Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7673776G>ACA000454TP53c.844C>T (p.Arg282Trp)
c.448C>T (p.Arg150Trp)
c.565C>T (p.Arg189Trp)
c.823C>T (p.Arg275Trp)
c.782+405C>T (n.782+405C>T)
c.727C>T (p.Arg243Trp)
c.367C>T (p.Arg123Trp)
c.811C>T (p.Arg271Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC
17g.7673776G>TCA497715987TP53c.844C>A (p.Arg282=)
c.448C>A (p.Arg150=)
c.565C>A (p.Arg189=)
c.823C>A (p.Arg275=)
c.782+405C>A (n.782+405C>A)
c.727C>A (p.Arg243=)
c.367C>A (p.Arg123=)
c.811C>A (p.Arg271=)
ClinVar dbSNP gnomAD v4 COSMIC
17g.7673776G>CCA000453TP53c.844C>G (p.Arg282Gly)
c.448C>G (p.Arg150Gly)
c.565C>G (p.Arg189Gly)
c.823C>G (p.Arg275Gly)
c.782+405C>G (n.782+405C>G)
c.727C>G (p.Arg243Gly)
c.367C>G (p.Arg123Gly)
c.811C>G (p.Arg271Gly)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched