Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.49619282A>T | CA400156918 | SPOP | c.304T>A (p.Phe102Ile) c.*153T>A (n.*153T>A) c.*247T>A (n.*247T>A) c.23T>A | dbSNP COSMIC |
17 | g.49619282A>C | CA16602969 | SPOP | c.304T>G (p.Phe102Val) c.*153T>G (n.*153T>G) c.*247T>G (n.*247T>G) c.23T>G | ClinVar dbSNP COSMIC |