| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Duplication (frameshift variant) | not provided +1 more | |
| | | Indel (frameshift variant) | Autosomal recessive retinitis pigmentosa | |
| | | Deletion (frameshift variant) | Retinal dystrophy +1 more | |
| | | Duplication (frameshift variant) | Retinitis pigmentosa 25 +3 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene