Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.32339121delCA020807BRCA2c.4766del (p.Pro1589GlnfsTer28)
c.4397del (p.Pro1466GlnfsTer28)
n.4766del
 ClinVar dbSNP
13g.32339121dupCA2697551760BRCA2c.4766dup (p.Cys1591ValfsTer2)
c.4397dup (p.Cys1468ValfsTer2)
n.4766dup
 ClinVar dbSNP

Number of alleles fetched