Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7675191A>TCA16602993TP53c.421T>A (p.Cys141Ser)
c.25T>A (p.Cys9Ser)
c.142T>A (p.Cys48Ser)
c.400T>A (p.Cys134Ser)
n.677T>A
c.304T>A (p.Cys102Ser)
c.-57T>A (n.-57T>A)
c.388T>A (p.Cys130Ser)
ClinVar dbSNP COSMIC
17g.7675191A>GCA16602991TP53c.421T>C (p.Cys141Arg)
c.25T>C (p.Cys9Arg)
c.142T>C (p.Cys48Arg)
c.400T>C (p.Cys134Arg)
n.677T>C
c.304T>C (p.Cys102Arg)
c.-57T>C (n.-57T>C)
c.388T>C (p.Cys130Arg)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7675191A>CCA16602992TP53c.421T>G (p.Cys141Gly)
c.25T>G (p.Cys9Gly)
c.142T>G (p.Cys48Gly)
c.400T>G (p.Cys134Gly)
n.677T>G
c.304T>G (p.Cys102Gly)
c.-57T>G (n.-57T>G)
c.388T>G (p.Cys130Gly)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched