Table 2 of Santana, Mol Vis 2009; 15:793-800.
Table 2. Cataract phenotypes, mutations, and polymorphisms identified in this study.
| Family ID |
Cataract phenotype |
Mutation | Polymorphism | ||||
|---|---|---|---|---|---|---|---|
| CRYAA | CRYGC | CRYGD | CRYAA | CRYGC | CRYGD | ||
| Family 1 | Nuclear+Microcornea | D2D | S119S | Y17Y, R95R | |||
| Family 2 | Lamellar | D2D | R95R | ||||
| Family 3 | Nuclear | D2D | Y17Y, R95R | ||||
| Family 4 | Nuclear | R12C | D2D | R95R | |||
| Family 5 | Lamellar | D2D | R95R | ||||
| Family 6 | Lamellar | Y17Y, R95R | |||||
| Family 7 | Nuclear | D2D | Y17Y, R95R | ||||
| Family 8 | Nuclear+Microcornea | D2D | Y17Y, R95R | ||||
| Family 9 | Nuclear | D2D | |||||
| Family 10 | Nuclear | Y56X | D2D | Y17Y, R95R | |||
| Family 11 | Lamellar | D2D | Y17Y | ||||