| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.49619326T>C | CA16602981 | SPOP | c.260A>G (p.Tyr87Cys) c.*109A>G (n.*109A>G) c.*203A>G (n.*203A>G) n.557A>G | ClinVar dbSNP COSMIC |
| 17 | g.49619326T>G | CA16602979 | SPOP | c.260A>C (p.Tyr87Ser) c.*109A>C (n.*109A>C) c.*203A>C (n.*203A>C) n.557A>C | ClinVar dbSNP COSMIC |