Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7675189G>T | CA397842565 | TP53 | c.423C>A (p.Cys141Ter) c.27C>A (p.Cys9Ter) c.144C>A (p.Cys48Ter) c.402C>A (p.Cys134Ter) n.679C>A c.306C>A (p.Cys102Ter) c.-55C>A (n.-55C>A) c.390C>A (p.Cys130Ter) | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7675189G>A | CA497925698 | TP53 | c.423C>T (p.Cys141=) c.27C>T (p.Cys9=) c.144C>T (p.Cys48=) c.402C>T (p.Cys134=) n.679C>T c.306C>T (p.Cys102=) c.-55C>T (n.-55C>T) c.390C>T (p.Cys130=) | ClinVar dbSNP COSMIC |
17 | g.7675189G>C | CA16602990 | TP53 | c.423C>G (p.Cys141Trp) c.27C>G (p.Cys9Trp) c.144C>G (p.Cys48Trp) c.402C>G (p.Cys134Trp) n.679C>G c.306C>G (p.Cys102Trp) c.-55C>G (n.-55C>G) c.390C>G (p.Cys130Trp) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |