Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7674251A>GCA16603002TP53c.712T>C (p.Cys238Arg)
c.316T>C (p.Cys106Arg)
c.433T>C (p.Cys145Arg)
c.691T>C (p.Cys231Arg)
c.595T>C (p.Cys199Arg)
c.235T>C (p.Cys79Arg)
c.679T>C (p.Cys227Arg)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674251A>TCA397839198TP53c.712T>A (p.Cys238Ser)
c.316T>A (p.Cys106Ser)
c.433T>A (p.Cys145Ser)
c.691T>A (p.Cys231Ser)
c.595T>A (p.Cys199Ser)
c.235T>A (p.Cys79Ser)
c.679T>A (p.Cys227Ser)
ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674251A>CCA16603003TP53c.712T>G (p.Cys238Gly)
c.316T>G (p.Cys106Gly)
c.433T>G (p.Cys145Gly)
c.691T>G (p.Cys231Gly)
c.595T>G (p.Cys199Gly)
c.235T>G (p.Cys79Gly)
c.679T>G (p.Cys227Gly)
ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched