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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
13
g.32336381del
CA014155
BRCA2
c.2026del (p.Cys676ValfsTer6)
c.1657del (p.Cys553ValfsTer6)
n.2026del
ClinVar
dbSNP
13
g.32336381T=
CA2082748768
BRCA2
c.2026T= (p.Cys676=)
c.1657T= (p.Cys553=)
n.2026T=
dbSNP
dbSNP
Number of alleles fetched
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