Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.32435232G>ACA473773277WT1c.129C>T (p.Gly43=)
c.114C>T (p.Gly38=)
n.308C>T
 gnomAD v4
11g.32435232G>CCA473773278WT1c.129C>G (p.Gly43=)
c.114C>G (p.Gly38=)
n.308C>G
 dbSNP
11g.32435232G>TCA473773279WT1c.129C>A (p.Gly43=)
c.114C>A (p.Gly38=)
n.308C>A
 gnomAD v4
11g.32435233C>ACA379966327WT1c.128G>T (p.Gly43Val)
c.113G>T (p.Gly38Val)
n.307G>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435233C=CA1962327409WT1c.128G= (p.Gly43=)
c.113G= (p.Gly38=)
n.307G=
11g.32435233C>GCA379966328WT1c.128G>C (p.Gly43Ala)
c.113G>C (p.Gly38Ala)
n.307G>C
11g.32435233C>TCA379966329WT1c.128G>A (p.Gly43Asp)
c.113G>A (p.Gly38Asp)
n.307G>A
 dbSNP gnomAD v4 COSMIC
11g.32435234C>ACA379966330WT1c.127G>T (p.Gly43Cys)
c.112G>T (p.Gly38Cys)
n.306G>T
 ClinVar dbSNP gnomAD v4
11g.32435234C=CA1962327410WT1c.127G= (p.Gly43=)
c.112G= (p.Gly38=)
n.306G=
11g.32435234C>GCA379966331WT1c.127G>C (p.Gly43Arg)
c.112G>C (p.Gly38Arg)
n.306G>C
 ClinVar gnomAD v4
11g.32435234C>TCA379966332WT1c.127G>A (p.Gly43Ser)
c.112G>A (p.Gly38Ser)
n.306G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435235G>ACA473773280WT1c.126C>T (p.Gly42=)
c.111C>T (p.Gly37=)
n.305C>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32435235G>CCA473773281WT1c.126C>G (p.Gly42=)
c.111C>G (p.Gly37=)
n.305C>G
11g.32435235G=CA1962327412WT1c.126C= (p.Gly42=)
c.111C= (p.Gly37=)
n.305C=
11g.32435235G>TCA473773282WT1c.126C>A (p.Gly42=)
c.111C>A (p.Gly37=)
n.305C>A
 ClinVar dbSNP gnomAD v4
11g.32435235_32435236delinsGCCA1962327411WT1c.125_126delinsGC (p.Gly42=)
c.110_111delinsGC (p.Gly37=)
n.304_305delinsGC
11g.32435236C>ACA379966333WT1c.125G>T (p.Gly42Val)
c.110G>T (p.Gly37Val)
n.304G>T
 gnomAD v4
11g.32435236C>GCA379966334WT1c.125G>C (p.Gly42Ala)
c.110G>C (p.Gly37Ala)
n.304G>C
11g.32435236C>TCA379966335WT1c.125G>A (p.Gly42Asp)
c.110G>A (p.Gly37Asp)
n.304G>A
 gnomAD v4
11g.32435238delCA598512810WT1c.125del (p.Gly42AlafsTer7)
c.110del (p.Gly37AlafsTer7)
n.304del
 dbSNP gnomAD v2 gnomAD v4
11g.32435237C>ACA379966336WT1c.124G>T (p.Gly42Cys)
c.109G>T (p.Gly37Cys)
n.303G>T
 gnomAD v4
11g.32435237C=CA1962327413WT1c.124G= (p.Gly42=)
c.109G= (p.Gly37=)
n.303G=
11g.32435237C>GCA379966337WT1c.124G>C (p.Gly42Arg)
c.109G>C (p.Gly37Arg)
n.303G>C
11g.32435237C>TCA064232WT1c.124G>A (p.Gly42Ser)
c.109G>A (p.Gly37Ser)
n.303G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32435238C>ACA473773283WT1c.123G>T (p.Pro41=)
c.108G>T (p.Pro36=)
n.302G>T
 gnomAD v4
11g.32435238C=CA1962327414WT1c.123G= (p.Pro41=)
c.108G= (p.Pro36=)
n.302G=
11g.32435238C>GCA017368WT1c.123G>C (p.Pro41=)
c.108G>C (p.Pro36=)
n.302G>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32435238C>TCA473773284WT1c.123G>A (p.Pro41=)
c.108G>A (p.Pro36=)
n.302G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435239G>ACA064128WT1c.122C>T (p.Pro41Leu)
c.107C>T (p.Pro36Leu)
n.301C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.32435239G>CCA379966339WT1c.122C>G (p.Pro41Arg)
c.107C>G (p.Pro36Arg)
n.301C>G
11g.32435239G=CA1962327415WT1c.122C= (p.Pro41=)
c.107C= (p.Pro36=)
n.301C=
11g.32435239G>TCA379966338WT1c.122C>A (p.Pro41Gln)
c.107C>A (p.Pro36Gln)
n.301C>A
 gnomAD v4
11g.32435241delCA2612989678WT1c.122del (p.Pro41ArgfsTer8)
c.107del (p.Pro36ArgfsTer8)
n.301del
 gnomAD v4
11g.32435240G>ACA219511447WT1c.121C>T (p.Pro41Ser)
c.106C>T (p.Pro36Ser)
n.300C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435240G>CCA379966341WT1c.121C>G (p.Pro41Ala)
c.106C>G (p.Pro36Ala)
n.300C>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32435240G=CA1962327416WT1c.121C= (p.Pro41=)
c.106C= (p.Pro36=)
n.300C=
11g.32435240G>TCA379966340WT1c.121C>A (p.Pro41Thr)
c.106C>A (p.Pro36Thr)
n.300C>A
 gnomAD v4
11g.32435241G>ACA473773285WT1c.120C>T (p.Asp40=)
c.105C>T (p.Asp35=)
n.299C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435241G>CCA379966342WT1c.120C>G (p.Asp40Glu)
c.105C>G (p.Asp35Glu)
n.299C>G
11g.32435241G=CA1962327417WT1c.120C= (p.Asp40=)
c.105C= (p.Asp35=)
n.299C=
11g.32435241G>TCA379966343WT1c.120C>A (p.Asp40Glu)
c.105C>A (p.Asp35Glu)
n.299C>A
 gnomAD v4
11g.32435241_32435251delinsGTCCCGGACTCCA1962327418WT1c.110_120delinsGAGTCCGGGAC (p.Gly37=)
c.95_105delinsGAGTCCGGGAC (p.Gly32=)
n.289_299delinsGAGTCCGGGAC
11g.32435242T>ACA379966344WT1c.119A>T (p.Asp40Val)
c.104A>T (p.Asp35Val)
n.298A>T
11g.32435242T>CCA379966345WT1c.119A>G (p.Asp40Gly)
c.104A>G (p.Asp35Gly)
n.298A>G
 dbSNP gnomAD v4
11g.32435242T>GCA379966346WT1c.119A>C (p.Asp40Ala)
c.104A>C (p.Asp35Ala)
n.298A>C
 ClinVar dbSNP gnomAD v4
11g.32435242_32435251delCA1962327419WT1c.110_119del (p.Gly37AlafsTer9)
c.95_104del (p.Gly32AlafsTer9)
n.289_298del
 dbSNP
11g.32435243C>ACA379966347WT1c.118G>T (p.Asp40Tyr)
c.103G>T (p.Asp35Tyr)
n.297G>T
 gnomAD v4
11g.32435243C=CA1962327420WT1c.118G= (p.Asp40=)
c.103G= (p.Asp35=)
n.297G=
11g.32435243C>GCA379966348WT1c.118G>C (p.Asp40His)
c.103G>C (p.Asp35His)
n.297G>C
 ClinVar dbSNP gnomAD v4
11g.32435243C>TCA379966349WT1c.118G>A (p.Asp40Asn)
c.103G>A (p.Asp35Asn)
n.297G>A
 gnomAD v4
11g.32435245delCA2499220932WT1c.118del (p.Asp40ThrfsTer9)
c.103del (p.Asp35ThrfsTer9)
n.297del
 ClinVar dbSNP gnomAD v4
11g.32435244C>ACA473773286WT1c.117G>T (p.Arg39=)
c.102G>T (p.Arg34=)
n.296G>T
 ClinVar gnomAD v4
11g.32435244C=CA1962327421WT1c.117G= (p.Arg39=)
c.102G= (p.Arg34=)
n.296G=
11g.32435244C>GCA473773287WT1c.117G>C (p.Arg39=)
c.102G>C (p.Arg34=)
n.296G>C
11g.32435244C>TCA219511451WT1c.117G>A (p.Arg39=)
c.102G>A (p.Arg34=)
n.296G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435245C>ACA379966352WT1c.116G>T (p.Arg39Leu)
c.101G>T (p.Arg34Leu)
n.295G>T
 dbSNP gnomAD v4
11g.32435245C=CA1962327422WT1c.116G= (p.Arg39=)
c.101G= (p.Arg34=)
n.295G=
11g.32435245C>GCA379966350WT1c.116G>C (p.Arg39Pro)
c.101G>C (p.Arg34Pro)
n.295G>C
 ClinVar dbSNP
11g.32435245C>TCA379966351WT1c.116G>A (p.Arg39Gln)
c.101G>A (p.Arg34Gln)
n.295G>A
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32435246G>ACA064047WT1c.115C>T (p.Arg39Trp)
c.100C>T (p.Arg34Trp)
n.294C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.32435246G>CCA379966353WT1c.115C>G (p.Arg39Gly)
c.100C>G (p.Arg34Gly)
n.294C>G
11g.32435246G=CA1962327423WT1c.115C= (p.Arg39=)
c.100C= (p.Arg34=)
n.294C=
11g.32435246G>TCA473773288WT1c.115C>A (p.Arg39=)
c.100C>A (p.Arg34=)
n.294C>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435247delCA2612989679WT1c.115del (p.Arg39GlyfsTer10)
c.100del (p.Arg34GlyfsTer10)
n.294del
 gnomAD v4
11g.32435247G>ACA473773289WT1c.114C>T (p.Val38=)
c.99C>T (p.Val33=)
n.293C>T
 gnomAD v4
11g.32435247G>CCA473773290WT1c.114C>G (p.Val38=)
c.99C>G (p.Val33=)
n.293C>G
 ClinVar
11g.32435247G>TCA473773291WT1c.114C>A (p.Val38=)
c.99C>A (p.Val33=)
n.293C>A
 gnomAD v4
11g.32435248A>CCA379966354WT1c.113T>G (p.Val38Gly)
c.98T>G (p.Val33Gly)
n.292T>G
 dbSNP
11g.32435248A>GCA379966355WT1c.113T>C (p.Val38Ala)
c.98T>C (p.Val33Ala)
n.292T>C
 gnomAD v4
11g.32435248A>TCA379966356WT1c.113T>A (p.Val38Asp)
c.98T>A (p.Val33Asp)
n.292T>A
 dbSNP
11g.32435249C>ACA379966357WT1c.112G>T (p.Val38Phe)
c.97G>T (p.Val33Phe)
n.291G>T
 ClinVar dbSNP gnomAD v4
11g.32435249C=CA1962327424WT1c.112G= (p.Val38=)
c.97G= (p.Val33=)
n.291G=
11g.32435249C>GCA379966359WT1c.112G>C (p.Val38Leu)
c.97G>C (p.Val33Leu)
n.291G>C
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435249C>TCA379966358WT1c.112G>A (p.Val38Ile)
c.97G>A (p.Val33Ile)
n.291G>A
 ClinVar gnomAD v4
11g.32435250T>ACA473773295WT1c.111A>T (p.Gly37=)
c.96A>T (p.Gly32=)
n.290A>T
11g.32435250T>CCA473773296WT1c.111A>G (p.Gly37=)
c.96A>G (p.Gly32=)
n.290A>G
 ClinVar dbSNP
11g.32435250T>GCA473773297WT1c.111A>C (p.Gly37=)
c.96A>C (p.Gly32=)
n.290A>C
11g.32435251C>ACA379966360WT1c.110G>T (p.Gly37Val)
c.95G>T (p.Gly32Val)
n.289G>T
 gnomAD v4
11g.32435251C=CA1962327425WT1c.110G= (p.Gly37=)
c.95G= (p.Gly32=)
n.289G=
11g.32435251C>GCA379966361WT1c.110G>C (p.Gly37Ala)
c.95G>C (p.Gly32Ala)
n.289G>C
 ClinVar dbSNP
11g.32435251C>TCA379966362WT1c.110G>A (p.Gly37Glu)
c.95G>A (p.Gly32Glu)
n.289G>A
 ClinVar gnomAD v4
11g.32435253delCA2612989680WT1c.110del (p.Gly37GlufsTer12)
c.95del (p.Gly32GlufsTer12)
n.289del
 gnomAD v4
11g.32435252C>ACA379966363WT1c.109G>T (p.Gly37Ter)
c.94G>T (p.Gly32Ter)
n.288G>T
 gnomAD v4
11g.32435252C=CA1962327426WT1c.109G= (p.Gly37=)
c.94G= (p.Gly32=)
n.288G=
11g.32435252C>GCA379966364WT1c.109G>C (p.Gly37Arg)
c.94G>C (p.Gly32Arg)
n.288G>C
 dbSNP
11g.32435252C>TCA379966365WT1c.109G>A (p.Gly37Arg)
c.94G>A (p.Gly32Arg)
n.288G>A
 ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
11g.32435253C>ACA379966366WT1c.108G>T (p.Gln36His)
c.93G>T (p.Gln31His)
n.287G>T
 dbSNP gnomAD v4
11g.32435253C>GCA379966367WT1c.108G>C (p.Gln36His)
c.93G>C (p.Gln31His)
n.287G>C
11g.32435253C>TCA473773302WT1c.108G>A (p.Gln36=)
c.93G>A (p.Gln31=)
n.287G>A
 ClinVar dbSNP gnomAD v4
11g.32435254T>ACA379966368WT1c.107A>T (p.Gln36Leu)
c.92A>T (p.Gln31Leu)
n.286A>T
 ClinVar dbSNP gnomAD v4
11g.32435254T>CCA379966369WT1c.107A>G (p.Gln36Arg)
c.92A>G (p.Gln31Arg)
n.286A>G
 gnomAD v4
11g.32435254T>GCA379966370WT1c.107A>C (p.Gln36Pro)
c.92A>C (p.Gln31Pro)
n.286A>C
11g.32435254T=CA1962327427WT1c.107A= (p.Gln36=)
c.92A= (p.Gln31=)
n.286A=
11g.32435255delCA2574790569WT1c.106del (p.Gln36ArgfsTer13)
c.91del (p.Gln31ArgfsTer13)
n.285del
11g.32435255G>ACA379966371WT1c.106C>T (p.Gln36Ter)
c.91C>T (p.Gln31Ter)
n.285C>T
 dbSNP
11g.32435255G>CCA379966373WT1c.106C>G (p.Gln36Glu)
c.91C>G (p.Gln31Glu)
n.285C>G
11g.32435255G>TCA379966372WT1c.106C>A (p.Gln36Lys)
c.91C>A (p.Gln31Lys)
n.285C>A
 gnomAD v4
11g.32435256C>ACA219511452WT1c.105G>T (p.Gln35His)
c.90G>T (p.Gln30His)
n.284G>T
 ClinVar dbSNP gnomAD v4
11g.32435256C=CA1962327428WT1c.105G= (p.Gln35=)
c.90G= (p.Gln30=)
n.284G=
11g.32435256C>GCA379966374WT1c.105G>C (p.Gln35His)
c.90G>C (p.Gln30His)
n.284G>C
 gnomAD v4
11g.32435256C>TCA473773306WT1c.105G>A (p.Gln35=)
c.90G>A (p.Gln30=)
n.284G>A
 gnomAD v4
11g.32435257T>ACA379966375WT1c.104A>T (p.Gln35Leu)
c.89A>T (p.Gln30Leu)
n.283A>T
11g.32435257T>CCA379966376WT1c.104A>G (p.Gln35Arg)
c.89A>G (p.Gln30Arg)
n.283A>G
 gnomAD v4
11g.32435257T>GCA379966377WT1c.104A>C (p.Gln35Pro)
c.89A>C (p.Gln30Pro)
n.283A>C
11g.32435258G>ACA379966378WT1c.103C>T (p.Gln35Ter)
c.88C>T (p.Gln30Ter)
n.282C>T
 gnomAD v4
11g.32435258G>CCA379966379WT1c.103C>G (p.Gln35Glu)
c.88C>G (p.Gln30Glu)
n.282C>G
11g.32435258G>TCA379966380WT1c.103C>A (p.Gln35Lys)
c.88C>A (p.Gln30Lys)
n.282C>A
 gnomAD v4
11g.32435259C>ACA379966381WT1c.102G>T (p.Glu34Asp)
c.87G>T (p.Glu29Asp)
n.281G>T
 gnomAD v4
11g.32435259C=CA1962327429WT1c.102G= (p.Glu34=)
c.87G= (p.Glu29=)
n.281G=
11g.32435259C>GCA379966382WT1c.102G>C (p.Glu34Asp)
c.87G>C (p.Glu29Asp)
n.281G>C
11g.32435259C>TCA065838WT1c.102G>A (p.Glu34=)
c.87G>A (p.Glu29=)
n.281G>A
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.32435260T>ACA379966385WT1c.101A>T (p.Glu34Val)
c.86A>T (p.Glu29Val)
n.280A>T
 gnomAD v4
11g.32435260T>CCA379966384WT1c.101A>G (p.Glu34Gly)
c.86A>G (p.Glu29Gly)
n.280A>G
 gnomAD v4
11g.32435260T>GCA379966383WT1c.101A>C (p.Glu34Ala)
c.86A>C (p.Glu29Ala)
n.280A>C
11g.32435261C>ACA379966386WT1c.100G>T (p.Glu34Ter)
c.85G>T (p.Glu29Ter)
n.279G>T
 gnomAD v4
11g.32435261C=CA1962327430WT1c.100G= (p.Glu34=)
c.85G= (p.Glu29=)
n.279G=
11g.32435261C>GCA379966387WT1c.100G>C (p.Glu34Gln)
c.85G>C (p.Glu29Gln)
n.279G>C
 dbSNP
11g.32435261C>TCA379966388WT1c.100G>A (p.Glu34Lys)
c.85G>A (p.Glu29Lys)
n.279G>A
11g.32435262T>ACA473773312WT1c.99A>T (p.Pro33=)
c.84A>T (p.Pro28=)
n.278A>T
 gnomAD v4
11g.32435262T>CCA473773314WT1c.99A>G (p.Pro33=)
c.84A>G (p.Pro28=)
n.278A>G
 ClinVar dbSNP gnomAD v4
11g.32435262T>GCA473773321WT1c.99A>C (p.Pro33=)
c.84A>C (p.Pro28=)
n.278A>C
11g.32435263G>ACA379966389WT1c.98C>T (p.Pro33Leu)
c.83C>T (p.Pro28Leu)
n.277C>T
 gnomAD v4
11g.32435263G>CCA379966390WT1c.98C>G (p.Pro33Arg)
c.83C>G (p.Pro28Arg)
n.277C>G
11g.32435263G>TCA379966391WT1c.98C>A (p.Pro33Gln)
c.83C>A (p.Pro28Gln)
n.277C>A
 ClinVar gnomAD v4
11g.32435264delCA2612989681WT1c.98del (p.Pro33GlnfsTer16)
c.83del (p.Pro28GlnfsTer16)
n.277del
 gnomAD v4
11g.32435264G>ACA379966392WT1c.97C>T (p.Pro33Ser)
c.82C>T (p.Pro28Ser)
n.276C>T
 dbSNP gnomAD v3 gnomAD v4
11g.32435264G>CCA379966393WT1c.97C>G (p.Pro33Ala)
c.82C>G (p.Pro28Ala)
n.276C>G
11g.32435264G=CA1962327431WT1c.97C= (p.Pro33=)
c.82C= (p.Pro28=)
n.276C=
11g.32435264G>TCA379966394WT1c.97C>A (p.Pro33Thr)
c.82C>A (p.Pro28Thr)
n.276C>A
 gnomAD v4
11g.32435265C>ACA379966395WT1c.96G>T (p.Gln32His)
c.81G>T (p.Gln27His)
n.275G>T
 gnomAD v4
11g.32435265C>GCA379966396WT1c.96G>C (p.Gln32His)
c.81G>C (p.Gln27His)
n.275G>C
11g.32435265C>TCA473773328WT1c.96G>A (p.Gln32=)
c.81G>A (p.Gln27=)
n.275G>A
 gnomAD v4
11g.32435266T>ACA379966399WT1c.95A>T (p.Gln32Leu)
c.80A>T (p.Gln27Leu)
n.274A>T
 gnomAD v4
11g.32435266T>CCA379966398WT1c.95A>G (p.Gln32Arg)
c.80A>G (p.Gln27Arg)
n.274A>G
 gnomAD v4
11g.32435266T>GCA379966397WT1c.95A>C (p.Gln32Pro)
c.80A>C (p.Gln27Pro)
n.274A>C
11g.32435267G>ACA379966400WT1c.94C>T (p.Gln32Ter)
c.79C>T (p.Gln27Ter)
n.273C>T
 dbSNP gnomAD v4
11g.32435267G>CCA379966402WT1c.94C>G (p.Gln32Glu)
c.79C>G (p.Gln27Glu)
n.273C>G
11g.32435267G>TCA379966401WT1c.94C>A (p.Gln32Lys)
c.79C>A (p.Gln27Lys)
n.273C>A
 ClinVar gnomAD v4
11g.32435268C>ACA379966403WT1c.93G>T (p.Gln31His)
c.78G>T (p.Gln26His)
n.272G>T
 gnomAD v4
11g.32435268C>GCA379966404WT1c.93G>C (p.Gln31His)
c.78G>C (p.Gln26His)
n.272G>C
11g.32435268C>TCA473773329WT1c.93G>A (p.Gln31=)
c.78G>A (p.Gln26=)
n.272G>A
 gnomAD v4
11g.32435269T>ACA379966405WT1c.92A>T (p.Gln31Leu)
c.77A>T (p.Gln26Leu)
n.271A>T
11g.32435269T>CCA379966406WT1c.92A>G (p.Gln31Arg)
c.77A>G (p.Gln26Arg)
n.271A>G
 dbSNP gnomAD v2 gnomAD v4
11g.32435269T>GCA379966407WT1c.92A>C (p.Gln31Pro)
c.77A>C (p.Gln26Pro)
n.271A>C
11g.32435269T=CA1962327432WT1c.92A= (p.Gln31=)
c.77A= (p.Gln26=)
n.271A=
11g.32435270G>ACA379966408WT1c.91C>T (p.Gln31Ter)
c.76C>T (p.Gln26Ter)
n.270C>T
 ClinVar dbSNP gnomAD v4
11g.32435270G>CCA219511455WT1c.91C>G (p.Gln31Glu)
c.76C>G (p.Gln26Glu)
n.270C>G
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435270G=CA1962327433WT1c.91C= (p.Gln31=)
c.76C= (p.Gln26=)
n.270C=
11g.32435270G>TCA379966409WT1c.91C>A (p.Gln31Lys)
c.76C>A (p.Gln26Lys)
n.270C>A
 gnomAD v4
11g.32435271T>ACA473773332WT1c.90A>T (p.Leu30=)
c.75A>T (p.Leu25=)
n.269A>T
11g.32435271T>CCA473773333WT1c.90A>G (p.Leu30=)
c.75A>G (p.Leu25=)
n.269A>G
11g.32435271T>GCA473773334WT1c.90A>C (p.Leu30=)
c.75A>C (p.Leu25=)
n.269A>C
11g.32435272A>CCA379966410WT1c.89T>G (p.Leu30Arg)
c.74T>G (p.Leu25Arg)
n.268T>G
11g.32435272A>GCA379966411WT1c.89T>C (p.Leu30Pro)
c.74T>C (p.Leu25Pro)
n.268T>C
 gnomAD v4
11g.32435272A>TCA379966412WT1c.89T>A (p.Leu30Gln)
c.74T>A (p.Leu25Gln)
n.268T>A
11g.32435273G>ACA473773338WT1c.88C>T (p.Leu30=)
c.73C>T (p.Leu25=)
n.267C>T
 gnomAD v4
11g.32435273G>CCA379966414WT1c.88C>G (p.Leu30Val)
c.73C>G (p.Leu25Val)
n.267C>G
11g.32435273G>TCA379966413WT1c.88C>A (p.Leu30Ile)
c.73C>A (p.Leu25Ile)
n.267C>A
 gnomAD v4
11g.32435274G>ACA473773340WT1c.87C>T (p.Cys29=)
c.72C>T (p.Cys24=)
n.266C>T
 ClinVar dbSNP gnomAD v4
11g.32435274G>CCA379966415WT1c.87C>G (p.Cys29Trp)
c.72C>G (p.Cys24Trp)
n.266C>G
11g.32435274G=CA1962327434WT1c.87C= (p.Cys29=)
c.72C= (p.Cys24=)
n.266C=
11g.32435274G>TCA379966416WT1c.87C>A (p.Cys29Ter)
c.72C>A (p.Cys24Ter)
n.266C>A
 ClinVar dbSNP gnomAD v4
11g.32435275C>ACA379966417WT1c.86G>T (p.Cys29Phe)
c.71G>T (p.Cys24Phe)
n.265G>T
 gnomAD v4 COSMIC
11g.32435275C=CA1962327435WT1c.86G= (p.Cys29=)
c.71G= (p.Cys24=)
n.265G=
11g.32435275C>GCA379966418WT1c.86G>C (p.Cys29Ser)
c.71G>C (p.Cys24Ser)
n.265G>C
11g.32435275C>TCA219511456WT1c.86G>A (p.Cys29Tyr)
c.71G>A (p.Cys24Tyr)
n.265G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435276A>CCA379966419WT1c.85T>G (p.Cys29Gly)
c.70T>G (p.Cys24Gly)
n.264T>G
 dbSNP
11g.32435276A>GCA379966420WT1c.85T>C (p.Cys29Arg)
c.70T>C (p.Cys24Arg)
n.264T>C
 gnomAD v4
11g.32435276A>TCA379966421WT1c.85T>A (p.Cys29Ser)
c.70T>A (p.Cys24Ser)
n.264T>A
11g.32435277C>ACA473773348WT1c.84G>T (p.Gly28=)
c.69G>T (p.Gly23=)
n.263G>T
 dbSNP gnomAD v2 gnomAD v4
11g.32435277C=CA1962327436WT1c.84G= (p.Gly28=)
c.69G= (p.Gly23=)
n.263G=
11g.32435277C>GCA473773350WT1c.84G>C (p.Gly28=)
c.69G>C (p.Gly23=)
n.263G>C
 ClinVar
11g.32435277C>TCA473773351WT1c.84G>A (p.Gly28=)
c.69G>A (p.Gly23=)
n.263G>A
 dbSNP gnomAD v2 gnomAD v4
11g.32435278C>ACA379966422WT1c.83G>T (p.Gly28Val)
c.68G>T (p.Gly23Val)
n.262G>T
 dbSNP gnomAD v4
11g.32435278C=CA1962327437WT1c.83G= (p.Gly28=)
c.68G= (p.Gly23=)
n.262G=
11g.32435278C>GCA379966423WT1c.83G>C (p.Gly28Ala)
c.68G>C (p.Gly23Ala)
n.262G>C
 dbSNP
11g.32435278C>TCA065499WT1c.83G>A (p.Gly28Glu)
c.68G>A (p.Gly23Glu)
n.262G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32435279C>ACA379966425WT1c.82G>T (p.Gly28Trp)
c.67G>T (p.Gly23Trp)
n.261G>T
 gnomAD v4
11g.32435279C>GCA379966426WT1c.82G>C (p.Gly28Arg)
c.67G>C (p.Gly23Arg)
n.261G>C
11g.32435279C>TCA379966424WT1c.82G>A (p.Gly28Arg)
c.67G>A (p.Gly23Arg)
n.261G>A
 gnomAD v4
11g.32435280A=CA1962327438WT1c.81T= (p.Pro27=)
c.66T= (p.Pro22=)
n.260T=
11g.32435280A>CCA473773356WT1c.81T>G (p.Pro27=)
c.66T>G (p.Pro22=)
n.260T>G
11g.32435280A>GCA065462WT1c.81T>C (p.Pro27=)
c.66T>C (p.Pro22=)
n.260T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32435280A>TCA473773357WT1c.81T>A (p.Pro27=)
c.66T>A (p.Pro22=)
n.260T>A
 gnomAD v4
11g.32435281G>ACA379966427WT1c.80C>T (p.Pro27Leu)
c.65C>T (p.Pro22Leu)
n.259C>T
11g.32435281G>CCA379966428WT1c.80C>G (p.Pro27Arg)
c.65C>G (p.Pro22Arg)
n.259C>G
11g.32435281G>TCA379966429WT1c.80C>A (p.Pro27His)
c.65C>A (p.Pro22His)
n.259C>A
 gnomAD v4
11g.32435283_32435287delCA2825001878WT1c.76_80del (p.Gly26TrpfsTer29)
c.61_65del (p.Gly21TrpfsTer29)
n.255_259del
 ClinVar
11g.32435282G>ACA379966432WT1c.79C>T (p.Pro27Ser)
c.64C>T (p.Pro22Ser)
n.258C>T
 ClinVar dbSNP gnomAD v4
11g.32435282G>CCA379966431WT1c.79C>G (p.Pro27Ala)
c.64C>G (p.Pro22Ala)
n.258C>G
11g.32435282G=CA1962327439WT1c.79C= (p.Pro27=)
c.64C= (p.Pro22=)
n.258C=
11g.32435282G>TCA379966430WT1c.79C>A (p.Pro27Thr)
c.64C>A (p.Pro22Thr)
n.258C>A
 gnomAD v4
11g.32435283C>ACA473773366WT1c.78G>T (p.Gly26=)
c.63G>T (p.Gly21=)
n.257G>T
 dbSNP gnomAD v4 COSMIC
11g.32435283C=CA1962327440WT1c.78G= (p.Gly26=)
c.63G= (p.Gly21=)
n.257G=
11g.32435283C>GCA473773365WT1c.78G>C (p.Gly26=)
c.63G>C (p.Gly21=)
n.257G>C
11g.32435283C>TCA473773363WT1c.78G>A (p.Gly26=)
c.63G>A (p.Gly21=)
n.257G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435284C>ACA379966433WT1c.77G>T (p.Gly26Val)
c.62G>T (p.Gly21Val)
n.256G>T
11g.32435284C=CA1962327441WT1c.77G= (p.Gly26=)
c.62G= (p.Gly21=)
n.256G=
11g.32435284C>GCA379966434WT1c.77G>C (p.Gly26Ala)
c.62G>C (p.Gly21Ala)
n.256G>C
11g.32435284C>TCA379966435WT1c.77G>A (p.Gly26Glu)
c.62G>A (p.Gly21Glu)
n.256G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
11g.32435285C>ACA379966436WT1c.76G>T (p.Gly26Trp)
c.61G>T (p.Gly21Trp)
n.255G>T
 gnomAD v4
11g.32435285C=CA1962327442WT1c.76G= (p.Gly26=)
c.61G= (p.Gly21=)
n.255G=
11g.32435285C>GCA379966437WT1c.76G>C (p.Gly26Arg)
c.61G>C (p.Gly21Arg)
n.255G>C
 ClinVar dbSNP
11g.32435285C>TCA379966438WT1c.76G>A (p.Gly26Arg)
c.61G>A (p.Gly21Arg)
n.255G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435286G>ACA473773368WT1c.75C>T (p.Ser25=)
c.60C>T (p.Ser20=)
n.254C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435286G>CCA473773370WT1c.75C>G (p.Ser25=)
c.60C>G (p.Ser20=)
n.254C>G
 ClinVar dbSNP
11g.32435286G=CA1962327443WT1c.75C= (p.Ser25=)
c.60C= (p.Ser20=)
n.254C=
11g.32435286G>TCA473773372WT1c.75C>A (p.Ser25=)
c.60C>A (p.Ser20=)
n.254C>A
 gnomAD v4
11g.32435287G>ACA379966439WT1c.74C>T (p.Ser25Phe)
c.59C>T (p.Ser20Phe)
n.253C>T
 gnomAD v4
11g.32435287G>CCA379966441WT1c.74C>G (p.Ser25Cys)
c.59C>G (p.Ser20Cys)
n.253C>G
11g.32435287G>TCA379966440WT1c.74C>A (p.Ser25Tyr)
c.59C>A (p.Ser20Tyr)
n.253C>A
11g.32435288A>CCA379966442WT1c.73T>G (p.Ser25Ala)
c.58T>G (p.Ser20Ala)
n.252T>G
11g.32435288A>GCA379966443WT1c.73T>C (p.Ser25Pro)
c.58T>C (p.Ser20Pro)
n.252T>C
 ClinVar gnomAD v4
11g.32435288A>TCA379966444WT1c.73T>A (p.Ser25Thr)
c.58T>A (p.Ser20Thr)
n.252T>A
11g.32435289G>ACA473773377WT1c.72C>T (p.Arg24=)
c.57C>T (p.Arg19=)
n.251C>T
 gnomAD v4
11g.32435289G>CCA473773378WT1c.72C>G (p.Arg24=)
c.57C>G (p.Arg19=)
n.251C>G
11g.32435289G>TCA473773380WT1c.72C>A (p.Arg24=)
c.57C>A (p.Arg19=)
n.251C>A
11g.32435290C>ACA379966445WT1c.71G>T (p.Arg24Leu)
c.56G>T (p.Arg19Leu)
n.250G>T
11g.32435290C=CA1962327444WT1c.71G= (p.Arg24=)
c.56G= (p.Arg19=)
n.250G=
11g.32435290C>GCA379966446WT1c.71G>C (p.Arg24Pro)
c.56G>C (p.Arg19Pro)
n.250G>C
 ClinVar dbSNP gnomAD v4
11g.32435290C>TCA379966447WT1c.71G>A (p.Arg24His)
c.56G>A (p.Arg19His)
n.250G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435291G>ACA10582914WT1c.70C>T (p.Arg24Cys)
c.55C>T (p.Arg19Cys)
n.249C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435291G>CCA379966448WT1c.70C>G (p.Arg24Gly)
c.55C>G (p.Arg19Gly)
n.249C>G
 ClinVar gnomAD v4
11g.32435291G=CA1962327445WT1c.70C= (p.Arg24=)
c.55C= (p.Arg19=)
n.249C=
11g.32435291G>TCA379966449WT1c.70C>A (p.Arg24Ser)
c.55C>A (p.Arg19Ser)
n.249C>A
 ClinVar gnomAD v4
11g.32435291_32435292delCA2825001879WT1c.69_70del (p.Arg24LeufsTer?)
c.54_55del (p.Arg19LeufsTer?)
n.248_249del
 ClinVar
11g.32435292G>ACA473773385WT1c.69C>T (p.Leu23=)
c.54C>T (p.Leu18=)
n.248C>T
11g.32435292G>CCA473773386WT1c.69C>G (p.Leu23=)
c.54C>G (p.Leu18=)
n.248C>G
 gnomAD v4
11g.32435292G=CA1962327446WT1c.69C= (p.Leu23=)
c.54C= (p.Leu18=)
n.248C=
11g.32435292G>TCA473773387WT1c.69C>A (p.Leu23=)
c.54C>A (p.Leu18=)
n.248C>A
 dbSNP gnomAD v2 gnomAD v4
11g.32435293A>CCA379966450WT1c.68T>G (p.Leu23Arg)
c.53T>G (p.Leu18Arg)
n.247T>G
11g.32435293A>GCA379966451WT1c.68T>C (p.Leu23Pro)
c.53T>C (p.Leu18Pro)
n.247T>C
11g.32435293A>TCA379966452WT1c.68T>A (p.Leu23His)
c.53T>A (p.Leu18His)
n.247T>A
11g.32435294G>ACA379966454WT1c.67C>T (p.Leu23Phe)
c.52C>T (p.Leu18Phe)
n.246C>T
 ClinVar dbSNP gnomAD v4
11g.32435294G>CCA379966455WT1c.67C>G (p.Leu23Val)
c.52C>G (p.Leu18Val)
n.246C>G
11g.32435294G>TCA379966453WT1c.67C>A (p.Leu23Ile)
c.52C>A (p.Leu18Ile)
n.246C>A
 gnomAD v4
11g.32435295C>ACA473773392WT1c.66G>T (p.Thr22=)
c.51G>T (p.Thr17=)
n.245G>T
 ClinVar dbSNP gnomAD v4
11g.32435295C=CA1962327447WT1c.66G= (p.Thr22=)
c.51G= (p.Thr17=)
n.245G=
11g.32435295C>GCA473773394WT1c.66G>C (p.Thr22=)
c.51G>C (p.Thr17=)
n.245G>C
 ClinVar gnomAD v4
11g.32435295C>TCA473773395WT1c.66G>A (p.Thr22=)
c.51G>A (p.Thr17=)
n.245G>A
 dbSNP
11g.32435296G>ACA379966456WT1c.65C>T (p.Thr22Met)
c.50C>T (p.Thr17Met)
n.244C>T
 dbSNP
11g.32435296G>CCA379966457WT1c.65C>G (p.Thr22Arg)
c.50C>G (p.Thr17Arg)
n.244C>G
 gnomAD v4
11g.32435296G>TCA379966458WT1c.65C>A (p.Thr22Lys)
c.50C>A (p.Thr17Lys)
n.244C>A
 ClinVar dbSNP
11g.32435297T>ACA379966459WT1c.64A>T (p.Thr22Ser)
c.49A>T (p.Thr17Ser)
n.243A>T
11g.32435297T>CCA379966460WT1c.64A>G (p.Thr22Ala)
c.49A>G (p.Thr17Ala)
n.243A>G
 ClinVar dbSNP
11g.32435297T>GCA379966461WT1c.64A>C (p.Thr22Pro)
c.49A>C (p.Thr17Pro)
n.243A>C
11g.32435298G>ACA473773400WT1c.63C>T (p.His21=)
c.48C>T (p.His16=)
n.242C>T
 ClinVar dbSNP gnomAD v4
11g.32435298G>CCA379966462WT1c.63C>G (p.His21Gln)
c.48C>G (p.His16Gln)
n.242C>G
11g.32435298G>TCA379966463WT1c.63C>A (p.His21Gln)
c.48C>A (p.His16Gln)
n.242C>A
11g.32435299T>ACA379966464WT1c.62A>T (p.His21Leu)
c.47A>T (p.His16Leu)
n.241A>T
 ClinVar dbSNP
11g.32435299T>CCA379966465WT1c.62A>G (p.His21Arg)
c.47A>G (p.His16Arg)
n.241A>G
 ClinVar dbSNP
11g.32435299T>GCA379966466WT1c.62A>C (p.His21Pro)
c.47A>C (p.His16Pro)
n.241A>C
11g.32435299T=CA1962327448WT1c.62A= (p.His21=)
c.47A= (p.His16=)
n.241A=
11g.32435300G>ACA379966467WT1c.61C>T (p.His21Tyr)
c.46C>T (p.His16Tyr)
n.240C>T
11g.32435300G>CCA379966468WT1c.61C>G (p.His21Asp)
c.46C>G (p.His16Asp)
n.240C>G
11g.32435300G>TCA379966469WT1c.61C>A (p.His21Asn)
c.46C>A (p.His16Asn)
n.240C>A
 gnomAD v4
11g.32435301C>ACA379966471WT1c.60G>T (p.Gln20His)
c.45G>T (p.Gln15His)
n.239G>T
 gnomAD v4
11g.32435301C>GCA379966470WT1c.60G>C (p.Gln20His)
c.45G>C (p.Gln15His)
n.239G>C
11g.32435301C>TCA473773407WT1c.60G>A (p.Gln20=)
c.45G>A (p.Gln15=)
n.239G>A
 gnomAD v4
11g.32435302T>ACA379966472WT1c.59A>T (p.Gln20Leu)
c.44A>T (p.Gln15Leu)
n.238A>T
 ClinVar
11g.32435302T>CCA379966473WT1c.59A>G (p.Gln20Arg)
c.44A>G (p.Gln15Arg)
n.238A>G
11g.32435302T>GCA379966474WT1c.59A>C (p.Gln20Pro)
c.44A>C (p.Gln15Pro)
n.238A>C
11g.32435302_32435303dupCA2612989682WT1c.58_59dup (p.Gln20HisfsTer30)
c.43_44dup (p.Gln15HisfsTer30)
n.237_238dup
 gnomAD v4
11g.32435303G>ACA379966475WT1c.58C>T (p.Gln20Ter)
c.43C>T (p.Gln15Ter)
n.237C>T
11g.32435303G>CCA379966476WT1c.58C>G (p.Gln20Glu)
c.43C>G (p.Gln15Glu)
n.237C>G
11g.32435303G>TCA379966477WT1c.58C>A (p.Gln20Lys)
c.43C>A (p.Gln15Lys)
n.237C>A
11g.32435304A>CCA473773416WT1c.57T>G (p.Ser19=)
c.42T>G (p.Ser14=)
n.236T>G
11g.32435304A>GCA473773415WT1c.57T>C (p.Ser19=)
c.42T>C (p.Ser14=)
n.236T>C
 gnomAD v4
11g.32435304A>TCA473773413WT1c.57T>A (p.Ser19=)
c.42T>A (p.Ser14=)
n.236T>A
11g.32435305G>ACA379966480WT1c.56C>T (p.Ser19Phe)
c.41C>T (p.Ser14Phe)
n.235C>T
 dbSNP
11g.32435305G>CCA379966479WT1c.56C>G (p.Ser19Cys)
c.41C>G (p.Ser14Cys)
n.235C>G
 ClinVar dbSNP
11g.32435305G>TCA379966478WT1c.56C>A (p.Ser19Tyr)
c.41C>A (p.Ser14Tyr)
n.235C>A
 gnomAD v4
11g.32435306A>CCA379966481WT1c.55T>G (p.Ser19Ala)
c.40T>G (p.Ser14Ala)
n.234T>G
11g.32435306A>GCA379966482WT1c.55T>C (p.Ser19Pro)
c.40T>C (p.Ser14Pro)
n.234T>C
11g.32435306A>TCA379966483WT1c.55T>A (p.Ser19Thr)
c.40T>A (p.Ser14Thr)
n.234T>A
11g.32435307C>ACA473773422WT1c.54G>T (p.Ala18=)
c.39G>T (p.Ala13=)
n.233G>T
11g.32435307C=CA1962327449WT1c.54G= (p.Ala18=)
c.39G= (p.Ala13=)
n.233G=
11g.32435307C>GCA473773423WT1c.54G>C (p.Ala18=)
c.39G>C (p.Ala13=)
n.233G>C
 dbSNP
11g.32435307C>TCA473773425WT1c.54G>A (p.Ala18=)
c.39G>A (p.Ala13=)
n.233G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435308G>ACA379966484WT1c.53C>T (p.Ala18Val)
c.38C>T (p.Ala13Val)
n.232C>T
 ClinVar dbSNP gnomAD v4
11g.32435308G>CCA379966485WT1c.53C>G (p.Ala18Gly)
c.38C>G (p.Ala13Gly)
n.232C>G
 dbSNP gnomAD v4
11g.32435308G=CA1962327450WT1c.53C= (p.Ala18=)
c.38C= (p.Ala13=)
n.232C=
11g.32435308G>TCA379966486WT1c.53C>A (p.Ala18Glu)
c.38C>A (p.Ala13Glu)
n.232C>A
 ClinVar
11g.32435309C>ACA379966487WT1c.52G>T (p.Ala18Ser)
c.37G>T (p.Ala13Ser)
n.231G>T
 ClinVar gnomAD v4
11g.32435309C=CA1962327451WT1c.52G= (p.Ala18=)
c.37G= (p.Ala13=)
n.231G=
11g.32435309C>GCA379966489WT1c.52G>C (p.Ala18Pro)
c.37G>C (p.Ala13Pro)
n.231G>C
 ClinVar dbSNP gnomAD v4
11g.32435309C>TCA379966488WT1c.52G>A (p.Ala18Thr)
c.37G>A (p.Ala13Thr)
n.231G>A
11g.32435310C>ACA473773433WT1c.51G>T (p.Pro17=)
c.36G>T (p.Pro12=)
n.230G>T
 gnomAD v4
11g.32435310C=CA1962327452WT1c.51G= (p.Pro17=)
c.36G= (p.Pro12=)
n.230G=
11g.32435310C>GCA473773434WT1c.51G>C (p.Pro17=)
c.36G>C (p.Pro12=)
n.230G>C
 ClinVar dbSNP gnomAD v4
11g.32435310C>TCA473773435WT1c.51G>A (p.Pro17=)
c.36G>A (p.Pro12=)
n.230G>A
 ClinVar dbSNP gnomAD v4
11g.32435311G>ACA379966490WT1c.50C>T (p.Pro17Leu)
c.35C>T (p.Pro12Leu)
n.229C>T
 ClinVar dbSNP
11g.32435311G>CCA379966491WT1c.50C>G (p.Pro17Arg)
c.35C>G (p.Pro12Arg)
n.229C>G
11g.32435311G=CA1962327453WT1c.50C= (p.Pro17=)
c.35C= (p.Pro12=)
n.229C=
11g.32435311G>TCA379966492WT1c.50C>A (p.Pro17Gln)
c.35C>A (p.Pro12Gln)
n.229C>A
11g.32435312G>ACA379966493WT1c.49C>T (p.Pro17Ser)
c.34C>T (p.Pro12Ser)
n.228C>T
 ClinVar dbSNP gnomAD v4
11g.32435312G>CCA379966494WT1c.49C>G (p.Pro17Ala)
c.34C>G (p.Pro12Ala)
n.228C>G
11g.32435312G=CA1962327454WT1c.49C= (p.Pro17=)
c.34C= (p.Pro12=)
n.228C=
11g.32435312G>TCA379966495WT1c.49C>A (p.Pro17Thr)
c.34C>A (p.Pro12Thr)
n.228C>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435313C>ACA379966497WT1c.48G>T (p.Glu16Asp)
c.33G>T (p.Glu11Asp)
n.227G>T
 gnomAD v4
11g.32435313C>GCA379966496WT1c.48G>C (p.Glu16Asp)
c.33G>C (p.Glu11Asp)
n.227G>C
11g.32435313C>TCA473773442WT1c.48G>A (p.Glu16=)
c.33G>A (p.Glu11=)
n.227G>A
 ClinVar
11g.32435314delCA2723472811WT1c.47del (p.Glu16GlyfsTer?)
c.32del (p.Glu11GlyfsTer?)
n.226del
 dbSNP
11g.32435314T>ACA379966498WT1c.47A>T (p.Glu16Val)
c.32A>T (p.Glu11Val)
n.226A>T
11g.32435314T>CCA379966499WT1c.47A>G (p.Glu16Gly)
c.32A>G (p.Glu11Gly)
n.226A>G
 dbSNP
11g.32435314T>GCA379966500WT1c.47A>C (p.Glu16Ala)
c.32A>C (p.Glu11Ala)
n.226A>C
 gnomAD v4
11g.32435314T=CA1962327455WT1c.47A= (p.Glu16=)
c.32A= (p.Glu11=)
n.226A=
11g.32435315C>ACA379966501WT1c.46G>T (p.Glu16Ter)
c.31G>T (p.Glu11Ter)
n.225G>T
11g.32435315C>GCA379966502WT1c.46G>C (p.Glu16Gln)
c.31G>C (p.Glu11Gln)
n.225G>C
11g.32435315C>TCA379966503WT1c.46G>A (p.Glu16Lys)
c.31G>A (p.Glu11Lys)
n.225G>A
 ClinVar dbSNP gnomAD v4
11g.32435316C>ACA473773447WT1c.45G>T (p.Pro15=)
c.30G>T (p.Pro10=)
n.224G>T
11g.32435316C=CA1962327456WT1c.45G= (p.Pro15=)
c.30G= (p.Pro10=)
n.224G=
11g.32435316C>GCA473773448WT1c.45G>C (p.Pro15=)
c.30G>C (p.Pro10=)
n.224G>C
11g.32435316C>TCA473773449WT1c.45G>A (p.Pro15=)
c.30G>A (p.Pro10=)
n.224G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435317G>ACA379966504WT1c.44C>T (p.Pro15Leu)
c.29C>T (p.Pro10Leu)
n.223C>T
 ClinVar dbSNP gnomAD v4
11g.32435317G>CCA379966506WT1c.44C>G (p.Pro15Arg)
c.29C>G (p.Pro10Arg)
n.223C>G
 gnomAD v4
11g.32435317G>TCA379966505WT1c.44C>A (p.Pro15Gln)
c.29C>A (p.Pro10Gln)
n.223C>A
11g.32435318G>ACA379966507WT1c.43C>T (p.Pro15Ser)
c.28C>T (p.Pro10Ser)
n.222C>T
 gnomAD v4
11g.32435318G>CCA379966508WT1c.43C>G (p.Pro15Ala)
c.28C>G (p.Pro10Ala)
n.222C>G
11g.32435318G>TCA379966509WT1c.43C>A (p.Pro15Thr)
c.28C>A (p.Pro10Thr)
n.222C>A
11g.32435319G>ACA473773452WT1c.42C>T (p.Val14=)
c.27C>T (p.Val9=)
n.221C>T
 ClinVar dbSNP gnomAD v4
11g.32435319G>CCA473773453WT1c.42C>G (p.Val14=)
c.27C>G (p.Val9=)
n.221C>G
 dbSNP gnomAD v2 gnomAD v4
11g.32435319G=CA1962327457WT1c.42C= (p.Val14=)
c.27C= (p.Val9=)
n.221C=
11g.32435319G>TCA473773454WT1c.42C>A (p.Val14=)
c.27C>A (p.Val9=)
n.221C>A
 gnomAD v4
11g.32435320A>CCA379966510WT1c.41T>G (p.Val14Gly)
c.26T>G (p.Val9Gly)
n.220T>G
11g.32435320A>GCA379966511WT1c.41T>C (p.Val14Ala)
c.26T>C (p.Val9Ala)
n.220T>C
 gnomAD v4
11g.32435320A>TCA379966512WT1c.41T>A (p.Val14Asp)
c.26T>A (p.Val9Asp)
n.220T>A
11g.32435321C>ACA379966513WT1c.40G>T (p.Val14Phe)
c.25G>T (p.Val9Phe)
n.219G>T
11g.32435321C>GCA379966514WT1c.40G>C (p.Val14Leu)
c.25G>C (p.Val9Leu)
n.219G>C
 ClinVar
11g.32435321C>TCA379966515WT1c.40G>A (p.Val14Ile)
c.25G>A (p.Val9Ile)
n.219G>A
11g.32435321dupCA2695201114WT1c.40dup (p.Val14GlyfsTer?)
c.25dup (p.Val9GlyfsTer?)
n.219dup
 ClinVar
11g.32435322A>CCA379966516WT1c.39T>G (p.Cys13Trp)
c.24T>G (p.Cys8Trp)
n.218T>G
11g.32435322A>GCA473773460WT1c.39T>C (p.Cys13=)
c.24T>C (p.Cys8=)
n.218T>C
11g.32435322A>TCA379966517WT1c.39T>A (p.Cys13Ter)
c.24T>A (p.Cys8Ter)
n.218T>A
11g.32435323C>ACA379966518WT1c.38G>T (p.Cys13Phe)
c.23G>T (p.Cys8Phe)
n.217G>T
11g.32435323C=CA1962327458WT1c.38G= (p.Cys13=)
c.23G= (p.Cys8=)
n.217G=
11g.32435323C>GCA379966520WT1c.38G>C (p.Cys13Ser)
c.23G>C (p.Cys8Ser)
n.217G>C
11g.32435323C>TCA379966519WT1c.38G>A (p.Cys13Tyr)
c.23G>A (p.Cys8Tyr)
n.217G>A
 dbSNP gnomAD v2 gnomAD v4
11g.32435324A>CCA379966521WT1c.37T>G (p.Cys13Gly)
c.22T>G (p.Cys8Gly)
n.216T>G
11g.32435324A>GCA379966522WT1c.37T>C (p.Cys13Arg)
c.22T>C (p.Cys8Arg)
n.216T>C
11g.32435324A>TCA379966523WT1c.37T>A (p.Cys13Ser)
c.22T>A (p.Cys8Ser)
n.216T>A
11g.32435325C>ACA473773465WT1c.36G>T (p.Thr12=)
c.21G>T (p.Thr7=)
n.215G>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435325C=CA1962327459WT1c.36G= (p.Thr12=)
c.21G= (p.Thr7=)
n.215G=
11g.32435325C>GCA473773467WT1c.36G>C (p.Thr12=)
c.21G>C (p.Thr7=)
n.215G>C
 ClinVar dbSNP gnomAD v4
11g.32435325C>TCA473773466WT1c.36G>A (p.Thr12=)
c.21G>A (p.Thr7=)
n.215G>A
 ClinVar
11g.32435326G>ACA379966524WT1c.35C>T (p.Thr12Met)
c.20C>T (p.Thr7Met)
n.214C>T
 ClinVar dbSNP gnomAD v4
11g.32435326G>CCA379966525WT1c.35C>G (p.Thr12Arg)
c.20C>G (p.Thr7Arg)
n.214C>G
11g.32435326G>TCA379966526WT1c.35C>A (p.Thr12Lys)
c.20C>A (p.Thr7Lys)
n.214C>A
 ClinVar gnomAD v4 COSMIC
11g.32435327T>ACA379966527WT1c.34A>T (p.Thr12Ser)
c.19A>T (p.Thr7Ser)
n.213A>T
 dbSNP
11g.32435327T>CCA219511507WT1c.34A>G (p.Thr12Ala)
c.19A>G (p.Thr7Ala)
n.213A>G
 ClinVar dbSNP gnomAD v4
11g.32435327T>GCA064742WT1c.34A>C (p.Thr12Pro)
c.19A>C (p.Thr7Pro)
n.213A>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32435327T=CA1962327460WT1c.34A= (p.Thr12=)
c.19A= (p.Thr7=)
n.213A=
11g.32435327_32435328delinsGTCA2573146221WT1c.33_34delinsAC (p.Thr12Pro)
c.18_19delinsAC (p.Thr7Pro)
n.212_213delinsAC
 ClinVar dbSNP
11g.32435328G>ACA473773478WT1c.33C>T (p.Ser11=)
c.18C>T (p.Ser6=)
n.212C>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32435328G>CCA473773479WT1c.33C>G (p.Ser11=)
c.18C>G (p.Ser6=)
n.212C>G
11g.32435328G=CA1962327461WT1c.33C= (p.Ser11=)
c.18C= (p.Ser6=)
n.212C=
11g.32435328G>TCA473773480WT1c.33C>A (p.Ser11=)
c.18C>A (p.Ser6=)
n.212C>A
 ClinVar
11g.32435329delCA2612989683WT1c.33del (p.Thr12ArgfsTer?)
c.18del (p.Thr7ArgfsTer?)
n.212del
 gnomAD v4
11g.32435329G>ACA379966528WT1c.32C>T (p.Ser11Phe)
c.17C>T (p.Ser6Phe)
n.211C>T
 ClinVar dbSNP
11g.32435329G>CCA379966529WT1c.32C>G (p.Ser11Cys)
c.17C>G (p.Ser6Cys)
n.211C>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435329G=CA1962327462WT1c.32C= (p.Ser11=)
c.17C= (p.Ser6=)
n.211C=
11g.32435329G>TCA379966530WT1c.32C>A (p.Ser11Tyr)
c.17C>A (p.Ser6Tyr)
n.211C>A
11g.32435330A>CCA379966531WT1c.31T>G (p.Ser11Ala)
c.16T>G (p.Ser6Ala)
n.210T>G
11g.32435330A>GCA379966532WT1c.31T>C (p.Ser11Pro)
c.16T>C (p.Ser6Pro)
n.210T>C
11g.32435330A>TCA379966533WT1c.31T>A (p.Ser11Thr)
c.16T>A (p.Ser6Thr)
n.210T>A
11g.32435331A>CCA473773488WT1c.30T>G (p.Ala10=)
c.15T>G (p.Ala5=)
n.209T>G
11g.32435331A>GCA473773489WT1c.30T>C (p.Ala10=)
c.15T>C (p.Ala5=)
n.209T>C
 gnomAD v4
11g.32435331A>TCA473773490WT1c.30T>A (p.Ala10=)
c.15T>A (p.Ala5=)
n.209T>A
11g.32435331_32435341delinsAGCCGGGTCCTCA1962327463WT1c.20_30delinsAGGACCCGGCT (p.Gln7=)
c.5_15delinsAGGACCCGGCT (p.Gln2=)
n.199_209delinsAGGACCCGGCT
11g.32435332G>ACA219511534WT1c.29C>T (p.Ala10Val)
c.14C>T (p.Ala5Val)
n.208C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435332G>CCA379966535WT1c.29C>G (p.Ala10Gly)
c.14C>G (p.Ala5Gly)
n.208C>G
11g.32435332G=CA1962327466WT1c.29C= (p.Ala10=)
c.14C= (p.Ala5=)
n.208C=
11g.32435332G>TCA379966534WT1c.29C>A (p.Ala10Asp)
c.14C>A (p.Ala5Asp)
n.208C>A
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32435332_32435333delinsATCA658658041WT1c.28_29delinsAT (p.Ala10Ile)
c.13_14delinsAT (p.Ala5Ile)
n.207_208delinsAT
 ClinVar dbSNP
11g.32435332_32435333delinsGCCA1962327465WT1c.28_29delinsGC (p.Ala10=)
c.13_14delinsGC (p.Ala5=)
n.207_208delinsGC
11g.32435332_32435333delinsTACA658797616WT1c.28_29delinsTA (p.Ala10Tyr)
c.13_14delinsTA (p.Ala5Tyr)
n.207_208delinsTA
 ClinVar dbSNP
11g.32435334_32435343delCA1962327464WT1c.20_29del (p.Gln7LeufsTer?)
c.5_14del (p.Gln2LeufsTer?)
n.199_208del
 dbSNP gnomAD v4

Number of alleles fetched