Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7676264C>ACA000025TP53c.105G>T (p.Leu35Phe)
n.105G>T (p.Leu35Phe)
n.361G>T
c.-21-1028G>T (p.=)
c.96+118G>T (p.=)
c.-13G>T (p.=)
ClinVar dbSNP COSMIC
17g.7676264C>GCA000024TP53c.105G>C (p.Leu35Phe)
n.105G>C (p.Leu35Phe)
n.361G>C
c.-21-1028G>C (p.=)
c.96+118G>C (p.=)
c.-13G>C (p.=)
ClinVar dbSNP gnomAD COSMIC

Number of alleles fetched