List of variants in gene FLCN reported as likely benign for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 90

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HGVS	dbSNP	gnomAD frequency
NM_144997.7(FLCN):c.1233G>A (p.Glu411=)	rs61750032	0.03557
NM_144997.7(FLCN):c.*393G>A	rs12602675	0.03206
NM_144997.7(FLCN):c.618+159C>T	rs72842537	0.02674
NM_144997.7(FLCN):c.1538+281_1538+284del	rs146159727	0.02671
NM_144997.7(FLCN):c.*442T>C	rs7224213	0.02480
NM_144997.7(FLCN):c.-24-243G>A	rs75336342	0.01141
NM_144997.7(FLCN):c.1538+235G>A	rs141383036	0.00804
NM_144997.7(FLCN):c.-176G>A	rs117215381	0.00772
NM_144997.7(FLCN):c.871+471C>T	rs75105639	0.00645
NM_144997.7(FLCN):c.1176+258C>T	rs116552501	0.00579
NM_144997.7(FLCN):c.249+174T>G	rs113071228	0.00526
NM_144997.7(FLCN):c.*223C>T	rs76272341	0.00495
NM_144997.7(FLCN):c.871+349A>G	rs147687712	0.00389
NM_144997.7(FLCN):c.-25+51C>T	rs531338403	0.00347
NM_144997.7(FLCN):c.1333G>A (p.Ala445Thr)	rs41419545	0.00217
NM_144997.7(FLCN):c.1414C>G (p.Pro472Ala)	rs151312899	0.00080
NM_144997.7(FLCN):c.959G>A (p.Arg320Gln)	rs143483053	0.00071
NM_144997.7(FLCN):c.397-12G>T	rs199958635	0.00063
NM_144997.7(FLCN):c.871+98C>T	rs144832463	0.00061
NM_144997.7(FLCN):c.*695C>T	rs775700421	0.00058
NM_144997.7(FLCN):c.871+47G>A	rs142934950	0.00058
NM_144997.7(FLCN):c.1269C>T (p.His423=)	rs41464156	0.00053
NM_144997.7(FLCN):c.397-21G>C	rs149414632	0.00038
NM_144997.7(FLCN):c.1201C>T (p.Arg401Cys)	rs143183215	0.00037
NM_144997.7(FLCN):c.619-20C>T	rs202217257	0.00037
NM_144997.7(FLCN):c.268G>T (p.Ala90Ser)	rs141140415	0.00029
NM_144997.7(FLCN):c.931C>T (p.Pro311Ser)	rs140246224	0.00029
NM_144997.7(FLCN):c.1149C>T (p.Leu383=)	rs150752548	0.00028
NM_144997.7(FLCN):c.715C>T (p.Arg239Cys)	rs78683075	0.00024
NM_144997.7(FLCN):c.1326C>T (p.His442=)	rs145004158	0.00023
NM_144997.7(FLCN):c.246C>T (p.Cys82=)	rs150712346	0.00020
NM_144997.7(FLCN):c.592G>A (p.Asp198Asn)	rs200168437	0.00019
NM_144997.7(FLCN):c.580C>T (p.Arg194Trp)	rs138070947	0.00017
NM_144997.7(FLCN):c.113G>T (p.Ser38Ile)	rs139418842	0.00016
NM_144997.7(FLCN):c.1278C>T (p.Ile426=)	rs41459448	0.00016
NM_144997.7(FLCN):c.1332C>T (p.Ala444=)	rs141283741	0.00015
NM_144997.7(FLCN):c.1281C>G (p.Pro427=)	rs372207262	0.00014
NM_144997.7(FLCN):c.1463C>T (p.Ala488Val)	rs200660337	0.00014
NM_144997.7(FLCN):c.977C>T (p.Pro326Leu)	rs138031155	0.00012
NM_144997.7(FLCN):c.1704G>A (p.Thr568=)	rs147554296	0.00011
NM_144997.7(FLCN):c.1539-6C>T	rs779028759	0.00009
NM_144997.7(FLCN):c.687C>T (p.Phe229=)	rs754710935	0.00008
NM_144997.7(FLCN):c.867C>T (p.Leu289=)	rs367562964	0.00007
NM_144997.7(FLCN):c.*1C>T	rs759292330	0.00006
NM_144997.7(FLCN):c.396+7C>T	rs781155484	0.00006
NM_144997.7(FLCN):c.444C>T (p.His148=)	rs376825814	0.00006
NM_144997.7(FLCN):c.78C>T (p.His26=)	rs746222481	0.00006
NM_144997.7(FLCN):c.1387T>C (p.Tyr463His)	rs770077517	0.00005
NM_144997.7(FLCN):c.1389C>T (p.Tyr463=)	rs137852929	0.00005
NM_144997.7(FLCN):c.1692C>T (p.His564=)	rs201810397	0.00005
NM_144997.7(FLCN):c.396+19G>A	rs767495491	0.00005
NM_144997.7(FLCN):c.1418T>C (p.Val473Ala)	rs144883828	0.00004
NM_144997.7(FLCN):c.645C>T (p.Cys215=)	rs772360950	0.00004
NM_144997.7(FLCN):c.992C>T (p.Ser331Phe)	rs202215080	0.00004
NM_144997.7(FLCN):c.1140C>T (p.Asp380=)	rs768454196	0.00003
NM_144997.7(FLCN):c.429C>T (p.Phe143=)	rs773792624	0.00003
NM_144997.7(FLCN):c.450T>C (p.Phe150=)	rs200672897	0.00003
NM_144997.7(FLCN):c.1021C>T (p.Arg341Trp)	rs770396757	0.00002
NM_144997.7(FLCN):c.222G>A (p.Pro74=)	rs770311645	0.00002
NM_144997.7(FLCN):c.720G>A (p.Ser240=)	rs186366202	0.00002
NM_144997.7(FLCN):c.1022G>A (p.Arg341Gln)	rs375352888	0.00001
NM_144997.7(FLCN):c.1059G>A (p.Arg353=)	rs751513488	0.00001
NM_144997.7(FLCN):c.1227C>T (p.Tyr409=)	rs561236067	0.00001
NM_144997.7(FLCN):c.1266G>A (p.Pro422=)	rs751013842	0.00001
NM_144997.7(FLCN):c.135G>A (p.Ala45=)	rs759930161	0.00001
NM_144997.7(FLCN):c.1419A>C (p.Val473=)	rs141036419	0.00001
NM_144997.7(FLCN):c.1464G>A (p.Ala488=)	rs747029882	0.00001
NM_144997.7(FLCN):c.1626C>T (p.Ser542=)	rs1433647771	0.00001
NM_144997.7(FLCN):c.207C>T (p.Val69=)	rs759772780	0.00001
NM_144997.7(FLCN):c.237G>A (p.Ser79=)	rs771650940	0.00001
NM_144997.7(FLCN):c.257G>A (p.Arg86Gln)	rs765550303	0.00001
NM_144997.7(FLCN):c.318C>T (p.Tyr106=)	rs773946854	0.00001
NM_144997.7(FLCN):c.42C>T (p.His14=)	rs766288960	0.00001
NM_144997.7(FLCN):c.702C>T (p.Asn234=)	rs1471089893	0.00001
NM_144997.7(FLCN):c.729G>A (p.Ser243=)	rs377261933	0.00001
NM_144997.7(FLCN):c.915A>G (p.Glu305=)	rs551034228	0.00001
NM_144997.7(FLCN):c.-227-4C>T
NM_144997.7(FLCN):c.-8A>G
NM_144997.7(FLCN):c.1177-186G>A	rs372508505
NM_144997.7(FLCN):c.12C>A (p.Ile4=)	rs752123350
NM_144997.7(FLCN):c.1314C>T (p.Ile438=)	rs771247255
NM_144997.7(FLCN):c.1350C>T (p.His450=)	rs753685944
NM_144997.7(FLCN):c.1433-20_1433-10del	rs1380029891
NM_144997.7(FLCN):c.1451A>G (p.Asn484Ser)	rs1010980331
NM_144997.7(FLCN):c.249+154GTTTT[2]	rs930172027
NM_144997.7(FLCN):c.249+265A>T	rs147232424
NM_144997.7(FLCN):c.619-230C>G	rs142465664
NM_144997.7(FLCN):c.75G>A (p.Leu25=)	rs200350612
NM_144997.7(FLCN):c.871+170_871+178del	rs750424403
NM_144997.7(FLCN):c.942A>G (p.Pro314=)

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