Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.1610691C>A | CA362558392 | FOXC1 | c.246C>A (p.Ser82Arg) | ClinVar dbSNP |
6 | g.1610691C>T | CA133389544 | FOXC1 | c.246C>T (p.Ser82=) | ClinVar dbSNP gnomAD v4 |
6 | g.1610691C>G | CA10588415 | FOXC1 | c.246C>G (p.Ser82Arg) | ClinVar dbSNP |