List of variants in gene FLCN reported as uncertain significance for not specified

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: 37

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_144997.7(FLCN):c.959G>A (p.Arg320Gln)	rs143483053	0.00071
NM_144997.7(FLCN):c.715C>T (p.Arg239Cys)	rs78683075	0.00024
NM_144997.7(FLCN):c.396+4A>G	rs370353839	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.580C>T (p.Arg194Trp)	rs138070947	0.00017
NM_144997.7(FLCN):c.113G>T (p.Ser38Ile)	rs139418842	0.00016
NM_144997.7(FLCN):c.1463C>T (p.Ala488Val)	rs200660337	0.00014
NM_144997.7(FLCN):c.552C>A (p.Asn184Lys)	rs143525924	0.00007
NM_144997.7(FLCN):c.802C>T (p.Arg268Trp)	rs762370059	0.00007
NM_144997.7(FLCN):c.1283C>T (p.Pro428Leu)	rs199889477	0.00006
NM_144997.7(FLCN):c.346C>A (p.Gln116Lys)	rs398124536	0.00005
NM_144997.7(FLCN):c.1513G>A (p.Val505Ile)	rs376715412	0.00004
NM_144997.7(FLCN):c.1637A>G (p.Asn546Ser)	rs775149348	0.00003
NM_144997.7(FLCN):c.1049G>A (p.Arg350Gln)	rs190786280	0.00002
NM_144997.7(FLCN):c.1084C>T (p.Arg362Cys)	rs557336321	0.00002
NM_144997.7(FLCN):c.1174C>T (p.Arg392Trp)	rs1060502374	0.00002
NM_144997.7(FLCN):c.703G>A (p.Gly235Ser)	rs200693409	0.00002
NM_144997.7(FLCN):c.1390G>A (p.Glu464Lys)	rs1471793185	0.00001
NM_144997.7(FLCN):c.1599G>C (p.Gln533His)	rs190965235	0.00001
NM_144997.7(FLCN):c.1635C>G (p.Asp545Glu)	rs760329266	0.00001
NM_144997.7(FLCN):c.169C>T (p.Arg57Trp)	rs746507528	0.00001
NM_144997.7(FLCN):c.1700C>T (p.Ser567Phe)	rs1466102804	0.00001
NM_144997.7(FLCN):c.410G>A (p.Arg137His)	rs1289872207	0.00001
NM_144997.7(FLCN):c.535C>T (p.Arg179Trp)	rs774358971	0.00001
NM_144997.7(FLCN):c.603G>T (p.Gln201His)	rs759405317	0.00001
NM_144997.7(FLCN):c.680C>T (p.Thr227Met)	rs747675386	0.00001
NM_144997.7(FLCN):c.1033G>C (p.Val345Leu)	rs2144893824
NM_144997.7(FLCN):c.1434G>A (p.Val478=)	rs1131690834
NM_144997.7(FLCN):c.1708C>T (p.Arg570Cys)	rs752161850
NM_144997.7(FLCN):c.187C>G (p.Pro63Ala)	rs2047305711
NM_144997.7(FLCN):c.424TTC[1] (p.Phe143del)	rs764153620
NM_144997.7(FLCN):c.457A>G (p.Ser153Gly)	rs1479341645
NM_144997.7(FLCN):c.52A>G (p.Thr18Ala)	rs761993256
NM_144997.7(FLCN):c.603G>C (p.Gln201His)
NM_144997.7(FLCN):c.659A>T (p.Gln220Leu)	rs2047129363
NM_144997.7(FLCN):c.665T>G (p.Met222Arg)	rs1555609889

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.