Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7674249A>TCA397839181TP53c.714T>A (p.Cys238Ter)
c.318T>A (p.Cys106Ter)
c.435T>A (p.Cys145Ter)
c.693T>A (p.Cys231Ter)
c.597T>A (p.Cys199Ter)
c.237T>A (p.Cys79Ter)
c.681T>A (p.Cys227Ter)
dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674249A>GCA497717529TP53c.714T>C (p.Cys238=)
c.318T>C (p.Cys106=)
c.435T>C (p.Cys145=)
c.693T>C (p.Cys231=)
c.597T>C (p.Cys199=)
c.237T>C (p.Cys79=)
c.681T>C (p.Cys227=)
dbSNP COSMIC
17g.7674249A>CCA000353TP53c.714T>G (p.Cys238Trp)
c.318T>G (p.Cys106Trp)
c.435T>G (p.Cys145Trp)
c.693T>G (p.Cys231Trp)
c.597T>G (p.Cys199Trp)
c.237T>G (p.Cys79Trp)
c.681T>G (p.Cys227Trp)
ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched