Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.127738431C>G | CA372279626 | MYC | c.169C>G (p.Pro57Ala) c.211C>G (p.Pro71Ala) c.214C>G (p.Pro72Ala) c.-132C>G (n.-132C>G) c.135C>G (p.Cys45Trp) | dbSNP COSMIC COSMIC |
8 | g.127738431C>T | CA122520 | MYC | c.169C>T (p.Pro57Ser) c.211C>T (p.Pro71Ser) c.214C>T (p.Pro72Ser) c.-132C>T (n.-132C>T) c.135C>T (p.Cys45=) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC |