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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
13
g.32336781T>G
CA015222
BRCA2
c.2426T>G (p.Leu809Ter)
c.2057T>G (p.Leu686Ter)
n.2426T>G
ClinVar
dbSNP
13
g.32336781T=
CA2082808509
BRCA2
c.2426T= (p.Leu809=)
c.2057T= (p.Leu686=)
n.2426T=
dbSNP
Number of alleles fetched
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