| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.7673805A>T | CA16603087 | TP53 | c.815T>A (p.Val272Glu) c.419T>A (p.Val140Glu) c.536T>A (p.Val179Glu) c.794T>A (p.Val265Glu) c.782+376T>A (n.782+376T>A) c.698T>A (p.Val233Glu) c.338T>A (p.Val113Glu) c.782T>A (p.Val261Glu) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7673805A>C | CA10580918 | TP53 | c.815T>G (p.Val272Gly) c.419T>G (p.Val140Gly) c.536T>G (p.Val179Gly) c.794T>G (p.Val265Gly) c.782+376T>G (n.782+376T>G) c.698T>G (p.Val233Gly) c.338T>G (p.Val113Gly) c.782T>G (p.Val261Gly) | ClinVar dbSNP gnomAD v4 |
| 17 | g.7673805A>G | CA397836997 | TP53 | c.815T>C (p.Val272Ala) c.419T>C (p.Val140Ala) c.536T>C (p.Val179Ala) c.794T>C (p.Val265Ala) c.782+376T>C (n.782+376T>C) c.698T>C (p.Val233Ala) c.338T>C (p.Val113Ala) c.782T>C (p.Val261Ala) | ClinVar dbSNP COSMIC |