Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7675084G>C | CA16602998 | TP53 | c.528C>G (p.Cys176Trp) c.132C>G (p.Cys44Trp) c.249C>G (p.Cys83Trp) c.507C>G (p.Cys169Trp) n.784C>G n.36C>G c.411C>G (p.Cys137Trp) c.51C>G (p.Cys17Trp) c.495C>G (p.Cys165Trp) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7675084G>T | CA397841425 | TP53 | c.528C>A (p.Cys176Ter) c.132C>A (p.Cys44Ter) c.249C>A (p.Cys83Ter) c.507C>A (p.Cys169Ter) n.784C>A n.36C>A c.411C>A (p.Cys137Ter) c.51C>A (p.Cys17Ter) c.495C>A (p.Cys165Ter) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7675084G>A | CA497925587 | TP53 | c.528C>T (p.Cys176=) c.132C>T (p.Cys44=) c.249C>T (p.Cys83=) c.507C>T (p.Cys169=) n.784C>T n.36C>T c.411C>T (p.Cys137=) c.51C>T (p.Cys17=) c.495C>T (p.Cys165=) | ClinVar dbSNP |