| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (nonsense +2 more) | See cases | |
| | | Deletion (frameshift variant +2 more) | See cases | |
| | | Single nucleotide variant (missense variant +2 more) | not provided +9 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene