Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.90088607T>A | CA16602873 | IDH2 | c.514A>T (p.Arg172Trp) c.358A>T (p.Arg120Trp) c.208-105A>T (n.208-105A>T) c.*139A>T (n.*139A>T) c.124A>T (p.Arg42Trp) | ClinVar dbSNP COSMIC |
15 | g.90088607T>C | CA16602874 | IDH2 | c.514A>G (p.Arg172Gly) c.358A>G (p.Arg120Gly) c.208-105A>G (n.208-105A>G) c.*139A>G (n.*139A>G) c.124A>G (p.Arg42Gly) | ClinVar dbSNP COSMIC |