| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome | |
| | | Single nucleotide variant (splice donor variant) | COQ4-related disorder +2 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene