List of variants in gene FLCN reported by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 28

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HGVS	dbSNP	gnomAD frequency
NM_144997.7(FLCN):c.1062+6C>T	rs8065832	0.47076
NM_144997.7(FLCN):c.397-14C>T	rs1736219	0.40309
NM_144997.7(FLCN):c.397-13G>A	rs3744123	0.07012
NM_144997.7(FLCN):c.1233G>A (p.Glu411=)	rs61750032	0.03557
NM_144997.7(FLCN):c.726A>T (p.Thr242=)	rs113938514	0.02907
NM_144997.7(FLCN):c.872-13A>G	rs114970273	0.01651
NM_144997.7(FLCN):c.1333G>A (p.Ala445Thr)	rs41419545	0.00217
NM_144997.7(FLCN):c.246C>T (p.Cys82=)	rs150712346	0.00020
NM_144997.7(FLCN):c.1523A>G (p.Lys508Arg)	rs199643834	0.00018
NM_144997.7(FLCN):c.113G>T (p.Ser38Ile)	rs139418842	0.00016
NM_144997.7(FLCN):c.977C>T (p.Pro326Leu)	rs138031155	0.00012
NM_144997.7(FLCN):c.1538+10A>C	rs12451312	0.00010
NM_144997.7(FLCN):c.779+9C>T	rs373504780	0.00009
NM_144997.7(FLCN):c.1387T>C (p.Tyr463His)	rs770077517	0.00005
NM_144997.7(FLCN):c.1390G>A (p.Glu464Lys)	rs1471793185	0.00001
NM_144997.7(FLCN):c.681G>A (p.Thr227=)	rs781035304	0.00001
NM_144997.7(FLCN):c.1252del (p.Leu418fs)	rs864622651
NM_144997.7(FLCN):c.1285dup (p.His429fs)	rs80338682
NM_144997.7(FLCN):c.1389C>G (p.Tyr463Ter)	rs137852929
NM_144997.7(FLCN):c.1432+2T>C	rs1567807517
NM_144997.7(FLCN):c.1616dup (p.Ala541fs)	rs2144810362
NM_144997.7(FLCN):c.250-2A>G	rs398124533
NM_144997.7(FLCN):c.256_269del (p.Ser87fs)	rs2145014205
NM_144997.7(FLCN):c.379dup (p.Arg127fs)	rs2145010446
NM_144997.7(FLCN):c.619-1G>A	rs1131690840
NM_144997.7(FLCN):c.634C>T (p.Gln212Ter)	rs558699420
NM_144997.7(FLCN):c.780G>A (p.Trp260Ter)	rs1131690826
NM_144997.7(FLCN):c.927_954dup (p.Gly319fs)	rs398124542

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