ClinVar Miner

List of variants in gene FLCN reported as likely benign for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 47
Download table as spreadsheet
HGVS dbSNP
NM_144997.7(FLCN):c.*17G>T rs115885284
NM_144997.7(FLCN):c.-29G>A rs151144873
NM_144997.7(FLCN):c.-45A>G rs571154058
NM_144997.7(FLCN):c.1059G>A (p.Arg353=) rs751513488
NM_144997.7(FLCN):c.1062+7G>A rs540198776
NM_144997.7(FLCN):c.1149C>T (p.Leu383=) rs150752548
NM_144997.7(FLCN):c.1176+14T>A rs757366854
NM_144997.7(FLCN):c.1177-21G>A rs150687840
NM_144997.7(FLCN):c.1227C>T (p.Tyr409=) rs561236067
NM_144997.7(FLCN):c.1269C>T (p.His423=) rs41464156
NM_144997.7(FLCN):c.1278C>T (p.Ile426=) rs41459448
NM_144997.7(FLCN):c.1281C>G (p.Pro427=) rs372207262
NM_144997.7(FLCN):c.1287C>T (p.His429=) rs374707789
NM_144997.7(FLCN):c.1300+12C>T rs565983064
NM_144997.7(FLCN):c.1300+15G>A rs751264915
NM_144997.7(FLCN):c.1301-18G>A rs186967236
NM_144997.7(FLCN):c.1332C>T (p.Ala444=) rs141283741
NM_144997.7(FLCN):c.1333G>A (p.Ala445Thr) rs41419545
NM_144997.7(FLCN):c.135G>A (p.Ala45=) rs759930161
NM_144997.7(FLCN):c.1389C>T (p.Tyr463=) rs137852929
NM_144997.7(FLCN):c.1414C>G (p.Pro472Ala) rs151312899
NM_144997.7(FLCN):c.1418T>C (p.Val473Ala) rs144883828
NM_144997.7(FLCN):c.1464G>A (p.Ala488=) rs747029882
NM_144997.7(FLCN):c.1494T>C (p.Asp498=) rs1555606990
NM_144997.7(FLCN):c.1509C>T (p.Cys503=) rs927844338
NM_144997.7(FLCN):c.1523A>G (p.Lys508Arg) rs199643834
NM_144997.7(FLCN):c.1557T>C (p.Phe519=) rs1555606453
NM_144997.7(FLCN):c.1692C>T (p.His564=) rs201810397
NM_144997.7(FLCN):c.1704G>A (p.Thr568=) rs147554296
NM_144997.7(FLCN):c.204C>T (p.Ser68=) rs371947198
NM_144997.7(FLCN):c.205G>A (p.Val69Ile) rs567617762
NM_144997.7(FLCN):c.249+13G>C rs200103733
NM_144997.7(FLCN):c.397-12G>T rs199958635
NM_144997.7(FLCN):c.42C>T (p.His14=) rs766288960
NM_144997.7(FLCN):c.450T>C (p.Phe150=) rs200672897
NM_144997.7(FLCN):c.592G>A (p.Asp198Asn) rs200168437
NM_144997.7(FLCN):c.618+15G>T rs1057522057
NM_144997.7(FLCN):c.619-20C>T rs202217257
NM_144997.7(FLCN):c.687C>T (p.Phe229=) rs754710935
NM_144997.7(FLCN):c.708C>T (p.Asn236=) rs750394475
NM_144997.7(FLCN):c.729G>A (p.Ser243=) rs377261933
NM_144997.7(FLCN):c.779+10G>A rs376357696
NM_144997.7(FLCN):c.871+16T>A rs116643153
NM_144997.7(FLCN):c.871+47G>A rs142934950
NM_144997.7(FLCN):c.954A>G (p.Glu318=) rs1555608573
NM_144997.7(FLCN):c.959G>A (p.Arg320Gln) rs143483053
NM_144997.7(FLCN):c.977C>T (p.Pro326Leu) rs138031155

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.