Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.32435044_32435048dupCA2573146229WT1c.314_318dup (p.Trp107ArgfsTer?)
c.299_303dup (p.Trp102ArgfsTer?)
n.493_497dup
 ClinVar dbSNP
11g.32435047G>ACA379965946WT1c.314C>T (p.Ala105Val)
c.299C>T (p.Ala100Val)
n.493C>T
 dbSNP gnomAD v4
11g.32435047G>CCA219511175WT1c.314C>G (p.Ala105Gly)
c.299C>G (p.Ala100Gly)
n.493C>G
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435047G=CA1962327296WT1c.314C= (p.Ala105=)
c.299C= (p.Ala100=)
n.493C=
11g.32435047G>TCA379965947WT1c.314C>A (p.Ala105Glu)
c.299C>A (p.Ala100Glu)
n.493C>A
 ClinVar dbSNP gnomAD v4
11g.32435048C>ACA379965948WT1c.313G>T (p.Ala105Ser)
c.298G>T (p.Ala100Ser)
n.492G>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435048C=CA1962327297WT1c.313G= (p.Ala105=)
c.298G= (p.Ala100=)
n.492G=
11g.32435048C>GCA379965949WT1c.313G>C (p.Ala105Pro)
c.298G>C (p.Ala100Pro)
n.492G>C
11g.32435048C>TCA379965950WT1c.313G>A (p.Ala105Thr)
c.298G>A (p.Ala100Thr)
n.492G>A
 ClinVar dbSNP gnomAD v4
11g.32435049C>ACA473773876WT1c.312G>T (p.Ala104=)
c.297G>T (p.Ala99=)
n.491G>T
 ClinVar gnomAD v4
11g.32435049C=CA1962327298WT1c.312G= (p.Ala104=)
c.297G= (p.Ala99=)
n.491G=
11g.32435049C>GCA473773878WT1c.312G>C (p.Ala104=)
c.297G>C (p.Ala99=)
n.491G>C
11g.32435049C>TCA473773879WT1c.312G>A (p.Ala104=)
c.297G>A (p.Ala99=)
n.491G>A
 ClinVar dbSNP gnomAD v4
11g.32435050G>ACA379965951WT1c.311C>T (p.Ala104Val)
c.296C>T (p.Ala99Val)
n.490C>T
 ClinVar gnomAD v4 COSMIC
11g.32435050G>CCA219511188WT1c.311C>G (p.Ala104Gly)
c.296C>G (p.Ala99Gly)
n.490C>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32435050G=CA1962327299WT1c.311C= (p.Ala104=)
c.296C= (p.Ala99=)
n.490C=
11g.32435050G>TCA379965952WT1c.311C>A (p.Ala104Glu)
c.296C>A (p.Ala99Glu)
n.490C>A
 gnomAD v4
11g.32435051C>ACA379965953WT1c.310G>T (p.Ala104Ser)
c.295G>T (p.Ala99Ser)
n.489G>T
 gnomAD v4
11g.32435051C=CA1962327300WT1c.310G= (p.Ala104=)
c.295G= (p.Ala99=)
n.489G=
11g.32435051C>GCA379965954WT1c.310G>C (p.Ala104Pro)
c.295G>C (p.Ala99Pro)
n.489G>C
 dbSNP
11g.32435051C>TCA379965955WT1c.310G>A (p.Ala104Thr)
c.295G>A (p.Ala99Thr)
n.489G>A
 ClinVar dbSNP gnomAD v4
11g.32435051dupCA2723468786WT1c.310dup (p.Ala104GlyfsTer?)
c.295dup (p.Ala99GlyfsTer?)
n.489dup
 dbSNP
11g.32435052G>ACA473773888WT1c.309C>T (p.Gly103=)
c.294C>T (p.Gly98=)
n.488C>T
 dbSNP gnomAD v4
11g.32435052G>CCA473773889WT1c.309C>G (p.Gly103=)
c.294C>G (p.Gly98=)
n.488C>G
 dbSNP
11g.32435052G=CA1962327301WT1c.309C= (p.Gly103=)
c.294C= (p.Gly98=)
n.488C=
11g.32435052G>TCA064811WT1c.309C>A (p.Gly103=)
c.294C>A (p.Gly98=)
n.488C>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32435053C>ACA379965958WT1c.308G>T (p.Gly103Val)
c.293G>T (p.Gly98Val)
n.487G>T
 gnomAD v4
11g.32435053C>GCA379965956WT1c.308G>C (p.Gly103Ala)
c.293G>C (p.Gly98Ala)
n.487G>C
11g.32435053C>TCA379965957WT1c.308G>A (p.Gly103Asp)
c.293G>A (p.Gly98Asp)
n.487G>A
 gnomAD v4
11g.32435054C>ACA379965959WT1c.307G>T (p.Gly103Cys)
c.292G>T (p.Gly98Cys)
n.486G>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435054C=CA1962327302WT1c.307G= (p.Gly103=)
c.292G= (p.Gly98=)
n.486G=
11g.32435054C>GCA379965960WT1c.307G>C (p.Gly103Arg)
c.292G>C (p.Gly98Arg)
n.486G>C
 gnomAD v4
11g.32435054C>TCA379965961WT1c.307G>A (p.Gly103Ser)
c.292G>A (p.Gly98Ser)
n.486G>A
 gnomAD v4
11g.32435055G>ACA473773896WT1c.306C>T (p.Ser102=)
c.291C>T (p.Ser97=)
n.485C>T
 dbSNP gnomAD v4
11g.32435055G>CCA379965962WT1c.306C>G (p.Ser102Arg)
c.291C>G (p.Ser97Arg)
n.485C>G
 dbSNP
11g.32435055G>TCA379965963WT1c.306C>A (p.Ser102Arg)
c.291C>A (p.Ser97Arg)
n.485C>A
 ClinVar gnomAD v4
11g.32435056C>ACA379965964WT1c.305G>T (p.Ser102Ile)
c.290G>T (p.Ser97Ile)
n.484G>T
 gnomAD v4
11g.32435056C=CA1962327303WT1c.305G= (p.Ser102=)
c.290G= (p.Ser97=)
n.484G=
11g.32435056C>GCA379965965WT1c.305G>C (p.Ser102Thr)
c.290G>C (p.Ser97Thr)
n.484G>C
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435056C>TCA379965966WT1c.305G>A (p.Ser102Asn)
c.290G>A (p.Ser97Asn)
n.484G>A
 ClinVar dbSNP gnomAD v4
11g.32435058_32435059insCCCTCCA2695213679WT1c.305_306insGGGAG (p.Ser102ArgfsTer?)
c.290_291insGGGAG (p.Ser97ArgfsTer?)
n.484_485insGGGAG
11g.32435057T>ACA379965967WT1c.304A>T (p.Ser102Cys)
c.289A>T (p.Ser97Cys)
n.483A>T
 dbSNP
11g.32435057T>CCA379965968WT1c.304A>G (p.Ser102Gly)
c.289A>G (p.Ser97Gly)
n.483A>G
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435057T>GCA379965969WT1c.304A>C (p.Ser102Arg)
c.289A>C (p.Ser97Arg)
n.483A>C
11g.32435057T=CA1962327304WT1c.304A= (p.Ser102=)
c.289A= (p.Ser97=)
n.483A=
11g.32435058C>ACA473773906WT1c.303G>T (p.Val101=)
c.288G>T (p.Val96=)
n.482G>T
 gnomAD v4
11g.32435058C>GCA473773907WT1c.303G>C (p.Val101=)
c.288G>C (p.Val96=)
n.482G>C
11g.32435058C>TCA473773908WT1c.303G>A (p.Val101=)
c.288G>A (p.Val96=)
n.482G>A
 ClinVar gnomAD v4
11g.32435059A>CCA379965972WT1c.302T>G (p.Val101Gly)
c.287T>G (p.Val96Gly)
n.481T>G
11g.32435059A>GCA379965970WT1c.302T>C (p.Val101Ala)
c.287T>C (p.Val96Ala)
n.481T>C
 gnomAD v4
11g.32435059A>TCA379965971WT1c.302T>A (p.Val101Glu)
c.287T>A (p.Val96Glu)
n.481T>A
 gnomAD v4
11g.32435059_32435062delCA645584491WT1c.299_302del (p.Pro100ArgfsTer?)
c.284_287del (p.Pro95ArgfsTer?)
n.478_481del
 COSMIC
11g.32435060C>ACA379965973WT1c.301G>T (p.Val101Leu)
c.286G>T (p.Val96Leu)
n.480G>T
 gnomAD v4
11g.32435060C=CA1962327305WT1c.301G= (p.Val101=)
c.286G= (p.Val96=)
n.480G=
11g.32435060C>GCA379965974WT1c.301G>C (p.Val101Leu)
c.286G>C (p.Val96Leu)
n.480G>C
 ClinVar dbSNP
11g.32435060C>TCA379965975WT1c.301G>A (p.Val101Met)
c.286G>A (p.Val96Met)
n.480G>A
 gnomAD v4
11g.32435061A=CA1962327306WT1c.300T= (p.Pro100=)
c.285T= (p.Pro95=)
n.479T=
11g.32435061A>CCA473773913WT1c.300T>G (p.Pro100=)
c.285T>G (p.Pro95=)
n.479T>G
 dbSNP gnomAD v4
11g.32435061A>GCA473773915WT1c.300T>C (p.Pro100=)
c.285T>C (p.Pro95=)
n.479T>C
 gnomAD v4
11g.32435061A>TCA473773916WT1c.300T>A (p.Pro100=)
c.285T>A (p.Pro95=)
n.479T>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435062G>ACA379965976WT1c.299C>T (p.Pro100Leu)
c.284C>T (p.Pro95Leu)
n.478C>T
 gnomAD v4
11g.32435062G>CCA379965977WT1c.299C>G (p.Pro100Arg)
c.284C>G (p.Pro95Arg)
n.478C>G
 ClinVar
11g.32435062G>TCA379965978WT1c.299C>A (p.Pro100His)
c.284C>A (p.Pro95His)
n.478C>A
 gnomAD v4
11g.32435063G>ACA219511235WT1c.298C>T (p.Pro100Ser)
c.283C>T (p.Pro95Ser)
n.477C>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32435063G>CCA379965979WT1c.298C>G (p.Pro100Ala)
c.283C>G (p.Pro95Ala)
n.477C>G
 ClinVar dbSNP gnomAD v4
11g.32435063G=CA1962327307WT1c.298C= (p.Pro100=)
c.283C= (p.Pro95=)
n.477C=
11g.32435063G>TCA379965980WT1c.298C>A (p.Pro100Thr)
c.283C>A (p.Pro95Thr)
n.477C>A
 ClinVar dbSNP gnomAD v4
11g.32435064C>ACA473773924WT1c.297G>T (p.Leu99=)
c.282G>T (p.Leu94=)
n.476G>T
 gnomAD v4
11g.32435064C=CA1962327308WT1c.297G= (p.Leu99=)
c.282G= (p.Leu94=)
n.476G=
11g.32435064C>GCA473773925WT1c.297G>C (p.Leu99=)
c.282G>C (p.Leu94=)
n.476G>C
 gnomAD v4
11g.32435064C>TCA473773926WT1c.297G>A (p.Leu99=)
c.282G>A (p.Leu94=)
n.476G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
11g.32435065A=CA1962327309WT1c.296T= (p.Leu99=)
c.281T= (p.Leu94=)
n.475T=
11g.32435065A>CCA379965981WT1c.296T>G (p.Leu99Arg)
c.281T>G (p.Leu94Arg)
n.475T>G
11g.32435065A>GCA379965982WT1c.296T>C (p.Leu99Pro)
c.281T>C (p.Leu94Pro)
n.475T>C
 ClinVar dbSNP gnomAD v4
11g.32435065A>TCA379965983WT1c.296T>A (p.Leu99Gln)
c.281T>A (p.Leu94Gln)
n.475T>A
 ClinVar dbSNP
11g.32435066G>ACA473773931WT1c.295C>T (p.Leu99=)
c.280C>T (p.Leu94=)
n.474C>T
 gnomAD v4
11g.32435066G>CCA379965985WT1c.295C>G (p.Leu99Val)
c.280C>G (p.Leu94Val)
n.474C>G
 ClinVar dbSNP
11g.32435066G=CA1962327310WT1c.295C= (p.Leu99=)
c.280C= (p.Leu94=)
n.474C=
11g.32435066G>TCA379965984WT1c.295C>A (p.Leu99Met)
c.280C>A (p.Leu94Met)
n.474C>A
 gnomAD v4
11g.32435067G>ACA219511241WT1c.294C>T (p.Ala98=)
c.279C>T (p.Ala93=)
n.473C>T
 ClinVar dbSNP gnomAD v4
11g.32435067G>CCA473773933WT1c.294C>G (p.Ala98=)
c.279C>G (p.Ala93=)
n.473C>G
11g.32435067G=CA1962327311WT1c.294C= (p.Ala98=)
c.279C= (p.Ala93=)
n.473C=
11g.32435067G>TCA473773934WT1c.294C>A (p.Ala98=)
c.279C>A (p.Ala93=)
n.473C>A
11g.32435068G>ACA379965986WT1c.293C>T (p.Ala98Val)
c.278C>T (p.Ala93Val)
n.472C>T
 ClinVar dbSNP gnomAD v4
11g.32435068G>CCA379965988WT1c.293C>G (p.Ala98Gly)
c.278C>G (p.Ala93Gly)
n.472C>G
 ClinVar dbSNP gnomAD v4
11g.32435068G=CA1962327312WT1c.293C= (p.Ala98=)
c.278C= (p.Ala93=)
n.472C=
11g.32435068G>TCA379965987WT1c.293C>A (p.Ala98Asp)
c.278C>A (p.Ala93Asp)
n.472C>A
 gnomAD v4
11g.32435069C>ACA379965989WT1c.292G>T (p.Ala98Ser)
c.277G>T (p.Ala93Ser)
n.471G>T
 dbSNP gnomAD v4
11g.32435069C>GCA379965990WT1c.292G>C (p.Ala98Pro)
c.277G>C (p.Ala93Pro)
n.471G>C
11g.32435069C>TCA379965991WT1c.292G>A (p.Ala98Thr)
c.277G>A (p.Ala93Thr)
n.471G>A
 gnomAD v4
11g.32435070A=CA1962327313WT1c.291T= (p.Cys97=)
c.276T= (p.Cys92=)
n.470T=
11g.32435070A>CCA064806WT1c.291T>G (p.Cys97Trp)
c.276T>G (p.Cys92Trp)
n.470T>G
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.32435070A>GCA473773939WT1c.291T>C (p.Cys97=)
c.276T>C (p.Cys92=)
n.470T>C
 ClinVar dbSNP gnomAD v4
11g.32435070A>TCA379965992WT1c.291T>A (p.Cys97Ter)
c.276T>A (p.Cys92Ter)
n.470T>A
11g.32435071C>ACA379965993WT1c.290G>T (p.Cys97Phe)
c.275G>T (p.Cys92Phe)
n.469G>T
 gnomAD v4
11g.32435071C=CA1962327314WT1c.290G= (p.Cys97=)
c.275G= (p.Cys92=)
n.469G=
11g.32435071C>GCA379965994WT1c.290G>C (p.Cys97Ser)
c.275G>C (p.Cys92Ser)
n.469G>C
 ClinVar dbSNP
11g.32435071C>TCA379965995WT1c.290G>A (p.Cys97Tyr)
c.275G>A (p.Cys92Tyr)
n.469G>A
 gnomAD v4
11g.32435072A=CA1962327315WT1c.289T= (p.Cys97=)
c.274T= (p.Cys92=)
n.468T=
11g.32435072A>CCA379965996WT1c.289T>G (p.Cys97Gly)
c.274T>G (p.Cys92Gly)
n.468T>G
 dbSNP
11g.32435072A>GCA379965997WT1c.289T>C (p.Cys97Arg)
c.274T>C (p.Cys92Arg)
n.468T>C
 ClinVar dbSNP gnomAD v4
11g.32435072A>TCA379965998WT1c.289T>A (p.Cys97Ser)
c.274T>A (p.Cys92Ser)
n.468T>A
11g.32435072_32435075delinsAGCCCA1962327316WT1c.286_289delinsGGCT (p.Gly96=)
c.271_274delinsGGCT (p.Gly91=)
n.465_468delinsGGCT
11g.32435072_32435073insTCCCA2580084184WT1c.288_289insGGA (p.Gly96_Cys97insGly)
c.273_274insGGA (p.Gly91_Cys92insGly)
n.467_468insGGA
 ClinVar
11g.32435073G>ACA473773942WT1c.288C>T (p.Gly96=)
c.273C>T (p.Gly91=)
n.467C>T
 dbSNP gnomAD v4
11g.32435073G>CCA473773943WT1c.288C>G (p.Gly96=)
c.273C>G (p.Gly91=)
n.467C>G
 ClinVar dbSNP gnomAD v4
11g.32435073G=CA1962327317WT1c.288C= (p.Gly96=)
c.273C= (p.Gly91=)
n.467C=
11g.32435073G>TCA473773944WT1c.288C>A (p.Gly96=)
c.273C>A (p.Gly91=)
n.467C>A
 gnomAD v4
11g.32435082_32435084dupCA2580615657WT1c.286_288dup (p.Gly96_Cys97insGly)
c.271_273dup (p.Gly91_Cys92insGly)
n.465_467dup
 ClinVar dbSNP gnomAD v4
11g.32435082_32435084delCA064802WT1c.286_288del (p.Gly96del)
c.271_273del (p.Gly91del)
n.465_467del
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32435073_32435074insTCCCA2825001877WT1c.287_288insGGA (p.Gly96_Cys97insAsp)
c.272_273insGGA (p.Gly91_Cys92insAsp)
n.466_467insGGA
 ClinVar
11g.32435074C>ACA379966001WT1c.287G>T (p.Gly96Val)
c.272G>T (p.Gly91Val)
n.466G>T
 gnomAD v4
11g.32435074C>GCA379965999WT1c.287G>C (p.Gly96Ala)
c.272G>C (p.Gly91Ala)
n.466G>C
11g.32435074C>TCA379966000WT1c.287G>A (p.Gly96Asp)
c.272G>A (p.Gly91Asp)
n.466G>A
 dbSNP gnomAD v4
11g.32435075C>ACA379966002WT1c.286G>T (p.Gly96Cys)
c.271G>T (p.Gly91Cys)
n.465G>T
 ClinVar dbSNP gnomAD v4
11g.32435075C=CA1962327318WT1c.286G= (p.Gly96=)
c.271G= (p.Gly91=)
n.465G=
11g.32435075C>GCA379966003WT1c.286G>C (p.Gly96Arg)
c.271G>C (p.Gly91Arg)
n.465G>C
11g.32435075C>TCA16613605WT1c.286G>A (p.Gly96Ser)
c.271G>A (p.Gly91Ser)
n.465G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435076G>ACA10638966WT1c.285C>T (p.Gly95=)
c.270C>T (p.Gly90=)
n.464C>T
 ClinVar dbSNP gnomAD v4
11g.32435076G>CCA473773947WT1c.285C>G (p.Gly95=)
c.270C>G (p.Gly90=)
n.464C>G
 dbSNP
11g.32435076G=CA1962327319WT1c.285C= (p.Gly95=)
c.270C= (p.Gly90=)
n.464C=
11g.32435076G>TCA473773948WT1c.285C>A (p.Gly95=)
c.270C>A (p.Gly90=)
n.464C>A
 gnomAD v4
11g.32435077C>ACA379966004WT1c.284G>T (p.Gly95Val)
c.269G>T (p.Gly90Val)
n.463G>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435077C=CA1962327320WT1c.284G= (p.Gly95=)
c.269G= (p.Gly90=)
n.463G=
11g.32435077C>GCA379966005WT1c.284G>C (p.Gly95Ala)
c.269G>C (p.Gly90Ala)
n.463G>C
 dbSNP
11g.32435077C>TCA379966006WT1c.284G>A (p.Gly95Asp)
c.269G>A (p.Gly90Asp)
n.463G>A
 ClinVar dbSNP gnomAD v4
11g.32435078C>ACA379966007WT1c.283G>T (p.Gly95Cys)
c.268G>T (p.Gly90Cys)
n.462G>T
 gnomAD v4
11g.32435078C>GCA379966008WT1c.283G>C (p.Gly95Arg)
c.268G>C (p.Gly90Arg)
n.462G>C
 dbSNP gnomAD v4
11g.32435078C>TCA379966009WT1c.283G>A (p.Gly95Ser)
c.268G>A (p.Gly90Ser)
n.462G>A
 dbSNP gnomAD v4
11g.32435079G>ACA473773952WT1c.282C>T (p.Gly94=)
c.267C>T (p.Gly89=)
n.461C>T
 ClinVar dbSNP gnomAD v4
11g.32435079G>CCA473773953WT1c.282C>G (p.Gly94=)
c.267C>G (p.Gly89=)
n.461C>G
 dbSNP
11g.32435079G=CA1962327321WT1c.282C= (p.Gly94=)
c.267C= (p.Gly89=)
n.461C=
11g.32435079G>TCA473773954WT1c.282C>A (p.Gly94=)
c.267C>A (p.Gly89=)
n.461C>A
 gnomAD v4
11g.32435080C>ACA379966012WT1c.281G>T (p.Gly94Val)
c.266G>T (p.Gly89Val)
n.460G>T
 gnomAD v4
11g.32435080C=CA1962327322WT1c.281G= (p.Gly94=)
c.266G= (p.Gly89=)
n.460G=
11g.32435080C>GCA379966011WT1c.281G>C (p.Gly94Ala)
c.266G>C (p.Gly89Ala)
n.460G>C
11g.32435080C>TCA379966010WT1c.281G>A (p.Gly94Asp)
c.266G>A (p.Gly89Asp)
n.460G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435081C>ACA379966014WT1c.280G>T (p.Gly94Cys)
c.265G>T (p.Gly89Cys)
n.459G>T
 gnomAD v4
11g.32435081C=CA1962327323WT1c.280G= (p.Gly94=)
c.265G= (p.Gly89=)
n.459G=
11g.32435081C>GCA379966013WT1c.280G>C (p.Gly94Arg)
c.265G>C (p.Gly89Arg)
n.459G>C
 gnomAD v4
11g.32435081C>TCA064798WT1c.280G>A (p.Gly94Ser)
c.265G>A (p.Gly89Ser)
n.459G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.32435082G>ACA473773960WT1c.279C>T (p.Gly93=)
c.264C>T (p.Gly88=)
n.458C>T
 ClinVar dbSNP gnomAD v4
11g.32435082G>CCA473773962WT1c.279C>G (p.Gly93=)
c.264C>G (p.Gly88=)
n.458C>G
 dbSNP
11g.32435082G=CA1962327324WT1c.279C= (p.Gly93=)
c.264C= (p.Gly88=)
n.458C=
11g.32435082G>TCA473773961WT1c.279C>A (p.Gly93=)
c.264C>A (p.Gly88=)
n.458C>A
 ClinVar dbSNP gnomAD v4
11g.32435084_32435112delCA2695213680WT1c.251_279del (p.Leu84ArgfsTer?)
c.236_264del (p.Leu79ArgfsTer?)
n.430_458del
11g.32435083C>ACA379966015WT1c.278G>T (p.Gly93Val)
c.263G>T (p.Gly88Val)
n.457G>T
 gnomAD v4
11g.32435083C=CA1962327325WT1c.278G= (p.Gly93=)
c.263G= (p.Gly88=)
n.457G=
11g.32435083C>GCA379966016WT1c.278G>C (p.Gly93Ala)
c.263G>C (p.Gly88Ala)
n.457G>C
 ClinVar dbSNP gnomAD v4
11g.32435083C>TCA379966017WT1c.278G>A (p.Gly93Asp)
c.263G>A (p.Gly88Asp)
n.457G>A
 ClinVar dbSNP gnomAD v4
11g.32435085_32435087delCA2612989581WT1c.276_278del (p.Gly93del)
c.261_263del (p.Gly88del)
n.455_457del
 gnomAD v4
11g.32435084C>ACA379966020WT1c.277G>T (p.Gly93Cys)
c.262G>T (p.Gly88Cys)
n.456G>T
 gnomAD v4
11g.32435084C>GCA379966019WT1c.277G>C (p.Gly93Arg)
c.262G>C (p.Gly88Arg)
n.456G>C
11g.32435084C>TCA379966018WT1c.277G>A (p.Gly93Ser)
c.262G>A (p.Gly88Ser)
n.456G>A
 gnomAD v4
11g.32435085delCA2573146230WT1c.276del (p.Gly93AlafsTer9)
c.261del (p.Gly88AlafsTer9)
n.455del
 ClinVar dbSNP
11g.32435085A>CCA473773968WT1c.276T>G (p.Gly92=)
c.261T>G (p.Gly87=)
n.455T>G
 dbSNP
11g.32435085A>GCA473773970WT1c.276T>C (p.Gly92=)
c.261T>C (p.Gly87=)
n.455T>C
 gnomAD v4
11g.32435085A>TCA473773972WT1c.276T>A (p.Gly92=)
c.261T>A (p.Gly87=)
n.455T>A
11g.32435086C>ACA379966021WT1c.275G>T (p.Gly92Val)
c.260G>T (p.Gly87Val)
n.454G>T
 gnomAD v4
11g.32435086C>GCA379966022WT1c.275G>C (p.Gly92Ala)
c.260G>C (p.Gly87Ala)
n.454G>C
11g.32435086C>TCA379966023WT1c.275G>A (p.Gly92Asp)
c.260G>A (p.Gly87Asp)
n.454G>A
 ClinVar
11g.32435088dupCA2740093680WT1c.275dup (p.Gly93TrpfsTer?)
c.260dup (p.Gly88TrpfsTer?)
n.454dup
 ClinVar
11g.32435088delCA2612989583WT1c.275del (p.Gly92ValfsTer10)
c.260del (p.Gly87ValfsTer10)
n.454del
 gnomAD v4
11g.32435087C>ACA379966024WT1c.274G>T (p.Gly92Cys)
c.259G>T (p.Gly87Cys)
n.453G>T
 gnomAD v4
11g.32435087C>GCA379966025WT1c.274G>C (p.Gly92Arg)
c.259G>C (p.Gly87Arg)
n.453G>C
11g.32435087C>TCA379966026WT1c.274G>A (p.Gly92Ser)
c.259G>A (p.Gly87Ser)
n.453G>A
 gnomAD v4
11g.32435088C>ACA473773977WT1c.273G>T (p.Leu91=)
c.258G>T (p.Leu86=)
n.452G>T
 dbSNP gnomAD v4
11g.32435088C=CA1962327326WT1c.273G= (p.Leu91=)
c.258G= (p.Leu86=)
n.452G=
11g.32435088C>GCA473773978WT1c.273G>C (p.Leu91=)
c.258G>C (p.Leu86=)
n.452G>C
11g.32435088C>TCA473773980WT1c.273G>A (p.Leu91=)
c.258G>A (p.Leu86=)
n.452G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435089A>CCA379966027WT1c.272T>G (p.Leu91Arg)
c.257T>G (p.Leu86Arg)
n.451T>G
11g.32435089A>GCA379966029WT1c.272T>C (p.Leu91Pro)
c.257T>C (p.Leu86Pro)
n.451T>C
 gnomAD v4
11g.32435089A>TCA379966028WT1c.272T>A (p.Leu91Gln)
c.257T>A (p.Leu86Gln)
n.451T>A
 gnomAD v4
11g.32435090G>ACA473773984WT1c.271C>T (p.Leu91=)
c.256C>T (p.Leu86=)
n.450C>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32435090G>CCA379966030WT1c.271C>G (p.Leu91Val)
c.256C>G (p.Leu86Val)
n.450C>G
 dbSNP
11g.32435090G=CA1962327327WT1c.271C= (p.Leu91=)
c.256C= (p.Leu86=)
n.450C=
11g.32435090G>TCA379966031WT1c.271C>A (p.Leu91Met)
c.256C>A (p.Leu86Met)
n.450C>A
 gnomAD v4
11g.32435094_32435098delCA645584492WT1c.267_271del (p.Ser90GlyfsTer?)
c.252_256del (p.Ser85GlyfsTer?)
n.446_450del
 COSMIC COSMIC
11g.32435091G>ACA473773986WT1c.270C>T (p.Ser90=)
c.255C>T (p.Ser85=)
n.449C>T
 ClinVar dbSNP gnomAD v4
11g.32435091G>CCA064793WT1c.270C>G (p.Ser90=)
c.255C>G (p.Ser85=)
n.449C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32435091G=CA1962327328WT1c.270C= (p.Ser90=)
c.255C= (p.Ser85=)
n.449C=
11g.32435091G>TCA473773987WT1c.270C>A (p.Ser90=)
c.255C>A (p.Ser85=)
n.449C>A
 gnomAD v4
11g.32435092G>ACA379966032WT1c.269C>T (p.Ser90Phe)
c.254C>T (p.Ser85Phe)
n.448C>T
 ClinVar dbSNP gnomAD v4
11g.32435092G>CCA379966033WT1c.269C>G (p.Ser90Cys)
c.254C>G (p.Ser85Cys)
n.448C>G
11g.32435092G=CA1962327329WT1c.269C= (p.Ser90=)
c.254C= (p.Ser85=)
n.448C=
11g.32435092G>TCA379966034WT1c.269C>A (p.Ser90Tyr)
c.254C>A (p.Ser85Tyr)
n.448C>A
 gnomAD v4
11g.32435093A=CA1962327330WT1c.268T= (p.Ser90=)
c.253T= (p.Ser85=)
n.447T=
11g.32435093A>CCA379966035WT1c.268T>G (p.Ser90Ala)
c.253T>G (p.Ser85Ala)
n.447T>G
11g.32435093A>GCA379966036WT1c.268T>C (p.Ser90Pro)
c.253T>C (p.Ser85Pro)
n.447T>C
 ClinVar dbSNP gnomAD v4
11g.32435093A>TCA379966037WT1c.268T>A (p.Ser90Thr)
c.253T>A (p.Ser85Thr)
n.447T>A
11g.32435094G>ACA473773990WT1c.267C>T (p.Pro89=)
c.252C>T (p.Pro84=)
n.446C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435094G>CCA473773995WT1c.267C>G (p.Pro89=)
c.252C>G (p.Pro84=)
n.446C>G
 gnomAD v4
11g.32435094G=CA1962327331WT1c.267C= (p.Pro89=)
c.252C= (p.Pro84=)
n.446C=
11g.32435094G>TCA473773996WT1c.267C>A (p.Pro89=)
c.252C>A (p.Pro84=)
n.446C>A
 gnomAD v4
11g.32435095G>ACA379966038WT1c.266C>T (p.Pro89Leu)
c.251C>T (p.Pro84Leu)
n.445C>T
 ClinVar dbSNP gnomAD v4
11g.32435095G>CCA379966039WT1c.266C>G (p.Pro89Arg)
c.251C>G (p.Pro84Arg)
n.445C>G
 ClinVar
11g.32435095G=CA1962327332WT1c.266C= (p.Pro89=)
c.251C= (p.Pro84=)
n.445C=
11g.32435095G>TCA379966040WT1c.266C>A (p.Pro89His)
c.251C>A (p.Pro84His)
n.445C>A
 gnomAD v4
11g.32435096G>ACA379966042WT1c.265C>T (p.Pro89Ser)
c.250C>T (p.Pro84Ser)
n.444C>T
 gnomAD v4
11g.32435096G>CCA379966043WT1c.265C>G (p.Pro89Ala)
c.250C>G (p.Pro84Ala)
n.444C>G
 dbSNP
11g.32435096G>TCA379966041WT1c.265C>A (p.Pro89Thr)
c.250C>A (p.Pro84Thr)
n.444C>A
 ClinVar gnomAD v4 COSMIC COSMIC
11g.32435096_32435098delCA2574790568WT1c.263_265del (p.Val88_Pro89delinsAla)
c.248_250del (p.Val83_Pro84delinsAla)
n.442_444del
11g.32435097G>ACA473774000WT1c.264C>T (p.Val88=)
c.249C>T (p.Val83=)
n.443C>T
 dbSNP gnomAD v2 gnomAD v4
11g.32435097G>CCA473774001WT1c.264C>G (p.Val88=)
c.249C>G (p.Val83=)
n.443C>G
 gnomAD v4
11g.32435097G=CA1962327333WT1c.264C= (p.Val88=)
c.249C= (p.Val83=)
n.443C=
11g.32435097G>TCA473774003WT1c.264C>A (p.Val88=)
c.249C>A (p.Val83=)
n.443C>A
 gnomAD v4
11g.32435098A>CCA379966044WT1c.263T>G (p.Val88Gly)
c.248T>G (p.Val83Gly)
n.442T>G
11g.32435098A>GCA379966045WT1c.263T>C (p.Val88Ala)
c.248T>C (p.Val83Ala)
n.442T>C
 dbSNP gnomAD v4
11g.32435098A>TCA379966046WT1c.263T>A (p.Val88Asp)
c.248T>A (p.Val83Asp)
n.442T>A
 ClinVar gnomAD v4
11g.32435099C>ACA379966047WT1c.262G>T (p.Val88Phe)
c.247G>T (p.Val83Phe)
n.441G>T
 ClinVar dbSNP gnomAD v4
11g.32435099C=CA1962327334WT1c.262G= (p.Val88=)
c.247G= (p.Val83=)
n.441G=
11g.32435099C>GCA379966048WT1c.262G>C (p.Val88Leu)
c.247G>C (p.Val83Leu)
n.441G>C
 gnomAD v4
11g.32435099C>TCA379966049WT1c.262G>A (p.Val88Ile)
c.247G>A (p.Val83Ile)
n.441G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435099_32435100delinsAACA2580084189WT1c.261_262delinsTT (p.Val88Phe)
c.246_247delinsTT (p.Val83Phe)
n.440_441delinsTT
 ClinVar
11g.32435100G>ACA473774006WT1c.261C>T (p.Ala87=)
c.246C>T (p.Ala82=)
n.440C>T
 ClinVar dbSNP gnomAD v4
11g.32435100G>CCA473774007WT1c.261C>G (p.Ala87=)
c.246C>G (p.Ala82=)
n.440C>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435100G=CA1962327335WT1c.261C= (p.Ala87=)
c.246C= (p.Ala82=)
n.440C=
11g.32435100G>TCA473774009WT1c.261C>A (p.Ala87=)
c.246C>A (p.Ala82=)
n.440C>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435101G>ACA379966052WT1c.260C>T (p.Ala87Val)
c.245C>T (p.Ala82Val)
n.439C>T
 dbSNP gnomAD v4
11g.32435101G>CCA379966051WT1c.260C>G (p.Ala87Gly)
c.245C>G (p.Ala82Gly)
n.439C>G
11g.32435101G>TCA379966050WT1c.260C>A (p.Ala87Asp)
c.245C>A (p.Ala82Asp)
n.439C>A
11g.32435102C>ACA379966053WT1c.259G>T (p.Ala87Ser)
c.244G>T (p.Ala82Ser)
n.438G>T
 gnomAD v4
11g.32435102C=CA1962327336WT1c.259G= (p.Ala87=)
c.244G= (p.Ala82=)
n.438G=
11g.32435102C>GCA379966054WT1c.259G>C (p.Ala87Pro)
c.244G>C (p.Ala82Pro)
n.438G>C
 dbSNP gnomAD v4
11g.32435102C>TCA064789WT1c.259G>A (p.Ala87Thr)
c.244G>A (p.Ala82Thr)
n.438G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32435103G>ACA473774014WT1c.258C>T (p.Pro86=)
c.243C>T (p.Pro81=)
n.437C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435103G>CCA473774015WT1c.258C>G (p.Pro86=)
c.243C>G (p.Pro81=)
n.437C>G
11g.32435103G=CA1962327337WT1c.258C= (p.Pro86=)
c.243C= (p.Pro81=)
n.437C=
11g.32435103G>TCA473774012WT1c.258C>A (p.Pro86=)
c.243C>A (p.Pro81=)
n.437C>A
 ClinVar dbSNP gnomAD v4
11g.32435105_32435106insGCCCGGGCGCCTGGGCA2790963048WT1c.258_259insAGGCGCCCGGGCCCC (p.Pro86_Ala87insArgArgProGlyPro)
c.243_244insAGGCGCCCGGGCCCC (p.Pro81_Ala82insArgArgProGlyPro)
n.437_438insAGGCGCCCGGGCCCC
11g.32435104G>ACA379966055WT1c.257C>T (p.Pro86Leu)
c.242C>T (p.Pro81Leu)
n.436C>T
 ClinVar gnomAD v4
11g.32435104G>CCA379966056WT1c.257C>G (p.Pro86Arg)
c.242C>G (p.Pro81Arg)
n.436C>G
11g.32435104G>TCA379966057WT1c.257C>A (p.Pro86His)
c.242C>A (p.Pro81His)
n.436C>A
 gnomAD v4
11g.32435105G>ACA379966058WT1c.256C>T (p.Pro86Ser)
c.241C>T (p.Pro81Ser)
n.435C>T
 dbSNP gnomAD v4 COSMIC COSMIC
11g.32435105G>CCA379966060WT1c.256C>G (p.Pro86Ala)
c.241C>G (p.Pro81Ala)
n.435C>G
11g.32435105G>TCA379966059WT1c.256C>A (p.Pro86Thr)
c.241C>A (p.Pro81Thr)
n.435C>A
 gnomAD v4
11g.32435106C>ACA473774031WT1c.255G>T (p.Leu85=)
c.240G>T (p.Leu80=)
n.434G>T
 gnomAD v4
11g.32435106C=CA1962327338WT1c.255G= (p.Leu85=)
c.240G= (p.Leu80=)
n.434G=
11g.32435106C>GCA473774024WT1c.255G>C (p.Leu85=)
c.240G>C (p.Leu80=)
n.434G>C
11g.32435106C>TCA473774023WT1c.255G>A (p.Leu85=)
c.240G>A (p.Leu80=)
n.434G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435107A>CCA379966061WT1c.254T>G (p.Leu85Arg)
c.239T>G (p.Leu80Arg)
n.433T>G
11g.32435107A>GCA379966062WT1c.254T>C (p.Leu85Pro)
c.239T>C (p.Leu80Pro)
n.433T>C
 ClinVar gnomAD v4
11g.32435107A>TCA379966063WT1c.254T>A (p.Leu85Gln)
c.239T>A (p.Leu80Gln)
n.433T>A
 gnomAD v4
11g.32435108G>ACA473774032WT1c.253C>T (p.Leu85=)
c.238C>T (p.Leu80=)
n.432C>T
 dbSNP gnomAD v4
11g.32435108G>CCA379966064WT1c.253C>G (p.Leu85Val)
c.238C>G (p.Leu80Val)
n.432C>G
11g.32435108G>TCA379966065WT1c.253C>A (p.Leu85Met)
c.238C>A (p.Leu80Met)
n.432C>A
 gnomAD v4
11g.32435109C>ACA473774035WT1c.252G>T (p.Leu84=)
c.237G>T (p.Leu79=)
n.431G>T
 dbSNP gnomAD v2 gnomAD v4
11g.32435109C=CA1962327339WT1c.252G= (p.Leu84=)
c.237G= (p.Leu79=)
n.431G=
11g.32435109C>GCA473774038WT1c.252G>C (p.Leu84=)
c.237G>C (p.Leu79=)
n.431G>C
11g.32435109C>TCA473774037WT1c.252G>A (p.Leu84=)
c.237G>A (p.Leu79=)
n.431G>A
 dbSNP gnomAD v4
11g.32435110A>CCA379966066WT1c.251T>G (p.Leu84Arg)
c.236T>G (p.Leu79Arg)
n.430T>G
 gnomAD v4
11g.32435110A>GCA379966067WT1c.251T>C (p.Leu84Pro)
c.236T>C (p.Leu79Pro)
n.430T>C
 gnomAD v4
11g.32435110A>TCA379966068WT1c.251T>A (p.Leu84Gln)
c.236T>A (p.Leu79Gln)
n.430T>A
11g.32435111G>ACA064783WT1c.250C>T (p.Leu84=)
c.235C>T (p.Leu79=)
n.429C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.32435111G>CCA379966069WT1c.250C>G (p.Leu84Val)
c.235C>G (p.Leu79Val)
n.429C>G
11g.32435111G=CA1962327340WT1c.250C= (p.Leu84=)
c.235C= (p.Leu79=)
n.429C=
11g.32435111G>TCA379966070WT1c.250C>A (p.Leu84Met)
c.235C>A (p.Leu79Met)
n.429C>A
 gnomAD v4
11g.32435112C>ACA473774039WT1c.249G>T (p.Ala83=)
c.234G>T (p.Ala78=)
n.428G>T
 ClinVar gnomAD v4
11g.32435112C=CA1962327341WT1c.249G= (p.Ala83=)
c.234G= (p.Ala78=)
n.428G=
11g.32435112C>GCA473774040WT1c.249G>C (p.Ala83=)
c.234G>C (p.Ala78=)
n.428G>C
 dbSNP gnomAD v2 gnomAD v4
11g.32435112C>TCA473774041WT1c.249G>A (p.Ala83=)
c.234G>A (p.Ala78=)
n.428G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435113G>ACA379966071WT1c.248C>T (p.Ala83Val)
c.233C>T (p.Ala78Val)
n.427C>T
 ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC
11g.32435113G>CCA379966073WT1c.248C>G (p.Ala83Gly)
c.233C>G (p.Ala78Gly)
n.427C>G
11g.32435113G=CA1962327342WT1c.248C= (p.Ala83=)
c.233C= (p.Ala78=)
n.427C=
11g.32435113G>TCA379966072WT1c.248C>A (p.Ala83Glu)
c.233C>A (p.Ala78Glu)
n.427C>A
 gnomAD v4
11g.32435113_32435114delinsAGCA2740093681WT1c.247_248delinsCT (p.Ala83Leu)
c.232_233delinsCT (p.Ala78Leu)
n.426_427delinsCT
 ClinVar
11g.32435114C>ACA10634698WT1c.247G>T (p.Ala83Ser)
c.232G>T (p.Ala78Ser)
n.426G>T
 ClinVar dbSNP gnomAD v4
11g.32435114C=CA1962327343WT1c.247G= (p.Ala83=)
c.232G= (p.Ala78=)
n.426G=
11g.32435114C>GCA379966074WT1c.247G>C (p.Ala83Pro)
c.232G>C (p.Ala78Pro)
n.426G>C
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435114C>TCA379966075WT1c.247G>A (p.Ala83Thr)
c.232G>A (p.Ala78Thr)
n.426G>A
 ClinVar gnomAD v4
11g.32435115G>ACA473774047WT1c.246C>T (p.Asn82=)
c.231C>T (p.Asn77=)
n.425C>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435115G>CCA379966076WT1c.246C>G (p.Asn82Lys)
c.231C>G (p.Asn77Lys)
n.425C>G
 ClinVar
11g.32435115G=CA1962327344WT1c.246C= (p.Asn82=)
c.231C= (p.Asn77=)
n.425C=
11g.32435115G>TCA379966077WT1c.246C>A (p.Asn82Lys)
c.231C>A (p.Asn77Lys)
n.425C>A
 ClinVar gnomAD v4
11g.32435116T>ACA379966078WT1c.245A>T (p.Asn82Ile)
c.230A>T (p.Asn77Ile)
n.424A>T
11g.32435116T>CCA379966079WT1c.245A>G (p.Asn82Ser)
c.230A>G (p.Asn77Ser)
n.424A>G
11g.32435116T>GCA379966080WT1c.245A>C (p.Asn82Thr)
c.230A>C (p.Asn77Thr)
n.424A>C
 dbSNP
11g.32435117T>ACA379966081WT1c.244A>T (p.Asn82Tyr)
c.229A>T (p.Asn77Tyr)
n.423A>T
11g.32435117T>CCA379966082WT1c.244A>G (p.Asn82Asp)
c.229A>G (p.Asn77Asp)
n.423A>G
 ClinVar gnomAD v4
11g.32435117T>GCA379966083WT1c.244A>C (p.Asn82His)
c.229A>C (p.Asn77His)
n.423A>C
11g.32435118C>ACA473774054WT1c.243G>T (p.Leu81=)
c.228G>T (p.Leu76=)
n.422G>T
 gnomAD v4
11g.32435118C>GCA473774055WT1c.243G>C (p.Leu81=)
c.228G>C (p.Leu76=)
n.422G>C
11g.32435118C>TCA473774056WT1c.243G>A (p.Leu81=)
c.228G>A (p.Leu76=)
n.422G>A
 gnomAD v4
11g.32435119A>CCA379966086WT1c.242T>G (p.Leu81Arg)
c.227T>G (p.Leu76Arg)
n.421T>G
 ClinVar dbSNP
11g.32435119A>GCA379966085WT1c.242T>C (p.Leu81Pro)
c.227T>C (p.Leu76Pro)
n.421T>C
 dbSNP gnomAD v4
11g.32435119A>TCA379966084WT1c.242T>A (p.Leu81Gln)
c.227T>A (p.Leu76Gln)
n.421T>A
 gnomAD v4
11g.32435120G>ACA473774057WT1c.241C>T (p.Leu81=)
c.226C>T (p.Leu76=)
n.420C>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435120G>CCA064777WT1c.241C>G (p.Leu81Val)
c.226C>G (p.Leu76Val)
n.420C>G
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.32435120G=CA1962327345WT1c.241C= (p.Leu81=)
c.226C= (p.Leu76=)
n.420C=
11g.32435120G>TCA379966087WT1c.241C>A (p.Leu81Met)
c.226C>A (p.Leu76Met)
n.420C>A
 ClinVar dbSNP gnomAD v4
11g.32435121G>ACA473774063WT1c.240C>T (p.Asp80=)
c.225C>T (p.Asp75=)
n.419C>T
 gnomAD v4
11g.32435121G>CCA379966088WT1c.240C>G (p.Asp80Glu)
c.225C>G (p.Asp75Glu)
n.419C>G
 ClinVar dbSNP gnomAD v4
11g.32435121G>TCA379966089WT1c.240C>A (p.Asp80Glu)
c.225C>A (p.Asp75Glu)
n.419C>A
 gnomAD v4
11g.32435122T>ACA379966090WT1c.239A>T (p.Asp80Val)
c.224A>T (p.Asp75Val)
n.418A>T
11g.32435122T>CCA379966091WT1c.239A>G (p.Asp80Gly)
c.224A>G (p.Asp75Gly)
n.418A>G
 ClinVar gnomAD v4
11g.32435122T>GCA379966092WT1c.239A>C (p.Asp80Ala)
c.224A>C (p.Asp75Ala)
n.418A>C
11g.32435123C>ACA379966093WT1c.238G>T (p.Asp80Tyr)
c.223G>T (p.Asp75Tyr)
n.417G>T
 gnomAD v4
11g.32435123C>GCA379966094WT1c.238G>C (p.Asp80His)
c.223G>C (p.Asp75His)
n.417G>C
 ClinVar
11g.32435123C>TCA379966095WT1c.238G>A (p.Asp80Asn)
c.223G>A (p.Asp75Asn)
n.417G>A
11g.32435125delCA2612989627WT1c.238del (p.Asp80ThrfsTer2)
c.223del (p.Asp75ThrfsTer2)
n.417del
 gnomAD v4
11g.32435124C>ACA473774070WT1c.237G>T (p.Arg79=)
c.222G>T (p.Arg74=)
n.416G>T
 gnomAD v4
11g.32435124C=CA1962327346WT1c.237G= (p.Arg79=)
c.222G= (p.Arg74=)
n.416G=
11g.32435124C>GCA473774074WT1c.237G>C (p.Arg79=)
c.222G>C (p.Arg74=)
n.416G>C
 ClinVar dbSNP gnomAD v4
11g.32435124C>TCA473774072WT1c.237G>A (p.Arg79=)
c.222G>A (p.Arg74=)
n.416G>A
 ClinVar gnomAD v4
11g.32435125C>ACA379966096WT1c.236G>T (p.Arg79Leu)
c.221G>T (p.Arg74Leu)
n.415G>T
 gnomAD v4
11g.32435125C=CA1962327347WT1c.236G= (p.Arg79=)
c.221G= (p.Arg74=)
n.415G=
11g.32435125C>GCA379966097WT1c.236G>C (p.Arg79Pro)
c.221G>C (p.Arg74Pro)
n.415G>C
 gnomAD v4
11g.32435125C>TCA379966098WT1c.236G>A (p.Arg79Gln)
c.221G>A (p.Arg74Gln)
n.415G>A
 ClinVar dbSNP gnomAD v4
11g.32435126G>ACA379966099WT1c.235C>T (p.Arg79Trp)
c.220C>T (p.Arg74Trp)
n.414C>T
 dbSNP gnomAD v4
11g.32435126G>CCA379966100WT1c.235C>G (p.Arg79Gly)
c.220C>G (p.Arg74Gly)
n.414C>G
11g.32435126G=CA1962327348WT1c.235C= (p.Arg79=)
c.220C= (p.Arg74=)
n.414C=
11g.32435126G>TCA473774078WT1c.235C>A (p.Arg79=)
c.220C>A (p.Arg74=)
n.414C>A
 gnomAD v4
11g.32435127C>ACA473774079WT1c.234G>T (p.Val78=)
c.219G>T (p.Val73=)
n.413G>T
 gnomAD v4
11g.32435127C>GCA473774082WT1c.234G>C (p.Val78=)
c.219G>C (p.Val73=)
n.413G>C
11g.32435127C>TCA473774084WT1c.234G>A (p.Val78=)
c.219G>A (p.Val73=)
n.413G>A
 gnomAD v4
11g.32435128A>CCA379966101WT1c.233T>G (p.Val78Gly)
c.218T>G (p.Val73Gly)
n.412T>G
11g.32435128A>GCA379966103WT1c.233T>C (p.Val78Ala)
c.218T>C (p.Val73Ala)
n.412T>C
 gnomAD v4
11g.32435128A>TCA379966102WT1c.233T>A (p.Val78Glu)
c.218T>A (p.Val73Glu)
n.412T>A
11g.32435129C>ACA379966104WT1c.232G>T (p.Val78Leu)
c.217G>T (p.Val73Leu)
n.411G>T
 ClinVar gnomAD v4
11g.32435129C=CA1962327349WT1c.232G= (p.Val78=)
c.217G= (p.Val73=)
n.411G=
11g.32435129C>GCA379966105WT1c.232G>C (p.Val78Leu)
c.217G>C (p.Val73Leu)
n.411G>C
 gnomAD v4
11g.32435129C>TCA379966106WT1c.232G>A (p.Val78Met)
c.217G>A (p.Val73Met)
n.411G>A
 ClinVar dbSNP gnomAD v4
11g.32435130G>ACA473774085WT1c.231C>T (p.Asp77=)
c.216C>T (p.Asp72=)
n.410C>T
 ClinVar dbSNP gnomAD v4
11g.32435130G>CCA379966107WT1c.231C>G (p.Asp77Glu)
c.216C>G (p.Asp72Glu)
n.410C>G
11g.32435130G=CA1962327350WT1c.231C= (p.Asp77=)
c.216C= (p.Asp72=)
n.410C=
11g.32435130G>TCA379966108WT1c.231C>A (p.Asp77Glu)
c.216C>A (p.Asp72Glu)
n.410C>A
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32435131T>ACA379966111WT1c.230A>T (p.Asp77Val)
c.215A>T (p.Asp72Val)
n.409A>T
 ClinVar dbSNP gnomAD v4
11g.32435131T>CCA379966110WT1c.230A>G (p.Asp77Gly)
c.215A>G (p.Asp72Gly)
n.409A>G
 gnomAD v4
11g.32435131T>GCA379966109WT1c.230A>C (p.Asp77Ala)
c.215A>C (p.Asp72Ala)
n.409A>C
11g.32435132C>ACA379966112WT1c.229G>T (p.Asp77Tyr)
c.214G>T (p.Asp72Tyr)
n.408G>T
 gnomAD v4
11g.32435132C>GCA379966113WT1c.229G>C (p.Asp77His)
c.214G>C (p.Asp72His)
n.408G>C
 gnomAD v4
11g.32435132C>TCA379966114WT1c.229G>A (p.Asp77Asn)
c.214G>A (p.Asp72Asn)
n.408G>A
 dbSNP gnomAD v4
11g.32435133G>ACA473774094WT1c.228C>T (p.Ser76=)
c.213C>T (p.Ser71=)
n.407C>T
 ClinVar dbSNP gnomAD v4
11g.32435133G>CCA473774098WT1c.228C>G (p.Ser76=)
c.213C>G (p.Ser71=)
n.407C>G
 ClinVar gnomAD v4
11g.32435133G>TCA473774100WT1c.228C>A (p.Ser76=)
c.213C>A (p.Ser71=)
n.407C>A
 gnomAD v4
11g.32435134G>ACA379966115WT1c.227C>T (p.Ser76Phe)
c.212C>T (p.Ser71Phe)
n.406C>T
 gnomAD v4
11g.32435134G>CCA379966116WT1c.227C>G (p.Ser76Cys)
c.212C>G (p.Ser71Cys)
n.406C>G
11g.32435134G>TCA379966117WT1c.227C>A (p.Ser76Tyr)
c.212C>A (p.Ser71Tyr)
n.406C>A
 gnomAD v4
11g.32435135A>CCA379966120WT1c.226T>G (p.Ser76Ala)
c.211T>G (p.Ser71Ala)
n.405T>G
11g.32435135A>GCA379966118WT1c.226T>C (p.Ser76Pro)
c.211T>C (p.Ser71Pro)
n.405T>C
 dbSNP
11g.32435135A>TCA379966119WT1c.226T>A (p.Ser76Thr)
c.211T>A (p.Ser71Thr)
n.405T>A
 dbSNP gnomAD v4
11g.32435136delCA2740093682WT1c.225del (p.Ser76ProfsTer6)
c.210del (p.Ser71ProfsTer6)
n.404del
 ClinVar
11g.32435136G>ACA473774105WT1c.225C>T (p.Gly75=)
c.210C>T (p.Gly70=)
n.404C>T
 ClinVar dbSNP
11g.32435136G>CCA473774106WT1c.225C>G (p.Gly75=)
c.210C>G (p.Gly70=)
n.404C>G
 ClinVar dbSNP
11g.32435136G=CA1962327351WT1c.225C= (p.Gly75=)
c.210C= (p.Gly70=)
n.404C=
11g.32435136G>TCA473774108WT1c.225C>A (p.Gly75=)
c.210C>A (p.Gly70=)
n.404C>A
 ClinVar dbSNP gnomAD v4
11g.32435137C>ACA379966121WT1c.224G>T (p.Gly75Val)
c.209G>T (p.Gly70Val)
n.403G>T
11g.32435137C=CA1962327352WT1c.224G= (p.Gly75=)
c.209G= (p.Gly70=)
n.403G=
11g.32435137C>GCA379966122WT1c.224G>C (p.Gly75Ala)
c.209G>C (p.Gly70Ala)
n.403G>C
 COSMIC COSMIC
11g.32435137C>TCA379966123WT1c.224G>A (p.Gly75Asp)
c.209G>A (p.Gly70Asp)
n.403G>A
 dbSNP gnomAD v2 gnomAD v4
11g.32435138C>ACA379966124WT1c.223G>T (p.Gly75Cys)
c.208G>T (p.Gly70Cys)
n.402G>T
 dbSNP gnomAD v4
11g.32435138C=CA1962327353WT1c.223G= (p.Gly75=)
c.208G= (p.Gly70=)
n.402G=
11g.32435138C>GCA379966125WT1c.223G>C (p.Gly75Arg)
c.208G>C (p.Gly70Arg)
n.402G>C
11g.32435138C>TCA064759WT1c.223G>A (p.Gly75Ser)
c.208G>A (p.Gly70Ser)
n.402G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32435139C>ACA379966126WT1c.222G>T (p.Met74Ile)
c.207G>T (p.Met69Ile)
n.401G>T
 dbSNP
11g.32435139C>GCA379966127WT1c.222G>C (p.Met74Ile)
c.207G>C (p.Met69Ile)
n.401G>C
11g.32435139C>TCA379966128WT1c.222G>A (p.Met74Ile)
c.207G>A (p.Met69Ile)
n.401G>A
 gnomAD v4
11g.32435140A>CCA379966129WT1c.221T>G (p.Met74Arg)
c.206T>G (p.Met69Arg)
n.400T>G
 dbSNP
11g.32435140A>GCA379966130WT1c.221T>C (p.Met74Thr)
c.206T>C (p.Met69Thr)
n.400T>C
 gnomAD v4
11g.32435140A>TCA379966131WT1c.221T>A (p.Met74Lys)
c.206T>A (p.Met69Lys)
n.400T>A
 dbSNP
11g.32435141T>ACA379966134WT1c.220A>T (p.Met74Leu)
c.205A>T (p.Met69Leu)
n.399A>T
 gnomAD v4
11g.32435141T>CCA379966132WT1c.220A>G (p.Met74Val)
c.205A>G (p.Met69Val)
n.399A>G
 ClinVar
11g.32435141T>GCA379966133WT1c.220A>C (p.Met74Leu)
c.205A>C (p.Met69Leu)
n.399A>C
11g.32435142T>ACA379966135WT1c.219A>T (p.Gln73His)
c.204A>T (p.Gln68His)
n.398A>T
11g.32435142T>CCA473774117WT1c.219A>G (p.Gln73=)
c.204A>G (p.Gln68=)
n.398A>G
 gnomAD v4
11g.32435142T>GCA379966136WT1c.219A>C (p.Gln73His)
c.204A>C (p.Gln68His)
n.398A>C
11g.32435143T>ACA219511297WT1c.218A>T (p.Gln73Leu)
c.203A>T (p.Gln68Leu)
n.397A>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435143T>CCA379966137WT1c.218A>G (p.Gln73Arg)
c.203A>G (p.Gln68Arg)
n.397A>G
11g.32435143T>GCA379966138WT1c.218A>C (p.Gln73Pro)
c.203A>C (p.Gln68Pro)
n.397A>C
11g.32435143T=CA1962327354WT1c.218A= (p.Gln73=)
c.203A= (p.Gln68=)
n.397A=
11g.32435144G>ACA379966139WT1c.217C>T (p.Gln73Ter)
c.202C>T (p.Gln68Ter)
n.396C>T
 gnomAD v4
11g.32435144G>CCA379966140WT1c.217C>G (p.Gln73Glu)
c.202C>G (p.Gln68Glu)
n.396C>G
11g.32435144G>TCA379966141WT1c.217C>A (p.Gln73Lys)
c.202C>A (p.Gln68Lys)
n.396C>A
 gnomAD v4
11g.32435145C>ACA064754WT1c.216G>T (p.Gln72His)
c.201G>T (p.Gln67His)
n.395G>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
11g.32435145C=CA1962327355WT1c.216G= (p.Gln72=)
c.201G= (p.Gln67=)
n.395G=
11g.32435145C>GCA379966142WT1c.216G>C (p.Gln72His)
c.201G>C (p.Gln67His)
n.395G>C
 ClinVar dbSNP gnomAD v4
11g.32435145C>TCA473774125WT1c.216G>A (p.Gln72=)
c.201G>A (p.Gln67=)
n.395G>A
 ClinVar gnomAD v4
11g.32435146T>ACA379966143WT1c.215A>T (p.Gln72Leu)
c.200A>T (p.Gln67Leu)
n.394A>T
 ClinVar dbSNP gnomAD v4
11g.32435146T>CCA379966144WT1c.215A>G (p.Gln72Arg)
c.200A>G (p.Gln67Arg)
n.394A>G
 gnomAD v4
11g.32435146T>GCA379966145WT1c.215A>C (p.Gln72Pro)
c.200A>C (p.Gln67Pro)
n.394A>C
11g.32435147G>ACA379966148WT1c.214C>T (p.Gln72Ter)
c.199C>T (p.Gln67Ter)
n.393C>T
 gnomAD v4
11g.32435147G>CCA379966146WT1c.214C>G (p.Gln72Glu)
c.199C>G (p.Gln67Glu)
n.393C>G
11g.32435147G>TCA379966147WT1c.214C>A (p.Gln72Lys)
c.199C>A (p.Gln67Lys)
n.393C>A
 gnomAD v4

Number of alleles fetched