| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.54285923G>C | CA356895025 | PDGFRA | c.2522G>C (p.Arg841Thr) c.1802G>C (p.Arg601Thr) c.2597G>C (p.Arg866Thr) c.2561G>C (p.Arg854Thr) | dbSNP |
| 4 | g.54285923G>A | CA16602638 | PDGFRA | c.2522G>A (p.Arg841Lys) c.1802G>A (p.Arg601Lys) c.2597G>A (p.Arg866Lys) c.2561G>A (p.Arg854Lys) | ClinVar dbSNP |