Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.40843845C>ACA9452573CYP2A6c.1436G>T (p.Gly479Val)
n.355G>T
c.119+42430C>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.40843845C=CA2336176434CYP2A6c.1436G= (p.Gly479=)
n.355G=
c.119+42430C=
19g.40843845C>GCA405959737CYP2A6c.1436G>C (p.Gly479Ala)
n.355G>C
c.119+42430C>G
19g.40843845C>TCA405959739CYP2A6c.1436G>A (p.Gly479Asp)
n.355G>A
c.119+42430C>T
19g.40843846C>ACA405959742CYP2A6c.1435G>T (p.Gly479Cys)
n.354G>T
c.119+42431C>A
19g.40843846C>GCA405959744CYP2A6c.1435G>C (p.Gly479Arg)
n.354G>C
c.119+42431C>G
19g.40843846C>TCA405959746CYP2A6c.1435G>A (p.Gly479Ser)
n.354G>A
c.119+42431C>T
gnomAD v4
19g.40843847C>ACA507525716CYP2A6c.1434G>T (p.Val478=)
n.353G>T
c.119+42432C>A
19g.40843847C>GCA507525715CYP2A6c.1434G>C (p.Val478=)
n.353G>C
c.119+42432C>G
19g.40843847C>TCA507525713CYP2A6c.1434G>A (p.Val478=)
n.353G>A
c.119+42432C>T
gnomAD v4
19g.40843848A>CCA405959752CYP2A6c.1433T>G (p.Val478Gly)
n.352T>G
c.119+42433A>C
19g.40843848A>GCA405959751CYP2A6c.1433T>C (p.Val478Ala)
n.352T>C
c.119+42433A>G
19g.40843848A>TCA405959749CYP2A6c.1433T>A (p.Val478Glu)
n.352T>A
c.119+42433A>T
19g.40843849C>ACA405959754CYP2A6c.1432G>T (p.Val478Leu)
n.351G>T
c.119+42434C>A
19g.40843849C>GCA405959757CYP2A6c.1432G>C (p.Val478Leu)
n.351G>C
c.119+42434C>G
19g.40843849C>TCA405959759CYP2A6c.1432G>A (p.Val478Met)
n.351G>A
c.119+42434C>T
gnomAD v4
19g.40843850G>ACA507525718CYP2A6c.1431C>T (p.His477=)
n.350C>T
c.119+42435G>A
gnomAD v4
19g.40843850G>CCA405959761CYP2A6c.1431C>G (p.His477Gln)
n.350C>G
c.119+42435G>C
19g.40843850G>TCA405959762CYP2A6c.1431C>A (p.His477Gln)
n.350C>A
c.119+42435G>T
gnomAD v4
19g.40843851T>ACA405959763CYP2A6c.1430A>T (p.His477Leu)
n.349A>T
c.119+42436T>A
19g.40843851T>CCA405959765CYP2A6c.1430A>G (p.His477Arg)
n.349A>G
c.119+42436T>C
19g.40843851T>GCA405959766CYP2A6c.1430A>C (p.His477Pro)
n.349A>C
c.119+42436T>G
19g.40843852G>ACA405959768CYP2A6c.1429C>T (p.His477Tyr)
n.348C>T
c.119+42437G>A
gnomAD v4
19g.40843852G>CCA405959770CYP2A6c.1429C>G (p.His477Asp)
n.348C>G
c.119+42437G>C
19g.40843852G>TCA405959771CYP2A6c.1429C>A (p.His477Asn)
n.348C>A
c.119+42437G>T
19g.40843852_40843853delinsGTCA2336176435CYP2A6c.1428_1429delinsAC (p.Lys476=)
n.347_348delinsAC
c.119+42437_119+42438delinsGT
19g.40843853T>ACA405959772CYP2A6c.1428A>T (p.Lys476Asn)
n.347A>T
c.119+42438T>A
19g.40843853T>CCA507525725CYP2A6c.1428A>G (p.Lys476=)
n.347A>G
c.119+42438T>C
19g.40843853T>GCA405959773CYP2A6c.1428A>C (p.Lys476Asn)
n.347A>C
c.119+42438T>G
19g.40843855delCA995923439CYP2A6c.1428del (p.Lys476AsnfsTer14)
n.347del
c.119+42440del
dbSNP gnomAD v3 gnomAD v4
19g.40843854T>ACA405959778CYP2A6c.1427A>T (p.Lys476Ile)
n.346A>T
c.119+42439T>A
19g.40843854T>CCA9452574CYP2A6c.1427A>G (p.Lys476Arg)
n.346A>G
c.119+42439T>C
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.40843854T>GCA405959776CYP2A6c.1427A>C (p.Lys476Thr)
n.346A>C
c.119+42439T>G
gnomAD v4
19g.40843854T=CA2336176436CYP2A6c.1427A= (p.Lys476=)
n.346A=
c.119+42439T=
19g.40843855T>ACA405959781CYP2A6c.1426A>T (p.Lys476Ter)
n.345A>T
c.119+42440T>A
19g.40843855T>CCA405959783CYP2A6c.1426A>G (p.Lys476Glu)
n.345A>G
c.119+42440T>C
19g.40843855T>GCA405959785CYP2A6c.1426A>C (p.Lys476Gln)
n.345A>C
c.119+42440T>G
19g.40843856G>ACA507525735CYP2A6c.1425C>T (p.Pro475=)
n.344C>T
c.119+42441G>A
dbSNP gnomAD v2 gnomAD v4
19g.40843856G>CCA507525733CYP2A6c.1425C>G (p.Pro475=)
n.344C>G
c.119+42441G>C
gnomAD v4
19g.40843856G=CA2336176437CYP2A6c.1425C= (p.Pro475=)
n.344C=
c.119+42441G=
19g.40843856G>TCA507525732CYP2A6c.1425C>A (p.Pro475=)
n.344C>A
c.119+42441G>T
19g.40843860dupCA2585203860CYP2A6c.1425dup (p.Lys476GlnfsTer?)
n.344dup
c.119+42445dup
gnomAD v4
19g.40843859_40843860delCA2585203861CYP2A6c.1424_1425del (p.Pro475GlnfsTer?)
n.343_344del
c.119+42444_119+42445del
gnomAD v4
19g.40843857G>ACA405959787CYP2A6c.1424C>T (p.Pro475Leu)
n.343C>T
c.119+42442G>A
19g.40843857G>CCA405959789CYP2A6c.1424C>G (p.Pro475Arg)
n.343C>G
c.119+42442G>C
19g.40843857G=CA2336176438CYP2A6c.1424C= (p.Pro475=)
n.343C=
c.119+42442G=
19g.40843857G>TCA405959792CYP2A6c.1424C>A (p.Pro475His)
n.343C>A
c.119+42442G>T
dbSNP gnomAD v3 gnomAD v4
19g.40843858G>ACA9452575CYP2A6c.1423C>T (p.Pro475Ser)
n.342C>T
c.119+42443G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.40843858G>CCA405959798CYP2A6c.1423C>G (p.Pro475Ala)
n.342C>G
c.119+42443G>C
19g.40843858G=CA2336176439CYP2A6c.1423C= (p.Pro475=)
n.342C=
c.119+42443G=

Number of alleles fetched