Chr Mutation (hg38) CAid Gene Transcript Linkouts
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
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)

Number of alleles fetched