| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.7673821G>C | CA397837125 | TP53 | c.799C>G (p.Arg267Gly) c.403C>G (p.Arg135Gly) c.520C>G (p.Arg174Gly) c.778C>G (p.Arg260Gly) c.782+360C>G (n.782+360C>G) c.682C>G (p.Arg228Gly) c.322C>G (p.Arg108Gly) c.766C>G (p.Arg256Gly) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7673821G>A | CA000423 | TP53 | c.799C>T (p.Arg267Trp) c.403C>T (p.Arg135Trp) c.520C>T (p.Arg174Trp) c.778C>T (p.Arg260Trp) c.782+360C>T (n.782+360C>T) c.682C>T (p.Arg228Trp) c.322C>T (p.Arg108Trp) c.766C>T (p.Arg256Trp) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC COSMIC |