| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Duplication | Early infantile epileptic encephalopathy with suppression bursts | |
| | | Deletion | Early infantile epileptic encephalopathy with suppression bursts | |
| | | Duplication | Developmental and epileptic encephalopathy, 33 +1 more | |
| | | Deletion | Autosomal dominant nocturnal frontal lobe epilepsy +1 more | |
| | | Duplication | Early infantile epileptic encephalopathy with suppression bursts +1 more | |
Click to view in NCBI Gene