Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.32363190A>GCA387748557BRCA2c.7988A>G (p.Glu2663Gly)
c.7619A>G (p.Glu2540Gly)
c.455A>G (p.Glu152Gly)
c.7996A>G (n.7996A>G)
c.553A>G
c.7892A>G (p.Glu2631Gly)
ClinVar dbSNP
13g.32363190A>TCA025385BRCA2c.7988A>T (p.Glu2663Val)
c.7619A>T (p.Glu2540Val)
c.455A>T (p.Glu152Val)
c.7996A>T (n.7996A>T)
c.553A>T
c.7892A>T (p.Glu2631Val)
ClinVar dbSNP gnomAD v4

Number of alleles fetched