| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +4 more | |
| | | Single nucleotide variant (synonymous variant) | Cowden syndrome 6 +1 more | |
| | | Single nucleotide variant (synonymous variant) | AKT1-related disorder +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (intron variant) | Cowden syndrome 6 +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cowden syndrome 6 +1 more | |
Click to view in NCBI Gene