Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.32434918T>ACA379965084WT1c.443A>T (p.Glu148Val)
c.428A>T (p.Glu143Val)
n.622A>T
11g.32434918T>CCA379965086WT1c.443A>G (p.Glu148Gly)
c.428A>G (p.Glu143Gly)
n.622A>G
11g.32434918T>GCA379965087WT1c.443A>C (p.Glu148Ala)
c.428A>C (p.Glu143Ala)
n.622A>C
11g.32434919C>ACA379965088WT1c.442G>T (p.Glu148Ter)
c.427G>T (p.Glu143Ter)
n.621G>T
COSMIC COSMIC
11g.32434919C>GCA379965090WT1c.442G>C (p.Glu148Gln)
c.427G>C (p.Glu143Gln)
n.621G>C
11g.32434919C>TCA379965092WT1c.442G>A (p.Glu148Lys)
c.427G>A (p.Glu143Lys)
n.621G>A
11g.32434920C>ACA379965093WT1c.441G>T (p.Gln147His)
c.426G>T (p.Gln142His)
n.620G>T
11g.32434920C>GCA379965094WT1c.441G>C (p.Gln147His)
c.426G>C (p.Gln142His)
n.620G>C
dbSNP
11g.32434920C>TCA473571803WT1c.441G>A (p.Gln147=)
c.426G>A (p.Gln142=)
n.620G>A
ClinVar
11g.32434921T>ACA379965096WT1c.440A>T (p.Gln147Leu)
c.425A>T (p.Gln142Leu)
n.619A>T
11g.32434921T>CCA064944WT1c.440A>G (p.Gln147Arg)
c.425A>G (p.Gln142Arg)
n.619A>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32434921T>GCA379965099WT1c.440A>C (p.Gln147Pro)
c.425A>C (p.Gln142Pro)
n.619A>C
ClinVar
11g.32434921T=CA1962327208WT1c.440A= (p.Gln147=)
c.425A= (p.Gln142=)
n.619A=
11g.32434922G>ACA379965624WT1c.439C>T (p.Gln147Ter)
c.424C>T (p.Gln142Ter)
n.618C>T
11g.32434922G>CCA16613373WT1c.439C>G (p.Gln147Glu)
c.424C>G (p.Gln142Glu)
n.618C>G
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32434922G=CA1962327209WT1c.439C= (p.Gln147=)
c.424C= (p.Gln142=)
n.618C=
11g.32434922G>TCA379965622WT1c.439C>A (p.Gln147Lys)
c.424C>A (p.Gln142Lys)
n.618C>A
gnomAD v4
11g.32434923T>ACA379965627WT1c.438A>T (p.Lys146Asn)
c.423A>T (p.Lys141Asn)
n.617A>T
11g.32434923T>CCA473773520WT1c.438A>G (p.Lys146=)
c.423A>G (p.Lys141=)
n.617A>G
11g.32434923T>GCA379965626WT1c.438A>C (p.Lys146Asn)
c.423A>C (p.Lys141Asn)
n.617A>C
11g.32434924T>ACA379965630WT1c.437A>T (p.Lys146Ile)
c.422A>T (p.Lys141Ile)
n.616A>T
11g.32434924T>CCA379965631WT1c.437A>G (p.Lys146Arg)
c.422A>G (p.Lys141Arg)
n.616A>G
11g.32434924T>GCA379965633WT1c.437A>C (p.Lys146Thr)
c.422A>C (p.Lys141Thr)
n.616A>C
11g.32434925T>ACA379965634WT1c.436A>T (p.Lys146Ter)
c.421A>T (p.Lys141Ter)
n.615A>T
11g.32434925T>CCA379965635WT1c.436A>G (p.Lys146Glu)
c.421A>G (p.Lys141Glu)
n.615A>G
11g.32434925T>GCA379965638WT1c.436A>C (p.Lys146Gln)
c.421A>C (p.Lys141Gln)
n.615A>C
ClinVar
11g.32434926G>ACA473773531WT1c.435C>T (p.Ile145=)
c.420C>T (p.Ile140=)
n.614C>T
dbSNP
11g.32434926G>CCA379965639WT1c.435C>G (p.Ile145Met)
c.420C>G (p.Ile140Met)
n.614C>G
11g.32434926G>TCA473773530WT1c.435C>A (p.Ile145=)
c.420C>A (p.Ile140=)
n.614C>A
gnomAD v4
11g.32434927A>CCA379965641WT1c.434T>G (p.Ile145Ser)
c.419T>G (p.Ile140Ser)
n.613T>G
11g.32434927A>GCA379965643WT1c.434T>C (p.Ile145Thr)
c.419T>C (p.Ile140Thr)
n.613T>C
11g.32434927A>TCA379965645WT1c.434T>A (p.Ile145Asn)
c.419T>A (p.Ile140Asn)
n.613T>A
11g.32434928T>ACA379965647WT1c.433A>T (p.Ile145Phe)
c.418A>T (p.Ile140Phe)
n.612A>T
11g.32434928T>CCA379965649WT1c.433A>G (p.Ile145Val)
c.418A>G (p.Ile140Val)
n.612A>G
ClinVar dbSNP gnomAD v4
11g.32434928T>GCA379965651WT1c.433A>C (p.Ile145Leu)
c.418A>C (p.Ile140Leu)
n.612A>C
11g.32434928_32434931delinsTGAACA1962327210WT1c.430_433delinsTTCA (p.Phe144=)
c.415_418delinsTTCA (p.Phe139=)
n.609_612delinsTTCA
11g.32434929G>ACA064939WT1c.432C>T (p.Phe144=)
c.417C>T (p.Phe139=)
n.611C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32434929G>CCA379965656WT1c.432C>G (p.Phe144Leu)
c.417C>G (p.Phe139Leu)
n.611C>G
11g.32434929G=CA1962327211WT1c.432C= (p.Phe144=)
c.417C= (p.Phe139=)
n.611C=
11g.32434929G>TCA379965654WT1c.432C>A (p.Phe144Leu)
c.417C>A (p.Phe139Leu)
n.611C>A
11g.32434930_32434932delCA598508257WT1c.430_432del (p.Phe144del)
c.415_417del (p.Phe139del)
n.609_611del
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32434930A>CCA379965657WT1c.431T>G (p.Phe144Cys)
c.416T>G (p.Phe139Cys)
n.610T>G
11g.32434930A>GCA379965658WT1c.431T>C (p.Phe144Ser)
c.416T>C (p.Phe139Ser)
n.610T>C
11g.32434930A>TCA379965662WT1c.431T>A (p.Phe144Tyr)
c.416T>A (p.Phe139Tyr)
n.610T>A
11g.32434931A>CCA379965664WT1c.430T>G (p.Phe144Val)
c.415T>G (p.Phe139Val)
n.609T>G
11g.32434931A>GCA379965666WT1c.430T>C (p.Phe144Leu)
c.415T>C (p.Phe139Leu)
n.609T>C
11g.32434931A>TCA379965668WT1c.430T>A (p.Phe144Ile)
c.415T>A (p.Phe139Ile)
n.609T>A
11g.32434932G>ACA473773556WT1c.429C>T (p.Ser143=)
c.414C>T (p.Ser138=)
n.608C>T
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32434932G>CCA064936WT1c.429C>G (p.Ser143=)
c.414C>G (p.Ser138=)
n.608C>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32434932G=CA1962327212WT1c.429C= (p.Ser143=)
c.414C= (p.Ser138=)
n.608C=
11g.32434932G>TCA473773561WT1c.429C>A (p.Ser143=)
c.414C>A (p.Ser138=)
n.608C>A
gnomAD v4
11g.32434934_32434946dupCA2695213676WT1c.417_429dup (p.Phe144AlafsTer?)
c.402_414dup (p.Phe139AlafsTer?)
n.596_608dup
11g.32434933G>ACA379965672WT1c.428C>T (p.Ser143Phe)
c.413C>T (p.Ser138Phe)
n.607C>T
11g.32434933G>CCA379965673WT1c.428C>G (p.Ser143Cys)
c.413C>G (p.Ser138Cys)
n.607C>G
ClinVar dbSNP
11g.32434933G=CA1962327213WT1c.428C= (p.Ser143=)
c.413C= (p.Ser138=)
n.607C=
11g.32434933G>TCA379965675WT1c.428C>A (p.Ser143Tyr)
c.413C>A (p.Ser138Tyr)
n.607C>A
11g.32434936_32434939delCA645584485WT1c.425_428del (p.His142ProfsTer20)
c.410_413del (p.His137ProfsTer20)
n.604_607del
COSMIC
11g.32434934A=CA1962327214WT1c.427T= (p.Ser143=)
c.412T= (p.Ser138=)
n.606T=
11g.32434934A>CCA379965679WT1c.427T>G (p.Ser143Ala)
c.412T>G (p.Ser138Ala)
n.606T>G
11g.32434934A>GCA379965677WT1c.427T>C (p.Ser143Pro)
c.412T>C (p.Ser138Pro)
n.606T>C
ClinVar dbSNP
11g.32434934A>TCA064931WT1c.427T>A (p.Ser143Thr)
c.412T>A (p.Ser138Thr)
n.606T>A
dbSNP ExAC gnomAD v2 gnomAD v4
11g.32434935G>ACA473773570WT1c.426C>T (p.His142=)
c.411C>T (p.His137=)
n.605C>T
dbSNP
11g.32434935G>CCA379965681WT1c.426C>G (p.His142Gln)
c.411C>G (p.His137Gln)
n.605C>G
ClinVar dbSNP
11g.32434935G=CA1962327215WT1c.426C= (p.His142=)
c.411C= (p.His137=)
n.605C=
11g.32434935G>TCA379965683WT1c.426C>A (p.His142Gln)
c.411C>A (p.His137Gln)
n.605C>A
11g.32434936T>ACA379965685WT1c.425A>T (p.His142Leu)
c.410A>T (p.His137Leu)
n.604A>T
ClinVar dbSNP
11g.32434936T>CCA379965686WT1c.425A>G (p.His142Arg)
c.410A>G (p.His137Arg)
n.604A>G
dbSNP
11g.32434936T>GCA379965687WT1c.425A>C (p.His142Pro)
c.410A>C (p.His137Pro)
n.604A>C
ClinVar dbSNP gnomAD v4 COSMIC COSMIC
11g.32434936T=CA1962327216WT1c.425A= (p.His142=)
c.410A= (p.His137=)
n.604A=
11g.32434936_32434938delinsGGCA645584486WT1c.423_425delinsCC (p.His142ProfsTer21)
c.408_410delinsCC (p.His137ProfsTer21)
n.602_604delinsCC
COSMIC
11g.32434937G>ACA379965690WT1c.424C>T (p.His142Tyr)
c.409C>T (p.His137Tyr)
n.603C>T
ClinVar
11g.32434937G>CCA379965692WT1c.424C>G (p.His142Asp)
c.409C>G (p.His137Asp)
n.603C>G
11g.32434937G>TCA379965693WT1c.424C>A (p.His142Asn)
c.409C>A (p.His137Asn)
n.603C>A
11g.32434938A=CA1962327217WT1c.423T= (p.Pro141=)
c.408T= (p.Pro136=)
n.602T=
11g.32434938A>CCA473773578WT1c.423T>G (p.Pro141=)
c.408T>G (p.Pro136=)
n.602T>G
ClinVar
11g.32434938A>GCA473773579WT1c.423T>C (p.Pro141=)
c.408T>C (p.Pro136=)
n.602T>C
dbSNP gnomAD v4
11g.32434938A>TCA473773586WT1c.423T>A (p.Pro141=)
c.408T>A (p.Pro136=)
n.602T>A
11g.32434938_32434941delinsAGGCCA1962327218WT1c.420_423delinsGCCT (p.Pro140=)
c.405_408delinsGCCT (p.Pro135=)
n.599_602delinsGCCT
11g.32434939G>ACA379965699WT1c.422C>T (p.Pro141Leu)
c.407C>T (p.Pro136Leu)
n.601C>T
ClinVar
11g.32434939G>CCA379965700WT1c.422C>G (p.Pro141Arg)
c.407C>G (p.Pro136Arg)
n.601C>G
gnomAD v4
11g.32434939G>TCA379965702WT1c.422C>A (p.Pro141His)
c.407C>A (p.Pro136His)
n.601C>A
11g.32434950_32434952dupCA5934336WT1c.420_422dup (p.Pro141_His142insPro)
c.405_407dup (p.Pro136_His137insPro)
n.599_601dup
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32434950_32434952delCA064917WT1c.420_422del (p.Pro141del)
c.405_407del (p.Pro136del)
n.599_601del
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32434947_32434964dupCA916081630WT1c.405_422dup (p.Pro141_His142insProProProProProPro)
c.390_407dup (p.Pro136_His137insProProProProProPro)
n.584_601dup
ClinVar dbSNP gnomAD v4
11g.32434940G>ACA064922WT1c.421C>T (p.Pro141Ser)
c.406C>T (p.Pro136Ser)
n.600C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32434940G>CCA379965705WT1c.421C>G (p.Pro141Ala)
c.406C>G (p.Pro136Ala)
n.600C>G
11g.32434940G=CA1962327219WT1c.421C= (p.Pro141=)
c.406C= (p.Pro136=)
n.600C=
11g.32434940G>TCA379965707WT1c.421C>A (p.Pro141Thr)
c.406C>A (p.Pro136Thr)
n.600C>A
11g.32434941C>ACA473773603WT1c.420G>T (p.Pro140=)
c.405G>T (p.Pro135=)
n.599G>T
ClinVar gnomAD v4
11g.32434941C=CA1962327220WT1c.420G= (p.Pro140=)
c.405G= (p.Pro135=)
n.599G=
11g.32434941C>GCA473773606WT1c.420G>C (p.Pro140=)
c.405G>C (p.Pro135=)
n.599G>C
dbSNP
11g.32434941C>TCA219511039WT1c.420G>A (p.Pro140=)
c.405G>A (p.Pro135=)
n.599G>A
dbSNP
11g.32434942G>ACA379965710WT1c.419C>T (p.Pro140Leu)
c.404C>T (p.Pro135Leu)
n.598C>T
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32434942G>CCA379965711WT1c.419C>G (p.Pro140Arg)
c.404C>G (p.Pro135Arg)
n.598C>G
11g.32434942G=CA1962327221WT1c.419C= (p.Pro140=)
c.404C= (p.Pro135=)
n.598C=
11g.32434942G>TCA379965712WT1c.419C>A (p.Pro140Gln)
c.404C>A (p.Pro135Gln)
n.598C>A
11g.32434944_32434955delCA2612989444WT1c.408_419del (p.Pro137_Pro140del)
c.393_404del (p.Pro132_Pro135del)
n.587_598del
gnomAD v4
11g.32434950_32434964delCA2573146227WT1c.405_419del (p.Pro136_Pro140del)
c.390_404del (p.Pro131_Pro135del)
n.584_598del
ClinVar dbSNP
11g.32434943G>ACA379965714WT1c.418C>T (p.Pro140Ser)
c.403C>T (p.Pro135Ser)
n.597C>T
dbSNP gnomAD v2
11g.32434943G>CCA379965716WT1c.418C>G (p.Pro140Ala)
c.403C>G (p.Pro135Ala)
n.597C>G
11g.32434943G=CA1962327222WT1c.418C= (p.Pro140=)
c.403C= (p.Pro135=)
n.597C=
11g.32434943G>TCA379965718WT1c.418C>A (p.Pro140Thr)
c.403C>A (p.Pro135Thr)
n.597C>A
11g.32434944C>ACA473773613WT1c.417G>T (p.Pro139=)
c.402G>T (p.Pro134=)
n.596G>T
ClinVar dbSNP
11g.32434944C=CA1962327223WT1c.417G= (p.Pro139=)
c.402G= (p.Pro134=)
n.596G=
11g.32434944C>GCA473773615WT1c.417G>C (p.Pro139=)
c.402G>C (p.Pro134=)
n.596G>C
dbSNP
11g.32434944C>TCA064912WT1c.417G>A (p.Pro139=)
c.402G>A (p.Pro134=)
n.596G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32434945G>ACA379965721WT1c.416C>T (p.Pro139Leu)
c.401C>T (p.Pro134Leu)
n.595C>T
gnomAD v4
11g.32434945G>CCA10582913WT1c.416C>G (p.Pro139Arg)
c.401C>G (p.Pro134Arg)
n.595C>G
ClinVar dbSNP gnomAD v4
11g.32434945G=CA1962327224WT1c.416C= (p.Pro139=)
c.401C= (p.Pro134=)
n.595C=
11g.32434945G>TCA379965724WT1c.416C>A (p.Pro139Gln)
c.401C>A (p.Pro134Gln)
n.595C>A
ClinVar gnomAD v4
11g.32434953_32434964dupCA675622615WT1c.405_416dup (p.Pro139_Pro140insProProProPro)
c.390_401dup (p.Pro134_Pro135insProProProPro)
n.584_595dup
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32434946G>ACA379965726WT1c.415C>T (p.Pro139Ser)
c.400C>T (p.Pro134Ser)
n.594C>T
11g.32434946G>CCA379965728WT1c.415C>G (p.Pro139Ala)
c.400C>G (p.Pro134Ala)
n.594C>G
11g.32434946G>TCA379965729WT1c.415C>A (p.Pro139Thr)
c.400C>A (p.Pro134Thr)
n.594C>A
gnomAD v4
11g.32434947C>ACA473773622WT1c.414G>T (p.Pro138=)
c.399G>T (p.Pro133=)
n.593G>T
11g.32434947C>GCA473773623WT1c.414G>C (p.Pro138=)
c.399G>C (p.Pro133=)
n.593G>C
dbSNP
11g.32434947C>TCA473773624WT1c.414G>A (p.Pro138=)
c.399G>A (p.Pro133=)
n.593G>A
ClinVar dbSNP gnomAD v4 COSMIC COSMIC
11g.32434948G>ACA379965733WT1c.413C>T (p.Pro138Leu)
c.398C>T (p.Pro133Leu)
n.592C>T
ClinVar gnomAD v4
11g.32434948G>CCA379965734WT1c.413C>G (p.Pro138Arg)
c.398C>G (p.Pro133Arg)
n.592C>G
ClinVar dbSNP
11g.32434948G=CA1962327225WT1c.413C= (p.Pro138=)
c.398C= (p.Pro133=)
n.592C=
11g.32434948G>TCA379965731WT1c.413C>A (p.Pro138Gln)
c.398C>A (p.Pro133Gln)
n.592C>A
ClinVar dbSNP gnomAD v4
11g.32434953_32434961dupCA2740093679WT1c.405_413dup (p.Pro138_Pro139insProProPro)
c.390_398dup (p.Pro133_Pro134insProProPro)
n.584_592dup
ClinVar
11g.32434949G>ACA064909WT1c.412C>T (p.Pro138Ser)
c.397C>T (p.Pro133Ser)
n.591C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32434949G>CCA379965736WT1c.412C>G (p.Pro138Ala)
c.397C>G (p.Pro133Ala)
n.591C>G
11g.32434949G=CA1962327226WT1c.412C= (p.Pro138=)
c.397C= (p.Pro133=)
n.591C=
11g.32434949G>TCA379965738WT1c.412C>A (p.Pro138Thr)
c.397C>A (p.Pro133Thr)
n.591C>A
ClinVar
11g.32434950delCA2612989498WT1c.411del (p.Pro138ArgfsTer25)
c.396del (p.Pro133ArgfsTer25)
n.590del
gnomAD v4
11g.32434950C>ACA473773631WT1c.411G>T (p.Pro137=)
c.396G>T (p.Pro132=)
n.590G>T
11g.32434950C=CA1962327227WT1c.411G= (p.Pro137=)
c.396G= (p.Pro132=)
n.590G=
11g.32434950C>GCA473773633WT1c.411G>C (p.Pro137=)
c.396G>C (p.Pro132=)
n.590G>C
ClinVar dbSNP gnomAD v4
11g.32434950C>TCA473773634WT1c.411G>A (p.Pro137=)
c.396G>A (p.Pro132=)
n.590G>A
dbSNP gnomAD v4
11g.32434951G>ACA379965739WT1c.410C>T (p.Pro137Leu)
c.395C>T (p.Pro132Leu)
n.589C>T
11g.32434951G>CCA379965741WT1c.410C>G (p.Pro137Arg)
c.395C>G (p.Pro132Arg)
n.589C>G
11g.32434951G=CA1962327228WT1c.410C= (p.Pro137=)
c.395C= (p.Pro132=)
n.589C=
11g.32434951G>TCA379965743WT1c.410C>A (p.Pro137Gln)
c.395C>A (p.Pro132Gln)
n.589C>A
dbSNP gnomAD v2 gnomAD v4
11g.32434951_32434952delinsTTCA645584487WT1c.409_410delinsAA (p.Pro137Lys)
c.394_395delinsAA (p.Pro132Lys)
n.588_589delinsAA
COSMIC COSMIC
11g.32434952_32434953insTGGCA2574790567WT1c.410_411insACC (p.Pro137_Pro138insPro)
c.395_396insACC (p.Pro132_Pro133insPro)
n.589_590insACC
11g.32434955dupCA2573320816WT1c.410dup (p.Pro138AlafsTer?)
c.395dup (p.Pro133AlafsTer?)
n.589dup
11g.32434955delCA2573334573WT1c.410del (p.Pro137ArgfsTer26)
c.395del (p.Pro132ArgfsTer26)
n.589del
ClinVar gnomAD v4
11g.32434952G>ACA379965749WT1c.409C>T (p.Pro137Ser)
c.394C>T (p.Pro132Ser)
n.588C>T
gnomAD v4
11g.32434952G>CCA379965745WT1c.409C>G (p.Pro137Ala)
c.394C>G (p.Pro132Ala)
n.588C>G
ClinVar dbSNP gnomAD v4
11g.32434952G=CA1962327229WT1c.409C= (p.Pro137=)
c.394C= (p.Pro132=)
n.588C=
11g.32434952G>TCA379965747WT1c.409C>A (p.Pro137Thr)
c.394C>A (p.Pro132Thr)
n.588C>A
11g.32434953G>ACA473773639WT1c.408C>T (p.Pro136=)
c.393C>T (p.Pro131=)
n.587C>T
ClinVar dbSNP gnomAD v4
11g.32434953G>CCA473773640WT1c.408C>G (p.Pro136=)
c.393C>G (p.Pro131=)
n.587C>G
gnomAD v4
11g.32434953G=CA1962327230WT1c.408C= (p.Pro136=)
c.393C= (p.Pro131=)
n.587C=
11g.32434953G>TCA473773642WT1c.408C>A (p.Pro136=)
c.393C>A (p.Pro131=)
n.587C>A
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32434954G>ACA379965751WT1c.407C>T (p.Pro136Leu)
c.392C>T (p.Pro131Leu)
n.586C>T
11g.32434954G>CCA379965753WT1c.407C>G (p.Pro136Arg)
c.392C>G (p.Pro131Arg)
n.586C>G
11g.32434954G>TCA379965755WT1c.407C>A (p.Pro136His)
c.392C>A (p.Pro131His)
n.586C>A
11g.32434955_32434956insCGGCA2580582997WT1c.407_408insGCC (p.Pro136_Pro137insPro)
c.392_393insGCC (p.Pro131_Pro132insPro)
n.586_587insGCC
11g.32434956_32434958dupCA1962327231WT1c.405_407dup (p.Pro136_Pro137insPro)
c.390_392dup (p.Pro131_Pro132insPro)
n.584_586dup
dbSNP
11g.32434964_32434978dupCA1962327232WT1c.393_407dup (p.Pro136_Pro137insAlaProProProPro)
c.378_392dup (p.Pro131_Pro132insAlaProProProPro)
n.572_586dup
ClinVar dbSNP gnomAD v4
11g.32434964_32434978delCA2499220923WT1c.393_407del (p.Ala132_Pro136del)
c.378_392del (p.Ala127_Pro131del)
n.572_586del
ClinVar dbSNP gnomAD v4
11g.32434955G>ACA379965757WT1c.406C>T (p.Pro136Ser)
c.391C>T (p.Pro131Ser)
n.585C>T
ClinVar dbSNP gnomAD v4
11g.32434955G>CCA379965759WT1c.406C>G (p.Pro136Ala)
c.391C>G (p.Pro131Ala)
n.585C>G
gnomAD v4
11g.32434955G=CA1962327233WT1c.406C= (p.Pro136=)
c.391C= (p.Pro131=)
n.585C=
11g.32434955G>TCA064905WT1c.406C>A (p.Pro136Thr)
c.391C>A (p.Pro131Thr)
n.585C>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.32434956T>ACA473773646WT1c.405A>T (p.Pro135=)
c.390A>T (p.Pro130=)
n.584A>T
dbSNP
11g.32434956T>CCA473773647WT1c.405A>G (p.Pro135=)
c.390A>G (p.Pro130=)
n.584A>G
gnomAD v4
11g.32434956T>GCA219511062WT1c.405A>C (p.Pro135=)
c.390A>C (p.Pro130=)
n.584A>C
dbSNP gnomAD v4
11g.32434956T=CA1962327234WT1c.405A= (p.Pro135=)
c.390A= (p.Pro130=)
n.584A=
11g.32434957G>ACA064898WT1c.404C>T (p.Pro135Leu)
c.389C>T (p.Pro130Leu)
n.583C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.32434957G>CCA379965765WT1c.404C>G (p.Pro135Arg)
c.389C>G (p.Pro130Arg)
n.583C>G
11g.32434957G=CA1962327235WT1c.404C= (p.Pro135=)
c.389C= (p.Pro130=)
n.583C=
11g.32434957G>TCA379965763WT1c.404C>A (p.Pro135Gln)
c.389C>A (p.Pro130Gln)
n.583C>A
gnomAD v4
11g.32434958G>ACA379965767WT1c.403C>T (p.Pro135Ser)
c.388C>T (p.Pro130Ser)
n.582C>T
dbSNP gnomAD v3 gnomAD v4
11g.32434958G>CCA379965769WT1c.403C>G (p.Pro135Ala)
c.388C>G (p.Pro130Ala)
n.582C>G
11g.32434958G=CA1962327236WT1c.403C= (p.Pro135=)
c.388C= (p.Pro130=)
n.582C=
11g.32434958G>TCA379965771WT1c.403C>A (p.Pro135Thr)
c.388C>A (p.Pro130Thr)
n.582C>A
gnomAD v4
11g.32434959C>ACA473773653WT1c.402G>T (p.Pro134=)
c.387G>T (p.Pro129=)
n.581G>T
ClinVar gnomAD v4
11g.32434959C=CA1962327237WT1c.402G= (p.Pro134=)
c.387G= (p.Pro129=)
n.581G=
11g.32434959C>GCA473773654WT1c.402G>C (p.Pro134=)
c.387G>C (p.Pro129=)
n.581G>C
dbSNP
11g.32434959C>TCA064893WT1c.402G>A (p.Pro134=)
c.387G>A (p.Pro129=)
n.581G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.32434964_32434965insGGGTGTCGGCGGCA2790963047WT1c.402_403insACACCCCCGCCG (p.Pro134_Pro135insThrProProPro)
c.387_388insACACCCCCGCCG (p.Pro129_Pro130insThrProProPro)
n.581_582insACACCCCCGCCG
11g.32434960G>ACA379965775WT1c.401C>T (p.Pro134Leu)
c.386C>T (p.Pro129Leu)
n.580C>T
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32434960G>CCA379965776WT1c.401C>G (p.Pro134Arg)
c.386C>G (p.Pro129Arg)
n.580C>G
ClinVar dbSNP
11g.32434960G=CA1962327238WT1c.401C= (p.Pro134=)
c.386C= (p.Pro129=)
n.580C=
11g.32434960G>TCA064889WT1c.401C>A (p.Pro134Gln)
c.386C>A (p.Pro129Gln)
n.580C>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.32434965_32434976dupCA2573146228WT1c.390_401dup (p.Pro134_Pro135insProAlaProPro)
c.375_386dup (p.Pro129_Pro130insProAlaProPro)
n.569_580dup
ClinVar dbSNP
11g.32434961G>ACA379965777WT1c.400C>T (p.Pro134Ser)
c.385C>T (p.Pro129Ser)
n.579C>T
ClinVar dbSNP gnomAD v4
11g.32434961G>CCA379965778WT1c.400C>G (p.Pro134Ala)
c.385C>G (p.Pro129Ala)
n.579C>G
11g.32434961G>TCA379965779WT1c.400C>A (p.Pro134Thr)
c.385C>A (p.Pro129Thr)
n.579C>A
gnomAD v4
11g.32434962C>ACA473773661WT1c.399G>T (p.Pro133=)
c.384G>T (p.Pro128=)
n.578G>T
ClinVar dbSNP gnomAD v4
11g.32434962C>GCA473773662WT1c.399G>C (p.Pro133=)
c.384G>C (p.Pro128=)
n.578G>C
dbSNP gnomAD v4
11g.32434962C>TCA473773663WT1c.399G>A (p.Pro133=)
c.384G>A (p.Pro128=)
n.578G>A
gnomAD v4
11g.32434963G>ACA064884WT1c.398C>T (p.Pro133Leu)
c.383C>T (p.Pro128Leu)
n.577C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32434963G>CCA379965780WT1c.398C>G (p.Pro133Arg)
c.383C>G (p.Pro128Arg)
n.577C>G
11g.32434963G=CA1962327239WT1c.398C= (p.Pro133=)
c.383C= (p.Pro128=)
n.577C=
11g.32434963G>TCA379965781WT1c.398C>A (p.Pro133Gln)
c.383C>A (p.Pro128Gln)
n.577C>A
ClinVar
11g.32434964G>ACA379965782WT1c.397C>T (p.Pro133Ser)
c.382C>T (p.Pro128Ser)
n.576C>T
ClinVar dbSNP
11g.32434964G>CCA379965784WT1c.397C>G (p.Pro133Ala)
c.382C>G (p.Pro128Ala)
n.576C>G
11g.32434964G=CA1962327240WT1c.397C= (p.Pro133=)
c.382C= (p.Pro128=)
n.576C=
11g.32434964G>TCA379965783WT1c.397C>A (p.Pro133Thr)
c.382C>A (p.Pro128Thr)
n.576C>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32434965A=CA1962327241WT1c.396T= (p.Ala132=)
c.381T= (p.Ala127=)
n.575T=
11g.32434965A>CCA473773668WT1c.396T>G (p.Ala132=)
c.381T>G (p.Ala127=)
n.575T>G
11g.32434965A>GCA473773666WT1c.396T>C (p.Ala132=)
c.381T>C (p.Ala127=)
n.575T>C
dbSNP gnomAD v4
11g.32434965A>TCA473773667WT1c.396T>A (p.Ala132=)
c.381T>A (p.Ala127=)
n.575T>A
11g.32434966G>ACA379965785WT1c.395C>T (p.Ala132Val)
c.380C>T (p.Ala127Val)
n.574C>T
11g.32434966G>CCA379965786WT1c.395C>G (p.Ala132Gly)
c.380C>G (p.Ala127Gly)
n.574C>G
ClinVar
11g.32434966G>TCA379965787WT1c.395C>A (p.Ala132Asp)
c.380C>A (p.Ala127Asp)
n.574C>A
11g.32434967C>ACA379965788WT1c.394G>T (p.Ala132Ser)
c.379G>T (p.Ala127Ser)
n.573G>T
ClinVar gnomAD v4
11g.32434967C=CA1962327242WT1c.394G= (p.Ala132=)
c.379G= (p.Ala127=)
n.573G=
11g.32434967C>GCA379965789WT1c.394G>C (p.Ala132Pro)
c.379G>C (p.Ala127Pro)
n.573G>C
dbSNP
11g.32434967C>TCA064879WT1c.394G>A (p.Ala132Thr)
c.379G>A (p.Ala127Thr)
n.573G>A
dbSNP ExAC gnomAD v2 gnomAD v4
11g.32434968C>ACA473773678WT1c.393G>T (p.Pro131=)
c.378G>T (p.Pro126=)
n.572G>T
ClinVar dbSNP gnomAD v4
11g.32434968C=CA1962327243WT1c.393G= (p.Pro131=)
c.378G= (p.Pro126=)
n.572G=
11g.32434968C>GCA473773681WT1c.393G>C (p.Pro131=)
c.378G>C (p.Pro126=)
n.572G>C
ClinVar dbSNP
11g.32434968C>TCA473773683WT1c.393G>A (p.Pro131=)
c.378G>A (p.Pro126=)
n.572G>A
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32434969G>ACA379965790WT1c.392C>T (p.Pro131Leu)
c.377C>T (p.Pro126Leu)
n.571C>T
ClinVar dbSNP gnomAD v4
11g.32434969G>CCA379965791WT1c.392C>G (p.Pro131Arg)
c.377C>G (p.Pro126Arg)
n.571C>G
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32434969G=CA1962327244WT1c.392C= (p.Pro131=)
c.377C= (p.Pro126=)
n.571C=
11g.32434969G>TCA379965792WT1c.392C>A (p.Pro131Gln)
c.377C>A (p.Pro126Gln)
n.571C>A
dbSNP gnomAD v4
11g.32434970delCA473773685WT1c.392del (p.Pro131ArgfsTer?)
c.377del (p.Pro126ArgfsTer?)
n.571del
COSMIC
11g.32434970G>ACA219511084WT1c.391C>T (p.Pro131Ser)
c.376C>T (p.Pro126Ser)
n.570C>T
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32434970G>CCA379965793WT1c.391C>G (p.Pro131Ala)
c.376C>G (p.Pro126Ala)
n.570C>G
11g.32434970G=CA1962327245WT1c.391C= (p.Pro131=)
c.376C= (p.Pro126=)
n.570C=
11g.32434970G>TCA219511089WT1c.391C>A (p.Pro131Thr)
c.376C>A (p.Pro126Thr)
n.570C>A
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32434971T>ACA473773688WT1c.390A>T (p.Pro130=)
c.375A>T (p.Pro125=)
n.569A>T
dbSNP
11g.32434971T>CCA10630774WT1c.390A>G (p.Pro130=)
c.375A>G (p.Pro125=)
n.569A>G
ClinVar dbSNP
11g.32434971T>GCA473773690WT1c.390A>C (p.Pro130=)
c.375A>C (p.Pro125=)
n.569A>C
ClinVar dbSNP
11g.32434971T=CA1962327246WT1c.390A= (p.Pro130=)
c.375A= (p.Pro125=)
n.569A=
11g.32434972G>ACA379965796WT1c.389C>T (p.Pro130Leu)
c.374C>T (p.Pro125Leu)
n.568C>T
ClinVar
11g.32434972G>CCA379965794WT1c.389C>G (p.Pro130Arg)
c.374C>G (p.Pro125Arg)
n.568C>G
dbSNP
11g.32434972G>TCA379965795WT1c.389C>A (p.Pro130Gln)
c.374C>A (p.Pro125Gln)
n.568C>A
gnomAD v4
11g.32434974_32434981delCA645584488WT1c.382_389del (p.Ala128ThrfsTer?)
c.367_374del (p.Ala123ThrfsTer?)
n.561_568del
COSMIC COSMIC
11g.32434973G>ACA379965797WT1c.388C>T (p.Pro130Ser)
c.373C>T (p.Pro125Ser)
n.567C>T
ClinVar dbSNP
11g.32434973G>CCA379965798WT1c.388C>G (p.Pro130Ala)
c.373C>G (p.Pro125Ala)
n.567C>G
11g.32434973G=CA1962327247WT1c.388C= (p.Pro130=)
c.373C= (p.Pro125=)
n.567C=
11g.32434973G>TCA379965799WT1c.388C>A (p.Pro130Thr)
c.373C>A (p.Pro125Thr)
n.567C>A
11g.32434974delCA473773701WT1c.387del (p.Pro130HisfsTer?)
c.372del (p.Pro125HisfsTer?)
n.566del
COSMIC
11g.32434974C>ACA473773702WT1c.387G>T (p.Pro129=)
c.372G>T (p.Pro124=)
n.566G>T
ClinVar dbSNP gnomAD v4
11g.32434974C=CA1962327248WT1c.387G= (p.Pro129=)
c.372G= (p.Pro124=)
n.566G=
11g.32434974C>GCA473773704WT1c.387G>C (p.Pro129=)
c.372G>C (p.Pro124=)
n.566G>C
dbSNP
11g.32434974C>TCA473773700WT1c.387G>A (p.Pro129=)
c.372G>A (p.Pro124=)
n.566G>A
dbSNP gnomAD v3 gnomAD v4
11g.32434975G>ACA064875WT1c.386C>T (p.Pro129Leu)
c.371C>T (p.Pro124Leu)
n.565C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32434975G>CCA379965800WT1c.386C>G (p.Pro129Arg)
c.371C>G (p.Pro124Arg)
n.565C>G
11g.32434975G=CA1962327249WT1c.386C= (p.Pro129=)
c.371C= (p.Pro124=)
n.565C=
11g.32434975G>TCA219511099WT1c.386C>A (p.Pro129Gln)
c.371C>A (p.Pro124Gln)
n.565C>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32434976G>ACA379965801WT1c.385C>T (p.Pro129Ser)
c.370C>T (p.Pro124Ser)
n.564C>T
dbSNP gnomAD v4
11g.32434976G>CCA379965802WT1c.385C>G (p.Pro129Ala)
c.370C>G (p.Pro124Ala)
n.564C>G
11g.32434976G>TCA379965803WT1c.385C>A (p.Pro129Thr)
c.370C>A (p.Pro124Thr)
n.564C>A
11g.32434978_32434987delCA2695213677WT1c.376_385del (p.Gly126ArgfsTer?)
c.361_370del (p.Gly121ArgfsTer?)
n.555_564del
11g.32434977C>ACA473773720WT1c.384G>T (p.Ala128=)
c.369G>T (p.Ala123=)
n.563G>T
11g.32434977C>GCA473773716WT1c.384G>C (p.Ala128=)
c.369G>C (p.Ala123=)
n.563G>C
dbSNP gnomAD v4
11g.32434977C>TCA473773718WT1c.384G>A (p.Ala128=)
c.369G>A (p.Ala123=)
n.563G>A
ClinVar dbSNP gnomAD v4
11g.32434978G>ACA379965804WT1c.383C>T (p.Ala128Val)
c.368C>T (p.Ala123Val)
n.562C>T
11g.32434978G>CCA379965805WT1c.383C>G (p.Ala128Gly)
c.368C>G (p.Ala123Gly)
n.562C>G
11g.32434978G=CA1962327250WT1c.383C= (p.Ala128=)
c.368C= (p.Ala123=)
n.562C=
11g.32434978G>TCA379965806WT1c.383C>A (p.Ala128Glu)
c.368C>A (p.Ala123Glu)
n.562C>A
ClinVar dbSNP gnomAD v4
11g.32434979C>ACA379965807WT1c.382G>T (p.Ala128Ser)
c.367G>T (p.Ala123Ser)
n.561G>T
11g.32434979C=CA1962327251WT1c.382G= (p.Ala128=)
c.367G= (p.Ala123=)
n.561G=
11g.32434979C>GCA379965809WT1c.382G>C (p.Ala128Pro)
c.367G>C (p.Ala123Pro)
n.561G>C
dbSNP
11g.32434979C>TCA379965808WT1c.382G>A (p.Ala128Thr)
c.367G>A (p.Ala123Thr)
n.561G>A
ClinVar dbSNP gnomAD v4 COSMIC COSMIC
11g.32434980G>ACA473773723WT1c.381C>T (p.Pro127=)
c.366C>T (p.Pro122=)
n.560C>T
ClinVar dbSNP gnomAD v4
11g.32434980G>CCA064867WT1c.381C>G (p.Pro127=)
c.366C>G (p.Pro122=)
n.560C>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32434980G=CA1962327252WT1c.381C= (p.Pro127=)
c.366C= (p.Pro122=)
n.560C=
11g.32434980G>TCA473773725WT1c.381C>A (p.Pro127=)
c.366C>A (p.Pro122=)
n.560C>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32434983delCA2695201112WT1c.381del (p.Ala128ArgfsTer?)
c.366del (p.Ala123ArgfsTer?)
n.560del
ClinVar
11g.32434981G>ACA379965810WT1c.380C>T (p.Pro127Leu)
c.365C>T (p.Pro122Leu)
n.559C>T
ClinVar gnomAD v4
11g.32434981G>CCA379965811WT1c.380C>G (p.Pro127Arg)
c.365C>G (p.Pro122Arg)
n.559C>G
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32434981G=CA1962327253WT1c.380C= (p.Pro127=)
c.365C= (p.Pro122=)
n.559C=
11g.32434981G>TCA379965812WT1c.380C>A (p.Pro127His)
c.365C>A (p.Pro122His)
n.559C>A
gnomAD v4
11g.32434982G>ACA379965813WT1c.379C>T (p.Pro127Ser)
c.364C>T (p.Pro122Ser)
n.558C>T
ClinVar dbSNP gnomAD v4
11g.32434982G>CCA379965814WT1c.379C>G (p.Pro127Ala)
c.364C>G (p.Pro122Ala)
n.558C>G
11g.32434982G=CA1962327254WT1c.379C= (p.Pro127=)
c.364C= (p.Pro122=)
n.558C=
11g.32434982G>TCA379965815WT1c.379C>A (p.Pro127Thr)
c.364C>A (p.Pro122Thr)
n.558C>A
ClinVar dbSNP gnomAD v4
11g.32434983G>ACA473773732WT1c.378C>T (p.Gly126=)
c.363C>T (p.Gly121=)
n.557C>T
gnomAD v4
11g.32434983G>CCA473773734WT1c.378C>G (p.Gly126=)
c.363C>G (p.Gly121=)
n.557C>G
11g.32434983G>TCA473773736WT1c.378C>A (p.Gly126=)
c.363C>A (p.Gly121=)
n.557C>A
11g.32434984C>ACA379965816WT1c.377G>T (p.Gly126Val)
c.362G>T (p.Gly121Val)
n.556G>T
gnomAD v4
11g.32434984C>GCA379965818WT1c.377G>C (p.Gly126Ala)
c.362G>C (p.Gly121Ala)
n.556G>C
ClinVar dbSNP
11g.32434984C>TCA379965817WT1c.377G>A (p.Gly126Asp)
c.362G>A (p.Gly121Asp)
n.556G>A
ClinVar dbSNP gnomAD v4
11g.32434985C>ACA379965819WT1c.376G>T (p.Gly126Cys)
c.361G>T (p.Gly121Cys)
n.555G>T
ClinVar dbSNP gnomAD v4
11g.32434985C=CA1962327255WT1c.376G= (p.Gly126=)
c.361G= (p.Gly121=)
n.555G=
11g.32434985C>GCA379965820WT1c.376G>C (p.Gly126Arg)
c.361G>C (p.Gly121Arg)
n.555G>C
ClinVar dbSNP gnomAD v4
11g.32434985C>TCA379965821WT1c.376G>A (p.Gly126Ser)
c.361G>A (p.Gly121Ser)
n.555G>A
ClinVar dbSNP gnomAD v4
11g.32434986G>ACA064860WT1c.375C>T (p.Gly125=)
c.360C>T (p.Gly120=)
n.554C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32434986G>CCA473773743WT1c.375C>G (p.Gly125=)
c.360C>G (p.Gly120=)
n.554C>G
dbSNP
11g.32434986G=CA1962327256WT1c.375C= (p.Gly125=)
c.360C= (p.Gly120=)
n.554C=
11g.32434986G>TCA473773745WT1c.375C>A (p.Gly125=)
c.360C>A (p.Gly120=)
n.554C>A
dbSNP gnomAD v4
11g.32434987C>ACA379965824WT1c.374G>T (p.Gly125Val)
c.359G>T (p.Gly120Val)
n.553G>T
11g.32434987C=CA1962327257WT1c.374G= (p.Gly125=)
c.359G= (p.Gly120=)
n.553G=
11g.32434987C>GCA379965822WT1c.374G>C (p.Gly125Ala)
c.359G>C (p.Gly120Ala)
n.553G>C
dbSNP
11g.32434987C>TCA379965823WT1c.374G>A (p.Gly125Asp)
c.359G>A (p.Gly120Asp)
n.553G>A
dbSNP gnomAD v4 COSMIC
11g.32434989delCA2612989553WT1c.374del (p.Gly125AlafsTer?)
c.359del (p.Gly120AlafsTer?)
n.553del
gnomAD v4
11g.32434988C>ACA379965825WT1c.373G>T (p.Gly125Cys)
c.358G>T (p.Gly120Cys)
n.552G>T
11g.32434988C=CA1962327258WT1c.373G= (p.Gly125=)
c.358G= (p.Gly120=)
n.552G=
11g.32434988C>GCA379965826WT1c.373G>C (p.Gly125Arg)
c.358G>C (p.Gly120Arg)
n.552G>C
dbSNP
11g.32434988C>TCA379965827WT1c.373G>A (p.Gly125Ser)
c.358G>A (p.Gly120Ser)
n.552G>A
dbSNP gnomAD v2 gnomAD v4
11g.32434989C>ACA379965828WT1c.372G>T (p.Leu124Phe)
c.357G>T (p.Leu119Phe)
n.551G>T
ClinVar
11g.32434989C>GCA379965829WT1c.372G>C (p.Leu124Phe)
c.357G>C (p.Leu119Phe)
n.551G>C
11g.32434989C>TCA473773753WT1c.372G>A (p.Leu124=)
c.357G>A (p.Leu119=)
n.551G>A
gnomAD v4
11g.32434990A>CCA379965830WT1c.371T>G (p.Leu124Trp)
c.356T>G (p.Leu119Trp)
n.550T>G
dbSNP
11g.32434990A>GCA379965831WT1c.371T>C (p.Leu124Ser)
c.356T>C (p.Leu119Ser)
n.550T>C
11g.32434990A>TCA379965832WT1c.371T>A (p.Leu124Ter)
c.356T>A (p.Leu119Ter)
n.550T>A
11g.32434991A>CCA379965833WT1c.370T>G (p.Leu124Val)
c.355T>G (p.Leu119Val)
n.549T>G
dbSNP
11g.32434991A>GCA473773757WT1c.370T>C (p.Leu124=)
c.355T>C (p.Leu119=)
n.549T>C
ClinVar gnomAD v4
11g.32434991A>TCA379965834WT1c.370T>A (p.Leu124Met)
c.355T>A (p.Leu119Met)
n.549T>A
11g.32434992C>ACA473773759WT1c.369G>T (p.Ser123=)
c.354G>T (p.Ser118=)
n.548G>T
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32434992C=CA1962327259WT1c.369G= (p.Ser123=)
c.354G= (p.Ser118=)
n.548G=
11g.32434992C>GCA473773761WT1c.369G>C (p.Ser123=)
c.354G>C (p.Ser118=)
n.548G>C
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32434992C>TCA473773762WT1c.369G>A (p.Ser123=)
c.354G>A (p.Ser118=)
n.548G>A
ClinVar dbSNP gnomAD v4
11g.32434993G>ACA379965835WT1c.368C>T (p.Ser123Leu)
c.353C>T (p.Ser118Leu)
n.547C>T
ClinVar dbSNP
11g.32434993G>CCA379965836WT1c.368C>G (p.Ser123Trp)
c.353C>G (p.Ser118Trp)
n.547C>G
dbSNP
11g.32434993G>TCA379965837WT1c.368C>A (p.Ser123Ter)
c.353C>A (p.Ser118Ter)
n.547C>A
ClinVar gnomAD v4
11g.32434994A>CCA379965838WT1c.367T>G (p.Ser123Ala)
c.352T>G (p.Ser118Ala)
n.546T>G
ClinVar dbSNP COSMIC COSMIC
11g.32434994A>GCA379965840WT1c.367T>C (p.Ser123Pro)
c.352T>C (p.Ser118Pro)
n.546T>C
dbSNP
11g.32434994A>TCA379965839WT1c.367T>A (p.Ser123Thr)
c.352T>A (p.Ser118Thr)
n.546T>A
11g.32434995C>ACA473773767WT1c.366G>T (p.Gly122=)
c.351G>T (p.Gly117=)
n.545G>T
ClinVar gnomAD v4
11g.32434995C=CA1962327260WT1c.366G= (p.Gly122=)
c.351G= (p.Gly117=)
n.545G=
11g.32434995C>GCA473773770WT1c.366G>C (p.Gly122=)
c.351G>C (p.Gly117=)
n.545G>C
dbSNP
11g.32434995C>TCA473773768WT1c.366G>A (p.Gly122=)
c.351G>A (p.Gly117=)
n.545G>A
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32434996C>ACA379965841WT1c.365G>T (p.Gly122Val)
c.350G>T (p.Gly117Val)
n.544G>T
gnomAD v4
11g.32434996C>GCA379965842WT1c.365G>C (p.Gly122Ala)
c.350G>C (p.Gly117Ala)
n.544G>C
11g.32434996C>TCA379965843WT1c.365G>A (p.Gly122Glu)
c.350G>A (p.Gly117Glu)
n.544G>A
gnomAD v4
11g.32434997C>ACA379965844WT1c.364G>T (p.Gly122Trp)
c.349G>T (p.Gly117Trp)
n.543G>T
gnomAD v4
11g.32434997C>GCA379965845WT1c.364G>C (p.Gly122Arg)
c.349G>C (p.Gly117Arg)
n.543G>C
gnomAD v4
11g.32434997C>TCA379965846WT1c.364G>A (p.Gly122Arg)
c.349G>A (p.Gly117Arg)
n.543G>A
gnomAD v4
11g.32434998G>ACA219511101WT1c.363C>T (p.Tyr121=)
c.348C>T (p.Tyr116=)
n.542C>T
ClinVar dbSNP gnomAD v4
11g.32434998G>CCA379965847WT1c.363C>G (p.Tyr121Ter)
c.348C>G (p.Tyr116Ter)
n.542C>G
dbSNP gnomAD v4 COSMIC
11g.32434998G=CA1962327261WT1c.363C= (p.Tyr121=)
c.348C= (p.Tyr116=)
n.542C=
11g.32434998G>TCA379965848WT1c.363C>A (p.Tyr121Ter)
c.348C>A (p.Tyr116Ter)
n.542C>A
ClinVar gnomAD v4 COSMIC
11g.32434999T>ACA379965849WT1c.362A>T (p.Tyr121Phe)
c.347A>T (p.Tyr116Phe)
n.541A>T
11g.32434999T>CCA379965850WT1c.362A>G (p.Tyr121Cys)
c.347A>G (p.Tyr116Cys)
n.541A>G
dbSNP
11g.32434999T>GCA379965851WT1c.362A>C (p.Tyr121Ser)
c.347A>C (p.Tyr116Ser)
n.541A>C
dbSNP
11g.32434999T=CA1962327262WT1c.362A= (p.Tyr121=)
c.347A= (p.Tyr116=)
n.541A=
11g.32435000A=CA1962327263WT1c.361T= (p.Tyr121=)
c.346T= (p.Tyr116=)
n.540T=
11g.32435000A>CCA219511102WT1c.361T>G (p.Tyr121Asp)
c.346T>G (p.Tyr116Asp)
n.540T>G
dbSNP
11g.32435000A>GCA379965853WT1c.361T>C (p.Tyr121His)
c.346T>C (p.Tyr116His)
n.540T>C
gnomAD v4
11g.32435000A>TCA379965852WT1c.361T>A (p.Tyr121Asn)
c.346T>A (p.Tyr116Asn)
n.540T>A
11g.32435001A>CCA473773778WT1c.360T>G (p.Ala120=)
c.345T>G (p.Ala115=)
n.539T>G
11g.32435001A>GCA473773779WT1c.360T>C (p.Ala120=)
c.345T>C (p.Ala115=)
n.539T>C
11g.32435001A>TCA473773780WT1c.360T>A (p.Ala120=)
c.345T>A (p.Ala115=)
n.539T>A
11g.32435002G>ACA379965854WT1c.359C>T (p.Ala120Val)
c.344C>T (p.Ala115Val)
n.538C>T
gnomAD v4
11g.32435002G>CCA379965855WT1c.359C>G (p.Ala120Gly)
c.344C>G (p.Ala115Gly)
n.538C>G
dbSNP
11g.32435002G>TCA379965856WT1c.359C>A (p.Ala120Asp)
c.344C>A (p.Ala115Asp)
n.538C>A
gnomAD v4
11g.32435003C>ACA379965857WT1c.358G>T (p.Ala120Ser)
c.343G>T (p.Ala115Ser)
n.537G>T
11g.32435003C=CA1962327264WT1c.358G= (p.Ala120=)
c.343G= (p.Ala115=)
n.537G=
11g.32435003C>GCA379965858WT1c.358G>C (p.Ala120Pro)
c.343G>C (p.Ala115Pro)
n.537G>C
dbSNP
11g.32435003C>TCA379965859WT1c.358G>A (p.Ala120Thr)
c.343G>A (p.Ala115Thr)
n.537G>A
ClinVar dbSNP gnomAD v4
11g.32435004C>ACA473773786WT1c.357G>T (p.Ser119=)
c.342G>T (p.Ser114=)
n.536G>T
ClinVar gnomAD v4
11g.32435004C=CA1962327265WT1c.357G= (p.Ser119=)
c.342G= (p.Ser114=)
n.536G=
11g.32435004C>GCA473773787WT1c.357G>C (p.Ser119=)
c.342G>C (p.Ser114=)
n.536G>C
dbSNP gnomAD v4
11g.32435004C>TCA473773788WT1c.357G>A (p.Ser119=)
c.342G>A (p.Ser114=)
n.536G>A
gnomAD v4
11g.32435005G>ACA379965860WT1c.356C>T (p.Ser119Leu)
c.341C>T (p.Ser114Leu)
n.535C>T
ClinVar gnomAD v4
11g.32435005G>CCA379965861WT1c.356C>G (p.Ser119Trp)
c.341C>G (p.Ser114Trp)
n.535C>G
ClinVar dbSNP
11g.32435005G=CA1962327266WT1c.356C= (p.Ser119=)
c.341C= (p.Ser114=)
n.535C=
11g.32435005G>TCA379965862WT1c.356C>A (p.Ser119Ter)
c.341C>A (p.Ser114Ter)
n.535C>A
COSMIC
11g.32435006A=CA1962327267WT1c.355T= (p.Ser119=)
c.340T= (p.Ser114=)
n.534T=
11g.32435006A>CCA379965863WT1c.355T>G (p.Ser119Ala)
c.340T>G (p.Ser114Ala)
n.534T>G
11g.32435006A>GCA379965864WT1c.355T>C (p.Ser119Pro)
c.340T>C (p.Ser114Pro)
n.534T>C
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435006A>TCA379965865WT1c.355T>A (p.Ser119Thr)
c.340T>A (p.Ser114Thr)
n.534T>A
gnomAD v4
11g.32435007A>CCA473773795WT1c.354T>G (p.Ala118=)
c.339T>G (p.Ala113=)
n.533T>G
dbSNP
11g.32435007A>GCA473773794WT1c.354T>C (p.Ala118=)
c.339T>C (p.Ala113=)
n.533T>C
dbSNP gnomAD v4
11g.32435007A>TCA473773793WT1c.354T>A (p.Ala118=)
c.339T>A (p.Ala113=)
n.533T>A
dbSNP
11g.32435008G>ACA064850WT1c.353C>T (p.Ala118Val)
c.338C>T (p.Ala113Val)
n.532C>T
dbSNP ExAC gnomAD v2 gnomAD v4
11g.32435008G>CCA379965867WT1c.353C>G (p.Ala118Gly)
c.338C>G (p.Ala113Gly)
n.532C>G
11g.32435008G=CA1962327268WT1c.353C= (p.Ala118=)
c.338C= (p.Ala113=)
n.532C=
11g.32435008G>TCA379965866WT1c.353C>A (p.Ala118Asp)
c.338C>A (p.Ala113Asp)
n.532C>A
gnomAD v4
11g.32435009C>ACA379965868WT1c.352G>T (p.Ala118Ser)
c.337G>T (p.Ala113Ser)
n.531G>T
gnomAD v4
11g.32435009C=CA1962327269WT1c.352G= (p.Ala118=)
c.337G= (p.Ala113=)
n.531G=
11g.32435009C>GCA379965870WT1c.352G>C (p.Ala118Pro)
c.337G>C (p.Ala113Pro)
n.531G>C
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32435009C>TCA379965869WT1c.352G>A (p.Ala118Thr)
c.337G>A (p.Ala113Thr)
n.531G>A
ClinVar dbSNP gnomAD v4
11g.32435010G>ACA473773799WT1c.351C>T (p.Gly117=)
c.336C>T (p.Gly112=)
n.530C>T
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435010G>CCA473773798WT1c.351C>G (p.Gly117=)
c.336C>G (p.Gly112=)
n.530C>G
11g.32435010G=CA1962327270WT1c.351C= (p.Gly117=)
c.336C= (p.Gly112=)
n.530C=
11g.32435010G>TCA473773797WT1c.351C>A (p.Gly117=)
c.336C>A (p.Gly112=)
n.530C>A
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32435011C>ACA379965871WT1c.350G>T (p.Gly117Val)
c.335G>T (p.Gly112Val)
n.529G>T
11g.32435011C=CA1962327271WT1c.350G= (p.Gly117=)
c.335G= (p.Gly112=)
n.529G=
11g.32435011C>GCA379965872WT1c.350G>C (p.Gly117Ala)
c.335G>C (p.Gly112Ala)
n.529G>C
dbSNP
11g.32435011C>TCA219511109WT1c.350G>A (p.Gly117Asp)
c.335G>A (p.Gly112Asp)
n.529G>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
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

Number of alleles fetched