Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.48981411C>ACA143725WNT1c.884C>A (p.Ser295Ter)
c.851C>A (p.Ser284Ter)
ClinVar dbSNP gnomAD v4
12g.48981411C>TCA384636690WNT1c.884C>T (p.Ser295Leu)
c.851C>T (p.Ser284Leu)
ClinVar dbSNP gnomAD v4
12g.48981411C=CA2034926115WNT1c.884C= (p.Ser295=)
c.851C= (p.Ser284=)
dbSNP

Number of alleles fetched