| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.52212730G>T | CA407183566 | PPP2R1A | c.668G>T (p.Arg223Leu) c.11G>T (p.Arg4Leu) n.492G>T c.590G>T (p.Arg197Leu) n.701G>T c.524G>T (p.Arg175Leu) c.548G>T (p.Arg183Leu) n.239G>T n.742G>T | dbSNP |
| 19 | g.52212730G>A | CA16602938 | PPP2R1A | c.668G>A (p.Arg223Gln) c.11G>A (p.Arg4Gln) n.492G>A c.590G>A (p.Arg197Gln) n.701G>A c.524G>A (p.Arg175Gln) c.548G>A (p.Arg183Gln) n.239G>A n.742G>A | ClinVar dbSNP COSMIC |
| 19 | g.52212730G>C | CA407183567 | PPP2R1A | c.668G>C (p.Arg223Pro) c.11G>C (p.Arg4Pro) n.492G>C c.590G>C (p.Arg197Pro) n.701G>C c.524G>C (p.Arg175Pro) c.548G>C (p.Arg183Pro) n.239G>C n.742G>C | ClinVar dbSNP COSMIC |