Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.49375576C>A | CA16602950 | RHOA | c.14G>T (p.Arg5Leu) n.294G>T c.-147-83G>T (n.-147-83G>T) | ClinVar dbSNP COSMIC |
3 | g.49375576C>G | CA352788296 | RHOA | c.14G>C (p.Arg5Pro) n.294G>C c.-147-83G>C (n.-147-83G>C) | dbSNP |
3 | g.49375576C>T | CA16602949 | RHOA | c.14G>A (p.Arg5Gln) n.294G>A c.-147-83G>A (n.-147-83G>A) | ClinVar dbSNP COSMIC |