Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7674233C>GCA16603024TP53c.730G>C (p.Gly244Arg)
c.334G>C (p.Gly112Arg)
c.451G>C (p.Gly151Arg)
c.709G>C (p.Gly237Arg)
c.613G>C (p.Gly205Arg)
c.253G>C (p.Gly85Arg)
c.697G>C (p.Gly233Arg)
ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674233C>TCA16603022TP53c.730G>A (p.Gly244Ser)
c.334G>A (p.Gly112Ser)
c.451G>A (p.Gly151Ser)
c.709G>A (p.Gly237Ser)
c.613G>A (p.Gly205Ser)
c.253G>A (p.Gly85Ser)
c.697G>A (p.Gly233Ser)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674233C>ACA16603021TP53c.730G>T (p.Gly244Cys)
c.334G>T (p.Gly112Cys)
c.451G>T (p.Gly151Cys)
c.709G>T (p.Gly237Cys)
c.613G>T (p.Gly205Cys)
c.253G>T (p.Gly85Cys)
c.697G>T (p.Gly233Cys)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched