List of variants in gene NDUFAF2 reported as uncertain significance for Mitochondrial complex I deficiency, nuclear type 1

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_174889.5(NDUFAF2):c.451G>A (p.Gly151Ser)	rs9885480	0.00369
NM_174889.5(NDUFAF2):c.422A>T (p.Glu141Val)	rs749677218	0.00011
NM_174889.5(NDUFAF2):c.131A>C (p.Gln44Pro)	rs775605330	0.00007
NM_174889.5(NDUFAF2):c.196G>C (p.Asp66His)	rs769579395	0.00005
NM_174889.5(NDUFAF2):c.423A>G (p.Glu141=)	rs550008432	0.00004
NM_174889.5(NDUFAF2):c.414T>A (p.Phe138Leu)	rs770172045	0.00003
NM_174889.5(NDUFAF2):c.98A>G (p.Tyr33Cys)	rs779872068	0.00002
NM_174889.5(NDUFAF2):c.100T>C (p.Tyr34His)	rs773988847	0.00001
NM_174889.5(NDUFAF2):c.128-14C>G	rs537327206
NM_174889.5(NDUFAF2):c.136A>G (p.Ile46Val)	rs1752321893

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