| | CRYGC, LOC100507443 (C130fs) | Duplication (frameshift variant) | Cataract 2, multiple types | |
| | CRYGC, LOC100507443 (N50S) | Single nucleotide variant (missense variant) | Cataract 2, multiple types | |
| | CRYGC, LOC100507443 (E135K) | Single nucleotide variant (missense variant) | Cataract 2, multiple types | |
| | CRYGC, LOC100507443 (V132fs) | Deletion (frameshift variant) | Cataract 2, multiple types | |
| | CRYGC, LOC100507443 (R142fs) | Deletion (frameshift variant) | Cataract 2, multiple types | |
| | CRYGC, LOC100507443 (S166F) | Single nucleotide variant (missense variant) | Developmental cataract +1 more | |
| | CRYGC, LOC100507443 (G129C) | Single nucleotide variant (missense variant) | Cataract 2, multiple types | |
| | CRYGC, LOC100507443 (W157*) | Single nucleotide variant (nonsense) | Cataract 2, multiple types | |
| | CRYGC, LOC100507443 (W157*) | Single nucleotide variant (nonsense) | not provided +1 more | |
| | CRYGC, LOC100507443 (R168W) | Single nucleotide variant (missense variant) | Nuclear pulverulent cataract +1 more | GConflicting classifications of pathogenicity |
| | CRYGC, LOC100507443 (C42fs) | Duplication (frameshift variant) | Cataract 2, multiple types | |