ClinVar for Gene (Select 201163) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3382013	NM_144997.7(FLCN):c.636del (p.Gln212fs)	FLCN (Q212fs +1 more)	Deletion (frameshift variant)	Familial spontaneous pneumothorax +3 more	GPathogenic
Select item 3381155	NM_144997.7(FLCN):c.819_824delinsGCTCGGACCG (p.Glu275fs)	FLCN (E275fs +1 more)	Indel (frameshift variant)	not provided	GLikely pathogenic
Select item 3380473	NM_144997.7(FLCN):c.1177-11_1177-4del	FLCN	Deletion (intron variant)	not provided	GUncertain significance
Select item 3369829	NM_144997.7(FLCN):c.-6G>A	FLCN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 3367673	NM_144997.7(FLCN):c.314A>T (p.Lys105Ile)	FLCN (K105I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3367667	NM_144997.7(FLCN):c.525C>T (p.Ile175=)	FLCN	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 3357935	NM_144997.7(FLCN):c.1177-22T>C	FLCN	Single nucleotide variant (intron variant)	FLCN-related disorder	GLikely benign
Select item 3356168	NM_144997.7(FLCN):c.-361C>T	FLCN	Single nucleotide variant (5 prime UTR variant)	FLCN-related disorder	GLikely benign
Select item 3354165	NM_144997.7(FLCN):c.871+130G>A	FLCN (R334Q)	Single nucleotide variant (missense variant +1 more)	FLCN-related disorder	GUncertain significance
Select item 3353063	NM_144997.7(FLCN):c.871+153G>A	FLCN (V342M)	Single nucleotide variant (missense variant +1 more)	FLCN-related disorder	GLikely benign
Select item 3352865	NM_144997.7(FLCN):c.871+129C>G	FLCN (R334G)	Single nucleotide variant (missense variant +1 more)	FLCN-related disorder	GLikely benign
Select item 3351525	NM_144997.7(FLCN):c.871+159T>C	FLCN	Single nucleotide variant (3 prime UTR variant +1 more)	FLCN-related disorder	GLikely benign
Select item 3350390	NM_144997.7(FLCN):c.397-323A>T	FLCN (M148L)	Single nucleotide variant (missense variant +1 more)	FLCN-related disorder	GUncertain significance
Select item 3346430	NM_144997.7(FLCN):c.1291C>T (p.Leu431Phe)	FLCN (L431F +1 more)	Single nucleotide variant (missense variant)	FLCN-related disorder	GUncertain significance
Select item 3345199	NM_144997.7(FLCN):c.98A>G (p.Asp33Gly)	FLCN (D33G)	Single nucleotide variant (missense variant)	FLCN-related disorder	GUncertain significance
Select item 3344214	NM_144997.7(FLCN):c.837dup (p.Glu280fs)	FLCN (E280fs +1 more)	Duplication (frameshift variant)	FLCN-related disorder	GLikely pathogenic
Select item 3343584	NM_144997.7(FLCN):c.-24-5C>T	FLCN	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 3343271	NM_144997.7(FLCN):c.968C>T (p.Thr323Ile)	FLCN (T323I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3343161	NM_144997.7(FLCN):c.1361G>T (p.Cys454Phe)	FLCN (C454F +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3341019	NM_144997.7(FLCN):c.1602G>T (p.Lys534Asn)	FLCN (K534N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3337115	NM_144997.7(FLCN):c.779+1G>A	FLCN	Single nucleotide variant (splice donor variant)	not provided	GLikely pathogenic
Select item 3279044	NM_144997.7(FLCN):c.336C>A (p.Pro112=)	FLCN	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3279043	NM_144997.7(FLCN):c.760C>A (p.Leu254Met)	FLCN (L254M +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3279042	NM_144997.7(FLCN):c.784C>T (p.Leu262=)	FLCN	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3279039	NM_144997.7(FLCN):c.182A>C (p.His61Pro)	FLCN (H61P)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3279038	NM_144997.7(FLCN):c.665T>C (p.Met222Thr)	FLCN (M222T +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3279037	NM_144997.7(FLCN):c.897_898dup (p.Asp300fs)	FLCN (D300fs +1 more)	Duplication (frameshift variant)	Hereditary cancer-predisposing syndrome	GPathogenic
Select item 3279036	NM_144997.7(FLCN):c.1076del (p.Pro359fs)	FLCN (P377fs +1 more)	Deletion (frameshift variant)	Hereditary cancer-predisposing syndrome	GPathogenic
Select item 3279035	NM_144997.7(FLCN):c.1232A>C (p.Glu411Ala)	FLCN (E429A +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3279034	NM_144997.7(FLCN):c.1561T>A (p.Phe521Ile)	FLCN (F521I +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3279033	NM_144997.7(FLCN):c.1202G>T (p.Arg401Leu)	FLCN (R419L +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3279032	NM_144997.7(FLCN):c.103A>G (p.Asn35Asp)	FLCN (N35D)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3279031	NM_144997.7(FLCN):c.269C>G (p.Ala90Gly)	FLCN (A90G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3279029	NM_144997.7(FLCN):c.764A>G (p.His255Arg)	FLCN (H255R +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3279028	NM_144997.7(FLCN):c.107A>T (p.Glu36Val)	FLCN (E36V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3279027	NM_144997.7(FLCN):c.560C>A (p.Pro187His)	FLCN (P205H +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3279026	NM_144997.7(FLCN):c.1581A>T (p.Arg527=)	FLCN	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
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 3279024	NM_144997.7(FLCN):c.918G>C (p.Glu306Asp)	FLCN (E324D +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3279022	NM_144997.7(FLCN):c.145G>T (p.Glu49Ter)	FLCN (E49*)	Single nucleotide variant (nonsense)	Hereditary cancer-predisposing syndrome	GPathogenic
Select item 3279021	NM_144997.7(FLCN):c.802C>G (p.Arg268Gly)	FLCN (R268G +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3279020	NM_144997.7(FLCN):c.855G>A (p.Gln285=)	FLCN	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3279019	NM_144997.7(FLCN):c.285T>G (p.Tyr95Ter)	FLCN (Y95*)	Single nucleotide variant (nonsense)	Hereditary cancer-predisposing syndrome	GPathogenic
Select item 3279017	NM_144997.7(FLCN):c.1614C>G (p.Ile538Met)	FLCN (I556M +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3279016	NM_144997.7(FLCN):c.1381A>G (p.Ser461Gly)	FLCN (S461G +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3279014	NM_144997.7(FLCN):c.642A>G (p.Gly214=)	FLCN	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3256335	NM_144997.7(FLCN):c.618+35G>C	FLCN	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 3256334	NM_144997.7(FLCN):c.1062+21G>A	FLCN	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 3256333	NM_144997.7(FLCN):c.1177-10T>C	FLCN	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 3256332	NM_144997.7(FLCN):c.1432+23T>A	FLCN	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 3256330	NM_144997.7(FLCN):c.1432+30T>C	FLCN	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 3256329	NM_144997.7(FLCN):c.1683C>G (p.Tyr561Ter)	FLCN (Y561* +1 more)	Single nucleotide variant (nonsense)	not specified	GUncertain significance
Select item 3254412	NM_144997.7(FLCN):c.340_349del (p.His114fs)	FLCN (H114fs)	Deletion (frameshift variant)	Birt-Hogg-Dube syndrome 1	GPathogenic
Select item 3254315	NM_144997.7(FLCN):c.619-2A>C	FLCN	Single nucleotide variant (splice acceptor variant)	Birt-Hogg-Dube syndrome 1	GLikely pathogenic
Select item 3242952	NC_000017.10:g.(?_17116969)_(17129656_?)dup	FLCN	Duplication	Birt-Hogg-Dube syndrome	GUncertain significance
Select item 3242951	NC_000017.10:g.(?_17127216)_(17140502_?)dup	FLCN	Duplication	Birt-Hogg-Dube syndrome	GUncertain significance
Select item 3242950	NC_000017.10:g.(?_17136102)_(17140502_?)dup	FLCN	Duplication	Birt-Hogg-Dube syndrome	GUncertain significance
Select item 3242949	NC_000017.10:g.(?_17140226)_(17140502_?)dup	FLCN	Duplication	Birt-Hogg-Dube syndrome	GUncertain significance
Select item 3242948	NC_000017.10:g.(?_17129480)_(17136215_?)del	FLCN	Deletion	Birt-Hogg-Dube syndrome	GPathogenic
Select item 3242947	NC_000017.10:g.(?_17118299)_(17119986_?)del	FLCN	Deletion	Birt-Hogg-Dube syndrome	GPathogenic
Select item 3242946	NC_000017.10:g.(?_17129480)_(17140502_?)del	FLCN	Deletion	Birt-Hogg-Dube syndrome	GPathogenic
Select item 3242945	NC_000017.10:g.(?_17135108)_(17135196_?)del	FLCN	Deletion	Birt-Hogg-Dube syndrome	GUncertain significance
Select item 3242944	NC_000017.10:g.(?_17116969)_(17117190_?)del	FLCN	Deletion	Birt-Hogg-Dube syndrome	GPathogenic
Select item 3241643	NM_144997.7(FLCN):c.1544T>C (p.Val515Ala)	FLCN (V515A +1 more)	Single nucleotide variant (missense variant)	Birt-Hogg-Dube syndrome 1	GUncertain significance
Select item 3241642	NM_144997.7(FLCN):c.1508G>A (p.Cys503Tyr)	FLCN (C503Y +1 more)	Single nucleotide variant (missense variant)	Birt-Hogg-Dube syndrome 1	GUncertain significance
Select item 3241641	NM_144997.7(FLCN):c.842_850del (p.Asp281_Leu283del)	FLCN	Deletion (inframe_deletion)	Birt-Hogg-Dube syndrome 1	GUncertain significance
Select item 3241640	NM_144997.7(FLCN):c.695A>G (p.Gln232Arg)	FLCN (Q232R +1 more)	Single nucleotide variant (missense variant)	Birt-Hogg-Dube syndrome 1	GUncertain significance
Select item 3241639	NM_144997.7(FLCN):c.53C>G (p.Thr18Ser)	FLCN (T18S)	Single nucleotide variant (missense variant)	Birt-Hogg-Dube syndrome 1	GUncertain significance
Select item 3241638	NM_144997.7(FLCN):c.94G>C (p.Gly32Arg)	FLCN (G32R)	Single nucleotide variant (missense variant)	Birt-Hogg-Dube syndrome 1	GUncertain significance
Select item 3241637	NM_144997.7(FLCN):c.820C>A (p.Leu274Met)	FLCN (L274M +1 more)	Single nucleotide variant (missense variant)	Birt-Hogg-Dube syndrome 1	GUncertain significance
Select item 3229263	NM_144997.7(FLCN):c.993_994delinsAT (p.Leu332Phe)	FLCN (L332F +1 more)	Indel (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3229262	NM_144997.7(FLCN):c.97dup (p.Asp33fs)	FLCN (D33fs)	Duplication (frameshift variant)	Hereditary cancer-predisposing syndrome	GPathogenic
Select item 3229261	NM_144997.7(FLCN):c.871+4A>G	FLCN (E292G)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3229260	NM_144997.7(FLCN):c.820C>T (p.Leu274=)	FLCN	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3229259	NM_144997.7(FLCN):c.750G>C (p.Leu250=)	FLCN	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3229258	NM_144997.7(FLCN):c.704G>A (p.Gly235Asp)	FLCN (G235D +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3229256	NM_144997.7(FLCN):c.639T>G (p.Phe213Leu)	FLCN (F213L +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3229255	NM_144997.7(FLCN):c.621G>A (p.Val207=)	FLCN	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3229254	NM_144997.7(FLCN):c.614T>A (p.Leu205His)	FLCN (L205H +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3229253	NM_144997.7(FLCN):c.550A>G (p.Asn184Asp)	FLCN (N184D +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3229252	NM_144997.7(FLCN):c.443A>G (p.His148Arg)	FLCN (H148R +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3229251	NM_144997.7(FLCN):c.425T>G (p.Phe142Cys)	FLCN (F142C +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3229250	NM_144997.7(FLCN):c.418C>A (p.Pro140Thr)	FLCN (P140T +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3229249	NM_144997.7(FLCN):c.399_405del (p.Cys134fs)	FLCN (C134fs +1 more)	Deletion (frameshift variant)	Hereditary cancer-predisposing syndrome	GPathogenic
Select item 3229248	NM_144997.7(FLCN):c.383_384delinsTT (p.Ser128Ile)	FLCN (S128I)	Indel (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3229247	NM_144997.7(FLCN):c.363C>T (p.Val121=)	FLCN	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3229246	NM_144997.7(FLCN):c.345C>T (p.Pro115=)	FLCN	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3229245	NM_144997.7(FLCN):c.336C>G (p.Pro112=)	FLCN	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3229244	NM_144997.7(FLCN):c.238G>A (p.Asp80Asn)	FLCN (D80N)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3229243	NM_144997.7(FLCN):c.206T>C (p.Val69Ala)	FLCN (V69A)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3229242	NM_144997.7(FLCN):c.200C>T (p.Ala67Val)	FLCN (A67V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	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 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 3229239	NM_144997.7(FLCN):c.1723_1729delinsCCACAGC (p.Ser575_Ser577delinsProGlnPro)	FLCN	Indel (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3229238	NM_144997.7(FLCN):c.1674C>T (p.Ser558=)	FLCN	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3229237	NM_144997.7(FLCN):c.1668C>T (p.Gly556=)	FLCN	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3229236	NM_144997.7(FLCN):c.1644G>A (p.Lys548=)	FLCN	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3229235	NM_144997.7(FLCN):c.1543G>T (p.Val515Leu)	FLCN (V515L +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3229234	NM_144997.7(FLCN):c.1527G>A (p.Glu509=)	FLCN	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3229233	NM_144997.7(FLCN):c.1467T>A (p.Ala489=)	FLCN	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign

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