List of variants in gene NCF4 reported as benign for immune system disorder

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: 19

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000631.5(NCF4):c.758+57T>C	rs2075939	0.86715
NM_000631.5(NCF4):c.627+34A>G	rs2072710	0.65446
NM_000631.5(NCF4):c.528+16A>G	rs2072708	0.64364
NM_000631.5(NCF4):c.735C>T (p.Tyr245=)	rs2072712	0.12064
NM_000631.5(NCF4):c.69G>A (p.Ser23=)	rs10854695	0.04124
NM_000631.5(NCF4):c.63C>T (p.Ala21=)	rs34373276	0.02859
NM_000631.5(NCF4):c.470+20G>C	rs6000454	0.02766
NM_000631.5(NCF4):c.628-14C>A	rs56071149	0.01126
NM_000631.5(NCF4):c.240T>C (p.Ser80=)	rs35431748	0.00749
NM_000631.5(NCF4):c.343-4A>G	rs79312013	0.00347
NM_000631.5(NCF4):c.705C>T (p.Asp235=)	rs150656826	0.00205
NM_000631.5(NCF4):c.271+7G>A	rs201881905	0.00127
NM_000631.5(NCF4):c.172C>T (p.Arg58Cys)	rs143532979	0.00103
NM_000631.5(NCF4):c.478G>A (p.Val160Met)	rs150103256	0.00093
NM_000631.5(NCF4):c.258G>A (p.Leu86=)
NM_000631.5(NCF4):c.32+1258T>C	rs4821544
NM_000631.5(NCF4):c.471-17del
NM_000631.5(NCF4):c.528+17C>A	rs36099901
NM_000631.5(NCF4):c.528+18G>C	rs6000455

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.