PDE6B p.Asp406=
c.1218C>T · rs148190219 · VCV349373
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 -13 | GERP -4.5 |
| Overall | ||
| CADD | 2.498 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
| Ancestry group | Frequency | 1 in |
|---|---|---|
| Finnishnot grpmax-eligible | 0.364% | 275 |
| Ashkenazi Jewishnot grpmax-eligible | 0.22% | 455 |
| Middle Easterngrpmax | 0.0825% | 1,212 |
| Remaining individualsnot grpmax-eligible | 0.0784% | 1,275 |
| Admixed American | 0.0733% | 1,364 |
| European (non-Finnish) | 0.0711% | 1,406 |
| African / African-American | 0.0133% | 7,505 |
| East Asian | 0.00892% | 11,216 |
| South Asian | 0.0011% | 91,088 |
Finnish shows a higher raw frequency than the grpmax group above it. gnomAD excludes bottlenecked groups — Finnish, Ashkenazi Jewish, Amish and “Remaining individuals” — from grpmax, because founder effects make their frequencies unrepresentative for filtering. The table is sorted by frequency, so an excluded group can sit above the grpmax row.
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.Asp406=
- Coding
- c.1218C>T
- MANE Select
- NM_000283
- dbSNP
- rs148190219
- Type
- single nucleotide variant
- Location
- chr4:656984 (GRCh38)
- Gene constraint
- LOEUF 1.238 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 89.72
- Residue 406
- the gaf 2 domain
Disease context
retinitis pigmentosa — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatmentsAlso linked: congenital stationary night blindness autosomal dominant 2
For Retinitis pigmentosa (Orphanet):
- Inheritance
- Autosomal dominant, Autosomal recessive, Mitochondrial inheritance
- Onset
- Adolescent, Adult, Childhood
- Prevalence
- 1-5 / 10 000 (Europe)
Similar variants
- PDE6B c.1060-1G>T Pathogenic/Likely pathogenic ★★ same condition
- PDE6B c.1107+3A>G Pathogenic/Likely pathogenic ★★ same condition
- PDE6B c.1832+1G>T Pathogenic ★★ same condition
- PDE6B c.1921-9C>G Pathogenic ★★ same condition
- PDE6B c.2021+2T>G Pathogenic/Likely pathogenic ★★ same condition
- PDE6B c.2193+1G>A Pathogenic ★★ same condition
- PDE6B p.Arg560Cys Pathogenic/Likely pathogenic ★★ same condition
- PDE6B p.Asp600Asn Pathogenic/Likely 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/pde6b-p-asp406 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown