CEP104 p.Thr186=
c.558G>A · rs2275822 · VCV1170110
Benign
Multiple submitters
Classification
Benign
ClinVar
Review
Multiple submitters ★★☆☆
ClinVar · 6 submitters
gnomAD v4.1
Common
common (popmax 44.2%, amr) — too common for a highly-penetrant pathogenic allele
Conditions
1
Joubert syndrome 25
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 | GERP -3.4 |
| Overall | ||
| CADD | 0.217 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
44.2%
Admixed American · 26,527/59,954 alleles
Filtering AF
43.9%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 43.9%
Overall
41.4%
666,543/1,610,982 alleles · common
| Ancestry group | Frequency | 1 in |
|---|---|---|
| Admixed Americangrpmax | 44.2% | 2 |
| European (non-Finnish) | 44% | 2 |
| Amishnot grpmax-eligible | 43.3% | 2 |
| Remaining individualsnot grpmax-eligible | 39.3% | 3 |
| East Asian | 37.5% | 3 |
| Middle Eastern | 34.6% | 3 |
| Ashkenazi Jewishnot grpmax-eligible | 34% | 3 |
| Finnishnot grpmax-eligible | 33.8% | 3 |
| South Asian | 30.7% | 3 |
| African / African-American | 24.6% | 4 |
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
- CEP104
- Protein
- p.Thr186=
- Coding
- c.558G>A
- MANE Select
- NM_014704
- dbSNP
- rs2275822
- Type
- single nucleotide variant
- Location
- chr1:3844915 (GRCh38)
- Gene constraint
- LOEUF 0.851 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 76.75 · 2 PDB
Similar variants
- CEP104 p.Arg299Ter Pathogenic/Likely pathogenic ★★ same condition
- CEP104 p.Arg55Ter Pathogenic/Likely pathogenic ★★ same condition
- CEP104 p.Glu627Ter Pathogenic/Likely pathogenic ★★ same condition
- CEP104 p.Lys270Ter Pathogenic/Likely pathogenic ★★ same condition
- CEP104 p.Tyr253Ter Pathogenic/Likely pathogenic ★★ same condition
- CEP104 c.1120-5T>A Uncertain significance ★★ same condition
- CEP104 p.Ala269Thr Uncertain significance ★★ ⚠ same condition
- CEP104 p.Ala28Val Uncertain significance ★★ ⚠ 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/cep104-p-thr186 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown