NM_000180.4(GUCY2D):c.2765A>G (p.Tyr922Cys) is a missense variant that replaces tyrosine with cysteine at position p.922, which is located within the guanylate cyclase catalytic domain that exhibits intolerance to missense variation (PM1_Supporting). This variant is absent from gnomAD v4.1.0 (PM2_Supporting). This variant has been reported in at least 1 proband with early-onset severe retinal dystrophy who harbored the variant in the compound heterozygous state confirmed in trans with the NM_000180.4(GUCY2D):c.2983C>T (p.Arg995Trp) variant, which was previously classified as likely pathogenic by the ClinGen LCA/eoRD VCEP (1 pt, PMID: 29844330, PM3). The computational predictor REVEL gives a score of 0.946 which is above the ClinGen LCA/eoRD VCEP threshold of ≥0.773 and predicts a damaging effect on RetGC-1 protein function (PP3_Moderate). The splicing impact predictor SpliceAI gives a score of 0.03 for splice donor gain, which is below the ClinGen LCA/eoRD VCEP recommended threshold of ≥0.2 and does not strongly predict an impact on splicing. In summary, this variant meets the criteria to be classified as likely pathogenic for GUCY2D-related recessive retinopathy based on the ACMG/AMP criteria applied, as specified by the ClinGen LCA/eoRD VCEP: PM2_Supporting, PM1_Supporting, PM3, and PP3_Moderate. (VCEP specifications version 1.0.0; date of approval 01/22/2025).