Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.47566721T>G | CA16602806 | ARAF | c.640T>G (p.Ser214Ala) c.649T>G (p.Ser217Ala) c.655T>G (p.Ser219Ala) c.-18T>G (n.-18T>G) | ClinVar dbSNP COSMIC |
X | g.47566721T>A | CA412813391 | ARAF | c.640T>A (p.Ser214Thr) c.649T>A (p.Ser217Thr) c.655T>A (p.Ser219Thr) c.-18T>A (n.-18T>A) | dbSNP COSMIC |