Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7674191C>T | CA000406 | TP53 | c.772G>A (p.Glu258Lys) c.376G>A (p.Glu126Lys) c.493G>A (p.Glu165Lys) c.751G>A (p.Glu251Lys) c.655G>A (p.Glu219Lys) c.295G>A (p.Glu99Lys) c.739G>A (p.Glu247Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.7674191C>G | CA397837688 | TP53 | c.772G>C (p.Glu258Gln) c.376G>C (p.Glu126Gln) c.493G>C (p.Glu165Gln) c.751G>C (p.Glu251Gln) c.655G>C (p.Glu219Gln) c.295G>C (p.Glu99Gln) c.739G>C (p.Glu247Gln) | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674191C>A | CA397837685 | TP53 | c.772G>T (p.Glu258Ter) c.376G>T (p.Glu126Ter) c.493G>T (p.Glu165Ter) c.751G>T (p.Glu251Ter) c.655G>T (p.Glu219Ter) c.295G>T (p.Glu99Ter) c.739G>T (p.Glu247Ter) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |