Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7673773G>CCA397836803TP53c.847C>G (p.Arg283Gly)
c.451C>G (p.Arg151Gly)
c.568C>G (p.Arg190Gly)
c.826C>G (p.Arg276Gly)
c.782+408C>G (n.782+408C>G)
c.730C>G (p.Arg244Gly)
c.370C>G (p.Arg124Gly)
c.814C>G (p.Arg272Gly)
ClinVar dbSNP COSMIC
17g.7673773G>ACA000457TP53c.847C>T (p.Arg283Cys)
c.451C>T (p.Arg151Cys)
c.568C>T (p.Arg190Cys)
c.826C>T (p.Arg276Cys)
c.782+408C>T (n.782+408C>T)
c.730C>T (p.Arg244Cys)
c.370C>T (p.Arg124Cys)
c.814C>T (p.Arg272Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.7673773G>TCA001486TP53c.847C>A (p.Arg283Ser)
c.451C>A (p.Arg151Ser)
c.568C>A (p.Arg190Ser)
c.826C>A (p.Arg276Ser)
c.782+408C>A (n.782+408C>A)
c.730C>A (p.Arg244Ser)
c.370C>A (p.Arg124Ser)
c.814C>A (p.Arg272Ser)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC

Number of alleles fetched