chr19:40849715 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.343+103A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849715 | |||||||
chr19:40849719 | C | A | 1 | a0001c0001t0001g0001 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.343+99G>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849719 | |||||||
chr19:40849721 | T | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+97A>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849721 | |||||||
chr19:40849731 | G | C | 1 | a0001c0001t0001g0001 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.343+87C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849731 | |||||||
chr19:40849733 | T | G | 1 | a0001c0001t0001g0001 | 8 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.343+85A>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849733 | |||||||
chr19:40849760 | G | C | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+58C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849760 | |||||||
chr19:40849771 | C | A | 1 | a0001c0001t0001g0001 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.343+47G>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849771 | |||||||
chr19:40849773 | T | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+45A>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849773 | |||||||
chr19:40849782 | A | G | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+36T>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849782 | |||||||
chr19:40849799 | C | A | 1 | a0001c0001t0001g0001 | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+19G>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849799 | |||||||
chr19:40849808 | AC | A | 1 | a0001c0001t0001g0001 | 17 | HG00639.hp2 HG01496.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.343+9delG | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 2/8 | chr19 | 40849808 | |||||||
chr19:40849991 | T | C | 1 | a0001c0001t0001g0001 | 11 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.181-11A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/8 | chr19 | 40849991 | |||||||
chr19:40849993 | G | A | 1 | a0001c0001t0001g0001 | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.181-13C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/8 | chr19 | 40849993 | |||||||
chr19:40850014 | A | C | 1 | a0001c0001t0001g0001 | 27 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.181-34T>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/8 | chr19 | 40850014 | |||||||
chr19:40850019 | T | C | 1 | a0001c0001t0001g0001 | 10 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.181-39A>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/8 | chr19 | 40850019 | |||||||
chr19:40850039 | G | C | 1 | a0001c0001t0001g0001 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.181-59C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/8 | chr19 | 40850039 | |||||||
chr19:40850053 | T | A | 1 | a0001c0001t0001g0001 | 10 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.181-73A>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/8 | chr19 | 40850053 | |||||||
chr19:40850056 | G | A | 1 | a0001c0001t0001g0001 | 10 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.181-76C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/8 | chr19 | 40850056 | |||||||
chr19:40850064 | G | C | 1 | a0001c0001t0001g0001 | 10 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.181-84C>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/8 | chr19 | 40850064 | |||||||
chr19:40850069 | G | A | 1 | a0001c0001t0001g0001 | 10 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.181-89C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/8 | chr19 | 40850069 | |||||||
chr19:40850071 | A | C | 1 | a0001c0001t0001g0001 | 9 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.181-91T>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/8 | chr19 | 40850071 | |||||||
chr19:40850119 | T | TCCTGGCT others(6): Show |
1 | a0001c0001t0001g0001 | 10 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.180+127_180+128ins others(13): Show |
CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/8 | chr19 | 40850119 | |||||||
chr19:40850121 | T | G | 1 | a0001c0001t0001g0001 | 10 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.180+126A>C | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/8 | chr19 | 40850121 | |||||||
chr19:40850144 | A | C | 1 | a0001c0001t0001g0001 | 14 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.180+103T>G | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/8 | chr19 | 40850144 | |||||||
chr19:40850149 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.180+98G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/8 | chr19 | 40850149 | |||||||
chr19:40850175 | C | T | 1 | a0001c0001t0001g0001 | 10 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.180+72G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/8 | chr19 | 40850175 | |||||||
chr19:40850190 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.180+57G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/8 | chr19 | 40850190 | |||||||
chr19:40850217 | C | T | 1 | a0001c0001t0001g0001 | 10 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.180+30G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/8 | chr19 | 40850217 | |||||||
chr19:40850218 | G | A | 1 | a0001c0001t0001g0001 | 17 | HG00639.hp2 HG01496.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.180+29C>T | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/8 | chr19 | 40850218 | |||||||
chr19:40850231 | C | T | 1 | a0001c0001t0001g0001 | 10 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.180+16G>A | CYP2A6 | ENSG00000255974.8 | transcript | ENST00000301141.10 | protein_coding | 1/8 | chr19 | 40850231 |