Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7673811A>CCA16603019TP53c.809T>G (p.Phe270Cys)
c.413T>G (p.Phe138Cys)
c.530T>G (p.Phe177Cys)
c.788T>G (p.Phe263Cys)
c.782+370T>G (n.782+370T>G)
c.692T>G (p.Phe231Cys)
c.332T>G (p.Phe111Cys)
c.776T>G (p.Phe259Cys)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673811A>TCA397837040TP53c.809T>A (p.Phe270Tyr)
c.413T>A (p.Phe138Tyr)
c.530T>A (p.Phe177Tyr)
c.788T>A (p.Phe263Tyr)
c.782+370T>A (n.782+370T>A)
c.692T>A (p.Phe231Tyr)
c.332T>A (p.Phe111Tyr)
c.776T>A (p.Phe259Tyr)
dbSNP COSMIC
17g.7673811A>GCA16603016TP53c.809T>C (p.Phe270Ser)
c.413T>C (p.Phe138Ser)
c.530T>C (p.Phe177Ser)
c.788T>C (p.Phe263Ser)
c.782+370T>C (n.782+370T>C)
c.692T>C (p.Phe231Ser)
c.332T>C (p.Phe111Ser)
c.776T>C (p.Phe259Ser)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched