List of variants in gene MIPEP reported as likely benign for combined oxidative phosphorylation deficiency

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_005932.4(MIPEP):c.1728+7A>G	rs186873433	0.00064
NM_005932.4(MIPEP):c.2092G>A (p.Val698Ile)	rs567713935	0.00004
NM_005932.4(MIPEP):c.1728+5G>T

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