Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.32434878_32434911delCA645584483WT1c.453_486del (p.Trp151Ter)
c.438_471del (p.Trp146Ter)
n.632_665del
COSMIC
11g.32434881C>ACA379964936WT1c.480G>T (p.Gln160His)
c.465G>T (p.Gln155His)
n.659G>T
11g.32434881C=CA1962327183WT1c.480G= (p.Gln160=)
c.465G= (p.Gln155=)
n.659G=
11g.32434881C>GCA379964937WT1c.480G>C (p.Gln160His)
c.465G>C (p.Gln155His)
n.659G>C
ClinVar dbSNP gnomAD v4
11g.32434881C>TCA064974WT1c.480G>A (p.Gln160=)
c.465G>A (p.Gln155=)
n.659G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32434882T>ACA379964940WT1c.479A>T (p.Gln160Leu)
c.464A>T (p.Gln155Leu)
n.658A>T
11g.32434882T>CCA379964941WT1c.479A>G (p.Gln160Arg)
c.464A>G (p.Gln155Arg)
n.658A>G
11g.32434882T>GCA379964943WT1c.479A>C (p.Gln160Pro)
c.464A>C (p.Gln155Pro)
n.658A>C
11g.32434883delCA473571694WT1c.478del (p.Gln160SerfsTer3)
c.463del (p.Gln155SerfsTer3)
n.657del
COSMIC
11g.32434883G>ACA379964944WT1c.478C>T (p.Gln160Ter)
c.463C>T (p.Gln155Ter)
n.657C>T
ClinVar dbSNP
11g.32434883G>CCA379964946WT1c.478C>G (p.Gln160Glu)
c.463C>G (p.Gln155Glu)
n.657C>G
ClinVar dbSNP
11g.32434883G=CA1962327184WT1c.478C= (p.Gln160=)
c.463C= (p.Gln155=)
n.657C=
11g.32434883G>TCA379964948WT1c.478C>A (p.Gln160Lys)
c.463C>A (p.Gln155Lys)
n.657C>A
11g.32434884C>ACA379964949WT1c.477G>T (p.Glu159Asp)
c.462G>T (p.Glu154Asp)
n.656G>T
11g.32434884C>GCA379964951WT1c.477G>C (p.Glu159Asp)
c.462G>C (p.Glu154Asp)
n.656G>C
ClinVar dbSNP
11g.32434884C>TCA473571698WT1c.477G>A (p.Glu159=)
c.462G>A (p.Glu154=)
n.656G>A
ClinVar dbSNP
11g.32434885T>ACA379964952WT1c.476A>T (p.Glu159Val)
c.461A>T (p.Glu154Val)
n.655A>T
11g.32434885T>CCA379964956WT1c.476A>G (p.Glu159Gly)
c.461A>G (p.Glu154Gly)
n.655A>G
ClinVar dbSNP
11g.32434885T>GCA379964954WT1c.476A>C (p.Glu159Ala)
c.461A>C (p.Glu154Ala)
n.655A>C
11g.32434885T=CA1962327185WT1c.476A= (p.Glu159=)
c.461A= (p.Glu154=)
n.655A=
11g.32434886C>ACA379964958WT1c.475G>T (p.Glu159Ter)
c.460G>T (p.Glu154Ter)
n.654G>T
11g.32434886C=CA1962327186WT1c.475G= (p.Glu159=)
c.460G= (p.Glu154=)
n.654G=
11g.32434886C>GCA379964959WT1c.475G>C (p.Glu159Gln)
c.460G>C (p.Glu154Gln)
n.654G>C
11g.32434886C>TCA064967WT1c.475G>A (p.Glu159Lys)
c.460G>A (p.Glu154Lys)
n.654G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32434887delCA2695213675WT1c.475del (p.Glu159SerfsTer4)
c.460del (p.Glu154SerfsTer4)
n.654del
11g.32434888_32434909delCA645584484WT1c.454_475del (p.Gly152SerfsTer4)
c.439_460del (p.Gly147SerfsTer4)
n.633_654del
COSMIC COSMIC
11g.32434887C>ACA379964962WT1c.474G>T (p.Glu158Asp)
c.459G>T (p.Glu153Asp)
n.653G>T
11g.32434887C=CA1962327187WT1c.474G= (p.Glu158=)
c.459G= (p.Glu153=)
n.653G=
11g.32434887C>GCA379964963WT1c.474G>C (p.Glu158Asp)
c.459G>C (p.Glu153Asp)
n.653G>C
dbSNP gnomAD v3 gnomAD v4
11g.32434887C>TCA219510972WT1c.474G>A (p.Glu158=)
c.459G>A (p.Glu153=)
n.653G>A
ClinVar dbSNP gnomAD v4
11g.32434888T>ACA379964965WT1c.473A>T (p.Glu158Val)
c.458A>T (p.Glu153Val)
n.652A>T
11g.32434888T>CCA379964966WT1c.473A>G (p.Glu158Gly)
c.458A>G (p.Glu153Gly)
n.652A>G
11g.32434888T>GCA379964968WT1c.473A>C (p.Glu158Ala)
c.458A>C (p.Glu153Ala)
n.652A>C
11g.32434889C>ACA379964969WT1c.472G>T (p.Glu158Ter)
c.457G>T (p.Glu153Ter)
n.651G>T
ClinVar dbSNP
11g.32434889C=CA1962327188WT1c.472G= (p.Glu158=)
c.457G= (p.Glu153=)
n.651G=
11g.32434889C>GCA379964971WT1c.472G>C (p.Glu158Gln)
c.457G>C (p.Glu153Gln)
n.651G>C
ClinVar dbSNP
11g.32434889C>TCA379964973WT1c.472G>A (p.Glu158Lys)
c.457G>A (p.Glu153Lys)
n.651G>A
ClinVar dbSNP gnomAD v4 COSMIC COSMIC
11g.32434890G>ACA064961WT1c.471C>T (p.His157=)
c.456C>T (p.His152=)
n.650C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC
11g.32434890G>CCA379964975WT1c.471C>G (p.His157Gln)
c.456C>G (p.His152Gln)
n.650C>G
ClinVar dbSNP gnomAD v4
11g.32434890G=CA1962327189WT1c.471C= (p.His157=)
c.456C= (p.His152=)
n.650C=
11g.32434890G>TCA379964974WT1c.471C>A (p.His157Gln)
c.456C>A (p.His152Gln)
n.650C>A
ClinVar dbSNP gnomAD v4
11g.32434891T>ACA379964976WT1c.470A>T (p.His157Leu)
c.455A>T (p.His152Leu)
n.649A>T
dbSNP
11g.32434891T>CCA379964977WT1c.470A>G (p.His157Arg)
c.455A>G (p.His152Arg)
n.649A>G
dbSNP
11g.32434891T>GCA379964979WT1c.470A>C (p.His157Pro)
c.455A>C (p.His152Pro)
n.649A>C
dbSNP
11g.32434892G>ACA379964981WT1c.469C>T (p.His157Tyr)
c.454C>T (p.His152Tyr)
n.648C>T
11g.32434892G>CCA379964983WT1c.469C>G (p.His157Asp)
c.454C>G (p.His152Asp)
n.648C>G
11g.32434892G>TCA379964986WT1c.469C>A (p.His157Asn)
c.454C>A (p.His152Asn)
n.648C>A
gnomAD v4
11g.32434893C>ACA16613331WT1c.468G>T (p.Pro156=)
c.453G>T (p.Pro151=)
n.647G>T
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32434893C=CA1962327190WT1c.468G= (p.Pro156=)
c.453G= (p.Pro151=)
n.647G=
11g.32434893C>GCA473571721WT1c.468G>C (p.Pro156=)
c.453G>C (p.Pro151=)
n.647G>C
gnomAD v4
11g.32434893C>TCA473571723WT1c.468G>A (p.Pro156=)
c.453G>A (p.Pro151=)
n.647G>A
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32434894G>ACA379964988WT1c.467C>T (p.Pro156Leu)
c.452C>T (p.Pro151Leu)
n.646C>T
ClinVar dbSNP gnomAD v4
11g.32434894G>CCA379964989WT1c.467C>G (p.Pro156Arg)
c.452C>G (p.Pro151Arg)
n.646C>G
11g.32434894G=CA1962327191WT1c.467C= (p.Pro156=)
c.452C= (p.Pro151=)
n.646C=
11g.32434894G>TCA379964991WT1c.467C>A (p.Pro156Gln)
c.452C>A (p.Pro151Gln)
n.646C>A
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32434895G>ACA379964993WT1c.466C>T (p.Pro156Ser)
c.451C>T (p.Pro151Ser)
n.645C>T
ClinVar dbSNP gnomAD v4
11g.32434895G>CCA379964995WT1c.466C>G (p.Pro156Ala)
c.451C>G (p.Pro151Ala)
n.645C>G
11g.32434895G=CA1962327192WT1c.466C= (p.Pro156=)
c.451C= (p.Pro151=)
n.645C=
11g.32434895G>TCA379964996WT1c.466C>A (p.Pro156Thr)
c.451C>A (p.Pro151Thr)
n.645C>A
gnomAD v4
11g.32434896C>ACA379965000WT1c.465G>T (p.Glu155Asp)
c.450G>T (p.Glu150Asp)
n.644G>T
11g.32434896C=CA1962327193WT1c.465G= (p.Glu155=)
c.450G= (p.Glu150=)
n.644G=
11g.32434896C>GCA379964998WT1c.465G>C (p.Glu155Asp)
c.450G>C (p.Glu150Asp)
n.644G>C
11g.32434896C>TCA473571731WT1c.465G>A (p.Glu155=)
c.450G>A (p.Glu150=)
n.644G>A
ClinVar dbSNP gnomAD v4
11g.32434897T>ACA379965001WT1c.464A>T (p.Glu155Val)
c.449A>T (p.Glu150Val)
n.643A>T
11g.32434897T>CCA379965004WT1c.464A>G (p.Glu155Gly)
c.449A>G (p.Glu150Gly)
n.643A>G
dbSNP
11g.32434897T>GCA379965003WT1c.464A>C (p.Glu155Ala)
c.449A>C (p.Glu150Ala)
n.643A>C
11g.32434898C>ACA379965006WT1c.463G>T (p.Glu155Ter)
c.448G>T (p.Glu150Ter)
n.642G>T
11g.32434898C=CA1962327194WT1c.463G= (p.Glu155=)
c.448G= (p.Glu150=)
n.642G=
11g.32434898C>GCA379965011WT1c.463G>C (p.Glu155Gln)
c.448G>C (p.Glu150Gln)
n.642G>C
11g.32434898C>TCA379965008WT1c.463G>A (p.Glu155Lys)
c.448G>A (p.Glu150Lys)
n.642G>A
ClinVar dbSNP
11g.32434899C>ACA473571737WT1c.462G>T (p.Ala154=)
c.447G>T (p.Ala149=)
n.641G>T
11g.32434899C>GCA473571738WT1c.462G>C (p.Ala154=)
c.447G>C (p.Ala149=)
n.641G>C
11g.32434899C>TCA473571739WT1c.462G>A (p.Ala154=)
c.447G>A (p.Ala149=)
n.641G>A
ClinVar dbSNP gnomAD v4
11g.32434902_32434903delCA2723464976WT1c.461_462del (p.Ala154GlyfsTer?)
c.446_447del (p.Ala149GlyfsTer?)
n.640_641del
dbSNP
11g.32434900G>ACA379965013WT1c.461C>T (p.Ala154Val)
c.446C>T (p.Ala149Val)
n.640C>T
ClinVar dbSNP gnomAD v4
11g.32434900G>CCA379965015WT1c.461C>G (p.Ala154Gly)
c.446C>G (p.Ala149Gly)
n.640C>G
dbSNP
11g.32434900G>TCA379965014WT1c.461C>A (p.Ala154Glu)
c.446C>A (p.Ala149Glu)
n.640C>A
11g.32434901C>ACA379965018WT1c.460G>T (p.Ala154Ser)
c.445G>T (p.Ala149Ser)
n.639G>T
gnomAD v4
11g.32434901C>GCA379965019WT1c.460G>C (p.Ala154Pro)
c.445G>C (p.Ala149Pro)
n.639G>C
11g.32434901C>TCA379965021WT1c.460G>A (p.Ala154Thr)
c.445G>A (p.Ala149Thr)
n.639G>A
ClinVar dbSNP gnomAD v4 COSMIC COSMIC
11g.32434902G>ACA473571744WT1c.459C>T (p.Gly153=)
c.444C>T (p.Gly148=)
n.638C>T
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32434902G>CCA473571747WT1c.459C>G (p.Gly153=)
c.444C>G (p.Gly148=)
n.638C>G
11g.32434902G=CA1962327195WT1c.459C= (p.Gly153=)
c.444C= (p.Gly148=)
n.638C=
11g.32434902G>TCA473571745WT1c.459C>A (p.Gly153=)
c.444C>A (p.Gly148=)
n.638C>A
11g.32434903C>ACA379965022WT1c.458G>T (p.Gly153Val)
c.443G>T (p.Gly148Val)
n.637G>T
11g.32434903C>GCA379965024WT1c.458G>C (p.Gly153Ala)
c.443G>C (p.Gly148Ala)
n.637G>C
11g.32434903C>TCA379965025WT1c.458G>A (p.Gly153Asp)
c.443G>A (p.Gly148Asp)
n.637G>A
11g.32434904C>ACA379965027WT1c.457G>T (p.Gly153Cys)
c.442G>T (p.Gly148Cys)
n.636G>T
gnomAD v4
11g.32434904C>GCA379965029WT1c.457G>C (p.Gly153Arg)
c.442G>C (p.Gly148Arg)
n.636G>C
11g.32434904C>TCA379965030WT1c.457G>A (p.Gly153Ser)
c.442G>A (p.Gly148Ser)
n.636G>A
gnomAD v4
11g.32434905G>ACA473571755WT1c.456C>T (p.Gly152=)
c.441C>T (p.Gly147=)
n.635C>T
ClinVar dbSNP COSMIC COSMIC
11g.32434905G>CCA473571756WT1c.456C>G (p.Gly152=)
c.441C>G (p.Gly147=)
n.635C>G
11g.32434905G>TCA473571758WT1c.456C>A (p.Gly152=)
c.441C>A (p.Gly147=)
n.635C>A
ClinVar dbSNP gnomAD v4
11g.32434906C>ACA379965032WT1c.455G>T (p.Gly152Val)
c.440G>T (p.Gly147Val)
n.634G>T
11g.32434906C=CA1962327196WT1c.455G= (p.Gly152=)
c.440G= (p.Gly147=)
n.634G=
11g.32434906C>GCA379965034WT1c.455G>C (p.Gly152Ala)
c.440G>C (p.Gly147Ala)
n.634G>C
11g.32434906C>TCA379965035WT1c.455G>A (p.Gly152Asp)
c.440G>A (p.Gly147Asp)
n.634G>A
ClinVar dbSNP
11g.32434909delCA2499220922WT1c.455del (p.Gly152AlafsTer11)
c.440del (p.Gly147AlafsTer11)
n.634del
ClinVar dbSNP
11g.32434907C>ACA379965037WT1c.454G>T (p.Gly152Cys)
c.439G>T (p.Gly147Cys)
n.633G>T
dbSNP
11g.32434907C=CA1962327197WT1c.454G= (p.Gly152=)
c.439G= (p.Gly147=)
n.633G=
11g.32434907C>GCA379965040WT1c.454G>C (p.Gly152Arg)
c.439G>C (p.Gly147Arg)
n.633G>C
11g.32434907C>TCA379965038WT1c.454G>A (p.Gly152Ser)
c.439G>A (p.Gly147Ser)
n.633G>A
gnomAD v4
11g.32434908C>ACA379965042WT1c.453G>T (p.Trp151Cys)
c.438G>T (p.Trp146Cys)
n.632G>T
dbSNP gnomAD v2 gnomAD v4
11g.32434908C=CA1962327198WT1c.453G= (p.Trp151=)
c.438G= (p.Trp146=)
n.632G=
11g.32434908C>GCA379965044WT1c.453G>C (p.Trp151Cys)
c.438G>C (p.Trp146Cys)
n.632G>C
11g.32434908C>TCA379965045WT1c.453G>A (p.Trp151Ter)
c.438G>A (p.Trp146Ter)
n.632G>A
ClinVar
11g.32434909C>ACA379965047WT1c.452G>T (p.Trp151Leu)
c.437G>T (p.Trp146Leu)
n.631G>T
gnomAD v4
11g.32434909C>GCA379965048WT1c.452G>C (p.Trp151Ser)
c.437G>C (p.Trp146Ser)
n.631G>C
11g.32434909C>TCA379965050WT1c.452G>A (p.Trp151Ter)
c.437G>A (p.Trp146Ter)
n.631G>A
11g.32434909_32434913delinsCAGCTCA1962327199WT1c.448_452delinsAGCTG (p.Ser150=)
c.433_437delinsAGCTG (p.Ser145=)
n.627_631delinsAGCTG
11g.32434910A=CA1962327200WT1c.451T= (p.Trp151=)
c.436T= (p.Trp146=)
n.630T=
11g.32434910A>CCA379965052WT1c.451T>G (p.Trp151Gly)
c.436T>G (p.Trp146Gly)
n.630T>G
ClinVar
11g.32434910A>GCA379965053WT1c.451T>C (p.Trp151Arg)
c.436T>C (p.Trp146Arg)
n.630T>C
11g.32434910A>TCA379965055WT1c.451T>A (p.Trp151Arg)
c.436T>A (p.Trp146Arg)
n.630T>A
ClinVar dbSNP
11g.32434910_32434913delCA598513625WT1c.448_451del (p.Ser150GlyfsTer12)
c.433_436del (p.Ser145GlyfsTer12)
n.627_630del
dbSNP gnomAD v2 gnomAD v4
11g.32434911G>ACA473571771WT1c.450C>T (p.Ser150=)
c.435C>T (p.Ser145=)
n.629C>T
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32434911G>CCA379965057WT1c.450C>G (p.Ser150Arg)
c.435C>G (p.Ser145Arg)
n.629C>G
dbSNP gnomAD v2 gnomAD v4
11g.32434911G=CA1962327201WT1c.450C= (p.Ser150=)
c.435C= (p.Ser145=)
n.629C=
11g.32434911G>TCA379965058WT1c.450C>A (p.Ser150Arg)
c.435C>A (p.Ser145Arg)
n.629C>A
ClinVar dbSNP
11g.32434912C>ACA379965060WT1c.449G>T (p.Ser150Ile)
c.434G>T (p.Ser145Ile)
n.628G>T
ClinVar
11g.32434912C=CA1962327202WT1c.449G= (p.Ser150=)
c.434G= (p.Ser145=)
n.628G=
11g.32434912C>GCA379965061WT1c.449G>C (p.Ser150Thr)
c.434G>C (p.Ser145Thr)
n.628G>C
11g.32434912C>TCA379965063WT1c.449G>A (p.Ser150Asn)
c.434G>A (p.Ser145Asn)
n.628G>A
ClinVar dbSNP gnomAD v4
11g.32434913T>ACA379965065WT1c.448A>T (p.Ser150Cys)
c.433A>T (p.Ser145Cys)
n.627A>T
dbSNP
11g.32434913T>CCA379965066WT1c.448A>G (p.Ser150Gly)
c.433A>G (p.Ser145Gly)
n.627A>G
ClinVar dbSNP gnomAD v4
11g.32434913T>GCA379965068WT1c.448A>C (p.Ser150Arg)
c.433A>C (p.Ser145Arg)
n.627A>C
11g.32434913T=CA1962327203WT1c.448A= (p.Ser150=)
c.433A= (p.Ser145=)
n.627A=
11g.32434914C>ACA219510988WT1c.447G>T (p.Pro149=)
c.432G>T (p.Pro144=)
n.626G>T
dbSNP gnomAD v4
11g.32434914C=CA1962327204WT1c.447G= (p.Pro149=)
c.432G= (p.Pro144=)
n.626G=
11g.32434914C>GCA473571783WT1c.447G>C (p.Pro149=)
c.432G>C (p.Pro144=)
n.626G>C
11g.32434914C>TCA473571785WT1c.447G>A (p.Pro149=)
c.432G>A (p.Pro144=)
n.626G>A
ClinVar
11g.32434915G>ACA379965070WT1c.446C>T (p.Pro149Leu)
c.431C>T (p.Pro144Leu)
n.625C>T
11g.32434915G>CCA379965071WT1c.446C>G (p.Pro149Arg)
c.431C>G (p.Pro144Arg)
n.625C>G
ClinVar dbSNP gnomAD v4
11g.32434915G=CA1962327205WT1c.446C= (p.Pro149=)
c.431C= (p.Pro144=)
n.625C=
11g.32434915G>TCA379965073WT1c.446C>A (p.Pro149Gln)
c.431C>A (p.Pro144Gln)
n.625C>A
ClinVar dbSNP gnomAD v4
11g.32434916G>ACA379965074WT1c.445C>T (p.Pro149Ser)
c.430C>T (p.Pro144Ser)
n.624C>T
ClinVar dbSNP
11g.32434916G>CCA379965076WT1c.445C>G (p.Pro149Ala)
c.430C>G (p.Pro144Ala)
n.624C>G
11g.32434916G=CA1962327206WT1c.445C= (p.Pro149=)
c.430C= (p.Pro144=)
n.624C=
11g.32434916G>TCA379965078WT1c.445C>A (p.Pro149Thr)
c.430C>A (p.Pro144Thr)
n.624C>A
gnomAD v4
11g.32434917C>ACA379965082WT1c.444G>T (p.Glu148Asp)
c.429G>T (p.Glu143Asp)
n.623G>T
gnomAD v4
11g.32434917C=CA1962327207WT1c.444G= (p.Glu148=)
c.429G= (p.Glu143=)
n.623G=
11g.32434917C>GCA379965080WT1c.444G>C (p.Glu148Asp)
c.429G>C (p.Glu143Asp)
n.623G>C
11g.32434917C>TCA064949WT1c.444G>A (p.Glu148=)
c.429G>A (p.Glu143=)
n.623G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
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

Number of alleles fetched