| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.54285926A>C | CA356895030 | PDGFRA | c.2525A>C (p.Asp842Ala) c.1805A>C (p.Asp602Ala) c.2600A>C (p.Asp867Ala) c.2564A>C (p.Asp855Ala) | dbSNP |
| 4 | g.54285926A>T | CA123194 | PDGFRA | c.2525A>T (p.Asp842Val) c.1805A>T (p.Asp602Val) c.2600A>T (p.Asp867Val) c.2564A>T (p.Asp855Val) | ClinVar dbSNP COSMIC |
| 4 | g.54285926A>G | CA356895031 | PDGFRA | c.2525A>G (p.Asp842Gly) c.1805A>G (p.Asp602Gly) c.2600A>G (p.Asp867Gly) c.2564A>G (p.Asp855Gly) | dbSNP |