List of variants in gene combination NCAPH2, SCO2, TYMP reported as benign for Mitochondrial complex IV 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_005138.3(SCO2):c.633A>C (p.Ala211=)	rs12148	0.63421
NM_005138.3(SCO2):c.776C>T (p.Ala259Val)	rs8139305	0.00949
NM_005138.3(SCO2):c.59G>C (p.Arg20Pro)	rs140523

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