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. Author manuscript; available in PMC: 2006 Jun 12.
Published in final edited form as: Invest Ophthalmol Vis Sci. 2004 Nov;45(11):3863–3870. doi: 10.1167/iovs.04-0590

TABLE 3.

Sequence Variants Identified in GCAP1 Gene

Protein Nucleotide Patient Diagnosis
None c.-26A>G 065-001 Achromatopsia
T114I c.341C>T 199-005 Atypical RP
I143NT c.428delTinsACAC 195-001 Cone degeneration
None g.IVS3+171delG 065-011* Achromatopsia
D189D c.577C>T 111-007 Achromatopsia
D189D c.577C>T 270-003 Macular degeneration
*

This patient was later shown to be a homozygote with the pathogenic mutation T383fs in the CNGB3 gene encoding β-subunit of the cone cGMP-gated channel (data not shown).