Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7674221G>C | CA16603069 | TP53 | c.742C>G (p.Arg248Gly) c.346C>G (p.Arg116Gly) c.463C>G (p.Arg155Gly) c.721C>G (p.Arg241Gly) c.625C>G (p.Arg209Gly) c.265C>G (p.Arg89Gly) c.709C>G (p.Arg237Gly) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674221G>A | CA000382 | TP53 | c.742C>T (p.Arg248Trp) c.346C>T (p.Arg116Trp) c.463C>T (p.Arg155Trp) c.721C>T (p.Arg241Trp) c.625C>T (p.Arg209Trp) c.265C>T (p.Arg89Trp) c.709C>T (p.Arg237Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674221G>T | CA497717294 | TP53 | c.742C>A (p.Arg248=) c.346C>A (p.Arg116=) c.463C>A (p.Arg155=) c.721C>A (p.Arg241=) c.625C>A (p.Arg209=) c.265C>A (p.Arg89=) c.709C>A (p.Arg237=) | ClinVar dbSNP COSMIC |