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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
13
g.32339641T>G
CA387784772
BRCA2
c.5286T>G (p.Tyr1762Ter)
c.4917T>G (p.Tyr1639Ter)
n.5286T>G
ClinVar
dbSNP
gnomAD v3
gnomAD v4
13
g.32339641T>A
CA021955
BRCA2
c.5286T>A (p.Tyr1762Ter)
c.4917T>A (p.Tyr1639Ter)
n.5286T>A
ClinVar
dbSNP
gnomAD v4
Number of alleles fetched
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