| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (frameshift variant) | Epilepsy, familial focal, with variable foci 2 | |
| | | Single nucleotide variant (missense variant) | Epilepsy, familial focal, with variable foci 2 | |
| | | Single nucleotide variant (intron variant) | Epilepsy, familial focal, with variable foci 2 | |
| | | Single nucleotide variant (nonsense) | Inborn genetic diseases +2 more | GConflicting classifications of pathogenicity |
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