Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7673740C>TCA397836516TP53c.880G>A (p.Glu294Lys)
c.484G>A (p.Glu162Lys)
c.601G>A (p.Glu201Lys)
c.859G>A (p.Glu287Lys)
c.782+441G>A (n.782+441G>A)
c.763G>A (p.Glu255Lys)
c.403G>A (p.Glu135Lys)
c.847G>A (p.Glu283Lys)
ClinVar dbSNP gnomAD v4 COSMIC
17g.7673740C>ACA16608665TP53c.880G>T (p.Glu294Ter)
c.484G>T (p.Glu162Ter)
c.601G>T (p.Glu201Ter)
c.859G>T (p.Glu287Ter)
c.782+441G>T (n.782+441G>T)
c.763G>T (p.Glu255Ter)
c.403G>T (p.Glu135Ter)
c.847G>T (p.Glu283Ter)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673740C>GCA397836519TP53c.880G>C (p.Glu294Gln)
c.484G>C (p.Glu162Gln)
c.601G>C (p.Glu201Gln)
c.859G>C (p.Glu287Gln)
c.782+441G>C (n.782+441G>C)
c.763G>C (p.Glu255Gln)
c.403G>C (p.Glu135Gln)
c.847G>C (p.Glu283Gln)
dbSNP COSMIC

Number of alleles fetched