| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.49619063A>G | CA16602973 | SPOP | c.398T>C (p.Phe133Ser) c.*247T>C (n.*247T>C) c.*341T>C (n.*341T>C) c.117T>C | ClinVar dbSNP COSMIC |
| 17 | g.49619063A>T | CA400156689 | SPOP | c.398T>A (p.Phe133Tyr) c.*247T>A (n.*247T>A) c.*341T>A (n.*341T>A) c.117T>A | dbSNP |
| 17 | g.49619063A>C | CA16602972 | SPOP | c.398T>G (p.Phe133Cys) c.*247T>G (n.*247T>G) c.*341T>G (n.*341T>G) c.117T>G | ClinVar dbSNP COSMIC |