| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.7673766T>G | CA397836731 | TP53 | c.854A>C (p.Glu285Ala) c.458A>C (p.Glu153Ala) c.575A>C (p.Glu192Ala) c.833A>C (p.Glu278Ala) c.782+415A>C (n.782+415A>C) c.737A>C (p.Glu246Ala) c.377A>C (p.Glu126Ala) c.821A>C (p.Glu274Ala) | dbSNP COSMIC |
| 17 | g.7673766T>A | CA000463 | TP53 | c.854A>T (p.Glu285Val) c.458A>T (p.Glu153Val) c.575A>T (p.Glu192Val) c.833A>T (p.Glu278Val) c.782+415A>T (n.782+415A>T) c.737A>T (p.Glu246Val) c.377A>T (p.Glu126Val) c.821A>T (p.Glu274Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7673766T>C | CA397836710 | TP53 | c.854A>G (p.Glu285Gly) c.458A>G (p.Glu153Gly) c.575A>G (p.Glu192Gly) c.833A>G (p.Glu278Gly) c.782+415A>G (n.782+415A>G) c.737A>G (p.Glu246Gly) c.377A>G (p.Glu126Gly) c.821A>G (p.Glu274Gly) | ClinVar dbSNP COSMIC COSMIC |