| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 8 | g.127738386C>T | CA16602745 | MYC | c.124C>T (p.Pro42Ser) c.166C>T (p.Pro56Ser) c.169C>T (p.Pro57Ser) c.-177C>T (n.-177C>T) c.90C>T (p.Ser30=) | ClinVar dbSNP gnomAD v4 |
| 8 | g.127738386C>G | CA372279502 | MYC | c.124C>G (p.Pro42Ala) c.166C>G (p.Pro56Ala) c.169C>G (p.Pro57Ala) c.-177C>G (n.-177C>G) c.90C>G (p.Ser30Arg) | dbSNP |
| 8 | g.127738386C= | CA1818466365 | MYC | c.124C= (p.Pro42=) c.166C= (p.Pro56=) c.169C= (p.Pro57=) c.-177C= (n.-177C=) c.90C= (p.Ser30=) | dbSNP |
| 8 | g.127738386C>A | CA372279501 | MYC | c.124C>A (p.Pro42Thr) c.166C>A (p.Pro56Thr) c.169C>A (p.Pro57Thr) c.-177C>A (n.-177C>A) c.90C>A (p.Ser30Arg) | dbSNP gnomAD v4 |