Chr Mutation (hg38) CAid Gene Transcript Linkouts
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)
 ClinVar 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
19g.41012478T>ACA9455492CYP2B6c.1145T>A (p.Ile382Asn)
c.1169T>A
c.437T>A (p.Ile146Asn)
n.640T>A
c.665T>A (p.Ile222Asn)
c.554T>A (p.Ile185Asn)
c.545T>A (p.Ile182Asn)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41012478T>CCA405984853CYP2B6c.1145T>C (p.Ile382Thr)
c.1169T>C
c.437T>C (p.Ile146Thr)
n.640T>C
c.665T>C (p.Ile222Thr)
c.554T>C (p.Ile185Thr)
c.545T>C (p.Ile182Thr)
19g.41012478T>GCA405984851CYP2B6c.1145T>G (p.Ile382Ser)
c.1169T>G
c.437T>G (p.Ile146Ser)
n.640T>G
c.665T>G (p.Ile222Ser)
c.554T>G (p.Ile185Ser)
c.545T>G (p.Ile182Ser)
19g.41012478T=CA2336260386CYP2B6c.1145T= (p.Ile382=)
c.1169T=
c.437T= (p.Ile146=)
n.640T=
c.665T= (p.Ile222=)
c.554T= (p.Ile185=)
c.545T= (p.Ile182=)
19g.41012479C>ACA507537738CYP2B6c.1146C>A (p.Ile382=)
c.1170C>A
c.438C>A (p.Ile146=)
n.641C>A
c.666C>A (p.Ile222=)
c.555C>A (p.Ile185=)
c.546C>A (p.Ile182=)
19g.41012479C>GCA405984857CYP2B6c.1146C>G (p.Ile382Met)
c.1170C>G
c.438C>G (p.Ile146Met)
n.641C>G
c.666C>G (p.Ile222Met)
c.555C>G (p.Ile185Met)
c.546C>G (p.Ile182Met)
19g.41012479C>TCA507537737CYP2B6c.1146C>T (p.Ile382=)
c.1170C>T
c.438C>T (p.Ile146=)
n.641C>T
c.666C>T (p.Ile222=)
c.555C>T (p.Ile185=)
c.546C>T (p.Ile182=)
 COSMIC
19g.41012480C>ACA405984860CYP2B6c.1147C>A (p.Pro383Thr)
c.1171C>A
c.439C>A (p.Pro147Thr)
n.642C>A
c.667C>A (p.Pro223Thr)
c.556C>A (p.Pro186Thr)
c.547C>A (p.Pro183Thr)
 COSMIC
19g.41012480C>GCA405984863CYP2B6c.1147C>G (p.Pro383Ala)
c.1171C>G
c.439C>G (p.Pro147Ala)
n.642C>G
c.667C>G (p.Pro223Ala)
c.556C>G (p.Pro186Ala)
c.547C>G (p.Pro183Ala)
19g.41012480C>TCA405984866CYP2B6c.1147C>T (p.Pro383Ser)
c.1171C>T
c.439C>T (p.Pro147Ser)
n.642C>T
c.667C>T (p.Pro223Ser)
c.556C>T (p.Pro186Ser)
c.547C>T (p.Pro183Ser)
 gnomAD v4 COSMIC
19g.41012481C>ACA405984869CYP2B6c.1148C>A (p.Pro383His)
c.1172C>A
c.440C>A (p.Pro147His)
n.643C>A
c.668C>A (p.Pro223His)
c.557C>A (p.Pro186His)
c.548C>A (p.Pro183His)
 gnomAD v4
19g.41012481C=CA2336260387CYP2B6c.1148C= (p.Pro383=)
c.1172C=
c.440C= (p.Pro147=)
n.643C=
c.668C= (p.Pro223=)
c.557C= (p.Pro186=)
c.548C= (p.Pro183=)
19g.41012481C>GCA405984875CYP2B6c.1148C>G (p.Pro383Arg)
c.1172C>G
c.440C>G (p.Pro147Arg)
n.643C>G
c.668C>G (p.Pro223Arg)
c.557C>G (p.Pro186Arg)
c.548C>G (p.Pro183Arg)
 dbSNP gnomAD v4
19g.41012481C>TCA405984872CYP2B6c.1148C>T (p.Pro383Leu)
c.1172C>T
c.440C>T (p.Pro147Leu)
n.643C>T
c.668C>T (p.Pro223Leu)
c.557C>T (p.Pro186Leu)
c.548C>T (p.Pro183Leu)
19g.41012482C>ACA507537741CYP2B6c.1149C>A (p.Pro383=)
c.1173C>A
c.441C>A (p.Pro147=)
n.644C>A
c.669C>A (p.Pro223=)
c.558C>A (p.Pro186=)
c.549C>A (p.Pro183=)
19g.41012482C=CA2336260388CYP2B6c.1149C= (p.Pro383=)
c.1173C=
c.441C= (p.Pro147=)
n.644C=
c.669C= (p.Pro223=)
c.558C= (p.Pro186=)
c.549C= (p.Pro183=)
19g.41012482C>GCA507537742CYP2B6c.1149C>G (p.Pro383=)
c.1173C>G
c.441C>G (p.Pro147=)
n.644C>G
c.669C>G (p.Pro223=)
c.558C>G (p.Pro186=)
c.549C>G (p.Pro183=)
19g.41012482C>TCA9455493CYP2B6c.1149C>T (p.Pro383=)
c.1173C>T
c.441C>T (p.Pro147=)
n.644C>T
c.669C>T (p.Pro223=)
c.558C>T (p.Pro186=)
c.549C>T (p.Pro183=)
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.41012483A>CCA405984881CYP2B6c.1150A>C (p.Lys384Gln)
c.1174A>C
c.442A>C (p.Lys148Gln)
n.645A>C
c.670A>C (p.Lys224Gln)
c.559A>C (p.Lys187Gln)
c.550A>C (p.Lys184Gln)
19g.41012483A>GCA405984883CYP2B6c.1150A>G (p.Lys384Glu)
c.1174A>G
c.442A>G (p.Lys148Glu)
n.645A>G
c.670A>G (p.Lys224Glu)
c.559A>G (p.Lys187Glu)
c.550A>G (p.Lys184Glu)
 gnomAD v4
19g.41012483A>TCA405984885CYP2B6c.1150A>T (p.Lys384Ter)
c.1174A>T
c.442A>T (p.Lys148Ter)
n.645A>T
c.670A>T (p.Lys224Ter)
c.559A>T (p.Lys187Ter)
c.550A>T (p.Lys184Ter)
19g.41012484A=CA2336260389CYP2B6c.1151A= (p.Lys384=)
c.1175A=
c.443A= (p.Lys148=)
n.646A=
c.671A= (p.Lys224=)
c.560A= (p.Lys187=)
c.551A= (p.Lys184=)
19g.41012484A>CCA405984889CYP2B6c.1151A>C (p.Lys384Thr)
c.1175A>C
c.443A>C (p.Lys148Thr)
n.646A>C
c.671A>C (p.Lys224Thr)
c.560A>C (p.Lys187Thr)
c.551A>C (p.Lys184Thr)
19g.41012484A>GCA308499249CYP2B6c.1151A>G (p.Lys384Arg)
c.1175A>G
c.443A>G (p.Lys148Arg)
n.646A>G
c.671A>G (p.Lys224Arg)
c.560A>G (p.Lys187Arg)
c.551A>G (p.Lys184Arg)
 dbSNP gnomAD v2 gnomAD v4
19g.41012484A>TCA405984894CYP2B6c.1151A>T (p.Lys384Met)
c.1175A>T
c.443A>T (p.Lys148Met)
n.646A>T
c.671A>T (p.Lys224Met)
c.560A>T (p.Lys187Met)
c.551A>T (p.Lys184Met)
19g.41012485G>ACA507537743CYP2B6c.1152G>A (p.Lys384=)
c.1176G>A
c.444G>A (p.Lys148=)
n.647G>A
c.672G>A (p.Lys224=)
c.561G>A (p.Lys187=)
c.552G>A (p.Lys184=)
19g.41012485G>CCA405984898CYP2B6c.1152G>C (p.Lys384Asn)
c.1176G>C
c.444G>C (p.Lys148Asn)
n.647G>C
c.672G>C (p.Lys224Asn)
c.561G>C (p.Lys187Asn)
c.552G>C (p.Lys184Asn)
19g.41012485G>TCA405984901CYP2B6c.1152G>T (p.Lys384Asn)
c.1176G>T
c.444G>T (p.Lys148Asn)
n.647G>T
c.672G>T (p.Lys224Asn)
c.561G>T (p.Lys187Asn)
c.552G>T (p.Lys184Asn)
19g.41012486G>ACA405984905CYP2B6c.1152+1G>A (n.1152+1G>A)
c.1176+1G>A
c.444+1G>A (n.444+1G>A)
n.647+1G>A
c.672+1G>A (n.672+1G>A)
c.561+1G>A (n.561+1G>A)
c.552+1G>A (n.552+1G>A)
19g.41012486G>CCA405984906CYP2B6c.1152+1G>C (n.1152+1G>C)
c.1176+1G>C
c.444+1G>C (n.444+1G>C)
n.647+1G>C
c.672+1G>C (n.672+1G>C)
c.561+1G>C (n.561+1G>C)
c.552+1G>C (n.552+1G>C)
 gnomAD v4
19g.41012486G>TCA405984907CYP2B6c.1152+1G>T (n.1152+1G>T)
c.1176+1G>T
c.444+1G>T (n.444+1G>T)
n.647+1G>T
c.672+1G>T (n.672+1G>T)
c.561+1G>T (n.561+1G>T)
c.552+1G>T (n.552+1G>T)
 COSMIC
19g.41012487T>ACA405984916CYP2B6c.1152+2T>A (n.1152+2T>A)
c.1176+2T>A
c.444+2T>A (n.444+2T>A)
n.647+2T>A
c.672+2T>A (n.672+2T>A)
c.561+2T>A (n.561+2T>A)
c.552+2T>A (n.552+2T>A)
19g.41012487T>CCA405984913CYP2B6c.1152+2T>C (n.1152+2T>C)
c.1176+2T>C
c.444+2T>C (n.444+2T>C)
n.647+2T>C
c.672+2T>C (n.672+2T>C)
c.561+2T>C (n.561+2T>C)
c.552+2T>C (n.552+2T>C)
19g.41012487T>GCA405984911CYP2B6c.1152+2T>G (n.1152+2T>G)
c.1176+2T>G
c.444+2T>G (n.444+2T>G)
n.647+2T>G
c.672+2T>G (n.672+2T>G)
c.561+2T>G (n.561+2T>G)
c.552+2T>G (n.552+2T>G)
19g.41012488A=CA2336260390CYP2B6c.1152+3A= (n.1152+3A=)
c.1176+3A=
c.444+3A= (n.444+3A=)
n.647+3A=
c.672+3A= (n.672+3A=)
c.561+3A= (n.561+3A=)
c.552+3A= (n.552+3A=)
19g.41012488A>GCA2336260391CYP2B6c.1152+3A>G (n.1152+3A>G)
c.1176+3A>G
c.444+3A>G (n.444+3A>G)
n.647+3A>G
c.672+3A>G (n.672+3A>G)
c.561+3A>G (n.561+3A>G)
c.552+3A>G (n.552+3A>G)
 dbSNP gnomAD v4
19g.41012492C>ACA9455494CYP2B6c.1152+7C>A (n.1152+7C>A)
c.1176+7C>A
c.444+7C>A (n.444+7C>A)
n.647+7C>A
c.672+7C>A (n.672+7C>A)
c.561+7C>A (n.561+7C>A)
c.552+7C>A (n.552+7C>A)
 dbSNP ExAC gnomAD v2
19g.41012492C=CA2336260392CYP2B6c.1152+7C= (n.1152+7C=)
c.1176+7C=
c.444+7C= (n.444+7C=)
n.647+7C=
c.672+7C= (n.672+7C=)
c.561+7C= (n.561+7C=)
c.552+7C= (n.552+7C=)
19g.41012492C>TCA9455495CYP2B6c.1152+7C>T (n.1152+7C>T)
c.1176+7C>T
c.444+7C>T (n.444+7C>T)
n.647+7C>T
c.672+7C>T (n.672+7C>T)
c.561+7C>T (n.561+7C>T)
c.552+7C>T (n.552+7C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.41012493C>ACA9455497CYP2B6c.1152+8C>A (n.1152+8C>A)
c.1176+8C>A
c.444+8C>A (n.444+8C>A)
n.647+8C>A
c.672+8C>A (n.672+8C>A)
c.561+8C>A (n.561+8C>A)
c.552+8C>A (n.552+8C>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41012493C=CA2336260393CYP2B6c.1152+8C= (n.1152+8C=)
c.1176+8C=
c.444+8C= (n.444+8C=)
n.647+8C=
c.672+8C= (n.672+8C=)
c.561+8C= (n.561+8C=)
c.552+8C= (n.552+8C=)
19g.41012493C>GCA2814422297CYP2B6c.1152+8C>G (n.1152+8C>G)
c.1176+8C>G
c.444+8C>G (n.444+8C>G)
n.647+8C>G
c.672+8C>G (n.672+8C>G)
c.561+8C>G (n.561+8C>G)
c.552+8C>G (n.552+8C>G)
19g.41012493C>TCA9455496CYP2B6c.1152+8C>T (n.1152+8C>T)
c.1176+8C>T
c.444+8C>T (n.444+8C>T)
n.647+8C>T
c.672+8C>T (n.672+8C>T)
c.561+8C>T (n.561+8C>T)
c.552+8C>T (n.552+8C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41012494G>ACA9455498CYP2B6c.1152+9G>A (n.1152+9G>A)
c.1176+9G>A
c.444+9G>A (n.444+9G>A)
n.647+9G>A
c.672+9G>A (n.672+9G>A)
c.561+9G>A (n.561+9G>A)
c.552+9G>A (n.552+9G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41012494G>CCA633469279CYP2B6c.1152+9G>C (n.1152+9G>C)
c.1176+9G>C
c.444+9G>C (n.444+9G>C)
n.647+9G>C
c.672+9G>C (n.672+9G>C)
c.561+9G>C (n.561+9G>C)
c.552+9G>C (n.552+9G>C)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41012494G=CA2336260394CYP2B6c.1152+9G= (n.1152+9G=)
c.1176+9G=
c.444+9G= (n.444+9G=)
n.647+9G=
c.672+9G= (n.672+9G=)
c.561+9G= (n.561+9G=)
c.552+9G= (n.552+9G=)
19g.41012494G>TCA2585217085CYP2B6c.1152+9G>T (n.1152+9G>T)
c.1176+9G>T
c.444+9G>T (n.444+9G>T)
n.647+9G>T
c.672+9G>T (n.672+9G>T)
c.561+9G>T (n.561+9G>T)
c.552+9G>T (n.552+9G>T)
 gnomAD v4
19g.41012496C>ACA9455499CYP2B6c.1152+11C>A (n.1152+11C>A)
c.1176+11C>A
c.444+11C>A (n.444+11C>A)
n.647+11C>A
c.672+11C>A (n.672+11C>A)
c.561+11C>A (n.561+11C>A)
c.552+11C>A (n.552+11C>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.41012496C=CA2336260395CYP2B6c.1152+11C= (n.1152+11C=)
c.1176+11C=
c.444+11C= (n.444+11C=)
n.647+11C=
c.672+11C= (n.672+11C=)
c.561+11C= (n.561+11C=)
c.552+11C= (n.552+11C=)
19g.41012499G>CCA2336260397CYP2B6c.1152+14G>C (n.1152+14G>C)
c.1176+14G>C
c.444+14G>C (n.444+14G>C)
n.647+14G>C
c.672+14G>C (n.672+14G>C)
c.561+14G>C (n.561+14G>C)
c.552+14G>C (n.552+14G>C)
 dbSNP
19g.41012499G=CA2336260396CYP2B6c.1152+14G= (n.1152+14G=)
c.1176+14G=
c.444+14G= (n.444+14G=)
n.647+14G=
c.672+14G= (n.672+14G=)
c.561+14G= (n.561+14G=)
c.552+14G= (n.552+14G=)
19g.41012500A=CA2336260398CYP2B6c.1152+15A= (n.1152+15A=)
c.1176+15A=
c.444+15A= (n.444+15A=)
n.647+15A=
c.672+15A= (n.672+15A=)
c.561+15A= (n.561+15A=)
c.552+15A= (n.552+15A=)
19g.41012500A>CCA2585217090CYP2B6c.1152+15A>C (n.1152+15A>C)
c.1176+15A>C
c.444+15A>C (n.444+15A>C)
n.647+15A>C
c.672+15A>C (n.672+15A>C)
c.561+15A>C (n.561+15A>C)
c.552+15A>C (n.552+15A>C)
 gnomAD v4
19g.41012500A>GCA2336260399CYP2B6c.1152+15A>G (n.1152+15A>G)
c.1176+15A>G
c.444+15A>G (n.444+15A>G)
n.647+15A>G
c.672+15A>G (n.672+15A>G)
c.561+15A>G (n.561+15A>G)
c.552+15A>G (n.552+15A>G)
 dbSNP
19g.41012501A=CA2336260400CYP2B6c.1152+16A= (n.1152+16A=)
c.1176+16A=
c.444+16A= (n.444+16A=)
n.647+16A=
c.672+16A= (n.672+16A=)
c.561+16A= (n.561+16A=)
c.552+16A= (n.552+16A=)
19g.41012501A>CCA2336260401CYP2B6c.1152+16A>C (n.1152+16A>C)
c.1176+16A>C
c.444+16A>C (n.444+16A>C)
n.647+16A>C
c.672+16A>C (n.672+16A>C)
c.561+16A>C (n.561+16A>C)
c.552+16A>C (n.552+16A>C)
 dbSNP
19g.41012501A>GCA9455500CYP2B6c.1152+16A>G (n.1152+16A>G)
c.1176+16A>G
c.444+16A>G (n.444+16A>G)
n.647+16A>G
c.672+16A>G (n.672+16A>G)
c.561+16A>G (n.561+16A>G)
c.552+16A>G (n.552+16A>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41012501_41012502delinsACCA2336260402CYP2B6c.1152+16_1152+17delinsAC (n.1152+16_1152+17delinsAC)
c.1176+16_1176+17delinsAC
c.444+16_444+17delinsAC (n.444+16_444+17delinsAC)
n.647+16_647+17delinsAC
c.672+16_672+17delinsAC (n.672+16_672+17delinsAC)
c.561+16_561+17delinsAC (n.561+16_561+17delinsAC)
c.552+16_552+17delinsAC (n.552+16_552+17delinsAC)
19g.41012502C=CA2336260404CYP2B6c.1152+17C= (n.1152+17C=)
c.1176+17C=
c.444+17C= (n.444+17C=)
n.647+17C=
c.672+17C= (n.672+17C=)
c.561+17C= (n.561+17C=)
c.552+17C= (n.552+17C=)
19g.41012502C>TCA882288982CYP2B6c.1152+17C>T (n.1152+17C>T)
c.1176+17C>T
c.444+17C>T (n.444+17C>T)
n.647+17C>T
c.672+17C>T (n.672+17C>T)
c.561+17C>T (n.561+17C>T)
c.552+17C>T (n.552+17C>T)
 dbSNP gnomAD v3 gnomAD v4
19g.41012505delCA2336260403CYP2B6c.1152+20del (n.1152+20del)
c.1176+20del
c.444+20del (n.444+20del)
n.647+20del
c.672+20del (n.672+20del)
c.561+20del (n.561+20del)
c.552+20del (n.552+20del)
 dbSNP gnomAD v4
19g.41012503C=CA2336260405CYP2B6c.1152+18C= (n.1152+18C=)
c.1176+18C=
c.444+18C= (n.444+18C=)
n.647+18C=
c.672+18C= (n.672+18C=)
c.561+18C= (n.561+18C=)
c.552+18C= (n.552+18C=)
19g.41012503C>GCA633469280CYP2B6c.1152+18C>G (n.1152+18C>G)
c.1176+18C>G
c.444+18C>G (n.444+18C>G)
n.647+18C>G
c.672+18C>G (n.672+18C>G)
c.561+18C>G (n.561+18C>G)
c.552+18C>G (n.552+18C>G)
 dbSNP gnomAD v2 gnomAD v4
19g.41012503C>TCA2585217096CYP2B6c.1152+18C>T (n.1152+18C>T)
c.1176+18C>T
c.444+18C>T (n.444+18C>T)
n.647+18C>T
c.672+18C>T (n.672+18C>T)
c.561+18C>T (n.561+18C>T)
c.552+18C>T (n.552+18C>T)
 gnomAD v4
19g.41012504C>ACA9455501CYP2B6c.1152+19C>A (n.1152+19C>A)
c.1176+19C>A
c.444+19C>A (n.444+19C>A)
n.647+19C>A
c.672+19C>A (n.672+19C>A)
c.561+19C>A (n.561+19C>A)
c.552+19C>A (n.552+19C>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41012504C=CA2336260406CYP2B6c.1152+19C= (n.1152+19C=)
c.1176+19C=
c.444+19C= (n.444+19C=)
n.647+19C=
c.672+19C= (n.672+19C=)
c.561+19C= (n.561+19C=)
c.552+19C= (n.552+19C=)
19g.41012505C>TCA2585217098CYP2B6c.1152+20C>T (n.1152+20C>T)
c.1176+20C>T
c.444+20C>T (n.444+20C>T)
n.647+20C>T
c.672+20C>T (n.672+20C>T)
c.561+20C>T (n.561+20C>T)
c.552+20C>T (n.552+20C>T)
 gnomAD v4
19g.41012506A=CA2336260407CYP2B6c.1152+21A= (n.1152+21A=)
c.1176+21A=
c.444+21A= (n.444+21A=)
n.647+21A=
c.672+21A= (n.672+21A=)
c.561+21A= (n.561+21A=)
c.552+21A= (n.552+21A=)
19g.41012506A>GCA9455502CYP2B6c.1152+21A>G (n.1152+21A>G)
c.1176+21A>G
c.444+21A>G (n.444+21A>G)
n.647+21A>G
c.672+21A>G (n.672+21A>G)
c.561+21A>G (n.561+21A>G)
c.552+21A>G (n.552+21A>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41012507T>CCA9455503CYP2B6c.1152+22T>C (n.1152+22T>C)
c.1176+22T>C
c.444+22T>C (n.444+22T>C)
n.647+22T>C
c.672+22T>C (n.672+22T>C)
c.561+22T>C (n.561+22T>C)
c.552+22T>C (n.552+22T>C)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41012507T=CA2336260408CYP2B6c.1152+22T= (n.1152+22T=)
c.1176+22T=
c.444+22T= (n.444+22T=)
n.647+22T=
c.672+22T= (n.672+22T=)
c.561+22T= (n.561+22T=)
c.552+22T= (n.552+22T=)
19g.41012508A=CA2336260409CYP2B6c.1152+23A= (n.1152+23A=)
c.1176+23A=
c.444+23A= (n.444+23A=)
n.647+23A=
c.672+23A= (n.672+23A=)
c.561+23A= (n.561+23A=)
c.552+23A= (n.552+23A=)
19g.41012508A>GCA9455504CYP2B6c.1152+23A>G (n.1152+23A>G)
c.1176+23A>G
c.444+23A>G (n.444+23A>G)
n.647+23A>G
c.672+23A>G (n.672+23A>G)
c.561+23A>G (n.561+23A>G)
c.552+23A>G (n.552+23A>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41012509G>ACA2814422303CYP2B6c.1152+24G>A (n.1152+24G>A)
c.1176+24G>A
c.444+24G>A (n.444+24G>A)
n.647+24G>A
c.672+24G>A (n.672+24G>A)
c.561+24G>A (n.561+24G>A)
c.552+24G>A (n.552+24G>A)
19g.41012509G=CA2336260410CYP2B6c.1152+24G= (n.1152+24G=)
c.1176+24G=
c.444+24G= (n.444+24G=)
n.647+24G=
c.672+24G= (n.672+24G=)
c.561+24G= (n.561+24G=)
c.552+24G= (n.552+24G=)
19g.41012509G>TCA9455505CYP2B6c.1152+24G>T (n.1152+24G>T)
c.1176+24G>T
c.444+24G>T (n.444+24G>T)
n.647+24G>T
c.672+24G>T (n.672+24G>T)
c.561+24G>T (n.561+24G>T)
c.552+24G>T (n.552+24G>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41012510C>ACA2585217105CYP2B6c.1152+25C>A (n.1152+25C>A)
c.1176+25C>A
c.444+25C>A (n.444+25C>A)
n.647+25C>A
c.672+25C>A (n.672+25C>A)
c.561+25C>A (n.561+25C>A)
c.552+25C>A (n.552+25C>A)
 gnomAD v4
19g.41012510C=CA2336260411CYP2B6c.1152+25C= (n.1152+25C=)
c.1176+25C=
c.444+25C= (n.444+25C=)
n.647+25C=
c.672+25C= (n.672+25C=)
c.561+25C= (n.561+25C=)
c.552+25C= (n.552+25C=)
19g.41012510C>TCA633469281CYP2B6c.1152+25C>T (n.1152+25C>T)
c.1176+25C>T
c.444+25C>T (n.444+25C>T)
n.647+25C>T
c.672+25C>T (n.672+25C>T)
c.561+25C>T (n.561+25C>T)
c.552+25C>T (n.552+25C>T)
 dbSNP gnomAD v2 gnomAD v4
19g.41012512C=CA2336260412CYP2B6c.1152+27C= (n.1152+27C=)
c.1176+27C=
c.444+27C= (n.444+27C=)
n.647+27C=
c.672+27C= (n.672+27C=)
c.561+27C= (n.561+27C=)
c.552+27C= (n.552+27C=)
19g.41012512C>TCA995929662CYP2B6c.1152+27C>T (n.1152+27C>T)
c.1176+27C>T
c.444+27C>T (n.444+27C>T)
n.647+27C>T
c.672+27C>T (n.672+27C>T)
c.561+27C>T (n.561+27C>T)
c.552+27C>T (n.552+27C>T)
 dbSNP gnomAD v3 gnomAD v4

Number of alleles fetched