| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.54274869T>G | CA356893078 | PDGFRA | c.1682T>G (p.Val561Gly) c.1018-56T>G (n.1018-56T>G) n.1500T>G c.1757T>G (p.Val586Gly) c.1721T>G (p.Val574Gly) | dbSNP |
| 4 | g.54274869T>C | CA16602796 | PDGFRA | c.1682T>C (p.Val561Ala) c.1018-56T>C (n.1018-56T>C) n.1500T>C c.1757T>C (p.Val586Ala) c.1721T>C (p.Val574Ala) | ClinVar dbSNP |
| 4 | g.54274869T>A | CA123203 | PDGFRA | c.1682T>A (p.Val561Asp) c.1018-56T>A (n.1018-56T>A) n.1500T>A c.1757T>A (p.Val586Asp) c.1721T>A (p.Val574Asp) | ClinVar dbSNP COSMIC |