| | | Single nucleotide variant (intron variant) | Retinitis pigmentosa 1 | |
| | | Deletion (frameshift variant) | Retinitis pigmentosa 1 | |
| | LOC126860392, RP1 (P1648fs) | Duplication (frameshift variant +1 more) | Retinitis pigmentosa 1 | |
| | | Single nucleotide variant (missense variant +1 more) | Retinitis pigmentosa 1 | |
| | | Deletion (frameshift variant +1 more) | Retinitis pigmentosa 1 | |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa 1 | |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa 1 | |
| | | Deletion (frameshift variant +1 more) | Retinitis pigmentosa 1 | |
| | | Single nucleotide variant (splice acceptor variant) | Retinitis pigmentosa 1 | |
| | | Indel (frameshift variant +1 more) | Retinitis pigmentosa 1 | |
| | LOC126860392, RP1 (R1668G) | Single nucleotide variant (missense variant +1 more) | Retinitis pigmentosa 1 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Retinitis pigmentosa 1 +1 more | |
| | | Duplication (frameshift variant +1 more) | Retinitis pigmentosa 1 +1 more | GPathogenic/Likely pathogenic |
| | LOC126860392, RP1 (E1750*) | Single nucleotide variant (nonsense +1 more) | Retinitis pigmentosa 1 | |
| | | Duplication (frameshift variant) | Retinitis pigmentosa 1 | |
| | | Single nucleotide variant (nonsense +1 more) | Retinitis pigmentosa 1 | |
| | | Deletion (frameshift variant +1 more) | Retinitis pigmentosa 1 | |
| | LOC126860392, RP1 (K1855fs) | Deletion (frameshift variant +1 more) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant +1 more) | Retinitis pigmentosa 1 | |
| | | Deletion (frameshift variant +1 more) | Retinitis pigmentosa 1 | |
| | | Deletion (inframe_deletion +1 more) | Retinitis pigmentosa 1 | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (nonsense) | not provided +1 more | |
| | | Deletion (frameshift variant +1 more) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +1 more | |
| | | Deletion (frameshift variant +1 more) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense +1 more) | Retinitis pigmentosa 1 | |
| | | Single nucleotide variant (nonsense +1 more) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Deletion | Retinitis pigmentosa 1 | |
| | | Deletion (intron variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant +1 more) | not provided +1 more | |
| | LOC126860392, RP1 (A1974fs) | Deletion (frameshift variant +1 more) | Retinitis pigmentosa 1 | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant +1 more) | Retinitis pigmentosa 1 | |
| | | Single nucleotide variant (nonsense +1 more) | Retinitis pigmentosa 1 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Retinitis pigmentosa 1 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | LOC126860392, RP1 (Y1636*) | Single nucleotide variant (nonsense +1 more) | Retinitis pigmentosa 1 | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +2 more | |
| | | Single nucleotide variant (nonsense +1 more) | Retinitis pigmentosa 1 +1 more | |
| | | Deletion (frameshift variant) | Retinitis pigmentosa 1 +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense +1 more) | Retinitis pigmentosa 1 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense +1 more) | Retinitis pigmentosa 1 | |
| | | Deletion (frameshift variant +1 more) | Retinitis pigmentosa +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant +1 more) | Retinitis pigmentosa 1 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Retinitis pigmentosa 1 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Retinitis pigmentosa 1 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Retinitis pigmentosa 1 | |
| | | Single nucleotide variant (intron variant) | Retinitis pigmentosa 1 | |
| | | Single nucleotide variant (missense variant +1 more) | Retinitis pigmentosa +2 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant +1 more) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Duplication (frameshift variant +1 more) | Retinitis pigmentosa +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense +1 more) | Autosomal recessive retinitis pigmentosa +1 more | |
| | | Single nucleotide variant (nonsense) | Retinitis pigmentosa 1 | |
| | | Single nucleotide variant (missense variant) | Retinal dystrophy +5 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (frameshift variant) | not provided | |
| | | Deletion (frameshift variant) | Retinitis pigmentosa 1 | |
| | | Single nucleotide variant (nonsense) | Retinal dystrophy +1 more | GPathogenic/Likely pathogenic |
| | LOC126860392, RP1 (D1702fs) | Deletion (frameshift variant) | Retinitis pigmentosa 1 | |
| | LOC126860392, RP1 (Y1673fs) | Deletion (frameshift variant) | not provided +2 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | Retinitis pigmentosa 1 +2 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | not provided | |
| | | Duplication (frameshift variant) | Retinal dystrophy +3 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | Retinitis pigmentosa 1 +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa +1 more | |
| | LOC126860392, RP1 (L1901F) | Single nucleotide variant (missense variant) | Retinitis pigmentosa 1 +2 more | |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa 1 +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +3 more | |
| | | Single nucleotide variant (synonymous variant) | Retinitis pigmentosa 1 +2 more | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | GConflicting classifications of pathogenicity |
| | | Duplication (frameshift variant) | not provided | |
| | | Deletion (frameshift variant) | Retinitis pigmentosa 1 +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Retinitis pigmentosa +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Retinal dystrophy +4 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | LOC126860392, RP1 (R1933*) | Single nucleotide variant (nonsense) | not specified +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Retinitis pigmentosa 1 +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Retinal dystrophy +4 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | |
| | LOC126860392, RP1 (S1691P) | Single nucleotide variant (missense variant) | Retinal dystrophy +4 more | |
| | LOC126860392, RP1 (A1670T) | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa +2 more | GConflicting classifications of pathogenicity |
| | | Duplication (nonsense) | Retinitis pigmentosa 1 | |
| | | Single nucleotide variant (missense variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa +4 more | |
| | | Single nucleotide variant (nonsense) | Retinitis pigmentosa 1 +1 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | Retinitis pigmentosa 1 | |
| | | Microsatellite (frameshift variant +1 more) | Retinal dystrophy +1 more | |
| | | Single nucleotide variant (nonsense) | not provided +2 more | |