For instance, we identified a heterozygous c.407G>A/p.Gly136Glu of the CLRN1 variant in a patient (as6) presenting with RP, a heterozygous c.1120G>A/p.Asp374Asn of the LSS variant in a patient (ju6) with cataract, and a heterozygous c.1255C>T/p.Arg419Cys of the TUB variant in a patient (li1) with RP. Here, CLRN1 is linked to retinitis pigmentosa 1.