| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.150117796G>A | CA343799 | PDGFRB | c.2959C>T (p.Arg987Trp) c.*2273C>T (n.*2273C>T) c.2767C>T (p.Arg923Trp) c.2476C>T (p.Arg826Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 5 | g.150117796G>C | CA361755914 | PDGFRB | c.2959C>G (p.Arg987Gly) c.*2273C>G (n.*2273C>G) c.2767C>G (p.Arg923Gly) c.2476C>G (p.Arg826Gly) | dbSNP |