| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.52212729C>G | CA16602939 | PPP2R1A | c.667C>G (p.Arg223Gly) c.10C>G (p.Arg4Gly) n.491C>G c.589C>G (p.Arg197Gly) n.700C>G c.523C>G (p.Arg175Gly) c.547C>G (p.Arg183Gly) n.238C>G n.741C>G | ClinVar dbSNP |
| 19 | g.52212729C>T | CA16602937 | PPP2R1A | c.667C>T (p.Arg223Trp) c.10C>T (p.Arg4Trp) n.491C>T c.589C>T (p.Arg197Trp) n.700C>T c.523C>T (p.Arg175Trp) c.547C>T (p.Arg183Trp) n.238C>T n.741C>T | ClinVar dbSNP COSMIC |