Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7675084G>CCA16602998TP53c.528C>G (p.Cys176Trp)
c.132C>G (p.Cys44Trp)
c.249C>G (p.Cys83Trp)
c.507C>G (p.Cys169Trp)
n.784C>G
n.36C>G
c.411C>G (p.Cys137Trp)
c.51C>G (p.Cys17Trp)
c.495C>G (p.Cys165Trp)
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7675084G>TCA397841425TP53c.528C>A (p.Cys176Ter)
c.132C>A (p.Cys44Ter)
c.249C>A (p.Cys83Ter)
c.507C>A (p.Cys169Ter)
n.784C>A
n.36C>A
c.411C>A (p.Cys137Ter)
c.51C>A (p.Cys17Ter)
c.495C>A (p.Cys165Ter)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7675084G>ACA497925587TP53c.528C>T (p.Cys176=)
c.132C>T (p.Cys44=)
c.249C>T (p.Cys83=)
c.507C>T (p.Cys169=)
n.784C>T
n.36C>T
c.411C>T (p.Cys137=)
c.51C>T (p.Cys17=)
c.495C>T (p.Cys165=)
dbSNP

Number of alleles fetched