Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.127738390C>T | CA16602893 | MYC | c.128C>T (p.Pro43Leu) c.170C>T (p.Pro57Leu) c.173C>T (p.Pro58Leu) c.-173C>T (n.-173C>T) c.94C>T (p.Arg32Trp) | ClinVar dbSNP |
8 | g.127738390C>G | CA372279511 | MYC | c.128C>G (p.Pro43Arg) c.170C>G (p.Pro57Arg) c.173C>G (p.Pro58Arg) c.-173C>G (n.-173C>G) c.94C>G (p.Arg32Gly) | dbSNP |