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. Author manuscript; available in PMC: 2019 Jan 1.
Published in final edited form as: Prog Retin Eye Res. 2017 Oct 16;62:1–23. doi: 10.1016/j.preteyeres.2017.10.002

Table 3. Clinical classification of rhodopsin RP mutations.

Class A phenotype refers to a severe early-onset loss of rod function. Class B refers to a milder phenotype, with retained rod function at least in certain retinal regions.

Phenotype Mutation Reference
Class A L88P1, L131P1, R135L/G/W2, E181K2, Q344P1, V345L2, P347L2 1Audo et al., (2010)
2Cideciyan et al., (1998)
3Iannaccone et al., (2006)
Class B N15S1, T17M2, P23H2, T58R2, Q64ter2, V87D2, G89D2, G106R2, P180A3, G188R3, D190G/Y2, T193M2, M207K2, Q312ter2, T342M2, Q344ter2 1Audo et al., (2010)
2Cideciyan et al., (1998)
3Iannaccone et al., (2006)