C.5836-2A> G that abolishes the acceptor splice site in intron 41 was previously reported in a CRD patient of a Chinese cohort.[6] C.1356+1G>A is being reported for the first time in a Stargardt disease-affected patient, although c.1356+1G>T was previously reported in age-related macular degeneration patients.[26] This signifies potential variability of phenotypic features associated with any ABCA4 mutation. The gene discussed is ABCA4; the disease is cone-rod dystrophy.