Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7673763T>ACA16603014TP53c.857A>T (p.Glu286Val)
c.461A>T (p.Glu154Val)
c.578A>T (p.Glu193Val)
c.836A>T (p.Glu279Val)
c.782+418A>T (n.782+418A>T)
c.740A>T (p.Glu247Val)
c.380A>T (p.Glu127Val)
c.824A>T (p.Glu275Val)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673763T>CCA16603012TP53c.857A>G (p.Glu286Gly)
c.461A>G (p.Glu154Gly)
c.578A>G (p.Glu193Gly)
c.836A>G (p.Glu279Gly)
c.782+418A>G (n.782+418A>G)
c.740A>G (p.Glu247Gly)
c.380A>G (p.Glu127Gly)
c.824A>G (p.Glu275Gly)
ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC
17g.7673763T>GCA16603015TP53c.857A>C (p.Glu286Ala)
c.461A>C (p.Glu154Ala)
c.578A>C (p.Glu193Ala)
c.836A>C (p.Glu279Ala)
c.782+418A>C (n.782+418A>C)
c.740A>C (p.Glu247Ala)
c.380A>C (p.Glu127Ala)
c.824A>C (p.Glu275Ala)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched