List of variants in gene FLCN reported as 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: 61

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HGVS	dbSNP	gnomAD frequency
NM_144997.7(FLCN):c.-113-226T>C	rs1736211	0.77993
NM_144997.7(FLCN):c.-25+100C>G	rs1736212	0.72868
NM_144997.6(FLCN):c.-487G>C	rs1736209	0.72552
NM_144997.7(FLCN):c.*557T>C	rs3803761	0.71694
NM_144997.7(FLCN):c.779+220T>C	rs1736221	0.58663
NM_144997.7(FLCN):c.1176+179A>G	rs7208065	0.51111
NM_144997.7(FLCN):c.1062+6C>T	rs8065832	0.47076
NM_144997.7(FLCN):c.-299C>T	rs1708629	0.44880
NM_144997.7(FLCN):c.1063-316A>G	rs4985752	0.44349
NM_144997.7(FLCN):c.397-14C>T	rs1736219	0.40309
NM_144997.7(FLCN):c.1433-38A>G	rs34235236	0.21634
NM_144997.7(FLCN):c.-227-200G>A	rs76045368	0.20419
NM_144997.7(FLCN):c.249+185A>C	rs55836267	0.17432
NM_144997.7(FLCN):c.1301-59C>T	rs34311146	0.13057
NM_144997.7(FLCN):c.871+226G>A	rs41400246	0.10424
NM_144997.7(FLCN):c.*425G>A	rs7224335	0.09952
NM_144997.7(FLCN):c.*356G>T	rs7224474	0.09138
NM_144997.7(FLCN):c.871+36G>A	rs3744124	0.07420
NM_144997.7(FLCN):c.397-13G>A	rs3744123	0.07012
NM_144997.7(FLCN):c.396+59T>C	rs41525346	0.06134
NM_144997.7(FLCN):c.-302G>A	rs41345949	0.05963
NM_144997.7(FLCN):c.-90A>G	rs8069957	0.04414
NM_144997.7(FLCN):c.779+241G>C	rs73284553	0.04391
NM_144997.7(FLCN):c.1176+68G>C	rs41364753	0.03697
NM_144997.7(FLCN):c.1538+131A>C	rs8073346	0.03692
NM_144997.7(FLCN):c.1233G>A (p.Glu411=)	rs61750032	0.03557
NM_144997.7(FLCN):c.-113-291A>G	rs77055033	0.03468
NM_144997.7(FLCN):c.779+214T>A	rs116390420	0.03452
NM_144997.7(FLCN):c.619-66C>T	rs2292527	0.03292
NM_144997.7(FLCN):c.726A>T (p.Thr242=)	rs113938514	0.02907
NM_144997.7(FLCN):c.1538+121C>T	rs41442248	0.02363
NM_144997.7(FLCN):c.1063-301A>C	rs79248566	0.02242
NM_144997.7(FLCN):c.872-13A>G	rs114970273	0.01651
NM_144997.7(FLCN):c.-78G>C	rs147598893	0.01648
NM_144997.7(FLCN):c.618+136C>G	rs116747558	0.01639
NM_144997.7(FLCN):c.1063-151G>A	rs74354336	0.01636
NM_144997.7(FLCN):c.1176+31G>A	rs41340844	0.01448
NM_144997.7(FLCN):c.1063-117C>T	rs4985751	0.00868
NM_144997.7(FLCN):c.-176G>A	rs117215381	0.00772
NM_144997.7(FLCN):c.1538+14T>G	rs112111994	0.00721
NM_144997.7(FLCN):c.1177-21G>A	rs150687840	0.00276
NM_144997.7(FLCN):c.1269C>T (p.His423=)	rs41464156	0.00053
NM_144997.7(FLCN):c.735A>C (p.Thr245=)	rs150175875	0.00032
NM_144997.7(FLCN):c.268G>T (p.Ala90Ser)	rs141140415	0.00029
NM_144997.7(FLCN):c.1326C>T (p.His442=)	rs145004158	0.00023
NM_144997.7(FLCN):c.1278C>T (p.Ile426=)	rs41459448	0.00016
NM_144997.7(FLCN):c.1539-6C>T	rs779028759	0.00009
NM_144997.7(FLCN):c.792G>A (p.Ala264=)	rs140500421	0.00008
NM_144997.7(FLCN):c.1389C>T (p.Tyr463=)	rs137852929	0.00005
NM_144997.7(FLCN):c.1300+12C>T	rs565983064	0.00004
NM_144997.7(FLCN):c.711C>T (p.Ala237=)	rs111258744	0.00004
NM_144997.7(FLCN):c.279G>A (p.Pro93=)	rs138688941	0.00002
NM_144997.7(FLCN):c.1227C>T (p.Tyr409=)	rs561236067	0.00001
NM_144997.7(FLCN):c.1464G>A (p.Ala488=)	rs747029882	0.00001
NM_144997.7(FLCN):c.83C>G (p.Pro28Arg)	rs780588085	0.00001
NM_144997.7(FLCN):c.-228+3_-228+21dup	rs370486376
NM_144997.7(FLCN):c.1063-172C>G	rs4985705
NM_144997.7(FLCN):c.1176+134G>C	rs41371953
NM_144997.7(FLCN):c.1539-294TCTT[3]	rs10681411
NM_144997.7(FLCN):c.250-288G>A	rs1708620
NM_144997.7(FLCN):c.75G>A (p.Leu25=)	rs200350612

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