Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.218890118C>A | CA2113956 | WNT10A | c.511C>A (p.Arg171Ser) c.264-2656C>A c.460C>A (p.Arg154Ser) c.415C>A (p.Arg139Ser) c.377-2656C>A (n.377-2656C>A) | dbSNP ExAC gnomAD v2 |
2 | g.218890118C>T | CA2113955 | WNT10A | c.511C>T (p.Arg171Cys) c.264-2656C>T c.460C>T (p.Arg154Cys) c.415C>T (p.Arg139Cys) c.377-2656C>T (n.377-2656C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |