ClinVar Miner

List of variants in gene FGD4 reported as likely benign for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
Download table as spreadsheet
HGVS dbSNP
NM_001304481.1(FGD4):c.20C>G (p.Thr7Ser) rs187853007
NM_001304481.1(FGD4):c.220C>A (p.Pro74Thr) rs199744649
NM_139241.3(FGD4):c.-246+9C>T rs531501340
NM_139241.3(FGD4):c.1191+13C>T rs557373932
NM_139241.3(FGD4):c.1366C>A (p.Pro456Thr) rs138160928
NM_139241.3(FGD4):c.1512-7A>G rs200542541
NM_139241.3(FGD4):c.1659C>G (p.Ala553=) rs188104446
NM_139241.3(FGD4):c.1711C>A (p.Pro571Thr) rs144693221
NM_139241.3(FGD4):c.1737G>A (p.Arg579=) rs372451301
NM_139241.3(FGD4):c.1761+8A>T rs761674021
NM_139241.3(FGD4):c.1782C>T (p.Ser594=) rs147136365
NM_139241.3(FGD4):c.1962G>A (p.Glu654=) rs201822384
NM_139241.3(FGD4):c.2040C>T (p.Pro680=) rs1314359233
NM_139241.3(FGD4):c.255A>T (p.Ala85=) rs139357821
NM_139241.3(FGD4):c.837-16dup rs368420700
NM_139241.3(FGD4):c.993+10C>T rs374656859

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.