Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7673767C>GCA397836740TP53c.853G>C (p.Glu285Gln)
c.457G>C (p.Glu153Gln)
c.574G>C (p.Glu192Gln)
c.832G>C (p.Glu278Gln)
c.782+414G>C (n.782+414G>C)
c.736G>C (p.Glu246Gln)
c.376G>C (p.Glu126Gln)
c.820G>C (p.Glu274Gln)
ClinVar dbSNP COSMIC
17g.7673767C>ACA397836737TP53c.853G>T (p.Glu285Ter)
c.457G>T (p.Glu153Ter)
c.574G>T (p.Glu192Ter)
c.832G>T (p.Glu278Ter)
c.782+414G>T (n.782+414G>T)
c.736G>T (p.Glu246Ter)
c.376G>T (p.Glu126Ter)
c.820G>T (p.Glu274Ter)
dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673767C>TCA16620615TP53c.853G>A (p.Glu285Lys)
c.457G>A (p.Glu153Lys)
c.574G>A (p.Glu192Lys)
c.832G>A (p.Glu278Lys)
c.782+414G>A (n.782+414G>A)
c.736G>A (p.Glu246Lys)
c.376G>A (p.Glu126Lys)
c.820G>A (p.Glu274Lys)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched