Table 3. List of variations unique to inherited cataract samples.
| Family | Location | Nucleotide position | Amino acid position |
|---|---|---|---|
| Family mt1A | MT-ND1 | T 4023 C | T 239 T |
| MT-T1 | T 4291 C | Non coding | |
| MT-ND4 | C 10797 T | P 13 L | |
| MT-CYB | T 15115 C | T 123 T | |
| Family mt2A | MT-ND1 | T 3394 C | Y 30 H |
| MT-ND1 | A 3511 G | T 69 A | |
| MT-ND1 | C 4171 T | L 289 L | |
| MT-ND5 | G 12372 A | L 12 L | |
| MT-ND5 | G 12501 A | M 55 M | |
| MT-ND5 | T 12696 C | Y 120 Y | |
| MT-ND5 | C 13943 T | T 536 M | |
| Family mt3A | MT-ND1 | A 3511 G | T 69 A |
The term ‘unique’ refers to mitochondrial sequence alterations found in inherited cataract samples while absent in unaffected members of the same family.