Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.1610823C>G | CA119634 | FOXC1 | c.378C>G (p.Ile126Met) | ClinVar dbSNP |
6 | g.1610823C>T | CA3614750 | FOXC1 | c.378C>T (p.Ile126=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.1610823C>A | CA3614749 | FOXC1 | c.378C>A (p.Ile126=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.1610823C= | CA1605822524 | FOXC1 | c.378C= (p.Ile126=) | dbSNP |