| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (nonsense) | not provided +1 more | |
| | | Single nucleotide variant (nonsense) | Carnitine acylcarnitine translocase deficiency +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice donor variant) | Carnitine acylcarnitine translocase deficiency | |
| | | Single nucleotide variant (5 prime UTR variant) | Carnitine acylcarnitine translocase deficiency | |
Click to view in NCBI Gene