ClinVar Miner

List of variants in gene FH reported as uncertain significance for Hereditary cancer-predisposing syndrome

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Total variants: 70
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HGVS dbSNP
NM_000143.3(FH):c.1013T>C (p.Ile338Thr) rs201975537
NM_000143.3(FH):c.1025T>C (p.Ile342Thr) rs201383596
NM_000143.3(FH):c.1045C>G (p.Pro349Ala) rs1254962869
NM_000143.3(FH):c.1046C>G (p.Pro349Arg) rs1553341017
NM_000143.3(FH):c.1049G>A (p.Arg350Gln) rs749316923
NM_000143.3(FH):c.1138A>G (p.Met380Val) rs587778362
NM_000143.3(FH):c.1154C>A (p.Ala385Asp) rs727503926
NM_000143.3(FH):c.1163T>C (p.Met388Thr) rs876660830
NM_000143.3(FH):c.1198A>G (p.Asn400Asp) rs1131691247
NM_000143.3(FH):c.1199A>G (p.Asn400Ser) rs764430466
NM_000143.3(FH):c.1216A>G (p.Asn406Asp) rs876659362
NM_000143.3(FH):c.1303G>A (p.Val435Met) rs147528200
NM_000143.3(FH):c.132+5G>A rs1060499627
NM_000143.3(FH):c.1366G>C (p.Val456Leu) rs200244096
NM_000143.3(FH):c.1389A>G (p.Ile463Met) rs876659472
NM_000143.3(FH):c.1391G>A (p.Gly464Glu) rs1131691250
NM_000143.3(FH):c.13C>T (p.Leu5Phe) rs1553342165
NM_000143.3(FH):c.1462G>A (p.Glu488Lys) rs201115573
NM_000143.3(FH):c.1472A>G (p.Tyr491Cys) rs773801940
NM_000143.3(FH):c.1480G>C (p.Ala494Pro) rs1553340508
NM_000143.3(FH):c.1506dup (p.Pro503fs) rs886041202
NM_000143.3(FH):c.1526C>T (p.Pro509Leu) rs1553340499
NM_000143.3(FH):c.154A>T (p.Ile52Leu) rs543844061
NM_000143.3(FH):c.190A>G (p.Asn64Asp) rs886046319
NM_000143.3(FH):c.194A>T (p.Asp65Val) rs145116688
NM_000143.3(FH):c.208G>A (p.Ala70Thr) rs587782207
NM_000143.3(FH):c.217G>A (p.Val73Met) rs201878591
NM_000143.3(FH):c.222A>T (p.Arg74Ser) rs146739519
NM_000143.3(FH):c.259C>T (p.Arg87Cys) rs139642944
NM_000143.3(FH):c.26C>G (p.Ala9Gly) rs766915154
NM_000143.3(FH):c.2T>G (p.Met1Arg) rs201261794
NM_000143.3(FH):c.305C>T (p.Ala102Val) rs61753295
NM_000143.3(FH):c.346A>T (p.Ile116Phe) rs201532589
NM_000143.3(FH):c.358A>G (p.Ile120Val) rs199641124
NM_000143.3(FH):c.37C>T (p.Pro13Ser) rs587778360
NM_000143.3(FH):c.404A>G (p.His135Arg) rs786202833
NM_000143.3(FH):c.40dup (p.Leu14fs) rs1060500900
NM_000143.3(FH):c.412C>G (p.Leu138Val) rs1466082062
NM_000143.3(FH):c.450T>A (p.Asn150Lys) rs1131691242
NM_000143.3(FH):c.50C>T (p.Ala17Val) rs111548093
NM_000143.3(FH):c.520C>A (p.Pro174Thr) rs1553341598
NM_000143.3(FH):c.535G>A (p.Asp179Asn) rs1553341588
NM_000143.3(FH):c.556A>T (p.Ser186Cys) rs1131691233
NM_000143.3(FH):c.580G>A (p.Ala194Thr) rs587782215
NM_000143.3(FH):c.586C>T (p.His196Tyr) rs1553341363
NM_000143.3(FH):c.587A>G (p.His196Arg) rs763601207
NM_000143.3(FH):c.593C>G (p.Ala198Gly) rs1414507017
NM_000143.3(FH):c.62C>G (p.Ala21Gly) rs1131691251
NM_000143.3(FH):c.648T>A (p.Asp216Glu) rs199536615
NM_000143.3(FH):c.692T>C (p.Ile231Thr) rs1335587342
NM_000143.3(FH):c.6C>G (p.Tyr2Ter) rs199971078
NM_000143.3(FH):c.700A>G (p.Thr234Ala) rs372505976
NM_000143.3(FH):c.702T>G (p.Thr234=) rs201083387
NM_000143.3(FH):c.722C>T (p.Pro241Leu) rs1553341319
NM_000143.3(FH):c.773C>T (p.Ala258Val) rs1553341166
NM_000143.3(FH):c.782G>T (p.Arg261Ile) rs61736558
NM_000143.3(FH):c.785T>G (p.Ile262Arg) rs786203177
NM_000143.3(FH):c.7C>G (p.Arg3Gly) rs202166344
NM_000143.3(FH):c.805A>G (p.Ile269Val) rs377015873
NM_000143.3(FH):c.809A>G (p.Tyr270Cys) rs202060616
NM_000143.3(FH):c.814C>A (p.Leu272Ile) rs779019570
NM_000143.3(FH):c.817G>A (p.Ala273Thr) rs772190176
NM_000143.3(FH):c.883G>A (p.Ala295Thr) rs145843819
NM_000143.3(FH):c.908T>C (p.Leu303Ser) rs201502246
NM_000143.3(FH):c.917T>C (p.Val306Ala) rs147991516
NM_000143.3(FH):c.925C>T (p.Pro309Ser) rs368849989
NM_000143.3(FH):c.92C>T (p.Ala31Val) rs876659347
NM_000143.3(FH):c.94G>T (p.Ala32Ser) rs1371664717
NM_000143.3(FH):c.986A>G (p.Asn329Ser) rs768483509
NM_000143.3(FH):c.98T>G (p.Val33Gly) rs1319755767

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