Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.1610901G>A | CA10603005 | FOXC1 | c.456G>A (p.Trp152Ter) | ClinVar dbSNP |
6 | g.1610901G>T | CA362558863 | FOXC1 | c.456G>T (p.Trp152Cys) | ClinVar dbSNP |
6 | g.1610901G= | CA1605822558 | FOXC1 | c.456G= (p.Trp152=) | dbSNP |