Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.48981458G>ACA384637286WNT1c.931G>A (p.Ala311Thr)
c.898G>A (p.Ala300Thr)
 gnomAD v4
12g.48981458G>CCA384637290WNT1c.931G>C (p.Ala311Pro)
c.898G>C (p.Ala300Pro)
12g.48981458G>TCA384637288WNT1c.931G>T (p.Ala311Ser)
c.898G>T (p.Ala300Ser)
 gnomAD v4
12g.48981459C>ACA384637292WNT1c.932C>A (p.Ala311Glu)
c.899C>A (p.Ala300Glu)
 gnomAD v4
12g.48981459C=CA2034926184WNT1c.932C= (p.Ala311=)
c.899C= (p.Ala300=)
12g.48981459C>GCA384637295WNT1c.932C>G (p.Ala311Gly)
c.899C>G (p.Ala300Gly)
12g.48981459C>TCA384637296WNT1c.932C>T (p.Ala311Val)
c.899C>T (p.Ala300Val)
 dbSNP gnomAD v2 gnomAD v4
12g.48981460A=CA2034926187WNT1c.933A= (p.Ala311=)
c.900A= (p.Ala300=)
12g.48981460A>CCA479704584WNT1c.933A>C (p.Ala311=)
c.900A>C (p.Ala300=)
 dbSNP
12g.48981460A>GCA479704585WNT1c.933A>G (p.Ala311=)
c.900A>G (p.Ala300=)
 gnomAD v4
12g.48981460A>TCA479704587WNT1c.933A>T (p.Ala311=)
c.900A>T (p.Ala300=)
12g.48981461G>ACA384637300WNT1c.934G>A (p.Gly312Arg)
c.901G>A (p.Gly301Arg)
 gnomAD v4
12g.48981461G>CCA384637302WNT1c.934G>C (p.Gly312Arg)
c.901G>C (p.Gly301Arg)
12g.48981461G>TCA384637310WNT1c.934G>T (p.Gly312Trp)
c.901G>T (p.Gly301Trp)
 gnomAD v4
12g.48981462G>ACA384637314WNT1c.935G>A (p.Gly312Glu)
c.902G>A (p.Gly301Glu)
12g.48981462G>CCA384637324WNT1c.935G>C (p.Gly312Ala)
c.902G>C (p.Gly301Ala)
 dbSNP gnomAD v2 gnomAD v4
12g.48981462G=CA2034926189WNT1c.935G= (p.Gly312=)
c.902G= (p.Gly301=)
12g.48981462G>TCA384637326WNT1c.935G>T (p.Gly312Val)
c.902G>T (p.Gly301Val)
 gnomAD v4
12g.48981463G>ACA479704588WNT1c.936G>A (p.Gly312=)
c.903G>A (p.Gly301=)
12g.48981463G>CCA479704591WNT1c.936G>C (p.Gly312=)
c.903G>C (p.Gly301=)
12g.48981463G>TCA479704589WNT1c.936G>T (p.Gly312=)
c.903G>T (p.Gly301=)
 gnomAD v4
12g.48981464C>ACA384637333WNT1c.937C>A (p.Arg313Ser)
c.904C>A (p.Arg302Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v4
12g.48981464C=CA2034926192WNT1c.937C= (p.Arg313=)
c.904C= (p.Arg302=)
12g.48981464C>GCA384637345WNT1c.937C>G (p.Arg313Gly)
c.904C>G (p.Arg302Gly)
12g.48981464C>TCA384637349WNT1c.937C>T (p.Arg313Cys)
c.904C>T (p.Arg302Cys)
 gnomAD v4
12g.48981465G>ACA384637352WNT1c.938G>A (p.Arg313His)
c.905G>A (p.Arg302His)
 gnomAD v4
12g.48981465G>CCA384637359WNT1c.938G>C (p.Arg313Pro)
c.905G>C (p.Arg302Pro)
12g.48981465G>TCA384637356WNT1c.938G>T (p.Arg313Leu)
c.905G>T (p.Arg302Leu)
12g.48981465_48981466delinsTTCA2580085682WNT1c.938_939delinsTT (p.Arg313Leu)
c.905_906delinsTT (p.Arg302Leu)
 ClinVar
12g.48981466C>ACA479704594WNT1c.939C>A (p.Arg313=)
c.906C>A (p.Arg302=)
12g.48981466C=CA2034926196WNT1c.939C= (p.Arg313=)
c.906C= (p.Arg302=)
12g.48981466C>GCA479704595WNT1c.939C>G (p.Arg313=)
c.906C>G (p.Arg302=)
12g.48981466C>TCA479704596WNT1c.939C>T (p.Arg313=)
c.906C>T (p.Arg302=)
 dbSNP gnomAD v2 gnomAD v4
12g.48981467G>ACA384637360WNT1c.940G>A (p.Ala314Thr)
c.907G>A (p.Ala303Thr)
 gnomAD v4
12g.48981467G>CCA384637361WNT1c.940G>C (p.Ala314Pro)
c.907G>C (p.Ala303Pro)
12g.48981467G=CA2034926199WNT1c.940G= (p.Ala314=)
c.907G= (p.Ala303=)
12g.48981467G>TCA6544492WNT1c.940G>T (p.Ala314Ser)
c.907G>T (p.Ala303Ser)
 dbSNP ExAC gnomAD v2 gnomAD v4
12g.48981468C>ACA384637364WNT1c.941C>A (p.Ala314Asp)
c.908C>A (p.Ala303Asp)
12g.48981468C=CA2034926201WNT1c.941C= (p.Ala314=)
c.908C= (p.Ala303=)
12g.48981468C>GCA384637377WNT1c.941C>G (p.Ala314Gly)
c.908C>G (p.Ala303Gly)
12g.48981468C>TCA384637380WNT1c.941C>T (p.Ala314Val)
c.908C>T (p.Ala303Val)
 dbSNP gnomAD v4
12g.48981469C>ACA479704600WNT1c.942C>A (p.Ala314=)
c.909C>A (p.Ala303=)
 gnomAD v4
12g.48981469C>GCA479704601WNT1c.942C>G (p.Ala314=)
c.909C>G (p.Ala303=)
12g.48981469C>TCA479704602WNT1c.942C>T (p.Ala314=)
c.909C>T (p.Ala303=)
 gnomAD v4
12g.48981470T>ACA384637396WNT1c.943T>A (p.Cys315Ser)
c.910T>A (p.Cys304Ser)
 gnomAD v4
12g.48981470T>CCA384637397WNT1c.943T>C (p.Cys315Arg)
c.910T>C (p.Cys304Arg)
 gnomAD v4
12g.48981470T>GCA384637398WNT1c.943T>G (p.Cys315Gly)
c.910T>G (p.Cys304Gly)
 dbSNP gnomAD v2 gnomAD v4
12g.48981470T=CA2034926205WNT1c.943T= (p.Cys315=)
c.910T= (p.Cys304=)
12g.48981471delCA2695216599WNT1c.944del (p.Cys315LeufsTer?)
c.911del (p.Cys304LeufsTer?)
12g.48981471G>ACA384637403WNT1c.944G>A (p.Cys315Tyr)
c.911G>A (p.Cys304Tyr)
 gnomAD v4
12g.48981471G>CCA384637425WNT1c.944G>C (p.Cys315Ser)
c.911G>C (p.Cys304Ser)
12g.48981471G>TCA384637400WNT1c.944G>T (p.Cys315Phe)
c.911G>T (p.Cys304Phe)
 ClinVar dbSNP gnomAD v4
12g.48981472T>ACA384637428WNT1c.945T>A (p.Cys315Ter)
c.912T>A (p.Cys304Ter)
12g.48981472T>CCA479704606WNT1c.945T>C (p.Cys315=)
c.912T>C (p.Cys304=)
12g.48981472T>GCA384637433WNT1c.945T>G (p.Cys315Trp)
c.912T>G (p.Cys304Trp)
12g.48981472T=CA2034926210WNT1c.945T= (p.Cys315=)
c.912T= (p.Cys304=)
12g.48981473A>CCA384637440WNT1c.946A>C (p.Asn316His)
c.913A>C (p.Asn305His)
12g.48981473A>GCA384637445WNT1c.946A>G (p.Asn316Asp)
c.913A>G (p.Asn305Asp)
 gnomAD v4
12g.48981473A>TCA384637447WNT1c.946A>T (p.Asn316Tyr)
c.913A>T (p.Asn305Tyr)
12g.48981473_48981476dupCA143727WNT1c.946_949dup (p.Ser317LysfsTer?)
c.913_916dup (p.Ser306LysfsTer?)
 ClinVar dbSNP
12g.48981474A>CCA384637489WNT1c.947A>C (p.Asn316Thr)
c.914A>C (p.Asn305Thr)
12g.48981474A>GCA384637454WNT1c.947A>G (p.Asn316Ser)
c.914A>G (p.Asn305Ser)
12g.48981474A>TCA384637473WNT1c.947A>T (p.Asn316Ile)
c.914A>T (p.Asn305Ile)
12g.48981475C>ACA384637490WNT1c.948C>A (p.Asn316Lys)
c.915C>A (p.Asn305Lys)
 gnomAD v4
12g.48981475C>GCA384637491WNT1c.948C>G (p.Asn316Lys)
c.915C>G (p.Asn305Lys)
12g.48981475C>TCA479704610WNT1c.948C>T (p.Asn316=)
c.915C>T (p.Asn305=)
 gnomAD v4
12g.48981476A>CCA384637493WNT1c.949A>C (p.Ser317Arg)
c.916A>C (p.Ser306Arg)
 gnomAD v4
12g.48981476A>GCA384637495WNT1c.949A>G (p.Ser317Gly)
c.916A>G (p.Ser306Gly)
12g.48981476A>TCA384637500WNT1c.949A>T (p.Ser317Cys)
c.916A>T (p.Ser306Cys)
12g.48981477G>ACA384637501WNT1c.950G>A (p.Ser317Asn)
c.917G>A (p.Ser306Asn)
 gnomAD v4
12g.48981477G>CCA384637503WNT1c.950G>C (p.Ser317Thr)
c.917G>C (p.Ser306Thr)
12g.48981477G=CA2034926218WNT1c.950G= (p.Ser317=)
c.917G= (p.Ser306=)
12g.48981477G>TCA384637502WNT1c.950G>T (p.Ser317Ile)
c.917G>T (p.Ser306Ile)
 dbSNP gnomAD v2 gnomAD v4
12g.48981478C>ACA384637505WNT1c.951C>A (p.Ser317Arg)
c.918C>A (p.Ser306Arg)
12g.48981478C>GCA384637509WNT1c.951C>G (p.Ser317Arg)
c.918C>G (p.Ser306Arg)
12g.48981478C>TCA479704612WNT1c.951C>T (p.Ser317=)
c.918C>T (p.Ser306=)
 gnomAD v4
12g.48981479T>ACA384637516WNT1c.952T>A (p.Ser318Thr)
c.919T>A (p.Ser307Thr)
12g.48981479T>CCA384637518WNT1c.952T>C (p.Ser318Pro)
c.919T>C (p.Ser307Pro)
12g.48981479T>GCA384637522WNT1c.952T>G (p.Ser318Ala)
c.919T>G (p.Ser307Ala)
12g.48981480C>ACA384637526WNT1c.953C>A (p.Ser318Ter)
c.920C>A (p.Ser307Ter)
 ClinVar dbSNP gnomAD v4
12g.48981480C=CA2034926220WNT1c.953C= (p.Ser318=)
c.920C= (p.Ser307=)
12g.48981480C>GCA384637528WNT1c.953C>G (p.Ser318Trp)
c.920C>G (p.Ser307Trp)
 ClinVar dbSNP gnomAD v4
12g.48981480C>TCA236608803WNT1c.953C>T (p.Ser318Leu)
c.920C>T (p.Ser307Leu)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.48981481G>ACA479704615WNT1c.954G>A (p.Ser318=)
c.921G>A (p.Ser307=)
 dbSNP
12g.48981481G>CCA479704616WNT1c.954G>C (p.Ser318=)
c.921G>C (p.Ser307=)
12g.48981481G=CA2034926225WNT1c.954G= (p.Ser318=)
c.921G= (p.Ser307=)
12g.48981481G>TCA479704617WNT1c.954G>T (p.Ser318=)
c.921G>T (p.Ser307=)
12g.48981482T>ACA384637531WNT1c.955T>A (p.Ser319Thr)
c.922T>A (p.Ser308Thr)
12g.48981482T>CCA384637533WNT1c.955T>C (p.Ser319Pro)
c.922T>C (p.Ser308Pro)
12g.48981482T>GCA384637537WNT1c.955T>G (p.Ser319Ala)
c.922T>G (p.Ser308Ala)
12g.48981483C>ACA384637546WNT1c.956C>A (p.Ser319Ter)
c.923C>A (p.Ser308Ter)
12g.48981483C>GCA384637544WNT1c.956C>G (p.Ser319Trp)
c.923C>G (p.Ser308Trp)
12g.48981483C>TCA384637541WNT1c.956C>T (p.Ser319Leu)
c.923C>T (p.Ser308Leu)
 gnomAD v4
12g.48981484G>ACA479704621WNT1c.957G>A (p.Ser319=)
c.924G>A (p.Ser308=)
 gnomAD v4
12g.48981484G>CCA479704623WNT1c.957G>C (p.Ser319=)
c.924G>C (p.Ser308=)
12g.48981484G>TCA479704625WNT1c.957G>T (p.Ser319=)
c.924G>T (p.Ser308=)
12g.48981485C>ACA384637549WNT1c.958C>A (p.Pro320Thr)
c.925C>A (p.Pro309Thr)
 gnomAD v4
12g.48981485C=CA2034926228WNT1c.958C= (p.Pro320=)
c.925C= (p.Pro309=)
12g.48981485C>GCA384637558WNT1c.958C>G (p.Pro320Ala)
c.925C>G (p.Pro309Ala)
 dbSNP gnomAD v2 gnomAD v4
12g.48981485C>TCA384637554WNT1c.958C>T (p.Pro320Ser)
c.925C>T (p.Pro309Ser)
 gnomAD v4
12g.48981486C>ACA384637564WNT1c.959C>A (p.Pro320His)
c.926C>A (p.Pro309His)
12g.48981486C>GCA384637569WNT1c.959C>G (p.Pro320Arg)
c.926C>G (p.Pro309Arg)
12g.48981486C>TCA384637572WNT1c.959C>T (p.Pro320Leu)
c.926C>T (p.Pro309Leu)
12g.48981487C>ACA479704629WNT1c.960C>A (p.Pro320=)
c.927C>A (p.Pro309=)
 gnomAD v4
12g.48981487C=CA2034926231WNT1c.960C= (p.Pro320=)
c.927C= (p.Pro309=)
12g.48981487C>GCA479704631WNT1c.960C>G (p.Pro320=)
c.927C>G (p.Pro309=)
 dbSNP
12g.48981487C>TCA479704632WNT1c.960C>T (p.Pro320=)
c.927C>T (p.Pro309=)
 dbSNP gnomAD v2 gnomAD v4
12g.48981488G>ACA384637578WNT1c.961G>A (p.Ala321Thr)
c.928G>A (p.Ala310Thr)
 dbSNP gnomAD v4
12g.48981488G>CCA384637580WNT1c.961G>C (p.Ala321Pro)
c.928G>C (p.Ala310Pro)
12g.48981488G=CA2034926234WNT1c.961G= (p.Ala321=)
c.928G= (p.Ala310=)
12g.48981488G>TCA384637583WNT1c.961G>T (p.Ala321Ser)
c.928G>T (p.Ala310Ser)
12g.48981489C>ACA384637586WNT1c.962C>A (p.Ala321Glu)
c.929C>A (p.Ala310Glu)
12g.48981489C>GCA384637591WNT1c.962C>G (p.Ala321Gly)
c.929C>G (p.Ala310Gly)
12g.48981489C>TCA384637605WNT1c.962C>T (p.Ala321Val)
c.929C>T (p.Ala310Val)
12g.48981490G>ACA479704357WNT1c.963G>A (p.Ala321=)
c.930G>A (p.Ala310=)
 dbSNP gnomAD v2 gnomAD v4 COSMIC
12g.48981490G>CCA479704358WNT1c.963G>C (p.Ala321=)
c.930G>C (p.Ala310=)
12g.48981490G=CA2034926238WNT1c.963G= (p.Ala321=)
c.930G= (p.Ala310=)
12g.48981490G>TCA479704359WNT1c.963G>T (p.Ala321=)
c.930G>T (p.Ala310=)
12g.48981491C>ACA384637610WNT1c.964C>A (p.Leu322Met)
c.931C>A (p.Leu311Met)
12g.48981491C>GCA384637619WNT1c.964C>G (p.Leu322Val)
c.931C>G (p.Leu311Val)
12g.48981491C>TCA479704360WNT1c.964C>T (p.Leu322=)
c.931C>T (p.Leu311=)
12g.48981492T>ACA384637631WNT1c.965T>A (p.Leu322Gln)
c.932T>A (p.Leu311Gln)
12g.48981492T>CCA384637627WNT1c.965T>C (p.Leu322Pro)
c.932T>C (p.Leu311Pro)
12g.48981492T>GCA384637629WNT1c.965T>G (p.Leu322Arg)
c.932T>G (p.Leu311Arg)
12g.48981493G>ACA479704364WNT1c.966G>A (p.Leu322=)
c.933G>A (p.Leu311=)
12g.48981493G>CCA479704366WNT1c.966G>C (p.Leu322=)
c.933G>C (p.Leu311=)
12g.48981493G>TCA479704365WNT1c.966G>T (p.Leu322=)
c.933G>T (p.Leu311=)
 gnomAD v4
12g.48981494G>ACA384637632WNT1c.967G>A (p.Asp323Asn)
c.934G>A (p.Asp312Asn)
12g.48981494G>CCA384637633WNT1c.967G>C (p.Asp323His)
c.934G>C (p.Asp312His)
12g.48981494G>TCA384637635WNT1c.967G>T (p.Asp323Tyr)
c.934G>T (p.Asp312Tyr)
12g.48981495A>CCA384637637WNT1c.968A>C (p.Asp323Ala)
c.935A>C (p.Asp312Ala)
12g.48981495A>GCA384637640WNT1c.968A>G (p.Asp323Gly)
c.935A>G (p.Asp312Gly)
12g.48981495A>TCA384637644WNT1c.968A>T (p.Asp323Val)
c.935A>T (p.Asp312Val)
12g.48981496C>ACA384637649WNT1c.969C>A (p.Asp323Glu)
c.936C>A (p.Asp312Glu)
12g.48981496C=CA2034926242WNT1c.969C= (p.Asp323=)
c.936C= (p.Asp312=)
12g.48981496C>GCA384637655WNT1c.969C>G (p.Asp323Glu)
c.936C>G (p.Asp312Glu)
 dbSNP gnomAD v3 gnomAD v4
12g.48981496C>TCA479704369WNT1c.969C>T (p.Asp323=)
c.936C>T (p.Asp312=)
 gnomAD v4
12g.48981497G>ACA384637659WNT1c.970G>A (p.Gly324Ser)
c.937G>A (p.Gly313Ser)
 gnomAD v4
12g.48981497G>CCA6544493WNT1c.970G>C (p.Gly324Arg)
c.937G>C (p.Gly313Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
12g.48981497G=CA2034926245WNT1c.970G= (p.Gly324=)
c.937G= (p.Gly313=)
12g.48981497G>TCA384637667WNT1c.970G>T (p.Gly324Cys)
c.937G>T (p.Gly313Cys)
12g.48981498G>ACA384637688WNT1c.971G>A (p.Gly324Asp)
c.938G>A (p.Gly313Asp)
 dbSNP gnomAD v2 gnomAD v4
12g.48981498G>CCA384637692WNT1c.971G>C (p.Gly324Ala)
c.938G>C (p.Gly313Ala)
 dbSNP
12g.48981498G=CA2034926251WNT1c.971G= (p.Gly324=)
c.938G= (p.Gly313=)
12g.48981498G>TCA384637672WNT1c.971G>T (p.Gly324Val)
c.938G>T (p.Gly313Val)
 gnomAD v4
12g.48981499C>ACA479704375WNT1c.972C>A (p.Gly324=)
c.939C>A (p.Gly313=)
 gnomAD v4
12g.48981499C>GCA479704376WNT1c.972C>G (p.Gly324=)
c.939C>G (p.Gly313=)
12g.48981499C>TCA479704377WNT1c.972C>T (p.Gly324=)
c.939C>T (p.Gly313=)
12g.48981500T>ACA384637701WNT1c.973T>A (p.Cys325Ser)
c.940T>A (p.Cys314Ser)
12g.48981500T>CCA384637704WNT1c.973T>C (p.Cys325Arg)
c.940T>C (p.Cys314Arg)
 gnomAD v4
12g.48981500T>GCA384637712WNT1c.973T>G (p.Cys325Gly)
c.940T>G (p.Cys314Gly)
12g.48981501G>ACA384637719WNT1c.974G>A (p.Cys325Tyr)
c.941G>A (p.Cys314Tyr)
 gnomAD v4
12g.48981501G>CCA384637724WNT1c.974G>C (p.Cys325Ser)
c.941G>C (p.Cys314Ser)
12g.48981501G>TCA384637727WNT1c.974G>T (p.Cys325Phe)
c.941G>T (p.Cys314Phe)
12g.48981502C>ACA384637729WNT1c.975C>A (p.Cys325Ter)
c.942C>A (p.Cys314Ter)
 gnomAD v4 COSMIC
12g.48981502C=CA2034926253WNT1c.975C= (p.Cys325=)
c.942C= (p.Cys314=)
12g.48981502C>GCA384637730WNT1c.975C>G (p.Cys325Trp)
c.942C>G (p.Cys314Trp)
12g.48981502C>TCA6544494WNT1c.975C>T (p.Cys325=)
c.942C>T (p.Cys314=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.48981503G>ACA384637767WNT1c.976G>A (p.Glu326Lys)
c.943G>A (p.Glu315Lys)
 ClinVar gnomAD v4
12g.48981503G>CCA384637780WNT1c.976G>C (p.Glu326Gln)
c.943G>C (p.Glu315Gln)
12g.48981503G>TCA384637785WNT1c.976G>T (p.Glu326Ter)
c.943G>T (p.Glu315Ter)
 gnomAD v4
12g.48981504A>CCA384637821WNT1c.977A>C (p.Glu326Ala)
c.944A>C (p.Glu315Ala)
12g.48981504A>GCA384637826WNT1c.977A>G (p.Glu326Gly)
c.944A>G (p.Glu315Gly)
12g.48981504A>TCA384637817WNT1c.977A>T (p.Glu326Val)
c.944A>T (p.Glu315Val)
12g.48981505G>ACA479704387WNT1c.978G>A (p.Glu326=)
c.945G>A (p.Glu315=)
12g.48981505G>CCA384637827WNT1c.978G>C (p.Glu326Asp)
c.945G>C (p.Glu315Asp)
12g.48981505G>TCA384637828WNT1c.978G>T (p.Glu326Asp)
c.945G>T (p.Glu315Asp)
 gnomAD v4
12g.48981506C>ACA384637830WNT1c.979C>A (p.Leu327Met)
c.946C>A (p.Leu316Met)
12g.48981506C>GCA384637835WNT1c.979C>G (p.Leu327Val)
c.946C>G (p.Leu316Val)
12g.48981506C>TCA479704392WNT1c.979C>T (p.Leu327=)
c.946C>T (p.Leu316=)
 gnomAD v4
12g.48981507T>ACA384637859WNT1c.980T>A (p.Leu327Gln)
c.947T>A (p.Leu316Gln)
12g.48981507T>CCA384637849WNT1c.980T>C (p.Leu327Pro)
c.947T>C (p.Leu316Pro)
 gnomAD v4
12g.48981507T>GCA384637848WNT1c.980T>G (p.Leu327Arg)
c.947T>G (p.Leu316Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v4
12g.48981507T=CA2034926256WNT1c.980T= (p.Leu327=)
c.947T= (p.Leu316=)
12g.48981508G>ACA479704393WNT1c.981G>A (p.Leu327=)
c.948G>A (p.Leu316=)
 gnomAD v4
12g.48981508G>CCA479704394WNT1c.981G>C (p.Leu327=)
c.948G>C (p.Leu316=)
12g.48981508G>TCA479704395WNT1c.981G>T (p.Leu327=)
c.948G>T (p.Leu316=)
 gnomAD v4
12g.48981509C>ACA384637862WNT1c.982C>A (p.Leu328Ile)
c.949C>A (p.Leu317Ile)
 gnomAD v4
12g.48981509C=CA2034926260WNT1c.982C= (p.Leu328=)
c.949C= (p.Leu317=)
12g.48981509C>GCA384637870WNT1c.982C>G (p.Leu328Val)
c.949C>G (p.Leu317Val)
12g.48981509C>TCA236608806WNT1c.982C>T (p.Leu328Phe)
c.949C>T (p.Leu317Phe)
 dbSNP
12g.48981510T>ACA384637899WNT1c.983T>A (p.Leu328His)
c.950T>A (p.Leu317His)
12g.48981510T>CCA384637909WNT1c.983T>C (p.Leu328Pro)
c.950T>C (p.Leu317Pro)
 gnomAD v4
12g.48981510T>GCA384637914WNT1c.983T>G (p.Leu328Arg)
c.950T>G (p.Leu317Arg)
 dbSNP
12g.48981510T=CA2034926262WNT1c.983T= (p.Leu328=)
c.950T= (p.Leu317=)
12g.48981511C>ACA479704397WNT1c.984C>A (p.Leu328=)
c.951C>A (p.Leu317=)
12g.48981511C>GCA479704398WNT1c.984C>G (p.Leu328=)
c.951C>G (p.Leu317=)
12g.48981511C>TCA479704399WNT1c.984C>T (p.Leu328=)
c.951C>T (p.Leu317=)
12g.48981512T>ACA384637921WNT1c.985T>A (p.Cys329Ser)
c.952T>A (p.Cys318Ser)
12g.48981512T>CCA384637919WNT1c.985T>C (p.Cys329Arg)
c.952T>C (p.Cys318Arg)
12g.48981512T>GCA384637917WNT1c.985T>G (p.Cys329Gly)
c.952T>G (p.Cys318Gly)
12g.48981513G>ACA384637926WNT1c.986G>A (p.Cys329Tyr)
c.953G>A (p.Cys318Tyr)
12g.48981513G>CCA384637943WNT1c.986G>C (p.Cys329Ser)
c.953G>C (p.Cys318Ser)
12g.48981513G>TCA384637930WNT1c.986G>T (p.Cys329Phe)
c.953G>T (p.Cys318Phe)
 gnomAD v4
12g.48981514C>ACA384637950WNT1c.987C>A (p.Cys329Ter)
c.954C>A (p.Cys318Ter)
 gnomAD v4
12g.48981514C=CA2034926266WNT1c.987C= (p.Cys329=)
c.954C= (p.Cys318=)
12g.48981514C>GCA384637952WNT1c.987C>G (p.Cys329Trp)
c.954C>G (p.Cys318Trp)
12g.48981514C>TCA479704403WNT1c.987C>T (p.Cys329=)
c.954C>T (p.Cys318=)
 dbSNP gnomAD v2 gnomAD v4
12g.48981515T>ACA384637957WNT1c.988T>A (p.Cys330Ser)
c.955T>A (p.Cys319Ser)
12g.48981515T>CCA384637965WNT1c.988T>C (p.Cys330Arg)
c.955T>C (p.Cys319Arg)
 ClinVar dbSNP gnomAD v4
12g.48981515T>GCA384637969WNT1c.988T>G (p.Cys330Gly)
c.955T>G (p.Cys319Gly)
12g.48981515T=CA2034926268WNT1c.988T= (p.Cys330=)
c.955T= (p.Cys319=)
12g.48981516G>ACA384637990WNT1c.989G>A (p.Cys330Tyr)
c.956G>A (p.Cys319Tyr)
 ClinVar dbSNP gnomAD v4
12g.48981516G>CCA384638017WNT1c.989G>C (p.Cys330Ser)
c.956G>C (p.Cys319Ser)
12g.48981516G=CA2034926271WNT1c.989G= (p.Cys330=)
c.956G= (p.Cys319=)
12g.48981516G>TCA384638024WNT1c.989G>T (p.Cys330Phe)
c.956G>T (p.Cys319Phe)
 gnomAD v4
12g.48981517C>ACA236608808WNT1c.990C>A (p.Cys330Ter)
c.957C>A (p.Cys319Ter)
 dbSNP gnomAD v2 gnomAD v4
12g.48981517C=CA2034926277WNT1c.990C= (p.Cys330=)
c.957C= (p.Cys319=)
12g.48981517C>GCA384638028WNT1c.990C>G (p.Cys330Trp)
c.957C>G (p.Cys319Trp)
12g.48981517C>TCA479704408WNT1c.990C>T (p.Cys330=)
c.957C>T (p.Cys319=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.48981518G>ACA384638029WNT1c.991G>A (p.Gly331Ser)
c.958G>A (p.Gly320Ser)
 dbSNP gnomAD v2 gnomAD v4 COSMIC
12g.48981518G>CCA384638031WNT1c.991G>C (p.Gly331Arg)
c.958G>C (p.Gly320Arg)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.48981518G=CA2034926280WNT1c.991G= (p.Gly331=)
c.958G= (p.Gly320=)
12g.48981518G>TCA384638035WNT1c.991G>T (p.Gly331Cys)
c.958G>T (p.Gly320Cys)
 gnomAD v4
12g.48981519G>ACA384638052WNT1c.992G>A (p.Gly331Asp)
c.959G>A (p.Gly320Asp)
 gnomAD v4
12g.48981519G>CCA384638046WNT1c.992G>C (p.Gly331Ala)
c.959G>C (p.Gly320Ala)
12g.48981519G>TCA384638041WNT1c.992G>T (p.Gly331Val)
c.959G>T (p.Gly320Val)
 gnomAD v4
12g.48981520C>ACA479704413WNT1c.993C>A (p.Gly331=)
c.960C>A (p.Gly320=)
12g.48981520C=CA2034902072WNT1c.993C= (p.Gly331=)
c.960C= (p.Gly320=)
12g.48981520C>GCA479704414WNT1c.993C>G (p.Gly331=)
c.960C>G (p.Gly320=)
12g.48981520C>TCA236608810WNT1c.993C>T (p.Gly331=)
c.960C>T (p.Gly320=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.48981521A=CA2034902073WNT1c.994A= (p.Arg332=)
c.961A= (p.Arg321=)
12g.48981521A>CCA6544495WNT1c.994A>C (p.Arg332=)
c.961A>C (p.Arg321=)
 ClinVar dbSNP ExAC gnomAD v3 gnomAD v4
12g.48981521A>GCA384638058WNT1c.994A>G (p.Arg332Gly)
c.961A>G (p.Arg321Gly)
 COSMIC
12g.48981521A>TCA384638061WNT1c.994A>T (p.Arg332Trp)
c.961A>T (p.Arg321Trp)
12g.48981522G>ACA384638095WNT1c.995G>A (p.Arg332Lys)
c.962G>A (p.Arg321Lys)
12g.48981522G>CCA384638100WNT1c.995G>C (p.Arg332Thr)
c.962G>C (p.Arg321Thr)
 gnomAD v4
12g.48981522G>TCA384638104WNT1c.995G>T (p.Arg332Met)
c.962G>T (p.Arg321Met)
 gnomAD v4
12g.48981525dupCA2618599448WNT1c.998dup (p.His334ProfsTer?)
c.965dup (p.His323ProfsTer?)
 gnomAD v4
12g.48981525delCA2618599454WNT1c.998del (p.Gly333AlafsTer?)
c.965del (p.Gly322AlafsTer?)
 gnomAD v4
12g.48981523G>ACA236608814WNT1c.996G>A (p.Arg332=)
c.963G>A (p.Arg321=)
 dbSNP gnomAD v2 gnomAD v4
12g.48981523G>CCA384638119WNT1c.996G>C (p.Arg332Ser)
c.963G>C (p.Arg321Ser)
12g.48981523G=CA2034902074WNT1c.996G= (p.Arg332=)
c.963G= (p.Arg321=)
12g.48981523G>TCA384638121WNT1c.996G>T (p.Arg332Ser)
c.963G>T (p.Arg321Ser)
 gnomAD v4
12g.48981524G>ACA384638122WNT1c.997G>A (p.Gly333Ser)
c.964G>A (p.Gly322Ser)
 gnomAD v4
12g.48981524G>CCA384638123WNT1c.997G>C (p.Gly333Arg)
c.964G>C (p.Gly322Arg)
12g.48981524G>TCA384638125WNT1c.997G>T (p.Gly333Cys)
c.964G>T (p.Gly322Cys)
12g.48981524_48981547delinsGGCCACCGCACGCGCACGCAGCGCCA2034902075WNT1c.997_1020delinsGGCCACCGCACGCGCACGCAGCGC (p.Gly333=)
c.964_987delinsGGCCACCGCACGCGCACGCAGCGC (p.Gly322=)
12g.48981525G>ACA384638139WNT1c.998G>A (p.Gly333Asp)
c.965G>A (p.Gly322Asp)
 gnomAD v4
12g.48981525G>CCA384638133WNT1c.998G>C (p.Gly333Ala)
c.965G>C (p.Gly322Ala)
12g.48981525G>TCA384638131WNT1c.998G>T (p.Gly333Val)
c.965G>T (p.Gly322Val)
 gnomAD v4
12g.48981526_48981548delCA947424479WNT1c.999_1021del (p.Thr336AlafsTer?)
c.966_988del (p.Thr325AlafsTer?)
 ClinVar dbSNP gnomAD v3 gnomAD v4
12g.48981526C>ACA479704422WNT1c.999C>A (p.Gly333=)
c.966C>A (p.Gly322=)
 gnomAD v4
12g.48981526C>GCA479704424WNT1c.999C>G (p.Gly333=)
c.966C>G (p.Gly322=)
12g.48981526C>TCA479704421WNT1c.999C>T (p.Gly333=)
c.966C>T (p.Gly322=)
 gnomAD v4
12g.48981526_48981549delinsCCACCGCACGCGCACGCAGCGCGTCA2034902076WNT1c.999_1022delinsCCACCGCACGCGCACGCAGCGCGT (p.Gly333=)
c.966_989delinsCCACCGCACGCGCACGCAGCGCGT (p.Gly322=)
12g.48981527C>ACA384638166WNT1c.1000C>A (p.His334Asn)
c.967C>A (p.His323Asn)
12g.48981527C>GCA384638153WNT1c.1000C>G (p.His334Asp)
c.967C>G (p.His323Asp)
12g.48981527C>TCA384638165WNT1c.1000C>T (p.His334Tyr)
c.967C>T (p.His323Tyr)
 dbSNP
12g.48981532_48981554delCA605233429WNT1c.1005_1027del (p.Thr336AlafsTer?)
c.972_994del (p.Thr325AlafsTer?)
 ClinVar dbSNP gnomAD v2 gnomAD v4
12g.48981528A>CCA384638167WNT1c.1001A>C (p.His334Pro)
c.968A>C (p.His323Pro)
12g.48981528A>GCA384638168WNT1c.1001A>G (p.His334Arg)
c.968A>G (p.His323Arg)
12g.48981528A>TCA384638170WNT1c.1001A>T (p.His334Leu)
c.968A>T (p.His323Leu)
12g.48981529C>ACA384638175WNT1c.1002C>A (p.His334Gln)
c.969C>A (p.His323Gln)
12g.48981529C>GCA384638177WNT1c.1002C>G (p.His334Gln)
c.969C>G (p.His323Gln)
12g.48981529C>TCA479704426WNT1c.1002C>T (p.His334=)
c.969C>T (p.His323=)
 gnomAD v4
12g.48981530C>ACA384638180WNT1c.1003C>A (p.Arg335Ser)
c.970C>A (p.Arg324Ser)
12g.48981530C=CA2034902077WNT1c.1003C= (p.Arg335=)
c.970C= (p.Arg324=)
12g.48981530C>GCA384638185WNT1c.1003C>G (p.Arg335Gly)
c.970C>G (p.Arg324Gly)
 dbSNP
12g.48981530C>TCA384638189WNT1c.1003C>T (p.Arg335Cys)
c.970C>T (p.Arg324Cys)
 gnomAD v4
12g.48981531G>ACA384638194WNT1c.1004G>A (p.Arg335His)
c.971G>A (p.Arg324His)
 gnomAD v4
12g.48981531G>CCA384638200WNT1c.1004G>C (p.Arg335Pro)
c.971G>C (p.Arg324Pro)
12g.48981531G=CA2034902078WNT1c.1004G= (p.Arg335=)
c.971G= (p.Arg324=)
12g.48981531G>TCA384638202WNT1c.1004G>T (p.Arg335Leu)
c.971G>T (p.Arg324Leu)
 dbSNP gnomAD v4
12g.48981532C>ACA479704431WNT1c.1005C>A (p.Arg335=)
c.972C>A (p.Arg324=)
 gnomAD v4
12g.48981532C>GCA479704433WNT1c.1005C>G (p.Arg335=)
c.972C>G (p.Arg324=)
 gnomAD v4
12g.48981532C>TCA479704432WNT1c.1005C>T (p.Arg335=)
c.972C>T (p.Arg324=)
12g.48981533A=CA2034902079WNT1c.1006A= (p.Thr336=)
c.973A= (p.Thr325=)
12g.48981533A>CCA384638216WNT1c.1006A>C (p.Thr336Pro)
c.973A>C (p.Thr325Pro)
 dbSNP gnomAD v3 gnomAD v4
12g.48981533A>GCA384638206WNT1c.1006A>G (p.Thr336Ala)
c.973A>G (p.Thr325Ala)
12g.48981533A>TCA384638209WNT1c.1006A>T (p.Thr336Ser)
c.973A>T (p.Thr325Ser)
12g.48981534C>ACA384638232WNT1c.1007C>A (p.Thr336Lys)
c.974C>A (p.Thr325Lys)
 gnomAD v4
12g.48981534C=CA2034902080WNT1c.1007C= (p.Thr336=)
c.974C= (p.Thr325=)
12g.48981534C>GCA384638233WNT1c.1007C>G (p.Thr336Arg)
c.974C>G (p.Thr325Arg)
12g.48981534C>TCA6544496WNT1c.1007C>T (p.Thr336Met)
c.974C>T (p.Thr325Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.48981535G>ACA479704440WNT1c.1008G>A (p.Thr336=)
c.975G>A (p.Thr325=)
 gnomAD v4
12g.48981535G>CCA479704441WNT1c.1008G>C (p.Thr336=)
c.975G>C (p.Thr325=)
12g.48981535G>TCA479704442WNT1c.1008G>T (p.Thr336=)
c.975G>T (p.Thr325=)
 gnomAD v4
12g.48981536C>ACA384638234WNT1c.1009C>A (p.Arg337Ser)
c.976C>A (p.Arg326Ser)
12g.48981536C>GCA384638255WNT1c.1009C>G (p.Arg337Gly)
c.976C>G (p.Arg326Gly)
12g.48981536C>TCA384638256WNT1c.1009C>T (p.Arg337Cys)
c.976C>T (p.Arg326Cys)
12g.48981537G>ACA384638276WNT1c.1010G>A (p.Arg337His)
c.977G>A (p.Arg326His)
 gnomAD v4
12g.48981537G>CCA384638281WNT1c.1010G>C (p.Arg337Pro)
c.977G>C (p.Arg326Pro)
12g.48981537G>TCA384638287WNT1c.1010G>T (p.Arg337Leu)
c.977G>T (p.Arg326Leu)
 gnomAD v4
12g.48981538C>ACA479704447WNT1c.1011C>A (p.Arg337=)
c.978C>A (p.Arg326=)
 gnomAD v4
12g.48981538C>GCA479704448WNT1c.1011C>G (p.Arg337=)
c.978C>G (p.Arg326=)
12g.48981538C>TCA479704449WNT1c.1011C>T (p.Arg337=)
c.978C>T (p.Arg326=)
12g.48981539A>CCA384638288WNT1c.1012A>C (p.Thr338Pro)
c.979A>C (p.Thr327Pro)
12g.48981539A>GCA384638289WNT1c.1012A>G (p.Thr338Ala)
c.979A>G (p.Thr327Ala)
 gnomAD v4
12g.48981539A>TCA384638290WNT1c.1012A>T (p.Thr338Ser)
c.979A>T (p.Thr327Ser)
12g.48981540C>ACA384638299WNT1c.1013C>A (p.Thr338Lys)
c.980C>A (p.Thr327Lys)
 gnomAD v4
12g.48981540C=CA2034902081WNT1c.1013C= (p.Thr338=)
c.980C= (p.Thr327=)
12g.48981540C>GCA384638295WNT1c.1013C>G (p.Thr338Arg)
c.980C>G (p.Thr327Arg)
 dbSNP gnomAD v3 gnomAD v4
12g.48981540C>TCA384638292WNT1c.1013C>T (p.Thr338Met)
c.980C>T (p.Thr327Met)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.48981541G>ACA479704453WNT1c.1014G>A (p.Thr338=)
c.981G>A (p.Thr327=)
 gnomAD v4
12g.48981541G>CCA479704454WNT1c.1014G>C (p.Thr338=)
c.981G>C (p.Thr327=)
12g.48981541G>TCA479704455WNT1c.1014G>T (p.Thr338=)
c.981G>T (p.Thr327=)
 gnomAD v4
12g.48981542C>ACA384638302WNT1c.1015C>A (p.Gln339Lys)
c.982C>A (p.Gln328Lys)
 gnomAD v4
12g.48981542C>GCA384638304WNT1c.1015C>G (p.Gln339Glu)
c.982C>G (p.Gln328Glu)
 gnomAD v4
12g.48981542C>TCA384638306WNT1c.1015C>T (p.Gln339Ter)
c.982C>T (p.Gln328Ter)
12g.48981543A>CCA384638332WNT1c.1016A>C (p.Gln339Pro)
c.983A>C (p.Gln328Pro)
 gnomAD v4
12g.48981543A>GCA384638335WNT1c.1016A>G (p.Gln339Arg)
c.983A>G (p.Gln328Arg)
12g.48981543A>TCA384638337WNT1c.1016A>T (p.Gln339Leu)
c.983A>T (p.Gln328Leu)
 gnomAD v4
12g.48981544G>ACA479704459WNT1c.1017G>A (p.Gln339=)
c.984G>A (p.Gln328=)
12g.48981544G>CCA384638349WNT1c.1017G>C (p.Gln339His)
c.984G>C (p.Gln328His)
12g.48981544G>TCA384638342WNT1c.1017G>T (p.Gln339His)
c.984G>T (p.Gln328His)
 gnomAD v4
12g.48981545C>ACA384638355WNT1c.1018C>A (p.Arg340Ser)
c.985C>A (p.Arg329Ser)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.48981545C=CA2034902082WNT1c.1018C= (p.Arg340=)
c.985C= (p.Arg329=)
12g.48981545C>GCA384638378WNT1c.1018C>G (p.Arg340Gly)
c.985C>G (p.Arg329Gly)
12g.48981545C>TCA384638386WNT1c.1018C>T (p.Arg340Cys)
c.985C>T (p.Arg329Cys)
 dbSNP gnomAD v2 gnomAD v4
12g.48981546G>ACA384638400WNT1c.1019G>A (p.Arg340His)
c.986G>A (p.Arg329His)
12g.48981546G>CCA6544497WNT1c.1019G>C (p.Arg340Pro)
c.986G>C (p.Arg329Pro)
 dbSNP ExAC gnomAD v2 gnomAD v4
12g.48981546G=CA2034902083WNT1c.1019G= (p.Arg340=)
c.986G= (p.Arg329=)
12g.48981546G>TCA384638420WNT1c.1019G>T (p.Arg340Leu)
c.986G>T (p.Arg329Leu)
12g.48981547C>ACA479704466WNT1c.1020C>A (p.Arg340=)
c.987C>A (p.Arg329=)
 gnomAD v4
12g.48981547C>GCA479704464WNT1c.1020C>G (p.Arg340=)
c.987C>G (p.Arg329=)
12g.48981547C>TCA479704465WNT1c.1020C>T (p.Arg340=)
c.987C>T (p.Arg329=)
 gnomAD v4
12g.48981548G>ACA384638455WNT1c.1021G>A (p.Val341Ile)
c.988G>A (p.Val330Ile)
 gnomAD v4
12g.48981548G>CCA384638428WNT1c.1021G>C (p.Val341Leu)
c.988G>C (p.Val330Leu)
12g.48981548G>TCA384638446WNT1c.1021G>T (p.Val341Phe)
c.988G>T (p.Val330Phe)
12g.48981549T>ACA384638465WNT1c.1022T>A (p.Val341Asp)
c.989T>A (p.Val330Asp)
12g.48981549T>CCA384638469WNT1c.1022T>C (p.Val341Ala)
c.989T>C (p.Val330Ala)
 dbSNP gnomAD v4
12g.48981549T>GCA384638474WNT1c.1022T>G (p.Val341Gly)
c.989T>G (p.Val330Gly)
12g.48981549T=CA2034902084WNT1c.1022T= (p.Val341=)
c.989T= (p.Val330=)
12g.48981550C>ACA479704471WNT1c.1023C>A (p.Val341=)
c.990C>A (p.Val330=)
 gnomAD v4
12g.48981550C=CA2034902085WNT1c.1023C= (p.Val341=)
c.990C= (p.Val330=)
12g.48981550C>GCA479704470WNT1c.1023C>G (p.Val341=)
c.990C>G (p.Val330=)
12g.48981550C>TCA479704469WNT1c.1023C>T (p.Val341=)
c.990C>T (p.Val330=)
 dbSNP gnomAD v2 gnomAD v4
12g.48981551A>CCA384638480WNT1c.1024A>C (p.Thr342Pro)
c.991A>C (p.Thr331Pro)
12g.48981551A>GCA384638481WNT1c.1024A>G (p.Thr342Ala)
c.991A>G (p.Thr331Ala)
 gnomAD v4
12g.48981551A>TCA384638482WNT1c.1024A>T (p.Thr342Ser)
c.991A>T (p.Thr331Ser)
12g.48981551_48981552delinsACCA2034902086WNT1c.1024_1025delinsAC (p.Thr342=)
c.991_992delinsAC (p.Thr331=)
12g.48981552C>ACA384638486WNT1c.1025C>A (p.Thr342Asn)
c.992C>A (p.Thr331Asn)
 gnomAD v4
12g.48981552C=CA2034902087WNT1c.1025C= (p.Thr342=)
c.992C= (p.Thr331=)
12g.48981552C>GCA6544498WNT1c.1025C>G (p.Thr342Ser)
c.992C>G (p.Thr331Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.48981552C>TCA384638493WNT1c.1025C>T (p.Thr342Ile)
c.992C>T (p.Thr331Ile)
12g.48981553delCA185909WNT1c.1026del (p.Glu343SerfsTer?)
c.993del (p.Glu332SerfsTer?)
 ClinVar dbSNP gnomAD v4
12g.48981553C>ACA479704478WNT1c.1026C>A (p.Thr342=)
c.993C>A (p.Thr331=)
 gnomAD v4
12g.48981553C>GCA479704480WNT1c.1026C>G (p.Thr342=)
c.993C>G (p.Thr331=)
12g.48981553C>TCA479704479WNT1c.1026C>T (p.Thr342=)
c.993C>T (p.Thr331=)
12g.48981554G>ACA384638502WNT1c.1027G>A (p.Glu343Lys)
c.994G>A (p.Glu332Lys)
 gnomAD v4
12g.48981554G>CCA6544499WNT1c.1027G>C (p.Glu343Gln)
c.994G>C (p.Glu332Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.48981554G=CA2034902088WNT1c.1027G= (p.Glu343=)
c.994G= (p.Glu332=)
12g.48981554G>TCA384638511WNT1c.1027G>T (p.Glu343Ter)
c.994G>T (p.Glu332Ter)
 gnomAD v4
12g.48981555A>CCA384638524WNT1c.1028A>C (p.Glu343Ala)
c.995A>C (p.Glu332Ala)
12g.48981555A>GCA384638538WNT1c.1028A>G (p.Glu343Gly)
c.995A>G (p.Glu332Gly)
12g.48981555A>TCA384638528WNT1c.1028A>T (p.Glu343Val)
c.995A>T (p.Glu332Val)
12g.48981556G>ACA479704487WNT1c.1029G>A (p.Glu343=)
c.996G>A (p.Glu332=)
12g.48981556G>CCA384638555WNT1c.1029G>C (p.Glu343Asp)
c.996G>C (p.Glu332Asp)
 dbSNP gnomAD v3 gnomAD v4
12g.48981556G=CA2034902089WNT1c.1029G= (p.Glu343=)
c.996G= (p.Glu332=)
12g.48981556G>TCA384638567WNT1c.1029G>T (p.Glu343Asp)
c.996G>T (p.Glu332Asp)
12g.48981557C>ACA384638575WNT1c.1030C>A (p.Arg344Ser)
c.997C>A (p.Arg333Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.48981557C=CA2034902090WNT1c.1030C= (p.Arg344=)
c.997C= (p.Arg333=)
12g.48981557C>GCA384638580WNT1c.1030C>G (p.Arg344Gly)
c.997C>G (p.Arg333Gly)
 gnomAD v4
12g.48981557C>TCA384638594WNT1c.1030C>T (p.Arg344Cys)
c.997C>T (p.Arg333Cys)
 gnomAD v4
12g.48981558G>ACA384638609WNT1c.1031G>A (p.Arg344His)
c.998G>A (p.Arg333His)
 dbSNP gnomAD v2 gnomAD v4
12g.48981558G>CCA384638611WNT1c.1031G>C (p.Arg344Pro)
c.998G>C (p.Arg333Pro)
12g.48981558G=CA2034902091WNT1c.1031G= (p.Arg344=)
c.998G= (p.Arg333=)
12g.48981558G>TCA384638612WNT1c.1031G>T (p.Arg344Leu)
c.998G>T (p.Arg333Leu)
 gnomAD v4

Number of alleles fetched