Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7673777G>C | CA10590135 | TP53 | c.843C>G (p.Asp281Glu) c.447C>G (p.Asp149Glu) c.564C>G (p.Asp188Glu) c.822C>G (p.Asp274Glu) c.782+404C>G (n.782+404C>G) c.726C>G (p.Asp242Glu) c.366C>G (p.Asp122Glu) c.810C>G (p.Asp270Glu) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
17 | g.7673777G>T | CA16615937 | TP53 | c.843C>A (p.Asp281Glu) c.447C>A (p.Asp149Glu) c.564C>A (p.Asp188Glu) c.822C>A (p.Asp274Glu) c.782+404C>A (n.782+404C>A) c.726C>A (p.Asp242Glu) c.366C>A (p.Asp122Glu) c.810C>A (p.Asp270Glu) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673777G>A | CA497715999 | TP53 | c.843C>T (p.Asp281=) c.447C>T (p.Asp149=) c.564C>T (p.Asp188=) c.822C>T (p.Asp274=) c.782+404C>T (n.782+404C>T) c.726C>T (p.Asp242=) c.366C>T (p.Asp122=) c.810C>T (p.Asp270=) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |