Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.1610825G>T | CA362558691 | FOXC1 | c.380G>T (p.Arg127Leu) | ClinVar dbSNP |
6 | g.1610825G>A | CA362558693 | FOXC1 | c.380G>A (p.Arg127His) | ClinVar dbSNP |
6 | g.1610825G= | CA1605822525 | FOXC1 | c.380G= (p.Arg127=) | dbSNP |