| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.218893145C>T | CA431417476 | WNT10A | c.1128C>T (p.Cys376=) c.635C>T c.1077C>T (p.Cys359=) c.1032C>T (p.Cys344=) c.748C>T (p.Leu250=) | ClinVar dbSNP |
| 2 | g.218893145C>A | CA116869 | WNT10A | c.1128C>A (p.Cys376Ter) c.635C>A c.1077C>A (p.Cys359Ter) c.1032C>A (p.Cys344Ter) c.748C>A (p.Leu250Met) | ClinVar dbSNP |
| 2 | g.218893145C>G | CA350591785 | WNT10A | c.1128C>G (p.Cys376Trp) c.635C>G c.1077C>G (p.Cys359Trp) c.1032C>G (p.Cys344Trp) c.748C>G (p.Leu250Val) | dbSNP |