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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
13
g.32337039del
CA016067
BRCA2
c.2684del (p.Ala895ValfsTer9)
c.2315del (p.Ala772ValfsTer9)
n.2684del
ClinVar
dbSNP
13
g.32337039C=
CA3200672639
BRCA2
c.2684C= (p.Ala895=)
c.2315C= (p.Ala772=)
n.2684C=
dbSNP
dbSNP
Number of alleles fetched
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