| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +2 more) | Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 +2 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant +2 more) | Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense +2 more) | Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 | |
| | | Deletion (splice donor variant) | Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 +1 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 | |
| | | Single nucleotide variant (missense variant +1 more) | Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 | |
| | | Deletion (frameshift variant +1 more) | Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GPathogenic/Likely pathogenic |
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