| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 8 | g.127738519A>C | CA122522 | MYC | c.257A>C (p.Asn86Thr) c.299A>C (p.Asn100Thr) c.302A>C (p.Asn101Thr) c.-44A>C (n.-44A>C) | ClinVar dbSNP |
| 8 | g.127738519A>G | CA372279826 | MYC | c.257A>G (p.Asn86Ser) c.299A>G (p.Asn100Ser) c.302A>G (p.Asn101Ser) c.-44A>G (n.-44A>G) | dbSNP |
| 8 | g.127738519A= | CA1818466598 | MYC | c.257A= (p.Asn86=) c.299A= (p.Asn100=) c.302A= (p.Asn101=) c.-44A= (n.-44A=) | dbSNP |
| 8 | g.127738519A>T | CA372279827 | MYC | c.257A>T (p.Asn86Ile) c.299A>T (p.Asn100Ile) c.302A>T (p.Asn101Ile) c.-44A>T (n.-44A>T) | dbSNP gnomAD v4 |