Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.127738447C>T | CA16602747 | MYC | c.185C>T (p.Ser62Phe) c.227C>T (p.Ser76Phe) c.230C>T (p.Ser77Phe) c.-116C>T (n.-116C>T) c.151C>T (p.Pro51Ser) | ClinVar dbSNP COSMIC COSMIC |
8 | g.127738447C>A | CA372279664 | MYC | c.185C>A (p.Ser62Tyr) c.227C>A (p.Ser76Tyr) c.230C>A (p.Ser77Tyr) c.-116C>A (n.-116C>A) c.151C>A (p.Pro51Thr) | dbSNP |
8 | g.127738447C>G | CA372279665 | MYC | c.185C>G (p.Ser62Cys) c.227C>G (p.Ser76Cys) c.230C>G (p.Ser77Cys) c.-116C>G (n.-116C>G) c.151C>G (p.Pro51Ala) | dbSNP gnomAD v4 |