| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal recessive 6 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided | |
Click to view in NCBI Gene