Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.47566722C>G | CA16602595 | ARAF | c.641C>G (p.Ser214Cys) c.650C>G (p.Ser217Cys) c.656C>G (p.Ser219Cys) c.-17C>G (n.-17C>G) | ClinVar dbSNP COSMIC |
X | g.47566722C>A | CA412813393 | ARAF | c.641C>A (p.Ser214Tyr) c.650C>A (p.Ser217Tyr) c.656C>A (p.Ser219Tyr) c.-17C>A (n.-17C>A) | dbSNP COSMIC |
X | g.47566722C>T | CA16602805 | ARAF | c.641C>T (p.Ser214Phe) c.650C>T (p.Ser217Phe) c.656C>T (p.Ser219Phe) c.-17C>T (n.-17C>T) | ClinVar dbSNP gnomAD v4 COSMIC |