Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.32435012C>ACA379965873WT1c.349G>T (p.Gly117Cys)
c.334G>T (p.Gly112Cys)
n.528G>T
 gnomAD v4
11g.32435012C=CA1962327272WT1c.349G= (p.Gly117=)
c.334G= (p.Gly112=)
n.528G=
11g.32435012C>GCA379965875WT1c.349G>C (p.Gly117Arg)
c.334G>C (p.Gly112Arg)
n.528G>C
 dbSNP
11g.32435012C>TCA379965874WT1c.349G>A (p.Gly117Ser)
c.334G>A (p.Gly112Ser)
n.528G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435013C>ACA473773802WT1c.348G>T (p.Pro116=)
c.333G>T (p.Pro111=)
n.527G>T
 gnomAD v4
11g.32435013C=CA1962327273WT1c.348G= (p.Pro116=)
c.333G= (p.Pro111=)
n.527G=
11g.32435013C>GCA473773804WT1c.348G>C (p.Pro116=)
c.333G>C (p.Pro111=)
n.527G>C
 ClinVar dbSNP gnomAD v4
11g.32435013C>TCA473773803WT1c.348G>A (p.Pro116=)
c.333G>A (p.Pro111=)
n.527G>A
 gnomAD v4
11g.32435014G>ACA10638965WT1c.347C>T (p.Pro116Leu)
c.332C>T (p.Pro111Leu)
n.526C>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435014G>CCA379965877WT1c.347C>G (p.Pro116Arg)
c.332C>G (p.Pro111Arg)
n.526C>G
 ClinVar dbSNP gnomAD v4
11g.32435014G=CA1962327274WT1c.347C= (p.Pro116=)
c.332C= (p.Pro111=)
n.526C=
11g.32435014G>TCA379965876WT1c.347C>A (p.Pro116Gln)
c.332C>A (p.Pro111Gln)
n.526C>A
 gnomAD v4
11g.32435018dupCA2612989557WT1c.347dup (p.Ala118ArgfsTer?)
c.332dup (p.Ala113ArgfsTer?)
n.526dup
 gnomAD v4
11g.32435018delCA2612989558WT1c.347del (p.Pro116ArgfsTer?)
c.332del (p.Pro111ArgfsTer?)
n.526del
 gnomAD v4
11g.32435015G>ACA379965878WT1c.346C>T (p.Pro116Ser)
c.331C>T (p.Pro111Ser)
n.525C>T
11g.32435015G>CCA379965879WT1c.346C>G (p.Pro116Ala)
c.331C>G (p.Pro111Ala)
n.525C>G
11g.32435015G=CA1962327275WT1c.346C= (p.Pro116=)
c.331C= (p.Pro111=)
n.525C=
11g.32435015G>TCA379965880WT1c.346C>A (p.Pro116Thr)
c.331C>A (p.Pro111Thr)
n.525C>A
 ClinVar dbSNP gnomAD v4
11g.32435015_32435016insACA2723467872WT1c.345_346insT (p.Pro116SerfsTer?)
c.330_331insT (p.Pro111SerfsTer?)
n.524_525insT
 dbSNP
11g.32435016G>ACA017474WT1c.345C>T (p.Pro115=)
c.330C>T (p.Pro110=)
n.524C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32435016G>CCA473773808WT1c.345C>G (p.Pro115=)
c.330C>G (p.Pro110=)
n.524C>G
 dbSNP
11g.32435016G=CA1962327276WT1c.345C= (p.Pro115=)
c.330C= (p.Pro110=)
n.524C=
11g.32435016G>TCA473773809WT1c.345C>A (p.Pro115=)
c.330C>A (p.Pro110=)
n.524C>A
 gnomAD v4
11g.32435017G>ACA379965881WT1c.344C>T (p.Pro115Leu)
c.329C>T (p.Pro110Leu)
n.523C>T
 gnomAD v4
11g.32435017G>CCA379965882WT1c.344C>G (p.Pro115Arg)
c.329C>G (p.Pro110Arg)
n.523C>G
11g.32435017G=CA1962327277WT1c.344C= (p.Pro115=)
c.329C= (p.Pro110=)
n.523C=
11g.32435017G>TCA379965883WT1c.344C>A (p.Pro115His)
c.329C>A (p.Pro110His)
n.523C>A
 ClinVar dbSNP gnomAD v4
11g.32435018G>ACA16613338WT1c.343C>T (p.Pro115Ser)
c.328C>T (p.Pro110Ser)
n.522C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435018G>CCA379965884WT1c.343C>G (p.Pro115Ala)
c.328C>G (p.Pro110Ala)
n.522C>G
11g.32435018G=CA1962327278WT1c.343C= (p.Pro115=)
c.328C= (p.Pro110=)
n.522C=
11g.32435018G>TCA379965885WT1c.343C>A (p.Pro115Thr)
c.328C>A (p.Pro110Thr)
n.522C>A
 ClinVar dbSNP
11g.32435019C>ACA473773813WT1c.342G>T (p.Ala114=)
c.327G>T (p.Ala109=)
n.521G>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435019C=CA1962327279WT1c.342G= (p.Ala114=)
c.327G= (p.Ala109=)
n.521G=
11g.32435019C>GCA473773814WT1c.342G>C (p.Ala114=)
c.327G>C (p.Ala109=)
n.521G>C
 ClinVar dbSNP gnomAD v4
11g.32435019C>TCA473773815WT1c.342G>A (p.Ala114=)
c.327G>A (p.Ala109=)
n.521G>A
 gnomAD v4
11g.32435020G>ACA379965888WT1c.341C>T (p.Ala114Val)
c.326C>T (p.Ala109Val)
n.520C>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435020G>CCA379965887WT1c.341C>G (p.Ala114Gly)
c.326C>G (p.Ala109Gly)
n.520C>G
 gnomAD v4
11g.32435020G=CA1962327280WT1c.341C= (p.Ala114=)
c.326C= (p.Ala109=)
n.520C=
11g.32435020G>TCA379965886WT1c.341C>A (p.Ala114Glu)
c.326C>A (p.Ala109Glu)
n.520C>A
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32435021C>ACA379965889WT1c.340G>T (p.Ala114Ser)
c.325G>T (p.Ala109Ser)
n.519G>T
 gnomAD v4
11g.32435021C=CA1962327281WT1c.340G= (p.Ala114=)
c.325G= (p.Ala109=)
n.519G=
11g.32435021C>GCA379965890WT1c.340G>C (p.Ala114Pro)
c.325G>C (p.Ala109Pro)
n.519G>C
11g.32435021C>TCA379965891WT1c.340G>A (p.Ala114Thr)
c.325G>A (p.Ala109Thr)
n.519G>A
 ClinVar dbSNP gnomAD v4
11g.32435022A>CCA379965892WT1c.339T>G (p.Phe113Leu)
c.324T>G (p.Phe108Leu)
n.518T>G
 gnomAD v4
11g.32435022A>GCA473773817WT1c.339T>C (p.Phe113=)
c.324T>C (p.Phe108=)
n.518T>C
 ClinVar dbSNP gnomAD v4
11g.32435022A>TCA379965893WT1c.339T>A (p.Phe113Leu)
c.324T>A (p.Phe108Leu)
n.518T>A
11g.32435022_32435023insGGCAACA645584490WT1c.339_340insTGCCT (p.Ala114CysfsTer?)
c.324_325insTGCCT (p.Ala109CysfsTer?)
n.518_519insTGCCT
 COSMIC COSMIC
11g.32435024dupCA645584489WT1c.339dup (p.Ala114CysfsTer?)
c.324dup (p.Ala109CysfsTer?)
n.518dup
 COSMIC
11g.32435024delCA2695213678WT1c.339del (p.Phe113LeufsTer?)
c.324del (p.Phe108LeufsTer?)
n.518del
11g.32435022_32435023insTCA473773819WT1c.338_339insA (p.Phe113LeufsTer?)
c.323_324insA (p.Phe108LeufsTer?)
n.517_518insA
11g.32435023A>CCA379965894WT1c.338T>G (p.Phe113Cys)
c.323T>G (p.Phe108Cys)
n.517T>G
11g.32435023A>GCA379965895WT1c.338T>C (p.Phe113Ser)
c.323T>C (p.Phe108Ser)
n.517T>C
 ClinVar gnomAD v4
11g.32435023A>TCA379965896WT1c.338T>A (p.Phe113Tyr)
c.323T>A (p.Phe108Tyr)
n.517T>A
 ClinVar
11g.32435024A=CA1962327282WT1c.337T= (p.Phe113=)
c.322T= (p.Phe108=)
n.516T=
11g.32435024A>CCA379965897WT1c.337T>G (p.Phe113Val)
c.322T>G (p.Phe108Val)
n.516T>G
11g.32435024A>GCA379965898WT1c.337T>C (p.Phe113Leu)
c.322T>C (p.Phe108Leu)
n.516T>C
 dbSNP
11g.32435024A>TCA379965899WT1c.337T>A (p.Phe113Ile)
c.322T>A (p.Phe108Ile)
n.516T>A
11g.32435025G>ACA473773824WT1c.336C>T (p.Asp112=)
c.321C>T (p.Asp107=)
n.515C>T
 ClinVar dbSNP gnomAD v4
11g.32435025G>CCA379965901WT1c.336C>G (p.Asp112Glu)
c.321C>G (p.Asp107Glu)
n.515C>G
 dbSNP
11g.32435025G>TCA379965900WT1c.336C>A (p.Asp112Glu)
c.321C>A (p.Asp107Glu)
n.515C>A
 gnomAD v4
11g.32435026T>ACA379965902WT1c.335A>T (p.Asp112Val)
c.320A>T (p.Asp107Val)
n.514A>T
 dbSNP
11g.32435026T>CCA379965903WT1c.335A>G (p.Asp112Gly)
c.320A>G (p.Asp107Gly)
n.514A>G
 dbSNP
11g.32435026T>GCA379965904WT1c.335A>C (p.Asp112Ala)
c.320A>C (p.Asp107Ala)
n.514A>C
 dbSNP
11g.32435026_32435027delinsTCCA1962327283WT1c.334_335delinsGA (p.Asp112=)
c.319_320delinsGA (p.Asp107=)
n.513_514delinsGA
11g.32435027C>ACA379965905WT1c.334G>T (p.Asp112Tyr)
c.319G>T (p.Asp107Tyr)
n.513G>T
 gnomAD v4
11g.32435027C=CA1962327284WT1c.334G= (p.Asp112=)
c.319G= (p.Asp107=)
n.513G=
11g.32435027C>GCA379965906WT1c.334G>C (p.Asp112His)
c.319G>C (p.Asp107His)
n.513G>C
11g.32435027C>TCA379965907WT1c.334G>A (p.Asp112Asn)
c.319G>A (p.Asp107Asn)
n.513G>A
 dbSNP
11g.32435028delCA658658040WT1c.334del (p.Asp112ThrfsTer?)
c.319del (p.Asp107ThrfsTer?)
n.513del
 ClinVar dbSNP gnomAD v4
11g.32435028C>ACA473773832WT1c.333G>T (p.Leu111=)
c.318G>T (p.Leu106=)
n.512G>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32435028C=CA1962327285WT1c.333G= (p.Leu111=)
c.318G= (p.Leu106=)
n.512G=
11g.32435028C>GCA473773833WT1c.333G>C (p.Leu111=)
c.318G>C (p.Leu106=)
n.512G>C
11g.32435028C>TCA473773834WT1c.333G>A (p.Leu111=)
c.318G>A (p.Leu106=)
n.512G>A
 gnomAD v4
11g.32435029delCA2695202566WT1c.332del (p.Leu111ArgfsTer?)
c.317del (p.Leu106ArgfsTer?)
n.511del
11g.32435029A>CCA379965910WT1c.332T>G (p.Leu111Arg)
c.317T>G (p.Leu106Arg)
n.511T>G
 dbSNP
11g.32435029A>GCA379965908WT1c.332T>C (p.Leu111Pro)
c.317T>C (p.Leu106Pro)
n.511T>C
 ClinVar gnomAD v4
11g.32435029A>TCA379965909WT1c.332T>A (p.Leu111Gln)
c.317T>A (p.Leu106Gln)
n.511T>A
11g.32435030G>ACA473773836WT1c.331C>T (p.Leu111=)
c.316C>T (p.Leu106=)
n.510C>T
 ClinVar dbSNP gnomAD v4
11g.32435030G>CCA379965911WT1c.331C>G (p.Leu111Val)
c.316C>G (p.Leu106Val)
n.510C>G
 dbSNP
11g.32435030G>TCA379965912WT1c.331C>A (p.Leu111Met)
c.316C>A (p.Leu106Met)
n.510C>A
 gnomAD v4
11g.32435031C>ACA473773838WT1c.330G>T (p.Val110=)
c.315G>T (p.Val105=)
n.509G>T
 gnomAD v4
11g.32435031C>GCA473773839WT1c.330G>C (p.Val110=)
c.315G>C (p.Val105=)
n.509G>C
11g.32435031C>TCA473773840WT1c.330G>A (p.Val110=)
c.315G>A (p.Val105=)
n.509G>A
 ClinVar
11g.32435032A=CA1962327286WT1c.329T= (p.Val110=)
c.314T= (p.Val105=)
n.508T=
11g.32435032A>CCA379965913WT1c.329T>G (p.Val110Gly)
c.314T>G (p.Val105Gly)
n.508T>G
 dbSNP
11g.32435032A>GCA379965914WT1c.329T>C (p.Val110Ala)
c.314T>C (p.Val105Ala)
n.508T>C
 ClinVar dbSNP gnomAD v4
11g.32435032A>TCA379965915WT1c.329T>A (p.Val110Glu)
c.314T>A (p.Val105Glu)
n.508T>A
 gnomAD v4
11g.32435033C>ACA379965916WT1c.328G>T (p.Val110Leu)
c.313G>T (p.Val105Leu)
n.507G>T
 gnomAD v4
11g.32435033C>GCA379965918WT1c.328G>C (p.Val110Leu)
c.313G>C (p.Val105Leu)
n.507G>C
11g.32435033C>TCA379965917WT1c.328G>A (p.Val110Met)
c.313G>A (p.Val105Met)
n.507G>A
 gnomAD v4
11g.32435034C>ACA473773843WT1c.327G>T (p.Pro109=)
c.312G>T (p.Pro104=)
n.506G>T
 dbSNP gnomAD v2 gnomAD v4
11g.32435034C=CA1962327287WT1c.327G= (p.Pro109=)
c.312G= (p.Pro104=)
n.506G=
11g.32435034C>GCA064841WT1c.327G>C (p.Pro109=)
c.312G>C (p.Pro104=)
n.506G>C
 ClinVar dbSNP ExAC gnomAD v3 gnomAD v4
11g.32435034C>TCA473773842WT1c.327G>A (p.Pro109=)
c.312G>A (p.Pro104=)
n.506G>A
 dbSNP gnomAD v4
11g.32435035G>ACA379965919WT1c.326C>T (p.Pro109Leu)
c.311C>T (p.Pro104Leu)
n.505C>T
 gnomAD v4
11g.32435035G>CCA379965920WT1c.326C>G (p.Pro109Arg)
c.311C>G (p.Pro104Arg)
n.505C>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32435035G=CA1962327288WT1c.326C= (p.Pro109=)
c.311C= (p.Pro104=)
n.505C=
11g.32435035G>TCA379965921WT1c.326C>A (p.Pro109Gln)
c.311C>A (p.Pro104Gln)
n.505C>A
 ClinVar dbSNP gnomAD v4
11g.32435036G>ACA379965922WT1c.325C>T (p.Pro109Ser)
c.310C>T (p.Pro104Ser)
n.504C>T
 ClinVar dbSNP gnomAD v4
11g.32435036G>CCA379965923WT1c.325C>G (p.Pro109Ala)
c.310C>G (p.Pro104Ala)
n.504C>G
 ClinVar dbSNP
11g.32435036G>TCA379965924WT1c.325C>A (p.Pro109Thr)
c.310C>A (p.Pro104Thr)
n.504C>A
 gnomAD v4
11g.32435037C>ACA473773846WT1c.324G>T (p.Ala108=)
c.309G>T (p.Ala103=)
n.503G>T
 dbSNP gnomAD v2 gnomAD v4
11g.32435037C=CA1962327289WT1c.324G= (p.Ala108=)
c.309G= (p.Ala103=)
n.503G=
11g.32435037C>GCA473773847WT1c.324G>C (p.Ala108=)
c.309G>C (p.Ala103=)
n.503G>C
11g.32435037C>TCA473773849WT1c.324G>A (p.Ala108=)
c.309G>A (p.Ala103=)
n.503G>A
 ClinVar dbSNP gnomAD v4
11g.32435038G>ACA379965925WT1c.323C>T (p.Ala108Val)
c.308C>T (p.Ala103Val)
n.502C>T
 dbSNP gnomAD v4
11g.32435038G>CCA379965926WT1c.323C>G (p.Ala108Gly)
c.308C>G (p.Ala103Gly)
n.502C>G
 dbSNP gnomAD v4
11g.32435038G>TCA379965927WT1c.323C>A (p.Ala108Glu)
c.308C>A (p.Ala103Glu)
n.502C>A
 gnomAD v4
11g.32435039C>ACA379965930WT1c.322G>T (p.Ala108Ser)
c.307G>T (p.Ala103Ser)
n.501G>T
 gnomAD v4
11g.32435039C=CA1962327290WT1c.322G= (p.Ala108=)
c.307G= (p.Ala103=)
n.501G=
11g.32435039C>GCA379965929WT1c.322G>C (p.Ala108Pro)
c.307G>C (p.Ala103Pro)
n.501G>C
11g.32435039C>TCA379965928WT1c.322G>A (p.Ala108Thr)
c.307G>A (p.Ala103Thr)
n.501G>A
 ClinVar dbSNP gnomAD v4
11g.32435040C>ACA379965931WT1c.321G>T (p.Trp107Cys)
c.306G>T (p.Trp102Cys)
n.500G>T
11g.32435040C>GCA379965933WT1c.321G>C (p.Trp107Cys)
c.306G>C (p.Trp102Cys)
n.500G>C
11g.32435040C>TCA379965932WT1c.321G>A (p.Trp107Ter)
c.306G>A (p.Trp102Ter)
n.500G>A
 gnomAD v3 gnomAD v4
11g.32435041C>ACA219511154WT1c.320G>T (p.Trp107Leu)
c.305G>T (p.Trp102Leu)
n.499G>T
 ClinVar dbSNP gnomAD v4
11g.32435041C=CA1962327291WT1c.320G= (p.Trp107=)
c.305G= (p.Trp102=)
n.499G=
11g.32435041C>GCA379965934WT1c.320G>C (p.Trp107Ser)
c.305G>C (p.Trp102Ser)
n.499G>C
11g.32435041C>TCA379965935WT1c.320G>A (p.Trp107Ter)
c.305G>A (p.Trp102Ter)
n.499G>A
 gnomAD v4
11g.32435042A=CA1962327292WT1c.319T= (p.Trp107=)
c.304T= (p.Trp102=)
n.498T=
11g.32435042A>CCA379965936WT1c.319T>G (p.Trp107Gly)
c.304T>G (p.Trp102Gly)
n.498T>G
 ClinVar dbSNP
11g.32435042A>GCA379965937WT1c.319T>C (p.Trp107Arg)
c.304T>C (p.Trp102Arg)
n.498T>C
11g.32435042A>TCA379965938WT1c.319T>A (p.Trp107Arg)
c.304T>A (p.Trp102Arg)
n.498T>A
11g.32435043C>ACA379965939WT1c.318G>T (p.Gln106His)
c.303G>T (p.Gln101His)
n.497G>T
 gnomAD v4
11g.32435043C>GCA379965940WT1c.318G>C (p.Gln106His)
c.303G>C (p.Gln101His)
n.497G>C
11g.32435043C>TCA473773857WT1c.318G>A (p.Gln106=)
c.303G>A (p.Gln101=)
n.497G>A
 gnomAD v4
11g.32435044_32435048dupCA2573146229WT1c.314_318dup (p.Trp107ArgfsTer?)
c.299_303dup (p.Trp102ArgfsTer?)
n.493_497dup
 ClinVar dbSNP
11g.32435044T>ACA379965941WT1c.317A>T (p.Gln106Leu)
c.302A>T (p.Gln101Leu)
n.496A>T
 dbSNP
11g.32435044T>CCA379965942WT1c.317A>G (p.Gln106Arg)
c.302A>G (p.Gln101Arg)
n.496A>G
 dbSNP gnomAD v4
11g.32435044T>GCA379965943WT1c.317A>C (p.Gln106Pro)
c.302A>C (p.Gln101Pro)
n.496A>C
11g.32435044T=CA1962327293WT1c.317A= (p.Gln106=)
c.302A= (p.Gln101=)
n.496A=
11g.32435045G>ACA379965945WT1c.316C>T (p.Gln106Ter)
c.301C>T (p.Gln101Ter)
n.495C>T
 gnomAD v4 COSMIC COSMIC
11g.32435045G>CCA379965944WT1c.316C>G (p.Gln106Glu)
c.301C>G (p.Gln101Glu)
n.495C>G
11g.32435045G=CA1962327294WT1c.316C= (p.Gln106=)
c.301C= (p.Gln101=)
n.495C=
11g.32435045G>TCA064832WT1c.316C>A (p.Gln106Lys)
c.301C>A (p.Gln101Lys)
n.495C>A
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.32435046C>ACA473773863WT1c.315G>T (p.Ala105=)
c.300G>T (p.Ala100=)
n.494G>T
 ClinVar dbSNP gnomAD v4
11g.32435046C=CA1962327295WT1c.315G= (p.Ala105=)
c.300G= (p.Ala100=)
n.494G=
11g.32435046C>GCA473773866WT1c.315G>C (p.Ala105=)
c.300G>C (p.Ala100=)
n.494G>C
11g.32435046C>TCA473773865WT1c.315G>A (p.Ala105=)
c.300G>A (p.Ala100=)
n.494G>A
 ClinVar dbSNP gnomAD v4
11g.32435047G>ACA379965946WT1c.314C>T (p.Ala105Val)
c.299C>T (p.Ala100Val)
n.493C>T
 dbSNP gnomAD v4
11g.32435047G>CCA219511175WT1c.314C>G (p.Ala105Gly)
c.299C>G (p.Ala100Gly)
n.493C>G
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435047G=CA1962327296WT1c.314C= (p.Ala105=)
c.299C= (p.Ala100=)
n.493C=
11g.32435047G>TCA379965947WT1c.314C>A (p.Ala105Glu)
c.299C>A (p.Ala100Glu)
n.493C>A
 ClinVar dbSNP gnomAD v4
11g.32435048C>ACA379965948WT1c.313G>T (p.Ala105Ser)
c.298G>T (p.Ala100Ser)
n.492G>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435048C=CA1962327297WT1c.313G= (p.Ala105=)
c.298G= (p.Ala100=)
n.492G=
11g.32435048C>GCA379965949WT1c.313G>C (p.Ala105Pro)
c.298G>C (p.Ala100Pro)
n.492G>C
11g.32435048C>TCA379965950WT1c.313G>A (p.Ala105Thr)
c.298G>A (p.Ala100Thr)
n.492G>A
 ClinVar dbSNP gnomAD v4
11g.32435049C>ACA473773876WT1c.312G>T (p.Ala104=)
c.297G>T (p.Ala99=)
n.491G>T
 ClinVar gnomAD v4
11g.32435049C=CA1962327298WT1c.312G= (p.Ala104=)
c.297G= (p.Ala99=)
n.491G=
11g.32435049C>GCA473773878WT1c.312G>C (p.Ala104=)
c.297G>C (p.Ala99=)
n.491G>C
11g.32435049C>TCA473773879WT1c.312G>A (p.Ala104=)
c.297G>A (p.Ala99=)
n.491G>A
 ClinVar dbSNP gnomAD v4
11g.32435050G>ACA379965951WT1c.311C>T (p.Ala104Val)
c.296C>T (p.Ala99Val)
n.490C>T
 ClinVar gnomAD v4 COSMIC
11g.32435050G>CCA219511188WT1c.311C>G (p.Ala104Gly)
c.296C>G (p.Ala99Gly)
n.490C>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32435050G=CA1962327299WT1c.311C= (p.Ala104=)
c.296C= (p.Ala99=)
n.490C=
11g.32435050G>TCA379965952WT1c.311C>A (p.Ala104Glu)
c.296C>A (p.Ala99Glu)
n.490C>A
 gnomAD v4
11g.32435051C>ACA379965953WT1c.310G>T (p.Ala104Ser)
c.295G>T (p.Ala99Ser)
n.489G>T
 gnomAD v4
11g.32435051C=CA1962327300WT1c.310G= (p.Ala104=)
c.295G= (p.Ala99=)
n.489G=
11g.32435051C>GCA379965954WT1c.310G>C (p.Ala104Pro)
c.295G>C (p.Ala99Pro)
n.489G>C
 dbSNP
11g.32435051C>TCA379965955WT1c.310G>A (p.Ala104Thr)
c.295G>A (p.Ala99Thr)
n.489G>A
 ClinVar dbSNP gnomAD v4
11g.32435051dupCA2723468786WT1c.310dup (p.Ala104GlyfsTer?)
c.295dup (p.Ala99GlyfsTer?)
n.489dup
 dbSNP
11g.32435052G>ACA473773888WT1c.309C>T (p.Gly103=)
c.294C>T (p.Gly98=)
n.488C>T
 dbSNP gnomAD v4
11g.32435052G>CCA473773889WT1c.309C>G (p.Gly103=)
c.294C>G (p.Gly98=)
n.488C>G
 dbSNP
11g.32435052G=CA1962327301WT1c.309C= (p.Gly103=)
c.294C= (p.Gly98=)
n.488C=
11g.32435052G>TCA064811WT1c.309C>A (p.Gly103=)
c.294C>A (p.Gly98=)
n.488C>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32435053C>ACA379965958WT1c.308G>T (p.Gly103Val)
c.293G>T (p.Gly98Val)
n.487G>T
 gnomAD v4
11g.32435053C>GCA379965956WT1c.308G>C (p.Gly103Ala)
c.293G>C (p.Gly98Ala)
n.487G>C
11g.32435053C>TCA379965957WT1c.308G>A (p.Gly103Asp)
c.293G>A (p.Gly98Asp)
n.487G>A
 gnomAD v4
11g.32435054C>ACA379965959WT1c.307G>T (p.Gly103Cys)
c.292G>T (p.Gly98Cys)
n.486G>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435054C=CA1962327302WT1c.307G= (p.Gly103=)
c.292G= (p.Gly98=)
n.486G=
11g.32435054C>GCA379965960WT1c.307G>C (p.Gly103Arg)
c.292G>C (p.Gly98Arg)
n.486G>C
 gnomAD v4
11g.32435054C>TCA379965961WT1c.307G>A (p.Gly103Ser)
c.292G>A (p.Gly98Ser)
n.486G>A
 gnomAD v4
11g.32435055G>ACA473773896WT1c.306C>T (p.Ser102=)
c.291C>T (p.Ser97=)
n.485C>T
 dbSNP gnomAD v4
11g.32435055G>CCA379965962WT1c.306C>G (p.Ser102Arg)
c.291C>G (p.Ser97Arg)
n.485C>G
 dbSNP
11g.32435055G>TCA379965963WT1c.306C>A (p.Ser102Arg)
c.291C>A (p.Ser97Arg)
n.485C>A
 ClinVar gnomAD v4
11g.32435056C>ACA379965964WT1c.305G>T (p.Ser102Ile)
c.290G>T (p.Ser97Ile)
n.484G>T
 gnomAD v4
11g.32435056C=CA1962327303WT1c.305G= (p.Ser102=)
c.290G= (p.Ser97=)
n.484G=
11g.32435056C>GCA379965965WT1c.305G>C (p.Ser102Thr)
c.290G>C (p.Ser97Thr)
n.484G>C
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435056C>TCA379965966WT1c.305G>A (p.Ser102Asn)
c.290G>A (p.Ser97Asn)
n.484G>A
 ClinVar dbSNP gnomAD v4
11g.32435058_32435059insCCCTCCA2695213679WT1c.305_306insGGGAG (p.Ser102ArgfsTer?)
c.290_291insGGGAG (p.Ser97ArgfsTer?)
n.484_485insGGGAG
11g.32435057T>ACA379965967WT1c.304A>T (p.Ser102Cys)
c.289A>T (p.Ser97Cys)
n.483A>T
 dbSNP
11g.32435057T>CCA379965968WT1c.304A>G (p.Ser102Gly)
c.289A>G (p.Ser97Gly)
n.483A>G
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435057T>GCA379965969WT1c.304A>C (p.Ser102Arg)
c.289A>C (p.Ser97Arg)
n.483A>C
11g.32435057T=CA1962327304WT1c.304A= (p.Ser102=)
c.289A= (p.Ser97=)
n.483A=
11g.32435058C>ACA473773906WT1c.303G>T (p.Val101=)
c.288G>T (p.Val96=)
n.482G>T
 gnomAD v4
11g.32435058C>GCA473773907WT1c.303G>C (p.Val101=)
c.288G>C (p.Val96=)
n.482G>C
11g.32435058C>TCA473773908WT1c.303G>A (p.Val101=)
c.288G>A (p.Val96=)
n.482G>A
 ClinVar gnomAD v4
11g.32435059A>CCA379965972WT1c.302T>G (p.Val101Gly)
c.287T>G (p.Val96Gly)
n.481T>G
11g.32435059A>GCA379965970WT1c.302T>C (p.Val101Ala)
c.287T>C (p.Val96Ala)
n.481T>C
 gnomAD v4
11g.32435059A>TCA379965971WT1c.302T>A (p.Val101Glu)
c.287T>A (p.Val96Glu)
n.481T>A
 gnomAD v4
11g.32435059_32435062delCA645584491WT1c.299_302del (p.Pro100ArgfsTer?)
c.284_287del (p.Pro95ArgfsTer?)
n.478_481del
 COSMIC
11g.32435060C>ACA379965973WT1c.301G>T (p.Val101Leu)
c.286G>T (p.Val96Leu)
n.480G>T
 gnomAD v4
11g.32435060C=CA1962327305WT1c.301G= (p.Val101=)
c.286G= (p.Val96=)
n.480G=
11g.32435060C>GCA379965974WT1c.301G>C (p.Val101Leu)
c.286G>C (p.Val96Leu)
n.480G>C
 ClinVar dbSNP
11g.32435060C>TCA379965975WT1c.301G>A (p.Val101Met)
c.286G>A (p.Val96Met)
n.480G>A
 gnomAD v4
11g.32435061A=CA1962327306WT1c.300T= (p.Pro100=)
c.285T= (p.Pro95=)
n.479T=
11g.32435061A>CCA473773913WT1c.300T>G (p.Pro100=)
c.285T>G (p.Pro95=)
n.479T>G
 dbSNP gnomAD v4
11g.32435061A>GCA473773915WT1c.300T>C (p.Pro100=)
c.285T>C (p.Pro95=)
n.479T>C
 gnomAD v4
11g.32435061A>TCA473773916WT1c.300T>A (p.Pro100=)
c.285T>A (p.Pro95=)
n.479T>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435062G>ACA379965976WT1c.299C>T (p.Pro100Leu)
c.284C>T (p.Pro95Leu)
n.478C>T
 gnomAD v4
11g.32435062G>CCA379965977WT1c.299C>G (p.Pro100Arg)
c.284C>G (p.Pro95Arg)
n.478C>G
 ClinVar
11g.32435062G>TCA379965978WT1c.299C>A (p.Pro100His)
c.284C>A (p.Pro95His)
n.478C>A
 gnomAD v4
11g.32435063G>ACA219511235WT1c.298C>T (p.Pro100Ser)
c.283C>T (p.Pro95Ser)
n.477C>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32435063G>CCA379965979WT1c.298C>G (p.Pro100Ala)
c.283C>G (p.Pro95Ala)
n.477C>G
 ClinVar dbSNP gnomAD v4
11g.32435063G=CA1962327307WT1c.298C= (p.Pro100=)
c.283C= (p.Pro95=)
n.477C=
11g.32435063G>TCA379965980WT1c.298C>A (p.Pro100Thr)
c.283C>A (p.Pro95Thr)
n.477C>A
 ClinVar dbSNP gnomAD v4
11g.32435064C>ACA473773924WT1c.297G>T (p.Leu99=)
c.282G>T (p.Leu94=)
n.476G>T
 gnomAD v4
11g.32435064C=CA1962327308WT1c.297G= (p.Leu99=)
c.282G= (p.Leu94=)
n.476G=
11g.32435064C>GCA473773925WT1c.297G>C (p.Leu99=)
c.282G>C (p.Leu94=)
n.476G>C
 gnomAD v4
11g.32435064C>TCA473773926WT1c.297G>A (p.Leu99=)
c.282G>A (p.Leu94=)
n.476G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
11g.32435065A=CA1962327309WT1c.296T= (p.Leu99=)
c.281T= (p.Leu94=)
n.475T=
11g.32435065A>CCA379965981WT1c.296T>G (p.Leu99Arg)
c.281T>G (p.Leu94Arg)
n.475T>G
11g.32435065A>GCA379965982WT1c.296T>C (p.Leu99Pro)
c.281T>C (p.Leu94Pro)
n.475T>C
 ClinVar dbSNP gnomAD v4
11g.32435065A>TCA379965983WT1c.296T>A (p.Leu99Gln)
c.281T>A (p.Leu94Gln)
n.475T>A
 ClinVar dbSNP
11g.32435066G>ACA473773931WT1c.295C>T (p.Leu99=)
c.280C>T (p.Leu94=)
n.474C>T
 gnomAD v4
11g.32435066G>CCA379965985WT1c.295C>G (p.Leu99Val)
c.280C>G (p.Leu94Val)
n.474C>G
 ClinVar dbSNP
11g.32435066G=CA1962327310WT1c.295C= (p.Leu99=)
c.280C= (p.Leu94=)
n.474C=
11g.32435066G>TCA379965984WT1c.295C>A (p.Leu99Met)
c.280C>A (p.Leu94Met)
n.474C>A
 gnomAD v4
11g.32435067G>ACA219511241WT1c.294C>T (p.Ala98=)
c.279C>T (p.Ala93=)
n.473C>T
 ClinVar dbSNP gnomAD v4
11g.32435067G>CCA473773933WT1c.294C>G (p.Ala98=)
c.279C>G (p.Ala93=)
n.473C>G
11g.32435067G=CA1962327311WT1c.294C= (p.Ala98=)
c.279C= (p.Ala93=)
n.473C=
11g.32435067G>TCA473773934WT1c.294C>A (p.Ala98=)
c.279C>A (p.Ala93=)
n.473C>A
11g.32435068G>ACA379965986WT1c.293C>T (p.Ala98Val)
c.278C>T (p.Ala93Val)
n.472C>T
 ClinVar dbSNP gnomAD v4
11g.32435068G>CCA379965988WT1c.293C>G (p.Ala98Gly)
c.278C>G (p.Ala93Gly)
n.472C>G
 ClinVar dbSNP gnomAD v4
11g.32435068G=CA1962327312WT1c.293C= (p.Ala98=)
c.278C= (p.Ala93=)
n.472C=
11g.32435068G>TCA379965987WT1c.293C>A (p.Ala98Asp)
c.278C>A (p.Ala93Asp)
n.472C>A
 gnomAD v4
11g.32435069C>ACA379965989WT1c.292G>T (p.Ala98Ser)
c.277G>T (p.Ala93Ser)
n.471G>T
 dbSNP gnomAD v4
11g.32435069C>GCA379965990WT1c.292G>C (p.Ala98Pro)
c.277G>C (p.Ala93Pro)
n.471G>C
11g.32435069C>TCA379965991WT1c.292G>A (p.Ala98Thr)
c.277G>A (p.Ala93Thr)
n.471G>A
 gnomAD v4
11g.32435070A=CA1962327313WT1c.291T= (p.Cys97=)
c.276T= (p.Cys92=)
n.470T=
11g.32435070A>CCA064806WT1c.291T>G (p.Cys97Trp)
c.276T>G (p.Cys92Trp)
n.470T>G
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.32435070A>GCA473773939WT1c.291T>C (p.Cys97=)
c.276T>C (p.Cys92=)
n.470T>C
 ClinVar dbSNP gnomAD v4
11g.32435070A>TCA379965992WT1c.291T>A (p.Cys97Ter)
c.276T>A (p.Cys92Ter)
n.470T>A
11g.32435071C>ACA379965993WT1c.290G>T (p.Cys97Phe)
c.275G>T (p.Cys92Phe)
n.469G>T
 gnomAD v4
11g.32435071C=CA1962327314WT1c.290G= (p.Cys97=)
c.275G= (p.Cys92=)
n.469G=
11g.32435071C>GCA379965994WT1c.290G>C (p.Cys97Ser)
c.275G>C (p.Cys92Ser)
n.469G>C
 ClinVar dbSNP
11g.32435071C>TCA379965995WT1c.290G>A (p.Cys97Tyr)
c.275G>A (p.Cys92Tyr)
n.469G>A
 gnomAD v4
11g.32435072A=CA1962327315WT1c.289T= (p.Cys97=)
c.274T= (p.Cys92=)
n.468T=
11g.32435072A>CCA379965996WT1c.289T>G (p.Cys97Gly)
c.274T>G (p.Cys92Gly)
n.468T>G
 dbSNP
11g.32435072A>GCA379965997WT1c.289T>C (p.Cys97Arg)
c.274T>C (p.Cys92Arg)
n.468T>C
 ClinVar dbSNP gnomAD v4
11g.32435072A>TCA379965998WT1c.289T>A (p.Cys97Ser)
c.274T>A (p.Cys92Ser)
n.468T>A
11g.32435072_32435075delinsAGCCCA1962327316WT1c.286_289delinsGGCT (p.Gly96=)
c.271_274delinsGGCT (p.Gly91=)
n.465_468delinsGGCT
11g.32435072_32435073insTCCCA2580084184WT1c.288_289insGGA (p.Gly96_Cys97insGly)
c.273_274insGGA (p.Gly91_Cys92insGly)
n.467_468insGGA
 ClinVar
11g.32435073G>ACA473773942WT1c.288C>T (p.Gly96=)
c.273C>T (p.Gly91=)
n.467C>T
 dbSNP gnomAD v4
11g.32435073G>CCA473773943WT1c.288C>G (p.Gly96=)
c.273C>G (p.Gly91=)
n.467C>G
 dbSNP gnomAD v4
11g.32435073G=CA1962327317WT1c.288C= (p.Gly96=)
c.273C= (p.Gly91=)
n.467C=
11g.32435073G>TCA473773944WT1c.288C>A (p.Gly96=)
c.273C>A (p.Gly91=)
n.467C>A
 gnomAD v4
11g.32435082_32435084dupCA2580615657WT1c.286_288dup (p.Gly96_Cys97insGly)
c.271_273dup (p.Gly91_Cys92insGly)
n.465_467dup
 ClinVar dbSNP gnomAD v4
11g.32435082_32435084delCA064802WT1c.286_288del (p.Gly96del)
c.271_273del (p.Gly91del)
n.465_467del
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32435074C>ACA379966001WT1c.287G>T (p.Gly96Val)
c.272G>T (p.Gly91Val)
n.466G>T
 gnomAD v4
11g.32435074C>GCA379965999WT1c.287G>C (p.Gly96Ala)
c.272G>C (p.Gly91Ala)
n.466G>C
11g.32435074C>TCA379966000WT1c.287G>A (p.Gly96Asp)
c.272G>A (p.Gly91Asp)
n.466G>A
 dbSNP gnomAD v4
11g.32435075C>ACA379966002WT1c.286G>T (p.Gly96Cys)
c.271G>T (p.Gly91Cys)
n.465G>T
 ClinVar dbSNP gnomAD v4
11g.32435075C=CA1962327318WT1c.286G= (p.Gly96=)
c.271G= (p.Gly91=)
n.465G=
11g.32435075C>GCA379966003WT1c.286G>C (p.Gly96Arg)
c.271G>C (p.Gly91Arg)
n.465G>C
11g.32435075C>TCA16613605WT1c.286G>A (p.Gly96Ser)
c.271G>A (p.Gly91Ser)
n.465G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435076G>ACA10638966WT1c.285C>T (p.Gly95=)
c.270C>T (p.Gly90=)
n.464C>T
 ClinVar dbSNP gnomAD v4
11g.32435076G>CCA473773947WT1c.285C>G (p.Gly95=)
c.270C>G (p.Gly90=)
n.464C>G
 dbSNP
11g.32435076G=CA1962327319WT1c.285C= (p.Gly95=)
c.270C= (p.Gly90=)
n.464C=
11g.32435076G>TCA473773948WT1c.285C>A (p.Gly95=)
c.270C>A (p.Gly90=)
n.464C>A
 gnomAD v4
11g.32435077C>ACA379966004WT1c.284G>T (p.Gly95Val)
c.269G>T (p.Gly90Val)
n.463G>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435077C=CA1962327320WT1c.284G= (p.Gly95=)
c.269G= (p.Gly90=)
n.463G=
11g.32435077C>GCA379966005WT1c.284G>C (p.Gly95Ala)
c.269G>C (p.Gly90Ala)
n.463G>C
 dbSNP
11g.32435077C>TCA379966006WT1c.284G>A (p.Gly95Asp)
c.269G>A (p.Gly90Asp)
n.463G>A
 ClinVar dbSNP gnomAD v4
11g.32435078C>ACA379966007WT1c.283G>T (p.Gly95Cys)
c.268G>T (p.Gly90Cys)
n.462G>T
 gnomAD v4
11g.32435078C>GCA379966008WT1c.283G>C (p.Gly95Arg)
c.268G>C (p.Gly90Arg)
n.462G>C
 dbSNP gnomAD v4
11g.32435078C>TCA379966009WT1c.283G>A (p.Gly95Ser)
c.268G>A (p.Gly90Ser)
n.462G>A
 dbSNP gnomAD v4
11g.32435079G>ACA473773952WT1c.282C>T (p.Gly94=)
c.267C>T (p.Gly89=)
n.461C>T
 ClinVar dbSNP gnomAD v4
11g.32435079G>CCA473773953WT1c.282C>G (p.Gly94=)
c.267C>G (p.Gly89=)
n.461C>G
 dbSNP
11g.32435079G=CA1962327321WT1c.282C= (p.Gly94=)
c.267C= (p.Gly89=)
n.461C=
11g.32435079G>TCA473773954WT1c.282C>A (p.Gly94=)
c.267C>A (p.Gly89=)
n.461C>A
 gnomAD v4
11g.32435080C>ACA379966012WT1c.281G>T (p.Gly94Val)
c.266G>T (p.Gly89Val)
n.460G>T
 gnomAD v4
11g.32435080C=CA1962327322WT1c.281G= (p.Gly94=)
c.266G= (p.Gly89=)
n.460G=
11g.32435080C>GCA379966011WT1c.281G>C (p.Gly94Ala)
c.266G>C (p.Gly89Ala)
n.460G>C
11g.32435080C>TCA379966010WT1c.281G>A (p.Gly94Asp)
c.266G>A (p.Gly89Asp)
n.460G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435081C>ACA379966014WT1c.280G>T (p.Gly94Cys)
c.265G>T (p.Gly89Cys)
n.459G>T
 gnomAD v4
11g.32435081C=CA1962327323WT1c.280G= (p.Gly94=)
c.265G= (p.Gly89=)
n.459G=
11g.32435081C>GCA379966013WT1c.280G>C (p.Gly94Arg)
c.265G>C (p.Gly89Arg)
n.459G>C
 gnomAD v4
11g.32435081C>TCA064798WT1c.280G>A (p.Gly94Ser)
c.265G>A (p.Gly89Ser)
n.459G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.32435082G>ACA473773960WT1c.279C>T (p.Gly93=)
c.264C>T (p.Gly88=)
n.458C>T
 ClinVar dbSNP gnomAD v4
11g.32435082G>CCA473773962WT1c.279C>G (p.Gly93=)
c.264C>G (p.Gly88=)
n.458C>G
 dbSNP
11g.32435082G=CA1962327324WT1c.279C= (p.Gly93=)
c.264C= (p.Gly88=)
n.458C=
11g.32435082G>TCA473773961WT1c.279C>A (p.Gly93=)
c.264C>A (p.Gly88=)
n.458C>A
 ClinVar dbSNP gnomAD v4
11g.32435084_32435112delCA2695213680WT1c.251_279del (p.Leu84ArgfsTer?)
c.236_264del (p.Leu79ArgfsTer?)
n.430_458del
11g.32435083C>ACA379966015WT1c.278G>T (p.Gly93Val)
c.263G>T (p.Gly88Val)
n.457G>T
 gnomAD v4
11g.32435083C=CA1962327325WT1c.278G= (p.Gly93=)
c.263G= (p.Gly88=)
n.457G=
11g.32435083C>GCA379966016WT1c.278G>C (p.Gly93Ala)
c.263G>C (p.Gly88Ala)
n.457G>C
 ClinVar dbSNP gnomAD v4
11g.32435083C>TCA379966017WT1c.278G>A (p.Gly93Asp)
c.263G>A (p.Gly88Asp)
n.457G>A
 ClinVar dbSNP gnomAD v4
11g.32435085_32435087delCA2612989581WT1c.276_278del (p.Gly93del)
c.261_263del (p.Gly88del)
n.455_457del
 gnomAD v4
11g.32435084C>ACA379966020WT1c.277G>T (p.Gly93Cys)
c.262G>T (p.Gly88Cys)
n.456G>T
 gnomAD v4
11g.32435084C>GCA379966019WT1c.277G>C (p.Gly93Arg)
c.262G>C (p.Gly88Arg)
n.456G>C
11g.32435084C>TCA379966018WT1c.277G>A (p.Gly93Ser)
c.262G>A (p.Gly88Ser)
n.456G>A
 gnomAD v4
11g.32435085delCA2573146230WT1c.276del (p.Gly93AlafsTer9)
c.261del (p.Gly88AlafsTer9)
n.455del
 ClinVar dbSNP
11g.32435085A>CCA473773968WT1c.276T>G (p.Gly92=)
c.261T>G (p.Gly87=)
n.455T>G
 dbSNP
11g.32435085A>GCA473773970WT1c.276T>C (p.Gly92=)
c.261T>C (p.Gly87=)
n.455T>C
 gnomAD v4
11g.32435085A>TCA473773972WT1c.276T>A (p.Gly92=)
c.261T>A (p.Gly87=)
n.455T>A
11g.32435086C>ACA379966021WT1c.275G>T (p.Gly92Val)
c.260G>T (p.Gly87Val)
n.454G>T
 gnomAD v4
11g.32435086C>GCA379966022WT1c.275G>C (p.Gly92Ala)
c.260G>C (p.Gly87Ala)
n.454G>C
11g.32435086C>TCA379966023WT1c.275G>A (p.Gly92Asp)
c.260G>A (p.Gly87Asp)
n.454G>A
11g.32435088dupCA2740093680WT1c.275dup (p.Gly93TrpfsTer?)
c.260dup (p.Gly88TrpfsTer?)
n.454dup
 ClinVar
11g.32435088delCA2612989583WT1c.275del (p.Gly92ValfsTer10)
c.260del (p.Gly87ValfsTer10)
n.454del
 gnomAD v4
11g.32435087C>ACA379966024WT1c.274G>T (p.Gly92Cys)
c.259G>T (p.Gly87Cys)
n.453G>T
 gnomAD v4
11g.32435087C>GCA379966025WT1c.274G>C (p.Gly92Arg)
c.259G>C (p.Gly87Arg)
n.453G>C
11g.32435087C>TCA379966026WT1c.274G>A (p.Gly92Ser)
c.259G>A (p.Gly87Ser)
n.453G>A
 gnomAD v4
11g.32435088C>ACA473773977WT1c.273G>T (p.Leu91=)
c.258G>T (p.Leu86=)
n.452G>T
 dbSNP gnomAD v4
11g.32435088C=CA1962327326WT1c.273G= (p.Leu91=)
c.258G= (p.Leu86=)
n.452G=
11g.32435088C>GCA473773978WT1c.273G>C (p.Leu91=)
c.258G>C (p.Leu86=)
n.452G>C
11g.32435088C>TCA473773980WT1c.273G>A (p.Leu91=)
c.258G>A (p.Leu86=)
n.452G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435089A>CCA379966027WT1c.272T>G (p.Leu91Arg)
c.257T>G (p.Leu86Arg)
n.451T>G
11g.32435089A>GCA379966029WT1c.272T>C (p.Leu91Pro)
c.257T>C (p.Leu86Pro)
n.451T>C
 gnomAD v4
11g.32435089A>TCA379966028WT1c.272T>A (p.Leu91Gln)
c.257T>A (p.Leu86Gln)
n.451T>A
 gnomAD v4
11g.32435090G>ACA473773984WT1c.271C>T (p.Leu91=)
c.256C>T (p.Leu86=)
n.450C>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32435090G>CCA379966030WT1c.271C>G (p.Leu91Val)
c.256C>G (p.Leu86Val)
n.450C>G
 dbSNP
11g.32435090G=CA1962327327WT1c.271C= (p.Leu91=)
c.256C= (p.Leu86=)
n.450C=
11g.32435090G>TCA379966031WT1c.271C>A (p.Leu91Met)
c.256C>A (p.Leu86Met)
n.450C>A
 gnomAD v4
11g.32435094_32435098delCA645584492WT1c.267_271del (p.Ser90GlyfsTer?)
c.252_256del (p.Ser85GlyfsTer?)
n.446_450del
 COSMIC COSMIC
11g.32435091G>ACA473773986WT1c.270C>T (p.Ser90=)
c.255C>T (p.Ser85=)
n.449C>T
 ClinVar dbSNP gnomAD v4
11g.32435091G>CCA064793WT1c.270C>G (p.Ser90=)
c.255C>G (p.Ser85=)
n.449C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32435091G=CA1962327328WT1c.270C= (p.Ser90=)
c.255C= (p.Ser85=)
n.449C=
11g.32435091G>TCA473773987WT1c.270C>A (p.Ser90=)
c.255C>A (p.Ser85=)
n.449C>A
 gnomAD v4
11g.32435092G>ACA379966032WT1c.269C>T (p.Ser90Phe)
c.254C>T (p.Ser85Phe)
n.448C>T
 ClinVar dbSNP gnomAD v4
11g.32435092G>CCA379966033WT1c.269C>G (p.Ser90Cys)
c.254C>G (p.Ser85Cys)
n.448C>G
11g.32435092G=CA1962327329WT1c.269C= (p.Ser90=)
c.254C= (p.Ser85=)
n.448C=
11g.32435092G>TCA379966034WT1c.269C>A (p.Ser90Tyr)
c.254C>A (p.Ser85Tyr)
n.448C>A
 gnomAD v4
11g.32435093A=CA1962327330WT1c.268T= (p.Ser90=)
c.253T= (p.Ser85=)
n.447T=
11g.32435093A>CCA379966035WT1c.268T>G (p.Ser90Ala)
c.253T>G (p.Ser85Ala)
n.447T>G
11g.32435093A>GCA379966036WT1c.268T>C (p.Ser90Pro)
c.253T>C (p.Ser85Pro)
n.447T>C
 ClinVar dbSNP gnomAD v4
11g.32435093A>TCA379966037WT1c.268T>A (p.Ser90Thr)
c.253T>A (p.Ser85Thr)
n.447T>A
11g.32435094G>ACA473773990WT1c.267C>T (p.Pro89=)
c.252C>T (p.Pro84=)
n.446C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435094G>CCA473773995WT1c.267C>G (p.Pro89=)
c.252C>G (p.Pro84=)
n.446C>G
 gnomAD v4
11g.32435094G=CA1962327331WT1c.267C= (p.Pro89=)
c.252C= (p.Pro84=)
n.446C=
11g.32435094G>TCA473773996WT1c.267C>A (p.Pro89=)
c.252C>A (p.Pro84=)
n.446C>A
 gnomAD v4
11g.32435095G>ACA379966038WT1c.266C>T (p.Pro89Leu)
c.251C>T (p.Pro84Leu)
n.445C>T
 ClinVar dbSNP gnomAD v4
11g.32435095G>CCA379966039WT1c.266C>G (p.Pro89Arg)
c.251C>G (p.Pro84Arg)
n.445C>G
11g.32435095G=CA1962327332WT1c.266C= (p.Pro89=)
c.251C= (p.Pro84=)
n.445C=
11g.32435095G>TCA379966040WT1c.266C>A (p.Pro89His)
c.251C>A (p.Pro84His)
n.445C>A
 gnomAD v4
11g.32435096G>ACA379966042WT1c.265C>T (p.Pro89Ser)
c.250C>T (p.Pro84Ser)
n.444C>T
 gnomAD v4
11g.32435096G>CCA379966043WT1c.265C>G (p.Pro89Ala)
c.250C>G (p.Pro84Ala)
n.444C>G
 dbSNP
11g.32435096G>TCA379966041WT1c.265C>A (p.Pro89Thr)
c.250C>A (p.Pro84Thr)
n.444C>A
 ClinVar gnomAD v4 COSMIC COSMIC
11g.32435096_32435098delCA2574790568WT1c.263_265del (p.Val88_Pro89delinsAla)
c.248_250del (p.Val83_Pro84delinsAla)
n.442_444del
11g.32435097G>ACA473774000WT1c.264C>T (p.Val88=)
c.249C>T (p.Val83=)
n.443C>T
 dbSNP gnomAD v2 gnomAD v4
11g.32435097G>CCA473774001WT1c.264C>G (p.Val88=)
c.249C>G (p.Val83=)
n.443C>G
 gnomAD v4
11g.32435097G=CA1962327333WT1c.264C= (p.Val88=)
c.249C= (p.Val83=)
n.443C=
11g.32435097G>TCA473774003WT1c.264C>A (p.Val88=)
c.249C>A (p.Val83=)
n.443C>A
 gnomAD v4
11g.32435098A>CCA379966044WT1c.263T>G (p.Val88Gly)
c.248T>G (p.Val83Gly)
n.442T>G
11g.32435098A>GCA379966045WT1c.263T>C (p.Val88Ala)
c.248T>C (p.Val83Ala)
n.442T>C
 dbSNP gnomAD v4
11g.32435098A>TCA379966046WT1c.263T>A (p.Val88Asp)
c.248T>A (p.Val83Asp)
n.442T>A
 ClinVar gnomAD v4
11g.32435099C>ACA379966047WT1c.262G>T (p.Val88Phe)
c.247G>T (p.Val83Phe)
n.441G>T
 ClinVar dbSNP gnomAD v4
11g.32435099C=CA1962327334WT1c.262G= (p.Val88=)
c.247G= (p.Val83=)
n.441G=
11g.32435099C>GCA379966048WT1c.262G>C (p.Val88Leu)
c.247G>C (p.Val83Leu)
n.441G>C
 gnomAD v4
11g.32435099C>TCA379966049WT1c.262G>A (p.Val88Ile)
c.247G>A (p.Val83Ile)
n.441G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435099_32435100delinsAACA2580084189WT1c.261_262delinsTT (p.Val88Phe)
c.246_247delinsTT (p.Val83Phe)
n.440_441delinsTT
 ClinVar
11g.32435100G>ACA473774006WT1c.261C>T (p.Ala87=)
c.246C>T (p.Ala82=)
n.440C>T
 ClinVar dbSNP gnomAD v4
11g.32435100G>CCA473774007WT1c.261C>G (p.Ala87=)
c.246C>G (p.Ala82=)
n.440C>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435100G=CA1962327335WT1c.261C= (p.Ala87=)
c.246C= (p.Ala82=)
n.440C=
11g.32435100G>TCA473774009WT1c.261C>A (p.Ala87=)
c.246C>A (p.Ala82=)
n.440C>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435101G>ACA379966052WT1c.260C>T (p.Ala87Val)
c.245C>T (p.Ala82Val)
n.439C>T
 dbSNP gnomAD v4
11g.32435101G>CCA379966051WT1c.260C>G (p.Ala87Gly)
c.245C>G (p.Ala82Gly)
n.439C>G
11g.32435101G>TCA379966050WT1c.260C>A (p.Ala87Asp)
c.245C>A (p.Ala82Asp)
n.439C>A
11g.32435102C>ACA379966053WT1c.259G>T (p.Ala87Ser)
c.244G>T (p.Ala82Ser)
n.438G>T
 gnomAD v4
11g.32435102C=CA1962327336WT1c.259G= (p.Ala87=)
c.244G= (p.Ala82=)
n.438G=
11g.32435102C>GCA379966054WT1c.259G>C (p.Ala87Pro)
c.244G>C (p.Ala82Pro)
n.438G>C
 dbSNP gnomAD v4
11g.32435102C>TCA064789WT1c.259G>A (p.Ala87Thr)
c.244G>A (p.Ala82Thr)
n.438G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32435103G>ACA473774014WT1c.258C>T (p.Pro86=)
c.243C>T (p.Pro81=)
n.437C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435103G>CCA473774015WT1c.258C>G (p.Pro86=)
c.243C>G (p.Pro81=)
n.437C>G
11g.32435103G=CA1962327337WT1c.258C= (p.Pro86=)
c.243C= (p.Pro81=)
n.437C=
11g.32435103G>TCA473774012WT1c.258C>A (p.Pro86=)
c.243C>A (p.Pro81=)
n.437C>A
 ClinVar dbSNP gnomAD v4
11g.32435105_32435106insGCCCGGGCGCCTGGGCA2790963048WT1c.258_259insAGGCGCCCGGGCCCC (p.Pro86_Ala87insArgArgProGlyPro)
c.243_244insAGGCGCCCGGGCCCC (p.Pro81_Ala82insArgArgProGlyPro)
n.437_438insAGGCGCCCGGGCCCC
11g.32435104G>ACA379966055WT1c.257C>T (p.Pro86Leu)
c.242C>T (p.Pro81Leu)
n.436C>T
 ClinVar gnomAD v4
11g.32435104G>CCA379966056WT1c.257C>G (p.Pro86Arg)
c.242C>G (p.Pro81Arg)
n.436C>G
11g.32435104G>TCA379966057WT1c.257C>A (p.Pro86His)
c.242C>A (p.Pro81His)
n.436C>A
 gnomAD v4
11g.32435105G>ACA379966058WT1c.256C>T (p.Pro86Ser)
c.241C>T (p.Pro81Ser)
n.435C>T
 dbSNP gnomAD v4 COSMIC COSMIC
11g.32435105G>CCA379966060WT1c.256C>G (p.Pro86Ala)
c.241C>G (p.Pro81Ala)
n.435C>G
11g.32435105G>TCA379966059WT1c.256C>A (p.Pro86Thr)
c.241C>A (p.Pro81Thr)
n.435C>A
 gnomAD v4
11g.32435106C>ACA473774031WT1c.255G>T (p.Leu85=)
c.240G>T (p.Leu80=)
n.434G>T
 gnomAD v4
11g.32435106C=CA1962327338WT1c.255G= (p.Leu85=)
c.240G= (p.Leu80=)
n.434G=
11g.32435106C>GCA473774024WT1c.255G>C (p.Leu85=)
c.240G>C (p.Leu80=)
n.434G>C
11g.32435106C>TCA473774023WT1c.255G>A (p.Leu85=)
c.240G>A (p.Leu80=)
n.434G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435107A>CCA379966061WT1c.254T>G (p.Leu85Arg)
c.239T>G (p.Leu80Arg)
n.433T>G
11g.32435107A>GCA379966062WT1c.254T>C (p.Leu85Pro)
c.239T>C (p.Leu80Pro)
n.433T>C
 ClinVar gnomAD v4
11g.32435107A>TCA379966063WT1c.254T>A (p.Leu85Gln)
c.239T>A (p.Leu80Gln)
n.433T>A
 gnomAD v4
11g.32435108G>ACA473774032WT1c.253C>T (p.Leu85=)
c.238C>T (p.Leu80=)
n.432C>T
 dbSNP gnomAD v4
11g.32435108G>CCA379966064WT1c.253C>G (p.Leu85Val)
c.238C>G (p.Leu80Val)
n.432C>G
11g.32435108G>TCA379966065WT1c.253C>A (p.Leu85Met)
c.238C>A (p.Leu80Met)
n.432C>A
 gnomAD v4
11g.32435109C>ACA473774035WT1c.252G>T (p.Leu84=)
c.237G>T (p.Leu79=)
n.431G>T
 dbSNP gnomAD v2 gnomAD v4
11g.32435109C=CA1962327339WT1c.252G= (p.Leu84=)
c.237G= (p.Leu79=)
n.431G=
11g.32435109C>GCA473774038WT1c.252G>C (p.Leu84=)
c.237G>C (p.Leu79=)
n.431G>C
11g.32435109C>TCA473774037WT1c.252G>A (p.Leu84=)
c.237G>A (p.Leu79=)
n.431G>A
 dbSNP gnomAD v4
11g.32435110A>CCA379966066WT1c.251T>G (p.Leu84Arg)
c.236T>G (p.Leu79Arg)
n.430T>G
 gnomAD v4
11g.32435110A>GCA379966067WT1c.251T>C (p.Leu84Pro)
c.236T>C (p.Leu79Pro)
n.430T>C
 gnomAD v4
11g.32435110A>TCA379966068WT1c.251T>A (p.Leu84Gln)
c.236T>A (p.Leu79Gln)
n.430T>A
11g.32435111G>ACA064783WT1c.250C>T (p.Leu84=)
c.235C>T (p.Leu79=)
n.429C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.32435111G>CCA379966069WT1c.250C>G (p.Leu84Val)
c.235C>G (p.Leu79Val)
n.429C>G
11g.32435111G=CA1962327340WT1c.250C= (p.Leu84=)
c.235C= (p.Leu79=)
n.429C=
11g.32435111G>TCA379966070WT1c.250C>A (p.Leu84Met)
c.235C>A (p.Leu79Met)
n.429C>A
 gnomAD v4
11g.32435112C>ACA473774039WT1c.249G>T (p.Ala83=)
c.234G>T (p.Ala78=)
n.428G>T
 ClinVar gnomAD v4
11g.32435112C=CA1962327341WT1c.249G= (p.Ala83=)
c.234G= (p.Ala78=)
n.428G=
11g.32435112C>GCA473774040WT1c.249G>C (p.Ala83=)
c.234G>C (p.Ala78=)
n.428G>C
 dbSNP gnomAD v2 gnomAD v4
11g.32435112C>TCA473774041WT1c.249G>A (p.Ala83=)
c.234G>A (p.Ala78=)
n.428G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4

Number of alleles fetched