Chr Mutation (hg38) CAid Gene Transcript Linkouts
22g.42128251_42128254delCA10264884CYP2D6c.612_615del (p.Thr205SerfsTer4)
c.765_768del (p.Thr256SerfsTer4)
c.432_435del (p.Thr145SerfsTer4)
c.699_702del (p.Thr234SerfsTer4)
n.1489_1492del
c.621_624del (p.Thr208SerfsTer4)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
22g.42128252_42128255delinsTAGCCA2406579046CYP2D6c.609_612delinsGCTA (p.Leu203=)
c.762_765delinsGCTA (p.Leu254=)
c.429_432delinsGCTA (p.Leu143=)
c.696_699delinsGCTA (p.Leu232=)
n.1486_1489delinsGCTA
c.618_621delinsGCTA (p.Leu206=)
22g.42128256_42128258dupCA639827953CYP2D6c.609_611dup (p.Leu204_Thr205insLeu)
c.762_764dup (p.Leu255_Thr256insLeu)
c.429_431dup (p.Leu144_Thr145insLeu)
c.696_698dup (p.Leu233_Thr234insLeu)
n.1486_1488dup
c.618_620dup (p.Leu207_Thr208insLeu)
dbSNP gnomAD v2 gnomAD v4
22g.42128256_42128258delCA639827954CYP2D6c.609_611del (p.Leu204del)
c.762_764del (p.Leu255del)
c.429_431del (p.Leu144del)
c.696_698del (p.Leu233del)
n.1486_1488del
c.618_620del (p.Leu207del)
dbSNP gnomAD v2
22g.42128254G>ACA10264887CYP2D6c.610C>T (p.Leu204=)
c.763C>T (p.Leu255=)
c.430C>T (p.Leu144=)
c.697C>T (p.Leu233=)
n.1487C>T
c.619C>T (p.Leu207=)
dbSNP ExAC gnomAD v2 gnomAD v4
22g.42128254G>CCA411773340CYP2D6c.610C>G (p.Leu204Val)
c.763C>G (p.Leu255Val)
c.430C>G (p.Leu144Val)
c.697C>G (p.Leu233Val)
n.1487C>G
c.619C>G (p.Leu207Val)
22g.42128254G=CA2406579048CYP2D6c.610C= (p.Leu204=)
c.763C= (p.Leu255=)
c.430C= (p.Leu144=)
c.697C= (p.Leu233=)
n.1487C=
c.619C= (p.Leu207=)
22g.42128254G>TCA411773341CYP2D6c.610C>A (p.Leu204Ile)
c.763C>A (p.Leu255Ile)
c.430C>A (p.Leu144Ile)
c.697C>A (p.Leu233Ile)
n.1487C>A
c.619C>A (p.Leu207Ile)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
22g.42128255C>ACA514800303CYP2D6c.609G>T (p.Leu203=)
c.762G>T (p.Leu254=)
c.429G>T (p.Leu143=)
c.696G>T (p.Leu232=)
n.1486G>T
c.618G>T (p.Leu206=)
22g.42128255C>GCA514800304CYP2D6c.609G>C (p.Leu203=)
c.762G>C (p.Leu254=)
c.429G>C (p.Leu143=)
c.696G>C (p.Leu232=)
n.1486G>C
c.618G>C (p.Leu206=)
22g.42128255C>TCA514800305CYP2D6c.609G>A (p.Leu203=)
c.762G>A (p.Leu254=)
c.429G>A (p.Leu143=)
c.696G>A (p.Leu232=)
n.1486G>A
c.618G>A (p.Leu206=)
dbSNP gnomAD v4
22g.42128256A=CA2406579049CYP2D6c.608T= (p.Leu203=)
c.761T= (p.Leu254=)
c.428T= (p.Leu143=)
c.695T= (p.Leu232=)
n.1485T=
c.617T= (p.Leu206=)
22g.42128256A>CCA411773348CYP2D6c.608T>G (p.Leu203Arg)
c.761T>G (p.Leu254Arg)
c.428T>G (p.Leu143Arg)
c.695T>G (p.Leu232Arg)
n.1485T>G
c.617T>G (p.Leu206Arg)
22g.42128256A>GCA411773344CYP2D6c.608T>C (p.Leu203Pro)
c.761T>C (p.Leu254Pro)
c.428T>C (p.Leu143Pro)
c.695T>C (p.Leu232Pro)
n.1485T>C
c.617T>C (p.Leu206Pro)
ClinVar dbSNP
22g.42128256A>TCA411773346CYP2D6c.608T>A (p.Leu203Gln)
c.761T>A (p.Leu254Gln)
c.428T>A (p.Leu143Gln)
c.695T>A (p.Leu232Gln)
n.1485T>A
c.617T>A (p.Leu206Gln)
22g.42128256_42128257delinsAGCA2406579050CYP2D6c.607_608delinsCT (p.Leu203=)
c.760_761delinsCT (p.Leu254=)
c.427_428delinsCT (p.Leu143=)
c.694_695delinsCT (p.Leu232=)
n.1484_1485delinsCT
c.616_617delinsCT (p.Leu206=)
22g.42128257delCA639827955CYP2D6c.607del (p.Leu203CysfsTer2)
c.760del (p.Leu254CysfsTer2)
c.427del (p.Leu143CysfsTer2)
c.694del (p.Leu232CysfsTer2)
n.1484del
c.616del (p.Leu206CysfsTer2)
dbSNP gnomAD v2 gnomAD v4
22g.42128257G>ACA514800306CYP2D6c.607C>T (p.Leu203=)
c.760C>T (p.Leu254=)
c.427C>T (p.Leu143=)
c.694C>T (p.Leu232=)
n.1484C>T
c.616C>T (p.Leu206=)
dbSNP
22g.42128257G>CCA411773350CYP2D6c.607C>G (p.Leu203Val)
c.760C>G (p.Leu254Val)
c.427C>G (p.Leu143Val)
c.694C>G (p.Leu232Val)
n.1484C>G
c.616C>G (p.Leu206Val)
dbSNP gnomAD v2 gnomAD v4
22g.42128257G=CA2406579051CYP2D6c.607C= (p.Leu203=)
c.760C= (p.Leu254=)
c.427C= (p.Leu143=)
c.694C= (p.Leu232=)
n.1484C=
c.616C= (p.Leu206=)
22g.42128257G>TCA411773352CYP2D6c.607C>A (p.Leu203Met)
c.760C>A (p.Leu254Met)
c.427C>A (p.Leu143Met)
c.694C>A (p.Leu232Met)
n.1484C>A
c.616C>A (p.Leu206Met)
22g.42128258C>ACA411773354CYP2D6c.606G>T (p.Glu202Asp)
c.759G>T (p.Glu253Asp)
c.426G>T (p.Glu142Asp)
c.693G>T (p.Glu231Asp)
n.1483G>T
c.615G>T (p.Glu205Asp)
22g.42128258C=CA2406579052CYP2D6c.606G= (p.Glu202=)
c.759G= (p.Glu253=)
c.426G= (p.Glu142=)
c.693G= (p.Glu231=)
n.1483G=
c.615G= (p.Glu205=)
22g.42128258C>GCA411773357CYP2D6c.606G>C (p.Glu202Asp)
c.759G>C (p.Glu253Asp)
c.426G>C (p.Glu142Asp)
c.693G>C (p.Glu231Asp)
n.1483G>C
c.615G>C (p.Glu205Asp)
22g.42128258C>TCA10264888CYP2D6c.606G>A (p.Glu202=)
c.759G>A (p.Glu253=)
c.426G>A (p.Glu142=)
c.693G>A (p.Glu231=)
n.1483G>A
c.615G>A (p.Glu205=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
22g.42128259delCA2657032109CYP2D6c.605del (p.Glu202GlyfsTer3)
c.758del (p.Glu253GlyfsTer3)
c.425del (p.Glu142GlyfsTer3)
c.692del (p.Glu231GlyfsTer3)
n.1482del
c.614del (p.Glu205GlyfsTer3)
gnomAD v4
22g.42128259T>ACA411773360CYP2D6c.605A>T (p.Glu202Val)
c.758A>T (p.Glu253Val)
c.425A>T (p.Glu142Val)
c.692A>T (p.Glu231Val)
n.1482A>T
c.614A>T (p.Glu205Val)
22g.42128259T>CCA411773362CYP2D6c.605A>G (p.Glu202Gly)
c.758A>G (p.Glu253Gly)
c.425A>G (p.Glu142Gly)
c.692A>G (p.Glu231Gly)
n.1482A>G
c.614A>G (p.Glu205Gly)
22g.42128259T>GCA411773364CYP2D6c.605A>C (p.Glu202Ala)
c.758A>C (p.Glu253Ala)
c.425A>C (p.Glu142Ala)
c.692A>C (p.Glu231Ala)
n.1482A>C
c.614A>C (p.Glu205Ala)
22g.42128259_42128261delinsTCACA2406579053CYP2D6c.603_605delinsTGA (p.Asp201=)
c.756_758delinsTGA (p.Asp252=)
c.423_425delinsTGA (p.Asp141=)
c.690_692delinsTGA (p.Asp230=)
n.1480_1482delinsTGA
c.612_614delinsTGA (p.Asp204=)
22g.42128260C>ACA411773367CYP2D6c.604G>T (p.Glu202Ter)
c.757G>T (p.Glu253Ter)
c.424G>T (p.Glu142Ter)
c.691G>T (p.Glu231Ter)
n.1481G>T
c.613G>T (p.Glu205Ter)
dbSNP
22g.42128260C>GCA411773369CYP2D6c.604G>C (p.Glu202Gln)
c.757G>C (p.Glu253Gln)
c.424G>C (p.Glu142Gln)
c.691G>C (p.Glu231Gln)
n.1481G>C
c.613G>C (p.Glu205Gln)
22g.42128260C>TCA411773370CYP2D6c.604G>A (p.Glu202Lys)
c.757G>A (p.Glu253Lys)
c.424G>A (p.Glu142Lys)
c.691G>A (p.Glu231Lys)
n.1481G>A
c.613G>A (p.Glu205Lys)
gnomAD v4
22g.42128260_42128261delCA639827956CYP2D6c.603_604del (p.Asp201GlufsTer5)
c.756_757del (p.Asp252GlufsTer5)
c.423_424del (p.Asp141GlufsTer5)
c.690_691del (p.Asp230GlufsTer5)
n.1480_1481del
c.612_613del (p.Asp204GlufsTer5)
dbSNP gnomAD v2 gnomAD v4
22g.42128261A=CA2406579054CYP2D6c.603T= (p.Asp201=)
c.756T= (p.Asp252=)
c.423T= (p.Asp141=)
c.690T= (p.Asp230=)
n.1480T=
c.612T= (p.Asp204=)
22g.42128261A>CCA411773371CYP2D6c.603T>G (p.Asp201Glu)
c.756T>G (p.Asp252Glu)
c.423T>G (p.Asp141Glu)
c.690T>G (p.Asp230Glu)
n.1480T>G
c.612T>G (p.Asp204Glu)
gnomAD v4
22g.42128261A>GCA514800307CYP2D6c.603T>C (p.Asp201=)
c.756T>C (p.Asp252=)
c.423T>C (p.Asp141=)
c.690T>C (p.Asp230=)
n.1480T>C
c.612T>C (p.Asp204=)
22g.42128261A>TCA10264889CYP2D6c.603T>A (p.Asp201Glu)
c.756T>A (p.Asp252Glu)
c.423T>A (p.Asp141Glu)
c.690T>A (p.Asp230Glu)
n.1480T>A
c.612T>A (p.Asp204Glu)
dbSNP ExAC gnomAD v2 gnomAD v4
22g.42128262T>ACA411773374CYP2D6c.602A>T (p.Asp201Val)
c.755A>T (p.Asp252Val)
c.422A>T (p.Asp141Val)
c.689A>T (p.Asp230Val)
n.1479A>T
c.611A>T (p.Asp204Val)
22g.42128262T>CCA411773377CYP2D6c.602A>G (p.Asp201Gly)
c.755A>G (p.Asp252Gly)
c.422A>G (p.Asp141Gly)
c.689A>G (p.Asp230Gly)
n.1479A>G
c.611A>G (p.Asp204Gly)
ClinVar dbSNP
22g.42128262T>GCA411773375CYP2D6c.602A>C (p.Asp201Ala)
c.755A>C (p.Asp252Ala)
c.422A>C (p.Asp141Ala)
c.689A>C (p.Asp230Ala)
n.1479A>C
c.611A>C (p.Asp204Ala)
22g.42128262T=CA2406579056CYP2D6c.602A= (p.Asp201=)
c.755A= (p.Asp252=)
c.422A= (p.Asp141=)
c.689A= (p.Asp230=)
n.1479A=
c.611A= (p.Asp204=)
22g.42128262_42128267delinsTCCAGCCA2406579055CYP2D6c.597_602delinsGCTGGA (p.Gln199=)
c.750_755delinsGCTGGA (p.Gln250=)
c.417_422delinsGCTGGA (p.Gln139=)
c.684_689delinsGCTGGA (p.Gln228=)
n.1474_1479delinsGCTGGA
c.606_611delinsGCTGGA (p.Gln202=)
22g.42128263C>ACA411773379CYP2D6c.601G>T (p.Asp201Tyr)
c.754G>T (p.Asp252Tyr)
c.421G>T (p.Asp141Tyr)
c.688G>T (p.Asp230Tyr)
n.1478G>T
c.610G>T (p.Asp204Tyr)
22g.42128263C=CA2406579057CYP2D6c.601G= (p.Asp201=)
c.754G= (p.Asp252=)
c.421G= (p.Asp141=)
c.688G= (p.Asp230=)
n.1478G=
c.610G= (p.Asp204=)
22g.42128263C>GCA411773380CYP2D6c.601G>C (p.Asp201His)
c.754G>C (p.Asp252His)
c.421G>C (p.Asp141His)
c.688G>C (p.Asp230His)
n.1478G>C
c.610G>C (p.Asp204His)
gnomAD v4
22g.42128263C>TCA411773381CYP2D6c.601G>A (p.Asp201Asn)
c.754G>A (p.Asp252Asn)
c.421G>A (p.Asp141Asn)
c.688G>A (p.Asp230Asn)
n.1478G>A
c.610G>A (p.Asp204Asn)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
22g.42128263_42128267delCA639827957CYP2D6c.597_601del (p.Leu200Ter)
c.750_754del (p.Leu251Ter)
c.417_421del (p.Leu140Ter)
c.684_688del (p.Leu229Ter)
n.1474_1478del
c.606_610del (p.Leu203Ter)
dbSNP gnomAD v2 gnomAD v4
22g.42128264C>ACA514800308CYP2D6c.600G>T (p.Leu200=)
c.753G>T (p.Leu251=)
c.420G>T (p.Leu140=)
c.687G>T (p.Leu229=)
n.1477G>T
c.609G>T (p.Leu203=)
22g.42128264C=CA2406579058CYP2D6c.600G= (p.Leu200=)
c.753G= (p.Leu251=)
c.420G= (p.Leu140=)
c.687G= (p.Leu229=)
n.1477G=
c.609G= (p.Leu203=)

Number of alleles fetched