Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7674200T>ACA16603041TP53c.763A>T (p.Ile255Phe)
c.367A>T (p.Ile123Phe)
c.484A>T (p.Ile162Phe)
c.742A>T (p.Ile248Phe)
c.646A>T (p.Ile216Phe)
c.286A>T (p.Ile96Phe)
c.730A>T (p.Ile244Phe)
ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674200T=CA2245951126TP53c.763A= (p.Ile255=)
c.367A= (p.Ile123=)
c.484A= (p.Ile162=)
c.742A= (p.Ile248=)
c.646A= (p.Ile216=)
c.286A= (p.Ile96=)
c.730A= (p.Ile244=)
dbSNP

Number of alleles fetched