List of variants in gene FGD4 reported by Eurofins NTD LLC (GA)

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 7

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001370298.3(FGD4):c.1971C>T (p.Ile657=)	rs61748364	0.00526
NM_001370298.3(FGD4):c.1296C>T (p.Phe432=)	rs151083690	0.00230
NM_001370298.3(FGD4):c.666A>T (p.Ala222=)	rs139357821	0.00161
NM_001370298.3(FGD4):c.2560G>A (p.Val854Met)	rs61753359	0.00131
NM_001370298.3(FGD4):c.2070C>G (p.Ala690=)	rs188104446	0.00106
NM_001370298.3(FGD4):c.2122C>A (p.Pro708Thr)	rs144693221
NM_001370298.3(FGD4):c.846C>G (p.Asp282Glu)	rs904582

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.