Chr Mutation (hg38) CAid Gene Transcript Linkouts
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
11g.32435333C>ACA379966536WT1c.28G>T (p.Ala10Ser)
c.13G>T (p.Ala5Ser)
n.207G>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32435333C=CA1962327467WT1c.28G= (p.Ala10=)
c.13G= (p.Ala5=)
n.207G=
11g.32435333C>GCA379966537WT1c.28G>C (p.Ala10Pro)
c.13G>C (p.Ala5Pro)
n.207G>C
 dbSNP gnomAD v3 gnomAD v4
11g.32435333C>TCA379966538WT1c.28G>A (p.Ala10Thr)
c.13G>A (p.Ala5Thr)
n.207G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435334C>ACA473773495WT1c.27G>T (p.Pro9=)
c.12G>T (p.Pro4=)
n.206G>T
 dbSNP
11g.32435334C=CA1962327468WT1c.27G= (p.Pro9=)
c.12G= (p.Pro4=)
n.206G=
11g.32435334C>GCA473773497WT1c.27G>C (p.Pro9=)
c.12G>C (p.Pro4=)
n.206G>C
 dbSNP gnomAD v4
11g.32435334C>TCA219511551WT1c.27G>A (p.Pro9=)
c.12G>A (p.Pro4=)
n.206G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435335G>ACA219511559WT1c.26C>T (p.Pro9Leu)
c.11C>T (p.Pro4Leu)
n.205C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435335G>CCA379966539WT1c.26C>G (p.Pro9Arg)
c.11C>G (p.Pro4Arg)
n.205C>G
 ClinVar dbSNP gnomAD v4
11g.32435335G=CA1962327469WT1c.26C= (p.Pro9=)
c.11C= (p.Pro4=)
n.205C=
11g.32435335G>TCA379966540WT1c.26C>A (p.Pro9Gln)
c.11C>A (p.Pro4Gln)
n.205C>A
11g.32435336G>ACA379966541WT1c.25C>T (p.Pro9Ser)
c.10C>T (p.Pro4Ser)
n.204C>T
 dbSNP
11g.32435336G>CCA379966542WT1c.25C>G (p.Pro9Ala)
c.10C>G (p.Pro4Ala)
n.204C>G
 ClinVar gnomAD v4
11g.32435336G=CA1962327470WT1c.25C= (p.Pro9=)
c.10C= (p.Pro4=)
n.204C=
11g.32435336G>TCA379966543WT1c.25C>A (p.Pro9Thr)
c.10C>A (p.Pro4Thr)
n.204C>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435337G>ACA473773499WT1c.24C>T (p.Asp8=)
c.9C>T (p.Asp3=)
n.203C>T
 ClinVar dbSNP
11g.32435337G>CCA379966544WT1c.24C>G (p.Asp8Glu)
c.9C>G (p.Asp3Glu)
n.203C>G
 ClinVar dbSNP
11g.32435337G=CA1962327471WT1c.24C= (p.Asp8=)
c.9C= (p.Asp3=)
n.203C=
11g.32435337G>TCA379966545WT1c.24C>A (p.Asp8Glu)
c.9C>A (p.Asp3Glu)
n.203C>A
 ClinVar dbSNP
11g.32435338T>ACA379966546WT1c.23A>T (p.Asp8Val)
c.8A>T (p.Asp3Val)
n.202A>T
 ClinVar
11g.32435338T>CCA379966548WT1c.23A>G (p.Asp8Gly)
c.8A>G (p.Asp3Gly)
n.202A>G
11g.32435338T>GCA379966547WT1c.23A>C (p.Asp8Ala)
c.8A>C (p.Asp3Ala)
n.202A>C
11g.32435339C>ACA379966549WT1c.22G>T (p.Asp8Tyr)
c.7G>T (p.Asp3Tyr)
n.201G>T
 gnomAD v4
11g.32435339C=CA1962327472WT1c.22G= (p.Asp8=)
c.7G= (p.Asp3=)
n.201G=
11g.32435339C>GCA379966550WT1c.22G>C (p.Asp8His)
c.7G>C (p.Asp3His)
n.201G>C
 dbSNP
11g.32435339C>TCA379966551WT1c.22G>A (p.Asp8Asn)
c.7G>A (p.Asp3Asn)
n.201G>A
11g.32435340C>ACA379966552WT1c.21G>T (p.Gln7His)
c.6G>T (p.Gln2His)
n.200G>T
11g.32435340C>GCA379966553WT1c.21G>C (p.Gln7His)
c.6G>C (p.Gln2His)
n.200G>C
11g.32435340C>TCA473773519WT1c.21G>A (p.Gln7=)
c.6G>A (p.Gln2=)
n.200G>A
11g.32435341T>ACA379966554WT1c.20A>T (p.Gln7Leu)
c.5A>T (p.Gln2Leu)
n.199A>T
11g.32435341T>CCA219511588WT1c.20A>G (p.Gln7Arg)
c.5A>G (p.Gln2Arg)
n.199A>G
 dbSNP
11g.32435341T>GCA379966555WT1c.20A>C (p.Gln7Pro)
c.5A>C (p.Gln2Pro)
n.199A>C
11g.32435341T=CA1962327473WT1c.20A= (p.Gln7=)
c.5A= (p.Gln2=)
n.199A=
11g.32435342G>ACA379966557WT1c.19C>T (p.Gln7Ter)
c.4C>T (p.Gln2Ter)
n.198C>T
 ClinVar dbSNP
11g.32435342G>CCA379966560WT1c.19C>G (p.Gln7Glu)
c.4C>G (p.Gln2Glu)
n.198C>G
11g.32435342G>TCA379966561WT1c.19C>A (p.Gln7Lys)
c.4C>A (p.Gln2Lys)
n.198C>A
 ClinVar dbSNP
11g.32435343C>ACA473773538WT1c.18G>T (p.Leu6=)
c.3G>T (p.Leu1=)
n.197G>T
 dbSNP gnomAD v4
11g.32435343C=CA1962327474WT1c.18G= (p.Leu6=)
c.3G= (p.Leu1=)
n.197G=
11g.32435343C>GCA473773539WT1c.18G>C (p.Leu6=)
c.3G>C (p.Leu1=)
n.197G>C
11g.32435343C>TCA473773542WT1c.18G>A (p.Leu6=)
c.3G>A (p.Leu1=)
n.197G>A
11g.32435344A=CA1962327475WT1c.17T= (p.Leu6=)
c.2T= (p.Leu1=)
n.196T=
11g.32435344A>CCA379966566WT1c.17T>G (p.Leu6Arg)
c.2T>G (p.Leu1Arg)
n.196T>G
 dbSNP gnomAD v3 gnomAD v4
11g.32435344A>GCA379966565WT1c.17T>C (p.Leu6Pro)
c.2T>C (p.Leu1Pro)
n.196T>C
 ClinVar
11g.32435344A>TCA379966563WT1c.17T>A (p.Leu6Gln)
c.2T>A (p.Leu1Gln)
n.196T>A
11g.32435344_32435345delinsCCCA2580084217WT1c.16_17delinsGG (p.Leu6Gly)
c.1_2delinsGG (p.Leu1Gly)
n.195_196delinsGG
 ClinVar
11g.32435345G>ACA473773546WT1c.16C>T (p.Leu6=)
c.1C>T (p.Leu1=)
n.195C>T
 ClinVar gnomAD v4
11g.32435345G>CCA379966568WT1c.16C>G (p.Leu6Val)
c.1C>G (p.Leu1Val)
n.195C>G
 dbSNP gnomAD v3 gnomAD v4
11g.32435345G=CA1962327476WT1c.16C= (p.Leu6=)
c.1C= (p.Leu1=)
n.195C=
11g.32435345G>TCA379966570WT1c.16C>A (p.Leu6Met)
c.1C>A (p.Leu1Met)
n.195C>A
 gnomAD v4
11g.32435347A=CA1962327477WT1c.14T= (p.Leu5=)
c.-2T= (n.-2T=)
n.193T=
11g.32435347A>GCA1962327478WT1c.14T>C (p.Leu5Ser)
c.-2T>C (n.-2T>C)
n.193T>C
 dbSNP
11g.32435348A>GCA2612989684WT1c.13T>C (p.Leu5=)
c.-3T>C (n.-3T>C)
n.192T>C
 gnomAD v4
11g.32435349G>ACA2612989685WT1c.12C>T (p.Leu4=)
c.-4C>T (n.-4C>T)
n.191C>T
 gnomAD v4
11g.32435349G>TCA2612989686WT1c.12C>A (p.Leu4=)
c.-4C>A (n.-4C>A)
n.191C>A
 gnomAD v4
11g.32435351G>ACA2723404706WT1c.10C>T (p.Leu4Phe)
c.-6C>T (n.-6C>T)
n.189C>T
 dbSNP
11g.32435351G>CCA598512816WT1c.10C>G (p.Leu4Val)
c.-6C>G (n.-6C>G)
n.189C>G
 dbSNP gnomAD v2 gnomAD v4
11g.32435351G=CA1962327479WT1c.10C= (p.Leu4=)
c.-6C= (n.-6C=)
n.189C=
11g.32435352delCA2790963049WT1c.10del (p.Leu4SerfsTer?)
c.-6del (n.-6del)
n.189del
11g.32435352G>ACA2612989687WT1c.9C>T (p.Phe3=)
c.-7C>T (n.-7C>T)
n.188C>T
 gnomAD v4
11g.32435354A=CA1962327480WT1c.7T= (p.Phe3=)
c.-9T= (n.-9T=)
n.186T=
11g.32435354A>CCA2790963050WT1c.7T>G (p.Phe3Val)
c.-9T>G (n.-9T>G)
n.186T>G
 ClinVar
11g.32435354A>GCA1962327481WT1c.7T>C (p.Phe3Leu)
c.-9T>C (n.-9T>C)
n.186T>C
 dbSNP
11g.32435355G>ACA675623683WT1c.6C>T (p.Asp2=)
c.-10C>T (n.-10C>T)
n.185C>T
 dbSNP gnomAD v3 gnomAD v4
11g.32435355G=CA1962327482WT1c.6C= (p.Asp2=)
c.-10C= (n.-10C=)
n.185C=

Number of alleles fetched