Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.41012377C>ACA405984421CYP2B6c.1044C>A (p.Tyr348Ter)
c.1068C>A
c.336C>A (p.Tyr112Ter)
n.539C>A
c.564C>A (p.Tyr188Ter)
c.453C>A (p.Tyr151Ter)
c.444C>A (p.Tyr148Ter)
19g.41012377C=CA2336260329CYP2B6c.1044C= (p.Tyr348=)
c.1068C=
c.336C= (p.Tyr112=)
n.539C=
c.564C= (p.Tyr188=)
c.453C= (p.Tyr151=)
c.444C= (p.Tyr148=)
19g.41012377C>GCA405984423CYP2B6c.1044C>G (p.Tyr348Ter)
c.1068C>G
c.336C>G (p.Tyr112Ter)
n.539C>G
c.564C>G (p.Tyr188Ter)
c.453C>G (p.Tyr151Ter)
c.444C>G (p.Tyr148Ter)
19g.41012377C>TCA9455460CYP2B6c.1044C>T (p.Tyr348=)
c.1068C>T
c.336C>T (p.Tyr112=)
n.539C>T
c.564C>T (p.Tyr188=)
c.453C>T (p.Tyr151=)
c.444C>T (p.Tyr148=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41012378A>CCA405984426CYP2B6c.1045A>C (p.Thr349Pro)
c.1069A>C
c.337A>C (p.Thr113Pro)
n.540A>C
c.565A>C (p.Thr189Pro)
c.454A>C (p.Thr152Pro)
c.445A>C (p.Thr149Pro)
19g.41012378A>GCA405984428CYP2B6c.1045A>G (p.Thr349Ala)
c.1069A>G
c.337A>G (p.Thr113Ala)
n.540A>G
c.565A>G (p.Thr189Ala)
c.454A>G (p.Thr152Ala)
c.445A>G (p.Thr149Ala)
 gnomAD v4
19g.41012378A>TCA405984429CYP2B6c.1045A>T (p.Thr349Ser)
c.1069A>T
c.337A>T (p.Thr113Ser)
n.540A>T
c.565A>T (p.Thr189Ser)
c.454A>T (p.Thr152Ser)
c.445A>T (p.Thr149Ser)
19g.41012379C>ACA405984431CYP2B6c.1046C>A (p.Thr349Lys)
c.1070C>A
c.338C>A (p.Thr113Lys)
n.541C>A
c.566C>A (p.Thr189Lys)
c.455C>A (p.Thr152Lys)
c.446C>A (p.Thr149Lys)
19g.41012379C=CA2336260330CYP2B6c.1046C= (p.Thr349=)
c.1070C=
c.338C= (p.Thr113=)
n.541C=
c.566C= (p.Thr189=)
c.455C= (p.Thr152=)
c.446C= (p.Thr149=)
19g.41012379C>GCA9455461CYP2B6c.1046C>G (p.Thr349Arg)
c.1070C>G
c.338C>G (p.Thr113Arg)
n.541C>G
c.566C>G (p.Thr189Arg)
c.455C>G (p.Thr152Arg)
c.446C>G (p.Thr149Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.41012379C>TCA405984434CYP2B6c.1046C>T (p.Thr349Ile)
c.1070C>T
c.338C>T (p.Thr113Ile)
n.541C>T
c.566C>T (p.Thr189Ile)
c.455C>T (p.Thr152Ile)
c.446C>T (p.Thr149Ile)
 gnomAD v4
19g.41012380A>CCA507537620CYP2B6c.1047A>C (p.Thr349=)
c.1071A>C
c.339A>C (p.Thr113=)
n.542A>C
c.567A>C (p.Thr189=)
c.456A>C (p.Thr152=)
c.447A>C (p.Thr149=)
19g.41012380A>GCA507537621CYP2B6c.1047A>G (p.Thr349=)
c.1071A>G
c.339A>G (p.Thr113=)
n.542A>G
c.567A>G (p.Thr189=)
c.456A>G (p.Thr152=)
c.447A>G (p.Thr149=)
19g.41012380A>TCA507537622CYP2B6c.1047A>T (p.Thr349=)
c.1071A>T
c.339A>T (p.Thr113=)
n.542A>T
c.567A>T (p.Thr189=)
c.456A>T (p.Thr152=)
c.447A>T (p.Thr149=)
19g.41012381G>ACA405984436CYP2B6c.1048G>A (p.Glu350Lys)
c.1072G>A
c.340G>A (p.Glu114Lys)
n.543G>A
c.568G>A (p.Glu190Lys)
c.457G>A (p.Glu153Lys)
c.448G>A (p.Glu150Lys)
 COSMIC
19g.41012381G>CCA405984438CYP2B6c.1048G>C (p.Glu350Gln)
c.1072G>C
c.340G>C (p.Glu114Gln)
n.543G>C
c.568G>C (p.Glu190Gln)
c.457G>C (p.Glu153Gln)
c.448G>C (p.Glu150Gln)
19g.41012381G=CA2336260331CYP2B6c.1048G= (p.Glu350=)
c.1072G=
c.340G= (p.Glu114=)
n.543G=
c.568G= (p.Glu190=)
c.457G= (p.Glu153=)
c.448G= (p.Glu150=)
19g.41012381G>TCA308499211CYP2B6c.1048G>T (p.Glu350Ter)
c.1072G>T
c.340G>T (p.Glu114Ter)
n.543G>T
c.568G>T (p.Glu190Ter)
c.457G>T (p.Glu153Ter)
c.448G>T (p.Glu150Ter)
 dbSNP gnomAD v4
19g.41012382delCA2585217067CYP2B6c.1049del (p.Glu350GlyfsTer?)
c.1073del
c.341del (p.Glu114GlyfsTer?)
n.544del
c.569del (p.Glu190GlyfsTer?)
c.458del (p.Glu153GlyfsTer?)
c.449del (p.Glu150GlyfsTer?)
 gnomAD v4
19g.41012382A=CA2336260332CYP2B6c.1049A= (p.Glu350=)
c.1073A=
c.341A= (p.Glu114=)
n.544A=
c.569A= (p.Glu190=)
c.458A= (p.Glu153=)
c.449A= (p.Glu150=)
19g.41012382A>CCA405984445CYP2B6c.1049A>C (p.Glu350Ala)
c.1073A>C
c.341A>C (p.Glu114Ala)
n.544A>C
c.569A>C (p.Glu190Ala)
c.458A>C (p.Glu153Ala)
c.449A>C (p.Glu150Ala)
19g.41012382A>GCA9455462CYP2B6c.1049A>G (p.Glu350Gly)
c.1073A>G
c.341A>G (p.Glu114Gly)
n.544A>G
c.569A>G (p.Glu190Gly)
c.458A>G (p.Glu153Gly)
c.449A>G (p.Glu150Gly)
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
19g.41012382A>TCA405984442CYP2B6c.1049A>T (p.Glu350Val)
c.1073A>T
c.341A>T (p.Glu114Val)
n.544A>T
c.569A>T (p.Glu190Val)
c.458A>T (p.Glu153Val)
c.449A>T (p.Glu150Val)
19g.41012383G>ACA9455464CYP2B6c.1050G>A (p.Glu350=)
c.1074G>A
c.342G>A (p.Glu114=)
n.545G>A
c.570G>A (p.Glu190=)
c.459G>A (p.Glu153=)
c.450G>A (p.Glu150=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41012383G>CCA405984448CYP2B6c.1050G>C (p.Glu350Asp)
c.1074G>C
c.342G>C (p.Glu114Asp)
n.545G>C
c.570G>C (p.Glu190Asp)
c.459G>C (p.Glu153Asp)
c.450G>C (p.Glu150Asp)
19g.41012383G=CA2336260333CYP2B6c.1050G= (p.Glu350=)
c.1074G=
c.342G= (p.Glu114=)
n.545G=
c.570G= (p.Glu190=)
c.459G= (p.Glu153=)
c.450G= (p.Glu150=)
19g.41012383G>TCA9455463CYP2B6c.1050G>T (p.Glu350Asp)
c.1074G>T
c.342G>T (p.Glu114Asp)
n.545G>T
c.570G>T (p.Glu190Asp)
c.459G>T (p.Glu153Asp)
c.450G>T (p.Glu150Asp)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41012384G>ACA405984451CYP2B6c.1051G>A (p.Ala351Thr)
c.1075G>A
c.343G>A (p.Ala115Thr)
n.546G>A
c.571G>A (p.Ala191Thr)
c.460G>A (p.Ala154Thr)
c.451G>A (p.Ala151Thr)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41012384G>CCA405984453CYP2B6c.1051G>C (p.Ala351Pro)
c.1075G>C
c.343G>C (p.Ala115Pro)
n.546G>C
c.571G>C (p.Ala191Pro)
c.460G>C (p.Ala154Pro)
c.451G>C (p.Ala151Pro)
 dbSNP
19g.41012384G=CA2336260334CYP2B6c.1051G= (p.Ala351=)
c.1075G=
c.343G= (p.Ala115=)
n.546G=
c.571G= (p.Ala191=)
c.460G= (p.Ala154=)
c.451G= (p.Ala151=)
19g.41012384G>TCA405984455CYP2B6c.1051G>T (p.Ala351Ser)
c.1075G>T
c.343G>T (p.Ala115Ser)
n.546G>T
c.571G>T (p.Ala191Ser)
c.460G>T (p.Ala154Ser)
c.451G>T (p.Ala151Ser)
19g.41012385C>ACA405984457CYP2B6c.1052C>A (p.Ala351Glu)
c.1076C>A
c.344C>A (p.Ala115Glu)
n.547C>A
c.572C>A (p.Ala191Glu)
c.461C>A (p.Ala154Glu)
c.452C>A (p.Ala151Glu)
19g.41012385C>GCA405984459CYP2B6c.1052C>G (p.Ala351Gly)
c.1076C>G
c.344C>G (p.Ala115Gly)
n.547C>G
c.572C>G (p.Ala191Gly)
c.461C>G (p.Ala154Gly)
c.452C>G (p.Ala151Gly)
19g.41012385C>TCA405984461CYP2B6c.1052C>T (p.Ala351Val)
c.1076C>T
c.344C>T (p.Ala115Val)
n.547C>T
c.572C>T (p.Ala191Val)
c.461C>T (p.Ala154Val)
c.452C>T (p.Ala151Val)
 gnomAD v4
19g.41012386A>CCA507537628CYP2B6c.1053A>C (p.Ala351=)
c.1077A>C
c.345A>C (p.Ala115=)
n.548A>C
c.573A>C (p.Ala191=)
c.462A>C (p.Ala154=)
c.453A>C (p.Ala151=)
19g.41012386A>GCA507537627CYP2B6c.1053A>G (p.Ala351=)
c.1077A>G
c.345A>G (p.Ala115=)
n.548A>G
c.573A>G (p.Ala191=)
c.462A>G (p.Ala154=)
c.453A>G (p.Ala151=)
19g.41012386A>TCA507537625CYP2B6c.1053A>T (p.Ala351=)
c.1077A>T
c.345A>T (p.Ala115=)
n.548A>T
c.573A>T (p.Ala191=)
c.462A>T (p.Ala154=)
c.453A>T (p.Ala151=)
19g.41012387G>ACA405984464CYP2B6c.1054G>A (p.Val352Ile)
c.1078G>A
c.346G>A (p.Val116Ile)
n.549G>A
c.574G>A (p.Val192Ile)
c.463G>A (p.Val155Ile)
c.454G>A (p.Val152Ile)
19g.41012387G>CCA405984466CYP2B6c.1054G>C (p.Val352Leu)
c.1078G>C
c.346G>C (p.Val116Leu)
n.549G>C
c.574G>C (p.Val192Leu)
c.463G>C (p.Val155Leu)
c.454G>C (p.Val152Leu)
19g.41012387G>TCA405984467CYP2B6c.1054G>T (p.Val352Phe)
c.1078G>T
c.346G>T (p.Val116Phe)
n.549G>T
c.574G>T (p.Val192Phe)
c.463G>T (p.Val155Phe)
c.454G>T (p.Val152Phe)
19g.41012388T>ACA405984470CYP2B6c.1055T>A (p.Val352Asp)
c.1079T>A
c.347T>A (p.Val116Asp)
n.550T>A
c.575T>A (p.Val192Asp)
c.464T>A (p.Val155Asp)
c.455T>A (p.Val152Asp)
19g.41012388T>CCA405984472CYP2B6c.1055T>C (p.Val352Ala)
c.1079T>C
c.347T>C (p.Val116Ala)
n.550T>C
c.575T>C (p.Val192Ala)
c.464T>C (p.Val155Ala)
c.455T>C (p.Val152Ala)
19g.41012388T>GCA405984474CYP2B6c.1055T>G (p.Val352Gly)
c.1079T>G
c.347T>G (p.Val116Gly)
n.550T>G
c.575T>G (p.Val192Gly)
c.464T>G (p.Val155Gly)
c.455T>G (p.Val152Gly)
 COSMIC
19g.41012389C>ACA507537631CYP2B6c.1056C>A (p.Val352=)
c.1080C>A
c.348C>A (p.Val116=)
n.551C>A
c.576C>A (p.Val192=)
c.465C>A (p.Val155=)
c.456C>A (p.Val152=)
19g.41012389C=CA2336260335CYP2B6c.1056C= (p.Val352=)
c.1080C=
c.348C= (p.Val116=)
n.551C=
c.576C= (p.Val192=)
c.465C= (p.Val155=)
c.456C= (p.Val152=)
19g.41012389C>GCA507537632CYP2B6c.1056C>G (p.Val352=)
c.1080C>G
c.348C>G (p.Val116=)
n.551C>G
c.576C>G (p.Val192=)
c.465C>G (p.Val155=)
c.456C>G (p.Val152=)
19g.41012389C>TCA308499215CYP2B6c.1056C>T (p.Val352=)
c.1080C>T
c.348C>T (p.Val116=)
n.551C>T
c.576C>T (p.Val192=)
c.465C>T (p.Val155=)
c.456C>T (p.Val152=)
 dbSNP gnomAD v4
19g.41012390A>CCA405984478CYP2B6c.1057A>C (p.Ile353Leu)
c.1081A>C
c.349A>C (p.Ile117Leu)
n.552A>C
c.577A>C (p.Ile193Leu)
c.466A>C (p.Ile156Leu)
c.457A>C (p.Ile153Leu)
19g.41012390A>GCA405984481CYP2B6c.1057A>G (p.Ile353Val)
c.1081A>G
c.349A>G (p.Ile117Val)
n.552A>G
c.577A>G (p.Ile193Val)
c.466A>G (p.Ile156Val)
c.457A>G (p.Ile153Val)
19g.41012390A>TCA405984480CYP2B6c.1057A>T (p.Ile353Phe)
c.1081A>T
c.349A>T (p.Ile117Phe)
n.552A>T
c.577A>T (p.Ile193Phe)
c.466A>T (p.Ile156Phe)
c.457A>T (p.Ile153Phe)
19g.41012391T>ACA405984484CYP2B6c.1058T>A (p.Ile353Asn)
c.1082T>A
c.350T>A (p.Ile117Asn)
n.553T>A
c.578T>A (p.Ile193Asn)
c.467T>A (p.Ile156Asn)
c.458T>A (p.Ile153Asn)
19g.41012391T>CCA405984486CYP2B6c.1058T>C (p.Ile353Thr)
c.1082T>C
c.350T>C (p.Ile117Thr)
n.553T>C
c.578T>C (p.Ile193Thr)
c.467T>C (p.Ile156Thr)
c.458T>C (p.Ile153Thr)
 gnomAD v4
19g.41012391T>GCA405984487CYP2B6c.1058T>G (p.Ile353Ser)
c.1082T>G
c.350T>G (p.Ile117Ser)
n.553T>G
c.578T>G (p.Ile193Ser)
c.467T>G (p.Ile156Ser)
c.458T>G (p.Ile153Ser)
19g.41012392C>ACA507537634CYP2B6c.1059C>A (p.Ile353=)
c.1083C>A
c.351C>A (p.Ile117=)
n.554C>A
c.579C>A (p.Ile193=)
c.468C>A (p.Ile156=)
c.459C>A (p.Ile153=)
19g.41012392C>GCA405984489CYP2B6c.1059C>G (p.Ile353Met)
c.1083C>G
c.351C>G (p.Ile117Met)
n.554C>G
c.579C>G (p.Ile193Met)
c.468C>G (p.Ile156Met)
c.459C>G (p.Ile153Met)
19g.41012392C>TCA507537635CYP2B6c.1059C>T (p.Ile353=)
c.1083C>T
c.351C>T (p.Ile117=)
n.554C>T
c.579C>T (p.Ile193=)
c.468C>T (p.Ile156=)
c.459C>T (p.Ile153=)
19g.41012393T>ACA405984491CYP2B6c.1060T>A (p.Tyr354Asn)
c.1084T>A
c.352T>A (p.Tyr118Asn)
n.555T>A
c.580T>A (p.Tyr194Asn)
c.469T>A (p.Tyr157Asn)
c.460T>A (p.Tyr154Asn)
19g.41012393T>CCA9455465CYP2B6c.1060T>C (p.Tyr354His)
c.1084T>C
c.352T>C (p.Tyr118His)
n.555T>C
c.580T>C (p.Tyr194His)
c.469T>C (p.Tyr157His)
c.460T>C (p.Tyr154His)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41012393T>GCA405984494CYP2B6c.1060T>G (p.Tyr354Asp)
c.1084T>G
c.352T>G (p.Tyr118Asp)
n.555T>G
c.580T>G (p.Tyr194Asp)
c.469T>G (p.Tyr157Asp)
c.460T>G (p.Tyr154Asp)
19g.41012393T=CA2336260336CYP2B6c.1060T= (p.Tyr354=)
c.1084T=
c.352T= (p.Tyr118=)
n.555T=
c.580T= (p.Tyr194=)
c.469T= (p.Tyr157=)
c.460T= (p.Tyr154=)
19g.41012394A=CA2336260337CYP2B6c.1061A= (p.Tyr354=)
c.1085A=
c.353A= (p.Tyr118=)
n.556A=
c.581A= (p.Tyr194=)
c.470A= (p.Tyr157=)
c.461A= (p.Tyr154=)
19g.41012394A>CCA405984496CYP2B6c.1061A>C (p.Tyr354Ser)
c.1085A>C
c.353A>C (p.Tyr118Ser)
n.556A>C
c.581A>C (p.Tyr194Ser)
c.470A>C (p.Tyr157Ser)
c.461A>C (p.Tyr154Ser)
19g.41012394A>GCA9455466CYP2B6c.1061A>G (p.Tyr354Cys)
c.1085A>G
c.353A>G (p.Tyr118Cys)
n.556A>G
c.581A>G (p.Tyr194Cys)
c.470A>G (p.Tyr157Cys)
c.461A>G (p.Tyr154Cys)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41012394A>TCA405984498CYP2B6c.1061A>T (p.Tyr354Phe)
c.1085A>T
c.353A>T (p.Tyr118Phe)
n.556A>T
c.581A>T (p.Tyr194Phe)
c.470A>T (p.Tyr157Phe)
c.461A>T (p.Tyr154Phe)
19g.41012395T>ACA405984502CYP2B6c.1062T>A (p.Tyr354Ter)
c.1086T>A
c.354T>A (p.Tyr118Ter)
n.557T>A
c.582T>A (p.Tyr194Ter)
c.471T>A (p.Tyr157Ter)
c.462T>A (p.Tyr154Ter)
19g.41012395T>CCA9455467CYP2B6c.1062T>C (p.Tyr354=)
c.1086T>C
c.354T>C (p.Tyr118=)
n.557T>C
c.582T>C (p.Tyr194=)
c.471T>C (p.Tyr157=)
c.462T>C (p.Tyr154=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41012395T>GCA405984500CYP2B6c.1062T>G (p.Tyr354Ter)
c.1086T>G
c.354T>G (p.Tyr118Ter)
n.557T>G
c.582T>G (p.Tyr194Ter)
c.471T>G (p.Tyr157Ter)
c.462T>G (p.Tyr154Ter)
 gnomAD v4
19g.41012395T=CA2336260338CYP2B6c.1062T= (p.Tyr354=)
c.1086T=
c.354T= (p.Tyr118=)
n.557T=
c.582T= (p.Tyr194=)
c.471T= (p.Tyr157=)
c.462T= (p.Tyr154=)
19g.41012395_41012398dupCA507537636CYP2B6c.1062_1065dup (p.Ile356Ter)
c.1086_1089dup
c.354_357dup (p.Ile120Ter)
n.557_560dup
c.582_585dup (p.Ile196Ter)
c.471_474dup (p.Ile159Ter)
c.462_465dup (p.Ile156Ter)
 dbSNP gnomAD v2 gnomAD v4
19g.41012396G>ACA9455468CYP2B6c.1063G>A (p.Glu355Lys)
c.1087G>A
c.355G>A (p.Glu119Lys)
n.558G>A
c.583G>A (p.Glu195Lys)
c.472G>A (p.Glu158Lys)
c.463G>A (p.Glu155Lys)
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.41012396G>CCA405984505CYP2B6c.1063G>C (p.Glu355Gln)
c.1087G>C
c.355G>C (p.Glu119Gln)
n.558G>C
c.583G>C (p.Glu195Gln)
c.472G>C (p.Glu158Gln)
c.463G>C (p.Glu155Gln)
19g.41012396G=CA2336260339CYP2B6c.1063G= (p.Glu355=)
c.1087G=
c.355G= (p.Glu119=)
n.558G=
c.583G= (p.Glu195=)
c.472G= (p.Glu158=)
c.463G= (p.Glu155=)
19g.41012396G>TCA405984507CYP2B6c.1063G>T (p.Glu355Ter)
c.1087G>T
c.355G>T (p.Glu119Ter)
n.558G>T
c.583G>T (p.Glu195Ter)
c.472G>T (p.Glu158Ter)
c.463G>T (p.Glu155Ter)
19g.41012397A>CCA405984510CYP2B6c.1064A>C (p.Glu355Ala)
c.1088A>C
c.356A>C (p.Glu119Ala)
n.559A>C
c.584A>C (p.Glu195Ala)
c.473A>C (p.Glu158Ala)
c.464A>C (p.Glu155Ala)
 gnomAD v4
19g.41012397A>GCA405984512CYP2B6c.1064A>G (p.Glu355Gly)
c.1088A>G
c.356A>G (p.Glu119Gly)
n.559A>G
c.584A>G (p.Glu195Gly)
c.473A>G (p.Glu158Gly)
c.464A>G (p.Glu155Gly)
19g.41012397A>TCA405984513CYP2B6c.1064A>T (p.Glu355Val)
c.1088A>T
c.356A>T (p.Glu119Val)
n.559A>T
c.584A>T (p.Glu195Val)
c.473A>T (p.Glu158Val)
c.464A>T (p.Glu155Val)
19g.41012398G>ACA507537639CYP2B6c.1065G>A (p.Glu355=)
c.1089G>A
c.357G>A (p.Glu119=)
n.560G>A
c.585G>A (p.Glu195=)
c.474G>A (p.Glu158=)
c.465G>A (p.Glu155=)
 gnomAD v4
19g.41012398G>CCA405984514CYP2B6c.1065G>C (p.Glu355Asp)
c.1089G>C
c.357G>C (p.Glu119Asp)
n.560G>C
c.585G>C (p.Glu195Asp)
c.474G>C (p.Glu158Asp)
c.465G>C (p.Glu155Asp)
19g.41012398G>TCA405984515CYP2B6c.1065G>T (p.Glu355Asp)
c.1089G>T
c.357G>T (p.Glu119Asp)
n.560G>T
c.585G>T (p.Glu195Asp)
c.474G>T (p.Glu158Asp)
c.465G>T (p.Glu155Asp)
19g.41012399A>CCA405984516CYP2B6c.1066A>C (p.Ile356Leu)
c.1090A>C
c.358A>C (p.Ile120Leu)
n.561A>C
c.586A>C (p.Ile196Leu)
c.475A>C (p.Ile159Leu)
c.466A>C (p.Ile156Leu)
19g.41012399A>GCA405984518CYP2B6c.1066A>G (p.Ile356Val)
c.1090A>G
c.358A>G (p.Ile120Val)
n.561A>G
c.586A>G (p.Ile196Val)
c.475A>G (p.Ile159Val)
c.466A>G (p.Ile156Val)
 gnomAD v4
19g.41012399A>TCA405984519CYP2B6c.1066A>T (p.Ile356Phe)
c.1090A>T
c.358A>T (p.Ile120Phe)
n.561A>T
c.586A>T (p.Ile196Phe)
c.475A>T (p.Ile159Phe)
c.466A>T (p.Ile156Phe)
19g.41012400T>ACA405984522CYP2B6c.1067T>A (p.Ile356Asn)
c.1091T>A
c.359T>A (p.Ile120Asn)
n.562T>A
c.587T>A (p.Ile196Asn)
c.476T>A (p.Ile159Asn)
c.467T>A (p.Ile156Asn)
19g.41012400T>CCA405984524CYP2B6c.1067T>C (p.Ile356Thr)
c.1091T>C
c.359T>C (p.Ile120Thr)
n.562T>C
c.587T>C (p.Ile196Thr)
c.476T>C (p.Ile159Thr)
c.467T>C (p.Ile156Thr)
19g.41012400T>GCA405984525CYP2B6c.1067T>G (p.Ile356Ser)
c.1091T>G
c.359T>G (p.Ile120Ser)
n.562T>G
c.587T>G (p.Ile196Ser)
c.476T>G (p.Ile159Ser)
c.467T>G (p.Ile156Ser)
 gnomAD v4
19g.41012401T>ACA507537642CYP2B6c.1068T>A (p.Ile356=)
c.1092T>A
c.360T>A (p.Ile120=)
n.563T>A
c.588T>A (p.Ile196=)
c.477T>A (p.Ile159=)
c.468T>A (p.Ile156=)
19g.41012401T>CCA507537643CYP2B6c.1068T>C (p.Ile356=)
c.1092T>C
c.360T>C (p.Ile120=)
n.563T>C
c.588T>C (p.Ile196=)
c.477T>C (p.Ile159=)
c.468T>C (p.Ile156=)
19g.41012401T>GCA405984528CYP2B6c.1068T>G (p.Ile356Met)
c.1092T>G
c.360T>G (p.Ile120Met)
n.563T>G
c.588T>G (p.Ile196Met)
c.477T>G (p.Ile159Met)
c.468T>G (p.Ile156Met)
19g.41012402C>ACA405984530CYP2B6c.1069C>A (p.Gln357Lys)
c.1093C>A
c.361C>A (p.Gln121Lys)
n.564C>A
c.589C>A (p.Gln197Lys)
c.478C>A (p.Gln160Lys)
c.469C>A (p.Gln157Lys)
19g.41012402C>GCA405984532CYP2B6c.1069C>G (p.Gln357Glu)
c.1093C>G
c.361C>G (p.Gln121Glu)
n.564C>G
c.589C>G (p.Gln197Glu)
c.478C>G (p.Gln160Glu)
c.469C>G (p.Gln157Glu)
19g.41012402C>TCA405984534CYP2B6c.1069C>T (p.Gln357Ter)
c.1093C>T
c.361C>T (p.Gln121Ter)
n.564C>T
c.589C>T (p.Gln197Ter)
c.478C>T (p.Gln160Ter)
c.469C>T (p.Gln157Ter)
19g.41012403A>CCA405984536CYP2B6c.1070A>C (p.Gln357Pro)
c.1094A>C
c.362A>C (p.Gln121Pro)
n.565A>C
c.590A>C (p.Gln197Pro)
c.479A>C (p.Gln160Pro)
c.470A>C (p.Gln157Pro)
19g.41012403A>GCA405984538CYP2B6c.1070A>G (p.Gln357Arg)
c.1094A>G
c.362A>G (p.Gln121Arg)
n.565A>G
c.590A>G (p.Gln197Arg)
c.479A>G (p.Gln160Arg)
c.470A>G (p.Gln157Arg)
19g.41012403A>TCA405984540CYP2B6c.1070A>T (p.Gln357Leu)
c.1094A>T
c.362A>T (p.Gln121Leu)
n.565A>T
c.590A>T (p.Gln197Leu)
c.479A>T (p.Gln160Leu)
c.470A>T (p.Gln157Leu)
19g.41012404G>ACA507537648CYP2B6c.1071G>A (p.Gln357=)
c.1095G>A
c.363G>A (p.Gln121=)
n.566G>A
c.591G>A (p.Gln197=)
c.480G>A (p.Gln160=)
c.471G>A (p.Gln157=)
19g.41012404G>CCA405984541CYP2B6c.1071G>C (p.Gln357His)
c.1095G>C
c.363G>C (p.Gln121His)
n.566G>C
c.591G>C (p.Gln197His)
c.480G>C (p.Gln160His)
c.471G>C (p.Gln157His)
 COSMIC
19g.41012404G>TCA405984543CYP2B6c.1071G>T (p.Gln357His)
c.1095G>T
c.363G>T (p.Gln121His)
n.566G>T
c.591G>T (p.Gln197His)
c.480G>T (p.Gln160His)
c.471G>T (p.Gln157His)
19g.41012405A>CCA507537649CYP2B6c.1072A>C (p.Arg358=)
c.1096A>C
c.364A>C (p.Arg122=)
n.567A>C
c.592A>C (p.Arg198=)
c.481A>C (p.Arg161=)
c.472A>C (p.Arg158=)
19g.41012405A>GCA405984546CYP2B6c.1072A>G (p.Arg358Gly)
c.1096A>G
c.364A>G (p.Arg122Gly)
n.567A>G
c.592A>G (p.Arg198Gly)
c.481A>G (p.Arg161Gly)
c.472A>G (p.Arg158Gly)
19g.41012405A>TCA405984547CYP2B6c.1072A>T (p.Arg358Ter)
c.1096A>T
c.364A>T (p.Arg122Ter)
n.567A>T
c.592A>T (p.Arg198Ter)
c.481A>T (p.Arg161Ter)
c.472A>T (p.Arg158Ter)
19g.41012406G>ACA405984549CYP2B6c.1073G>A (p.Arg358Lys)
c.1097G>A
c.365G>A (p.Arg122Lys)
n.568G>A
c.593G>A (p.Arg198Lys)
c.482G>A (p.Arg161Lys)
c.473G>A (p.Arg158Lys)
19g.41012406G>CCA405984551CYP2B6c.1073G>C (p.Arg358Thr)
c.1097G>C
c.365G>C (p.Arg122Thr)
n.568G>C
c.593G>C (p.Arg198Thr)
c.482G>C (p.Arg161Thr)
c.473G>C (p.Arg158Thr)
19g.41012406G>TCA405984552CYP2B6c.1073G>T (p.Arg358Ile)
c.1097G>T
c.365G>T (p.Arg122Ile)
n.568G>T
c.593G>T (p.Arg198Ile)
c.482G>T (p.Arg161Ile)
c.473G>T (p.Arg158Ile)
 COSMIC
19g.41012407A>CCA405984555CYP2B6c.1074A>C (p.Arg358Ser)
c.1098A>C
c.366A>C (p.Arg122Ser)
n.569A>C
c.594A>C (p.Arg198Ser)
c.483A>C (p.Arg161Ser)
c.474A>C (p.Arg158Ser)
19g.41012407A>GCA507537651CYP2B6c.1074A>G (p.Arg358=)
c.1098A>G
c.366A>G (p.Arg122=)
n.569A>G
c.594A>G (p.Arg198=)
c.483A>G (p.Arg161=)
c.474A>G (p.Arg158=)
19g.41012407A>TCA405984556CYP2B6c.1074A>T (p.Arg358Ser)
c.1098A>T
c.366A>T (p.Arg122Ser)
n.569A>T
c.594A>T (p.Arg198Ser)
c.483A>T (p.Arg161Ser)
c.474A>T (p.Arg158Ser)
19g.41012408T>ACA405984557CYP2B6c.1075T>A (p.Phe359Ile)
c.1099T>A
c.367T>A (p.Phe123Ile)
n.570T>A
c.595T>A (p.Phe199Ile)
c.484T>A (p.Phe162Ile)
c.475T>A (p.Phe159Ile)
19g.41012408T>CCA9455469CYP2B6c.1075T>C (p.Phe359Leu)
c.1099T>C
c.367T>C (p.Phe123Leu)
n.570T>C
c.595T>C (p.Phe199Leu)
c.484T>C (p.Phe162Leu)
c.475T>C (p.Phe159Leu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41012408T>GCA405984559CYP2B6c.1075T>G (p.Phe359Val)
c.1099T>G
c.367T>G (p.Phe123Val)
n.570T>G
c.595T>G (p.Phe199Val)
c.484T>G (p.Phe162Val)
c.475T>G (p.Phe159Val)
19g.41012408T=CA2336260340CYP2B6c.1075T= (p.Phe359=)
c.1099T=
c.367T= (p.Phe123=)
n.570T=
c.595T= (p.Phe199=)
c.484T= (p.Phe162=)
c.475T= (p.Phe159=)
19g.41012409T>ACA405984562CYP2B6c.1076T>A (p.Phe359Tyr)
c.1100T>A
c.368T>A (p.Phe123Tyr)
n.571T>A
c.596T>A (p.Phe199Tyr)
c.485T>A (p.Phe162Tyr)
c.476T>A (p.Phe159Tyr)
19g.41012409T>CCA405984564CYP2B6c.1076T>C (p.Phe359Ser)
c.1100T>C
c.368T>C (p.Phe123Ser)
n.571T>C
c.596T>C (p.Phe199Ser)
c.485T>C (p.Phe162Ser)
c.476T>C (p.Phe159Ser)
19g.41012409T>GCA405984566CYP2B6c.1076T>G (p.Phe359Cys)
c.1100T>G
c.368T>G (p.Phe123Cys)
n.571T>G
c.596T>G (p.Phe199Cys)
c.485T>G (p.Phe162Cys)
c.476T>G (p.Phe159Cys)
19g.41012410T>ACA405984567CYP2B6c.1077T>A (p.Phe359Leu)
c.1101T>A
c.369T>A (p.Phe123Leu)
n.572T>A
c.597T>A (p.Phe199Leu)
c.486T>A (p.Phe162Leu)
c.477T>A (p.Phe159Leu)
19g.41012410T>CCA507537656CYP2B6c.1077T>C (p.Phe359=)
c.1101T>C
c.369T>C (p.Phe123=)
n.572T>C
c.597T>C (p.Phe199=)
c.486T>C (p.Phe162=)
c.477T>C (p.Phe159=)
19g.41012410T>GCA405984569CYP2B6c.1077T>G (p.Phe359Leu)
c.1101T>G
c.369T>G (p.Phe123Leu)
n.572T>G
c.597T>G (p.Phe199Leu)
c.486T>G (p.Phe162Leu)
c.477T>G (p.Phe159Leu)
19g.41012411T>ACA405984571CYP2B6c.1078T>A (p.Ser360Thr)
c.1102T>A
c.370T>A (p.Ser124Thr)
n.573T>A
c.598T>A (p.Ser200Thr)
c.487T>A (p.Ser163Thr)
c.478T>A (p.Ser160Thr)
19g.41012411T>CCA405984573CYP2B6c.1078T>C (p.Ser360Pro)
c.1102T>C
c.370T>C (p.Ser124Pro)
n.573T>C
c.598T>C (p.Ser200Pro)
c.487T>C (p.Ser163Pro)
c.478T>C (p.Ser160Pro)
 gnomAD v4
19g.41012411T>GCA9455470CYP2B6c.1078T>G (p.Ser360Ala)
c.1102T>G
c.370T>G (p.Ser124Ala)
n.573T>G
c.598T>G (p.Ser200Ala)
c.487T>G (p.Ser163Ala)
c.478T>G (p.Ser160Ala)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41012411T=CA2336260341CYP2B6c.1078T= (p.Ser360=)
c.1102T=
c.370T= (p.Ser124=)
n.573T=
c.598T= (p.Ser200=)
c.487T= (p.Ser163=)
c.478T= (p.Ser160=)
19g.41012412C>ACA405984576CYP2B6c.1079C>A (p.Ser360Tyr)
c.1103C>A
c.371C>A (p.Ser124Tyr)
n.574C>A
c.599C>A (p.Ser200Tyr)
c.488C>A (p.Ser163Tyr)
c.479C>A (p.Ser160Tyr)
 dbSNP gnomAD v3 gnomAD v4
19g.41012412C=CA2336260342CYP2B6c.1079C= (p.Ser360=)
c.1103C=
c.371C= (p.Ser124=)
n.574C=
c.599C= (p.Ser200=)
c.488C= (p.Ser163=)
c.479C= (p.Ser160=)
19g.41012412C>GCA405984577CYP2B6c.1079C>G (p.Ser360Cys)
c.1103C>G
c.371C>G (p.Ser124Cys)
n.574C>G
c.599C>G (p.Ser200Cys)
c.488C>G (p.Ser163Cys)
c.479C>G (p.Ser160Cys)
19g.41012412C>TCA405984579CYP2B6c.1079C>T (p.Ser360Phe)
c.1103C>T
c.371C>T (p.Ser124Phe)
n.574C>T
c.599C>T (p.Ser200Phe)
c.488C>T (p.Ser163Phe)
c.479C>T (p.Ser160Phe)
19g.41012413C>ACA507537658CYP2B6c.1080C>A (p.Ser360=)
c.1104C>A
c.372C>A (p.Ser124=)
n.575C>A
c.600C>A (p.Ser200=)
c.489C>A (p.Ser163=)
c.480C>A (p.Ser160=)
19g.41012413C=CA2336260343CYP2B6c.1080C= (p.Ser360=)
c.1104C=
c.372C= (p.Ser124=)
n.575C=
c.600C= (p.Ser200=)
c.489C= (p.Ser163=)
c.480C= (p.Ser160=)
19g.41012413C>GCA507537659CYP2B6c.1080C>G (p.Ser360=)
c.1104C>G
c.372C>G (p.Ser124=)
n.575C>G
c.600C>G (p.Ser200=)
c.489C>G (p.Ser163=)
c.480C>G (p.Ser160=)
19g.41012413C>TCA9455471CYP2B6c.1080C>T (p.Ser360=)
c.1104C>T
c.372C>T (p.Ser124=)
n.575C>T
c.600C>T (p.Ser200=)
c.489C>T (p.Ser163=)
c.480C>T (p.Ser160=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41012414G>ACA9455472CYP2B6c.1081G>A (p.Asp361Asn)
c.1105G>A
c.373G>A (p.Asp125Asn)
n.576G>A
c.601G>A (p.Asp201Asn)
c.490G>A (p.Asp164Asn)
c.481G>A (p.Asp161Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41012414G>CCA405984582CYP2B6c.1081G>C (p.Asp361His)
c.1105G>C
c.373G>C (p.Asp125His)
n.576G>C
c.601G>C (p.Asp201His)
c.490G>C (p.Asp164His)
c.481G>C (p.Asp161His)
19g.41012414G=CA2336260344CYP2B6c.1081G= (p.Asp361=)
c.1105G=
c.373G= (p.Asp125=)
n.576G=
c.601G= (p.Asp201=)
c.490G= (p.Asp164=)
c.481G= (p.Asp161=)
19g.41012414G>TCA405984584CYP2B6c.1081G>T (p.Asp361Tyr)
c.1105G>T
c.373G>T (p.Asp125Tyr)
n.576G>T
c.601G>T (p.Asp201Tyr)
c.490G>T (p.Asp164Tyr)
c.481G>T (p.Asp161Tyr)
 dbSNP gnomAD v2 gnomAD v4
19g.41012415A=CA2336260345CYP2B6c.1082A= (p.Asp361=)
c.1106A=
c.374A= (p.Asp125=)
n.577A=
c.602A= (p.Asp201=)
c.491A= (p.Asp164=)
c.482A= (p.Asp161=)
19g.41012415A>CCA405984588CYP2B6c.1082A>C (p.Asp361Ala)
c.1106A>C
c.374A>C (p.Asp125Ala)
n.577A>C
c.602A>C (p.Asp201Ala)
c.491A>C (p.Asp164Ala)
c.482A>C (p.Asp161Ala)
 gnomAD v4
19g.41012415A>GCA405984589CYP2B6c.1082A>G (p.Asp361Gly)
c.1106A>G
c.374A>G (p.Asp125Gly)
n.577A>G
c.602A>G (p.Asp201Gly)
c.491A>G (p.Asp164Gly)
c.482A>G (p.Asp161Gly)
19g.41012415A>TCA405984591CYP2B6c.1082A>T (p.Asp361Val)
c.1106A>T
c.374A>T (p.Asp125Val)
n.577A>T
c.602A>T (p.Asp201Val)
c.491A>T (p.Asp164Val)
c.482A>T (p.Asp161Val)
 dbSNP gnomAD v3 gnomAD v4
19g.41012416C>ACA405984593CYP2B6c.1083C>A (p.Asp361Glu)
c.1107C>A
c.375C>A (p.Asp125Glu)
n.578C>A
c.603C>A (p.Asp201Glu)
c.492C>A (p.Asp164Glu)
c.483C>A (p.Asp161Glu)
 gnomAD v4
19g.41012416C=CA2336260346CYP2B6c.1083C= (p.Asp361=)
c.1107C=
c.375C= (p.Asp125=)
n.578C=
c.603C= (p.Asp201=)
c.492C= (p.Asp164=)
c.483C= (p.Asp161=)
19g.41012416C>GCA405984595CYP2B6c.1083C>G (p.Asp361Glu)
c.1107C>G
c.375C>G (p.Asp125Glu)
n.578C>G
c.603C>G (p.Asp201Glu)
c.492C>G (p.Asp164Glu)
c.483C>G (p.Asp161Glu)
19g.41012416C>TCA507537661CYP2B6c.1083C>T (p.Asp361=)
c.1107C>T
c.375C>T (p.Asp125=)
n.578C>T
c.603C>T (p.Asp201=)
c.492C>T (p.Asp164=)
c.483C>T (p.Asp161=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41012417C>ACA405984597CYP2B6c.1084C>A (p.Leu362Ile)
c.1108C>A
c.376C>A (p.Leu126Ile)
n.579C>A
c.604C>A (p.Leu202Ile)
c.493C>A (p.Leu165Ile)
c.484C>A (p.Leu162Ile)
 dbSNP gnomAD v3 gnomAD v4
19g.41012417C=CA2336260347CYP2B6c.1084C= (p.Leu362=)
c.1108C=
c.376C= (p.Leu126=)
n.579C=
c.604C= (p.Leu202=)
c.493C= (p.Leu165=)
c.484C= (p.Leu162=)
19g.41012417C>GCA405984599CYP2B6c.1084C>G (p.Leu362Val)
c.1108C>G
c.376C>G (p.Leu126Val)
n.579C>G
c.604C>G (p.Leu202Val)
c.493C>G (p.Leu165Val)
c.484C>G (p.Leu162Val)
19g.41012417C>TCA405984601CYP2B6c.1084C>T (p.Leu362Phe)
c.1108C>T
c.376C>T (p.Leu126Phe)
n.579C>T
c.604C>T (p.Leu202Phe)
c.493C>T (p.Leu165Phe)
c.484C>T (p.Leu162Phe)
19g.41012418T>ACA9455473CYP2B6c.1085T>A (p.Leu362His)
c.1109T>A
c.377T>A (p.Leu126His)
n.580T>A
c.605T>A (p.Leu202His)
c.494T>A (p.Leu165His)
c.485T>A (p.Leu162His)
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.41012418T>CCA405984604CYP2B6c.1085T>C (p.Leu362Pro)
c.1109T>C
c.377T>C (p.Leu126Pro)
n.580T>C
c.605T>C (p.Leu202Pro)
c.494T>C (p.Leu165Pro)
c.485T>C (p.Leu162Pro)
19g.41012418T>GCA405984606CYP2B6c.1085T>G (p.Leu362Arg)
c.1109T>G
c.377T>G (p.Leu126Arg)
n.580T>G
c.605T>G (p.Leu202Arg)
c.494T>G (p.Leu165Arg)
c.485T>G (p.Leu162Arg)
19g.41012418T=CA2336260348CYP2B6c.1085T= (p.Leu362=)
c.1109T=
c.377T= (p.Leu126=)
n.580T=
c.605T= (p.Leu202=)
c.494T= (p.Leu165=)
c.485T= (p.Leu162=)
19g.41012419T>ACA507537664CYP2B6c.1086T>A (p.Leu362=)
c.1110T>A
c.378T>A (p.Leu126=)
n.581T>A
c.606T>A (p.Leu202=)
c.495T>A (p.Leu165=)
c.486T>A (p.Leu162=)
19g.41012419T>CCA507537666CYP2B6c.1086T>C (p.Leu362=)
c.1110T>C
c.378T>C (p.Leu126=)
n.581T>C
c.606T>C (p.Leu202=)
c.495T>C (p.Leu165=)
c.486T>C (p.Leu162=)
19g.41012419T>GCA507537667CYP2B6c.1086T>G (p.Leu362=)
c.1110T>G
c.378T>G (p.Leu126=)
n.581T>G
c.606T>G (p.Leu202=)
c.495T>G (p.Leu165=)
c.486T>G (p.Leu162=)
19g.41012420C>ACA405984612CYP2B6c.1087C>A (p.Leu363Ile)
c.1111C>A
c.379C>A (p.Leu127Ile)
n.582C>A
c.607C>A (p.Leu203Ile)
c.496C>A (p.Leu166Ile)
c.487C>A (p.Leu163Ile)
19g.41012420C=CA2336260349CYP2B6c.1087C= (p.Leu363=)
c.1111C=
c.379C= (p.Leu127=)
n.582C=
c.607C= (p.Leu203=)
c.496C= (p.Leu166=)
c.487C= (p.Leu163=)
19g.41012420C>GCA405984610CYP2B6c.1087C>G (p.Leu363Val)
c.1111C>G
c.379C>G (p.Leu127Val)
n.582C>G
c.607C>G (p.Leu203Val)
c.496C>G (p.Leu166Val)
c.487C>G (p.Leu163Val)
19g.41012420C>TCA405984609CYP2B6c.1087C>T (p.Leu363Phe)
c.1111C>T
c.379C>T (p.Leu127Phe)
n.582C>T
c.607C>T (p.Leu203Phe)
c.496C>T (p.Leu166Phe)
c.487C>T (p.Leu163Phe)
 dbSNP gnomAD v4
19g.41012421T>ACA405984618CYP2B6c.1088T>A (p.Leu363His)
c.1112T>A
c.380T>A (p.Leu127His)
n.583T>A
c.608T>A (p.Leu203His)
c.497T>A (p.Leu166His)
c.488T>A (p.Leu163His)
19g.41012421T>CCA405984614CYP2B6c.1088T>C (p.Leu363Pro)
c.1112T>C
c.380T>C (p.Leu127Pro)
n.583T>C
c.608T>C (p.Leu203Pro)
c.497T>C (p.Leu166Pro)
c.488T>C (p.Leu163Pro)
19g.41012421T>GCA405984616CYP2B6c.1088T>G (p.Leu363Arg)
c.1112T>G
c.380T>G (p.Leu127Arg)
n.583T>G
c.608T>G (p.Leu203Arg)
c.497T>G (p.Leu166Arg)
c.488T>G (p.Leu163Arg)
19g.41012422C>ACA9455474CYP2B6c.1089C>A (p.Leu363=)
c.1113C>A
c.381C>A (p.Leu127=)
n.584C>A
c.609C>A (p.Leu203=)
c.498C>A (p.Leu166=)
c.489C>A (p.Leu163=)
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.41012422C=CA2336260350CYP2B6c.1089C= (p.Leu363=)
c.1113C=
c.381C= (p.Leu127=)
n.584C=
c.609C= (p.Leu203=)
c.498C= (p.Leu166=)
c.489C= (p.Leu163=)
19g.41012422C>GCA507537669CYP2B6c.1089C>G (p.Leu363=)
c.1113C>G
c.381C>G (p.Leu127=)
n.584C>G
c.609C>G (p.Leu203=)
c.498C>G (p.Leu166=)
c.489C>G (p.Leu163=)
19g.41012422C>TCA507537670CYP2B6c.1089C>T (p.Leu363=)
c.1113C>T
c.381C>T (p.Leu127=)
n.584C>T
c.609C>T (p.Leu203=)
c.498C>T (p.Leu166=)
c.489C>T (p.Leu163=)
 COSMIC
19g.41012423C>ACA9455475CYP2B6c.1090C>A (p.Pro364Thr)
c.1114C>A
c.382C>A (p.Pro128Thr)
n.585C>A
c.610C>A (p.Pro204Thr)
c.499C>A (p.Pro167Thr)
c.490C>A (p.Pro164Thr)
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.41012423C=CA2336260351CYP2B6c.1090C= (p.Pro364=)
c.1114C=
c.382C= (p.Pro128=)
n.585C=
c.610C= (p.Pro204=)
c.499C= (p.Pro167=)
c.490C= (p.Pro164=)
19g.41012423C>GCA405984621CYP2B6c.1090C>G (p.Pro364Ala)
c.1114C>G
c.382C>G (p.Pro128Ala)
n.585C>G
c.610C>G (p.Pro204Ala)
c.499C>G (p.Pro167Ala)
c.490C>G (p.Pro164Ala)
19g.41012423C>TCA405984622CYP2B6c.1090C>T (p.Pro364Ser)
c.1114C>T
c.382C>T (p.Pro128Ser)
n.585C>T
c.610C>T (p.Pro204Ser)
c.499C>T (p.Pro167Ser)
c.490C>T (p.Pro164Ser)
 gnomAD v4 COSMIC
19g.41012424C>ACA405984624CYP2B6c.1091C>A (p.Pro364His)
c.1115C>A
c.383C>A (p.Pro128His)
n.586C>A
c.611C>A (p.Pro204His)
c.500C>A (p.Pro167His)
c.491C>A (p.Pro164His)
19g.41012424C>GCA405984625CYP2B6c.1091C>G (p.Pro364Arg)
c.1115C>G
c.383C>G (p.Pro128Arg)
n.586C>G
c.611C>G (p.Pro204Arg)
c.500C>G (p.Pro167Arg)
c.491C>G (p.Pro164Arg)
 gnomAD v4
19g.41012424C>TCA405984627CYP2B6c.1091C>T (p.Pro364Leu)
c.1115C>T
c.383C>T (p.Pro128Leu)
n.586C>T
c.611C>T (p.Pro204Leu)
c.500C>T (p.Pro167Leu)
c.491C>T (p.Pro164Leu)
 gnomAD v4 COSMIC
19g.41012425C>ACA507537672CYP2B6c.1092C>A (p.Pro364=)
c.1116C>A
c.384C>A (p.Pro128=)
n.587C>A
c.612C>A (p.Pro204=)
c.501C>A (p.Pro167=)
c.492C>A (p.Pro164=)
19g.41012425C=CA2336260352CYP2B6c.1092C= (p.Pro364=)
c.1116C=
c.384C= (p.Pro128=)
n.587C=
c.612C= (p.Pro204=)
c.501C= (p.Pro167=)
c.492C= (p.Pro164=)
19g.41012425C>GCA507537673CYP2B6c.1092C>G (p.Pro364=)
c.1116C>G
c.384C>G (p.Pro128=)
n.587C>G
c.612C>G (p.Pro204=)
c.501C>G (p.Pro167=)
c.492C>G (p.Pro164=)
19g.41012425C>TCA9455476CYP2B6c.1092C>T (p.Pro364=)
c.1116C>T
c.384C>T (p.Pro128=)
n.587C>T
c.612C>T (p.Pro204=)
c.501C>T (p.Pro167=)
c.492C>T (p.Pro164=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41012426A=CA2336260353CYP2B6c.1093A= (p.Met365=)
c.1117A=
c.385A= (p.Met129=)
n.588A=
c.613A= (p.Met205=)
c.502A= (p.Met168=)
c.493A= (p.Met165=)
19g.41012426A>CCA405984631CYP2B6c.1093A>C (p.Met365Leu)
c.1117A>C
c.385A>C (p.Met129Leu)
n.588A>C
c.613A>C (p.Met205Leu)
c.502A>C (p.Met168Leu)
c.493A>C (p.Met165Leu)
19g.41012426A>GCA405984632CYP2B6c.1093A>G (p.Met365Val)
c.1117A>G
c.385A>G (p.Met129Val)
n.588A>G
c.613A>G (p.Met205Val)
c.502A>G (p.Met168Val)
c.493A>G (p.Met165Val)
 dbSNP gnomAD v2 gnomAD v4
19g.41012426A>TCA405984634CYP2B6c.1093A>T (p.Met365Leu)
c.1117A>T
c.385A>T (p.Met129Leu)
n.588A>T
c.613A>T (p.Met205Leu)
c.502A>T (p.Met168Leu)
c.493A>T (p.Met165Leu)
 gnomAD v4
19g.41012427T>ACA405984637CYP2B6c.1094T>A (p.Met365Lys)
c.1118T>A
c.386T>A (p.Met129Lys)
n.589T>A
c.614T>A (p.Met205Lys)
c.503T>A (p.Met168Lys)
c.494T>A (p.Met165Lys)
19g.41012427T>CCA405984635CYP2B6c.1094T>C (p.Met365Thr)
c.1118T>C
c.386T>C (p.Met129Thr)
n.589T>C
c.614T>C (p.Met205Thr)
c.503T>C (p.Met168Thr)
c.494T>C (p.Met165Thr)
19g.41012427T>GCA308499228CYP2B6c.1094T>G (p.Met365Arg)
c.1118T>G
c.386T>G (p.Met129Arg)
n.589T>G
c.614T>G (p.Met205Arg)
c.503T>G (p.Met168Arg)
c.494T>G (p.Met165Arg)
 dbSNP gnomAD v4
19g.41012427T=CA2336260354CYP2B6c.1094T= (p.Met365=)
c.1118T=
c.386T= (p.Met129=)
n.589T=
c.614T= (p.Met205=)
c.503T= (p.Met168=)
c.494T= (p.Met165=)
19g.41012428G>ACA405984639CYP2B6c.1095G>A (p.Met365Ile)
c.1119G>A
c.387G>A (p.Met129Ile)
n.590G>A
c.615G>A (p.Met205Ile)
c.504G>A (p.Met168Ile)
c.495G>A (p.Met165Ile)
19g.41012428G>CCA405984640CYP2B6c.1095G>C (p.Met365Ile)
c.1119G>C
c.387G>C (p.Met129Ile)
n.590G>C
c.615G>C (p.Met205Ile)
c.504G>C (p.Met168Ile)
c.495G>C (p.Met165Ile)
19g.41012428G>TCA405984643CYP2B6c.1095G>T (p.Met365Ile)
c.1119G>T
c.387G>T (p.Met129Ile)
n.590G>T
c.615G>T (p.Met205Ile)
c.504G>T (p.Met168Ile)
c.495G>T (p.Met165Ile)
19g.41012429G>ACA405984645CYP2B6c.1096G>A (p.Gly366Ser)
c.1120G>A
c.388G>A (p.Gly130Ser)
n.591G>A
c.616G>A (p.Gly206Ser)
c.505G>A (p.Gly169Ser)
c.496G>A (p.Gly166Ser)
19g.41012429G>CCA405984647CYP2B6c.1096G>C (p.Gly366Arg)
c.1120G>C
c.388G>C (p.Gly130Arg)
n.591G>C
c.616G>C (p.Gly206Arg)
c.505G>C (p.Gly169Arg)
c.496G>C (p.Gly166Arg)
19g.41012429G=CA2336260355CYP2B6c.1096G= (p.Gly366=)
c.1120G=
c.388G= (p.Gly130=)
n.591G=
c.616G= (p.Gly206=)
c.505G= (p.Gly169=)
c.496G= (p.Gly166=)
19g.41012429G>TCA405984649CYP2B6c.1096G>T (p.Gly366Cys)
c.1120G>T
c.388G>T (p.Gly130Cys)
n.591G>T
c.616G>T (p.Gly206Cys)
c.505G>T (p.Gly169Cys)
c.496G>T (p.Gly166Cys)
 dbSNP
19g.41012430G>ACA9455477CYP2B6c.1097G>A (p.Gly366Asp)
c.1121G>A
c.389G>A (p.Gly130Asp)
n.592G>A
c.617G>A (p.Gly206Asp)
c.506G>A (p.Gly169Asp)
c.497G>A (p.Gly166Asp)
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.41012430G>CCA405984652CYP2B6c.1097G>C (p.Gly366Ala)
c.1121G>C
c.389G>C (p.Gly130Ala)
n.592G>C
c.617G>C (p.Gly206Ala)
c.506G>C (p.Gly169Ala)
c.497G>C (p.Gly166Ala)
 gnomAD v4
19g.41012430G=CA2336260356CYP2B6c.1097G= (p.Gly366=)
c.1121G=
c.389G= (p.Gly130=)
n.592G=
c.617G= (p.Gly206=)
c.506G= (p.Gly169=)
c.497G= (p.Gly166=)
19g.41012430G>TCA405984653CYP2B6c.1097G>T (p.Gly366Val)
c.1121G>T
c.389G>T (p.Gly130Val)
n.592G>T
c.617G>T (p.Gly206Val)
c.506G>T (p.Gly169Val)
c.497G>T (p.Gly166Val)
19g.41012431T>ACA507537678CYP2B6c.1098T>A (p.Gly366=)
c.1122T>A
c.390T>A (p.Gly130=)
n.593T>A
c.618T>A (p.Gly206=)
c.507T>A (p.Gly169=)
c.498T>A (p.Gly166=)
19g.41012431T>CCA507537680CYP2B6c.1098T>C (p.Gly366=)
c.1122T>C
c.390T>C (p.Gly130=)
n.593T>C
c.618T>C (p.Gly206=)
c.507T>C (p.Gly169=)
c.498T>C (p.Gly166=)
 gnomAD v4
19g.41012431T>GCA9455478CYP2B6c.1098T>G (p.Gly366=)
c.1122T>G
c.390T>G (p.Gly130=)
n.593T>G
c.618T>G (p.Gly206=)
c.507T>G (p.Gly169=)
c.498T>G (p.Gly166=)
 dbSNP ExAC gnomAD v2
19g.41012431T=CA2336260357CYP2B6c.1098T= (p.Gly366=)
c.1122T=
c.390T= (p.Gly130=)
n.593T=
c.618T= (p.Gly206=)
c.507T= (p.Gly169=)
c.498T= (p.Gly166=)
19g.41012432G>ACA405984656CYP2B6c.1099G>A (p.Val367Met)
c.1123G>A
c.391G>A (p.Val131Met)
n.594G>A
c.619G>A (p.Val207Met)
c.508G>A (p.Val170Met)
c.499G>A (p.Val167Met)
19g.41012432G>CCA405984658CYP2B6c.1099G>C (p.Val367Leu)
c.1123G>C
c.391G>C (p.Val131Leu)
n.594G>C
c.619G>C (p.Val207Leu)
c.508G>C (p.Val170Leu)
c.499G>C (p.Val167Leu)
19g.41012432G=CA2336260358CYP2B6c.1099G= (p.Val367=)
c.1123G=
c.391G= (p.Val131=)
n.594G=
c.619G= (p.Val207=)
c.508G= (p.Val170=)
c.499G= (p.Val167=)
19g.41012432G>TCA9455479CYP2B6c.1099G>T (p.Val367Leu)
c.1123G>T
c.391G>T (p.Val131Leu)
n.594G>T
c.619G>T (p.Val207Leu)
c.508G>T (p.Val170Leu)
c.499G>T (p.Val167Leu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41012433T>ACA405984663CYP2B6c.1100T>A (p.Val367Glu)
c.1124T>A
c.392T>A (p.Val131Glu)
n.595T>A
c.620T>A (p.Val207Glu)
c.509T>A (p.Val170Glu)
c.500T>A (p.Val167Glu)
19g.41012433T>CCA405984665CYP2B6c.1100T>C (p.Val367Ala)
c.1124T>C
c.392T>C (p.Val131Ala)
n.595T>C
c.620T>C (p.Val207Ala)
c.509T>C (p.Val170Ala)
c.500T>C (p.Val167Ala)
19g.41012433T>GCA405984661CYP2B6c.1100T>G (p.Val367Gly)
c.1124T>G
c.392T>G (p.Val131Gly)
n.595T>G
c.620T>G (p.Val207Gly)
c.509T>G (p.Val170Gly)
c.500T>G (p.Val167Gly)
19g.41012434G>ACA9455480CYP2B6c.1101G>A (p.Val367=)
c.1125G>A
c.393G>A (p.Val131=)
n.596G>A
c.621G>A (p.Val207=)
c.510G>A (p.Val170=)
c.501G>A (p.Val167=)
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.41012434G>CCA507537685CYP2B6c.1101G>C (p.Val367=)
c.1125G>C
c.393G>C (p.Val131=)
n.596G>C
c.621G>C (p.Val207=)
c.510G>C (p.Val170=)
c.501G>C (p.Val167=)
19g.41012434G=CA2336260359CYP2B6c.1101G= (p.Val367=)
c.1125G=
c.393G= (p.Val131=)
n.596G=
c.621G= (p.Val207=)
c.510G= (p.Val170=)
c.501G= (p.Val167=)
19g.41012434G>TCA507537684CYP2B6c.1101G>T (p.Val367=)
c.1125G>T
c.393G>T (p.Val131=)
n.596G>T
c.621G>T (p.Val207=)
c.510G>T (p.Val170=)
c.501G>T (p.Val167=)
19g.41012435C>ACA405984671CYP2B6c.1102C>A (p.Pro368Thr)
c.1126C>A
c.394C>A (p.Pro132Thr)
n.597C>A
c.622C>A (p.Pro208Thr)
c.511C>A (p.Pro171Thr)
c.502C>A (p.Pro168Thr)
 gnomAD v4
19g.41012435C=CA2336260360CYP2B6c.1102C= (p.Pro368=)
c.1126C=
c.394C= (p.Pro132=)
n.597C=
c.622C= (p.Pro208=)
c.511C= (p.Pro171=)
c.502C= (p.Pro168=)
19g.41012435C>GCA405984667CYP2B6c.1102C>G (p.Pro368Ala)
c.1126C>G
c.394C>G (p.Pro132Ala)
n.597C>G
c.622C>G (p.Pro208Ala)
c.511C>G (p.Pro171Ala)
c.502C>G (p.Pro168Ala)
19g.41012435C>TCA405984669CYP2B6c.1102C>T (p.Pro368Ser)
c.1126C>T
c.394C>T (p.Pro132Ser)
n.597C>T
c.622C>T (p.Pro208Ser)
c.511C>T (p.Pro171Ser)
c.502C>T (p.Pro168Ser)
 dbSNP gnomAD v4
19g.41012436C>ACA405984673CYP2B6c.1103C>A (p.Pro368His)
c.1127C>A
c.395C>A (p.Pro132His)
n.598C>A
c.623C>A (p.Pro208His)
c.512C>A (p.Pro171His)
c.503C>A (p.Pro168His)
19g.41012436C=CA2336260361CYP2B6c.1103C= (p.Pro368=)
c.1127C=
c.395C= (p.Pro132=)
n.598C=
c.623C= (p.Pro208=)
c.512C= (p.Pro171=)
c.503C= (p.Pro168=)
19g.41012436C>GCA405984675CYP2B6c.1103C>G (p.Pro368Arg)
c.1127C>G
c.395C>G (p.Pro132Arg)
n.598C>G
c.623C>G (p.Pro208Arg)
c.512C>G (p.Pro171Arg)
c.503C>G (p.Pro168Arg)
19g.41012436C>TCA9455481CYP2B6c.1103C>T (p.Pro368Leu)
c.1127C>T
c.395C>T (p.Pro132Leu)
n.598C>T
c.623C>T (p.Pro208Leu)
c.512C>T (p.Pro171Leu)
c.503C>T (p.Pro168Leu)
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.41012437C>ACA507537688CYP2B6c.1104C>A (p.Pro368=)
c.1128C>A
c.396C>A (p.Pro132=)
n.599C>A
c.624C>A (p.Pro208=)
c.513C>A (p.Pro171=)
c.504C>A (p.Pro168=)
19g.41012437C>GCA507537691CYP2B6c.1104C>G (p.Pro368=)
c.1128C>G
c.396C>G (p.Pro132=)
n.599C>G
c.624C>G (p.Pro208=)
c.513C>G (p.Pro171=)
c.504C>G (p.Pro168=)
19g.41012437C>TCA507537689CYP2B6c.1104C>T (p.Pro368=)
c.1128C>T
c.396C>T (p.Pro132=)
n.599C>T
c.624C>T (p.Pro208=)
c.513C>T (p.Pro171=)
c.504C>T (p.Pro168=)
19g.41012438C>ACA405984678CYP2B6c.1105C>A (p.His369Asn)
c.1129C>A
c.397C>A (p.His133Asn)
n.600C>A
c.625C>A (p.His209Asn)
c.514C>A (p.His172Asn)
c.505C>A (p.His169Asn)
19g.41012438C=CA2336260362CYP2B6c.1105C= (p.His369=)
c.1129C=
c.397C= (p.His133=)
n.600C=
c.625C= (p.His209=)
c.514C= (p.His172=)
c.505C= (p.His169=)
19g.41012438C>GCA405984680CYP2B6c.1105C>G (p.His369Asp)
c.1129C>G
c.397C>G (p.His133Asp)
n.600C>G
c.625C>G (p.His209Asp)
c.514C>G (p.His172Asp)
c.505C>G (p.His169Asp)
19g.41012438C>TCA9455482CYP2B6c.1105C>T (p.His369Tyr)
c.1129C>T
c.397C>T (p.His133Tyr)
n.600C>T
c.625C>T (p.His209Tyr)
c.514C>T (p.His172Tyr)
c.505C>T (p.His169Tyr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.41012439A>CCA405984683CYP2B6c.1106A>C (p.His369Pro)
c.1130A>C
c.398A>C (p.His133Pro)
n.601A>C
c.626A>C (p.His209Pro)
c.515A>C (p.His172Pro)
c.506A>C (p.His169Pro)
19g.41012439A>GCA405984684CYP2B6c.1106A>G (p.His369Arg)
c.1130A>G
c.398A>G (p.His133Arg)
n.601A>G
c.626A>G (p.His209Arg)
c.515A>G (p.His172Arg)
c.506A>G (p.His169Arg)
19g.41012439A>TCA405984686CYP2B6c.1106A>T (p.His369Leu)
c.1130A>T
c.398A>T (p.His133Leu)
n.601A>T
c.626A>T (p.His209Leu)
c.515A>T (p.His172Leu)
c.506A>T (p.His169Leu)
19g.41012440C>ACA405984688CYP2B6c.1107C>A (p.His369Gln)
c.1131C>A
c.399C>A (p.His133Gln)
n.602C>A
c.627C>A (p.His209Gln)
c.516C>A (p.His172Gln)
c.507C>A (p.His169Gln)
19g.41012440C=CA2336260363CYP2B6c.1107C= (p.His369=)
c.1131C=
c.399C= (p.His133=)
n.602C=
c.627C= (p.His209=)
c.516C= (p.His172=)
c.507C= (p.His169=)
19g.41012440C>GCA405984690CYP2B6c.1107C>G (p.His369Gln)
c.1131C>G
c.399C>G (p.His133Gln)
n.602C>G
c.627C>G (p.His209Gln)
c.516C>G (p.His172Gln)
c.507C>G (p.His169Gln)
19g.41012440C>TCA507537695CYP2B6c.1107C>T (p.His369=)
c.1131C>T
c.399C>T (p.His133=)
n.602C>T
c.627C>T (p.His209=)
c.516C>T (p.His172=)
c.507C>T (p.His169=)
 dbSNP gnomAD v4
19g.41012441A>CCA405984692CYP2B6c.1108A>C (p.Ile370Leu)
c.1132A>C
c.400A>C (p.Ile134Leu)
n.603A>C
c.628A>C (p.Ile210Leu)
c.517A>C (p.Ile173Leu)
c.508A>C (p.Ile170Leu)
19g.41012441A>GCA405984696CYP2B6c.1108A>G (p.Ile370Val)
c.1132A>G
c.400A>G (p.Ile134Val)
n.603A>G
c.628A>G (p.Ile210Val)
c.517A>G (p.Ile173Val)
c.508A>G (p.Ile170Val)
 gnomAD v4
19g.41012441A>TCA405984694CYP2B6c.1108A>T (p.Ile370Phe)
c.1132A>T
c.400A>T (p.Ile134Phe)
n.603A>T
c.628A>T (p.Ile210Phe)
c.517A>T (p.Ile173Phe)
c.508A>T (p.Ile170Phe)
19g.41012442T>ACA405984698CYP2B6c.1109T>A (p.Ile370Asn)
c.1133T>A
c.401T>A (p.Ile134Asn)
n.604T>A
c.629T>A (p.Ile210Asn)
c.518T>A (p.Ile173Asn)
c.509T>A (p.Ile170Asn)
19g.41012442T>CCA405984700CYP2B6c.1109T>C (p.Ile370Thr)
c.1133T>C
c.401T>C (p.Ile134Thr)
n.604T>C
c.629T>C (p.Ile210Thr)
c.518T>C (p.Ile173Thr)
c.509T>C (p.Ile170Thr)
19g.41012442T>GCA405984702CYP2B6c.1109T>G (p.Ile370Ser)
c.1133T>G
c.401T>G (p.Ile134Ser)
n.604T>G
c.629T>G (p.Ile210Ser)
c.518T>G (p.Ile173Ser)
c.509T>G (p.Ile170Ser)
19g.41012442_41012445delCA2814422291CYP2B6c.1109_1112del (p.Ile370ThrfsTer22)
c.1133_1136del
c.401_404del (p.Ile134ThrfsTer22)
n.604_607del
c.1109_1112del (p.Ile370ThrfsTer21)
c.1109_1112del (p.Ile370ThrfsTer15)
c.1109_1112del (p.Ile370ThrfsTer?)
c.629_632del (p.Ile210ThrfsTer22)
c.518_521del (p.Ile173ThrfsTer22)
c.509_512del (p.Ile170ThrfsTer22)
19g.41012443T>ACA507537698CYP2B6c.1110T>A (p.Ile370=)
c.1134T>A
c.402T>A (p.Ile134=)
n.605T>A
c.630T>A (p.Ile210=)
c.519T>A (p.Ile173=)
c.510T>A (p.Ile170=)
19g.41012443T>CCA507537699CYP2B6c.1110T>C (p.Ile370=)
c.1134T>C
c.402T>C (p.Ile134=)
n.605T>C
c.630T>C (p.Ile210=)
c.519T>C (p.Ile173=)
c.510T>C (p.Ile170=)
 dbSNP gnomAD v4
19g.41012443T>GCA405984704CYP2B6c.1110T>G (p.Ile370Met)
c.1134T>G
c.402T>G (p.Ile134Met)
n.605T>G
c.630T>G (p.Ile210Met)
c.519T>G (p.Ile173Met)
c.510T>G (p.Ile170Met)
19g.41012443T=CA2336260364CYP2B6c.1110T= (p.Ile370=)
c.1134T=
c.402T= (p.Ile134=)
n.605T=
c.630T= (p.Ile210=)
c.519T= (p.Ile173=)
c.510T= (p.Ile170=)
19g.41012444G>ACA405984706CYP2B6c.1111G>A (p.Val371Ile)
c.1135G>A
c.403G>A (p.Val135Ile)
n.606G>A
c.631G>A (p.Val211Ile)
c.520G>A (p.Val174Ile)
c.511G>A (p.Val171Ile)
19g.41012444G>CCA405984708CYP2B6c.1111G>C (p.Val371Leu)
c.1135G>C
c.403G>C (p.Val135Leu)
n.606G>C
c.631G>C (p.Val211Leu)
c.520G>C (p.Val174Leu)
c.511G>C (p.Val171Leu)
19g.41012444G=CA2336260365CYP2B6c.1111G= (p.Val371=)
c.1135G=
c.403G= (p.Val135=)
n.606G=
c.631G= (p.Val211=)
c.520G= (p.Val174=)
c.511G= (p.Val171=)
19g.41012444G>TCA9455483CYP2B6c.1111G>T (p.Val371Phe)
c.1135G>T
c.403G>T (p.Val135Phe)
n.606G>T
c.631G>T (p.Val211Phe)
c.520G>T (p.Val174Phe)
c.511G>T (p.Val171Phe)
 dbSNP ExAC gnomAD v3 gnomAD v4
19g.41012445T>ACA405984711CYP2B6c.1112T>A (p.Val371Asp)
c.1136T>A
c.404T>A (p.Val135Asp)
n.607T>A
c.632T>A (p.Val211Asp)
c.521T>A (p.Val174Asp)
c.512T>A (p.Val171Asp)
19g.41012445T>CCA405984713CYP2B6c.1112T>C (p.Val371Ala)
c.1136T>C
c.404T>C (p.Val135Ala)
n.607T>C
c.632T>C (p.Val211Ala)
c.521T>C (p.Val174Ala)
c.512T>C (p.Val171Ala)
 gnomAD v4
19g.41012445T>GCA405984715CYP2B6c.1112T>G (p.Val371Gly)
c.1136T>G
c.404T>G (p.Val135Gly)
n.607T>G
c.632T>G (p.Val211Gly)
c.521T>G (p.Val174Gly)
c.512T>G (p.Val171Gly)
19g.41012446C>ACA507537700CYP2B6c.1113C>A (p.Val371=)
c.1137C>A
c.405C>A (p.Val135=)
n.608C>A
c.633C>A (p.Val211=)
c.522C>A (p.Val174=)
c.513C>A (p.Val171=)
19g.41012446C>GCA507537701CYP2B6c.1113C>G (p.Val371=)
c.1137C>G
c.405C>G (p.Val135=)
n.608C>G
c.633C>G (p.Val211=)
c.522C>G (p.Val174=)
c.513C>G (p.Val171=)
19g.41012446C>TCA507537703CYP2B6c.1113C>T (p.Val371=)
c.1137C>T
c.405C>T (p.Val135=)
n.608C>T
c.633C>T (p.Val211=)
c.522C>T (p.Val174=)
c.513C>T (p.Val171=)
19g.41012447A=CA2336260366CYP2B6c.1114A= (p.Thr372=)
c.1138A=
c.406A= (p.Thr136=)
n.609A=
c.634A= (p.Thr212=)
c.523A= (p.Thr175=)
c.514A= (p.Thr172=)
19g.41012447A>CCA405984717CYP2B6c.1114A>C (p.Thr372Pro)
c.1138A>C
c.406A>C (p.Thr136Pro)
n.609A>C
c.634A>C (p.Thr212Pro)
c.523A>C (p.Thr175Pro)
c.514A>C (p.Thr172Pro)
19g.41012447A>GCA9455484CYP2B6c.1114A>G (p.Thr372Ala)
c.1138A>G
c.406A>G (p.Thr136Ala)
n.609A>G
c.634A>G (p.Thr212Ala)
c.523A>G (p.Thr175Ala)
c.514A>G (p.Thr172Ala)
 dbSNP ExAC gnomAD v2
19g.41012447A>TCA405984716CYP2B6c.1114A>T (p.Thr372Ser)
c.1138A>T
c.406A>T (p.Thr136Ser)
n.609A>T
c.634A>T (p.Thr212Ser)
c.523A>T (p.Thr175Ser)
c.514A>T (p.Thr172Ser)
19g.41012448C>ACA405984720CYP2B6c.1115C>A (p.Thr372Asn)
c.1139C>A
c.407C>A (p.Thr136Asn)
n.610C>A
c.635C>A (p.Thr212Asn)
c.524C>A (p.Thr175Asn)
c.515C>A (p.Thr172Asn)
19g.41012448C>GCA405984721CYP2B6c.1115C>G (p.Thr372Ser)
c.1139C>G
c.407C>G (p.Thr136Ser)
n.610C>G
c.635C>G (p.Thr212Ser)
c.524C>G (p.Thr175Ser)
c.515C>G (p.Thr172Ser)
19g.41012448C>TCA405984723CYP2B6c.1115C>T (p.Thr372Ile)
c.1139C>T
c.407C>T (p.Thr136Ile)
n.610C>T
c.635C>T (p.Thr212Ile)
c.524C>T (p.Thr175Ile)
c.515C>T (p.Thr172Ile)
19g.41012449C>ACA507537704CYP2B6c.1116C>A (p.Thr372=)
c.1140C>A
c.408C>A (p.Thr136=)
n.611C>A
c.636C>A (p.Thr212=)
c.525C>A (p.Thr175=)
c.516C>A (p.Thr172=)
19g.41012449C=CA2336260367CYP2B6c.1116C= (p.Thr372=)
c.1140C=
c.408C= (p.Thr136=)
n.611C=
c.636C= (p.Thr212=)
c.525C= (p.Thr175=)
c.516C= (p.Thr172=)
19g.41012449C>GCA507537705CYP2B6c.1116C>G (p.Thr372=)
c.1140C>G
c.408C>G (p.Thr136=)
n.611C>G
c.636C>G (p.Thr212=)
c.525C>G (p.Thr175=)
c.516C>G (p.Thr172=)
19g.41012449C>TCA9455485CYP2B6c.1116C>T (p.Thr372=)
c.1140C>T
c.408C>T (p.Thr136=)
n.611C>T
c.636C>T (p.Thr212=)
c.525C>T (p.Thr175=)
c.516C>T (p.Thr172=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41012450C>ACA405984725CYP2B6c.1117C>A (p.Gln373Lys)
c.1141C>A
c.409C>A (p.Gln137Lys)
n.612C>A
c.637C>A (p.Gln213Lys)
c.526C>A (p.Gln176Lys)
c.517C>A (p.Gln173Lys)
19g.41012450C>GCA405984726CYP2B6c.1117C>G (p.Gln373Glu)
c.1141C>G
c.409C>G (p.Gln137Glu)
n.612C>G
c.637C>G (p.Gln213Glu)
c.526C>G (p.Gln176Glu)
c.517C>G (p.Gln173Glu)
19g.41012450C>TCA405984728CYP2B6c.1117C>T (p.Gln373Ter)
c.1141C>T
c.409C>T (p.Gln137Ter)
n.612C>T
c.637C>T (p.Gln213Ter)
c.526C>T (p.Gln176Ter)
c.517C>T (p.Gln173Ter)
 gnomAD v4
19g.41012451A>CCA405984729CYP2B6c.1118A>C (p.Gln373Pro)
c.1142A>C
c.410A>C (p.Gln137Pro)
n.613A>C
c.638A>C (p.Gln213Pro)
c.527A>C (p.Gln176Pro)
c.518A>C (p.Gln173Pro)
19g.41012451A>GCA405984731CYP2B6c.1118A>G (p.Gln373Arg)
c.1142A>G
c.410A>G (p.Gln137Arg)
n.613A>G
c.638A>G (p.Gln213Arg)
c.527A>G (p.Gln176Arg)
c.518A>G (p.Gln173Arg)
19g.41012451A>TCA405984733CYP2B6c.1118A>T (p.Gln373Leu)
c.1142A>T
c.410A>T (p.Gln137Leu)
n.613A>T
c.638A>T (p.Gln213Leu)
c.527A>T (p.Gln176Leu)
c.518A>T (p.Gln173Leu)
19g.41012452A=CA2336260368CYP2B6c.1119A= (p.Gln373=)
c.1143A=
c.411A= (p.Gln137=)
n.614A=
c.639A= (p.Gln213=)
c.528A= (p.Gln176=)
c.519A= (p.Gln173=)
19g.41012452A>CCA405984735CYP2B6c.1119A>C (p.Gln373His)
c.1143A>C
c.411A>C (p.Gln137His)
n.614A>C
c.639A>C (p.Gln213His)
c.528A>C (p.Gln176His)
c.519A>C (p.Gln173His)
19g.41012452A>GCA507537707CYP2B6c.1119A>G (p.Gln373=)
c.1143A>G
c.411A>G (p.Gln137=)
n.614A>G
c.639A>G (p.Gln213=)
c.528A>G (p.Gln176=)
c.519A>G (p.Gln173=)
 dbSNP gnomAD v3 gnomAD v4
19g.41012452A>TCA405984737CYP2B6c.1119A>T (p.Gln373His)
c.1143A>T
c.411A>T (p.Gln137His)
n.614A>T
c.639A>T (p.Gln213His)
c.528A>T (p.Gln176His)
c.519A>T (p.Gln173His)
19g.41012453C>ACA9455486CYP2B6c.1120C>A (p.His374Asn)
c.1144C>A
c.412C>A (p.His138Asn)
n.615C>A
c.640C>A (p.His214Asn)
c.529C>A (p.His177Asn)
c.520C>A (p.His174Asn)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41012453C=CA2336260369CYP2B6c.1120C= (p.His374=)
c.1144C=
c.412C= (p.His138=)
n.615C=
c.640C= (p.His214=)
c.529C= (p.His177=)
c.520C= (p.His174=)
19g.41012453C>GCA405984740CYP2B6c.1120C>G (p.His374Asp)
c.1144C>G
c.412C>G (p.His138Asp)
n.615C>G
c.640C>G (p.His214Asp)
c.529C>G (p.His177Asp)
c.520C>G (p.His174Asp)
19g.41012453C>TCA405984739CYP2B6c.1120C>T (p.His374Tyr)
c.1144C>T
c.412C>T (p.His138Tyr)
n.615C>T
c.640C>T (p.His214Tyr)
c.529C>T (p.His177Tyr)
c.520C>T (p.His174Tyr)
19g.41012454A=CA2336260370CYP2B6c.1121A= (p.His374=)
c.1145A=
c.413A= (p.His138=)
n.616A=
c.641A= (p.His214=)
c.530A= (p.His177=)
c.521A= (p.His174=)
19g.41012454A>CCA405984742CYP2B6c.1121A>C (p.His374Pro)
c.1145A>C
c.413A>C (p.His138Pro)
n.616A>C
c.641A>C (p.His214Pro)
c.530A>C (p.His177Pro)
c.521A>C (p.His174Pro)
 dbSNP gnomAD v4
19g.41012454A>GCA405984743CYP2B6c.1121A>G (p.His374Arg)
c.1145A>G
c.413A>G (p.His138Arg)
n.616A>G
c.641A>G (p.His214Arg)
c.530A>G (p.His177Arg)
c.521A>G (p.His174Arg)
19g.41012454A>TCA405984745CYP2B6c.1121A>T (p.His374Leu)
c.1145A>T
c.413A>T (p.His138Leu)
n.616A>T
c.641A>T (p.His214Leu)
c.530A>T (p.His177Leu)
c.521A>T (p.His174Leu)
19g.41012455C>ACA405984748CYP2B6c.1122C>A (p.His374Gln)
c.1146C>A
c.414C>A (p.His138Gln)
n.617C>A
c.642C>A (p.His214Gln)
c.531C>A (p.His177Gln)
c.522C>A (p.His174Gln)
19g.41012455C>GCA405984749CYP2B6c.1122C>G (p.His374Gln)
c.1146C>G
c.414C>G (p.His138Gln)
n.617C>G
c.642C>G (p.His214Gln)
c.531C>G (p.His177Gln)
c.522C>G (p.His174Gln)
19g.41012455C>TCA507537711CYP2B6c.1122C>T (p.His374=)
c.1146C>T
c.414C>T (p.His138=)
n.617C>T
c.642C>T (p.His214=)
c.531C>T (p.His177=)
c.522C>T (p.His174=)
 gnomAD v4
19g.41012456A>CCA405984755CYP2B6c.1123A>C (p.Thr375Pro)
c.1147A>C
c.415A>C (p.Thr139Pro)
n.618A>C
c.643A>C (p.Thr215Pro)
c.532A>C (p.Thr178Pro)
c.523A>C (p.Thr175Pro)
19g.41012456A>GCA405984752CYP2B6c.1123A>G (p.Thr375Ala)
c.1147A>G
c.415A>G (p.Thr139Ala)
n.618A>G
c.643A>G (p.Thr215Ala)
c.532A>G (p.Thr178Ala)
c.523A>G (p.Thr175Ala)
19g.41012456A>TCA405984754CYP2B6c.1123A>T (p.Thr375Ser)
c.1147A>T
c.415A>T (p.Thr139Ser)
n.618A>T
c.643A>T (p.Thr215Ser)
c.532A>T (p.Thr178Ser)
c.523A>T (p.Thr175Ser)
19g.41012457C>ACA405984757CYP2B6c.1124C>A (p.Thr375Asn)
c.1148C>A
c.416C>A (p.Thr139Asn)
n.619C>A
c.644C>A (p.Thr215Asn)
c.533C>A (p.Thr178Asn)
c.524C>A (p.Thr175Asn)
 dbSNP gnomAD v2 gnomAD v4
19g.41012457C=CA2336260371CYP2B6c.1124C= (p.Thr375=)
c.1148C=
c.416C= (p.Thr139=)
n.619C=
c.644C= (p.Thr215=)
c.533C= (p.Thr178=)
c.524C= (p.Thr175=)
19g.41012457C>GCA405984760CYP2B6c.1124C>G (p.Thr375Ser)
c.1148C>G
c.416C>G (p.Thr139Ser)
n.619C>G
c.644C>G (p.Thr215Ser)
c.533C>G (p.Thr178Ser)
c.524C>G (p.Thr175Ser)
19g.41012457C>TCA405984762CYP2B6c.1124C>T (p.Thr375Ile)
c.1148C>T
c.416C>T (p.Thr139Ile)
n.619C>T
c.644C>T (p.Thr215Ile)
c.533C>T (p.Thr178Ile)
c.524C>T (p.Thr175Ile)
19g.41012458C>ACA507537717CYP2B6c.1125C>A (p.Thr375=)
c.1149C>A
c.417C>A (p.Thr139=)
n.620C>A
c.645C>A (p.Thr215=)
c.534C>A (p.Thr178=)
c.525C>A (p.Thr175=)
19g.41012458C>GCA507537715CYP2B6c.1125C>G (p.Thr375=)
c.1149C>G
c.417C>G (p.Thr139=)
n.620C>G
c.645C>G (p.Thr215=)
c.534C>G (p.Thr178=)
c.525C>G (p.Thr175=)
19g.41012458C>TCA507537713CYP2B6c.1125C>T (p.Thr375=)
c.1149C>T
c.417C>T (p.Thr139=)
n.620C>T
c.645C>T (p.Thr215=)
c.534C>T (p.Thr178=)
c.525C>T (p.Thr175=)
19g.41012459A=CA2336260372CYP2B6c.1126A= (p.Ser376=)
c.1150A=
c.418A= (p.Ser140=)
n.621A=
c.646A= (p.Ser216=)
c.535A= (p.Ser179=)
c.526A= (p.Ser176=)
19g.41012459A>CCA405984764CYP2B6c.1126A>C (p.Ser376Arg)
c.1150A>C
c.418A>C (p.Ser140Arg)
n.621A>C
c.646A>C (p.Ser216Arg)
c.535A>C (p.Ser179Arg)
c.526A>C (p.Ser176Arg)
19g.41012459A>GCA9455487CYP2B6c.1126A>G (p.Ser376Gly)
c.1150A>G
c.418A>G (p.Ser140Gly)
n.621A>G
c.646A>G (p.Ser216Gly)
c.535A>G (p.Ser179Gly)
c.526A>G (p.Ser176Gly)
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.41012459A>TCA405984767CYP2B6c.1126A>T (p.Ser376Cys)
c.1150A>T
c.418A>T (p.Ser140Cys)
n.621A>T
c.646A>T (p.Ser216Cys)
c.535A>T (p.Ser179Cys)
c.526A>T (p.Ser176Cys)
19g.41012460G>ACA405984771CYP2B6c.1127G>A (p.Ser376Asn)
c.1151G>A
c.419G>A (p.Ser140Asn)
n.622G>A
c.647G>A (p.Ser216Asn)
c.536G>A (p.Ser179Asn)
c.527G>A (p.Ser176Asn)
 dbSNP gnomAD v2 gnomAD v4
19g.41012460G>CCA405984773CYP2B6c.1127G>C (p.Ser376Thr)
c.1151G>C
c.419G>C (p.Ser140Thr)
n.622G>C
c.647G>C (p.Ser216Thr)
c.536G>C (p.Ser179Thr)
c.527G>C (p.Ser176Thr)
19g.41012460G=CA2336260373CYP2B6c.1127G= (p.Ser376=)
c.1151G=
c.419G= (p.Ser140=)
n.622G=
c.647G= (p.Ser216=)
c.536G= (p.Ser179=)
c.527G= (p.Ser176=)
19g.41012460G>TCA405984769CYP2B6c.1127G>T (p.Ser376Ile)
c.1151G>T
c.419G>T (p.Ser140Ile)
n.622G>T
c.647G>T (p.Ser216Ile)
c.536G>T (p.Ser179Ile)
c.527G>T (p.Ser176Ile)
19g.41012461C>ACA405984777CYP2B6c.1128C>A (p.Ser376Arg)
c.1152C>A
c.420C>A (p.Ser140Arg)
n.623C>A
c.648C>A (p.Ser216Arg)
c.537C>A (p.Ser179Arg)
c.528C>A (p.Ser176Arg)
 dbSNP gnomAD v2
19g.41012461C=CA2336260374CYP2B6c.1128C= (p.Ser376=)
c.1152C=
c.420C= (p.Ser140=)
n.623C=
c.648C= (p.Ser216=)
c.537C= (p.Ser179=)
c.528C= (p.Ser176=)
19g.41012461C>GCA405984775CYP2B6c.1128C>G (p.Ser376Arg)
c.1152C>G
c.420C>G (p.Ser140Arg)
n.623C>G
c.648C>G (p.Ser216Arg)
c.537C>G (p.Ser179Arg)
c.528C>G (p.Ser176Arg)
19g.41012461C>TCA507537720CYP2B6c.1128C>T (p.Ser376=)
c.1152C>T
c.420C>T (p.Ser140=)
n.623C>T
c.648C>T (p.Ser216=)
c.537C>T (p.Ser179=)
c.528C>T (p.Ser176=)
19g.41012462T>ACA405984781CYP2B6c.1129T>A (p.Phe377Ile)
c.1153T>A
c.421T>A (p.Phe141Ile)
n.624T>A
c.649T>A (p.Phe217Ile)
c.538T>A (p.Phe180Ile)
c.529T>A (p.Phe177Ile)
19g.41012462T>CCA405984780CYP2B6c.1129T>C (p.Phe377Leu)
c.1153T>C
c.421T>C (p.Phe141Leu)
n.624T>C
c.649T>C (p.Phe217Leu)
c.538T>C (p.Phe180Leu)
c.529T>C (p.Phe177Leu)
19g.41012462T>GCA405984783CYP2B6c.1129T>G (p.Phe377Val)
c.1153T>G
c.421T>G (p.Phe141Val)
n.624T>G
c.649T>G (p.Phe217Val)
c.538T>G (p.Phe180Val)
c.529T>G (p.Phe177Val)
19g.41012463T>ACA405984785CYP2B6c.1130T>A (p.Phe377Tyr)
c.1154T>A
c.422T>A (p.Phe141Tyr)
n.625T>A
c.650T>A (p.Phe217Tyr)
c.539T>A (p.Phe180Tyr)
c.530T>A (p.Phe177Tyr)
19g.41012463T>CCA405984787CYP2B6c.1130T>C (p.Phe377Ser)
c.1154T>C
c.422T>C (p.Phe141Ser)
n.625T>C
c.650T>C (p.Phe217Ser)
c.539T>C (p.Phe180Ser)
c.530T>C (p.Phe177Ser)
19g.41012463T>GCA405984788CYP2B6c.1130T>G (p.Phe377Cys)
c.1154T>G
c.422T>G (p.Phe141Cys)
n.625T>G
c.650T>G (p.Phe217Cys)
c.539T>G (p.Phe180Cys)
c.530T>G (p.Phe177Cys)
19g.41012464C>ACA405984791CYP2B6c.1131C>A (p.Phe377Leu)
c.1155C>A
c.423C>A (p.Phe141Leu)
n.626C>A
c.651C>A (p.Phe217Leu)
c.540C>A (p.Phe180Leu)
c.531C>A (p.Phe177Leu)
19g.41012464C>GCA405984792CYP2B6c.1131C>G (p.Phe377Leu)
c.1155C>G
c.423C>G (p.Phe141Leu)
n.626C>G
c.651C>G (p.Phe217Leu)
c.540C>G (p.Phe180Leu)
c.531C>G (p.Phe177Leu)
19g.41012464C>TCA507537721CYP2B6c.1131C>T (p.Phe377=)
c.1155C>T
c.423C>T (p.Phe141=)
n.626C>T
c.651C>T (p.Phe217=)
c.540C>T (p.Phe180=)
c.531C>T (p.Phe177=)
 COSMIC
19g.41012465C>ACA507537722CYP2B6c.1132C>A (p.Arg378=)
c.1156C>A
c.424C>A (p.Arg142=)
n.627C>A
c.652C>A (p.Arg218=)
c.541C>A (p.Arg181=)
c.532C>A (p.Arg178=)
19g.41012465C=CA2336260375CYP2B6c.1132C= (p.Arg378=)
c.1156C=
c.424C= (p.Arg142=)
n.627C=
c.652C= (p.Arg218=)
c.541C= (p.Arg181=)
c.532C= (p.Arg178=)
19g.41012465C>GCA405984794CYP2B6c.1132C>G (p.Arg378Gly)
c.1156C>G
c.424C>G (p.Arg142Gly)
n.627C>G
c.652C>G (p.Arg218Gly)
c.541C>G (p.Arg181Gly)
c.532C>G (p.Arg178Gly)
19g.41012465C>TCA233033CYP2B6c.1132C>T (p.Arg378Ter)
c.1156C>T
c.424C>T (p.Arg142Ter)
n.627C>T
c.652C>T (p.Arg218Ter)
c.541C>T (p.Arg181Ter)
c.532C>T (p.Arg178Ter)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.41012466G>ACA9455488CYP2B6c.1133G>A (p.Arg378Gln)
c.1157G>A
c.425G>A (p.Arg142Gln)
n.628G>A
c.653G>A (p.Arg218Gln)
c.542G>A (p.Arg181Gln)
c.533G>A (p.Arg178Gln)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41012466G>CCA405984798CYP2B6c.1133G>C (p.Arg378Pro)
c.1157G>C
c.425G>C (p.Arg142Pro)
n.628G>C
c.653G>C (p.Arg218Pro)
c.542G>C (p.Arg181Pro)
c.533G>C (p.Arg178Pro)
19g.41012466G=CA2336260376CYP2B6c.1133G= (p.Arg378=)
c.1157G=
c.425G= (p.Arg142=)
n.628G=
c.653G= (p.Arg218=)
c.542G= (p.Arg181=)
c.533G= (p.Arg178=)
19g.41012466G>TCA405984801CYP2B6c.1133G>T (p.Arg378Leu)
c.1157G>T
c.425G>T (p.Arg142Leu)
n.628G>T
c.653G>T (p.Arg218Leu)
c.542G>T (p.Arg181Leu)
c.533G>T (p.Arg178Leu)
 COSMIC
19g.41012467A>CCA507537723CYP2B6c.1134A>C (p.Arg378=)
c.1158A>C
c.426A>C (p.Arg142=)
n.629A>C
c.654A>C (p.Arg218=)
c.543A>C (p.Arg181=)
c.534A>C (p.Arg178=)
19g.41012467A>GCA507537725CYP2B6c.1134A>G (p.Arg378=)
c.1158A>G
c.426A>G (p.Arg142=)
n.629A>G
c.654A>G (p.Arg218=)
c.543A>G (p.Arg181=)
c.534A>G (p.Arg178=)
19g.41012467A>TCA507537726CYP2B6c.1134A>T (p.Arg378=)
c.1158A>T
c.426A>T (p.Arg142=)
n.629A>T
c.654A>T (p.Arg218=)
c.543A>T (p.Arg181=)
c.534A>T (p.Arg178=)
19g.41012467_41012468delinsAGCA2336260377CYP2B6c.1134_1135delinsAG (p.Arg378=)
c.1158_1159delinsAG
c.426_427delinsAG (p.Arg142=)
n.629_630delinsAG
c.654_655delinsAG (p.Arg218=)
c.543_544delinsAG (p.Arg181=)
c.534_535delinsAG (p.Arg178=)
19g.41012468G>ACA405984806CYP2B6c.1135G>A (p.Gly379Arg)
c.1159G>A
c.427G>A (p.Gly143Arg)
n.630G>A
c.655G>A (p.Gly219Arg)
c.544G>A (p.Gly182Arg)
c.535G>A (p.Gly179Arg)
19g.41012468G>CCA405984805CYP2B6c.1135G>C (p.Gly379Arg)
c.1159G>C
c.427G>C (p.Gly143Arg)
n.630G>C
c.655G>C (p.Gly219Arg)
c.544G>C (p.Gly182Arg)
c.535G>C (p.Gly179Arg)
19g.41012468G=CA2336260378CYP2B6c.1135G= (p.Gly379=)
c.1159G=
c.427G= (p.Gly143=)
n.630G=
c.655G= (p.Gly219=)
c.544G= (p.Gly182=)
c.535G= (p.Gly179=)
19g.41012468G>TCA405984803CYP2B6c.1135G>T (p.Gly379Trp)
c.1159G>T
c.427G>T (p.Gly143Trp)
n.630G>T
c.655G>T (p.Gly219Trp)
c.544G>T (p.Gly182Trp)
c.535G>T (p.Gly179Trp)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41012470delCA507537727CYP2B6c.1137del (p.Tyr380ThrfsTer13)
c.1161del
c.429del (p.Tyr144ThrfsTer13)
n.632del
c.1137del (p.Tyr380ThrfsTer12)
c.1137del (p.Tyr380ThrfsTer6)
c.1137del (p.Tyr380ThrfsTer?)
c.657del (p.Tyr220ThrfsTer13)
c.546del (p.Tyr183ThrfsTer13)
c.537del (p.Tyr180ThrfsTer13)
 dbSNP gnomAD v2 gnomAD v4
19g.41012469G>ACA405984809CYP2B6c.1136G>A (p.Gly379Glu)
c.1160G>A
c.428G>A (p.Gly143Glu)
n.631G>A
c.656G>A (p.Gly219Glu)
c.545G>A (p.Gly182Glu)
c.536G>A (p.Gly179Glu)
 gnomAD v4
19g.41012469G>CCA405984811CYP2B6c.1136G>C (p.Gly379Ala)
c.1160G>C
c.428G>C (p.Gly143Ala)
n.631G>C
c.656G>C (p.Gly219Ala)
c.545G>C (p.Gly182Ala)
c.536G>C (p.Gly179Ala)
 dbSNP
19g.41012469G=CA2336260379CYP2B6c.1136G= (p.Gly379=)
c.1160G=
c.428G= (p.Gly143=)
n.631G=
c.656G= (p.Gly219=)
c.545G= (p.Gly182=)
c.536G= (p.Gly179=)
19g.41012469G>TCA405984812CYP2B6c.1136G>T (p.Gly379Val)
c.1160G>T
c.428G>T (p.Gly143Val)
n.631G>T
c.656G>T (p.Gly219Val)
c.545G>T (p.Gly182Val)
c.536G>T (p.Gly179Val)
19g.41012470G>ACA507537729CYP2B6c.1137G>A (p.Gly379=)
c.1161G>A
c.429G>A (p.Gly143=)
n.632G>A
c.657G>A (p.Gly219=)
c.546G>A (p.Gly182=)
c.537G>A (p.Gly179=)
 gnomAD v4
19g.41012470G>CCA507537730CYP2B6c.1137G>C (p.Gly379=)
c.1161G>C
c.429G>C (p.Gly143=)
n.632G>C
c.657G>C (p.Gly219=)
c.546G>C (p.Gly182=)
c.537G>C (p.Gly179=)
19g.41012470G=CA2336260380CYP2B6c.1137G= (p.Gly379=)
c.1161G=
c.429G= (p.Gly143=)
n.632G=
c.657G= (p.Gly219=)
c.546G= (p.Gly182=)
c.537G= (p.Gly179=)
19g.41012470G>TCA507537731CYP2B6c.1137G>T (p.Gly379=)
c.1161G>T
c.429G>T (p.Gly143=)
n.632G>T
c.657G>T (p.Gly219=)
c.546G>T (p.Gly182=)
c.537G>T (p.Gly179=)
 dbSNP gnomAD v4
19g.41012471T>ACA405984815CYP2B6c.1138T>A (p.Tyr380Asn)
c.1162T>A
c.430T>A (p.Tyr144Asn)
n.633T>A
c.658T>A (p.Tyr220Asn)
c.547T>A (p.Tyr183Asn)
c.538T>A (p.Tyr180Asn)
19g.41012471T>CCA9455489CYP2B6c.1138T>C (p.Tyr380His)
c.1162T>C
c.430T>C (p.Tyr144His)
n.633T>C
c.658T>C (p.Tyr220His)
c.547T>C (p.Tyr183His)
c.538T>C (p.Tyr180His)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41012471T>GCA405984817CYP2B6c.1138T>G (p.Tyr380Asp)
c.1162T>G
c.430T>G (p.Tyr144Asp)
n.633T>G
c.658T>G (p.Tyr220Asp)
c.547T>G (p.Tyr183Asp)
c.538T>G (p.Tyr180Asp)
19g.41012471T=CA2336260381CYP2B6c.1138T= (p.Tyr380=)
c.1162T=
c.430T= (p.Tyr144=)
n.633T=
c.658T= (p.Tyr220=)
c.547T= (p.Tyr183=)
c.538T= (p.Tyr180=)
19g.41012472A>CCA405984820CYP2B6c.1139A>C (p.Tyr380Ser)
c.1163A>C
c.431A>C (p.Tyr144Ser)
n.634A>C
c.659A>C (p.Tyr220Ser)
c.548A>C (p.Tyr183Ser)
c.539A>C (p.Tyr180Ser)
19g.41012472A>GCA405984821CYP2B6c.1139A>G (p.Tyr380Cys)
c.1163A>G
c.431A>G (p.Tyr144Cys)
n.634A>G
c.659A>G (p.Tyr220Cys)
c.548A>G (p.Tyr183Cys)
c.539A>G (p.Tyr180Cys)
19g.41012472A>TCA405984823CYP2B6c.1139A>T (p.Tyr380Phe)
c.1163A>T
c.431A>T (p.Tyr144Phe)
n.634A>T
c.659A>T (p.Tyr220Phe)
c.548A>T (p.Tyr183Phe)
c.539A>T (p.Tyr180Phe)
19g.41012473C>ACA405984825CYP2B6c.1140C>A (p.Tyr380Ter)
c.1164C>A
c.432C>A (p.Tyr144Ter)
n.635C>A
c.660C>A (p.Tyr220Ter)
c.549C>A (p.Tyr183Ter)
c.540C>A (p.Tyr180Ter)
19g.41012473C=CA2336260382CYP2B6c.1140C= (p.Tyr380=)
c.1164C=
c.432C= (p.Tyr144=)
n.635C=
c.660C= (p.Tyr220=)
c.549C= (p.Tyr183=)
c.540C= (p.Tyr180=)
19g.41012473C>GCA405984827CYP2B6c.1140C>G (p.Tyr380Ter)
c.1164C>G
c.432C>G (p.Tyr144Ter)
n.635C>G
c.660C>G (p.Tyr220Ter)
c.549C>G (p.Tyr183Ter)
c.540C>G (p.Tyr180Ter)
19g.41012473C>TCA9455490CYP2B6c.1140C>T (p.Tyr380=)
c.1164C>T
c.432C>T (p.Tyr144=)
n.635C>T
c.660C>T (p.Tyr220=)
c.549C>T (p.Tyr183=)
c.540C>T (p.Tyr180=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41012474delCA2585217068CYP2B6c.1141del (p.Ile381SerfsTer12)
c.1165del
c.433del (p.Ile145SerfsTer12)
n.636del
c.1141del (p.Ile381SerfsTer11)
c.1141del (p.Ile381SerfsTer5)
c.1141del (p.Ile381SerfsTer?)
c.661del (p.Ile221SerfsTer12)
c.550del (p.Ile184SerfsTer12)
c.541del (p.Ile181SerfsTer12)
 gnomAD v4
19g.41012474A=CA2336260383CYP2B6c.1141A= (p.Ile381=)
c.1165A=
c.433A= (p.Ile145=)
n.636A=
c.661A= (p.Ile221=)
c.550A= (p.Ile184=)
c.541A= (p.Ile181=)
19g.41012474A>CCA9455491CYP2B6c.1141A>C (p.Ile381Leu)
c.1165A>C
c.433A>C (p.Ile145Leu)
n.636A>C
c.661A>C (p.Ile221Leu)
c.550A>C (p.Ile184Leu)
c.541A>C (p.Ile181Leu)
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.41012474A>GCA405984832CYP2B6c.1141A>G (p.Ile381Val)
c.1165A>G
c.433A>G (p.Ile145Val)
n.636A>G
c.661A>G (p.Ile221Val)
c.550A>G (p.Ile184Val)
c.541A>G (p.Ile181Val)
 dbSNP
19g.41012474A>TCA405984830CYP2B6c.1141A>T (p.Ile381Phe)
c.1165A>T
c.433A>T (p.Ile145Phe)
n.636A>T
c.661A>T (p.Ile221Phe)
c.550A>T (p.Ile184Phe)
c.541A>T (p.Ile181Phe)
19g.41012475T>ACA405984835CYP2B6c.1142T>A (p.Ile381Asn)
c.1166T>A
c.434T>A (p.Ile145Asn)
n.637T>A
c.662T>A (p.Ile221Asn)
c.551T>A (p.Ile184Asn)
c.542T>A (p.Ile181Asn)
 gnomAD v4
19g.41012475T>CCA405984836CYP2B6c.1142T>C (p.Ile381Thr)
c.1166T>C
c.434T>C (p.Ile145Thr)
n.637T>C
c.662T>C (p.Ile221Thr)
c.551T>C (p.Ile184Thr)
c.542T>C (p.Ile181Thr)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41012475T>GCA405984838CYP2B6c.1142T>G (p.Ile381Ser)
c.1166T>G
c.434T>G (p.Ile145Ser)
n.637T>G
c.662T>G (p.Ile221Ser)
c.551T>G (p.Ile184Ser)
c.542T>G (p.Ile181Ser)
19g.41012475T=CA2336260384CYP2B6c.1142T= (p.Ile381=)
c.1166T=
c.434T= (p.Ile145=)
n.637T=
c.662T= (p.Ile221=)
c.551T= (p.Ile184=)
c.542T= (p.Ile181=)
19g.41012476C>ACA507537735CYP2B6c.1143C>A (p.Ile381=)
c.1167C>A
c.435C>A (p.Ile145=)
n.638C>A
c.663C>A (p.Ile221=)
c.552C>A (p.Ile184=)
c.543C>A (p.Ile181=)
19g.41012476C>GCA405984840CYP2B6c.1143C>G (p.Ile381Met)
c.1167C>G
c.435C>G (p.Ile145Met)
n.638C>G
c.663C>G (p.Ile221Met)
c.552C>G (p.Ile184Met)
c.543C>G (p.Ile181Met)
19g.41012476C>TCA507537736CYP2B6c.1143C>T (p.Ile381=)
c.1167C>T
c.435C>T (p.Ile145=)
n.638C>T
c.663C>T (p.Ile221=)
c.552C>T (p.Ile184=)
c.543C>T (p.Ile181=)
 gnomAD v4
19g.41012476_41012493delCA2585217072CYP2B6c.1143_1152+8del
c.1167_1176+8del
c.435_444+8del
n.638_647+8del
c.663_672+8del
c.552_561+8del
c.543_552+8del
 gnomAD v4
19g.41012477A=CA2336260385CYP2B6c.1144A= (p.Ile382=)
c.1168A=
c.436A= (p.Ile146=)
n.639A=
c.664A= (p.Ile222=)
c.553A= (p.Ile185=)
c.544A= (p.Ile182=)
19g.41012477A>CCA405984842CYP2B6c.1144A>C (p.Ile382Leu)
c.1168A>C
c.436A>C (p.Ile146Leu)
n.639A>C
c.664A>C (p.Ile222Leu)
c.553A>C (p.Ile185Leu)
c.544A>C (p.Ile182Leu)
19g.41012477A>GCA405984844CYP2B6c.1144A>G (p.Ile382Val)
c.1168A>G
c.436A>G (p.Ile146Val)
n.639A>G
c.664A>G (p.Ile222Val)
c.553A>G (p.Ile185Val)
c.544A>G (p.Ile182Val)
 gnomAD v4
19g.41012477A>TCA405984846CYP2B6c.1144A>T (p.Ile382Phe)
c.1168A>T
c.436A>T (p.Ile146Phe)
n.639A>T
c.664A>T (p.Ile222Phe)
c.553A>T (p.Ile185Phe)
c.544A>T (p.Ile182Phe)
 dbSNP

Number of alleles fetched