Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.41009349_41009366dupCA2336258737CYP2B6c.776_793dup (p.Leu264_Ile265insSerAlaProLysAspLeu)
c.800_817dup
c.257-2949_257-2932dup (n.257-2949_257-2932dup)
c.485-2949_485-2932dup (n.485-2949_485-2932dup)
c.185_202dup (p.Leu67_Ile68insSerAlaProLysAspLeu)
c.365-2949_365-2932dup (n.365-2949_365-2932dup)
dbSNP
19g.41009358A=CA2336258759CYP2B6c.785A= (p.Lys262=)
c.809A=
c.257-2940A= (n.257-2940A=)
c.485-2940A= (n.485-2940A=)
c.194A= (p.Lys65=)
c.365-2940A= (n.365-2940A=)
19g.41009358A>CCA405980725CYP2B6c.785A>C (p.Lys262Thr)
c.809A>C
c.257-2940A>C (n.257-2940A>C)
c.485-2940A>C (n.485-2940A>C)
c.194A>C (p.Lys65Thr)
c.365-2940A>C (n.365-2940A>C)
19g.41009358A>GCA230624CYP2B6c.785A>G (p.Lys262Arg)
c.809A>G
c.257-2940A>G (n.257-2940A>G)
c.485-2940A>G (n.485-2940A>G)
c.194A>G (p.Lys65Arg)
c.365-2940A>G (n.365-2940A>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41009358A>TCA405980728CYP2B6c.785A>T (p.Lys262Met)
c.809A>T
c.257-2940A>T (n.257-2940A>T)
c.485-2940A>T (n.485-2940A>T)
c.194A>T (p.Lys65Met)
c.365-2940A>T (n.365-2940A>T)
dbSNP gnomAD v4
19g.41009359_41009361dupCA2336258758CYP2B6c.786_788dup (p.Lys262_Asp263insGlu)
c.810_812dup
c.257-2939_257-2937dup (n.257-2939_257-2937dup)
c.485-2939_485-2937dup (n.485-2939_485-2937dup)
c.195_197dup (p.Lys65_Asp66insGlu)
c.365-2939_365-2937dup (n.365-2939_365-2937dup)
dbSNP
19g.41009359G>ACA507535577CYP2B6c.786G>A (p.Lys262=)
c.810G>A
c.257-2939G>A (n.257-2939G>A)
c.485-2939G>A (n.485-2939G>A)
c.195G>A (p.Lys65=)
c.365-2939G>A (n.365-2939G>A)
gnomAD v4 COSMIC
19g.41009359G>CCA405980730CYP2B6c.786G>C (p.Lys262Asn)
c.810G>C
c.257-2939G>C (n.257-2939G>C)
c.485-2939G>C (n.485-2939G>C)
c.195G>C (p.Lys65Asn)
c.365-2939G>C (n.365-2939G>C)
19g.41009359G>TCA405980733CYP2B6c.786G>T (p.Lys262Asn)
c.810G>T
c.257-2939G>T (n.257-2939G>T)
c.485-2939G>T (n.485-2939G>T)
c.195G>T (p.Lys65Asn)
c.365-2939G>T (n.365-2939G>T)
19g.41009360G>ACA405980736CYP2B6c.787G>A (p.Asp263Asn)
c.811G>A
c.257-2938G>A (n.257-2938G>A)
c.485-2938G>A (n.485-2938G>A)
c.196G>A (p.Asp66Asn)
c.365-2938G>A (n.365-2938G>A)
gnomAD v4
19g.41009360G>CCA405980738CYP2B6c.787G>C (p.Asp263His)
c.811G>C
c.257-2938G>C (n.257-2938G>C)
c.485-2938G>C (n.485-2938G>C)
c.196G>C (p.Asp66His)
c.365-2938G>C (n.365-2938G>C)
19g.41009360G>TCA405980740CYP2B6c.787G>T (p.Asp263Tyr)
c.811G>T
c.257-2938G>T (n.257-2938G>T)
c.485-2938G>T (n.485-2938G>T)
c.196G>T (p.Asp66Tyr)
c.365-2938G>T (n.365-2938G>T)
19g.41009361A=CA2336258765CYP2B6c.788A= (p.Asp263=)
c.812A=
c.257-2937A= (n.257-2937A=)
c.485-2937A= (n.485-2937A=)
c.197A= (p.Asp66=)
c.365-2937A= (n.365-2937A=)
19g.41009361A>CCA405980742CYP2B6c.788A>C (p.Asp263Ala)
c.812A>C
c.257-2937A>C (n.257-2937A>C)
c.485-2937A>C (n.485-2937A>C)
c.197A>C (p.Asp66Ala)
c.365-2937A>C (n.365-2937A>C)
gnomAD v4
19g.41009361A>GCA405980750CYP2B6c.788A>G (p.Asp263Gly)
c.812A>G
c.257-2937A>G (n.257-2937A>G)
c.485-2937A>G (n.485-2937A>G)
c.197A>G (p.Asp66Gly)
c.365-2937A>G (n.365-2937A>G)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41009361A>TCA405980752CYP2B6c.788A>T (p.Asp263Val)
c.812A>T
c.257-2937A>T (n.257-2937A>T)
c.485-2937A>T (n.485-2937A>T)
c.197A>T (p.Asp66Val)
c.365-2937A>T (n.365-2937A>T)
19g.41009362C>ACA405980754CYP2B6c.789C>A (p.Asp263Glu)
c.813C>A
c.257-2936C>A (n.257-2936C>A)
c.485-2936C>A (n.485-2936C>A)
c.198C>A (p.Asp66Glu)
c.365-2936C>A (n.365-2936C>A)
ClinVar
19g.41009362C>GCA405980753CYP2B6c.789C>G (p.Asp263Glu)
c.813C>G
c.257-2936C>G (n.257-2936C>G)
c.485-2936C>G (n.485-2936C>G)
c.198C>G (p.Asp66Glu)
c.365-2936C>G (n.365-2936C>G)
19g.41009362C>TCA507535588CYP2B6c.789C>T (p.Asp263=)
c.813C>T
c.257-2936C>T (n.257-2936C>T)
c.485-2936C>T (n.485-2936C>T)
c.198C>T (p.Asp66=)
c.365-2936C>T (n.365-2936C>T)
19g.41009363C>ACA308498417CYP2B6c.790C>A (p.Leu264Ile)
c.814C>A
c.257-2935C>A (n.257-2935C>A)
c.485-2935C>A (n.485-2935C>A)
c.199C>A (p.Leu67Ile)
c.365-2935C>A (n.365-2935C>A)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41009363C=CA2336258770CYP2B6c.790C= (p.Leu264=)
c.814C=
c.257-2935C= (n.257-2935C=)
c.485-2935C= (n.485-2935C=)
c.199C= (p.Leu67=)
c.365-2935C= (n.365-2935C=)
19g.41009363C>GCA405980758CYP2B6c.790C>G (p.Leu264Val)
c.814C>G
c.257-2935C>G (n.257-2935C>G)
c.485-2935C>G (n.485-2935C>G)
c.199C>G (p.Leu67Val)
c.365-2935C>G (n.365-2935C>G)
19g.41009363C>TCA405980759CYP2B6c.790C>T (p.Leu264Phe)
c.814C>T
c.257-2935C>T (n.257-2935C>T)
c.485-2935C>T (n.485-2935C>T)
c.199C>T (p.Leu67Phe)
c.365-2935C>T (n.365-2935C>T)
19g.41009364_41009365delCA2520215766CYP2B6c.791_792del (p.Leu264HisfsTer18)
c.815_816del
c.257-2934_257-2933del (n.257-2934_257-2933del)
c.485-2934_485-2933del (n.485-2934_485-2933del)
c.200_201del (p.Leu67HisfsTer18)
c.365-2934_365-2933del (n.365-2934_365-2933del)
19g.41009364T>ACA405980762CYP2B6c.791T>A (p.Leu264His)
c.815T>A
c.257-2934T>A (n.257-2934T>A)
c.485-2934T>A (n.485-2934T>A)
c.200T>A (p.Leu67His)
c.365-2934T>A (n.365-2934T>A)
gnomAD v4
19g.41009364T>CCA405980764CYP2B6c.791T>C (p.Leu264Pro)
c.815T>C
c.257-2934T>C (n.257-2934T>C)
c.485-2934T>C (n.485-2934T>C)
c.200T>C (p.Leu67Pro)
c.365-2934T>C (n.365-2934T>C)
19g.41009364T>GCA405980765CYP2B6c.791T>G (p.Leu264Arg)
c.815T>G
c.257-2934T>G (n.257-2934T>G)
c.485-2934T>G (n.485-2934T>G)
c.200T>G (p.Leu67Arg)
c.365-2934T>G (n.365-2934T>G)
19g.41009365C>ACA507535594CYP2B6c.792C>A (p.Leu264=)
c.816C>A
c.257-2933C>A (n.257-2933C>A)
c.485-2933C>A (n.485-2933C>A)
c.201C>A (p.Leu67=)
c.365-2933C>A (n.365-2933C>A)
19g.41009365C>GCA507535595CYP2B6c.792C>G (p.Leu264=)
c.816C>G
c.257-2933C>G (n.257-2933C>G)
c.485-2933C>G (n.485-2933C>G)
c.201C>G (p.Leu67=)
c.365-2933C>G (n.365-2933C>G)
19g.41009365C>TCA507535596CYP2B6c.792C>T (p.Leu264=)
c.816C>T
c.257-2933C>T (n.257-2933C>T)
c.485-2933C>T (n.485-2933C>T)
c.201C>T (p.Leu67=)
c.365-2933C>T (n.365-2933C>T)
19g.41009366A>CCA405980767CYP2B6c.793A>C (p.Ile265Leu)
c.817A>C
c.257-2932A>C (n.257-2932A>C)
c.485-2932A>C (n.485-2932A>C)
c.202A>C (p.Ile68Leu)
c.365-2932A>C (n.365-2932A>C)
gnomAD v4
19g.41009366A>GCA405980769CYP2B6c.793A>G (p.Ile265Val)
c.817A>G
c.257-2932A>G (n.257-2932A>G)
c.485-2932A>G (n.485-2932A>G)
c.202A>G (p.Ile68Val)
c.365-2932A>G (n.365-2932A>G)
gnomAD v4
19g.41009366A>TCA405980771CYP2B6c.793A>T (p.Ile265Phe)
c.817A>T
c.257-2932A>T (n.257-2932A>T)
c.485-2932A>T (n.485-2932A>T)
c.202A>T (p.Ile68Phe)
c.365-2932A>T (n.365-2932A>T)
19g.41009367T>ACA405980772CYP2B6c.794T>A (p.Ile265Asn)
c.818T>A
c.257-2931T>A (n.257-2931T>A)
c.485-2931T>A (n.485-2931T>A)
c.203T>A (p.Ile68Asn)
c.365-2931T>A (n.365-2931T>A)
19g.41009367T>CCA405980773CYP2B6c.794T>C (p.Ile265Thr)
c.818T>C
c.257-2931T>C (n.257-2931T>C)
c.485-2931T>C (n.485-2931T>C)
c.203T>C (p.Ile68Thr)
c.365-2931T>C (n.365-2931T>C)
19g.41009367T>GCA405980774CYP2B6c.794T>G (p.Ile265Ser)
c.818T>G
c.257-2931T>G (n.257-2931T>G)
c.485-2931T>G (n.485-2931T>G)
c.203T>G (p.Ile68Ser)
c.365-2931T>G (n.365-2931T>G)
19g.41009368C>ACA507535605CYP2B6c.795C>A (p.Ile265=)
c.819C>A
c.257-2930C>A (n.257-2930C>A)
c.485-2930C>A (n.485-2930C>A)
c.204C>A (p.Ile68=)
c.365-2930C>A (n.365-2930C>A)
dbSNP gnomAD v3 gnomAD v4
19g.41009368C=CA2336258774CYP2B6c.795C= (p.Ile265=)
c.819C=
c.257-2930C= (n.257-2930C=)
c.485-2930C= (n.485-2930C=)
c.204C= (p.Ile68=)
c.365-2930C= (n.365-2930C=)
19g.41009368C>GCA308498419CYP2B6c.795C>G (p.Ile265Met)
c.819C>G
c.257-2930C>G (n.257-2930C>G)
c.485-2930C>G (n.485-2930C>G)
c.204C>G (p.Ile68Met)
c.365-2930C>G (n.365-2930C>G)
dbSNP gnomAD v4
19g.41009368C>TCA9455336CYP2B6c.795C>T (p.Ile265=)
c.819C>T
c.257-2930C>T (n.257-2930C>T)
c.485-2930C>T (n.485-2930C>T)
c.204C>T (p.Ile68=)
c.365-2930C>T (n.365-2930C>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41009369G>ACA9455337CYP2B6c.796G>A (p.Asp266Asn)
c.820G>A
c.257-2929G>A (n.257-2929G>A)
c.485-2929G>A (n.485-2929G>A)
c.205G>A (p.Asp69Asn)
c.365-2929G>A (n.365-2929G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.41009369G>CCA405980780CYP2B6c.796G>C (p.Asp266His)
c.820G>C
c.257-2929G>C (n.257-2929G>C)
c.485-2929G>C (n.485-2929G>C)
c.205G>C (p.Asp69His)
c.365-2929G>C (n.365-2929G>C)
19g.41009369G=CA2336258778CYP2B6c.796G= (p.Asp266=)
c.820G=
c.257-2929G= (n.257-2929G=)
c.485-2929G= (n.485-2929G=)
c.205G= (p.Asp69=)
c.365-2929G= (n.365-2929G=)
19g.41009369G>TCA405980781CYP2B6c.796G>T (p.Asp266Tyr)
c.820G>T
c.257-2929G>T (n.257-2929G>T)
c.485-2929G>T (n.485-2929G>T)
c.205G>T (p.Asp69Tyr)
c.365-2929G>T (n.365-2929G>T)
19g.41009370A=CA2336258782CYP2B6c.797A= (p.Asp266=)
c.821A=
c.257-2928A= (n.257-2928A=)
c.485-2928A= (n.485-2928A=)
c.206A= (p.Asp69=)
c.365-2928A= (n.365-2928A=)
19g.41009370A>CCA405980784CYP2B6c.797A>C (p.Asp266Ala)
c.821A>C
c.257-2928A>C (n.257-2928A>C)
c.485-2928A>C (n.485-2928A>C)
c.206A>C (p.Asp69Ala)
c.365-2928A>C (n.365-2928A>C)
dbSNP gnomAD v4
19g.41009370A>GCA405980785CYP2B6c.797A>G (p.Asp266Gly)
c.821A>G
c.257-2928A>G (n.257-2928A>G)
c.485-2928A>G (n.485-2928A>G)
c.206A>G (p.Asp69Gly)
c.365-2928A>G (n.365-2928A>G)
19g.41009370A>TCA9455338CYP2B6c.797A>T (p.Asp266Val)
c.821A>T
c.257-2928A>T (n.257-2928A>T)
c.485-2928A>T (n.485-2928A>T)
c.206A>T (p.Asp69Val)
c.365-2928A>T (n.365-2928A>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.41009371C>ACA405980787CYP2B6c.798C>A (p.Asp266Glu)
c.822C>A
c.257-2927C>A (n.257-2927C>A)
c.485-2927C>A (n.485-2927C>A)
c.207C>A (p.Asp69Glu)
c.365-2927C>A (n.365-2927C>A)
19g.41009371C=CA2336258785CYP2B6c.798C= (p.Asp266=)
c.822C=
c.257-2927C= (n.257-2927C=)
c.485-2927C= (n.485-2927C=)
c.207C= (p.Asp69=)
c.365-2927C= (n.365-2927C=)

Number of alleles fetched