List of variants in gene FGD4 reported as likely benign for Inborn genetic diseases

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 27

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.1143G>A (p.Ser381=)	rs34555341	0.00517
NM_001370298.3(FGD4):c.1296C>T (p.Phe432=)	rs151083690	0.00214
NM_001370298.3(FGD4):c.647C>T (p.Thr216Ile)	rs145115430	0.00213
NM_001370298.3(FGD4):c.1777C>A (p.Pro593Thr)	rs138160928	0.00168
NM_001370298.3(FGD4):c.666A>T (p.Ala222=)	rs139357821	0.00152
NM_001370298.3(FGD4):c.2070C>G (p.Ala690=)	rs188104446	0.00106
NM_001370298.3(FGD4):c.740T>C (p.Leu247Pro)	rs142609007	0.00033
NM_001370298.3(FGD4):c.785C>T (p.Thr262Met)	rs200732890	0.00030
NM_001370298.3(FGD4):c.890G>A (p.Gly297Asp)	rs201826412	0.00024
NM_001370298.3(FGD4):c.2193C>T (p.Ser731=)	rs147136365	0.00021
NM_001370298.3(FGD4):c.2625T>C (p.Ala875=)	rs200144770	0.00018
NM_001370298.3(FGD4):c.1046A>G (p.Asn349Ser)	rs147969494	0.00014
NM_001370298.3(FGD4):c.1075G>A (p.Val359Ile)	rs528790143	0.00011
NM_001370298.3(FGD4):c.2517C>T (p.Ser839=)	rs777555137	0.00009
NM_001370298.3(FGD4):c.603A>G (p.Gln201=)	rs771558628	0.00008
NM_001370298.3(FGD4):c.433T>C (p.Ser145Pro)	rs369365466	0.00004
NM_001370298.3(FGD4):c.2373G>A (p.Glu791=)	rs201822384	0.00003
NM_001370298.3(FGD4):c.1194T>C (p.Asn398=)	rs201678865	0.00002
NM_001370298.3(FGD4):c.2133A>G (p.Ala711=)	rs771910342	0.00001
NM_001370298.3(FGD4):c.2148G>A (p.Arg716=)	rs372451301	0.00001
NM_001370298.3(FGD4):c.1971C>A (p.Ile657=)	rs61748364
NM_001370298.3(FGD4):c.2122C>A (p.Pro708Thr)	rs144693221
NM_001370298.3(FGD4):c.2361T>G (p.Leu787=)	rs1358873743
NM_001370298.3(FGD4):c.559C>T (p.Pro187Ser)	rs2540545878
NM_001370298.3(FGD4):c.828T>A (p.Pro276=)	rs1295234161
NM_001370298.3(FGD4):c.892A>G (p.Ile298Val)	rs769174179

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.