ClinVar Miner

List of variants in gene FLCN studied for none provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
Download table as spreadsheet
NM_144997.7(FLCN):c.1333G>A (p.Ala445Thr) rs41419545
NM_144997.7(FLCN):c.1419A>C (p.Val473=) rs141036419
NM_144997.7(FLCN):c.1697T>C (p.Met566Thr)
NM_144997.7(FLCN):c.268G>T (p.Ala90Ser) rs141140415
NM_144997.7(FLCN):c.33C>G (p.Cys11Trp)
NM_144997.7(FLCN):c.726A>T (p.Thr242=) rs113938514
NM_144997.7(FLCN):c.872-13A>G rs114970273
NM_144997.7(FLCN):c.890_893del (p.Glu297fs) rs398124541
NM_144997.7(FLCN):c.955_956insCCCCTGTGTTGCCAGAGAGTACAGAAAG (p.Gly319fs) rs1597591793

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.