Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.48981526_48981549delinsCCACCGCACGCGCACGCAGCGCGTCA2034902076WNT1c.999_1022delinsCCACCGCACGCGCACGCAGCGCGT (p.Gly333=)
c.966_989delinsCCACCGCACGCGCACGCAGCGCGT (p.Gly322=)
12g.48981532_48981554delCA605233429WNT1c.1005_1027del (p.Thr336AlafsTer?)
c.972_994del (p.Thr325AlafsTer?)
ClinVar dbSNP gnomAD v2 gnomAD v4
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
12g.48981559C>ACA479704490WNT1c.1032C>A (p.Arg344=)
c.999C>A (p.Arg333=)
12g.48981559C>GCA479704491WNT1c.1032C>G (p.Arg344=)
c.999C>G (p.Arg333=)
12g.48981559C>TCA479704492WNT1c.1032C>T (p.Arg344=)
c.999C>T (p.Arg333=)
gnomAD v4
12g.48981560delCA2618599574WNT1c.1033del (p.Cys345AlafsTer?)
c.1000del (p.Cys334AlafsTer?)
gnomAD v4
12g.48981560T>ACA384638614WNT1c.1033T>A (p.Cys345Ser)
c.1000T>A (p.Cys334Ser)
12g.48981560T>CCA236608820WNT1c.1033T>C (p.Cys345Arg)
c.1000T>C (p.Cys334Arg)
dbSNP gnomAD v4
12g.48981560T>GCA384638628WNT1c.1033T>G (p.Cys345Gly)
c.1000T>G (p.Cys334Gly)
dbSNP
12g.48981560T=CA2034902092WNT1c.1033T= (p.Cys345=)
c.1000T= (p.Cys334=)
12g.48981561G>ACA384638633WNT1c.1034G>A (p.Cys345Tyr)
c.1001G>A (p.Cys334Tyr)
gnomAD v4
12g.48981561G>CCA384638635WNT1c.1034G>C (p.Cys345Ser)
c.1001G>C (p.Cys334Ser)
12g.48981561G>TCA384638639WNT1c.1034G>T (p.Cys345Phe)
c.1001G>T (p.Cys334Phe)
12g.48981562C>ACA384638643WNT1c.1035C>A (p.Cys345Ter)
c.1002C>A (p.Cys334Ter)
gnomAD v4
12g.48981562C>GCA384638647WNT1c.1035C>G (p.Cys345Trp)
c.1002C>G (p.Cys334Trp)
12g.48981562C>TCA479704495WNT1c.1035C>T (p.Cys345=)
c.1002C>T (p.Cys334=)
gnomAD v4
12g.48981563A>CCA384638669WNT1c.1036A>C (p.Asn346His)
c.1003A>C (p.Asn335His)
12g.48981563A>GCA384638671WNT1c.1036A>G (p.Asn346Asp)
c.1003A>G (p.Asn335Asp)
12g.48981563A>TCA384638680WNT1c.1036A>T (p.Asn346Tyr)
c.1003A>T (p.Asn335Tyr)
gnomAD v4
12g.48981564A>CCA384638685WNT1c.1037A>C (p.Asn346Thr)
c.1004A>C (p.Asn335Thr)
ClinVar dbSNP
12g.48981564A>GCA384638688WNT1c.1037A>G (p.Asn346Ser)
c.1004A>G (p.Asn335Ser)
12g.48981564A>TCA384638691WNT1c.1037A>T (p.Asn346Ile)
c.1004A>T (p.Asn335Ile)
12g.48981565C>ACA384638703WNT1c.1038C>A (p.Asn346Lys)
c.1005C>A (p.Asn335Lys)
gnomAD v4
12g.48981565C>GCA384638704WNT1c.1038C>G (p.Asn346Lys)
c.1005C>G (p.Asn335Lys)
12g.48981565C>TCA479704501WNT1c.1038C>T (p.Asn346=)
c.1005C>T (p.Asn335=)
12g.48981566T>ACA384638705WNT1c.1039T>A (p.Cys347Ser)
c.1006T>A (p.Cys336Ser)
12g.48981566T>CCA384638706WNT1c.1039T>C (p.Cys347Arg)
c.1006T>C (p.Cys336Arg)
gnomAD v4
12g.48981566T>GCA384638713WNT1c.1039T>G (p.Cys347Gly)
c.1006T>G (p.Cys336Gly)
gnomAD v4
12g.48981567G>ACA384638717WNT1c.1040G>A (p.Cys347Tyr)
c.1007G>A (p.Cys336Tyr)
gnomAD v4
12g.48981567G>CCA384638720WNT1c.1040G>C (p.Cys347Ser)
c.1007G>C (p.Cys336Ser)
12g.48981567G>TCA384638718WNT1c.1040G>T (p.Cys347Phe)
c.1007G>T (p.Cys336Phe)
12g.48981568C>ACA384638724WNT1c.1041C>A (p.Cys347Ter)
c.1008C>A (p.Cys336Ter)
gnomAD v4
12g.48981568C=CA2034902093WNT1c.1041C= (p.Cys347=)
c.1008C= (p.Cys336=)
12g.48981568C>GCA384638732WNT1c.1041C>G (p.Cys347Trp)
c.1008C>G (p.Cys336Trp)
12g.48981568C>TCA479704506WNT1c.1041C>T (p.Cys347=)
c.1008C>T (p.Cys336=)
dbSNP gnomAD v2 gnomAD v4
12g.48981569A=CA2034902094WNT1c.1042A= (p.Thr348=)
c.1009A= (p.Thr337=)
12g.48981569A>CCA6544500WNT1c.1042A>C (p.Thr348Pro)
c.1009A>C (p.Thr337Pro)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.48981569A>GCA384638738WNT1c.1042A>G (p.Thr348Ala)
c.1009A>G (p.Thr337Ala)
dbSNP gnomAD v4
12g.48981569A>TCA384638750WNT1c.1042A>T (p.Thr348Ser)
c.1009A>T (p.Thr337Ser)
12g.48981570C>ACA384638754WNT1c.1043C>A (p.Thr348Asn)
c.1010C>A (p.Thr337Asn)
gnomAD v4
12g.48981570C=CA2034902095WNT1c.1043C= (p.Thr348=)
c.1010C= (p.Thr337=)
12g.48981570C>GCA384638758WNT1c.1043C>G (p.Thr348Ser)
c.1010C>G (p.Thr337Ser)
12g.48981570C>TCA384638760WNT1c.1043C>T (p.Thr348Ile)
c.1010C>T (p.Thr337Ile)
dbSNP gnomAD v2
12g.48981572_48981575delCA2575143759WNT1c.1045_1048del (p.Phe349ThrfsTer?)
c.1012_1015del (p.Phe338ThrfsTer?)
12g.48981571C>ACA479704516WNT1c.1044C>A (p.Thr348=)
c.1011C>A (p.Thr337=)
gnomAD v4
12g.48981571C=CA2034902096WNT1c.1044C= (p.Thr348=)
c.1011C= (p.Thr337=)
12g.48981571C>GCA479704513WNT1c.1044C>G (p.Thr348=)
c.1011C>G (p.Thr337=)
12g.48981571C>TCA479704511WNT1c.1044C>T (p.Thr348=)
c.1011C>T (p.Thr337=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.48981572T>ACA384638764WNT1c.1045T>A (p.Phe349Ile)
c.1012T>A (p.Phe338Ile)
12g.48981572T>CCA384638770WNT1c.1045T>C (p.Phe349Leu)
c.1012T>C (p.Phe338Leu)
12g.48981572T>GCA384638775WNT1c.1045T>G (p.Phe349Val)
c.1012T>G (p.Phe338Val)
12g.48981573T>ACA384638778WNT1c.1046T>A (p.Phe349Tyr)
c.1013T>A (p.Phe338Tyr)
12g.48981573T>CCA384638782WNT1c.1046T>C (p.Phe349Ser)
c.1013T>C (p.Phe338Ser)
12g.48981573T>GCA384638793WNT1c.1046T>G (p.Phe349Cys)
c.1013T>G (p.Phe338Cys)
12g.48981574C>ACA384638804WNT1c.1047C>A (p.Phe349Leu)
c.1014C>A (p.Phe338Leu)
gnomAD v4
12g.48981574C=CA2034902097WNT1c.1047C= (p.Phe349=)
c.1014C= (p.Phe338=)
12g.48981574C>GCA384638803WNT1c.1047C>G (p.Phe349Leu)
c.1014C>G (p.Phe338Leu)
12g.48981574C>TCA479704522WNT1c.1047C>T (p.Phe349=)
c.1014C>T (p.Phe338=)
dbSNP gnomAD v2
12g.48981575C>ACA384638806WNT1c.1048C>A (p.His350Asn)
c.1015C>A (p.His339Asn)
gnomAD v4
12g.48981575C=CA2034902098WNT1c.1048C= (p.His350=)
c.1015C= (p.His339=)
12g.48981575C>GCA384638809WNT1c.1048C>G (p.His350Asp)
c.1015C>G (p.His339Asp)
gnomAD v4
12g.48981575C>TCA384638811WNT1c.1048C>T (p.His350Tyr)
c.1015C>T (p.His339Tyr)
dbSNP gnomAD v4
12g.48981576A>CCA384638815WNT1c.1049A>C (p.His350Pro)
c.1016A>C (p.His339Pro)
12g.48981576A>GCA384638820WNT1c.1049A>G (p.His350Arg)
c.1016A>G (p.His339Arg)
gnomAD v4
12g.48981576A>TCA384638835WNT1c.1049A>T (p.His350Leu)
c.1016A>T (p.His339Leu)
12g.48981577C>ACA384638855WNT1c.1050C>A (p.His350Gln)
c.1017C>A (p.His339Gln)
gnomAD v4
12g.48981577C>GCA384638854WNT1c.1050C>G (p.His350Gln)
c.1017C>G (p.His339Gln)
12g.48981577C>TCA479704526WNT1c.1050C>T (p.His350=)
c.1017C>T (p.His339=)
gnomAD v4
12g.48981578T>ACA384638856WNT1c.1051T>A (p.Trp351Arg)
c.1018T>A (p.Trp340Arg)
gnomAD v4
12g.48981578T>CCA384638857WNT1c.1051T>C (p.Trp351Arg)
c.1018T>C (p.Trp340Arg)
gnomAD v4
12g.48981578T>GCA16607302WNT1c.1051T>G (p.Trp351Gly)
c.1018T>G (p.Trp340Gly)
ClinVar dbSNP
12g.48981578T=CA2034902099WNT1c.1051T= (p.Trp351=)
c.1018T= (p.Trp340=)
12g.48981579G>ACA384638893WNT1c.1052G>A (p.Trp351Ter)
c.1019G>A (p.Trp340Ter)
gnomAD v4
12g.48981579G>CCA384638896WNT1c.1052G>C (p.Trp351Ser)
c.1019G>C (p.Trp340Ser)
12g.48981579G>TCA384638916WNT1c.1052G>T (p.Trp351Leu)
c.1019G>T (p.Trp340Leu)
gnomAD v4
12g.48981580G>ACA384638931WNT1c.1053G>A (p.Trp351Ter)
c.1020G>A (p.Trp340Ter)
12g.48981580G>CCA384638923WNT1c.1053G>C (p.Trp351Cys)
c.1020G>C (p.Trp340Cys)
dbSNP gnomAD v2 gnomAD v4
12g.48981580G=CA2034902100WNT1c.1053G= (p.Trp351=)
c.1020G= (p.Trp340=)
12g.48981580G>TCA384638929WNT1c.1053G>T (p.Trp351Cys)
c.1020G>T (p.Trp340Cys)
gnomAD v4
12g.48981581T>ACA384638935WNT1c.1054T>A (p.Cys352Ser)
c.1021T>A (p.Cys341Ser)
12g.48981581T>CCA384638947WNT1c.1054T>C (p.Cys352Arg)
c.1021T>C (p.Cys341Arg)
12g.48981581T>GCA384638953WNT1c.1054T>G (p.Cys352Gly)
c.1021T>G (p.Cys341Gly)
12g.48981582G>ACA384638957WNT1c.1055G>A (p.Cys352Tyr)
c.1022G>A (p.Cys341Tyr)
gnomAD v4
12g.48981582G>CCA384638962WNT1c.1055G>C (p.Cys352Ser)
c.1022G>C (p.Cys341Ser)
12g.48981582G>TCA384638966WNT1c.1055G>T (p.Cys352Phe)
c.1022G>T (p.Cys341Phe)
dbSNP gnomAD v4
12g.48981583C>ACA384638973WNT1c.1056C>A (p.Cys352Ter)
c.1023C>A (p.Cys341Ter)
gnomAD v4
12g.48981583C>GCA384638971WNT1c.1056C>G (p.Cys352Trp)
c.1023C>G (p.Cys341Trp)
12g.48981583C>TCA479704533WNT1c.1056C>T (p.Cys352=)
c.1023C>T (p.Cys341=)
gnomAD v4
12g.48981584T>ACA384638976WNT1c.1057T>A (p.Cys353Ser)
c.1024T>A (p.Cys342Ser)
12g.48981584T>CCA384638977WNT1c.1057T>C (p.Cys353Arg)
c.1024T>C (p.Cys342Arg)
gnomAD v4
12g.48981584T>GCA384638978WNT1c.1057T>G (p.Cys353Gly)
c.1024T>G (p.Cys342Gly)
12g.48981585G>ACA384638979WNT1c.1058G>A (p.Cys353Tyr)
c.1025G>A (p.Cys342Tyr)
gnomAD v4
12g.48981585G>CCA384638983WNT1c.1058G>C (p.Cys353Ser)
c.1025G>C (p.Cys342Ser)
12g.48981585G>TCA384639001WNT1c.1058G>T (p.Cys353Phe)
c.1025G>T (p.Cys342Phe)
gnomAD v4
12g.48981585_48981586delinsGCCA2034902101WNT1c.1058_1059delinsGC (p.Cys353=)
c.1025_1026delinsGC (p.Cys342=)
12g.48981586C>ACA384639007WNT1c.1059C>A (p.Cys353Ter)
c.1026C>A (p.Cys342Ter)
dbSNP gnomAD v2 gnomAD v4
12g.48981586C=CA2034902102WNT1c.1059C= (p.Cys353=)
c.1026C= (p.Cys342=)
12g.48981586C>GCA384639014WNT1c.1059C>G (p.Cys353Trp)
c.1026C>G (p.Cys342Trp)
ClinVar
12g.48981586C>TCA6544501WNT1c.1059C>T (p.Cys353=)
c.1026C>T (p.Cys342=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.48981587delCA605233430WNT1c.1060del (p.His354ThrfsTer?)
c.1027del (p.His343ThrfsTer?)
ClinVar dbSNP gnomAD v2 gnomAD v4
12g.48981586_48981588delinsCCACA2034902103WNT1c.1059_1061delinsCCA (p.Cys353=)
c.1026_1028delinsCCA (p.Cys342=)
12g.48981587C>ACA384639019WNT1c.1060C>A (p.His354Asn)
c.1027C>A (p.His343Asn)
gnomAD v4
12g.48981587C>GCA384639023WNT1c.1060C>G (p.His354Asp)
c.1027C>G (p.His343Asp)
12g.48981587C>TCA384639034WNT1c.1060C>T (p.His354Tyr)
c.1027C>T (p.His343Tyr)
gnomAD v4
12g.48981587_48981588delinsGCA658797896WNT1c.1060_1061delinsG (p.His354AlafsTer?)
c.1027_1028delinsG (p.His343AlafsTer?)
ClinVar dbSNP
12g.48981588A=CA2034902104WNT1c.1061A= (p.His354=)
c.1028A= (p.His343=)
12g.48981588A>CCA384639041WNT1c.1061A>C (p.His354Pro)
c.1028A>C (p.His343Pro)
12g.48981588A>GCA384639046WNT1c.1061A>G (p.His354Arg)
c.1028A>G (p.His343Arg)
dbSNP gnomAD v4
12g.48981588A>TCA384639050WNT1c.1061A>T (p.His354Leu)
c.1028A>T (p.His343Leu)
ClinVar dbSNP gnomAD v4
12g.48981589C>ACA384639062WNT1c.1062C>A (p.His354Gln)
c.1029C>A (p.His343Gln)
gnomAD v4
12g.48981589C>GCA384639065WNT1c.1062C>G (p.His354Gln)
c.1029C>G (p.His343Gln)
12g.48981589C>TCA479704538WNT1c.1062C>T (p.His354=)
c.1029C>T (p.His343=)
gnomAD v4
12g.48981590G>ACA384639070WNT1c.1063G>A (p.Val355Ile)
c.1030G>A (p.Val344Ile)
gnomAD v4
12g.48981590G>CCA384639074WNT1c.1063G>C (p.Val355Leu)
c.1030G>C (p.Val344Leu)
dbSNP gnomAD v3 gnomAD v4
12g.48981590G=CA2034902105WNT1c.1063G= (p.Val355=)
c.1030G= (p.Val344=)
12g.48981590G>TCA143728WNT1c.1063G>T (p.Val355Phe)
c.1030G>T (p.Val344Phe)
ClinVar dbSNP gnomAD v4
12g.48981591T>ACA384639077WNT1c.1064T>A (p.Val355Asp)
c.1031T>A (p.Val344Asp)
12g.48981591T>CCA236608826WNT1c.1064T>C (p.Val355Ala)
c.1031T>C (p.Val344Ala)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.48981591T>GCA384639078WNT1c.1064T>G (p.Val355Gly)
c.1031T>G (p.Val344Gly)
ClinVar
12g.48981591T=CA2034902106WNT1c.1064T= (p.Val355=)
c.1031T= (p.Val344=)
12g.48981592C>ACA479704542WNT1c.1065C>A (p.Val355=)
c.1032C>A (p.Val344=)
gnomAD v4
12g.48981592C>GCA479704543WNT1c.1065C>G (p.Val355=)
c.1032C>G (p.Val344=)
gnomAD v4
12g.48981592C>TCA479704544WNT1c.1065C>T (p.Val355=)
c.1032C>T (p.Val344=)
gnomAD v4
12g.48981593A>CCA384639081WNT1c.1066A>C (p.Ser356Arg)
c.1033A>C (p.Ser345Arg)
12g.48981593A>GCA384639083WNT1c.1066A>G (p.Ser356Gly)
c.1033A>G (p.Ser345Gly)
12g.48981593A>TCA384639082WNT1c.1066A>T (p.Ser356Cys)
c.1033A>T (p.Ser345Cys)
12g.48981594G>ACA384639084WNT1c.1067G>A (p.Ser356Asn)
c.1034G>A (p.Ser345Asn)
gnomAD v4
12g.48981594G>CCA384639087WNT1c.1067G>C (p.Ser356Thr)
c.1034G>C (p.Ser345Thr)
12g.48981594G>TCA384639091WNT1c.1067G>T (p.Ser356Ile)
c.1034G>T (p.Ser345Ile)
gnomAD v4
12g.48981595C>ACA384639100WNT1c.1068C>A (p.Ser356Arg)
c.1035C>A (p.Ser345Arg)
gnomAD v4
12g.48981595C>GCA384639103WNT1c.1068C>G (p.Ser356Arg)
c.1035C>G (p.Ser345Arg)
12g.48981595C>TCA479704550WNT1c.1068C>T (p.Ser356=)
c.1035C>T (p.Ser345=)
12g.48981596T>ACA384639108WNT1c.1069T>A (p.Cys357Ser)
c.1036T>A (p.Cys346Ser)
12g.48981596T>CCA384639111WNT1c.1069T>C (p.Cys357Arg)
c.1036T>C (p.Cys346Arg)
12g.48981596T>GCA384639112WNT1c.1069T>G (p.Cys357Gly)
c.1036T>G (p.Cys346Gly)
12g.48981597G>ACA384639116WNT1c.1070G>A (p.Cys357Tyr)
c.1037G>A (p.Cys346Tyr)
gnomAD v4
12g.48981597G>CCA384639119WNT1c.1070G>C (p.Cys357Ser)
c.1037G>C (p.Cys346Ser)
12g.48981597G>TCA384639123WNT1c.1070G>T (p.Cys357Phe)
c.1037G>T (p.Cys346Phe)
gnomAD v4
12g.48981598C>ACA384639128WNT1c.1071C>A (p.Cys357Ter)
c.1038C>A (p.Cys346Ter)
gnomAD v4
12g.48981598C>GCA384639126WNT1c.1071C>G (p.Cys357Trp)
c.1038C>G (p.Cys346Trp)
12g.48981598C>TCA479704554WNT1c.1071C>T (p.Cys357=)
c.1038C>T (p.Cys346=)
gnomAD v4
12g.48981599C>ACA384639132WNT1c.1072C>A (p.Arg358Ser)
c.1039C>A (p.Arg347Ser)
gnomAD v4
12g.48981599C=CA2034902107WNT1c.1072C= (p.Arg358=)
c.1039C= (p.Arg347=)
12g.48981599C>GCA384639134WNT1c.1072C>G (p.Arg358Gly)
c.1039C>G (p.Arg347Gly)
12g.48981599C>TCA384639135WNT1c.1072C>T (p.Arg358Cys)
c.1039C>T (p.Arg347Cys)
dbSNP gnomAD v2 gnomAD v4
12g.48981600_48981601delCA2618599708WNT1c.1073_1074del (p.Arg358GlnfsTer?)
c.1040_1041del (p.Arg347GlnfsTer?)
gnomAD v4
12g.48981600G>ACA6544502WNT1c.1073G>A (p.Arg358His)
c.1040G>A (p.Arg347His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.48981600G>CCA384639136WNT1c.1073G>C (p.Arg358Pro)
c.1040G>C (p.Arg347Pro)
12g.48981600G=CA2034902108WNT1c.1073G= (p.Arg358=)
c.1040G= (p.Arg347=)
12g.48981600G>TCA384639137WNT1c.1073G>T (p.Arg358Leu)
c.1040G>T (p.Arg347Leu)
12g.48981601C>ACA479704561WNT1c.1074C>A (p.Arg358=)
c.1041C>A (p.Arg347=)
dbSNP gnomAD v3 gnomAD v4
12g.48981601C=CA2034902109WNT1c.1074C= (p.Arg358=)
c.1041C= (p.Arg347=)
12g.48981601C>GCA479704563WNT1c.1074C>G (p.Arg358=)
c.1041C>G (p.Arg347=)
12g.48981601C>TCA479704562WNT1c.1074C>T (p.Arg358=)
c.1041C>T (p.Arg347=)
gnomAD v4
12g.48981602A=CA2034902110WNT1c.1075A= (p.Asn359=)
c.1042A= (p.Asn348=)
12g.48981602A>CCA384639140WNT1c.1075A>C (p.Asn359His)
c.1042A>C (p.Asn348His)
12g.48981602A>GCA6544503WNT1c.1075A>G (p.Asn359Asp)
c.1042A>G (p.Asn348Asp)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.48981602A>TCA384639141WNT1c.1075A>T (p.Asn359Tyr)
c.1042A>T (p.Asn348Tyr)
12g.48981603A=CA2034902111WNT1c.1076A= (p.Asn359=)
c.1043A= (p.Asn348=)
12g.48981603A>CCA384639142WNT1c.1076A>C (p.Asn359Thr)
c.1043A>C (p.Asn348Thr)
12g.48981603A>GCA6544504WNT1c.1076A>G (p.Asn359Ser)
c.1043A>G (p.Asn348Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.48981603A>TCA384639144WNT1c.1076A>T (p.Asn359Ile)
c.1043A>T (p.Asn348Ile)
gnomAD v4
12g.48981604C>ACA384639151WNT1c.1077C>A (p.Asn359Lys)
c.1044C>A (p.Asn348Lys)
gnomAD v4
12g.48981604C>GCA384639148WNT1c.1077C>G (p.Asn359Lys)
c.1044C>G (p.Asn348Lys)
12g.48981604C>TCA479704568WNT1c.1077C>T (p.Asn359=)
c.1044C>T (p.Asn348=)
12g.48981605T>ACA384639155WNT1c.1078T>A (p.Cys360Ser)
c.1045T>A (p.Cys349Ser)
12g.48981605T>CCA384639157WNT1c.1078T>C (p.Cys360Arg)
c.1045T>C (p.Cys349Arg)
gnomAD v4
12g.48981605T>GCA384639162WNT1c.1078T>G (p.Cys360Gly)
c.1045T>G (p.Cys349Gly)
12g.48981606G>ACA384639165WNT1c.1079G>A (p.Cys360Tyr)
c.1046G>A (p.Cys349Tyr)
dbSNP gnomAD v4
12g.48981606G>CCA384639168WNT1c.1079G>C (p.Cys360Ser)
c.1046G>C (p.Cys349Ser)
12g.48981606G=CA2034902112WNT1c.1079G= (p.Cys360=)
c.1046G= (p.Cys349=)
12g.48981606G>TCA384639171WNT1c.1079G>T (p.Cys360Phe)
c.1046G>T (p.Cys349Phe)
ClinVar gnomAD v4
12g.48981607C>ACA384639179WNT1c.1080C>A (p.Cys360Ter)
c.1047C>A (p.Cys349Ter)
gnomAD v4
12g.48981607C>GCA384639177WNT1c.1080C>G (p.Cys360Trp)
c.1047C>G (p.Cys349Trp)
12g.48981607C>TCA479704572WNT1c.1080C>T (p.Cys360=)
c.1047C>T (p.Cys349=)
gnomAD v4
12g.48981608A>CCA384639180WNT1c.1081A>C (p.Thr361Pro)
c.1048A>C (p.Thr350Pro)
12g.48981608A>GCA384639181WNT1c.1081A>G (p.Thr361Ala)
c.1048A>G (p.Thr350Ala)
gnomAD v4
12g.48981608A>TCA384639182WNT1c.1081A>T (p.Thr361Ser)
c.1048A>T (p.Thr350Ser)
12g.48981609C>ACA384639185WNT1c.1082C>A (p.Thr361Lys)
c.1049C>A (p.Thr350Lys)
gnomAD v4
12g.48981609C=CA2034902113WNT1c.1082C= (p.Thr361=)
c.1049C= (p.Thr350=)
12g.48981609C>GCA384639205WNT1c.1082C>G (p.Thr361Arg)
c.1049C>G (p.Thr350Arg)
dbSNP
12g.48981609C>TCA236608831WNT1c.1082C>T (p.Thr361Met)
c.1049C>T (p.Thr350Met)
dbSNP gnomAD v3 gnomAD v4
12g.48981610G>ACA479704577WNT1c.1083G>A (p.Thr361=)
c.1050G>A (p.Thr350=)
gnomAD v4
12g.48981610G>CCA479704578WNT1c.1083G>C (p.Thr361=)
c.1050G>C (p.Thr350=)
gnomAD v4
12g.48981610G>TCA479704579WNT1c.1083G>T (p.Thr361=)
c.1050G>T (p.Thr350=)
gnomAD v4
12g.48981611C>ACA384639215WNT1c.1084C>A (p.His362Asn)
c.1051C>A (p.His351Asn)
gnomAD v4
12g.48981611C>GCA384639220WNT1c.1084C>G (p.His362Asp)
c.1051C>G (p.His351Asp)
12g.48981611C>TCA384639218WNT1c.1084C>T (p.His362Tyr)
c.1051C>T (p.His351Tyr)
gnomAD v4
12g.48981612A>CCA384639223WNT1c.1085A>C (p.His362Pro)
c.1052A>C (p.His351Pro)
12g.48981612A>GCA384639224WNT1c.1085A>G (p.His362Arg)
c.1052A>G (p.His351Arg)
gnomAD v4
12g.48981612A>TCA384639226WNT1c.1085A>T (p.His362Leu)
c.1052A>T (p.His351Leu)
12g.48981613C>ACA384639229WNT1c.1086C>A (p.His362Gln)
c.1053C>A (p.His351Gln)
dbSNP gnomAD v2 gnomAD v4
12g.48981613C=CA2034902114WNT1c.1086C= (p.His362=)
c.1053C= (p.His351=)
12g.48981613C>GCA384639234WNT1c.1086C>G (p.His362Gln)
c.1053C>G (p.His351Gln)
12g.48981613C>TCA479704586WNT1c.1086C>T (p.His362=)
c.1053C>T (p.His351=)
gnomAD v4
12g.48981614A>CCA384639238WNT1c.1087A>C (p.Thr363Pro)
c.1054A>C (p.Thr352Pro)
12g.48981614A>GCA384639244WNT1c.1087A>G (p.Thr363Ala)
c.1054A>G (p.Thr352Ala)
gnomAD v4
12g.48981614A>TCA384639246WNT1c.1087A>T (p.Thr363Ser)
c.1054A>T (p.Thr352Ser)
12g.48981615C>ACA384639249WNT1c.1088C>A (p.Thr363Lys)
c.1055C>A (p.Thr352Lys)
gnomAD v4
12g.48981615C>GCA384639252WNT1c.1088C>G (p.Thr363Arg)
c.1055C>G (p.Thr352Arg)
12g.48981615C>TCA384639256WNT1c.1088C>T (p.Thr363Met)
c.1055C>T (p.Thr352Met)
gnomAD v4
12g.48981616G>ACA479704590WNT1c.1089G>A (p.Thr363=)
c.1056G>A (p.Thr352=)
gnomAD v4
12g.48981616G>CCA479704592WNT1c.1089G>C (p.Thr363=)
c.1056G>C (p.Thr352=)
12g.48981616G>TCA479704593WNT1c.1089G>T (p.Thr363=)
c.1056G>T (p.Thr352=)
gnomAD v4
12g.48981617C>ACA384639269WNT1c.1090C>A (p.Arg364Ser)
c.1057C>A (p.Arg353Ser)
gnomAD v4
12g.48981617C=CA2034902115WNT1c.1090C= (p.Arg364=)
c.1057C= (p.Arg353=)
12g.48981617C>GCA384639272WNT1c.1090C>G (p.Arg364Gly)
c.1057C>G (p.Arg353Gly)
ClinVar dbSNP gnomAD v2 gnomAD v4
12g.48981617C>TCA384639262WNT1c.1090C>T (p.Arg364Cys)
c.1057C>T (p.Arg353Cys)
dbSNP gnomAD v2 gnomAD v4
12g.48981618G>ACA384639301WNT1c.1091G>A (p.Arg364His)
c.1058G>A (p.Arg353His)
dbSNP gnomAD v2 gnomAD v4
12g.48981618G>CCA384639299WNT1c.1091G>C (p.Arg364Pro)
c.1058G>C (p.Arg353Pro)
12g.48981618G=CA2034902116WNT1c.1091G= (p.Arg364=)
c.1058G= (p.Arg353=)
12g.48981618G>TCA384639302WNT1c.1091G>T (p.Arg364Leu)
c.1058G>T (p.Arg353Leu)
gnomAD v4
12g.48981619C>ACA479704597WNT1c.1092C>A (p.Arg364=)
c.1059C>A (p.Arg353=)
gnomAD v4
12g.48981619C=CA2034902117WNT1c.1092C= (p.Arg364=)
c.1059C= (p.Arg353=)
12g.48981619C>GCA479704598WNT1c.1092C>G (p.Arg364=)
c.1059C>G (p.Arg353=)
12g.48981619C>TCA479704599WNT1c.1092C>T (p.Arg364=)
c.1059C>T (p.Arg353=)
dbSNP
12g.48981620G>ACA384639305WNT1c.1093G>A (p.Val365Ile)
c.1060G>A (p.Val354Ile)
ClinVar dbSNP gnomAD v2 gnomAD v4
12g.48981620G>CCA384639311WNT1c.1093G>C (p.Val365Leu)
c.1060G>C (p.Val354Leu)
gnomAD v4
12g.48981620G=CA2034902118WNT1c.1093G= (p.Val365=)
c.1060G= (p.Val354=)
12g.48981620G>TCA384639309WNT1c.1093G>T (p.Val365Leu)
c.1060G>T (p.Val354Leu)
gnomAD v4
12g.48981621T>ACA384639312WNT1c.1094T>A (p.Val365Glu)
c.1061T>A (p.Val354Glu)
gnomAD v4
12g.48981621T>CCA384639313WNT1c.1094T>C (p.Val365Ala)
c.1061T>C (p.Val354Ala)
12g.48981621T>GCA384639314WNT1c.1094T>G (p.Val365Gly)
c.1061T>G (p.Val354Gly)
12g.48981622A=CA2034902119WNT1c.1095A= (p.Val365=)
c.1062A= (p.Val354=)
12g.48981622A>CCA236608833WNT1c.1095A>C (p.Val365=)
c.1062A>C (p.Val354=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.48981622A>GCA479704603WNT1c.1095A>G (p.Val365=)
c.1062A>G (p.Val354=)
gnomAD v4
12g.48981622A>TCA479704604WNT1c.1095A>T (p.Val365=)
c.1062A>T (p.Val354=)
12g.48981623C>ACA384639320WNT1c.1096C>A (p.Leu366Met)
c.1063C>A (p.Leu355Met)
gnomAD v4
12g.48981623C=CA2034902120WNT1c.1096C= (p.Leu366=)
c.1063C= (p.Leu355=)
12g.48981623C>GCA384639321WNT1c.1096C>G (p.Leu366Val)
c.1063C>G (p.Leu355Val)
12g.48981623C>TCA479704605WNT1c.1096C>T (p.Leu366=)
c.1063C>T (p.Leu355=)
dbSNP gnomAD v2 gnomAD v4
12g.48981624T>ACA384639323WNT1c.1097T>A (p.Leu366Gln)
c.1064T>A (p.Leu355Gln)
12g.48981624T>CCA384639327WNT1c.1097T>C (p.Leu366Pro)
c.1064T>C (p.Leu355Pro)
gnomAD v4
12g.48981624T>GCA384639330WNT1c.1097T>G (p.Leu366Arg)
c.1064T>G (p.Leu355Arg)
12g.48981625G>ACA479704607WNT1c.1098G>A (p.Leu366=)
c.1065G>A (p.Leu355=)
gnomAD v4
12g.48981625G>CCA479704608WNT1c.1098G>C (p.Leu366=)
c.1065G>C (p.Leu355=)
12g.48981625G>TCA479704609WNT1c.1098G>T (p.Leu366=)
c.1065G>T (p.Leu355=)
gnomAD v4
12g.48981626C>ACA384639333WNT1c.1099C>A (p.His367Asn)
c.1066C>A (p.His356Asn)
gnomAD v4
12g.48981626C>GCA384639334WNT1c.1099C>G (p.His367Asp)
c.1066C>G (p.His356Asp)
12g.48981626C>TCA384639336WNT1c.1099C>T (p.His367Tyr)
c.1066C>T (p.His356Tyr)
gnomAD v4
12g.48981627A=CA2034902121WNT1c.1100A= (p.His367=)
c.1067A= (p.His356=)
12g.48981627A>CCA384639341WNT1c.1100A>C (p.His367Pro)
c.1067A>C (p.His356Pro)
12g.48981627A>GCA384639348WNT1c.1100A>G (p.His367Arg)
c.1067A>G (p.His356Arg)
dbSNP
12g.48981627A>TCA384639345WNT1c.1100A>T (p.His367Leu)
c.1067A>T (p.His356Leu)
12g.48981628C>ACA384639351WNT1c.1101C>A (p.His367Gln)
c.1068C>A (p.His356Gln)
dbSNP gnomAD v4
12g.48981628C=CA2034902122WNT1c.1101C= (p.His367=)
c.1068C= (p.His356=)
12g.48981628C>GCA384639358WNT1c.1101C>G (p.His367Gln)
c.1068C>G (p.His356Gln)
12g.48981628C>TCA479704611WNT1c.1101C>T (p.His367=)
c.1068C>T (p.His356=)
gnomAD v4 COSMIC
12g.48981629G>ACA384639365WNT1c.1102G>A (p.Glu368Lys)
c.1069G>A (p.Glu357Lys)
dbSNP gnomAD v3 gnomAD v4
12g.48981629G>CCA384639378WNT1c.1102G>C (p.Glu368Gln)
c.1069G>C (p.Glu357Gln)
12g.48981629G=CA2034902123WNT1c.1102G= (p.Glu368=)
c.1069G= (p.Glu357=)
12g.48981629G>TCA384639382WNT1c.1102G>T (p.Glu368Ter)
c.1069G>T (p.Glu357Ter)
gnomAD v4
12g.48981630A>CCA384639386WNT1c.1103A>C (p.Glu368Ala)
c.1070A>C (p.Glu357Ala)
12g.48981630A>GCA384639389WNT1c.1103A>G (p.Glu368Gly)
c.1070A>G (p.Glu357Gly)
12g.48981630A>TCA384639394WNT1c.1103A>T (p.Glu368Val)
c.1070A>T (p.Glu357Val)
12g.48981631G>ACA479704614WNT1c.1104G>A (p.Glu368=)
c.1071G>A (p.Glu357=)
gnomAD v4
12g.48981631G>CCA384639398WNT1c.1104G>C (p.Glu368Asp)
c.1071G>C (p.Glu357Asp)
12g.48981631G>TCA384639401WNT1c.1104G>T (p.Glu368Asp)
c.1071G>T (p.Glu357Asp)
gnomAD v4
12g.48981632T>ACA384639406WNT1c.1105T>A (p.Cys369Ser)
c.1072T>A (p.Cys358Ser)
12g.48981632T>CCA384639407WNT1c.1105T>C (p.Cys369Arg)
c.1072T>C (p.Cys358Arg)
12g.48981632T>GCA384639404WNT1c.1105T>G (p.Cys369Gly)
c.1072T>G (p.Cys358Gly)
ClinVar
12g.48981633G>ACA384639409WNT1c.1106G>A (p.Cys369Tyr)
c.1073G>A (p.Cys358Tyr)
gnomAD v4
12g.48981633G>CCA384639412WNT1c.1106G>C (p.Cys369Ser)
c.1073G>C (p.Cys358Ser)
12g.48981633G=CA2034902124WNT1c.1106G= (p.Cys369=)
c.1073G= (p.Cys358=)
12g.48981633G>TCA384639414WNT1c.1106G>T (p.Cys369Phe)
c.1073G>T (p.Cys358Phe)
dbSNP gnomAD v2 gnomAD v4
12g.48981634T>ACA384639423WNT1c.1107T>A (p.Cys369Ter)
c.1074T>A (p.Cys358Ter)
gnomAD v4
12g.48981634T>CCA479704618WNT1c.1107T>C (p.Cys369=)
c.1074T>C (p.Cys358=)
gnomAD v4
12g.48981634T>GCA384639439WNT1c.1107T>G (p.Cys369Trp)
c.1074T>G (p.Cys358Trp)
12g.48981635C>ACA384639441WNT1c.1108C>A (p.Leu370Met)
c.1075C>A (p.Leu359Met)
gnomAD v4
12g.48981635C=CA2034902125WNT1c.1108C= (p.Leu370=)
c.1075C= (p.Leu359=)
12g.48981635C>GCA236608835WNT1c.1108C>G (p.Leu370Val)
c.1075C>G (p.Leu359Val)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.48981635C>TCA479704619WNT1c.1108C>T (p.Leu370=)
c.1075C>T (p.Leu359=)
gnomAD v4
12g.48981636T>ACA384639446WNT1c.1109T>A (p.Leu370Gln)
c.1076T>A (p.Leu359Gln)
gnomAD v4
12g.48981636T>CCA384639449WNT1c.1109T>C (p.Leu370Pro)
c.1076T>C (p.Leu359Pro)
gnomAD v4
12g.48981636T>GCA384639451WNT1c.1109T>G (p.Leu370Arg)
c.1076T>G (p.Leu359Arg)
12g.48981638_48981639delCA2618599717WNT1c.1111_1112del (p.Ter371ArgextTer?)
c.1078_1079del (p.Ter360=)
gnomAD v4
12g.48981637G>ACA479704628WNT1c.1110G>A (p.Leu370=)
c.1077G>A (p.Leu359=)
gnomAD v4
12g.48981637G>CCA479704627WNT1c.1110G>C (p.Leu370=)
c.1077G>C (p.Leu359=)
12g.48981637G>TCA479704626WNT1c.1110G>T (p.Leu370=)
c.1077G>T (p.Leu359=)
gnomAD v4
12g.48981638T>ACA384639452WNT1c.1111T>A (p.Ter371Arg)
c.1078T>A (p.Ter360Arg)
dbSNP gnomAD v2 gnomAD v4
12g.48981638T>CCA384639453WNT1c.1111T>C (p.Ter371Arg)
c.1078T>C (p.Ter360Arg)
gnomAD v4
12g.48981638T>GCA384639455WNT1c.1111T>G (p.Ter371Gly)
c.1078T>G (p.Ter360Gly)
12g.48981638T=CA2034902126WNT1c.1111T= (p.Ter371=)
c.1078T= (p.Ter360=)
12g.48981639G>ACA479704630WNT1c.1112G>A (p.Ter371=)
c.1079G>A (p.Ter360=)
dbSNP gnomAD v3 gnomAD v4
12g.48981639G>CCA384639462WNT1c.1112G>C (p.Ter371Ser)
c.1079G>C (p.Ter360Ser)
12g.48981639G=CA2034902127WNT1c.1112G= (p.Ter371=)
c.1079G= (p.Ter360=)
12g.48981639G>TCA384639458WNT1c.1112G>T (p.Ter371Leu)
c.1079G>T (p.Ter360Leu)
gnomAD v4
12g.48981640A>CCA384639465WNT1c.1113A>C (p.Ter371Cys)
c.1080A>C (p.Ter360Cys)
12g.48981640A>GCA384639467WNT1c.1113A>G (p.Ter371Trp)
c.1080A>G (p.Ter360Trp)
gnomAD v4
12g.48981640A>TCA384639469WNT1c.1113A>T (p.Ter371Cys)
c.1080A>T (p.Ter360Cys)
dbSNP gnomAD v4
12g.48981641G>ACA2618599727WNT1c.*1G>A (n.*1G>A)
gnomAD v4
12g.48981641G>TCA2618599729WNT1c.*1G>T (n.*1G>T)
gnomAD v4
12g.48981642G>ACA605233431WNT1c.*2G>A (n.*2G>A)
dbSNP gnomAD v2 gnomAD v4
12g.48981642G=CA2034902128WNT1c.*2G= (n.*2G=)
12g.48981642G>TCA2618599733WNT1c.*2G>T (n.*2G>T)
gnomAD v4
12g.48981643C>ACA2618599735WNT1c.*3C>A (n.*3C>A)
gnomAD v4
12g.48981643C>TCA2618599736WNT1c.*3C>T (n.*3C>T)
gnomAD v4
12g.48981644G>ACA605233432WNT1c.*4G>A (n.*4G>A)
dbSNP gnomAD v2 gnomAD v4
12g.48981644G=CA2034902129WNT1c.*4G= (n.*4G=)
12g.48981644G>TCA2034902130WNT1c.*4G>T (n.*4G>T)
dbSNP gnomAD v4
12g.48981645C>ACA2618599742WNT1c.*5C>A (n.*5C>A)
gnomAD v4
12g.48981645C>TCA2618599744WNT1c.*5C>T (n.*5C>T)
gnomAD v4
12g.48981646T>CCA2575143761WNT1c.*6T>C (n.*6T>C)
gnomAD v4
12g.48981647G>ACA236608837WNT1c.*7G>A (n.*7G>A)
dbSNP gnomAD v2 gnomAD v4
12g.48981647G>CCA2575143762WNT1c.*7G>C (n.*7G>C)
12g.48981647G=CA2034902131WNT1c.*7G= (n.*7G=)
12g.48981647G>TCA2618599750WNT1c.*7G>T (n.*7G>T)
gnomAD v4
12g.48981648C>ACA236608839WNT1c.*8C>A (n.*8C>A)
dbSNP gnomAD v4
12g.48981648C=CA2034902132WNT1c.*8C= (n.*8C=)
12g.48981648C>TCA2575143763WNT1c.*8C>T (n.*8C>T)
gnomAD v4
12g.48981649G>ACA6544505WNT1c.*9G>A (n.*9G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.48981649G=CA2034902133WNT1c.*9G= (n.*9G=)
12g.48981649G>TCA2618599759WNT1c.*9G>T (n.*9G>T)
gnomAD v4

Number of alleles fetched