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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
13
g.32337824G>T
CA018132
BRCA2
c.3469G>T (p.Glu1157Ter)
c.3100G>T (p.Glu1034Ter)
n.3469G>T
ClinVar
dbSNP
13
g.32337824G=
CA2082817545
BRCA2
c.3469G= (p.Glu1157=)
c.3100G= (p.Glu1034=)
n.3469G=
dbSNP
Number of alleles fetched
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