Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7676037A>TCA16603051TP53c.332T>A (p.Leu111Gln)
c.-21-801T>A (n.-21-801T>A)
c.96+345T>A (n.96+345T>A)
n.588T>A
c.215T>A (p.Leu72Gln)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676037A>GCA16603049TP53c.332T>C (p.Leu111Pro)
c.-21-801T>C (n.-21-801T>C)
c.96+345T>C (n.96+345T>C)
n.588T>C
c.215T>C (p.Leu72Pro)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676037A>CCA16603050TP53c.332T>G (p.Leu111Arg)
c.-21-801T>G (n.-21-801T>G)
c.96+345T>G (n.96+345T>G)
n.588T>G
c.215T>G (p.Leu72Arg)
ClinVar dbSNP

Number of alleles fetched