| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 8 | g.127738995C>G | CA16602748 | MYC | c.733C>G (p.Pro245Ala) c.775C>G (p.Pro259Ala) c.778C>G (p.Pro260Ala) c.433C>G (p.Pro145Ala) | ClinVar dbSNP gnomAD v4 |
| 8 | g.127738995C>T | CA372280843 | MYC | c.733C>T (p.Pro245Ser) c.775C>T (p.Pro259Ser) c.778C>T (p.Pro260Ser) c.433C>T (p.Pro145Ser) | dbSNP gnomAD v4 |
| 8 | g.127738995C>A | CA372280842 | MYC | c.733C>A (p.Pro245Thr) c.775C>A (p.Pro259Thr) c.778C>A (p.Pro260Thr) c.433C>A (p.Pro145Thr) | dbSNP |