Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7673791A>CCA397836909TP53c.829T>G (p.Cys277Gly)
c.433T>G (p.Cys145Gly)
c.550T>G (p.Cys184Gly)
c.808T>G (p.Cys270Gly)
c.782+390T>G (n.782+390T>G)
c.712T>G (p.Cys238Gly)
c.352T>G (p.Cys118Gly)
c.796T>G (p.Cys266Gly)
dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673791A>TCA397836911TP53c.829T>A (p.Cys277Ser)
c.433T>A (p.Cys145Ser)
c.550T>A (p.Cys184Ser)
c.808T>A (p.Cys270Ser)
c.782+390T>A (n.782+390T>A)
c.712T>A (p.Cys238Ser)
c.352T>A (p.Cys118Ser)
c.796T>A (p.Cys266Ser)
dbSNP
17g.7673791A>GCA16620617TP53c.829T>C (p.Cys277Arg)
c.433T>C (p.Cys145Arg)
c.550T>C (p.Cys184Arg)
c.808T>C (p.Cys270Arg)
c.782+390T>C (n.782+390T>C)
c.712T>C (p.Cys238Arg)
c.352T>C (p.Cys118Arg)
c.796T>C (p.Cys266Arg)
ClinVar dbSNP gnomAD v4 COSMIC

Number of alleles fetched