Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.32356514G>ACA025130BRCA2c.7522G>A (p.Gly2508Ser)
c.7153G>A (p.Gly2385Ser)
c.87G>A
n.7522G>A
c.7426G>A (p.Gly2476Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32356514G>CCA387743535BRCA2c.7522G>C (p.Gly2508Arg)
c.7153G>C (p.Gly2385Arg)
c.87G>C
n.7522G>C
c.7426G>C (p.Gly2476Arg)
ClinVar dbSNP
13g.32356514G>TCA387743536BRCA2c.7522G>T (p.Gly2508Cys)
c.7153G>T (p.Gly2385Cys)
c.87G>T
n.7522G>T
c.7426G>T (p.Gly2476Cys)
dbSNP

Number of alleles fetched