Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.90088605C>G | CA16602460 | IDH2 | c.516G>C (p.Arg172Ser) c.360G>C (p.Arg120Ser) c.208-103G>C (n.208-103G>C) c.*141G>C (n.*141G>C) c.126G>C (p.Arg42Ser) | ClinVar dbSNP gnomAD v4 COSMIC |
15 | g.90088605C>A | CA393802238 | IDH2 | c.516G>T (p.Arg172Ser) c.360G>T (p.Arg120Ser) c.208-103G>T (n.208-103G>T) c.*141G>T (n.*141G>T) c.126G>T (p.Arg42Ser) | ClinVar dbSNP COSMIC |
15 | g.90088605C>T | CA492298026 | IDH2 | c.516G>A (p.Arg172=) c.360G>A (p.Arg120=) c.208-103G>A (n.208-103G>A) c.*141G>A (n.*141G>A) c.126G>A (p.Arg42=) | dbSNP gnomAD v4 COSMIC |