| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.54277977T>G | CA356893745 | PDGFRA | c.1973T>G (p.Val658Gly) n.211T>G c.1253T>G (p.Val418Gly) n.399T>G n.1791T>G c.2048T>G (p.Val683Gly) c.2012T>G (p.Val671Gly) | dbSNP |
| 4 | g.54277977T>C | CA16602637 | PDGFRA | c.1973T>C (p.Val658Ala) n.211T>C c.1253T>C (p.Val418Ala) n.399T>C n.1791T>C c.2048T>C (p.Val683Ala) c.2012T>C (p.Val671Ala) | ClinVar dbSNP |