PDE6B p.Arg235=
c.705C>T · rs760596729 · VCV1603475
Likely benign
Multiple submitters
Classification
Likely benign
ClinVar
Review
Multiple submitters ★★☆☆
ClinVar · 2 submitters
gnomAD v4.1
Rare
very rare (popmax 0.0019%, nfe)
Computational evidence
| Protein change | ||
| Missense predictors do not apply to this variant type; conservation carries the signal. | ||
| Splicing | ||
| SpliceAI | — | not assessed · no allele here is in the release |
|---|---|---|
| Constraint at this position | ||
| Conservation | phyloP -4.2 | GERP -4.2 |
| Overall | ||
| CADD | 3.37 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.0019%
European (non-Finnish) · 22/1,160,528 alleles
Filtering AF
0.00124%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 0.00106%
Overall
0.0016%
23/1,440,312 alleles · very rare
| Ancestry group | Frequency | 1 in |
|---|---|---|
| European (non-Finnish)grpmax | 0.0019% | 52,751 |
| Remaining individualsnot grpmax-eligible | 0.00162% | 61,812 |
Rarity supports pathogenicity (ACMG PM2); frequency above a disease-specific BA1/BS1 threshold argues against it. A variant frequent in one ancestry group can be near-absent in others, so a single global figure can mislead.
Variant & gene context
- Gene
- PDE6B
- Protein
- p.Arg235=
- Coding
- c.705C>T
- MANE Select
- NM_000283
- dbSNP
- rs760596729
- Type
- single nucleotide variant
- Location
- chr4:635963 (GRCh38)
- Gene constraint
- LOEUF 1.238 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 89.72
- Residue 235
- the gaf 2 domain
Similar variants
- PDE6B p.Arg235Cys Uncertain significance ★★ ⚠ same residue
- PDE6B p.Arg235His Uncertain significance ★★ ⚠ same residue
- PDE6B p.Arg235Pro Uncertain significance ★ ⚠ same residue
- PDE6B p.Arg235fs Pathogenic ★ same residue
- PDE6B c.1059+2T>G Likely pathogenic ★★ same type
- PDE6B c.1060-1G>T Pathogenic/Likely pathogenic ★★ same type
- PDE6B c.1107+1G>T Likely pathogenic ★★ same type
- PDE6B c.1107+3A>G Pathogenic/Likely pathogenic ★★ same type
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/pde6b-p-arg235 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown