Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.1610837C>T | CA119632 | FOXC1 | c.392C>T (p.Ser131Leu) | ClinVar dbSNP |
6 | g.1610837C>G | CA362558718 | FOXC1 | c.392C>G (p.Ser131Trp) | ClinVar dbSNP |
6 | g.1610837C= | CA1605822531 | FOXC1 | c.392C= (p.Ser131=) | dbSNP |
6 | g.1610837C>A | CA362558717 | FOXC1 | c.392C>A (p.Ser131Ter) | ClinVar dbSNP |