| | | Single nucleotide variant (missense variant) | not provided +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy, 14 +2 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nocturnal frontal lobe epilepsy 5 | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nocturnal frontal lobe epilepsy 5 | |
| | | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy, 14 +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy, 14 +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nocturnal frontal lobe epilepsy 5 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Developmental and epileptic encephalopathy, 14 +1 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nocturnal frontal lobe epilepsy 5 +1 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nocturnal frontal lobe epilepsy 5 +2 more | |
| | | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy, 14 | |
| | | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy, 14 +2 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nocturnal frontal lobe epilepsy 5 +1 more | |