Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7674221G>CCA16603069TP53c.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
17g.7674221G>ACA000382TP53c.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
17g.7674221G>TCA497717294TP53c.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

Number of alleles fetched