List of variants in gene FLCN reported as benign for Birt-Hogg-Dube syndrome

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: 72

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HGVS	dbSNP	gnomAD frequency
NM_144997.6(FLCN):c.-487G>C	rs1736209	0.72552
NM_144997.7(FLCN):c.*1403T>C	rs7218795	0.72029
NM_144997.7(FLCN):c.*557T>C	rs3803761	0.71694
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.397-14C>T	rs1736219	0.40309
NM_144997.7(FLCN):c.1433-38A>G	rs34235236	0.21634
NM_144997.7(FLCN):c.*1336G>T	rs7218992	0.12032
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.*914C>T	rs7223831	0.04505
NM_144997.7(FLCN):c.-90A>G	rs8069957	0.04414
NM_144997.7(FLCN):c.-93C>T	rs115413827	0.03572
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.726A>T (p.Thr242=)	rs113938514	0.02907
NM_144997.7(FLCN):c.-97C>T	rs114481741	0.02691
NM_144997.7(FLCN):c.*956A>G	rs141650706	0.02638
NM_144997.7(FLCN):c.*442T>C	rs7224213	0.02480
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.-176G>A	rs117215381	0.00772
NM_144997.7(FLCN):c.1538+14T>G	rs112111994	0.00721
NM_144997.7(FLCN):c.*911G>A	rs571893996	0.00356
NM_144997.7(FLCN):c.1177-21G>A	rs150687840	0.00276
NM_144997.7(FLCN):c.-480G>C	rs564584154	0.00265
NM_144997.7(FLCN):c.*526T>C	rs574547835	0.00235
NM_144997.7(FLCN):c.1333G>A (p.Ala445Thr)	rs41419545	0.00217
NM_144997.7(FLCN):c.-29G>A	rs151144873	0.00213
NM_144997.7(FLCN):c.871+16T>A	rs116643153	0.00146
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+47G>A	rs142934950	0.00058
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.1149C>T (p.Leu383=)	rs150752548	0.00028
NM_144997.7(FLCN):c.*178A>G	rs145430714	0.00026
NM_144997.7(FLCN):c.715C>T (p.Arg239Cys)	rs78683075	0.00024
NM_144997.7(FLCN):c.*379G>A	rs117436649	0.00021
NM_144997.7(FLCN):c.1176+15T>C	rs550870270	0.00020
NM_144997.7(FLCN):c.592G>A (p.Asp198Asn)	rs200168437	0.00019
NM_144997.7(FLCN):c.1523A>G (p.Lys508Arg)	rs199643834	0.00018
NM_144997.7(FLCN):c.*528G>A	rs184006653	0.00017
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.1538+10A>C	rs12451312	0.00010
NM_144997.7(FLCN):c.779+9C>T	rs373504780	0.00009
NM_144997.7(FLCN):c.1300+14C>T	rs200823760	0.00005
NM_144997.7(FLCN):c.1692C>T (p.His564=)	rs201810397	0.00005
NM_144997.7(FLCN):c.249+13G>C	rs200103733	0.00005
NM_144997.7(FLCN):c.708C>T (p.Asn236=)	rs750394475	0.00005
NM_144997.7(FLCN):c.*4G>A	rs770795599	0.00004
NM_144997.7(FLCN):c.1300+12C>T	rs565983064	0.00004
NM_144997.7(FLCN):c.1428C>G (p.Asp476Glu)	rs756944795	0.00004
NM_144997.7(FLCN):c.1580G>A (p.Arg527Gln)	rs777826268	0.00003
NM_144997.7(FLCN):c.450T>C (p.Phe150=)	rs200672897	0.00003
NM_144997.7(FLCN):c.-430C>T	rs553452028	0.00001
NM_144997.7(FLCN):c.1464G>A (p.Ala488=)	rs747029882	0.00001
NM_144997.7(FLCN):c.1539-16T>G	rs553673947	0.00001
NM_144997.7(FLCN):c.*1182dup	rs199535675
NM_144997.7(FLCN):c.-134C>T	rs116581458
NM_144997.7(FLCN):c.1432+12del
NM_144997.7(FLCN):c.1432+12dup	rs2144836206
NM_144997.7(FLCN):c.75G>A (p.Leu25=)	rs200350612

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