ClinVar Miner

List of variants in gene FLCN studied for not provided

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Total variants: 113
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HGVS dbSNP
NM_144997.5(FLCN):c.1021delC (p.Arg341Glyfs) rs1060502368
NM_144997.5(FLCN):c.1060C>T (p.Gln354Ter) rs398124523
NM_144997.5(FLCN):c.1062+2T>C rs886039370
NM_144997.5(FLCN):c.1062+2T>G rs886039370
NM_144997.5(FLCN):c.1117C>T (p.Gln373Ter) rs398124524
NM_144997.5(FLCN):c.113delG (p.Ser38Ilefs) rs878855212
NM_144997.5(FLCN):c.1177-2A>G rs1057520528
NM_144997.5(FLCN):c.1177-5_1177-3delCTC rs767671406
NM_144997.5(FLCN):c.1179delC (p.Met394Cysfs) rs398124525
NM_144997.5(FLCN):c.1198G>T (p.Val400Phe) rs148257120
NM_144997.5(FLCN):c.1203dupC (p.Ile402Hisfs) rs398124526
NM_144997.5(FLCN):c.1219delA (p.Ser407Alafs) rs878855213
NM_144997.5(FLCN):c.1227C>A (p.Tyr409Ter) rs561236067
NM_144997.5(FLCN):c.1227C>G (p.Tyr409Ter) rs561236067
NM_144997.5(FLCN):c.1245C>A (p.Cys415Ter) rs748148728
NM_144997.5(FLCN):c.1252delC (p.Leu418Trpfs) rs864622651
NM_144997.5(FLCN):c.1253T>C (p.Leu418Pro) rs879255674
NM_144997.5(FLCN):c.127G>T (p.Glu43Ter) rs1555611494
NM_144997.5(FLCN):c.1285_1286insG (p.His429Argfs) rs1555607651
NM_144997.5(FLCN):c.1285delC (p.His429Thrfs) rs80338682
NM_144997.5(FLCN):c.1285dupC (p.His429Profs) rs80338682
NM_144997.5(FLCN):c.1286dupA (p.His429Glnfs) rs879255675
NM_144997.5(FLCN):c.1300+2T>G rs1064793766
NM_144997.5(FLCN):c.1300G>T (p.Glu434Ter) rs1266098984
NM_144997.5(FLCN):c.1305delT (p.Phe435Leufs) rs398124527
NM_144997.5(FLCN):c.1318_1334dup17 (p.Leu449Glnfs) rs879255677
NM_144997.5(FLCN):c.1333G>A (p.Ala445Thr) rs41419545
NM_144997.5(FLCN):c.1379_1380delTC (p.Leu460Glnfs) rs1064793128
NM_144997.5(FLCN):c.1389C>G (p.Tyr463Ter) rs137852929
NM_144997.5(FLCN):c.1429C>T (p.Arg477Ter) rs879255678
NM_144997.5(FLCN):c.1430G>A (p.Arg477Gln) rs748878853
NM_144997.5(FLCN):c.1432+1G>A rs755959303
NM_144997.5(FLCN):c.1433-2A>G rs398124528
NM_144997.5(FLCN):c.1504C>T (p.Gln502Ter) rs886042033
NM_144997.5(FLCN):c.1522_1524delAAG (p.Lys508del) rs398124529
NM_144997.5(FLCN):c.1528_1530delGAG (p.Glu510del) rs879255681
NM_144997.5(FLCN):c.1532G>A (p.Trp511Ter) rs879255682
NM_144997.5(FLCN):c.1539-16_1539-12delTTTTG rs398124531
NM_144997.5(FLCN):c.1539-2A>G rs878855214
NM_144997.5(FLCN):c.1540A>T (p.Lys514Ter) rs886041478
NM_144997.5(FLCN):c.1578_1599del22 (p.Ser526Argfs) rs1057518043
NM_144997.5(FLCN):c.1579C>T (p.Arg527Ter) rs879255683
NM_144997.5(FLCN):c.1584delC (p.Glu530Argfs) rs1131690827
NM_144997.5(FLCN):c.158delA (p.Gln53Argfs) rs1131690825
NM_144997.5(FLCN):c.1597C>T (p.Gln533Ter) rs398124532
NM_144997.5(FLCN):c.1601delA (p.Lys534Serfs) rs886039371
NM_144997.5(FLCN):c.171dupG (p.Met58Aspfs) rs886041203
NM_144997.5(FLCN):c.189delC (p.Ala64Glnfs) rs876660611
NM_144997.5(FLCN):c.233delA (p.Lys78Serfs) rs1555611377
NM_144997.5(FLCN):c.235_238delTCGG (p.Ser79Thrfs) rs750146811
NM_144997.5(FLCN):c.241_242delAT (p.Met81Valfs) rs1057518147
NM_144997.5(FLCN):c.246C>T (p.Cys82=) rs150712346
NM_144997.5(FLCN):c.247G>A (p.Glu83Lys) rs757060348
NM_144997.5(FLCN):c.249+5G>A rs1064793127
NM_144997.5(FLCN):c.250-1G>A rs786202081
NM_144997.5(FLCN):c.250-2A>G rs398124533
NM_144997.5(FLCN):c.296delA (p.Asp99Valfs) rs398124534
NM_144997.5(FLCN):c.33C>A (p.Cys11Ter) rs754616167
NM_144997.5(FLCN):c.346C>T (p.Gln116Ter) rs398124536
NM_144997.5(FLCN):c.347dupA (p.Leu117Alafs) rs776896550
NM_144997.5(FLCN):c.429C>G (p.Phe143Leu) rs773792624
NM_144997.5(FLCN):c.469_471delTTC (p.Phe157del) rs786203218
NM_144997.5(FLCN):c.499C>T (p.Gln167Ter) rs587782069
NM_144997.5(FLCN):c.49delC (p.Arg17Alafs) rs758385503
NM_144997.5(FLCN):c.50G>C (p.Arg17Pro) rs398124537
NM_144997.5(FLCN):c.521_527delCCATCAT (p.Thr174Argfs) rs1085307478
NM_144997.5(FLCN):c.552C>A (p.Asn184Lys) rs143525924
NM_144997.5(FLCN):c.557G>A (p.Trp186Ter) rs876658409
NM_144997.5(FLCN):c.584delG (p.Gly195Glufs) rs878855217
NM_144997.5(FLCN):c.59delT (p.Phe20Serfs) rs876658390
NM_144997.5(FLCN):c.632_633delAGinsC (p.Glu211Alafs) rs879255661
NM_144997.5(FLCN):c.649C>T (p.Gln217Ter) rs1555609899
NM_144997.5(FLCN):c.708delC (p.Asn236Lysfs) rs886039369
NM_144997.5(FLCN):c.715C>T (p.Arg239Cys) rs78683075
NM_144997.5(FLCN):c.75G>A (p.Leu25=) rs200350612
NM_144997.5(FLCN):c.763C>T (p.His255Tyr) rs879255664
NM_144997.5(FLCN):c.779+1G>T rs758175953
NM_144997.5(FLCN):c.780-1G>T rs878855218
NM_144997.5(FLCN):c.780-2A>G rs1555609514
NM_144997.5(FLCN):c.871+16T>A rs116643153
NM_144997.5(FLCN):c.871+47G>A rs142934950
NM_144997.5(FLCN):c.872-13A>G rs114970273
NM_144997.5(FLCN):c.875T>G (p.Leu292Ter) rs879255668
NM_144997.5(FLCN):c.890_893delAAAG (p.Glu297Alafs) rs398124541
NM_144997.5(FLCN):c.927dupA (p.Ala310Serfs) rs879255669
NM_144997.5(FLCN):c.932_933delCT (p.Pro311Argfs) rs1555608614
NM_144997.5(FLCN):c.932delC (p.Pro311Leufs) rs1555608617
NM_144997.5(FLCN):c.97G>C (p.Asp33His) rs386833401
NM_144997.5:c.1188delC
NM_144997.5:c.594_596delTGA
NM_144997.6(FLCN):c.1062+6C>T rs8065832
NM_144997.6(FLCN):c.1149C>T (p.Leu383=) rs150752548
NM_144997.6(FLCN):c.1233G>A (p.Glu411=) rs61750032
NM_144997.6(FLCN):c.1329_1332dup (p.Ala445Serfs) rs1085307771
NM_144997.6(FLCN):c.1523A>G (p.Lys508Arg) rs199643834
NM_144997.6(FLCN):c.1533G>A (p.Trp511Ter) rs398124530
NM_144997.6(FLCN):c.268G>T (p.Ala90Ser) rs141140415
NM_144997.6(FLCN):c.319_320delGTinsCAC (p.Val107Hisfs) rs398124535
NM_144997.6(FLCN):c.396+59T>C rs41525346
NM_144997.6(FLCN):c.397-13G>A rs3744123
NM_144997.6(FLCN):c.397-14C>T rs1736219
NM_144997.6(FLCN):c.451G>A (p.Val151Met) rs147164515
NM_144997.6(FLCN):c.49dup (p.Arg17Profs) rs758385503
NM_144997.6(FLCN):c.583G>T (p.Gly195Ter)
NM_144997.6(FLCN):c.586A>G (p.Ile196Val) rs201078144
NM_144997.6(FLCN):c.610_611delGCinsTA (p.Ala204Ter) rs398124538
NM_144997.6(FLCN):c.726A>T (p.Thr242=) rs113938514
NM_144997.6(FLCN):c.828_829dup (p.Ala277Valfs) rs398124539
NM_144997.6(FLCN):c.83dup (p.Leu29Thrfs) rs398124540
NM_144997.6(FLCN):c.871+36G>A rs3744124
NM_144997.6(FLCN):c.927_954dup (p.Gly319Serfs) rs398124542
NM_144997.6(FLCN):c.959G>A (p.Arg320Gln) rs143483053
NM_144997.6(FLCN):c.977C>T (p.Pro326Leu) rs138031155

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