| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Congenital hyperammonemia, type I | |
| | | Deletion (frameshift variant +1 more) | Pulmonary hypertension, neonatal, susceptibility to +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Congenital hyperammonemia, type I | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant +1 more) | Congenital hyperammonemia, type I +1 more | GConflicting classifications of pathogenicity |
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