Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.48981363delCA2618599013WNT1c.836del (p.Pro279ArgfsTer?)
c.827+9del (n.827+9del)
gnomAD v4
12g.48981362C>ACA384635914WNT1c.835C>A (p.Pro279Thr)
c.827+8C>A (n.827+8C>A)
gnomAD v4
12g.48981362C=CA2034926055WNT1c.835C= (p.Pro279=)
c.827+8C= (n.827+8C=)
12g.48981362C>GCA384635923WNT1c.835C>G (p.Pro279Ala)
c.827+8C>G (n.827+8C>G)
12g.48981362C>TCA384635925WNT1c.835C>T (p.Pro279Ser)
c.827+8C>T (n.827+8C>T)
dbSNP gnomAD v4
12g.48981363C>ACA384635935WNT1c.836C>A (p.Pro279Gln)
c.827+9C>A (n.827+9C>A)
dbSNP gnomAD v4
12g.48981363C=CA2034926057WNT1c.836C= (p.Pro279=)
c.827+9C= (n.827+9C=)
12g.48981363C>GCA236608777WNT1c.836C>G (p.Pro279Arg)
c.827+9C>G (n.827+9C>G)
dbSNP gnomAD v2 gnomAD v4
12g.48981363C>TCA384635953WNT1c.836C>T (p.Pro279Leu)
c.827+9C>T (n.827+9C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.48981364G>ACA479704415WNT1c.837G>A (p.Pro279=)
c.827+10G>A (n.827+10G>A)
gnomAD v4
12g.48981364G>CCA479704416WNT1c.837G>C (p.Pro279=)
c.827+10G>C (n.827+10G>C)
12g.48981364G=CA2034926059WNT1c.837G= (p.Pro279=)
c.827+10G= (n.827+10G=)
12g.48981364G>TCA479704417WNT1c.837G>T (p.Pro279=)
c.827+10G>T (n.827+10G>T)
dbSNP gnomAD v4
12g.48981365G>ACA384635967WNT1c.838G>A (p.Ala280Thr)
c.827+11G>A (n.827+11G>A)
dbSNP gnomAD v4
12g.48981365G>CCA384635980WNT1c.838G>C (p.Ala280Pro)
c.827+11G>C (n.827+11G>C)
dbSNP gnomAD v4
12g.48981365G=CA2034926060WNT1c.838G= (p.Ala280=)
c.827+11G= (n.827+11G=)
12g.48981365G>TCA384635977WNT1c.838G>T (p.Ala280Ser)
c.827+11G>T (n.827+11G>T)
gnomAD v4
12g.48981366C>ACA384635983WNT1c.839C>A (p.Ala280Asp)
c.827+12C>A (n.827+12C>A)
gnomAD v4
12g.48981366C=CA2034926062WNT1c.839C= (p.Ala280=)
c.827+12C= (n.827+12C=)
12g.48981366C>GCA384635993WNT1c.839C>G (p.Ala280Gly)
c.827+12C>G (n.827+12C>G)
dbSNP gnomAD v2
12g.48981366C>TCA384635997WNT1c.839C>T (p.Ala280Val)
c.827+12C>T (n.827+12C>T)
dbSNP gnomAD v4
12g.48981367C>ACA479704418WNT1c.840C>A (p.Ala280=)
c.827+13C>A (n.827+13C>A)
gnomAD v4
12g.48981367C>GCA479704419WNT1c.840C>G (p.Ala280=)
c.827+13C>G (n.827+13C>G)
12g.48981367C>TCA479704420WNT1c.840C>T (p.Ala280=)
c.827+13C>T (n.827+13C>T)
gnomAD v4
12g.48981368C>ACA384636003WNT1c.841C>A (p.His281Asn)
c.827+14C>A (n.827+14C>A)
gnomAD v4
12g.48981368C=CA2034926064WNT1c.841C= (p.His281=)
c.827+14C= (n.827+14C=)
12g.48981368C>GCA384636007WNT1c.841C>G (p.His281Asp)
c.827+14C>G (n.827+14C>G)
12g.48981368C>TCA384636015WNT1c.841C>T (p.His281Tyr)
c.827+14C>T (n.827+14C>T)
dbSNP gnomAD v2 gnomAD v4
12g.48981369A>CCA384636024WNT1c.842A>C (p.His281Pro)
c.827+15A>C (n.827+15A>C)
12g.48981369A>GCA384636031WNT1c.842A>G (p.His281Arg)
c.827+15A>G (n.827+15A>G)
gnomAD v4
12g.48981369A>TCA384636039WNT1c.842A>T (p.His281Leu)
c.827+15A>T (n.827+15A>T)
12g.48981370C>ACA384636049WNT1c.843C>A (p.His281Gln)
c.827+16C>A (n.827+16C>A)
gnomAD v4
12g.48981370C>GCA384636058WNT1c.843C>G (p.His281Gln)
c.827+16C>G (n.827+16C>G)
gnomAD v4
12g.48981370C>TCA479704425WNT1c.843C>T (p.His281=)
c.827+16C>T (n.827+16C>T)
gnomAD v4
12g.48981371A>CCA384636083WNT1c.844A>C (p.Lys282Gln)
c.828-17A>C (n.828-17A>C)
12g.48981371A>GCA384636088WNT1c.844A>G (p.Lys282Glu)
c.828-17A>G (n.828-17A>G)
gnomAD v4
12g.48981371A>TCA384636067WNT1c.844A>T (p.Lys282Ter)
c.828-17A>T (n.828-17A>T)
12g.48981372A>CCA384636094WNT1c.845A>C (p.Lys282Thr)
c.828-16A>C (n.828-16A>C)
12g.48981372A>GCA384636095WNT1c.845A>G (p.Lys282Arg)
c.828-16A>G (n.828-16A>G)
gnomAD v4
12g.48981372A>TCA384636096WNT1c.845A>T (p.Lys282Ile)
c.828-16A>T (n.828-16A>T)
gnomAD v4
12g.48981373A=CA2034926066WNT1c.846A= (p.Lys282=)
c.828-15A= (n.828-15A=)
12g.48981373A>CCA384636102WNT1c.846A>C (p.Lys282Asn)
c.828-15A>C (n.828-15A>C)
12g.48981373A>GCA6544484WNT1c.846A>G (p.Lys282=)
c.828-15A>G (n.828-15A>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.48981373A>TCA384636105WNT1c.846A>T (p.Lys282Asn)
c.828-15A>T (n.828-15A>T)
12g.48981374C>ACA384636116WNT1c.847C>A (p.Pro283Thr)
c.828-14C>A (n.828-14C>A)
gnomAD v4
12g.48981374C>GCA384636106WNT1c.847C>G (p.Pro283Ala)
c.828-14C>G (n.828-14C>G)
12g.48981374C>TCA384636111WNT1c.847C>T (p.Pro283Ser)
c.828-14C>T (n.828-14C>T)
gnomAD v4
12g.48981375C>ACA384636121WNT1c.848C>A (p.Pro283Gln)
c.828-13C>A (n.828-13C>A)
dbSNP gnomAD v4
12g.48981375C=CA2034926068WNT1c.848C= (p.Pro283=)
c.828-13C= (n.828-13C=)
12g.48981375C>GCA384636130WNT1c.848C>G (p.Pro283Arg)
c.828-13C>G (n.828-13C>G)
gnomAD v4
12g.48981375C>TCA384636132WNT1c.848C>T (p.Pro283Leu)
c.828-13C>T (n.828-13C>T)
dbSNP gnomAD v4
12g.48981376G>ACA479704438WNT1c.849G>A (p.Pro283=)
c.828-12G>A (n.828-12G>A)
gnomAD v4
12g.48981376G>CCA479704436WNT1c.849G>C (p.Pro283=)
c.828-12G>C (n.828-12G>C)
12g.48981376G=CA2034926070WNT1c.849G= (p.Pro283=)
c.828-12G= (n.828-12G=)
12g.48981376G>TCA479704434WNT1c.849G>T (p.Pro283=)
c.828-12G>T (n.828-12G>T)
dbSNP gnomAD v4
12g.48981377C>ACA384636139WNT1c.850C>A (p.Pro284Thr)
c.828-11C>A (n.828-11C>A)
gnomAD v4
12g.48981377C=CA2034926071WNT1c.850C= (p.Pro284=)
c.828-11C= (n.828-11C=)
12g.48981377C>GCA384636141WNT1c.850C>G (p.Pro284Ala)
c.828-11C>G (n.828-11C>G)
12g.48981377C>TCA6544485WNT1c.850C>T (p.Pro284Ser)
c.828-11C>T (n.828-11C>T)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.48981378C>ACA384636147WNT1c.851C>A (p.Pro284His)
c.828-10C>A (n.828-10C>A)
12g.48981378C>GCA384636164WNT1c.851C>G (p.Pro284Arg)
c.828-10C>G (n.828-10C>G)
12g.48981378C>TCA384636155WNT1c.851C>T (p.Pro284Leu)
c.828-10C>T (n.828-10C>T)
gnomAD v4
12g.48981379C>ACA479704443WNT1c.852C>A (p.Pro284=)
c.828-9C>A (n.828-9C>A)
gnomAD v4
12g.48981379C=CA2034926073WNT1c.852C= (p.Pro284=)
c.828-9C= (n.828-9C=)
12g.48981379C>GCA479704444WNT1c.852C>G (p.Pro284=)
c.828-9C>G (n.828-9C>G)
12g.48981379C>TCA479704445WNT1c.852C>T (p.Pro284=)
c.828-9C>T (n.828-9C>T)
dbSNP gnomAD v2 gnomAD v4
12g.48981380delCA2618599082WNT1c.853del (p.Ser285ProfsTer?)
c.828-8del (n.828-8del)
gnomAD v4
12g.48981380T>ACA384636172WNT1c.853T>A (p.Ser285Thr)
c.828-8T>A (n.828-8T>A)
gnomAD v4
12g.48981380T>CCA384636184WNT1c.853T>C (p.Ser285Pro)
c.828-8T>C (n.828-8T>C)
gnomAD v4
12g.48981380T>GCA384636191WNT1c.853T>G (p.Ser285Ala)
c.828-8T>G (n.828-8T>G)
12g.48981380T=CA2034926075WNT1c.853T= (p.Ser285=)
c.828-8T= (n.828-8T=)
12g.48981381C>ACA384636192WNT1c.854C>A (p.Ser285Tyr)
c.828-7C>A (n.828-7C>A)
dbSNP gnomAD v4
12g.48981381C=CA2034926078WNT1c.854C= (p.Ser285=)
c.828-7C= (n.828-7C=)
12g.48981381C>GCA6544486WNT1c.854C>G (p.Ser285Cys)
c.828-7C>G (n.828-7C>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.48981381C>TCA384636197WNT1c.854C>T (p.Ser285Phe)
c.828-7C>T (n.828-7C>T)
gnomAD v4
12g.48981386dupCA143720WNT1c.859dup (p.His287ProfsTer30)
c.828-2dup (n.828-2dup)
ClinVar dbSNP gnomAD v4
12g.48981386delCA645574753WNT1c.859del (p.His287ThrfsTer?)
c.828-2del (n.828-2del)
gnomAD v4 COSMIC
12g.48981382C>ACA479704450WNT1c.855C>A (p.Ser285=)
c.828-6C>A (n.828-6C>A)
gnomAD v4 COSMIC
12g.48981382C=CA2034926080WNT1c.855C= (p.Ser285=)
c.828-6C= (n.828-6C=)
12g.48981382C>GCA479704451WNT1c.855C>G (p.Ser285=)
c.828-6C>G (n.828-6C>G)
dbSNP gnomAD v4
12g.48981382C>TCA479704452WNT1c.855C>T (p.Ser285=)
c.828-6C>T (n.828-6C>T)
dbSNP gnomAD v4
12g.48981383C>ACA236608785WNT1c.856C>A (p.Pro286Thr)
c.828-5C>A (n.828-5C>A)
dbSNP gnomAD v4
12g.48981383C=CA2034926082WNT1c.856C= (p.Pro286=)
c.828-5C= (n.828-5C=)
12g.48981383C>GCA384636206WNT1c.856C>G (p.Pro286Ala)
c.828-5C>G (n.828-5C>G)
12g.48981383C>TCA6544487WNT1c.856C>T (p.Pro286Ser)
c.828-5C>T (n.828-5C>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.48981384C>ACA236608788WNT1c.857C>A (p.Pro286His)
c.828-4C>A (n.828-4C>A)
dbSNP gnomAD v4
12g.48981384C=CA2034926085WNT1c.857C= (p.Pro286=)
c.828-4C= (n.828-4C=)
12g.48981384C>GCA384636231WNT1c.857C>G (p.Pro286Arg)
c.828-4C>G (n.828-4C>G)
dbSNP gnomAD v2 gnomAD v4
12g.48981384C>TCA384636242WNT1c.857C>T (p.Pro286Leu)
c.828-4C>T (n.828-4C>T)
dbSNP gnomAD v2 gnomAD v4
12g.48981385C>ACA236608790WNT1c.858C>A (p.Pro286=)
c.828-3C>A (n.828-3C>A)
ClinVar dbSNP gnomAD v3 gnomAD v4
12g.48981385C=CA2034926087WNT1c.858C= (p.Pro286=)
c.828-3C= (n.828-3C=)
12g.48981385C>GCA479704457WNT1c.858C>G (p.Pro286=)
c.828-3C>G (n.828-3C>G)
ClinVar dbSNP gnomAD v2 gnomAD v4
12g.48981385C>TCA479704458WNT1c.858C>T (p.Pro286=)
c.828-3C>T (n.828-3C>T)
gnomAD v4
12g.48981386C>ACA384636257WNT1c.859C>A (p.His287Asn)
c.828-2C>A (n.828-2C>A)
dbSNP gnomAD v3 gnomAD v4
12g.48981386C=CA2034926088WNT1c.859C= (p.His287=)
c.828-2C= (n.828-2C=)
12g.48981386C>GCA6544488WNT1c.859C>G (p.His287Asp)
c.828-2C>G (n.828-2C>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.48981386C>TCA6544489WNT1c.859C>T (p.His287Tyr)
c.828-2C>T (n.828-2C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.48981387A>CCA384636321WNT1c.860A>C (p.His287Pro)
c.828-1A>C (n.828-1A>C)
12g.48981387A>GCA384636324WNT1c.860A>G (p.His287Arg)
c.828-1A>G (n.828-1A>G)
12g.48981387A>TCA384636329WNT1c.860A>T (p.His287Leu)
c.828-1A>T (n.828-1A>T)
12g.48981387dupCA2573148647WNT1c.860dup (p.His287GlnfsTer30)
c.828-1dup (n.828-1dup)
ClinVar dbSNP
12g.48981388C>ACA384636332WNT1c.861C>A (p.His287Gln)
c.828C>A (p.Pro276=)
gnomAD v4
12g.48981388C>GCA384636333WNT1c.861C>G (p.His287Gln)
c.828C>G (p.Pro276=)
12g.48981388C>TCA479704463WNT1c.861C>T (p.His287=)
c.828C>T (p.Pro276=)
gnomAD v4
12g.48981389G>ACA236608797WNT1c.862G>A (p.Asp288Asn)
c.829G>A (p.Asp277Asn)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.48981389G>CCA384636351WNT1c.862G>C (p.Asp288His)
c.829G>C (p.Asp277His)
12g.48981389G=CA2034926091WNT1c.862G= (p.Asp288=)
c.829G= (p.Asp277=)
12g.48981389G>TCA384636356WNT1c.862G>T (p.Asp288Tyr)
c.829G>T (p.Asp277Tyr)
12g.48981390A>CCA384636359WNT1c.863A>C (p.Asp288Ala)
c.830A>C (p.Asp277Ala)
12g.48981390A>GCA384636361WNT1c.863A>G (p.Asp288Gly)
c.830A>G (p.Asp277Gly)
gnomAD v4
12g.48981390A>TCA384636365WNT1c.863A>T (p.Asp288Val)
c.830A>T (p.Asp277Val)
gnomAD v4
12g.48981391C>ACA384636370WNT1c.864C>A (p.Asp288Glu)
c.831C>A (p.Asp277Glu)
gnomAD v4
12g.48981391C=CA2034926094WNT1c.864C= (p.Asp288=)
c.831C= (p.Asp277=)
12g.48981391C>GCA384636372WNT1c.864C>G (p.Asp288Glu)
c.831C>G (p.Asp277Glu)
12g.48981391C>TCA479704468WNT1c.864C>T (p.Asp288=)
c.831C>T (p.Asp277=)
dbSNP gnomAD v2 gnomAD v4
12g.48981392C>ACA384636413WNT1c.865C>A (p.Leu289Ile)
c.832C>A (p.Leu278Ile)
gnomAD v4
12g.48981392C>GCA384636390WNT1c.865C>G (p.Leu289Val)
c.832C>G (p.Leu278Val)
12g.48981392C>TCA384636407WNT1c.865C>T (p.Leu289Phe)
c.832C>T (p.Leu278Phe)
12g.48981393T>ACA384636433WNT1c.866T>A (p.Leu289His)
c.833T>A (p.Leu278His)
12g.48981393T>CCA384636440WNT1c.866T>C (p.Leu289Pro)
c.833T>C (p.Leu278Pro)
gnomAD v4
12g.48981393T>GCA384636446WNT1c.866T>G (p.Leu289Arg)
c.833T>G (p.Leu278Arg)
12g.48981394C>ACA479704475WNT1c.867C>A (p.Leu289=)
c.834C>A (p.Leu278=)
gnomAD v4
12g.48981394C>GCA479704476WNT1c.867C>G (p.Leu289=)
c.834C>G (p.Leu278=)
12g.48981394C>TCA479704477WNT1c.867C>T (p.Leu289=)
c.834C>T (p.Leu278=)
gnomAD v4
12g.48981395G>ACA384636450WNT1c.868G>A (p.Val290Ile)
c.835G>A (p.Val279Ile)
dbSNP gnomAD v3 gnomAD v4
12g.48981395G>CCA384636456WNT1c.868G>C (p.Val290Leu)
c.835G>C (p.Val279Leu)
gnomAD v4
12g.48981395G=CA2034926096WNT1c.868G= (p.Val290=)
c.835G= (p.Val279=)
12g.48981395G>TCA384636459WNT1c.868G>T (p.Val290Phe)
c.835G>T (p.Val279Phe)
gnomAD v4
12g.48981396T>ACA384636462WNT1c.869T>A (p.Val290Asp)
c.836T>A (p.Val279Asp)
12g.48981396T>CCA384636467WNT1c.869T>C (p.Val290Ala)
c.836T>C (p.Val279Ala)
gnomAD v4
12g.48981396T>GCA384636470WNT1c.869T>G (p.Val290Gly)
c.836T>G (p.Val279Gly)
12g.48981397C>ACA479704486WNT1c.870C>A (p.Val290=)
c.837C>A (p.Val279=)
gnomAD v4
12g.48981397C>GCA479704485WNT1c.870C>G (p.Val290=)
c.837C>G (p.Val279=)
12g.48981397C>TCA479704484WNT1c.870C>T (p.Val290=)
c.837C>T (p.Val279=)
12g.48981398T>ACA384636472WNT1c.871T>A (p.Tyr291Asn)
c.838T>A (p.Tyr280Asn)
gnomAD v4
12g.48981398T>CCA384636473WNT1c.871T>C (p.Tyr291His)
c.838T>C (p.Tyr280His)
gnomAD v4
12g.48981398T>GCA384636476WNT1c.871T>G (p.Tyr291Asp)
c.838T>G (p.Tyr280Asp)
12g.48981399A=CA2034926099WNT1c.872A= (p.Tyr291=)
c.839A= (p.Tyr280=)
12g.48981399A>CCA384636502WNT1c.872A>C (p.Tyr291Ser)
c.839A>C (p.Tyr280Ser)
12g.48981399A>GCA384636504WNT1c.872A>G (p.Tyr291Cys)
c.839A>G (p.Tyr280Cys)
12g.48981399A>TCA384636484WNT1c.872A>T (p.Tyr291Phe)
c.839A>T (p.Tyr280Phe)
dbSNP gnomAD v2 gnomAD v4
12g.48981400C>ACA384636507WNT1c.873C>A (p.Tyr291Ter)
c.840C>A (p.Tyr280Ter)
gnomAD v4
12g.48981400C=CA2034926103WNT1c.873C= (p.Tyr291=)
c.840C= (p.Tyr280=)
12g.48981400C>GCA384636505WNT1c.873C>G (p.Tyr291Ter)
c.840C>G (p.Tyr280Ter)
gnomAD v4
12g.48981400C>TCA479704489WNT1c.873C>T (p.Tyr291=)
c.840C>T (p.Tyr280=)
dbSNP
12g.48981401T>ACA384636513WNT1c.874T>A (p.Phe292Ile)
c.841T>A (p.Phe281Ile)
gnomAD v4
12g.48981401T>CCA384636522WNT1c.874T>C (p.Phe292Leu)
c.841T>C (p.Phe281Leu)
dbSNP gnomAD v2 gnomAD v4
12g.48981401T>GCA384636526WNT1c.874T>G (p.Phe292Val)
c.841T>G (p.Phe281Val)
ClinVar dbSNP gnomAD v4
12g.48981401T=CA2034926108WNT1c.874T= (p.Phe292=)
c.841T= (p.Phe281=)
12g.48981402T>ACA384636531WNT1c.875T>A (p.Phe292Tyr)
c.842T>A (p.Phe281Tyr)
gnomAD v4
12g.48981402T>CCA384636533WNT1c.875T>C (p.Phe292Ser)
c.842T>C (p.Phe281Ser)
gnomAD v4
12g.48981402T>GCA384636535WNT1c.875T>G (p.Phe292Cys)
c.842T>G (p.Phe281Cys)
12g.48981403C>ACA236608799WNT1c.876C>A (p.Phe292Leu)
c.843C>A (p.Phe281Leu)
dbSNP gnomAD v4
12g.48981403C=CA2034926110WNT1c.876C= (p.Phe292=)
c.843C= (p.Phe281=)
12g.48981403C>GCA384636545WNT1c.876C>G (p.Phe292Leu)
c.843C>G (p.Phe281Leu)
ClinVar dbSNP gnomAD v4
12g.48981403C>TCA479704493WNT1c.876C>T (p.Phe292=)
c.843C>T (p.Phe281=)
dbSNP gnomAD v4
12g.48981404G>ACA384636550WNT1c.877G>A (p.Glu293Lys)
c.844G>A (p.Glu282Lys)
gnomAD v4
12g.48981404G>CCA384636572WNT1c.877G>C (p.Glu293Gln)
c.844G>C (p.Glu282Gln)
gnomAD v4
12g.48981404G>TCA384636577WNT1c.877G>T (p.Glu293Ter)
c.844G>T (p.Glu282Ter)
gnomAD v4
12g.48981405A>CCA384636601WNT1c.878A>C (p.Glu293Ala)
c.845A>C (p.Glu282Ala)
12g.48981405A>GCA384636588WNT1c.878A>G (p.Glu293Gly)
c.845A>G (p.Glu282Gly)
12g.48981405A>TCA384636582WNT1c.878A>T (p.Glu293Val)
c.845A>T (p.Glu282Val)
12g.48981406G>ACA479704496WNT1c.879G>A (p.Glu293=)
c.846G>A (p.Glu282=)
gnomAD v4
12g.48981406G>CCA384636605WNT1c.879G>C (p.Glu293Asp)
c.846G>C (p.Glu282Asp)
12g.48981406G=CA2034926112WNT1c.879G= (p.Glu293=)
c.846G= (p.Glu282=)
12g.48981406G>TCA384636618WNT1c.879G>T (p.Glu293Asp)
c.846G>T (p.Glu282Asp)
dbSNP gnomAD v4
12g.48981407A>CCA384636624WNT1c.880A>C (p.Lys294Gln)
c.847A>C (p.Lys283Gln)
12g.48981407A>GCA384636631WNT1c.880A>G (p.Lys294Glu)
c.847A>G (p.Lys283Glu)
gnomAD v4
12g.48981407A>TCA384636641WNT1c.880A>T (p.Lys294Ter)
c.847A>T (p.Lys283Ter)
12g.48981408A>CCA384636650WNT1c.881A>C (p.Lys294Thr)
c.848A>C (p.Lys283Thr)
12g.48981408A>GCA384636651WNT1c.881A>G (p.Lys294Arg)
c.848A>G (p.Lys283Arg)
gnomAD v4
12g.48981408A>TCA384636653WNT1c.881A>T (p.Lys294Ile)
c.848A>T (p.Lys283Ile)
ClinVar gnomAD v4
12g.48981409A>CCA384636662WNT1c.882A>C (p.Lys294Asn)
c.849A>C (p.Lys283Asn)
12g.48981409A>GCA479704502WNT1c.882A>G (p.Lys294=)
c.849A>G (p.Lys283=)
12g.48981409A>TCA384636663WNT1c.882A>T (p.Lys294Asn)
c.849A>T (p.Lys283Asn)
12g.48981410T>ACA384636667WNT1c.883T>A (p.Ser295Thr)
c.850T>A (p.Ser284Thr)
12g.48981410T>CCA384636668WNT1c.883T>C (p.Ser295Pro)
c.850T>C (p.Ser284Pro)
gnomAD v4
12g.48981410T>GCA384636671WNT1c.883T>G (p.Ser295Ala)
c.850T>G (p.Ser284Ala)
12g.48981411C>ACA143725WNT1c.884C>A (p.Ser295Ter)
c.851C>A (p.Ser284Ter)
ClinVar dbSNP gnomAD v4
12g.48981411C=CA2034926115WNT1c.884C= (p.Ser295=)
c.851C= (p.Ser284=)
12g.48981411C>GCA384636691WNT1c.884C>G (p.Ser295Trp)
c.851C>G (p.Ser284Trp)
12g.48981411C>TCA384636690WNT1c.884C>T (p.Ser295Leu)
c.851C>T (p.Ser284Leu)
ClinVar gnomAD v4
12g.48981412G>ACA479704507WNT1c.885G>A (p.Ser295=)
c.852G>A (p.Ser284=)
gnomAD v4
12g.48981412G>CCA479704508WNT1c.885G>C (p.Ser295=)
c.852G>C (p.Ser284=)
12g.48981412G>TCA479704509WNT1c.885G>T (p.Ser295=)
c.852G>T (p.Ser284=)
gnomAD v4
12g.48981413C>ACA384636700WNT1c.886C>A (p.Pro296Thr)
c.853C>A (p.Pro285Thr)
gnomAD v4
12g.48981413C>GCA384636698WNT1c.886C>G (p.Pro296Ala)
c.853C>G (p.Pro285Ala)
12g.48981413C>TCA384636699WNT1c.886C>T (p.Pro296Ser)
c.853C>T (p.Pro285Ser)
gnomAD v4
12g.48981414C>ACA384636713WNT1c.887C>A (p.Pro296His)
c.854C>A (p.Pro285His)
gnomAD v4
12g.48981414C>GCA384636722WNT1c.887C>G (p.Pro296Arg)
c.854C>G (p.Pro285Arg)
12g.48981414C>TCA384636725WNT1c.887C>T (p.Pro296Leu)
c.854C>T (p.Pro285Leu)
gnomAD v4
12g.48981415C>ACA479704512WNT1c.888C>A (p.Pro296=)
c.855C>A (p.Pro285=)
gnomAD v4
12g.48981415C>GCA479704514WNT1c.888C>G (p.Pro296=)
c.855C>G (p.Pro285=)
gnomAD v4
12g.48981415C>TCA479704517WNT1c.888C>T (p.Pro296=)
c.855C>T (p.Pro285=)
gnomAD v4
12g.48981416A>CCA384636741WNT1c.889A>C (p.Asn297His)
c.856A>C (p.Asn286His)
12g.48981416A>GCA384636749WNT1c.889A>G (p.Asn297Asp)
c.856A>G (p.Asn286Asp)
gnomAD v4
12g.48981416A>TCA384636751WNT1c.889A>T (p.Asn297Tyr)
c.856A>T (p.Asn286Tyr)
12g.48981417A>CCA384636752WNT1c.890A>C (p.Asn297Thr)
c.857A>C (p.Asn286Thr)
gnomAD v4
12g.48981417A>GCA384636755WNT1c.890A>G (p.Asn297Ser)
c.857A>G (p.Asn286Ser)
12g.48981417A>TCA384636760WNT1c.890A>T (p.Asn297Ile)
c.857A>T (p.Asn286Ile)
12g.48981418C>ACA384636761WNT1c.891C>A (p.Asn297Lys)
c.858C>A (p.Asn286Lys)
12g.48981418C=CA2034926120WNT1c.891C= (p.Asn297=)
c.858C= (p.Asn286=)
12g.48981418C>GCA384636762WNT1c.891C>G (p.Asn297Lys)
c.858C>G (p.Asn286Lys)
12g.48981418C>TCA479704520WNT1c.891C>T (p.Asn297=)
c.858C>T (p.Asn286=)
dbSNP
12g.48981419T>ACA384636788WNT1c.892T>A (p.Phe298Ile)
c.859T>A (p.Phe287Ile)
gnomAD v4
12g.48981419T>CCA384636766WNT1c.892T>C (p.Phe298Leu)
c.859T>C (p.Phe287Leu)
gnomAD v4
12g.48981419T>GCA384636777WNT1c.892T>G (p.Phe298Val)
c.859T>G (p.Phe287Val)
12g.48981420T>ACA384636796WNT1c.893T>A (p.Phe298Tyr)
c.860T>A (p.Phe287Tyr)
12g.48981420T>CCA384636825WNT1c.893T>C (p.Phe298Ser)
c.860T>C (p.Phe287Ser)
12g.48981420T>GCA384636831WNT1c.893T>G (p.Phe298Cys)
c.860T>G (p.Phe287Cys)
ClinVar dbSNP
12g.48981421C>ACA384636840WNT1c.894C>A (p.Phe298Leu)
c.861C>A (p.Phe287Leu)
gnomAD v4
12g.48981421C>GCA384636846WNT1c.894C>G (p.Phe298Leu)
c.861C>G (p.Phe287Leu)
gnomAD v4
12g.48981421C>TCA479704523WNT1c.894C>T (p.Phe298=)
c.861C>T (p.Phe287=)
gnomAD v4
12g.48981422T>ACA384636852WNT1c.895T>A (p.Cys299Ser)
c.862T>A (p.Cys288Ser)
12g.48981422T>CCA384636853WNT1c.895T>C (p.Cys299Arg)
c.862T>C (p.Cys288Arg)
dbSNP
12g.48981422T>GCA384636854WNT1c.895T>G (p.Cys299Gly)
c.862T>G (p.Cys288Gly)
12g.48981422T=CA2034926124WNT1c.895T= (p.Cys299=)
c.862T= (p.Cys288=)
12g.48981423G>ACA384636856WNT1c.896G>A (p.Cys299Tyr)
c.863G>A (p.Cys288Tyr)
gnomAD v4
12g.48981423G>CCA384636858WNT1c.896G>C (p.Cys299Ser)
c.863G>C (p.Cys288Ser)
12g.48981423G>TCA384636870WNT1c.896G>T (p.Cys299Phe)
c.863G>T (p.Cys288Phe)
12g.48981424C>ACA384636886WNT1c.897C>A (p.Cys299Ter)
c.864C>A (p.Cys288Ter)
gnomAD v4
12g.48981424C=CA2034926127WNT1c.897C= (p.Cys299=)
c.864C= (p.Cys288=)
12g.48981424C>GCA384636887WNT1c.897C>G (p.Cys299Trp)
c.864C>G (p.Cys288Trp)
12g.48981424C>TCA479704528WNT1c.897C>T (p.Cys299=)
c.864C>T (p.Cys288=)
dbSNP gnomAD v2 gnomAD v4
12g.48981425A=CA2034926131WNT1c.898A= (p.Thr300=)
c.865A= (p.Thr289=)
12g.48981425A>CCA384636895WNT1c.898A>C (p.Thr300Pro)
c.865A>C (p.Thr289Pro)
12g.48981425A>GCA384636896WNT1c.898A>G (p.Thr300Ala)
c.865A>G (p.Thr289Ala)
dbSNP
12g.48981425A>TCA384636890WNT1c.898A>T (p.Thr300Ser)
c.865A>T (p.Thr289Ser)
12g.48981426C>ACA6544490WNT1c.899C>A (p.Thr300Lys)
c.866C>A (p.Thr289Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.48981426C=CA2034926135WNT1c.899C= (p.Thr300=)
c.866C= (p.Thr289=)
12g.48981426C>GCA384636910WNT1c.899C>G (p.Thr300Arg)
c.866C>G (p.Thr289Arg)
gnomAD v4
12g.48981426C>TCA384636898WNT1c.899C>T (p.Thr300Met)
c.866C>T (p.Thr289Met)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.48981427G>ACA479704529WNT1c.900G>A (p.Thr300=)
c.867G>A (p.Thr289=)
dbSNP gnomAD v2 gnomAD v4
12g.48981427G>CCA479704530WNT1c.900G>C (p.Thr300=)
c.867G>C (p.Thr289=)
12g.48981427G=CA2034926139WNT1c.900G= (p.Thr300=)
c.867G= (p.Thr289=)
12g.48981427G>TCA479704531WNT1c.900G>T (p.Thr300=)
c.867G>T (p.Thr289=)
gnomAD v4
12g.48981428T>ACA384636931WNT1c.901T>A (p.Tyr301Asn)
c.868T>A (p.Tyr290Asn)
dbSNP gnomAD v2 gnomAD v4
12g.48981428T>CCA384636944WNT1c.901T>C (p.Tyr301His)
c.868T>C (p.Tyr290His)
12g.48981428T>GCA384636967WNT1c.901T>G (p.Tyr301Asp)
c.868T>G (p.Tyr290Asp)
12g.48981428T=CA2034926143WNT1c.901T= (p.Tyr301=)
c.868T= (p.Tyr290=)
12g.48981429A>CCA384636980WNT1c.902A>C (p.Tyr301Ser)
c.869A>C (p.Tyr290Ser)
12g.48981429A>GCA384636982WNT1c.902A>G (p.Tyr301Cys)
c.869A>G (p.Tyr290Cys)
gnomAD v4
12g.48981429A>TCA384636986WNT1c.902A>T (p.Tyr301Phe)
c.869A>T (p.Tyr290Phe)
12g.48981430C>ACA384636991WNT1c.903C>A (p.Tyr301Ter)
c.870C>A (p.Tyr290Ter)
gnomAD v4
12g.48981430C>GCA384637013WNT1c.903C>G (p.Tyr301Ter)
c.870C>G (p.Tyr290Ter)
12g.48981430C>TCA479704534WNT1c.903C>T (p.Tyr301=)
c.870C>T (p.Tyr290=)
gnomAD v4
12g.48981431A=CA2034926145WNT1c.904A= (p.Ser302=)
c.871A= (p.Ser291=)
12g.48981431A>CCA384637041WNT1c.904A>C (p.Ser302Arg)
c.871A>C (p.Ser291Arg)
dbSNP gnomAD v3 gnomAD v4
12g.48981431A>GCA384637043WNT1c.904A>G (p.Ser302Gly)
c.871A>G (p.Ser291Gly)
gnomAD v4
12g.48981431A>TCA384637046WNT1c.904A>T (p.Ser302Cys)
c.871A>T (p.Ser291Cys)
12g.48981432G>ACA384637060WNT1c.905G>A (p.Ser302Asn)
c.872G>A (p.Ser291Asn)
12g.48981432G>CCA384637050WNT1c.905G>C (p.Ser302Thr)
c.872G>C (p.Ser291Thr)
12g.48981432G>TCA384637055WNT1c.905G>T (p.Ser302Ile)
c.872G>T (p.Ser291Ile)
gnomAD v4
12g.48981433C>ACA384637090WNT1c.906C>A (p.Ser302Arg)
c.873C>A (p.Ser291Arg)
gnomAD v4
12g.48981433C=CA2034926149WNT1c.906C= (p.Ser302=)
c.873C= (p.Ser291=)
12g.48981433C>GCA384637097WNT1c.906C>G (p.Ser302Arg)
c.873C>G (p.Ser291Arg)
12g.48981433C>TCA479704537WNT1c.906C>T (p.Ser302=)
c.873C>T (p.Ser291=)
dbSNP gnomAD v2 gnomAD v4
12g.48981434G>ACA384637110WNT1c.907G>A (p.Gly303Arg)
c.874G>A (p.Gly292Arg)
gnomAD v4
12g.48981434G>CCA384637112WNT1c.907G>C (p.Gly303Arg)
c.874G>C (p.Gly292Arg)
12g.48981434G=CA2034926151WNT1c.907G= (p.Gly303=)
c.874G= (p.Gly292=)
12g.48981434G>TCA384637116WNT1c.907G>T (p.Gly303Ter)
c.874G>T (p.Gly292Ter)
ClinVar dbSNP gnomAD v4
12g.48981435G>ACA384637126WNT1c.908G>A (p.Gly303Glu)
c.875G>A (p.Gly292Glu)
dbSNP gnomAD v2 gnomAD v4
12g.48981435G>CCA384637134WNT1c.908G>C (p.Gly303Ala)
c.875G>C (p.Gly292Ala)
12g.48981435G=CA2034926155WNT1c.908G= (p.Gly303=)
c.875G= (p.Gly292=)
12g.48981435G>TCA384637138WNT1c.908G>T (p.Gly303Val)
c.875G>T (p.Gly292Val)
gnomAD v4
12g.48981435_48981436insGAAGCA2528286812WNT1c.908_909insGAAG (p.Arg304LysfsTer14)
c.875_876insGAAG (p.Arg293LysfsTer14)
12g.48981436A=CA2034926157WNT1c.909A= (p.Gly303=)
c.876A= (p.Gly292=)
12g.48981436A>CCA479704539WNT1c.909A>C (p.Gly303=)
c.876A>C (p.Gly292=)
12g.48981436A>GCA479704540WNT1c.909A>G (p.Gly303=)
c.876A>G (p.Gly292=)
12g.48981436A>TCA479704541WNT1c.909A>T (p.Gly303=)
c.876A>T (p.Gly292=)
dbSNP
12g.48981437C>ACA384637139WNT1c.910C>A (p.Arg304Ser)
c.877C>A (p.Arg293Ser)
gnomAD v4
12g.48981437C=CA2034926158WNT1c.910C= (p.Arg304=)
c.877C= (p.Arg293=)
12g.48981437C>GCA384637140WNT1c.910C>G (p.Arg304Gly)
c.877C>G (p.Arg293Gly)
12g.48981437C>TCA236608800WNT1c.910C>T (p.Arg304Cys)
c.877C>T (p.Arg293Cys)
dbSNP gnomAD v4
12g.48981437_48981440delCA2504225729WNT1c.910_913del (p.Arg304TrpfsTer?)
c.877_880del (p.Arg293TrpfsTer?)
12g.48981438G>ACA384637154WNT1c.911G>A (p.Arg304His)
c.878G>A (p.Arg293His)
gnomAD v4
12g.48981438G>CCA384637155WNT1c.911G>C (p.Arg304Pro)
c.878G>C (p.Arg293Pro)
12g.48981438G>TCA384637153WNT1c.911G>T (p.Arg304Leu)
c.878G>T (p.Arg293Leu)
gnomAD v4
12g.48981439C>ACA479704545WNT1c.912C>A (p.Arg304=)
c.879C>A (p.Arg293=)
gnomAD v4
12g.48981439C=CA2034926161WNT1c.912C= (p.Arg304=)
c.879C= (p.Arg293=)
12g.48981439C>GCA479704546WNT1c.912C>G (p.Arg304=)
c.879C>G (p.Arg293=)
12g.48981439C>TCA479704547WNT1c.912C>T (p.Arg304=)
c.879C>T (p.Arg293=)
ClinVar dbSNP gnomAD v2 gnomAD v4
12g.48981440C>ACA384637156WNT1c.913C>A (p.Leu305Met)
c.880C>A (p.Leu294Met)
12g.48981440C=CA2034926163WNT1c.913C= (p.Leu305=)
c.880C= (p.Leu294=)
12g.48981440C>GCA6544491WNT1c.913C>G (p.Leu305Val)
c.880C>G (p.Leu294Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.48981440C>TCA479704548WNT1c.913C>T (p.Leu305=)
c.880C>T (p.Leu294=)
12g.48981441T>ACA384637169WNT1c.914T>A (p.Leu305Gln)
c.881T>A (p.Leu294Gln)
12g.48981441T>CCA236608801WNT1c.914T>C (p.Leu305Pro)
c.881T>C (p.Leu294Pro)
dbSNP gnomAD v3 gnomAD v4
12g.48981441T>GCA384637176WNT1c.914T>G (p.Leu305Arg)
c.881T>G (p.Leu294Arg)
12g.48981441T=CA2034926166WNT1c.914T= (p.Leu305=)
c.881T= (p.Leu294=)
12g.48981442G>ACA479704551WNT1c.915G>A (p.Leu305=)
c.882G>A (p.Leu294=)
gnomAD v4
12g.48981442G>CCA479704552WNT1c.915G>C (p.Leu305=)
c.882G>C (p.Leu294=)
12g.48981442G>TCA479704553WNT1c.915G>T (p.Leu305=)
c.882G>T (p.Leu294=)
gnomAD v4
12g.48981443G>ACA384637188WNT1c.916G>A (p.Gly306Ser)
c.883G>A (p.Gly295Ser)
12g.48981443G>CCA384637184WNT1c.916G>C (p.Gly306Arg)
c.883G>C (p.Gly295Arg)
12g.48981443G>TCA384637183WNT1c.916G>T (p.Gly306Cys)
c.883G>T (p.Gly295Cys)
12g.48981444G>ACA384637191WNT1c.917G>A (p.Gly306Asp)
c.884G>A (p.Gly295Asp)
gnomAD v4
12g.48981444G>CCA384637202WNT1c.917G>C (p.Gly306Ala)
c.884G>C (p.Gly295Ala)
12g.48981444G>TCA384637215WNT1c.917G>T (p.Gly306Val)
c.884G>T (p.Gly295Val)
gnomAD v4
12g.48981445C>ACA479704555WNT1c.918C>A (p.Gly306=)
c.885C>A (p.Gly295=)
gnomAD v4
12g.48981445C>GCA479704557WNT1c.918C>G (p.Gly306=)
c.885C>G (p.Gly295=)
12g.48981445C>TCA479704559WNT1c.918C>T (p.Gly306=)
c.885C>T (p.Gly295=)
gnomAD v4
12g.48981446A>CCA384637220WNT1c.919A>C (p.Thr307Pro)
c.886A>C (p.Thr296Pro)
12g.48981446A>GCA384637224WNT1c.919A>G (p.Thr307Ala)
c.886A>G (p.Thr296Ala)
gnomAD v4
12g.48981446A>TCA384637230WNT1c.919A>T (p.Thr307Ser)
c.886A>T (p.Thr296Ser)
12g.48981447C>ACA384637234WNT1c.920C>A (p.Thr307Lys)
c.887C>A (p.Thr296Lys)
gnomAD v4
12g.48981447C>GCA384637246WNT1c.920C>G (p.Thr307Arg)
c.887C>G (p.Thr296Arg)
12g.48981447C>TCA384637243WNT1c.920C>T (p.Thr307Ile)
c.887C>T (p.Thr296Ile)
12g.48981448A=CA2034926169WNT1c.921A= (p.Thr307=)
c.888A= (p.Thr296=)
12g.48981448A>CCA479704564WNT1c.921A>C (p.Thr307=)
c.888A>C (p.Thr296=)
dbSNP gnomAD v2 gnomAD v4
12g.48981448A>GCA479704565WNT1c.921A>G (p.Thr307=)
c.888A>G (p.Thr296=)
12g.48981448A>TCA479704566WNT1c.921A>T (p.Thr307=)
c.888A>T (p.Thr296=)
12g.48981449G>ACA384637252WNT1c.922G>A (p.Ala308Thr)
c.889G>A (p.Ala297Thr)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.48981449G>CCA384637255WNT1c.922G>C (p.Ala308Pro)
c.889G>C (p.Ala297Pro)
12g.48981449G=CA2034926172WNT1c.922G= (p.Ala308=)
c.889G= (p.Ala297=)
12g.48981449G>TCA384637256WNT1c.922G>T (p.Ala308Ser)
c.889G>T (p.Ala297Ser)
gnomAD v4
12g.48981450C>ACA384637257WNT1c.923C>A (p.Ala308Glu)
c.890C>A (p.Ala297Glu)
gnomAD v4
12g.48981450C=CA2034926175WNT1c.923C= (p.Ala308=)
c.890C= (p.Ala297=)
12g.48981450C>GCA384637258WNT1c.923C>G (p.Ala308Gly)
c.890C>G (p.Ala297Gly)
dbSNP gnomAD v2 gnomAD v4
12g.48981450C>TCA384637261WNT1c.923C>T (p.Ala308Val)
c.890C>T (p.Ala297Val)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.48981451A>CCA479704569WNT1c.924A>C (p.Ala308=)
c.891A>C (p.Ala297=)
12g.48981451A>GCA479704571WNT1c.924A>G (p.Ala308=)
c.891A>G (p.Ala297=)
gnomAD v4
12g.48981451A>TCA479704570WNT1c.924A>T (p.Ala308=)
c.891A>T (p.Ala297=)
gnomAD v4
12g.48981452G>ACA384637265WNT1c.925G>A (p.Gly309Ser)
c.892G>A (p.Gly298Ser)
gnomAD v4
12g.48981452G>CCA384637266WNT1c.925G>C (p.Gly309Arg)
c.892G>C (p.Gly298Arg)
12g.48981452G>TCA384637268WNT1c.925G>T (p.Gly309Cys)
c.892G>T (p.Gly298Cys)
gnomAD v4
12g.48981453G>ACA384637272WNT1c.926G>A (p.Gly309Asp)
c.893G>A (p.Gly298Asp)
gnomAD v4
12g.48981453G>CCA384637273WNT1c.926G>C (p.Gly309Ala)
c.893G>C (p.Gly298Ala)
12g.48981453G>TCA384637276WNT1c.926G>T (p.Gly309Val)
c.893G>T (p.Gly298Val)
12g.48981454C>ACA479704573WNT1c.927C>A (p.Gly309=)
c.894C>A (p.Gly298=)
ClinVar gnomAD v4
12g.48981454C>GCA479704575WNT1c.927C>G (p.Gly309=)
c.894C>G (p.Gly298=)
12g.48981454C>TCA479704576WNT1c.927C>T (p.Gly309=)
c.894C>T (p.Gly298=)
gnomAD v4
12g.48981455A>CCA384637278WNT1c.928A>C (p.Thr310Pro)
c.895A>C (p.Thr299Pro)
12g.48981455A>GCA384637280WNT1c.928A>G (p.Thr310Ala)
c.895A>G (p.Thr299Ala)
12g.48981455A>TCA384637279WNT1c.928A>T (p.Thr310Ser)
c.895A>T (p.Thr299Ser)
gnomAD v4
12g.48981456C>ACA384637281WNT1c.929C>A (p.Thr310Lys)
c.896C>A (p.Thr299Lys)
gnomAD v4
12g.48981456C=CA2034926178WNT1c.929C= (p.Thr310=)
c.896C= (p.Thr299=)
12g.48981456C>GCA384637284WNT1c.929C>G (p.Thr310Arg)
c.896C>G (p.Thr299Arg)
12g.48981456C>TCA384637282WNT1c.929C>T (p.Thr310Met)
c.896C>T (p.Thr299Met)
dbSNP gnomAD v3 gnomAD v4
12g.48981457G>ACA479704580WNT1c.930G>A (p.Thr310=)
c.897G>A (p.Thr299=)
gnomAD v4
12g.48981457G>CCA479704581WNT1c.930G>C (p.Thr310=)
c.897G>C (p.Thr299=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.48981457G=CA2034926182WNT1c.930G= (p.Thr310=)
c.897G= (p.Thr299=)
12g.48981457G>TCA479704582WNT1c.930G>T (p.Thr310=)
c.897G>T (p.Thr299=)
dbSNP gnomAD v3 gnomAD v4
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

Number of alleles fetched