Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7674884A>TCA16603086TP53c.647T>A (p.Val216Glu)
c.251T>A (p.Val84Glu)
c.368T>A (p.Val123Glu)
c.626T>A (p.Val209Glu)
n.903T>A
n.67+169T>A
c.530T>A (p.Val177Glu)
c.170T>A (p.Val57Glu)
c.614T>A (p.Val205Glu)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674884A>GCA397839975TP53c.647T>C (p.Val216Ala)
c.251T>C (p.Val84Ala)
c.368T>C (p.Val123Ala)
c.626T>C (p.Val209Ala)
n.903T>C
n.67+169T>C
c.530T>C (p.Val177Ala)
c.170T>C (p.Val57Ala)
c.614T>C (p.Val205Ala)
dbSNP COSMIC
17g.7674884A>CCA16603085TP53c.647T>G (p.Val216Gly)
c.251T>G (p.Val84Gly)
c.368T>G (p.Val123Gly)
c.626T>G (p.Val209Gly)
n.903T>G
n.67+169T>G
c.530T>G (p.Val177Gly)
c.170T>G (p.Val57Gly)
c.614T>G (p.Val205Gly)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched