| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.90088702C>T | CA124277 | IDH2 | c.419G>A (p.Arg140Gln) c.263G>A (p.Arg88Gln) c.208-200G>A (n.208-200G>A) c.*44G>A (n.*44G>A) c.29G>A (p.Arg10Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.90088702C>A | CA16602463 | IDH2 | c.419G>T (p.Arg140Leu) c.263G>T (p.Arg88Leu) c.208-200G>T (n.208-200G>T) c.*44G>T (n.*44G>T) c.29G>T (p.Arg10Leu) | ClinVar dbSNP gnomAD v4 COSMIC |
| 15 | g.90088702C>G | CA393802432 | IDH2 | c.419G>C (p.Arg140Pro) c.263G>C (p.Arg88Pro) c.208-200G>C (n.208-200G>C) c.*44G>C (n.*44G>C) c.29G>C (p.Arg10Pro) | dbSNP |