Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7673777G>CCA10590135TP53c.843C>G (p.Asp281Glu)
c.447C>G (p.Asp149Glu)
c.564C>G (p.Asp188Glu)
c.822C>G (p.Asp274Glu)
c.782+404C>G (n.782+404C>G)
c.726C>G (p.Asp242Glu)
c.366C>G (p.Asp122Glu)
c.810C>G (p.Asp270Glu)
ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC
17g.7673777G>TCA16615937TP53c.843C>A (p.Asp281Glu)
c.447C>A (p.Asp149Glu)
c.564C>A (p.Asp188Glu)
c.822C>A (p.Asp274Glu)
c.782+404C>A (n.782+404C>A)
c.726C>A (p.Asp242Glu)
c.366C>A (p.Asp122Glu)
c.810C>A (p.Asp270Glu)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673777G>ACA497715999TP53c.843C>T (p.Asp281=)
c.447C>T (p.Asp149=)
c.564C>T (p.Asp188=)
c.822C>T (p.Asp274=)
c.782+404C>T (n.782+404C>T)
c.726C>T (p.Asp242=)
c.366C>T (p.Asp122=)
c.810C>T (p.Asp270=)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched