Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.32434833delCA473571504WT1c.528del (p.Ala177ProfsTer?)
c.513del (p.Ala172ProfsTer?)
n.707del
 COSMIC
11g.32434833T>ACA473571507WT1c.528A>T (p.Thr176=)
c.513A>T (p.Thr171=)
n.707A>T
11g.32434833T>CCA473571501WT1c.528A>G (p.Thr176=)
c.513A>G (p.Thr171=)
n.707A>G
 dbSNP gnomAD v2 gnomAD v4
11g.32434833T>GCA473571506WT1c.528A>C (p.Thr176=)
c.513A>C (p.Thr171=)
n.707A>C
11g.32434833T=CA1962327161WT1c.528A= (p.Thr176=)
c.513A= (p.Thr171=)
n.707A=
11g.32434834G>ACA379964768WT1c.527C>T (p.Thr176Ile)
c.512C>T (p.Thr171Ile)
n.706C>T
 ClinVar dbSNP gnomAD v4
11g.32434834G>CCA379964769WT1c.527C>G (p.Thr176Arg)
c.512C>G (p.Thr171Arg)
n.706C>G
 gnomAD v4
11g.32434834G=CA1962327162WT1c.527C= (p.Thr176=)
c.512C= (p.Thr171=)
n.706C=
11g.32434834G>TCA379964771WT1c.527C>A (p.Thr176Lys)
c.512C>A (p.Thr171Lys)
n.706C>A
11g.32434835T>ACA379964773WT1c.526A>T (p.Thr176Ser)
c.511A>T (p.Thr171Ser)
n.705A>T
 dbSNP
11g.32434835T>CCA379964774WT1c.526A>G (p.Thr176Ala)
c.511A>G (p.Thr171Ala)
n.705A>G
11g.32434835T>GCA379964776WT1c.526A>C (p.Thr176Pro)
c.511A>C (p.Thr171Pro)
n.705A>C
 dbSNP
11g.32434836G>ACA473571523WT1c.525C>T (p.Gly175=)
c.510C>T (p.Gly170=)
n.704C>T
 gnomAD v4 COSMIC COSMIC
11g.32434836G>CCA473571524WT1c.525C>G (p.Gly175=)
c.510C>G (p.Gly170=)
n.704C>G
 COSMIC COSMIC
11g.32434836G>TCA473571526WT1c.525C>A (p.Gly175=)
c.510C>A (p.Gly170=)
n.704C>A
 gnomAD v4
11g.32434837C>ACA379964777WT1c.524G>T (p.Gly175Val)
c.509G>T (p.Gly170Val)
n.703G>T
11g.32434837C=CA1962327163WT1c.524G= (p.Gly175=)
c.509G= (p.Gly170=)
n.703G=
11g.32434837C>GCA379964779WT1c.524G>C (p.Gly175Ala)
c.509G>C (p.Gly170Ala)
n.703G>C
11g.32434837C>TCA379964781WT1c.524G>A (p.Gly175Asp)
c.509G>A (p.Gly170Asp)
n.703G>A
 ClinVar dbSNP gnomAD v4
11g.32434838C>ACA379964782WT1c.523G>T (p.Gly175Cys)
c.508G>T (p.Gly170Cys)
n.702G>T
 ClinVar dbSNP
11g.32434838C=CA1962327164WT1c.523G= (p.Gly175=)
c.508G= (p.Gly170=)
n.702G=
11g.32434838C>GCA379964783WT1c.523G>C (p.Gly175Arg)
c.508G>C (p.Gly170Arg)
n.702G>C
11g.32434838C>TCA379964784WT1c.523G>A (p.Gly175Ser)
c.508G>A (p.Gly170Ser)
n.702G>A
11g.32434839A=CA1962327165WT1c.522T= (p.Thr174=)
c.507T= (p.Thr169=)
n.701T=
11g.32434839A>CCA473571533WT1c.522T>G (p.Thr174=)
c.507T>G (p.Thr169=)
n.701T>G
 ClinVar
11g.32434839A>GCA065022WT1c.522T>C (p.Thr174=)
c.507T>C (p.Thr169=)
n.701T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.32434839A>TCA473571538WT1c.522T>A (p.Thr174=)
c.507T>A (p.Thr169=)
n.701T>A
11g.32434840G>ACA379964789WT1c.521C>T (p.Thr174Ile)
c.506C>T (p.Thr169Ile)
n.700C>T
11g.32434840G>CCA379964788WT1c.521C>G (p.Thr174Ser)
c.506C>G (p.Thr169Ser)
n.700C>G
11g.32434840G>TCA379964787WT1c.521C>A (p.Thr174Asn)
c.506C>A (p.Thr169Asn)
n.700C>A
11g.32434841T>ACA379964791WT1c.520A>T (p.Thr174Ser)
c.505A>T (p.Thr169Ser)
n.699A>T
11g.32434841T>CCA379964793WT1c.520A>G (p.Thr174Ala)
c.505A>G (p.Thr169Ala)
n.699A>G
 ClinVar dbSNP gnomAD v4
11g.32434841T>GCA219510924WT1c.520A>C (p.Thr174Pro)
c.505A>C (p.Thr169Pro)
n.699A>C
 dbSNP
11g.32434841T=CA1962327166WT1c.520A= (p.Thr174=)
c.505A= (p.Thr169=)
n.699A=
11g.32434841_32434842insAGCCA2612989398WT1c.519_520insGCT (p.Phe173_Thr174insAla)
c.504_505insGCT (p.Phe168_Thr169insAla)
n.698_699insGCT
 gnomAD v4
11g.32434842G>ACA473571543WT1c.519C>T (p.Phe173=)
c.504C>T (p.Phe168=)
n.698C>T
11g.32434842G>CCA379964795WT1c.519C>G (p.Phe173Leu)
c.504C>G (p.Phe168Leu)
n.698C>G
11g.32434842G>TCA379964796WT1c.519C>A (p.Phe173Leu)
c.504C>A (p.Phe168Leu)
n.698C>A
 ClinVar
11g.32434843A>CCA379964798WT1c.518T>G (p.Phe173Cys)
c.503T>G (p.Phe168Cys)
n.697T>G
11g.32434843A>GCA379964800WT1c.518T>C (p.Phe173Ser)
c.503T>C (p.Phe168Ser)
n.697T>C
11g.32434843A>TCA379964802WT1c.518T>A (p.Phe173Tyr)
c.503T>A (p.Phe168Tyr)
n.697T>A
11g.32434843_32434844insCCA2612989399WT1c.517_518insG (p.Phe173CysfsTer?)
c.502_503insG (p.Phe168CysfsTer?)
n.696_697insG
 gnomAD v4
11g.32434844A>CCA379964803WT1c.517T>G (p.Phe173Val)
c.502T>G (p.Phe168Val)
n.696T>G
11g.32434844A>GCA379964804WT1c.517T>C (p.Phe173Leu)
c.502T>C (p.Phe168Leu)
n.696T>C
11g.32434844A>TCA379964805WT1c.517T>A (p.Phe173Ile)
c.502T>A (p.Phe168Ile)
n.696T>A
11g.32434844_32434845insGGCA2612989400WT1c.516_517insCC (p.Phe173ProfsTer?)
c.501_502insCC (p.Phe168ProfsTer?)
n.695_696insCC
 gnomAD v4
11g.32434845C>ACA379964806WT1c.516G>T (p.Gln172His)
c.501G>T (p.Gln167His)
n.695G>T
11g.32434845C>GCA379964807WT1c.516G>C (p.Gln172His)
c.501G>C (p.Gln167His)
n.695G>C
 gnomAD v4
11g.32434845C>TCA473571559WT1c.516G>A (p.Gln172=)
c.501G>A (p.Gln167=)
n.695G>A
11g.32434846T>ACA379964809WT1c.515A>T (p.Gln172Leu)
c.500A>T (p.Gln167Leu)
n.694A>T
11g.32434846T>CCA379964812WT1c.515A>G (p.Gln172Arg)
c.500A>G (p.Gln167Arg)
n.694A>G
11g.32434846T>GCA379964810WT1c.515A>C (p.Gln172Pro)
c.500A>C (p.Gln167Pro)
n.694A>C
11g.32434846_32434847insCCCA2612989401WT1c.514_515insGG (p.Gln172ArgfsTer?)
c.499_500insGG (p.Gln167ArgfsTer?)
n.693_694insGG
 gnomAD v4
11g.32434847G>ACA379964814WT1c.514C>T (p.Gln172Ter)
c.499C>T (p.Gln167Ter)
n.693C>T
 ClinVar
11g.32434847G>CCA379964815WT1c.514C>G (p.Gln172Glu)
c.499C>G (p.Gln167Glu)
n.693C>G
11g.32434847G>TCA379964816WT1c.514C>A (p.Gln172Lys)
c.499C>A (p.Gln167Lys)
n.693C>A
11g.32434848delCA2580084154WT1c.514del (p.Gln172SerfsTer?)
c.499del (p.Gln167SerfsTer?)
n.693del
 ClinVar dbSNP
11g.32434848G>ACA473571566WT1c.513C>T (p.Gly171=)
c.498C>T (p.Gly166=)
n.692C>T
 ClinVar dbSNP
11g.32434848G>CCA473571568WT1c.513C>G (p.Gly171=)
c.498C>G (p.Gly166=)
n.692C>G
11g.32434848G=CA1962327167WT1c.513C= (p.Gly171=)
c.498C= (p.Gly166=)
n.692C=
11g.32434848G>TCA065010WT1c.513C>A (p.Gly171=)
c.498C>A (p.Gly166=)
n.692C>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32434849C>ACA379964820WT1c.512G>T (p.Gly171Val)
c.497G>T (p.Gly166Val)
n.691G>T
 ClinVar dbSNP
11g.32434849C=CA1962327168WT1c.512G= (p.Gly171=)
c.497G= (p.Gly166=)
n.691G=
11g.32434849C>GCA379964821WT1c.512G>C (p.Gly171Ala)
c.497G>C (p.Gly166Ala)
n.691G>C
11g.32434849C>TCA379964822WT1c.512G>A (p.Gly171Asp)
c.497G>A (p.Gly166Asp)
n.691G>A
 gnomAD v4
11g.32434850C>ACA379964824WT1c.511G>T (p.Gly171Cys)
c.496G>T (p.Gly166Cys)
n.690G>T
11g.32434850C>GCA379964828WT1c.511G>C (p.Gly171Arg)
c.496G>C (p.Gly166Arg)
n.690G>C
 ClinVar dbSNP
11g.32434850C>TCA379964826WT1c.511G>A (p.Gly171Ser)
c.496G>A (p.Gly166Ser)
n.690G>A
 dbSNP
11g.32434850_32434854delinsACAGTGCA2580084156WT1c.507_511delinsCACTGT (p.Ser170ThrfsTer?)
c.492_496delinsCACTGT (p.Ser165ThrfsTer?)
n.686_690delinsCACTGT
 ClinVar
11g.32434851G>ACA065003WT1c.510C>T (p.Ser170=)
c.495C>T (p.Ser165=)
n.689C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC
11g.32434851G>CCA473571577WT1c.510C>G (p.Ser170=)
c.495C>G (p.Ser165=)
n.689C>G
 ClinVar dbSNP
11g.32434851G=CA1962327169WT1c.510C= (p.Ser170=)
c.495C= (p.Ser165=)
n.689C=
11g.32434851G>TCA473571578WT1c.510C>A (p.Ser170=)
c.495C>A (p.Ser165=)
n.689C>A
 gnomAD v4
11g.32434852G>ACA379964830WT1c.509C>T (p.Ser170Phe)
c.494C>T (p.Ser165Phe)
n.688C>T
 COSMIC COSMIC
11g.32434852G>CCA379964831WT1c.509C>G (p.Ser170Cys)
c.494C>G (p.Ser165Cys)
n.688C>G
11g.32434852G>TCA379964832WT1c.509C>A (p.Ser170Tyr)
c.494C>A (p.Ser165Tyr)
n.688C>A
11g.32434853A>CCA379964837WT1c.508T>G (p.Ser170Ala)
c.493T>G (p.Ser165Ala)
n.687T>G
11g.32434853A>GCA379964834WT1c.508T>C (p.Ser170Pro)
c.493T>C (p.Ser165Pro)
n.687T>C
11g.32434853A>TCA379964835WT1c.508T>A (p.Ser170Thr)
c.493T>A (p.Ser165Thr)
n.687T>A
11g.32434854A>CCA379964839WT1c.507T>G (p.Phe169Leu)
c.492T>G (p.Phe164Leu)
n.686T>G
11g.32434854A>GCA473571585WT1c.507T>C (p.Phe169=)
c.492T>C (p.Phe164=)
n.686T>C
11g.32434854A>TCA379964841WT1c.507T>A (p.Phe169Leu)
c.492T>A (p.Phe164Leu)
n.686T>A
11g.32434855A>CCA379964842WT1c.506T>G (p.Phe169Cys)
c.491T>G (p.Phe164Cys)
n.685T>G
11g.32434855A>GCA379964844WT1c.506T>C (p.Phe169Ser)
c.491T>C (p.Phe164Ser)
n.685T>C
 ClinVar
11g.32434855A>TCA379964845WT1c.506T>A (p.Phe169Tyr)
c.491T>A (p.Phe164Tyr)
n.685T>A
11g.32434856A>CCA379964847WT1c.505T>G (p.Phe169Val)
c.490T>G (p.Phe164Val)
n.684T>G
11g.32434856A>GCA379964848WT1c.505T>C (p.Phe169Leu)
c.490T>C (p.Phe164Leu)
n.684T>C
 ClinVar dbSNP
11g.32434856A>TCA379964850WT1c.505T>A (p.Phe169Ile)
c.490T>A (p.Phe164Ile)
n.684T>A
11g.32434857G>ACA473571593WT1c.504C>T (p.His168=)
c.489C>T (p.His163=)
n.683C>T
11g.32434857G>CCA379964851WT1c.504C>G (p.His168Gln)
c.489C>G (p.His163Gln)
n.683C>G
11g.32434857G>TCA379964853WT1c.504C>A (p.His168Gln)
c.489C>A (p.His163Gln)
n.683C>A
11g.32434858T>ACA379964855WT1c.503A>T (p.His168Leu)
c.488A>T (p.His163Leu)
n.682A>T
 dbSNP
11g.32434858T>CCA064994WT1c.503A>G (p.His168Arg)
c.488A>G (p.His163Arg)
n.682A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.32434858T>GCA379964857WT1c.503A>C (p.His168Pro)
c.488A>C (p.His163Pro)
n.682A>C
11g.32434858T=CA1962327170WT1c.503A= (p.His168=)
c.488A= (p.His163=)
n.682A=
11g.32434859G>ACA379964862WT1c.502C>T (p.His168Tyr)
c.487C>T (p.His163Tyr)
n.681C>T
 gnomAD v4
11g.32434859G>CCA379964859WT1c.502C>G (p.His168Asp)
c.487C>G (p.His163Asp)
n.681C>G
11g.32434859G>TCA379964860WT1c.502C>A (p.His168Asn)
c.487C>A (p.His163Asn)
n.681C>A
11g.32434860G>ACA473571604WT1c.501C>T (p.Val167=)
c.486C>T (p.Val162=)
n.680C>T
11g.32434860G>CCA473571607WT1c.501C>G (p.Val167=)
c.486C>G (p.Val162=)
n.680C>G
 dbSNP
11g.32434860G>TCA473571605WT1c.501C>A (p.Val167=)
c.486C>A (p.Val162=)
n.680C>A
11g.32434861A=CA1962327171WT1c.500T= (p.Val167=)
c.485T= (p.Val162=)
n.679T=
11g.32434861A>CCA379964864WT1c.500T>G (p.Val167Gly)
c.485T>G (p.Val162Gly)
n.679T>G
11g.32434861A>GCA379964865WT1c.500T>C (p.Val167Ala)
c.485T>C (p.Val162Ala)
n.679T>C
 ClinVar
11g.32434861A>TCA379964866WT1c.500T>A (p.Val167Asp)
c.485T>A (p.Val162Asp)
n.679T>A
 ClinVar dbSNP
11g.32434862_32434863delCA2695213674WT1c.499_500del (p.Val167ProfsTer?)
c.484_485del (p.Val162ProfsTer?)
n.678_679del
11g.32434862C>ACA379964868WT1c.499G>T (p.Val167Phe)
c.484G>T (p.Val162Phe)
n.678G>T
11g.32434862C=CA1962327172WT1c.499G= (p.Val167=)
c.484G= (p.Val162=)
n.678G=
11g.32434862C>GCA379964870WT1c.499G>C (p.Val167Leu)
c.484G>C (p.Val162Leu)
n.678G>C
 dbSNP
11g.32434862C>TCA379964871WT1c.499G>A (p.Val167Ile)
c.484G>A (p.Val162Ile)
n.678G>A
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32434863A=CA1962327173WT1c.498T= (p.Thr166=)
c.483T= (p.Thr161=)
n.677T=
11g.32434863A>CCA473571616WT1c.498T>G (p.Thr166=)
c.483T>G (p.Thr161=)
n.677T>G
11g.32434863A>GCA473571619WT1c.498T>C (p.Thr166=)
c.483T>C (p.Thr161=)
n.677T>C
 ClinVar dbSNP
11g.32434863A>TCA473571623WT1c.498T>A (p.Thr166=)
c.483T>A (p.Thr161=)
n.677T>A
11g.32434864G>ACA379964875WT1c.497C>T (p.Thr166Ile)
c.482C>T (p.Thr161Ile)
n.676C>T
 dbSNP
11g.32434864G>CCA379964872WT1c.497C>G (p.Thr166Ser)
c.482C>G (p.Thr161Ser)
n.676C>G
 ClinVar
11g.32434864G>TCA379964873WT1c.497C>A (p.Thr166Asn)
c.482C>A (p.Thr161Asn)
n.676C>A
11g.32434865T>ACA379964878WT1c.496A>T (p.Thr166Ser)
c.481A>T (p.Thr161Ser)
n.675A>T
11g.32434865T>CCA379964879WT1c.496A>G (p.Thr166Ala)
c.481A>G (p.Thr161Ala)
n.675A>G
 ClinVar dbSNP
11g.32434865T>GCA379964880WT1c.496A>C (p.Thr166Pro)
c.481A>C (p.Thr161Pro)
n.675A>C
11g.32434865T=CA1962327174WT1c.496A= (p.Thr166=)
c.481A= (p.Thr161=)
n.675A=
11g.32434866G>ACA473571631WT1c.495C>T (p.Phe165=)
c.480C>T (p.Phe160=)
n.674C>T
11g.32434866G>CCA379964882WT1c.495C>G (p.Phe165Leu)
c.480C>G (p.Phe160Leu)
n.674C>G
11g.32434866G>TCA379964883WT1c.495C>A (p.Phe165Leu)
c.480C>A (p.Phe160Leu)
n.674C>A
11g.32434867A>CCA379964885WT1c.494T>G (p.Phe165Cys)
c.479T>G (p.Phe160Cys)
n.673T>G
11g.32434867A>GCA379964888WT1c.494T>C (p.Phe165Ser)
c.479T>C (p.Phe160Ser)
n.673T>C
 dbSNP
11g.32434867A>TCA379964886WT1c.494T>A (p.Phe165Tyr)
c.479T>A (p.Phe160Tyr)
n.673T>A
11g.32434868A>CCA379964890WT1c.493T>G (p.Phe165Val)
c.478T>G (p.Phe160Val)
n.672T>G
11g.32434868A>GCA379964892WT1c.493T>C (p.Phe165Leu)
c.478T>C (p.Phe160Leu)
n.672T>C
 gnomAD v4
11g.32434868A>TCA379964893WT1c.493T>A (p.Phe165Ile)
c.478T>A (p.Phe160Ile)
n.672T>A
11g.32434869G>ACA473571639WT1c.492C>T (p.Ala164=)
c.477C>T (p.Ala159=)
n.671C>T
11g.32434869G>CCA473571645WT1c.492C>G (p.Ala164=)
c.477C>G (p.Ala159=)
n.671C>G
 dbSNP
11g.32434869G>TCA473571647WT1c.492C>A (p.Ala164=)
c.477C>A (p.Ala159=)
n.671C>A
11g.32434870G>ACA379964895WT1c.491C>T (p.Ala164Val)
c.476C>T (p.Ala159Val)
n.670C>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32434870G>CCA379964896WT1c.491C>G (p.Ala164Gly)
c.476C>G (p.Ala159Gly)
n.670C>G
11g.32434870G=CA1962327175WT1c.491C= (p.Ala164=)
c.476C= (p.Ala159=)
n.670C=
11g.32434870G>TCA379964898WT1c.491C>A (p.Ala164Asp)
c.476C>A (p.Ala159Asp)
n.670C>A
11g.32434871C>ACA219510930WT1c.490G>T (p.Ala164Ser)
c.475G>T (p.Ala159Ser)
n.669G>T
 dbSNP gnomAD v4
11g.32434871C=CA1962327176WT1c.490G= (p.Ala164=)
c.475G= (p.Ala159=)
n.669G=
11g.32434871C>GCA379964899WT1c.490G>C (p.Ala164Pro)
c.475G>C (p.Ala159Pro)
n.669G>C
 ClinVar dbSNP
11g.32434871C>TCA379964900WT1c.490G>A (p.Ala164Thr)
c.475G>A (p.Ala159Thr)
n.669G>A
 dbSNP gnomAD v3 gnomAD v4
11g.32434872G>ACA219510935WT1c.489C>T (p.Ser163=)
c.474C>T (p.Ser158=)
n.668C>T
 ClinVar dbSNP gnomAD v4
11g.32434872G>CCA379964901WT1c.489C>G (p.Ser163Arg)
c.474C>G (p.Ser158Arg)
n.668C>G
 ClinVar
11g.32434872G=CA1962327177WT1c.489C= (p.Ser163=)
c.474C= (p.Ser158=)
n.668C=
11g.32434872G>TCA379964903WT1c.489C>A (p.Ser163Arg)
c.474C>A (p.Ser158Arg)
n.668C>A
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32434873C>ACA379964905WT1c.488G>T (p.Ser163Ile)
c.473G>T (p.Ser158Ile)
n.667G>T
11g.32434873C=CA1962327178WT1c.488G= (p.Ser163=)
c.473G= (p.Ser158=)
n.667G=
11g.32434873C>GCA379964907WT1c.488G>C (p.Ser163Thr)
c.473G>C (p.Ser158Thr)
n.667G>C
 dbSNP gnomAD v3 gnomAD v4
11g.32434873C>TCA379964906WT1c.488G>A (p.Ser163Asn)
c.473G>A (p.Ser158Asn)
n.667G>A
 ClinVar dbSNP
11g.32434874T>ACA379964909WT1c.487A>T (p.Ser163Cys)
c.472A>T (p.Ser158Cys)
n.666A>T
11g.32434874T>CCA379964911WT1c.487A>G (p.Ser163Gly)
c.472A>G (p.Ser158Gly)
n.666A>G
 dbSNP
11g.32434874T>GCA379964913WT1c.487A>C (p.Ser163Arg)
c.472A>C (p.Ser158Arg)
n.666A>C
11g.32434875C>ACA473571666WT1c.486G>T (p.Leu162=)
c.471G>T (p.Leu157=)
n.665G>T
 dbSNP
11g.32434875C=CA1962327179WT1c.486G= (p.Leu162=)
c.471G= (p.Leu157=)
n.665G=
11g.32434875C>GCA473571667WT1c.486G>C (p.Leu162=)
c.471G>C (p.Leu157=)
n.665G>C
11g.32434875C>TCA473571668WT1c.486G>A (p.Leu162=)
c.471G>A (p.Leu157=)
n.665G>A
11g.32434878_32434911delCA645584483WT1c.453_486del (p.Trp151Ter)
c.438_471del (p.Trp146Ter)
n.632_665del
 COSMIC
11g.32434876A>CCA379964914WT1c.485T>G (p.Leu162Arg)
c.470T>G (p.Leu157Arg)
n.664T>G
 gnomAD v4
11g.32434876A>GCA379964915WT1c.485T>C (p.Leu162Pro)
c.470T>C (p.Leu157Pro)
n.664T>C
 gnomAD v4
11g.32434876A>TCA379964917WT1c.485T>A (p.Leu162Gln)
c.470T>A (p.Leu157Gln)
n.664T>A
11g.32434877G>ACA064984WT1c.484C>T (p.Leu162=)
c.469C>T (p.Leu157=)
n.663C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.32434877G>CCA379964920WT1c.484C>G (p.Leu162Val)
c.469C>G (p.Leu157Val)
n.663C>G
 dbSNP gnomAD v4
11g.32434877G=CA1962327180WT1c.484C= (p.Leu162=)
c.469C= (p.Leu157=)
n.663C=
11g.32434877G>TCA379964919WT1c.484C>A (p.Leu162Met)
c.469C>A (p.Leu157Met)
n.663C>A
11g.32434878G>ACA064979WT1c.483C>T (p.Cys161=)
c.468C>T (p.Cys156=)
n.662C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.32434878G>CCA379964922WT1c.483C>G (p.Cys161Trp)
c.468C>G (p.Cys156Trp)
n.662C>G
11g.32434878G=CA1962327181WT1c.483C= (p.Cys161=)
c.468C= (p.Cys156=)
n.662C=
11g.32434878G>TCA379964924WT1c.483C>A (p.Cys161Ter)
c.468C>A (p.Cys156Ter)
n.662C>A
11g.32434879C>ACA379964926WT1c.482G>T (p.Cys161Phe)
c.467G>T (p.Cys156Phe)
n.661G>T
 ClinVar dbSNP
11g.32434879C=CA1962327182WT1c.482G= (p.Cys161=)
c.467G= (p.Cys156=)
n.661G=
11g.32434879C>GCA379964928WT1c.482G>C (p.Cys161Ser)
c.467G>C (p.Cys156Ser)
n.661G>C
11g.32434879C>TCA379964929WT1c.482G>A (p.Cys161Tyr)
c.467G>A (p.Cys156Tyr)
n.661G>A
 dbSNP gnomAD v4
11g.32434880A>CCA379964931WT1c.481T>G (p.Cys161Gly)
c.466T>G (p.Cys156Gly)
n.660T>G
 ClinVar
11g.32434880A>GCA379964934WT1c.481T>C (p.Cys161Arg)
c.466T>C (p.Cys156Arg)
n.660T>C
11g.32434880A>TCA379964932WT1c.481T>A (p.Cys161Ser)
c.466T>A (p.Cys156Ser)
n.660T>A
 dbSNP
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

Number of alleles fetched