| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (splice acceptor variant +1 more) | Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency | |
| | | Single nucleotide variant (missense variant +1 more) | Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
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