| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (missense variant) | Autosomal dominant nocturnal frontal lobe epilepsy 3 +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal dominant nocturnal frontal lobe epilepsy 3 +3 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal dominant nocturnal frontal lobe epilepsy +5 more | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant nocturnal frontal lobe epilepsy +3 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +5 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
Click to view in NCBI Gene