Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7676044A>CCA16608667TP53c.325T>G (p.Phe109Val)
c.-21-808T>G (n.-21-808T>G)
c.96+338T>G (n.96+338T>G)
n.581T>G
c.208T>G (p.Phe70Val)
ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676044A>TCA397844614TP53c.325T>A (p.Phe109Ile)
c.-21-808T>A (n.-21-808T>A)
c.96+338T>A (n.96+338T>A)
n.581T>A
c.208T>A (p.Phe70Ile)
ClinVar dbSNP
17g.7676044A=CA2245933360TP53c.325T= (p.Phe109=)
c.-21-808T= (n.-21-808T=)
c.96+338T= (n.96+338T=)
n.581T=
c.208T= (p.Phe70=)
dbSNP

Number of alleles fetched