P56S (p.Pro56Ser) variant of RPE65 (Retinoid isomerohydrolase)
P56S (p.Pro56Ser) in RPE65 (Retinoid isomerohydrolase) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Leber congenital amaurosis 2; Retinitis pigmentosa 20. The record also includes variant effect predictions, published literature, and structural context.
P56S (p.Pro56Ser) variant details
- p.Pro56Ser
- rs1193374066
- ClinGen CA340749095
- ClinVar RCV003118341
- Ensembl rs1193374066
- Uncertain significance
- Leber congenital amaurosis 2; Retinitis pigmentosa 20
- Missense
- MutPred 0.35
- ClinVar: Uncertain significance (Leber congenital amaurosis 2; Retinitis pigmentosa 20)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- Cited in: Nonsyndromic Leber Congenital Amaurosis / Early-Onset Severe Retinal Dystrophy Overview. (PMID 30285347)
- Cited in: Autosomal Recessive RPE65-Related Retinal Degeneration. (PMID 31725251)