| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 8 | g.127738393C>T | CA4875243 | MYC | c.131C>T (p.Ala44Val) c.173C>T (p.Ala58Val) c.176C>T (p.Ala59Val) c.-170C>T (n.-170C>T) c.97C>T (p.Arg33Cys) | ClinVar dbSNP ExAC gnomAD v2 COSMIC COSMIC |
| 8 | g.127738393C>G | CA372279519 | MYC | c.131C>G (p.Ala44Gly) c.173C>G (p.Ala58Gly) c.176C>G (p.Ala59Gly) c.-170C>G (n.-170C>G) c.97C>G (p.Arg33Gly) | dbSNP |
| 8 | g.127738393C>A | CA372279518 | MYC | c.131C>A (p.Ala44Glu) c.173C>A (p.Ala58Glu) c.176C>A (p.Ala59Glu) c.-170C>A (n.-170C>A) c.97C>A (p.Arg33Ser) | dbSNP gnomAD v4 |