List of variants in gene TIMM22 reported as pathogenic for combined oxidative phosphorylation deficiency

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

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_013337.4(TIMM22):c.97G>C (p.Val33Leu)	rs149879547	0.00440
NM_013337.4(TIMM22):c.75C>A (p.Tyr25Ter)	rs754537066	0.00004

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