Table 4. Summary of mutations identified in LIM2 associated with cataractogenesis.

No	Nucleotide Change	Amino Acid Change	Exon	Cataractogenesis Onset	Cataract Phenotype	Additional Phenotypes	Ethnicity	Reference
1	c.313T>G	p.F105V	3	Presenile	pulverulent cortical/ nuclear	-	Iraqi/Arab	[17]
2	c.587G>A	p.G154E	4/5	Congenital	total	nystagmus; dense amblyopia	Indian	[31]
3	c.233G>A	p.G78D	3	Congenital	nuclear	nystagmus	Pakistani	current study