| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.54285925G>T | CA16602703 | PDGFRA | c.2524G>T (p.Asp842Tyr) c.1804G>T (p.Asp602Tyr) c.2599G>T (p.Asp867Tyr) c.2563G>T (p.Asp855Tyr) | ClinVar dbSNP COSMIC |
| 4 | g.54285925G>C | CA356895028 | PDGFRA | c.2524G>C (p.Asp842His) c.1804G>C (p.Asp602His) c.2599G>C (p.Asp867His) c.2563G>C (p.Asp855His) | dbSNP COSMIC |
| 4 | g.54285925G>A | CA356895029 | PDGFRA | c.2524G>A (p.Asp842Asn) c.1804G>A (p.Asp602Asn) c.2599G>A (p.Asp867Asn) c.2563G>A (p.Asp855Asn) | dbSNP |