Is CUL4B p.Pro191= (c.573A>G) pathogenic?

CUL4B p.Pro191= (c.573A>G) is classified Likely benign in CUL4B (ClinVar, Single submitter, 1 submitter; last evaluated 2023-08-02). Very rare (popmax 0.00487%, nfe); Associated with X-linked intellectual disability, Cabezas type.

What condition is associated with CUL4B p.Pro191= (c.573A>G)?

CUL4B p.Pro191= (c.573A>G) is associated with X-linked intellectual disability, Cabezas type (ClinVar).

How common is CUL4B p.Pro191= (c.573A>G) in the general population?

CUL4B p.Pro191= (c.573A>G) is very rare (popmax 0.00487%, nfe) (gnomAD).

CUL4B p.Pro191=

c.573A>G · rs776364726 · VCV2739968

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Rare

very rare (popmax 0.00487%, nfe)

Conditions

X-linked intellectual disability, Cabezas type

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 -0.41	GERP -0.86, phastCons 0.21
Overall
CADD	11.14	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.00487% European (non-Finnish) · 43/883,091 alleles

Filtering AF 0.00367% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00326%

Overall 0.00385% 46/1,195,646 alleles · very rare

Ancestry group	Frequency	1 in
European (non-Finnish)grpmax	0.00487%	20,537
South Asian	0.00354%	28,225
Remaining individualsnot grpmax-eligible	0.00212%	47,123

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: CUL4B
Protein: p.Pro191=
Coding: c.573A>G
MANE Select: NM_001079872
dbSNP: rs776364726
Type: single nucleotide variant
Location: chrX:120558023 (GRCh38)
Structure: AlphaFold pLDDT 80.02 · 5 PDB

Full CUL4B gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

X-linked intellectual disability, Cabezas type — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

CUL4B p.Arg351Ter Likely pathogenic ★★ same condition
CUL4B p.Arg370Ter Pathogenic ★★ same condition
CUL4B p.Gln241Ter Pathogenic ★★ same condition
CUL4B p.Thr813= Pathogenic/Likely pathogenic ★★ same condition
CUL4B c.2592+3A>T Uncertain significance ★★ same condition
CUL4B c.777-3C>T Uncertain significance ★★ same condition
CUL4B p.Ala16Pro Uncertain significance ★★ ⚠ same condition
CUL4B p.Cys712Arg 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/cul4b-p-pro191 (accessed [today's date]).

Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown