List of variants in gene FLCN reported as likely benign for adenocarcinoma

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: 26

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HGVS	dbSNP	gnomAD frequency
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.619-20C>T	rs202217257	0.00037
NM_144997.7(FLCN):c.1326C>T (p.His442=)	rs145004158	0.00023
NM_144997.7(FLCN):c.1176+15T>C	rs550870270	0.00020
NM_144997.7(FLCN):c.1062+7G>A	rs540198776	0.00016
NM_144997.7(FLCN):c.1278C>T (p.Ile426=)	rs41459448	0.00016
NM_144997.7(FLCN):c.1432+8C>T	rs201898226	0.00009
NM_144997.7(FLCN):c.779+9C>T	rs373504780	0.00009
NM_144997.7(FLCN):c.792G>A (p.Ala264=)	rs140500421	0.00008
NM_144997.7(FLCN):c.867C>T (p.Leu289=)	rs367562964	0.00007
NM_144997.7(FLCN):c.396+7C>T	rs781155484	0.00006
NM_144997.7(FLCN):c.1692C>T (p.His564=)	rs201810397	0.00005
NM_144997.7(FLCN):c.1068G>T (p.Leu356=)	rs534904034	0.00004
NM_144997.7(FLCN):c.645C>T (p.Cys215=)	rs772360950	0.00004
NM_144997.7(FLCN):c.1380C>T (p.Leu460=)	rs773581294	0.00003
NM_144997.7(FLCN):c.450T>C (p.Phe150=)	rs200672897	0.00003
NM_144997.7(FLCN):c.1227C>T (p.Tyr409=)	rs561236067	0.00001
NM_144997.7(FLCN):c.1301-8T>C	rs571192457	0.00001
NM_144997.7(FLCN):c.1539-11G>C	rs368472222	0.00001
NM_144997.7(FLCN):c.619-8C>T	rs1274815686	0.00001
NM_144997.7(FLCN):c.780-13C>T	rs777670469	0.00001
NM_144997.7(FLCN):c.981A>G (p.Ala327=)	rs763078516	0.00001
NM_144997.7(FLCN):c.1353T>C (p.Pro451=)	rs1597580172
NM_144997.7(FLCN):c.756G>A (p.Ala252=)	rs746664975
NM_144997.7(FLCN):c.871+13T>C	rs770537219

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