| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | Epileptic encephalopathy, infantile or early childhood, 2 +1 more | |
| | | Single nucleotide variant (missense variant) | Epileptic encephalopathy, infantile or early childhood, 2 +2 more | GConflicting classifications of pathogenicity |
| | | Deletion (intron variant) | Epileptic encephalopathy, infantile or early childhood, 2 +1 more | |
Click to view in NCBI Gene