| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Duplication | not provided | |
| | | Single nucleotide variant (missense variant) | Epilepsy, familial focal, with variable foci 4 | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Microsatellite (inframe_deletion) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Developmental and epileptic encephalopathy, 62 +1 more | |
| | | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy, 62 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
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