Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7674191C>TCA000406TP53c.772G>A (p.Glu258Lys)
c.376G>A (p.Glu126Lys)
c.493G>A (p.Glu165Lys)
c.751G>A (p.Glu251Lys)
c.655G>A (p.Glu219Lys)
c.295G>A (p.Glu99Lys)
c.739G>A (p.Glu247Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17g.7674191C>GCA397837688TP53c.772G>C (p.Glu258Gln)
c.376G>C (p.Glu126Gln)
c.493G>C (p.Glu165Gln)
c.751G>C (p.Glu251Gln)
c.655G>C (p.Glu219Gln)
c.295G>C (p.Glu99Gln)
c.739G>C (p.Glu247Gln)
dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674191C>ACA397837685TP53c.772G>T (p.Glu258Ter)
c.376G>T (p.Glu126Ter)
c.493G>T (p.Glu165Ter)
c.751G>T (p.Glu251Ter)
c.655G>T (p.Glu219Ter)
c.295G>T (p.Glu99Ter)
c.739G>T (p.Glu247Ter)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched