| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Combined oxidative phosphorylation defect type 20 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (intron variant) | Combined oxidative phosphorylation defect type 20 | |
| | | Single nucleotide variant (nonsense) | Combined oxidative phosphorylation defect type 20 | |
Click to view in NCBI Gene