Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7674886A>TCA397839990TP53c.645T>A (p.Ser215Arg)
c.249T>A (p.Ser83Arg)
c.366T>A (p.Ser122Arg)
c.624T>A (p.Ser208Arg)
n.901T>A
n.67+167T>A
c.528T>A (p.Ser176Arg)
c.168T>A (p.Ser56Arg)
c.612T>A (p.Ser204Arg)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674886A>GCA497925298TP53c.645T>C (p.Ser215=)
c.249T>C (p.Ser83=)
c.366T>C (p.Ser122=)
c.624T>C (p.Ser208=)
n.901T>C
n.67+167T>C
c.528T>C (p.Ser176=)
c.168T>C (p.Ser56=)
c.612T>C (p.Ser204=)
ClinVar dbSNP COSMIC
17g.7674886A>CCA16603076TP53c.645T>G (p.Ser215Arg)
c.249T>G (p.Ser83Arg)
c.366T>G (p.Ser122Arg)
c.624T>G (p.Ser208Arg)
n.901T>G
n.67+167T>G
c.528T>G (p.Ser176Arg)
c.168T>G (p.Ser56Arg)
c.612T>G (p.Ser204Arg)
ClinVar dbSNP gnomAD v4 COSMIC COSMIC

Number of alleles fetched