| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Duplication (frameshift variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Tuberous sclerosis 1 +1 more | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Duplication (frameshift variant) | not provided | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (nonsense) | Tuberous sclerosis 1 +4 more | |
| | | Deletion (frameshift variant) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (splice donor variant) | not provided | |
| | | Single nucleotide variant (nonsense +1 more) | not provided | |
| | | Duplication (frameshift variant) | not provided +5 more | |
| | | Single nucleotide variant (nonsense) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Tuberous sclerosis 1 +1 more | GConflicting classifications of pathogenicity |
| | | Duplication (5 prime UTR variant +1 more) | not provided | |
| | | Microsatellite (frameshift variant +2 more) | not provided | |
| | | Single nucleotide variant (intron variant +1 more) | Tuberous sclerosis 1 +1 more | |
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