| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.7674965G>C | CA397840857 | TP53 | c.566C>G (p.Ala189Gly) c.170C>G (p.Ala57Gly) c.287C>G (p.Ala96Gly) c.545C>G (p.Ala182Gly) n.822C>G n.67+88C>G c.449C>G (p.Ala150Gly) c.89C>G (p.Ala30Gly) c.533C>G (p.Ala178Gly) | ClinVar dbSNP COSMIC |
| 17 | g.7674965G>A | CA000270 | TP53 | c.566C>T (p.Ala189Val) c.170C>T (p.Ala57Val) c.287C>T (p.Ala96Val) c.545C>T (p.Ala182Val) n.822C>T n.67+88C>T c.449C>T (p.Ala150Val) c.89C>T (p.Ala30Val) c.533C>T (p.Ala178Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |