| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.49619070A>G | CA400156701 | SPOP | c.391T>C (p.Trp131Arg) c.*240T>C (n.*240T>C) c.*334T>C (n.*334T>C) c.110T>C | dbSNP COSMIC |
| 17 | g.49619070A>C | CA16602975 | SPOP | c.391T>G (p.Trp131Gly) c.*240T>G (n.*240T>G) c.*334T>G (n.*334T>G) c.110T>G | ClinVar dbSNP COSMIC |
| 17 | g.49619070A>T | CA16602977 | SPOP | c.391T>A (p.Trp131Arg) c.*240T>A (n.*240T>A) c.*334T>A (n.*334T>A) c.110T>A | ClinVar dbSNP |