List of variants reported as likely pathogenic for combined oxidative phosphorylation deficiency by Randwick Genomics Laboratory, Prince of Wales Hospital Sydney, Australia, New South Wales Health Pathology

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_005932.4(MIPEP):c.1534C>G (p.His512Asp)	rs779598020	0.00006
NM_005932.4(MIPEP):c.1259T>C (p.Leu420Pro)	rs1869287041

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