| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.54285937G>C | CA356895055 | PDGFRA | c.2536G>C (p.Asp846His) c.1816G>C (p.Asp606His) c.2611G>C (p.Asp871His) c.2575G>C (p.Asp859His) | dbSNP |
| 4 | g.54285937G>T | CA123218 | PDGFRA | c.2536G>T (p.Asp846Tyr) c.1816G>T (p.Asp606Tyr) c.2611G>T (p.Asp871Tyr) c.2575G>T (p.Asp859Tyr) | ClinVar dbSNP COSMIC |
| 4 | g.54285937G>A | CA356895054 | PDGFRA | c.2536G>A (p.Asp846Asn) c.1816G>A (p.Asp606Asn) c.2611G>A (p.Asp871Asn) c.2575G>A (p.Asp859Asn) | ClinVar dbSNP |