FLCN[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 322033	NM_144997.7(FLCN):c.*1403T>C	FLCN	Single nucleotide variant (3 prime UTR variant)	Birt-Hogg-Dube syndrome +2 more	GBenign
Select item 322034	NM_144997.7(FLCN):c.*1336G>T	FLCN	Single nucleotide variant (3 prime UTR variant)	Birt-Hogg-Dube syndrome +2 more	GBenign
Select item 322035	NM_144997.7(FLCN):c.*1273C>T	FLCN	Single nucleotide variant (3 prime UTR variant)	Familial spontaneous pneumothorax +1 more	GUncertain significance
Select item 322036	NM_144997.7(FLCN):c.*1182dup	FLCN	Duplication (3 prime UTR variant)	Spontaneous pneumothorax +1 more	GBenign
Select item 322037	NM_144997.7(FLCN):c.*1179dup	FLCN	Duplication (3 prime UTR variant)	Spontaneous pneumothorax +1 more	GUncertain significance
Select item 322038	NM_144997.7(FLCN):c.*1179T>A	FLCN	Single nucleotide variant (3 prime UTR variant)	Familial spontaneous pneumothorax +1 more	GUncertain significance
Select item 889505	NM_144997.7(FLCN):c.*1101C>G	FLCN	Single nucleotide variant (3 prime UTR variant)	Birt-Hogg-Dube syndrome +1 more	GUncertain significance
Select item 889506	NM_144997.7(FLCN):c.*1035T>C	FLCN	Single nucleotide variant (3 prime UTR variant)	Birt-Hogg-Dube syndrome +1 more	GUncertain significance
Select item 322039	NM_144997.7(FLCN):c.*967T>C	FLCN	Single nucleotide variant (3 prime UTR variant)	Familial spontaneous pneumothorax +1 more	GUncertain significance
Select item 322040	NM_144997.7(FLCN):c.*956A>G	FLCN	Single nucleotide variant (3 prime UTR variant)	Birt-Hogg-Dube syndrome +1 more	GBenign
Select item 890168	NM_144997.7(FLCN):c.*915G>T	FLCN	Single nucleotide variant (3 prime UTR variant)	Birt-Hogg-Dube syndrome +1 more	GUncertain significance
Select item 322041	NM_144997.7(FLCN):c.*914C>T	FLCN	Single nucleotide variant (3 prime UTR variant)	Familial spontaneous pneumothorax +1 more	GBenign
Select item 322042	NM_144997.7(FLCN):c.*911G>A	FLCN	Single nucleotide variant (3 prime UTR variant)	Familial spontaneous pneumothorax +1 more	GBenign/Likely benign
Select item 322043	NM_144997.7(FLCN):c.*887T>C	FLCN	Single nucleotide variant (3 prime UTR variant)	Familial spontaneous pneumothorax +1 more	GUncertain significance
Select item 890749	NM_144997.7(FLCN):c.*846C>T	FLCN	Single nucleotide variant (3 prime UTR variant)	Birt-Hogg-Dube syndrome +1 more	GUncertain significance
Select item 322044	NM_144997.7(FLCN):c.*739C>T	FLCN	Single nucleotide variant (3 prime UTR variant)	Familial spontaneous pneumothorax +1 more	GUncertain significance
Select item 322045	NM_144997.7(FLCN):c.695_696del	FLCN	Deletion (3 prime UTR variant)	Spontaneous pneumothorax +1 more	GUncertain significance
Select item 322046	NM_144997.7(FLCN):c.*695C>T	FLCN	Single nucleotide variant (3 prime UTR variant)	Birt-Hogg-Dube syndrome +2 more	GConflicting classifications of pathogenicity
Select item 322047	NM_144997.7(FLCN):c.*634A>C	FLCN	Single nucleotide variant (3 prime UTR variant)	Familial spontaneous pneumothorax +1 more	GUncertain significance
Select item 322048	NM_144997.7(FLCN):c.*557T>C	FLCN	Single nucleotide variant (3 prime UTR variant)	Birt-Hogg-Dube syndrome +2 more	GBenign
Select item 322049	NM_144997.7(FLCN):c.*528G>A	FLCN	Single nucleotide variant (3 prime UTR variant)	Birt-Hogg-Dube syndrome +1 more	GConflicting classifications of pathogenicity
Select item 322050	NM_144997.7(FLCN):c.*526T>C	FLCN	Single nucleotide variant (3 prime UTR variant)	Familial spontaneous pneumothorax +1 more	GBenign/Likely benign
Select item 322051	NM_144997.7(FLCN):c.*442T>C	FLCN	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GBenign/Likely benign
Select item 322052	NM_144997.7(FLCN):c.*425G>A	FLCN	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GBenign
Select item 322053	NM_144997.7(FLCN):c.*393G>A	FLCN	Single nucleotide variant (3 prime UTR variant)	Birt-Hogg-Dube syndrome +2 more	GBenign/Likely benign
Select item 322054	NM_144997.7(FLCN):c.*379G>A	FLCN	Single nucleotide variant (3 prime UTR variant)	Familial spontaneous pneumothorax +1 more	GConflicting classifications of pathogenicity
Select item 322055	NM_144997.7(FLCN):c.*356G>T	FLCN	Single nucleotide variant (3 prime UTR variant)	Birt-Hogg-Dube syndrome +2 more	GBenign
Select item 322056	NM_144997.7(FLCN):c.*340G>A	FLCN	Single nucleotide variant (3 prime UTR variant)	Familial spontaneous pneumothorax +1 more	GUncertain significance
Select item 890789	NM_144997.7(FLCN):c.*339C>T	FLCN	Single nucleotide variant (3 prime UTR variant)	Birt-Hogg-Dube syndrome +1 more	GUncertain significance
Select item 322057	NM_144997.7(FLCN):c.*333C>T	FLCN	Single nucleotide variant (3 prime UTR variant)	Familial spontaneous pneumothorax +1 more	GUncertain significance
Select item 322058	NM_144997.7(FLCN):c.*290C>T	FLCN	Single nucleotide variant (3 prime UTR variant)	Birt-Hogg-Dube syndrome +1 more	GUncertain significance
Select item 322059	NM_144997.7(FLCN):c.*224G>A	FLCN	Single nucleotide variant (3 prime UTR variant)	Familial spontaneous pneumothorax +2 more	GUncertain significance
Select item 1209300	NM_144997.7(FLCN):c.*223C>T	FLCN	Single nucleotide variant (3 prime UTR variant)	not provided	GLikely benign
Select item 892027	NM_144997.7(FLCN):c.*178A>C	FLCN	Single nucleotide variant (3 prime UTR variant)	Birt-Hogg-Dube syndrome +1 more	GUncertain significance
Select item 322060	NM_144997.7(FLCN):c.*178A>G	FLCN	Single nucleotide variant (3 prime UTR variant)	Familial spontaneous pneumothorax +1 more	GConflicting classifications of pathogenicity
Select item 892028	NM_144997.7(FLCN):c.*140C>T	FLCN	Single nucleotide variant (3 prime UTR variant)	Birt-Hogg-Dube syndrome +1 more	GUncertain significance
Select item 892029	NM_144997.7(FLCN):c.*29G>A	FLCN	Single nucleotide variant (3 prime UTR variant)	Birt-Hogg-Dube syndrome +1 more	GUncertain significance
Select item 387053	NM_144997.7(FLCN):c.*17G>T	FLCN	Single nucleotide variant (3 prime UTR variant)	not specified	GBenign/Likely benign
Select item 664451	NC_000017.11:g.(?_17213645)_(17213866_?)del	FLCN	Deletion	Birt-Hogg-Dube syndrome	GPathogenic
Select item 664449	NC_000017.10:g.(?_17116959)_(17124952_?)dup	FLCN	Duplication	Birt-Hogg-Dube syndrome	GUncertain significance
Select item 659589	NC_000017.10:g.(?_17116959)_(17136215_?)dup	FLCN	Duplication	Birt-Hogg-Dube syndrome	GUncertain significance
Select item 642628	NC_000017.11:g.(?_17213645)_(17237188_?)del	FLCN	Deletion	Birt-Hogg-Dube syndrome	GPathogenic
Select item 639366	NC_000017.10:g.(?_17116959)_(17140502_?)dup	FLCN	Duplication	Birt-Hogg-Dube syndrome	GUncertain significance
Select item 530023	NC_000017.10:g.(?_17116963)_(17131457_?)dup	FLCN	Duplication	Birt-Hogg-Dube syndrome	GUncertain significance
Select item 530022	NC_000017.10:g.(?_17116963)_(17120502_?)dup	FLCN	Duplication	Birt-Hogg-Dube syndrome	GUncertain significance
Select item 485622	NM_144997.7(FLCN):c.*5T>C	FLCN	Single nucleotide variant (3 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 888566	NM_144997.7(FLCN):c.*4G>A	FLCN	Single nucleotide variant (3 prime UTR variant)	Birt-Hogg-Dube syndrome +2 more	GConflicting classifications of pathogenicity
Select item 1802907	NM_144997.7(FLCN):c.*2C>T	FLCN	Single nucleotide variant (3 prime UTR variant)	not specified	GLikely benign
Select item 1196117	NM_144997.7(FLCN):c.*1C>T	FLCN	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3379	NM_144997.7(FLCN):c.(871+1_872-1)_(*1_?)del	FLCN	Deletion	Familial spontaneous pneumothorax	GPathogenic
Select item 1010800	NM_144997.7(FLCN):c.1737C>G (p.Asn579Lys)	FLCN (N579K +1 more)	Single nucleotide variant (missense variant)	Birt-Hogg-Dube syndrome	GUncertain significance
Select item 530016	NM_144997.7(FLCN):c.1737C>T (p.Asn579=)	FLCN	Single nucleotide variant (synonymous variant)	Birt-Hogg-Dube syndrome	GLikely benign
Select item 1779040	NM_144997.7(FLCN):c.1734G>A (p.Arg578=)	FLCN	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 819964	NM_144997.7(FLCN):c.1733G>A (p.Arg578Gln)	FLCN (R578Q +1 more)	Single nucleotide variant (missense variant)	Birt-Hogg-Dube syndrome +5 more	GUncertain significance
Select item 651362	NM_144997.7(FLCN):c.1732C>T (p.Arg578Trp)	FLCN (R596W +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 851704	NM_144997.7(FLCN):c.1730C>T (p.Ser577Phe)	FLCN (S595F +1 more)	Single nucleotide variant (missense variant)	Birt-Hogg-Dube syndrome	GUncertain significance
Select item 3229239	NM_144997.7(FLCN):c.1723_1729delinsCCACAGC (p.Ser575_Ser577delinsProGlnPro)	FLCN	Indel (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1778931	NM_144997.7(FLCN):c.1729T>G (p.Ser577Ala)	FLCN (S595A +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1425769	NM_144997.7(FLCN):c.1729T>C (p.Ser577Pro)	FLCN (S577P +1 more)	Single nucleotide variant (missense variant)	Birt-Hogg-Dube syndrome	GUncertain significance
Select item 3279025	NM_144997.7(FLCN):c.1728G>A (p.Glu576=)	FLCN	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 1420988	NM_144997.7(FLCN):c.1728G>T (p.Glu576Asp)	FLCN (E576D +1 more)	Single nucleotide variant (missense variant)	Birt-Hogg-Dube syndrome	GUncertain significance
Select item 2496514	NM_144997.7(FLCN):c.1727A>G (p.Glu576Gly)	FLCN (E576G +1 more)	Single nucleotide variant (missense variant)	Birt-Hogg-Dube syndrome +1 more	GUncertain significance
Select item 3229241	NM_144997.7(FLCN):c.1726G>C (p.Glu576Gln)	FLCN (E576Q +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 707812	NM_144997.7(FLCN):c.1725G>A (p.Ser575=)	FLCN	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 1059893	NM_144997.7(FLCN):c.1724C>T (p.Ser575Leu)	FLCN (S575L +1 more)	Single nucleotide variant (missense variant)	Birt-Hogg-Dube syndrome +1 more	GUncertain significance
Select item 3229240	NM_144997.7(FLCN):c.1723T>C (p.Ser575Pro)	FLCN (S575P +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 944338	NM_144997.7(FLCN):c.1721C>T (p.Ala574Val)	FLCN (A592V +1 more)	Single nucleotide variant (missense variant)	Birt-Hogg-Dube syndrome +1 more	GUncertain significance
Select item 2624777	NM_144997.7(FLCN):c.1720G>A (p.Ala574Thr)	FLCN (A574T +1 more)	Single nucleotide variant (missense variant)	Birt-Hogg-Dube syndrome +1 more	GUncertain significance
Select item 2681946	NM_144997.7(FLCN):c.1719A>G (p.Thr573=)	FLCN	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1052892	NM_144997.7(FLCN):c.1718C>T (p.Thr573Ile)	FLCN (T573I +1 more)	Single nucleotide variant (missense variant)	Birt-Hogg-Dube syndrome	GUncertain significance
Select item 1011921	NM_144997.7(FLCN):c.1717A>T (p.Thr573Ser)	FLCN (T573S +1 more)	Single nucleotide variant (missense variant)	Birt-Hogg-Dube syndrome	GUncertain significance
Select item 643740	NM_144997.7(FLCN):c.1717A>G (p.Thr573Ala)	FLCN (T573A +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1778631	NM_144997.7(FLCN):c.1716C>T (p.Pro572=)	FLCN	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 988470	NM_144997.7(FLCN):c.1716del (p.Thr573fs)	FLCN (T573fs +1 more)	Deletion (frameshift variant)	not provided	GLikely pathogenic
Select item 653717	NM_144997.7(FLCN):c.1715C>A (p.Pro572His)	FLCN (P572H +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +5 more	GUncertain significance
Select item 656775	NM_144997.7(FLCN):c.1714C>T (p.Pro572Ser)	FLCN (P590S +1 more)	Single nucleotide variant (missense variant)	Birt-Hogg-Dube syndrome	GUncertain significance
Select item 460607	NM_144997.7(FLCN):c.1714C>G (p.Pro572Ala)	FLCN (P572A +1 more)	Single nucleotide variant (missense variant)	Birt-Hogg-Dube syndrome	GUncertain significance
Select item 1778602	NM_144997.7(FLCN):c.1713C>T (p.Ser571=)	FLCN	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2131850	NM_144997.7(FLCN):c.1654_1709dup (p.Ser571_Pro572insGlyTerSer)	FLCN	Duplication (nonsense +1 more)	Birt-Hogg-Dube syndrome +1 more	GUncertain significance
Select item 1153440	NM_144997.7(FLCN):c.1710C>T (p.Arg570=)	FLCN	Single nucleotide variant (synonymous variant)	Birt-Hogg-Dube syndrome	GLikely benign
Select item 1043559	NM_144997.7(FLCN):c.1709G>T (p.Arg570Leu)	FLCN (R588L +1 more)	Single nucleotide variant (missense variant)	Birt-Hogg-Dube syndrome 1 +6 more	GConflicting classifications of pathogenicity
Select item 229915	NM_144997.7(FLCN):c.1709G>A (p.Arg570His)	FLCN (R570H +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +6 more	GConflicting classifications of pathogenicity
Select item 819901	NM_144997.7(FLCN):c.1708C>T (p.Arg570Cys)	FLCN (R570C +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 749853	NM_144997.7(FLCN):c.1707C>T (p.Val569=)	FLCN	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 1474976	NM_144997.7(FLCN):c.1706T>C (p.Val569Ala)	FLCN (V569A +1 more)	Single nucleotide variant (missense variant)	Birt-Hogg-Dube syndrome	GUncertain significance
Select item 1087486	NM_144997.7(FLCN):c.1704G>C (p.Thr568=)	FLCN	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 415623	NM_144997.7(FLCN):c.1704G>A (p.Thr568=)	FLCN	Single nucleotide variant (synonymous variant)	Birt-Hogg-Dube syndrome +2 more	GLikely benign
Select item 2850429	NM_144997.7(FLCN):c.1703C>G (p.Thr568Arg)	FLCN (T568R +1 more)	Single nucleotide variant (missense variant)	Birt-Hogg-Dube syndrome	GUncertain significance
Select item 460606	NM_144997.7(FLCN):c.1703C>T (p.Thr568Met)	FLCN (T568M +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 232328	NM_144997.7(FLCN):c.1702A>G (p.Thr568Ala)	FLCN (T568A +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 938559	NM_144997.7(FLCN):c.1700C>T (p.Ser567Phe)	FLCN (S567F +1 more)	Single nucleotide variant (missense variant)	Birt-Hogg-Dube syndrome 1 +4 more	GConflicting classifications of pathogenicity
Select item 1961169	NM_144997.7(FLCN):c.1698G>A (p.Met566Ile)	FLCN (M566I +1 more)	Single nucleotide variant (missense variant)	Birt-Hogg-Dube syndrome	GUncertain significance
Select item 993694	NM_144997.7(FLCN):c.1697T>C (p.Met566Thr)	FLCN (M566T +1 more)	Single nucleotide variant (missense variant)	Birt-Hogg-Dube syndrome 1 +3 more	GUncertain significance
Select item 1970227	NM_144997.7(FLCN):c.1696A>G (p.Met566Val)	FLCN (M584V +1 more)	Single nucleotide variant (missense variant)	Birt-Hogg-Dube syndrome	GUncertain significance
Select item 1124032	NM_144997.7(FLCN):c.1695C>G (p.Leu565=)	FLCN	Single nucleotide variant (synonymous variant)	Birt-Hogg-Dube syndrome	GLikely benign
Select item 1778180	NM_144997.7(FLCN):c.1693C>T (p.Leu565Phe)	FLCN (L583F +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2037757	NM_144997.7(FLCN):c.1692C>G (p.His564Gln)	FLCN (H564Q +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 184907	NM_144997.7(FLCN):c.1692C>T (p.His564=)	FLCN	Single nucleotide variant (synonymous variant)	not specified +7 more	GBenign/Likely benign
Select item 2157084	NM_144997.7(FLCN):c.1691A>C (p.His564Pro)	FLCN (H582P +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1778140	NM_144997.7(FLCN):c.1691A>T (p.His564Leu)	FLCN (H564L +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance

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