Chr Mutation (hg38) CAid Gene Transcript Linkouts
22g.42128851G>ACA411773913CYP2D6c.446C>T (p.Pro149Leu)
c.599C>T (p.Pro200Leu)
c.266C>T (p.Pro89Leu)
c.533C>T (p.Pro178Leu)
n.1323C>T
c.455C>T (p.Pro152Leu)
22g.42128851G>CCA411773914CYP2D6c.446C>G (p.Pro149Arg)
c.599C>G (p.Pro200Arg)
c.266C>G (p.Pro89Arg)
c.533C>G (p.Pro178Arg)
n.1323C>G
c.455C>G (p.Pro152Arg)
22g.42128851G=CA2406579519CYP2D6c.446C= (p.Pro149=)
c.599C= (p.Pro200=)
c.266C= (p.Pro89=)
c.533C= (p.Pro178=)
n.1323C=
c.455C= (p.Pro152=)
22g.42128851G>TCA411773915CYP2D6c.446C>A (p.Pro149His)
c.599C>A (p.Pro200His)
c.266C>A (p.Pro89His)
c.533C>A (p.Pro178His)
n.1323C>A
c.455C>A (p.Pro152His)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
22g.42128852G>ACA411773916CYP2D6c.445C>T (p.Pro149Ser)
c.598C>T (p.Pro200Ser)
c.265C>T (p.Pro89Ser)
c.532C>T (p.Pro178Ser)
n.1322C>T
c.454C>T (p.Pro152Ser)
ClinVar dbSNP gnomAD v4
22g.42128852G>CCA10265013CYP2D6c.445C>G (p.Pro149Ala)
c.598C>G (p.Pro200Ala)
c.265C>G (p.Pro89Ala)
c.532C>G (p.Pro178Ala)
n.1322C>G
c.454C>G (p.Pro152Ala)
dbSNP ExAC gnomAD v2 gnomAD v4
22g.42128852G=CA2406579520CYP2D6c.445C= (p.Pro149=)
c.598C= (p.Pro200=)
c.265C= (p.Pro89=)
c.532C= (p.Pro178=)
n.1322C=
c.454C= (p.Pro152=)
22g.42128852G>TCA411773917CYP2D6c.445C>A (p.Pro149Thr)
c.598C>A (p.Pro200Thr)
c.265C>A (p.Pro89Thr)
c.532C>A (p.Pro178Thr)
n.1322C>A
c.454C>A (p.Pro152Thr)
dbSNP gnomAD v2 gnomAD v4
22g.42128853G>ACA10265014CYP2D6c.444C>T (p.Asp148=)
c.597C>T (p.Asp199=)
c.264C>T (p.Asp88=)
c.531C>T (p.Asp177=)
n.1321C>T
c.453C>T (p.Asp151=)
dbSNP ExAC gnomAD v2 gnomAD v4
22g.42128853G>CCA411773918CYP2D6c.444C>G (p.Asp148Glu)
c.597C>G (p.Asp199Glu)
c.264C>G (p.Asp88Glu)
c.531C>G (p.Asp177Glu)
n.1321C>G
c.453C>G (p.Asp151Glu)
dbSNP
22g.42128853G=CA2406579521CYP2D6c.444C= (p.Asp148=)
c.597C= (p.Asp199=)
c.264C= (p.Asp88=)
c.531C= (p.Asp177=)
n.1321C=
c.453C= (p.Asp151=)
22g.42128853G>TCA411773919CYP2D6c.444C>A (p.Asp148Glu)
c.597C>A (p.Asp199Glu)
c.264C>A (p.Asp88Glu)
c.531C>A (p.Asp177Glu)
n.1321C>A
c.453C>A (p.Asp151Glu)
22g.42128858_42128860delCA2657033654CYP2D6c.442_444del (p.Asp148del)
c.595_597del (p.Asp199del)
c.262_264del (p.Asp88del)
c.529_531del (p.Asp177del)
n.1319_1321del
c.451_453del (p.Asp151del)
gnomAD v4
22g.42128854T>ACA411773920CYP2D6c.443A>T (p.Asp148Val)
c.596A>T (p.Asp199Val)
c.263A>T (p.Asp88Val)
c.530A>T (p.Asp177Val)
n.1320A>T
c.452A>T (p.Asp151Val)
dbSNP
22g.42128854T>CCA411773921CYP2D6c.443A>G (p.Asp148Gly)
c.596A>G (p.Asp199Gly)
c.263A>G (p.Asp88Gly)
c.530A>G (p.Asp177Gly)
n.1320A>G
c.452A>G (p.Asp151Gly)
22g.42128854T>GCA10265015CYP2D6c.443A>C (p.Asp148Ala)
c.596A>C (p.Asp199Ala)
c.263A>C (p.Asp88Ala)
c.530A>C (p.Asp177Ala)
n.1320A>C
c.452A>C (p.Asp151Ala)
dbSNP ExAC gnomAD v2 gnomAD v4
22g.42128854T=CA2406579522CYP2D6c.443A= (p.Asp148=)
c.596A= (p.Asp199=)
c.263A= (p.Asp88=)
c.530A= (p.Asp177=)
n.1320A=
c.452A= (p.Asp151=)
22g.42128855C>ACA10265016CYP2D6c.442G>T (p.Asp148Tyr)
c.595G>T (p.Asp199Tyr)
c.262G>T (p.Asp88Tyr)
c.529G>T (p.Asp177Tyr)
n.1319G>T
c.451G>T (p.Asp151Tyr)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
22g.42128855C=CA2406579523CYP2D6c.442G= (p.Asp148=)
c.595G= (p.Asp199=)
c.262G= (p.Asp88=)
c.529G= (p.Asp177=)
n.1319G=
c.451G= (p.Asp151=)
22g.42128855C>GCA411773923CYP2D6c.442G>C (p.Asp148His)
c.595G>C (p.Asp199His)
c.262G>C (p.Asp88His)
c.529G>C (p.Asp177His)
n.1319G>C
c.451G>C (p.Asp151His)
dbSNP gnomAD v4
22g.42128855C>TCA411773922CYP2D6c.442G>A (p.Asp148Asn)
c.595G>A (p.Asp199Asn)
c.262G>A (p.Asp88Asn)
c.529G>A (p.Asp177Asn)
n.1319G>A
c.451G>A (p.Asp151Asn)
dbSNP gnomAD v4
22g.42128855_42128862delCA2738247943CYP2D6c.435_442del (p.Tyr146ProfsTer?)
c.588_595del (p.Tyr197ProfsTer?)
c.255_262del (p.Tyr86ProfsTer?)
c.522_529del (p.Tyr175ProfsTer?)
n.1312_1319del
c.444_451del (p.Tyr149ProfsTer?)
dbSNP
22g.42128856G>ACA10265017CYP2D6c.441C>T (p.Asp147=)
c.594C>T (p.Asp198=)
c.261C>T (p.Asp87=)
c.528C>T (p.Asp176=)
n.1318C>T
c.450C>T (p.Asp150=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
22g.42128856G>CCA411773924CYP2D6c.441C>G (p.Asp147Glu)
c.594C>G (p.Asp198Glu)
c.261C>G (p.Asp87Glu)
c.528C>G (p.Asp176Glu)
n.1318C>G
c.450C>G (p.Asp150Glu)
dbSNP gnomAD v4
22g.42128856G=CA2406579524CYP2D6c.441C= (p.Asp147=)
c.594C= (p.Asp198=)
c.261C= (p.Asp87=)
c.528C= (p.Asp176=)
n.1318C=
c.450C= (p.Asp150=)
22g.42128856G>TCA411773925CYP2D6c.441C>A (p.Asp147Glu)
c.594C>A (p.Asp198Glu)
c.261C>A (p.Asp87Glu)
c.528C>A (p.Asp176Glu)
n.1318C>A
c.450C>A (p.Asp150Glu)
dbSNP
22g.42128857T>ACA411773926CYP2D6c.440A>T (p.Asp147Val)
c.593A>T (p.Asp198Val)
c.260A>T (p.Asp87Val)
c.527A>T (p.Asp176Val)
n.1317A>T
c.449A>T (p.Asp150Val)
dbSNP
22g.42128857T>CCA411773927CYP2D6c.440A>G (p.Asp147Gly)
c.593A>G (p.Asp198Gly)
c.260A>G (p.Asp87Gly)
c.527A>G (p.Asp176Gly)
n.1317A>G
c.449A>G (p.Asp150Gly)
dbSNP gnomAD v3 gnomAD v4
22g.42128857T>GCA411773928CYP2D6c.440A>C (p.Asp147Ala)
c.593A>C (p.Asp198Ala)
c.260A>C (p.Asp87Ala)
c.527A>C (p.Asp176Ala)
n.1317A>C
c.449A>C (p.Asp150Ala)
dbSNP
22g.42128857T=CA2406579525CYP2D6c.440A= (p.Asp147=)
c.593A= (p.Asp198=)
c.260A= (p.Asp87=)
c.527A= (p.Asp176=)
n.1317A=
c.449A= (p.Asp150=)
22g.42128858C>ACA411773930CYP2D6c.439G>T (p.Asp147Tyr)
c.592G>T (p.Asp198Tyr)
c.259G>T (p.Asp87Tyr)
c.526G>T (p.Asp176Tyr)
n.1316G>T
c.448G>T (p.Asp150Tyr)
dbSNP
22g.42128858C=CA2406579526CYP2D6c.439G= (p.Asp147=)
c.592G= (p.Asp198=)
c.259G= (p.Asp87=)
c.526G= (p.Asp176=)
n.1316G=
c.448G= (p.Asp150=)
22g.42128858C>GCA411773929CYP2D6c.439G>C (p.Asp147His)
c.592G>C (p.Asp198His)
c.259G>C (p.Asp87His)
c.526G>C (p.Asp176His)
n.1316G>C
c.448G>C (p.Asp150His)
dbSNP gnomAD v4
22g.42128858C>TCA10265018CYP2D6c.439G>A (p.Asp147Asn)
c.592G>A (p.Asp198Asn)
c.259G>A (p.Asp87Asn)
c.526G>A (p.Asp176Asn)
n.1316G>A
c.448G>A (p.Asp150Asn)
dbSNP ExAC gnomAD v2 gnomAD v4
22g.42128859G>ACA10265019CYP2D6c.438C>T (p.Tyr146=)
c.591C>T (p.Tyr197=)
c.258C>T (p.Tyr86=)
c.525C>T (p.Tyr175=)
n.1315C>T
c.447C>T (p.Tyr149=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
22g.42128859G>CCA411773931CYP2D6c.438C>G (p.Tyr146Ter)
c.591C>G (p.Tyr197Ter)
c.258C>G (p.Tyr86Ter)
c.525C>G (p.Tyr175Ter)
n.1315C>G
c.447C>G (p.Tyr149Ter)
dbSNP gnomAD v2 gnomAD v4
22g.42128859G=CA2406579527CYP2D6c.438C= (p.Tyr146=)
c.591C= (p.Tyr197=)
c.258C= (p.Tyr86=)
c.525C= (p.Tyr175=)
n.1315C=
c.447C= (p.Tyr149=)
22g.42128859G>TCA411773932CYP2D6c.438C>A (p.Tyr146Ter)
c.591C>A (p.Tyr197Ter)
c.258C>A (p.Tyr86Ter)
c.525C>A (p.Tyr175Ter)
n.1315C>A
c.447C>A (p.Tyr149Ter)
22g.42128860T>ACA411773933CYP2D6c.437A>T (p.Tyr146Phe)
c.590A>T (p.Tyr197Phe)
c.257A>T (p.Tyr86Phe)
c.524A>T (p.Tyr175Phe)
n.1314A>T
c.446A>T (p.Tyr149Phe)
dbSNP
22g.42128860T>CCA411773934CYP2D6c.437A>G (p.Tyr146Cys)
c.590A>G (p.Tyr197Cys)
c.257A>G (p.Tyr86Cys)
c.524A>G (p.Tyr175Cys)
n.1314A>G
c.446A>G (p.Tyr149Cys)
dbSNP
22g.42128860T>GCA411773935CYP2D6c.437A>C (p.Tyr146Ser)
c.590A>C (p.Tyr197Ser)
c.257A>C (p.Tyr86Ser)
c.524A>C (p.Tyr175Ser)
n.1314A>C
c.446A>C (p.Tyr149Ser)
dbSNP
22g.42128860T=CA2406579528CYP2D6c.437A= (p.Tyr146=)
c.590A= (p.Tyr197=)
c.257A= (p.Tyr86=)
c.524A= (p.Tyr175=)
n.1314A=
c.446A= (p.Tyr149=)
22g.42128861A=CA2406579529CYP2D6c.436T= (p.Tyr146=)
c.589T= (p.Tyr197=)
c.256T= (p.Tyr86=)
c.523T= (p.Tyr175=)
n.1313T=
c.445T= (p.Tyr149=)
22g.42128861A>CCA411773936CYP2D6c.436T>G (p.Tyr146Asp)
c.589T>G (p.Tyr197Asp)
c.256T>G (p.Tyr86Asp)
c.523T>G (p.Tyr175Asp)
n.1313T>G
c.445T>G (p.Tyr149Asp)
22g.42128861A>GCA411773938CYP2D6c.436T>C (p.Tyr146His)
c.589T>C (p.Tyr197His)
c.256T>C (p.Tyr86His)
c.523T>C (p.Tyr175His)
n.1313T>C
c.445T>C (p.Tyr149His)
dbSNP gnomAD v3 gnomAD v4
22g.42128861A>TCA411773937CYP2D6c.436T>A (p.Tyr146Asn)
c.589T>A (p.Tyr197Asn)
c.256T>A (p.Tyr86Asn)
c.523T>A (p.Tyr175Asn)
n.1313T>A
c.445T>A (p.Tyr149Asn)
dbSNP
22g.42128862C>ACA411773939CYP2D6c.435G>T (p.Glu145Asp)
c.588G>T (p.Glu196Asp)
c.255G>T (p.Glu85Asp)
c.522G>T (p.Glu174Asp)
n.1312G>T
c.444G>T (p.Glu148Asp)
dbSNP gnomAD v4
22g.42128862C=CA2406579530CYP2D6c.435G= (p.Glu145=)
c.588G= (p.Glu196=)
c.255G= (p.Glu85=)
c.522G= (p.Glu174=)
n.1312G=
c.444G= (p.Glu148=)
22g.42128862C>GCA411773940CYP2D6c.435G>C (p.Glu145Asp)
c.588G>C (p.Glu196Asp)
c.255G>C (p.Glu85Asp)
c.522G>C (p.Glu174Asp)
n.1312G>C
c.444G>C (p.Glu148Asp)
dbSNP gnomAD v4
22g.42128862C>TCA10265020CYP2D6c.435G>A (p.Glu145=)
c.588G>A (p.Glu196=)
c.255G>A (p.Glu85=)
c.522G>A (p.Glu174=)
n.1312G>A
c.444G>A (p.Glu148=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched