Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.48981590G>TCA143728WNT1c.1063G>T (p.Val355Phe)
c.1030G>T (p.Val344Phe)
 ClinVar dbSNP gnomAD v4
12g.48981590G>CCA384639074WNT1c.1063G>C (p.Val355Leu)
c.1030G>C (p.Val344Leu)
 dbSNP gnomAD v3 gnomAD v4

Number of alleles fetched