ClinVar Miner

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

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Total variants: 76
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HGVS dbSNP
NM_144997.7(FLCN):c.*5T>C rs1555606300
NM_144997.7(FLCN):c.1021C>T (p.Arg341Trp) rs770396757
NM_144997.7(FLCN):c.1048C>T (p.Arg350Trp) rs1261069493
NM_144997.7(FLCN):c.1049G>A (p.Arg350Gln) rs190786280
NM_144997.7(FLCN):c.1084C>T (p.Arg362Cys) rs557336321
NM_144997.7(FLCN):c.1085G>T (p.Arg362Leu) rs559055296
NM_144997.7(FLCN):c.1087A>T (p.Met363Leu) rs1313891453
NM_144997.7(FLCN):c.1100A>G (p.His367Arg) rs1555607981
NM_144997.7(FLCN):c.1133G>A (p.Ser378Asn) rs769489773
NM_144997.7(FLCN):c.116C>G (p.Pro39Arg) rs1197656765
NM_144997.7(FLCN):c.1171C>T (p.Leu391Phe) rs1555607942
NM_144997.7(FLCN):c.1175G>A (p.Arg392Gln) rs570066243
NM_144997.7(FLCN):c.1270G>A (p.Val424Met) rs1264775833
NM_144997.7(FLCN):c.1274A>G (p.Gln425Arg) rs786203348
NM_144997.7(FLCN):c.1279C>A (p.Pro427Thr) rs773986076
NM_144997.7(FLCN):c.1283C>A (p.Pro428His) rs199889477
NM_144997.7(FLCN):c.1283C>G (p.Pro428Arg) rs199889477
NM_144997.7(FLCN):c.1283C>T (p.Pro428Leu) rs199889477
NM_144997.7(FLCN):c.1285C>G (p.His429Asp) rs375082054
NM_144997.7(FLCN):c.1285C>T (p.His429Tyr) rs375082054
NM_144997.7(FLCN):c.1330G>A (p.Ala444Thr) rs876660342
NM_144997.7(FLCN):c.134C>G (p.Ala45Gly) rs556510460
NM_144997.7(FLCN):c.134C>T (p.Ala45Val) rs556510460
NM_144997.7(FLCN):c.1358G>A (p.Gly453Glu) rs1555607217
NM_144997.7(FLCN):c.1364A>G (p.Glu455Gly) rs199786696
NM_144997.7(FLCN):c.1387T>C (p.Tyr463His) rs770077517
NM_144997.7(FLCN):c.139G>C (p.Glu47Gln) rs369115472
NM_144997.7(FLCN):c.1428C>G (p.Asp476Glu) rs756944795
NM_144997.7(FLCN):c.1432+5G>C rs786203179
NM_144997.7(FLCN):c.1433-5C>A rs781046590
NM_144997.7(FLCN):c.1434G>A (p.Val478=) rs1131690834
NM_144997.7(FLCN):c.1463C>T (p.Ala488Val) rs200660337
NM_144997.7(FLCN):c.1513G>A (p.Val505Ile) rs376715412
NM_144997.7(FLCN):c.1539-5T>G rs876658649
NM_144997.7(FLCN):c.1543G>A (p.Val515Met) rs1415483886
NM_144997.7(FLCN):c.1580G>A (p.Arg527Gln) rs777826268
NM_144997.7(FLCN):c.1593_1594CA[2] (p.Gln533fs) rs876660810
NM_144997.7(FLCN):c.1635C>G (p.Asp545Glu) rs760329266
NM_144997.7(FLCN):c.1637A>G (p.Asn546Ser) rs775149348
NM_144997.7(FLCN):c.1644G>C (p.Lys548Asn) rs771847652
NM_144997.7(FLCN):c.164A>G (p.Asn55Ser) rs876660119
NM_144997.7(FLCN):c.1657T>C (p.Trp553Arg) rs1131690833
NM_144997.7(FLCN):c.1685A>G (p.Lys562Arg) rs749359334
NM_144997.7(FLCN):c.1690C>T (p.His564Tyr) rs1555606350
NM_144997.7(FLCN):c.1702A>G (p.Thr568Ala) rs748337450
NM_144997.7(FLCN):c.1709G>A (p.Arg570His) rs201056799
NM_144997.7(FLCN):c.205G>A (p.Val69Ile) rs567617762
NM_144997.7(FLCN):c.208G>A (p.Glu70Lys) rs554247745
NM_144997.7(FLCN):c.249+4A>G rs753648691
NM_144997.7(FLCN):c.256C>T (p.Arg86Trp) rs1327627870
NM_144997.7(FLCN):c.278C>T (p.Pro93Leu) rs766548696
NM_144997.7(FLCN):c.302A>C (p.Glu101Ala) rs958255980
NM_144997.7(FLCN):c.304A>T (p.Thr102Ser) rs1555610938
NM_144997.7(FLCN):c.346C>A (p.Gln116Lys) rs398124536
NM_144997.7(FLCN):c.379C>T (p.Arg127Trp) rs1274919531
NM_144997.7(FLCN):c.396+4A>G rs370353839
NM_144997.7(FLCN):c.421A>G (p.Ile141Val) rs375921200
NM_144997.7(FLCN):c.429C>G (p.Phe143Leu) rs773792624
NM_144997.7(FLCN):c.461A>T (p.His154Leu) rs1555610310
NM_144997.7(FLCN):c.59T>A (p.Phe20Tyr) rs1555611550
NM_144997.7(FLCN):c.604G>A (p.Gly202Ser) rs774491699
NM_144997.7(FLCN):c.610G>A (p.Ala204Thr) rs1456509027
NM_144997.7(FLCN):c.633G>C (p.Glu211Asp) rs876659927
NM_144997.7(FLCN):c.65C>T (p.Thr22Met) rs768734584
NM_144997.7(FLCN):c.673G>A (p.Ala225Thr) rs769250170
NM_144997.7(FLCN):c.707A>G (p.Asn236Ser) rs1194767470
NM_144997.7(FLCN):c.716G>A (p.Arg239His) rs753948488
NM_144997.7(FLCN):c.748C>A (p.Leu250Met) rs898441209
NM_144997.7(FLCN):c.766A>T (p.Thr256Ser) rs876658799
NM_144997.7(FLCN):c.779+5C>T rs745645385
NM_144997.7(FLCN):c.789G>C (p.Lys263Asn) rs1483962771
NM_144997.7(FLCN):c.844A>T (p.Thr282Ser) rs876658621
NM_144997.7(FLCN):c.872A>G (p.Asp291Gly) rs1201672985
NM_144997.7(FLCN):c.931C>T (p.Pro311Ser) rs140246224
NM_144997.7(FLCN):c.955G>C (p.Gly319Arg) rs753491072
NM_144997.7(FLCN):c.97G>T (p.Asp33Tyr) rs386833401

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