Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.150124300A>T | CA361764702 | PDGFRB | c.1973T>A (p.Leu658His) n.608T>A c.*1287T>A (n.*1287T>A) c.1781T>A (p.Leu594His) c.1490T>A (p.Leu497His) | dbSNP |
5 | g.150124300A>G | CA343798 | PDGFRB | c.1973T>C (p.Leu658Pro) n.608T>C c.*1287T>C (n.*1287T>C) c.1781T>C (p.Leu594Pro) c.1490T>C (p.Leu497Pro) | ClinVar dbSNP |