Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7674238C>GCA001776TP53c.725G>C (p.Cys242Ser)
c.329G>C (p.Cys110Ser)
c.446G>C (p.Cys149Ser)
c.704G>C (p.Cys235Ser)
c.608G>C (p.Cys203Ser)
c.248G>C (p.Cys83Ser)
c.692G>C (p.Cys231Ser)
ClinVar dbSNP ExAC gnomAD v2 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674238C>ACA501203TP53c.725G>T (p.Cys242Phe)
c.329G>T (p.Cys110Phe)
c.446G>T (p.Cys149Phe)
c.704G>T (p.Cys235Phe)
c.608G>T (p.Cys203Phe)
c.248G>T (p.Cys83Phe)
c.692G>T (p.Cys231Phe)
ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674238C>TCA000361TP53c.725G>A (p.Cys242Tyr)
c.329G>A (p.Cys110Tyr)
c.446G>A (p.Cys149Tyr)
c.704G>A (p.Cys235Tyr)
c.608G>A (p.Cys203Tyr)
c.248G>A (p.Cys83Tyr)
c.692G>A (p.Cys231Tyr)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched