Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.127738434A>C | CA4875250 | MYC | c.172A>C (p.Thr58Pro) c.214A>C (p.Thr72Pro) c.217A>C (p.Thr73Pro) c.-129A>C (n.-129A>C) c.138A>C (p.Pro46=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.127738434A>G | CA372279633 | MYC | c.172A>G (p.Thr58Ala) c.214A>G (p.Thr72Ala) c.217A>G (p.Thr73Ala) c.-129A>G (n.-129A>G) c.138A>G (p.Pro46=) | ClinVar dbSNP COSMIC COSMIC |