| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (splice acceptor variant +1 more) | Hypomyelination and Congenital Cataract | |
| | | Single nucleotide variant (splice donor variant) | Hypomyelination and Congenital Cataract | |
| | | Single nucleotide variant (missense variant) | Hypomyelination and Congenital Cataract | |
| | | Single nucleotide variant (splice donor variant) | Hypomyelination and Congenital Cataract | |
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