DCAF4 p.Pro51=
c.153G>A · VCV4009602
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
rare (popmax 0.263%, mid)
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 -4.5 | GERP -5.2 |
| Overall | ||
| CADD | 1.147 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.263%
Middle Eastern · 16/6,080 alleles
Filtering AF
0.165%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 0.134%
Overall
0.00261%
42/1,611,948 alleles · rare
exomes 29/1,459,726 · genomes 13/152,222 · joint denominator
| Ancestry group | Frequency | 1 in |
|---|---|---|
| Middle Easterngrpmax | 0.263% | 380 |
| African / African-American | 0.02% | 4,992 |
| Admixed American | 0.00167% | 59,818 |
| European (non-Finnish) | 0.000848% | 117,914 |
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
- DCAF4
- Protein
- p.Pro51=
- Coding
- c.153G>A
- MANE Select
- NM_015604
- Type
- single nucleotide variant
- Location
- chr14:72939862 (GRCh38)
- Gene constraint
- LOEUF 0.787 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 77.34 · 1 PDB
- Residue 51
- the 'disordered' region
Similar variants
- DCAF4 p.Ser28= Benign ★★ same type
- DCAF4 p.Ser325Gly Likely benign ★★ same type
- DCAF4 p.Ala125Val Uncertain significance ★ ⚠ same type
- DCAF4 p.Ala168Gly Uncertain significance ★ ⚠ same type
- DCAF4 p.Ala179Thr Uncertain significance ★ ⚠ same type
- DCAF4 p.Ala233Val Uncertain significance ★ ⚠ same type
- DCAF4 p.Ala285Ser Uncertain significance ★ ⚠ same type
- DCAF4 p.Ala461Thr 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/dcaf4-p-pro51 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown