WDR11 p.Pro1102=
c.3306T>G · VCV4909809
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
very rare (popmax 8.47e-05%, 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 -1.6 | GERP -0.39 |
| Overall | ||
| CADD | 3.537 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
8.47e-05%
European (non-Finnish) · 1/1,180,042 alleles
Overall
6.19e-05%
1/1,614,212 alleles · very rare
exomes 1/1,461,892 · genomes 0/152,320 · joint denominator
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
- WDR11
- Protein
- p.Pro1102=
- Coding
- c.3306T>G
- MANE Select
- NM_018117
- Type
- single nucleotide variant
- Location
- chr10:120905890 (GRCh38)
- Gene constraint
- LOEUF 0.617 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 83.75 · 4 PDB
- Residue 1102
- a turn; a UniProt-annotated variant site (in mrt78; no protein detected in homozygous patient cells)
Similar variants
- WDR11 p.Pro1102Ala Uncertain significance ★★ ⚠ same residue
- WDR11 p.Gln419Ter Pathogenic ★★ same type
- WDR11 p.Ala1076Thr Uncertain significance ★★ ⚠ same type
- WDR11 p.Ala1203Thr Uncertain significance ★★ ⚠ same type
- WDR11 p.Ala26Thr Uncertain significance ★★ ⚠ same type
- WDR11 p.Ala954Val Uncertain significance ★★ ⚠ same type
- WDR11 p.Ala974Val Uncertain significance ★★ ⚠ same type
- WDR11 p.Arg1185Trp Uncertain significance ★★ ⚠ 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/wdr11-p-pro1102 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown