| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Deletion (inframe_deletion) | Choroidal dystrophy, central areolar, 1 +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Night blindness, congenital stationary, type1i +5 more | |
| | | Single nucleotide variant (missense variant) | Cone-rod dystrophy 6 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cone-rod dystrophy 6 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Leber congenital amaurosis 1 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Leber congenital amaurosis 1 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cone-rod dystrophy 6 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Leber congenital amaurosis 1 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cone-rod dystrophy 6 +1 more | |
| | | Single nucleotide variant (missense variant) | Leber congenital amaurosis 1 +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +7 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene