ClinVar Miner

List of variants in gene FLCN reported as uncertain significance by Ambry Genetics

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ClinVar version:
Total variants: 172
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HGVS dbSNP
NM_144997.7(FLCN):c.*5T>C rs1555606300
NM_144997.7(FLCN):c.1018C>T (p.Pro340Ser)
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.1066C>G (p.Leu356Val) rs757313788
NM_144997.7(FLCN):c.106G>C (p.Glu36Gln)
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.1102G>A (p.Val368Ile)
NM_144997.7(FLCN):c.1108A>G (p.Met370Val)
NM_144997.7(FLCN):c.1117C>A (p.Gln373Lys)
NM_144997.7(FLCN):c.1133G>A (p.Ser378Asn) rs769489773
NM_144997.7(FLCN):c.113G>T (p.Ser38Ile) rs139418842
NM_144997.7(FLCN):c.1160C>T (p.Ala387Val) rs1431737113
NM_144997.7(FLCN):c.1168G>A (p.Val390Ile)
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.1174C>T (p.Arg392Trp) rs1060502374
NM_144997.7(FLCN):c.1175G>A (p.Arg392Gln) rs570066243
NM_144997.7(FLCN):c.1198G>T (p.Val400Phe) rs148257120
NM_144997.7(FLCN):c.1199T>C (p.Val400Ala) rs760079073
NM_144997.7(FLCN):c.1202G>A (p.Arg401His)
NM_144997.7(FLCN):c.1216A>G (p.Ser406Gly) rs528541881
NM_144997.7(FLCN):c.1224G>T (p.Gln408His) rs774142829
NM_144997.7(FLCN):c.1241G>A (p.Arg414Gln)
NM_144997.7(FLCN):c.1247A>G (p.Asn416Ser)
NM_144997.7(FLCN):c.124G>C (p.Gly42Arg)
NM_144997.7(FLCN):c.125G>A (p.Gly42Asp) rs999239742
NM_144997.7(FLCN):c.1265C>T (p.Pro422Leu) rs565447853
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.1280C>T (p.Pro427Leu) rs766218250
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>A (p.His429Asn)
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.1288G>A (p.Val430Met)
NM_144997.7(FLCN):c.1298C>T (p.Ser433Leu) rs1060502372
NM_144997.7(FLCN):c.1315G>A (p.Val439Met)
NM_144997.7(FLCN):c.1330G>A (p.Ala444Thr) rs876660342
NM_144997.7(FLCN):c.1333G>T (p.Ala445Ser)
NM_144997.7(FLCN):c.1337G>A (p.Arg446His)
NM_144997.7(FLCN):c.134C>A (p.Ala45Glu)
NM_144997.7(FLCN):c.134C>T (p.Ala45Val) rs556510460
NM_144997.7(FLCN):c.1354G>T (p.Val452Leu)
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.1365G>T (p.Glu455Asp)
NM_144997.7(FLCN):c.1373A>G (p.Gln458Arg) rs150439088
NM_144997.7(FLCN):c.1376C>T (p.Ser459Phe) rs377468280
NM_144997.7(FLCN):c.1383C>G (p.Ser461Arg)
NM_144997.7(FLCN):c.1387T>C (p.Tyr463His) rs770077517
NM_144997.7(FLCN):c.1394T>C (p.Phe465Ser)
NM_144997.7(FLCN):c.139G>C (p.Glu47Gln) rs369115472
NM_144997.7(FLCN):c.1402A>G (p.Thr468Ala)
NM_144997.7(FLCN):c.1415C>T (p.Pro472Leu) rs1180118315
NM_144997.7(FLCN):c.1428C>G (p.Asp476Glu) rs756944795
NM_144997.7(FLCN):c.1430G>A (p.Arg477Gln) rs748878853
NM_144997.7(FLCN):c.1432+3G>T
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.1462G>A (p.Ala488Thr)
NM_144997.7(FLCN):c.1487C>G (p.Ser496Cys)
NM_144997.7(FLCN):c.1513G>A (p.Val505Ile) rs376715412
NM_144997.7(FLCN):c.1519C>T (p.Leu507Phe)
NM_144997.7(FLCN):c.1525G>A (p.Glu509Lys)
NM_144997.7(FLCN):c.1527G>T (p.Glu509Asp)
NM_144997.7(FLCN):c.1539-5T>G rs876658649
NM_144997.7(FLCN):c.1543G>A (p.Val515Met) rs1415483886
NM_144997.7(FLCN):c.1565C>T (p.Thr522Ile)
NM_144997.7(FLCN):c.1579_1580insA (p.Arg527fs) rs753009073
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.1594A>C (p.Thr532Pro)
NM_144997.7(FLCN):c.1627G>A (p.Glu543Lys) rs776389684
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.1685A>G (p.Lys562Arg) rs749359334
NM_144997.7(FLCN):c.1689del (p.His564fs) rs1314645884
NM_144997.7(FLCN):c.1690C>T (p.His564Tyr) rs1555606350
NM_144997.7(FLCN):c.169C>T (p.Arg57Trp) rs746507528
NM_144997.7(FLCN):c.1702A>G (p.Thr568Ala) rs748337450
NM_144997.7(FLCN):c.1708C>T (p.Arg570Cys)
NM_144997.7(FLCN):c.1709G>A (p.Arg570His) rs201056799
NM_144997.7(FLCN):c.170G>A (p.Arg57Gln) rs749770193
NM_144997.7(FLCN):c.1733G>A (p.Arg578Gln)
NM_144997.7(FLCN):c.175C>T (p.Arg59Cys) rs778275358
NM_144997.7(FLCN):c.176G>A (p.Arg59His) rs374969279
NM_144997.7(FLCN):c.176G>T (p.Arg59Leu)
NM_144997.7(FLCN):c.197G>A (p.Gly66Glu) rs753787458
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.223G>A (p.Gly75Arg)
NM_144997.7(FLCN):c.249+4A>G rs753648691
NM_144997.7(FLCN):c.250-4A>G
NM_144997.7(FLCN):c.256C>T (p.Arg86Trp) rs1327627870
NM_144997.7(FLCN):c.257G>A (p.Arg86Gln) rs765550303
NM_144997.7(FLCN):c.268G>A (p.Ala90Thr)
NM_144997.7(FLCN):c.274C>T (p.His92Tyr) rs755107067
NM_144997.7(FLCN):c.278C>T (p.Pro93Leu) rs766548696
NM_144997.7(FLCN):c.284A>G (p.Tyr95Cys) rs1555610947
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.311T>C (p.Ile104Thr)
NM_144997.7(FLCN):c.326A>G (p.His109Arg)
NM_144997.7(FLCN):c.341A>G (p.His114Arg)
NM_144997.7(FLCN):c.379C>T (p.Arg127Trp) rs1274919531
NM_144997.7(FLCN):c.396G>A (p.Glu132=)
NM_144997.7(FLCN):c.409C>T (p.Arg137Cys)
NM_144997.7(FLCN):c.410G>A (p.Arg137His) rs1289872207
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.43G>A (p.Gly15Ser)
NM_144997.7(FLCN):c.451G>A (p.Val151Met) rs147164515
NM_144997.7(FLCN):c.461A>T (p.His154Leu) rs1555610310
NM_144997.7(FLCN):c.482G>A (p.Ser161Asn)
NM_144997.7(FLCN):c.498C>G (p.Phe166Leu) rs1040675580
NM_144997.7(FLCN):c.501G>C (p.Gln167His) rs772775816
NM_144997.7(FLCN):c.517A>G (p.Ile173Val)
NM_144997.7(FLCN):c.527T>C (p.Met176Thr)
NM_144997.7(FLCN):c.535C>T (p.Arg179Trp) rs774358971
NM_144997.7(FLCN):c.586A>G (p.Ile196Val) rs201078144
NM_144997.7(FLCN):c.598C>T (p.Leu200Phe)
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.611C>T (p.Ala204Val)
NM_144997.7(FLCN):c.614T>C (p.Leu205Pro) rs878855219
NM_144997.7(FLCN):c.62G>A (p.Cys21Tyr)
NM_144997.7(FLCN):c.633G>C (p.Glu211Asp) rs876659927
NM_144997.7(FLCN):c.634C>A (p.Gln212Lys) rs558699420
NM_144997.7(FLCN):c.65C>T (p.Thr22Met) rs768734584
NM_144997.7(FLCN):c.669_671delinsGCACAGCGTGCTCAG (p.Asn223_Thr224delinsLysHisSerValLeuArg)
NM_144997.7(FLCN):c.673G>A (p.Ala225Thr) rs769250170
NM_144997.7(FLCN):c.703G>A (p.Gly235Ser)
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.721C>G (p.Leu241Val)
NM_144997.7(FLCN):c.734C>A (p.Thr245Lys)
NM_144997.7(FLCN):c.738T>G (p.Ser246Arg)
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.802C>T (p.Arg268Trp)
NM_144997.7(FLCN):c.826G>A (p.Gly276Ser)
NM_144997.7(FLCN):c.82C>T (p.Pro28Ser) rs749758787
NM_144997.7(FLCN):c.832C>G (p.Pro278Ala)
NM_144997.7(FLCN):c.83C>G (p.Pro28Arg) rs780588085
NM_144997.7(FLCN):c.844A>T (p.Thr282Ser) rs876658621
NM_144997.7(FLCN):c.845C>T (p.Thr282Ile)
NM_144997.7(FLCN):c.872-3C>T rs1555608676
NM_144997.7(FLCN):c.872A>G (p.Asp291Gly) rs1201672985
NM_144997.7(FLCN):c.873T>G (p.Asp291Glu)
NM_144997.7(FLCN):c.931C>T (p.Pro311Ser) rs140246224
NM_144997.7(FLCN):c.952G>A (p.Glu318Lys) rs756787389
NM_144997.7(FLCN):c.955G>C (p.Gly319Arg) rs753491072
NM_144997.7(FLCN):c.95G>A (p.Gly32Glu) rs587778366
NM_144997.7(FLCN):c.971A>G (p.Gln324Arg)
NM_144997.7(FLCN):c.97G>C (p.Asp33His) rs386833401
NM_144997.7(FLCN):c.97G>T (p.Asp33Tyr) rs386833401
NM_144997.7(FLCN):c.992C>T (p.Ser331Phe)
NM_144997.7(FLCN):c.99T>A (p.Asp33Glu)

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