PRPH2 p.Arg220Pro
c.659G>C · rs61755810 · VCV860907
Pathogenic/Likely pathogenic
Multiple submitters
Classification
Pathogenic/Likely pathogenic
ClinVar
Review
Multiple submitters ★★☆☆
ClinVar · 5 submitters
gnomAD v4.1
Absent
absent from gnomAD v4.1
Conditions
3
patterned dystrophy of the retinal pigment epithelium
Computational evidence
| Protein change | ||
| Missense predictors do not apply to this variant type; conservation carries the signal. | ||
| REVEL | 0.882 | moderately pathogenic-leaning |
|---|---|---|
| Splicing | ||
| SpliceAI | <0.2 | no splice effect predicted · four deltas, not one · how we know |
| Constraint at this position | ||
| Conservation | phyloP 7.6 | GERP 1.6, phastCons 1 |
| Regional constraint | o/e 0.98 | unconstrained · MANE · 24 kb · p 0.64 · regional, not allelic |
| Overall | ||
| CADD | 32.0 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Absent from gnomAD v4.1. Not observed in any sequenced alleles — a rarity signal (ACMG PM2-supporting), not evidence of pathogenicity on its own.
Variant & gene context
- Gene
- PRPH2
- Protein
- p.Arg220Pro
- Coding
- c.659G>C
- MANE Select
- NM_000322
- dbSNP
- rs61755810
- Type
- single nucleotide variant
- Location
- chr6:42704534 (GRCh38)
- Gene constraint
- LOEUF 0.773 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 87.56 · 1 PDB
- Residue 220
- a UniProt-annotated variant site (in mdpt1; increased protein expression); a UniProt-annotated variant site (in mdpt1)
Similar variants
- PRPH2 p.Arg220Gln Pathogenic/Likely pathogenic ★★ same residue
- PRPH2 p.Arg220Trp Conflicting classifications of pathogenicity ★ same residue
- PRPH2 p.Arg220= Likely benign ★★ same residue
- PRPH2 p.Arg220Gly Conflicting classifications of pathogenicity ★ same residue
- PRPH2 c.581+1G>A Pathogenic ★★ same condition
- PRPH2 c.582-1G>A Pathogenic/Likely pathogenic ★★ same condition
- PRPH2 c.582-2A>T Pathogenic ★★ same condition
- PRPH2 c.828+3A>T Pathogenic ★★ same condition
Built on 18 open, versioned datasets — ClinVar, gnomAD, AlphaMissense, REVEL, ClinGen & more — plus Sugi Variant's own cross-source analysis. Source data 2026-01–2026-10, ClinVar 2026-10. Full sources & versions →
Cite Sugi Variant
Gür T. Sugi Variant: A Deterministic Per-Variant Germline Reference from a Knowledge Graph for Humans and AI Agents. 2026. doi:10.5281/zenodo.21509445. This variant: https://sugi.bio/variant/prph2-p-arg220pro (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown