Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.32363259T>CCA025427BRCA2c.8057T>C (p.Leu2686Pro)
c.7688T>C (p.Leu2563Pro)
c.524T>C (p.Leu175Pro)
c.8065T>C (n.8065T>C)
c.622T>C
c.7961T>C (p.Leu2654Pro)
ClinVar dbSNP gnomAD v4
13g.32363259T>GCA387749102BRCA2c.8057T>G (p.Leu2686Arg)
c.7688T>G (p.Leu2563Arg)
c.524T>G (p.Leu175Arg)
c.8065T>G (n.8065T>G)
c.622T>G
c.7961T>G (p.Leu2654Arg)
ClinVar dbSNP
13g.32363259T>ACA387749100BRCA2c.8057T>A (p.Leu2686His)
c.7688T>A (p.Leu2563His)
c.524T>A (p.Leu175His)
c.8065T>A (n.8065T>A)
c.622T>A
c.7961T>A (p.Leu2654His)
dbSNP

Number of alleles fetched