| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (frameshift variant +1 more) | Autosomal dominant epilepsy with auditory features +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Epilepsy, familial temporal lobe, 1 +1 more | |
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