Table 2.

Summary of genetic variation in familial aniridic patients

S No	Systematic Name	Codon	Exon/Intron	Domain	Common Name patient ID	Type of Mutation	Interpretation	Gene bank Accession No.
01	c.1080 C>T	R240X	exon 9	Homeodomain	ANF/6-1 female	Premature termination	Arginine to stop codon	--
03	c.1174del TG	271	exon 10	PST region	ANF/2-1 female	Deletion	Novel mutation	DQ251040
05	c.710del C	116	exon 6	Paired domain	ANF/7-1 male	Deletion	Novel mutation	DQ251039
07	c.406delTT	15	exon 5	Paired domain	ANF9-1female	Deletion	Novel mutation	DQ251038
09	c.393ins5	11	exon 5	Paired domain	ANF8-1 male	Insertion	Novel mutation	DQ251037