ClinVar Miner

List of variants reported as uncertain significance for Breast-ovarian cancer, familial 2 by Fulgent Genetics,Fulgent Genetics

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Total variants: 10
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HGVS dbSNP
NM_000059.3(BRCA2):c.1568A>G (p.His523Arg) rs80358443
NM_000059.3(BRCA2):c.2157T>A (p.Asn719Lys) rs1064797382
NM_000059.3(BRCA2):c.2918C>T (p.Ser973Leu) rs397507296
NM_000059.3(BRCA2):c.4594G>T (p.Val1532Phe) rs80358693
NM_000059.3(BRCA2):c.551T>C (p.Leu184Pro) rs80358775
NM_000059.3(BRCA2):c.5552T>G (p.Ile1851Ser) rs80358776
NM_000059.3(BRCA2):c.6263C>T (p.Thr2088Ile) rs767567428
NM_000059.3(BRCA2):c.7463G>A (p.Arg2488Lys) rs80358968
NM_000059.3(BRCA2):c.7628A>G (p.Tyr2543Cys) rs431825354
NM_000059.3(BRCA2):c.9292T>C (p.Tyr3098His) rs41293521

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