| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Congenital myasthenic syndrome 9 +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Congenital myasthenic syndrome 9 +2 more | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Fetal akinesia deformation sequence 1 +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Fetal akinesia deformation sequence 1 +2 more | |
| | | Insertion (inframe_insertion) | Fetal akinesia deformation sequence 1 +2 more | |
| | | Single nucleotide variant (missense variant) | Fetal akinesia deformation sequence 1 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Fetal akinesia deformation sequence 1 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Congenital myasthenic syndrome 9 +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GPathogenic/Likely pathogenic |
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