| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.54285934C>T | CA16602639 | PDGFRA | c.2533C>T (p.His845Tyr) c.1813C>T (p.His605Tyr) c.2608C>T (p.His870Tyr) c.2572C>T (p.His858Tyr) | ClinVar dbSNP COSMIC |
| 4 | g.54285934C>G | CA356895049 | PDGFRA | c.2533C>G (p.His845Asp) c.1813C>G (p.His605Asp) c.2608C>G (p.His870Asp) c.2572C>G (p.His858Asp) | dbSNP |