| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.7674218T>A | CA000389 | TP53 | c.745A>T (p.Arg249Trp) c.349A>T (p.Arg117Trp) c.466A>T (p.Arg156Trp) c.724A>T (p.Arg242Trp) c.466A>T c.628A>T (p.Arg210Trp) c.268A>T (p.Arg90Trp) c.712A>T (p.Arg238Trp) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7674218T>C | CA16603071 | TP53 | c.745A>G (p.Arg249Gly) c.349A>G (p.Arg117Gly) c.466A>G (p.Arg156Gly) c.724A>G (p.Arg242Gly) c.466A>G c.628A>G (p.Arg210Gly) c.268A>G (p.Arg90Gly) c.712A>G (p.Arg238Gly) | ClinVar dbSNP gnomAD v4 |