| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (missense variant +1 more) | Combined oxidative phosphorylation deficiency 35 | |
| | | Single nucleotide variant (nonsense +2 more) | TRIT1-related disorder +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +2 more) | Combined oxidative phosphorylation deficiency 35 +1 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene