ClinVar Miner

List of variants reported as uncertain significance for Familial cancer of breast; Breast-ovarian cancer, familial 1; Pancreatic cancer 4; FANCONI ANEMIA, COMPLEMENTATION GROUP S by Fulgent Genetics,Fulgent Genetics

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Total variants: 20
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NM_007294.3(BRCA1):c.4096+3A>G rs80358015
NM_007294.4(BRCA1):c.1381T>C (p.Phe461Leu) rs62625300
NM_007294.4(BRCA1):c.1745C>T (p.Thr582Met) rs786202386
NM_007294.4(BRCA1):c.2050C>T (p.Pro684Ser) rs397508934
NM_007294.4(BRCA1):c.20G>A (p.Arg7His) rs144792613
NM_007294.4(BRCA1):c.2663A>C (p.His888Pro) rs876658843
NM_007294.4(BRCA1):c.3080G>C (p.Ser1027Thr) rs80357386
NM_007294.4(BRCA1):c.3104T>C (p.Val1035Ala) rs1555588389
NM_007294.4(BRCA1):c.3403C>G (p.Gln1135Glu) rs80357136
NM_007294.4(BRCA1):c.3424G>C (p.Ala1142Pro) rs80357101
NM_007294.4(BRCA1):c.3555G>T (p.Glu1185Asp) rs587779368
NM_007294.4(BRCA1):c.3649T>C (p.Ser1217Pro) rs273900712
NM_007294.4(BRCA1):c.4231A>G (p.Met1411Val) rs587781768
NM_007294.4(BRCA1):c.446A>C (p.Glu149Ala) rs397507233
NM_007294.4(BRCA1):c.4654T>C (p.Tyr1552His) rs1265352633
NM_007294.4(BRCA1):c.5056C>T (p.His1686Tyr) rs1555579648
NM_007294.4(BRCA1):c.5068A>C (p.Lys1690Gln) rs397507239
NM_007294.4(BRCA1):c.527C>T (p.Thr176Met) rs587782747
NM_007294.4(BRCA1):c.5470A>G (p.Ile1824Val) rs587782026
NM_007294.4(BRCA1):c.851A>G (p.Gln284Arg) rs80357039

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