Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7675094A>TCA16603083TP53c.518T>A (p.Val173Glu)
c.122T>A (p.Val41Glu)
c.239T>A (p.Val80Glu)
c.497T>A (p.Val166Glu)
n.774T>A
n.26T>A
c.401T>A (p.Val134Glu)
c.41T>A (p.Val14Glu)
c.485T>A (p.Val162Glu)
ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7675094A>GCA16602486TP53c.518T>C (p.Val173Ala)
c.122T>C (p.Val41Ala)
c.239T>C (p.Val80Ala)
c.497T>C (p.Val166Ala)
n.774T>C
n.26T>C
c.401T>C (p.Val134Ala)
c.41T>C (p.Val14Ala)
c.485T>C (p.Val162Ala)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7675094A>CCA16602485TP53c.518T>G (p.Val173Gly)
c.122T>G (p.Val41Gly)
c.239T>G (p.Val80Gly)
c.497T>G (p.Val166Gly)
n.774T>G
n.26T>G
c.401T>G (p.Val134Gly)
c.41T>G (p.Val14Gly)
c.485T>G (p.Val162Gly)
ClinVar dbSNP gnomAD v4

Number of alleles fetched