Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7675071G>ACA000257TP53c.541C>T (p.Arg181Cys)
c.145C>T (p.Arg49Cys)
c.262C>T (p.Arg88Cys)
c.520C>T (p.Arg174Cys)
n.797C>T
n.49C>T
c.424C>T (p.Arg142Cys)
c.64C>T (p.Arg22Cys)
c.508C>T (p.Arg170Cys)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7675071G>TCA10580940TP53c.541C>A (p.Arg181Ser)
c.145C>A (p.Arg49Ser)
c.262C>A (p.Arg88Ser)
c.520C>A (p.Arg174Ser)
n.797C>A
n.49C>A
c.424C>A (p.Arg142Ser)
c.64C>A (p.Arg22Ser)
c.508C>A (p.Arg170Ser)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched