Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.54285925_54285926delinsAT | CA16602522 | PDGFRA | c.2524_2525delinsAT (p.Asp842Ile) c.1804_1805delinsAT (p.Asp602Ile) c.2599_2600delinsAT (p.Asp867Ile) c.2563_2564delinsAT (p.Asp855Ile) | ClinVar dbSNP COSMIC |
4 | g.54285925_54285926delinsTT | CA645526432 | PDGFRA | c.2524_2525delinsTT (p.Asp842Phe) c.1804_1805delinsTT (p.Asp602Phe) c.2599_2600delinsTT (p.Asp867Phe) c.2563_2564delinsTT (p.Asp855Phe) | dbSNP COSMIC |