Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.32340524G>TCA023712BRCA2c.6169G>T (p.Gly2057Ter)
c.5800G>T (p.Gly1934Ter)
n.6169G>T
 ClinVar dbSNP
13g.32340524G>ACA387788354BRCA2c.6169G>A (p.Gly2057Arg)
c.5800G>A (p.Gly1934Arg)
n.6169G>A
 ClinVar dbSNP

Number of alleles fetched