ClinVar Miner

List of variants in gene FGD4 reported as uncertain significance by Inherited Neuropathy Consortium

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 14
Download table as spreadsheet
NM_001370298.3(FGD4):c.2039_2040del (p.Glu680fs) rs1565921326
NM_001370298.3(FGD4):c.2298_2302del (p.Lys767fs) rs751035912
NM_139241.3(FGD4):c.1132+1G>A rs1592388367
NM_139241.3(FGD4):c.1325G>A (p.Arg442His) rs281865063
NM_139241.3(FGD4):c.1698G>A (p.Met566Ile) rs281865064
NM_139241.3(FGD4):c.1762-2A>G rs281865065
NM_139241.3(FGD4):c.1772G>A (p.Trp591Ter) rs1592488602
NM_139241.3(FGD4):c.1886_1889del (p.Arg629fs) rs1592489096
NM_139241.3(FGD4):c.1890_1894del (p.Lys630fs) rs1592489165
NM_139241.3(FGD4):c.514dup (p.Ala172fs) rs1565869918
NM_139241.3(FGD4):c.837-1G>A rs1592368399
NM_139241.3(FGD4):c.837-2A>G rs1592368395
NM_139241.3(FGD4):c.893T>C (p.Met298Thr) rs63749871
NM_139241.3(FGD4):c.893T>G (p.Met298Arg) rs63749871

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.